WorldWideScience

Sample records for atmospheric trace gases

  1. Atmospheric trace gases monitoring by UV-vis spectroscopic techniques

    Science.gov (United States)

    Xie, Pinhua; Li, Ang; Wu, Fengcheng; Qin, Min; Hu, Rezhi; Xu, Jin; Si, Fuqi; Liu, Jianguo; Liu, Wenqing

    2016-04-01

    Due to rapidly economic development, air pollution has become an important issue in China. Phenomena such as regional haze in winter and high O3 concentration in summer are strongly related to increasing trace species. For better understanding the air pollution formation, it is necessary to know spatial and temporal distribution of trace species in the atmosphere. UV-vis spectroscopic techniques are of great advantages for trace species monitoring to meet several requirements, e.g. versatility, high sensitivity, good temporal resolution and field applicability. We have studied and developed various trace gases monitoring techniques and instruments based on UV-vis spectroscopic technique for in-situ measurements and remote sensing, e.g. LP-DOAS, IBBCEAS, CRDS, MAX-DOAS and mobile DOAS for NO2, SO2, HCHO, HONO, NO3, and N2O5 etc. The principle, instrumentation and inversion algorithm are presented. As typical applications of these techniques, investigation of the evolution of HONO and NO3 radicals over Beijing area, measurements of regional pollution in NCP and YRD are discussed in the aspects of HONO and nocturnal NO3 radical characteristics, trace gases (NO2, SO2 etc.) temporal and spatial distribution, pollution transport pathway, emission sources.

  2. Atmospheric trace gases and global climate - A seasonal model study

    Science.gov (United States)

    Wang, Wei-Chyung; Molnar, Gyula; Ko, Malcolm K. W.; Goldenberg, Steven; Sze, Nien Dak

    1990-01-01

    Atmospheric models with seasonal cycles are used to study the possible near-future changes in latitudinal and vertical distributions of atmospheric ozone and temperature caused by increases of trace gases. It is found that increases of CFCs, CH4, and N2O may add to the surface warming from increased CO2. Calculations based on projected trends of CO2, N2O, CH4, and CFCs show that the annual mean and global mean surface temperature could warm by as much as 2.5 C by the year 2050, with larger warming at high latitudes. The results suggest that the warming in the lower stratosphere and upper troposphere is much larger than that at the surface, especially during the summer season.

  3. Remote sensing of atmospheric trace gases by diode laser spectroscopy

    Science.gov (United States)

    Liu, Jianguo; Kan, Ruifeng; He, Yabai; He, Ying; Zhang, Yujun; Xie, Pinhua; liu, Wenqing

    2016-04-01

    Gaseous ammonia is the most abundant alkaline trace gas in the atmosphere. In order to study its role in acid deposition and aerosol formation, as well as its influence on the regional air quality and atmospheric visibility, several instruments has been developed based on TDLAS (Tunable Diode Laser Absorption Spectroscopy) techniques. In this paper, a long open path TDLAS system and a continuous-wave CRDS (Cavity-Ring down Spectroscopy) system are presented. The long open path system has been developed for NH3 in-situ monitoring by combining wavelength modulation with harmonic detection techniques to obtain the necessary detection sensitivity. The prototype instrument has been used to monitor atmospheric NH3 concentration at an urban site near Beijing National Stadium during Beijing Olympics in 2008, and recently used to measure the fluxes of NH3 from farm fields by flux-gradient method. The detection limit for ammonia is proved approximately 3ppb for a total path length of 456m. The continuous-wave, rapidly swept CRDS system has been developed for localized atmospheric sensing of trace gases at remote sites. Passive open-path optical sensor units could be coupled by optical fiber over distances of >1 km to a single transmitter/receiver console incorporating a photodetector and a swept-frequency diode laser tuned to molecule-specific near-infrared wavelengths. A noise-limited minimum detectable mixing ratio of ~11 ppbv is attained for ammonia at atmospheric pressure. The developed instruments are deployable in agricultural, industrial, and natural atmospheric environments.

  4. Measurement of Trace Gases in the Atmosphere of Venus Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Southwest Sciences proposes to develop small, lightweight, low power instrumentation for the in situ balloon-borne measurement of several trace gases of importance...

  5. Trace gases in the atmosphere over Russian cities

    Science.gov (United States)

    Elansky, Nikolai F.; Lavrova, Olga V.; Skorokhod, Andrey I.; Belikov, Igor B.

    2016-10-01

    Multiyear observational data (obtained at the mobile railroad laboratory in the course of the 1995-2010 TROICA experiments) on the composition and state of the atmosphere were used to study the features of both spatial and temporal variations in the contents of trace gases in the surface air layer over Russian cities. The obtained characteristics of urban air noticeably differ from those obtained at stationary stations. The emission fluxes of NOx, CO, and CH4 and their integral emissions from large cities have been estimated on the basis of observational data obtained at the mobile laboratory. The values of these emission fluxes reflect the state of urban infrastructure. The integral urban emissions of CO depend on the city size and vary from 50 Gg yr-1 for Yaroslavl to 130 Gg yr-1 for Yekaterinburg. For most cities, they agree with the EDGAR v4.2 data within the limits of experimental error. The agreement is worse for the emissions of NOx. The EDGAR v4.2 data on the emissions of CH4 seem to be overestimated.

  6. Wet precipitation scavenging of soluble atmospheric trace gases due to chemical absorption in inhomogeneous atmosphere

    Science.gov (United States)

    Elperin, Tov; Fominykh, Andrew; Krasovitov, Boris

    2017-02-01

    We analyze the effects of irreversible chemical reactions of the first and higher orders and aqueous-phase dissociation reactions on the rate of trace gas scavenging by rain in the atmosphere with non-uniform concentration and temperature. We employ an one-dimensional model of precipitation scavenging of chemically active soluble gaseous pollutants that is valid for small gradients of temperature and concentration in the atmosphere. It is demonstrated that transient altitudinal distribution of concentration under the influence of rain is determined by the partial hyperbolic differential equation of the first order. Scavenging coefficients are calculated for wet removal of chlorine, nitrogen dioxide and sulfur dioxide for the exponential and linear initial altitudinal distributions of trace gases concentration in the atmosphere and linear and uniform altitudinal temperature distributions. Theoretical predictions of the dependence of the magnitude of the scavenging coefficient on rain intensity for sulfur dioxide are in a good agreement with the available atmospheric measurements.

  7. Laboratory infrared spectroscopy of some important atmospheric trace gases

    Science.gov (United States)

    Zou, Qunjun

    -broadened line widths has been determined for the lines in both bands. Assuming a similar power law relationship, the temperature- dependence of the self- and air-induced line shifts, an exponent Π, has also been determined. The absorption cross-sections have been measured for C2F 6 under the conditions appropriate to the terrestrial atmosphere, with temperatures in the range of 180 to 296 K, and the broadening pressures in the range of 30 to 760 torr. The measured band strengths (in units of 10 -16 cm-molecule-1) of the 8.0 and 8.95 μm bands are 1.636 +/- 0.003 and 0.467 +/- 0.0018, respectively. The highly accurate spectroscopic parameters obtained in this work, many of which have not been reported previously, can be applied to the remote sensing and radiative transfer modeling of the terrestrial atmosphere. The data are also compared with the results in the literature reported by other investigators.

  8. An overview of current issues in the uptake of atmospheric trace gases by aerosols and clouds

    Science.gov (United States)

    Kolb, C. E.; Cox, R. A.; Abbatt, J. P. D.; Ammann, M.; Davis, E. J.; Donaldson, D. J.; Garrett, B. C.; George, C.; Griffiths, P. T.; Hanson, D. R.; Kulmala, M.; McFiggans, G.; Pöschl, U.; Riipinen, I.; Rossi, M. J.; Rudich, Y.; Wagner, P. E.; Winkler, P. M.; Worsnop, D. R.; O'Dowd, C. D.

    2010-11-01

    A workshop was held in the framework of the ACCENT (Atmospheric Composition Change - a European Network) Joint Research Programme on "Aerosols" and the Programme on "Access to Laboratory Data". The aim of the workshop was to hold "Gordon Conference" type discussion covering accommodation and reactive uptake of water vapour and trace pollutant gases on condensed phase atmospheric materials. The scope was to review and define the current state of knowledge of accommodation coefficients for water vapour on water droplet and ice surfaces, and uptake of trace gas species on a variety of different surfaces characteristic of the atmospheric condensed phase particulate matter and cloud droplets. Twenty-six scientists participated in this meeting through presentations, discussions and the development of a consensus review. In this review we present an analysis of the state of knowledge on the thermal and mass accommodation coefficient for water vapour on aqueous droplets and ice and a survey of current state-of the-art of reactive uptake of trace gases on a range of liquid and solid atmospheric droplets and particles. The review recommends consistent definitions of the various parameters that are needed for quantitative representation of the range of gas/condensed surface kinetic processes important for the atmosphere and identifies topics that require additional research.

  9. An overview of current issues in the uptake of atmospheric trace gases by aerosols and clouds

    Directory of Open Access Journals (Sweden)

    C. E. Kolb

    2010-11-01

    Full Text Available A workshop was held in the framework of the ACCENT (Atmospheric Composition Change – a European Network Joint Research Programme on "Aerosols" and the Programme on "Access to Laboratory Data". The aim of the workshop was to hold "Gordon Conference" type discussion covering accommodation and reactive uptake of water vapour and trace pollutant gases on condensed phase atmospheric materials. The scope was to review and define the current state of knowledge of accommodation coefficients for water vapour on water droplet and ice surfaces, and uptake of trace gas species on a variety of different surfaces characteristic of the atmospheric condensed phase particulate matter and cloud droplets. Twenty-six scientists participated in this meeting through presentations, discussions and the development of a consensus review.

    In this review we present an analysis of the state of knowledge on the thermal and mass accommodation coefficient for water vapour on aqueous droplets and ice and a survey of current state-of the-art of reactive uptake of trace gases on a range of liquid and solid atmospheric droplets and particles. The review recommends consistent definitions of the various parameters that are needed for quantitative representation of the range of gas/condensed surface kinetic processes important for the atmosphere and identifies topics that require additional research.

  10. An overview of current issues in the uptake of atmospheric trace gases by aerosols and clouds

    Directory of Open Access Journals (Sweden)

    C. E. Kolb

    2010-04-01

    Full Text Available A workshop was held in the framework of the ACCENT (Atmospheric Composition Change – a European Network Joint Research Programme on "Aerosols" and the Programme on "Access to Laboratory Data". The aim of the workshop was to hold "Gordon Conference" type discussion covering accommodation and reactive uptake of water vapour and trace pollutant gases on condensed phase atmospheric materials. The scope was to review and define the current state of knowledge of accommodation coefficients for water vapour on water droplet and ice surfaces, and uptake of trace gas species on a variety of different surfaces characteristic of the atmospheric condensed phase particulate matter and cloud droplets. Twenty-six scientists participated in this meeting through presentations, discussions and the development of a consensus review.

    In this review we present an analysis of the state of knowledge on the thermal and mass accommodation coefficient for water vapour on aqueous droplets and ice and a survey of current state-of the-art of reactive uptake of trace gases on a range of liquid and solid atmospheric droplets and particles. The review recommends consistent definitions of the various parameters that are needed for quantitative representation of the range of gas/condensed surface kinetic processes important for the atmosphere and identifies topics that require additional research.

  11. Potential for the use of reconstructed IASI radiances in the detection of atmospheric trace gases

    Directory of Open Access Journals (Sweden)

    N. C. Atkinson

    2010-07-01

    Full Text Available Principal component (PC analysis has received considerable attention as a technique for the extraction of meteorological signals from hyperspectral infra-red sounders such as the Infrared Atmospheric Sounding Interferometer (IASI and the Atmospheric Infrared Sounder (AIRS. In addition to achieving substantial bit-volume reductions for dissemination purposes, the technique can also be used to generate reconstructed radiances in which random instrument noise has been reduced. Studies on PC analysis of hyperspectral infrared sounder data have been undertaken in the context of numerical weather prediction, instrument monitoring and geophysical variable retrieval, as well as data compression. This study examines the potential of PC analysis for chemistry applications.

    A major concern in the use of PC analysis for chemistry is that the spectral features associated with trace gases may not be well represented in the reconstructed spectra, either due to deficiencies in the training set or due to the limited number of PC scores used in the radiance reconstruction. In this paper we show examples of reconstructed IASI radiances for several trace gases: ammonia, sulphur dioxide, methane and carbon monoxide. It is shown that care must be taken in the selection of spectra for the initial training set: an iterative technique, in which outlier spectra are added to a base training set, gives the best results. For the four trace gases examined, key features of the chemical signatures are retained in the reconstructed radiances, whilst achieving a substantial reduction in instrument noise.

    A new regional re-transmission service for IASI is scheduled to start in 2010, as part of the EUMETSAT Advanced Retransmission Service (EARS. For this EARS-IASI service it is intended to include PC scores as part of the data stream. The paper describes the generation of the reference eigenvectors for this new service.

  12. Detectability of trace gases in the Martian atmosphere using gas correlation filter radiometry

    Science.gov (United States)

    Sinclair, J.; Irwin, P. G. J.; Wilson, E.; Calcutt, S.

    2015-10-01

    We present the results of radiative transfer simulations of a gas correlation filter radiometer (GCFR) in the detection of trace species in the Martian atmosphere. We investigated two scenarios: 1) nadir and/or limb sounding from a Mars orbiter in the thermal infrared, 2) solar occultation measurements in the near-infrared from the Martian surface. In both scenarios, a GCFR would allow detection of trace gases at a lower concentration than that detectable by a conventional filter radiometer. In nadir/limb sounding, we find that CH4, SO2, N2O, C2H2 and CH3OH are detectable at concentrations lower than previously-derived upper limits. From solar occultation measurements, we find that CH4, SO2, C2H2, C2H6 are detectable at concentrations lower than previously-derived upper limits but only in low dust conditions.

  13. Sensitivity of net thermal flux to the abundance of trace gases in the lower atmosphere of Venus

    Science.gov (United States)

    Lee, Yeon Joo; Sagawa, Hideo; Haus, Rainer; Stefani, Stefania; Imamura, Takeshi; Titov, Dmitrij V.; Piccioni, Giuseppe

    2016-09-01

    We calculated the net thermal flux in the atmosphere of Venus from the surface to 100 km altitude. Our atmospheric model was carefully constructed especially for altitudes below the clouds (Venus using 20-50 ppmv H2O, suggesting that the high H2O abundance of 200 ppmv derived in the earlier analysis is not required. Our sensitivity study shows that the trace gases SO2, H2O, and OCS are effective thermal agents, while CO and HCl influences are rather weak. We suggest that the influence of the former three gases should be taken into account to estimate the net radiative energy in the deep atmosphere.

  14. Carbon dioxide Information Analysis Center and World Data Center: A for Atmospheric trace gases. Annual progress report, FY 1994

    Energy Technology Data Exchange (ETDEWEB)

    Burtis, M.D. [comp.] [Tennessee Univ., Knoxville, TN (United States). Energy, Environment and Resources Center; Cushman, R.M.; Boden, T.A.; Jones, S.B.; Nelson, T.R.; Stoss, F.W. [Oak Ridge National Lab., TN (United States)

    1995-03-01

    This report summarizes the activities and accomplishments made by the Carbon Dioxide Information Analysis Center and World Data Center-A for Atmospheric Trace Gases during the fiscal year 1994. Topics discussed in this report include; organization and staff, user services, systems, communications, Collaborative efforts with China, networking, ocean data and activities of the World Data Center-A.

  15. Miniaturized Gas Correlation Radiometer for the Detection of Trace Gases in the Martian Atmosphere

    Science.gov (United States)

    Melroy, H.; Wilson, E. L.; Georgieva, E.

    2012-12-01

    We present a miniaturized and simplified version of a gas correlation radiometer (GCR) capable of simultaneously mapping multiple trace gases and identifying active regions on the Mars surface. Gas correlation radiometry (GCR) has been shown to be a sensitive and versatile method for detecting trace gases in Earth's atmosphere. Reduction of the size and mass of the GCR was achieved by implementing compact, light-weight 1 mm inner diameter hollow-core optical fibers (hollow waveguides) as the gas correlation cells. In a comparison with an Earth orbiting CO2 GCR instrument, exchanging the 10 m multipass cells with hollow waveguide gas correlation cells of equivalent pathlength reduces the mass from ~150 kg to ~0.5 kg, and reduces the volume from 1.9 m x 1.3 m x 0.86 m to a small bundle of fiber coils approximately 1 meter in diameter by 0.05 m in height (mass and volume reductions of >99%). A unique feature of this instrument is its stackable module design, with a single module for each trace gas. Each of the modules is self-contained, and fundamentally identical; differing by the bandpass filter wavelength range and gas mixtures inside the hollow-waveguide absorption cells. The current configuration contains four stacked modules for simultaneous measurements of methane (CH4), formaldehyde (H2CO), water vapor (H2O), and deuterated water vapor (HDO) but could easily be expanded to include measurements of additional species of interest including nitrous oxide (N2O), hydrogen sulfide (H2S), methanol (CH3OH), and sulfur dioxide (SO2), as well as carbon dioxide (CO2) for a simultaneous measure of mass balance. Preliminary results indicate that a 1 ppb detection limit is possible for both formaldehyde and methane with one second of averaging. Using non-optimized components, we have demonstrated an instrument sensitivity equivalent to ~30 ppb for formaldehyde, and ~500 ppb for methane. We expect custom bandpass filters and 6 m long waveguides to significantly improve these

  16. Miniaturized Gas Correlation Radiometer for the Detection of Trace Gases in the Martian Atmosphere

    Science.gov (United States)

    Melroy, Hilary R.; Wilson, Emily L.; Georgieva, Elena

    2012-01-01

    We present a miniaturized and simplified version of a gas correlation radiometer (GCR) capable of simultaneously mapping multiple trace gases and identifying active regions on the Mars surface. Gas correlation radiometry (GCR) has been shown to be a sensitive and versatile method for detecting trace gases in Earth's atmosphere. Reduction of the size and mass of the GCR was achieved by implementing compact, light-weight 1 mm inner diameter hollow-core optical fibers (hollow waveguides) as the gas correlation cells. In a comparison with an Earth orbiting CO2 GCR instrument, exchanging the 10 m multipass cells with hollow waveguide gas correlation cells of equivalent path length reduces the mass from approximately 150 kg to approximately 0.5 kg, and reduces the volume from 1.9 m x 1.3 m x 0.86 m to a small bundle of fiber coils approximately 1 meter in diameter by 0.05 m in height (mass and volume reductions of greater than 99%). A unique feature of this instrument is its stackable module design, with a single module for each trace gas. Each of the modules is self-contained, and fundamentally identical; differing by the bandpass filter wavelength range and gas mixtures inside the hollow-waveguide absorption cells. The current configuration contains four stacked modules for simultaneous measurements of methane (CH4), formaldehyde (H2CO), water vapor (H2O), and deuterated water vapor (HDO) but could easily be expanded to include measurements of additional species of interest including nitrous oxide (N2O), hydrogen sulfide (H2S), methanol (CH3OH), and sulfur dioxide (SO2), as well as carbon dioxide (CO2) for a simultaneous measure of mass balance. Preliminary results indicate that a 1 ppb detection limit is possible for both formaldehyde and methane with one second of averaging. Using non-optimized components, we have demonstrated an instrument sensitivity equivalent to approximately 30 ppb for formaldehyde, and approximately 500 ppb for methane. We expect custom

  17. Airborne multi-axis DOAS measurements of atmospheric trace gases on CARIBIC long-distance flights

    Directory of Open Access Journals (Sweden)

    B. Dix

    2009-11-01

    Full Text Available A DOAS (Differential Optical Absorption Spectroscopy instrument was implemented and operated onboard a long-distance passenger aircraft within the framework of the CARIBIC project (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container. The instrument was designed to keep weight, size and power consumption low and to comply with civil aviation regulations. It records spectra of scattered light from three viewing directions (nadir, 10° above and below horizon using a miniaturized telescope system. The telescopes are integrated in the main pylon of the inlet system which is mounted at the belly of the aircraft. Fibre bundles transmit light from the telescopes to spectrograph-detector units inside the DOAS container instrument. The latter is part of the removable CARIBIC instrument container, which is installed monthly on the aircraft for a series of measurement flights.

    During 30 flight operations within three years, measurements of HCHO, HONO, NO2, BrO, O3 and the oxygen dimer O4 were conducted. All of these trace gases except BrO could be analysed with a 30 s time resolution. HONO was detected for the first time in a deep convective cloud over central Asia, while BrO, NO2 and O3 could be observed in tropopause fold regions. Biomass burning signatures over South America could be seen and measurements during ascent and descent provided information on boundary layer trace gas profiles (e.g. NO2 or HCHO.

  18. Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 2000 Annual Report

    Energy Technology Data Exchange (ETDEWEB)

    Cushman, R.M.

    2001-11-15

    The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO{sub 2}) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO{sub 2} and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea levels.

  19. Compilation and evaluation of gas phase diffusion coefficients of reactive trace gases in the atmosphere: volume 1. Inorganic compounds

    Science.gov (United States)

    Tang, M. J.; Cox, R. A.; Kalberer, M.

    2014-09-01

    Diffusion of gas molecules to the surface is the first step for all gas-surface reactions. Gas phase diffusion can influence and sometimes even limit the overall rates of these reactions; however, there is no database of the gas phase diffusion coefficients of atmospheric reactive trace gases. Here we compile and evaluate, for the first time, the diffusivities (pressure-independent diffusion coefficients) of atmospheric inorganic reactive trace gases reported in the literature. The measured diffusivities are then compared with estimated values using a semi-empirical method developed by Fuller et al. (1966). The diffusivities estimated using Fuller's method are typically found to be in good agreement with the measured values within ±30%, and therefore Fuller's method can be used to estimate the diffusivities of trace gases for which experimental data are not available. The two experimental methods used in the atmospheric chemistry community to measure the gas phase diffusion coefficients are also discussed. A different version of this compilation/evaluation, which will be updated when new data become available, is uploaded online (google.com/site/mingjintang/home/diffusion"target="_blank">https://sites.google.com/site/mingjintang/home/diffusion).

  20. Synthesis of corrected multi-wavelength spectrometers for atmospheric trace gases

    Institute of Scientific and Technical Information of China (English)

    Hikmat H.Asadov; Islam M.Mirzabalayev; Davud Z.Aliyev; Javid A.Agayev; Sima R.Azimova; Nabi A.Nabiyev; Sevinj N.Abdullayeva

    2009-01-01

    The method for synthesis of corrected three-wavelengths spectrometers for trace gas components of atmo sphere on the basis of development of mathematical model has been suggested.The classification table for possible structures of corrected spectrometers is considered.The synthesis allows to reveal some new variants for development of three-wavelength spectrometers for trace gas components of atmosphere.For experimental checkup of achieved theoretical results,a laboratory pattern of three-wavelength spectrometer is developed and tested.

  1. Spatial Variability of Trace Gases During DISCOVER-AQ: Planning for Geostationary Observations of Atmospheric Composition

    Science.gov (United States)

    Follette-Cook, Melanie B.; Pickering, K.; Crawford, J.; Appel, W.; Diskin, G.; Fried, A.; Loughner, C.; Pfister, G.; Weinheimer, A.

    2015-01-01

    Results from an in-depth analysis of trace gas variability in MD indicated that the variability in this region was large enough to be observable by a TEMPO-like instrument. The variability observed in MD is relatively similar to the other three campaigns with a few exceptions: CO variability in CA was much higher than in the other regions; HCHO variability in CA and CO was much lower; MD showed the lowest variability in NO2All model simulations do a reasonable job simulating O3 variability. For CO, the CACO simulations largely under over estimate the variability in the observations. The variability in HCHO is underestimated for every campaign. NO2 variability is slightly overestimated in MD, more so in CO. The TX simulation underestimates the variability in each trace gas. This is most likely due to missing emissions sources (C. Loughner, manuscript in preparation).Future Work: Where reasonable, we will use these model outputs to further explore the resolvability from space of these key trace gases using analyses of tropospheric column amounts relative to satellite precision requirements, similar to Follette-Cook et al. (2015).

  2. Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases, Fiscal Year 2002 Annual Report

    Energy Technology Data Exchange (ETDEWEB)

    Cushman, R.M.

    2003-08-28

    The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including atmospheric concentrations and atmospheric emissions of carbon dioxide (CO{sub 2}) and other radiatively active gases; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea levels.

  3. A Novel Miniaturised Infrared Imaging Spectrometer for the Measurement of Atmospheric Trace Gases

    Science.gov (United States)

    Mortimer, A. H.

    2012-04-01

    A novel, ultra-compact Static Imaging Fourier Transform Spectrometer, SIFTS, with no moving parts has been developed for the remote and in-situ detection of atmospheric gases. This technique has previously been demonstrated in the visible spectral region (400 to 1100nm) using a CCD detector. This paper the author presents the results of the infrared version of the SIFTS instrument, which uses an uncooled microbolometer detector array to measure infrared spectra (7 to 14μm) with a resolution of up 4 cm-1 and temporal resolution of 30Hz. The technique is based on a static optical configuration whereby light is split into two paths and made to recombine along a focal plane producing an interference pattern. The spectral information is returned using a detector array to digitally capture the interferogram which can then be processed into a spectrum by the application of a Fourier transform. The novel optical design has reduced the optics required to only 3 optical components and the detector array, to generate and measure the interferogram. The experimental performance of the SIFTS instrument has verified the theoretical models, which has shown that the spectral resolution is for the infrared instrument is 4cm-1. The Connes advantage, inherent to the Michelson spectrometer Fourier Transform Spectrometer (FTS), whereby the spectral wavelength accuracy is referenced to a stabilised laser has also been demonstrated in the SIFTS instrument. This has been implemented through the use of an expanded internal laser diode with Distributed Bragg Reflector (DFB) which acts as the calibration source used to maintain the wavelength stability of the SIFTS instrument. As there are no moving components, the instrument is compact, light and insensitive to mechanical vibration, additionally the speed of measurement is determined by the frame rate of the detector array. Thus, this instrument has a temporal advantage over common Michelson FTIR instruments. For example, this technique has

  4. Carbon Dioxide Information Analysis Center and World Data Center-A for atmospheric trace gases: FY 1993 activities

    Energy Technology Data Exchange (ETDEWEB)

    Cushman, R.M. [Oak Ridge National Lab., TN (United States). Carbon Dioxide Information Analysis Center; Stoss, F.W. [Oak Ridge National Lab., TN (United States). Carbon Dioxide Information Analysis Center]|[Univ. of Tennessee, Knoxville, TN (United States). Energy, Environment, and Resources Center

    1994-01-01

    During the course of a fiscal year, Oak Ridge National Laboratory`s Carbon Dioxide Information Analysis Center (CDIAC) distributes thousands of specialty publications-numeric data packages (NDPs), computer model packages (CMPs), technical reports, public communication publications, newsletters, article reprints, and reference books-in response to requests for information related to global environmental issues, primarily those pertaining to climate change. CDIAC`s staff also provide technical responses to specific inquiries related to carbon dioxide (CO{sub 2}), other trace gases, and climate. Hundreds of referrals to other researchers, policy analysts, information specialists, or organizations are also facilitated by CDIAC`s staff. This report provides an account of the activities accomplished by CDIAC (including World Data Center-A for Atmospheric Trace Gases) during the period October 1, 1992, to September 30, 1993. An organizational overview of CDIAC and its staff is supplemented by a detailed description of inquiries received and CDIAC`s response to those inquiries. An analysis and description of the preparation and distribution of NDPS, CMPS, technical reports, newsletters, fact sheets, specialty publications, and reprints are provided. Comments and descriptions of CDIAC`s information management systems, professional networking, and special bilateral agreements are also presented.

