Concentrations and (delta)13C values of atmospheric CO2 from oceanic atmosphere through time: polluted and non-polluted areas

International Nuclear Information System (INIS)

Longinelli, Antonio; Selmo, Enrico; Lenaz, Renzo; Ori, Carlo

2005-01-01

CO 2 is one of the primary agents of global climate changes. The increase of atmospheric CO 2 concentration is essentially related to human-induced emissions and, particularly, to the burning of fossil fuel whose (delta) 13 C values are quite negative. Consequently, an increase of the CO 2 concentration in the atmosphere should be paralleled by a decrease of its (delta) 13 C. Continuous and/or spot measurements of CO 2 concentrations were repeatedly carried out during the last decade and in the same period of the year along hemispheric courses from Italy to Antarctica on a vessel of the Italian National Research Program in Antarctica. During these expeditions, discrete air samples were also collected in 4-l Pyrex flasks in order to carry out precise carbon isotope analyses on atmospheric CO 2 from different areas, including theoretically 'clean' open ocean areas, with the main purpose of comparing these open ocean results with the results obtained by the National Oceanic and Atmospheric Administration/World Meteorological Organization (NOAA/WMO) at land-based stations. According to the data obtained for these two variables, a relatively large atmospheric pollution is apparent in the Mediterranean area where the CO 2 concentration has reached the value of 384 ppmv while quite negative (delta) 13 C values have been measured only occasionally. In this area, southerly winds probably help to reduce the effect of atmospheric pollution even though, despite a large variability of CO 2 concentrations, these values are consistently higher than those measured in open ocean areas by a few ppmv to about 10 ppmv. A marked, though non-continuous, pollution is apparent in the area of the Bab-el-Mandeb strait where (delta) 13 C values considerably more negative than in the Central and Southern Red Sea were measured. The concentration of atmospheric CO 2 over the Central Indian Ocean increased from about 361 ppmv at the end of 1996 to about 373 ppmv at the end of 2003 (mean growth

Rising atmospheric CO2 concentration may imply higher risk of Fusarium mycotoxin contamination of wheat grains.

Science.gov (United States)

Bencze, Szilvia; Puskás, Katalin; Vida, Gyula; Karsai, Ildikó; Balla, Krisztina; Komáromi, Judit; Veisz, Ottó

2017-08-01

Increasing atmospheric CO 2 concentration not only has a direct impact on plants but also affects plant-pathogen interactions. Due to economic and health-related problems, special concern was given thus in the present work to the effect of elevated CO 2 (750 μmol mol -1 ) level on the Fusarium culmorum infection and mycotoxin contamination of wheat. Despite the fact that disease severity was found to be not or little affected by elevated CO 2 in most varieties, as the spread of Fusarium increased only in one variety, spike grain number and/or grain weight decreased significantly at elevated CO 2 in all the varieties, indicating that Fusarium infection generally had a more dramatic impact on the grain yield at elevated CO 2 than at the ambient level. Likewise, grain deoxynivalenol (DON) content was usually considerably higher at elevated CO 2 than at the ambient level in the single-floret inoculation treatment, suggesting that the toxin content is not in direct relation to the level of Fusarium infection. In the whole-spike inoculation, DON production did not change, decreased or increased depending on the variety × experiment interaction. Cooler (18 °C) conditions delayed rachis penetration while 20 °C maximum temperature caused striking increases in the mycotoxin contents, resulting in extremely high DON values and also in a dramatic triggering of the grain zearalenone contamination at elevated CO 2 . The results indicate that future environmental conditions, such as rising CO 2 levels, may increase the threat of grain mycotoxin contamination.

Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant

Energy Technology Data Exchange (ETDEWEB)

Akata, Naofumi, E-mail: nao@ies.or.jp [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan); Kakiuchi, Hideki [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan); Shima, Nagayoshi [Entex Inc., 1-2-8 Asahi, Kashiwa, Chiba 277-0852 (Japan); Iyogi, Takashi [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan); Momoshima, Noriyuki [Radioisotope Center, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581 (Japan); Hisamatsu, Shun' ichi [Department of Radioecology, Institute for Environmental Sciences, 1-7 Ienomae, Obuchi, Rokkasho, Aomori 039-3212 (Japan)

2011-09-15

This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH{sub 3}T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH{sub 3}T concentrations. The HT and CH{sub 3}T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Ostlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH{sub 3}T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH{sub 4} to estimate global warming in its 2007 report. The longer environmental half-life of CH{sub 3}T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. - Highlights: > We observed background tritium concentrations in atmospheric environment at Rokkasho, Japan. > Tritium concentration in precipitation was high in spring and low in summer. > The

Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant

International Nuclear Information System (INIS)

Akata, Naofumi; Kakiuchi, Hideki; Shima, Nagayoshi; Iyogi, Takashi; Momoshima, Noriyuki; Hisamatsu, Shun'ichi

2011-01-01

This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH 3 T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH 3 T concentrations. The HT and CH 3 T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Ostlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH 3 T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH 4 to estimate global warming in its 2007 report. The longer environmental half-life of CH 3 T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. - Highlights: → We observed background tritium concentrations in atmospheric environment at Rokkasho, Japan. → Tritium concentration in precipitation was high in spring and low in summer. → The atmospheric HT

Concentration of elements in atmospheric aerosol in Bratislava

International Nuclear Information System (INIS)

Meresova, J.; Florek, M.; Holy, K.; Sykora, I.; Frontasyeva, M.V.; Pavlov, S.S.

2006-01-01

The concentrations of 41 chemical elements (heavy metals, rare earths, and actinides) were determined in atmospheric aerosol using nuclear and related analytical techniques. The sampling location in Bratislava (Slovak Republic). The main goal of this study is the quantification of the atmospheric pollution and its trend. The elemental content in filters was measured using instrumental neutron activation analysis at IBR-2 reactor in JINR Dubna and by atomic absorption spectrometry in Bratislava. The obtained results confirm the decreasing trend of pollution by most of the heavy metals in Bratislava atmosphere, and they are compared with the contents of pollutants in atmosphere of other cities. We determined also the composition of clear filter materials. (Authors)

Variation of atmospheric 210Pb concentration in the inland area of Chinese continent

International Nuclear Information System (INIS)

Doi, Taeko; Sato, Jun.

1995-01-01

Atmospheric concentrations of 210 Pb and their variations over Urumqi, Lanzhou and Baotou, cities located in inland area of Chinese continent, were observed for a period of 1 year in 1992. The monthly average concentrations ranged from 0.27 to 4.57 mBq/m 3 . The concentrations over these cities in winter were several times higher than that observed at Tsukuba Science City, Japan, and the range of variation was also larger. The variations in concentration over the 3 localities were similar to each other, showing the same seasonal variation pattern: low concentration appeared in summer and high in winter. This variation pattern was different from that observed at Tsukuba Science City. The variations in concentration over Chinese continent, where precipitation is much lower than that in Japan, correlated quite well with the variation in precipitation. (author)

Monitoring of mercury concentration in atmosphere in Usti nad Labem

International Nuclear Information System (INIS)

Synek, V.; Baloch, T.; Otcenasek, J.; Kremlova, S.; Subrt, P.

2007-01-01

This study elaborates the observation of mercury pollution of the atmosphere in the city of Usti nad Labem. The biggest source of the polluting mercury in Usti nad Labem is the chlor-alkali production in the factory of Spolchemie Inc. The method of mercury determination applied is based on capturing the mercury contented in a volume of the air on an amalgamator and measuring the mercury by an atomic absorption spectrometer (Perkin -Elmer 4100ZL) equipped with a special adapter after a thermal release of the mercury from the amalgamator. The basic characteristics of this method were evaluated; e.g. the limit of detection and limit of determination are, respectively, 0.43 and 1.4 ng/m 3 , the relative expanded uncertainty is 28 %. The work gives results of long-term (1998-2006) observations in a few localities in Usti nad Labem situated in various distances from the mercury source (e.g. means of 28.6 and 14.1 ng/m3 were obtained, respectively, in places 350 and 700 m far from the electrolysis plant) and also in a different city (Duchcov). The cases with a higher mercury concentration are very frequent so the sets of the obtained results have lognormal distributions. This study statistically compares the total level and variability of the mercury concentrations in the time series. It also investigates their trends, correlations between them and meteorological influences upon the levels of mercury concentration in the air. The effect of the mercury emission from the chlor-alkali plant is dominant. It as the only factor determines when the cases with a high mercury concentration in the atmosphere occur. (author)

Relationship between carbon-14 concentrations in tree-ring cellulose and atmospheric CO2

International Nuclear Information System (INIS)

Yamada, Yoshimune; Yasuike, Kaeko; Komura, Kazuhisa

2008-01-01

Concentrations of organically-bound 14 C in the tree-ring cellulose of a Japanese Cedar (Cryptomeria japonica) grown in a rural region of Kanazawa, Ishikawa prefecture, Japan (36.5degN, 136.7degE), were measured for the ring-years from 1989 to 1998 to study relationship between 14 C concentrations in tree-ring cellulose and atmospheric CO 2 in a narrow region. An interesting result in comparing our data of tree-ring cellulose with those of atmospheric CO 2 is that the 14 C concentration in tree-ring cellulose was close to the corresponding average from mid-June to early September of 14 C concentrations in atmospheric CO 2 . Furthermore, the 14 C concentrations in tree-ring cellulose were found to be merely influenced by the drastic decrease of 14 C concentrations in atmospheric CO 2 in winter, which might be caused by air pollution from the Asian continent and additional local fossil fuel contribution. These results suggest that the 14 C concentration in tree-ring cellulose for a given growing year reflects the 14 C concentrations of atmospheric CO 2 during the warm summer months. (author)

Influence of ship emission on atmospheric pollutant concentration around Osaka Bay, Japan

International Nuclear Information System (INIS)

Kondo, A.; Yamaguchi, K.; Nishikawa, E.

1999-01-01

Marine traffic in Osaka Bay is very intensified and much atmosphere pollutant (SO x and NO x ) from ships is released but there is no regulation about the ship emission. In this paper, we investigated the emission amounts of SO x NO x and HC from car, factory and ships in Osaka bay area and estimated the influence of the ship emission on the atmospheric pollutant concentration, using both the meteorological prediction model and the atmospheric pollutant concentration prediction model including the dry deposition and the chemical reaction. In Osaka bay area, the emission amounts of SO x and NO x from ships were about 30% of the total emission amounts, respectively. Using these emission data, the atmospheric pollutant concentration was simulated on a summer fine day when high oxidant concentration was measured at several observatories and was compared with the observed data. Though some differences were seen between the simulated results and the observed data, the diurnal variation agreed reasonably. The second simulation was carried out except for the ship emission and we estimated the influence of the ship emission on the atmospheric pollutant concentration. It was found that the ship emission raised SO 2 , NO 2 and NO concentration not only in shore area but also in 40km inland. (Author)

The determinants of atmospheric SO2 concentrations. Reconsidering the environmental Kuznets curve

International Nuclear Information System (INIS)

Kaufmann, Robert K.; Davidsdottir, Brynhildur; Garnham, Sophie; Pauly, Peter

1998-01-01

This analysis explores the effects of income and the spatial intensity of economic activity on the atmospheric concentration of sulfur dioxide. The results indicate that there is a U-shaped relation between income and atmospheric concentration of SO 2 and an inverted U-shaped relation between the spatial intensity of economic activity and SO 2 concentrations. These results suggest that the spatial intensity of economic activity, rather than income, provides the impetus for policies and technologies that reduce SO 2 emissions. Based on this result, the atmospheric concentration of SO 2 in developing nations may decline faster than indicated by previous analyses. The potential for this decline depends on the rate at which income grows relative to population. The trade-off between the effects of income gains and the spatial intensity of economic activity on the atmospheric concentration of SO 2 is consistent with the notion that environmental problems can be ameliorated by slowing population growth and increasing income levels

Seasonal trends in vegetation and atmospheric concentrations of PAHs and PBDEs near a sanitary landfill

Science.gov (United States)

St-Amand, Annick D.; Mayer, Paul M.; Blais, Jules M.

Spruce needle and atmospheric (gaseous and particulate-bound) concentrations were surveyed near a sanitary landfill from February 2004 to June 2005. The influence of several parameters such as temperature, relative humidity, wind speed and direction, as well as increased domestic heating during the winter was assessed. In general, polybrominated diphenyl ethers (PBDE) and polycyclic aromatic hydrocarbons (PAH) concentrations in spruce needles increased over time and decreased following snowmelt with a minimum coinciding with bud burst of deciduous trees. Atmospheric concentrations of PBDE and PAH, both particulate-bound and gaseous phase, were linked to daily weather events and thus showed more variability than those in spruce needles. Highest PAH concentrations were encountered during the winter, likely reflecting increased emission from heating homes. Pseudo Clausius-Clapeyron plots revealed higher PBDE gaseous concentrations with increasing temperature, but showed no correlation between PAH gaseous concentrations and temperature as this effect was obscured by seasonal emission patterns. Finally, air mass back trajectories and local wind directions revealed that particulate-bound PBDEs, along with both gaseous and particulate-bound PAHs were from local sources, whereas gaseous PBDEs were likely from distant sources.

Comparison of atmosphere/aquatic environment concentration ratio of volatile chlorinated hydrocarbons between temperate regions and Antarctica.

Science.gov (United States)

Zoccolillo, Lelio; Amendola, Luca; Insogna, Susanna

2009-09-01

For the purpose of understanding the transport and deposition mechanisms and the air-water distribution of some volatile chlorinated hydrocarbons (VCHCs), their atmosphere/aquatic environment concentration ratio was evaluated. In addition, for the purpose of differentiating VCHC behaviour in a temperate climate from its behaviour in a polar climate, the atmosphere/aquatic environment concentration ratio evaluated in matrices from temperate zones was compared with the concentration ratio evaluated in Antarctic matrices. In order to perform air samplings also at rigid Antarctic temperatures, the sampling apparatus, consisting of a diaphragm pump and canisters, was suitably modified. Chloroform, 1,1,1-trichloroethane, tetrachloromethane, 1,1,2-trichloroethylene and tetrachloroethylene were measured in air, water and snow using specific techniques composed of a purpose-made cryofocusing-trap-injector (for air samples) and a modified purge-and-trap injector (for aqueous samples) coupled to a gas chromatograph with mass spectrometric detection operating in selected ion monitoring mode. The VCHCs were retrieved in all the investigated matrices, both Italian and Antarctic, with concentrations varying from tens to thousands of ng m(-3) in air and from digits to hundreds of ng kg(-1) in water and snow. The atmosphere/aquatic environment concentration ratios were always found to be lower than 1. In particular, the Italian air/water concentration ratios were smaller than the Antarctic ones, by reason of the higher atmospheric photochemical activity in temperate zones. On the other hand, the Antarctic air/snow concentration ratios proved to be largely in favour of snow with respect to the Italian ratios, thus corroborating the hypothesis of a more efficient VCHC deposition mechanism and accumulation on Antarctic snow.

Effectiveness of Emission Controls to Reduce the Atmospheric Concentrations of Mercury.

Science.gov (United States)

Castro, Mark S; Sherwell, John

2015-12-15

Coal-fired power plants in the United States are required to reduce their emissions of mercury (Hg) into the atmosphere to lower the exposure of Hg to humans. The effectiveness of power-plant emission controls on the atmospheric concentrations of Hg in the United States is largely unknown because there are few long-term high-quality atmospheric Hg data sets. Here, we present the atmospheric concentrations of Hg and sulfur dioxide (SO2) measured from 2006 to 2015 at a relatively pristine location in western Maryland that is several (>50 km) kilometers downwind of power plants in Ohio, Pennsylvania, and West Virginia. Annual average atmospheric concentrations of gaseous oxidized mercury (GOM), SO2, fine particulate mercury (PBM2.5), and gaseous elemental mercury (GEM) declined by 75%, 75%, 43%, and 13%, respectively, and were strongly correlated with power-plant Hg emissions from the upwind states. These results provide compelling evidence that reductions in Hg emissions from power plants in the United States had their intended impact to reduce regional Hg pollution.

Seasonal variation in diurnal atmospheric grass pollen concentration profiles

DEFF Research Database (Denmark)

Peel, Robert George; Ørby, Pia Viuf; Skjøth, Carsten Ambelas

2014-01-01

the time of day when peak concentrations are most likely to occur using seasonally averaged diurnal profiles. Atmospheric pollen loads are highly dependent upon emissions, and different species of grass are known to flower and emit pollen at different times of the day and during different periods......In this study, the diurnal atmospheric grass pollen concentration profile within the Danish city of Aarhus was shown to change in a systematic manner as the pollen season progressed. Although diurnal grass pollen profiles can differ greatly from day-to-day, it is common practice to establish...... of the pollen season. Pollen concentrations are also influenced by meteorological factors - directly through those parameters that govern pollen dispersion and transport, and indirectly through the weather-driven flowering process. We found that three different profiles dominated the grass pollen season...

A 40-year record of Northern Hemisphere atmospheric carbon monoxide concentration and isotope ratios from the firn at Greenland Summit.

Science.gov (United States)

Place, P., Jr.; Petrenko, V. V.; Vimont, I.; Buizert, C.; Lang, P. M.; Edwards, J.; Harth, C. M.; Hmiel, B.; Mak, J. E.; Novelli, P. C.; Brook, E.; Weiss, R. F.; Vaughn, B. H.; White, J. W. C.

2014-12-01

Carbon Monoxide (CO) is an important atmospheric trace gas that affects the oxidative capacity of the atmosphere and contributes indirectly to climate forcing by being a major sink of tropospheric OH. A good understanding of the past atmospheric CO budget is therefore important for climate models attempting to characterize recent changes in the atmosphere. Previous work at NEEM, Greenland provided the first reconstructions of Arctic atmospheric history of CO concentration and stable isotope ratios (δC18O and δ13CO) from firn air, dating to the 1950s. In this new study, firn air was sampled from eighteen depth levels through the firn column at Summit, Greenland (in May 2013), yielding a second, independent record of Arctic CO concentration and isotopic ratios. Carbon monoxide stable isotope ratios were analyzed on replicate samples and using a newly developed system with improved precision allowing for a more robust reconstruction. The new CO concentration and stable isotope results overall confirm the earlier findings from NEEM, with a CO concentration peak around the 1970s and higher δC18O and δ13CO values associated with peak CO. Modeling and interpretation of the data are in progress.

Ionization rates and profiles of electron concentration in Martian atmosphere

International Nuclear Information System (INIS)

Komitov, B.; Spasov, S.; Gogoshev, M.

1981-01-01

The ionization and vertical profiles of electron concentration in the Martian atmosphere are calculated as functions of the solar zenith angles varying from O deg to 90 deg. A neutral atmospheric model based on direct mass-spectometric measurements from the Viking-1 landing modul is employed in the calculation. The Earth data of the ionization solar flux at the same level of the solar activity and for the month of the Viking-1 measurements reduced for the Mars orbit are used. The numerical result for the photoionization rates and quasi-equilibrium electron-concentration profiles in the upper Martian atmosphere at different solar zenith angles from 0 deg to 100 deg are presented. It is shown that the maxima of both quantities decrease and move towards the upper atmosphere regions. The calculated electron density at the zenith solar angle of 40 deg are compared to Viking-1 experimental data and a good agreement is achieved

Elevated atmospheric carbon dioxide concentrations promote ant tending of aphids.

Science.gov (United States)

Kremer, Jenni M M; Nooten, Sabine S; Cook, James M; Ryalls, James M W; Barton, Craig V M; Johnson, Scott N

2018-04-27

Animal mutualisms, which involve beneficial interactions between individuals of different species, are common in nature. Insect-insect mutualism, for example, is widely regarded as a keystone ecological interaction. Some mutualisms are anticipated to be modified by climate change, but the focus has largely been on plant-microbe and plant-animal mutualisms rather than those between animals. Ant-aphid mutualisms, whereby ants tend aphids to harvest their honeydew excretions and, in return, provide protection for the aphids, are widespread. The mutualism is heavily influenced by the quality and quantity of honeydew produced by aphids, which is directly affected by host plant quality. As predicted increases in concentrations of atmospheric carbon dioxide (eCO 2 ) are widely reported to affect plant nutritional chemistry, this may also alter honeydew quality and hence the nature of ant-aphid mutualisms. Using glasshouse chambers and field-based open-top chambers, we determined the effect of eCO 2 on the growth and nutritional quality (foliar amino acids) of lucerne (Medicago sativa). We determined how cowpea aphid (Aphis craccivora) populations and honeydew production were impacted when feeding on such plants and how this affected the tending behaviour of ants (Iridomyrmex sp.). eCO 2 stimulated plant growth but decreased concentrations of foliar amino acids by 29% and 14% on aphid-infested plants and aphid-free plants, respectively. Despite the deterioration in host plant quality under eCO 2 , aphids maintained performance and populations were unchanged by eCO 2 . Aphids induced higher concentrations of amino acids (glutamine, asparagine, glutamic acid and aspartic acid) important for endosymbiont-mediated synthesis of essential amino acids. Aphids feeding under eCO 2 also produced over three times more honeydew than aphids feeding under ambient CO 2 , suggesting they were imbibing more phloem sap at eCO 2 . The frequency of ant tending of aphids more than doubled in

Factors controlling temporal variability of near-ground atmospheric 222Rn concentration over central Europe

Science.gov (United States)

Zimnoch, M.; Wach, P.; Chmura, L.; Gorczyca, Z.; Rozanski, K.; Godlowska, J.; Mazur, J.; Kozak, K.; Jeričević, A.

2014-09-01

Concentration of radon (222Rn) in the near-ground atmosphere has been measured quasi-continuously from January 2005 to December 2009 at two continental sites in Europe: Heidelberg (south-west Germany) and Krakow (southern Poland). The atmosphere was sampled at ca. 30 and 20 m above the local ground. Both stations were equipped with identical instruments. Regular observations of 222Rn were supplemented by measurements of surface fluxes of this gas in the Krakow urban area, using two different approaches. The measured concentrations of 222Rn varied at both sites in a wide range, from less than 2.0 Bq m-3 to approximately 40 Bq m-3 in Krakow and 35 Bq m-3 in Heidelberg. The mean 222Rn content in Krakow, when averaged over the entire observation period, was 30% higher than in Heidelberg (5.86 ± 0.09 and 4.50 ± 0.07 Bq m-3, respectively). Distinct seasonality of 222Rn signal is visible in the obtained time series of 222Rn concentration, with higher values recorded generally during late summer and autumn. The surface 222Rn fluxes measured in Krakow also revealed a distinct seasonality, with broad maximum observed during summer and early autumn and minimum during the winter. When averaged over a 5-year observation period, the night-time surface 222Rn flux was equal to 46.8 ± 2.4 Bq m-2 h-1. Although the atmospheric 222Rn levels at Heidelberg and Krakow appeared to be controlled primarily by local factors, it was possible to evaluate the "continental effect" in atmospheric 222Rn content between both sites, related to gradual build-up of 222Rn concentration in the air masses travelling between Heidelberg and Krakow. The mean value of this build-up was equal to 0.78 ± 0.12 Bq m-3. The measured minimum 222Rn concentrations at both sites and the difference between them was interpreted in the framework of a simple box model coupled with HYSPLIT (Hybrid Single Particle Lagrangian Integrated Trajectory) analysis of air mass trajectories. The best fit of experimental data was

Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant.

Science.gov (United States)

Akata, Naofumi; Kakiuchi, Hideki; Shima, Nagayoshi; Iyogi, Takashi; Momoshima, Noriyuki; Hisamatsu, Shun'ichi

2011-09-01

This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH(3)T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH(3)T concentrations. The HT and CH(3)T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Östlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH(3)T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH(4) to estimate global warming in its 2007 report. The longer environmental half-life of CH(3)T suggested its supply from other sources than past nuclear weapon testing in the atmosphere. Copyright © 2011 Elsevier Ltd. All rights reserved.

Control methods of radon and its progeny concentration in indoor atmosphere

International Nuclear Information System (INIS)

Ramachandran, T.V.; Subba Ramu, M.C.

1990-01-01

Exposure to radon-222 and its progeny in indoor atmosphere can result in significant inhalation risk to the population particularly to those living in houses with much higher levels of Rn. There are three methods generally used for the control of Rn and its progeny concentration in the indoor environment: (1) restricting the radon entry, (2) reduction of indoor radon concentration by ventilation or by aircleaning and (3) removal of airborne radon progeny by aerosol reduction. Prominent process of radon entry in most of the residence appears to be the pressure driven flow of soil gas through cracks or through other openings in the basements slab or subfloor. Sealing off these openings or ventilation of the slab or subfloor spaces are the methods of reducing the radon entry rate. Indoor radon progeny levels can also be reduced by decreasing the aerosol load in the dwellings. The results of a few experiments carried out to study the reduction in the working level concentration of radon, by decreasing the aerosol load are discussed in this paper. (author). 9 tabs., 8 figs., 37 refs

Effect of light and atmosphere on the cultivation of the golden oyster culinary-medicinal mushroom, Pleurotus citrinopileatus (higher Basidiomycetes).

Science.gov (United States)

Hu, Shu-Hui; Wu, Chiu-Yeh; Chen, Yu-Kuei; Wang, Jinn-Chyi; Chang, Sue-Joan

2013-01-01

With an aim to explore the productivity and quality of the fruiting body of culinary-medicinal golden oyster mushroom Pleurotus citrinopileatus, the carbon dioxide (CO₂) concentration of the ambient atmosphere was adjusted and a light-emitting diode panel was used to illuminate the colonized mycelium at different wavelengths. Biological efficiency and yield were higher at CO₂ levels of 0.05 and 0.1% than other tested CO₂ levels, and the mature fruiting body showed the highest yellow value at a CO₂ level of 0.1% (of all tested CO₂ levels). The highest biological efficiency and yield was obtained at the 720-nm wavelength. The ergosterol content of the pileus of the fruiting body was higher than that of the stipe in any flush time at a 720-nm wavelength of light and a CO₂ concentration of 0.1%. The decreased percentages of cellulose and lignin at the appearance of primordia were larger than those of mycelial growth duration. The fruiting quality of P. citrinopileatus might thus be enhanced by 720-nm illumination and an atmosphere with a CO₂ concentration of 0.1 to 0.15%.

Global atmospheric concentrations and source strength of ethane

Science.gov (United States)

Blake, D. R.; Rowland, F. S.

1986-01-01

A study of the variation in ethane (C2H6) concentration between northern and southern latitudes over three years is presented together with a new estimate of its source strength. Ethane concentrations vary from 0.07 to 2 p.p.b.v. (parts per billion by volume) in air samples collected in remote surface locations in the Pacific (latitude 71 N-47 S) in all four seasons between September 1984 and June 1985. The variations are consistent with southerly transport from sources located chiefly in the Northern Hemisphere, further modified by seasonal variations in the strength of the reaction of C2H6 with OH radicals. These global data can be combined with concurrent data for CH4 and the laboratory reaction rates of each with OH to provide an estimate of three months as the average atmospheric lifetime for C2H6 and 13 + or - 3 Mtons for its annual atmospheric release.

Exchange of carbonyl sulfide (OCS) between soils and atmosphere under various CO2 concentrations

Science.gov (United States)

Bunk, Rüdiger; Behrendt, Thomas; Yi, Zhigang; Andreae, Meinrat O.; Kesselmeier, Jürgen

2017-06-01

A new continuous integrated cavity output spectroscopy analyzer and an automated soil chamber system were used to investigate the exchange processes of carbonyl sulfide (OCS) between soils and the atmosphere under laboratory conditions. The exchange patterns of OCS between soils and the atmosphere were found to be highly dependent on soil moisture and ambient CO2 concentration. With increasing soil moisture, OCS exchange ranged from emission under dry conditions to an uptake within an optimum moisture range, followed again by emission at high soil moisture. Elevated CO2 was found to have a significant impact on the exchange rate and direction as tested with several soils. There is a clear tendency toward a release of OCS at higher CO2 levels (up to 7600 ppm), which are typical for the upper few centimeters within soils. At high soil moisture, the release of OCS increased sharply. Measurements after chloroform vapor application show that there is a biotic component to the observed OCS exchange. Furthermore, soil treatment with the fungi inhibitor nystatin showed that fungi might be the dominant OCS consumers in the soils we examined. We discuss the influence of soil moisture and elevated CO2 on the OCS exchange as a change in the activity of microbial communities. Physical factors such as diffusivity that are governed by soil moisture also play a role. Comparing KM values of the enzymes to projected soil water CO2 concentrations showed that competitive inhibition is unlikely for carbonic anhydrase and PEPCO but might occur for RubisCO at higher CO2 concentrations.

Atmospheric conditions during high ragweed pollen concentrations in Zagreb, Croatia

Science.gov (United States)

Prtenjak, Maja Telišman; Srnec, Lidija; Peternel, Renata; Madžarević, Valentina; Hrga, Ivana; Stjepanović, Barbara

2012-11-01

We examined the atmospheric conditions favourable to the occurrence of maximum concentrations of ragweed pollen with an extremely high risk of producing allergy. Over the 2002-2009 period, daily pollen data collected in Zagreb were used to identify two periods of high pollen concentration (> 600 grains/m3) for our analysis: period A (3-4 September 2002) and period B (6-7 September 2003). Synoptic conditions in both periods were very similar: Croatia was under the influence of a lower sector high pressure system moving slowly eastward over Eastern Europe. During the 2002-2009 period, this type of weather pattern (on ~ 70% of days), in conjunction with almost non-gradient surface pressure conditions in the area (on ~ 30% of days) characterised days when the daily pollen concentrations were higher than 400 grains/m3. Numerical experiments using a mesoscale model at fine resolution showed successful multi-day simulations reproducing the local topographic influence on wind flow and in reasonable agreement with available observations. According to the model, the relatively weak synoptic flow (predominantly from the eastern direction) allowed local thermal circulations to develop over Zagreb during both high pollen episodes. Two-hour pollen concentrations and 48-h back-trajectories indicated that regional-range transport of pollen grains from the central Pannonian Plain was the cause of the high pollen concentrations during period A. During period B, the north-westward regional-range transport in Zagreb was supplemented significantly by pronounced horizontal recirculation of pollen grains. This recirculation happened within the diurnal local circulation over the city, causing a late-evening increase in pollen concentration.

Control of radon and its progeny concentration in indoor atmosphere

International Nuclear Information System (INIS)

Ramachandran, T.V.; Subbaramu, M.C.

1986-01-01

Exposure to radon daughter concentration in indoor atmosphere can result in a significant risk to the general public. There are two generally used methods for the control of radon and progeny concentration in the indoor atmosphere, namely restriction of radon entry and reduction of indoor radon and its progeny concentration by ventilation or by air cleaning. Predominant radon entry process in most of the dwellings appears to be by pressure driven flow of soil gas through cracks or other openings in the basement slab or subfloors. Sealing these openings or ventilation of the subslab or subfloor space are the methods for reducing the radon entry rates. Indoor radon concentration can also be reduced by increasing the ventilation and by using charcoal filters for the removal of radon gas in indoor air by absorption. Concentration of radon progeny, which are responsible for most of the health risks associatd with radon exposure can also be controlled by the use of electrostatic or mechanical filters. This study describes briefly the above control strategies used for reducing the inhalation doses to persons in dwellings. (author). 9 refs., 2 tables

Determination of atmospheric concentrations of xenon radioisotopes. Progress report

International Nuclear Information System (INIS)

Abel, K.H.; Panisko, M.E.; Hensley, W.K.; Bowyer, T.W.; Perkins, R.W.

1995-07-01

Determination of radioactive xenon concentrations in the atmosphere over a two year period has been performed as part of a research program to develop real-time measurement capabilities. The initial measurements were made to develop, prove, and validate the authors technical approach, while the longer-term measurements are being undertaken to establish natural background concentrations and variability with time. The results reported were made using noble gas fraction (typically 90% Kr and 10% Xe by weight) gas samples obtained from a commercial air-reduction plant in the northeastern US over a two-year interval beginning in the fall of 1993. The concentrated gas samples were typically obtained during a 6--8 hour interval at the commercial reduction plant and were shipped overnight to their laboratory. Analysis was typically completed approximately 24 hours after sampling. The analytical separation process typically took approximately 6 hours and gamma-ray spectrometric measurements were conducted for intervals ranging from 3 to 16 hours. The technical approach involved removal of potentially interfering radon daughter radionuclides using a molecular sieve at room temperature, followed by cryogenic concentration of noble gases using a chilled (-76 C) activated carbon molecular sieve. During initial measurements both molecular sieve materials were contained in 30 foot x 1/4 inch gas chromatography columns for analytical separations. Krypton was separated from Xenon during the analytical procedure by warming the activated carbon molecular sieve to room temperature after initial noble gas concentration and actively pumping it away. Xenon-133 adsorbed to the activated charcoal molecular sieve was then quantified via its 81 keV gamma-ray using initially a p-type intrinsic germanium detector and later a higher efficiency (64% relative to a 3 inch x 3 inch sodium iodide) n-type intrinsic germanium detector

HO2 measurements at atmospheric concentrations using a chemical ionization mass spectrometry

Science.gov (United States)

Albrecht, S.; Novelli, A.; Hofzumahaus, A.; Kang, S.; Baker, Y.; Mentel, T. F.; Fuchs, H.

2017-12-01

Correct and precise measurements of atmospheric radical species are necessary for a better understanding of the oxidative capacity of the atmosphere. Due to the reactivity of radicals, and their consequent low concentrations, direct measurements of these species are particularly challenging and have been proven in the past to be affected by interfering species. Here we present a chemical ionization source coupled to an APi-HR-TOF-MS (Aerodyne Research Inc.), which has a limit of detection for HO2 radicals well below its atmospheric concentrations ( 1 x 108 molecules cm-3). The instrument was calibrated with a well-established and characterized HO2 calibration source in use for the laser induced fluorescence instrument in the Forschungszentrum Jülich. Within the source, a well characterized amount of HO2 radicals is produced after photolysis of water by a mercury lamp. In addition, several experiments were performed in the atmosphere simulation chamber SAPHIR at the Forschungszentrum Jülich to test for potential interferences. Measurements of HO2 radicals were concurrently detected by a laser induced fluorescence instrument allowing for the comparison of measurements within the two different and independent techniques for various atmospheric conditions regarding concentrations of O3, NOx and VOCs. Results from the intercomparison together with the calibration procedure of the instrument and laboratory characterization will be presented.

Effect of wind speed and relative humidity on atmospheric dust concentrations in semi-arid climates.

Science.gov (United States)

Csavina, Janae; Field, Jason; Félix, Omar; Corral-Avitia, Alba Y; Sáez, A Eduardo; Betterton, Eric A

2014-07-15

Atmospheric particulate have deleterious impacts on human health. Predicting dust and aerosol emission and transport would be helpful to reduce harmful impacts but, despite numerous studies, prediction of dust events and contaminant transport in dust remains challenging. In this work, we show that relative humidity and wind speed are both determinants in atmospheric dust concentration. Observations of atmospheric dust concentrations in Green Valley, AZ, USA, and Juárez, Chihuahua, México, show that PM10 concentrations are not directly correlated with wind speed or relative humidity separately. However, selecting the data for high wind speeds (>4m/s at 10 m elevation), a definite trend is observed between dust concentration and relative humidity: dust concentration increases with relative humidity, reaching a maximum around 25% and it subsequently decreases with relative humidity. Models for dust storm forecasting may be improved by utilizing atmospheric humidity and wind speed as main drivers for dust generation and transport. Copyright © 2014 Elsevier B.V. All rights reserved.

Atmospheric concentrations and trends of poly- and perfluoroalkyl substances (PFAS) and volatile methyl siloxanes (VMS) over 7 years of sampling in the Global Atmospheric Passive Sampling (GAPS) network.

Science.gov (United States)

Rauert, Cassandra; Shoieb, Mahiba; Schuster, Jasmin K; Eng, Anita; Harner, Tom

2018-07-01

Poly- and per-fluoroalkyl substances (PFAS) and volatile methyl siloxanes (VMS) were monitored at 21 sites in the Global Atmospheric Passive Sampling (GAPS) Network. Atmospheric concentrations previously reported from 2009 were compared to concentrations measured at these sites in 2013 and 2015, to assess trends over 7 years of monitoring. Concentrations of the fluorotelomer alcohols (FTOHs) and fluorinated sulfonamides and sulfonamidoethanols (FOSAs and FOSEs) were stable at these sites from 2009 to 2015 with no significant difference (p > 0.05) in concentrations. Elevated concentrations of all the neutral PFAS were detected at the urban sites as compared to the polar/background sites. The perfluorosulfonic acids (PFSAs), meanwhile, saw a significant increase (p  0.05). Concentrations of the PFSAs and the PFCAs were similar at all location types, showing the global reach of these persistent compounds. Concentrations of the cyclic VMS (cVMS) were at least an order of magnitude higher than the linear VMS (lVMS) and the PFAS. Octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5) and dodecamethylcyclohexasiloxane (D6) saw a weak significant increase in concentrations from 2009 to 2013 (p < 0.05), however, hexamethylcyclotrisiloxane (D3) had a strong significant decrease in concentrations from 2009 to 2015 (p < 0.01). Copyright © 2018 The Authors. Published by Elsevier Ltd.. All rights reserved.

Tritium concentration reducing method in atmosphere in nuclear reactor containment facility

International Nuclear Information System (INIS)

Hirasawa, Yoshiya; Kigoshi, Yasutane; Yonenaga, Haruo.

1992-01-01

A portion of water content in an atmosphere is condensed by a condensation/evaporation device disposed in a nuclear reactor containment building and then a portion of the condensed water is evaporated in the atmosphere. A portion of hydrogen nuclides constituting the evaporated water content is subjected to isotopic exchange with tritium nuclides in the atmosphere. A portion of water content in the atmosphere applied with the isotopic exchange is condensed in the condensation/evaporation device. That is, the hydrogen nuclides in steams are applied with isotopic exchange with tritium nuclides, and steams incorporating tritium nuclides are condensed again in the condensation/evaporation device, to transfer the tritium nuclides in the atmosphere to condensed water. The condensed water is recovered without releasing the tritium nuclides to the outside of the reactor containment building, thereby enabling to reduce the tritium concentration in the atmosphere. (N.H.)

A revised method to calculate the concentration time integral of atmospheric pollutants

International Nuclear Information System (INIS)

Voelz, E.; Schultz, H.

1980-01-01

It is possible to calculate the spreading of a plume in the atmosphere under nonstationary and nonhomogeneous conditions by introducing the ''particle-in-cell'' method (PIC). This is a numerical method by which the transport of and the diffusion in the plume is reproduced in such a way, that particles representing the concentration are moved time step-wise in restricted regions (cells) and separately with the advection velocity and the diffusion velocity. This has a systematical advantage over the steady state Gaussian plume model usually used. The fixed-point concentration time integral is calculated directly instead of being substituted by the locally integrated concentration at a constant time as is done in the Gaussian model. In this way inaccuracies due to the above mentioned computational techniques may be avoided for short-time emissions, as may be seen by the fact that both integrals do not lead to the same results. Also the PIC method enables one to consider the height-dependent wind speed and its variations while the Gaussian model can be used only with averaged wind data. The concentration time integral calculated by the PIC method results in higher maximum values in shorter distances to the source. This is an effect often observed in measurements. (author)

Source contributions to atmospheric fine carbon particle concentrations

Science.gov (United States)

Andrew Gray, H.; Cass, Glen R.

A Lagrangian particle-in-cell air quality model has been developed that facilitates the study of source contributions to atmospheric fine elemental carbon and fine primary total carbon particle concentrations. Model performance was tested using spatially and temporally resolved emissions and air quality data gathered for this purpose in the Los Angeles area for the year 1982. It was shown that black elemental carbon (EC) particle concentrations in that city were dominated by emissions from diesel engines including both on-highway and off-highway applications. Fine primary total carbon particle concentrations (TC=EC+organic carbon) resulted from the accumulation of small increments from a great variety of emission source types including both gasoline and diesel powered highway vehicles, stationary source fuel oil and gas combustion, industrial processes, paved road dust, fireplaces, cigarettes and food cooking (e.g. charbroilers). Strategies for black elemental carbon particle concentration control will of necessity need to focus on diesel engines, while controls directed at total carbon particle concentrations will have to be diversified over a great many source types.

Atmospheric concentration of 210Pb at Beijing and Chengdu, the People's Republic of China

International Nuclear Information System (INIS)

Sato, Shin; Sato, Jun; Doi, Taeko

2000-01-01

Atmospheric concentrations of 210 Pb were observed in the eastern area of the People's Republic of China with aerosol samples. Observations were carried out intermittently during the period from April, 1989 to December, 1992 at Beijing and Chengdu. The atmospheric concentrations of 210 Pb ranged from 0.9 to 4.6 mBq/m 3 at Beijing and from 1.4 to 7.8 mBq/m 3 at Chengdu, respectively, which were in the similar level to those observed previously in the inland area of the Chinese Continent. Seasonal variations of the 210 Pb concentration show the 'one-peak' variation pattern: the maximum levels were recorded in winter season. Small additional rises in the atmospheric 210 Pb concentrations observed in the period from spring to autumn seasons may be due to complicated meteorology with high pressure systems at Beijing and due to the topographical situation at Chengdu. (author)

Suspended Particulates Concentration (PM10 under Unstable Atmospheric Conditions over Subtropical Urban Area (Qena, Egypt

Directory of Open Access Journals (Sweden)

M. El-Nouby Adam

2013-01-01

Full Text Available The main purpose of this study is to evaluate the suspended particulates (PM10 in the atmosphere under unstable atmospheric conditions. The variation of PM10 was investigated and primary statistics were employed. The results show that, the PM10 concentrations values ranged from 6.00 to 646.74 μg m−3. The average value of PM10 is equal to 114.32 μg m−3. The high values were recorded in April and May (155.17 μg m−3 and 171.82 μg m−3, respectively and the low values were noted in February and December (73.86 μg m−3 and 74.05 μg m−3, respectively. The average value of PM10 of the hot season (125.35 × 10−6 g m−3 was higher than its value for the cold season (89.27 μg m−3. In addition, the effect of weather elements (air temperature, humidity and wind on the concentration of PM10 was determined. The multiple R between PM10 and these elements ranged from 0.05 to 0.47 and its value increased to reach 0.73 for the monthly average of the database used. Finally, the PM10 concentrations were grouped depending on their associated atmospheric stability class. These average values were equal to 122.80 ± 9 μg m−3 (highly unstable or convective, 109.37 ± 12 μg m−3 (moderately unstable and 104.42 ± 15 μg m−3 (slightly unstable.

Evidence of precursor phenomena in the Kobe earthquake obtained from atmospheric radon concentration

Energy Technology Data Exchange (ETDEWEB)

Yasuoka, Yumi [Kobe Pharmaceutical University, 4-19-1 Mtoyamakitama-machi, Higashinada-ku, Kobe, Hyogo 658-8558 (Japan)]. E-mail: yasuoka@kobepharma-u.ac.jp; Igarashi, George [Science Research Center for Prediction of Earthquakes and Volcanic Eruptions, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575 (Japan); Ishikawa, Testuo [National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan); Tokonami, Shinji [National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan); Shinogi, Masaki [Kobe Pharmaceutical University, 4-19-1 Mtoyamakitama-machi, Higashinada-ku, Kobe, Hyogo 658-8558 (Japan)

2006-06-15

Atmospheric {sup 222}Rn concentrations were determined over a 10a period, which included the date of the Kobe, Japan earthquake, on January 17th 1995. It was found that the seismically related {sup 222}Rn anomaly was higher than the 99% confidence limits for the residual value of atmospheric {sup 222}Rn which had been observed 2 months before. The residual {sup 222}Rn concentration, in which residual values of the daily minimum are the difference between each normal {sup 222}Rn concentration (calculated from January 1984 to December 1993) and the daily minimum {sup 222}Rn concentration (January 1994 to January 1995), was calculated by applying the exponential smoothing method to the residual values for each day. It was found that the fluctuations of the residual values can be fitted very well to a log-periodic oscillation model. The real residual values stopped increasing at 1994.999 (December 31st 1994), which corresponds with the critical point (t {sub c}) of best fit model. This anomalous {sup 222}Rn variation can be seen as the result of local stresses, not primary stresses which directly lead to the Kobe earthquake. On the other hand, when the critical exponent (z) and the radial frequency ({omega}) of the model were simultaneously fixed 0.2 {<=} z {<=} 0.6 and 6 {<=} {omega} {<=} 12, t {sub c} (critical point) was between January 13th 1995 and January 27th 1995. The Kobe earthquake occurrence date (January 17th 1995) is within this range. Therefore this anomalous {sup 222}Rn variation can also be seen as the result of primary stresses which possibly led to the Kobe earthquake. There is a distinct possibility that similar statistical oscillations will be detected in other measurements such as microseismicity, tectonic strain, fluctuation in the ground level, or changes in groundwater elevations and composition.

Temporal variability of atmospheric radon-222 concentration at Gosan Station, Jeju Island, Korea, during 2009-2013

Energy Technology Data Exchange (ETDEWEB)

Song, Jung Min; Kim, Won Hyung; Kang, Chang Hee [Dept. of Chemistry, Jeju National University, Jeju (Korea, Republic of); Lee, Hae Young; Lee, Chul Kyu [Korea Global Atmosphere Watch Center, Korea Meteorological Administration, ChungNam (Korea, Republic of); Chambers, S.; Williams, A. G. [Australian Nuclear Science and Technology Organisation, Kirrawee DC (Australia)

2015-02-15

Atmospheric radon-222 (radon) measurements were made from 2009 to 2013 at the Gosan station of Jeju Island, one of the cleanest regions in Korea, in order to characterize the temporal variability (on diurnal, seasonal, and annual scales) and analyze the influence of changing air mass transport pathways on observed radon concentrations. The mean hourly radon concentration over the whole period was 2441 ± 1037 mBq/m{sup 3}. The seasonal cycle of radon at the Gosan station was characterized by a fall maximum and summer minimum, consistent with a reduction in nonfrozen terrestrial fetch from fall to summer. In order, the seasonal mean radon concentrations were 2962 mBq/m{sup 3} (fall) >2907 mBq/m{sup 3} (winter) >2219 mBq/m{sup 3} (spring) >1756 mBq/m{sup 3} (summer). Based on a 5-year composite, the maximum mean monthly radon concentration in October (3100 mBq/m{sup 3}) was more than twice the July minimum (1471 mBq/m{sup 3}). Diurnal composite radon concentrations for the whole period increased throughout the night to a maximum of 2788 mBq/m{sup 3} at around 7 a.m., and then gradually decreased to a minimum of 2050 mBq/m{sup 3} at around 3 p.m. The winter diurnal cycle had a small amplitude due to the low variability in atmospheric mixing depth associated with recent air mass fetch over the Yellow Sea. The diurnal cycle in summer, however, exhibited a relatively large amplitude due to changes in atmospheric mixing depth associated with recent fetch over Jeju Island. Back trajectory analysis showed that high radon events were typically associated with long-term air mass fetch over continental Asia. Specifically, the average radon concentration of air masses originating from China was about 2.4 times higher than that of air masses originating from the North Pacific Ocean.

Temporal variability of atmospheric radon-222 concentration at Gosan Station, Jeju Island, Korea, during 2009-2013

International Nuclear Information System (INIS)

Song, Jung Min; Kim, Won Hyung; Kang, Chang Hee; Lee, Hae Young; Lee, Chul Kyu; Chambers, S.; Williams, A. G.

2015-01-01

Atmospheric radon-222 (radon) measurements were made from 2009 to 2013 at the Gosan station of Jeju Island, one of the cleanest regions in Korea, in order to characterize the temporal variability (on diurnal, seasonal, and annual scales) and analyze the influence of changing air mass transport pathways on observed radon concentrations. The mean hourly radon concentration over the whole period was 2441 ± 1037 mBq/m"3. The seasonal cycle of radon at the Gosan station was characterized by a fall maximum and summer minimum, consistent with a reduction in nonfrozen terrestrial fetch from fall to summer. In order, the seasonal mean radon concentrations were 2962 mBq/m"3 (fall) >2907 mBq/m"3 (winter) >2219 mBq/m"3 (spring) >1756 mBq/m"3 (summer). Based on a 5-year composite, the maximum mean monthly radon concentration in October (3100 mBq/m"3) was more than twice the July minimum (1471 mBq/m"3). Diurnal composite radon concentrations for the whole period increased throughout the night to a maximum of 2788 mBq/m"3 at around 7 a.m., and then gradually decreased to a minimum of 2050 mBq/m"3 at around 3 p.m. The winter diurnal cycle had a small amplitude due to the low variability in atmospheric mixing depth associated with recent air mass fetch over the Yellow Sea. The diurnal cycle in summer, however, exhibited a relatively large amplitude due to changes in atmospheric mixing depth associated with recent fetch over Jeju Island. Back trajectory analysis showed that high radon events were typically associated with long-term air mass fetch over continental Asia. Specifically, the average radon concentration of air masses originating from China was about 2.4 times higher than that of air masses originating from the North Pacific Ocean

Concentration of 7Be in the lower atmosphere and fallout rate in Tokai

International Nuclear Information System (INIS)

Amano, Hikaru; Kasai, Atsushi

1981-01-01

Beryllium-7, cosmic ray produced radioactivity, its monthly average concentration in the lower atmosphere and monthly fallout rate were measured in Tokai, Japan. Then, the monthly variations were compared with those of fission products due to nuclear detonations in the atmosphere. The concentration of 7 Be in the lower atmosphere ranged from 0.5 x 10 -1 pCi/m 3 to 2.5 x 10 -1 pCi/m 3 in Tokai between the observed period, 1975 - 1977. The fallout rate of 7 Be vibrated widely, its range was from the detection limits to 1.2 x 10 4 pCi/m 2 . The monthly variations were not always the same with variations of the fission products. Fallout rate of 7 Be depended on the rain strongly. The concentration of 7 Be in the rain was measured, too. Then the range was from 9.2 pCi/l to 1.9 x 10 2 pCi/l between the observed period 1976.9 - 1977.2. (author)

The optimal atmospheric CO2 concentration for the growth of winter wheat (Triticum aestivum).

Science.gov (United States)

Xu, Ming

2015-07-20

This study examined the optimal atmospheric CO2 concentration of the CO2 fertilization effect on the growth of winter wheat with growth chambers where the CO2 concentration was controlled at 400, 600, 800, 1000, and 1200 ppm respectively. I found that initial increase in atmospheric CO2 concentration dramatically enhanced winter wheat growth through the CO2 fertilization effect. However, this CO2 fertilization effect was substantially compromised with further increase in CO2 concentration, demonstrating an optimal CO2 concentration of 889.6, 909.4, and 894.2 ppm for aboveground, belowground, and total biomass, respectively, and 967.8 ppm for leaf photosynthesis. Also, high CO2 concentrations exceeding the optima not only reduced leaf stomatal density, length and conductance, but also changed the spatial distribution pattern of stomata on leaves. In addition, high CO2 concentration also decreased the maximum carboxylation rate (Vc(max)) and the maximum electron transport rate (J(max)) of leaf photosynthesis. However, the high CO2 concentration had little effect on leaf length and plant height. The optimal CO2 fertilization effect found in this study can be used as an indicator in selecting and breeding new wheat strains in adapting to future high atmospheric CO2 concentrations and climate change. Copyright © 2015. Published by Elsevier GmbH.

Atmospheric relative concentrations in building wakes

International Nuclear Information System (INIS)

Ramsdell, J.V. Jr.; Simonen, C.A.; Smyth, S.B.

1995-05-01

This report documents the ARCON95 computer code developed for the U.S. Nuclear Regulatory Commission Office of Nuclear Regulatory Research for use in control room habitability assessments. The document includes a user's guide to the code, a description of the technical basis for the code, and a programmer's guide to the code. The ARCON95 code uses hourly meteorological data and recently developed methods for estimating dispersion in the vicinity of buildings to calculate relative concentrations at control room air intakes that would be exceeded no more five percent of the time. These concentrations are calculated for averaging periods ranging from one hour to 30 days in duration. Relative concentrations calculated by ARCON95 are significantly lower than concentrations calculated using the currently accepted procedure when winds are less than two meters per second. For higher wind speeds, ARCON95 calculates about the same concentrations as the current procedure

Studies of atmospheric pollutants concentration factors from La Reina reactor

International Nuclear Information System (INIS)

Vera, I.; Alegria, E.

1983-01-01

Results of an atmospheric diffusion model for pollutant gases re shown, in which the nuclear reactor of the La Reina Nuclear Centre is considered as the emitting source. The model uses a gaussian shape steady state cloud of concentration of pollutants and actual topographical and meteorological statistics data os the zone. Expected and maximum probable concentration factors are computed in a polar lattice in 16 wind directions. It was found that peaks for expected concentration factors and maximum probable concentration factors at ground level fall within the N and ESE directions at distances where hills or mountains reach the emitted cloud. A discussion of the practical value of these calculations is given. (Author)

Studies of atmospheric pollutants concentration factors from La Reina reactor

Energy Technology Data Exchange (ETDEWEB)

Vera, I; Alegria, E [Comision Chilena de Energia Nuclear, Santiago. Div. de Seguridade Nuclear y Radioproteccion

1983-11-01

Results of an atmospheric diffusion model for pollutant gases are shown, in which the nuclear reactor of the La Reina Nuclear Centre is considered as the emitting source. The model uses a gaussian shape steady state cloud of concentration of pollutants and actual topographical and meteorological statistics data of the zone. Expected and maximum probable concentration factors are computed in a polar lattice in 16 wind directions. It was found that peaks for expected concentration factors and maximum probable concentration factors at ground level fall within the N and ESE directions at distances where hills or mountains reach the emitted cloud. A discussion of the practical value of these calculations is given.

PAHs concentration and toxicity in organic solvent extracts of atmospheric particulate matter and sea sediments.

Science.gov (United States)

Ozaki, Noriatsu; Takeuchi, Shin-ya; Kojima, Keisuke; Kindaichi, Tomonori; Komatsu, Toshiko; Fukushima, Takehiko

2012-01-01

The concentration of polycyclic aromatic hydrocarbons (PAHs) and the toxicity to marine bacteria (Vibrio fischeri) were measured for the organic solvent extracts of sea sediments collected from an urban watershed area (Hiroshima Bay) of Japan and compared with the concentrations and toxicity of atmospheric particulate matter (PM). In atmospheric PM, the PAHs concentration was highest in fine particulate matter (FPM) collected during cold seasons. The concentrations of sea sediments were 0.01-0.001 times those of atmospheric PM. 1/EC50 was 1-10 L g(-1) PM for atmospheric PM and 0.1-1 L g(-1) dry solids for sea sediments. These results imply that toxic substances from atmospheric PM are diluted several tens or hundreds of times in sea sediments. The ratio of the 1/EC50 to PAHs concentration ((1/EC50)/16PAHs) was stable for all sea sediments (0.1-1 L μg(-1) 16PAHs) and was the same order of magnitude as that of FPM and coarse particulate matter (CPM). The ratio of sediments collected from the west was more similar to that of CPM while that from the east was more similar to FPM, possibly because of hydraulic differences among water bodies. The PAHs concentration pattern analyses (principal component analysis and isomer ratio analysis) were conducted and the results showed that the PAHs pattern in sea sediments was quite different to that of FPM and CPM. Comparison with previously conducted PAHs analyses suggested that biomass burning residues comprised a major portion of these other sources.

Volume concentration of 41 elements in ground level of atmosphere in Bratislava

International Nuclear Information System (INIS)

Florek, M.; Meresova, J.; Holy, K.; Sykora, I.; Frontasyeva, M. V.; Pavlov, S. S.

2006-01-01

The concentrations of 41 chemical elements (heavy metals, rare earths, and actinides) were determined in atmospheric aerosol using nuclear and related analytical techniques. The sampling location was in Bratislava (Slovak Republic). The main goal of this study is the quantification of the atmospheric pollution and its trend. The elemental content in filters was measured using instrumental neutron activation analysis at IBR-2 reactor in JINR Dubna and by atomic absorption spectrometry in Bratislava. The obtained results confirmed the decreasing trend of pollution by most of the heavy metals in Bratislava atmosphere, and they are compared with the contents of pollutants in atmosphere of other cities. We determined also the composition of clear filter materials. (authors)

Effect of Mechanical Alloying Atmospheres and Oxygen Concentration on Mechanical Properties of ODS Ferritic Steels

International Nuclear Information System (INIS)

Noh, Sanghoon; Choi, Byoungkwon; Han, Changhee; Kim, Kibaik; Kang, Sukhoon; Chun, Youngbum; Kim, Taekyu

2013-01-01

Finely dispersed nano-oxide particles with a high number density in the homogeneous grain matrix are essential to achieve superior mechanical properties at high temperatures, and these unique microstructures can be obtained through the mechanical alloying (MA) and hot consolidation process. The microstructure and mechanical property of ODS steel significantly depends on its powder property and the purity after the MA process. These contents should be carefully controlled to improve the mechanical property at elevated temperature. In particular, appropriate the control of oxygen concentration improves the mechanical property of ODS steel at high temperature. An effective method is to control the mechanical alloying atmosphere by high purity inert gas. In the present study, the effects of mechanical alloying atmospheres and oxygen concentration on the mechanical property of ODS steel were investigated. ODS ferritic alloys were fabricated in various atmospheres, and the HIP process was used to investigate the effects of MA atmospheres and oxygen concentration on the microstructure and mechanical property. ODS ferritic alloys milled in an Ar-H 2 mixture, and He is effective to reduce the excess oxygen concentration. The YH 2 addition made an extremely reduced oxygen concentration by the internal oxygen reduction reaction and resulted in a homogeneous microstructure and superior creep strength

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.

Monitoring network of atmospheric Radon-222 concentration in East Asia and backward trajectory analysis of Radon-222 concentration trend at a small solitary island on pacific ocean

International Nuclear Information System (INIS)

Ohkura, Takehisa; Yamazawa, Hiromi; Moriizumi, Jun; Hirao, Shigekazu; Iida, Takao; Guo Qiuju; Tohjima, Yasunori

2009-01-01

A monitoring network of atmospheric 222 Rn concentration as a tracer for long-range transport in East Asia was established. Atmospheric 222 Rn concentration at Beijing, which is located on China Continent was 10-20 Bq m -3 , at Nagoya, which is located on edge of terrestrial area was 3-10 Bq m -3 and at Hachijo-jima and Hateruma-jima, which are solitary islands in Pacific Ocean was 0.5-3 Bq m -3 , respectively. The atmospheric 222 Rn concentration variations were different from sites. The 222 Rn concentration was the lowest in the summer and the highest in the winter except Nagoya where the highest was observed in the autumn and the lowest in the spring. Diurnal variations were measured at Beijing and Nagoya. In contrast, diurnal variations were not measured but several-day-cycle variations were measured at Hachijo-jima and Hateruma-jima. It was pointed out by this study that the several-day-cycle variations at Hachijo-jima were dependent on synoptic-scale atmospheric disturbance. 222 Rn concentration increased rapidly after a cold front passed through Hachijo-jima. Backward trajectory analysis of the relationship between atmospheric 222 Rn concentrations at Hachijo-jima and transport pathway of air mass indicates that air mass transported from China and Siberia has high concentration 222 Rn and air mass transported from Pacific Ocean has low concentration 222 Rn. In winter, atmospheric 222 Rn concentrations at Hachijo-jima is dependent on vertical transport pathway rather than horizontal transport pathway. (author)

Source, concentration, and distribution of elemental mercury in the atmosphere in Toronto, Canada

International Nuclear Information System (INIS)

Cairns, Elaine; Tharumakulasingam, Kavitharan; Athar, Makshoof; Yousaf, Muhammad; Cheng, Irene; Huang, Y.; Lu, Julia; Yap, Dave

2011-01-01

Atmospheric gaseous elemental mercury [GEM] at 1.8, 4, and 59 m above ground, in parking lots, and in indoor and outdoor air was measured in Toronto City, Canada from May 2008-July 2009. The average GEM value at 1.8 m was 1.89 ± 0.62 ng m -3 . The GEM values increased with elevation. The average GEM in underground parking lots ranged from 1.37 to 7.86 ng m -3 and was higher than those observed from the surface parking lots. The GEM in the indoor air ranged from 1.21 to 28.50 ng m -3 , was higher in the laboratories than in the offices, and was much higher than that in the outdoor air. All these indicate that buildings serve as sources of mercury to the urban atmosphere. More studies are needed to estimate the contribution of urban areas to the atmospheric mercury budget and the impact of indoor air on outdoor air quality and human health. - Highlights: → Buildings served as mercury sources to urban atmosphere. → Atmospheric mercury level increased with increasing height in the street canyon. → Emission from vehicles and ground surfaces was not the major sources of Hg to urban air. → Mercury levels were higher in indoor than outdoor air and in laboratories than in offices. → Mercury levels were higher in the outdoor air near building walls. - Buildings serve as sources of gaseous elemental mercury and research is needed to quantify the emission and to assess the impact of indoor air on outdoor air quality and human health.