  5. Atmospheric Chemistry and Greenhouse Gases

    Energy Technology Data Exchange (ETDEWEB)

    Ehhalt, D.; Prather, M.; Dentener, F.; Derwent, R.; Dlugokencky, Edward J.; Holland, E.; Isaksen, I.; Katima, J.; Kirchhoff, V.; Matson, P.; Midgley, P.; Wang, M.; Berntsen, T.; Bey, I.; Brasseur, G.; Buja, L.; Collins, W. J.; Daniel, J. S.; DeMore, W. B.; Derek, N.; Dickerson, R.; Etheridge, D.; Feichter, J.; Fraser, P.; Friedl, R.; Fuglestvedt, J.; Gauss, M.; Grenfell, L.; Grubler, Arnulf; Harris, N.; Hauglustaine, D.; Horowitz, L.; Jackman, C.; Jacob, D.; Jaegle, L.; Jain, Atul K.; Kanakidou, M.; Karlsdottir, S.; Ko, M.; Kurylo, M.; Lawrence, M.; Logan, J. A.; Manning, M.; Mauzerall, D.; McConnell, J.; Mickley, L. J.; Montzka, S.; Muller, J. F.; Olivier, J.; Pickering, K.; Pitari, G.; Roelofs, G.-J.; Rogers, H.; Rognerud, B.; Smith, Steven J.; Solomon, S.; Staehelin, J.; Steele, P.; Stevenson, D. S.; Sundet, J.; Thompson, A.; van Weele, M.; von Kuhlmann, R.; Wang, Y.; Weisenstein, D. K.; Wigley, T. M.; Wild, O.; Wuebbles, D.J.; Yantosca, R.; Joos, Fortunat; McFarland, M.

    2001-10-01

    Chapter 4 of the IPCC Third Assessment Report Climate Change 2001: The Scientific Basis. Sections include: Executive Summary 2414.1 Introduction 2434.2 Trace Gases: Current Observations, Trends and Budgets 2484.3 Projections of Future Emissions 2664.4 Projections of Atmospheric Composition for the 21st Century 2674.5 Open Questions 2774.6 Overall Impact of Global Atmospheric Chemistry Change 279

  6. Atmospheric transport and chemistry of trace gases in LMDz5B: evaluation and implications for inverse modelling

    Directory of Open Access Journals (Sweden)

    R. Locatelli

    2014-07-01

    Full Text Available Representation of atmospheric transport is a major source of error in the estimation of greenhouse gas sources and sinks by inverse modelling. Here we assess the impact on trace gas mole fractions of the new physical parameterisations recently implemented in the Atmospheric Global Climate Model LMDz to improve vertical diffusion, mesoscale mixing by thermal plumes in the planetary boundary layer (PBL, and deep convection in the troposphere. At the same time, the horizontal and vertical resolution of the model used in the inverse system has been increased. The aim of this paper is to evaluate the impact of these developments on the representation of trace gas transport and chemistry, and to anticipate the implications for inversions of greenhouse gas emissions using such an updated model. Comparison of a one-dimensional version of LMDz with large eddy simulations shows that the thermal scheme simulates shallow convective tracer transport in the PBL over land very efficiently, and much better than previous versions of the model. This result is confirmed in three dimensional simulations, by a much improved reproduction of the Radon-222 diurnal cycle. However, the enhanced dynamics of tracer concentrations induces a stronger sensitivity of the new LMDz configuration to external meteorological forcings. At larger scales, the inter-hemispheric exchange is slightly slower when using the new version of the model, bringing them closer to observations. The increase in the vertical resolution (from 19 to 39 layers significantly improves the representation of stratosphere/troposphere exchange. Furthermore, changes in atmospheric thermodynamic variables, such as temperature, due to changes in the PBL mixing, significantly modify chemical reaction rates and the equilibrium value of reactive trace gases. One implication of LMDz model developments for future inversions of greenhouse gas emissions is the ability of the updated system to assimilate a larger

  7. Investigating atmospheric transport processes of trace gases with ICON-ART on different scales

    Science.gov (United States)

    Schröter, Jennifer; Ruhnke, Roland; Rieger, Daniel; Vogel, Heike; Vogel, Bernhard

    2016-04-01

    We have extended the global ICON [1] (ICOsahedral Nonhydrostatic) modelling framework by introducing ICON-ART [2]. ICON is jointly developed by the German Weather Service (DWD) and Max-Planck-Institute for Meteorology (MPI-M), and is used for numerical weather prediction as well as for future climate predictions. ICON-ART is developed at the KIT with the goal to simulate interactions between trace substances and the state of the atmosphere. For the dynamics (transport and diffusion) of gaseous tracers, the original ICON tracer framework is used. A process splitting approach separates the physical processes. In this study, we present results of the ICON-ART extension, including the full gas-phase chemistry module. This module uses the kpp formalism [3] to generate chemistry modules and the photolysis module is based on Cloud-J7.3 [4]. Photolysis rates are calculated online based on the meteorological state of the atmosphere, as well as on the actual ozone profile and cloud optical parameters. Two simulations are performed with ICON-ART. The first one with physics parameterisations for the numerical weather prediction (NWP) and the second one with that for climate simulation in order to investigate the dynamical influence on the distribution of long-lived as well as of short-lived species by comparing both simulations. The results are evaluated with other model results and with observation. In addition to that, we use aircraft campaign data to validate the results on the regional scale for short term simulations by using the NWP physics. [1] Zängl, G., Reinert, D., Ripodas, P., and Baldauf, M.: The ICON (ICOsahedral Non-hydrostatic) modelling framework of DWD and MPI-M: Description of the non-hydrostatic dynamicalcore, Q. J. Roy. Meteor. Soc,141, 563-579, doi:10.1002/qj.2378, 2015 [2] Rieger, D., Bangert, M., Bischoff-Gauss, I., Förstner, J., Lundgren, K., Reinert, D., Schröter, J., Vogel, H., Zängl, G., Ruhnke, R., and Vogel, B.: ICON-ART 1.0 - a new online

  8. A kinetic chemistry tagging technique and its application to modelling the stable isotopic composition of atmospheric trace gases

    Directory of Open Access Journals (Sweden)

    S. Gromov

    2010-02-01

    Full Text Available Isotope composition, in many cases, holds unique information on sources, chemical modification and sinks of atmospheric trace gases. Vital to the interpretation and use of an increasing number of isotope analyses is appropriate modelling. However, the exact implementation of isotopic information is a challenge, and often studies use simplifications which limit their applicability. Here we confer a thorough isotopic extension to MECCA, a comprehensive kinetic chemistry sub-model. To this end, we devise a generic tagging technique for the kinetic chemistry mechanisms implemented as the sub-submodel MECCA-TAG. The technique constitutes a diagnostic tool that can benefit the investigation of various aspects of kinetic chemistry schemes; at the same time, the designed numerical optimisation reduces the computational effort while keeping important details unaffected. We further focus specifically on the modelling of stable isotopic composition, including the required extensions of the approach. The results of MECCA-TAG are evaluated against the reference sub-submodel MECCA-DBL, which is implicitly full-detailed, but necessarily is sub-optimal in practical applications due to its high computational demands. Furthermore, we evaluate the elaborate carbon and oxygen isotopic mechanism by simulating the multi-isotope composition of CO and other trace gases in the CAABA/MECCA box-model. The mechanism realistically simulates the oxygen isotope composition of key species resulting from the interchange with ozone and main atmospheric reservoirs, as well as the carbon isotope signature transfer. The model adequately reproduces the isotope chemistry features for CO under the limitation of the modelling domain. In particular, the mass-independently fractionated (MIF composition of CO due to reactions of ozone with unsaturated hydrocarbons (a source effect versus its intrinsic MIF enrichment induced in the removal reaction via oxidation by OH is assessed. As for

  9. Ratios among atmospheric trace gases together with winds imply exploitable information for bird navigation: a model elucidating experimental results

    Science.gov (United States)

    Wallraff, H. G.

    2013-11-01

    A model of avian goal-oriented navigation is described that is based on two empirical findings building a bridge from ornithology to atmospheric chemistry. (1) To orient their courses homeward from distant unfamiliar areas, homing pigeons require long-term exposure to undisturbed winds at the home site and olfactory access to the environmental air at home and abroad. (2) Above Germany, ratios among some atmospheric trace gases vary along differently oriented spatial gradients as well as depending on wind direction. The model emulates finding (1) by utilising the analysed air samples on which finding (2) is based. Starting with an available set of 46 omnipresent compounds, virtual pigeons determine the profile of relative weights among them at each of 96 sites regularly distributed around a central home site within a radius of 200 km and compare this profile with corresponding profiles determined at home under varying wind conditions. Referring to particular similarities and dissimilarities depending on home-wind direction, they try to estimate, at each site, the compass direction they should fly in order to approach home. To make the model work, an iterative algorithm imitates evolution by modifying sensitivity to the individual compounds stepwise at random. In the course of thousands of trial-and-error steps it gradually improves homeward orientation by selecting smaller sets of most useful and optimally weighted substances from whose proportional configurations at home and abroad it finally derives navigational performances similar to those accomplished by real pigeons. It is concluded that the dynamic chemical atmosphere most likely contains sufficient spatial information for home-finding over hundreds of kilometres of unfamiliar terrain. The underlying chemo-atmospheric processes remain to be clarified.

  10. Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 1999 Annual Report

    Energy Technology Data Exchange (ETDEWEB)

    Cushman, R.M.

    2000-03-31

    The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global-change data and information analysis center of the Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has--since its inception in 1982--enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO{sub 2}) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO{sub 2} and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea level. CDIAC is located within the Environmental Sciences Division (ESD) at Oak Ridge National Laboratory (ORNL) in Oak Ridge, Tennessee. CDIAC is co-located with ESD researchers investigating global-change topics, such as the global carbon cycle and the effects of carbon dioxide on vegetation. CDIAC staff are also connected with current ORNL research on related topics, such as renewable energy and supercomputing technologies. CDIAC is supported by the Environmental Sciences Division (Jerry Elwood, Acting Director) of DOE's Office of Biological and Environmental Research. CDIAC's FY 1999 budget was 2.2M dollars. CDIAC represents the DOE in the multi-agency Global Change Data and Information System. Bobbi Parra, and Wanda Ferrell on an interim basis, is DOE's Program Manager with responsibility for CDIAC. CDIAC comprises three groups, Global Change Data, Computer Systems, and

  11. Carbon Dioxide Information Analysis Center and World Data Center for Atmospheric Trace Gases Fiscal Year 2001 Annual Report

    Energy Technology Data Exchange (ETDEWEB)

    Cushman, R.M.

    2002-10-15

    The Carbon Dioxide Information Analysis Center (CDIAC), which includes the World Data Center (WDC) for Atmospheric Trace Gases, is the primary global change data and information analysis center of the U.S. Department of Energy (DOE). More than just an archive of data sets and publications, CDIAC has, since its inception in 1982, enhanced the value of its holdings through intensive quality assurance, documentation, and integration. Whereas many traditional data centers are discipline-based (for example, meteorology or oceanography), CDIAC's scope includes potentially anything and everything that would be of value to users concerned with the greenhouse effect and global climate change, including concentrations of carbon dioxide (CO{sub 2}) and other radiatively active gases in the atmosphere; the role of the terrestrial biosphere and the oceans in the biogeochemical cycles of greenhouse gases; emissions of CO{sub 2} and other trace gases to the atmosphere; long-term climate trends; the effects of elevated CO{sub 2} on vegetation; and the vulnerability of coastal areas to rising sea levels. CDIAC is located within the Environmental Sciences Division (ESD) at Oak Ridge National Laboratory (ORNL) in Oak Ridge, Tennessee. CDIAC is co-located with ESD researchers investigating global-change topics, such as the global carbon cycle and the effects of carbon dioxide on climate and vegetation. CDIAC staff are also connected with current ORNL research on related topics, such as renewable energy and supercomputing technologies. CDIAC is supported by the Environmental Sciences Division (Jerry Elwood, Director) of DOE's Office of Biological and Environmental Research. CDIAC represents DOE in the multi-agency Global Change Data and Information System (GCDIS). Wanda Ferrell is DOE's Program Manager with overall responsibility for CDIAC. Roger Dahlman is responsible for CDIAC's AmeriFlux tasks, and Anna Palmisano for CDIAC's Ocean Data tasks. CDIAC is made

  12. A kinetic chemistry tagging technique and its application to modelling the stable isotopic composition of atmospheric trace gases

    Directory of Open Access Journals (Sweden)

    S. Gromov

    2010-08-01

    Full Text Available Isotope composition, in many cases, holds unique information on the sources, chemical modification and sinks of atmospheric trace gases. Vital to the interpretation and use of an increasing number of isotope analyses is appropriate modelling. However, the exact implementation of isotopic information in chemistry-climate models is a challenge, and often studies use simplifications which limit their applicability. Here we implement a thorough isotopic extension in MECCA, a comprehensive kinetic chemistry sub-model. To this end, we devise a generic tagging technique for the kinetic chemistry mechanisms implemented as the sub-submodel MECCA-TAG. The technique is diagnostic and numerically efficient and supports the investigation of various aspects of kinetic chemistry schemes. We focus specifically on the application to the modelling of stable isotopic composition. The results of MECCA-TAG are evaluated against the reference sub-submodel MECCA-DBL, which is implicitly full-detailed, but computationally expensive and thus sub-optimal in practical applications. Furthermore, we evaluate the elaborate carbon and oxygen isotopic mechanism by simulating the multi-isotope composition of CO and other trace gases in the CAABA/MECCA box-model. The mechanism realistically simulates the oxygen isotope composition of key species, as well as the carbon isotope signature transfer. The model adequately reproduces the isotope chemistry features for CO, taking into account the limits of the modelling domain. In particular, the mass-independently fractionated (MIF composition of CO due to reactions of ozone with unsaturated hydrocarbons (a source effect versus its intrinsic MIF enrichment induced in the removal reaction via oxidation by OH is assessed. The simulated ozone source effect was up to +1‰ in Δ17O(CO. The versatile modelling framework we employ (the Modular Earth Submodel System, MESSy opens the way for implementation of the novel detailed

  13. A broadband cavity ringdown spectrometer for in-situ measurements of atmospheric trace gases

    Directory of Open Access Journals (Sweden)

    M. Bitter

    2005-01-01

    Full Text Available This paper describes a broadband cavity ringdown spectrometer and its deployment during the 2002 North Atlantic Marine Boundary Layer Experiment (NAMBLEX to measure ambient concentrations of NO3, N2O5, I2 and OIO at the Mace Head Atmospheric Research Station, Co. Galway, Ireland. The effective absorption path lengths accessible with the spectrometer generally exceeded 10 km, enabling sensitive localised ``point' measurements of atmospheric absorbers to be made adjacent to the other instruments monitoring chemically related species at the same site. For the majority of observations, the spectrometer was used in an open path configuration thereby avoiding surface losses of reactive species. A subset of observations targeted the N2O5 molecule by detecting the additional NO3 formed by the thermal dissociation of N2O5. In all cases the concentrations of the atmospheric absorbers were retrieved by fitting the differential structure in the broadband cavity ringdown spectra using a methodology adapted from long path differential optical absorption spectroscopy. The uncertainty of the retrieval depends crucially on the correct treatment and fitting of the absorption bands due to water vapour, a topic that is discussed in the context of analysing broadband cavity ringdown spectra. The quality of the measurements and the retrieval method are illustrated with representative spectra acquired during NAMBLEX in spectral regions around 660 nm (NO3 and N2O5 and 570 nm (I2 and OIO. Typical detection limits were 1 pptv for NO3 in an integration time of 100 s, 4 pptv for OIO and 20 pptv for I2 in an integration time of 10 min. Additionally, the concentrations of atmospheric water vapour and the aerosol optical extinction were retrieved in both spectral regions. A companion paper in this issue presents the time series of the measurements and discusses their significance for understanding the variability of short lived nitrogen and iodine compounds in the marine

  14. Development of Mid-Infrared Lasers for the Measurement of Trace Atmospheric Gases

    Science.gov (United States)

    Hannun, R. A.; Witinski, M. F.; Forouhar, S.; Anderson, J.

    2012-12-01

    In order to thoroughly characterize atmospheric composition at all altitudes, an unprecedented scientific and technical effort is needed. Essential to the advancement of both satellite and in situ science are improvements in continuous wave (CW) and high-power pulsed laser systems in the infrared spectral region integrated with miniaturized electronic and optical components, allowing for the deployment of single mode light sources aboard satellite and UAV platforms. Sources in the the spectral region from 2.8 μm to 3.5 μm are crucial to the sensitive and precise quantification of several atmospherically relevant species, including: OH, H2O, H218O, HDO, CH4, 13CH4, CO2, CH2O, and C2H6, all of which present strong fundamental vibrational absorptions in this mid-infrared range. Currently, however, a massive technology gap exists in both CW and pulsed laser systems within this spectral window. Recent developments include the advancement of CW tunable diode technology using new solid state materials to improve electron hole localization, and the initial integration of these lasers into miniaturized optoelectronic systems ideal for in situ deployment. In addition, high-power pulsed light sources have been produced using optical parametric generation (OPG). A single-frequency Nd:YAG pumps a nonlinear crystal, injection seeded with a diode laser to enhance efficiency and reduce the bandwidth of the output radiation, creating a light source ideal for LIDAR and other remote sensing applications.

  15. Fourier Transform Infrared (FT-IR) Spectroscopy of Atmospheric Trace Gases HCl, NO and SO2

    Science.gov (United States)

    Haridass, C.; Aw-Musse, A.; Dowdye, E.; Bandyopadhyay, C.; Misra, P.; Okabe, H.

    1998-01-01

    Fourier Transform Infrared (FT-IR) spectral data have been recorded in the spectral region 400-4000/cm of hydrogen chloride and sulfur dioxide with I/cm resolution and of nitric oxide with 0.25 cm-i resolution, under quasi-static conditions, when the sample gas was passed through tubings of aluminum, copper, stainless steel and teflon. The absorbance was measured for the rotational lines of the fundamental bands of (1)H(35)Cl and (1)H(37)Cl for pressures in the range 100-1000 Torr and for the (14)N(16)O molecule in the range 100-300 Torr. The absorbance was also measured for individual rotational lines corresponding to the three modes of vibrations (upsilon(sub 1) - symmetric stretch, upsilon(sub 2) - symmetric bend, upsilon(sub 3) - anti-symmetric stretch) of the SO2 molecule in the pressure range 25-150 Torr. A graph of absorbance versus pressure was plotted for the observed rotational transitions of the three atmospherically significant molecules, and it was found that the absorbance was linearly proportional to the pressure range chosen, thereby validating Beer's law. The absorption cross-sections were determined from the graphical slopes for each rotational transition recorded for the HCl, NO and SO2 species. Qualitative and quantitative spectral changes in the FT-IR data will be discussed to identify and characterize various tubing materials with respect to their absorption features.

  16. Air Quality Impacts of Atmospheric Particles & Trace Gases: Field Studies in Diverse Environments

    Science.gov (United States)

    Mwaniki, George R.

    Air pollution impacts occur at all scales, meaning that policies and air quality management practices must be implemented and coordinated at the local, regional, national, and global scales. This dissertation is part of a continuing effort to improve our understanding of various air quality related issues in different environments. The dissertation consists of four studies. In the first study, wintertime chemical composition of water-soluble particulate matter with aerodynamic diameter less than 2.5 microm (PM2.5) was monitored in the Treasure Valley region near Boise, Idaho. This study was aimed at understanding the major drivers of wintertime PM2.5 within the locality of Boise and its suburbs. From this study, organics and particulate nitrate were the dominant contributors to the PM2.5 mass during wintertime. In the second study, particle size distribution, light scattering coefficient, speciated water soluble PM2.5, and cloud condensation nuclei (CCN) concentration were monitored in a mixed deciduous forest in Northern Michigan during the Community Atmosphere-Biosphere Interactions Experiment (CABINEX-2009). The overall goal of this study was to understand on how emissions of biogenic volatile organic compounds (BVOC) affect the gas-phase and particle-phase chemistry in the near-canopy environment, and the implications on local and regional air quality. From this study aerosol derived from the oxidation of BVOCs exhibited reduced hygroscopicity and CCN activation potential compared to aerosols derived from anthropogenic activities. The third study employed the eddy covariance (EC) technique to understand source-sink interactions of carbon dioxide (CO2), methane (CH 4), carbon monoxide (CO) and nitrous oxide (N2O) in Xi'an, China. In this study urban vegetation were found to play a major role in regulating CO2 emissions within the city while vehicular activities were a major driver for CO and CH4 fluxes. In the fourth study, visibility degradation effects of

  17. Greenhouse Trace Gases in Deadwood

    Science.gov (United States)

    Covey, Kristofer; Bueno de Mesquita, Cliff; Oberle, Brad; Maynard, Dan; Bettigole, Charles; Crowther, Thomas; Duguid, Marlyse; Steven, Blaire; Zanne, Amy; Lapin, Marc; Ashton, Mark; Oliver, Chad; Lee, Xuhui; Bradford, Mark

    2016-04-01

    Deadwood, long recognized as playing an important role in carbon cycling in forest ecosystems, is more recently drawing attention for its potential role in the cycling of other greenhouse trace gases. We report data from four independent studies measuring internal gas concentrations in deadwood in in three Quercus dominated upland forest systems in the Northeastern and Central United States. Mean methane concentrations in deadwood were 23 times atmospheric levels, indicating a lower bound, mean radial wood surface area flux of ~6 x 10-4 μmol CH4 m-2 s-1. Site, decay class, diameter, and species were all highly significant predictors of methane abundance in deadwood, and log diameter and decay stage interacted as important controls limiting methane concentrations in the smallest and most decayed logs. Nitrous oxide concentrations were negatively correlated with methane and on average ~25% lower than ambient, indicating net consumption of nitrous oxide. These data suggest nonstructural carbohydrates fuel archaeal methanogens and confirm the potential for widespread in situ methanogenesis in both living and deadwood. Applying this understanding to estimate methane emissions from microbial activity in living trees implies a potential global flux of 65.6±12.0 Tg CH4 yr-1, more than 20 times greater than currently considered.

  18. Year-round retrievals of trace gases in the Arctic using the Extended-range Atmospheric Emitted Radiance Interferometer

    Directory of Open Access Journals (Sweden)

    Z. Mariani

    2013-06-01

    Full Text Available The Extended-range Atmospheric Emitted Radiance Interferometer (E-AERI was installed at the Polar Environment Atmospheric Research Laboratory (PEARL at Eureka, Nunavut, Canada in October 2008. Spectra from the E-AERI provide information about the radiative balance and budgets of trace gases in the Canadian high Arctic. Measurements are taken every 7 min year-round, including polar night when the solar-viewing spectrometers at PEARL are not operated. This allows E-AERI measurements to fill the gap in the PEARL dataset during the four months of polar night. Measurements were taken year-round in 2008–2009 at the PEARL Ridge Lab, which is 610 m a.s.l. (above sea-level, and from 2011 onwards at the Zero-Altitude PEARL Auxiliary Lab (0PAL, which is at sea level 15 km from the Ridge Lab. Total columns of O3, CO, CH4, and N2O have been retrieved using a modified version of the SFIT2 retrieval algorithm adapted for emission spectra. This provides the first ground-based nighttime measurements of these species at Eureka. Changes in the total columns driven by photochemistry and dynamics are observed. Analyses of E-AERI retrievals indicate accurate spectral fits (root-mean-square residuals consistent with noise and a 10–15% uncertainty in the total column, depending on the trace gas. O3 comparisons between the E-AERI and a Bruker IFS 125HR Fourier transform infrared (FTIR spectrometer, three Brewer spectrophotometers, two UV-visible ground-based spectrometers, and a System D'Analyse par Observations Zenithales (SAOZ at PEARL are made from 2008–2009 and for 2011. 125HR CO, CH4, and N2O columns are also compared with the E-AERI measurements. Mean relative differences between the E-AERI and the other spectrometers are 1–10% (14% is for the un-smoothed profiles, which are less than the E-AERI's total column uncertainties. The E-AERI O3 and CO measurements are well correlated with the other spectrometers (r > 0.92 with the 125HR. The 24 h diurnal cycle

  19. Polar night retrievals of trace gases in the Arctic using the Extended-range Atmospheric Emitted Radiance Interferometer

    Directory of Open Access Journals (Sweden)

    Z. Mariani

    2013-01-01

    Full Text Available The Extended-range Atmospheric Emitted Radiance Interferometer (E-AERI was installed at the Polar Environment Atmospheric Research Laboratory (PEARL at Eureka, Nunavut, Canada in October 2008. Spectra from the E-AERI provide information about the radiative balance and budgets of trace gases in the Canadian high Arctic. Measurements are taken every seven minutes year-round, including polar night when the solar-viewing spectrometers at PEARL are not operated. This allows E-AERI measurements to fill the gap in the PEARL dataset during the four months of polar night. Measurements were taken year-round in 2008–2009 at the PEARL Ridge Lab, which is 610 m above sea-level, and from 2011-onwards at the Zero-Altitude PEARL Auxiliary Lab (0PAL, which is 15 km from the Ridge Lab at sea level. Total columns of O3, CO, CH4, and N2O have been retrieved using a modified version of the SFIT2 retrieval algorithm adapted for emission spectra. This provides the first nighttime measurements of these species at Eureka. Changes in the total columns driven by photochemistry and dynamics are observed. Analyses of E-AERI retrievals indicate accurate spectral fits (root-mean-square residuals < 1.5% and a 10–15% uncertainty in the total column, depending on the trace gas. O3 comparisons between the E-AERI and a Bruker IFS 125HR Fourier transform infrared (FTIR spectrometer, three Brewer spectrophotometers, two UV-visible ground-based spectrometers, and a System D'Analyse par Observations Zenithales (SAOZ at PEARL are made from 2008–2009 and for 2011. 125HR CO, CH4, and N2O columns are also compared with the E-AERI measurements. Mean relative differences between the E-AERI and the other spectrometers are 1–14% (depending on the gas, which are less than the E-AERI's total column uncertainties. The E-AERI O3 and CO measurements are well correlated with the other spectrometers; the best

  20. Uncertainties in the current knowledge of some atmospheric trace gases associated with U.S. agriculture: a review.

    Science.gov (United States)

    Krupa, Sagar; Booker, Fitzerald; Bowersox, Van; Lehmann, Christopher; Lehmann, Chris Topher; Grantz, David

    2008-08-01

    Approximately 80 different crop species are grown in the United States in widely differing geographic areas, climatic and edaphic conditions, and management practices. Although the majority of cultivated acreage in the United States is planted with only about 10 primary crops, uncertainties associated with trace gas emissions arise from: (1) limited data availability, (2) inaccurate estimates because of large temporal and spatial variability in trace gas composition and magnitude of trace gas emissions from agricultural activities, (3) differing characteristics of pollutant emissions from highly dispersed animal feed-lots, and (4) limited understanding of the emissions of semi-volatile organic compounds (SVOCs) associated with agriculture. Although emission issues are of concern, so also is atmospheric deposition to cropping systems, including wet and dry nitrogen, minerals, and organic compounds. These can have feedback effects on trace gas emissions. Overall, the many gaps in our understanding of these aspects of agricultural systems deserve serious attention.

  1. Basic characteristics of atmospheric particles, trace gases and meteorology in a relatively clean Southern African Savannah environment

    Directory of Open Access Journals (Sweden)

    L. Laakso

    2008-08-01

    Full Text Available We have analyzed one year (July 2006–July 2007 of measurement data from a relatively clean background site located in dry savannah in South Africa. The annual-median trace gas concentrations were equal to 0.7 ppb for SO2, 1.4 ppb for NOx, 36 ppb for O3 and 105 ppb for CO. The corresponding PM1, PM2.5 and PM10 concentrations were 9.0, 10.5 and 18.8 μg m−3, and the annual median total particle number concentration in the size range 10–840 nm was 2340 cm−3. During Easterly winds, influence of industrial sources approximately 150 km away from the measurement site was clearly visible, especially in SO2 and NOx concentrations. Of gases, NOx and CO had a clear annual, and SO2, NOx and O3 clear diurnal cycle. Atmospheric new-particle formation was observed to take place in more than 90% of the analyzed days. The days with no new particle formation were cloudy or rainy days. The formation rate of 10 nm particles varied in the range of 0.1–28 cm−3 s−1 (median 1.9 cm−3 s−1 and nucleation mode particle growth rates were in the range 3–21 nm h−1 (median 8.5 nm h−1. Due to high formation and growth rates, observed new particle formation gives a significant contribute to the number of cloud condensation nuclei budget, having a potential to affect the regional climate forcing patterns.

  2. High resolution imaging Fourier transform spectrometer with no moving components for the measurement of atmospheric trace gases

    Science.gov (United States)

    Mortimer, H.

    2014-12-01

    A high resolution Static Imaging Fourier Transform Spectrometer, SIFTS, with no moving parts has been developed for the detection of atmospheric gases. The instrument has been shown to have high spectral resolution (4 cm-1) and temporal resolution (10kHz) resolution in both the mid and near infrared and moderate spectral resolution (14cm-1) in the visible. This instrument has been developed for the remote sensing and in-situ measurements of atmospheric gases. It has been identified that due to the low mass and compact size of the instrument system, that the SIFTS could be deployed as a remote sensing instrument onboard a Earth Observation satellite or Unmanned Aerial Vehicle (UAV), or conversely as a radiosonde instrument for in-situ measurements of atmospheric gases. The technique is based on a static optical configuration whereby light is split into two paths and made to recombine along a focal plane producing an interference pattern. The spectral information is returned using a detector array to digitally capture the interferogram which can then be processed into a spectrum by applying a Fourier transform. As there are no moving components, the speed of measurement is determined by the frame rate of the detector array. Thus, this instrument has a temporal advantage over common Michelson FTIR instruments. Using a high speed Toshiba CCD line array, sensitive over the spectral region of 400 - 1100nm, spectra have been recorded at a rate of one every 100 microseconds. Using an uncooled microbolometer infrared detector array, sensitive over the spectral region of 2 to 15μm, the gases NH3, O3 and CH4 have been used to demonstrate the sensitivity of the SIFTS instrument. It has been shown that the Signal to Noise of the SIFTSMIR is >1200 using an integration time of 77msec. The novel optical design has reduced the optics to only 3 optical components, and the detector array, to generate and measure the interferogram. The experimental performance of the SIFTS instrument

  3. Off-axis measurements of atmospheric trace gases by use of an airborne ultraviolet-visible spectrometer.

    Science.gov (United States)

    Petritoli, Andrea; Ravegnani, Fabrizio; Giovanelli, Giorgio; Bortoli, Daniele; Bonafè, Ubaldo; Kostadinov, Ivan; Oulanovsky, Alexey

    2002-09-20

    An airborne UV-visible spectrometer, the Gas Analyzer Spectrometer Correlating Optical Differences, airborne version (GASCOD/A4pi) was successfully operated during the Airborne Polar Experiment, Geophysica Aircraft in Antarctica airborne campaign from Ushuaia (54 degrees 49' S, 68 degrees 18' W), Argentina in southern spring 1999. The instrument measured scattered solar radiation through three optical windows with a narrow field of view (FOV), one from the zenith, two from the horizontal, as well as actinic fluxes through 2pi FOV radiometric heads. Only a few airborne measurements of scattered solar radiation at different angles from the zenith are available in the literature. With our configuration we attempted to obtain the average line-of-sight concentrations of detectable trace gases. The retrieval method, based on differential optical absorption spectroscopy, is described and results for ozone are shown and compared with measurements from an in situ instrument as the first method of validation.

  4. A pre-processor of trace gases and aerosols emission fields for regional and global atmospheric chemistry models

    Directory of Open Access Journals (Sweden)

    S. R. Freitas

    2010-06-01

    Full Text Available The pre-processor PREP-CHEM-SRC presented in the paper is a comprehensive tool aiming at preparing emissions fields of trace gases and aerosols for use in regional or global transport models. The emissions considered are urban/industrial, biogenic, biomass burning, volcanic, biofuel use and burning from agricultural waste sources from most recent databases or from satellite fire detections for biomass burning. A plumerise model is used to derive the height of smoke emissions from satellite fire products. The pre-processor provides emission fields interpolated onto the transport model grid. Several map projections can be chosen. The way to include these emissions in transport models is also detailed. The pre-processor is coded using Fortran 90 and C and is driven by a namelist allowing the user to choose the type of emissions and the database.

  5. CU AMAX-DOAS applications in cloud-free and cloudy atmospheres: innovative Scattered Sun Light observations of trace gases and aerosol extinction

    Science.gov (United States)

    Volkamer, R.; Baidar, S.; Coburn, S.; Dix, B. K.; Oetjen, H.; Ortega, I.; Sinreich, R.; Atmospeclab

    2011-12-01

    An innovative airborne scanning multi-axis differential optical absorption spectroscopy (CU AMAX-DOAS) instrument has been developed at the University of Colorado, Boulder. The instrument collects scattered sunlight spectra in a sequence of discrete viewing angles, and employs the DOAS method (inherently calibrated, and selective) to simultaneously retrieve multiple trace gases, e.g., nitrogen dioxide (NO2), nitrous acid (HONO), formaldehyde (HCHO), glyoxal (CHOCHO), bromine oxide (BrO), iodine oxide (IO), chlorine dioxide (OClO), water vapor (H2O), and oxygen dimers (O4, at 360nm, 477nm, and 632nm) differential slant column densities (dSCD). Vertical profiles of these gases and multi-spectral aerosol extinction are inferred by combining Monte-Carlo Radiative Transfer Modelling (RTM) and optimal estimation techniques to construct a model atmosphere that can in principle represent 3D clouds and aerosols. The atmospheric state of this model atmosphere is constrained by observations of O4 dSCDs, Raman Scattering Probability (RSP), and intensity ratios, i.e., quantities that depend solely on relative intensity changes, without need for a direct sun view, or absolute radiance calibration. We show results from ongoing validation efforts (NOAA TwinOtter aircraft during CalNex and CARES), and demonstrate vertical profile retrievals (NSF/NCAR GV over the tropical Pacific Ocean) in both cloud-free and cloudy atmospheres.

  6. Soil and litter exchange of reactive trace gases

    Science.gov (United States)

    The soil and litter play an important role in the exchange of trace gases between terrestrial ecosystems and the atmosphere. - The exchange of ammonia between vegetation and the atmosphere is highly influenced by soil and litter emissions especially in managed ecosystems (grassla...

  7. Greenhouse effect of trace gases, 1970-1980

    Science.gov (United States)

    Lacis, A.; Hansen, J.; Lee, P.; Lebedeff, S.; Mitchell, T.

    1981-01-01

    Increased abundances were measured for several trace atmospheric gases in the decade 1970-1980. The equilibrium greenhouse warming for the measured increments of CH4, chlorofluorocarbons and N2O is between 50% and 100% of the equilibrium warming for the measured increase of atmospheric CO2 during the same 10 years. The combined warming of CO2 and trace gases should exceed natural global temperature variability in the 1980's and cause the global mean temperature to rise above the maximum of the late 1930's.

  8. Study of trace gases in the Martian atmosphere: Groundbased observation using SUBARU/IRCS and development of radiative transfer model for MEX/PFS limb observation

    Science.gov (United States)

    Aoki, S.; Nakagawa, H.; Kasaba, Y.; Giuranna, M.; Geminale, A.; Sindoni, G.; Sagawa, H.; Mendrok, J.; Kasai, Y.; Formisano, V.

    2012-09-01

    We observed Martian atmosphere to investigate CH4, H2O, and HDO on 30 November 2011, 4-5 January 2012, and 12 April 2012 using SUBARU/ IRCS. This observation aims to verify CH4 on Mars, constrain its source, and investigate the distribution of H2O/HDO ratio. Our observation covered possible source areas of CH4, i.e. the areas where the extend plumes of CH4 were detected by previous groundbased and MEX/PFS observations [1,2] and the potential mud volcanism areas [3,4]. This paper will show some preliminary results. Vertical profiles of these trace gases are crucial for understanding their chemistry and transportation. Limb observations by MEX/PFS are a powerful tool to retrieve vertical profiles of H2O, CO, and CH4. For this purpose, we adapted the SARTre model, a radiative transfer code which includes multiple scattering for limb geometry observations developed for the terrestrial atmosphere [5], to the Martian atmosphere. In order to validate our model, SARTre model for Martian limb, we first compared of our synthetic spectra in nadir geometry with the result from ARS [6] which has been widely used for previous studies of MEX/PFS nadir-observation. We concluded that the difference between them is small offset (below 3%) in the spectral range between 3000 and 3030 cm-1.

  9. Fiscal Year 1998 Annual Report, Carbon Dioxide Information Analysis Center, World Data Center -- A for Atmospheric Trace Gases

    Energy Technology Data Exchange (ETDEWEB)

    Cushman, R.M.; Boden, T.A.; Hook, L.A.; Jones, S.B.; Kaiser, D.P.; Nelson, T.R.

    1999-03-01

    Once again, the most recent fiscal year was a productive one for the Carbon Dioxide Information Analysis Center (CDIAC) at Oak Ridge National Laboratory (ORNL), as well as a year for change. The FY 1998 in Review section in this report summarizes quite a few new and updated data and information products, and the ''What's Coming in FY 1999'' section describes our plans for this new fiscal year. During FY 1998, CDIAC began a data-management system for AmeriFlux, a long-term study of carbon fluxes between the terrestrial biosphere of the Western Hemisphere and the atmosphere. The specific objectives of AmeriFlux are to establish an infrastructure for guiding, collecting, synthesizing, and disseminating long-term measurements of CO{sub 2}, water, and energy exchange from a variety of ecosystems; collect critical new information to help define the current global CO{sub 2} budget; enable improved predictions of future concentrations of atmospheric CO{sub 2}; and enhance understanding of carbon fluxes. Net Ecosystem Production (NEP), and carbon sequestration in the terrestrial biosphere. The data-management system, available from CDIAC'S AmeriFlux home page (http://cdiac.esd.ornl.gov/programs/ameriflux/ ) is intended to provide consistent, quality-assured, and documented data across all AmeriFlux sites in the US, Canada, Costa Rica, and Brazil. It is being developed by Antoinette Brenkert and Tom Boden, with assistance from Susan Holladay (who joined CDIAC specifically to support the AmeriFlux data-management effort).

  10. Impacts of aerosols on the chemistry of atmospheric trace gases: a case study of peroxides and HO2 radicals

    Directory of Open Access Journals (Sweden)

    H. Liang

    2013-06-01

    Full Text Available Field measurements of atmospheric peroxides were obtained during the summer on two consecutive years over urban Beijing, and focused on the impacts of aerosols on the chemistry of peroxide compounds and hydroperoxyl radicals (HO2. The major peroxides were determined to be hydrogen peroxide (H2O2, methyl hydroperoxide (MHP, and peroxyacetic acid (PAA. A negative correlation was found between H2O2 and PAA in rainwater, providing evidence for a conversion between H2O2 and PAA in the aqueous phase. A standard gas phase chemistry model based on the NCAR Master Mechanism provided a good reproduction of the observed H2O2 profile on non-haze days but greatly overpredicted the H2O2 level on haze days. We attribute this overprediction to the reactive uptake of HO2 by the aerosols, since there was greatly enhanced aerosol loading and aerosol liquid water content on haze days. The discrepancy between the observed and modeled H2O2 can be diminished by adding to the model a newly proposed transition metal ion catalytic mechanism of HO2 in aqueous aerosols. This confirms the importance of the aerosol uptake of HO2 and the subsequent aqueous phase reactions in the reduction of H2O2. The closure of HO2 and H2O2 between the gas and aerosol phases suggests that the aerosols do not have a net reactive uptake of H2O2, because the conversion of HO2 to H2O2 on aerosols compensates for the H2O2 loss. Laboratory studies for the aerosol uptake of H2O2 in the presence of HO2 are urgently required to better understand the aerosol uptake of H2O2 in the real atmosphere.

  11. Climate change and trace gases.

    Science.gov (United States)

    Hansen, James; Sato, Makiko; Kharecha, Pushker; Russell, Gary; Lea, David W; Siddall, Mark

    2007-07-15

    Palaeoclimate data show that the Earth's climate is remarkably sensitive to global forcings. Positive feedbacks predominate. This allows the entire planet to be whipsawed between climate states. One feedback, the 'albedo flip' property of ice/water, provides a powerful trigger mechanism. A climate forcing that 'flips' the albedo of a sufficient portion of an ice sheet can spark a cataclysm. Inertia of ice sheet and ocean provides only moderate delay to ice sheet disintegration and a burst of added global warming. Recent greenhouse gas (GHG) emissions place the Earth perilously close to dramatic climate change that could run out of our control, with great dangers for humans and other creatures. Carbon dioxide (CO2) is the largest human-made climate forcing, but other trace constituents are also important. Only intense simultaneous efforts to slow CO2 emissions and reduce non-CO2 forcings can keep climate within or near the range of the past million years. The most important of the non-CO2 forcings is methane (CH4), as it causes the second largest human-made GHG climate forcing and is the principal cause of increased tropospheric ozone (O3), which is the third largest GHG forcing. Nitrous oxide (N2O) should also be a focus of climate mitigation efforts. Black carbon ('black soot') has a high global warming potential (approx. 2000, 500 and 200 for 20, 100 and 500 years, respectively) and deserves greater attention. Some forcings are especially effective at high latitudes, so concerted efforts to reduce their emissions could preserve Arctic ice, while also having major benefits for human health, agricultural productivity and the global environment.

  12. Greenhouse effect of chlorofluorocarbons and other trace gases

    Science.gov (United States)

    Hansen, James; Lacis, Andrew; Prather, Michael

    1989-01-01

    A comparison is made of the radiative (greenhouse) forcing of the climate system due to changes of atmospheric chlorofluorocarbons and other trace gases. It is found that CFCs, defined to include chlorofluorocarbons, chlorocarbons, and fluorocarbons, now provide about one-quater of current annual increases in anthropogenic greenhouse climate forcing. If the growth rates of CFC production in the early 1970s had continued to the present, current annual growth of climate forcing due to CFCs would exceed that due to CO2.

  13. Method for detecting trace impurities in gases

    Science.gov (United States)

    Freund, S.M.; Maier, W.B. II; Holland, R.F.; Beattie, W.H.

    A technique for considerably improving the sensitivity and specificity of infrared spectrometry as applied to quantitative determination of trace impurities in various carrier or solvent gases is presented. A gas to be examined for impurities is liquefied and infrared absorption spectra of the liquid are obtained. Spectral simplification and number densities of impurities in the optical path are substantially higher than are obtainable in similar gas-phase analyses. Carbon dioxide impurity (approx. 2 ppM) present in commercial Xe and ppM levels of Freon 12 and vinyl chloride added to liquefied air are used to illustrate the method.

  14. Latitudinal distribution of trace gases from biomass burning emissions

    Energy Technology Data Exchange (ETDEWEB)

    Ridder, Theo; Warneke, Thorsten [Institut fuer Umweltphysik, Universitaet Bremen, Otto-Hahn-Allee 1, 28359 Bremen (Germany); Gerbig, Christoph; Jordan, Armin; Rothe, Michael [Max-Planck-Institut fuer Biogeochemie, Hans-Knoell-Str. 10, 07745 Jena (Germany); Schrems, Otto [Alfred-Wegener-Institut fuer Polar- und Meeresforschung, Am Handelshafen 12, 27570 Bremerhaven (Germany)

    2009-07-01

    We study the latitudinal distribution of trace gases in the atmosphere with ground-based Fourier Transform InfraRed (FTIR) Spectrometry and in situ measurements. Our measurements have been performed during several ship cruises on the Atlantic (55 N - 30 S) between the years 1995 and 2005 on board of the research vessel Polarstern. Here we report on the latitudinal variability of trace gases originating from biomass burning emissions. We analyze the distribution of these gases for recent cruises and compare it to the results from former trips. Thereby we concentrate on the distribution of carbon monoxide (CO), which is a suitable tracer for biomass burning. We compare our data to in situ measurements, which have been accomplished during some of our cruises. In situ measurements have been performed by flask sampling and were analyzed by gas chromatography and mass spectrometry. In addition we studied the backward trajectories of air masses to reveal the origin of enhanced trace gas concentrations due to biomass burning emissions.

  15. Influence of orographically induced transport process on the structure of the atmospheric boundary layer and on the distribution of trace gases; Einfluss orographisch induzierter Transportprozesse auf die Struktur der atmosphaerischen Grenzschicht und die Verteilung von Spurengasen

    Energy Technology Data Exchange (ETDEWEB)

    Kossmann, M.

    1998-04-01

    The influence of terrain on the structure of the atmospheric boundary-layer and the distribution of trace gases during periods of high atmospheric pressure was studied by means of meteorological and air-chemical data collected in September 1992 during the TRACT experiment in the transition area between the upper Rhine valley and the northern Black Forest. The emphasis was on the investigation of the development of the convective boundary layer, the formation of thermally induced circulation systems, and the orographic exchange between the atmospheric boundary layer and the free troposphere. Thanks to the extensive measurements, phenomena not yet described in literature could be verified by case studies, and processes that had only been established qualitatively could be quantified. (orig.)

  16. Epiphytic cryptogams as a source of bioaerosols and trace gases

    Science.gov (United States)

    Ruckteschler, Nina; Hrabe de Angelis, Isabella; Zartman, Charles E.; Araùjo, Alessandro; Pöschl, Ulrich; Manzi, Antonio O.; Andreae, Meinrat O.; Pöhlker, Christopher; Weber, Bettina

    2016-04-01

    Cryptogamic covers comprise (cyano-)bacteria, algae, lichens, bryophytes, fungi, and archaea in varying proportions. These organisms do not form flowers, but reproduce by spores or cell cleavage with these reproductive units being dispersed via the atmosphere. As so-called poikilohydric organisms they are unable to regulate their water content, and their physiological activity pattern mainly follows the external water conditions. We hypothesize, that both spore dispersal and the release of trace gases are governed by the moisture patterns of these organisms and thus they could have a greater impact on the atmosphere than previously thought. In order to test this hypothesis, we initiated experiments at the study site Amazonian Tall Tower Observatory (ATTO) in September 2014. We installed microclimate sensors in epiphytic cryptogams at four different heights of a tree to monitor the activity patterns of these organisms. Self-developed moisture probes are used to analyze the water status of the organisms accompanied by light and temperature sensors. The continuously logged data are linked to ongoing measurements of trace gases and particulate bioaerosols to analyze these for the relevance of cryptogams. Here, we are particularly interested in diurnal cycles of coarse mode particles and the atmospheric abundance of fine potassium-rich particles from a currently unknown biogenic source. Based upon the results of this field study we also investigate the bioaerosol and trace gas release patterns of cryptogamic covers under controlled conditions. With this combined approach of field and laboratory experiments we aim to disclose the role of cryptogamic covers in bioaerosol and trace gas release patterns in the Amazonian rainforest.

  17. Climate-chemical interactions and greenhouse effects of trace gases

    Science.gov (United States)

    Shi, Guang-Yu; Fan, Xiao-Biao

    1994-01-01

    A completely coupled one-dimensional radiative-convective (RC) and photochemical-diffusion (PC) model has been developed recently and used to study the climate-chemical interactions. The importance of radiative-chemical interactions within the troposphere and stratosphere has been examined in some detail. We find that increases of radiatively and/or chemically active trace gases such as CO2, CH4 and N2O have both the direct effects and the indirect effects on climate change by changing the atmospheric O3 profile through their interaction with chemical processes in the atmosphere. It is also found that the climatic effect of ozone depends strongly on its vertical distribution throughout the troposphere and stratosphere, as well on its column amount in the atmosphere.

  18. Greenhouse effects due to man-made perturbations of trace gases

    Science.gov (United States)

    Wang, W. C.; Yung, Y. L.; Lacis, A. A.; Mo, T.; Hansen, J. E.

    1976-01-01

    Nitrous oxide, methane, ammonia, and a number of other trace constituents of the earth's atmosphere have infrared absorption bands in the spectral range from 7 to 14 microns. Despite their small amounts, these gases can have a significant effect on the thermal structure of the atmosphere by transmitting most of the thermal radiation from the earth's surface to the lower atmosphere. In the present paper, this greenhouse effect is computed for a number of trace gases. The nature and climatic implications of possible changes in the concentrations of N2O, CH4, NH3, and HNO3 are discussed.

  19. Escape of atmospheric gases from the Moon

    Indian Academy of Sciences (India)

    Da Dao-an; Yang Ya-tian

    2005-12-01

    The escape rate of atmospheric molecules on the Moon is calculated.Based on the assumption that the rates of emission and escape of gases attain equilibrium, the ratio of molecular number densities during day and night, 0/0, can be explained. The plausible emission rate of helium and radioactive elements present in the Moon has also been calculated.

  20. Trace Gases, CO2, Climate, and the Greenhouse Effect.

    Science.gov (United States)

    Aubrecht, Gordon J., II

    1988-01-01

    Reports carbon dioxide and other trace gases can be the cause of the Greenhouse Effect. Discusses some effects of the temperature change and suggests some solutions. Included are several diagrams, graphs, and a table. (YP)

  1. Measurements of trace gases above the tropical forests....

    Science.gov (United States)

    Nicolas-Perea, V.; Monks, P. S.

    2009-04-01

    Measurements of trace gases above the tropical forests; A comparison between ozone levels in the forest and the oil palm plantation areas using the BAe -146 aircraft. The atmospheric composition of Sabah region (Borneo) was sampled using the FAAM BAE-146 instrumented aircraft during July 2008 as part of the OP3 (Oxidant particle photochemical processes above a South East Asia tropical rain forest) project. Tropical forests play an important role in the carbon and energy balance of the Earth (which determine global climate) and are themselves vulnerable to climate change. The tropical biosphere is one of the main sources of reactive trace gas emissions into the global atmosphere, and understanding the role of ozone in these areas is of major importance given the rapid changes in land-use in the tropics. This poster presents preliminary ozone concentrations results collected using the FAAM BAE 146 instrumented aircraft over some of Malaysia most extended oil palm plantations; comparing these with the results recorded when flying over forest areas. Oil palm is becoming one of the most widespread tropical crops; in Malaysia 13% of the land area (4.3Mha) is now oil palm plantations (MPOCP, 2008) compared with 1% in 1974 (FAO, 2005). This poster is expected to show very significant ozone concentrations over the two different landscapes. The set-up of the instruments, the specific sampling sites, as well as the land cover areas will be described.

  2. Ground-based Measurements of Vertical Profiles and Columns of Atmospheric Trace Gases Over Toronto Using a New High-Resolution Fourier Transform Infrared Spectrometer

    Science.gov (United States)

    Wiacek, A.; Yashcov, D.; Strong, K.; Boudreau, L.; Rochette, L.; Roy, C.