Air mass origins by back trajectory analysis for evaluating atmospheric 210Pb concentrations at Rokkasho, Aomori, Japan

International Nuclear Information System (INIS)

Akata, N.; Kawabata, H.; Hasegawa, H.; Kondo, K.; Chikuchi, Y.; Hisamatsu, S.; Inaba, J.; Sato, T.

2009-01-01

Atmospheric concentrations of 210 Pb change with various factors such as meso-scale meteorological conditions. We have already reported the biweekly atmospheric 210 Pb concentrations in Rokkasho, Japan for 5 years and found that they had clear seasonal variations: low concentrations in summer and high values in winter to spring. To study the reasons for the seasonal variations, the origins of the air mass flowing to Rokkasho were analyzed by 3-D backward air mass trajectory analysis. Routes of the calculated trajectories were classified into four regions: northeastern and southeastern Asian Continent, sea and other regions. The atmospheric 210 Pb concentrations were well correlated with the frequency of the routes through the northeastern Asian Continent. A non-linear multiple regression analysis of the 210 Pb concentrations and the relative frequencies of the four routes showed good fitting of the predicted values to the observed ones, and indicated that the atmospheric 210 Pb concentrations in Rokkasho depended on the frequency of the air mass from the northeastern Asian Continent. (author)

Short-Chain Chlorinated Paraffins in Zurich, Switzerland--Atmospheric Concentrations and Emissions.

Science.gov (United States)

Diefenbacher, Pascal S; Bogdal, Christian; Gerecke, Andreas C; Glüge, Juliane; Schmid, Peter; Scheringer, Martin; Hungerbühler, Konrad

2015-08-18

Short-chain chlorinated paraffins (SCCPs) are of concern due to their potential for adverse health effects, bioaccumulation, persistence, and long-range transport. Data on concentrations of SCCPs in urban areas and underlying emissions are still scarce. In this study, we investigated the levels and spatial distribution of SCCPs in air, based on two separate, spatially resolved sampling campaigns in the city of Zurich, Switzerland. SCCP concentrations in air ranged from 1.8 to 17 ng·m(-3) (spring 2011) and 1.1 to 42 ng·m(-3) (spring 2013) with medians of 4.3 and 2.7 ng·m(-3), respectively. Both data sets show that atmospheric SCCP levels in Zurich can vary substantially and may be influenced by a number of localized sources within this urban area. Additionally, continuous measurements of atmospheric concentrations performed at one representative sampling site in the city center from 2011 to 2013 showed strong seasonal variations with high SCCP concentrations in summer and lower levels in winter. A long-term dynamic multimedia environmental fate model was parametrized to simulate the seasonal trends of SCCP concentrations in air and to back-calculate urban emissions. Resulting annual SCCP emissions in the city of Zurich accounted for 218-321 kg, which indicates that large SCCP stocks are present in urban areas of industrialized countries.

The Superstatistical Nature and Interoccurrence Time of Atmospheric Mercury Concentration Fluctuations

Science.gov (United States)

The probability density function (PDF) of the time intervals between subsequent extreme events in atmospheric Hg0 concentration data series from different latitudes has been investigated. The Hg0 dynamic possesses a long-term memory autocorrelation function. Above a fixed thresh...

Higher Atmosphere Heating due to black carbon Over the Northern Part of India

Science.gov (United States)

Tiwari, S.; Singh, S., , Dr

2017-12-01

Light-absorbing, atmospheric particles have gained greater attention in recent years because of their direct and indirect impacts on regional and global climate. Atmospheric black carbon (BC) aerosol (also called soot particle) is a leading climate warming agent, yet uncertainties in the global direct aerosol radiative forcing remain large. Based on a year of aerosol absorption measurements at seven wavelengths, BC concentrations were investigated in Dhanbad, the coal capital of India. Coal is routinely burned for cooking and residential heat as well as in small industries. The mean daily concentrations of ultraviolet-absorbing black carbon measured at 370 nm (UVBC) and black carbon measured at 880 nm (BC) were 9.8 ± 5.7 and 6.5 ± 3.8 μg m-3, respectively. The difference between UVBC and BC, Delta-C, is an indicator of biomass or residential coal burning and averaged 3.29 ± 4.61 μg m-3. An alternative approach uses the calculation of the Angstrom Exponent (AE) to estimate the amounts of biomass/coal and traffic BC. Biomass/coal burning contributed 87% and fossil fuel combustion contributed 13% to the annual average BC concentration. In the post-monsoon season, potential source contribution function analysis showed that air masses came from the central and northwestern Indo-Gangetic Plains resulting in mean UVBC values of 10.9 μg m-3 and BC of 7.2 μg m-3. The mean winter UVBC and BC concentrations were 15.0 and 10.1 μg m-3, respectively. These highest values were largely driven by local sources under conditions of poor dispersion. The direct radiative forcing (DRF) due to UVBC and BC at the surface (SFC) and the top of the atmosphere (TOA) were calculated. The mean atmospheric heating rates due to UVBC and BC were estimated to be 1.40°K day-1 and 1.18°K day-1, respectively. This high heating rate may affect the monsoon circulation in this region.

Metal concentrations in homing pigeon lung tissue as a biomonitor of atmospheric pollution.

Science.gov (United States)

Cui, Jia; Halbrook, Richard S; Zang, Shuying; Han, Shuang; Li, Xinyu

2018-03-01

Atmospheric pollution in urban areas is a major worldwide concern with potential adverse impacts on wildlife and humans. Biomonitoring can provide direct evidence of the bioavailability and bioaccumulation of toxic metals in the environment that is not available with mechanical air monitoring. The current study continues our evaluation of the usefulness of homing pigeon lung tissue as a biomonitor of atmospheric pollution. Homing pigeons (1-2, 5-6, and 9-10+ year old (yo)) collected from Guangzhou during 2015 were necropsied and concentrations of cadmium (Cd), lead (Pb), and mercury (Hg) were measured in lung tissue. Lung Cd and Pb concentrations were significantly greater in 9-10+-year-old pigeons compared with those in other age groups, indicating their bioavailability and bioaccumulation. Lung Pb and Cd concentrations measured in 5-yo pigeons collected from Guangzhou during 2015 were significantly lower than concentrations reported in 5-yo homing pigeons collected from Guangzhou during 2011 and correlated with concentrations measured using mechanical air monitoring. In addition to temporal differences, spatial differences in concentrations of Cd, Pb, and Hg reported in ambient air samples and in pigeon lung tissues collected from Beijing and Guangzhou are discussed.

Atmospheric CO2 Concentration Measurements with Clouds from an Airborne Lidar

Science.gov (United States)

Mao, J.; Abshire, J. B.; Kawa, S. R.; Riris, H.; Allan, G. R.; Hasselbrack, W. E.; Numata, K.; Chen, J. R.; Sun, X.; DiGangi, J. P.; Choi, Y.

2017-12-01

Globally distributed atmospheric CO2 concentration measurements with high precision, low bias and full seasonal sampling are crucial to advance carbon cycle sciences. However, two thirds of the Earth's surface is typically covered by clouds, and passive remote sensing approaches from space are limited to cloud-free scenes. NASA Goddard is developing a pulsed, integrated-path differential absorption (IPDA) lidar approach to measure atmospheric column CO2 concentrations, XCO2, from space as a candidate for NASA's ASCENDS mission. Measurements of time-resolved laser backscatter profiles from the atmosphere also allow this technique to estimate XCO2 and range to cloud tops in addition to those to the ground with precise knowledge of the photon path-length. We demonstrate this measurement capability using airborne lidar measurements from summer 2017 ASCENDS airborne science campaign in Alaska. We show retrievals of XCO2 to ground and to a variety of cloud tops. We will also demonstrate how the partial column XCO2 to cloud tops and cloud slicing approach help resolving vertical and horizontal gradient of CO2 in cloudy conditions. The XCO2 retrievals from the lidar are validated against in situ measurements and compared to the Goddard Parameterized Chemistry Transport Model (PCTM) simulations. Adding this measurement capability to the future lidar mission for XCO2 will provide full global and seasonal data coverage and some information about vertical structure of CO2. This unique facility is expected to benefit atmospheric transport process studies, carbon data assimilation in models, and global and regional carbon flux estimation.

Time-scale invariant changes in atmospheric radon concentration and crustal strain prior to a large earthquake

Directory of Open Access Journals (Sweden)

Y. Kawada

2007-01-01

Full Text Available Prior to large earthquakes (e.g. 1995 Kobe earthquake, Japan, an increase in the atmospheric radon concentration is observed, and this increase in the rate follows a power-law of the time-to-earthquake (time-to-failure. This phenomenon corresponds to the increase in the radon migration in crust and the exhalation into atmosphere. An irreversible thermodynamic model including time-scale invariance clarifies that the increases in the pressure of the advecting radon and permeability (hydraulic conductivity in the crustal rocks are caused by the temporal changes in the power-law of the crustal strain (or cumulative Benioff strain, which is associated with damage evolution such as microcracking or changing porosity. As the result, the radon flux and the atmospheric radon concentration can show a temporal power-law increase. The concentration of atmospheric radon can be used as a proxy for the seismic precursory processes associated with crustal dynamics.

New instruments and methods for measuring the concentration of radioactive products in the atmosphere; Appareils recents et methodes nouvelles pour la mesure de la concentration des produits radioactifs dans l'atmosphere

Energy Technology Data Exchange (ETDEWEB)

Jehanno, C; Blanc, A; Lallemant, C; Roux, G [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1959-07-01

Different recorders for radioactive aerosols have been developed for measuring the pollution of the atmosphere in laboratories or the external atmosphere. EAR 600. - Allows continuous measurement, instantaneously and 3 to 10 hours after sampling, of concentrations of {alpha} or {beta} emitting aerosols varying between some 10{sup -11} and some 10{sup -8} curie per cubic metre of air. EAR 800. - Allows continuous measurement of concentration of {alpha} emitting aerosols varying between 10{sup -11} and 10{sup -5} curie per cubic metre of air and concentration of {beta} emitting aerosols from 10{sup -11} to 10{sup -1} curie per cubic metre of air. EAR Plutonium. - Allows detection after several minutes of 1000 MPD (2 x 10{sup -9} curie par cubic metre), and after 8 hours 1 MPD (2 x 10{sup -12} curie per cubic metre). Two methods are used to separate the activity due to plutonium from that due to the descendants of radon and thoron: a) by amplitude discrimination, b) by RaC-RaC' and ThC-ThC' ({alpha} {beta} ) coincidences. SP4. This system, mounted on a jeep, allows the measurement of irradiation produced on the ground by the smoke from the piles. The sensitivity is 5{mu}R/h. A.D.I.R. - This autonomous and portable instrument is designed for the instantaneous measurement of the radon content of the atmosphere in mines. It allows the measurement of contents in air varying between 0.4 and 400 x 10{sup -10} curie per litre of air (0.4 and 400 MPD). The measurement of radioactive fall-out is carried out after collection of this activity by a special rain gauge which comprises an adhesive surface and a tube containing ion exchange resins. The radioactivity of the fall-out varies between some 10{sup -9} and some 10{sup -7} curie per square metre per month. Concentrations in fission products of the atmosphere are measured after collecting on filter paper. Concentrations measured in air at ground level vary between 10{sup -13} and 10{sup -12} curie per cubic metre. (author

Estimating Terrestrial Wood Biomass from Observed Concentrations of Atmospheric Carbon Dioxide

NARCIS (Netherlands)

Schaefer, K. M.; Peters, W.; Carvalhais, N.; van der Werf, G.; Miller, J.

2008-01-01

We estimate terrestrial disequilibrium state and wood biomass from observed concentrations of atmospheric CO2 using the CarbonTracker system coupled to the SiBCASA biophysical model. Starting with a priori estimates of carbon flux from the land, ocean, and fossil fuels, CarbonTracker estimates net

A terrestrial biosphere model optimized to atmospheric CO2 concentration and above ground woody biomass

Science.gov (United States)

Saito, M.; Ito, A.; Maksyutov, S. S.

2013-12-01

This study documents an optimization of a prognostic biosphere model (VISIT; Vegetation Integrative Similator for Trace gases) to observations of atmospheric CO2 concentration and above ground woody biomass by using a Bayesian inversion method combined with an atmospheric tracer transport model (NIES-TM; National Institute for Environmental Studies / Frontier Research Center for Global Change (NIES/FRCGC) off-line global atmospheric tracer transport model). The assimilated observations include 74 station records of surface atmospheric CO2 concentration and aggregated grid data sets of above ground woody biomass (AGB) and net primary productivity (NPP) over the globe. Both the biosphere model and the atmospheric transport model are used at a horizontal resolution of 2.5 deg x 2.5 deg grid with temporal resolutions of a day and an hour, respectively. The atmospheric transport model simulates atmospheric CO2 concentration with nine vertical levels using daily net ecosystem CO2 exchange rate (NEE) from the biosphere model, oceanic CO2 flux, and fossil fuel emission inventory. The models are driven by meteorological data from JRA-25 (Japanese 25-year ReAnalysis) and JCDAS (JMA Climate Data Assimilation System). Statistically optimum physiological parameters in the biosphere model are found by iterative minimization of the corresponding Bayesian cost function. We select thirteen physiological parameter with high sensitivity to NEE, NPP, and AGB for the minimization. Given the optimized physiological parameters, the model shows error reductions in seasonal variation of the CO2 concentrations especially in the northern hemisphere due to abundant observation stations, while errors remain at a few stations that are located in coastal coastal area and stations in the southern hemisphere. The model also produces moderate estimates of the mean magnitudes and probability distributions in AGB and NPP for each biome. However, the model fails in the simulation of the terrestrial

Cast Stone Formulation At Higher Sodium Concentrations

International Nuclear Information System (INIS)

Fox, K. M.; Edwards, T. A.; Roberts, K. B.

2013-01-01

concentration in the salt solution reduced the time to peak heat flow, and reducing the amount of slag in the premix increased the time to peak heat flow. These observations may help to describe some of the cured properties of the samples, in particular the differences in compressive strength observed after 28 and 90 days of curing. Samples were cured for at least 28 days at ambient temperature in the laboratory prior to cured properties analyses. The low activity waste form for disposal at the Hanford Site is required to have a compressive strength of at least 500 psi. After 28 days of curing, several of the test mixes had mean compressive strengths that were below the 500 psi requirement. Higher sodium concentrations and higher water to premix ratios led to reduced compressive strength. Higher fly ash concentrations decreased the compressive strength after 28 days of curing. This may be explained in that the cementitious phases matured more quickly in the mixes with higher concentrations of slag, as evidenced by the data for the time to peak heat generation. All of the test mixes exhibited higher mean compressive strengths after 90 days of curing, with only one composition having a mean compressive strength of less than 500 psi. Leach indices were determined for the test mixes for contaminants of interest. The leaching performance of the mixes evaluated in this study was not particularly sensitive to the factors used in the experimental design. This may be beneficial in demonstrating that the performance of the waste form is robust with respect to changes in the mix composition. The results of this study demonstrate the potential to achieve significantly higher waste loadings in Cast Stone and other low temperature, cementitious waste forms. Additional work is needed to elucidate the hydration mechanisms occurring in Cast Stone formulated with highly concentrated salt solutions since these reactions are responsible for determining the performance of the cured waste form. The

Cast Stone Formulation At Higher Sodium Concentrations

International Nuclear Information System (INIS)

Fox, K. M.; Roberts, K. A.; Edwards, T. B.

2014-01-01

concentration in the salt solution reduced the time to peak heat flow, and reducing the amount of slag in the premix increased the time to peak heat flow. These observations may help to describe some of the cured properties of the samples, in particular the differences in compressive strength observed after 28 and 90 days of curing. Samples were cured for at least 28 days at ambient temperature in the laboratory prior to cured properties analyses. The low activity waste form for disposal at the Hanford Site is required to have a compressive strength of at least 500 psi. After 28 days of curing, several of the test mixes had mean compressive strengths that were below the 500 psi requirement. Higher sodium concentrations and higher water to premix ratios led to reduced compressive strength. Higher fly ash concentrations decreased the compressive strength after 28 days of curing. This may be explained in that the cementitious phases matured more quickly in the mixes with higher concentrations of slag, as evidenced by the data for the time to peak heat generation. All of the test mixes exhibited higher mean compressive strengths after 90 days of curing, with only one composition having a mean compressive strength of less than 500 psi. Leachability indices were determined for the test mixes for contaminants of interest. The leaching performance of the mixes evaluated in this study was not particularly sensitive to the factors used in the experimental design. This may be beneficial in demonstrating that the performance of the waste form is robust with respect to changes in the mix composition. The results of this study demonstrate the potential to achieve significantly higher waste loadings in Cast Stone and other low temperature, cementitious waste forms. Additional work is needed to elucidate the hydration mechanisms occurring in Cast Stone formulated with highly concentrated salt solutions since these reactions are responsible for determining the performance of the cured waste

Cast Stone Formulation At Higher Sodium Concentrations

Energy Technology Data Exchange (ETDEWEB)

Fox, K. M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Roberts, K. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Edwards, T. B. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2014-02-28

concentration in the salt solution reduced the time to peak heat flow, and reducing the amount of slag in the premix increased the time to peak heat flow. These observations may help to describe some of the cured properties of the samples, in particular the differences in compressive strength observed after 28 and 90 days of curing. Samples were cured for at least 28 days at ambient temperature in the laboratory prior to cured properties analyses. The low activity waste form for disposal at the Hanford Site is required to have a compressive strength of at least 500 psi. After 28 days of curing, several of the test mixes had mean compressive strengths that were below the 500 psi requirement. Higher sodium concentrations and higher water to premix ratios led to reduced compressive strength. Higher fly ash concentrations decreased the compressive strength after 28 days of curing. This may be explained in that the cementitious phases matured more quickly in the mixes with higher concentrations of slag, as evidenced by the data for the time to peak heat generation. All of the test mixes exhibited higher mean compressive strengths after 90 days of curing, with only one composition having a mean compressive strength of less than 500 psi. Leachability indices were determined for the test mixes for contaminants of interest. The leaching performance of the mixes evaluated in this study was not particularly sensitive to the factors used in the experimental design. This may be beneficial in demonstrating that the performance of the waste form is robust with respect to changes in the mix composition. The results of this study demonstrate the potential to achieve significantly higher waste loadings in Cast Stone and other low temperature, cementitious waste forms. Additional work is needed to elucidate the hydration mechanisms occurring in Cast Stone formulated with highly concentrated salt solutions since these reactions are responsible for determining the performance of the cured waste

Cast Stone Formulation At Higher Sodium Concentrations

Energy Technology Data Exchange (ETDEWEB)

Fox, K. M.; Edwards, T. A.; Roberts, K. B.

2013-10-02

concentration in the salt solution reduced the time to peak heat flow, and reducing the amount of slag in the premix increased the time to peak heat flow. These observations may help to describe some of the cured properties of the samples, in particular the differences in compressive strength observed after 28 and 90 days of curing. Samples were cured for at least 28 days at ambient temperature in the laboratory prior to cured properties analyses. The low activity waste form for disposal at the Hanford Site is required to have a compressive strength of at least 500 psi. After 28 days of curing, several of the test mixes had mean compressive strengths that were below the 500 psi requirement. Higher sodium concentrations and higher water to premix ratios led to reduced compressive strength. Higher fly ash concentrations decreased the compressive strength after 28 days of curing. This may be explained in that the cementitious phases matured more quickly in the mixes with higher concentrations of slag, as evidenced by the data for the time to peak heat generation. All of the test mixes exhibited higher mean compressive strengths after 90 days of curing, with only one composition having a mean compressive strength of less than 500 psi. Leach indices were determined for the test mixes for contaminants of interest. The leaching performance of the mixes evaluated in this study was not particularly sensitive to the factors used in the experimental design. This may be beneficial in demonstrating that the performance of the waste form is robust with respect to changes in the mix composition. The results of this study demonstrate the potential to achieve significantly higher waste loadings in Cast Stone and other low temperature, cementitious waste forms. Additional work is needed to elucidate the hydration mechanisms occurring in Cast Stone formulated with highly concentrated salt solutions since these reactions are responsible for determining the performance of the cured waste form. The

Cast Stone Formulation At Higher Sodium Concentrations

Energy Technology Data Exchange (ETDEWEB)

Fox, K. M.; Roberts, K. A.; Edwards, T. B.

2013-09-17

concentration in the salt solution reduced the time to peak heat flow, and reducing the amount of slag in the premix increased the time to peak heat flow. These observations may help to describe some of the cured properties of the samples, in particular the differences in compressive strength observed after 28 and 90 days of curing. Samples were cured for at least 28 days at ambient temperature in the laboratory prior to cured properties analyses. The low activity waste form for disposal at the Hanford Site is required to have a compressive strength of at least 500 psi. After 28 days of curing, several of the test mixes had mean compressive strengths that were below the 500 psi requirement. Higher sodium concentrations and higher water to premix ratios led to reduced compressive strength. Higher fly ash concentrations decreased the compressive strength after 28 days of curing. This may be explained in that the cementitious phases matured more quickly in the mixes with higher concentrations of slag, as evidenced by the data for the time to peak heat generation. All of the test mixes exhibited higher mean compressive strengths after 90 days of curing, with only one composition having a mean compressive strength of less than 500 psi. Leach indices were determined for the test mixes for contaminants of interest. The leaching performance of the mixes evaluated in this study was not particularly sensitive to the factors used in the experimental design. This may be beneficial in demonstrating that the performance of the waste form is robust with respect to changes in the mix composition. The results of this study demonstrate the potential to achieve significantly higher waste loadings in Cast Stone and other low temperature, cementitious waste forms. Additional work is needed to elucidate the hydration mechanisms occurring in Cast Stone formulated with highly concentrated salt solutions since these reactions are responsible for determining the performance of the cured waste form. The

Results of long-term measurement of 222Rn concentrations in outdoor atmosphere

International Nuclear Information System (INIS)

Holy, K.; Boehm, R.; Polaskova, A.; Hola, O.

1998-01-01

Results are reported of the authors' long-term measurement of 222 Rn concentrations in the outdoor atmosphere. The measurements started in 1987 and were performed at a height of 1.5 m over a grass-covered ground surface, using till 1991 a Lucas type scintillation chamber and later a large volume scintillation chamber. Graphs are presented and discussed of the course of average monthly radon concentration in 1987-1996 and of annual courses of radon concentration for different time intervals of the day over 1991 to 1995. (A.K.)

Development of a 10 Hz measurement system for atmospheric aerosol concentration

International Nuclear Information System (INIS)

Bouarouri, Assia

2014-01-01

The goal is to develop an aerosol charger based on a corona discharge for atmospheric concentration measurements (10 3 -10 5 cm -3 ) within a response time of 100 ms. Two ion sources, point-to-hole and wire-to-slit have been characterized. The increase of the ion flow in the post-discharge by EHD ion confinement in both the discharge gap and the hole has been shown. At first, using an experimental survey driven in two mixing configurations, concentric and face-to-face, we have confirmed the aerosol diffusion charging law which depends on aerosol diameter and N i .t product, with N i , the ions concentration and t, the charging time. Thus, the originality of this charger relies on the very high heterogeneity of unipolar ion densities (N i 0 ≥10 9 cm -3 ) required to compensate the charging time of 50 ms. In these conditions, we have shown that aerosol diameter and the charging dynamic (which depends also on the diameter) control the aerosol trajectory. The chargers have, next, been compared in different operating conditions, mainly in terms of the maximal charging and the minimal losses. In the chosen charger (point-to-hole ion source and concentric mixing), the relations charge/mobility and losses according to diameter have been characterized. We have also shown the linearity of the charged particles current with the aerosol concentration which allows the current-concentration data inversion. The preliminary measurement system composed by the charger, the separator and the particle current measurements, satisfies the objectives of the study in terms of the concentration detection limit (10 3 cm -3 ) and the response time (100 ms). We have thus shown the feasibility of an atmospheric aerosol concentration measurement system at 10 Hz using a corona discharge charger provided that the separation power is improved. Furthermore, knowing that aerosol losses are negligible and the lower limit of the partial charging, the developed charger is adaptable with other

Climatology of atmospheric PM10 concentration in the Po Valley

Science.gov (United States)

Bigi, A.; Ghermandi, G.

2014-01-01

The limits to atmospheric pollutant concentration set by the European Commission provide a challenging target for the municipalities in the Po Valley, because of the characteristic climatic conditions and high population density of this region. In order to assess climatology and trends in the concentration of atmospheric particles in the Po Valley, a dataset of PM10 data from 41 sites across the Po Valley have been analysed, including both traffic and background sites (either urban, suburban or rural). Of these 41 sites, 18 with 10 yr or longer record have been analysed for long term trend in de-seasonalized monthly means, in annual quantiles and in monthly frequency distribution. A widespread significant decreasing trend has been observed at most sites, up to few percent per year, by Generalised Least Square and Theil-Sen method. All 41 sites have been tested for significant weekly periodicity by Kruskal-Wallis test for mean anomalies and by Wilcoxon test for weekend effect magnitude. A significant weekly periodicity has been observed for most PM10 series, particularly in summer and ascribed mainly to anthropic particulate emissions. A cluster analysis has been applied in order to highlight stations sharing similar pollution conditions over the reference period. Five clusters have been found, two gathering the metropolitan areas of Torino and Milano and their respective nearby sites and the other three clusters gathering north-east, north-west and central Po Valley sites respectively. Finally the observed trends in atmospheric PM10 have been compared to trends in provincial emissions of particulates and PM precursors, and analysed along with data on vehicular fleet age, composition and fuel sales. Significant basin-wide drop in emissions occurred for gaseous pollutants, contrarily to emissions of PM10 and PM2.5, whose drop resulted low and restricted to few provinces. It is not clear whether the decrease for only gaseous emissions is sufficient to explain the

Possible future scenarios for atmospheric concentration of greenhouse gases. A simplified thermodynamic approach

International Nuclear Information System (INIS)

Angulo-Brown, F.; Sanchez-Salas, N.; Barranco-Jimenez, M.A.; Rosales, M.A.

2009-01-01

Most of the increase in concentrations of greenhouse gases in the Earth's atmosphere is mainly due to anthropogenic activities. This is particularly significant in the case of CO 2 . The atmospheric concentration of CO 2 has systematically increased since the Industrial Revolution (260 ppm), with a remarkable raise after the 1970s until the present day (380 ppm). If this increasing tendency is maintained, the last report of the Intergovernmental Panel on Climate Change (IPCC) estimates that, for the year 2100, the CO 2 concentration can augment up to approximately 675 ppm. In this work it is assumed that the quantity of anthropogenic greenhouse gases emitted to the Earth's atmosphere is proportional to the quantity of heat rejected to the environment by internal combustion heat engines. It is also assumed that this increasing tendency of CO 2 due to men's activity stems from a mode of energy production mainly based on a maximum-power output paradigm. With these hypotheses, a thermoeconomic optimization of a thermal engine model under two regimes of performance: the maximum-power regime and the so-called ecological function criterion is presented. This last regime consists in maximizing a function that represents a good compromise between high power output and low entropy production. It is showed that, under maximum ecological conditions, the emissions of thermal energy to the environment are reduced approximately up to 50%. Thus working under this mode of performance the slope of the curves of CO 2 concentration, for instance, drastically diminishes. A simple qualitative criterion to design ecological taxes is also suggested. (author)

Gaseous polycyclic aromatic hydrocarbon concentrations are higher in urban forests than adjacent open areas during summer but not in winter – Exploratory study

International Nuclear Information System (INIS)

Viippola, Viljami; Rantalainen, Anna-Lea; Yli-Pelkonen, Vesa; Tervo, Peatta; Setälä, Heikki

2016-01-01

While the potential of plants to uptake polycyclic aromatic hydrocarbons (PAHs) is widely acknowledged, empirical evidence of the effects of this process on local atmospheric PAH concentrations and human health is tenuous. We measured gaseous PAH concentrations using passive samplers in urban tree-covered areas and adjacent open, treeless areas in a near-road environment in Finland to gain information on the ability of urban vegetation to improve air quality. The ability of urban, mostly deciduous, vegetation to affect PAHs was season dependent: during summer, concentrations were significantly higher in tree-covered areas, while in the fall, concentrations in open areas exceeded those in tree-covered areas. During winter, concentrations in tree-covered areas were either lower or did not differ from those in open areas. Results of this study imply that the commonly believed notion that trees unequivocally improve air quality does not apply to PAHs studied here. - Highlights: • Urban tree-cover increases gaseous PAH concentrations during summertime. • Elevated PAH concentrations do not clearly correspond with vegetation properties. • Tree-cover attenuates seasonal PAH concentration fluctuation. - Higher ambient gaseous PAH concentrations were detected within urban tree cover as compared to open areas during summertime.

A review of studies on atmospheric mercury in China.

Science.gov (United States)

Fu, Xuewu; Feng, Xinbin; Sommar, Jonas; Wang, Shaofeng

2012-04-01

Due to the fast developing economy, mercury (Hg) emissions to the atmosphere from Chinese mainland have increased rapidly in recent years. Consequently, this issue has received a considerable attention internationally. This paper reviews the current understanding of and knowledge on atmospheric Hg emissions, distribution and transport in China. The magnitude of Hg emissions to the atmosphere from Chinese anthropogenic sources has been estimated to be in the range of 500-700 tons per year, whereby comprising a significant proportion of the globe total anthropogenic emissions. Emissions of Hg from natural surfaces including bare soil, water, and vegetation covered soil tend in a comparison to be higher in China than in Europe and North America, indicating the importance of this source category. Atmospheric Hg exhibits a significant concentration variability among urban, semi-remote, and remote areas. Total Gaseous Mercury (TGM) concentrations in urban areas of China were often 1.5 - 5 folds higher compared to the corresponding settings in North America and Europe. In turn, particulate mercury (PHg) concentrations in urban areas of China were up to two orders of magnitude higher compared to North America and Europe. Atmospheric observations made at strictly remote sites in China also include the presence of occasional high concentrations of TGM, and the more short-lived fractions PHg and Reactive Gaseous Mercury (RGM). Accordingly, Hg deposition fluxes tended to be higher in China, with remote areas and urban areas being 1-2 times and 1-2 magnitude higher than those in North America and Europe, respectively. Crown Copyright © 2011. Published by Elsevier B.V. All rights reserved.

Influence of some atmospheric variables on the concentration and particle size distribution of sulfate in urban air

Energy Technology Data Exchange (ETDEWEB)

Wagman, J; Lee, Jr, R E; Axt, C J

1967-01-01

Variations in the particle size distribution and concentration of atmospheric sulfate during a week in each of four cities were assessed with regard to the influence of such factors as location, humidity, sulfur dioxide level and time of day. Average sulfate mass median equivalent diameters (MMD) in Cincinnati, Chicago and Fairfax (Ohio) were nearly the same (0.42 micron) despite large differences in sulfate concentration and heterodispersity. A higher MMD (0.66 micron) in downtown Philadelphia was at least partly attributable to the presence of dust generated by road construction near the sampling site. Sulfate MMD generally increased with increasing relative humidity, whereas sulfate concentration was more closely correlated with absolute humidity except when SO/sub 2/ levels exceeded 3pphm. Periodic variations in the sulfate parameters at the different locations were characterized by the lack of a consistent pattern and could not be explained on the basis of humidity changes alone.

An approach for verifying biogenic greenhouse gas emissions inventories with atmospheric CO2 concentration data

International Nuclear Information System (INIS)

Ogle, Stephen M; Davis, Kenneth; Lauvaux, Thomas; Miles, Natasha L; Richardson, Scott; Schuh, Andrew; Cooley, Dan; Breidt, F Jay; West, Tristram O; Heath, Linda S; Smith, James E; McCarty, Jessica L; Gurney, Kevin R; Tans, Pieter; Denning, A Scott

2015-01-01

Verifying national greenhouse gas (GHG) emissions inventories is a critical step to ensure that reported emissions data to the United Nations Framework Convention on Climate Change (UNFCCC) are accurate and representative of a country’s contribution to GHG concentrations in the atmosphere. Furthermore, verifying biogenic fluxes provides a check on estimated emissions associated with managing lands for carbon sequestration and other activities, which often have large uncertainties. We report here on the challenges and results associated with a case study using atmospheric measurements of CO 2 concentrations and inverse modeling to verify nationally-reported biogenic CO 2 emissions. The biogenic CO 2 emissions inventory was compiled for the Mid-Continent region of United States based on methods and data used by the US government for reporting to the UNFCCC, along with additional sources and sinks to produce a full carbon balance. The biogenic emissions inventory produced an estimated flux of −408 ± 136 Tg CO 2 for the entire study region, which was not statistically different from the biogenic flux of −478 ± 146 Tg CO 2 that was estimated using the atmospheric CO 2 concentration data. At sub-regional scales, the spatial density of atmospheric observations did not appear sufficient to verify emissions in general. However, a difference between the inventory and inversion results was found in one isolated area of West-central Wisconsin. This part of the region is dominated by forestlands, suggesting that further investigation may be warranted into the forest C stock or harvested wood product data from this portion of the study area. The results suggest that observations of atmospheric CO 2 concentration data and inverse modeling could be used to verify biogenic emissions, and provide more confidence in biogenic GHG emissions reporting to the UNFCCC. (letter)

Determining How Atmospheric Carbon Dioxide Concentrations Have Changed during the History of the Earth

Science.gov (United States)

Badger, Marcus P. S.; Pancost, Richard D.; Harrison, Timothy G.

2011-01-01

The reconstruction of ancient atmospheric carbon dioxide concentrations is essential to understanding the history of the Earth and life. It is also an important guide to identifying the sensitivity of the Earth system to this greenhouse gas and, therefore, constraining its future impact on climate. However, determining the concentration of…

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.

Temporal variations in elemental concentrations of atmospheric aerosols in Mexico City

International Nuclear Information System (INIS)

Aldape U, F.

1992-05-01

Measurements are reported of elemental concentrations of airborne particulates in Mexico City and their time variation over a one-week period in the spring of 1988. Proton-induced X-ray emission analysis, PIXE, was used to analyse the atmospheric aerosols which were bombarded with 2.5 MeV protons from the 12 MV Tandem Van de Graaff accelerator at the National Institute of Nuclear Research, ININ. Variations in the elemental concentrations were observed over the time period studied. An intercomparison was made in the case of the element lead with PIXE results obtained at the Crocker Nuclear Laboratory, CNL, University of California for the same set of samples. Excellent agreement was obtained both for the time variation of the relative concentration and the absolute lead concentrations. These results give added confidence to the protocol adopted at ININ. (Author)

Estimation of maximum credible atmospheric radioactivity concentrations and dose rates from nuclear tests

International Nuclear Information System (INIS)

Telegadas, K.

1979-01-01

A simple technique is presented for estimating maximum credible gross beta air concentrations from nuclear detonations in the atmosphere, based on aircraft sampling of radioactivity following each Chinese nuclear test from 1964 to 1976. The calculated concentration is a function of the total yield and fission yield, initial vertical radioactivity distribution, time after detonation, and rate of horizontal spread of the debris with time. calculated maximum credible concentrations are compared with the highest concentrations measured during aircraft sampling. The technique provides a reasonable estimate of maximum air concentrations from 1 to 10 days after a detonation. An estimate of the whole-body external gamma dose rate corresponding to the maximum credible gross beta concentration is also given. (author)

Deep Sea Memory of High Atmospheric CO2 Concentration

Science.gov (United States)

Mathesius, Sabine; Hofmann, Matthias; Caldeira, Ken; Schellnhuber, Hans Joachim

2015-04-01

Carbon dioxide removal (CDR) from the atmosphere has been proposed as a powerful measure to mitigate global warming and ocean acidification. Planetary-scale interventions of that kind are often portrayed as "last-resort strategies", which need to weigh in if humankind keeps on enhancing the climate-system stock of CO2. Yet even if CDR could restore atmospheric CO2 to substantially lower concentrations, would it really qualify to undo the critical impacts of past emissions? In the study presented here, we employed an Earth System Model of Intermediate Complexity (EMIC) to investigate how CDR might erase the emissions legacy in the marine environment, focusing on pH, temperature and dissolved oxygen. Against a background of a world following the RCP8.5 emissions path ("business-as-usual") for centuries, we simulated the effects of two massive CDR interventions with CO2 extraction rates of 5 GtC yr-1 and 25 GtC yr-1, respectively, starting in 2250. We found that the 5 GtC yr-1 scheme would have only minor ameliorative influence on the oceans, even after several centuries of application. By way of contrast, the extreme 25 GtC yr-1 scheme eventually leads to tangible improvements. However, even with such an aggressive measure, past CO2 emissions leave a substantial legacy in the marine environment within the simulated period (i.e., until 2700). In summary, our study demonstrates that anthropogenic alterations of the oceans, caused by continued business-as-usual emissions, may not be reversed on a multi-centennial time scale by the most aspirational geoengineering measures. We also found that a transition from the RCP8.5 state to the state of a strong mitigation scenario (RCP2.6) is not possible, even under the assumption of extreme extraction rates (25 GtC yr-1). This is explicitly demonstrated by simulating additional scenarios, starting CDR already in 2150 and operating until the atmospheric CO2 concentration reaches 280 ppm and 180 ppm, respectively. The simulated

The determination of carbon dioxide concentration using atmospheric pressure ionization mass spectrometry/isotopic dilution and errors in concentration measurements caused by dryers.

Science.gov (United States)

DeLacy, Brendan G; Bandy, Alan R

2008-01-01

An atmospheric pressure ionization mass spectrometry/isotopically labeled standard (APIMS/ILS) method has been developed for the determination of carbon dioxide (CO(2)) concentration. Descriptions of the instrumental components, the ionization chemistry, and the statistics associated with the analytical method are provided. This method represents an alternative to the nondispersive infrared (NDIR) technique, which is currently used in the atmospheric community to determine atmospheric CO(2) concentrations. The APIMS/ILS and NDIR methods exhibit a decreased sensitivity for CO(2) in the presence of water vapor. Therefore, dryers such as a nafion dryer are used to remove water before detection. The APIMS/ILS method measures mixing ratios and demonstrates linearity and range in the presence or absence of a dryer. The NDIR technique, on the other hand, measures molar concentrations. The second half of this paper describes errors in molar concentration measurements that are caused by drying. An equation describing the errors was derived from the ideal gas law, the conservation of mass, and Dalton's Law. The purpose of this derivation was to quantify errors in the NDIR technique that are caused by drying. Laboratory experiments were conducted to verify the errors created solely by the dryer in CO(2) concentration measurements post-dryer. The laboratory experiments verified the theoretically predicted errors in the derived equations. There are numerous references in the literature that describe the use of a dryer in conjunction with the NDIR technique. However, these references do not address the errors that are caused by drying.

RELATIONSHIP BETWEEN ATMOSPHERIC CO_2 AND CH_4 CONCENTRATIONS AT SYOWA STATION, ANTARCTICA

OpenAIRE

アオキ, シュウジ; ナカザワ, タカキヨ; ムラヤマ, ショウヘイ; シミズ, アキラ; ハヤシ, マサヒコ; イワイ, クニモト; Shuhji, AOKI; Takakiyo, NAKAZAWA; Shohei, MURAYAMA; Akira, SHIMIZU; Masahiko, HAYASHI; Kunimoto, IWAI

1994-01-01

Precise measurements of the atmospheric CO_2 and CH_4 concentrations have been continued at Syowa Station since 1984 and 1987,respectively. Measured concentrations show secular increase, together with seasonal cycle and irregular variations. Negative correlation is clearly seen between the secular trends of the CO_2 and CH_4 concentrations. The increase rates of CO_2 and CH_4 show oscillations with periods of 2.3 to 2.8 years. The phases of the average seasonal cycles of CO_2 and CH_4 coincid...

Atmospheric concentrations of persistent organic pollutants over the Pacific Ocean near southern Taiwan and the northern Philippines.

Science.gov (United States)

Chao, How-Ran; Lin, Ding-Yan; Chen, Kuang-Yu; Gou, Yan-Yu; Chiou, Tsyr-Huei; Lee, Wen-Jhy; Chen, Shui-Jen; Wang, Lin-Chi

2014-09-01

This study investigates the atmospheric occurrence of persistent organic pollutants (POPs) over the Pacific Ocean near southern Taiwan and the northern Philippines. We determined sixty-six compounds, including polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), dioxin-like polychlorinated biphenyls (DLPCBs), polybrominated diphenyl ethers (PBDEs), as well as polychlorinated diphenyl ethers (PCDEs), polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs), and polybrominated biphenyls (PBBs), in air samples simultaneously collected from the offshore oceanic atmosphere (n=6) and over a rural area (n=2). We calculated the atmospheric World Health Organization 2005 toxic equivalency levels (WHO2005-TEQ), for the total dioxin-like POPs, including PCDD/Fs, DLPCBs, and PBDD/Fs, being 0.00612 pg WHO2005-TEQ/m(3) and 0.0138 pg WHO2005-TEQ/m(3) over the ocean and land, respectively. We found unexpected lower averaged atmospheric PBDE concentrations in the rural area (15.9 pg/m(3)) than over the ocean (31.1 pg/m(3)) due to higher levels of the BDE209 congener, although the difference was not statistically significant. We have compared and reported our field results with previously published datasets over the global oceans, which suggest PCBs and PBDEs are the dominant chemical contaminants in the global oceanic atmosphere among these halogenated POPs (e.g. PCBs and Σdi-hepta PBDEs could be found in the range of 0.09-48.7 and 8.07-94.0 pg/m(3), respectively, including our dataset). However, there are still very few investigations on the global atmospheric levels of PBDD/Fs, PCDEs and PBBs and our data sums to these earlier studies. Finally, we point out that the halogenated POPs originated from Taiwan or the continental East Asia which could easily reach remote ocean sites via atmospheric transport. Copyright © 2014 Elsevier B.V. All rights reserved.

The measurement of airborne rodon daughter concentrations in the atmosphere

International Nuclear Information System (INIS)

Ha, C.W.; Lee, J.K.; Moon, P.S.

1979-01-01

A simple method for determining the airborne concentration of radon daughter products has been developed, which is based on gross alpha counting of the air filter collections at several time intervals after completion of air sampling. The concentration of each nuclide is then obtained from an equation involving the alpha disintegrations, the sampling time, and the known numerical coefficients. The state of radioactive disequilibrium is also inventigated. The atmosphere sampled in the TRIGA Mark-III reactor room was largely in disequilibrium. The extent of radioactive disequilibrium between radon daughter products seems likely depend on sampling times associated with turbulence conditions. The data obtained here will certainly provide useful information on the evaluation of internal exposure and calibration of effluent monitoring instruments. (author)

Atmospheric concentrations of halogenated flame retardants at two remote locations: The Canadian High Arctic and the Tibetan Plateau

International Nuclear Information System (INIS)

Xiao Hang; Shen Li; Su, Yushan; Barresi, Enzo; DeJong, Maryl; Hung, Hayley; Lei, Ying-Duan; Wania, Frank; Reiner, Eric J.; Sverko, Ed; Kang, Shi-Chang

2012-01-01

Atmospheric concentrations of halogenated flame retardants (FRs) were monitored for approximately one year at two remote stations, namely Nam Co on the Tibetan Plateau and Alert in the Canadian High Arctic. BDE-47 and 99 were the dominant polybrominated diphenyl ether (PBDE) congeners at both sites. Atmospheric PBDE concentrations in Nam Co were generally lower than those at Alert. While significant seasonal variations were observed for PBDEs at Alert, the FR concentrations at Nam Co showed no significant seasonality, even though air masses originated from distinctly different regions during different seasons. This suggests that FRs in Tibet do not have regional sources, but are reflective of truly global background contamination. Three new FRs, namely 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), 2-ethyl-1-hexyl-2,3,4,5-tetrabromobenzoate (EHTeBB) and bis(2-ethyl-1-hexyl)tetrabromophthalate (TBPH) were detected at relatively high concentrations at both sites. This is the first report of these FRs in the remote global atmosphere and suggests significant potential for long-range atmospheric transport. - Highlights: ► First year-round measurements of FRs in the atmosphere of the Tibetan Plateau. ► PBDEs in Tibet are reflective of truly global background levels. ► Orographic precipitation limits the transport of particle-bound chemicals. ► First study of BTBPE, EHTeBB and TBPH in the Arctic and Tibetan air. ► These new FRs may have significant long-range atmospheric transport potential. - Several brominated flame retardants (BTBPE, EHTeBB, TBPH) were present in the atmosphere of the Arctic and the Tibetan Plateau at levels similar to those of the PBDEs.

Atmospheric reactive nitrogen concentrations at ten sites with contrasting land use in an arid region of central Asia

Directory of Open Access Journals (Sweden)

K. H. Li

2012-10-01

Full Text Available Atmospheric concentrations of reactive nitrogen (N_r species from 2009 to 2011 are reported for ten sites in Xinjiang, China, an arid region of central Asia. Concentrations of NH₃, NO₂, particulate ammonium and nitrate (pNH₄⁺ and pNO₃⁻ showed large spatial and seasonal variation and averaged 7.71, 9.68, 1.81 and 1.13 μg N m⁻³, and PM₁₀ concentrations averaged 249.2 μg m⁻³ across all sites. Lower NH₃ concentrations and higher NO₂, pNH₄⁺ and pNO₃⁻ concentrations were found in winter, reflecting serious air pollution due to domestic heating in winter and other anthropogenic sources such as increased emissions from motor traffic and industry. The increasing order of total concentrations of N_r species was alpine grassland; desert, desert-oasis ecotone; desert in an oasis; farmland; suburban and urban ecosystems. Lower ratios of secondary particles (NH₄⁺ and NO₃⁻ were found in the desert and desert-oasis ecotone, while urban and suburban areas had higher ratios, which implied that anthropogenic activities have greatly influenced local air quality and must be controlled.

Atmospheric fate of poly- and perfluorinated alkyl substances (PFASs): I. Day–night patterns of air concentrations in summer in Zurich, Switzerland

International Nuclear Information System (INIS)

Müller, Claudia E.; Gerecke, Andreas C.; Bogdal, Christian; Wang, Zhanyun; Scheringer, Martin; Hungerbühler, Konrad

2012-01-01

Poly- and perfluorinated alkyl substances (PFASs) are anthropogenic pollutants ubiquitously found in the environment. Volatile PFASs are likely transported atmospherically over long ranges, but identification and quantification of emission sources is a challenging task. In this work, special meteorological conditions were utilized to quantify atmospheric emissions of Zurich City, Switzerland with a dual approach of modeling and field measurements. During high pressure systems in summer, a stable nocturnal boundary layer is formed in which pollutants are enriched. For volatile PFASs, a diel pattern of high concentrations in the night and low concentrations during the day was observed in Zurich, which is likely due to the atmospheric boundary layer dynamics. These results enable to model the emission source strength of Zurich City with a multimedia mass balance model in an accompanying paper. Cluster analyses suggested that perfluorocarboxylates (PFCAs) are a result of degradation of volatile precursors and direct emissions. - Highlights: ► Atmospheric PFAS concentrations in Zurich increase during the night. ► Diel concentration dynamics are likely due to stable nocturnal boundary layer. ► City is a source of PFASs to the atmosphere. ► 8:2 FTOH concentrations are high: up to 1200 pg/m 3 . ► PFAA concentrations are correlated with ozone, not particulate matter. - Semivolatile PFAS concentrations follow a diel trend in Zurich City in stable summer conditions likely due to atmospheric boundary layer effects and urban emissions.

A study on the environmental behavior of global air pollutants based on the continuous measurements of atmospheric radon concentrations

International Nuclear Information System (INIS)

Iida, Takao; Yamazawa, Hiromi

2003-01-01

Radon is a useful natural radioactive tracer of air transportation of atmospheric pollution, since radon is a noble gas and chemically inert. The atmospheric radon concentration is usually measured by a high-sensitivity electrostatic collection method or a two-filter method. The variations of radon concentrations observed over a solitary island and in the upper atmosphere are suitable for comparing with those of air pollutants. Some numerical simulation models were used to study the radon global transport in the atmosphere. In East Asia, atmospheric radon and air pollutants are transported with the air stream from the continent of China to the Northwestern Pacific Ocean. It is necessary to clarify the transport mechanism from both radon observations at various locations and numerical simulation. (author)

Study of the effects of atmospheric parameters on ground radon concentration by track technique

International Nuclear Information System (INIS)

Tidjani, Adams

1988-01-01

Radon emanation was continuously monitored for 24 months, accompanied by measurements of atmospheric parameters. Integrated measurments of radon concentrations have been performed with LR-115 cellulose nitrate track detectors. The monitoring was conducted at 16 sites distributed around the Dakar University area. Observed changes in radon concentration are interpreted as being caused by changes in meteorological conditions and ocean tides. (author)

HTO and OBT activity concentrations in soil at the historical atmospheric HT release site (Chalk River Laboratories)

International Nuclear Information System (INIS)

Kim, S.B.; Bredlaw, M.; Korolevych, V.Y.

2012-01-01

Tritium is routinely released by the Chalk River Laboratories (CRL) nuclear facilities. Three International HT release experiments have been conducted at the CRL site in the past. The site has not been disturbed since the last historical atmospheric testing in 1994 and presents an opportunity to assess the retention of tritium in soil. This study is devoted to the measurement of HTO and OBT activity concentration profiles in the subsurface 25 cm of soil. In terms of soil HTO, there is no evidence from the past HT release experiments that HTO was retained. The HTO activity concentration in the soil pore water appears similar to concentrations found in background areas in Ontario. In contrast, OBT activity concentrations in soil at the same site were significantly higher than HTO activity concentrations in soil. Elevated OBT appears to reside in the top layer of the soil (0–5 cm). In addition, OBT activity concentrations in the top soil layer did not fluctuate much with season, again, quite in contrast with soil HTO. This result suggests that OBT activity concentrations retained the signature of the historical tritium releases. Highlights: ► At the historical HT release site, HTO and OBT activity concentrations in soil depths were investigated. ► Most organically bound tritium exists in the top layer of the soil. ► The results indicated that OBT activity concentrations can be reflective of historical tritium releases into the environment.

Relationship between atmospheric ammonia concentration and nitrogen content in terricolous lichen (Cladonia portentosa)

DEFF Research Database (Denmark)

Nielsen, Knud Erik; Andersen, Helle Vibeke; Strandberg, Morten Tune

2014-01-01

From April 2006 to April 2007, the geographical and seasonal variation in nitrogen content in terricolous lichen (Cladonia portentosa) and atmospheric ammonia concentrations were measured at five heathland sites. The seasonal variation in the nitrogen content of the lichen was small, even though...... there was a large seasonal variation in the air concentration of ammonia. A sizable local variation in the nitrogen content of the lichen was found even at the scale of a few kilometres. The nitrogen content in the lichen showed a high correlation to the yearly mean value of the measured ammonia concentration...

Atmospheric Mercury Concentrations Near Salmon Falls Creek Reservoir - Phase 1

Energy Technology Data Exchange (ETDEWEB)

M. L. Abbott

2005-10-01

Elemental and reactive gaseous mercury (EGM/RGM) were measured in ambient air concentrations over a two-week period in July/August 2005 near Salmon Falls Creek Reservoir, a popular fishery located 50 km southwest of Twin Falls, Idaho. A fish consumption advisory for mercury was posted at the reservoir in 2002 by the Idaho Department of Health and Welfare. The air measurements were part of a multi-media (water, sediment, precipitation, air) study initiated by the Idaho Department of Environmental Quality and the U.S. Environmental Protection Agency (EPA) Region 10 to identify potential sources of mercury contamination to the reservoir. The sampling site is located about 150 km northeast of large gold mining operations in Nevada, which are known to emit large amounts of mercury to the atmosphere (est. 2,200 kg/y from EPA 2003 Toxic Release Inventory). The work was co-funded by the Idaho National Laboratory’s Community Assistance Program and has a secondary objective to better understand mercury inputs to the environment near the INL, which lies approximately 230 km to the northeast. Sampling results showed that both EGM and RGM concentrations were significantly elevated (~ 30 – 70%, P<0.05) compared to known regional background concentrations. Elevated short-term RGM concentrations (the primary form that deposits) were likely due to atmospheric oxidation of high EGM concentrations, which suggests that EGM loading from upwind sources could increase Hg deposition in the area. Back-trajectory analyses indicated that elevated EGM and RGM occurred when air parcels came out of north-central and northeastern Nevada. One EGM peak occurred when the air parcels came out of northwestern Utah. Background concentrations occurred when the air was from upwind locations in Idaho (both northwest and northeast). Based on 2003 EPA Toxic Release Inventory data, it is likely that most of the observed peaks were from Nevada gold mine sources. Emissions from known large natural mercury

Relationships between Atmospheric Transport Regimes and PCB Concentrations in the Air at Zeppelin, Spitsbergen.

Science.gov (United States)

Ubl, Sandy; Scheringer, Martin; Hungerbühler, Konrad

2017-09-05

Polychlorinated biphenyls (PCBs) are persistent hazardous chemicals that are still detected in the atmosphere and other environmental media, although their production has been banned for several decades. At the long-term monitoring site, Zeppelin at Spitsbergen, different PCB congeners have been continuously measured for more than a decade. However, it is not clear what factors determine the seasonal and interannual variability of different (lighter versus heavier) PCB congeners. To investigate the influence of atmospheric transport patterns on PCB-28 and PCB-101 concentrations at Zeppelin, we applied the Lagrangian Particle Dispersion Model FLEXPART and calculated "footprints" that indicate the potential source regions of air arriving at Zeppelin. By means of a cluster analysis, we assigned groups of similar footprints to different transport regimes and analyzed the PCB concentrations according to the transport regimes. The concentrations of both PCB congeners are affected by the different transport regimes. For PCB-101, the origin of air masses from the European continent is primarily related to high concentrations; elevated PCB-101 concentrations in winter can be explained by the high frequency of this transport regime in winter, whereas PCB-101 concentrations are low when air is arriving from the oceans. For PCB-28, in contrast, concentrations are high during summer when air is mainly arriving from the oceans but low when air is arriving from the continents. The most likely explanation of this finding is that local emissions of PCB-28 mask the effect of long-range transport and determine the concentrations measured at Zeppelin.

Trace element concentrations in higher fungi

International Nuclear Information System (INIS)

Byrne, A.R.; Ravnik, V.; Kosta, L.

1976-01-01

The concentrations of ten trace elements, As, Br, Cd, Cu, Hg, I, Mn, Se, Zn and V, have been determined in up to 27 species of higher fungi from several sites in Slovenia, Yugoslavia. Analyses were based on destructive neutron activation techniques. Data are presented and compared with the concentrations found in soils. Previously values were non-existent or scanty for these elements, so that the data represent typical levels for basidiomycetes. In addition to confirming high levels of mercury in many species, the survey also found that cadmium is accumulated to a surprising extent by most fungi, the average value being 5 ppm. Among other accumulations found was bromine by the genus Amanita, and selenium by edible Boletus. Correlation analysis between all pairs of trace elements gave values for r of from 0.75 to 0.43 for 7 pairs (Cu and Hg, 0.75; Se and As, 0.69). As well as these features of biochemical interest, the values found and the pattern of accumulation suggest potential uses of fungi in environmental studies

Concentrations of organochlorine pesticides, polybrominated diphenyl ethers and perfluorinated compounds in the atmosphere of North Greenland

DEFF Research Database (Denmark)

Bossi, Rossana; Vorkamp, Katrin; Skov, Henrik

2016-01-01

Atmospheric concentrations of organochlorine pesticides (OCPs), polybrominated diphenyl ethers (PBDEs) and neutral per- and polyfluoroalkyl substances (PFAS) have been measured at Villum Research Station, Station Nord (North Greenland) in the period 2008–2013. Atmospheric concentrations of OCPs...... for neutral PFAS we present for the first time a multiyear series of measurements for North Greenland. The average sum of the seven measured neutral PFAS (∑7PFAS) ranged from 1.82 to 32.1 pg m−3. The most abundant compound was 8:2 FTOH (44% of ∑7PFAS), followed by 6:2 FTOH and 10:2 FTOH. Perfluoroalkyl...

Concentrations of benzene, toluene, ethylbenzene and o-xylene in soil and atmospheric precipitations in the cities of Almaty and Astana

Directory of Open Access Journals (Sweden)

Dina Orazbayeva

2016-06-01

Full Text Available BTEX (benzene, toluene, ethylbenzene, xylene is one of the most dangerous groups of organic toxicants in terms of emissions and risks to public health. BTEX are present in almost all technogenic and natural objects. The greatest risk to public health is caused by BTEX contamination of cities characterized by high population densities and emissions to the environment. The aim of this work was to determine the concentrations of benzene, toluene, ethylbenzene and o-xylene in samples of soils and atmospheric precipitations selected in the cities of Almaty and Astana. Screening and quantification of analytes was performed by gas chromatography - mass spectrometry. Solid-phase microextraction was used for sample preparation. In the soil samples collected in the cities of Almaty and Astana, the concentrations of analytes ranged from 29.9 to 455 ng/g for benzene, from 9.9 to 375 ng/g for toluene, from 1.8 to 386 ng/g for ethylbenzene, and from 2.4 to 217 ng/g for o-xylene. Concentrations of BTEX in samples of atmospheric precipitations varied in the range of 8.2-21.2 ng/g for benzene; 0.8-5.1 ng/g for toluene; 0.1-1.1 ng/g for ethylbenzene; and 0.2-0.5 ng/g for o-xylene. BTEX concentrations in analyzed soil samples were in average ten times higher than those measured in European cities.

Atmospheric concentrations of 7Be and 210Pb in Granada, Spain

International Nuclear Information System (INIS)

Azahra, M.; Gonzalez-Gomez, C.; Instituto Andaluz de Ciencias de la Tierra, Granada; Lopez-Penalver, J.J.; Camacho-Garcia, M.A.; El Bardouni, T.; Boukhal, H.