    2002-12-01

    The University of Toronto Atmospheric Observatory (TAO) has recently been established at Toronto, Canada. TAO includes several instruments, with a DA8 Fourier Transform Spectrometer (DA8 FTS, manufactured by ABB Bomem Inc., Québec, Canada) serving as the primary instrument at the facility. The geographic position of TAO (43.66°N, 79.40°W) makes it well suited for long-term measurements of mid-latitude stratospheric ozone and related species, while its urban setting enables measurements of tropospheric pollution. The DA8 FTS is based on a Michelson interferometer with a maximum optical path difference of 250 cm, providing a maximum unapodized resolution of 0.0026 cm-1. It is currently equipped with KBr and CaF2 beamsplitters, and InSb and HgCdTe detectors, for coverage of the spectral range from 700 to 4100 cm-1. A new heliostat (manufactured by Aim Controls Inc., California, USA) provides active solar tracking, collecting the incoming solar radiation and directing it into the FTS. The TAO DA8 FTS incorporates a new optical design recently developed by ABB Bomem Inc., which results in a fixed optical axis through the beamsplitter (and a fixed focal point on the detector) as well as a more stable modulation efficiency. The new instrument optics will be discussed. Next, the performance of the instrument will be examined in the context of standard NDSC (Network for the Detection of Stratospheric Change) trace gas column and vertical profile retrieval techniques, which use least squares fitting algorithms (SFIT, SFIT2). TAO has been operational (weather permitting) since October 2001. We have been retrieving columns and vertical profiles of HCl, HF, CH4, OCS, C2H6, CO, N2O and NO2 since May 2002. A detailed error analysis of retrieved columns and vertical profiles has been undertaken for the above species. Future plans for the TAO FTS include comparing our measurements with satellite measurements made by MOPITT, OSIRIS, and the upcoming ACE and MAESTRO instruments

  3. Measurements of atmospheric trace gases by means of matrix-isolation-spectroscopy. Final report. Atmosphaerische Spurengasmessungen mittels Matrix-Isolations-Spektroskopie. Abschlussbericht

    Energy Technology Data Exchange (ETDEWEB)

    Wilson, S.; Griffith, D.; Schuster, G.; Helas, G.

    1988-12-01

    The report describes the results and general experience of project No. 0743188 0 (ATP 88). The method of matrix isolation spectroscopy is described, as are the flights funded during this project. This is followed by tables of the samples taken, by trace elements. Finally, the data measured during all flights are summarized. (orig.).

  4. Use of satellite data to constrain the model-calculated atmospheric lifetime for N2O - Implications for other trace gases

    Science.gov (United States)

    Ko, Malcolm K. W.; Sze, Nien Dak; Weisenstein, Debra K.

    1991-01-01

    Model calculations of the zonal-mean concentrations of N2O in the upper stratosphere are presented showing that about 80 percent of N2O is removed in the stratosphere between 30 deg N and 30 deg S. A comparison of calculated N2O values with remote data on N2O concentrations obtained from Nimbus 7 SAMS instrument indicated that the two-dimensional model of Ko and Sze (1982) may have underestimated the concentration of N2O in the tropical lower stratosphere. It is concluded that the calculated lifetimes for N2O and chlorofluorocarbon-source gases could be 30 percent shorter than previously reported values.

  5. The Global Atmosphere Watch reactive gases measurement network

    Directory of Open Access Journals (Sweden)

    Martin G. Schultz

    2015-10-01

    Full Text Available Abstract Long-term observations of reactive gases in the troposphere are important for understanding trace gas cycles and the oxidation capacity of the atmosphere, assessing impacts of emission changes, verifying numerical model simulations, and quantifying the interactions between short-lived compounds and climate change. The World Meteorological Organization’s (WMO Global Atmosphere Watch (GAW program coordinates a global network of surface stations some of which have measured reactive gases for more than 40 years. Gas species included under this umbrella are ozone, carbon monoxide, nitrogen oxides, and volatile organic compounds (VOCs. There are many challenges involved in setting-up and maintaining such a network over many decades and to ensure that data are of high quality, regularly updated and made easily accessible to users. This overview describes the GAW surface station network of reactive gases, its unique quality management framework, and discusses the data that are available from the central archive. Highlights of data use from the published literature are reviewed, and a brief outlook into the future of GAW is given. This manuscript constitutes the overview of a special feature on GAW reactive gases observations with individual papers reporting on research and data analysis of particular substances being covered by the program.

  6. Rain scavenging of soluble gases by non-evaporating and evaporating droplets from inhomogeneous atmosphere

    Science.gov (United States)

    Elperin, Tov; Fominykh, Andrew; Krasovitov, Boris

    2013-11-01

    We suggest a one-dimensional model of precipitation scavenging of soluble gaseous pollutants by non-evaporating and evaporating droplets that is valid for arbitrary initial vertical distribution of soluble trace gases in the atmosphere. It is shown that for low gradients of soluble trace gases in the atmosphere, scavenging of gaseous pollutants is governed by a linear wave equation that describes propagation of a wave in one direction. The derived equation is solved by the method of characteristics. Scavenging coefficient and the rates of precipitation scavenging are calculated for wet removal of sulfur dioxide (SO2) and ammonia (NH3) using measured initial distributions of trace gases. It is shown that scavenging coefficient for arbitrary initial vertical distribution of soluble trace gases in the atmosphere is non-stationary and height-dependent. In case of exponential initial distribution of soluble trace gases in the atmosphere, scavenging coefficient for non-evaporating droplets in the region between the ground and the position of a scavenging front is a product of rainfall rate, solubility parameter, and the growth constant in the formula for the initial profile of a soluble trace gas in the atmosphere. This expression yields the same estimate of scavenging coefficient for sulfur dioxide scavenging by rain as field estimates presented in McMahon and Denison (1979). It is demonstrated that the smaller the slope of the concentration profile the higher the value of a scavenging coefficient.

  7. Development of Optical Parametric Amplifier for Lidar Measurements of Trace Gases on Earth and Mars

    Science.gov (United States)

    Numata, Kenji; Riris, Haris; Li, Steve; Wu, Stewart; Kawa, Stephen R.; Krainak, Michael; Abshire, James

    2011-01-01

    Trace gases in planetary atmospheres offer important clues as to the origins of the planet's hydrology, geology. atmosphere. and potential for biology. Wc report on the development effort of a nanosecond-pulsed optical parametric amplifier (OPA) for remote trace gas measurements for Mars and Earth. The OP A output light is single frequency with high spectral purity and is widely tunable both at 1600 nm and 3300 nm with an optical-optical conversion efficiency of approximately 40%. We demonstrated open-path atmospheric measurements ofCH4 (3291 nm and 1651 nm). CO2 (1573 nm), H20 (1652 nm) with this laser source.

  8. Adsorption of Atmospheric Gases on Pu Surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Nelson, A J; Holliday, K S; Stanford, J A; Grant, W K; Erler, R G; Allen, P G; McLean, W; Roussel, P

    2012-03-29

    Surface adsorption represents a competition between collision and scattering processes that depend on surface energy, surface structure and temperature. The surface reactivity of the actinides can add additional complexity due to radiological dissociation of the gas and electronic structure. Here we elucidate the chemical bonding of gas molecules adsorbed on Pu metal and oxide surfaces. Atmospheric gas reactions were studied at 190 and 300 K using x-ray photoelectron spectroscopy. Evolution of the Pu 4f and O 1s core-level states were studied as a function of gas dose rates to generate a set of Langmuir isotherms. Results show that the initial gas dose forms Pu{sub 2}O{sub 3} on the Pu metal surface followed by the formation of PuO{sub 2} resulting in a layered oxide structure. This work represents the first steps in determining the activation energy for adsorption of various atmospheric gases on Pu.

  9. Long-Term Changes of Tropospheric Trace Gases over Pakistan Derived From Multiple Satellite Instruments

    Science.gov (United States)

    Zeb, Naila; Fahim Khokhar, Muhammad; Murtaza, Rabbia; Noreen, Asma; Khalid, Tameem

    2016-07-01

    in June (Summer/Monsoon). For NO2, the highest concentrations are observed during Winter and the lowest concentrations are found in Summer/Monsoon. Like TOC, the HCHO showed seasonal maxima during summer and minima during winter. The expected sources are the crop residue burning, biomass/fossil fuel burning for heating purposes, urbanization, industrialization and meterological variations. Further focus is made on exploring the association of trace gases in atmosphere and their source identification.

  10. Measuring Viscosities of Gases at Atmospheric Pressure

    Science.gov (United States)

    Singh, Jag J.; Mall, Gerald H.; Hoshang, Chegini

    1987-01-01

    Variant of general capillary method for measuring viscosities of unknown gases based on use of thermal mass-flowmeter section for direct measurement of pressure drops. In technique, flowmeter serves dual role, providing data for determining volume flow rates and serving as well-characterized capillary-tube section for measurement of differential pressures across it. New method simple, sensitive, and adaptable for absolute or relative viscosity measurements of low-pressure gases. Suited for very complex hydrocarbon mixtures where limitations of classical theory and compositional errors make theoretical calculations less reliable.

  11. Fuel characteristics and trace gases produced through biomass burning

    Directory of Open Access Journals (Sweden)

    BAMBANG HERO SAHARJO

    2010-01-01

    Full Text Available Saharjo BH, Sudo S, Yonemura S, Tsuruta H (2010 Fuel characteristics and trace gases produced through biomass burning. Biodiversitas 11: 40-45. Indonesian 1997/1998 forest fires resulted in forest destruction totally 10 million ha with cost damaged about US$ 10 billion, where more than 1 Gt CO2 has been released during the fire episode and elevating Indonesia to one of the largest polluters of carbon in the world where 22% of world’s carbon dioxide produced. It has been found that 80-90% of the fire comes from estate crops and industrial forest plantation area belongs to the companies which using fire illegally for the land preparation. Because using fire is cheap, easy and quick and also support the companies purpose in achieving yearly planted area target. Forest management and land use practices in Sumatra and Kalimantan have evolved very rapidly over the past three decades. Poor logging practices resulted in large amounts of waste will left in the forest, greatly elevating fire hazard. Failure by the government and concessionaires to protect logged forests and close old logging roads led to and invasion of the forest by agricultural settlers whose land clearances practices increased the risk of fire. Several field experiments had been done in order to know the quality and the quantity of trace produced during biomass burning in peat grass, peat soil and alang-alang grassland located in South Sumatra, Indonesia. Result of research show that different characteristics of fuel burned will have the different level also in trace gasses produced. Peat grass with higher fuel load burned produce more trace gasses compared to alang-alang grassland and peat soil.

  12. Emissions of organic trace gases from savanna fires in southern Africa during the 1992 Southern African Fire Atmosphere Research Initiative and their impact on the formation of tropospheric ozone

    Science.gov (United States)

    Koppmann, R.; Khedim, A.; Rudolph, J.; Poppe, D.; Andreae, M. O.; Helas, G.; Welling, M.; Zenker, T.

    1997-08-01

    CO, CH4, and organic trace gases were measured in air samples collected during several flights with a DC-3 aircraft through the plumes from savanna fires and agricultural fires during the SAFARI 92 campaign in southern Africa in September and October 1992. In all samples a variety of higher molecular weight organic compounds was found, most of which are very reactive. More than 70 of the roughly 140 major components present could be identified. Typically, mixing ratios of several hundred parts per billion carbon of organic compounds were measured inside the plumes, corresponding to an emission ratio of total organic carbon relative to CO2 of up to 1%. About 50% of these emissions were in the form of oxygenated and unsaturated compounds. The contributions of still unknown compounds to the total emission of organic compounds add up to another 20-30%. The observed emission ratios relative to CO2 show a considerable variation depending on the fuel type and the burning stages of the fire. The lowest value of the emission ratio of the sum of all identified organic compounds relative to CO2 was found for a sugar cane fire with (1.7±0.7)×10-3 (ppb C/ppb CO2). For a large savanna fire in Kruger National Park the ratio was (7.4±1.6)×10-3 (ppb C/ppb CO2). The highest value was (13.7±0.9)×10-3 (ppb C/ppb CO2) for an uncontrolled fire of mainly wood and shrub in the Drakensberg region. Results of model calculations show that in biomass-burning plumes, reactive organic compounds contribute significantly to the formation of ozone, especially during the initial phase of photochemical processing.

  13. Biosignature Gases in H2-Dominated Atmospheres on Rocky Exoplanets

    CERN Document Server

    Seager, S; Hu, R

    2013-01-01

    (Abridged) Super Earth exoplanets are being discovered with increasing frequency and some will be able to retain stable H2-dominated atmospheres. We study biosignature gases on exoplanets with thin H2 atmospheres and habitable surface temperatures, by using a model atmosphere with photochemistry, and biomass estimate framework for evaluating the plausibilty of a range of biosignature gas candidates. We find that photochemically produced H atoms are the most abundant reactive species in H2 atmospheres. In atmospheres with high CO2 levels, atomic O is the major destructive species for some molecules. In sun-Earth-like UV radiation environments, H (and in some cases O) will rapidly destroy nearly all biosignature gases of interest. The lower UV fluxes from UV quiet M stars would produce a lower concentration of H (or O) for the same scenario, enabling some biosignature gases to accumulate. The favorability of low-UV radiation environments to in an H2 atmosphere is closely analogous to the case of oxidized atmosp...

  14. Physics of Atmospheric Electric Discharges in Gases: An Informal Introduction

    CERN Document Server

    Treumann, R A; Parrot, M

    2007-01-01

    A short account of the physics of electrical discharges in gases is given in view of its historical evolution and application to planetary atmospheres. As such it serves as an introduction to the articles on particular aspects of electric discharges contained in this book, in particular in the chapters on lightning and the violent discharges which in the recent two decades have been observed to take place in Earth's upper atmosphere. In addition of briefly reviewing the early history of gas discharge physics we discuss the main parameters affecting violent atmospheric discharges like collision frequency, mean free path and critical electric field strength. Any discharge current in the atmosphere is clearly carried only by electrons. Above the lower bound of the mesosphere the electrons must be considered magnetized with the conductivity becoming a tensor. Moreover, the collisional mean free path in the upper atmosphere becomes relatively large which lowers the critical electric field there and more easily ena...

  15. MAX-DOAS aerosol and trace gases measurements in megacities in China

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xin [Institut fuer Energie- und Klimaforschung, Forschungszentrum Juelich (Germany); College of Environmental Science and Engineering Peking University, Beijing (China); Brauers, Theo [Institut fuer Energie- und Klimaforschung, Forschungszentrum Juelich (Germany); Shao, Min [College of Environmental Science and Engineering Peking University, Beijing (China)

    2011-07-01

    Multi Axis Differential Optical Absorption Spectroscopy (MAXDOAS) is a new remote sensing technique to measure atmospheric trace gases. Compared to other areas in the world, the atmospheric observations in megacities in China are rather limited. We present MAX-DOAS measurements at four sites in Beijing and Guangzhou in 2006 and 2008. At each site, the scattered sunlight was recorded at 7 elevation angles for about 1 months. Using the zenith spectrum as reference, the Differential Slant Column Densities (DSCDs) of HCHO, CHOCHO, O{sub 4} and NO{sub 2} at offaxis viewing geometries were derived from the DOAS fit. These DSCDs were simulated using a backward Monte Carlo radiative transfer model. The aerosol and trace gas profiles were defined by 3 parameters: the integrated quantities (T), the height of the surface layer (H), and the fraction of T below H. We fitted the modeled values to the measured values at the corresponding viewing geometries by varying the 3 parameters. The aerosol extinction and the boundary layer height were successfully retrieved from the measured O{sub 4} DSCDs as well as ground level concentrations of CHOCHO, HCHO, and NO{sub 2}, the latter being compared to simultaneous in-situ measurements.

  16. Characteristics of Fine Particles in an Urban Atmosphere—Relationships with Meteorological Parameters and Trace Gases

    Directory of Open Access Journals (Sweden)

    Tianhao Zhang

    2016-08-01

    Full Text Available Atmospheric fine particles (diameter < 1 μm attract a growing global health concern and have increased in urban areas that have a strong link to nucleation, traffic emissions, and industrial emissions. To reveal the characteristics of fine particles in an industrial city of a developing country, two-year measurements of particle number size distribution (15.1 nm–661 nm, meteorological parameters, and trace gases were made in the city of Wuhan located in central China from June 2012 to May 2014. The annual average particle number concentrations in the nucleation mode (15.1 nm–30 nm, Aitken mode (30 nm–100 nm, and accumulation mode (100 nm–661 nm reached 4923 cm−3, 12193 cm−3 and 4801 cm−3, respectively. Based on Pearson coefficients between particle number concentrations and meteorological parameters, precipitation and temperature both had significantly negative relationships with particle number concentrations, whereas atmospheric pressure was positively correlated with the particle number concentrations. The diurnal variation of number concentration in nucleation mode particles correlated closely with photochemical processes in all four seasons. At the same time, distinct growth of particles from nucleation mode to Aitken mode was only found in spring, summer, and autumn. The two peaks of Aitken mode and accumulation mode particles in morning and evening corresponded obviously to traffic exhaust emissions peaks. A phenomenon of “repeated, short-lived” nucleation events have been created to explain the durability of high particle concentrations, which was instigated by exogenous pollutants, during winter in a case analysis of Wuhan. Measurements of hourly trace gases and segmental meteorological factors were applied as proxies for complex chemical reactions and dense industrial activities. The results of this study offer reasonable estimations of particle impacts and provide references for emissions control strategies in

  17. The CU Airborne MAX-DOAS instrument: vertical profiling of aerosol extinction and trace gases

    Science.gov (United States)

    Baidar, S.; Oetjen, H.; Coburn, S.; Dix, B.; Ortega, I.; Sinreich, R.; Volkamer, R.

    2013-03-01

    The University of Colorado Airborne Multi-Axis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS) instrument uses solar stray light to detect and quantify multiple trace gases, including nitrogen dioxide (NO2), glyoxal (CHOCHO), formaldehyde (HCHO), water vapor (H2O), nitrous acid (HONO), iodine monoxide (IO), bromine monoxide (BrO), and oxygen dimers (O4) at multiple wavelengths (absorption bands at 360, 477, 577, 632 nm) simultaneously in the open atmosphere. The instrument is unique as it (1) features a motion compensation system that decouples the telescope field of view from aircraft movements in real time (CHOCHO, HCHO, and H2O concentrations and aerosol extinction coefficients, ɛ, at 477 nm calculated from O4 measurements from a low approach at Brackett airfield inside the South Coast Air Basin (SCAB) are presented. These profiles contain ~12 degrees of freedom (DOF) over a 3.5 km altitude range, an independent information approximately every 250 m. The boundary layer NO2 concentration, and the integral aerosol extinction over height (aerosol optical depth, AOD) agrees well with nearby ground-based in situ NO2 measurement, and AERONET station. The detection limits of NO2, CHOCHO, HCHO, H2O442, ϵ360, ϵ477 for 30 s integration time spectra recorded forward of the plane are 5 ppt, 3 ppt, 100 ppt, 42 ppm, 0.004 km-1, 0.002 km-1 in the free troposphere (FT), and 30 ppt, 16 ppt, 540 ppt, 252 ppm, 0.012 km-1, 0.006 km-1 inside the boundary layer (BL), respectively. Mobile column observations of trace gases and aerosols are complimentary to in situ observations, and help bridge the spatial scales that are probed by satellites and ground-based observations, and predicted by atmospheric models.

  18. Development of 2-D-MAX-DOAS and retrievals of trace gases and aerosols optical properties

    Science.gov (United States)

    Ortega, Ivan

    Air pollution is a major problem worldwide that adversely a_ects human health, impacts ecosystems and climate. In the atmosphere, there are hundreds of important compounds participating in complex atmospheric reactions linked to air quality and climate. Aerosols are relevant because they modify the radiation balance, a_ect clouds, and thus Earth albedo. The amount of aerosol is often characterized by the vertical integral through the entire height of the atmosphere of the logarithm fraction of incident light that is extinguished called Aerosol Optical Depth (AOD). The AOD at 550 nm (AOD550) over land is 0.19 (multi annual global mean), and that over oceans is 0.13. About 43 % of the Earth surface shows AOD550 smaller than 0.1. There is a need for measurement techniques that are optimized to measure aerosol optical properties under low AOD conditions, sample spatial scales that resemble satellite ground-pixels and atmospheric models, and help integrate remote sensing and in-situ observations to obtain optical closure on the effects of aerosols and trace gases in our changing environment. In this work, I present the recent development of the University of Colorado two dimensional (2-D) Multi-AXis Differential Optical Absorption Spectroscopy (2-D-MAX-DOAS) instrument to measure the azimuth and altitude distribution of trace gases and aerosol optical properties simultaneously with a single instrument. The instrument measures solar scattered light from any direction in the sky, including direct sun light in the hyperspectral domain. In Chapter 2, I describe the capabilities of 2-D measurements in the context of retrievals of azimuth distributions of nitrogen dioxide (NO2), formaldehyde (HCHO), and glyoxal (CHOCHO), which are precursors for tropospheric O3 and aerosols. The measurements were carried out during the Multi-Axis DOAS Comparison campaign for Aerosols and Trace gases (MAD-CAT) campaign in Mainz, Germany and show the ability to bridge spatial scales to

  19. Exomars orbiter science and data-relay mission / looking for trace gases on Mars

    Science.gov (United States)

    Fratacci, Olivier

    EXOMARS Orbiter Module: looking for trace gas on Mars and providing data relay support for future Mars Surface assets O.Fratacci, M.Mesrine, H.Renault, Thales Alenia Space France B.Musetti, M.Montagna, Thales Alenia Space Italy M.Kesselmann, M.Barczewski OHB P.Mitschdoerfer, D.Dellantonio Euro-pean Space Agency / ESTEC The European Space Agency (ESA) in a joint cooperation with NASA, will launch in 2016 the EXOMARS spacecraft composite to develop European landing technologies and provide a science orbiter with data-relay capability around Mars until end 2022. The spacecraft composite is composed of the Orbitr Module (OM), provided by TAS-France, an entry descent and landing demonstrator module (EDM) provided by TAS-Italy, and a set of six scientific payloads to be selected by the JPL during 2010. Recent observations of the planet Mars have indicated detection of methane as well as temporal, perhaps spatial variability in the detected signal while current photochemical models cannot explain the presence of methane in the atmosphere of Mars nor its reported rapid variations in space and time. The triple scientific objectives that drive the selection of these six instruments for the Exomars 2016 mission is to detect trace gases in Mars atmosphere, to characterise their spatial and temporal variation and to explore the source of the key trace gases (e.g. methane) on the surface. The launch is scheduled in January 2016 from Kennedy Space Center (KSC) using an ATLAS V 421 launcher with a total launch mass of 4.4 tons. After release of the EDM on Mars, the OM will perform the Mars Orbit Insertion manoeuvre and then reduce its elliptic orbit by implementing the first European Aerobraking around Mars for about 6 to 9 months, to finally end on a circular 400x400km orbit with an altitude in the range of 350km to 420km. From this orbit, a science phase will follow lasting 2 years in which the Mars atmosphere and surface is continuously observed. Science instruments composed of

  20. MASERATI: a new rocket-borne diode laser absorption spectrometer for in-situ measurement of trace gases in the middle and upper atmosphere; MASERATI: Ein neues raketengetragenes Diodenlaser-Absorptionsspektrometer zur in situ-Messung von Spurengasen in der mittleren und oberen Atmosphaere

    Energy Technology Data Exchange (ETDEWEB)

    Lucke, H. von

    1999-09-01

    MASERATI (middle atmosphere spectrometric experiment on Rockets for the analysis of trace gas influences) is the first rocket-borne tunable diode laser absorption spectrometer (TDLAS). It was developed to measure water vapor and carbon dioxide in the altitude range from 50 to 90 km and 120 km, respectively. Infrared absorption spectroscopy using two laser diodes is applied to measure both trace gases simultaneously. The laser beams are sent into an open multiple-pass absorption setup mounted on top of the sounding rocket. High sensitivity is achieved by means of frequency modulation and lock-in techniques. The results of several tests performed in the laboratory demonstrate that the instrument is capable of detecting relative absorbances down to 10{sup -4} - 10{sup -5} when integrating spectra for 1 s. Two almost identical MASERATI instruments have been built and launched on sounding rockets from the Andoeya rocket range (69 N, 16 E) in northern Norway during winter 1997/98. The results of these flights demonstrate that MASERATI is a new suitable tool for in situ studies of the mesosphere and lower thermosphere. (orig.)

  1. Miniaturized Laser Heterodyne Radiometer (LHR) for Measurements of Greenhouse Gases in the Atmospheric Column

    Science.gov (United States)

    Steel, Emily; McLinden, Matthew

    2012-01-01

    This passive laser heterodyne radiometer (LHR) instrument simultaneously measures multiple trace gases in the atmospheric column including carbon dioxide (CO2) and methane (CH4), and resolves their concentrations at different altitudes. This instrument has been designed to operate in tandem with the passive aerosol sensor currently used in AERONET (an established network of more than 450 ground aerosol monitoring instruments worldwide). Because aerosols induce a radiative effect that influences terrestrial carbon exchange, simultaneous detection of aerosols with these key carbon cycle gases offers a uniquely comprehensive measurement approach. Laser heterodyne radiometry is a technique for detecting weak signals that was adapted from radio receiver technology. In a radio receiver, a weak input signal from a radio antenna is mixed with a stronger local oscillator signal. The mixed signal (beat note, or intermediate frequency) has a frequency equal to the difference between the input signal and the local oscillator. The intermediate frequency is amplified and sent to a detector that extracts the audio from the signal. In the LHR instrument described here, sunlight that has undergone absorption by the trace gas is mixed with laser light at a frequency matched to a trace gas absorption feature in the infrared (IR). Mixing results in a beat signal in the RF (radio frequency) region that can be related to the atmospheric concentration. For a one-second integration, the estimated column sensitivities are 0.1 ppmv for CO2, and Greenhouse gases Observational SATellite). The only network that currently measures CO2 and CH4 in the atmospheric column is TCCON (Total Carbon Column Observing Network), and only two of its 16 operational sites are in the United States. TCCON data is used for validation of GOSAT data, and will be used for OCO-2 validation. While these Fourier-transform spectrometers (FTS) can measure the largest range of trace gases, the network is severely limited

  2. Knudsen cell: Investigations about the uptake of important traces gases on ambient airborne mineral dust

    Science.gov (United States)

    Horn, Sabrina; Herrmann, Hartmut

    2013-04-01

    Mineral dust constitutes one of the largest mass fractions of natural aerosol. Its emission is estimated between 800 - 2000 Tg/a]. The dust is emitted through sand and dust storms in the arid regions of our planet, in particular by the great desserts such as the Sahara. The complex chemical composition of mineral dust is similar to crust material, because the dust is produced by soil erosion. The main components of mineral dust are SiO2 and Al2O3, whereas the active oxides (Fe2O3, TiO2) show some variety in content due to the dust source region. Mineral dust particles can be transported over several 1000 km and during its transport the surface can be changed by the uptake of water vapor and trace gases. On such modified surfaces homo- and heterogeneous reactions can occur. Trace gas uptakes play an important role in atmospheric chemistry as sinks or sources for several gaseous species. Hence, it is necessary to study these reactions. Among several experimental setups, the Knudsen cell is one of the promising tools to study reactive uptakes from the gas phase and the release of products formed by dust surface-mediated reactions. The Knudsen cell, implemented by Golden et al. in 1975, is a high vacuum flow reactor operating under molecular flow conditions, i.e., gas-wall collisions are highly preferred over gas-gas collisions. Despite several Knudsen cell studies examining the reaction between different traces gases and model dust surfaces constituted of not more than a few components, no measurements utilizing collected ambient mineral dust are done so far. For a better understanding of the chemistry on mineral dust surfaces gas uptake measurements will be done with a Knudsen cell. The first measurements are done with isopropanol on TiO2. Afterwards there are studies with different substrates like, Al2O3 (α- and γ-phase), FeO2, Arizona test dust, air collected mineral dust from the Cap Verde islands. In the beginning SO2, NO2 and HNO3 will be used.

  3. The CU Airborne MAX-DOAS instrument: vertical profiling of aerosol extinction and trace gases

    Directory of Open Access Journals (Sweden)

    S. Baidar

    2013-03-01

    Full Text Available The University of Colorado Airborne Multi-Axis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS instrument uses solar stray light to detect and quantify multiple trace gases, including nitrogen dioxide (NO2, glyoxal (CHOCHO, formaldehyde (HCHO, water vapor (H2O, nitrous acid (HONO, iodine monoxide (IO, bromine monoxide (BrO, and oxygen dimers (O4 at multiple wavelengths (absorption bands at 360, 477, 577, 632 nm simultaneously in the open atmosphere. The instrument is unique as it (1 features a motion compensation system that decouples the telescope field of view from aircraft movements in real time ( The instrument is described, and data from flights over California during the CalNex (California Research at the Nexus of Air Quality and Climate Change and CARES (Carbonaceous Aerosols and Radiative Effects Study air quality field campaigns is presented. Horizontal distributions of NO2 VCD (below the aircraft maps are sampled with typically 1 km resolution, and show good agreement with two ground-based MAX-DOAS instruments (slope = 0.95 ± 0.09, R2 = 0.86. As a case study vertical profiles of NO2, CHOCHO, HCHO, and H2O concentrations and aerosol extinction coefficients, ε, at 477 nm calculated from O4 measurements from a low approach at Brackett airfield inside the South Coast Air Basin (SCAB are presented. These profiles contain ~12 degrees of freedom (DOF over a 3.5 km altitude range, an independent information approximately every 250 m. The boundary layer NO2 concentration, and the integral aerosol extinction over height (aerosol optical depth, AOD agrees well with nearby ground-based in situ NO2 measurement, and AERONET station. The detection limits of NO2, CHOCHO, HCHO, H2O442, ϵ360, ϵ477 for 30 s integration time spectra recorded forward of the plane are 5 ppt, 3 ppt, 100 ppt, 42 ppm, 0.004 km−1, 0.002 km−1 in the free troposphere (FT, and 30 ppt, 16 ppt, 540 ppt, 252 ppm, 0.012 km−1, 0.006 km−1

  4. Remote sensing of atmospheric greenhouse gases: bridging spatial scales

    Science.gov (United States)

    Humpage, N.; Boesch, H.; Parker, R.; Hewson, W.; Sembhi, H.; Somkuti, P.; Webb, A.; Palmer, P. I.; Feng, L.

    2015-12-01

    Observed atmospheric variations of greenhouse gases (GHG) are determined by surface-atmosphere exchange, and atmospheric chemistry and transport. These processes occur over a wide spectrum of spatial and temporal scales. Confronting atmospheric transport models and ultimately improving the fidelity of surface flux estimates demands an integrated observing system that captures these scales. We will discuss using data the role of GHG remote sensing instruments and argue that our ability to deploy them from the ground and to fly them on satellite, aircraft, and unmanned airborne vehicles (UAV) mean that they represent the ideal technology to bridge the observed scales of variability. We will discuss a five-year record of global-scale column observations of CO2 and CH4 from the Japanese GOSAT satellite instrument that is available from University of Leicester as part of the ESA Climate Change Initiative. We will showcase new CO2 and CH4 column data that was collected by our shortwave infrared spectrometer GHOST oboard the NASA Global Hak during a regional survey over the eastern Pacific during early spring 2015, which included coincident overpasses from GOSAT and the NASA OCO-2. These data are being used to test atmospheric transport models over remote regions and to help validate satellite observations over the oceans. We will also discuss GHOST data collected on the UK Dornier 226 research aircraft to measure local-scale measurements over Leicester city centre, a major power plant, and downwind of a controlled Cumbrian heathland fire. Finally, we will report preliminary results from a new ground-based Fourier transform spectrometer station at Harwell (80 km west of London). We anticipate that this site will eventually join the TCCON network, which has been used to validation of satellite observations.

  5. In situ measurements and modeling of reactive trace gases in a small biomass burning plume

    Science.gov (United States)

    Müller, Markus; Anderson, Bruce E.; Beyersdorf, Andreas J.; Crawford, James H.; Diskin, Glenn S.; Eichler, Philipp; Fried, Alan; Keutsch, Frank N.; Mikoviny, Tomas; Thornhill, Kenneth L.; Walega, James G.; Weinheimer, Andrew J.; Yang, Melissa; Yokelson, Robert J.; Wisthaler, Armin

    2016-03-01

    An instrumented NASA P-3B aircraft was used for airborne sampling of trace gases in a plume that had emanated from a small forest understory fire in Georgia, USA. The plume was sampled at its origin to derive emission factors and followed ˜ 13.6 km downwind to observe chemical changes during the first hour of atmospheric aging. The P-3B payload included a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS), which measured non-methane organic gases (NMOGs) at unprecedented spatiotemporal resolution (10 m spatial/0.1 s temporal). Quantitative emission data are reported for CO2, CO, NO, NO2, HONO, NH3, and 16 NMOGs (formaldehyde, methanol, acetonitrile, propene, acetaldehyde, formic acid, acetone plus its isomer propanal, acetic acid plus its isomer glycolaldehyde, furan, isoprene plus isomeric pentadienes and cyclopentene, methyl vinyl ketone plus its isomers crotonaldehyde and methacrolein, methylglyoxal, hydroxy acetone plus its isomers methyl acetate and propionic acid, benzene, 2,3-butanedione, and 2-furfural) with molar emission ratios relative to CO larger than 1 ppbV ppmV-1. Formaldehyde, acetaldehyde, 2-furfural, and methanol dominated NMOG emissions. No NMOGs with more than 10 carbon atoms were observed at mixing ratios larger than 50 pptV ppmV-1 CO. Downwind plume chemistry was investigated using the observations and a 0-D photochemical box model simulation. The model was run on a nearly explicit chemical mechanism (MCM v3.3) and initialized with measured emission data. Ozone formation during the first hour of atmospheric aging was well captured by the model, with carbonyls (formaldehyde, acetaldehyde, 2,3-butanedione, methylglyoxal, 2-furfural) in addition to CO and CH4 being the main drivers of peroxy radical chemistry. The model also accurately reproduced the sequestration of NOx into peroxyacetyl nitrate (PAN) and the OH-initiated degradation of furan and 2-furfural at an average OH concentration of 7.45 ± 1.07 × 106 cm-3 in the

  6. Effects of traces of molecular gases (hydrogen, nitrogen) in glow discharges in noble gases

    Science.gov (United States)

    Steers, E. B. M.; Smid, P.; Hoffmann, V.

    2008-07-01

    The "Grimm" type of low pressure glow discharge source, introduced some forty years ago, has proved to be a versatile analytical source. A flat sample is used as the cathode and placed about 0.2mm away from the end of a hollow tubular anode leading to an obstructed discharge. When the source was first developed, it was used for the direct analysis of solid metallic samples by optical emission spectroscopy (OES), normally with argon as the plasma gas; it was soon found that, using suitable electrical parameters, the cathode material was sputtered uniformly from a circular crater of diameter equal to that of the tubular anode, so that the technique could be used for compositional depth profile analysis (CDPA). Over the years the capability and applications of the technique have steadily increased. The use of rf powered discharges now permits the analysis of non-conducting layers and samples; improved instrumental design now allows CDPA of ever thinner layers (e.g. resolution of layers 5 nm thick in multilayer stacks is possible). For the original bulk material application, pre-sputtering could be used to remove any surface contamination but for CDPA, analysis must start immediately the discharge is ignited, so that any surface contamination can introduce molecular gases into the plasma gas and have significant analytical consequences, especially for very thin layers; in addition, many types of samples now analysed contain molecular gases as components (either as occluded gas, or e.g. as a nitride or oxide), and this gas enters the discharge when the sample is sputtered. It is therefore important to investigate the effect of such foreign gases on the discharge, in particular on the spectral intensities and hence the analytical results. The presentation will concentrate mainly on the effect of hydrogen in argon discharges, in the concentration range 0-2 % v/v but other gas mixtures (e.g. Ar/N_2, Ne/H_2) will be considered for comparison. In general, the introduction of

  7. Observations of trace gases and aerosols over the Indian Ocean during the monsoon transition period

    Digital Repository Service at National Institute of Oceanography (India)

    Mandal, T.K.; Khan, A; Ahammed, Y.N; Tanwar, R.S.; Parmar, R.S.; Zalpuri, K.S.; Gupta, P.K.; Jain, S.L.; Singh, R.; Mitra, A; Garg, S.C.; Suryanarayana, A; Murty, V.S.N; DileepKumar, M.; Shepherd, A.J.

    Characteristics of trace gases (O sub(3), CO, CO sub(2), CH sub(4) and N sub(2)O) and aerosols (particle size of 2.5 micron) were studied over the Arabian Sea, equatorial Indian Ocean and southwest part of the Bay of Bengal during the monsoon...

  8. A sensitivity study for far infrared balloon-borne limb emission sounding of stratospheric trace gases

    Directory of Open Access Journals (Sweden)

    J. Xu

    2013-05-01

    Full Text Available This paper presents a sensitivity study performed for trace gases retrieval from synthetic observations by TELIS (TErahertz and submillimeter LImb Sounder which is a stratospheric balloon-borne cryogenic heterodyne spectrometer. Issues pertaining to hydroxyl radical (OH retrieval from the far infrared measurements by the 1.8 THz channel are addressed. The study is conducted by a retrieval code PILS (Profile Inversion for Limb Sounding developed to solve the nonlinear inverse problems arising in the analysis of infrared/microwave limb sounding measurements. PILS combines a line-by-line forward model with automatic differentiation for computing Jacobians and employs regularized nonlinear least squares inversion. We examine the application of direct and iterative regularization methods and evaluate the performance of single- and multi-profile retrievals. Sensitivities to expected errors in calibration procedure, instrumental knowledge and atmospheric profiles have been analyzed. Nonlinearity effect, inaccurate sideband ratio, and pointing error turned out to be the dominant error sources. Furthermore, the capability of multi-channel simultaneous retrieval from the far infrared and submillimeter data has been investigated. The errors and averaging kernels infer that the quality of the obtained hydrogen chloride (HCl can be improved by significantly better exploitation of information from the observations.

  9. Convective Transport of Trace Gases in the Maritime Continent

    Science.gov (United States)

    Harris, Neil

    2015-04-01

    Passage of air through the Tropical Tropopause Layer (TTL) is the major route for troposphere to stratosphere transport. The UK CAST (Co-ordinated Airborne Studies in the Tropics) campaign took place in the West Pacific in January/February 2014. The field campaign was based mainly in Guam (13.5oN, 144.8oE) and had three components: CAST with the NERC FAAM BAe-146 research aircraft; the NASA ATTREX project based around the Global Hawk; the NCAR-led CONTRAST campaign based around the Gulfstream V (HIAPER) aircraft. Together, these aircraft were able to make detailed measurements of atmospheric structure and composition from the ocean surface to 20 km. The CAST team also made ground-based and ozonesonde measurements at the ARM site on Manus Island in Papua New Guinea during February 2014, and halocarbon measurements were made at several West Pacific sites. I will present an overview of the CAST campaign along with the results of high resolution global Unified Model studies and NAME (Numerical Atmospheric-dispersion Modelling Environment) trajectory calculations to look at the transport of air into the TTL in convective systems over the Maritime continent and West Pacific. I will focus on the transport of air from in and around the boundary layer and will assess the possible importance of natural and anthropogenic emissions for TTL composition.

  10. Measurements of organic gases during aerosol formation events in the boreal forest atmosphere during QUEST

    Directory of Open Access Journals (Sweden)

    K. Sellegri

    2004-08-01

    Full Text Available Biogenic VOCs are important in the growth and possibly also in the formation of atmospheric aerosol particles. In this work, we present 10 min-time resolution measurements of organic trace gases at Hyytiälä, Finland during March 2002. The measurements were part of the project QUEST (Quantification of Aerosol Nucleation in the European Boundary Layer and took place during a two-week period when nucleation events occurred with various intensities nearly every day. Using a ground-based Chemical Ionization Mass Spectrometer (CIMS instrument, the following trace gases were detected: acetone, TMA, DMA, mass 68 amu (candidate=isoprene, monoterpenes, Methyl Vinyl Ketone (MVK and Methacrolein (MaCR, cis-3-hexenyl acetate and MonoTerpene Oxidation Products (MTOP. For all of them except for the amines, we present daily variations during different classes of event days, and non-event days. Isoprene, monoterpenes, MVK+MaCR, cis-3-hexenyl acetate and MTOP are found to show significant correlations with the condensational sink (CS, which indicates that a fraction of these compounds are participating to the growth of the nucleated particles and generally secondary organic aerosol formation. Moreover, the terpene oxidation products (TOP (MVK, MaCR and MTOP show a higher ratio to the CS on event days compared to non-event days, indicating that their abundance relative to the surface of aerosol available is higher on nucleation days.

  11. A novel aircraft-based tandem mass spectrometer for atmospheric ion and trace gas measurements

    Science.gov (United States)

    Moehler, O.; Reiner, Th.; Arnold, F.

    1993-05-01

    The general design and operation of a novel aircraft-based triple-quadrupole mass spectrometer (TQMS) developed for the improved detection and collisional analysis of atmospheric ions and trace gases are described. The instrument is also suitable for laboratory collision-induced dissociation measurements, studies of ion-molecule reactions, and analytical applications. Highly sensitive and selective trace gas detection by chemical ionization mass spectrometry is also possible using a novel ion injection technique. Result of aircraft-based measurements made with the TQMS are summarized.

  12. Anaerobic Metabolism: Linkages to Trace Gases and Aerobic Processes

    Science.gov (United States)

    Megonigal, J. P.; Hines, M. E.; Visscher, P. T.

    2003-12-01

    Life evolved and flourished in the absence of molecular oxygen (O2). As the O2 content of the atmosphere rose to the present level of 21% beginning about two billion years ago, anaerobic metabolism was gradually supplanted by aerobic metabolism. Anaerobic environments have persisted on Earth despite the transformation to an oxidized state because of the combined influence of water and organic matter. Molecular oxygen diffuses about 104 times more slowly through water than air, and organic matter supports a large biotic O2 demand that consumes the supply faster than it is replaced by diffusion. Such conditions exist in wetlands, rivers, estuaries, coastal marine sediments, aquifers, anoxic water columns, sewage digesters, landfills, the intestinal tracts of animals, and the rumen of herbivores. Anaerobic microsites are also embedded in oxic environments such as upland soils and marine water columns. Appreciable rates of aerobic respiration are restricted to areas that are in direct contact with air or those inhabited by organisms that produce O2.Rising atmospheric O2 reduced the global area of anaerobic habitat, but enhanced the overall rate of anaerobic metabolism (at least on an area basis) by increasing the supply of electron donors and acceptors. Organic carbon production increased dramatically, as did oxidized forms of nitrogen, manganese, iron, sulfur, and many other elements. In contemporary anaerobic ecosystems, nearly all of the reducing power is derived from photosynthesis, and most of it eventually returns to O2, the most electronegative electron acceptor that is abundant. This photosynthetically driven redox gradient has been thoroughly exploited by aerobic and anaerobic microorganisms for metabolism. The same is true of hydrothermal vents (Tunnicliffe, 1992) and some deep subsurface environments ( Chapelle et al., 2002), where thermal energy is the ultimate source of the reducing power.Although anaerobic habitats are currently a small fraction of Earth

  13. A Nanoparticulate Photocatalytic Filter for Removal of Trace Contaminant Gases Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Maintaining a healthy atmosphere in closed life support systems is essential for crew well being and success of space missions. Current trace contaminant control...

  14. A Nanoparticulate Photocatalytic Filter for Removal of Trace Contaminant Gases Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Maintaining a healthy atmosphere in closed life support systems is necessary for the well being of the crew and success of a space mission. Current trace contaminant...

  15. 1988 Pilot Institute on Global Change on trace gases and the biosphere

    Energy Technology Data Exchange (ETDEWEB)

    Eddy, J.A.; Moore, B. III

    1998-07-01

    This proposal seeks multi-agency funding to conduct an international, multidisciplinary 1988 Pilot Institute on Global Change to take place from August 7 through 21, 1988, on the topic: Trace Gases and the Biosphere. The institute, to be held in Snowmass, Colorado, is envisioned as a pilot version of a continuing series of institutes on Global Change (IGC). This proposal seeks support for the 1988 pilot institute only. The concept and structure for the continuing series, and the definition of the 1988 pilot institute, were developed at an intensive and multidisciplinary Summer Institute Planning Meeting in Boulder, Colorado, on August 24--25, 1987. The theme for the 1988 PIGC, Trace Gases and the Biosphere, will focus a concerted, high-level multidisciplinary effort on a scientific problem central to the Global Change Program. Dramatic year-to-year increases in the global concentrations of radiatively-active trace gases such as methane and carbon dioxide are now well documented. The predicted climatic effects of these changes lend special urgency to efforts to study the biospheric sources and sinks of these gases and to clarify their interactions and role in the geosphere-biosphere system.

  16. A Fourier transform infrared trace gas analyser for atmospheric applications

    Directory of Open Access Journals (Sweden)

    D. W. T. Griffith

    2012-05-01

    Full Text Available Concern in recent decades about human impacts on Earth's climate has led to the need for improved and expanded measurement capabilities for greenhouse gases in the atmosphere. In this paper we describe in detail an in situ trace gas analyser based on Fourier Transform Infrared (FTIR spectroscopy that is capable of simultaneous and continuous measurements of carbon dioxide (CO2, methane (CH4, carbon monoxide (CO, nitrous oxide (N2O and 13C in CO2 in air with high precision and accuracy. Stable water isotopes can also be measured in undried airstreams. The analyser is automated and allows unattended operation with minimal operator intervention. Precision and accuracy meet and exceed the compatibility targets set by the World Meteorological Organisation – Global Atmosphere Watch Programme for baseline measurements in the unpolluted troposphere for all species except 13C in CO2.

    The analyser is mobile and well suited to fixed sites, tower measurements, mobile platforms and campaign-based measurements. The isotopic specificity of the optically-based technique and analysis allows application of the analyser in isotopic tracer experiments, for example 13C in CO2 and 15N in N2O. We review a number of applications illustrating use of the analyser in clean air monitoring, micrometeorological flux and tower measurements, mobile measurements on a train, and soil flux chamber measurements.

  17. Relationship between epiphytic lichens, trace elements and gaseous atmospheric pollutants

    NARCIS (Netherlands)

    Dobben, van H.F.; Wamelink, G.W.W.; Braak, ter C.J.F.

    2001-01-01

    A study was conducted to determine the joint effect of gaseous atmospheric pollutants and trace elements on epiphytic lichens. We used our data to test the hypothesis that lichens are generally insensitive to toxic effects of trace elements, and can therefore be used as accumulator organisms to esti

  18. Quantum cascade laser-based spectrometer for high sensitive measurements of trace gases in air

    Institute of Scientific and Technical Information of China (English)

    Yuanyuan Tang; Wenqing Liu; Ruifeng Kan; Yujun Zhang; Dong Chen; Shuai Zhang; Jun Ruan

    2012-01-01

    A quantum cascade (QC) laser-based spectrometer is developed to measure trace gases in air.The proposed spectrometer is tested for N2O,and the results presented in this letter.This system takes advantage of recent technology in QC lasers by utilizing intra-pulse scan spectroscopy,which allows high sensitive measurement.Without calibration gases,the gas concentration can be calculated with scan integration and the corresponding values from the HITRAN04 database.By analyzing the Allan variance,a detection limit of 2 ppb is obtained.Continuous measurement of N2O sampled from ambient air shows the applicability of the proposed system for the field measurements of gases of environmental concern.

  19. WMO WDCGG data report. GAW data. Volume IV - greenhouse gases and other atmospheric gases. WDCGG No. 25

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-03-01

    The report contains data on the concentrations of greenhouse gases and related gases in the atmosphere and the oceans. This report contains monthly and annual mean values collected from January 1998 to October 2000 on global, regional and local scales, together with information on observation stations. Gases include: carbon dioxide, methane, nitrous oxide, carbon monoxide, nitrogen dioxide, nitrogen monoxide, sulphur dioxide, chlorofluorocarbons, tetrachloroethane, trichloroethane and trichloromethane. Trends in concentrations and growth rates presented mainly in graphical form for observation stations around the world. Tables list concentrations of gases, over periods covered at all reporting stations with average growth rates per year and also regression equations of trends. Geographical locations of observation stations are also listed.

  20. Two-dimensional observation of atmospheric trace gases based on the differential optical absorption sp ectroscopy technique%基于差分吸收光谱技术的大气痕量气体二维观测方法∗

    Institute of Scientific and Technical Information of China (English)

    刘进; 邹莹; 司福祺; 周海金; 窦科; 王煜; 刘文清

    2015-01-01

    A two-dimensional observation method of atmospheric trace gases based on differential optical absorption spec-troscopy technique is reported in this paper. The conventional multi-axis differential absorption spectrum system is improved to make the telescope point to different directions. Thereby, the trace gas information of different azimuthal angles and consequently the distribution and variation of pollution gases around the measurement point can be obtained simultaneously. Using this method, NO2 concentration and distribution as well as O4 slant column densities are ob-tained. High degree of similarity is shown between O4 slant column density simulated by radiation transfer model and the measured data. Based on the measured O4 data, light path information can also be extracted. By combining with radiation transfer model, the light path differences caused by different profile modifications are corrected. The corrected NO2 slant column density is further converted into the volume mixing ratio. By comparing the calculated NO2 mixing ratio with the long-path-differential optical absorption spectroscopy data, the results show good consistency with each other.%基于差分吸收光谱技术,对大气痕量气体二维观测方法进行研究。对常规多轴差分吸收光谱系统进行改进,使望远镜可指向不同方位角,获取测量点各方位角上的痕量气体信息,从而更直观地了解测量点四周污染气体分布及其演变情况。主要对NO2浓度分布进行了研究,同时获取了不同方位角上的O4斜柱浓度;采用辐射传输模型模拟计算O4斜柱浓度并与实测数据对比,结果表明二者具有高度相关性,验证了大气中O4分布的稳定性;基于实测O4数据提取光路信息,结合辐射传输模型对NO2和O4因廓线不同造成的散射路径差异进行修正,将NO2斜柱浓度进一步转化为体积混合比,获得了不同方位角上NO2浓度分布图。将计算结果与

  1. Assessment of TRACE Condensation Model Against Reflux Condensation Tests with Noncondensable Gases

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Kyung Won; Cheong, Ae Ju; Shin, Andong; Suh, Nam Duk [Korea Institute of Nuclear Safety, Daejeon (Korea, Republic of)

    2015-05-15

    The TRACE is the latest in a series of advanced, best-estimated reactor systems code developed by U.S. Nuclear Regulatory Commission for analyzing transient and steady-state neutronic-thermal-hydraulic behavior in light water reactors. This special model is expected to replace the default model in a future code release after sufficient testing has been completed. This study assesses the special condensation model of TRACE 5.0-patch4 against the counter-current flow configuration. For this purpose, the predicted results of special model are compared to the experimental and to those of default model. The KAST reflux condensation test with NC gases are used in this assessment. We assessed the special model for film condensation of TRACE 5.0-patch4 against the data of the reflux condensation test in the presence of NC gases. The special condensation model of TRACE provides a reasonable estimate of HTC with good agreement at the low inlet steam flow rate.

  2. L'effet de serre par le CO2 et les gaz traces Greenhouse Effect from CO2 and Trace Gases

    Directory of Open Access Journals (Sweden)

    Bertrand A.

    2006-11-01

    , mainly from combustion and deforestation, and have been progressively accumulating in the Earth's atmosphere, could result in a greenhouse effect that could cause the heating up of the Earth by several degrees in the 21st century. The climatic consequences (melting of ice, etc. would be disastrous. Therefore, we examined the leading parameters involved in this phenomenon: nature of the greenhouse effect, carbon cycle, CO2 transfer on a worldwide scale, trace gases, climatic consequences of the greenhouse effect due to CO2 and trace gases. We reached the following conclusions:(a The CO2 and trace-gas concentration in the atmosphere increases exponentially in the absence of any regulations, and this occurs at the same time as human production of the same substances also at an exponential rate. (b No increase has as yet been detected in the Earth's average temperature due to the greenhouse effect. Moreover, since 1940 we have been going through a period of cooling. (c Human activity also produces antagonistic cooling effects (effect of dust in the atmosphere, etc. that are rather poorly understood. (d The study of ancient climates indicates a regular succession of cool and warm periods, which should reassure us about any sudden and irreversible change in the climate. (e However, it is absolutely necessary to improve our fundamental understanding of the main factors governing the Earth's climate (chemistry of the atmosphere, ocean/ atmosphere transfers, etc. and eventually to limit the production of some trace gases (Freon, in particular.