2004-01-01

Aerosols samples in near-surface air of Granada (Spain) were collected on a weekly basis. The seasonal 210 Pb and 7 Be concentrations were determined during the five-year period, from October 1993 to September 1997. The elements, despite their different origin and their different distribution throughout the atmosphere, present the same seasonal variation. There was a tendency for a maximum during the summer season and a minimum during fall and/or winter. Concentration of 7 Be and 210 Pb and meteorological data have been used in order to determine the periods of the potential radioactive pollution. Deposition of 7 Be occurs primarily by precipitation except during the investigation periods where precipitation was scarce and irregular. (author)

Background concentrations and fluxes of atmospheric ammonia over a deciduous forest

DEFF Research Database (Denmark)

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

2015-01-01

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

Detection of atmospheric tritium by scintillation. Variations in its concentration in France

International Nuclear Information System (INIS)

Bibron, R.

1964-06-01

The tritium released into the atmosphere as a result of the explosion of thermonuclear devices is a useful radioactive tracer for the study of certain geophysical problems. The low concentrations found however call for the use of extremely sensitive detectors. Two detection methods using liquid scintillators are described. In the first method, the sample is introduced into the scintillator in liquid form, after prior concentration of the tritium by electrolysis. In the second method the tritium is incorporated into the scintillator solvent molecule by chemical synthesis. In the last part of the report are examined the variations in the tritium concentration in rain-water and of the free hydrogen in the air in France. A discussion is then made of the seasonal variations in the case of rain-water and these are compared to the variations in the strontium-90 concentrations. (author) [fr

Technical Note: Long-term memory effect in the atmospheric CO2 concentration at Mauna Loa

Directory of Open Access Journals (Sweden)

C. Varotsos

2007-01-01

Full Text Available The monthly mean values of the atmospheric carbon dioxide concentration derived from in-situ air samples collected at Mauna Loa Observatory, Hawaii, USA during 1958–2004 (the longest continuous record available in the world are analyzed by employing the detrended fluctuation analysis to detect scaling behavior in this time series. The main result is that the fluctuations of carbon dioxide concentrations exhibit long-range power-law correlations (long memory with lag times ranging from four months to eleven years, which correspond to 1/f noise. This result indicates that random perturbations in the carbon dioxide concentrations give rise to noise, characterized by a frequency spectrum following a power-law with exponent that approaches to one; the latter shows that the correlation times grow strongly. This feature is pointing out that a correctly rescaled subset of the original time series of the carbon dioxide concentrations resembles the original time series. Finally, the power-law relationship derived from the real measurements of the carbon dioxide concentrations could also serve as a tool to improve the confidence of the atmospheric chemistry-transport and global climate models.

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

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P. Shokri Ragheb

2016-07-01

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

Organic Nitrogen in Atmospheric Drops and Particles: Concentrations, (Limited) Speciation, and Chemical Transformations

Science.gov (United States)

Anastasio, C.; Zhang, Q.

2003-12-01

While quite a bit is known of the concentrations, speciation, and chemistry of inorganic forms of nitrogen in the atmosphere, the same cannot be said for organic forms. Despite this, there is growing evidence that organic N (ON) is ubiquitous in the atmosphere, especially in atmospheric condensed phases such as fog/cloud drops and aerosol particles. Although the major compounds that make up organic N are generally unknown, as are the sources of these compounds, it is clear that there are significant fluxes of ON between the atmosphere and ecosystems. It also appears that organic N can have significant effects in both spheres. The goal of our recent work in this area has been to better describe the atmospheric component of the biogeochemistry of organic nitrogen. Based on particle, gas, and fogwater samples from Northern California we have made three major findings: 1) Organic N represents a significant component, approximately 20%, of the total atmospheric N loading in these samples. This is broadly consistent with studies from other locations. 2) Amino compounds, primarily as combined amino acids, account for approximately 20% of the measured ON in our condensed phase samples. Given the properties of amino acids, these compounds could significantly affect the chemical and physical properties of atmospheric particles. 3) Organic nitrogen in atmospheric particles and drops is transformed to inorganic forms - primarily ammonium, nitrate, and nitrogen oxides (NOx) - during exposure to sunlight and/or ozone. These chemical reactions likely increase the bioavailability of the condensed phase nitrogen pool and enhance its biological effects after deposition to ecosystems.

The role and importance of ozone for atmospheric chemistry and methods for measuring its concentration

Directory of Open Access Journals (Sweden)

Marković Dragan M.

2003-01-01

Full Text Available Depending on where ozone resides, it can protect or harm life on Earth. The thin layer of ozone that surrounds Earth acts as a shield protecting the planet from irradiation by UV light. When it is close to the planet's surface, ozone is a powerful photochemical oxidant that damage, icons frescos, museum exhibits, rubber, plastic and all plant and animal life. Besides the basic properties of some methods for determining the ozone concentration in working and living conditions, this paper presents a detailed description of the electrochemical method. The basic properties of the electrochemical method are used in the construction of mobile equipment for determining the sum of oxidants in the atmosphere. The equipment was used for testing the determination of the ozone concentration in working rooms, where the concentration was at a high level and caused by UV radiation or electrostatic discharge. According to the obtained results, it can be concluded that this equipment for determining the ozone concentration in the atmosphere is very powerful and reproducible in measurements.

Analysis of atmospheric concentrations of radon and thoron using beta counting technique

International Nuclear Information System (INIS)

Islam, G.S.; Basunia, S.M.

1995-05-01

This paper presents a detailed theory and experimental procedure for measurement and analysis of mixed radon and thoron in the environment. The technique has been successfully applied to the study of seasonal variations of radon and thoron in Rajshahi atmosphere during the years 1989-1991. The maximum radon concentration in outdoor air was observed in the winter from December to January while the indoor radon concentration was found to be maximum during the monsoon months of July and August. The implication of results is briefly discussed in the paper. (author). 4 refs, 6 figs, 2 tabs

Qualitative aspects of biomonitoring: Sphagnum auriculatum response vs. aerosol metal concentrations (Pb, Ca, Cr, Cu, Fe, Mn, Ni and Zn) in the Porto urban atmosphere

International Nuclear Information System (INIS)

Teresa, M.; Vasconcelos, S.D.; Tavares Laquipai, H.M.F.

2000-01-01

Bags of S. auriculatum and a low-volume aerosol sampler provided with 0.8 μm pore size filters were exposed, in parallel, to the atmosphere of Porto, at different sampling points and in different periods of time, between 1991 and 1997. The levels of lead in the moss (weekly samples) and in the filters (daily samples) were determined by atomic absorption spectrophotometry and the results were compared. Living S. auriculatum exposed in bags to the Porto atmosphere died in several weeks (about a month), but continued to sorb metals from the atmosphere for about another month. In dry weather periods (relative humidity ≤ 76%) the rate of lead uptake by moss was approximately constant and proportional to the levels of the metal in atmospheric aerosols. A converting factor [CF=parallel-Pb-parallel moss (μg/g.day)/ parallel-Pb-parallel air (μg/m 3 )] allowed conversion of the lead levels in S. auriculatum to those in the atmospheric aerosols. Because the moss fixed lead from gas, aerosol and particulate matter, the rate of sorption depends markedly on the distance to the lead sources (mainly traffic) and on surrounding obstacles which retain particles. Therefore, specific calibration by mechanic monitoring, at each sampling point is required in a first stage of biomonitoring, when moss bag samplers are used to provide quantitative information about lead levels in the atmosphere. The mean Pb levels were ≤ 0.5 μg/m 3 and approximately constants at each sample point up to January 1996. After that date it decreased about 50%, in consequence of the reduction of the Pb concentration in leaded gasoline. In wet weather periods, higher but irregular rate of lead uptake was observed. In contrast, the lead levels in atmospheric aerosols decreased when the humidity increased due to wet deposition. Therefore, no proportionality between lead levels in the moss and in air were found. For about two months, in 1994, during a dry weather period, the levels of Ca, Cr, Cu, Fe, Mn, Ni

Atmospheric aerosol sampling campaign in Budapest and K-puszta. Part 1. Elemental concentrations and size distributions

International Nuclear Information System (INIS)

Dobos, E.; Borbely-Kiss, I.; Kertesz, Zs.; Szabo, Gy.; Salma, I.

2004-01-01

Complete text of publication follows. Atmospheric aerosol samples were collected in a sampling campaign from 24 July to 1 Au- gust, 2003 in Hungary. The sampling were performed in two places simultaneously: in Budapest (urban site) and K-puszta (remote area). Two PIXE International 7-stage cascade impactors were used for aerosol sampling with 24 hours duration. These impactors separate the aerosol into 7 size ranges. The elemental concentrations of the samples were obtained by proton-induced X-ray Emission (PIXE) analysis. Size distributions of S, Si, Ca, W, Zn, Pb and Fe elements were investigated in K-puszta and in Budapest. Average rates (shown in Table 1) of the elemental concentrations was calculated for each stage (in %) from the obtained distributions. The elements can be grouped into two parts on the basis of these data. The majority of the particle containing Fe, Si, Ca, (Ti) are in the 2-8 μm size range (first group). These soil origin elements were found usually in higher concentration in Budapest than in K-puszta (Fig.1.). The second group consisted of S, Pb and (W). The majority of these elements was found in the 0.25-1 μm size range and was much higher in Budapest than in K-puszta. W was measured only in samples collected in Budapest. Zn has uniform distribution in Budapest and does not belong to the above mentioned groups. This work was supported by the National Research and Development Program (NRDP 3/005/2001). (author)

[Atmospheric Polybrominated Diphenyl Ethers in Eight Cities of China: Pollution Characteristics and Human Exposure].

Science.gov (United States)

Lin, Hai-tao; Li, Qi-lu; Zhang, Gan; Li, Jun

2016-01-15

The gas and particle samples of eight cities were collected by high flow active air sampler in the Eastern and Western China and eight congeners of polybrominated diphenyl ethers were analyzed. The results showed that the concentration of BDE-28 (tri-BDE) in the gas-phase (three bromide components) was the highest, which was different from previous studies where BDE-99 and-47 were the predominant homologues in the gas-phase while the concentration of BDE-209 [(25.4 ± 124) pg · m⁻³] in particle-phase was the highest. The atmospheric concentrations of PBDEs in Beijing and Guangzhou were relatively higher, especially the BDE-209 concentration in particle phases of Guangzhou was two orders higher than those of other cities. However, the atmospheric concentrations of PBDEs declined significantly when compared with the data from previous studies. Meanwhile, the results indicated that the gas-phase concentrations decreased slowly and the particle-phase concentrations decreased rapidly. Combined with the results of correlation analysis, this phenomenon might be ascribed to the ceased commercial production of penta- and octa-BDE, the light degradation of high bromide components and reduced concentrations of atmospheric particles in urban area. Inhalation exposure for infants was about 2-3 times higher than that of adults. This reflected that the potential health risk of atmospheric PBDEs in city for residents, especially infants and young children, should not be ignored.

Growth under elevated atmospheric CO(2) concentration accelerates leaf senescence in sunflower (Helianthus annuus L.) plants.

Science.gov (United States)

de la Mata, Lourdes; Cabello, Purificación; de la Haba, Purificación; Agüera, Eloísa

2012-09-15

Some morphogenetic and metabolic processes were sensitive to a high atmospheric CO(2) concentration during sunflower primary leaf ontogeny. Young leaves of sunflower plants growing under elevated CO(2) concentration exhibited increased growth, as reflected by the high specific leaf mass referred to as dry weight in young leaves (16 days). The content of photosynthetic pigments decreased with leaf development, especially in plants grown under elevated CO(2) concentrations, suggesting that high CO(2) accelerates chlorophyll degradation, and also possibly leaf senescence. Elevated CO(2) concentration increased the oxidative stress in sunflower plants by increasing H(2)O(2) levels and decreasing activity of antioxidant enzymes such as catalase and ascorbate peroxidase. The loss of plant defenses probably increases the concentration of reactive oxygen species in the chloroplast, decreasing the photosynthetic pigment content as a result. Elevated CO(2) concentration was found to boost photosynthetic CO(2) fixation, especially in young leaves. High CO(2) also increased the starch and soluble sugar contents (glucose and fructose) and the C/N ratio during sunflower primary leaf development. At the beginning of senescence, we observed a strong increase in the hexoses to sucrose ratio that was especially marked at high CO(2) concentration. These results indicate that elevated CO(2) concentration could promote leaf senescence in sunflower plants by affecting the soluble sugar levels, the C/N ratio and the oxidative status during leaf ontogeny. It is likely that systemic signals produced in plants grown with elevated CO(2), lead to early senescence and a higher oxidation state of the cells of these plant leaves. Copyright © 2012 Elsevier GmbH. All rights reserved.

Atmospheric chlorinated polycyclic aromatic hydrocarbons in East Asia.

Science.gov (United States)

Kakimoto, Kensaku; Nagayoshi, Haruna; Konishi, Yoshimasa; Kajimura, Keiji; Ohura, Takeshi; Hayakawa, Kazuichi; Toriba, Akira

2014-09-01

This study estimates atmospheric concentrations of chlorinated polycyclic aromatic hydrocarbons (ClPAHs) and polycyclic aromatic hydrocarbons (PAHs) in East Asia using a Gas Chromatograph with High Resolution Mass Spectrometer (GC-HRMS). ClPAHs are ubiquitously generated from PAHs through substitution, and some ClPAHs show higher aryl hydrocarbon receptor (AhR)-mediated activities than their parent PAHs. Atmospheric particles were collected using a high-volume air sampler equipped with a quartz-fiber filter. We determined the ClPAH concentrations of atmospheric particles collected in Japan (Sapporo, Sagamihara, Kanazawa, and Kitakyushu), Korea (Busan), and China (Beijing). The concentrations of ClPAHs were highest in the winter Beijing sample, where the total mean concentration was approximately 15-70 times higher than in the winter samples from Japan and Korea. The concentrations of Σ19ClPAHs and Σ9PAHs were significantly correlated in the Kanazawa and the Busan samples. This indicates that within those cities ClPAHs and PAHs share the same origin, implying direct chlorination of parent PAHs. Toxic equivalent concentrations (TEQs) of the total ClPAHs and PAHs were lowest in Kanazawa in the summer, reaching 1.18 and 2610fg-TEQm(-3) respectively, and highest in Beijing in the winter, reaching 627 and 4240000fg-TEQm(-3) respectively. Copyright © 2014 Elsevier Ltd. All rights reserved.

Development of an atmospheric 214Bi measuring instrument

International Nuclear Information System (INIS)

1975-01-01

Part of the radiation environment encountered during airborne gamma ray surveys is produced by 214 Bi existing in the atmosphere. The 214 Bi atmospheric concentration changes with time and location, and should be measured to process the acquired data correctly. Three methods of atmospheric 214 Bi measurement are evaluated in this work. These are: (1) an 11 1 / 2 '' dia. x 4'' thick NaI(Tl) crystal shielded from ground radiation, (2) a negatively charged wire to collect radioactive ions, and (3) a high volume air sampler collecting particulate matter on filter paper. The shielded detector and filter paper methods yield good results with the shielded detector producing a factor of about 10 times higher counting rate. The charged wire method gave very low counting rates where the shielded detector counting rates were about a factor of 100 times higher, and the results did not correlate with the 214 Bi atmospheric concentration as determined by the other two methods. The theory necessary to understand the collection and decay of the airborne radioactivity using the charged wire and filter paper methods is developed

Correlations between atmospheric aerosol trace element concentrations and red tide at Port Aransas, Texas, on the Gulf of Mexico

International Nuclear Information System (INIS)

Biegalski, S.R.; Villareal, T.A.

2005-01-01

Neutron activation analysis (NAA) was employed as an analytical technique to measure atmospheric aerosol concentrations of trace metals in Port Aransas, TX on the Gulf of Mexico. The sources of atmospheric aerosols and the seasonal variation of the sources are explored. High atmospheric iron concentrations are then shown to have a possible correlation to the occurrences of red tide in this region. The data shows that this correlation is plausible, but due to the many factors that affect red tide growth a definitive conclusion may not be reached. The period of study for these measurements was September 12, 2000 to January 4, 2002. (author)

Double Compressions of Atmospheric Depth by Geopotential Tendency, Vorticity, and Atmospheric Boundary Layer Affected Abrupt High Particulate Matter Concentrations at a Coastal City for a Yellow Dust Period in October

Directory of Open Access Journals (Sweden)

Hyo Choi

2014-01-01

Full Text Available Using GRIMM-aerosol sampler, NOAA-HYSPLIT model, and 3D-WRF-3.3 model, the transportation of dusts from Gobi Desert toward Gangneung city, Korea was investigated from 09:00 LST October 27 to 04:00 LST October 28, 2003. Maximum PM10 (PM2.5, PM1 concentration was detected with 3.8 (3.4, 14.1 times higher magnitude than one in non-Yellow Dust period. The combination of dusts transported from the desert under westerly wind with particulate matters and gases from vehicles on the road of the city caused high PM concentrations near the ground surface at 09:00 LST and their maxima at 17:00 LST near sunset with further pollutants from heating boilers in the resident area. Positive geopotential tendency at the 500 hPa level of the city (∂Φ/∂t; m day−1 corresponding to negative vorticity of -4×10-5 sec−1 (-2.5×10-5 sec−1 at 0900 LST (21:00 LST; at night was +83 m day−1 (+30 m day−1 and it caused atmospheric depth between 500 hPa level and the ground surface to be vertically expanded. However, its net reduction to −53 m/12 hrs until 21:00 LST indicated synoptic-scale atmospheric layer to be vertical shrunken, resulting in the increase of PM concentrations at 17:00 LST. Simultaneously, much shallower microscale stable nocturnal surface inversion layer (NSIL than daytime thermal internal boundary layer induced particulate matters to be merged inside the NSIL, resulting in maximum PM concentrations at 17:00 LST.

Large-scale coherent structures of suspended dust concentration in the neutral atmospheric surface layer: A large-eddy simulation study

Science.gov (United States)

Zhang, Yangyue; Hu, Ruifeng; Zheng, Xiaojing

2018-04-01

Dust particles can remain suspended in the atmospheric boundary layer, motions of which are primarily determined by turbulent diffusion and gravitational settling. Little is known about the spatial organizations of suspended dust concentration and how turbulent coherent motions contribute to the vertical transport of dust particles. Numerous studies in recent years have revealed that large- and very-large-scale motions in the logarithmic region of laboratory-scale turbulent boundary layers also exist in the high Reynolds number atmospheric boundary layer, but their influence on dust transport is still unclear. In this study, numerical simulations of dust transport in a neutral atmospheric boundary layer based on an Eulerian modeling approach and large-eddy simulation technique are performed to investigate the coherent structures of dust concentration. The instantaneous fields confirm the existence of very long meandering streaks of dust concentration, with alternating high- and low-concentration regions. A strong negative correlation between the streamwise velocity and concentration and a mild positive correlation between the vertical velocity and concentration are observed. The spatial length scales and inclination angles of concentration structures are determined, compared with their flow counterparts. The conditionally averaged fields vividly depict that high- and low-concentration events are accompanied by a pair of counter-rotating quasi-streamwise vortices, with a downwash inside the low-concentration region and an upwash inside the high-concentration region. Through the quadrant analysis, it is indicated that the vertical dust transport is closely related to the large-scale roll modes, and ejections in high-concentration regions are the major mechanisms for the upward motions of dust particles.

Atmospheric concentrations, distributions and air-soil exchange tendencies of PAHs and PCBs in a heavily industrialized area in Kocaeli, Turkey.

Science.gov (United States)

Cetin, Banu; Yurdakul, Sema; Keles, Melek; Celik, Isil; Ozturk, Fatma; Dogan, Cevdet

2017-09-01

Dilovasi is one of the heavily industrialized areas in Turkey with serious environmental problems. In this study, the atmospheric concentration of PAHs and PCBs were measured for a whole year at 23 sites. The average ambient air Σ 15 PAH and Σ 41 PCB concentrations were found as 285 ± 431 ng m -3 and 4152 ± 6072 pg m -3 , respectively. PAH concentrations increased with decreasing temperature especially in urban areas, indicating the impact of residential heating. However, PCB concentrations mostly increased with temperature probably due to enhanced volatilization from their sources. The gradient obtained for PCBs, rural air were higher in industrial-urban areas than rural sites, showing that soil was a secondary source for PAHs. Fugacity ratios of PCBs were mostly <1.0 for the whole sampling period. Although the source/sink tendency of soil for some PCBs depends on their volatility, considering the whole data, PCBs were generally deposited to soil. Copyright © 2017 Elsevier Ltd. All rights reserved.

Corrosion of bismuth-based superconductor wires by some atmospheric agents

International Nuclear Information System (INIS)

Ben Azzouz, F.; M'chirgui, A.; Ben Salem, M.; Yangui, B.; Lamine, C.; Nitsche, S.; Boulesteix, C.

2000-01-01

Superconducting wires (SWs) were previously prepared in our group by heat treatment of bismuth-based superconductor coatings on a metal core. This paper presents an analysis of the corrosion process by some atmospheric agents on the SWs. SWs with different concentrations of a (Bi, Pb)-2223 phase have been exposed to water vapour saturated air, to pure water vapour or to dry carbon dioxide. Each of these atmospheric agents was found to act differently on the SWs. However, all the studied corrosion processes present a high sensitivity to the concentration of the (Bi, Pb)-2223 phase. For a higher concentration of this phase, the SWs are less sensitive to atmospheric agents. (author)

Prediction on long-term mean and mean square pollutant concentrations in an urban atmosphere

Energy Technology Data Exchange (ETDEWEB)

Kumar, S; Lamb, R G; Seinfeld, J H

1976-01-01

The general problem of predicting long-term average (say yearly) pollutant concentrations in an urban atmosphere is formulated. The pollutant concentration can be viewed as a random process, the complete description of which requires knowledge of its probability density function, which is unknown. The mean concentration is the first moment of the concentration distribution, and at present there exist a number of models for predicting the long-term mean concentration of an inert pollutant. The second moment, or mean square concentration, indicates additional features of the distribution, such as the level of fluctuations about the mean. In the paper a model proposed by Lamb for the long-term mean concentration is reviewed, and a new model for prediction of the long-term mean square concentration of an inert air pollutant is derived. The properties and uses of the model are discussed, and the equations defining the model are presented in a form for direct application to an urban area.

Comparison of atmospheric concentrations of sulphur and nitrogen compounds, chloride and base cations at Ahtari and Hyytiala, Finland

Energy Technology Data Exchange (ETDEWEB)

Ruoho-Airola, T. [Finnish Meteorological Institute, Helsinki (Finland)

2012-11-01

Seven-year (2003-2009) time series of atmospheric SO{sub 2}, SO{sub 4}{sup 2-}, NO{sub 3}-, NH{sub 4}{sup +} and Cl{sup -} concentrations as well as four-year time series of atmospheric Na{sup +}, K{sup +}, Ca{sup 2+} and Mg{sup 2+} concentrations from Ahtari and Hyytiala background stations in southern Finland, located within 85 km of each other were compared. At Ahtari the air sampler was located in a clearing within a young forest, while at Hyytiala it was within dense forest stands. Pearson's correlations between the time series were very strong (r{sub P} {>=} 0.9) for SO{sub 2}, SO{sub 4}{sup 2-}, NO{sub 3}{sup -}, NH{sub 4}{sup +}, Cl{sup -} and Ca{sup 2+}, strong (r{sub P} > 0.8) for Na{sup +} and Mg{sup 2+} and week (r{sub P} = 0.65) for K{sup +}. The concentrations recorded at Hyytiala were on average 0.8-1.0 times those at Ahtari, although for K{sup +} and Ca{sup 2+} the ratios were higher. The GLS-ARMA method used takes into account the seasonal behaviour and serial correlation in the air quality time series, which revealed similar seasonal and temporal behaviour for S and N compounds and Cl- at both stations. As a result of the dense seasonalization of the time series, the part of the data heavily influenced by local agricultural sources could be identified. This enables elimination of the minimal part of the data affected and the use of the remaining data for further studies on a more regional level. (orig.)

RISING ATMOSPHERIC CO2 AND CARBON SEQUESTRATION IN FORESTS

Science.gov (United States)

Rising CO2 concentrations in the Earth's atmosphere could alter Earth's climate system, but it is thought that higher concentrations may improve plant growth by way of the fertilization effect. Forests, an important part of the Earth's carbon cycle, are postulated to sequester a...

Evaluation of atmospheric particulate concentrations derived from analysis of ratio Thematic Mapper data

Science.gov (United States)

Carnahan, W. H.; Mausel, P. W.; Zhou, G. P.

1984-01-01

An approach for atmospheric particulate concentration evaluation above urban areas using ratio Thematic Mapper (TM) data is discussed. October 25, 1982 TM data over Chicago, IL are analyzed using TM band ratios of 1/2, 1/3, 1/4, 1/5, and 1/6 and particulate concentration estimates derived from TM ratios are tested over low reflective turbid water sites and highly reflective concrete highways. From analysis of the data it is evident that for water, the pattern of increasing particulate concentration is associated with decreasing ratio values in all band combinations used. Over concrete features, the TM band 1/4 ratio values follow the predicted pattern, while the TM band 1/6 has ratios which are reversed from anticipated values.

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

Relative effects of climate and source strength on atmospheric lead concentrations in Auckland, New Zealand

Science.gov (United States)

Power, H. C.; de Freitas, C. R.; Hay, J. E.

1992-06-01

Atmospheric lead levels were examined to assess the consequences of the 46 percent reduction in the lead content of premium grade petrol in New Zealand. Since this change was implemented in July 1986 observed levels of atmospheric lead decreased by 38 percent, but all or part of this reduction may have been due to factors other than fluctuations in lead emissions, notably variations in climate. Analysis of detailed atmospheric lead, meteorological and traffic data measured contemporaneously provided insight into the atmospheric processes influencing lead levels in Auckland and formed the basis of a statistical model capable of predicting monthly lead concentrations. The model was used to predict lead levels in Auckland for the period July 1986 through to July 1989 in the absence of any reduction in the lead content of petrol. Comparison with values observed for the same period showed that all of the reduction in atmospheric lead levels since July 1986 can be attributed to the reduction in the lead content of petrol. Policy planning implications of such a finding are considered.

Observed atmospheric total column ozone distribution from SCIAMACHY over Peninsular Malaysia

International Nuclear Information System (INIS)

Chooi, T K; San, L H; Jafri, M Z M

2014-01-01

The increase in atmospheric ozone has received great attention because it degrades air quality and brings hazard to human health and ecosystems. The aim of this study was to assess the seasonal variations of ozone concentrations in Peninsular Malaysia from January 2003 to December 2009 using Scanning Imaging Absorption Spectrometer for Atmospheric Cartography (SCIAMACHY). Level-2 data of total column ozone WFMD version 1.0 with spatial resolution 1° × 1.25° were acquired through SCIAMACHY. Analysis for trend of five selected sites exhibit strong seasonal variation in atmospheric ozone concentrations, where there is a significant difference between northeast monsoon and southwest monsoon. The highest ozone values occurred over industrial and congested urban zones (280.97 DU) on August at Bayan Lepas. The lowest ozone values were observed during northeast monsoon on December at Subang (233.08 DU). In addition, the local meteorological factors also bring an impact on the atmospheric ozone. During northeast monsoon, with the higher rate of precipitation, higher relative humidity, low temperature, and less sunlight hours let to the lowest ozone concentrations. Inversely, the highest ozone concentrations observed during southwest monsoon, with the low precipitation rate, lower relative humidity, higher temperature, and more sunlight hours. Back trajectories analysis is carried out, in order to trace the path of the air parcels with high ozone concentration event, suggesting cluster of trajectory (from southwest of the study area) caused by the anthropogenic sources associated with biogenic emissions from large tropical forests, which can make important contribution to regional and global pollution

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.

Radiation-use of a forest exposed to elevated concentrations of atmospheric carbon dioxide

International Nuclear Information System (INIS)

DeLucia, E. H.; George, K.; Hamilton, J. G.

2002-01-01

Radiation-use efficiency of growth (defined as biomass accumulation per unit of absorbed photosynthetically active radiation) of loblobby pine forest plots exposed to ambient or elevated atmospheric carbon dioxide concentration was compared. Biomass accumulation of the dominant loblobby pines was calculated from monthly measurements of tree growth and site-specific allometric measurements. Leaf area index was estimated by optical, allometric and interfall methods, depending on species. Results showed that depending on tree height, elevated carbon dioxide did not alter the above-ground biomass allocation in loblobby pine. Leaf area index estimates by the different methods were found to vary significantly, but elevated carbon dioxide had only a slight effect on leaf area index in the first three years of this study. The 27 per cent increase in radiation-use efficiency of growth in response to carbon dioxide enrichment is believed to have been caused primarily by the stimulation of biomass increment. It was concluded that long-term increases in atmospheric carbon dioxide concentration can increase the radiation-use efficiency of growth in closed canopy forests, but the magnitude and duration of this increase in uncertain. 57 refs., 2 tabs., 3 figs

Optical remote sensing of properties and concentrations of atmospheric trace constituents

Science.gov (United States)

Vladutescu, Daniela Viviana

The effect of human activities on the global climate may lead to large disturbances of the economic, social and political circumstances in the middle and long term. Understanding the dynamics of the Earth's climate is therefore of high importance and one of the major scientific challenges of our time. The estimation of the contribution of the Earth's climate system components needs observation and continuous monitoring of various atmospheric physical and chemical parameters. Temperature, water vapor and greenhouse gases concentration, aerosol and clouds loads, and atmospheric dynamics are parameters of particular importance in this respect. The quantification of the anthropogenic influence on the dynamics of these above-mentioned parameters is of crucial importance nowadays but still affected by significant uncertainties. In the present context of these huge uncertainties in our understanding of how these different atmospheric compounds contribute to the radiative forcing, a significant part of my research interest is related to the following topics: (1) Development of lidar (Light Detection and Ranging)-based remote sensing techniques for monitoring atmospheric compounds and processes; (2) Aerosols hygroscopic properties and atmospheric modeling; (3) Water vapor mixing ratio and relative humidity estimation in the troposphere; (4) Characterization of the long-range transported aerosols; (5) Ambient gases detection using Fourier Transform Interferometers (FTIR); (6) Design of inexpensive Fabry Perot Interferometer for visible and near infrared for land and ocean surface remote sensing applications. The lidar-based remote sensing measurement techniques for the monitoring of climate change parameters where implemented at the City College of the City University of New York (CCNY/CUNY) LIDAR station and are presented in the second section of the paper. The geographical location of the CCNY lidar station is 40.86N, -73.86W. Among the lidar retrievals one important

Impact of marine mercury cycling on coastal atmospheric mercury concentrations in the North- and Baltic Sea region

Directory of Open Access Journals (Sweden)

Johannes Bieser

2016-06-01

Full Text Available Abstract The cycling of mercury between ocean and atmosphere is an important part of the global Hg cycle. Here we study the regional contribution of the air-sea exchange in the North- and Baltic Sea region. We use a newly developed coupled regional chemistry transport modeling (CTM system to determine the flux between atmosphere and ocean based on the meteorological model COSMO-CLM, the ocean-ecosystem model ECOSMO, the atmospheric CTM CMAQ and a newly developed module for mercury partitioning and speciation in the ocean (MECOSMO. The model was evaluated using atmospheric observations of gaseous elemental mercury (GEM, surface concentrations of dissolved gaseous mercury (DGM, and air-sea flux (ASF calculations based on observations made on seven cruises in the western and central Baltic Sea and three cruises in the North Sea performed between 1991 and 2006. It was shown that the model is in good agreement with observations: DGM (Normalized Mean Bias NMB=-0.27 N=413, ASF (NMB=-0.32, N=413, GEM (NMB=0.07, N=2359. Generally, the model was able to reproduce the seasonal DGM cycle with the best agreement during winter and autumn (NMBWinter=-0.26, NMBSpring=-0.41, NMBSummer=-0.29, NMBAutumn=-0.03. The modelled mercury evasion from the Baltic Sea ranged from 3400 to 4000 kg/a for the simulation period 1994–2007 which is on the lower end of previous estimates. Modelled atmospheric deposition, river inflow and air-sea exchange lead to an annual net Hg accumulation in the Baltic Sea of 500 to 1000 kg/a. For the North Sea the model calculates an annual mercury flux into the atmosphere between 5700 and 6000 kg/a. The mercury flux from the ocean influenced coastal atmospheric mercury concentrations. Running CMAQ coupled with the ocean model lead to better agreement with GEM observations. Directly at the coast GEM concentrations could be increased by up to 10% on annual average and observed peaks could be reproduced much better. At stations 100km downwind

The influence of small-scale variations in isoprene concentrations on atmospheric chemistry over a tropical rainforest

Directory of Open Access Journals (Sweden)

T. A. M. Pugh

2011-05-01

Full Text Available Biogenic volatile organic compounds (BVOCs such as isoprene constitute a large proportion of the global atmospheric oxidant sink. Their reactions in the atmosphere contribute to processes such as ozone production and secondary organic aerosol formation. However, over the tropical rainforest, where 50 % of the global emissions of BVOCs are believed to occur, atmospheric chemistry models have been unable to simulate concurrently the measured daytime concentration of isoprene and that of its principal oxidant, hydroxyl (OH. One reason for this model-measurement discrepancy may be incomplete mixing of isoprene within the convective boundary layer, leading to patchiness or segregation in isoprene and OH mixing ratios and average concentrations that appear to be incompatible with each other. One way of capturing this effect in models of atmospheric chemistry is to use a reduced effective rate constant for their reaction. Recent studies comparing atmospheric chemistry global/box models with field measurements have suggested that this effective rate reduction may be as large as 50 %; which is at the upper limit of that calculated using large eddy simulation models. To date there has only been one field campaign worldwide that has reported co-located measurements of isoprene and OH at the necessary temporal resolution to calculate the segregation of these compounds. However many campaigns have recorded sufficiently high resolution isoprene measurements to capture the small-scale fluctuations in its concentration. Assuming uniform distributions of other OH production and loss processes, we use a box model of atmospheric chemistry, constrained by the spectrum of isoprene concentrations measured, as a virtual instrument, to estimate the variability in OH at a point and hence, to estimate the segregation intensity of isoprene and OH from high-frequency isoprene time series. The method successfully reproduces the only directly observed segregation, using

Historical record of concentrations of atmospheric trace components deduced from a glacier in the Alps

International Nuclear Information System (INIS)

Doescher, A.

1996-07-01

A 109 m ice core from a high-alpine glacier (Colle Gnifetti, Monte Rosa massif, 4440 m a.s.l., Switzerland) was used to reconstruct the history of atmospheric trace components. Concentrations of the anions chloride, nitrate, sulfate and the cations sodium, ammonium, potassium, magnesium and calcium were measured with 2.5-5.0 cm resolution in the top 70 m of a 109 m long of the ice core. Dating of the ice core was performed using stratigraphic markers such as historically known Saharan dust events, the atomic bomb horizon and volcanic eruptions and supplemented with the 210 Pb nuclear dating. The record covers the time period from about 1755-1981. The concentrations of nitrate and sulfate show an exponential increase from 1930 and 1870 until 1965, respectively. The factors of increase were 2.3±0.3 and 5.8±0.9, respectively. The chloride concentrations remained constant during this period. A good agreement between the concentrations of sulfate, which were corrected for the contribution of seasalt and mineral dust and the European SO 2 -emissions was found for the last 100 years. The concentrations of sodium, potassium, magnesium and calcium did not show a trend. The concentrations of ammonium increased exponentially between 1870 and 1960 by a factor of 2.2±0.4. The different sources of the trace components were identified using correlation analysis. Sodium and chloride originated from seasalt, magnesium and calcium from geologic erosion. For both, the industrial and pre-industrial period, the dominant source of ammonium and nitrate was conversion of the gaseous precursors NH 3 and HNO 3 . Sulfate concentrations in the industrial period originated from the anthropogenically emitted SO 2 , whereas in the pre-industrial period the geologic source dominated. The Colle Gnifetti accumulates mainly summer snow, and therefore, several test drillings were performed to find a new site with higher accumulation rate. (author) figs., 17 tabs., 50 refs

Atmospheric concentrations of organochlorine pesticides, polybrominated diphenyl ethers and polychloronaphthalenes in Nuuk, South-West Greenland

Science.gov (United States)

Bossi, Rossana; Skov, Henrik; Vorkamp, Katrin; Christensen, Jesper; Rastogi, Suresh C.; Egeløv, Axel; Petersen, Dorthe

Atmospheric concentrations of organochlorine pesticides (OCs), polybrominated diphenyl ethers (PBDEs) and polychloronaphthalenes (PCNs) were measured for the first time in Nuuk, Greenland in 2004 and 2005. The annual mean concentrations of the measured OCs were: α-HCH 20.2 pg m -3, γ-HCH (lindane) 5.1 pg m -3, endosulfan 4.8 pg m -3 and dieldrin 1.9 pg m -3. Concentrations of Σ-chlordanes, DDEs and heptachlor epoxide were generally similar and lower than those of α-HCH and γ-HCH. The concentrations of most chlorinated pesticides did not show any clear seasonal variation, with the exception of γ-HCH, which had maximum concentration in August in both years. The average annual mean for ΣPBDEs was 1.14 ± 0.81 pg m -3. The predominant congeners measured in Nuuk were BDE-47 and BDE-99 followed by BDE-100, -153 and -28, indicating the use of penta-BDE technical products as the main source. A clear seasonal variation of PBDE concentrations was observed with maximum concentrations occurring in the summer months. The ΣPCNs concentrations ranged between 0.062 and 0.258 pg m -3 with an annual mean concentration of 0.161 ± 0.004 pg m -3. The PCNs profile was dominated by the tetra-PCNs (74% of the annual mean) and the penta-PCNs (18% of the annual mean). A seasonal trend for ΣPCNs was not observed. Atmospheric concentrations of the investigated compounds were correlated with temperature and anthropogenic CO in order to obtain information about their transport pattern. Positive correlations were found between CO and chlordanes, p, p'-DDE and trifluralin, while a negative correlation was found for γ-HCH. A significant correlation with temperature variations was found for dieldrin, heptachlor epoxide, α-HCH, γ-HCH, BDE-47, BDE-99 and tetra-PCNs, which indicates that re-emission of these compounds from previously contaminated surfaces as an important factor for the observed variations in concentrations.

Effects of atmospheric composition on respiratory behavior, weight loss, and appearance of Camembert-type cheeses during chamber ripening.

Science.gov (United States)

Picque, D; Leclercq-Perlat, M-N; Corrieu, G

2006-08-01

Respiratory activity, weight loss, and appearance of Camembert-type cheeses were studied during chamber ripening in relation to atmospheric composition. Cheese ripening was carried out in chambers under continuously renewed, periodically renewed, or nonrenewed gaseous atmospheres or under a CO(2) concentration kept constant at either 2 or 6% throughout the chamber-ripening process. It was found that overall atmospheric composition, and especially CO(2) concentration, of the ripening chamber affected respiratory activity. When CO(2) was maintained at either 2 or 6%, O(2) consumption and CO(2) production (and their kinetics) were higher compared with ripening trials carried out without regulating CO(2) concentration over time. Global weight loss was maximal under continuously renewed atmospheric conditions. In this case, the airflow increased exchanges between cheeses and the atmosphere. The ratio between water evaporation and CO(2) release also depended on atmospheric composition, especially CO(2) concentration. The thickening of the creamy underrind increased more quickly when CO(2) was present in the chamber from the beginning of the ripening process. However, CO(2) concentrations higher than 2% negatively influenced the appearance of the cheeses.

Contributions of Organic Sources to Atmospheric Aerosol Particle Concentrations and Growth

Science.gov (United States)

Russell, L. M.

2017-12-01

Organic molecules are important contributors to aerosol particle mass and number concentrations through primary emissions as well as secondary growth in the atmosphere. New techniques for measuring organic aerosol components in atmospheric particles have improved measurements of this contribution in the last 20 years, including Scanning Transmission X-ray Microscopy Near Edge X-ray Absorption Fine Structure (STXM-NEXAFS), Fourier Transform Infrared spectroscopy (FTIR), and High-Resolution Aerosol Mass Spectrometry (AMS). STXM-NEXAFS individual aerosol particle composition illustrated the variety of morphology of organic components in marine aerosols, the inherent relationships between organic composition and shape, and the links between atmospheric aerosol composition and particles produced in smog chambers. This type of single particle microscopy has also added to size distribution measurements by providing evidence of how surface-controlled and bulk-controlled processes contribute to the growth of particles in the atmosphere. FTIR analysis of organic functional groups are sufficient to distinguish combustion, marine, and terrestrial organic particle sources and to show that each of those types of sources has a surprisingly similar organic functional group composition over four different oceans and four different continents. Augmenting the limited sampling of these off-line techniques with side-by-side inter-comparisons to online AMS provides complementary composition information and consistent quantitative attribution to sources (despite some clear method differences). Single-particle AMS techniques using light scattering and event trigger modes have now also characterized the types of particles found in urban, marine, and ship emission aerosols. Most recently, by combining with off-line techniques, single particle composition measurements have separated and quantified the contributions of organic, sulfate and salt components from ocean biogenic and sea spray

Atmospheric CO{sub 2}, trace gas and CN concentrations in Vaerrioe

Energy Technology Data Exchange (ETDEWEB)

Ahonen, T; Aalto, P; Kulmala, M; Rannik, U; Vesala, T [Helsinki Univ. (Finland). Dept. of Physics; Hari, P; Pohja, T [Helsinki Univ. (Finland). Dept. of Forest Ecology

1996-12-31

The Vaerrioe environmental measurement station is founded in 1991. The aim of the station is to obtain more information on air quality influenced by Kola industrial areas and effects of pollutants on photosynthesis in subarctic climate. In the station air quality and meteorological quantities are measured together with photosynthesis, which makes it quite unique in comparison with other measurement stations located in northern Finland. The measurements also provide information of aerosol and trace gas concentrations in order to study the direct and indirect aerosol effects on climate. These measurements also increase the knowledge of atmospheric chemistry and deposition in subarctic conditions

Atmospheric CO{sub 2}, trace gas and CN concentrations in Vaerrioe

Energy Technology Data Exchange (ETDEWEB)

Ahonen, T.; Aalto, P.; Kulmala, M.; Rannik, U.; Vesala, T. [Helsinki Univ. (Finland). Dept. of Physics; Hari, P.; Pohja, T. [Helsinki Univ. (Finland). Dept. of Forest Ecology

1995-12-31

The Vaerrioe environmental measurement station is founded in 1991. The aim of the station is to obtain more information on air quality influenced by Kola industrial areas and effects of pollutants on photosynthesis in subarctic climate. In the station air quality and meteorological quantities are measured together with photosynthesis, which makes it quite unique in comparison with other measurement stations located in northern Finland. The measurements also provide information of aerosol and trace gas concentrations in order to study the direct and indirect aerosol effects on climate. These measurements also increase the knowledge of atmospheric chemistry and deposition in subarctic conditions

Surface ozone concentrations in Europe: Links with the regional-scale atmospheric circulation

Science.gov (United States)

Davies, T. D.; Kelly, P. M.; Low, P. S.; Pierce, C. E.

1992-06-01

Daily surface ozone observations from 1978 (1976 for some analyses) to 1988 for Bottesford (United Kingdom), Cabauw, Kloosterburen (The Netherlands), Hohenpeissenberg, Neuglobsow, Hamburg, and Arkona (Germany) are used to analyze links between surface ozone variations and the atmospheric circulation. A daily Europe-wide synoptic classification highlights marked differences between surface ozone/meteorology relationships in summer and winter. These relationships are characterized by correlations between daily surface ozone concentrations at each station and a local subregional surface pressure gradient (a wind speed index). Although there are geographical variations, which are explicable in terms of regional climatology, there are distinct annual cycles. In summer, the surface ozone/wind speed relationship exhibits the expected negative sign; however, in winter, the relationship is, in the main, strongly positive, especially at those stations which are more influenced by the vigorous westerlies. Spring and autumn exhibit negative, positive, or transitional (between summer and winter) behavior, depending on geographical position. It is suggested that these relationships reflect the importance of vertical exchange from the free troposphere to the surface in the nonsummer months. Composite surface pressure patterns and surface pressure anomaly (from the long-term mean) patterns associated with high surface ozone concentrations on daily and seasonal time scales are consistent with the surface ozone/wind speed relationships. Moreover, they demonstrate that high surface ozone concentrations, in a climatological time frame, can be associated with mean surface pressure patterns which have a synoptic reality and are robust. Such an approach may be useful in interpreting past variations in surface ozone and may help to isolate the effect of human activity. It is also possible that assessments can be made of the effect of projected future changes in the atmospheric circulation

Atmospheric mercury deposition to forests in the eastern USA.

Science.gov (United States)

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

2017-09-01

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

The sensitivity of stand-scale photosynthesis and transpiration to changes in atmospheric CO2 concentration and climate

Science.gov (United States)

Kruijt, B.; Barton, C.; Rey, A.; Jarvis, P. G.

The 3-dimensional forest model MAESTRO was used to simulate daily and annual photosynthesis and transpiration fluxes of forest stands and the sensitivity of these fluxes to potential changes in atmospheric CO2 concentration ([CO2]), temperature, water stress and phenology. The effects of possible feed-backs from increased leaf area and limitations to leaf nutrition were simulated by imposing changes in leaf area and nitrogen content. Two different tree species were considered: Picea sitchensis (Bong.) Carr., a conifer with long needle longevity and large leaf area, and Betula pendula Roth., a broad-leaved deciduous species with an open canopy and small leaf area. Canopy photosynthetic production in trees was predicted to increase with atmospheric [CO2] and length of the growing season and to decrease with increased water stress. Associated increases in leaf area increased production further only in the B. pendula canopy, where the original leaf area was relatively small. Assumed limitations in N uptake affected B. pendula more than P. sitchensis. The effect of increased temperature was shown to depend on leaf area and nitrogen content. The different sensitivities of the two species were related to their very different canopy structure. Increased [CO2] reduced transpiration, but larger leaf area, early leaf growth, and higher temperature all led to increased water use. These effects were limited by feedbacks from soil water stress. The simulations suggest that, with the projected climate change, there is some increase in stand annual `water use efficiency', but the actual water losses to the atmosphere may not always decrease.

Measuring atmospheric ammonia with remote sensing campaign: Part 1 - Characterisation of vertical ammonia concentration profile in the centre of The Netherlands

Science.gov (United States)

Dammers, E.; Schaap, M.; Haaima, M.; Palm, M.; Wichink Kruit, R. J.; Volten, H.; Hensen, A.; Swart, D.; Erisman, J. W.

2017-11-01

Ammonia (NH3) is difficult to monitor at atmospheric concentrations due its high solubility and reactivity and the strong spatial and temporal variations of its concentrations. Monitoring is mostly performed using passive samplers or filter packs with daily coverage at best. Only at a few sites ammonia is measured with more expensive wet chemical or spectroscopic measurement techniques. Instruments using an open path show the most potential as these avoid the use of inlets and thus the interactions of NH3 with tubing, filters, and inlets. Measurements on the vertical distribution of NH3 are even scarcer, with only a few available airborne and tower measurements. Satellite observations of NH3 show potential to be used for real-time monitoring as these have global coverage often with daily overpasses. Unfortunately, validation of satellite NH3 products representing the total atmospheric column with ground based instruments measuring in situ NH3 has been troublesome due to a lack of knowledge about the vertical distribution. Validation with FTIR instruments has shown potential but has been performed for only a limited number of stations. In this study we report on measurements performed during the Measuring atmospheric Ammonia with Remote Sensing (MARS) field campaign at Cabauw, the Netherlands. The aim of the campaign was to improve the general understanding of the vertical distribution of NH3. An approach was taken using four mini-DOAS instruments installed in the meteorological tower at Cabauw, supplemented by measurements with a MARGA and a mobile FTIR instrument. The measurements between May and October 2014 showed large variations in the concentrations and maximum concentrations reached up to 240 μg m-3. The lower three mini-DOAS and MARGA measurements showed large differences on an hourly basis, which were shown to originate from multiple measurement artefacts of the MARGA. The mini-DOAS concentrations varied sharply between the different levels with the lower

Applications of Ground-based Mobile Atmospheric Monitoring: Real-time Characterization of Source Emissions and Ambient Concentrations

Science.gov (United States)

Goetz, J. Douglas

Gas and particle phase atmospheric pollution are known to impact human and environmental health as well as contribute to climate forcing. While many atmospheric pollutants are regulated or controlled in the developed world uncertainty still remains regarding the impacts from under characterized emission sources, the interaction of anthropogenic and naturally occurring pollution, and the chemical and physical evolution of emissions in the atmosphere, among many other uncertainties. Because of the complexity of atmospheric pollution many types of monitoring have been implemented in the past, but none are capable of perfectly characterizing the atmosphere and each monitoring type has known benefits and disadvantages. Ground-based mobile monitoring with fast-response in-situ instrumentation has been used in the past for a number of applications that fill data gaps not possible with other types of atmospheric monitoring. In this work, ground-based mobile monitoring was implemented to quantify emissions from under characterized emission sources using both moving and portable applications, and used in a novel way for the characterization of ambient concentrations. In the Marcellus Shale region of Pennsylvania two mobile platforms were used to estimate emission rates from infrastructure associated with the production and transmission of natural gas using two unique methods. One campaign investigated emissions of aerosols, volatile organic compounds (VOCs), methane, carbon monoxide (CO), nitrogen dioxide (NO2), and carbon dioxide (CO 2) from natural gas wells, well development practices, and compressor stations using tracer release ratio methods and a developed fenceline tracer release correction factor. Another campaign investigated emissions of methane from Marcellus Shale gas wells and infrastructure associated with two large national transmission pipelines using the "Point Source Gaussian" method described in the EPA OTM-33a. During both campaigns ambient concentrations

Variation of atmospheric tritium concentration in three chemical forms at Toki, Japan: 2004-12.

Science.gov (United States)

Tanaka, M; Uda, T

2015-11-01

Atmospheric tritium concentrations of HTO, HT and CH3T have been measured at Toki, Japan, for the environmental impact assessment of tritium for a fusion test facility. According to the data from 2004 to 2012, the concentrations of HT and HTO in water vapour tend to increase in spring. The seasonal variation in HT concentration at Toki was compared with the H2 concentration between 1990 and 2005 at Tae-ahn Peninsula, Republic of Korea, which is at approximately the same latitude as Toki. The monthly average of HT-specific activity varied from 1.24 × 10(5) to 1.76 × 10(5) TU. The peak of the monthly average H2 concentration did not match that of HT. This indicates that the mechanism of the production or the source of HT might be different from the production mechanism of H2. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Atmospheric concentrations of organochlorine pesticides, polybrominated diphenyl ethers and polychloronaphthalenes in Nuuk, South-West Greenland

DEFF Research Database (Denmark)

Bossi, Rossana; Skov, Henrik; Vorkamp, Katrin

2008-01-01

Atmospheric concentrations of organochlorine pesticides (OCs), polybrominated diphenyl ethers (PBDEs) and polychloronaphthalenes (PCNs) were measured for the first time in Nuuk, Greenland in 2004 and 2005. The annual mean concentrations af the measured OCs were: α-HCH 20.2 pg m-3, Υ-HCH (lindane) 5......-HCH, which had maximum concentration in August in both years. The average annual mean for ΣPBDEs was 1.14 ± 0.81 pg m-3. The predominant congeners measured in Nuuk were BDE-47 and BDE-99 followed by BDE-100, -153 and -28, indicating the use of penta-BDE technical products as the main source. A clear seasonal...

Determination of equivalent mixing height and atmospheric stability assessment

International Nuclear Information System (INIS)

Simon, J.; Bulko, M.; Holy, K.

2007-01-01

Atmospheric stability is an indicator that reflects the intensity of boundary layer mixing processes. This feature of the atmosphere is especially important since it defines dispersive atmospheric conditions and provides information on how effectively the anthropogenic pollution will be transferred to the higher levels of the atmosphere. The assessment of atmospheric dispersiveness plays a crucial role in the protection of air quality and public health in big cities. The presented paper deals with determination of atmospheric stability via so called Equivalent Mixing Height (EMH) quantity using a radioactive noble gas 222 Rn. A method of deriving a link between 222 Rn activity concentration, eddy diffusion coefficient and EMH using fluid mechanics is also outlined in this work. (authors)

Atmospheric concentration of 210Pb in East Asia and its contribution to Japanese islands by long-range transport

International Nuclear Information System (INIS)

Doi, Taeko; Sato, Shin; Sato, Jun

2007-01-01

Atmospheric 210 Pb is a long-lived progeny of 222 Rn generated from the earth's crust and exists as adsorbed onto the surface of aerosol particles. The distribution of atmospheric 210 Pb in East Asia reflects (1) the concentration levels in continental and maritime air masses and (2) the spatial extent of the continental air mass. This paper reviews the previously observed results on seasonal variation of 210 Pb concentration at several sites of Japan, Korea and China to evaluate the contribution of continental to Japanese atmosphere, and the specific activity of 210 Pb in the main components of aerosol samples and discusses from the view point of the Japanese islands. The authors conclude that aerosols from continental East Asia in winter contain more soil particles with low specific radioactivity of 210 Pb than the aerosols in Japan and that the natural radionuclide is extremely useful tracer for researches on meteorological phenomena and global transfer of environmental pollution. (S. Ohno)

An approach for verifying biogenic greenhouse gas emissions inventories with atmospheric CO2 concentration data

Science.gov (United States)

Stephen M Ogle; Kenneth Davis; Thomas Lauvaux; Andrew Schuh; Dan Cooley; Tristram O West; Linda S Heath; Natasha L Miles; Scott Richardson; F Jay Breidt; James E Smith; Jessica L McCarty; Kevin R Gurney; Pieter Tans; A Scott. Denning

2015-01-01

Verifying national greenhouse gas (GHG) emissions inventories is a critical step to ensure that reported emissions data to the United Nations Framework Convention on Climate Change (UNFCCC) are accurate and representative of a country's contribution to GHG concentrations in the atmosphere. Furthermore, verifying biogenic fluxes provides a check on estimated...

CARVE Measurements of Atmospheric Methane Concentrations and Emissions in Arctic and Boreal Alaska

Science.gov (United States)

Miller, C. E.; Miller, J. B.; Chang, R. Y.; Sweeney, C.; Karion, A.; Wofsy, S. C.; Henderson, J.; Eluszkiewicz, J.; Mountain, M.; Oechel, W. C.

2013-12-01

The Carbon in Arctic Reservoirs Vulnerability Experiment (CARVE) is a NASA Earth Ventures (EV-1) investigation designed to quantify correlations between atmospheric and surface state variables for the Alaskan terrestrial ecosystems through intensive seasonal aircraft campaigns, ground-based observations, and analysis sustained over a 5-year mission. CARVE bridges critical gaps in our knowledge and understanding of Arctic ecosystems, linkages between the Arctic hydrologic and terrestrial carbon cycles, and the feedbacks from fires and thawing permafrost. We present CARVE airborne measurements of spatial and temporal patterns in atmospheric CH4 concentrations and estimated surface-atmosphere emissions for Arctic and Boreal Alaska. Continuous in situ CH4, CO2 and CO data are supplemented by periodic whole air flask samples from which 13CH4 and non-methane hydrocarbons are used to assess the relative contributions of wetlands, fossil fuel combustion, and oil and gas production to the observed CH4 signals. The CARVE project has also initiated monthly 14CH4 sampling at Barrow, AK (BRW) and the CARVE Tower in Fox, AK (CRV) to evaluate seasonal changes in the fraction of old carbon being mobilized via methanogenesis.

Study of the superficial ozone concentrations in the atmosphere of Comunidad de Madrid using passive samplers

Directory of Open Access Journals (Sweden)

D. Galán Madruga

2001-06-01

Full Text Available The ozone is a secondary atmospheric pollutant which is generated for photochemical reactions of volatil organic compounds (VOC’s and nitrogen oxides (NOx. In Spain the ozone is a big problem as a consequence of the solar radiation to reach high levels. Exposure over a period of time to elevated ozone concentrations can cause damage in the public health and alterations in the vegetation.The aim of this study is to carry out the development and validation of a measurement method to let asses the superficial ozone levels in the Comunidad de Madrid, by identifing the zones more significants, where to measure with UV photometric monitors (automatics methods this pollutant and where the health and the vegetation can be affected. To such effect, passive samplers are used, which have glass fiber filters coated with a solution of sodium nitrite, potassium carbonate, glycerol and water. The nitrite ion in the presence of ozone is oxidized to nitrato ion, which it is extrated with ultrapure water and analyzed for ion chromatography, by seen proportional to the concentration existing in the sampling point.The results of validation from field tests indicate a excellent correlation between the passive and the automatic method.The higher superficial ozone concentrations are placed in rural zones, distanced of emission focus of primary pollutants (nitrogen oxides and volatil organic compounds... principally in direction soutwest and northwest of the Comunidad of Madrid.

Carbon assimilation in Eucalyptus urophylla grown under high atmospheric CO2 concentrations: A proteomics perspective.

Science.gov (United States)

Santos, Bruna Marques Dos; Balbuena, Tiago Santana

2017-01-06

Photosynthetic organisms may be drastically affected by the future climate projections of a considerable increase in CO 2 concentrations. Growth under a high concentration of CO 2 could stimulate carbon assimilation-especially in C3-type plants. We used a proteomics approach to test the hypothesis of an increase in the abundance of the enzymes involved in carbon assimilation in Eucalyptus urophylla plants grown under conditions of high atmospheric CO 2 . Our strategy allowed the profiling of all Calvin-Benson cycle enzymes and associated protein species. Among the 816 isolated proteins, those involved in carbon fixation were found to be the most abundant ones. An increase in the abundance of six key enzymes out of the eleven core enzymes involved in carbon fixation was detected in plants grown at a high CO 2 concentration. Proteome changes were corroborated by the detection of a decrease in the stomatal aperture and in the vascular bundle area in Eucalyptus urophylla plantlets grown in an environment of high atmospheric CO 2 . Our proteomics approach indicates a positive metabolic response regarding carbon fixation in a CO 2 -enriched atmosphere. The slight but significant increase in the abundance of the Calvin enzymes suggests that stomatal closure did not prevent an increase in the carbon assimilation rates. The sample enrichment strategy and data analysis used here enabled the identification of all enzymes and most protein isoforms involved in the Calvin-Benson-Bessham cycle in Eucalyptus urophylla. Upon growth in CO 2 -enriched chambers, Eucalyptus urophylla plantlets responded by reducing the vascular bundle area and stomatal aperture size and by increasing the abundance of six of the eleven core enzymes involved in carbon fixation. Our proteome approach provides an estimate on how a commercially important C3-type plant would respond to an increase in CO 2 concentrations. Additionally, confirmation at the protein level of the predicted genes involved in

Temporal and seasonal variation of atmospheric concentrations of currently used pesticides in Champagne in the centre of Reims from 2012 to 2015

Science.gov (United States)

Villiot, A.; Chrétien, E.; Drab-Sommesous, E.; Rivière, E.; Chakir, A.; Roth, E.