  3. Numerical sensitivity study of the nocturnal low-level jet over a forest canopy and implications for nocturnal surface exchange of carbon dioxide and other trace gases

    DEFF Research Database (Denmark)

    Sogachev, Andrey; Leclerc, M.Y.; Duarte, H.F.

    2010-01-01

    in the nocturnal boundary layer, several studies demonstrated the role of nocturnal jets in transporting moisture, ozone, and other trace gases between the biosphere and the lower atmosphere (Mathieu et al., 2005; Karipot et al., 2006; 2007; 2008; 2009). This study suggests that SCADIS, because of its simplicity...... and low computational demand, has potential as a research tool regarding surface–atmosphere gaseous exchange in the nocturnal boundary layer, especially if carbon dioxide, water vapor, ozone and other gases are released or deposited inside the forest canopy.......The development of a wind speed maximum in the nocturnal boundary layer, commonly referred to as a low-level jet (LLJ) (Blackadar, 1957), is a common feature of the vertical structure of the atmospheric boundary layer (ABL) and impacts the meteorology and the local climate of a region. A variety...

  4. Dynamics of a geothermal field traced by noble gases: Cerro Prieto, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Mazor, E. (Weizmann Inst. of Science, Rehovot, Israel); Truesdell, A.H.

    1981-01-01

    Noble gases have been measured mass spectrometrically in samples collected during 1977 from producing wells at Cerro Prieto. Positive correlations between concentrations of radiogenic (He, /sup 40/Ar) and atmospheric noble gases (Ne, Ar, and Kr) suggest the following dynamic model: the geothermal fluids originated from meteoric water penetrated to more than 2500 m depth (below the level of first boiling) and mixed with radiogenic helium and argon-40 formed in the aquifer rocks. Subsequently, small amounts of steam were lost by a Raleigh process (0 to 3%) and mixing with shallow cold water occurred (0 to 30%). Noble gases are sensitive tracers of boiling in the initial stages of 0 to 3% steam separation and complement other tracers, such as Cl or temperature, which are effective only beyond this range.

  5. Dynamics of a geothermal field traced by noble gases: Cerro Prieto, Mexico

    Science.gov (United States)

    Mazor, E.; Truesdell, A.H.

    1984-01-01

    Noble gases have been measured mass spectrometrically in samples collected during 1977 from producing wells at Cerro Prieto. Positive correlations between concentrations of radiogenic (He and 40Ar) and atmospheric noble gases (Ne, Ar and Kr) suggest the following dynamic model: the geothermal fluids originated from meteoric water that penetrated to more than 2500 m depth (below the level of first boiling) and mixed with radiogenic He and 40Ar formed in the aquifer rocks. Subsequently, small amounts of steam were lost by a Raleigh process (0 - 30%) and mixing with shallow cold water occurred (0 - 30%). Noble gases are sensitive tracers of boiling in the initial stages of 0 - 3% steam separation and complement other tracers, such as C1 or temperature, which are effective only beyond this range. ?? 1984.

  6. One year observations of atmospheric reactive gases (O3, CO, NOx, SO2) at Jang Bogo base in Terra Nova Bay, Antarctica

    Science.gov (United States)

    Siek Rhee, Tae; Seo, Sora

    2016-04-01

    Antarctica is a remote area surrounded by the Southern Ocean and far from the influence of human activities, giving us unique opportunity to investigate the background variation of trace gases which are sensitive to the human activities. Korean Antarctic base, Jang Bogo, was established as a unique permanent overwintering base in Terra Nova Bay in February, 2014. One year later, we installed a package of instruments to monitor atmospheric trace gases at the base, which includes long-lived greenhouse gases, CO2, CH4, and N2O, and reactive gases, O3, CO, NOx, and SO2. The atmospheric chemistry observatory, where these scientific instruments were installed, is located ca. 1 km far from the main building and power plant, minimizing the influence of pollution that may come from the operation of the base. Here we focus on the reactive gases measured in-situ at the base; O3 displays a typical seasonal variation with high in winter and low in summer with seasonal amplitude of ~18 ppb, CO was high in September at ~56 ppb, probably implying the invasion of lower latitude air mass with biomass burning, and low in late summer due to photochemical oxidation. NO did not show clear seasonal variation, but SO2 reveals larger values in summer than in winter. We will discuss potential atmospheric processes behind these first observations of reactive gases in Terra Nova Bay, Antarctica.

  7. 3-DoF MAX-DOAS: A new method for deriving free tropospheric columns of marine trace gases from ground

    Science.gov (United States)

    Coburn, S.; Baidar, S.; Ortega, I.; Sinreich, R.; Volkamer, R.

    2013-12-01

    Current retrievals of Multi-AXis Differential Optical Absorption Spectroscopy (MAX-DOAS) measurements from the surface focus on retrieving boundary layer vertical profiles and vertical column amounts of atmospheric trace gases in the lower atmosphere. We have expanded these retrievals, and combine a high signal-to-noise MAX-DOAS instrument with an in-depth treatment of radiative transfer modeling of the suns movement to show that we can decouple the partial vertical column of trace gases located in the free troposphere from that in the boundary layer. The approach is demonstrated using our long-term (9 months) of MAX-DOAS observations of iodine oxide (IO), bromine oxide (BrO), glyoxal (CHOCHO) and formaldehyde (HCHO) near Pensacola, FL. Boundary layer profiles are derived from measurements at shallow looking elevation angles. In a second inversion we utilize MAX-DOAS angles still containing information above the boundary layer in order to assess total tropospheric columns (up to ~13km). The free tropospheric column is then derived by difference of the total column minus the boundary layer partial column. We apply this technique to several trace gases measured in the coastal marine troposphere including IO, BrO, CHOCHO, and HCHO, and discuss implications of our findings in context with recent aircraft observations by the TORERO project.

  8. Analytical representation of elastic scattering cross sections of low energy electrons by atmospheric gases

    Science.gov (United States)

    Ivanov, V. Y.; Sipov, N. K.; Shneyder, V. A.

    1977-01-01

    Analytical representations of the elastic scattering cross sections of electrons with energies of 0.01-1 keV in atmospheric gases of N2, O2, O are given. These representations are suitable for the Monte Carlo method.

  9. Atmospheric transport of trace elements and nutrients to the oceans

    Science.gov (United States)

    Jickells, T. D.; Baker, A. R.; Chance, R.

    2016-11-01

    This paper reviews atmospheric inputs of trace elements and nutrients to the oceans in the context of the GEOTRACES programme and provides new data from two Atlantic GEOTRACES cruises. We consider the deposition of nitrogen to the oceans, which is now dominated by anthropogenic emissions, the deposition of mineral dust and related trace elements, and the deposition of other trace elements which have a mixture of anthropogenic and dust sources. We then consider the solubility (as a surrogate for bioavailability) of the various elements. We consider briefly the sources, atmospheric transport and transformations of these elements and how this results in strong spatial deposition gradients. Solubility of the trace elements also varies systematically between elements, reflecting their sources and cycling, and for some trace elements there are also systematic gradients in solubility related to dust loading. Together, these effects create strong spatial gradients in the inputs of bioavailable trace elements to the oceans, and we are only just beginning to understand how these affect ocean biogeochemistry. This article is part of the themed issue 'Biological and climatic impacts of ocean trace element chemistry'.

  10. Pi-MAX: a new parametrized algorithm to retrieve vertical profiles of trace gases and aerosols from MAX-DOAS measurements

    Science.gov (United States)

    Remmers, Julia; Beirle, Steffen; Doerner, Steffen; Wagner, Thomas

    2013-04-01

    Multi-Axis (MAX-) DOAS instruments observe scattered sunlight under various mostly slant elevation angles. From such observations information on tropospheric profiles of trace gases and aerosols can be retrieved. MAX-DOAS observations can be used to quantify emissions and to study chemical processes in the atmosphere. Measuring (horizontally and vertically) averaged concentrations the technique can be used as a link between in-situ and satellite measurements. Thus satellite observations of tropospheric trace gases can be validated. IMAX (Parametrized Inversion for MAX-DOAS measurements) is a parametrized method to retrieve vertical profiles of trace gases (such as H2O, NO2, HCHO, CHOCHO) and aerosols. No online calculations are necessary, since look-up tables (LUT) calculated with a Monte Carlo based radiative Transport Model are used. In this manner it is user-friendly, easy to distribute and applicable to every measurement location. The here shown measurements took place in the Maldives in March, 2012, during the CARDEX campaign. Simultaneous sun photometry-, Lidar- and UAV-measurements provide the possibility to validate the new algorithm. We present time series of profiles of trace gas concentrations and aerosol extinction We discuss the effects of clouds on the retrieved results.

  11. Analysis of Process Gases and Trace Contaminants in Membrane-Aerated Gaseous Effluent Streams.

    Science.gov (United States)

    Coutts, Janelle L.; Lunn, Griffin Michael; Meyer, Caitlin E.

    2015-01-01

    In membrane-aerated biofilm reactors (MABRs), hollow fibers are used to supply oxygen to the biofilms and bulk fluid. A pressure and concentration gradient between the inner volume of the fibers and the reactor reservoir drives oxygen mass transport across the fibers toward the bulk solution, providing the fiber-adhered biofilm with oxygen. Conversely, bacterial metabolic gases from the bulk liquid, as well as from the biofilm, move opposite to the flow of oxygen, entering the hollow fiber and out of the reactor. Metabolic gases are excellent indicators of biofilm vitality, and can aid in microbial identification. Certain gases can be indicative of system perturbations and control anomalies, or potentially unwanted biological processes occurring within the reactor. In confined environments, such as those found during spaceflight, it is important to understand what compounds are being stripped from the reactor and potentially released into the crew cabin to determine the appropriateness or the requirement for additional mitigation factors. Reactor effluent gas analysis focused on samples provided from Kennedy Space Center's sub-scale MABRs, as well as Johnson Space Center's full-scale MABRs, using infrared spectroscopy and gas chromatography techniques. Process gases, such as carbon dioxide, oxygen, nitrogen, nitrogen dioxide, and nitrous oxide, were quantified to monitor reactor operations. Solid Phase Microextraction (SPME) GC-MS analysis was used to identify trace volatile compounds. Compounds of interest were subsequently quantified. Reactor supply air was examined to establish target compound baseline concentrations. Concentration levels were compared to average ISS concentration values and/or Spacecraft Maximum Allowable Concentration (SMAC) levels where appropriate. Based on a review of to-date results, current trace contaminant control systems (TCCS) currently on board the ISS should be able to handle the added load from bioreactor systems without the need

  12. Trace Molecules in Giant Planet Atmospheres

    Science.gov (United States)

    Huestis, D. L.; Smith, G. P.

    2010-12-01

    Chemical kinetics matters in the upper atmospheres of giant planets in our solar system and in extrasolar systems. The composition of a volume of gas depends not only on where it is, but also on how it got there. The giant planets in our own solar system still have much to teach us about what we will be observing on extrasolar giant planets and how to interpret what we observe. Some molecules, such as CO, C2H2, C2H6, PH3, and NH3, which we call tracer molecules, provide remotely observable signatures of vertical transport. PH3 and NH3 especially have complicated thermochemistry and chemical kinetics that, until recently, have been poorly understood. Based on analysis of recent literature, we have identified new chemical mechanisms for interconverting NH3 and N2 and for interconverting PH3 and NH4-H2PO4.

  13. Evolution of trace gases and particles emitted by a chaparral fire in California

    Directory of Open Access Journals (Sweden)

    S. K. Akagi

    2011-08-01

    Full Text Available Biomass burning (BB is a major global source of trace gases and particles. Accurately representing the production and evolution of these emissions is an important goal for atmospheric chemical transport models. We measured a suite of gases and aerosols emitted from an 81 ha prescribed fire in chaparral fuels on the central coast of California, US on 17 November 2009. We also measured post-emission chemical changes in the isolated downwind plume for ~4 h of smoke aging. The measurements were carried out on board a Twin Otter aircraft outfitted with an airborne Fourier transform infrared spectrometer (AFTIR, aerosol mass spectrometer (AMS, single particle soot photometer (SP2, nephelometer, LiCor CO2 analyzer, a chemiluminescence ozone instrument, and a wing-mounted meteorological probe. Our measurements included: CO2; CO; NOx; NH3; non-methane organic compounds; organic aerosol (OA; inorganic aerosol (nitrate, ammonium, sulfate, and chloride; aerosol light scattering; refractory black carbon (rBC; and ambient temperature, relative humidity, barometric pressure, and three-dimensional wind velocity. The molar ratio of excess O3 to excess CO in the plume (ΔO3/ΔCO increased from −0.005 to 0.102 in 4.5 h. Excess acetic and formic acid (normalized to excess CO increased by factors of 1.7 ± 0.4 and 7.3 ± 3.0 (respectively over the same aging period. Based on the rapid decay of C2H4 we infer an in-plume average OH concentration of 5.3 (±1.0 × 106 molecules cm−3, consistent with previous studies showing elevated OH concentrations in biomass burning plumes. Ammonium, nitrate, and sulfate all increased with plume aging. The observed ammonium increase was a factor of 3.9 ± 2.6 in about 4 h, but accounted for just ~36 % of the gaseous ammonia lost on a molar basis. Some of the gas phase NH3 loss may have been due to condensation

  14. Evolution of trace gases and particles emitted by a chaparral fire in California

    Directory of Open Access Journals (Sweden)

    C. E. Wold

    2012-02-01

    Full Text Available Biomass burning (BB is a major global source of trace gases and particles. Accurately representing the production and evolution of these emissions is an important goal for atmospheric chemical transport models. We measured a suite of gases and aerosols emitted from an 81 hectare prescribed fire in chaparral fuels on the central coast of California, US on 17 November 2009. We also measured physical and chemical changes that occurred in the isolated downwind plume in the first ~4 h after emission. The measurements were carried out onboard a Twin Otter aircraft outfitted with an airborne Fourier transform infrared spectrometer (AFTIR, aerosol mass spectrometer (AMS, single particle soot photometer (SP2, nephelometer, LiCor CO2 analyzer, a chemiluminescence ozone instrument, and a wing-mounted meteorological probe. Our measurements included: CO2; CO; NOx; NH3; non-methane organic compounds; organic aerosol (OA; inorganic aerosol (nitrate, ammonium, sulfate, and chloride; aerosol light scattering; refractory black carbon (rBC; and ambient temperature, relative humidity, barometric pressure, and three-dimensional wind velocity. The molar ratio of excess O3 to excess CO in the plume (ΔO3/ΔCO increased from −5.13 (±1.13 × 10−3 to 10.2 (±2.16 × 10−2 in ~4.5 h following smoke emission. Excess acetic and formic acid (normalized to excess CO increased by factors of 1.73 ± 0.43 and 7.34 ± 3.03 (respectively over the same time since emission. Based on the rapid decay of C2H4 we infer an in-plume average OH concentration of 5.27 (±0.97 × 106 molec cm−3, consistent with previous studies showing elevated OH concentrations in biomass burning plumes. Ammonium, nitrate, and sulfate all increased over the course of 4 h. The observed ammonium increase was a factor of 3.90 ± 2.93 in about 4 h, but accounted for just ~36

  15. WMO WDCGG data catalogue. GAW data. Volume IV - Greenhouse gases and other atmospheric gases

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-03-01

    The fourth issue of the data catalogue gives information on measurement methods, instruments, and data handling procedures for recording data on greenhouse gases at the observation stations submitting data to the WDCGG up to December 2000. Chapter 1 gives details of the observation stations; Chapter 2, the data index, is prepared to give notice of the data. Chapter 3 contains detail of the observation programme: category and location, date when observation started, instrument manufacturers, characteristics of instrument system calibration methods, and data selection procedures. It gives references on the observation programme at each station. Gases measured are: carbon dioxide, methane, nitrous oxide, chlorofluorocarbons, hydrochlorofluorocarbons, hydrofluorocarbons, tetrachloromethane, trichloroethane, trichloromethane, carbon monoxide, nitrogen monoxide, nitrogen oxides, odd nitrogen, nitrogen dioxide, sulphur dioxide, volatile organic compounds (VOCs), organic peroxides, hydrogen peroxide, and isotopes ({sup 13}C). 3 apps.

  16. The ray-tracing mapping operator in an asymmetric atmosphere

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    In a spherically symmetric atmosphere, the refractive index profile is retrieved from bending angle measurements through Abel integral transform. As horizontal refractivity inhomogeneity becomes significant in the moist low atmosphere, the error in refractivity profile obtained from Abel inversion reaches about 10%. One way to avoid this error is to directly assimilate bending angle profile into numerical weather models. This paper discusses the 2D ray-tracing mapping operator for bending angle in an asymmetric atmosphere. Through simulating computations, the retrieval error of the refractivity in horizontal inhomogeneity is assessed. The step length of 4 rank Runge-Kutta method is also tested.

  17. Atmospheric contamination: A possible source for heavy noble gases in basalts from Loihi Seamount, Hawaii

    Energy Technology Data Exchange (ETDEWEB)

    Patterson, D.B.; Honda, M.; McDougall, I. (Australian National Univ., Canberra (Australia))

    1990-05-01

    Re-evaluation of available noble gas data obtained from the glassy rims of basalts from Loihi Seamount, Hawaii, shows that contamination of magmas prior to eruption, by addition of a significant component of atmosphere-derived heavy noble gases, is a plausible explanation for the observed atmosphere-like isotopic compositions of Ne, Ar, Kr, and Xe. The most likely source for the atmospheric component is interaction of the magma with seawater carrying dissolved atmosphere-derived noble gases. The possibility of a significant atmospheric component in Loihi samples suggests that the observed heavy noble gas compositions may not be representative of the mantle source of Loihi magmas. While leaving open the question of the noble gas composition in the source region, atmospheric contamination provides a valid alternative to the interpretation that the mantle source region of Loihi magmas has an atmosphere-like noble gas composition.

  18. The CU Airborne MAX-DOAS instrument: ground based validation, and vertical profiling of aerosol extinction and trace gases

    Science.gov (United States)

    Baidar, S.; Oetjen, H.; Coburn, S.; Dix, B.; Ortega, I.; Sinreich, R.; Volkamer, R.

    2012-09-01

    The University of Colorado Airborne Multi Axis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS) instrument uses solar stray light remote sensing to detect and quantify multiple trace gases, including nitrogen dioxide (NO2), glyoxal (CHOCHO), formaldehyde (HCHO), water vapor (H2O), nitrous acid (HONO), iodine monoxide (IO), bromine monoxide (BrO), and oxygen dimers (O4) at multiple wavelengths (360 nm, 477 nm, 577 nm and 632 nm) simultaneously, and sensitively in the open atmosphere. The instrument is unique, in that it presents the first systematic implementation of MAX-DOAS on research aircraft, i.e. (1) includes measurements of solar stray light photons from nadir, zenith, and multiple elevation angles forward and below the plane by the same spectrometer/detector system, and (2) features a motion compensation system that decouples the telescope field of view (FOV) from aircraft movements in real-time (CHOCHO, HCHO, and H2O mixing ratios and aerosol extinction coefficients, ɛ, at 477nm calculated from O4 measurements from a low approach at Brackett airfield inside the South Coast Air Basin (SCAB) are presented. These profiles contain ~ 12 degrees of freedom (DOF) over a 3.5 km altitude range, independent of signal-to-noise at which the trace gas is detected. The boundary layer NO2 concentration, and the integral aerosol extinction over height (aerosol optical depth, AOD) agrees well with nearby ground-based in-situ NO2 measurement, and AERONET station. The detection limits of NO2, CHOCHO, HCHO, ɛ360, ɛ477 from 30 s integration time spectra recorded forward of the plane are 5 ppt, 3 ppt, 100 ppt, 0.004 km-1, 0.002 km-1 in the free troposphere (FT), and 30 ppt, 16 ppt, 540 ppt, 0.012 km-1, 0.006 km-1 inside the boundary layer (BL), respectively. Mobile column observations of trace gases and aerosols are complimentary to in-situ observations, and help bridge the spatial scales probed by ground-based observations, satellites, and predicted by atmospheric

  19. Application of cascade lasers to detection of trace gaseous atmospheric pollutants

    Science.gov (United States)

    Miczuga, Marcin; Kopczyński, Krzysztof

    2016-12-01

    Understanding the impact of gaseous pollutants on the earth's atmosphere, as well as more and more felt by mankind negative effects of its contamination, result in increasing the level of environmental awareness and contribute to the intensification of actions aimed at reducing the emission of harmful gases into the atmosphere. At the same time, the extensive studies are conducted in order to continuously monitor the level of air contamination with harmful gases and the industry compliance with the standards limited the amount of emitted pollutants. Over recent years, there has been increasing use of cascade lasers and multi-pass cells in optical systems detecting the gaseous atmospheric pollutants and measuring the gas concentrations. The paper presents the use of a tunable quantum cascade laser as a source of the IR radiation in an advanced detection system enabling the trace gaseous atmospheric pollutants to be identified. Apart from the laser, the main elements of the system are: a multi-pass cell, an IR detector and a module for control and analysis. Operation of the system is exemplified by measuring the level of the air pollution with ammonia, carbon oxide and nitrous oxide.

  20. Effect of noble gases on an atmospheric greenhouse /Titan/.

    Science.gov (United States)

    Cess, R.; Owen, T.

    1973-01-01

    Several models for the atmosphere of Titan have been investigated, taking into account various combinations of neon and argon. The investigation shows that the addition of large amounts of Ne and/or Ar will substantially reduce the hydrogen abundance required for a given greenhouse effect. The fact that a large amount of neon should be present if the atmosphere is a relic of the solar nebula is an especially attractive feature of the models, because it is hard to justify appropriate abundances of other enhancing agents.

  1. Redistribution of trace gases by convective clouds - mixed-phase processes

    Directory of Open Access Journals (Sweden)

    Y. Yin

    2002-01-01

    Full Text Available The efficiency of gas transport to the free and upper troposphere in convective clouds is investigated in an axisymmetric dynamic cloud model with detailed microphysics. In particular, we examine the sensitivity of gas transport to the treatment of gas uptake by different ice hydrometeors. Two parameters are used to describe this uptake. The gas retention coefficient defines the fraction of dissolved gas that is retained in an ice particle upon freezing, which includes also the riming process. We also define a gas burial efficiency defining the amount of gas entrapped in ice crystals growing by vapour diffusion. Model calculations are performed for continental and maritime clouds using a complete range of gas solubilities, retention coefficients and burial efficiencies. The results show that the magnitude of the gas retention coefficient is much more important for gas transport in maritime clouds than in continental clouds. The cause of this difference lies in the different microphysical processes dominating the formation and evolution of hydrometeors in the two cloud types. For highly soluble gases, the amount of gas transported to the free troposphere in maritime clouds falls approximately linearly by a factor of 12 as the retention coefficient is varied between 0 and 1. Gas transport is relatively insensitive to the magnitude of the gas burial efficiency. However, the burial efficiency strongly controls the concentration of trace gases inside anvil ice crystals, which subsequently form cirrus clouds.

  2. Redistribution of trace gases by convective clouds – mixed-phase processes

    Directory of Open Access Journals (Sweden)

    Y. Yin

    2002-06-01

    Full Text Available The efficiency of gas transport to the free and upper troposphere in convective clouds is investigated in an axisymmetric dynamic cloud model with detailed microphysics. In particular, we examine the sensitivity of gas transport to the treatment of gas uptake by different ice hydrometeors. Two parameters are used to describe this uptake. The gas retention coefficient defines the fraction of dissolved gas that is retained in an ice particle upon freezing, which includes also the riming process. We also define a gas burial efficiency defining the amount of gas entrapped in ice crystals growing by vapour diffusion. Model calculations are performed for continental and maritime clouds using a complete range of gas solubilities, retention coefficients and burial efficiencies. The results show that the magnitude of the gas retention coefficient is much more important for gas transport in maritime clouds than in continental clouds. The cause of this difference lies in the different microphysical processes dominating the formation and evolution of hydrometeors in the two cloud types. For highly soluble gases, the amount of gas transported to the free troposphere in maritime clouds falls approximately linearly by a factor of 12 as the retention coefficient is varied between 0 and 1. Gas transport is relatively insensitive to the magnitude of the gas burial efficiency. However, the burial efficiency strongly controls the concentration of trace gases inside anvil ice crystals, which subsequently form cirrus clouds.

  3. Continuous measurements of greenhouse gases and atmospheric oxygen at the Namib Desert Atmospheric Observatory

    Science.gov (United States)

    Morgan, E. J.; Lavrič, J. V.; Seifert, T.; Chicoine, T.; Day, A.; Gomez, J.; Logan, R.; Sack, J.; Shuuya, T.; Uushona, E. G.; Vincent, K.; Schultz, U.; Brunke, E.-G.; Labuschagne, C.; Thompson, R. L.; Schmidt, S.; Manning, A. C.; Heimann, M.

    2015-02-01

    A new coastal background site has been established for observations of greenhouse gases (GHGs) in the central Namib Desert at Gobabeb, Namibia. The location of the site was chosen to provide observations for a data-poor region in the global sampling network for GHGs. Semi-automated, continuous measurements of carbon dioxide, methane, nitrous oxide, carbon monoxide, atmospheric oxygen, and basic meteorology are made at a height of 21 m a.g.l., 50 km from the coast at the northern border of the Namib Sand Sea. Atmospheric oxygen is measured with a differential fuel cell analyzer (DFCA). Carbon dioxide and methane are measured with an early-model cavity ring-down spectrometer (CRDS); nitrous oxide and carbon monoxide are measured with an off-axis integrated cavity output spectrometer (OA-ICOS). Instrument-specific water corrections are employed for both the CRDS and OA-ICOS instruments in lieu of drying. The performance and measurement uncertainties are discussed in detail. As the station is located in a remote desert environment, there are some particular challenges, namely fine dust, high diurnal temperature variability, and minimal infrastructure. The gas handling system and calibration scheme were tailored to best fit the conditions of the site. The CRDS and DFCA provide data of acceptable quality when base requirements for operation are met, specifically adequate temperature control in the laboratory and regular supply of electricity. In the case of the OA-ICOS instrument, performance is significantly improved through the implementation of a drift correction through frequent measurements of a working tank.