2018-02-01

For four years (2012-2015), pesticides were analyzed in atmospheric samples in the Centre of Reims (France). Among the analyzed substances, 28 have been quantified at least one time during the 4 sampling years. The annual cumulated pesticide concentrations were respectively 158.8, 38.5, 84.5 and 86.6 ng m-3 from 2012 to 2015, showing a great variability in the presence of pesticides in the atmosphere of the Centre of Reims. The top nine pesticides quantified in the atmosphere were cymoxanil, chlorothalonil and prosulfocarb reaching concentrations up to 13-14 ng m-3 and folpel, cyazofamid, fluazinam, pendimethalin, fenpropidin and spiroxamine reaching concentrations between 1 and 5 ng m-3. Among the nine predominant pesticides, seven of them were fungicides especially used against septoriose, mildew and oïdium occurring as well in vineyard and arable crops. Herbicides quantified were those which are used in arable crops. Insecticides especially carbaryl, chlorpyrifos ethyl and lindane were negligible in the atmosphere. The role of meteorological conditions in the development of diseases and the application rates of pesticide was related to the presence of pesticide in the atmosphere.

Evaluation of modified atmosphere bag and sulphur dioxide concentrations applied on highbush blueberries fruit (Vaccinium corymbosum L.) cv. Emerald

OpenAIRE

Rodríguez, Mario; Wyss, Anddy; Hormazábal, Nelson

2015-01-01

Aiming to evaluate techniques for modified atmosphere and application of sulphur anhydride upon parameters of quality of postharvest on blueberry fruit (Vaccinium corymbosum L.) cv. Emerald, an experiment of six treatments was conducted, given by the combination of two factors, modified atmosphere (with and without) and different concentrations of sulphur dioxide (generated by 0, 1 and 2 g of sodium metabisulphite) during 7, 14, 21 and 28 days at 0 °C. The dose of 2 g of modified atmosphere s...

Tritium concentration analysis in atmospheric precipitation in Serbia.

Science.gov (United States)

Janković, Marija M; Janković, Bojan Ž; Todorović, Dragana J; Ignjatović, Ljubiša M

2012-01-01

Tritium activity concentration were monitored in monthly precipitation at five locations in Serbia (Meteorological Station of Belgrade at Zeleno Brdo, Vinča Institute of Nuclear Sciences, Smederevska Palanka, Kraljevo and Niš) over 2005, using electrolytic enrichment and liquid scintillation counting. The obtained concentrations ranged from 3.36 to 127.02 TU. The activity values obtained in samples collected at Zeleno Brdo were lower or close to the minimum detectable activity (MDA), which has a value of 3.36 TU. Significantly higher tritium levels were obtained in samples collected in Vinča Institute of Nuclear Sciences compared with samples from the other investigated locations. Amount of precipitation were also recorded. A good linear correlation (r = 0.75) for Zeleno Brdo and VINS between their tritium activity was obtained. It was found that the value of the symmetrical index n (which indicates the magnitude of tritium content changes with time (months) through its second derivative) is the highest for Vinča Institute of Nuclear Sciences compared to other locations, which is in accordance with the fact that the highest concentrations of tritium were obtained in the samples from the cited place.

Concentration and isotope composition of atmospheric methane in Walbrzych Coal District

International Nuclear Information System (INIS)

Korus, A.; Necki, J.; Kotarba, M.

2002-01-01

The closure of hard coal mines in the Walbrzych Coal District led to the reconstruction of carboniferous groundwater horizon and migration of carbon dioxide and methane upward to the surface. Migration of methane is facilitated by systems of fractures, faults and by dense network of shafts, which still remain in connection with the surface. Measurement of the isotopic composition (δ 13 CH 4 ) of methane together with its concentration in atmosphere, yield useful information on the contribution of anthropogenic sources to regional budget of methane. A two component-mixing model was applied to distinguish anthropogenic source. The result of the study, current parameters of anthropogenic source are presented. (author)

Atmosphere composition changes, solar irradiance variations, and changing forest tree growth

International Nuclear Information System (INIS)

Chalupa, V.

1997-01-01

The paper deals with changes in the Earth's atmosphere composition, which greatly influence the growth and health condition of forests. Impacts of increasing concentrations of greenhouse gases and anthropogenic aerosols on future climate changes are assessed. In the past forty years increasing assimilation of CO2 by forests growing in temperature and boreal zones in the Northern Hemisphere was observed. Increasing trends in diameter, height and volume growth of forest trees were found in the Central, Western and Northern Europe. Causes of higher increments are not exactly known, however, the results of present measurements indicate that higher air temperature, nitrogen deposition in forest soils and raising atmospheric CO2 concentration participated in increased growth of forests

Short-term 222Rn activity concentration changes in underground spaces with limited air exchange with the atmosphere

Science.gov (United States)

Fijałkowska-Lichwa, L.; Przylibski, T. A.

2011-04-01

The authors investigated short-time changes in 222Rn activity concentration occurring yearly in two underground tourist facilities with limited air exchange with the atmosphere. One of them is Niedźwiedzia (Bear) Cave in Kletno, Poland - a natural space equipped with locks ensuring isolation from the atmosphere. The other site is Fluorite Adit in Kletno, a section of a disused uranium mine. This adit is equipped with a mechanical ventilation system, operated periodically outside the opening times (at night). Both sites are situated within the same metamorphic rock complex, at similar altitudes, about 2 km apart. The measurements conducted revealed spring and autumn occurrence of convective air movements. In Bear Cave, this process causes a reduction in 222Rn activity concentration in the daytime, i.e. when tourists, guides and other staff are present in the cave. From the point of view of radiation protection, this is the best situation. For the rest of the year, daily concentrations of 222Rn activity in the cave are very stable. In Fluorite Adit, on the other hand, significant variations in daily 222Rn activity concentrations are recorded almost all year round. These changes are determined by the periods of activity and inactivity of mechanical ventilation. Unfortunately this is inactive in the daytime, which results in the highest values of 222Rn activity concentration at the times when tourists and staff are present in the adit. Slightly lower concentrations of radon in Fluorite Adit are recorded in the winter season, when convective air movements carry a substantial amount of radon out into the atmosphere. The incorrect usage of mechanical ventilation in Fluorite Adit results in the most unfavourable conditions in terms of radiation protection. The staff working in that facility are exposed practically throughout the year to the highest 222Rn activity concentrations, both at work (in the adit) and at home (outside their working hours). Therefore, not very well

1.6 μm DIAL Measurement and Back Trajectory Analysis of CO2 Concentration Profiles in the Lower-Atmosphere

Science.gov (United States)

Shibata, Y.; Nagasawa, C.; Abo, M.

2016-12-01

Carbon dioxide (CO2) is the primary greenhouse gas emitted through human activities. In addition to the ground level CO2 network, vertical CO2 concentration profiles also play an important role for the estimation of the carbon budget and global warming in the inversion method. Especially, for the detailed analysis of forest carbon dynamics and CO2 fluxes of urban area, vertical CO2 concentration profiles with high spatial and temporal resolution in the lower atmosphere have been conducted by a differential absorption lidar (DIAL). We have observed several vertical profiles of CO2 concentrations for nighttime and daytime from 0.25 to 2.5 km altitude with range resolution of 300 m and integration time of 1 hour. In order to extract information on the origin of the CO2 masses, one day back trajectories were calculated by using a three dimensional (3-D) atmospheric transport model. In many cases, CO2 low concentration layers of over 1.5km altitude were flown by westerly winds from the forest. In another case, high concentration layers of CO2 were flown from the urban areas. As the spectra of absorption lines of any molecules are influenced basically by the temperature in the atmosphere, laser beams of three wavelengths around a CO2 absorption spectrum are transmitted alternately to the atmosphere for simultaneous measurements of CO2 concentration and temperature profiles. Moreover, a few processing algorithms of CO2-DIAL are also performed for improvement of measurement accuracy. For computation of trajectories and drawing their figures, the JRA-25 data provided by the cooperative research project for the JRA-25 long-term reanalysis of the Japan Meteorological Agency (JMA) and the Central Research Institute of Electric Power Industry (CRIEPI) and the NIPR trajectory model (Tomikawa and Sato, 2005; http://firp-nitram.nipr.ac.jp) were used. This work was financially supported by the System Development Program for Advanced Measurement and Analysis of the Japan Science and

HARAD, Decay Isotope Concentration from Atmospheric Noble-Gas Release

International Nuclear Information System (INIS)

Moore, R.E.

1986-01-01

1 - Description of problem or function: HARAD calculates concentrations of radioactive daughters in air following the atmospheric release of a parent radionuclide for a variety of release heights and meteorological conditions. It can be applied most profitably to the assessment of doses to man from the noble gases such as Rn-222, Rn-220, and Xe and Kr isotopes. These gases can produce significant quantities of short-lived particulate daughters in an airborne plume, which are the major contributors to dose. The simultaneous processes of radioactive decay, buildup and environmental loss due to wet and dry deposition on ground surfaces are calculated for a daughter chain in an airborne plume as it is dispersed downwind from a point of release of a parent. 2 - Method of solution: The code evaluates the analytic solution to the set of coupled first order differential equations describing time variation of the concentration of a chain of radionuclides. The analytic solutions assume that the coefficient describing the fractional rate of dry deposition is constant with time. To account for the variation the time coordinate is automatically divided into intervals and a set of average values are used. 3 - Restrictions on the complexity of the problem: - The maximum length of decay chain is 10 nuclides; calculations can be made at a maximum of 24 downwind distances

Summer–winter concentrations and gas-particle partitioning of short chain chlorinated paraffins in the atmosphere of an urban setting

International Nuclear Information System (INIS)

Wang Thanh; Han Shanlong; Yuan Bo; Zeng Lixi; Li Yingming; Wang Yawei; Jiang Guibin

2012-01-01

Short chain chlorinated paraffins (SCCPs) are semi-volatile chemicals that are considered persistent in the environment, potential toxic and subject to long-range transport. This study investigates the concentrations and gas-particle partitioning of SCCPs at an urban site in Beijing during summer and wintertime. The total atmospheric SCCP levels ranged 1.9–33.0 ng/m 3 during wintertime. Significantly higher levels were found during the summer (range 112–332 ng/m 3 ). The average fraction of total SCCPs in the particle phase (φ) was 0.67 during wintertime but decreased significantly during the summer (φ = 0.06). The ten and eleven carbon chain homologues with five to eight chlorine atoms were the predominant SCCP formula groups in air. Significant linear correlations were found between the gas-particle partition coefficients and the predicted subcooled vapor pressures and octanol–air partition coefficients. The gas-particle partitioning of SCCPs was further investigated and compared with both the Junge–Pankow adsorption and K oa -based absorption models. - Highlights: ► Short chain chlorinated paraffins were investigated in air samples from Beijing. ► Higher levels of SCCPs were found in air during summertime than wintertime. ► Relevant physical–chemical properties were estimated by SPARC and EPI Suite. ► Obtained data were used to model the gas-particle partitioning of SCCPs. - Atmospheric levels and gas-particle partitioning of SCCPs in Beijing, China.

Atmospheric mercury deposition to forests in the eastern USA

International Nuclear Information System (INIS)

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

2017-01-01

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

Study of particle size and trace metal distribution in atmospheric aerosols of islamabad

International Nuclear Information System (INIS)

Shah, M.H.; Shaheen, N.

2009-01-01

Atmospheric aerosol samples were collected on glass fibre filters using high volume air samplers Half of each aerosol sample was solubilized in nitric acid/hydrochloric acid based wet digestion method and the concentration of trace metals was determined through flame atomic absorption spectrophotometer. Among the eight trace metals analyzed, mean concentration recorded for Zn (844 ng/m3), Fe (642 ng/m3) and Pb (253 ng/m3), was found to be higher than mean levels of Mn, Cr and Co. The size distribution of the collected particulate samples was carried out on mastersizer, which revealed PM/sub 100-10/ as the major fraction (55 %) followed by PM/sub 2.5-10/ (28 %). The correlation study evidenced a strong tendency of trace metals to be associated with fine particulate fractions. The atmospheric trace metal levels showed that the mean metal concentrations in the atmosphere of Islamabad are far higher than background and European urban sites mainly due to the anthropogenic emissions. (author)

Detection of atmospheric tritium by scintillation. Variations in its concentration in France; Detection du tritium atmospherique par scintillation. Evolution de sa concentration en France

Energy Technology Data Exchange (ETDEWEB)

Bibron, R [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1964-06-01

The tritium released into the atmosphere as a result of the explosion of thermonuclear devices is a useful radioactive tracer for the study of certain geophysical problems. The low concentrations found however call for the use of extremely sensitive detectors. Two detection methods using liquid scintillators are described. In the first method, the sample is introduced into the scintillator in liquid form, after prior concentration of the tritium by electrolysis. In the second method the tritium is incorporated into the scintillator solvent molecule by chemical synthesis. In the last part of the report are examined the variations in the tritium concentration in rain-water and of the free hydrogen in the air in France. A discussion is then made of the seasonal variations in the case of rain-water and these are compared to the variations in the strontium-90 concentrations. (author) [French] Le tritium introduit dans l'atmosphere par les explosions d'armes thermonucleaires est un traceur radioactif Interessant pour l'etude de certains problemes de geophysique. Les faibles concentrations rencontrees obligent toutefois a utiliser des detecteurs extremement sensibles. On decrit deux methodes de detection utilisant des scintillateurs liquides. Dans la premiere methode, l'echantillon est introduit dans le scintillateur, sous forme aqueuse, apres une concentration prealable du tritium par electrolyse. Dans la seconde methode, le tritium est incorpore a la molecule du solvant du scintillateur par synthese chimique. Dans la derniere partie du rapport, on examine l'evolution de la concentration du tritium dans les eaux de precipitation et l'hydrogene libre de l'air en France. On discute ensuite les variations saisonnieres dans le cas des eaux de precipitation et on les compare aux variations du strontium 90. (auteur)

Detection of atmospheric tritium by scintillation. Variations in its concentration in France; Detection du tritium atmospherique par scintillation. Evolution de sa concentration en France

Energy Technology Data Exchange (ETDEWEB)

Bibron, R. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1964-06-01

The tritium released into the atmosphere as a result of the explosion of thermonuclear devices is a useful radioactive tracer for the study of certain geophysical problems. The low concentrations found however call for the use of extremely sensitive detectors. Two detection methods using liquid scintillators are described. In the first method, the sample is introduced into the scintillator in liquid form, after prior concentration of the tritium by electrolysis. In the second method the tritium is incorporated into the scintillator solvent molecule by chemical synthesis. In the last part of the report are examined the variations in the tritium concentration in rain-water and of the free hydrogen in the air in France. A discussion is then made of the seasonal variations in the case of rain-water and these are compared to the variations in the strontium-90 concentrations. (author) [French] Le tritium introduit dans l'atmosphere par les explosions d'armes thermonucleaires est un traceur radioactif Interessant pour l'etude de certains problemes de geophysique. Les faibles concentrations rencontrees obligent toutefois a utiliser des detecteurs extremement sensibles. On decrit deux methodes de detection utilisant des scintillateurs liquides. Dans la premiere methode, l'echantillon est introduit dans le scintillateur, sous forme aqueuse, apres une concentration prealable du tritium par electrolyse. Dans la seconde methode, le tritium est incorpore a la molecule du solvant du scintillateur par synthese chimique. Dans la derniere partie du rapport, on examine l'evolution de la concentration du tritium dans les eaux de precipitation et l'hydrogene libre de l'air en France. On discute ensuite les variations saisonnieres dans le cas des eaux de precipitation et on les compare aux variations du strontium 90. (auteur)

Carbon dioxide assimilation in Danish crops (wheat and maize) and its dependency on increasing temperature and elevated atmospheric CO2 concentration

International Nuclear Information System (INIS)

Soegaard, H.; Boegh, E.

2001-01-01

Eddy correlation measurements of atmospheric CO 2 fluxes have been recorded over a number of crops throughout the growing season. These data have been used for validating a mechanistic photosynthesis model, which is used together with one of the most wide spread soil respiration equations. The combined model, is applied for analysing the temperature- and CO 2 -dependency of field crops. To get an idea of the potential range in the sensitivity of agricultural crops to atmospheric change, two crops with contrasting biochemical and physiological properties were selected for the present analysis: winter wheat (Triticum aestivum cv. Hereward) and maize (Zea mayz cv. Loft). While wheat, which is a C 3 -species, is the most common Danish crop (covering 25% of the Danish agricultural area), maize is interesting because it is a C 4 -plant which uses another CO 2 pathway in the dry matter production. The photosynthetic process of C 4 -plants has a higher temperature optimum compared to C 3 -plants. This could give C 4 plants more favourable conditions in the future. The model applied in this paper is utilized to evaluate whether increasing atmospheric CO 2 concentrations have contributed to the general increase in grain yield observed in Denmark since the late sixties. (LN)

Inter-annual variability of the atmospheric carbon dioxide concentrations as simulated with global terrestrial biosphere models and an atmospheric transport model

Energy Technology Data Exchange (ETDEWEB)

Fujita, Daisuke; Saeki, Tazu; Nakazawa, Takakiyo [Tohoku Univ., Sendai (Japan). Center for Atmospheric and Oceanic Studies; Ishizawa, Misa; Maksyutov, Shamil [Inst. for Global Change Research, Yokohama (Japan). Frontier Research System for Global Change; Thornton, Peter E. [National Center for Atmospheric Research, Boulder, CO (United States). Climate and Global Dynamics Div.

2003-04-01

Seasonal and inter-annual variations of atmospheric CO{sub 2} for the period from 1961 to 1997 have been simulated using a global tracer transport model driven by a new version of the Biome BioGeochemical Cycle model (Biome-BGC). Biome-BGC was forced by daily temperature and precipitation from the NCEP reanalysis dataset, and the calculated monthly-averaged CO{sub 2} fluxes were used as input to the global transport model. Results from an inter-comparison with the Carnegie-Ames-Stanford Approach model (CASA) and the Simulation model of Carbon CYCLE in Land Ecosystems (Sim-CYCLE) model are also reported. The phase of the seasonal cycle in the Northern Hemisphere was reproduced generally well by Biome-BGC, although the amplitude was smaller compared to the observations and to the other biosphere models. The CO{sub 2} time series simulated by Biome-BGC were compared to the global CO{sub 2} concentration anomalies from the observations at Mauna Loa and the South Pole. The modeled concentration anomalies matched the phase of the inter-annual variations in the atmospheric CO{sub 2} observations; however, the modeled amplitude was lower than the observed value in several cases. The result suggests that a significant part of the inter-annual variability in the global carbon cycle can be accounted for by the terrestrial biosphere models. Simulations performed with another climate-based model, Sim-CYCLE, produced a larger amplitude of inter-annual variability in atmospheric CO{sub 2}, making the amplitude closer to the observed range, but with a more visible phase mismatch in a number of time periods. This may indicate the need to increase the Biome-BGC model sensitivity to seasonal and inter-annual changes in temperature and precipitation.

Inter-annual variability of the atmospheric carbon dioxide concentrations as simulated with global terrestrial biosphere models and an atmospheric transport model

International Nuclear Information System (INIS)

Fujita, Daisuke; Saeki, Tazu; Nakazawa, Takakiyo; Ishizawa, Misa; Maksyutov, Shamil; Thornton, Peter E.

2003-01-01

Seasonal and inter-annual variations of atmospheric CO 2 for the period from 1961 to 1997 have been simulated using a global tracer transport model driven by a new version of the Biome BioGeochemical Cycle model (Biome-BGC). Biome-BGC was forced by daily temperature and precipitation from the NCEP reanalysis dataset, and the calculated monthly-averaged CO 2 fluxes were used as input to the global transport model. Results from an inter-comparison with the Carnegie-Ames-Stanford Approach model (CASA) and the Simulation model of Carbon CYCLE in Land Ecosystems (Sim-CYCLE) model are also reported. The phase of the seasonal cycle in the Northern Hemisphere was reproduced generally well by Biome-BGC, although the amplitude was smaller compared to the observations and to the other biosphere models. The CO 2 time series simulated by Biome-BGC were compared to the global CO 2 concentration anomalies from the observations at Mauna Loa and the South Pole. The modeled concentration anomalies matched the phase of the inter-annual variations in the atmospheric CO 2 observations; however, the modeled amplitude was lower than the observed value in several cases. The result suggests that a significant part of the inter-annual variability in the global carbon cycle can be accounted for by the terrestrial biosphere models. Simulations performed with another climate-based model, Sim-CYCLE, produced a larger amplitude of inter-annual variability in atmospheric CO 2 , making the amplitude closer to the observed range, but with a more visible phase mismatch in a number of time periods. This may indicate the need to increase the Biome-BGC model sensitivity to seasonal and inter-annual changes in temperature and precipitation

Seasonal variations in the concentration and solubility of elements in atmospheric particulate matter: a case study in Northern Italy

Directory of Open Access Journals (Sweden)

Canepari S.

2013-04-01

Full Text Available Atmospheric particulate matter is characterized by a variety of chemical components, generally produced by different sources. Chemical fractionation of elements, namely the determination of their extractable and residual fractions, may reliably increase the selectivity of some elements as tracers of specific PM sources. Seasonal variations of atmospheric particulate matter concentration in PM10 and PM2.5, of elemental concentration in PM10 and PM2.5, of the extractable and residual fraction of elements in different size fractions in the range 0.18 – 18 μm are reported in this paper. The effect of the ageing of the air masses is discussed.

Atmospheric pollutants monitoring by analysis of epiphytic lichens

International Nuclear Information System (INIS)

Fuga, Alessandra; Saiki, Mitiko; Marcelli, Marcelo P.; Saldiva, Paulo H.N.

2008-01-01

The Canoparmelia texana epiphytic lichenized fungi was used to monitor atmospheric pollution in the Sao Paulo metropolitan region, SP, Brazil. The cluster analysis applied to the element concentration values confirmed the site groups of different levels of pollution due to industrial and vehicular emissions. In the distribution maps of element concentrations, higher concentrations of Ba and Mn were observed in the vicinity of industries and of a petrochemical complex. The highest concentration of Co found in lichens from the Sao Miguel Paulista site is due to the emissions from a metallurgical processing plant that produces this element. For Br and Zn, the highest concentrations could be associated both to vehicular and industrial emissions. Exploratory analyses revealed that the accumulation of toxic elements in C. texana may be of use in evaluating the human risk of cardiopulmonary mortality due to prolonged exposure to ambient levels of air pollution. - Canoparmelia texana lichenized fungi is a valuable biomonitor for atmospheric pollution

Growth and {delta}{sup 13}C responses to increasing atmospheric carbon dioxide concentrations for several crop species

Energy Technology Data Exchange (ETDEWEB)

Hanba, Y.T.; Wada, E. [Center for Ecological Research, Kyoto University, Kyoto (Japan); Osaki, M.; Nakamura, T. [Faculty of Agriculture, Hokkaido University, Hokkaido (Japan)

1996-04-01

The responses of plant growth and carbon isotope discrimination ({Delta}) to elevated atmospheric CO{sub 2} concentrations for several crop species (lettuce: Lactuca sativa L.; corn: Zea Mays L. var. P3540, wheat: Triticum aestivum L. var Haruyutaka; and soybean: Glycine Max (L). Merr. var. Kitamusume) were investigated. Shoot relative growth rate was used to indicate plant growth, and {delta}{sup 13}C value of leaf materials in corn (C4 species) was used to calculate {Delta} for C3 species. Plant growth was stimulated by enriched CO{sub 2}, while {Delta} remained almost constant as CO{sub 2} concentration changed. {Delta} showed interspecific difference, and the plant species of larger {Delta} had larger relative growth rates. Relative growth rates of the plants of larger {Delta} were stimulated by CO{sub 2} enrichment more than those of the plants of smaller {Delta}. We propose that plant {Delta} could be a possible parameter to assess the interspecific difference of plant response to the increasing atmospheric CO{sub 2} concentrations. 3 figs., 2 tabs., 25 refs.

Atmospheric concentration characteristics and gas-particle partitioning of PCBs in a rural area of eastern Germany

International Nuclear Information System (INIS)

Mandalakis, Manolis; Stephanou, Euripides G.

2007-01-01

Atmospheric concentrations of polychlorinated biphenyls (PCBs) were measured in 14 successive daytime and nighttime air samples collected from Melpitz, a rural site in eastern Germany. The average total concentration of PCBs was 110+/-80pgm -3 and they were predominately present in the gas phase (∼95%). Composition of individual congeners closely resembled those of Clophen A30 and Aroclor 1232. Partial vapor pressures of PCBs were well correlated with temperature and the steep slopes obtained from Clausius-Clapeyron plots (-4500 to -8000) indicated that evaporation from adjacent land surfaces still controls the atmospheric levels of these pollutants. Particle-gas partitioning coefficients (K P ) of PCBs were well correlated with the respective sub-cooled vapor pressures (P L o ), but the slopes obtained from logK P versus logP L o plots (-0.16 to -0.59) deviated significantly from the expected value of -1. Overall, gas-particle partitioning of PCBs was better simulated by Junge-Pankow than octanol/air partition coefficient-based model

Differences in energy expenditures and growth dilution explain higher PCB concentrations in male summer flounder

Science.gov (United States)

Madenjian, Charles P.; Jensen, Olaf P.; Rediske, Richard R.; O'Keefe, James P.; Vastano, Anthony R.; Pothoven, Steven A.

2016-01-01

Comparison of polychlorinated biphenyl (PCB) concentrations between the sexes of mature fish may reveal important behavioral and physiological differences between the sexes. We determined whole-fish PCB concentrations in 23 female summer flounder Paralichthys dentatus and 27 male summer flounder from New Jersey coastal waters. To investigate the potential for differences in diet or habitat utilization between the sexes, carbon and nitrogen stable isotope ratios were also determined. In 5 of the 23 female summer flounder, PCB concentrations in the somatic tissue and ovaries were determined. In addition, we used bioenergetics modeling to assess the contribution of the growth dilution effect to the observed difference in PCB concentrations between the sexes. Whole-fish PCB concentrations for females and males averaged 87 and 124 ng/g, respectively; thus males were 43% higher in PCB concentration compared with females. Carbon and nitrogen stable isotope ratios did not significantly differ between the sexes, suggesting that diet composition and habitat utilization did not vary between the sexes. Based on PCB determinations in the somatic tissue and ovaries, we predicted that PCB concentration of females would increase by 0.6%, on average, immediately after spawning due to release of eggs. Thus, the change in PCB concentration due to release of eggs did not explain the higher PCB concentrations observed in males. Bioenergetics modeling results indicated that the growth dilution effect could account for males being 19% higher in PCB concentration compared with females. Thus, the bulk of the observed difference in PCB concentrations between the sexes was not explained by growth dilution. We concluded that a higher rate of energy expenditure in males, stemming from greater activity and a greater resting metabolic rate, was most likely the primary driver for the observed difference in PCB concentrations between the sexes.

Differences in Energy Expenditures and Growth Dilution Explain Higher PCB Concentrations in Male Summer Flounder.

Directory of Open Access Journals (Sweden)

Charles P Madenjian

Full Text Available Comparison of polychlorinated biphenyl (PCB concentrations between the sexes of mature fish may reveal important behavioral and physiological differences between the sexes. We determined whole-fish PCB concentrations in 23 female summer flounder Paralichthys dentatus and 27 male summer flounder from New Jersey coastal waters. To investigate the potential for differences in diet or habitat utilization between the sexes, carbon and nitrogen stable isotope ratios were also determined. In 5 of the 23 female summer flounder, PCB concentrations in the somatic tissue and ovaries were determined. In addition, we used bioenergetics modeling to assess the contribution of the growth dilution effect to the observed difference in PCB concentrations between the sexes. Whole-fish PCB concentrations for females and males averaged 87 and 124 ng/g, respectively; thus males were 43% higher in PCB concentration compared with females. Carbon and nitrogen stable isotope ratios did not significantly differ between the sexes, suggesting that diet composition and habitat utilization did not vary between the sexes. Based on PCB determinations in the somatic tissue and ovaries, we predicted that PCB concentration of females would increase by 0.6%, on average, immediately after spawning due to release of eggs. Thus, the change in PCB concentration due to release of eggs did not explain the higher PCB concentrations observed in males. Bioenergetics modeling results indicated that the growth dilution effect could account for males being 19% higher in PCB concentration compared with females. Thus, the bulk of the observed difference in PCB concentrations between the sexes was not explained by growth dilution. We concluded that a higher rate of energy expenditure in males, stemming from greater activity and a greater resting metabolic rate, was most likely the primary driver for the observed difference in PCB concentrations between the sexes.

Quantitative Analysis of Major Factors Affecting Black Carbon Transport and Concentrations in the Unique Atmospheric Structures of Urban Environment

Science.gov (United States)

Liang, Marissa Shuang

Black carbon (BC) from vehicular emission in transportation is a principal component of particulate matters ≤ 2.5 mum (PM2.5). PM2.5 and other diesel emission pollutants (e.g., NOx) are regulated by the Clean Air Act (CAA) according to the National Ambient Air Quality standards (NAAQS). This doctoral dissertation details a study on transport behaviors of black carbon and PM2.5 from transportation routes, their relations with the atmospheric structure of an urban formation, and their relations with the use of biodiesel fuels. The results have implications to near-road risk assessment and to the development of sustainable transportation solutions in urban centers. The first part of study quantified near-roadside black carbon transport as a function of particulate matter (PM) size and composition, as well as microclimatic variables (temperature and wind fields) at the interstate highway I-75 in northern Cincinnati, Ohio. Among variables examined, wind speed and direction significantly affect the roadside transport of black carbon and hence its effective emission factor. Observed non-Gaussian dispersion occurred during low wind and for wind directions at acute angles or upwind to the receptors, mostly occurring in the morning hours. Meandering of air pollutant mass under thermal inversion is likely the driving force. In contrary, Gaussian distribution predominated in daytime of strong downwinds. The roles of urban atmospheric structure, wind fields, and the urban heat island (UHI) effects were further examined on pollutant dispersion and transport. Spatiotemporal variations of traffic flow, atmospheric structure, ambient temperature and PM2.5 concentration data from 14 EPA-certified NAAQS monitoring stations, were analyzed in relation to land-use in the Cincinnati metropolitan area. The results show a decade-long UHI effects with higher interior temperature than that in exurban, and a prominent nocturnal thermal inversion frequent in urban boundary layer. The

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

Control of atmospheric CO2 concentrations by 2050: A calculation on the emission rights of different countries

Institute of Scientific and Technical Information of China (English)

无

2009-01-01

This paper is to provide quantitative data on some critical issues in anticipation of the forthcoming international negotiations in Denmark on the control of atmospheric CO2 concentrations. Instead of letting only a small number of countries dominate a few controversial dialogues about emissions reductions, a comprehensive global system must be established based on emissions allowances for different countries, to realize the long-term goal of controlling global atmospheric CO2 concentrations. That a system rooted in "cumulative emissions per capita," the best conception of the "common but differentiated responsibilities" principle affirmed by the Kyoto Protocol according to fundamental standards of fairness and justice, was demonstrated. Based on calculations of various countries’ cumulative emissions per capita, estimates of their cumulative emissions from 1900 to 2005, and their annual emissions allowances into the future (2006―2050), a 470 ppmv atmospheric CO2 concentration target was set. According to the following four objective indicators―total emissions allowance from 1900 to 2050, actual emissions from 1900 to 2005, emissions levels in 2005, and the average growth rate of emissions from 1996 to 2005―all countries and regions whose population was more than 300000 in 2005 were divided into four main groups: countries with emissions deficits, countries and regions needing to reduce their gross emissions, countries and regions needing to reduce their emissions growth rates, and countries that can maintain the current emissions growth rates. Based on this proposal, most G8 countries by 2005 had already expended their 2050 emissions allowances. The accu-mulated financial value based on emissions has reached more than 5.5 trillion US dollars (20 dollars per ton of CO2). Even if these countries could achieve their ambitious emissions reduction targets in the future, their per capita emissions from 2006 to 2050 would still be much higher than those of

Modeling concentrations and fluxes of atmospheric CO₂ in the North East Atlantic region

DEFF Research Database (Denmark)

Geels, C.; Christensen, J.H.; Hansen, A.W.

2001-01-01

As part of the Danish NEAREX project a three-dimensional Eulerian hemispheric air pollution model is used to study the transport and concentrations of atmospheric CO2 in the North East Atlantic region. The model domain covers the major part of the Northern Hemisphere and currently the model...

Use of a Simple GIS-Based Model in Mapping the Atmospheric Concentration of γ-HCH in Europe

Directory of Open Access Journals (Sweden)

Pilar Vizcaino

2014-10-01

Full Text Available The state-of-the-art of atmospheric contaminant transport modeling provides accurate estimation of chemical concentrations. However, existing complex models, sophisticated in terms of process description and potentially highly accurate, may entail expensive setups and require very detailed input data. In contexts where detailed predictions are not needed (e.g., for regulatory risk assessment or life cycle impact assessment of chemicals, simple models allowing quick evaluation of contaminants may be preferable. The goal of this paper is to illustrate and critically discuss the use of a simple equation proposed by Pistocchi and Galmarini (2010, which can be implemented through basic GIS functions, to predict atmospheric concentrations of lindane (γ-HCH in Europe from both local and remote sources. Concentrations were computed for 1995 and 2005 assuming different modes of use of lindane and consequently different spatial patterns of emissions. Results were compared with those from the well-established MSCE-POP model (2005 developed within EMEP (European Monitoring and Evaluation Programme, and with available monitoring data, showing acceptable correspondence in terms of the orders of magnitude and spatial distribution of concentrations, especially when the background effect of emissions from extracontinental sources, estimated using the same equation, is added to European emissions.

Potential ocean–atmosphere preconditioning of late autumn Barents-Kara sea ice concentration anomaly

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Martin P. King

2016-02-01

Full Text Available Many recent studies have revealed the importance of the climatic state in November on the seasonal climate of the subsequent winter. In particular, it has been shown that interannual variability of sea ice concentration (SIC over the Barents-Kara (BK seas in November is linked to winter atmospheric circulation anomaly that projects on the North Atlantic Oscillation. Understanding the lead–lag processes involving the different components of the climate system from autumn to winter is therefore important. This note presents dynamical interpretation for the ice-ocean–atmosphere relationships that can affect the BK SIC anomaly in late autumn. It is found that cyclonic (anticyclonic wind anomaly over the Arctic in October, by Ekman drift, can be responsible for positive (negative SIC in the BK seas in November. The results also suggest that ocean heat transport via the Barents Sea Opening in September and October can contribute to BK SIC anomaly in November.

Fire feedbacks over geological time and the evolution of atmospheric oxygen concentration

Science.gov (United States)

Mills, B.; Belcher, C.; Lenton, T. M.

2017-12-01

During the 4.5 billion year history of the Earth, the concentration of oxygen in the atmosphere has risen from trace levels to today's 21%. Yet over the last 400 million years, O2 concentration appears to have remained within a relatively narrow range (around 15% - 30%), despite dramatic changes in the nature of global biogeochemical cycling. This stability has been crucial for continued animal evolution, and is thought to have arisen through feedbacks between oxygen, wildfire and plant productivity: the strong oxygen- dependence of fire initiation and spread means that global photosynthetic primary productivity is suppressed when oxygen levels are high, and enhanced when levels are low. We present biogeochemical modelling of the long term carbon and oxygen cycles, which aims to capture the operation of the wildfire feedback alongside other key processes. We find that wildfire can effectively stabilize long term oxygen concentrations, but that the nature of this feedback has changed as plant evolution has provided different fuels. Specifically, the evolution of early angiosperms during the Cretaceous period provided new understory fuels that more easily facilitated crown and canopy fires. Adding these dynamics to our model produces a more stable system over long timescales, and the model predicts that oxygen concentration has declined towards the present day - a prediction that is supported by other independent estimates.

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.

Carbon-13 isotopic abundance and concentration of atmospheric methane for background air in the Southern and Northern Hemispheres from 1978 to 1989

International Nuclear Information System (INIS)

Stevens, C.M.; Sepanski; Morris, L.J.

1995-03-01

Atmospheric methane (CH 4 ) may become an increasingly important contributor to global warming in future years. Its atmospheric concentration has risen, doubling over the past several hundred years, and additional methane is thought to have a much greater effect on climate, on a per molecule basis, than additional C0 2 at present day concentrations (Shine et al. 1990). The causes of the increase of atmospheric CH 4 have been difficult to ascertain because of a lack of quantitative knowledge of the fluxes (i.e., net emissions) from the numerous anthropogenic and natural sources. The goal of CH 4 isotopic studies is to provide a constraint (and so reduce the uncertainties) in estimating the relative fluxes from the various isotopically distinct sources, whose combined fluxes must result in the measured atmospheric isotopic composition, after the fractionating effect of the atmospheric removal process is considered. In addition, knowledge of the spatial and temporal changes in the isotopic composition of atmospheric CH 4 , along with estimates of the fluxes from some of the major sources, makes it possible to calculate growth rates for sources whose temporal emissions trends would be difficult to measure directly

Formation of the lunar helium corona and atmosphere

Science.gov (United States)

Hodges, R. R., Jr.

1977-01-01

Helium is one of the dominant gases of the lunar atmosphere. Its presence is easily identified in data from the mass spectrometer at the Apollo 17 landing site. The major part of these data was obtained in lunar nighttime, where helium concentration reaches the maximum of its diurnal cyclic variation. The large night to day concentration ratio agrees with the basic theory of exospheric lateral transport reported by Hodges and Johnson (1968). A reasonable fraction of atmospheric helium atoms has a velocity in excess of the gravitational escape velocity. The result is a short average lifetime and a tenuous helium atmosphere. A description is presented of an investigation which shows that the atmosphere of the moon has two distinct components including low energy atoms, which are gravitationally bound in trajectories that intersect the lunar surface, and higher energy atoms, which are trapped in satellite orbits. The total helium abundance in the lunar corona is shown to be about 1.3 times 10 to the 30th power atoms.

Be-7 concentration in garden and wild vegetables in Japan

International Nuclear Information System (INIS)

Nobuhiko Ito; Iwao Kunugijama; Yoshinori Furukawa.

1996-01-01

Beryllium-7 is a natural radionuclide produced by cosmic rays. Be-7 is found vividly in the atmosphere, so the concentrations in airborne particles were analyzed by many investigators. It is known that airborne particles with Be-7 in the atmosphere fall slowly to the ground and adhere to plant surface. However, Be-7 concentrations of foods were not measured too much. So we measured Be-7 concentrations of garden vegetables, wild vegetables, grasses, beef and milk, and calculated internal exposure dose from Be-7. Beryllium-7 concentrations of plant samples are shown. Beryllium-7 concentrations of garden vegetables were from 0.2 to 25.3 Bq/kg, and concentrations of wild vegetables were from 0.8 to 23.5 Bq/kg. There is no difference in Be-7 concentrations between garden vegetables and wild vegetables. Leaf vegetables have almost higher concentration of Be-7. Though Matteuccia Struthiopteris and Pteridium aquilinum are ferns, their eatable stages are sprouts. The relationship between surface area and Be-7 concentration in some vegetable leaves gathered simultaneously at the same farm is shown. Beryllium-7 concentrations of leaves correlate significantly with the surface area/weight ratios. What high concentration vegetables have proportionately broad leaves suggests that atmospheric Be-7 particles adhere to surface of leaves. (author)

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

Science.gov (United States)

Han, Qin

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

On the formation of sulphuric acid – amine clusters in varying atmospheric conditions and its influence on atmospheric new particle formation

Directory of Open Access Journals (Sweden)

I. K. Ortega

2012-10-01

Full Text Available Sulphuric acid is a key component in atmospheric new particle formation. However, sulphuric acid alone does not form stable enough clusters to initiate particle formation in atmospheric conditions. Strong bases, such as amines, have been suggested to stabilize sulphuric acid clusters and thus participate in particle formation. We modelled the formation rate of clusters with two sulphuric acid and two amine molecules (JA2B2 at varying atmospherically relevant conditions with respect to concentrations of sulphuric acid ([H2SO4], dimethylamine ([DMA] and trimethylamine ([TMA], temperature and relative humidity (RH. We also tested how the model results change if we assume that the clusters with two sulphuric acid and two amine molecules would act as seeds for heterogeneous nucleation of organic vapours (other than amines with higher atmospheric concentrations than sulphuric acid. The modelled formation rates JA2B2 were functions of sulphuric acid concentration with close to quadratic dependence, which is in good agreement with atmospheric observations of the connection between the particle formation rate and sulphuric acid concentration. The coefficients KA2B2 connecting the cluster formation rate and sulphuric acid concentrations as JA2B2=KA2B2[H2SO4]2 turned out to depend also on amine concentrations, temperature and relative humidity. We compared the modelled coefficients KA2B2 with the corresponding coefficients calculated from the atmospheric observations (Kobs from environments with varying temperatures and levels of anthropogenic influence. By taking into account the modelled behaviour of JA2B2 as a function of [H2SO4], temperature and RH, the atmospheric particle formation rate was reproduced more closely than with the traditional semi-empirical formulae based on sulphuric acid concentration only. The formation rates of clusters with two sulphuric acid and two amine molecules with different amine compositions (DMA or TMA or one of both had

CLIMATE CHANGE. Long-term climate forcing by atmospheric oxygen concentrations.

Science.gov (United States)

Poulsen, Christopher J; Tabor, Clay; White, Joseph D

2015-06-12

The percentage of oxygen in Earth's atmosphere varied between 10% and 35% throughout the Phanerozoic. These changes have been linked to the evolution, radiation, and size of animals but have not been considered to affect climate. We conducted simulations showing that modulation of the partial pressure of oxygen (pO2), as a result of its contribution to atmospheric mass and density, influences the optical depth of the atmosphere. Under low pO2 and a reduced-density atmosphere, shortwave scattering by air molecules and clouds is less frequent, leading to a substantial increase in surface shortwave forcing. Through feedbacks involving latent heat fluxes to the atmosphere and marine stratus clouds, surface shortwave forcing drives increases in atmospheric water vapor and global precipitation, enhances greenhouse forcing, and raises global surface temperature. Our results implicate pO2 as an important factor in climate forcing throughout geologic time. Copyright © 2015, American Association for the Advancement of Science.

Long-term trend and variability of atmospheric PM10 concentration in the Po Valley

Science.gov (United States)

Bigi, A.; Ghermandi, G.

2014-05-01

The limits to atmospheric pollutant concentration set by the European Commission provide a challenging target for the municipalities in the Po Valley, because of the characteristic climatic conditions and high population density of this region. In order to assess climatology and trends in the concentration of atmospheric particles in the Po Valley, a data set of PM10 data from 41 sites across the Po Valley have been analysed, including both traffic and background sites (either urban, suburban or rural). Of these 41 sites, 18 with 10 yr or longer record have been analysed for long-term trend in deseasonalized monthly means, in annual quantiles and in monthly frequency distribution. A widespread significant decreasing trend has been observed at most sites, up to a few percent per year, by a generalized least squares and Theil-Sen method. All 41 sites have been tested for significant weekly periodicity by Kruskal-Wallis test for mean anomalies and by Wilcoxon test for weekend effect magnitude. A significant weekly periodicity has been observed for most PM10 series, particularly in summer and ascribed mainly to anthropic particulate emissions. A cluster analysis has been applied in order to highlight stations sharing similar pollution conditions over the reference period. Five clusters have been found, two encompassing the metropolitan areas of Turin and Milan and their respective nearby sites and the other three clusters gathering northeast, northwest and central Po Valley sites respectively. Finally, the observed trends in atmospheric PM10 have been compared to trends in provincial emissions of particulates and PM precursors, and analysed along with data on vehicular fleet age, composition and fuel sales. A significant basin-wide drop in emissions occurred for gaseous pollutants, contrarily to emissions of PM10 and PM2.5, whose drop was low and restricted to a few provinces. It is not clear whether the decrease for only gaseous emissions is sufficient to explain the

Atmospheric concentrations of 7Be, 10Be and 210Pb in northeast Asia

International Nuclear Information System (INIS)

Yamagata, T.; Tada, W.; T saito; Nagai, H.; Murayama, M.; Momoshima, N.; Matsuzaki, H.

2005-01-01

Cosmogenic nuclides 7 Be (T 1/2 = 53.3 d) and 10 Be (T 1/2 = 1.5 X 10 6 y) are very useful tracer for the aerosols originated in the upper atmosphere, In the case of 10 Be in surface air, however, two components from upper troposphere and from re-suspended dust from soil are mixed. We try to divide these sources, in order to know an interpretation of aerosol drives. To try to separate the two different source of 10 Be, we use 210 Pb (T 1/2 = 22.3y), progeny of 222 Rn, as continental component. In this study, the distribution of these nuclides in aerosols collected in the Northwest pacific and adjacent seas by employing the research Vessels as cut off the re-suspended dusts from soil are reported. Since research expeditions are mostly short term, continuous observation is very difficult. So we observed at Tokyo and Hachijo-Island, remote island located 300 km south from Tokyo, in 2002-2004. Seasonal variations for 7 Be, 10 Be and 210 Pb concentration were similar pattern at Tokyo and Hachijo-Island. The concentrations were high in April and October to November and low in July to August. Although 210 Pb concentration showed the seasonal variation similar to 7 Be concentration, the average 210 Pb concentration of Tokyo showed the value high about 35% as compared with Hachijo-Island, while the average 7 Be concentration having been mostly in agreement at both points. For the distribution of these nuclide, 7 Be and 10 Be concentrations in ocean air showed strong latitude dependence but 210 Pb concentration depend on distance from continent.

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

not possible to conclude that the actual contamination by zinc is due to atmospheric deposition or spill. However, some samples in this same area present lightly higher zinc concentration in topsoil than in subsoil indicating a cursory atmospheric deposition. Regarding to lead, one of the industrial areas showed a very active atmospheric deposition, with concentrations higher than 900 mg/kg in topsoil decreasing until less than 10 mg/kg to 30 cm depth. Oppositely, the lead concentration in natural soil is constant in the profile. On the other hand, the range of cadmium concentrations in the different depths of the profiles was, generally, low. Only one sample from the industrial area shows high concentration in the first centimetre of soil, decreasing quickly with the depth, supporting the hypothesis that the atmospheric deposition is the main pathway of cadmium contamination. Studding the copper concentration, only in agricultural soil atmospheric deposition is observed, probably due to application of pesticides. Oppositely to the rest of metals, manganese increases its concentration with the depth in natural soil, probably due to that the parent material (metamorphic rock) is rich in this metal. In the case of chromium has not been detected atmospheric deposition in any sampling point. Finally, only one sample located at the industrial area, nickel concentration shows a higher level in topsoil than subsoil, indicating atmospheric deposition. Acknowledgements: to "Fundación Séneca" of "Comunidad Autónoma de Murcia" for its financial support

Nutrient concentrations in a Littorella uniflora community at higher CO₂ concentrations and reduced light intensities

DEFF Research Database (Denmark)

Andersen, T.; Pedersen, O.; Andersen, F. Ø.

2005-01-01

laboratory experiments with isoetid vegetation (Littorella uniflora) where water column CO2 and light could be manipulated in order to test whether (i) light and CO2 availability affect nutrient concentrations in isoetid vegetation, and (ii) if changes in light and CO2 climate affect fluxes of inorganic...... nitrogen (N) and phosphorus (P) from sediment to water column, which potentially could result in increased growth of epiphytic algae. 3. The results showed that the standing stocks of phosphorus and nitrogen in the L. uniflora vegetation were significantly influenced by CO2 concentration and light...... intensity. Both standing stocks of P and N were significantly higher in the mesocosm treatments with high CO2 concentration than in those at low CO2 concentration. Similarly, standing stocks of P and N enhanced with increasing light intensity. 4. Measurements of nutrient fluxes both in the field...

Ten years of continual monitoring of 222Rn concentration in Bratislava atmosphere

International Nuclear Information System (INIS)

Holy, K.; Bosa, I.; Polaskova, A.; Boehm, R.; Ondo-Estok, D.; Bulko, M.; Hola, O.

2003-01-01

By the continual monitoring we obtained the extensive set of radon data in Bratislava atmosphere covering the time period of 1991 - 2000. The average annual radon activity concentrations varied from 4.1 to 7.2 Bq/m 3 . In the years 1996 - 1999 the decreasing of the average annual radon concentration was observed. The average daily courses of the radon activity concentration for individual months calculated on the basis of all data from 1991 - 2000 have a form of waves with the maximum in morning hours and with the minimum in the afternoon. The maximal amplitude of daily wave was found out in August (2.9 Bq/m 3 ) and minimal in December (0.5 Bq/m 3 ). The average daily wave obtained as the mean off all data from years 1991 - 2000 reaches the maximum between 4 and 6 a. m. and the minimum between 2 and 4 p. m. The Rn-222 activity concentration reaches its average daily value equal to 5.6 Bq/m 3 at about 10 a. m and at 9 p. m. The amplitude of average daily wave is equal to 1.5 Bq/m 3 . The average annual radon course calculated on the basis of all the measured data reaches the minimum in April and the maximum in October with seasonal variation from 3.9 to 6.9 Bq/m 3 . The annual radon courses differ from each other for various periods of the day. (authors)

Evaporative crystallization of salts from Electrodialysis concentrated brine at atmospheric and subatmospheric pressures

Science.gov (United States)

Wang, Dong; Du, Wei; Cheng, Penggao; Tang, Na; Wang, Xuekui

2018-02-01

A large amount of concentrated brine was produced as by-product during the process of the electrodialysis seawater desalination. In this study, the crystallization sequences of different salts from the brine through evaporative crystallization at both atmospheric and subatmospheric pressures were investigated in detail. The profile of the boiling temperature with density and the relationship between the boiling temperature and the pressure were recorded. The combination of Powder X-Ray Diffraction and the polarizing microscope was employed to identify the salts in the solid form. It can be inferred that NaCl crystallized out firstly and then MgSO4·6H2O and CaSO4 precipitate in order at both atmospheric and subatmospheric pressures, and it should be noticed that CaSO4 crystallized as anhydrate at 70°C and 90°C while as dihydrate at 50°C. At the end of all the experiments the precipitation rates of CaSO4 and NaCl have reached to more than 95% while MgSO4 only reached to about 60%.

Effect of elevated atmospheric CO2 concentration on growth and leaf litter decomposition of Quercus acutissima and Fraxinus rhynchophylla.

Directory of Open Access Journals (Sweden)

Sangsub Cha

Full Text Available The atmospheric carbon dioxide (CO2 level is expected to increase substantially, which may change the global climate and carbon dynamics in ecosystems. We examined the effects of an elevated atmospheric CO2 level on the growth of Quercus acutissima and Fraxinus rhynchophylla seedlings. We investigated changes in the chemical composition of leaf litter, as well as litter decomposition. Q. acutissima and F. rhynchophylla did not show differences in dry weight between ambient CO2 and enriched CO2 treatments, but they exhibited different patterns of carbon allocation, namely, lower shoot/root ratio (S/R and decreased specific leaf area (SLA under CO2-enriched conditions. The elevated CO2 concentration significantly reduced the nitrogen concentration in leaf litter while increasing lignin concentrations and carbon/nitrogen (C/N and lignin/N ratios. The microbial biomass associated with decomposing Q. acutissima leaf litter was suppressed in CO2 enrichment chambers, while that of F. rhynchophylla was not. The leaf litter of Q. acutissima from the CO2-enriched chambers, in contrast with F. rhynchophylla, contained much lower nutrient concentrations than that of the litter in the ambient air chambers. Consequently, poorer litter quality suppressed decomposition.

Effect of elevated atmospheric CO2 concentration on growth and leaf litter decomposition of Quercus acutissima and Fraxinus rhynchophylla.

Science.gov (United States)

Cha, Sangsub; Chae, Hee-Myung; Lee, Sang-Hoon; Shim, Jae-Kuk

2017-01-01

The atmospheric carbon dioxide (CO2) level is expected to increase substantially, which may change the global climate and carbon dynamics in ecosystems. We examined the effects of an elevated atmospheric CO2 level on the growth of Quercus acutissima and Fraxinus rhynchophylla seedlings. We investigated changes in the chemical composition of leaf litter, as well as litter decomposition. Q. acutissima and F. rhynchophylla did not show differences in dry weight between ambient CO2 and enriched CO2 treatments, but they exhibited different patterns of carbon allocation, namely, lower shoot/root ratio (S/R) and decreased specific leaf area (SLA) under CO2-enriched conditions. The elevated CO2 concentration significantly reduced the nitrogen concentration in leaf litter while increasing lignin concentrations and carbon/nitrogen (C/N) and lignin/N ratios. The microbial biomass associated with decomposing Q. acutissima leaf litter was suppressed in CO2 enrichment chambers, while that of F. rhynchophylla was not. The leaf litter of Q. acutissima from the CO2-enriched chambers, in contrast with F. rhynchophylla, contained much lower nutrient concentrations than that of the litter in the ambient air chambers. Consequently, poorer litter quality suppressed decomposition.

Reconstruction of Atmospheric Tracer Releases with Optimal Resolution Features: Concentration Data Assimilation

Science.gov (United States)

Singh, Sarvesh Kumar; Turbelin, Gregory; Issartel, Jean-Pierre; Kumar, Pramod; Feiz, Amir Ali

2015-04-01

The fast growing urbanization, industrialization and military developments increase the risk towards the human environment and ecology. This is realized in several past mortality incidents, for instance, Chernobyl nuclear explosion (Ukraine), Bhopal gas leak (India), Fukushima-Daichi radionuclide release (Japan), etc. To reduce the threat and exposure to the hazardous contaminants, a fast and preliminary identification of unknown releases is required by the responsible authorities for the emergency preparedness and air quality analysis. Often, an early detection of such contaminants is pursued by a distributed sensor network. However, identifying the origin and strength of unknown releases following the sensor reported concentrations is a challenging task. This requires an optimal strategy to integrate the measured concentrations with the predictions given by the atmospheric dispersion models. This is an inverse problem. The measured concentrations are insufficient and atmospheric dispersion models suffer from inaccuracy due to the lack of process understanding, turbulence uncertainties, etc. These lead to a loss of information in the reconstruction process and thus, affect the resolution, stability and uniqueness of the retrieved source. An additional well known issue is the numerical artifact arisen at the measurement locations due to the strong concentration gradient and dissipative nature of the concentration. Thus, assimilation techniques are desired which can lead to an optimal retrieval of the unknown releases. In general, this is facilitated within the Bayesian inference and optimization framework with a suitable choice of a priori information, regularization constraints, measurement and background error statistics. An inversion technique is introduced here for an optimal reconstruction of unknown releases using limited concentration measurements. This is based on adjoint representation of the source-receptor relationship and utilization of a weight

Changes in gas exchange characteristics during the life span of giant sequoia: Implications for response to current and future concentrations of atmospheric ozone

Energy Technology Data Exchange (ETDEWEB)

Grulke, N.E.; Miller, P.R. (USDA Forest Service, Riverside, CA (United States))

Native stands of giant sequoia are being exposed to relatively high concentrations of atmospheric ozone produced in urban and agricultural areas upwind. The expected change in environmental conditions over the next 100 y is likely to be unprecendented in the life span (ca 2,500 y) of giant sequoia. Changes in the physiological responses of three age classes of giant sequoia (current year, 12 y and 25 y) to different concentrations of ozone were determined, and age-related differences in sensitivity to pollutants were assessed by examining physiological changes (gas exchange, water use efficiency) across the life span of giant sequoia. The CO[sub 2] exchange rate (CER) was greater in current year (12.1 [mu]mol CO[sub 2]/m[sup 2]s) and 2 year old seedlings (4.8 [mu]mol CO[sub 2]/m[sup 2]s) than in all older trees (average of 3.0 [mu]mol CO[sub 2]/m[sup 2]s). Dark respiration was highest for current year seedlings and was increased twofold in symptotic individuals exposed to elevated ozone concentrations. Stomatal conductance was greater in current-year and 2 year old seedlings (335 and 200 mmol H[sub 2]O/m[sup 2]s), respectively, than in all older trees (50 mmol H[sub 2]O/m[sup 2]s), indicating that the ozone concentration in substomatol cavities is higher in young seedlings than in older trees. Significant changes in water use efficiency occurred in trees between ages 5 and 20 years. It is concluded that giant sequoia seedlings are sensitive to atmospheric ozone until they are ca 5 y old. Low conductance, high water use efficiency, and compact mesophyll all contribute to a natural ozone tolerance, or defense, or both, in foliage of older trees. 11 refs., 1 fig., 1 tab.

Effects of oxygen concentration on atmospheric pressure dielectric barrier discharge in Argon-Oxygen Mixture

Science.gov (United States)

Li, Xuechun; Li, Dian; Wang, Younian

2016-09-01

A dielectric barrier discharge (DBD) can generate a low-temperature plasma easily at atmospheric pressure and has been investigated for applications in trials in cancer therapy, sterilization, air pollution control, etc. It has been confirmed that reactive oxygen species (ROS) play a key role in the processes. In this work, we use a fluid model to simulate the plasma characteristics for DBD in argon-oxygen mixture. The effects of oxygen concentration on the plasma characteristics have been discussed. The evolution mechanism of ROS has been systematically analyzed. It was found that the ground state oxygen atoms and oxygen molecular ions are the dominated oxygen species under the considered oxygen concentrations. With the oxygen concentration increasing, the densities of electrons, argon atomic ions, resonance state argon atoms, metastable state argon atoms and excited state argon atoms all show a trend of decline. The oxygen molecular ions density is high and little influenced by the oxygen concentration. Ground state oxygen atoms density tends to increase before falling. The ozone density increases significantly. Increasing the oxygen concentration, the discharge mode begins to change gradually from the glow discharge mode to Townsend discharge mode. Project supported by the National Natural Science Foundation of China (Grant No. 11175034).

Spatial and temporal variability of atmospheric mercury concentrations emitted from a coal-fired power plant in Mexico.

Science.gov (United States)

García, Gilberto Fuentes; Álvarez, Humberto Bravo; Echeverría, Rodolfo Sosa; de Alba, Sergio Rosas; Rueda, Víctor Magaña; Dosantos, Ernesto Caetano; Cruz, Gustavo Vázquez

2017-09-01

Atmospheric mercury in the environment as a result of the consumption of fossil fuels, such as coal used in electricity generation, has gained increased attention worldwide because of its toxicity, atmospheric persistence, and bioaccumulation. Determining or predicting the concentration of this pollutant in ambient air is essential for determining sensitive areas requiring health protection. This study investigated the spatiotemporal variability of gaseous elemental mercury (GEM) concentrations and its dry deposition surrounding the Presidente Plutarco Elías Calles (CETEPEC) coal-fired power plant, located on Mexico's Pacific coast. The CALPUFF dispersion model was applied on the basis of the daily consumption of coal during 2013 for each generating unit in the power plant and considering the local scale. The established 300-ng/m 3 annual average risk factor considered by the U.S. Department of Health and Human Services (U.S. DHHS) and Integrated Risk Information System (IRIS) must not be exceeded to meet satisfactory air quality levels. An area of 65 × 60 km was evaluated, and the results show that the risk level for mercury vapor was not exceeded because the annual average concentration was 2.8 ng/m 3 . Although the predicted risk level was not exceeded, continuous monitoring studies of GEM and of particulates in the atmosphere, soil, and water may be necessary to identify the concentration of this pollutant, specifically that resulting from coal-fired power plants operated in environmental areas of interest in Mexico. The dry mercury deposition was low in the study area; according to the CALPUFF model, the annual average was 1.40E-2 ng/m 2 /sec. These results represent a starting point for Mexico's government to implement the Minamata Convention on Mercury, which Mexico signed in 2013. The obtained concentrations of mercury from a bigger coal-fired plant in Mexico, through the application of the CALPUFF dispersion model by the mercury emissions, are below the

Atmospheric Concentrations of Persistent Organic Pollutants in the Southern Ocean

Science.gov (United States)

Vlahos, P.; Edson, J.; Cifuentes, A.; McGillis, W. R.; Zappa, C.

2008-12-01

Long-range transport of persistent organic pollutant (POPs) is a global concern. Remote regions such as the Southern Ocean are greatly under-sampled though critical components in understanding POPs cycling. Over 20 high-volume air samples were collected in the Southern Ocean aboard the RV Brown during the GASEX III experiment between Mar 05 to April 9 2008. The relatively stationary platform (51S,38W) enabled the collection of a unique atmospheric time series at this open ocean station. Air sampling was also conducted across transects from Punto Arenas, Chile and to Montevideo, Uruguay. Samples were collected using glass sleeves packed with poly-urethane foam plugs and C-18 resin in order to collect target organic pollutants (per-fluorinated compounds, currently and historically used pesticides) in this under-sampled region. Here we present POPs concentrations and trends over the sampled period and compare variations with air parcel back trajectories to establish potential origins of their long-range transport.

Response of biomass and nitrogen yield of white clover to radiation and atmospheric CO2 concentration

International Nuclear Information System (INIS)

Manderscheid, R.; Bender, J.; Schenk, U.; Weigel, H.J.

1997-01-01

The objectives of the present study were to test (i) whether the effect of season-long CO 2 enrichment on plant dry matter production of white clover (Trifolium repens cv. Karina) depends on the temperature or can solely be explained by changes in radiation use efficiency, and (ii) whether the atmospheric CO 2 concentration affects the relationship between tissue %N and plant biomass. Plants were grown in pots with adequate nutrient and water supply and were exposed to ambient and above ambient CO 2 concentrations (approximately +80 ppm, +160 ppm, +280 ppm) in open-top chambers for two seasons. Nitrogen fertilizer was given only before the experiment started to promote N 2 fixation. Plants were clipped to a height of 5 cm, when the canopy had reached a height of about 20 cm and when the CO 2 effect had not been diminished due to self-shading of the leaves. Photon exposure (400–700 nm) measured above the canopy was linearly related to the above ground biomass, the leaf area index and the nitrogen yield (r 2 > 0.94). The slopes of the curves depended on the CO 2 concentration. Since most of the radiation (>90%) was absorbed by the foliage, the slopes were used to calculate the CO 2 effect on the radiation use efficiency of biomass production, which is shown to increase curvilinearly between 380 and 660 ppm CO 2 from 2.7 g MJ −1 to 3.9 g MJ −1 . CO 2 enrichment increased above ground biomass by increasing the leaf number, the individual leaf weight and the leaf area; specific leaf weight was not affected. The relative CO 2 response varied between harvests; there was a slight but not significant positive relationship with mean daytime temperature. At the beginning of the season, plant nitrogen concentration in the above ground biomass was decreased by CO 2 enrichment. However, at later growth stages, when the plants depended solely on N 2 fixation, nitrogen concentration was found to be increased when the nitrogen concentration value was adjusted for the decrease

Regional scale variations of atmospheric CO2 and CH4 from satellite observation

International Nuclear Information System (INIS)

Ru, F; Lei, L; Guan, X; Bu, R; Qi, J

2014-01-01

To identify the sources, sinks and changes of atmospheric CO 2 and CH 4 , this study investigates the spatio-temporal changes of atmospheric CO 2 and CH 4 concentration on the regional scale by the satellite observations. In this paper, choosing the land region of China as the study area, we investigate the spatio-temporal changes of atmospheric CO 2 and CH 4 concentrations using the data of the CO 2 dry air mixing ratio (XCO 2 ), and the CH 4 dry air mixing ratio (XCH 4 ), retrieved by the Greenhouse Gases Observing Satellite (GOSAT) from Jan. 2010 to Dec. 2012. The results show that (1) both XCO 2 and XCH 4 show higher concentrations in southeastern regions than that in the northwestern, and tend to yearly increasing from 2010 to 2013; (2) XCO 2 shows obvious seasonal change with higher values in the spring than that in summer. The seasonal peak-to-peak amplitude is 8 ppm and the annual growth is about 2 ppm. XCH 4 , however, does not show a seasonal change; (3) With regard to different land-use backgrounds, XCO 2 shows larger concentrations over the areas of urban agglomeration than that over the grasslands and deserts, and XCH 4 shows lower concentrations over deserts than that over the Yangtze River Delta region and Sichuan Basin

Tritium concentrations in tree ring cellulose

International Nuclear Information System (INIS)

Kaji, Toshio; Momoshima, Noriyuki; Takashima, Yoshimasa.

1989-01-01

Measurements of tritium (tissue bound tritium; TBT) concentration in tree rings are presented and discussed. Such measurement is expected to provide a useful means of estimating the tritium level in the environment in the past. The concentration of tritium bound in the tissue (TBT) in a tree ring considered to reflect the environmental tritium level in the area at the time of the formation of the ring, while the concentration of tritium in the free water in the tissue represents the current environmental tritium level. First, tritium concentration in tree ring cellulose sampled from a cedar tree grown in a typical environment in Fukuoka Prefecture is compared with the tritium concentration in precipitation in Tokyo. Results show that the year-to-year variations in the tritium concentration in the tree rings agree well with those in precipitation. The maximum concentration, which occurred in 1963, is attibuted to atmospheric nuclear testing which was performed frequently during the 1961 - 1963 period. Measurement is also made of the tritium concentration in tree ring cellulose sampled from a pine tree grown near the Isotope Center of Kyushu University (Fukuoka). Results indicate that the background level is higher probably due to the release of tritium from the facilities around the pine tree. Thus, measurement of tritium in tree ring cellulose clearly shows the year-to-year variation in the tritium concentration in the atmosphere. (N.K.)

Northern European trees show a progressively diminishing response to increasing atmospheric carbon dioxide concentrations

CSIR Research Space (South Africa)

Waterhouse, JS

2004-04-01

Full Text Available Reviews 23 (2004) 803?810 Northern European trees show a progressively diminishing response to increasing atmospheric carbon dioxide concentrations J.S. Waterhousea,*, V.R. Switsura,b, A.C. Barkera, A.H.C. Cartera,b,{, D.L. Hemmingc, N.J. Loaderd, I..., V.R., Waterhouse, J.S., Heaton, T.H.E., Carter, A.H.C., 1998. Climatic variation andthe stable carbon isotope composition of tree ring cellulose: an intercomparison of Quercus robur, Fagus sylvatica and Pinus silvestris. Tellus 50B, 25?33. J.ggi, M...

Neutral polyfluoroalkyl substances in the atmosphere over the northern South China Sea.

Science.gov (United States)

Lai, Senchao; Song, Junwei; Song, Tianli; Huang, Zhijiong; Zhang, Yingyi; Zhao, Yan; Liu, Guicheng; Zheng, Junyu; Mi, Wenying; Tang, Jianhui; Zou, Shichun; Ebinghaus, Ralf; Xie, Zhiyong

2016-07-01

Neutral Polyfluoroalkyl substances (PFASs) in the atmosphere were measured during a cruise campaign over the northern South China Sea (SCS) from September to October 2013. Four groups of PFASs, i.e., fluorotelomer alcohols (FTOHs), fluorotelomer acrylates (FTAs), fluorooctane sulfonamides (FOSAs) and fluorooctane sulfonamidoethanols (FASEs), were detected in gas samples. FTOHs was the predominant PFAS group, accounting for 95.2-99.3% of total PFASs (ΣPFASs), while the other PFASs accounted for a small fraction of ΣPFASs. The concentrations of ΣPFASs ranged from 18.0 to 109.9 pg m(-3) with an average of 54.5 pg m(-3). The concentrations are comparable to those reported in other marine atmosphere. Higher concentrations of ΣPFASs were observed in the continental-influenced samples than those in other samples, pointing to the substantial contribution of anthropogenic sources. Long-range transport is suggested to be a major pathway for introducing gaseous PFASs into the atmosphere over the northern SCS. In order to further understand the fate of gaseous PFASs during transport, the atmospheric decay of neutral PFASs under the influence of reaction with OH radicals and atmospheric physical processes were estimated. Concentrations of 8:2 FTOH, 6:2 FTOH and MeFBSE from selected source region to the atmosphere over the SCS after long-range transport were predicted and compared with the observed concentrations. It suggests that the reaction with OH radicals may play an important role in the atmospheric decay of PFAS during long-range transport, especially for shorted-lived species. Moreover, the influence of atmospheric physical processes on the decay of PFAS should be further considered. Copyright © 2016 Elsevier Ltd. All rights reserved.

Change in the atmospheric concentration of greenhouse gases

International Nuclear Information System (INIS)

GARREC, Jean-Pierre

2000-01-01

With the constant increase in industrial and agricultural activities since the beginning of the 20. Century, human societies have altered the chemical composition of the atmosphere both in their immediate vicinity and further afar. The most preoccupying problem today is the increase in the so-called greenhouse gases (CO 2 , CH 4 , N 2 O, CFC, O 3 ). Indeed, these pollutant gases generally have long life cycles and consequently have for the first time produced a change in the composition of the atmosphere on a global scale inducing deferred effects such as a likely change in the earth's climate. (author)

Influence of long-range atmospheric transport pathways and climate teleconnection patterns on the variability of surface 210Pb and 7Be concentrations in southwestern Europe.

Science.gov (United States)

Grossi, C; Ballester, J; Serrano, I; Galmarini, S; Camacho, A; Curcoll, R; Morguí, J A; Rodò, X; Duch, M A

2016-12-01

The variability of the atmospheric concentration of the 7 Be and 210 Pb radionuclides is strongly linked to the origin of air masses, the strength of their sources and the processes of wet and dry deposition. It has been shown how these processes and their variability are strongly affected by climate change. Thus, a deeper knowledge of the relationship between the atmospheric radionuclides variability measured close to the ground and these atmospheric processes could help in the analysis of climate scenarios. In the present study, we analyze the atmospheric variability of a 14-year time series of 7 Be and 210 Pb in a Mediterranean coastal city using a synergy of different indicators and tools such as: the local meteorological conditions, global and regional climate indexes and a lagrangian atmospheric transport model. We particularly focus on the relationships between the main pathways of air masses and sun spots occurrence, the variability of the local relative humidity and temperature conditions, and the main modes of regional climate variability, such as the North Atlantic Oscillation (NAO) and the Western Mediterranean Oscillation (WeMO). The variability of the observed atmospheric concentrations of both 7 Be and 210 Pb radionuclides was found to be mainly positively associated to the local climate conditions of temperature and to the pathways of air masses arriving at the station. Measured radionuclide concentrations significantly increase when air masses travel at low tropospheric levels from central Europe and the western part of the Iberian Peninsula, while low concentrations are associated with westerly air masses. We found a significant negative correlation between the WeMO index and the atmospheric variability of both radionuclides and no significant association was observed for the NAO index. Copyright © 2016 Elsevier Ltd. All rights reserved.

Environmental and Body Concentrations of Heavy Metals at Sites Near and Distant from Industrial Complexes in Ulsan, Korea.

Science.gov (United States)

Sung, Joo Hyun; Oh, Inbo; Kim, Ahra; Lee, Jiho; Sim, Chang Sun; Yoo, Cheolin; Park, Sang Jin; Kim, Geun Bae; Kim, Yangho

2018-01-29

Industrial pollution may affect the heavy metal body burden of people living near industrial complexes. We determined the average concentrations of atmospheric heavy metals in areas close to and distant from industrial complexes in Korea, and the body concentrations of these heavy metals in residents living near and distant from these facilities. The atmospheric data of heavy metals (lead and cadmium) were from the Regional Air Monitoring Network in Ulsan. We recruited 1,148 participants, 872 who lived near an industrial complex ("exposed" group) and 276 who lived distant from industrial complexes ("non-exposed" group), and measured their concentrations of blood lead, urinary cadmium, and urinary total mercury. The results showed that atmospheric and human concentrations of heavy metals were higher in areas near industrial complexes. In addition, residents living near industrial complexes had higher individual and combined concentrations (cadmium + lead + mercury) of heavy metals. We conclude that residents living near industrial complexes are exposed to high concentrations of heavy metals, and should be carefully monitored. © 2018 The Korean Academy of Medical Sciences.

Daily changes of radon concentration in soil gas under influence of atmospheric factors: room temperature, soil surface temperature and relative humidity

International Nuclear Information System (INIS)

Lara, Evelise G.; Oliveira, Arno Heeren de

2015-01-01

This work aims at relating the daily change in the radon concentration in soil gas in a Red Yellow Acrisol (SiBCS) under influence of atmospheric factors: room temperature, soil surface temperature and relative humidity. The 226 Ra, 232 Th, U content and permeability were also performed. The measurements of radon soil gas were carried out by using an AlphaGUARD monitor. The 226 Ra activity concentration was made by Gamma Spectrometry (HPGe); the permeability was carried out using the RADON-JOK permeameter and ICP-MS analysis to 232 Th and U content. The soil permeability is 5.0 x 10 -12 , which is considered average. The 226 Ra (22.2 ± 0.3 Bq.m -3 ); U content (73.4 ± 3.6 Bq.kg -1 ) and 232 Th content (55.3 ± 4.0 Bq.kg -1 ) were considered above of average concentrations, according to mean values for soils typical (~ 35.0 Bq.kg -1 ) by UNSCEAR. The results showed a difference of 26.0% between the highest and the lowest concentration of radon in soil gas: at midnight (15.5 ± 1.0 kBq.m -3 ) and 3:00 pm, the highest mean radon concentration (21.0 ± 1.0 kBq.m -3 ). The room temperature and surface soil temperature showed equivalent behavior and the surface soil temperature slightly below room temperature during the entire monitoring time. Nevertheless, the relative humidity showed the highest cyclical behavior, showing a higher relationship with the radon concentration in soil gas. (author)

Seasonal variations of aerosol residence time in the lower atmospheric boundary layer

International Nuclear Information System (INIS)

Ahmed, A.A.; Mohamed, A.; Ali, A.E.; Barakat, A.; Abd El-Hady, M.; El-Hussein, A.

2004-01-01

During a one year period, from Jan. 2002 up to Dec. 2002, approximately 130 air samples were analyzed to determine the atmospheric air activity concentrations of short- and long-lived ( 222 Rn) decay products 214 Pb and 210 Pb. The samples were taken by using a single-filter technique and γ-spectrometry was applied to determine the activity concentrations. A seasonal fluctuation in the concentration of 214 Pb and 210 Pb in surface air was observed. The activity concentrations of both radionuclides were observed to be relatively higher during the winter/autumn season than in spring/summer season. The mean activity concentration of 214 Pb and 210 Pb within the whole year was found to be 1.4±0.27 Bq m -3 and 1.2±0.15 mBq m -3 , respectively. Different 210 Pb: 214 Pb activity ratios during the year varied between 1.78x10 -4 and 1.6x10 -3 with a mean value of 8.9x10 -4 ±7.6x10 -5 . From the ratio between the activity concentrations of the radon decay products 214 Pb and 210 Pb a mean residence time (MRT) of aerosol particles in the atmosphere of about 10.5±0.91 d could be estimated. The seasonal variation pattern shows relatively higher values of MRT in spring/summer season than in winter/autumn season. The MRT data together with relative humidity (RH), air temperature (T) and wind speed (WS), were used for a comprehensive regression analysis of its seasonal variation in the atmospheric air

Persistent organic pollutants in the atmosphere - spatial and temporal variations

Energy Technology Data Exchange (ETDEWEB)

Backe, Cecilia

2001-05-01

significant relationships were found between air and soil concentrations of PCBs, or between deposition and soil concentrations. From fugacity quotient calculations it was shown that the soil- and air compartments for most of the sampling-areas were close to equilibrium. However, for some areas there was an outgassing of PCBs from the soil and at one site a tendency for a transport of PCBs from the air to the soil was observed. Within the Baltic Sea region a latitudinal gradient of PCBs in the atmosphere was revealed, with higher levels in the south. Further evidence of the global distillation theory was shown in a study with higher atmospheric levels of DDT in a tropical region in comparison with DDT levels in a temperate region. In accordance with the theory, DDT levels were high in fish from the temperate region, but low in fish from the tropical region.

Diagnostic of N2(A) concentration in high velocity nitrogen afterglow at atmospheric pressure

Science.gov (United States)

Pointu, Anne-Marie; Mintusov, Evgeny

2009-10-01

An optical emission diagnostic was used to measure N2(A) concentration in a high velocity (1000 cm/s) N2 flowing afterglow of corona discharge at atmospheric pressure, used for biological decontamination. Introducing impurities of NO (measured at different axial distances and for different values of NO injected flow. Moreover, it has been demonstrated that N2(A) creation comes from N+N+N2 atom recombination with a global rate around 2e-33 cm^6/s, a result which agrees with literature, as well as N2(A) loss mechanisms were confirmed to go via quenching with O and N atoms. The order of magnitude of obtained N2(A) concentration, about 1e11 cm-3, coincides with the results of direct measurement (by Vegard-Kaplan band), using a spectrometer of better resolution.

Atmospheric wet deposition of mercury in North America

Energy Technology Data Exchange (ETDEWEB)

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

1999-07-01

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

Temporal and vertical variations radon and its progeny related to atmospheric electrical conductivity

International Nuclear Information System (INIS)

Pruthvi Rani, K.S.; Chandrashekara, M.S.; Paramesh, L.

2015-01-01

Atmospheric radon, its progeny, electrical conductivity and meteorological parameters such as wind, temperature, humidity, pressure and rainfall were continuously monitored during 2012 to 2014 at one location in Mysuru city. The annual mean atmospheric radon concentration at the study location was found to be 16.4 Bqm -3 . The diurnal cycle of radon and its progeny show a peak in the early morning hours followed by a drastic decrease after sunrise and rising to a second peak in the afternoon. It was found that the stability of the atmosphere and ambient temperature played a major role in the diurnal variations. Higher concentrations of radon and its progeny were observed in winter and lower values in summer. This may due to the variations in origin of air mass and meteorological parameters. Wind direction analyses reveal that in sectors with air which has spent a longer period over the granitic region and low wind speeds will lead to higher concentrations of radon. Atmospheric electrical conductivity near the ground is mainly due to the ionization from radon and its progeny. The diurnal variations of conductivity and ionization rate due to radon and its individual progeny were of similar trend. In addition its significant dependence on meteorological parameters is confirmed. The vertical variations of atmospheric electrical conductivity were studied at different heights up to 250 m from the ground level. Higher values were observed close to the ground surface, there was a rapid reduction up to about 10 m and beyond that the conductivity gradually decreases. The diurnal conductivity cycle is studied at 10 m and 100 m showed the expected similar trend at both the heights but early morning maxima were considerably different, this confirms the accumulation of radon gas close to the ground surface during night time leading to increase of conductivity values. (author)

POSSIBLE RAMIFICATIONS OF HIGHER MERCURY CONCENTRATIONS IN FILLET TISSUE OF SKINNIER FISH

Science.gov (United States)

Mercury concentrations were found to be statistically higher in the fillet tissue of the skinnier individuals of a fish species (striped bass) that was experiencing starvation when collected from Lake Mead, which is located on the Arizona-Nevada border. This is considered a conse...

Future concentrations of atmospheric greenhouse gases CO2, CFC and CH4 - an assessment on the educational level

International Nuclear Information System (INIS)

Hoppenau, S.

1992-01-01

A model on the educational level is described to estimate effective future atmospheric CO 2 concentrations. The effects of chlorofluorocarbon and methane emission and deforestation are taken into account. The influence of different emission scenarios on the time evolution of greenhouse-gas concentration are illustrated. Future global energy policies are discussed both under the aspects of rising world population and the reduction in global CO 2 emissions. The model can be handled on a PC or even on a pocket calculator

Annual atmospheric mercury species in downtown Toronto, Canada.

Science.gov (United States)

Song, Xinjie; Cheng, Irene; Lu, Julia

2009-03-01

Real-time concentrations of atmospheric gaseous elemental mercury (GEM), reactive gaseous mercury (RGM), and mercury associated with particles having sizes RGM were 4.5 +/- 3.1 ng m(-3) (99.2%), 21.5 +/- 16.4 pg m(-3) (0.5%) and 14.2 +/- 13.2 pg m(-3) (0.3%), respectively. The concentrations for all the measured Hg species were highly variable throughout the year and were lower in winter than in the other three seasons. The maximum concentrations of Hg species were observed in June and were a result of the high number of Hg spikes (using [GEM] >10 ng m(-3) as an indicator) that occurred in the month. Nighttime (between 9pm-6am) concentrations of Hg species were higher than those of daytime. The results revealed: (1) an urban area is a continuous source of Hg species that have the potential to pose impacts on local, regional and global scales; (2) local/regional anthropogenic sources contributed significantly to the levels and the distributions of the Hg species in the urban atmosphere. More studies are needed to identify and quantify the anthropogenic sources of Hg and the Hg species emitted from these sources; (3) surface emission and photochemical reactions (including the reactions involving ozone) did not have significant influence on the levels of Hg species and their distribution in the urban atmosphere.

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

Science.gov (United States)

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

2017-12-01

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

Coal char combustion under a CO{sub 2}-rich atmosphere: Implications for pulverized coal injection in a blast furnace

Energy Technology Data Exchange (ETDEWEB)

Borrego, A.G.; Casal, M.D. [Instituto Nacional del Carbon, CSIC. P.O. Box 73, 33080 Oviedo (Spain); Osorio, E.; Vilela, A.C.F. [Laboratorio de Siderurgia, DEMET/PPGEM - Universidade Federal do Rio Grande do Sul. P.O. Box 15021, 91501-970 Porto Alegre (Brazil)

2008-11-15

Pulverized coal injection (PCI) is employed in blast furnace tuyeres attempting to maximize the injection rate without increasing the amount of unburned char inside the stack of the blast furnace. When coal is injected with air through the injection lance, the resolidified char will burn in an atmosphere with a progressively lower oxygen content and higher CO{sub 2} concentration. In this study an experimental approach was followed to separate the combustion process into two distinct devolatilization and combustion steps. Initially coal was injected into a drop tube furnace (DTF) operating at 1300 C in an atmosphere with a low oxygen concentration to ensure the combustion of volatiles and prevent the formation of soot. Then the char was refired into the DTF at the same temperature under two different atmospheres O{sub 2}/N{sub 2} (typical combustion) and O{sub 2}/CO{sub 2} (oxy-combustion) with the same oxygen concentration. Coal injection was also performed under a higher oxygen concentration in atmospheres typical for both combustion and oxy-combustion. The fuels tested comprised a petroleum coke and coals currently used for PCI injection ranging from high volatile to low volatile bituminous rank. Thermogravimetric analyses and microscopy techniques were used to establish the reactivity and appearance of the chars. Overall similar burnouts were achieved with N{sub 2} and CO{sub 2} for similar oxygen concentrations and therefore no loss in burnout should be expected as a result of enrichment in CO{sub 2} in the blast furnace gas. The advantage of increasing the amount of oxygen in a reacting atmosphere during burnout was found to be greater, the higher the rank of the coal. (author)

Atmospheric particulate matter size distribution and concentration in West Virginia coal mining and non-mining areas.

Science.gov (United States)

Kurth, Laura M; McCawley, Michael; Hendryx, Michael; Lusk, Stephanie

2014-07-01

People who live in Appalachian areas where coal mining is prominent have increased health problems compared with people in non-mining areas of Appalachia. Coal mines and related mining activities result in the production of atmospheric particulate matter (PM) that is associated with human health effects. There is a gap in research regarding particle size concentration and distribution to determine respiratory dose around coal mining and non-mining areas. Mass- and number-based size distributions were determined with an Aerodynamic Particle Size and Scanning Mobility Particle Sizer to calculate lung deposition around mining and non-mining areas of West Virginia. Particle number concentrations and deposited lung dose were significantly greater around mining areas compared with non-mining areas, demonstrating elevated risks to humans. The greater dose was correlated with elevated disease rates in the West Virginia mining areas. Number concentrations in the mining areas were comparable to a previously documented urban area where number concentration was associated with respiratory and cardiovascular disease.

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.

Sampling of Atmospheric Precipitation and Deposits for Analysis of Atmospheric Pollution

OpenAIRE

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

2006-01-01

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

Higher aluminum concentration in Alzheimer's disease after Box-Cox data transformation.

Science.gov (United States)

Rusina, Robert; Matěj, Radoslav; Kašparová, Lucie; Kukal, Jaromír; Urban, Pavel

2011-11-01

Evidence regarding the role of mercury and aluminum in the pathogenesis of Alzheimer's disease (AD) remains controversial. The aims of our project were to investigate the content of the selected metals in brain tissue samples and the use of a specific mathematical transform to eliminate the disadvantage of a strong positive skew in the original data distribution. In this study, we used atomic absorption spectrophotometry to determine mercury and aluminum concentrations in the hippocampus and associative visual cortex of 29 neuropathologically confirmed AD and 27 age-matched controls. The Box-Cox data transformation was used for statistical evaluation. AD brains had higher mean aluminum concentrations in the hippocampus than controls (0.357 vs. 0.090 μg/g; P = 0.039) after data transformation. Results for mercury were not significant. Original data regarding microelement concentrations are heavily skewed and do not pass the normality test in general. A Box-Cox transformation can eliminate this disadvantage and allow parametric testing.

Atmospheric Dispersion of Various Types of Iodine in UAE in February and August

Energy Technology Data Exchange (ETDEWEB)

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

2013-05-15

The distribution ratio of these three types of iodine being released to the atmosphere under accident scenario is still not clearly reported because of its complex kinetics of chemical and physical process in the accidental condition. In this research, the dispersion behaviors of three kinds of iodine in the atmosphere have been considered in the UAE environment in winter and summer situations. Higher ground level concentration on the same downwind distance from the source appears in summer because of lower wind speed than that of winter. More lateral spreading of vertical downwind direction in summer has been confirmed because of less stable air than that of winter. Higher ground level concentrations have been appeared in order of particle type, organic gas type and elemental gas type of I-131 with given assumptions.

The Inflammatory Radicular Cysts Have Higher Concentration of TNF-α in Comparison to Odontogenic Keratocysts (Odontogenic Tumour

Directory of Open Access Journals (Sweden)

Vladimir Jurisic

2007-01-01

Full Text Available TNF-α is a pleiotropic cytokine that is considered as a primary modifier of inflammatory and immune reaction in response to various inflammatory diseases and tumour. We investigated levels of TNF-α in 43 radicular cysts and 15 odontogenic keratocysts, obtained from patients undergoing surgery, under local anaesthesia, and after aspiration of cystic fluid from non-ruptured cysts. TNF-α is elevated in both cysts’ fluid, but higher values were found in radicular cysts in comparison to keratocysts. The significantly higher concentration of TNF-α was associated with smaller radicular cysts, higher protein concentration, higher presence of inflammatory cells in peri cystic tissues, and the degree of vascularisation and cysts wall thickness (Mann-Whitney U-test, p<0.05. No correlation was found based on these parameters in odontogenic keratocyst, but all cysts have detectable concentrations of TNF-α. We here for the first time present that a difference in the concentration of TNF-α exists between these two cystic types.

Record high peaks in PCB concentrations in the Arctic atmosphere due to long-range transport of biomass burning emissions

Directory of Open Access Journals (Sweden)

S. Eckhardt

2007-08-01

Full Text Available Soils and forests in the boreal region of the Northern Hemisphere are recognised as having a large capacity for storing air-borne Persistent Organic Pollutants (POPs, such as the polychlorinated biphenyls (PCBs. Following reductions of primary emissions of various legacy POPs, there is an increasing interest and debate about the relative importance of secondary re-emissions on the atmospheric levels of POPs. In spring of 2006, biomass burning emissions from agricultural fires in Eastern Europe were transported to the Zeppelin station on Svalbard, where record-high levels of many air pollutants were recorded (Stohl et al., 2007. Here we report on the extremely high concentrations of PCBs that were also measured during this period. 21 out of 32 PCB congeners were enhanced by more than two standard deviations above the long-term mean concentrations. In July 2004, about 5.8 million hectare of boreal forest burned in North America, emitting a pollution plume which reached the Zeppelin station after a travel time of 3–4 weeks (Stohl et al., 2006. Again, 12 PCB congeners were elevated above the long-term mean by more than two standard deviations, with the less chlorinated congeners being most strongly affected. We propose that these abnormally high concentrations were caused by biomass burning emissions. Based on enhancement ratios with carbon monoxide and known emissions factors for this species, we estimate that 130 and 66 μg PCBs were released per kilogram dry matter burned, respectively. To our knowledge, this is the first study relating atmospheric PCB enhancements with biomass burning. The strong effects on observed concentrations far away from the sources, suggest that biomass burning is an important source of PCBs for the atmosphere.

Higher milk fat content is associated with higher 25-hydroxyvitamin D concentration in early childhood.

Science.gov (United States)

Vanderhout, Shelley M; Birken, Catherine S; Parkin, Patricia C; Lebovic, Gerald; Chen, Yang; O'Connor, Deborah L; Maguire, Jonathon L

2016-05-01

Current guidelines for cow's milk consumption in children older than age 2 years suggest 1% or 2% milk to reduce the risk of obesity. Given that milk is the main dietary source of vitamin D for North American children and that vitamin D is fat soluble, we hypothesized 25-hydroxyvitamin D (25(OH)D) concentration to be positively associated with the fat content of milk. The objective was to determine the relationship between the fat content of milk consumed and the serum 25(OH)D concentration; our secondary objective was to explore the role that the volume of milk consumed played in this relationship. We completed a cross-sectional study of children aged 12-72 months in the TARGetKids! research network. Multivariable linear regression was used to test the association between milk fat content and child 25(OH)D, adjusted for clinically relevant covariates. The interaction between volume of milk and fat content was examined. Two thousand eight hundred fifty-seven children were included in the analysis. The fat content of milk was positively associated with 25(OH)D (p = 0.03), and the interaction between the volume of milk consumed and the milk fat content was statistically significant (p = 0.005). Children who drank 1% milk needed 2.46 cups (95% confidence interval (CI) 2.38-2.54) of milk to have a 25(OH)D concentration similar to that of children who drank 1 cup of homogenized milk (3.25% fat). Children who consumed 1% milk had 2.05 (95% CI 1.73-2.42) times higher odds of having a 25(OH)D concentration <50 nmol/L compared with children who consumed homogenized milk. In conclusion, recommendations for children to drink lower-fat milk (1% or 2%) may compromise serum 25(OH)D levels and may require study to ensure optimal childhood health.

Concentration and behavior of radiocesium in higher basidiomycetes in some Kanto and the Koshin districts, Japan

International Nuclear Information System (INIS)

Sugiyama, Hideo; Iwashima, Kiyoshi; Shibata, Hisashi.

1990-01-01

Concentration of 137 Cs, 134 Cs and potassium were measured in several higher fungi and in substrates, soils, woods and litters in some Kanto and the Koshin districts, Japan, following the Chernobyl accident during October to November 1989. 137 Cs concentrations in fungi were in the range of 0.7-101 Bq kg -1 · fresh. Maximum 137 Cs level in them was observed in Boletopsis leucomelas (Pers.: Fr.) Fayod. Significantly higher levels of concentration ratios of 137 Cs in fungi to substrates (e.g.; 137 Cs concentration · fresh in fungus/ 137 Cs concentration · dry in soil), 10 -1 to 10 x 10 -1 , were found nearly 10 to 1000 times as much as leaf vegetables, root crops and potatoes to substrates. It was confirmed that levels of concentration ratios of potassium were similar to those of 137 Cs. In all fungi, 134 Cs which released from the Chernobyl accident and is not present in nuclear weapons fallout was not detected. (author)

Relating Nimbus-7 37 GHz data to global land-surface evaporation, primary productivity and the atmospheric CO2 concentration

Science.gov (United States)

Choudhury, B. J.

1988-01-01

Global observations at 37 GHz by the Nimbus-7 SMMR are related to zonal variations of land surface evaporation and primary productivity, as well as to temporal variations of atmospheric CO2 concentration. The temporal variation of CO2 concentration and the zonal variations of evaporation and primary productivity are shown to be highly correlated with the satellite sensor data. The potential usefulness of the 37-GHz data for global biospheric and climate studies is noted.

Three years (2008-2010) of measurements of atmospheric concentrations of organochlorine pesticides (OCPs) at Station Nord, North-East Greenland

DEFF Research Database (Denmark)

Bossi, R.; Skjoth, C. A.; Skov, H.

2013-01-01

the Clausius-Clapeyron equation in order to obtain information about their transport properties. The correlation between atmospheric concentrations and temperature was not significant for endosulfan I, gamma-HCH and p,p'-DDT, which indicates that direct transport from direct sources is the dominating transport...

Atmospheric relative concentrations in building wakes

International Nuclear Information System (INIS)

Ramsdell, J.V. Jr.; Simonen, C.A.

1997-05-01

This report documents the ARCON96 computer code developed for the U.S. Nuclear Regulatory Commission Office of Nuclear Reactor Regulation for potential use in control room habitability assessments. It includes a user's guide to the code, a description of the technical basis for the code, and a programmer's guide to the code. The ARCON96 code uses hourly meteorological data and recently developed methods for estimating dispersion in the vicinity of buildings to calculate relative concentrations at control room air intakes that would be exceeded no more than five percent of the time. The concentrations are calculated for averaging periods ranging from one hour to 30 days in duration. ARCON96 is a revised version of ARCON95, which was developed for the NRC Office of Nuclear Regulatory Research. Changes in the code permit users to simulate releases from area sources as well as point sources. The method of averaging concentrations for periods longer than 2 hours has also been changed. The change in averaging procedures increases relative concentrations for these averaging periods. In general, the increase in concentrations is less than a factor of two. The increase is greatest for relatively short averaging periods, for example 0 to 8 hours and diminishes as the duration of the averaging period increases

Daily changes of radon concentration in soil gas under influence of atmospheric factors: room temperature, soil surface temperature and relative humidity

Energy Technology Data Exchange (ETDEWEB)

Lara, Evelise G.; Oliveira, Arno Heeren de, E-mail: evelise.lara@gmail.com, E-mail: heeren@nuclear.ufmg.br [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Departamento de Engenharia Nuclear; Rocha, Zildete; Rios, Francisco Javier, E-mail: rochaz@cdtn.br, E-mail: javier@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

2015-07-01

This work aims at relating the daily change in the radon concentration in soil gas in a Red Yellow Acrisol (SiBCS) under influence of atmospheric factors: room temperature, soil surface temperature and relative humidity. The {sup 226}Ra, {sup 232}Th, U content and permeability were also performed. The measurements of radon soil gas were carried out by using an AlphaGUARD monitor. The {sup 226}Ra activity concentration was made by Gamma Spectrometry (HPGe); the permeability was carried out using the RADON-JOK permeameter and ICP-MS analysis to {sup 232}Th and U content. The soil permeability is 5.0 x 10{sup -12}, which is considered average. The {sup 226}Ra (22.2 ± 0.3 Bq.m{sup -3}); U content (73.4 ± 3.6 Bq.kg{sup -1}) and {sup 232}Th content (55.3 ± 4.0 Bq.kg{sup -1}) were considered above of average concentrations, according to mean values for soils typical (~ 35.0 Bq.kg{sup -1}) by UNSCEAR. The results showed a difference of 26.0% between the highest and the lowest concentration of radon in soil gas: at midnight (15.5 ± 1.0 kBq.m{sup -3}) and 3:00 pm, the highest mean radon concentration (21.0 ± 1.0 kBq.m{sup -3}). The room temperature and surface soil temperature showed equivalent behavior and the surface soil temperature slightly below room temperature during the entire monitoring time. Nevertheless, the relative humidity showed the highest cyclical behavior, showing a higher relationship with the radon concentration in soil gas. (author)

CONCENTRATION OF HARMFUL SUBSTANCES REDUCING IN SURFACE LAYER OF ATMOSPHERE AT RHEOSTAT LOCOMOTIVE TESTS

Directory of Open Access Journals (Sweden)

E. A. Bondar

2010-06-01

Full Text Available It is shown that at present an acceptable way of reducing the concentration of harmful substances in the surface layer of the atmosphere at rheostat tests of locomotives is their dispersion in a large volume of air. Channels, installed above an exhaust pipe of diesel locomotive with a break at the gas flow, work as ejectors. We have solved jointly the equation of aerodynamic characteristics of the ejector device and the equation of diffusion of gases; as a result the calculated dependence for determining the necessary height of ejector device has been obtained.

Declining Atmospheric pCO2 During the Late Miocene and Early Pliocene: New Insights from Paired Alkenone and Coccolith Stable Isotope Barometry

Science.gov (United States)

Phelps, S. R.; Polissar, P. J.; deMenocal, P. B.; Swann, J. P.; Guo, M. Y.; Stoll, H. M.

2015-12-01

The relationship between atmospheric CO2 concentrations and climate is broadly understood for the Cenozoic era: warmer periods are associated with higher atmospheric carbon dioxide. This understanding is supported by atmospheric samples of the past 800,000 years from ice cores, which suggest CO2 levels play a key role in regulating global climate on glacial interglacial timescales as well. In this context, the late Miocene poses a challenge: sea-surface temperatures indicate substantial global warmth, though existing data suggest atmospheric CO2 concentrations were lower than pre-industrial values. Recent work using the stable carbon and oxygen isotopic composition of coccolith calcite has demonstrated these organisms began actively diverting inorganic carbon away from calcification and to the site of photosynthesis during the late Miocene. This process occurs in culture experiments in response to low aqueous CO2 concentrations, and suggests decreasing atmospheric pCO2 values during the late Miocene. Here we present new data from ODP Site 806 in the western equatorial Pacific Ocean that supports declining atmospheric CO2 across the late Miocene. Carbon isotope values of coccolith calcite from Site 806 demonstrate carbon limitation and re-allocation of inorganic carbon to photosynthesis starting between ~8 and 6 Ma. The timing of this limitation at Site 806 precedes shifts at other ODP sites, reflecting the higher mixed layer temperature and resultant lower CO2 solubility at Site 806. New measurements of carbon isotope values from alkenones at Site 806 show an increase in photosynthetic carbon fractionation (ɛp) accompanied the carbon limitation evident from coccolith calcite stable isotope data. While higher ɛp is typically interpreted as higher CO2 concentrations, at Site 806, our data suggest it reflects enhancement of chloroplast CO2 from active carbon transport by the coccolithophore algae in response to lower CO2 concentrations. Our new data from ODP Site

Temporal variations of atmospheric CO2 concentration in a temperate deciduous forest in central Japan

International Nuclear Information System (INIS)

Murayama, Shohei; Saigusa, Nobuko; Yamamoto, Susumu; Kondo, Hiroaki; Eguchi, Yozo; Chan, Douglas

2003-01-01

In order to examine the temporal variation of the atmospheric CO 2 concentration in a temperate deciduous forest, and its relationship with meteorological conditions, continuous measurements of CO 2 and meteorological parameters have been made since 1993 on a tower at Takayama in the central part of Japan. In addition to an average secular increase in atmospheric CO 2 of 1.8 ppm/yr, diurnal variation with a maximum during the night-time to early morning and a minimum in the afternoon is observed from late spring to early fall; the diurnal cycle is not so clearly observed in the remaining seasons of the year. A concentration difference between above and below the canopy, and its diurnal variation, can also be seen clearly in summer. Daily mean concentration data show a prominent seasonal cycle. The maximum and the minimum of the seasonal cycle occur in April and from mid August to mid September, respectively. Day-to-day changes in the diurnal cycle of CO 2 are highly dependent on the day-to-day variations in meteorological conditions. However, CO 2 variations on longer time scales (>10 d) appear to be linearly related to changes in respiration. At Takayama, variations in the 10-d standard deviation of daily mean CO 2 data and 10-d averaged respiration show distinct relationships with soil temperature during spring and fall seasons. In spring, respiration has a stronger exponential dependence on soil temperature than in fall. Interestingly, in summer when soil temperature becomes greater than about 15 deg C, biological respiration becomes more variable and independent of the soil temperature. Thus, at the Takayama site, the Q10 relationship is seasonally dependent, and does not represent well the biological respiration process when the soil temperature rises above 15 deg C

Results of concentration measurements of artificial radioactive aerosols in the lower atmosphere; Resultats des mesures de concentration, dans la basse atmosphere, des aerosols radioactifs artificiels

Energy Technology Data Exchange (ETDEWEB)

Ardouin, B; Jehanno, C; Labeyrie, J; Lambert, G; Tanaevsky, O; Vassy, E [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1963-07-01

This report gives the results of the measurements of artificial gross-{beta}-radioactivity in aerosols in the lower atmosphere; these measurements have been made by the Electronic Physics Service of the Electronic Department, and by the Atmospheric Physics Laboratory of the Paris Science Faculty. The measurements were begun in September 1956 and were continued in an increasing number of stations both in France and in the rest of the world. The present report deals with the period up to the end of august 1961, that is up to the end of the nuclear moratorium. After recalling the constitution and the properties of radioactive aerosols present in the atmosphere, the authors describe the measurement methods, estimate their accuracy and discuss various aspects of the results. (authors) [French] Ce rapport contient les resultats des mesures de radioactivite {beta} globale d'origine artificielle des aerosols dans la basse atmosphere, effectuees conjointement par le Service d'Electronique Physique du Departement d'Electronique et le Laboratoire de Physique de l'Atmosphere de la Faculte des Sciences de Paris. Les mesures ont commence en septembre 1956 et ont ete poursuivies dans un nombre croissant de stations, tant en France que dans le reste du monde. Le present rapport s'arrete a la fin aout 1961, c'est-a-dire au moment de la reprise des essais nucleaires. Apres avoir rappele la constitution et les proprietes des aerosols radioactifs presents dans l'atmosphere, les auteurs indiquent les methodes de mesure utilisees, evaluent leur precision et discutent les differents aspects des resultats de leurs mesures. (auteurs)

Elevated atmospheric carbon dioxide concentration: effects of increased carbon input in a Lolium perenne soil on microorganisms and decomposition

NARCIS (Netherlands)

Ginkel, van J.H.; Gorissen, A.; Polci, D.

2000-01-01

Effects of ambient and elevated atmospheric CO2 concentrations (350 and 700 μl l-1) on net carbon input into soil, the production of root-derived material and the subsequent microbial transformation were investigated. Perennial ryegrass plants (L. perenne L.) were labelled in a continuously labelled

Global atmospheric changes.

OpenAIRE

Piver, W T

1991-01-01

Increasing concentrations of CO2 and other greenhouse gases in the atmosphere can be directly related to global warming. In terms of human health, because a major cause of increasing atmospheric concentrations of CO2 is the increased combustion of fossil fuels, global warming also may result in increases in air pollutants, acid deposition, and exposure to ultraviolet (UV) radiation. To understand better the impacts of global warming phenomena on human health, this review emphasizes the proces...

Impacts of Mercury Pollution Controls on Atmospheric Mercury Concentration and Occupational Mercury Exposure in a Hospital.

Science.gov (United States)

Li, Ping; Yang, Yan; Xiong, Wuyan

2015-12-01

Mercury (Hg) and Hg-containing products are used in a wide range of settings in hospitals. Hg pollution control measures were carried out in the pediatric ward of a hospital to decrease the possibility of Hg pollution occurring and to decrease occupational Hg exposure. Total gaseous Hg (TGM) concentrations in the pediatric ward and hair and urine Hg concentrations for the pediatric staff were determined before and after the Hg pollution control measures had been implemented. A questionnaire survey performed indicated that the pediatric staff had little understanding of Hg pollution and that appropriate disposal techniques were not always used after Hg leakage. TGM concentrations in the pediatric ward and urine Hg (UHg) concentrations for the pediatric staff were 25.7 and 22.2% lower, respectively, after the Hg pollution control measures had been implemented than before, which indicated that the control measures were effective. However, TGM concentrations in the pediatric ward remained significantly higher than background concentrations and UHg concentrations for the pediatric staff were remained significantly higher than the concentrations in control group, indicating continued existence of certain Hg pollution.

Beryllium-7 in near-surface atmospheric aerosols in mid-latitude (40 deg N) city Beijing, China

International Nuclear Information System (INIS)

Keyan Tan; Yongliang Yang; Xiaohua Zhu; Shu Chen; Xingchun Jiao; Nan Gai; Yi Huang

2013-01-01

A high-volume air sampler and a high-resolution gamma-ray spectrometer have been used to measure the activity of 7 Be in near-surface atmospheric aerosols at sampling frequency of 3 days week for 1 year from August 2009 to July 2010 at Beijing in the mid-latitude region of East Asia monsoon. The measurements indicate that the average concentration of 7 Be was 8.39 ± 0.49 mBq m -3 , which was significantly higher than values reported for other cities in the East Asia monsoon region and in the world during the same period. The maximum and minimum of the weekly means of 7 Be concentration were observed in September and May, respectively. The 7 Be concentrations varied in accordance with the monsoon phases. Low but frequent wet precipitation may have caused lower 7 Be observed in July when southeasterly was prevailing. Higher seasonal mean of 7 Be concentrations in autumn could be attributed to the abnormal atmospheric circulation in autumn 2009. (author)

Variable conductivity and embolism in roots and branches of four contrasting tree species and their impacts on whole-plant hydraulic performance under future atmospheric CO2 concentration

International Nuclear Information System (INIS)

Domec, J.C.; North Carolina State Univ., Raleigh, NC; Schafer, K.; Oren, R.; Kim, H.S.; McCarthy, H.R.

2010-01-01

Tree growth and wood quality are being affected by changes in atmospheric carbon dioxide (CO 2 ) concentrations and precipitation regimes. Plant photosynthesis is likely to be higher under elevated atmospheric CO 2 concentrations, thereby increasing the availability of carbohydrates for growth. This study quantified the effect of elevated CO 2 concentration on anatomical and functional traits related to water transport, gas exchange, water economy and drought tolerance. The conditions under which embolism in the xylem of roots and branches are most likely to occur were investigated on 4 tree species at the Duke Forest free-air CO 2 enrichment (FACE) facility. The trees occupied different canopy strata and represented different xylem types. The study determined whether different xylem anatomies result in a wide range of hydraulic conductance and difference in resistance to cavitation. The link between liquid and gas-phase transport and how it is affected by elevated CO 2 was then quantified. Physiological changes observed under elevated CO 2 were not clearly related to structural change in the xylem of any of the species. The study showed that in some species, elevated CO 2 changed the hydraulic pathways, most likely structurally, thereby affecting the liquid phase transport and reducing stomatal conductance. The results provided a better understanding of the physiological and anatomical mechanisms that determine the responses of tree species to drought, and more generally to global change. 96 refs., 3 tabs., 8 figs.

Cocaine use is associated with a higher prevalence of elevated ST2 concentrations.

Science.gov (United States)

van Wijk, Xander M R; Vittinghoff, Eric; Wu, Alan H B; Lynch, Kara L; Riley, Elise D

2017-09-01

Cocaine is a well-known risk factor for acute cardiac events, but the effects in users outside of acute events are less clear. We investigated a possible association between cocaine use and the concentration of a novel biomarker for cardiac stress and heart failure, ST2. A case-control study was conducted to compare ST2 concentrations by the presence of cocaine in patients presenting for care, but not cardiac care, at an urban safety net hospital. In samples taken from 100 cocaine-positive and 100 cocaine-negative patients, the presence of cocaine was associated with ST2 concentrations>35ng/mL. Serum concentrations of benzoylecgonine, a major cocaine metabolite, were significantly correlated with ST2 concentrations. Cocaine use is associated with subclinical cardiac stress and damage outside of acute cardiac events. This information could add to better stratification of cocaine users with elevated ST2 concentrations who may be at higher risk for developing heart failure and other cardiac complications. Copyright © 2017 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.

Using nitrogen concentration and isotopic composition in lichens to spatially assess the relative contribution of atmospheric nitrogen sources in complex landscapes

International Nuclear Information System (INIS)

Pinho, P.; Barros, C.; Augusto, S.; Pereira, M.J.

2017-01-01

Reactive nitrogen (Nr) is an important driver of global change, causing alterations in ecosystem biodiversity and functionality. Environmental assessments require monitoring the emission and deposition of both the amount and types of Nr. This is especially important in heterogeneous landscapes, as different land-cover types emit particular forms of Nr to the atmosphere, which can impact ecosystems distinctively. Such assessments require high spatial resolution maps that also integrate temporal variations, and can only be feasibly achieved by using ecological indicators. Our aim was to rank land-cover types according to the amount and form of emitted atmospheric Nr in a complex landscape with multiple sources of N. To do so, we measured and mapped nitrogen concentration and isotopic composition in lichen thalli, which we then related to land-cover data. Results suggested that, at the landscape scale, intensive agriculture and urban areas were the most important sources of Nr to the atmosphere. Additionally, the ocean greatly influences Nr in land, by providing air with low Nr concentration and a unique isotopic composition. These results have important consequences for managing air pollution at the regional level, as they provide critical information for modeling Nr emission and deposition across regional as well as continental scales. - Highlights: • Which land-cover types are reactive nitrogen sources or sinks at a landscape level? • Nitrogen concentration and isotopic composition were analyzed in lichens. • This allowed determination of the main nitrogen sources: agricultural and urban areas. • Marine sources provided persistent low concentrations of reactive nitrogen. • The typical signature of each source was also determined. - Reactive-nitrogen concentration and isotopic composition in lichens were used to rank Nr sources at a landscape level.

Natural and anthropogenic pollution of the global atmosphere

International Nuclear Information System (INIS)

Jaworowski, Z.

1999-01-01

Results of determination of natural radionuclides, fission products and heavy metals in contemporary and pre-industrial ice from 14 glaciers in Southern and Northern Hemisphere, and in aerosols collected during three decades from seven altitudes between 0 and 15 km in the troposphere and atmosphere, were used for determinations of fluxes of man-made and natural pollutants into the global atmosphere. For these determinations 137 Cs from nuclear explosions and natural 210 Pb were used as tracers. Concentration of natural radionuclides and heavy metals in ice deposited before industrial revolution were higher than the contemporary precipitation presented as firn in high mountain and polar glaciers. This is due probably to volcanic activity which was higher before the first part of 20 th century. Man-made contribution to the total atmospheric flux is now 3.5% for 226 Ra, 12% for U, 7.4% for Pb, 011% for Cd, 62% for V and 5.8 for Hg. The mass of annual global wet precipitation, determined for the first time with radioactive tracers, is 5.7·10 1 7 kg. In Poland the lowest concentration of stable lead in human bones is now in highly industrialized southern districts. Lead level in medieval human bones from these districts reached up to 370 μg/g. Its current average level in inhabitants of southern Poland is 3.5 μg/g, i. e. similar as 1800 years ago. (author)

Relationship between atmospheric pollution in the residential area and concentrations of polycyclic aromatic hydrocarbons (PAHs) in human breast milk.

Science.gov (United States)

Pulkrabova, Jana; Stupak, Michal; Svarcova, Andrea; Rossner, Pavel; Rossnerova, Andrea; Ambroz, Antonin; Sram, Radim; Hajslova, Jana

2016-08-15

Human milk is an important source of beneficial nutrients and antibodies for newborns and infants and, under certain circumstances, its analysis may provide information on mothers' and infants' exposure to various contaminants. In the presented study, we have introduced the new analytical approach for analysis of 24 highly occurring polycyclic aromatic hydrocarbons (PAHs) in this indicator matrix. The sample preparation procedure is based on an ethyl acetate extraction of milk; the transfer of analytes into an organic layer is enhanced by addition of inorganic salts, i.e. sodium chloride and magnesium sulphate. Following the clean-up of a crude extract on silica SPE columns, gas chromatography coupled to triple quadrupole mass spectrometry is used for PAH identification and quantitation. The average recoveries of targeted PAHs from spiked samples were in the range of 68-110% with repeatabilities below 30% and method quantitation limits ranging from 0.03 to 0.3ng/g lipid weight. This newly validated method was successfully applied for analyses of 324 human milk samples collected from nonsmoking women during two sampling periods (summer and winter) in two residential areas in the Czech Republic differing in atmospheric pollution by PAHs. From 24 targeted analytes 17 were detected at least in one sample. Phenantherene, fluoranthrene, pyrene and fluorene were the most abundant compounds found at average concentration of 13.81, 1.80, 0.86, and 2.01ng/g lipid weight respectively. Comparing the data from two sampling periods, in both areas higher concentrations were measured in samples collected during winter. Also in the highly industrialized locality with heavily contaminated air PAH amounts in milk were higher than in the control locality. These first data on PAH concentrations in human milk collected in the Czech Republic are comparable with measurements for nonsmoking women reported earlier in the United States but significantly lower than results from China, Turkey

A new procedure for estimating the cell temperature of a high concentrator photovoltaic grid connected system based on atmospheric parameters

International Nuclear Information System (INIS)

Fernández, Eduardo F.; Almonacid, Florencia

2015-01-01

Highlights: • Concentrating grid-connected systems are working at maximum power point. • The operating cell temperature is inherently lower than at open circuit. • Two novel methods for estimating the cell temperature are proposed. • Both predict the operating cell temperature from atmospheric parameters. • Experimental results show that both methods perform effectively. - Abstract: The working cell temperature of high concentrator photovoltaic systems is a crucial parameter when analysing their performance and reliability. At the same time, due to the special features of this technology, the direct measurement of the cell temperature is very complex and is usually obtained by using different indirect methods. High concentrator photovoltaic modules in a system are operating at maximum power since they are connected to an inverter. So that, their cell temperature is lower than the cell temperature of a module at open-circuit voltage since an important part of the light power density is converted into electricity. In this paper, a procedure for indirectly estimating the cell temperature of a high concentrator photovoltaic system from atmospheric parameters is addressed. Therefore, this new procedure has the advantage that is valid for estimating the cell temperature of a system at any location of interest if the atmospheric parameters are available. To achieve this goal, two different methods are proposed: one based on simple mathematical relationships and another based on artificial intelligent techniques. Results show that both methods predicts the cell temperature of a module connected to an inverter with a low margin of error with a normalised root mean square error lower or equal than 3.3%, an absolute root mean square error lower or equal than 2 °C, a mean absolute error lower or equal then 1.5 °C, and a mean bias error and a mean relative error almost equal to 0%

Feedback mechanisms between snow and atmospheric mercury: Results and observations from field campaigns on the Antarctic plateau.

Science.gov (United States)

Spolaor, Andrea; Angot, Hélène; Roman, Marco; Dommergue, Aurélien; Scarchilli, Claudio; Vardè, Massimiliano; Del Guasta, Massimo; Pedeli, Xanthi; Varin, Cristiano; Sprovieri, Francesca; Magand, Olivier; Legrand, Michel; Barbante, Carlo; Cairns, Warren R L

2018-04-01

The Antarctic Plateau snowpack is an important environment for the mercury geochemical cycle. We have extensively characterized and compared the changes in surface snow and atmospheric mercury concentrations that occur at Dome C. Three summer sampling campaigns were conducted between 2013 and 2016. The three campaigns had different meteorological conditions that significantly affected mercury deposition processes and its abundance in surface snow. In the absence of snow deposition events, the surface mercury concentration remained stable with narrow oscillations, while an increase in precipitation results in a higher mercury variability. The Hg concentrations detected confirm that snowfall can act as a mercury atmospheric scavenger. A high temporal resolution sampling experiment showed that surface concentration changes are connected with the diurnal solar radiation cycle. Mercury in surface snow is highly dynamic and it could decrease by up to 90% within 4/6 h. A negative relationship between surface snow mercury and atmospheric concentrations has been detected suggesting a mutual dynamic exchange between these two environments. Mercury concentrations were also compared with the Br concentrations in surface and deeper snow, results suggest that Br could have an active role in Hg deposition, particularly when air masses are from coastal areas. This research presents new information on the presence of Hg in surface and deeper snow layers, improving our understanding of atmospheric Hg deposition to the snow surface and the possible role of re-emission on the atmospheric Hg concentration. Copyright © 2018 Elsevier Ltd. All rights reserved.

Case study of the atmospheric dispersion of emissions from UPPR/CDTN, Brazil

International Nuclear Information System (INIS)

Barreto, Alberto A.; Cesar, Raisa H.S.; Maleta, Paulo G.M.; Grossi, Pablo A.

2015-01-01

This work presents a study of the atmospheric dispersion of emissions released during activities of production and research of radiopharmaceuticals in the Center of Nuclear Technology Development (CDTN), localized in Belo Horizonte, Minas Gerais - Brazil. The installation, 'Unidade de Producao e Pesquisa de Radiofarmacos' (UPPR), was considered operating full time during a year. The general goal was to evaluate the radiological environmental impact due to these atmospheric emissions. The pollutants studied were the radionuclides F-18, C-11 and N-13. The meteorological view evaluated was a period of 365 days, simulated from the dates of a typical meteorological year. It was applied the dispersion model ARTM (Atmospheric Radionuclide Transport Model). The atmospheric emissions from UPPR were estimated for the simulation based in an extremely conservative operation condition. Others important data raised and analyzed were: topography, obstacles (buildings) and the land occupation around the CDTN. Among the main results, it is important to emphasize the estimate of the radionuclide concentration and the dose value calculated from these concentration. These results were compared with the dose restriction limit set by the standard CNEN 3.01. Areas of higher concentration were identified and are being used as reference for the positioning of the concentration's monitor of the pollutant by the Radiological Environmental Monitoring Program (PMA). (author)

Correlation between meteorological conditions and the concentration of radionuclides in the ground layer of atmospheric air

International Nuclear Information System (INIS)

Krajny, E.; Osrodka, L.; Wojtylak, M.; Michalik, B.; Skowronek, J.

2001-01-01

The main goal of this work was to find correlation between the concentrations of radionuclides in outdoor air and the meteorological conditions like: atmospheric pressure, wind velocity and amount of precipitation. Because the sampling period of radionuclides concentrations in air was relatively long (7 days), the average levels of meteorological parameters have been calculated within the same time. Data of radionuclide concentrations and meteorological data have been analyzed in order to find statistical correlation. The regression analysis and one of AI methods, known as neural network, were applied. In general, analysis of the gathered data does not show any strong correlation between the meteorological conditions and the concentrations of the radionuclides in air. A slightly stronger correlation we found for radionuclides with relatively short half-lives. The only positive correlation has been found between the 7 Be concentration and air temperature (at the significance level α = 0.05). In our opinion, the lack of correlation was caused by a too long sampling time in measurements of radionuclides in outdoor air (a whole week). Results of analysis received by means of the artificial neuron network are better. We were able to find certain groups of meteorological conditions, related with the corresponding concentrations of particular radionuclides in air. Preliminary measurements of radon progeny concentration support the thesis that the link between changes of meteorological parameters and concentrations of radionuclides in ambient air must exist. (author)

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

Science.gov (United States)

Rossini, Paolo; Matteucci, Gabriele; Guerzoni, Stefano

2010-01-01

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

Atmospheric formaldehyde and acetaldehyde at the campus University of Hiroshima, Japan

Directory of Open Access Journals (Sweden)

Sonia Naomi Nomi

2010-09-01

Full Text Available Ambient levels of formaldehyde (HCHO and acetaldehyde (CH3CHO were measured at Hiroshima (Japan during spring and summer of 2005. Measurements of O3, NOx, and SO2 were simultaneously conducted, in an attempt to identify temporal profiles and sources for these aldehydes. Atmospheric aldehydes were collected using C18 silica gel cartridges coated with an acidic solution of 2, 4-dinitrophenylhydrazine (2,4-DNPH and analyzed by high performance liquid chromatography with UV/VIS detection adjusted to 360 nm. Summer concentrations were higher than spring levels. FA concentrations during spring period ranged from 0.50 to 1.05 ppb and AA concentrations ranged from 0.17 to 1.31 ppb; during summer their concentrations ranged from 1.55 to 4.12 ppb and 0. 34 to 2.03 ppb. Average FA/AA in spring and summer were 3.09 and 3.72 suggesting biogenic emissions of aldehydes. The levels of FA and AA, their temporal variations, and their concentration ratio (FA/AA indicated that photochemical reactions contributed significantly to the formation of atmospheric aldehydes at the study site.