  4. How primitive are the gases in Titan's atmosphere?

    Science.gov (United States)

    Owen, T

    1987-01-01

    Titan's atmosphere contains a mixture of nitrogen, methane, argon, hydrogen, simple hydrocarbons and nitriles, carbon monoxide, and carbon dioxide. Sources of nitrogen may be as a product of the photodissociation of ammonia or trapped in the ices that formed the satellite. Reasons for the abundance of deuterium are examined and its association with nitrogen on Titan is explained.

  5. Possible cometary origin of heavy noble gases in the atmospheres of Venus, earth, and Mars

    Science.gov (United States)

    Owen, Tobias; Bar-Nun, Akiva; Kleinfeld, Idit

    1992-01-01

    Due consideration of the probable history of the Martian atmosphere, as well as noble-gas data from the Mars-derived SNC meteorites and from laboratory tests on the trapping of noble gases in ice, are the bases of the presently hypothesized domination of noble gases in the atmospheres of all terrestrial planets by a mixture of internal components and a contribution from comets. If verified, this hypothesis would underscore the significance of impacts for these planets' volatile inventories. The sizes of the hypothesized comets are of the order of 120 km for Venus and only 80 km for that which struck the earth.

  6. High spatial resolution imaging of methane and other trace gases with the airborne Hyperspectral Thermal Emission Spectrometer (HyTES)

    Science.gov (United States)

    Hulley, Glynn C.; Duren, Riley M.; Hopkins, Francesca M.; Hook, Simon J.; Vance, Nick; Guillevic, Pierre; Johnson, William R.; Eng, Bjorn T.; Mihaly, Jonathan M.; Jovanovic, Veljko M.; Chazanoff, Seth L.; Staniszewski, Zak K.; Kuai, Le; Worden, John; Frankenberg, Christian; Rivera, Gerardo; Aubrey, Andrew D.; Miller, Charles E.; Malakar, Nabin K.; Sánchez Tomás, Juan M.; Holmes, Kendall T.

    2016-06-01

    Currently large uncertainties exist associated with the attribution and quantification of fugitive emissions of criteria pollutants and greenhouse gases such as methane across large regions and key economic sectors. In this study, data from the airborne Hyperspectral Thermal Emission Spectrometer (HyTES) have been used to develop robust and reliable techniques for the detection and wide-area mapping of emission plumes of methane and other atmospheric trace gas species over challenging and diverse environmental conditions with high spatial resolution that permits direct attribution to sources. HyTES is a pushbroom imaging spectrometer with high spectral resolution (256 bands from 7.5 to 12 µm), wide swath (1-2 km), and high spatial resolution (˜ 2 m at 1 km altitude) that incorporates new thermal infrared (TIR) remote sensing technologies. In this study we introduce a hybrid clutter matched filter (CMF) and plume dilation algorithm applied to HyTES observations to efficiently detect and characterize the spatial structures of individual plumes of CH4, H2S, NH3, NO2, and SO2 emitters. The sensitivity and field of regard of HyTES allows rapid and frequent airborne surveys of large areas including facilities not readily accessible from the surface. The HyTES CMF algorithm produces plume intensity images of methane and other gases from strong emission sources. The combination of high spatial resolution and multi-species imaging capability provides source attribution in complex environments. The CMF-based detection of strong emission sources over large areas is a fast and powerful tool needed to focus on more computationally intensive retrieval algorithms to quantify emissions with error estimates, and is useful for expediting mitigation efforts and addressing critical science questions.

  7. Miniaturized Hollow-Waveguide Gas Correlation Radiometer (GCR) for Trace Gas Detection in the Martian Atmosphere

    Science.gov (United States)

    Wilson, Emily L.; Georgieva, E. M.; Melroy, H. R.

    2012-01-01

    Gas correlation radiometry (GCR) has been shown to be a sensitive and versatile method for detecting trace gases in Earth's atmosphere. Here, we present a miniaturized and simplified version of this instrument capable of mapping multiple trace gases and identifying active regions on the Mars surface. Reduction of the size and mass of the GCR instrument has been achieved by implementing a lightweight, 1 mm inner diameter hollow-core optical fiber (hollow waveguide) for the gas correlation cell. Based on a comparison with an Earth orbiting CO2 gas correlation instrument, replacement of the 10 meter mUltipass cell with hollow waveguide of equivalent pathlength reduces the cell mass from approx 150 kg to approx 0.5 kg, and reduces the volume from 1.9 m x 1.3 m x 0.86 m to a small bundle of fiber coils approximately I meter in diameter by 0.05 m in height (mass and volume reductions of >99%). This modular instrument technique can be expanded to include measurements of additional species of interest including nitrous oxide (N2O), hydrogen sulfide (H2S), methanol (CH3OH), and sulfur dioxide (SO2), as well as carbon dioxide (CO2) for a simultaneous measure of mass balance.

  8. The CU Airborne MAX-DOAS instrument: ground based validation, and vertical profiling of aerosol extinction and trace gases

    Directory of Open Access Journals (Sweden)

    S. Baidar

    2012-09-01

    Full Text Available The University of Colorado Airborne Multi Axis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS instrument uses solar stray light remote sensing to detect and quantify multiple trace gases, including nitrogen dioxide (NO2, glyoxal (CHOCHO, formaldehyde (HCHO, water vapor (H2O, nitrous acid (HONO, iodine monoxide (IO, bromine monoxide (BrO, and oxygen dimers (O4 at multiple wavelengths (360 nm, 477 nm, 577 nm and 632 nm simultaneously, and sensitively in the open atmosphere. The instrument is unique, in that it presents the first systematic implementation of MAX-DOAS on research aircraft, i.e. (1 includes measurements of solar stray light photons from nadir, zenith, and multiple elevation angles forward and below the plane by the same spectrometer/detector system, and (2 features a motion compensation system that decouples the telescope field of view (FOV from aircraft movements in real-time (< 0.35° accuracy. Sets of solar stray light spectra collected from nadir to zenith scans provide some vertical profile information within 2 km above and below the aircraft altitude, and the vertical column density (VCD below the aircraft is measured in nadir view. Maximum information about vertical profiles is derived simultaneously for trace gas concentrations and aerosol extinction coefficients over similar spatial scales and with a vertical resolution of typically 250 m during aircraft ascent/descent.

    The instrument is described, and data from flights over California during the CalNex and CARES air quality field campaigns is presented. Horizontal distributions of NO2 VCDs (below the aircraft maps are sampled with typically 1 km resolution, and show good agreement with two ground based CU MAX-DOAS instruments (slope 0.95 ± 0.09, R2 = 0.86. As a case study vertical profiles of NO2, CHOCHO, HCHO, and H2O mixing ratios and aerosol extinction coefficients

  9. THE INTEGRITY OF THE ICE RECORD OF GREENHOUSE GASES WITH A SPECIAL FOCUS ON ATMOSPHERIC CO2

    Directory of Open Access Journals (Sweden)

    Dominique Raynaud

    2012-01-01

    Full Text Available Over the last 25 years, the ice core record has provided a unique and precious archive of past changes in three important greenhouse gases: carbon dioxide CO2, methane CH4 and nitrous oxide N2O. Recovering the Vostok ice core has played a major role, being the first ice record showing the variations of CO2 and CH4 during a full glacial-interglacial cycle, and a few years later being extended to three more cycles. This information, by revealing the tight coupling between climate and carbon cycle during the last glacial-interglacial cycles, has become a benchmark against which climate and carbon cycle models can be tested. The purpose of the present work is to discuss the degree of integrity of the ice core record of greenhouse gases and to assess to which degree it provides an accurate reconstruction of the past atmospheric changes. The various processes potentially affecting the integrity of the record are discussed. They include the interactions of trace gases with precipitation or firn grains, the effect of summer-melting at the surface of the ice sheet, the diffusion and the gravitational setting of gases in the open spaces of the firn, the physical, chemical and biological interactions between the air trapped and the ice matrix, the role of the transformation of air bubbles into air hydrates with depth in the ice column. Providing to select an appropriate sampling site, to take specific precautions during storage and transportation of the ice cores, and to select ice of good quality, the ice core record of initial atmospheric gases is hardly affected by the processes listed above. Such conclusion is strongly supported by the remarkable agreement of global signals like CO2 or CH4 measured in different cores taken at different locations. Finally, I bring back here the history of how the ice core record of atmospheric CO2 has been obtained, from the pioneering times to today, and summarize the main conclusions reached in terms of climate

  10. Measurement of gas/water uptake coefficients for trace gases active in the marine environment

    Energy Technology Data Exchange (ETDEWEB)

    Davidovits, P. (Boston Coll., Chestnut Hill, MA (United States). Dept. of Chemistry); Worsnop, D.W.; Zahniser, M.S.; Kolb, C.E. (Aerodyne Research, Inc., Billerica, MA (United States). Center for Chemical and Environmental Physics)

    1992-02-01

    Ocean produced reduced sulfur compounds including dimethylsulfide (DMS), hydrogen sulfide (H{sub 2}S), carbon disulfide (CS{sub 2}), methyl mercaptan (CH{sub 3}CH) and carbonyl sulfide (OCS) deliver a sulfur burden to the atmosphere which is roughly equal to sulfur oxides produced by fossil fuel combustion. These species and their oxidation products dimethyl sulfoxide (DMSO), dimethyl sulfone (DMSO{sub 2}) and methane sulfonic acid (MSA) dominate aerosol and CCN production in clean marine air. Furthermore, oxidation of reduced sulfur species will be strongly influenced by NO{sub x}/O{sub 3} chemistry in marine atmospheres. The multiphase chemical processes for these species must be understood in order to study the evolving role of combustion produced sulfur oxides over the oceans. We have measured the chemical and physical parameters affecting the uptake of reduced sulfur compounds, their oxidation products, ozone, and nitrogen oxides by the ocean's surface, and marine clouds, fogs, and aerosols. These parameters include: gas/surface mass accommodation coefficients; physical and chemically modified (effective) Henry's law constants; and surface and liquid phase reaction constants. These parameters are critical to understanding both the interaction of gaseous trace species with cloud and fog droplets and the deposition of trace gaseous species to dew covered, fresh water and marine surfaces.

  11. European emissions of halogenated greenhouse gases inferred from atmospheric measurements.

    Science.gov (United States)

    Keller, Christoph A; Hill, Matthias; Vollmer, Martin K; Henne, Stephan; Brunner, Dominik; Reimann, Stefan; O'Doherty, Simon; Arduini, Jgor; Maione, Michela; Ferenczi, Zita; Haszpra, Laszlo; Manning, Alistair J; Peter, Thomas

    2012-01-01

    European emissions of nine representative halocarbons (CFC-11, CFC-12, Halon 1211, HCFC-141b, HCFC-142b, HCFC-22, HFC-125, HFC-134a, HFC-152a) are derived for the year 2009 by combining long-term observations in Switzerland, Italy, and Ireland with campaign measurements from Hungary. For the first time, halocarbon emissions over Eastern Europe are assessed by top-down methods, and these results are compared to Western European emissions. The employed inversion method builds on least-squares optimization linking atmospheric observations with calculations from the Lagrangian particle dispersion model FLEXPART. The aggregated halocarbon emissions over the study area are estimated at 125 (106-150) Tg of CO(2) equiv/y, of which the hydrofluorocarbons (HFCs) make up the most important fraction with 41% (31-52%). We find that chlorofluorocarbon (CFC) emissions from banks are still significant and account for 35% (27-43%) of total halocarbon emissions in Europe. The regional differences in per capita emissions are only small for the HFCs, while emissions of CFCs and hydrochlorofluorocarbons (HCFCs) tend to be higher in Western Europe compared to Eastern Europe. In total, the inferred per capita emissions are similar to estimates for China, but 3.5 (2.3-4.5) times lower than for the United States. Our study demonstrates the large benefits of adding a strategically well placed measurement site to the existing European observation network of halocarbons, as it extends the coverage of the inversion domain toward Eastern Europe and helps to better constrain the emissions over Central Europe.

  12. A Fourier transform infrared trace gas and isotope analyser for atmospheric applications

    Directory of Open Access Journals (Sweden)

    D. W. T. Griffith

    2012-10-01

    Full Text Available Concern in recent decades about human impacts on Earth's climate has led to the need for improved and expanded measurement capabilities of greenhouse gases in the atmosphere. In this paper we describe in detail an in situ trace gas analyser based on Fourier Transform Infrared (FTIR spectroscopy that is capable of simultaneous and continuous measurements of carbon dioxide (CO2, methane (CH4, carbon monoxide (CO, nitrous oxide (N2O and 13C in CO2 in air with high precision. High accuracy is established by reference to measurements of standard reference gases. Stable water isotopes can also be measured in undried airstreams. The analyser is automated and allows unattended operation with minimal operator intervention. Precision and accuracy meet and exceed the compatibility targets set by the World Meteorological Organisation – Global Atmosphere Watch for baseline measurements in the unpolluted troposphere for all species except 13C in CO2.

    The analyser is mobile and well suited to fixed sites, tower measurements, mobile platforms and campaign-based measurements. The isotopic specificity of the optically-based technique and analysis allows its application in isotopic tracer experiments, for example in tracing variations of 13C in CO2 and 15N in N2O. We review a number of applications illustrating use of the analyser in clean air monitoring, micrometeorological flux and tower measurements, mobile measurements on a train, and soil flux chamber measurements.

  13. Limitations of wind extraction from 4-D-Var assimilation of trace gases

    Directory of Open Access Journals (Sweden)

    D. R. Allen

    2012-12-01

    Full Text Available Time-dependent variational data assimilation allows the possibility of extracting wind information from observations of long-lived trace gases. Since trace gas observations are not available at sufficient resolution for deriving feature-track winds, they must be combined with model background information to produce an analysis. If done with time-dependent variational assimilation, wind information may be extracted via the adjoint of the linearized tracer continuity equation. This paper presents idealized experiments that illustrate the mechanics of tracer-wind extraction and demonstrate some of the limitations of this procedure. We first examine tracer-wind extraction using a simple one-dimensional advection equation. The analytic solution for a single trace gas observation is discussed along with numerical solutions for multiple observations. The limitations of tracer-wind extraction are then explored using highly idealized ozone experiments performed with a development version of the Navy Global Environmental Model (NAVGEM in which stratospheric globally-distributed hourly stratospheric ozone profiles are assimilated in a single 6-h update cycle in January 2009. Starting with perfect background ozone conditions, but imperfect dynamical conditions, ozone errors develop over the 6-h background window. Wind increments are introduced in the analysis in order to reduce the differences between background ozone and ozone observations. For "perfect" observations (unbiased and no random error, this results in root mean square (RMS vector wind error reductions of up to ∼ 3 m s−1 in the winter hemisphere and tropics. Wind extraction is more difficult in the summer hemisphere due to weak ozone gradients and smaller background wind errors. The limitations of wind extraction are also explored for observations with imposed random errors and for limited sampling patterns. As expected, the amount of wind information extracted degrades as

  14. Retrieval of vertical profiles of multiple trace gases from MAX-DOAS observations during the MADCAT Campaign in Mainz, Germany

    Science.gov (United States)

    Wang, Yang; Xie, Pinhua; Wagner, Thomas; Li, Ang; Luo, Yuhan; Remmers, Julia; Horbanski, Martin; Friess, Udo

    2014-05-01

    In order to promote the development of passive DOAS technique and solve some critical problems including e.g. accurate retrievals of trace gas slant column densities (SCD), profile retrievals of trace gases and aerosol, and the effects of cloud, the Multi Axis DOAS-Comparison campaign for Aerosols and Trace gases (MAD-CAT) was held at the Max-Planck institute for Chemistry in Mainz, Germany from June to August 2013. Within this campaign, spectra of scattered sun light were taken by our two-dimensional scanning MAX-DOAS (2D-MAX-DOAS) instrument and a Mini-MAX-DOAS instrument from the Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences. In this presentation, firstly we show the retrieved differential SCDs of O4, NO2, HCHO, HONO and CHOCHO based on the observations of the 2D-MAX-DOAS. Based on these dSCDs we acquired the vertical profiles of these trace gases and aerosol extinction using optimal estimation method. We compare the aerosol optical depth (AOD) from MAX-DOAS with simultaneous observations from an AERONET instrument as well as the near surface volume mixing ratio (VMR) of NO2 from MAX-DOAS with those from a CE-DOAS instrument from the IUP Heidelberg group and found in general good agreement. In addition we apply a cloud classification scheme based on our MAX-DOAS observations to identify different kinds of weather during the MAD-CAT campaign.

  15. On the detectability of trace chemical species in the martian atmosphere using gas correlation filter radiometry

    Science.gov (United States)

    Sinclair, J. A.; Irwin, P. G. J.; Calcutt, S. B.; Wilson, E. L.

    2015-11-01

    The martian atmosphere is host to many trace gases including water (H2O) and its isotopologues, methane (CH4) and potentially sulphur dioxide (SO2), nitrous oxide (N2O) and further organic compounds, which would serve as indirect tracers of geological, chemical and biological processes on Mars. With exception of the recent detection of CH4 by Curiosity, previous detections of these species have been unsuccessful or considered tentative due to the low concentrations of these species in the atmosphere (∼10-9 partial pressures), limited spectral resolving power and/or signal-to-noise and the challenge of discriminating between telluric and martian features when observing from the Earth. In this study, we present radiative transfer simulations of an alternative method for detection of trace gas species - the gas correlation radiometry method. Two potential observing scenarios were explored where a gas correlation filter radiometer (GCFR) instrument: (1) performs nadir and/or limb sounding of the martian atmosphere in the thermal infrared (200-2000 cm-1 from an orbiting spacecraft or (2) performs solar occultation measurements in the near-infrared (2000-5000 cm-1) from a lander on the martian surface. In both scenarios, simulations of a narrowband filter radiometer (without gas correlation) were also generated to serve as a comparison. From a spacecraft, we find that a gas correlation filter radiometer, in comparison to a filter radiometer (FR), offers a greater discrimination between temperature and dust, a greater discrimination between H2O and HDO, and would allow detection of N2O and CH3OH at concentrations of ∼10 ppbv and ∼2 ppbv, respectively, which are lower than previously-derived upper limits. However, the lowest retrievable concentration of SO2 (approximately 2 ppbv) is comparable with previous upper limits and CH4 is only detectable at concentrations of approximately 10 ppbv, which is an order of magnitude higher than the concentration recently measured

  16. A simple method to estimate entropy of atmospheric gases from their action

    CERN Document Server

    Kennedy, Ivan R; Rose, Michael T; Crossan, Angus N

    2015-01-01

    A convenient model for estimating the total entropy ({\\Sigma}Si) of atmospheric gases based on physical action is proposed. This realistic approach is fully consistent with statistical mechanics, but uses the properties of translational, rotational and vibrational action to partition the entropy. When all sources of action are computed as appropriate non-linear functions, the total input of thermal energy ({\\Sigma}SiT) required to sustain a chemical system at specific temperatures (T) and pressures (p) can be estimated, yielding results in close agreement with published experimental third law values. Thermodynamic properties of gases including enthalpy, Gibbs energy and Helmholtz energy can be easily calculated from simple molecular and physical properties. We propose that these values for entropy are employed both chemically for reactions and physically for computing atmospheric profiles, the latter based on steady state heat flow equilibrating thermodynamics with gravity. We also predict that this applicati...

  17. Neural-estimator for the surface emission rate of atmospheric gases

    CERN Document Server

    Paes, F F

    2009-01-01

    The emission rate of minority atmospheric gases is inferred by a new approach based on neural networks. The neural network applied is the multi-layer perceptron with backpropagation algorithm for learning. The identification of these surface fluxes is an inverse problem. A comparison between the new neural-inversion and regularized inverse solution id performed. The results obtained from the neural networks are significantly better. In addition, the inversion with the neural netwroks is fster than regularized approaches, after training.

  18. Optical propagation in linear media atmospheric gases and particles, solid-state components, and water

    CERN Document Server

    Thomas, Michael E

    2006-01-01

    PART I: Background Theory and Measurement. 1. Optical Electromagnetics I. 2. Optical Electromagnetics II. 3. Spectroscopy of Matter. 4. Electrodynamics I: Macroscopic Interaction of Light and Matter. 5. Electrodynamics II: Microscopic Interaction of Light and Matter. 6. Experimental Techniques. PART II: Practical Models for Various Media. 7. Optical Propagation in Gases and the Atmosphere of the Earth. 8. Optical Propagation in Solids. 9. Optical Propagation in Liquids. 10. Particle Absorption and Scatter. 11. Propagation Background and Noise

  19. Airborne observations of trace gases over boreal Canada during BORTAS: campaign climatology, airmass analysis and enhancement ratios

    Directory of Open Access Journals (Sweden)

    S. J. O'Shea

    2013-05-01

    Full Text Available In situ airborne measurements were made over Eastern Canada in summer 2011 as part of the BORTAS experiment (Quantifying the impact of BOReal forest fires on Tropospheric oxidants over the Atlantic using Aircraft and~Satellites. In this paper we present observations of greenhouse gases (CO2 and CH4 and other biomass burning tracers and related trace gases, both climatologically and through case studies, as recorded on board the FAAM BAe-146 research aircraft. Vertical profiles of CO2 were generally characterised by depleted boundary layer concentrations relative to the free troposphere, consistent with terrestrial biospheric uptake. In contrast, CH4 concentrations were found to rise with decreasing altitude due to strong local and regional surface sources. We use coincident tracer-tracer correlations and a Lagrangian trajectory model to characterise and differentiate air mass history of intercepted plumes. In particular, CO, HCN and CH3CN were used to identify air masses that have been recently influenced by biomass burning. Concentrations of CO2 were found to have a mean tropospheric, campaign-average concentration of 384.8 ppm (ranging between 371.5 and 397.1 ppm, whilst CH4 concentrations had a mean value of 1859 ppb (ranging between 1797 and 1968 ppb, representing the episodic sampling of local fire plumes. CH4 and CO2 concentrations during BORTAS were found to be broadly comparable to previous measurements in the region during the regional burning season and with reanalysed composition fields from the EU Monitoring Atmospheric Composition and Change (MACC project. By examining individual case studies we were able to quantify emissions from biomass burning. Using both near-field (1 day sampling, boreal forest fire plumes were identified throughout the troposphere. Fresh plumes from fires in Northwest Ontario yield emission factors for CH4 and CO2 of 8.5 ± 0.9 g (kg dry matter−1 and 1512 g ± 185 g (kg dry matter−1, respectively. We have

  20. Luminescence studies of trace gases through metastable transfer in cold helium jets

    Science.gov (United States)

    Wilde, Scott Colton

    Among the elements, Helium has the largest steps among its internal energy structure that can keep for long periods of time, hence the metastable helium moniker. It is referred to as a "nano-grenade" in some circles because of how much energy it can deliver to a space roughly the size of an atom. This work demonstrates a method to create metastable helium abundantly and it is used to excite trace amounts of oxygen to the point where the signal received from the oxygen was larger than the signal received from the helium in a cold atomized jet. Further cooling of the jet and turbulence added by a liquid helium surface worked to increase the oxygen signal and decrease the helium signal. This work investigates the possibility of forming a strong metastable helium source from a flowing helium gas jet excited by passing through ring electrodes introduced into a cryogenic environment using evaporated helium as a buffer gas. Prior study of luminescence from trace gases at cold helium temperatures is virtually absent and so it is the motivation for this work to blaze the trail in this subject. The absence of ionic oxygen spectral lines from the transfer of energy that was well over the first ionization potential of oxygen made for a deeper understanding of collision dynamics with multiple collision partners. This opened the possibility of using the high energy states of oxygen after metastable transfer as a lasing transition previously unavailable and a preliminary analysis suggested that the threshold for lasing action should be easily overcome if feedback were introduced by an optical cavity. To better understand the thermodynamics of the jet it was proposed to use diatomic nitrogen as an in situ thermometer, investigating whether the rotational degrees of freedom of the nitrogen molecule were in thermal equilibrium with the surrounding environment. If the gas was truly in thermodynamic equilibrium then the temperature given by the method of using collisions of a buffer

  1. Long term measurements of submicrometer urban aerosols: statistical analysis for correlations with meteorological conditions and trace gases

    Directory of Open Access Journals (Sweden)

    B. Wehner

    2003-01-01

    Full Text Available Long-term measurements (over 4 years of particle number size distributions (submicrometer particles, 3-800 nm in diameter, trace gases (NO, NO2, and O3, and meteorological parameters (global radiation, wind speed and direction, atmospheric pressure, etc. were taken in a moderately polluted site in the city of Leipzig (Germany. The resulting complex data set was analyzed with respect to seasonal, weekly, and diurnal variation of the submicrometer aerosol. Car traffic produced a peak in the number size distribution at around 20 nm particle diameter during morning rush hour on weekdays. A second peak at 10-15 nm particle diameter occurred around noon during summer, confirmed by high correlation between concentration of particles less than 20 nm and the global radiation. This new-particle formation at noon was correlated with the amount of global radiation. A high concentration of accumulation mode particles (between 100 and 800 nm, which are associated with large particle-surface area, might prevent this formation. Such high particle concentration in the ultrafine region (particles smaller than 20 nm in diameter was not detected in the particle mass, and thus, particle mass concentration is not suitable for determining the diurnal patterns of particles. In summer, statistical time series analysis showed a cyclic pattern of ultrafine particles with a period of one day and confirmed the correlation with global radiation. Principal component analysis (PCA revealed a strong correlation between the particle concentration for 20-800 nm particles and the NO- and NO2-concentrations, indicating the influence of combustion processes on this broad size range, in particular during winter. In addition, PCA also revealed that particle concentration depended on meteorological conditions such as wind speed and wind direction, although the dependence differed with particle size class.