Impact of atmospheric boundary layer depth variability and wind reversal on the diurnal variability of aerosol concentration at a valley site

Energy Technology Data Exchange (ETDEWEB)

Pal, S., E-mail: sp5hd@Virginia.EDU; Lee, T.R.; Phelps, S.; De Wekker, S.F.J.

2014-10-15

The development of the atmospheric boundary layer (ABL) plays a key role in affecting the variability of atmospheric constituents such as aerosols, greenhouse gases, water vapor, and ozone. In general, the concentration of any tracers within the ABL varies due to the changes in the mixing volume (i.e. ABL depth). In this study, we investigate the impact on the near-surface aerosol concentration in a valley site of 1) the boundary layer dilution due to vertical mixing and 2) changes in the wind patterns. We use a data set obtained during a 10-day field campaign in which a number of remote sensing and in-situ instruments were deployed, including a ground-based aerosol lidar system for monitoring of the ABL top height (z{sub i}), a particle counter to determine the number concentration of aerosol particles at eight different size ranges, and tower-based standard meteorological instruments. Results show a clearly visible decreasing trend of the mean daytime z{sub i} from 2900 m AGL (above ground level) to 2200 m AGL during a three-day period which resulted in increased near-surface pollutant concentrations. An inverse relationship exists between the z{sub i} and the fine fraction (0.3–0.7 μm) accumulation mode particles (AMP) on some days due to the dilution effect in a well-mixed ABL. These days are characterized by the absence of daytime upvalley winds and the presence of northwesterly synoptic-driven winds. In contrast, on the days with an onset of an upvalley wind circulation after the morning transition, the wind-driven local transport mechanism outweighs the ABL-dilution effect in determining the variability of AMP concentration. The interplay between the ABL depth evolution and the onset of the upvalley wind during the morning transition period significantly governs the air quality in a valley and could be an important component in the studies of mountain meteorology and air quality. - Highlights: • Role of atmospheric boundary layer depth on particle

Determination of atmospheric SO/sub 2/ concentrations that are dangerous to plant life

Energy Technology Data Exchange (ETDEWEB)

Stratmann, H

1963-01-01

Controlled climate experiments indicate that the reaction of plants is not simply proportional to the project of SO/sub 2/ concentration and exposure time, and the degree of damage inflicted increases in proportion to this product as the concentration itself increases. A determining factor is the fact that plants, even when kept in a controlled climate, undergo a diurnal cycle of sensitivity. High concentrations for a shorter time do more damage than low concentrations for a longer exposure time, indicating the existence of concentration peaks. Although most cultivated plants are resistant to night exposure, a night exposure immediately following a daylight exposure causes a multiplication of damages, as does a succession of peak concentrations. It has also been discovered that plants whose leaves are not fully developed suffer a higher degree of SO damage than those whose leaves are fully matured. In the case of deciduous trees, sensitivity increases in proportion to the development of the leaves, until full leaf maturity is reached. Older trees are more resistant to SO/sub 2/.

Atmospheric correction of satellite data

Science.gov (United States)

Shmirko, Konstantin; Bobrikov, Alexey; Pavlov, Andrey

2015-11-01

Atmosphere responses for more than 90% of all radiation measured by satellite. Due to this, atmospheric correction plays an important role in separating water leaving radiance from the signal, evaluating concentration of various water pigments (chlorophyll-A, DOM, CDOM, etc). The elimination of atmospheric intrinsic radiance from remote sensing signal referred to as atmospheric correction.

Seasonal variation of radon daughters concentrations in the atmosphere and in precipitation at the Japanese coast of the Sea of Japan

International Nuclear Information System (INIS)

Nishikawa, T.; Okabe, S.; Aoki, M.

1988-01-01

The atmospheric radon daughters concentration at Fukui in the Japanese coastal region of the Sea of Japan shows a seasonal variation whose high values appear in summer and low values in winter. On the other hand, the radon daughters concentration in precipitation at Fukui and that in the maritime atmosphere over the Sea of Japan are high in winter and low in summer. It is concluded from these phenomena that the greater part of the continental radon and its daughters are transported by seasonal winds from Siberia and China to Japan across the Sea of Japan in winter. However, when the air masses approach the shore, the cumulonimbus grows and the heavy snowfall scavenges out the radon daughters from the air masses in large quantities at the Japanese coastal region of the Sea of Japan. (author)

Positive feedback between increasing atmospheric CO2 and ecosystem productivity

Science.gov (United States)

Gelfand, I.; Hamilton, S. K.; Robertson, G. P.

2009-12-01

Increasing atmospheric CO2 will likely affect both the hydrologic cycle and ecosystem productivity. Current assumptions that increasing CO2 will lead to increased ecosystem productivity and plant water use efficiency (WUE) are driving optimistic predictions of higher crop yields as well as greater availability of freshwater resources due to a decrease in evapotranspiration. The plant physiological response that drives these effects is believed to be an increase in carbon uptake either by (a) stronger CO2 gradient between the stomata and the atmosphere, or by (b) reduced CO2 limitation of enzymatic carboxylation within the leaf. The (a) scenario will lead to increased water use efficiency (WUE) in plants. However, evidence for increased WUE is mostly based on modeling studies, and experiments producing a short duration or step-wise increase in CO2 concentration (e.g. free-air CO2 enrichment). We hypothesize that the increase in atmospheric CO2 concentration is having a positive effect on ecosystem productivity and WUE. To investigate this hypothesis, we analyzed meteorological, ANPP, and soil CO2 flux datasets together with carbon isotopic ratio (13C/12C) of archived plant samples from the long term ecological research (LTER) program at Kellogg Biological Station. The datasets were collected between 1989 and 2007 (corresponding to an increase in atmospheric CO2 concentration of ~33 ppmv at Mauna Loa). Wheat (Triticum aestivum) samples taken from 1989 and 2007 show a significant decrease in the C isotope discrimination factor (Δ) over time. Stomatal conductance is directly related to Δ, and thus Δ is inversely related to plant intrinsic WUE (iWUE). Historical changes in the 13C/12C ratio (δ13C) in samples of a perennial forb, Canada goldenrod (Solidago canadensis), taken from adjacent successional fields, indicate changes in Δ upon uptake of CO2 as well. These temporal trends in Δ suggest a positive feedback between the increasing CO2 concentration in the

Global atmospheric changes.

Science.gov (United States)

Piver, W T

1991-12-01

Increasing concentrations of CO2 and other greenhouse gases in the atmosphere can be directly related to global warming. In terms of human health, because a major cause of increasing atmospheric concentrations of CO2 is the increased combustion of fossil fuels, global warming also may result in increases in air pollutants, acid deposition, and exposure to ultraviolet (UV) radiation. To understand better the impacts of global warming phenomena on human health, this review emphasizes the processes that are responsible for the greenhouse effect, air pollution, acid deposition, and increased exposure to UV radiation.

Summer-winter concentrations and gas-particle partitioning of short chain chlorinated paraffins in the atmosphere of an urban setting.

Science.gov (United States)

Wang, Thanh; Han, Shanlong; Yuan, Bo; Zeng, Lixi; Li, Yingming; Wang, Yawei; Jiang, Guibin

2012-12-01

Short chain chlorinated paraffins (SCCPs) are semi-volatile chemicals that are considered persistent in the environment, potential toxic and subject to long-range transport. This study investigates the concentrations and gas-particle partitioning of SCCPs at an urban site in Beijing during summer and wintertime. The total atmospheric SCCP levels ranged 1.9-33.0 ng/m(3) during wintertime. Significantly higher levels were found during the summer (range 112-332 ng/m(3)). The average fraction of total SCCPs in the particle phase (ϕ) was 0.67 during wintertime but decreased significantly during the summer (ϕ = 0.06). The ten and eleven carbon chain homologues with five to eight chlorine atoms were the predominant SCCP formula groups in air. Significant linear correlations were found between the gas-particle partition coefficients and the predicted subcooled vapor pressures and octanol-air partition coefficients. The gas-particle partitioning of SCCPs was further investigated and compared with both the Junge-Pankow adsorption and K(oa)-based absorption models. Copyright © 2012 Elsevier Ltd. All rights reserved.

Higher prices at Canadian gas pumps: international crude oil prices or local market concentration? An empirical investigation

International Nuclear Information System (INIS)

Anindya Sen

2003-01-01

There is little consensus on whether higher retail gasoline prices in Canada are the result of international crude oil price fluctuations or local market power exercised by large vertically-integrated firms. I find that although both increasing local market concentration and higher average monthly wholesale prices are positively and significantly associated with higher retail prices, wholesale prices are more important than local market concentration. Similarly, crude oil prices are more important than the number of local wholesalers in determining wholesale prices. These results suggest that movements in gasoline prices are largely the result of input price fluctuations rather than local market structure. (author)

Void growth suppression by dislocation impurity atmospheres

International Nuclear Information System (INIS)

Weertman, J.; Green, W.V.

1976-01-01

A detailed calculation is given of the effect of an impurity atmosphere on void growth under irradiation damage conditions. Norris has proposed that such an atmosphere can suppress void growth. The hydrostatic stress field of a dislocation that is surrounded by an impurity atmosphere was found and used to calculate the change in the effective radius of a dislocation line as a sink for interstitials and vacancies. The calculation of the impurity concentration in a Cottrell cloud takes into account the change in hydrostatic pressure produced by the presence of the cloud itself. It is found that void growth is eliminated whenever dislocations are surrounded by a condensed atmosphere of either oversized substitutional impurity atoms or interstitial impurity atoms. A condensed atmosphere will form whenever the average impurity concentration is larger than a critical concentration

Distribution of atmospheric mercury in northern Southeast Asia and South China Sea during Dongsha Experiment

Science.gov (United States)

Sheu, Guey-Rong; Lin, Neng-Huei; Lee, Chung-Te; Wang, Jia-Lin; Chuang, Ming-Tung; Wang, Sheng-Hsiang; Chi, Kai Hsine; Ou-Yang, Chang-Feng

2013-10-01

Northern South China Sea (SCS) is adjacent to major atmospheric mercury (Hg) emission source regions; however, studies concerning regional atmospheric Hg distribution and cycling are very limited. Accordingly, measurements of atmospheric Hg were conducted in March and April during the 2010 Dongsha Experiment to study its spatial and temporal distribution. Atmospheric Hg was measured at Hengchun and Dongsha Island (Taiwan), Da Nang (Vietnam), Chiang Mai (Thailand) and over the northern SCS. Atmospheric Hg concentrations ranged between 1.54 and 6.83 ng m-3, mostly higher than the Northern Hemisphere background value. Regional wind fields and backward trajectories indicated that the atmospheric Hg concentrations over northern SCS should principally reflect the export of the East Asian Hg emissions by northeast monsoon. However, significantly elevated Hg concentrations were always observed at Da Nang, possibly due to the influence of local Hg emissions. Chiang Mai is located in the intense biomass burning region in northern Thailand. Therefore, atmospheric Hg concentrations at Chiang Mai reflected the influence of regional biomass burning Hg emissions. Two dust storms were encountered at Dongsha Island, one on March 16 and the other on March 21, with atmospheric Hg enhancements. Compared with the 2008 summer values, elevated Hg levels were observed at Dongsha Island in the spring of 2010. Summer air masses were mainly from the deep SCS, representing relatively clean marine air. On the other hand, air masses were from the north in spring, passing eastern China or Taiwan prior to reaching Dongsha Island. Results of this research thus demonstrated the transport of atmospheric Hg from the East Asian continent to northern SCS by regional monsoon activity in spring, but special events, such as biomass burning and dust storms, can also cause enhancements of ambient Hg levels.

Factors Controlling the Distribution of Atmospheric Mercury in the East Asian Free Troposphere

Science.gov (United States)

Sheu, G.; Lee, C.; Lin, N.; Wang, J.; Ouyang, C.

2008-12-01

Taiwan is located to the downwind side of both East and Southeast Asia, which are the major anthropogenic mercury (Hg) source region worldwide. Also, it has been suggested that mountain-top monitoring sites, which are frequently in the free troposphere, are essential to the understanding of the global Hg transport. Accordingly, continuous measurements of atmospheric Hg have been conducting at Lulin Atmospheric Background Station (LABS, 2862 m a.s.l.) in Taiwan since April 13, 2006 to study the trans-boundary transport and transformation of Hg in the free troposphere. Three types of atmospheric Hg, including gaseous elemental Hg (GEM), reactive gaseous Hg (RGM), and particulate Hg (PHg), are measured using the Tekran 2537A/1130/1135 speciation system. Diurnal variations in the concentrations of GEM, RGM, ozone, and water vapor (WV) mixing ratio indicated the influence of boundary layer air in daytime and the subsidence of free tropospheric air masses from higher altitudes at night. Seasonal variation in GEM concentrations was evident with elevated concentrations usually observed between fall and spring when air masses were more or less under the influence of Asian continent. Low summer GEM values were associated with marine air masses. Spikes of RGM were frequently detected between midnight and early morning with concurrent decreases in GEM and WV mixing ratio and increases in ozone concentrations, suggesting the oxidation of GEM and formation of RGM in free troposphere. Concentrations of PHg were usually low; however, elevated concentrations were detected in spring when the Southeast Asian biomass burning plumes affected the LABS. Analysis of the collected data indicate that at LABS the distribution of atmospheric Hg is dynamically controlled by background atmosphere, exchange and mixing of free troposphere/boundary layer air, chemical transformation, and long-range transport from East and Southeast Asia.

Spatial and Temporal Variability of CO2 and CH4 Concentrations in the Atmospheric Surface Layer over West Siberia

Science.gov (United States)

Belan, Boris D.; Machida, Toshinobu; Sasakawa, Motoki; Davydov, Denis K.; Fofonov, Alexander V.; Krasnov, Oleg A.; Maksyutov, Shamil; Arshinov, Mikhail Yu.

2015-04-01

The investigation of greenhouse gas behavior in the atmosphere plays a key role in predicting the global changes of Earth's climate. In this connection, of particular importance is the study of the distribution of sources/sinks of trace gases in the atmospheric surface layer over the different regions of the globe. In order to fill a gap in the data on greenhouse gas concentrations in Russia, National Institute for Environmental Studies (NIES, Japan) and Institute of Atmospheric Optics (IAO SB RAS, Russia) established a network for GHG monitoring (JR-STATION, Japan-Russia Siberian Tall Tower Inland Observation Network). Gas analyzers and meteorological sensors were mounted at radio relay towers located in different regions of West Siberia. The checking equipment was placed in containers at the tower base. In the containers, the climatic parameters optimal for gas analyzer operation were maintained. The work on the network development started in 2001. Since at each of the sites the measurement duration could be different, in this paper we present the data of the greenhouse gas monitoring for eight sites which give the primary idea on the spatial distribution and temporal dynamics of CO2 and CH4 in the atmospheric surface layer over West Siberia. The analysis of the data showed that the average increase in concentration of carbon dioxide by results of our measurements in this territory increases within 1.95 - 2.53 ppm/year, depending on the area. The analysis of long-term data testifies about existence of growth of concentration of methane within 3.2 - 7.2 ppb / year. The presence of a distributed network of the sites operating in the monitoring regime makes it possible not only to investigate the temporal dynamics of CO2 and CH4 at each site and to determine the spatial differences between the concentrations by comparing the data, but also to plot the distribution charts for different moments of time. This work was supported by the Global Environment Research

Comparative cardiopulmonary effects of particulate matter- and ozone-enhanced smog atmospheres in mice

Science.gov (United States)

This study was conducted to compare the cardiac effects of particulate matter (PM)-enhanced and ozone(O3)-enhanced smog atmospheres in mice. We hypothesized that O3-enhanced smog would cause greater cardiac dysfunction than PM-enhanced smog due to the higher concentrations of irr...

Joint Application of Concentrations and Isotopic Signatures to Investigate the Global Atmospheric Carbon Monoxide Budget: Inverse Modeling Approach

Science.gov (United States)

Park, K.; Mak, J. E.; Emmons, L. K.

2008-12-01

Carbon monoxide is not only an important component for determining the atmospheric oxidizing capacity but also a key trace gas in the atmospheric chemistry of the Earth's background environment. The global CO cycle and its change are closely related to both the change of CO mixing ratio and the change of source strength. Previously, to estimate the global CO budget, most top-down estimation techniques have been applied the concentrations of CO solely. Since CO from certain sources has a unique isotopic signature, its isotopes provide additional information to constrain its sources. Thus, coupling the concentration and isotope fraction information enables to tightly constrain CO flux by its sources and allows better estimations on the global CO budget. MOZART4 (Model for Ozone And Related chemical Tracers), a 3-D global chemical transport model developed at NCAR, MPI for meteorology and NOAA/GFDL and is used to simulate the global CO concentration and its isotopic signature. Also, a tracer version of MOZART4 which tagged for C16O and C18O from each region and each source was developed to see their contributions to the atmosphere efficiently. Based on the nine-year-simulation results we analyze the influences of each source of CO to the isotopic signature and the concentration. Especially, the evaluations are focused on the oxygen isotope of CO (δ18O), which has not been extensively studied yet. To validate the model performance, CO concentrations and isotopic signatures measured from MPI, NIWA and our lab are compared to the modeled results. The MOZART4 reproduced observational data fairly well; especially in mid to high latitude northern hemisphere. Bayesian inversion techniques have been used to estimate the global CO budget with combining observed and modeled CO concentration. However, previous studies show significant differences in their estimations on CO source strengths. Because, in addition to the CO mixing ratio, isotopic signatures are independent tracers

The influence of atmospheric circulation on the air pollution concentration and temperature inversion in Sosnowiec. Case study

Directory of Open Access Journals (Sweden)

Widawski Artur

2015-06-01

Full Text Available Sosnowiec is located in the Katowice Region, which is the most urbanized and industrialized region in Poland. Urban areas of such character favor enhancement of pollution concentration in the atmosphere and the consequent emergence of smog. Local meteorological and circulation conditions significantly influence not only on the air pollution level but also change air temperature considerably in their centers and immediate vicinities. The synoptic situation also plays the major role in dispersal and concentration of air pollutants and changes in temperature profile. One of the most important are the near-ground (100 m inversions of temperature revealed their highest values on clear winter days and sometimes stay still for the whole day and night. Air temperature inversions in Sosnowiec occur mainly during anticyclone stagnation (Ca-anticyclone centre and Ka-anticyclonic ridge and in anticyclones with air advection from the south and southwest (Sa and SWa which cause significantly increase of air pollution values. The detailed evaluation of the influence of circulation types on the appearance of a particular concentration of pollutants carried out in this work has confirmed the predominant influence of individual circulation types on the development of air pollution levels at the Katowice region. This paper presents research case study results of the thermal structure of the near-ground atmospheric layer (100 m and air pollution parameters (PM10, SO2, NO, NO2 changes in selected days of 2005 year according to regional synoptic circulation types. The changes in urban environment must be taken into account in analyses of multiyear trends of air temperature and air conditions on the regional and global scales.

Using nitrogen concentration and isotopic composition in lichens to spatially assess the relative contribution of atmospheric nitrogen sources in complex landscapes.

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Pinho, P; Barros, C; Augusto, S; Pereira, M J; Máguas, C; Branquinho, C

2017-11-01

Reactive nitrogen (Nr) is an important driver of global change, causing alterations in ecosystem biodiversity and functionality. Environmental assessments require monitoring the emission and deposition of both the amount and types of Nr. This is especially important in heterogeneous landscapes, as different land-cover types emit particular forms of Nr to the atmosphere, which can impact ecosystems distinctively. Such assessments require high spatial resolution maps that also integrate temporal variations, and can only be feasibly achieved by using ecological indicators. Our aim was to rank land-cover types according to the amount and form of emitted atmospheric Nr in a complex landscape with multiple sources of N. To do so, we measured and mapped nitrogen concentration and isotopic composition in lichen thalli, which we then related to land-cover data. Results suggested that, at the landscape scale, intensive agriculture and urban areas were the most important sources of Nr to the atmosphere. Additionally, the ocean greatly influences Nr in land, by providing air with low Nr concentration and a unique isotopic composition. These results have important consequences for managing air pollution at the regional level, as they provide critical information for modeling Nr emission and deposition across regional as well as continental scales. Copyright © 2017 Elsevier Ltd. All rights reserved.

Long-term decline of global atmospheric ethane concentrations and implications for methane.

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Simpson, Isobel J; Sulbaek Andersen, Mads P; Meinardi, Simone; Bruhwiler, Lori; Blake, Nicola J; Helmig, Detlev; Rowland, F Sherwood; Blake, Donald R

2012-08-23

After methane, ethane is the most abundant hydrocarbon in the remote atmosphere. It is a precursor to tropospheric ozone and it influences the atmosphere's oxidative capacity through its reaction with the hydroxyl radical, ethane's primary atmospheric sink. Here we present the longest continuous record of global atmospheric ethane levels. We show that global ethane emission rates decreased from 14.3 to 11.3 teragrams per year, or by 21 per cent, from 1984 to 2010. We attribute this to decreasing fugitive emissions from ethane's fossil fuel source--most probably decreased venting and flaring of natural gas in oil fields--rather than a decline in its other major sources, biofuel use and biomass burning. Ethane's major emission sources are shared with methane, and recent studies have disagreed on whether reduced fossil fuel or microbial emissions have caused methane's atmospheric growth rate to slow. Our findings suggest that reduced fugitive fossil fuel emissions account for at least 10-21 teragrams per year (30-70 per cent) of the decrease in methane's global emissions, significantly contributing to methane's slowing atmospheric growth rate since the mid-1980s.

The study of azaarene behavior over atmosphere of subtropical city(Keelung)

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Liu, Chih Yun

2017-04-01

In this study, we collected the Total Suspended Particulates (TSP) from July 2014 to February 2016 in the subtropical city (Keelung), and researched azaarene behavior over atmosphere. Polycyclic Aromatic Compounds (PAHs) are ubiquitous pollutants in the environment; they have known carcinogens and/or mutagens, mainly produce from incomplete combustion. Azaarenes are polycyclic aromatic hydrocarbon derivative compounds in which a carbon atom in one of the aromatic rings is substituted by a nitrogen atom. Organism exposure to azaarenes occurs through inhalation of polluted air and by ingestion of food and/or water containing combustion products and accumulate in the body. Total azaarene concentration (16 individual compound concentration of the aggregate) is between 0.92 to 3.76 μg/m3, results showed that the concentration of azaarenes have significant seasonal variation, they have higher concentration in the cold month. In molecular weight, the highest proportion is the molecular weight equal to 143(ΣMQ) and then the molecular weight equal to 179(BAP), ΣMQ would rise from 30% 40% to 40% 50% during the cold month and warm months. Compared to ring number, 2-rings are biggest part, the smallest is 4-rings, its ratio has slight variation, but primary species is 2-rings. Emissions from transportation, local housing heating, factories burning fossil fuels and dust from Mainland south air mass are pollutant, their sources and climate conditions can affect concentration and composition of compound. There are highly significant correlation between 3-rings and 4-rings, which suggests that there are similar source strengths and transport mechanisms for these compounds. Correlation between concentration of azaarenes and ambient temperature is negative moderation, with concentration of atmospheric suspended particles is positive moderate correlation. Finally, we establish the relationship between the three parameters to predict concentration of azaarenes over atmosphere of

Contribution of various carbon sources toward isoprene biosynthesis in poplar leaves mediated by altered atmospheric CO2 concentrations.

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Amy M Trowbridge

Full Text Available Biogenically released isoprene plays important roles in both tropospheric photochemistry and plant metabolism. We performed a (13CO(2-labeling study using proton-transfer-reaction mass spectrometry (PTR-MS to examine the kinetics of recently assimilated photosynthate into isoprene emitted from poplar (Populus × canescens trees grown and measured at different atmospheric CO(2 concentrations. This is the first study to explicitly consider the effects of altered atmospheric CO(2 concentration on carbon partitioning to isoprene biosynthesis. We studied changes in the proportion of labeled carbon as a function of time in two mass fragments, M41(+, which represents, in part, substrate derived from pyruvate, and M69(+, which represents the whole unlabeled isoprene molecule. We observed a trend of slower (13C incorporation into isoprene carbon derived from pyruvate, consistent with the previously hypothesized origin of chloroplastic pyruvate from cytosolic phosphenolpyruvate (PEP. Trees grown under sub-ambient CO(2 (190 ppmv had rates of isoprene emission and rates of labeling of M41(+ and M69(+ that were nearly twice those observed in trees grown under elevated CO(2 (590 ppmv. However, they also demonstrated the lowest proportion of completely labeled isoprene molecules. These results suggest that under reduced atmospheric CO(2 availability, more carbon from stored/older carbon sources is involved in isoprene biosynthesis, and this carbon most likely enters the isoprene biosynthesis pathway through the pyruvate substrate. We offer direct evidence that extra-chloroplastic rather than chloroplastic carbon sources are mobilized to increase the availability of pyruvate required to up-regulate the isoprene biosynthesis pathway when trees are grown under sub-ambient CO(2.

Atmospheric BTEX-concentrations in an area with intensive street traffic

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Buczynska, Anna Jolanta; Krata, Agnieszka; Stranger, Marianne; Locateli Godoi, Ana Flavia; Kontozova-Deutsch, Velichka; Bencs, László; Naveau, Inge; Roekens, Edward; Van Grieken, René

The major threat to clean air in developed and industrializing countries is now posed by traffic emissions. The effects of traffic road modifications on the air quality are, however, rarely reported in the literature. The aim of this study was to determine the influence of the modernization and renovation of a traffic artery in the region of Mortsel (Antwerp, Belgium) on the concentration of volatile organic compounds such as: benzene, toluene, ethylbenzene and m-, p-, o-xylenes (BTEX). The original goal of the reconstruction works was to reduce the traffic lanes of one of the busiest streets in Antwerp, in order to discourage the road traffic and in consequence also to improve the air quality in this region. The average concentrations of BTEX before these works in 2003 were: 1.6, 7.0, 0.9, 2.3, and 0.9 μg/m 3, for benzene, toluene, ethylbenzene, m + p xylenes, and o-xylene, respectively. However, after the completion of the works, in 2005, they were slightly higher: 2.5, 9.5, 1.6, 3.4, and 1.3 μg/m 3, respectively. The scatter plots of benzene against toluene, ethylbenzene and xylenes in 2003 and 2005 showed very good correlations. This fact indicated that all of the measured compounds originated from the same source, namely the road traffic. Moreover, the data obtained from an air-monitoring station at less than 6 km distance from the sampling site (operated by the Flemish Environment Agency, and located in Borgerhout, Antwerp), confirmed the lack of influence of background concentrations of BTEX. The obtained results led to the conclusion that the reduction of the number of traffic lanes had apparently increased the traffic jams and also increased the emission from cars. Therefore, these modernization works had even a negative impact on the local concentration of traffic-related pollutants as BTEX.

Verification of atmospheric diffusion models with data of atmospheric diffusion experiments

International Nuclear Information System (INIS)

Hato, Shinji; Homma, Toshimitsu

2009-02-01

The atmospheric diffusion experiments were implemented by Japan Atomic Energy Research Institute (JAERI) around Mount Tsukuba in 1989 and 1990, and the tracer gas concentration were monitored. In this study, the Gauss Plume Model and RAMS/HYPACT that are meteorological forecast code and atmospheric diffusion code with detailed physical law are made a comparison between monitored concentration. In conclusion, the Gauss Plume Model is better than RAM/HYPACT even complex topography if the estimation is around tens of kilometer form release point and the change in weather is constant for short time. This reason is difference of wind between RAMS and observation. (author)

Atmospheric transport of urban-derived NHx: Evidence from nitrogen concentration and δ15N in epilithic mosses at Guiyang, SW China

International Nuclear Information System (INIS)

Liu Xueyan; Xiao Huayun; Liu Congqiang; Li Youyi; Xiao Hongwei

2008-01-01

Nitrogen concentration and δ 15 N in 175 epilithic moss samples were investigated along four directions from urban to rural sites in Guiyang, SW China. The spatial variations of moss N concentration and δ 15 N revealed that atmospheric N deposition is dominated by NH x -N from two major sources (urban sewage NH 3 and agricultural NH 3 ), the deposition of urban-derived NH x followed a point source pattern characterized by an exponential decline with distance from the urban center, while the agricultural-derived NH x was shown to be a non-point source. The relationship between moss N concentration and distance (y = 1.5e -0.13x + 1.26) indicated that the maximum transporting distance of urban-derived NH x averaged 41 km from the urban center, and it could be determined from the relationship between moss δ 15 N and distance [y = 2.54 ln(x) - 12.227] that urban-derived NH x was proportionally lower than agricultural-derived NH x in N deposition at sites beyond 17.2 km from the urban center. Consequently, the variation of urban-derived NH x with distance from the urban center could be modeled as y = 56.272e -0.116x - 0.481 in the Guiyang area. - Tissue N concentration and δ 15 N in epilithic mosses may be indicators for atmospheric transport of urban-derived NH x

Estimating the atmospheric concentration of Criegee intermediates and their possible interference in a FAGE-LIF instrument

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Novelli, Anna; Hens, Korbinian; Tatum Ernest, Cheryl; Martinez, Monica; Nölscher, Anke C.; Sinha, Vinayak; Paasonen, Pauli; Petäjä, Tuukka; Sipilä, Mikko; Elste, Thomas; Plass-Dülmer, Christian; Phillips, Gavin J.; Kubistin, Dagmar; Williams, Jonathan; Vereecken, Luc; Lelieveld, Jos; Harder, Hartwig

2017-06-01

We analysed the extensive dataset from the HUMPPA-COPEC 2010 and the HOPE 2012 field campaigns in the boreal forest and rural environments of Finland and Germany, respectively, and estimated the abundance of stabilised Criegee intermediates (SCIs) in the lower troposphere. Based on laboratory tests, we propose that the background OH signal observed in our IPI-LIF-FAGE instrument during the aforementioned campaigns is caused at least partially by SCIs. This hypothesis is based on observed correlations with temperature and with concentrations of unsaturated volatile organic compounds and ozone. Just like SCIs, the background OH concentration can be removed through the addition of sulfur dioxide. SCIs also add to the previously underestimated production rate of sulfuric acid. An average estimate of the SCI concentration of ˜ 5.0 × 104 molecules cm-3 (with an order of magnitude uncertainty) is calculated for the two environments. This implies a very low ambient concentration of SCIs, though, over the boreal forest, significant for the conversion of SO2 into H2SO4. The large uncertainties in these calculations, owing to the many unknowns in the chemistry of Criegee intermediates, emphasise the need to better understand these processes and their potential effect on the self-cleaning capacity of the atmosphere.

Atmospheric mercury concentrations observed at ground-based monitoring sites globally distributed in the framework of the GMOS network

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F. Sprovieri

2016-09-01

Full Text Available Long-term monitoring of data of ambient mercury (Hg on a global scale to assess its emission, transport, atmospheric chemistry, and deposition processes is vital to understanding the impact of Hg pollution on the environment. The Global Mercury Observation System (GMOS project was funded by the European Commission (http://www.gmos.eu and started in November 2010 with the overall goal to develop a coordinated global observing system to monitor Hg on a global scale, including a large network of ground-based monitoring stations, ad hoc periodic oceanographic cruises and measurement flights in the lower and upper troposphere as well as in the lower stratosphere. To date, more than 40 ground-based monitoring sites constitute the global network covering many regions where little to no observational data were available before GMOS. This work presents atmospheric Hg concentrations recorded worldwide in the framework of the GMOS project (2010–2015, analyzing Hg measurement results in terms of temporal trends, seasonality and comparability within the network. Major findings highlighted in this paper include a clear gradient of Hg concentrations between the Northern and Southern hemispheres, confirming that the gradient observed is mostly driven by local and regional sources, which can be anthropogenic, natural or a combination of both.

Observed and Modeled Tritium Concentrations in the Terrestrial Food Chain near a Continuous Atmospheric Source

International Nuclear Information System (INIS)

Davis, P.A.; Kim, S.B.; Chouhan, S.L.; Workman, W.J.G.

2005-01-01

Tritium concentrations were measured in a large number of environmental and biological samples collected during 2002 at two dairy farms and a hobby farm near Pickering Nuclear Generating Station in Ontario, Canada. The data cover most compartments of the terrestrial food chain in an agricultural setting and include detailed information on the diets of the local farm animals. Ratios of plant OBT concentration to air moisture HTO varied between 0.12 and 0.56, and were generally higher for the forage crops collected at the dairy farms than for the garden vegetables sampled at the hobby farm. Animal OBT to air HTO ratios were more uniform, ranging from 0.18 to 0.45, and were generally higher for the milk and beef samples from the dairy farms than for the chicken products from the hobby farm. The observed OBT concentrations in plants and animals were compared with predictions of IMPACT, the model used by the Canadian nuclear industry to calculate annual average doses due to routine releases. The model performed well on average for the animal endpoints but overestimated concentrations in plants by a factor of 2

Leaching of a copper flotation concentrate with ammonium persulfate in an autoclave system

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Deniz Turan, M.; Soner Altundoğan, H.

2014-09-01

The leaching behavior of a copper flotation concentrate was investigated using ammonium persulfate (APS) in an autoclave system. The decomposition products of APS, active oxygen, and acidic medium were used to extract metals from the concentrate. Leaching experiments were performed to compare the availability of APS as an oxidizing agent for leaching of the concentrate under atmospheric conditions and in an autoclave system. Leaching temperature and APS concentration were found to be important parameters in both leaching systems. Atmospheric leaching studies showed that the metal extractions increased with the increase in APS concentration and temperature (up to 333 K). A similar tendency was determined in the autoclave studies up to 423 K. It was also determined that the metal extractions decreased at temperatures above 423 K due to the passivation of the particle surface by molten elemental sulfur. The results showed that higher copper extractions could be achieved using an autoclave system.

THE SENSITIVITY OF THE GREENHOUSE EFFECT TO CHANGES IN THE CONCENTRATION OF GASES IN PLANETARY ATMOSPHERES

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Smadar Bressler

2013-12-01

Full Text Available We present a radiative transfer model for Earth-Like-Planets (ELP. The model allows the assessment of the effect of a change in the concentration of an atmospheric component, especially a greenhouse gas (GHG, on the surface temperature of a planet. The model is based on the separation between the contribution of the short wavelength molecular absorption and the long wavelength one. A unique feature of the model is the condition of energy conservation at every point in the atmosphere. The radiative transfer equation is solved in the two stream approximation without assuming the existence of an LTE in any wavelength range. The model allows us to solve the Simpson paradox, whereby the greenhouse effect (GHE has no temperature limit. On the contrary, we show that the temperature saturates, and its value depends primarily on the distance of the planet from the central star. We also show how the relative humidity affects the surface temperature of a planet and explain why the effect is smaller than the one derived when the above assumptions are neglected.

Comparison of atmospheric CH4 concentration observed by GOSAT and in-situ measurements in Thailand and India

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Hayashida, S.; Ono, A.; Ishikawa, S.; Terao, Y.; Takeuchi, W.

2012-12-01

The concentration of atmospheric methane (CH4) has more than doubled since pre-industrial levels and the observed long-term changes in the CH4 concentration have been attributed to anthropogenic activity. However, despite the importance of atmospheric CH4 in global warming, the strength of individual sources of CH4 remains highly uncertain [e.g.,Dlugokencky et al., 2011]. To characterize and quantify the emissions of CH4 especially in Monsoon Asia and Siberia, which are the most important regions as CH4 source, we started a new project, "Characterization and Quantification of global methane emissions by utilizing GOSAT and in-situ measurements " by support of the Environment Research and Technology Development Fund (ERTDF) from June 2012 under the umbrella of Ministry of Environment Japan. The projects includes (1) satellite data applications, (2) in-situ measurements in Siberia, over Western Pacific and in Monsoon Asia, (3) development of the inverse model to derive CH4 emissions by top-down approach, and (4) flux measurements in Siberia and Asia to improve the bottom-up inventories. As an initiatory approach in the project, we started air sampling in Thailand and India where there are only a few CH4 data of direct sampling with high precision. We took eight air samples at Kohn Kaen and Pimai in Thailand on June 9 and 10, 2012. The high CH4 concentration near rice paddy field contrasted to the lower CH4 concentration near Cassava field. We are planning to take more samples in India in mid-August. The satellite CH4 data including GOSAT and SCIAMACHY are also compared with the Land Surface Water Coverage (LSWC) and the Normalized Difference Vegetation Index (NDVI). The analysis revealed the seasonal variation in of xCH4 is closely related to the variation of the LSWC, coupled with NDVI. However, the satellite measurements are all column-averaged mixing ratio (xCH4), and therefore do not necessarily reflect high CH4 concentration near the surface over the emission

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

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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 Carbon Dioxide and the Global Carbon Cycle: The Key Uncertainties

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Peng, T. H.; Post, W. M.; DeAngelis, D. L.; Dale, V. H.; Farrell, M. P.

1987-12-01

The biogeochemical cycling of carbon between its sources and sinks determines the rate of increase in atmospheric CO{sub 2} concentrations. The observed increase in atmospheric CO{sub 2} content is less than the estimated release from fossil fuel consumption and deforestation. This discrepancy can be explained by interactions between the atmosphere and other global carbon reservoirs such as the oceans, and the terrestrial biosphere including soils. Undoubtedly, the oceans have been the most important sinks for CO{sub 2} produced by man. But, the physical, chemical, and biological processes of oceans are complex and, therefore, credible estimates of CO{sub 2} uptake can probably only come from mathematical models. Unfortunately, one- and two-dimensional ocean models do not allow for enough CO{sub 2} uptake to accurately account for known releases. Thus, they produce higher concentrations of atmospheric CO{sub 2} than was historically the case. More complex three-dimensional models, while currently being developed, may make better use of existing tracer data than do one- and two-dimensional models and will also incorporate climate feedback effects to provide a more realistic view of ocean dynamics and CO{sub 2} fluxes. The instability of current models to estimate accurately oceanic uptake of CO{sub 2} creates one of the key uncertainties in predictions of atmospheric CO{sub 2} increases and climate responses over the next 100 to 200 years.

Characteristics of coupled atmosphere-ocean CO2 sensitivity experiments with different ocean formulations

International Nuclear Information System (INIS)

Washington, W.M.; Meehl, G.A.

1990-01-01

The Community Climate Model at the National Center for Atmospheric Research has been coupled to a simple mixed-layer ocean model and to a coarse-grid ocean general circulation model (OGCM). This paper compares the responses of simulated climate to increases of atmospheric carbon dioxide (CO 2 ) in these two coupled models. Three types of simulations were run: (1) control runs with both ocean models, with CO 2 held constant at present-day concentrations, (2) instantaneous doubling of atmospheric CO 2 (from 330 to 660 ppm) with both ocean models, and (3) a gradually increasing (transient) CO 2 concentration starting at 330 ppm and increasing linearly at 1% per year, with the OGCM. The mixed-layer and OGCM cases exhibit increases of 3.5 C and 1.6 C, respectively, in globally averaged surface air temperature for the instantaneous doubling cases. The transient-forcing case warms 0.7 C by the end of 30 years. The mixed-layer ocean yields warmer-than-observed tropical temperatures and colder-than-observed temperatures in the higher latitudes. The coarse-grid OGCM simulates lower-than-observed sea surface temperatures (SSTs) in the tropics and higher-than-observed SSTs and reduced sea-ice extent at higher latitudes. Sensitivity in the OGCM after 30 years is much lower than in simulations with the same atmosphere coupled to a 50-m slab-ocean mixed layer. The OGCM simulates a weaker thermohaline circulation with doubled CO 2 as the high-latitude ocean-surface layer warms and freshens and the westerly wind stress decreases. Convective overturning in the OGCM decreases substantially with CO 2 warming

Characteristics of coupled atmosphere-ocean CO2 sensitivity experiments with different ocean formulations

International Nuclear Information System (INIS)

Washington, W.M.; Meehl, G.A.

1991-01-01

The Community Climate Model at the National Center for Atmospheric Research has been coupled to a simple mixed-layer ocean model and to a coarse-grid ocean general circulation model (OGCM). This paper compares the responses of simulated climate to increases of atmospheric carbon dioxide (CO 2 ) in these two coupled models. Three types of simulations were run: (1) control runs with both ocean models, with CO 2 held constant at present-day concentrations, (2) instantaneous doubling of atmospheric CO 2 (from 330 to 660 ppm) with both ocean models, and (3) a gradually increasing (transient) CO 2 concentration starting at 330 ppm and increasing linearly at 1% per year, with the OGCM. The mixed-layer and OGCM cases exhibit increases of 3.5 C and 1.6 C, respectively, in globally averaged surface air temperature for the instantaneous doubling cases. The transient-forcing case warms 0.7 C by the end of 30 years. The mixed-layer ocean yields warmer-than-observed tropical temperatures and colder-than-observed temperatures in the higher latitudes. The coarse-grid OGCM simulates lower-than-observed sea surface temperatures (SSTs) in the tropics and higher-than-observed SSTs and reduced sea-ice extent at higher latitudes. Sensitivity in the OGCM after 30 years is much lower than in simulations with the same atmosphere coupled to a 50-m slab-ocean mixed layer. The OGCM simulates a weaker thermohaline circulation with doubled CO 2 as the high-latitude ocean-surface layer warms and freshens and the westerly wind stress decreases. Convective overturning in the OGCM decreases substantially with CO 2 warming. 46 refs.; 20 figs.; 1 tab

The global carbon cycle change: Le Chatelier principle in the response of biota to changing CO2 concentration in the atmosphere

International Nuclear Information System (INIS)

Gorshkov, V.G.; Sherman, S.G.; Kondratyev, K.Y.

1990-01-01

The long-term existence of natural biota in the environment means that such a system is stable with respect to external disturbances. This system must follow the Le Chatelier principle which is based on the processes that compensate the disturbing effects. The use of the Le Chatelier principle makes it possible to choose between contradictory observational data. Available observational data on variations of the concentration of rare carbon isotopes in various media show that the oceanic biota follows the Le Chatelier principle and absorbs about half the carbon which the ocean gets from the atmosphere, compensating an increment of carbon in the atmosphere caused by an anthropogenic impact. The strongly anthropogenetically disturbed land biota does not follow the Le Chatelier principle, starting from the middle of this century. The land biota not only cannot absorb excess carbon accumulated in the atmosphere: it ejects carbon to the atmosphere in quantities equal to halved emission of carbon through fossil fuel burning. All the quantitative results considered in this paper have been obtained without using models of the biota and of the ocean

The Structure and Composition of Io's Atmosphere

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Smyth, W. H.; Marconi, M. L.

2011-12-01

Io's atmosphere is thought to be generated principally by sublimation on the dayside and by multiple volcanoes scattered throughout its surface and more concentrated near the equator. While SO2 seems to be the principle product of these sources, many other chemical species are placed into the atmosphere by these sources, including substantial amounts of SO and S2 as well as smaller but observationally significant amounts of Na bearing molecules. These species in turn interact strongly with the torus plasma generating additional species such as O2, S, O, and Na. The strong interaction of the torus plasma with the neutral atmosphere not only exerts a profound effect on the composition of Io's atmosphere but also strongly affects the dynamics and thermodynamics of Io's atmosphere, particularly at higher altitudes. In addition, as Io orbits Jupiter, the change in location of the sublimation region and the eclipse of Io as it passes through Jupiter's shadow result in substantial variation in the atmosphere. A complex time-dependent three-dimensional atmosphere with strong spatial compositional variation is created. Here we extend the two-dimensional multispecies Navier-Stokes model of Smyth and Wong (2004) to three-dimensions, include two volcanic sources similar to Pele and Loki, and include the effect of Io's movement around Jupiter on sublimation. The effects of the torus plasma are also included as in Smyth and Wong. We will present the overall composition and structure of the atmosphere, O to S ratios in the upper atmosphere, and discuss a potential issue with the O2 abundance. Smyth, W.H. and M.C. Wong, Icarus 171, 171-182, 2004.

Atmospheric mercury cycles in northern Wisconsin

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Watras, C. J.; Morrison, K. A.; Rubsam, J. L.; Rodger, B.

Total gaseous mercury (TGM) in the lower atmosphere of northern Wisconsin exhibits strong annual and diurnal cycles similar to those previously reported for other rural monitoring sites across mid-latitude North America. Annually, TGM was highest in late winter and then gradually declined until late summer. During 2002-04, the average TGM concentration was 1.4 ± 0.2 (SD) ng m -3, and the amplitude of the annual cycle was 0.4 ng m -3 (˜30% of the long-term mean). The diurnal cycle was characterized by increasing TGM concentrations during the morning followed by decreases during the afternoon and night. The diurnal amplitude was variable but it was largest in spring and summer, when daily TGM oscillations of 20-40% were not uncommon. Notably, we also observed a diurnal cycle for TGM indoors in a room ventilated through an open window. Even though TGM concentrations were an order of magnitude higher indoors, (presumably due to historical practices within the building: e.g. latex paint, fluorescent lamps, thermometers), the diurnal cycle was remarkably similar to that observed outdoors. The indoor cycle was not directly attributable to human activity, the metabolic activity of vegetation or diurnal atmospheric dynamics; but it was related to changes in temperature and oxidants in outdoor air that infiltrated the room. Although there was an obvious difference in the proximal source of indoor and outdoor TGM, similarities in behavior suggest that common TGM cycles may be driven largely by adsorption/desorption reactions involving solid surfaces, such as leaves, snow, dust and walls. Such behavior would imply a short residence time for Hg in the lower atmosphere and intense recycling - consistent with the "ping-pong ball" or "multi-hop" conceptual models proposed by others.

Higher Leptin but Not Human Milk Macronutrient Concentration Distinguishes Normal-Weight from Obese Mothers at 1-Month Postpartum.

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De Luca, Arnaud; Frasquet-Darrieux, Marine; Gaud, Marie-Agnès; Christin, Patricia; Boquien, Clair-Yves; Millet, Christine; Herviou, Manon; Darmaun, Dominique; Robins, Richard J; Ingrand, Pierre; Hankard, Régis

2016-01-01

Exclusively breastfed infants born to obese mothers have previously been shown to gain less weight by 1-month postpartum than infants of normal-weight mothers. Our hypothesis is that human milk composition and volume may differ between obese and normal-weight mothers. To compare human milk leptin, macronutrient concentration, and volume in obese and normal-weight mothers. Mother and infant characteristics were studied as secondary aims. This cross-sectional observational study compared 50 obese mothers matched for age, parity, ethnic origin, and educational level with 50 normal-weight mothers. Leptin, macronutrient human milk concentration, and milk volume were determined at 1 month in exclusively breastfed infants. Mother characteristics and infant growth were recorded. Human milk leptin concentration was higher in obese mothers than normal-weight mothers (4.8±2.7 vs. 2.5±1.5 ng.mL-1, pobese and normal-weight mothers in protein, lipid, carbohydrate content, and volume, nor in infant weight gain. Leptin concentration was higher in the milk of obese mothers than that of normal-weight mothers, but macronutrient concentration was not. It remains to be established whether the higher leptin content impacts on infant growth beyond the 1-month of the study period.

[Study on atmospheric VOCs in Gongga Mountain base station].

Science.gov (United States)

Zhang, Jun-Ke; Wang, Yue-Si; Wu, Fang-Kun; Sun, Jie

2012-12-01

Volatile organic compounds (VOCs) play important roles in the atmosphere as precursors of secondary air pollutants. The regional background concentrations and variation characteristics of VOCs in the atmosphere of southwestern China were studied. Meanwhile, a receptor model based on principal component analysis (PCA) was used to identify the major sources of VOCs. Weekly samples were collected in 2007 in the Gongga Mountain base station and analyzed with a three-stage preconcentration method coupled with GC-MS. The annual mean concentration of TVOCs and NMHCs were 9.40 x 10(-9) +/- 4.55 x 10(-9) and 7.73 x 10(-9) +/- 4.43 x 10(-9), respectively. Aromatic hydrocarbons provided the largest contribution to TVOCs (37.3%), follow by alkanes (30.0%) and halogenated hydrocarbons (19.8%), the smallest contribution was from alkenes (12.9%). Three major sources were resolved by the receptor model, traffic sources, biogenic sources and combustion sources. The seasonal variation of TVOCs in this area was obviously, and the order was autumn > winter > spring > summer. TVOCs concentration in autumn was very significantly higher than that in summer (P station emission characteristic.

Flurbiprofen concentration in soft tissues is higher after topical application than after oral administration

Science.gov (United States)

Kai, Shuken; Kondo, Eiji; Kawaguchi, Yasuyuki; Kitamura, Nobuto; Yasuda, Kazunori

2013-01-01

Aim To compare tissue concentrations of flurbiprofen resulting from topical application and oral administration according to the regulatory approved dosing guidelines. Method Sixteen patients were included in this study. Each patient was randomly assigned to the topical application or oral administration group. In each group, a pair of tapes or a tablet, containing a total of 40 mg flurbiprofen, was administered twice at 16 and 2 h before the surgery. Results The flurbiprofen concentration in the fat, tendon, muscle and periosteum tissues was significantly higher (P flurbiprofen to the human body, particularly to soft tissues near the body surface. PMID:22822928

Measurements of gaseous mercury exchanges at the sediment-water, water-atmosphere and sediment-atmosphere interfaces of a tidal environment (Arcachon Bay, France).

Science.gov (United States)

Bouchet, Sylvain; Tessier, Emmanuel; Monperrus, Mathilde; Bridou, Romain; Clavier, Jacques; Thouzeau, Gerard; Amouroux, David

2011-05-01

The elemental mercury evasion from non-impacted natural areas is of significant importance in the global Hg cycle due to their large spatial coverage. Intertidal areas represent a dynamic environment promoting the transformations of Hg species and their subsequent redistribution. A major challenge remains in providing reliable data on Hg species variability and fluxes under typical transient tidal conditions found in such environment. Field experiments were thus carried out to allow the assessment and comparison of the magnitude of the gaseous Hg fluxes at the three interfaces, sediment-water, sediment-atmosphere and water-atmosphere of a mesotidal temperate lagoon (Arcachon Bay, Aquitaine, France) over three distinct seasonal conditions. The fluxes between the sediment-water and the sediment-atmosphere interfaces were directly evaluated with field flux chambers, respectively static or dynamic. Water-atmosphere fluxes were evaluated from ambient concentrations using a gas exchange model. The fluxes at the sediment-water interface ranged from -5.0 to 5.1 ng m(-2) h(-1) and appeared mainly controlled by diffusion. The occurrence of macrophytic covers (i.e.Zostera noltii sp.) enhanced the fluxes under light radiations. The first direct measurements of sediment-atmosphere fluxes are reported here. The exchanges were more intense and variable than the two other interfaces, ranging between -78 and 40 ng m(-2) h(-1) and were mostly driven by the overlying atmospheric Hg concentrations and superficial sediment temperature. The exchanges between the water column and the atmosphere, computed as a function of wind speed and gaseous mercury saturation ranged from 0.4 to 14.5 ng m(-2) h(-1). The flux intensities recorded over the intertidal sediments periodically exposed to the atmosphere were roughly 2 to 3 times higher than the fluxes of the other interfaces. The evasion of elemental mercury from emerged intertidal sediments is probably a significant pathway for Hg evasion in

The Concentrations and Reduction of Airborne Particulate Matter (PM10, PM2.5, PM1 at Shelterbelt Site in Beijing

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Jungang Chen

2015-05-01

Full Text Available Particulate matter is a serious source of air pollution in urban areas, where it exerts adverse effects on human health. This article focuses on the study of subduction of shelterbelts for atmospheric particulates. The results suggest that (1 the PM mass concentration is higher in the morning or both morning and noon inside the shelterbelts and lower mass concentrations at other times; (2 the particle mass concentration inside shelterbelt is higher than outside; (3 the particle interception efficiency of the two forest belts over the three months in descending order was PM10 > PM1 > PM2.5; and (4 the two shelterbelts captured air pollutants at rates of 1496.285 and 909.075 kg/month and the major atmospheric pollutant in Beijing city is PM10. Future research directions are to study PM mass concentration variation of shelterbelt with different tree species and different configuration.

Effects of biochemical and physical processes on concentrations and size distributions of dimethylaminium and trimethylaminium in atmospheric particles from marginal seas of China to the northwest Pacific Ocean

Science.gov (United States)

Hu, Q.; Yao, X.; Qu, K.; Cui, Z.; Gao, H.; Xie, H.

2017-12-01

This study aim to assess the effects of concentrations and size distributions of aminium ions in atmospheric particles from offshore to open oceans. Size-segregated dimethylaminium (DMA+) and trimethylaminium (TMA+) in atmospheric particles were measured during March-May, 2014. One cruise was over marginal seas of China, in which the concentrations of DMA+ and TMA+ in PM0.056-10 varied from 0.08 nmol m-3 to 0.43 nmol m-3 and from 0.10 to 0.27 nmol m-3, respectively. The two ions both had good positive correlations with subsurface chlorophyll-a maximum and salinity, respectively. The highest concentrations of (DMA+ + TMA+) were observed during cyanobacteria bloom period which happened in subsurface water. The results implied that the concentrations of DMA+ (TMA+) in marine atmospheric particles might be influenced by phytoplankton quantities and species in subsurface seawater. Another cruise was carried out from marginal seas of China to the northwest Pacific Ocean (NWPO). The concentrations of DMA+ and TMA+ in PM0.056-1.8 varied from 0.19 nmol m-3 to 1.53 nmol m-3 and from 0.57 to 3.85 nmol m-3, respectively. The highest (lowest) concentrations of (DMA+ + TMA+) were observed near the cyclonic (anticyclonic) eddy, indicating that the cyclonic (anticyclonic) eddy with high (low) chlorophyll-a enhanced (suppressed) DMA+ (TMA+) production in atmospheric particles. In addition, the dominant particle modes less than 0.2 μm for DMA+ (TMA+) were observed, ie., 0.13±0.02 μm for DMA+ over marginal seas of China, and 0.08±0.00 μm for TMA+ in NWPO, but if they were emitted via bubble bursting needed to be further researched.

Atmospheric Oxygen Concentrations for the Past 350 Myr Modeled from the δ13C of C3 Land Plants

Science.gov (United States)

Nordt, L.; Breecker, D.

2016-12-01

Numerous studies have focused on the systematic collection of long-term d13C records from marine sediments, but no such isotopic compilation exists for C3 land plants. Consequently, we gathered a meta-data base of 8003 plant-derived δ13C values (ISOORG) from various carbon sources binned into 5 myr time steps. The results of this investigation were reported in a recent publication showing that most δ13C sources co-vary with ten CIEs during the last 400 myr. For this paper we culled ISOORG to produce ISOORG16-H that contains 7025 plant-derived δ13C values from paleo-moist environments to reflect secular controls on the δ13C of C3 plants. We then constructed atmospheric pO2 curves for the past 350 myr using prior experimental work showing a direct relationship between the Δ13C of C3 plants and pO2 concentration. Periods of hyperoxia (25-30% pO2) were identified from 300-250, 225-190, and 110-105 myr, and intervals of hypoxia (10-15% pO2) from 350-345, 245-230, and 185-115 myr. During the last 150 myr, pO2 stabilized at 17-24% except for a notable positive excursion from 110-105 myr. Hyperoxia, apparently from widespread carbon burial, supports the notion of insect gigantism during the Late Paleozoic. Hypoxia during the early Triassic correlates with the coal gap following the collapse of Paleozoic ecosystems. Rising pO2 in the late Triassic seems to reflect renewed carbon burial from reorganization of Mesozoic ecosystems. The middle Mesozoic is characterized by low pO2 during an intense greenhouse interval, with ambient conditions ensuing thereafter possibly linked to carbon burial from the radiation of angiosperms. pO2 concentrations >14% suggest wildfires persisted through the study interval except possibly at 160 and 140 myr. Intervals of low pO2 concentration were likely accompanied by lower atmospheric pressure and higher temperatures, particularly from 245-230 myr and 180-120 myr. Our O2 reconstructions conform with GEOCARBSULF, but not with proxy

Concentration, distribution and source apportionment of atmospheric polycyclic aromatic hydrocarbons in the southeast suburb of Beijing, China.

Science.gov (United States)

Zhang, Shucai; Zhang, Wei; Wang, Kaiyan; Shen, Yating; Hu, Lianwu; Wang, Xuejun

2009-04-01

Total suspended particle samples and gas phase samples were collected at three representative sampling sites in the southeastern suburb of Beijing from March 2005 to January 2006. The samples were analyzed for 16 US EPA priority PAHs using GC/MS. Concentrations of Sigma PAHs in particle and gas phases were 0.21-1.18 x 10(3) ng m(-3) and 9.5 x 10(2) ng-1.03 x 10(5) ng m(-3), respectively. PAH concentrations displayed seasonal variation in the order of winter>spring>autumn>summer for particle phase, and winter>autumn>summer>spring for gas phase. Partial correlation analysis indicates that PAH concentrations in particle phase are negatively correlated with temperature and positively correlated with air pollution index of SO(2). No significant correlation is observed between gas phase PAHs and the auxiliary parameters. Sources of PAH are identified through principal component analysis, and source contributions are estimated through multiple linear regression. Major sources of atmospheric PAHs in the study area include coal combustion, coke industry, vehicular emission and natural gas combustion.

Size resolved mass concentration and elemental composition of atmospheric aerosols over the Eastern Mediterranean area

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J. Smolík

2003-01-01

Full Text Available A Berner low pressure impactor was used to collect size-segregated aerosol samples at Finokalia, located on the north-eastern coast of Crete, Greece during July 2000 and January 2001. Several samples were also collected during the summer campaign aboard the research vessel "AEGAIEO" in the Aegean Sea. Gravimetric analysis and inversion techniques yielded daily PM1 and PM10 mass concentrations. The samples were also analysed by PIXE giving the elemental size distributions of Al, Si, K, Ca, Ti, Mn, Fe, Sr, S, Cl, Ni, V, Cu, Cr, Zn, and Pb. The crustal elements and sea-salt had a unimodal supermicron size distribution. Sulphur was found predominantly in submicron fractions. K, V, and Ni exhibited a bimodal distribution with a submicron mode produced by forest fires and oil combustion. The anthropogenic elements had broad and not well-defined distributions. The time series for PM1 and PM10 mass and elemental concentrations showed both daily and seasonal variation. Higher mass concentrations were observed during two incursions of Saharan dust, whilst higher concentrations of S, Cu, Zn, and Pb were encountered in samples collected in air masses arriving from northern Greece or the western coast of Turkey. Elevated concentrations of chlorine were found in samples with air masses either originating above the Atlantic Ocean and arriving at Finokalia via western Europe or recirculating over the western coast of the Black Sea.

Atmospheric tritium. Measurement and application

International Nuclear Information System (INIS)

Frejaville, Gerard

1967-02-01

The possible origins of atmospheric tritium are reviewed and discussed. A description is given of enrichment (electrolysis and thermal diffusion) and counting (gas counters and liquid scintillation counters) processes which can be used for determining atmospheric tritium concentrations. A series of examples illustrates the use of atmospheric tritium for resolving a certain number of hydrological and glaciological problems. (author) [fr

Export of Atmospheric Mercury from East Asia Observed at Various Monitoring Sites in Taiwan

Science.gov (United States)

Sheu, G.; Lin, N.; Wang, J.; Lee, C.; Chang, S.

2009-12-01

East Asia is the major atmospheric mercury (Hg) source region in the world due to the excessive coal combustion, industrial emission, and biomass burning in this area. Nonetheless, studies concerning the export of atmospheric Hg from East Asia are still limited. Accordingly, atmospheric Hg has been measured at various sites in Taiwan to study its temporal and spatial distribution, and the significance of long-range transport from the East Asian continent as well. Here we report the data collected in Fu-guei-jiao (121.97°E, 25.47°N, ~30 m a.s.l.), Mt. Bamboo (121.54°E, 25.19°N, 1025 m a.s.l.), and Lulin Atmospheric Background Station (LABS; 120.87°E, 23.47°N, 2862 m a.s.l.) to discuss the atmospheric Hg export from the East Asian continent. Twenty-four hour-integrated total atmospheric Hg (THg) samples were manually collected in Fu-guei-jiao and Mt. Bamboo in 2007-2008 and quantified by dual amalgamation CVAFS. On the other hand, continuous measurements of gaseous elemental Hg (GEM), reactive gaseous Hg (RGM), and particulate Hg (PHg) at LABS began since April 13, 2006 using the Tekran 2537A/1130/1135 speciation system. Mean(±S.D.) THg concentrations were 2.09±0.71 and 1.86±0.50 ng m-3 for Fu-guei-jiao and Mt. Bamboo, respectively. At LABS between April 2006 and April 2009, the mean(±S.D.) concentrations of GEM, RGM and PHg were 1.77±0.54 ng m-3, 22.4±43.8 pg m-3 and 6.3±10.9 pg m-3, respectively. Evident seasonal distribution in THg/GEM concentrations was observed at all sites with higher values usually occurred between fall and spring when the air masses were mainly from the East Asian continent, indicating the influence of the East Asian atmospheric Hg outflow. This also demonstrated that the atmospheric Hg export is occurring both in the boundary layer and in the free troposphere. Concentrations of PHg were usually low at LABS; however, elevated values were detected in spring when the Indochina Peninsula biomass burning plumes frequently affected

Atmospheric benzene and toluene

International Nuclear Information System (INIS)

Rasmussen, R.A.; Khalil, M.A.K.

1983-01-01

Atmospheric concentrations of benzene (C 6 H 6 ) and toluene (C 7 H 8 )have been observed at nine remote locations of the world ranging in latitude from inside the arctic circle to the south pole. The observations span all seasons at each location. In the northern hemisphere it is observed that C 6 H 6 and C 7 H 8 are most abundant during winter and least abundant during summer. Based on the limited data available, such cycles are not observed in the tropics. These findings are consistent with the expected latitudinal and seasonal variations of OH radicals which cause benzene and toluene to be removed from the atmosphere. The latitude distribution shows high concentrations at mid latitude and low levels in the southern hemisphere. This finding is consistent with the present understanding that the sources of benzene and toluene are primarily anthropogenic. The observed concentration distribution and varibility are consistent with the short expected atmospheric lifetime of the order of months for benzene and days for toluene

Elevated atmospheric CO2 concentration leads to increased whole-plant isoprene emission in hybrid aspen (Populus tremula × Populus tremuloides).

Science.gov (United States)

Sun, Zhihong; Niinemets, Ülo; Hüve, Katja; Rasulov, Bahtijor; Noe, Steffen M

2013-05-01

Effects of elevated atmospheric [CO2] on plant isoprene emissions are controversial. Relying on leaf-scale measurements, most models simulating isoprene emissions in future higher [CO2] atmospheres suggest reduced emission fluxes. However, combined effects of elevated [CO2] on leaf area growth, net assimilation and isoprene emission rates have rarely been studied on the canopy scale, but stimulation of leaf area growth may largely compensate for possible [CO2] inhibition reported at the leaf scale. This study tests the hypothesis that stimulated leaf area growth leads to increased canopy isoprene emission rates. We studied the dynamics of canopy growth, and net assimilation and isoprene emission rates in hybrid aspen (Populus tremula × Populus tremuloides) grown under 380 and 780 μmol mol(-1) [CO2]. A theoretical framework based on the Chapman-Richards function to model canopy growth and numerically compare the growth dynamics among ambient and elevated atmospheric [CO2]-grown plants was developed. Plants grown under elevated [CO2] had higher C : N ratio, and greater total leaf area, and canopy net assimilation and isoprene emission rates. During ontogeny, these key canopy characteristics developed faster and stabilized earlier under elevated [CO2]. However, on a leaf area basis, foliage physiological traits remained in a transient state over the whole experiment. These results demonstrate that canopy-scale dynamics importantly complements the leaf-scale processes, and that isoprene emissions may actually increase under higher [CO2] as a result of enhanced leaf area production. © 2013 The Authors. New Phytologist © 2013 New Phytologist Trust.

Remote measurement of atmospheric pollutants

Science.gov (United States)

Allario, F.; Hoell, J.; Seals, R. K.

1979-01-01

The concentration and vertical distribution of atmospheric ammonia and ozone are remotely sensed, using dual-C02-laser multichannel infrared Heterodyne Spectrometer (1HS). Innovation makes atmospheric pollution measurements possible with nearly-quantum-noise-limited sensitivity and ultrafine spectral resolution.

Serum vitamin E concentrations among highly functioning hip fracture patients are higher than in nonfracture controls.

Science.gov (United States)

D'Adamo, Christopher R; Shardell, Michelle D; Hicks, Gregory E; Orwig, Denise L; Hochberg, Marc C; Semba, Richard D; Yu-Yahiro, Janet A; Ferrucci, Luigi; Magaziner, Jay S; Miller, Ram R

2011-03-01

fracture patients demonstrated higher vitamin E concentrations. Thus, the relatively high degree of function among this cohort of hip fracture patients may explain their higher-than-expected vitamin E concentrations. Copyright © 2011 Elsevier Inc. All rights reserved.

OZONE CONCENTRATION ATTRIBUTABLE PREMATURE DEATH IN POLAND

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Krzysztof Skotak

2010-03-01

Full Text Available Ozone in the lower part of the atmosphere (troposphere, strong photochemical oxidant, is not directly emitted to the atmosphere but formed through a series of complex reactions. Ozone concentrations depends on ozone precursors air contamination (mainly nitrogen dioxide and non-methane volatile organic compounds and meteorological conditions (temperature and solar radiation. The main sectors emitted ozone precursors are road transport, power and heat generation plants, household (heating, industry, and petrol storage and distribution. Ozone and some of its precursors are also transported long distances in the atmosphere and are therefore considered a transboundary problem. As a result, the ozone concentrations are often low in busy urban areas and higher in suburban and rural areas. Nowadays, instead of particulate matter, ozone is one of the most widespread global air pollution problems. In and around urban areas, relatively large gradients of ozone can be observed. Because of its high reactivity in elevated concentrations ozone causes serious health problems and damage to ecosystems, agricultural crops and materials. Main ill-health endpoints as a results of ozone concentrations can be characterised as an effect of pulmonary and cardiovascular system, time morbidity and mortality series, development of atherosclerosis and asthma and finally reduction in life expectancy. The associations with increased daily mortality due to ozone concentrations are confirmed by many researches and epidemiological studies. Estimation of the level selected ill-health endpoints (mortality in total and due to cardiovascular and respiratory causes as a result of the short-term ozone exposure in Poland was the main aim of the project. Final results have been done based on estimation method elaborated by WHO, ozone measurements from National Air Quality Monitoring System and statistical information such as mortality rate and populations. All analysis have been done in

Modeled atmospheric radon concentrations from uranium mines

Energy Technology Data Exchange (ETDEWEB)

Droppo, J.G.

1985-04-01

Uranium mining and milling operations result in the release of radon from numerous sources of various types and strengths. The US Environmental Protection Agency (EPA) under the Clean Air Act, is assessing the health impact of air emissions of radon from underground uranium mines. In this case, the radon emissions may impact workers and residents in the mine vicinity. To aid in this assessment, the EPA needs to know how mine releases can affect the radon concentrations at populated locations. To obtain this type of information, Pacific Northwest Laboratory used the radon emissions, release characteristics and local meterological conditions for a number of mines to model incremental radon concentrations. Long-term, average, incremental radon concentrations were computed based on the best available information on release rates, plume rise parameters, number and locations of vents, and local dispersion climatology. Calculations are made for a model mine, individual mines, and multiple mines. Our approach was to start with a general case and then consider specific cases for comparison. A model underground uranium mine was used to provide definition of the order of magnitude of typical impacts. Then computations were made for specific mines using the best mine-specific information available for each mine. These case study results are expressed as predicted incremental radon concentration contours plotted on maps with local population data from a previous study. Finally, the effect of possible overlap of radon releases from nearby mines was studied by calculating cumulative radon concentrations for multiple mines in a region with many mines. The dispersion model, modeling assumptions, data sources, computational procedures, and results are documented in this report. 7 refs., 27 figs., 18 tabs.

Modeled atmospheric radon concentrations from uranium mines

International Nuclear Information System (INIS)

Droppo, J.G.

1985-04-01

Uranium mining and milling operations result in the release of radon from numerous sources of various types and strengths. The US Environmental Protection Agency (EPA) under the Clean Air Act, is assessing the health impact of air emissions of radon from underground uranium mines. In this case, the radon emissions may impact workers and residents in the mine vicinity. To aid in this assessment, the EPA needs to know how mine releases can affect the radon concentrations at populated locations. To obtain this type of information, Pacific Northwest Laboratory used the radon emissions, release characteristics and local meterological conditions for a number of mines to model incremental radon concentrations. Long-term, average, incremental radon concentrations were computed based on the best available information on release rates, plume rise parameters, number and locations of vents, and local dispersion climatology. Calculations are made for a model mine, individual mines, and multiple mines. Our approach was to start with a general case and then consider specific cases for comparison. A model underground uranium mine was used to provide definition of the order of magnitude of typical impacts. Then computations were made for specific mines using the best mine-specific information available for each mine. These case study results are expressed as predicted incremental radon concentration contours plotted on maps with local population data from a previous study. Finally, the effect of possible overlap of radon releases from nearby mines was studied by calculating cumulative radon concentrations for multiple mines in a region with many mines. The dispersion model, modeling assumptions, data sources, computational procedures, and results are documented in this report. 7 refs., 27 figs., 18 tabs

Polychlorinated biphenyls and polybrominated diphenyl ethers in the North American atmosphere

International Nuclear Information System (INIS)

Shen Li; Wania, Frank; Lei, Ying D.; Teixeira, Camilla; Muir, Derek C.G.; Xiao, Hang

2006-01-01

To assess the spatial concentration variability of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in the atmosphere on a large continental scale, their annually integrated air concentrations were determined in 2000/2001 using XAD-based passive air samplers (PAS). The network included 40 stations in Canada, the United States, Mexico, Belize and Costa Rica, and covered 72 degrees of latitude and longitude. Total concentrations of PCB and PBDE congeners ranged from below the detection limit to 130 ng PAS -1 and 24 ng PAS -1 , respectively. PCBs displayed a large variation between urban, rural and remote sites, whereas PBDEs did not follow such a pattern. Open burning of 'Penta'-containing waste may have contributed to the PBDEs detected in the air samples from rural and remote areas. Air from the Canadian Arctic had a relatively higher percentage of lighter PCB congeners than air sampled in the tropical region, which is interpreted as evidence for global fractionation. - A continental passive air sampling network reveals atmospheric distribution patterns of two classes of industrial chemicals

Effectiveness of carbon dioxide removal in lowering atmospheric CO2 and reversing global warming in the context of 1.5 degrees

Science.gov (United States)

Zickfeld, K.; Azevedo, D.

2017-12-01

The majority of emissions scenarios that limit warming to 2°C, and nearly all emission scenarios that do not exceed 1.5°C warming by the year 2100 require artificial removal of CO2 from the atmosphere. Carbon dioxide removal (CDR) technologies in these scenarios are required to offset emissions from sectors that are difficult or costly to decarbonize and to generate global `net negative' emissions, allowing to compensate for earlier emissions and to meet long-term climate stabilization targets after overshoot. Only a few studies have explored the Earth system response to CDR and large uncertainties exist regarding the effect of CDR on the carbon cycle and its effectiveness in reversing climate impacts after overshoot. Here we explore the effectiveness of CDR in lowering atmospheric CO2 ("carbon cycle effectiveness") and cool global climate ("cooling effectiveness"). We force the University of Victoria Earth System Climate Model, a model of intermediate complexity, with a set of negative CO2 emissions pulses of different magnitude and applied from different background atmospheric CO2 concentrations. We find the carbon cycle effectiveness of CDR - defined as the change in atmospheric CO2 per unit CO2 removed - decreases with the amount of CO2 removed from the atmosphere and increases at higher background CO2 concentrations from which CDR is applied due to nonlinear responses of carbon sinks to CO2 and climate. The cooling effectiveness - defined as the change in global mean surface air temperature per unit CO2 removed - on the other hand, is largely insensitive to the amount of CO2 removed, but decreases if CDR is applied at higher atmospheric CO2 concentrations, due to the logarithmic relationship between atmospheric CO2 and radiative forcing. Based on our results we conclude that CDR is more effective in restoring a lower atmospheric CO2 concentration and reversing impacts directly linked to CO2 at lower levels of overshoot. CDR's effectiveness in restoring a

The Global Land-Ocean Temperature Index in Relation to Sunspot Number, the Atlantic Multidecadal Oscillation Index, the Mauna Loa Atmospheric Concentration of CO2, and Anthropogenic Carbon Emissions

Science.gov (United States)

Wilson, Robert M.

2013-01-01

Global warming/climate change has been a subject of scientific interest since the early 19th century. In particular, increases in the atmospheric concentration of carbon dioxide (CO2) have long been thought to account for Earth's increased warming, although the lack of a dependable set of observational data was apparent as late as the mid 1950s. However, beginning in the late 1950s, being associated with the International Geophysical Year, the opportunity arose to begin accurate continuous monitoring of the Earth's atmospheric concentration of CO2. Consequently, it is now well established that the atmospheric concentration of CO2, while varying seasonally within any particular year, has steadily increased over time. Associated with this rising trend in the atmospheric concentration of CO2 is a rising trend in the surface-air and sea-surface temperatures (SSTs). This Technical Publication (TP) examines the statistical relationships between 10-year moving averages (10-yma) of the Global Land-Ocean Temperature Index (GLOTI), sunspot number (SSN), the Atlantic Multidecadal Oscillation (AMO) index, and the Mauna Loa CO2 (MLCO2) index for the common interval 1964-2006, where the 10-yma values are used to indicate trends in the data. Scatter plots using the 10-yma values between GLOTI and each of the other parameters are determined, both as single-variate and multivariate fits. Scatter plots are also determined for MLCO2 using single-variate and bivariate (BV) fits, based on the GLOTI alone and the GLOTI in combination with the AMO index. On the basis of the inferred preferential fits for MLCO2, estimates for MLCO2 are determined for the interval 1885-1964, thereby yielding an estimate of the preindustrial level of atmospheric concentration of CO2. Lastly, 10-yma values of MLCO2 are compared against 10-yma estimates of the total carbon emissions (TCE) to determine the likelihood that manmade sources of carbon emissions are indeed responsible for the recent warming now

Aerosols radioactivity in the Bratislava atmosphere

International Nuclear Information System (INIS)

Sykora, I.; Chudy, M.; Durana, L.; Holy, K.; Meresova, J.

2001-01-01

In our laboratory we measured temporal variation of 7 Be concentration in the atmosphere in period 1977 -1994 years. The aerosols were collected through every month at Hydrometeorological Institute in Bratislava-Koliba, latitude 48 grad 10' and altitude 286 m above sea level. Since end of year 2000 we have started to continue monitoring radioactivity of atmosphere aerosols in new locality in Bratislava-Mlynska dolina. Beside 7 Be we measured also 210 Pb radionuclide aerosols concentration. For measured values 7 Be concentrations are considered corrections for decay radionuclide during the time of filters collection, time between end of collection and measurement and decay during the time of measurement. Obtained results for 7 Be concentrations in aerosols shows seasonal summer maximum, but for 210 Pb concentration in aerosols the seasonal variations are not evident. The temporal variations of this radionuclide which is originated in ground-level atmosphere are more sensitive on meteorological factors and can be also influenced by the industrial activity. For better understanding is needed long term monitoring. (authors)

Evaluation of correlating factors between 238U concentration measured in fine and course atmospheric particles

International Nuclear Information System (INIS)

Peixoto, Claudia Marques; Jacomino, Vanusa Maria Feliciano; Barreto, Alberto Avelar; Dias, Vagner Silva; Dias, Fabiana Ferrari

2009-01-01

Air quality is ever more important in function of the enormous proportion of human actions that have affected the environment over the last two centuries. Particulate material is one among many pollutants that can cause great risk to human health and the environment. It can be classified as: Total Suspended Particles (TSP), defined simply as particles with less than 50 μm aerodynamic diameter (one group of these particles can be inhaled and may cause health problems, while others may unfavorably affect the population's quality of life, interfering in environmental conditions and impairing normal community activities); and Inhalable Particles (PM 10 ), defined as those particles with less than 10 μm aerodynamic diameter. These particles penetrate the respiratory system and can reach pulmonary alveoli due to their small size, causing serious health damage. The Nuclear Technology Development Center (CDTN) has monitored air quality around its installations since 2000. CDTN's Environmental Monitoring Program (EMP) includes monitoring radioactivity levels contained in atmospheric TSP. In order to optimize its program, CDTN is carrying out a study to estimate the correlation between concentrations of particulate material measured in TSP and those measured in PM 10 , PI 2.5 and PI 1 , as well as determination of activity concentration for each controlled radionuclide in all parts. The objective of this study is to present preliminary results and report 238 U activity concentration results. (author)

Dynamics of radioactive lead isotopes in the global environmental atmosphere

International Nuclear Information System (INIS)

Koike, Yuya; Kosako, Toshiso

2006-01-01

Fundamental information of radioactive lead isotopes, which used as the atmospheric tracer in the global environmental atmosphere, is reviewed. Emanation and exhalation of Rn and Tn, parent nuclide, is stated. Some reports on measurement and application of short-lived lead isotopes are reported. Transfer of radioactive lead isotopes in the atmosphere, vertical profiles of radon, thoron, and short-lived lead isotopes for different turbulent mixing conditions, deposition to aerosol, basic processes of Rn decay product behavior in air defining 'unattached' and 'aerosol-attached' activities, seasonal variation of atmospheric 210 Pb concentration at Beijing and Chengdu, seasonal variation of atmospheric 212 Pb concentration at several observation sites in Japan Islands, and variation in the atmospheric concentration of 212 Pb along with SO 2 are shown. (S.Y.)

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.

A Department of Atmospheric and Planetary Sciences at Hampton University

Science.gov (United States)

Paterson, W. R.; McCormick, M. P.; Russell, J. M.; Anderson, J.; Kireev, S.; Loughman, R. P.; Smith, W. L.

2006-12-01

With this presentation we discuss the status of plans for a Department of Atmospheric and Planetary Sciences at Hampton University. Hampton University is a privately endowed, non-profit, non-sectarian, co-educational, and historically black university with 38 baccalaureate, 14 masters, and 4 doctoral degree programs. The graduate program in physics currently offers advanced degrees with concentration in Atmospheric Science. The 10 students now enrolled benefit substantially from the research experience and infrastructure resident in the university's Center for Atmospheric Sciences (CAS), which is celebrating its tenth anniversary. Promoting a greater diversity of participants in geosciences is an important objective for CAS. To accomplish this, we require reliable pipelines of students into the program. One such pipeline is our undergraduate minor in Space, Earth, and Atmospheric Sciences (SEAS minor). This minor concentraton of study is contributing to awareness of geosciences on the Hampton University campus, and beyond, as our students matriculate and join the workforce, or pursue higher degrees. However, the current graduate program, with its emphasis on physics, is not necessarily optimal for atmospheric scientists, and it limits our ability to recruit students who do not have a physics degree. To increase the base of candidate students, we have proposed creation of a Department of Atmospheric and Planetary Sciences, which could attract students from a broader range of academic disciplines. The revised curriculum would provide for greater concentration in atmospheric and planetary sciences, yet maintain a degree of flexibility to allow for coursework in physics or other areas to meet the needs of individual students. The department would offer the M.S. and Ph.D. degrees, and maintain the SEAS minor. The university's administration and faculty have approved our plan for this new department pending authorization by the university's board of trustees, which will

Response of the rhizosphere prokaryotic community of barley (Hordeum vulgare L.) to elevated atmospheric CO2 concentration in open-top chambers.

Science.gov (United States)

Szoboszlay, Márton; Näther, Astrid; Mitterbauer, Esther; Bender, Jürgen; Weigel, Hans-Joachim; Tebbe, Christoph C

2017-08-01

The effect of elevated atmospheric CO 2 concentration [CO 2 ] on the diversity and composition of the prokaryotic community inhabiting the rhizosphere of winter barley (Hordeum vulgare L.) was investigated in a field experiment, using open-top chambers. Rhizosphere samples were collected at anthesis (flowering stage) from six chambers with ambient [CO 2 ] (approximately 400 ppm) and six chambers with elevated [CO 2 ] (700 ppm). The V4 region of the 16S rRNA gene was PCR-amplified from the extracted DNA and sequenced on an Illumina MiSeq instrument. Above-ground plant biomass was not affected by elevated [CO 2 ] at anthesis, but plants exposed to elevated [CO 2 ] had significantly higher grain yield. The composition of the rhizosphere prokaryotic communities was very similar under ambient and elevated [CO 2 ]. The dominant taxa were Bacteroidetes, Actinobacteria, Alpha-, Gamma-, and Betaproteobacteria. Elevated [CO 2 ] resulted in lower prokaryotic diversity in the rhizosphere, but did not cause a significant difference in community structure. © 2017 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd.

The ~ 2400-year cycle in atmospheric radiocarbon concentration: bispectrum of 14C data over the last 8000 years

Directory of Open Access Journals (Sweden)

S. S. Vasiliev

2002-01-01

Full Text Available We have carried out power spectrum, time-spectrum and bispectrum analyses of the long-term series of the radiocarbon concentrations deduced from measurements of the radiocarbon content in tree rings for the last 8000 years. Classical harmonic analysis of this time series shows a number of periods: 2400, 940, 710, 570, 500, 420, 360, 230, 210 and 190 years. A principle feature of the time series is the long period of ~ 2400 years, which is well known. The lines with periods of 710, 420 and 210 years are found to be the primary secular components of power spectrum. The complicated structure of the observed power spectrum is the result of ~ 2400-year modulation of primary secular components. The modulation induces the appearance of two side lines for every primary one, namely lines with periods of 940 and 570 years, of 500 and 360 years, and 230 and 190 years. The bispectral analysis shows that the parameters of carbon exchange system varied with the ~ 2400-year period during the last 8000 years. Variations of these parameters appear to be a climate effect on the rate of transfer of 14C between the atmosphere and the the ocean.Key words. Meteorology and atmospheric dynamics (climatology; ocean-atmosphere interaction; paleoclimatology

Molecular dynamics simulation of the local concentration and structure in multicomponent aerosol nanoparticles under atmospheric conditions.

Science.gov (United States)

Karadima, Katerina S; Mavrantzas, Vlasis G; Pandis, Spyros N

2017-06-28

Molecular dynamics (MD) simulations were employed to investigate the local structure and local concentration in atmospheric nanoparticles consisting of an organic compound (cis-pinonic acid or n-C 30 H 62 ), sulfate and ammonium ions, and water. Simulations in the isothermal-isobaric (NPT) statistical ensemble under atmospheric conditions with a prespecified number of molecules of the abovementioned compounds led to the formation of a nanoparticle. Calculations of the density profiles of all the chemical species in the nanoparticle, the corresponding radial pair distribution functions, and their mobility inside the nanoparticle revealed strong interactions developing between sulfate and ammonium ions. However, sulfate and ammonium ions prefer to populate the central part of the nanoparticle under the simulated conditions, whereas organic molecules like to reside at its outer surface. Sulfate and ammonium ions were practically immobile; in contrast, the organic molecules exhibited appreciable mobility at the outer surface of the nanoparticle. When the organic compound was a normal alkane (e.g. n-C 30 H 62 ), a well-organized (crystalline-like) phase was rapidly formed at the free surface of the nanoparticle and remained separate from the rest of the species.

Trends in atmospheric ammonium concentrations in relation to atmospheric sulfate and local agriculture.

Science.gov (United States)

Kelly, Victoria R; Lovett, Gary M; Weathers, Kathleen C; Likens, Gene E

2005-06-01

Ammonium (NH(4)(+)) concentrations in air and precipitation at the Institute of Ecosystem Studies (IES) in southeastern New York, USA declined over an 11-year period from 1988 to 1999, but increased from 1999 to 2001. These trends in particulate NH(4)(+) correlated well with trends in particulate SO(4)(2-) over the 1988-2001 period. The NH(4)(+) trends were not as well correlated with local cattle and milk production, which declined continuously throughout the period. This suggests that regional transport of SO(4)(2-) may have a greater impact on concentrations of NH(4)(+) and subsequent deposition than local agricultural emissions of NH(3). Ammonium concentrations in precipitation correlated significantly with precipitation SO(4)(2-) concentrations for the 1984-2001 period although NH(4)(+) in precipitation increased after 1999 and SO(4)(2-) in precipitation continued to decline after 1999. The correlation between NH(4)(+) and SO(4)(2-) was stronger for particulates than for precipitation. Particulate NH(4)(+) concentrations were also correlated with particulate SO(4)(2-) concentrations at 31 of 35 eastern U.S. CASTNet sites that had at least 10 years of data. Air concentrations of NH(4)(+) and SO(4)(2-) were more strongly correlated at the sites that were located within an agricultural landscape than in forested sites. At most of the sites there was either no trend or a decrease in NH(4)(+) dry deposition during the 1988-2001 period. The sites that showed an increasing trend in NH(4)(+) dry deposition were generally located in the southeastern U.S. The results of this study suggest that, in the northeastern U.S., air concentrations of NH(4)(+) and subsequent deposition may be more closely linked to SO(4)(2-) and thus SO(2) emissions than with NH(3) emissions. These results also suggest that reductions in S emissions have reduced NH(4)(+) transport to and NH(4)(+)-N deposition in the Northeast.

Regional atmospheric budgets of reduced nitrogen over the British isles assessed using a multi-layer atmospheric transport model

NARCIS (Netherlands)

Fournier, N.; Tang, Y.S.; Dragosits, U.; Kluizenaar, Y.de; Sutton, M.A.

2005-01-01

Atmospheric budgets of reduced nitrogen for the major political regions of the British Isles are investigated with a multi-layer atmospheric transport model. The model is validated against measurements of NH3 concentration and is developed to provide atmospheric budgets for defined subdomains of the

Polychlorinated biphenyl concentrations, accumulation rates in soil from atmospheric deposition and analysis of their affecting landscape variables along an urban-rural gradient in Shanghai, China.

Science.gov (United States)

Fang, Shubo; Cui, Qu; Matherne, Brian; Hou, Aixin

2017-11-01

This study initiated an in-situ soil experimental system to quantify the annual dynamics of polychlorinated biphenyl (PCB) congener's concentrations and accumulation rates in soil from atmosphere deposition in a rural-urban fringe, and correlated them by landscape physical and demographic variables in the area. The results showed that the concentrations of all PCB congeners significantly increased with the sampling time (p urban center. The moderate average concentrations along the gradient for PCB 8, 18, and 28 were 31.003, 18.825, and 19.505 ng g-1, respectively. Tetra-CBs including PCB 44, 52, 66, and 77 were 10.243, 31.214, 8.330 and 9.530 ng g-1, respectively. Penta-CBs including PCB 101, 105, 118, and 126 were 9.465, 7.896, 17.703, and 6.363 ng g-1, respectively. Hexa-CBs including PCB 128, 138, 153, 170, 180, and 187 were 6.798, 11.522, 4.969, 6.722, 6.317, and 8.243 ng g-1 respectively. PCB 195, 206, and 209 were 8.259, 9.506, and 14.169 ng g-1, respectively. Most of the PCB congeners had a higher accumulation rate approximately 28 km from the urban center. The computed variables were found to affect the soil PCB concentrations with a threshold effect (p urban sprawling (i.e. built-up areas expanding) were the sources of PCBs. Copyright © 2017 Elsevier Ltd. All rights reserved.

Diurnal Variation of Radon Concentration in the Postojna Cave

International Nuclear Information System (INIS)

Gregoric, A.; Vaupotic, J.

2011-01-01

seasonal variations of radon concentration. Diurnal variations are noticed only under special atmospheric conditions and depend mostly on the outside air temperature variation. On average, radon concentrations were in the ranges of 500 - 2500 Bq m -3 and 500 - 7000 Bq m -3 at site P1 and P2, respectively. On a long-time scale similar effect of atmospheric conditions is often observed at both sites. However, local morphology and characteristics of the cave at the site cause different short-time variations of radon concentration. Thus, radon concentrations are lower and more stable at the Great Mountain hall, whereas they are higher and with more pronounced diurnal and seasonal variations in the Beautiful Caves. (author)

Effects of elevated atmospheric CO2 concentration on leaf dark respiration of Xanthium strumarium in light and in darkness.

Science.gov (United States)

Wang, X; Lewis, J D; Tissue, D T; Seemann, J R; Griffin, K L

2001-02-27

Leaf dark respiration (R) is an important component of plant carbon balance, but the effects of rising atmospheric CO(2) on leaf R during illumination are largely unknown. We studied the effects of elevated CO(2) on leaf R in light (R(L)) and in darkness (R(D)) in Xanthium strumarium at different developmental stages. Leaf R(L) was estimated by using the Kok method, whereas leaf R(D) was measured as the rate of CO(2) efflux at zero light. Leaf R(L) and R(D) were significantly higher at elevated than at ambient CO(2) throughout the growing period. Elevated CO(2) increased the ratio of leaf R(L) to net photosynthesis at saturated light (A(max)) when plants were young and also after flowering, but the ratio of leaf R(D) to A(max) was unaffected by CO(2) levels. Leaf R(N) was significantly higher at the beginning but significantly lower at the end of the growing period in elevated CO(2)-grown plants. The ratio of leaf R(L) to R(D) was used to estimate the effect of light on leaf R during the day. We found that light inhibited leaf R at both CO(2) concentrations but to a lesser degree for elevated (17-24%) than for ambient (29-35%) CO(2)-grown plants, presumably because elevated CO(2)-grown plants had a higher demand for energy and carbon skeletons than ambient CO(2)-grown plants in light. Our results suggest that using the CO(2) efflux rate, determined by shading leaves during the day, as a measure for leaf R is likely to underestimate carbon loss from elevated CO(2)-grown plants.

Electric field measurement in an atmospheric or higher pressure gas by coherent Raman scattering of nitrogen

International Nuclear Information System (INIS)

Ito, Tsuyohito; Kobayashi, Kazunobu; Hamaguchi, Satoshi; Mueller, Sarah; Luggenhoelscher, Dirk; Czarnetzki, Uwe

2009-01-01

The feasibility of electric field measurement based on field-induced coherent Raman scattering is demonstrated for the first time in a nitrogen containing gas at atmospheric or higher pressure, including open air. The technique is especially useful for the determination of temporal and spatial profiles of the electric field in air-based microdischarges, where nitrogen is abundant. In our current experimental setup, the minimum detectable field strength in open air is about 100 V mm -1 , which is sufficiently small compared with the average field present in typical microdischarges. No further knowledge of other gas/plasma parameters such as the nitrogen density is required. (fast track communication)

The counteracting effects of elevated atmospheric CO2 concentrations and drought episodes: Studies of enchytraeid communities in a dry heathland

DEFF Research Database (Denmark)

Maraldo, Kristine; Krogh, Paul Henning; Linden, Leon

2010-01-01

The potential impacts of interactions of multiple climate change factors in soil ecosystems have received little attention. Most studies have addressed effects of single factors such as increased temperature or atmospheric CO2 but little is known about how such environmental factors will interact...... impact of drought on the enchytraeids, compared to the year with a wet summer and autumn (2007). Our study emphasises the importance of multi-factorial experimental design as a means to investigate effects of climatic changes.......The potential impacts of interactions of multiple climate change factors in soil ecosystems have received little attention. Most studies have addressed effects of single factors such as increased temperature or atmospheric CO2 but little is known about how such environmental factors will interact....... In the present study we investigate the effects of in situ exposure to elevated atmospheric CO2 concentration, increased temperatures and prolonged drought episodes on field communities of Enchytraeidae (Oligochaeta) in a dry heathland (Brandbjerg, Denmark). Increased CO2 had a positive effect on enchytraeid...

Observation and analysis of speciated atmospheric mercury in Shangri-La, Tibetan Plateau, China

Science.gov (United States)

Zhang, H.; Fu, X. W.; Lin, C.-J.; Wang, X.; Feng, X. B.

2015-01-01

This study reports the concentrations and potential sources of speciated atmospheric mercury at the Shangri-La Atmosphere Watch Regional Station (SAWRS), a pristine high-altitude site (3580 m a.s.l.) in Tibetan Plateau, China. Total gaseous mercury (TGM, defined as the sum of gaseous elemental mercury, GEM, and gaseous oxidized mercury, GOM), GOM and particulate-bound mercury (PBM) were monitored from November 2009 to November 2010 to investigate the characteristics and potential influence of the Indian summer monsoon (ISM) and the Westerlies on atmospheric transport of mercury. The mean concentrations (± standard deviation) of TGM, PBM and GOM were 2.55 ± 0.73 ng m-3, 38.82 ± 31.26 pg m-3 and 8.22 ± 7.90 pg m-3, respectively. A notable seasonal pattern of TGM concentrations was observed with higher concentrations at the beginning and the end of the ISM season. High TGM concentrations (> 2.5 ng m-3) were associated with the transport of dry air that carried regional anthropogenic emissions from both Chinese domestic and foreign (e.g., Myanmar, Bay of Bengal, and northern India) sources based on analysis of HYSPLIT4 back trajectories. Somewhat lower PBM and GOM levels during the ISM period were attributed to the enhanced wet scavenging. The high GOM and PBM were likely caused by local photo-chemical transformation under low RH and the domestic biofuel burning in cold seasons.

Atmospheric concentrations, sources and gas-particle partitioning of PAHs in Beijing after the 29th Olympic Games

Energy Technology Data Exchange (ETDEWEB)

Ma Wanli [International Joint Research Center for Persistent Toxic Substances (IJRC-PTS), State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Sun Dezhi [International Joint Research Center for Persistent Toxic Substances (IJRC-PTS), State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083 (China); Shen Weiguo [College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083 (China); Yang Meng [IJRC-PTS, Dalian Maritime University, Dalian (China); Qi Hong; Liu Liyan; Shen Jimin [International Joint Research Center for Persistent Toxic Substances (IJRC-PTS), State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Li Yifan, E-mail: ijrc_pts_paper@yahoo.com [International Joint Research Center for Persistent Toxic Substances (IJRC-PTS), State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Science and Technology Branch, Environment Canada, Toronto, Ontario M3H5T4 (Canada)

2011-07-15

A comprehensive sampling campaign was carried out to study atmospheric concentration of polycyclic aromatic hydrocarbons (PAHs) in Beijing and to evaluate the effectiveness of source control strategies in reducing PAHs pollution after the 29th Olympic Games. The sub-cooled liquid vapor pressure (logP{sub L}{sup o})-based model and octanol-air partition coefficient (K{sub oa})-based model were applied based on each seasonal dateset. Regression analysis among log K{sub P}, logP{sub L}{sup o} and log K{sub oa} exhibited high significant correlations for four seasons. Source factors were identified by principle component analysis and contributions were further estimated by multiple linear regression. Pyrogenic sources and coke oven emission were identified as major sources for both the non-heating and heating seasons. As compared with literatures, the mean PAH concentrations before and after the 29th Olympic Games were reduced by more than 60%, indicating that the source control measures were effective for reducing PAHs pollution in Beijing. - Highlights: > This is the first comprehensive study of PAHs in atmosphere after the 29th Olympics in Beijing, China. > The air quality before and after 29th Olympics has attracted much attention worldwide. > The study was helpful for other countries to understand how the Olympics affected PAHs emissions. > The study would act as a case study to know the effects that big events can impose on the host cities. - The source control measures implemented before and during the 29th Olympic Games were effective for reducing the emissions of air pollutants in Beijing.

Using native epiphytic ferns to estimate the atmospheric mercury levels in a small-scale gold mining area of West Java, Indonesia.

Science.gov (United States)

Kono, Yuriko; Rahajoe, Joeni S; Hidayati, Nuril; Kodamatani, Hitoshi; Tomiyasu, Takashi

2012-09-01

Mercury pollution is caused by artisanal and small-scale gold mining (ASGM) operations along the Cikaniki River (West Java, Indonesia). The atmosphere is one of the primary media through which mercury can disperse. In this study, atmospheric mercury levels are estimated using the native epiphytic fern Asplenium nidus complex (A. nidus) as a biomonitor; these estimates shed light on the atmospheric dispersion of mercury released during mining. Samples were collected from 8 sites along the Cikaniki Basin during September-November, 2008 and September-November, 2009. The A. nidus fronds that were attached to tree trunks 1-3m above the ground were collected and measured for total mercury concentration using cold vapor atomic absorption spectrometry (CVAAS) after acid-digestion. The atmospheric mercury was collected using porous gold collectors, and the concentrations were determined using double-amalgam CVAAS. The highest atmospheric mercury concentration, 1.8 × 10(3) ± 1.6 × 10(3) ngm(-3), was observed at the mining hot spot, and the lowest concentration of mercury, 5.6 ± 2.0 ngm(-3), was observed at the remote site from the Cikaniki River in 2009. The mercury concentrations in A. nidus were higher at the mining village (5.4 × 10(3) ± 1.6 × 10(3) ngg(-1)) than at the remote site (70 ± 30 ngg(-1)). The distribution of mercury in A. nidus was similar to that in the atmosphere; a significant correlation was observed between the mercury concentrations in the air and in A. nidus (r=0.895, P<0.001, n=14). The mercury levels in the atmosphere can be estimated from the mercury concentration in A. nidus using a regression equation: log (Hg(A.nidu)/ngg(-1))=0.740 log (Hg(Air)/ngm (-3)) - 1.324. Copyright © 2012 Elsevier Ltd. All rights reserved.

Atmospheric concentrations and phase partitioning of polycyclic aromatic hydrocarbons in Izmir, Turkey

Energy Technology Data Exchange (ETDEWEB)

Demircioglu, Eylem; Odabasi, Mustafa [Faculty of Engineering, Department of Environmental Engineering, Dokuz Eylul University, Izmir (Turkey); Sofuoglu, Aysun [Faculty of Engineering, Department of Chemical Engineering, Izmir Institute of Technology, Gulbahce-Urla (Turkey)

2011-04-15

Ambient air polycyclic aromatic hydrocarbon (PAH) samples were collected at a suburban (n = 63) and at an urban site (n = 14) in Izmir, Turkey. Average gas-phase total PAH (sum {sub 14}PAH) concentrations were 23.5 ng m{sup -3} for suburban and 109.7 ng m{sup -3} for urban sites while average particle-phase total PAH concentrations were 12.3 and 34.5 ng m{sup -3} for suburban and urban sites, respectively. Higher ambient PAH concentrations were measured in the gas-phase and sum {sub 14}PAH concentrations were dominated by lower molecular weight PAHs. Multiple linear regression analysis indicated that the meteorological parameters were effective on ambient PAH concentrations. Emission sources of particle-phase PAHs were investigated using a diagnostic plot of fluorene (FLN)/(fluorine + pyrene; PY) versus indeno[1,2,3-cd]PY/(indeno[1,2,3-cd]PY + benzo[g,h,i]perylene) and several diagnostic ratios. These approaches have indicated that traffic emissions (petroleum combustion) were the dominant PAH sources at both sites for summer and winter seasons. Experimental gas-particle partition coefficients (K{sub P}) were compared to the predictions of octanol-air (K{sub OA}) and soot-air (K{sub SA}) partition coefficient models. The correlations between experimental and modeled K{sub P} values were significant (r{sup 2} = 0.79 and 0.94 for suburban and urban sites, respectively, p < 0.01). Octanol-based absorptive partitioning model predicted lower partition coefficients especially for relatively volatile PAHs. However, overall there was a relatively good agreement between the measured K{sub P} and soot-based model predictions. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Influence of Superparameterization and a Higher-Order Turbulence Closure on Rainfall Bias Over Amazonia in Community Atmosphere Model Version 5: How Parameterization Changes Rainfall

Energy Technology Data Exchange (ETDEWEB)

Zhang, Kai [Jackson School of Geosciences, University of Texas at Austin, Austin TX USA; Fu, Rong [Jackson School of Geosciences, University of Texas at Austin, Austin TX USA; Department of Atmospheric and Oceanic Sciences, University of California, Los Angeles CA USA; Shaikh, Muhammad J. [Jackson School of Geosciences, University of Texas at Austin, Austin TX USA; Ghan, Steven [Pacific Northwest National Laboratory, Richland WA USA; Wang, Minghuai [Institute for Climate and Global Change Research and School of Atmospheric Sciences, Nanjing University, Nanjing China; Collaborative Innovation Center of Climate Change, Nanjing China; Leung, L. Ruby [Pacific Northwest National Laboratory, Richland WA USA; Dickinson, Robert E. [Jackson School of Geosciences, University of Texas at Austin, Austin TX USA; Marengo, Jose [Centro Nacional de Monitoramento e Alertas aos Desastres Naturais, São Jose dos Campos Brazil

2017-09-21

We evaluate the Community Atmosphere Model Version 5 (CAM5) with a higher-order turbulence closure scheme, named Cloud Layers Unified By Binomials (CLUBB), and a Multiscale Modeling Framework (MMF) with two different microphysics configurations to investigate their influences on rainfall simulations over Southern Amazonia. The two different microphysics configurations in MMF are the one-moment cloud microphysics without aerosol treatment (SAM1MOM) and two-moment cloud microphysics coupled with aerosol treatment (SAM2MOM). Results show that both MMF-SAM2MOM and CLUBB effectively reduce the low biases of rainfall, mainly during the wet season. The CLUBB reduces low biases of humidity in the lower troposphere with further reduced shallow clouds. The latter enables more surface solar flux, leading to stronger convection and more rainfall. MMF, especially MMF-SAM2MOM, unstablizes the atmosphere with more moisture and higher atmospheric temperatures in the atmospheric boundary layer, allowing the growth of more extreme convection and further generating more deep convection. MMF-SAM2MOM significantly increases rainfall in the afternoon, but it does not reduce the early bias of the diurnal rainfall peak; LUBB, on the other hand, delays the afternoon peak time and produces more precipitation in the early morning, due to more realistic gradual transition between shallow and deep convection. MMF appears to be able to realistically capture the observed increase of relative humidity prior to deep convection, especially with its two-moment configuration. In contrast, in CAM5 and CAM5 with CLUBB, occurrence of deep convection in these models appears to be a result of stronger heating rather than higher relative humidity.

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

Serum concentration of alpha-1 antitrypsin is significantly higher in colorectal cancer patients than in healthy controls

International Nuclear Information System (INIS)

Pérez-Holanda, Sergio; Blanco, Ignacio; Menéndez, Manuel; Rodrigo, Luis

2014-01-01

The association between alpha-1 antitrypsin (AAT) deficiency and colorectal cancer (CRC) is currently controversial. The present study compares AAT serum concentrations and gene frequencies between a group of CRC patients and a control group of healthy unrelated people (HUP). 267 CRC subjects (63% males, 72 ± 10 years old) were enlisted from a Hospital Clinic setting in Asturias, Spain. The HUP group comprised 327 subjects (67% males, mean age 70 ± 7.5 years old) from the same geographical region. Outcome measures were AAT serum concentrations measured by nephelometry, and AAT phenotyping characterization by isoelectric focusing. Significantly higher serum concentrations were found among CRC (208 ± 60) than in HUP individuals (144 ± 20.5) (p = 0.0001). No differences were found in the phenotypic distribution of the Pi*S and Pi*Z allelic frequencies (p = 0.639), although the frequency of Pi*Z was higher in CRC (21%) than in HUP subjects (15%). The only statistically significant finding in this study was the markedly higher AAT serum concentrations found in CRC subjects compared with HUP controls, irrespective of whether their Pi* phenotype was normal (Pi*MM) or deficient (Pi*MS, Pi*MZ and Pi*SZ). Although there was a trend towards the more deficient Pi* phenotype the more advanced the tumor, the results were inconclusive due to the small sample size. Consequently, more powerful studies are needed to reach firmer conclusions on this matter

Biosphere-Atmosphere Exchange of NOx and O3 in Central Amazon

Science.gov (United States)

Wiedemann, K. T.; Swofsy, S. C.; Munger, J. W.; Saleska, S. R.; Rizzo, L. V.; Silva Campos, K.

2017-12-01

The primary source of atmospheric OH is the photolysis of O3 in the presence of water vapor. NOx gases are the main precursors of O3 and OH. In NOx-rich environments that have both high humidity and high solar radiation, OH concentrations are enhanced, making tropical forests dominant in global oxidation of long lived gases. The Amazon rain forest has a unique combination of vegetation with diverse characteristics, climate, and a dynamic land use, factors that altogether govern the emission and fate of trace gases, particle formation and atmospheric chemistry. Understanding the interactions among the mechanisms that govern local precursor emissions will lead to a better description of the local atmospheric chemistry and its global impacts. As part of the GoAmazon project, an array of complementary measurements was conducted in a research site in central Amazon, near Santarem (PA, Brazil), inside the Tapajos National Forest. The research site is surrounded by intact rain forest in a 6km radius, and a 45m canopy. The 67m tower was assembled in the site in 2001 for flux measurements (CO2 and H2O). In mid 2014 additional instrumentation were added, measuring NOx, O3, CH4, and SO2 fluxes and profiles. The low concentrations of SO2 (up to 0.1ppb during the peak of the dry season), and a small vertical gradient, suggest the predominance of biogenic sources. O3 show no significant seasonality between the daytime and nighttime vertical profiles, but occasional nighttime high concentrations for levels below canopy were observed. Hourly ozone fluxes suggest a production of O3 under canopy. NO soil emissions are indicated by concentrations in the ppb range for lower profile levels, decreasing to a few hundreds ppt above the canopy, and emission rates of NO from Amazonian soils may be higher than expected from earlier measurements. Daytime data indicate that not all of this NOx escapes to the atmosphere, however. Fluxes of NO average 133x109 molec cm-2 s-1, a factor of 4 higher

Seasonal associations and atmospheric transport distances of Fusarium collected with unmanned aerial vehicles and ground-based sampling devices

Science.gov (United States)

Schmale, David; Ross, Shane; Lin, Binbin

2014-05-01

Spores of fungi in the genus Fusarium may be transported through the atmosphere over long distances. Members of this genus are important pathogens and mycotoxin producers. New information is needed to characterize seasonal trends in atmospheric loads of Fusarium and to pinpoint the source(s) of inoculum at both local (farm) and regional (state or country) scales. Spores of Fusarium were collected from the atmosphere in an agricultural ecosystem in Blacksburg, VA, USA using a Burkard volumetric sampler (BVS) 1 m above ground level and autonomous unmanned aerial vehicles (UAVs) 100 m above ground level. More than 2,200 colony forming units (CFUs) of Fusarium were collected during 104 BVS sampling periods and 180 UAV sampling periods over four calendar years (2009-2012). Spore concentrations ranged from 0 to 13 and 0 to 23 spores m-3 for the BVS and the UAVs, respectively. Spore concentrations were generally higher in the fall, spring, and summer, and lower in the winter. Spore concentrations from the BVS were generally higher than those from the UAVs for both seasonal and hourly collections. Some of the species of Fusarium identified from our collections have not been previously reported in the state of Virginia. A Gaussian plume transport model was used to estimate distances to the potential inoculum source(s) by season. This work extends previous studies showing an association between atmospheric transport barriers (Lagrangian coherent structures or LCSs) and the movement of Fusarium in the lower atmosphere. An increased understanding of the aerobiology of Fusarium may contribute to new and improved control strategies for diseases causes by fusaria in the future.

Does carbon isotope data help explain atmospheric CO2 concentrations during glacial periods?

International Nuclear Information System (INIS)

Alverson, K.; Le Grand, P.

2002-01-01

An inverse ocean box modeling approach is used to address the question of what may have caused decreased atmospheric CO 2 concentration during glacial periods. The inverse procedure seeks solutions that are consistent, within prescribed uncertainties, with both available paleodata constraints and box model conservation equations while relaxing traditional assumptions such as exact steady state and precise prescription of uncertain model parameters. Decreased ventilation of Southern Ocean deep water, decreased Southern Ocean air-sea gas exchange, and enhanced high latitude biological pumping are all shown to be individually capable of explaining available paleodata constraints provided that significant calcium carbonate compensation is allowed. None of the scenarios require more than a very minor (order 1 deg. C) glacial reduction in low to mid latitude sea surface temperature although scenarios with larger changes are equally plausible. One explanation for the fairly wide range of plausible solutions is that most paleo-data directly constrain the inventory of paleo-tracers but only indirectly constrain their fluxes. Because the various scenarios that have been proposed to explain pCO 2 levels during the last glacial maximum are distinguished primarily by different fluxes, the data, including ocean 13 C concentrations, do not allow one to confidently chose between them. Oceanic 14 C data for the last glacial maximum, which can constrain water mass fluxes, present an excellent potential solution to this problem if their reliability is demonstrated in the future. (author)

On the influence of atmospheric super-saturation layer on China's heavy haze-fog events

Science.gov (United States)

Wang, Jizhi; Yang, Yuanqin; Zhang, Xiaoye; Liu, Hua; Che, Huizheng; Shen, Xiaojing; Wang, Yaqiang

2017-12-01

With the background of global change, the air quality in Earth's atmosphere has significantly decreased. The North China Plain (NCP), Yangtze River Delta (YRD), Pearl River Delta (PRD) and Si-Chuan Basin (SCB) are the major areas suffering the decreasing air quality and frequent pollution events in recent years. Studying the effect of meteorological conditions on the concentration of pollution aerosols in these pollution sensitive regions is a hot focus now. This paper analyses the characteristics of atmospheric super-saturation and the corresponding H_PMLs (height of supersaturated pollution mixing layer), investigating their contribution to the frequently-seen heavy haze-fog weather. The results suggest that: (1) in the above-mentioned pollution sensitive regions in China, super-saturated layers repeatedly appear in the low altitude and the peak value of supersaturation S can reach 6-10%, which makes pollution particles into the wet adiabatic uplift process in the stable-static atmosphere. After low-level atmosphere reaches the super-saturation state below the H_PMLs, meteorological condition contributes to humidification and condensation of pollution particles. (2) Caculation of condensation function Fc, one of PLAM sensetive parameter, indicates that super-saturation state helps promote condensation, beneficial to the formation of Condensational Kink (CK) in the pollution sensitive areas. This favors the formation of new aerosol particles and intensities the cumulative growth of aerosol concentration. (3) By calculating the convective inhibition energy on average │CIN│ > 1.0 × 104 J kg-1, we found the value is about 100 times higher than the stable critical value. The uplifting diffusion of the particles is inhibited by the ambient airflow. So, this is the important reason for the aggravation and persistence of aerosol pollutants in local areas. (4) H_PMLs is negatively correlated to the pollution meteorological condition index PLAM which can describe the

Effect of traffic restriction on atmospheric particle concentrations and their size distributions in urban Lanzhou, Northwestern China.

Science.gov (United States)

Zhao, Suping; Yu, Ye; Liu, Na; He, Jianjun; Chen, Jinbei

2014-02-01

During the 2012 Lanzhou International Marathon, the local government made a significant effort to improve traffic conditions and air quality by implementing traffic restriction measures. To evaluate the direct effect of these measures on urban air quality, especially particle concentrations and their size distributions, atmospheric particle size distributions (0.5-20 microm) obtained using an aerodynamic particle sizer (model 3321, TSI, USA) in June 2012 were analyzed. It was found that the particle number, surface area and volume concentrations for size range 0.5-10 microm were (15.0 +/- 2.1) cm(-3), (11.8 +/- 2.6) microm2/cm3 and (1.9 +/- 0.6) microm2/cm3, respectively, on the traffic-restricted day (Sunday), which is 63.2%, 53.0% and 47.2% lower than those on a normal Sunday. For number and surface area concentrations, the most affected size range was 0.5-0.7 and 0.5-0.8 microm, respectively, while for volume concentration, the most affected size ranges were 0.5-0.8, 1.7-2.0 and 5.0-5.4 microm. Number and volume concentrations of particles in size range 0.5-1.0 microm correlated well with the number of non-CNG (Compressed Natural Gas) powered vehicles, while their correlation with the number of CNG-powered vehicles was very low, suggesting that reasonable urban traffic controls along with vehicle technology improvements could play an important role in improving urban air quality.

An advanced analysis and modelling the air pollutant concentration temporal dynamics in atmosphere of the industrial cities: Odessa city

Science.gov (United States)

Buyadzhi, V. V.; Glushkov, A. V.; Khetselius, O. Yu; Ternovsky, V. B.; Serga, I. N.; Bykowszczenko, N.

2017-10-01

Results of analysis and modelling the air pollutant (dioxide of nitrogen) concentration temporal dynamics in atmosphere of the industrial city Odessa are presented for the first time and based on computing by nonlinear methods of the chaos and dynamical systems theories. A chaotic behaviour is discovered and investigated. To reconstruct the corresponding strange chaotic attractor, the time delay and embedding dimension are computed. The former is determined by the methods of autocorrelation function and average mutual information, and the latter is calculated by means of correlation dimension method and algorithm of false nearest neighbours. It is shown that low-dimensional chaos exists in the nitrogen dioxide concentration time series under investigation. Further, the Lyapunov’s exponents spectrum, Kaplan-Yorke dimension and Kolmogorov entropy are computed.

A glossary of atmospheric science

International Nuclear Information System (INIS)

1996-09-01

This book concentrates on the glossary of atmospheric science, which contains summary, for enactment and deliberation on choosing special glossary on atmospheric science in Korea, examiner for the glossary on atmospheric science, reference, explanatory notes and a lot of glossary on atmospheric science. It also has an appendix on commercial abbreviation, prefix, unit, wavelength and the number o vibrations of electromagnetic waves, ICAO classified catalogue on cloud, list of varietal cloud and list of local wind. It has explanation of the glossary in English, Korea, China and Japan.

[Influence of elevated atmospheric CO2 concentration on photosynthesis and leaf nitrogen partition in process of photosynthetic carbon cycle in Musa paradisiaca].

Science.gov (United States)

Sun, G; Zhao, P; Zeng, X; Peng, S

2001-06-01

The photosynthetic rate (Pn) in leaves of Musa paradisiaca grown under elevated CO2 concentration (700 +/- 56 microliters.L-1) for one week was 5.14 +/- 0.32 mumol.m-2.s-1, 22.1% higher than that under ambient CO2 concentration, while under elevated CO2 concentration for 8 week, the Pn decreased by 18.1%. It can be inferred that the photosynthetic acclimation to elevated CO2 concentration and the Pn inhibition occurred in leaves of M. paradisiaca. The respiration rate in light (Rd) was lower in leaves under higher CO2 concentration, compared with that under ambient CO2 concentration. If the respiration in light was not included, the difference in CO2 compensation point for the leaves of both plants was not significant. Under higher CO2 concentration for 8 weeks, the maximum carboxylation rate(Vcmax) and electron transportation rate (J) in leaves decreased respectively by 30.5% and 14.8%, compared with that under ambient CO2 concentration. The calculated apparent quantum yield (alpha) in leaves under elevated CO2 concentration according to the initial slope of Pn/PAR was reduced to 0.014 +/- 0.010 molCO2.mol-1 quanta, compared with the value of 0.025 +/- 0.005 molCO2.mol-1 quanta in the control. The efficiency of light energy conversion also decreased from 0.203 to 0.136 electrons.quanta-1 in plants under elevated CO2 concentration. A lower partitioning coefficient for leaf nitrogen in Rubisco, bioenergetics and thylakoid light-harvesting components was observed in plants under higher CO2 concentration. The results indicated that the multi-process of photosynthesis was suppressed significantly by a long-term (8 weeks) higher CO2 concentration incubation.

Atmospheric transport of persistent semi-volatile organic chemicals to the Arctic and cold condensation in the mid-troposphere – Part 1: 2-D modeling in mean atmosphere

Directory of Open Access Journals (Sweden)

J. Ma

2010-08-01

Full Text Available In the first part of this study for revisiting the cold condensation effect on global distribution of semi-volatile organic chemicals (SVOCs, the atmospheric transport of SVOCs to the Arctic in the mid-troposphere in a mean meridional atmospheric circulation over the Northern Hemisphere was simulated by a two-dimensional (2-D atmospheric transport model. Results show that under the mean meridional atmospheric circulation the long-range atmospheric transport of SVOCs from warm latitudes to the Arctic occurs primarily in the mid-troposphere. Although major sources are in low and mid-latitude soils, the modeled air concentration of SVOCs in the mid-troposphere is of the same order as or higher than that near the surface, demonstrating that the mid-troposphere is an important pathway and reservoir of SVOCs. The cold condensation of the chemicals is also likely to take place in the mid-troposphere over a source region of SVOCs in warm low latitudes through interacting with clouds. We demonstrate that the temperature dependent vapour pressure and atmospheric degradation rate of SVOCs exhibit similarities between lower atmosphere over the Arctic and the mid-troposphere over a tropical region. Frequent occurrence of atmospheric ascending motion and convection over warm latitudes carry the chemicals to a higher altitude where some of these chemicals may partition onto solid or aqueous phase through interaction with atmospheric aerosols, cloud water droplets and ice particles, and become more persistent at lower temperatures. Stronger winds in the mid-troposphere then convey solid and aqueous phase chemicals to the Arctic where they sink by large-scale descending motion and wet deposition. Using calculated water droplet-air partitioning coefficient of several persistent organic semi-volatile chemicals under a mean air temperature profile from the equator to the North Pole we propose that clouds are likely important sorbing media for SVOCs and pathway of

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.

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

Seasonal associations and atmospheric transport distances of fungi in the genus Fusarium collected with unmanned aerial vehicles and ground-based sampling devices

Science.gov (United States)

Lin, Binbin; Ross, Shane D.; Prussin, Aaron J.; Schmale, David G.

2014-09-01

Spores of fungi in the genus Fusarium may be transported through the atmosphere over long distances. New information is needed to characterize seasonal trends in atmospheric loads of Fusarium and to pinpoint the source(s) of inoculum at both local (farm) and regional (state or country) scales. We hypothesized that (1) atmospheric concentrations of Fusarium spores in an agricultural ecosystem vary with height and season and (2) transport distances from potential inoculum source(s) vary with season. To test these hypotheses, spores of Fusarium were collected from the atmosphere in an agricultural ecosystem in Blacksburg, VA, USA using a Burkard volumetric sampler (BVS) 1 m above ground level and autonomous unmanned aerial vehicles (UAVs) 100 m above ground level. More than 2200 colony forming units (CFUs) of Fusarium were collected during 104 BVS sampling periods and 180 UAV sampling periods over four calendar years (2009-2012). Spore concentrations ranged from 0 to 13 and 0 to 23 spores m-3 for the BVS and the UAVs, respectively. Spore concentrations were generally higher in the fall, spring, and summer, and lower in the winter. Spore concentrations from the BVS were generally higher than those from the UAVs for both seasonal and hourly collections. A Gaussian plume transport model was used to estimate distances to the potential inoculum source(s) by season, and produced mean transport distances of 1.4 km for the spring, 1.7 km for the summer, 1.2 km for the fall, and 4.1 km for the winter. Environmental signatures that predict atmospheric loads of Fusarium could inform disease spread, air pollution, and climate change.

Elevated atmospheric ozone increases concentration of insecticidal Bacillus thuringiensis (Bt) Cry1Ac protein in Bt Brassica napus and reduces feeding of a Bt target herbivore on the non-transgenic parent

International Nuclear Information System (INIS)

Himanen, Sari J.; Nerg, Anne-Marja; Nissinen, Anne; Stewart, C. Neal; Poppy, Guy M.; Holopainen, Jarmo K.

2009-01-01

Sustained cultivation of Bacillus thuringiensis (Bt) transgenic crops requires stable transgene expression under variable abiotic conditions. We studied the interactions of Bt toxin production and chronic ozone exposure in Bt cry1Ac-transgenic oilseed rape and found that the insect resistance trait is robust under ozone elevations. Bt Cry1Ac concentrations were higher in the leaves of Bt oilseed rape grown under elevated ozone compared to control treatment, measured either per leaf fresh weight or per total soluble protein of leaves. The mean relative growth rate of a Bt target herbivore, Plutella xylostella L. larvae was negative on Bt plants in all ozone treatments. On the non-transgenic plants, larval feeding damage was reduced under elevated ozone. Our results indicate the need for monitoring fluctuations in Bt toxin concentrations to reveal the potential of ozone exposure for altering dosing of Bt proteins to target and non-target herbivores in field environments experiencing increasing ozone pollution. - Elevated atmospheric ozone can induce fluctuations in insecticidal protein concentrations in transgenic plants

Elevated atmospheric ozone increases concentration of insecticidal Bacillus thuringiensis (Bt) Cry1Ac protein in Bt Brassica napus and reduces feeding of a Bt target herbivore on the non-transgenic parent

Energy Technology Data Exchange (ETDEWEB)

Himanen, Sari J. [University of Kuopio, Department of Environmental Science, P.O. Box 1627, FIN-70211 Kuopio (Finland)], E-mail: sari.himanen@uku.fi; Nerg, Anne-Marja [University of Kuopio, Department of Environmental Science, P.O. Box 1627, FIN-70211 Kuopio (Finland); Nissinen, Anne [University of Kuopio, Department of Environmental Science, P.O. Box 1627, FIN-70211 Kuopio (Finland); MTT Agrifood Research Finland, Plant Protection, FIN-31600 Jokioinen (Finland); Stewart, C. Neal [University of Tennessee, Department of Plant Sciences, Knoxville, TN 37996-4561 (United States); Poppy, Guy M. [University of Southampton, School of Biological Sciences, Southampton SO16 7PX (United Kingdom); Holopainen, Jarmo K. [University of Kuopio, Department of Environmental Science, P.O. Box 1627, FIN-70211 Kuopio (Finland)

2009-01-15

Sustained cultivation of Bacillus thuringiensis (Bt) transgenic crops requires stable transgene expression under variable abiotic conditions. We studied the interactions of Bt toxin production and chronic ozone exposure in Bt cry1Ac-transgenic oilseed rape and found that the insect resistance trait is robust under ozone elevations. Bt Cry1Ac concentrations were higher in the leaves of Bt oilseed rape grown under elevated ozone compared to control treatment, measured either per leaf fresh weight or per total soluble protein of leaves. The mean relative growth rate of a Bt target herbivore, Plutella xylostella L. larvae was negative on Bt plants in all ozone treatments. On the non-transgenic plants, larval feeding damage was reduced under elevated ozone. Our results indicate the need for monitoring fluctuations in Bt toxin concentrations to reveal the potential of ozone exposure for altering dosing of Bt proteins to target and non-target herbivores in field environments experiencing increasing ozone pollution. - Elevated atmospheric ozone can induce fluctuations in insecticidal protein concentrations in transgenic plants.

Impacts of heterogeneous reactions to atmospheric peroxides: Observations and budget analysis study

Science.gov (United States)

Qin, Mengru; Chen, Zhongming; Shen, Hengqing; Li, Huan; Wu, Huihui; Wang, Yin

2018-06-01

Atmospheric peroxides play important roles in atmospheric chemistry, acting as reactive oxidants and reservoirs of HOX and ROX radicals. Field measurements of atmospheric peroxides were conducted over urban Beijing from 2015 to 2016, including dust storm days, haze days and different seasons. We employed a box model based on RACM2 mechanism to conduct concentration simulation and budget analysis of hydrogen peroxide (H2O2) and peroxyacetic acid (PAA). In this study, heterogeneous reaction is found to be a significant sink for atmospheric H2O2 and PAA in urban Beijing. Here, we recommend a suitable uptake coefficient formula considering the water effect for model research of peroxides. It is found that H2O2 and PAA unexpectedly maintained considerable concentrations on haze days, even higher than that on non-haze days. This phenomenon is mainly ascribed to relatively high levels of volatile organic compounds and ozone on haze days. In addition, high levels of water vapor in pollution episode can promote not only the heterogeneous uptake to aerosol phase but also the production of H2O2. Atmospheric PAA formation is suggested to be sensitive to alkenes and NOX in urban Beijing. In particular, with the help of peroxides, sulfate formation rate from heterogeneous uptake could increase by ∼4 times on haze days, indicating the potential effect of peroxides on enhancement of aerosol oxidative property and secondary sulfate formation.

Ship-Based Measurements of Atmospheric Mercury Concentrations over the Baltic Sea

Directory of Open Access Journals (Sweden)

Hanna Hoglind

2018-02-01

Full Text Available Mercury is a toxic pollutant emitted from both natural sources and through human activities. A global interest in atmospheric mercury has risen ever since the discovery of the Minamata disease in 1956. Properties of gaseous elemental mercury enable long range transport, which can cause pollution even in pristine environments. Gaseous elemental mercury (GEM was measured from winter 2016 to spring 2017 over the Baltic Sea. A Tekran 2357A mercury analyser was installed aboard the research and icebreaking vessel Oden for the purpose of continuous measurements of gaseous mercury in ambient air. Measurements were performed during a campaign along the Swedish east coast and in the Bothnian Bay near Lulea during the icebreaking season. Data was evaluated from Gothenburg using plotting software, and back trajectories for air masses were calculated. The GEM average of 1.36 ± 0.054 ng/m3 during winter and 1.29 ± 0.140 ng/m3 during spring was calculated as well as a total average of 1.36 ± 0.16 ng/m3. Back trajectories showed a possible correlation of anthropogenic sources elevating the mercury background level in some areas. There were also indications of depleted air, i.e., air with lower concentrations than average, being transported from the Arctic to northern Sweden, resulting in a drop in GEM levels.

Variations of Rn-222 concentration in the Bratislava air

International Nuclear Information System (INIS)

Holy, K.; Bohm, R.; Polaskova, A.

1996-01-01

222 Rn is produced by alpha decay of 222 Ra in roil. A small fraction of totally produced 222 Rn escapes from coil particles into soil air. Then 222 Rn is transported predominantly by molecular diffusion into outdoor atmosphere. The radon concentration in the outdoor atmosphere is not stable. It varies irregularly depending on meteorological conditions. However there were found out regular daily and remand variations of 222 Rn concentration in outdoor atmosphere. These variations were measured in numerous works and results are summarized f.e. in work of Gesell. A simple model described the annual variations of 222 Rn concentration war published by Minato. A mathematical analysis of daily course of 222 Rn concentration in outdoor atmosphere was realized by Garzon et al. Some results of our study of 222 Rn variations in outdoor atmosphere of Bratislava are shown in this report. (author)

Influence of the Southeast Asian biomass burnings on the atmospheric persistent organic pollutants observed at near sources and receptor site

Science.gov (United States)

Chang, Shun-Shiang; Lee, Wen-Jhy; Wang, Lin-Chi; Lin, Neng-Huei; Chang-Chien, Guo-Ping

2013-10-01

Persistent organic pollutants (POPs) such as PCDD/Fs, PCBs, PBDD/Fs, PBBs and PBDEs are bio-accumulative, toxic, and susceptible to long-range transport (LRT). This study is the first that comprehensively discusses the long-range atmospheric transport behavior of these five groups of POPs. The main goal is to investigate the atmospheric characteristics of these POPs at the biomass burning sites of Chiang Mai in Thailand, and Da Nang in Vietnam, as well as the influence of the Southeast Asian biomass burnings on the Lulin Atmospheric Background Station (LABS) in Taiwan. Biomass burning in Southeast Asia is usually carried to remove the residues of agricultural activities. The ambient air in Da Nang seems to be more seriously affected by the local biomass burnings than that in Chiang Mai. The elevated atmospheric brominated POP (PBDD/Fs, PBBs and PBDEs) concentrations in Da Nang were attributed to the biomass burning and viewed as mostly unrelated to the local use of brominated flame retardants. In the spring of 2010, the mean atmospheric concentrations in LABS during the first and second Intensive Observation Periods (IOPs) were 0.00428 and 0.00232 pg I-TEQ Nm-3 for PCDD/Fs, 0.000311 and 0.000282 pg WHO-TEQ m-3 for PCBs, 0.000379 and 0.000449 pg TEQ Nm-3 for total PBDD/Fs, 0.0208 and 0.0163 pg Nm-3 for total PBBs, and 109 and 18.2 pg Nm-3 for total PBDEs, respectively. These values represent the above concentrations due to the Southeast Asian biomass burnings. The affected atmospheric POP concentrations at the LABS were still at least one order lower than those in other atmospheric environments, except for the PBDE concentrations during the first IOP (109 pg Nm-3), which was surprisingly higher than those in Taiwanese metal complex areas (93.9 pg Nm-3) and urban areas (34.7 pg Nm-3). Atmospheric POP concentrations do not seem to dramatically decrease during long-range transport, and the reasons for this need to be further investigated.

Seasonal variation in radon concentration in the atmosphere simultaneously measured in Donghae on Korean peninsula, Matsue on Shimane peninsula, and Oki island in the sea of Japan

International Nuclear Information System (INIS)

Yoshioka, Katsuhiro; Iida, Takao; Kim, Yoon Shin

2008-01-01

We measured simultaneously radon concentration in the atmosphere at Donghae, Oki Island and Matsue. In Donghae, radon concentration had peaks in the winter and summer and lower values in the spring. It was the highest in the winter and lowest in the summer in Oki Island, in Matsue, the highest in the fall and lowest in the summer. The timing and frequency of arrival air mass from the ocean and the land were different among the three measuring points. The highest values in Donghae and Oki Island were because of effects of radon flow from Eurasian continent in the winter. The inversion layer often formed in the atmospheric boundary layer over the land area around the Sea of Japan caused the peak values in the summer in Donghae. The atmosphere over Oki Island is always mixed with that over the ocean because the island is small. Radon escaping from the ground of the island does not stay with the surface layer even at night, therefore, diurnal variation was almost none throughout the year. Air mass with low radon concentration coming from the Pacific Ocean caused the lowest values in the summer. In Matsue, the peak was found in the fall in which occurrences of surface inversion layer is most common in the year. (author)

Proterozoic atmospheric oxygen

DEFF Research Database (Denmark)

Canfield, Donald Eugene

2014-01-01

This article is concerned with the evolution of atmospheric oxygen concentrations through the Proterozoic Eon. In particular, this article will seek to place the history of atmospheric oxygenation through the Proterozoic Eon in the context of the evolving physical environment including the history...... of continental growth and volcanic outgassing, as well as biogeochemical processing of elements within the oceans. The author will seek to explore constraints on the history of oxygenation and understand which processes have regulated oxygen through this eon....

Higher blood harmane (1-methyl-9H-pyrido[3,4-b]indole) concentrations correlate with lower olfactory scores in essential tremor.

Science.gov (United States)

Louis, Elan D; Rios, Eileen; Pellegrino, Kathryn M; Jiang, Wendy; Factor-Litvak, Pam; Zheng, Wei

2008-05-01

Harmane (1-methyl-9H-pyrido[3,4-b]indole), a neurotoxin, may be an environmental risk factor for essential tremor (ET). Harmane and related chemicals are toxic to the cerebellum. Whether it is through this mechanism (cerebellar toxicity) that harmane leads to ET is unknown. Impaired olfaction may be a feature of cerebellar disease. To determine whether blood harmane concentrations correlate with olfactory test scores in patients with ET. Blood harmane concentrations were quantified using high performance liquid chromatography. Odor identification testing was performed with the University of Pennsylvania Smell Identification Test (UPSIT). In 83 ET cases, higher log blood harmane concentration was correlated with lower UPSIT score (rho=-0.46, p<0.001). 25/40 (62.5%) cases with high log blood harmane concentration (based on a median split) had low UPSIT scores (based on a median split) vs. 12/43 (27.9%) ET cases with low log blood harmane concentration (adjusted odd ratios (OR) 4.04, 95% confidence intervals (CI) 1.42-11.50, p=0.009). When compared with the low log blood harmane tertile, the odds of olfactory dysfunction were 2.64 times higher in cases in the middle tertile and 10.95 times higher in cases in the high tertile. In 69 control subjects, higher log blood harmane concentration was not correlated with lower UPSIT score (rho=0.12, p=0.32). Blood harmane concentrations were correlated with UPSIT scores in ET cases but not controls. These analyses set the stage for postmortem studies to further explore the role of harmane as a cerebellar toxin in ET.

Options for cost-effectively reducing atmospheric methane concentrations from anthropogenic biomass sources

International Nuclear Information System (INIS)

Roos, K.F.; Jacobs, C.; Orlic, M.

1993-01-01

Methane is a major greenhouse gas, second only to carbon dioxide in its contribution to future global warming. Methane concentrations have more than doubled over the last two centuries and continue to rise annually. These increases are largely correlated with increasing human populations. Methane emissions from human related activities currently account for about 70 percent of annual emissions. Of these human related emissions, biomass sources account for about 75 percent and non-biomass sources about 25 percent. Because methane has a shorter lifetime than other major greenhouse gases, efforts to reduce methane emissions may fairly quickly be translated into lower atmospheric concentrations of methane and lower levels of radiative forcing. This fairly quick response would have the benefit of slowing the rate of climate change and hence allow natural ecosystems more time to adapt. Importantly, methane may be cost-effectively reduced from a number of biomass and non-biomass sources in the United States and worldwide. Methane is a valuable fuel, not just a waste by-product, and often systems may be reconfigured to reap the fuel value of the methane and more than justify the necessary expenditures. Such options for reducing methane emission from biomass sources exist for landfills, livestock manures, and ruminant livestock, and have been implemented to varying degrees in countries around the world. However, there are a number of barriers that hinder the more widespread use of technologies, including institutional, financial, regulatory, informational, and other barriers. This paper describes an array of available options that may be cost-effectively implemented to reduce methane emissions from biomass sources. This paper also discusses a number of programs that have been developed in the United States and internationally to promote the implementation of these methane reduction options and overcome existing barriers

Monoterpene and herbivore-induced emissions from cabbage plants grown at elevated atmospheric CO 2 concentration

Science.gov (United States)

Vuorinen, Terhi; Reddy, G. V. P.; Nerg, Anne-Marja; Holopainen, Jarmo K.

The warming of the lower atmosphere due to elevating CO 2 concentration may increase volatile organic compound (VOC) emissions from plants. Also, direct effects of elevated CO 2 on plant secondary metabolism are expected to lead to increased VOC emissions due to allocation of excess carbon on secondary metabolites, of which many are volatile. We investigated how growing at doubled ambient CO 2 concentration affects emissions from cabbage plants ( Brassica oleracea subsp. capitata) damaged by either the leaf-chewing larvae of crucifer specialist diamondback moth ( Plutella xylostella L.) or generalist Egyptian cotton leafworm ( Spodoptera littoralis (Boisduval)). The emission from cabbage cv. Lennox grown in both CO 2 concentrations, consisted mainly of monoterpenes (sabinene, limonene, α-thujene, 1,8-cineole, β-pinene, myrcene, α-pinene and γ-terpinene). ( Z)-3-Hexenyl acetate, sesquiterpene ( E, E)- α-farnesene and homoterpene ( E)-4,8-dimethyl-1,3,7-nonatriene (DMNT) were emitted mainly from herbivore-damaged plants. Plants grown at 720 μmol mol -1 of CO 2 had significantly lower total monoterpene emissions per shoot dry weight than plants grown at 360 μmol mol -1 of CO 2, while damage by both herbivores significantly increased the total monoterpene emissions compared to intact plants. ( Z)-3-Hexenyl acetate, ( E, E)- α-farnesene and DMNT emissions per shoot dry weight were not affected by the growth at elevated CO 2. The emission of DMNT was significantly enhanced from plants damaged by the specialist P. xylostella compared to the plants damaged by the generalist S. littoralis. The relative proportions of total monoterpenes and total herbivore-induced compounds of total VOCs did not change due to the growth at elevated CO 2, while insect damage increased significantly the proportion of induced compounds. The results suggest that VOC emissions that are induced by the leaf-chewing herbivores will not be influenced by elevated CO 2 concentration.

Enrichment of radon and carbon dioxide in the open atmosphere of an Australian coal seam gas field.

Science.gov (United States)

Tait, Douglas R; Santos, Isaac R; Maher, Damien T; Cyronak, Tyler J; Davis, Rachael J

2013-04-02

Atmospheric radon ((222)Rn) and carbon dioxide (CO2) concentrations were used to gain insight into fugitive emissions in an Australian coal seam gas (CSG) field (Surat Basin, Tara region, Queensland). (222)Rn and CO2 concentrations were observed for 24 h within and outside the gas field. Both (222)Rn and CO2 concentrations followed a diurnal cycle with night time concentrations higher than day time concentrations. Average CO2 concentrations over the 24-h period ranged from ~390 ppm at the control site to ~467 ppm near the center of the gas field. A ~3 fold increase in maximum (222)Rn concentration was observed inside the gas field compared to outside of it. There was a significant relationship between maximum and average (222)Rn concentrations and the number of gas wells within a 3 km radius of the sampling sites (n = 5 stations; p gas field related to both point (well heads, pipelines, etc.) and diffuse soil sources. Radon may be useful in monitoring enhanced soil gas fluxes to the atmosphere due to changes in the geological structure associated with wells and hydraulic fracturing in CSG fields.

Natural and Anthropogenic Influences on Atmospheric Aerosol Variability

Energy Technology Data Exchange (ETDEWEB)

Asmi, A.

2012-07-01

Aerosol particles are everywhere in the atmosphere. They are a key factor in many important processes in the atmosphere, including cloud formation, scattering of incoming solar radiation and air chemistry. The aerosol particles have relatively short lifetimes in lower atmosphere, typically from days to weeks, and thus they have a high spatial and temporal variability. This thesis concentrates on the extent and reasons of sub-micron aerosol particle variability in the lower atmosphere, using both global atmospheric models and analysis of observational data. Aerosol number size distributions in the lower atmosphere are affected strongly by the new particle formation. Perhaps more importantly, a strong influence new particle formation is also evident in the cloud condensation nuclei (CCN) concentrations, suggesting a major role of the sulphuric acid driven new particle formation in the climate system. In this thesis, the sub-micron aerosol number size distributions in the European regional background air were characterized for the first time from consistent, homogenized and comparable datasets. Some recent studies have suggested that differences in aerosol emissions between weekdays could also affect the weather via aerosol-cloud interactions. In this thesis, the weekday-to-weekday variation of CCN sized aerosol number concentrations in Europe were found to be much smaller than expected from earlier studies, based on particle mass measurements. This result suggests that a lack of week-day variability in meteorology is not necessarily a sign of weak aerosol-cloud interactions. An analysis of statistically significant trends in past decades of measured aerosol number concentrations from Europe, North America, Pacific islands and Antarctica generally show decreases in concentrations. The analysis of these changes show that a potential explanation for the decreasing trends is the general reduction of anthropogenic emissions, especially SO{sub 2}, although a combination of

Higher stability in forest-atmosphere exchange observed in a structurally diverse forest.

Science.gov (United States)

Tamrakar, R.; Rayment, M.; Moyano, F.; Herbst, M.; Mund, M.; Knohl, A.

2016-12-01

We tested the hypothesis that structurally diverse forests have greater stability on exchange processes with the atmosphere compared to forests with less diverse structure. In a case study, we assessed how net ecosystem exchange (NEE) and normalized maximum assimilation (Amax) varied over time in two forests in Germany based on 11 years of continuous eddy flux measurements. The two sites differ in structure as well as in species composition: one (Hainich) is an unmanaged, uneven-aged and heterogeneous mixed beech forest (65% beech), the other (Leinefelde) is a managed, even-aged and homogeneous pure beech stand. The two selected forests are of similar mean ages (about 130 years old) and exposed to similar air temperatures and vapour pressure deficits. Even though Hainich (the unmanaged forest) received higher rainfall (720 ± 134 mm vs 599±166 mm), the soil water availability showed no significant difference between both sites. Based on detailed biomass inventory, trees in Hainich are well distributed in all diameter at breast height (dbh) classes (10 to 90cm dbh) whereas in Leinefelde (the managed forest) trees are mostly confined to dbh classes of 40 to 55 cm. Our results showed a strong difference in inter-annual variability of NEE, which was lower in the unmanaged than in the managed site (coefficient of variation (CV) of 0.13 and 0.27, respectively). The lowest NEE was observed in both sites in 2004, a mast year and a year after the strong summer drought of 2003. The variation in the inter-annual normalized maximum assimilation (Amax) was lower in Hainich (standard deviation of 2.5 compared to 3.9 µmol m-2 s-1). Also, the seasonal course of Amax differed between the two forests which could explain why the mixed forest was more affected by the late summer drought of 2003, despite showing a more conservative carbon budget than the pure stand in the long term. The interannual anomaly in Amax was correlated with fruit production, the latter being larger in

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

Increasing surface ozone concentrations in the background atmosphere of Southern China, 1994–2007

Directory of Open Access Journals (Sweden)

T. Wang

2009-08-01

Full Text Available Tropospheric ozone is of great importance with regard to air quality, atmospheric chemistry, and climate change. In this paper we report the first continuous record of surface ozone in the background atmosphere of South China. The data were obtained from 1994 to 2007 at a coastal site in Hong Kong, which is strongly influenced by the outflow of Asian continental air during the winter and the inflow of maritime air from the subtropics in the summer. Three methods are used to derive the rate of change in ozone. A linear fit to the 14-year record shows that the ozone concentration increased by 0.58 ppbv/yr, whereas comparing means in years 1994–2000 and 2001–2007 gives an increase of 0.87 ppbv/yr for a 7-year period. The ozone changes in air masses from various source regions are also examined. Using local wind and carbon monoxide (CO data to filter out local influence, we find that ozone increased by 0.94 ppbv/yr from 1994–2000 to 2001–2007 in air masses from Eastern China, with similar changes in the other two continent-influenced air-mass groups, but no statistically significant change in the marine air. An examination of the nitrogen dioxide (NO₂ column obtained from GOME and SCIAMACHY reveals an increase in atmospheric NO₂ in China's three fastest developing coastal regions, whereas NO₂ in other parts of Asia decreased during the same period, and no obvious trend over the main shipping routes in the South China Sea was indicated. Thus the observed increase in background ozone in Hong Kong is most likely due to the increased emissions of NO₂ (and possibly volatile organic compounds (VOCs as well in the upwind coastal regions of mainland China. The CO data at Hok Tsui showed less definitive changes compared to the satellite NO₂ column. The increase in background ozone likely made a strong contribution (81% to the rate of increase in "total ozone" at an urban site in Hong Kong

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.

A Coupled Soil-Atmosphere Model of H2O2 on Mars

Science.gov (United States)

Bullock, Mark A.; Stoker, Carol R.; Mckay, Christopher P.; Zent, Aaron P.

1994-01-01

The Viking Gas Chromatograph Mass Spectrometer failed to detect organic compounds on Mars, and both the Viking Labeled Release and the Viking Gas Exchange experiments indicated a reactive soil surface. These results have led to the widespread belief that there are oxidants in the martian soil. Since H2O2 is produced by photochemical processes in the atmosphere of Mars, and has been shown in the laboratory to reproduce closely the Viking LR results, it is a likely candidate for a martian soil oxidant. Here, we report on the results of a coupled soil/atmosphere transport model for H202 on Mars. Upon diffusing into the soil, its concentration is determined by the extent to which it is adsorbed and by the rate at which it is catalytically destroyed. An analytical model for calculating the distribution of H202 in the martian atmosphere and soil is developed. The concentration of H202 in the soil is shown to go to zero at a finite depth, a consequence of the nonlinear soil diffusion equation. The model is parameterized in terms of an unknown quantity, the lifetime of H202 against heterogeneous catalytic destruction in the soil. Calculated concentrations are compared with a H202 concentration of 30 nmoles/cu cm, inferred from the Viking Labeled Release experiment. A significant result of this model is that for a wide range of H202 lifetimes (up to 105 years), the extinction depth was found to be less than 3 m. The maximum possible concentration in the top 4 cm is calculated to be approx. 240 nmoles/cu cm, achieved with lifetimes of greater than 1000 years. Concentrations higher than 30 nmoles/cu cm require lifetimes of greater than 4.3 terrestrial years. For a wide range of H202 lifetimes, it was found that the atmospheric concentration is only weakly coupled with soil loss processes. Losses to the soil become significant only when lifetimes are less than a few hours. If there are depths below which H202 is not transported, it is plausible that organic compounds

Modeling the response of forest isoprene emissions to future increases in atmospheric CO2 concentration and changes in climate (Invited)

Science.gov (United States)

Monson, R. K.; Heald, C. L.; Guenther, A. B.; Wilkinson, M.

2009-12-01

Isoprene emissions from plants to the atmosphere are sensitive to changes in temperature, light and atmospheric CO2 concentration in both the short- (seconds-to-minutes) and long-term (hours-to-months). We now understand that the different time constants for these responses are due to controls by different sets of biochemical and physiological processes n leaves. Progress has been made in the past few years toward converting this process-level understanding into quantitative models. In this talk, we consider this progress with special emphasis on the short- and long-term responses to atmospheric CO2 concentration and temperature. A new biochemically-based model is presented for describing the CO2 responses, and the model is deployed in a global context to predict interactions between the influences of temperature and CO2 on the global isoprene emission rate. The model is based on the theory of enzyme-substrate kinetics, particularly with regard to those reactions that produce puruvate or glyceraldehyde 3-phosphate, the two chloroplastic substrates for isoprene biosynthesis. In the global model, when we accounted for CO2 inhibition of isoprene emission in the long-term response, we observed little impact on present-day global isoprene emission (increase from 508 to 523 Tg C yr-1). However, the large increases in future isoprene emissions predicted from past models which are due to a projected warmer climate, were entirely offset by including the CO2 effects. The isoprene emission response to CO2 was dominated by the long-term growth environment effect, with modulations of 10% or less from the short-term effect. We use this analysis as a framework for grounding future global models of isoprene emission in biochemical and physiological observations.

Observations of the uptake of carbonyl sulfide (COS by trees under elevated atmospheric carbon dioxide concentrations

Directory of Open Access Journals (Sweden)

L. Sandoval-Soto

2012-08-01

Full Text Available Global change forces ecosystems to adapt to elevated atmospheric concentrations of carbon dioxide (CO₂. We understand that carbonyl sulfide (COS, a trace gas which is involved in building up the stratospheric sulfate aerosol layer, is taken up by vegetation with the same triad of the enzymes which are metabolizing CO₂, i.e. ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco, phosphoenolpyruvate carboxylase (PEP-Co and carbonic anhydrase (CA. Therefore, we discuss a physiological/biochemical acclimation of these enzymes affecting the sink strength of vegetation for COS. We investigated the acclimation of two European tree species, Fagus sylvatica and Quercus ilex, grown inside chambers under elevated CO₂, and determined the exchange characteristics and the content of CA after a 1–2 yr period of acclimation from 350 ppm to 800 ppm CO₂. We demonstrate that a compensation point, by definition, does not exist. Instead, we propose to discuss a point of uptake affinity (PUA. The results indicate that such a PUA, the CA activity and the deposition velocities may change and may cause a decrease of the COS uptake by plant ecosystems, at least as long as the enzyme acclimation to CO₂ is not surpassed by an increase of atmospheric COS. As a consequence, the atmospheric COS level may rise causing an increase of the radiative forcing in the troposphere. However, this increase is counterbalanced by the stronger input of this trace gas into the stratosphere causing a stronger energy reflection by the stratospheric sulfur aerosol into space (Brühl et al., 2012. These data are very preliminary but may trigger a discussion on COS uptake acclimation to foster measurements with modern analytical instruments.

Atmospheric BTEX concentrations in the vicinity of the crude oil refinery of the Baltic region.

Science.gov (United States)

Baltrėnas, Pranas; Baltrėnaitė, Edita; Serevičienė, Vaida; Pereira, Paulo

2011-11-01

Among chemical industries, petroleum refineries have been identified as large emitters of a wide variety of pollutants. Benzene, toluene, ethylbenzene, and xylene (BTEX) form an important group of aromatic volatile organic compounds (VOCs) because of their role in the troposphere chemistry and the risk posed to human health. A very large crude oil refinery of the Baltic States (200,000 bbl/day) is situated in the northern, rural part of Lithuania, 10 km from the town of Mažeikiai (Lithuania). The objectives of this study were: (1) to determine of atmospheric levels of BTEX in the region rural and urban parts at the vicinity of the crude oil refinery; and (2) to investigate the effect of meteorological parameters (wind speed, wind direction, temperature, pressure, humidity) on the concentrations measured. The averaged concentration of benzene varied from 2.12 ppbv in the rural areas to 2.75 ppbv in the urban areas where the traffic was determined to be a dominant source of BTEX emissions. Our study showed that concentration of benzene, as strictly regulated air pollutant by EU Directive 2008/50/EC, did not exceed the limit of 5 ppbv in the region in the vicinity of the crude oil refinery during the investigated period. No significant change in air quality in the vicinity of the oil refinery was discovered, however, an impact of the industry on the background air quality was detected. The T/B ratio (0.50-0.81) that was much lower than 2.0, identified other sources of pollution than traffic.

Regularities in the behavior of radioactive aerosols in the near-earth atmosphere

Energy Technology Data Exchange (ETDEWEB)

Makhonko, K.P.; Avramenko, A.S.; Martynenko, V.P.; Volokitin, A.A.; Rabotnova, F.A.

1979-10-01

The relationship is considered between the power of nuclear explosions and mean annual magnitudes of surface concentrations and atmospheric fallout of long-lived isotopes which are products of these explosions. The role of Chinese nuclear explosions in pollution of the atmosphere over the territory of the USSR is demonstrated. Regularities are discussed about the annual course of concentrations of products of atmospheric nuclear explosions, features in concentration distribution over the territory of the USSR as well as the impact of the amount and type of atmospheric precipitation upon the formation of radioactive fallout.

Effects of long-term elevated atmospheric CO2 concentrations on Pinus ponderosa

International Nuclear Information System (INIS)

Surano, K.A.; Kercher, J.R.

1993-01-01

This report details the results from an experiment of the effects of long-term elevated atmospheric CO 2 concentrations on ponderosa pine (Pinus ponderosa Laws.) saplings and seedlings. The study began in 1983 as a pilot study designed to explore the feasibility of using open-top chambers for continuous multi-year exposures on sapling-sized trees and to examine possible CO 2 responses so that future research could be adequately designed. however, following the first year of exposure, preliminary results from the study indicated that measurements of CO 2 responses should be intensified. Open-top chambers proved suitable for use in multiyear exposures of mature trees. With respect to the preliminary examination of CO 2 responses, many interesting observations were made. The nature of the preliminary results suggests that future long-term field CO 2 exposures on perennial species may be critical to the understanding and preparation for future environments. Other research reported here attempted to adapt an existing western coniferous forest growth and succession model for use in elevated CO 2 scenarios using differential species responses, and assessed the usefulness of the model in that regard. Seven papers have been processed separately for inclusion in the appropriate data bases

Tracer chemistry in the laboratory and the atmosphere

International Nuclear Information System (INIS)

Rowland, F.S.

1994-01-01

The steady bombardment of the Earth's atmosphere by cosmic radiation induces numerous radioactive species in the atmosphere of which the best known are 14 C and T. Others of interest include 7 Be, 10 Be, and several isotopes of chlorine. The eventual formation of 14 CO 2 and its subsequent significance for archaeological dating were brilliantly established by Willard Libby in the 1940s. However, the initial reactions of nascent 14 C in a mixture of N 2 and O 2 produce 14 CO, as shown first in the lab. and then in the atmosphere. Because cosmic ray production rates are essentially constant in a given location, the observed concentration of 14 CO provides an excellent tool for studying the removal process, oxidation by HO to form 14 CO 2 . Because 14 CO 2 becomes incorporated into all living biological species, other molecules become labeled with 14 C as well, including 14 CH 4 . Measurement of the 14 C radioactivity of such molecules in the atmosphere allows apportionment of sources between biological and fossil fuel origins. Tritium atoms are also formed by cosmic radiation, and can subsequently be incorporated into the chemical forms HT and HTO. Although most T atoms from cosmic radiation are found as HTO, the much higher specific radioactivity of HT provides interesting insights into atmospheric processes. Lab. studies furnish important clues for understanding the atmospheric routes. The differences in radioactive half-lives cause the terrestrial locations of cosmic ray induced 7 Be and 10 Be to be primarily the atmosphere and the oceans, respectively. In a comparable manner, the chemistry of atmospheric radiochlorine divides between the very long-lived 36 Cl and three isotopes with half-lives less than an hour, 34m Cl, 38 Cl and 39 Cl

Barrier effects of remote high mountain on atmospheric metal transport in the eastern Tibetan Plateau.

Science.gov (United States)

Bing, Haijian; Zhou, Jun; Wu, Yanhong; Luo, Xiaosan; Xiang, Zhongxiang; Sun, Hongyang; Wang, Jipeng; Zhu, He

2018-07-01

Anthropogenic metals adsorbed on suspended fine particles can be deposited on remote and inaccessible high mountains by long-range atmospheric transport. In this study, we investigated the cadmium (Cd) and lead (Pb) in the soils, mosses and rainfall of three transects on the Gongga Mountain, eastern Tibetan Plateau, to understand the mountain interception effects on their atmospheric transport. The concentrations of Cd and Pb in the soils and mosses displayed a pattern of eastern transect>northern transect>western transect. The distribution of Cd and Pb on the eastern transect increased from 2000 to 2900m a.s.l. (above sea level), decreased toward the timberline, and increased again with altitude; on the northern transect, it generally decreased with altitude whereas a distribution trend was not clearly observed on the western transect. The Cd and Pb concentrations in the rainfall of the eastern transect generally decreased with altitude, and they were higher inside forests than outside forests and temporally higher in the winter than the summer. The Pb isotopic ratios coupled with moss bio-monitoring distinguished anthropogenic sources of Cd and Pb on the eastern and northern transects, whereas bedrock weathering was the main source of Cd and Pb on the western transect. We proposed a conceptual model to delineate the effects of terrain, local climate and vegetation on the transport of atmospheric metals. Our results highlighted the high mountains in the eastern Tibetan Plateau as an effective natural barrier limiting atmospheric metal transport. Copyright © 2018 Elsevier B.V. All rights reserved.

Assessment of the performance of a compact concentric spectrometer system for Atmospheric Differential Optical Absorption Spectroscopy

Science.gov (United States)

Whyte, C.; Leigh, R. J.; Lobb, D.; Williams, T.; Remedios, J. J.; Cutter, M.; Monks, P. S.

2009-12-01

A breadboard demonstrator of a novel UV/VIS grating spectrometer has been developed based upon a concentric arrangement of a spherical meniscus lens, concave spherical mirror and curved diffraction grating suitable for a range of atmospheric remote sensing applications from the ground or space. The spectrometer is compact and provides high optical efficiency and performance benefits over traditional instruments. The concentric design is capable of handling high relative apertures, owing to spherical aberration and comma being near zero at all surfaces. The design also provides correction for transverse chromatic aberration and distortion, in addition to correcting for the distortion called "smile", the curvature of the slit image formed at each wavelength. These properties render this design capable of superior spectral and spatial performance with size and weight budgets significantly lower than standard configurations. This form of spectrometer design offers the potential for exceptionally compact instrument for differential optical absorption spectroscopy (DOAS) applications from LEO, GEO, HAP or ground-based platforms. The breadboard demonstrator has been shown to offer high throughput and a stable Gaussian line shape with a spectral range from 300 to 450 nm at 0.5 nm resolution, suitable for a number of typical DOAS applications.

Influence of long-range transboundary transport on atmospheric water vapor mercury collected at the largest city of Tibet

Energy Technology Data Exchange (ETDEWEB)

Huang, Jie [Key Laboratory of Tibetan Environment Changes and Land Surface Processes, Institute of Tibetan Plateau Research, Chinese Academy of Sciences, Beijing 100101 (China); CAS Center for Excellence in Tibetan Plateau Earth Sciences, Chinese Academy of Sciences, Beijing 100101 (China); Laboratory of Green Chemistry, Lappeenranta University of Technology, Sammonkatu 12, Mikkeli FI 50130 (Finland); Kang, Shichang, E-mail: shichang.kang@lzb.ac.cn [State Key Laboratory of Cryospheric Sciences, Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou 730000 (China); CAS Center for Excellence in Tibetan Plateau Earth Sciences, Chinese Academy of Sciences, Beijing 100101 (China); Tian, Lide [Key Laboratory of Tibetan Environment Changes and Land Surface Processes, Institute of Tibetan Plateau Research, Chinese Academy of Sciences, Beijing 100101 (China); CAS Center for Excellence in Tibetan Plateau Earth Sciences, Chinese Academy of Sciences, Beijing 100101 (China); Guo, Junming [Key Laboratory of Tibetan Environment Changes and Land Surface Processes, Institute of Tibetan Plateau Research, Chinese Academy of Sciences, Beijing 100101 (China); Graduate University of the Chinese Academy of Sciences, Beijing 100049 (China); Zhang, Qianggong; Cong, Zhiyuan [Key Laboratory of Tibetan Environment Changes and Land Surface Processes, Institute of Tibetan Plateau Research, Chinese Academy of Sciences, Beijing 100101 (China); CAS Center for Excellence in Tibetan Plateau Earth Sciences, Chinese Academy of Sciences, Beijing 100101 (China); Sillanpää, Mika [Laboratory of Green Chemistry, Lappeenranta University of Technology, Sammonkatu 12, Mikkeli FI 50130 (Finland); and others

2016-10-01

Monsoon circulation is an important process that affects long-range transboundary transport of anthropogenic contaminants such as mercury (Hg). During the Indian monsoon season of 2013, a total of 92 and 26 atmospheric water vapor samples were collected at Lhasa, the largest city of the Tibet, for Hg and major ions analysis, respectively. The relatively low pH/high electronic conductivity values, together with the fact that NH{sub 4}{sup +} in atmospheric water vapor was even higher than that determined in precipitation of Lhasa, indicated the effects of anthropogenic perturbations through long-range transboundary atmospheric transport. Concentrations of Hg in atmospheric water vapor ranged from 2.5 to 73.7 ng L{sup −1}, with an average of 12.5 ng L{sup −1}. The elevated Hg and major ions concentrations, and electronic conductivity values were generally associated with weak acidic samples, and Hg mainly loaded with anthropogenic ions such as NH{sub 4}{sup +}. The results of principal component analysis and trajectory analysis suggested that anthropogenic emissions from the Indian subcontinent may have largely contributed to the determined Hg in atmospheric water vapor. Furthermore, our study reconfirmed that below-cloud scavenging contribution was significant for precipitation Hg in Lhasa, and evaluated that on average 74.1% of the Hg in precipitation could be accounted for by below-cloud scavenging. - Highlights: • The low pH/high electronic conductivity was found in atmospheric water vapor. • Anthropogenic NH{sub 4}{sup +} was higher than that determined in precipitation of Lhasa. • Elevated Hg and major ions levels were usually associated with weak acidic samples. • Hg in atmospheric water vapor was largely influenced by transboundary transport. • Below-cloud scavenging accounted for most Hg in precipitation.

Influence of long-range transboundary transport on atmospheric water vapor mercury collected at the largest city of Tibet

International Nuclear Information System (INIS)

Huang, Jie; Kang, Shichang; Tian, Lide; Guo, Junming; Zhang, Qianggong; Cong, Zhiyuan; Sillanpää, Mika

2016-01-01

Monsoon circulation is an important process that affects long-range transboundary transport of anthropogenic contaminants such as mercury (Hg). During the Indian monsoon season of 2013, a total of 92 and 26 atmospheric water vapor samples were collected at Lhasa, the largest city of the Tibet, for Hg and major ions analysis, respectively. The relatively low pH/high electronic conductivity values, together with the fact that NH_4"+ in atmospheric water vapor was even higher than that determined in precipitation of Lhasa, indicated the effects of anthropogenic perturbations through long-range transboundary atmospheric transport. Concentrations of Hg in atmospheric water vapor ranged from 2.5 to 73.7 ng L"−"1, with an average of 12.5 ng L"−"1. The elevated Hg and major ions concentrations, and electronic conductivity values were generally associated with weak acidic samples, and Hg mainly loaded with anthropogenic ions such as NH_4"+. The results of principal component analysis and trajectory analysis suggested that anthropogenic emissions from the Indian subcontinent may have largely contributed to the determined Hg in atmospheric water vapor. Furthermore, our study reconfirmed that below-cloud scavenging contribution was significant for precipitation Hg in Lhasa, and evaluated that on average 74.1% of the Hg in precipitation could be accounted for by below-cloud scavenging. - Highlights: • The low pH/high electronic conductivity was found in atmospheric water vapor. • Anthropogenic NH_4"+ was higher than that determined in precipitation of Lhasa. • Elevated Hg and major ions levels were usually associated with weak acidic samples. • Hg in atmospheric water vapor was largely influenced by transboundary transport. • Below-cloud scavenging accounted for most Hg in precipitation.

Particulate matter and polycyclic aromatic hydrocarbons in a selected athletic hall: ambient concentrations, origin and effects on human health

Science.gov (United States)

Kuskowska, Karolina; Rogula-Kozłowska, Wioletta; Rogula-Kopiec, Patrycja

2018-01-01

The paper presents the results of research on the concentration of 16 polycyclic aromatic hydrocarbons (PAHs) associated with total suspended particles (TSP) and their respirable fraction (PM4) in one of the Warsaw sports halls. Samples of dust were collected for 15 days simultaneously inside and outside (atmospheric air) of the sports hall. The obtained data allowed calculating diagnostic ratios indicating the origin of the PAHs and selected indicators of cumulative exposure to the PAH mixture. Both PM and PAH in the surveyed area were derived from the combustion of solid fuels; this involved pollution both in the atmospheric air and in the air inside the sports hall. It has been shown that the exposure of sports hall users to PAHs is significantly higher than the exposure resulting from concentrations recorded in the atmospheric air.

Intercomparison study of atmospheric methane and carbon dioxide concentrations measured at the Ebre River Delta Station

Science.gov (United States)

Occhipinti, Paola; Morguí, Josep Anton; Àgueda, Alba; Batet, Oscar; Borràs, Sílvia; Cañas, Lídia; Curcoll, Roger; Grossi, Claudia; Nofuentes, Manel; Vazquez, Eusebi; Rodó, Xavier

2015-04-01

In the framework of the ClimaDat project, IC3 has established a network of eight monitoring stations across the Iberian Peninsula and the Canarian Archipelago with the aim of studying climate processes. The monitoring station at the Ebre River Delta (DEC3) is located in the Ebre River Delta Natural Park (40° 44' N; 0° 47' E) and it is characterized by the typical North-Western Mediterranean climate. Since 2013, atmospheric greenhouse gases (GHG) and 222Rn tracer gas together with the meteorological parameters are continuously measured from a 10 m a.g.l. height tower. Atmospheric GHG (CO2, CH4, CO and N2O) concentrations are determined using a Picarro analyzer G2301 (CO2 and CH4) and a modified gas chromatograph (GC) Agilent 6890N (CO2, CH4, CO and N2O). Open data access is available from the www.climadat.es website. Data collected at the DEC3 station are also submitted to the InGOS platform since this station is part of the InGOS European infrastructure project. Researchers from the Laboratory of the Atmosphere and the Oceans (LAO) at IC3 have performed an intercomparison study at the DEC3 site between three different Picarro analyzers (two Picarro G2301 and one Picarro G2301M), a Los Gatos Research (LGR) analyzer and the GC system already installed at the station. The aim of this study is to compare and assess the measuring agreement between the four optical gas analyzers and the GC. In the first part of the experiment, all instruments have been calibrated using NOAA gases as primary standards analyzing five Praxair provided targets to evaluate the precision of the measuring instruments. Max Plank Institute (MPI) gases have been used as secondary standards for the GC whereas Praxair provided tanks are used as secondary standards for the Picarro and the LGR analyzers. In the second part of the experiment, atmospheric GHG were measured from natural atmospheric air taken from a 10 m a.g.l. inlet. Daily cycles of GHG measurements were carried out using different

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.

Can rising CO2 concentrations in the atmosphere mitigate the impact of drought years on tree growth?

Science.gov (United States)

Achim, Alexis; Plumpton, Heather; Auty, David; Ogee, Jerome; MacCarthy, Heather; Bert, Didier; Domec, Jean-Christophe; Oren, Ram; Wingate, Lisa

2015-04-01

Atmospheric CO2 concentrations and nitrogen deposition rates have increased substantially over the last century and are expected to continue unabated. As a result, terrestrial ecosystems will experience warmer temperatures and some may even experience droughts of a more intense and frequent nature that could lead to widespread forest mortality. Thus there is mounting pressure to understand and predict how forest growth will be affected by such environmental interactions in the future. In this study we used annual tree growth data from the Duke Free Air CO2 Enrichment (FACE) experiment to determine the effects of elevated atmospheric CO2 concentration (+200 ppm) and Nitrogen fertilisation (11.2 g of N m-2 yr-1) on the stem biomass increments of mature loblolly pine (Pinus taeda L.) trees from 1996 to 2010. A non-linear mixed-effects model was developed to provide estimates of annual ring specific gravity in all trees using cambial age and annual ring width as explanatory variables. Elevated CO2 did not have a significant effect on annual ring specific gravity, but N fertilisation caused a slight decrease of approximately 2% compared to the non-fertilised in both the ambient and CO2-elevated plots. When basal area increments were multiplied by wood specific gravity predictions to provide estimates of stem biomass, there was a 40% increase in the CO2-elevated plots compared to those in ambient conditions. This difference remained relatively stable until the application of the fertilisation treatment, which caused a further increase in biomass increments that peaked after three years. Unexpectedly the magnitude of this second response was similar in the CO2-elevated and ambient plots (about 25% in each after 3 years), suggesting that there was no interaction between the concentration of CO2 and the availability of soil N on biomass increments. Importantly, during drier years when annual precipitation was less than 1000 mm we observed a significant decrease in annual

Impact of atmospheric boundary layer depth variability and wind reversal on the diurnal variability of aerosol concentration at a valley site.

Science.gov (United States)

Pal, S; Lee, T R; Phelps, S; De Wekker, S F J

2014-10-15

The development of the atmospheric boundary layer (ABL) plays a key role in affecting the variability of atmospheric constituents such as aerosols, greenhouse gases, water vapor, and ozone. In general, the concentration of any tracers within the ABL varies due to the changes in the mixing volume (i.e. ABL depth). In this study, we investigate the impact on the near-surface aerosol concentration in a valley site of 1) the boundary layer dilution due to vertical mixing and 2) changes in the wind patterns. We use a data set obtained during a 10-day field campaign in which a number of remote sensing and in-situ instruments were deployed, including a ground-based aerosol lidar system for monitoring of the ABL top height (zi), a particle counter to determine the number concentration of aerosol particles at eight different size ranges, and tower-based standard meteorological instruments. Results show a clearly visible decreasing trend of the mean daytime zi from 2900 m AGL (above ground level) to 2200 m AGL during a three-day period which resulted in increased near-surface pollutant concentrations. An inverse relationship exists between the zi and the fine fraction (0.3-0.7 μm) accumulation mode particles (AMP) on some days due to the dilution effect in a well-mixed ABL. These days are characterized by the absence of daytime upvalley winds and the presence of northwesterly synoptic-driven winds. In contrast, on the days with an onset of an upvalley wind circulation after the morning transition, the wind-driven local transport mechanism outweighs the ABL-dilution effect in determining the variability of AMP concentration. The interplay between the ABL depth evolution and the onset of the upvalley wind during the morning transition period significantly governs the air quality in a valley and could be an important component in the studies of mountain meteorology and air quality. Copyright © 2014 Elsevier B.V. All rights reserved.

Ecological aspects of Moessbauer study of iron-containing atmospheric aerosols

International Nuclear Information System (INIS)

Kopcewicz, B.; Kopcewicz, M.

2000-01-01

Moessbauer spectroscopy was applied to analyze the iron compounds in atmospheric aerosol. Seasonal variations of iron concentration in atmospheric air measured over twenty years in Poland are discussed. It was observed that the concentration of iron sulfides (FeS, FeS 2 ) related to coal combustion dropped significantly, however, concentration of iron oxides and iron oxyhydroxides related to fuel combustion increased

Review on occurrence and behavior of PCDD/Fs and dl-PCBs in atmosphere of East Asia

Science.gov (United States)

Trinh, Minh Man; Chang, Moo Been

2018-05-01

This paper reviews the data from studies mainly published after 2000 to provide the current understanding of the physicochemical properties, atmospheric occurrence, gas/particle partitioning, fate and temporal trends in atmospheric matrix of PCDD/Fs and dl-PCBs of East Asia. Ambient PCDD/Fs and dl-PCBs concentrations in East Asia are found to be tens to hundreds times higher than that measured in Europe and North America. After strict regulations on PCDD/Fs and dl-PCBs emissions are enacted, the concentrations of these compounds decrease dramatically in Eastern Asian countries. In general, most of PCDD/Fs distribute in particle phase while dl-PCBs majorly exist in gas phase. Three main factors including physicochemical properties of the compounds, properties of particle and atmospheric condition affect the gas/particle partitioning of PCDD/Fs and dl-PCBs. The accuracy of absorption and adsorption models on predicting gas/particle partitioning of PCDD/Fs and dl-PCBs is evaluated. Gas-phase compounds are mostly removed from the atmosphere via reactions with OH radicals while those in particle phase are majorly removed by wet/dry deposition processes. The effects of removing processes and long-range transport on gas/particle partitioning are also discussed.

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

A comparison of atmospheric composition using the Carbon Bond and Regional Atmospheric Chemistry Mechanisms

Directory of Open Access Journals (Sweden)

G. Sarwar

2013-10-01

Full Text Available We incorporate the recently developed Regional Atmospheric Chemistry Mechanism (version 2, RACM2 into the Community Multiscale Air Quality modeling system for comparison with the existing 2005 Carbon Bond mechanism with updated toluene chemistry (CB05TU. Compared to CB05TU, RACM2 enhances the domain-wide monthly mean hydroxyl radical concentrations by 46% and nitric acid by 26%. However, it reduces hydrogen peroxide by 2%, peroxyacetic acid by 94%, methyl hydrogen peroxide by 19%, peroxyacetyl nitrate by 40%, and organic nitrate by 41%. RACM2 enhances ozone compared to CB05TU at all ambient levels. Although it exhibited greater overestimates at lower observed concentrations, it displayed an improved performance at higher observed concentrations. The RACM2 ozone predictions are also supported by increased ozone production efficiency that agrees better with observations. Compared to CB05TU, RACM2 enhances the domain-wide monthly mean sulfate by 10%, nitrate by 6%, ammonium by 10%, anthropogenic secondary organic aerosols by 42%, biogenic secondary organic aerosols by 5%, and in-cloud secondary organic aerosols by 7%. Increased inorganic and organic aerosols with RACM2 agree better with observed data. Any air pollution control strategies developed using the two mechanisms do not differ appreciably.

Evaluation of three atmospheric dispersion models using tracer release experiment data

International Nuclear Information System (INIS)

Daoo, V.J.; Oza, R.B.; Pandit, G.G.; Sadasivan, S.; Venkat Raj, V.

2004-01-01

Performance of three atmospheric dispersion models viz: (1) Gaussian Plume Model (GPM), (2) Equi-Distance PUFF Model (EDPUFFM) and (3) Particle Trajectory Model (PTM) is evaluated using field data collected from a tracer (SF 6 ) release experiment. The experiment was conducted within the campus of the Bhabha Atomic Research Centre (BARC), located at Trombay, Mumbai, India. The three models used are currently in operation at the BARC. The first one is a standard, well-documented empirical model while the other two models have been developed at the Bhabha Atomic Research Centre. The PTM is a numerical model while the EDPUFFM is a hybrid model combining both the numerical and analytical techniques. The procedure for evaluation is as per the recommendations of 1980 AMS (American Meteorological Society) workshop on atmospheric dispersion models performance evaluation. In addition, linear regression analysis has also been carried out. The regression analysis reveals that on an average, the EDPUFFM and the GPM predictions are higher by a factor of about 1.5 while the PTM predictions are lower by a factor of about 4. Comparison of various performance measures reveals that the performance of the EDPUFFM is marginally better than that of the GPM while the PTM performance is comparatively poor. The uncertainty factors obtained in this study, especially for higher concentration range ( > 100 ppt) are similar to those obtained in other validation study carried out elsewhere to validate the GPM predictions. However, for lower concentration range and for the conditions after the source is switched off, all the three models perform poorly in predicting the concentration. (author)

Experimental Observation of Strongly Bound Dimers of Sulfuric Acid: Application to Nucleation in the Atmosphere

DEFF Research Database (Denmark)

Petaja, Tuukka; Sipila, Mikko; Paasonen, Pauli

2011-01-01

rate was clearly higher than the measured new particle formation rate at similar to 1.5 nmsuggesting that the rate limiting step for the nucleation takes place after the dimerization step. The quantum chemical calculations suggested that even in the ultraclean conditions there exist (a) stabilizing...... compound(s) with (a) concentration(s) high enough to prevent the dimer evaporation. Such a stabilizing compound should be abundant enough in any natural environment and would therefore not limit the formation of sulfuric acid dimers in the atmosphere....

Measurement of atmospheric CO2 column concentrations to cloud tops with a pulsed multi-wavelength airborne lidar

Science.gov (United States)

Mao, Jianping; Ramanathan, Anand; Abshire, James B.; Kawa, Stephan R.; Riris, Haris; Allan, Graham R.; Rodriguez, Michael; Hasselbrack, William E.; Sun, Xiaoli; Numata, Kenji; Chen, Jeff; Choi, Yonghoon; Yang, Mei Ying Melissa

2018-01-01

We have measured the column-averaged atmospheric CO2 mixing ratio to a variety of cloud tops by using an airborne pulsed multi-wavelength integrated-path differential absorption (IPDA) lidar. Airborne measurements were made at altitudes up to 13 km during the 2011, 2013 and 2014 NASA Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) science campaigns flown in the United States West and Midwest and were compared to those from an in situ sensor. Analysis of the lidar backscatter profiles shows the average cloud top reflectance was ˜ 5 % for the CO2 measurement at 1572.335 nm except to cirrus clouds, which had lower reflectance. The energies for 1 µs wide laser pulses reflected from cloud tops were sufficient to allow clear identification of CO2 absorption line shape and then to allow retrievals of atmospheric column CO2 from the aircraft to cloud tops more than 90 % of the time. Retrievals from the CO2 measurements to cloud tops had minimal bias but larger standard deviations when compared to those made to the ground, depending on cloud top roughness and reflectance. The measurements show this new capability helps resolve CO2 horizontal and vertical gradients in the atmosphere. When used with nearby full-column measurements to ground, the CO2 measurements to cloud tops can be used to estimate the partial-column CO2 concentration below clouds, which should lead to better estimates of surface carbon sources and sinks. This additional capability of the range-resolved CO2 IPDA lidar technique provides a new benefit for studying the carbon cycle in future airborne and space-based CO2 missions.

Measurement of Atmospheric CO2 Column Concentrations to Cloud Tops With a Pulsed Multi-Wavelength Airborne Lidar

Science.gov (United States)

Mao, Jianping; Ramanathan, Anand; Abshire, James B.; Kawa, Stephan R.; Riris, Haris; Allan, Graham R.; Rodriguez, Michael R.; Hasselbrack, William E.; Sun, Xiaoli; Numata, Kenji;

Brominated flame retardants in the urban atmosphere of Northeast China: Concentrations, temperature dependence and gas-particle partitioning

Energy Technology Data Exchange (ETDEWEB)

Qi, Hong; Li, Wen-Long; Liu, Li-Yan; Song, Wei-Wei; Ma, Wan-Li, E-mail: mawanli002@163.com; Li, Yi-Fan, E-mail: ijrc_pts_paper@yahoo.com

2014-09-01

57 pairs of air samples (gas and particle phases) were collected using a high volume air sampler in a typical city of Northeast China. Brominated flame retardants (BFRs) including 13 polybrominated diphenyl ethers (PBDEs, including BDEs 17, 28, 47, 49, 66, 85, 99, 100, 138, 153, 154, 183, and 209) and 9 alternative BFRs (p-TBX, PBBZ, PBT, PBEB, DPTE, HBBZ, γ-HBCD, BTBPE, and DBDPE) were analyzed. The annual average total concentrations of the 13 PBDEs and the 9 alternative BFRs were 69 pg/m{sup 3} and 180 pg/m{sup 3}, respectively. BDE 209 and γ-HBCD were the dominant congeners, according to the one-year study. The partial pressure of BFRs in the gas phase was significantly correlated with the ambient temperature, except for BDE 85, γ-HBCD and DBDPE, indicating the important influence of ambient temperature on the behavior of BFRs in the atmosphere. It was found that the gas–particle partitioning coefficients (logK{sub p}) for most low molecular weight BFRs were highly temperature dependent as well. Gas–particle partitioning coefficients (logK{sub p}) also correlated with the sub-cooled liquid vapor pressure (logP{sub L}{sup o}). Our results indicated that absorption into organic matter is the main control mechanism for the gas–particle partitioning of atmospheric PBDEs. - Highlights: • Both PBDEs and alternative BFRs were analyzed in the atmosphere of Northeast China. • Partial pressure of BFRs was significantly correlated with the ambient temperature. • A strong temperature dependence of gas-particle partitioning was found. • Absorption into organic matter was the control mechanism for G-P partitioning.

Ecosystem-atmosphere exchange of carbon in a heathland under future climatic conditions