  2. A versatile, refrigerant- and cryogen-free cryofocusing-thermodesorption unit for preconcentration of traces gases in air

    Science.gov (United States)

    Obersteiner, Florian; Bönisch, Harald; Keber, Timo; O'Doherty, Simon; Engel, Andreas

    2016-10-01

    We present a compact and versatile cryofocusing-thermodesorption unit, which we developed for quantitative analysis of halogenated trace gases in ambient air. Possible applications include aircraft-based in situ measurements, in situ monitoring and laboratory operation for the analysis of flask samples. Analytes are trapped on adsorptive material cooled by a Stirling cooler to low temperatures (e.g. -80 °C) and subsequently desorbed by rapid heating of the adsorptive material (e.g. +200 °C). The set-up involves neither the exchange of adsorption tubes nor any further condensation or refocusing steps. No moving parts are used that would require vacuum insulation. This allows for a simple and robust design. Reliable operation is ensured by the Stirling cooler, which neither contains a liquid refrigerant nor requires refilling a cryogen. At the same time, it allows for significantly lower adsorption temperatures compared to commonly used Peltier elements. We use gas chromatography - mass spectrometry (GC-MS) for separation and detection of the preconcentrated analytes after splitless injection. A substance boiling point range of approximately -80 to +150 °C and a substance mixing ratio range of less than 1 ppt (pmol mol-1) to more than 500 ppt in preconcentrated sample volumes of 0.1 to 10 L of ambient air is covered, depending on the application and its analytical demands. We present the instrumental design of the preconcentration unit and demonstrate capabilities and performance through the examination of analyte breakthrough during adsorption, repeatability of desorption and analyte residues in blank tests. Examples of application are taken from the analysis of flask samples collected at Mace Head Atmospheric Research Station in Ireland using our laboratory GC-MS instruments and by data obtained during a research flight with our in situ aircraft instrument GhOST-MS (Gas chromatograph for the Observation of Tracers - coupled with a Mass Spectrometer).

  3. Adsorption and reaction of trace gas-phase organic compounds on atmospheric water film surfaces: a critical review.

    Science.gov (United States)

    Donaldson, D J; Valsaraj, Kalliat T

    2010-02-01

    The air-water interface in atmospheric water films of aerosols and hydrometeors (fog, mist, ice, rain, and snow) presents an important surface for the adsorption and reaction of many organic trace gases and gaseous reactive oxidants (hydroxyl radical (OH(.)), ozone (O(3)), singlet oxygen (O(2)((1)Delta(g))), nitrate radicals (NO(3)(.)), and peroxy radicals (RO(2)(.)). Knowledge of the air-water interface partition constant of hydrophobic organic species is necessary for elucidating the significance of the interface in atmospheric fate and transport. Various methods of assessing both experimental and theoretical values of the thermodynamic partition constant and adsorption isotherm are described in this review. Further, the reactivity of trace gases with gas-phase oxidants (ozone and singlet oxygen) at the interface is summarized. Oxidation products are likely to be more water-soluble and precursors for secondary organic aerosols in hydrometeors. Estimation of characteristic times shows that heterogeneous photooxidation in water films can compete effectively with homogeneous gas-phase reactions for molecules in the atmosphere. This provides further support to the existing thesis that reactions of organic compounds at the air-water interface should be considered in gas-phase tropospheric chemistry.

  4. Integrated method for the measurement of trace atmospheric bases

    Directory of Open Access Journals (Sweden)

    D. Key

    2011-09-01

    Full Text Available Nitrogenous atmospheric bases are thought to play a key role in the global nitrogen cycle, but their sources, transport, and sinks remain poorly understood. Of the many methods available to measure such compounds in ambient air, few meet the current need of being applicable to the complete range of potential analytes and fewer still are convenient to implement using instrumentation that is standard to most laboratories. In this work, an integrated approach to measuring trace atmospheric nitrogenous bases has been developed and validated. The method uses a simple acid scrubbing step to capture and concentrate the bases as their phosphite salts, which then are derivatized and analyzed using GC/MS and/or LC/MS. The advantages of both techniques in the context of the present measurements are discussed. The approach is sensitive, selective, reproducible, as well as convenient to implement and has been validated for different sampling strategies. The limits of detection for the families of tested compounds are suitable for ambient measurement applications, as supported by field measurements in an urban park and in the exhaust of on-road vehicles.

  5. Computerized atmospheric trace contaminant control simulation for manned spacecraft

    Science.gov (United States)

    Perry, J. L.

    1993-01-01

    Buildup of atmospheric trace contaminants in enclosed volumes such as a spacecraft may lead to potentially serious health problems for the crew members. For this reason, active control methods must be implemented to minimize the concentration of atmospheric contaminants to levels that are considered safe for prolonged, continuous exposure. Designing hardware to accomplish this has traditionally required extensive testing to characterize and select appropriate control technologies. Data collected since the Apollo project can now be used in a computerized performance simulation to predict the performance and life of contamination control hardware to allow for initial technology screening, performance prediction, and operations and contingency studies to determine the most suitable hardware approach before specific design and testing activities begin. The program, written in FORTRAN 77, provides contaminant removal rate, total mass removed, and per pass efficiency for each control device for discrete time intervals. In addition, projected cabin concentration is provided. Input and output data are manipulated using commercial spreadsheet and data graphing software. These results can then be used in analyzing hardware design parameters such as sizing and flow rate, overall process performance and program economics. Test performance may also be predicted to aid test design.

  6. The airborne mass spectrometer AIMS – Part 2: Measurements of trace gases with stratospheric or tropospheric origin in the UTLS

    Directory of Open Access Journals (Sweden)

    T. Jurkat

    2016-04-01

    an isotopically labeled 34SO2 standard. In addition, we report on trace gas measurements of HONO, which is sensitive to the reaction with SF5−. The detection limit for the various trace gases is in the low 10 pptv range at a 1 s time resolution with an overall uncertainty of the measurement of the order of 20 %. AIMS has been integrated and successfully operated on the DLR research aircraft Falcon and HALO (High Altitude LOng range research aircraft. As an example, measurements conducted during the TACTS/ESMVal (Transport and Composition of the LMS/UT and Earth System Model Validation mission with HALO in 2012 are presented, focusing on a classification of tropospheric and stratospheric influences in the UTLS region. The combination of AIMS measurements with other measurement techniques yields a comprehensive picture of the sulfur, chlorine and reactive nitrogen oxide budget in the UTLS. The different trace gases measured with AIMS exhibit the potential to gain a better understanding of the trace gas origin and variability at and near the tropopause.

  7. An approach to noble-gas isotopic compositions in natural gases and gas-source tracing in the Ordos Basin, China

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Isotopic compositions of noble gases, i.e. He Ar Kr and Xe, are measured in natural gases from the Zhongbu gasfield in the Ordos Basin. And heavy noble-gas isotopes (Kr, Xe) are here first used in geochemically studying natural gases and gas-source correlation. Isotopic compositions of heavy noble gases in natural gases, especially Xe, show two-source mixing in the Zhongbu gasfield. Gas sources are somewhat different in the northeast and the southwest of the gasfield. Generally, the gas source of the Lower Paleozoic makes a greater contribution in the southwest than in the northeast in the field. Two kinds of gases can be differentiated from isotopic compositions of heavy noble gases and from their relation with the Ar isotopic composition, Therefore, the comprehensive study on isotopic compositions of light and heavy noble gases can supply more useful information on gas-source correlation and tracing.

  8. Numerical modelling of the transport of trace gases including methane in the subsurface of Mars

    Science.gov (United States)

    Stevens, Adam H.; Patel, Manish R.; Lewis, Stephen R.

    2015-04-01

    We model the transport of gas through the martian subsurface in order to quantify the timescales of release of a trace gas with a source at depth using a Fickian model of diffusion through a putative martian regolith column. The model is then applied to the case of methane to determine if diffusive transport of gas can explain previous observations of methane in the martian atmosphere. We investigate which parameters in the model have the greatest effect on transport timescales and show that the calculated diffusivity is very sensitive to the pressure profile of the subsurface, but relatively insensitive to the temperature profile, though diffusive transport may be affected by other temperature dependent properties of the subsurface such as the local vapour pressure. Uncertainties in the structure and physical conditions of the martian subsurface also introduce uncertainties in the timescales calculated. It was found that methane may take several hundred thousand Mars-years to diffuse from a source at depth. Purely diffusive transport cannot explain transient release that varies on timescales of less than one martian year from sources such as serpentinization or methanogenic organisms at depths of more than 2 km. However, diffusion of gas released by the destabilisation of methane clathrate hydrates close to the surface, for example caused by transient mass wasting events or erosion, could produce a rapidly varying flux of methane into the atmosphere of more than 10-3 kg m-2 s-1 over a duration of less than half a martian year, consistent with observations of martian methane variability. Seismic events, magmatic intrusions or impacts could also potentially produce similar patterns of release, but are far more complex to simulate.

  9. Climate relevant trace gases (N2O and CH4) in the Eurasian Basin (Arctic Ocean)

    Science.gov (United States)

    Verdugo, Josefa; Damm, Ellen; Snoeijs, Pauline; Díez, Beatriz; Farías, Laura

    2016-11-01

    The concentration of greenhouse gases, including nitrous oxide (N2O), methane (CH4), and compounds such as total dimethylsulfoniopropionate (DMSPt), along with other oceanographic variables were measured in the ice-covered Arctic Ocean within the Eurasian Basin (EAB). The EAB is affected by the perennial ice-pack and has seasonal microalgal blooms, which in turn may stimulate microbes involved in trace gas cycling. Data collection was carried out on board the LOMROG III cruise during the boreal summer of 2012. Water samples were collected from the surface to the bottom layer (reaching 4300 m depth) along a South-North transect (SNT), from 82.19°N, 8.75°E to 89.26°N, 58.84°W, crossing the EAB through the Nansen and Amundsen Basins. The Polar Mixed Layer and halocline waters along the SNT showed a heterogeneous distribution of N2O, CH4 and DMSPt, fluctuating between 42-111 and 27-649% saturation for N2O and CH4, respectively; and from 3.5 to 58.9 nmol L-1 for DMSPt. Spatial patterns revealed that while CH4 and DMSPt peaked in the Nansen Basin, N2O was higher in the Amundsen Basin. In the Atlantic Intermediate Water and Arctic Deep Water N2O and CH4 distributions were also heterogeneous with saturations between 52% and 106% and 28% and 340%, respectively. Remarkably, the Amundsen Basin contained less CH4 than the Nansen Basin and while both basins were mostly under-saturated in N2O. We propose that part of the CH4 and N2O may be microbiologically consumed via methanotrophy, denitrification, or even diazotrophy, as intermediate and deep waters move throughout EAB associated with the overturning water mass circulation. This study contributes to baseline information on gas distribution in a region that is increasingly subject to rapid environmental changes, and that has an important role on global ocean circulation and climate regulation.

  10. Massive impact-induced release of carbon and sulfur gases in the early Earth's atmosphere

    Science.gov (United States)

    Marchi, S.; Black, B. A.; Elkins-Tanton, L. T.; Bottke, W. F.

    2016-09-01

    Recent revisions to our understanding of the collisional history of the Hadean and early-Archean Earth indicate that large collisions may have been an important geophysical process. In this work we show that the early bombardment flux of large impactors (>100 km) facilitated the atmospheric release of greenhouse gases (particularly CO2) from Earth's mantle. Depending on the timescale for the drawdown of atmospheric CO2, the Earth's surface could have been subject to prolonged clement surface conditions or multiple freeze-thaw cycles. The bombardment also delivered and redistributed to the surface large quantities of sulfur, one of the most important elements for life. The stochastic occurrence of large collisions could provide insights on why the Earth and Venus, considered Earth's twin planet, exhibit radically different atmospheres.

  11. A comprehensive study of different gases in inductively coupled plasma torch operating at one atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Punjabi, Sangeeta B. [Electrical Engineering Department, V. J.T.I, Matunga, Mumbai 400019 (India); Department of Physics, University of Mumbai, Kalina, Santacruz(E) 400098 (India); Joshi, N. K. [Faculty of Engineering and technology, MITS, lakshmangarh, (Sikar), Rajasthan 332311 (India); Mangalvedekar, H. A.; Lande, B. K. [Electrical Engineering Department, V. J.T.I, Matunga, Mumbai 400019 (India); Das, A. K. [Laser and Plasma Technology Division, BARC, Mumbai 400085 (India); Kothari, D. C. [Department of Physics, University of Mumbai, Kalina, Santacruz(E) 400098 (India)

    2012-01-15

    A numerical study is done to understand the possible operating regimes of RF-ICP torch (3 MHz, 50 kW) using different gases for plasma formation at atmospheric pressure. A two dimensional numerical simulation of RF-ICP torch using argon, nitrogen, oxygen, and air as plasma gas has been investigated using computational fluid dynamic (CFD) software fluent{sup (c)}. The operating parameters varied here are central gas flow, sheath gas flow, RF-power dissipated in plasma, and plasma gas. The temperature contours, flow field, axial, and radial velocity profiles were investigated under different operating conditions. The plasma resistance, inductance of the torch, and the heat distribution for various plasma gases have also been investigated. The plasma impedance of ICP torch varies with different operating parameters and plays an important role for RF oscillator design and power coupling. These studies will be useful to decide the design criteria for ICP torches required for different material processing applications.

  12. The state of greenhouse gases in the atmosphere using global observations through 2014

    Science.gov (United States)

    Tarasova, Oksana; Koide, Hiroshi; Dlugokencky, Ed

    2016-04-01

    We present results from the eleventh annual Greenhouse Gas Bulletin (http://www.wmo.int/pages/prog/arep/gaw/ghg/GHGbulletin.html) of the World Meteorological Organization (WMO). The results are based on research and observations performed by laboratories contributing to the WMO Global Atmosphere Watch (GAW) Programme (www.wmo.int/gaw). The Bulletin presents results of global analyses of observational data collected according to GAW recommended practices and submitted to the World Data Center for Greenhouse Gases (WDCGG). Bulletins are prepared by the WMO/GAW Scientific Advisory Group for Greenhouse Gases (http://www.wmo.int/pages/prog/arep/gaw/ScientificAdvisoryGroups.html) in collaboration with WDCGG. Observations used for global analysis are collected at more than 100 marine and terrestrial sites worldwide for CO2 and CH4 and at a smaller number of sites for other greenhouse gases. Globally averaged dry-air mole fractions of CO2, CH4 and N2O derived from this network reached new highs in 2014, at 397.7±0.1 ppm, 1833±1 ppb and 327.1±0.1 ppb respectively. These values constitute 143%, 254% and 121% of pre-industrial (before 1750) levels. The atmospheric increase of CO2 from 2013 to 2014 was 1.9 ppm, which is smaller than the increase from 2012 to 2013 and the average growth rate for the past decade (˜2.06 ppm per year), but larger than the average growth rate for the 1990s (˜1.5 ppm per year). Smaller growth in 2014 compared with other recent years is most likely related to a relatively small net change in large fluxes between the atmosphere and terrestrial biosphere. The rise of atmospheric CO2 has been only about a half of what is expected if all excess CO2 from burning fossil-fuels stayed in the air. The other half has been absorbed by the land biosphere and the oceans, leading to ocean acidification. For both CH4 and N2O the increases from 2013 to 2014 were larger than those observed from 2012 to 2013 and the mean rates over the past 10 years. The National

  13. Atmospheric composition change: Ecosystems-Atmosphere interactions

    NARCIS (Netherlands)

    Fowler, D.; Pilegaard, K.; Sutton, M.A.; Ambus, P.; Raivonen, M.; Duyzer, J.; Simpson, D.; Fagerli, H.; Fuzzi, S.; Schjoerring, J.K.; Granier, C.; Neftel, A.; Isaksen, I.S.A.; Laj, P.; Maione, M.; Monks, P.S.; Burkhardt, J.; Daemmgen, U.; Neirynck, J.; Personne, E.; Wichink Kruit, R.J.; Butterbach-Bahl, K.; Flechard, C.; Tuovinen, J.P.; Coyle, M.; Gerosa, G.; Loubet, B.; Altimir, N.; Gruenhage, L.; Ammann, C.; Cieslik, S.; Paoletti, E.; Mikkelsen, T.N.; Ro-Poulsen, H.; Cellier, P.; Cape, J.N.; Horvath, L.; Loreto, F.; Niinemets, U.; Palmer, P.I.; Rinne, J.; Misztal, P.; Nemitz, E.; Nilsson, D.; Pryor, S.; Gallagher, M.W.; Vesala, T.; Skiba, U.; Brueggemann, N.; Zechmeister-Boltenstern, S.; Williams, J.; O'Dowd, C.; Facchini, M.C.; Leeuw, de G.; Flossman, A.; Chaumerliac, N.; Erisman, J.W.

    2009-01-01

    Ecosystems and the atmosphere: This review describes the state of understanding the processes involved in the exchange of trace gases and aerosols between the earth's surface and the atmosphere. The gases covered include NO, NO2, HONO, HNO3, NH3, SO2, DMS, Biogenic VOC, O-3, CH4, N2O and particles i

  14. Condition of Retrieving Vertical Column Density of Atmospheric Pollution Gases by Using Scattered Solar Radiation

    Institute of Scientific and Technical Information of China (English)

    ZUO Sao-Yi

    2009-01-01

    We present a method to monitor the vertical column density (VCD) of atmospheric pollution gases by using the scattered solar radiation. The necessary condition of capturing the useful scattered solar radiation is achieved. The condition is only dependent on the solar elevation angle, while independent of the solar azimuth angle, which could greatly simply the capturing equipment and procedure. Under the condition, the VCD of tropospheric NO2 in Chengdu, China is retrieved from the scattered solar radiation, which is dose to that from the direct solar radiation.

  15. Technical Note: A new global database of trace gases and aerosols from multiple sources of high vertical resolution measurements

    Directory of Open Access Journals (Sweden)

    G. E. Bodeker

    2008-09-01

    Full Text Available A new database of trace gases and aerosols with global coverage, derived from high vertical resolution profile measurements, has been assembled as a collection of binary data files; hereafter referred to as the "Binary DataBase of Profiles" (BDBP. Version 1.0 of the BDBP, described here, includes measurements from different satellite- (HALOE, POAM II and III, SAGE I and II and ground-based measurement systems (ozonesondes. In addition to the primary product of ozone, secondary measurements of other trace gases, aerosol extinction, and temperature are included. All data are subjected to very strict quality control and for every measurement a percentage error on the measurement is included. To facilitate analyses, each measurement is added to 3 different instances (3 different grids of the database where measurements are indexed by: (1 geographic latitude, longitude, altitude (in 1 km steps and time, (2 geographic latitude, longitude, pressure (at levels ~1 km apart and time, (3 equivalent latitude, potential temperature (8 levels from 300 K to 650 K and time.

    In contrast to existing zonal mean databases, by including a wider range of measurement sources (both satellite and ozonesondes, the BDBP is sufficiently dense to permit calculation of changes in ozone by latitude, longitude and altitude. In addition, by including other trace gases such as water vapour, this database can be used for comprehensive radiative transfer calculations. By providing the original measurements rather than derived monthly means, the BDBP is applicable to a wider range of applications than databases containing only monthly mean data. Monthly mean zonal mean ozone concentrations calculated from the BDBP are compared with the database of Randel and Wu, which has been used in many earlier analyses. As opposed to that database which is generated from regression model fits, the BDBP uses the original (quality controlled measurements with no smoothing applied in any

  16. Biomass burning emissions of trace gases and particles in marine air at Cape Grim, Tasmania

    Science.gov (United States)

    Lawson, S. J.; Keywood, M. D.; Galbally, I. E.; Gras, J. L.; Cainey, J. M.; Cope, M. E.; Krummel, P. B.; Fraser, P. J.; Steele, L. P.; Bentley, S. T.; Meyer, C. P.; Ristovski, Z.; Goldstein, A. H.

    2015-12-01

    (ΔO3 / ΔCO 0.001-0.074). A short-lived increase in NMOCs by a factor of 10 corresponded with a large CO enhancement, an increase of the NMOC / CO emission ratio (ER) by a factor of 2-4 and a halving of the BC / CO ratio. Rainfall on Robbins Island was observed by radar during this period which likely resulted in a lower fire combustion efficiency, and higher emission of compounds associated with smouldering. This highlights the importance of relatively minor meteorological events on BB emission ratios. Emission factors (EFs) were derived for a range of trace gases, some never before reported for Australian fires, (including hydrogen, phenol and toluene) using the carbon mass balance method. This provides a unique set of EFs for Australian coastal heathland fires. Methyl halide EFs were higher than EFs reported from other studies in Australia and the Northern Hemisphere which is likely due to high halogen content in vegetation on Robbins Island. This work demonstrates the substantial impact that BB plumes can have on the composition of marine air, and the significant changes that can occur as the plume interacts with terrestrial, aged urban and marine emission sources.

  17. New SI-traceable reference gas mixtures for fluorinated gases at atmospheric concentration

    Science.gov (United States)

    Guillevic, Myriam; Wyss, Simon A.; Pascale, Céline; Vollmer, Martin K.; Niederhauser, Bernhard; Reimann, Stefan

    2016-04-01

    In order to better support the monitoring of greenhouse gases in the atmosphere, we develop a method to produce reference gas mixtures for fluorinated gases (F-gases, i.e. gases containing fluorine atoms) in a SI-traceable way, meaning that the amount of substance fraction in mole per mole is traceable to SI-units. These research activities are conducted in the framework of the HIGHGAS and AtmoChem-ECV projects. First, single-component mixtures in synthetic air at ~85 nmol/mol (ppb) are generated for HFC-125 (pentafluoroethane, a widely used HFC) and HFC-1234yf (2,3,3,3-tetrafluoropropene, a car air conditioner fluid of growing importance). These mixtures are first dynamically produced by permeation: a permeator containing the pure substance loses mass linearly over time under a constant gas flow, in the permeation chamber of a magnetic suspension balance, which is regularly calibrated. This primary mixture is then pressurised into Silconert2000-coated stainless steel cylinders by cryo-filling. In a second step these mixtures are dynamically diluted using 2 subsequent dilution steps piloted by mass flow controllers (MFC) and pressure controllers. The assigned mixture concentration is calculated mostly based on the permeator mass loss, on the carrier gas purity and on the MFCs flows. An uncertainty budget is presented, resulting in an expanded uncertainty of 2% for the HFC-125 reference mixture and of 2.5% for the HFC-1234yf mixture (95% confidence interval). The final gas, with near-atmospheric concentration (17.11 pmol/mol for HFC-125, 2.14 pmol/mol for HFC-1234yf) is then measured with Medusa-GC/MS technology against standards calibrated on existing reference scales. The assigned values of the dynamic standards are in excellent agreement with measurements vs the existing reference scales, SIO-14 from the Scripps Institution of Oceanography for HFC-125 and Empa-2013 for HFC-1234yf. Moreover, the Medusa-GC/MS measurements show the excellent purity of the SI

  18. Biomass Burning: The Cycling of Gases and Particulates from the Biosphere to the Atmosphere

    Science.gov (United States)

    Levine, J. S.

    2003-12-01

    Biomass burning is both a process of geochemical cycling of gases and particulates from the biosphere to the atmosphere and a process of global change. In the preface to the book, One Earth, One Future: Our Changing Global Environment (National Academy of Sciences, 1990), Dr. Frank Press, the President of the National Academy of Sciences, writes: "Human activities are transforming the global environment, and these global changes have many faces: ozone depletion, tropical deforestation, acid deposition, and increased atmospheric concentrations of gases that trap heat and may warm the global climate."It is interesting to note that all four global change "faces" identified by Dr. Press have a common thread - they are all caused by biomass burning.Biomass burning or vegetation burning is the burning of living and dead vegetation and includes human-initiated burning and natural lightning-induced burning. The bulk of the world's biomass burning occurs in the tropics - in the tropical forests of South America and Southeast Asia and in the savannasof Africa and South America. The majority of the biomass burning, primarily in the tropics (perhaps as much as 90%), is believed to be human initiated for land clearing and land-use change. Natural fires triggered by atmospheric lightning only accounts for ˜10% of all fires (Andreae, 1991). As will be discussed, a significant amount of biomass burning occurs in the boreal forests of Russia, Canada, and Alaska.Biomass burning is a significant source of gases and particulates to the regional and global atmosphere (Crutzen et al., 1979; Seiler and Crutzen, 1980; Crutzen and Andreae, 1990; Levine et al., 1995). Its burning is truly a multidiscipline subject, encompassing the following areas: fire ecology, fire measurements, fire modeling, fire combustion, remote sensing, fire combustion gaseous and particulate emissions, the atmospheric transport of these emissions, and the chemical and climatic impacts of these emissions. Recently

  19. The terrestrial biosphere as a net source of greenhouse gases to the atmosphere.

    Science.gov (United States)

    Tian, Hanqin; Lu, Chaoqun; Ciais, Philippe; Michalak, Anna M; Canadell, Josep G; Saikawa, Eri; Huntzinger, Deborah N; Gurney, Kevin R; Sitch, Stephen; Zhang, Bowen; Yang, Jia; Bousquet, Philippe; Bruhwiler, Lori; Chen, Guangsheng; Dlugokencky, Edward; Friedlingstein, Pierre; Melillo, Jerry; Pan, Shufen; Poulter, Benjamin; Prinn, Ronald; Saunois, Marielle; Schwalm, Christopher R; Wofsy, Steven C

    2016-03-10

    The terrestrial biosphere can release or absorb the greenhouse gases, carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O), and therefore has an important role in regulating atmospheric composition and climate. Anthropogenic activities such as land-use change, agriculture and waste management have altered terrestrial biogenic greenhouse gas fluxes, and the resulting increases in methane and nitrous oxide emissions in particular can contribute to climate change. The terrestrial biogenic fluxes of individual greenhouse gases have been studied extensively, but the net biogenic greenhouse gas balance resulting from anthropogenic activities and its effect on the climate system remains uncertain. Here we use bottom-up (inventory, statistical extrapolation of local flux measurements, and process-based modelling) and top-down (atmospheric inversions) approaches to quantify the global net biogenic greenhouse gas balance between 1981 and 2010 resulting from anthropogenic activities and its effect on the climate system. We find that the cumulative warming capacity of concurrent biogenic methane and nitrous oxide emissions is a factor of about two larger than the cooling effect resulting from the global land carbon dioxide uptake from 2001 to 2010. This results in a net positive cumulative impact of the three greenhouse gases on the planetary energy budget, with a best estimate (in petagrams of CO2 equivalent per year) of 3.9 ± 3.8 (top down) and 5.4 ± 4.8 (bottom up) based on the GWP100 metric (global warming potential on a 100-year time horizon). Our findings suggest that a reduction in agricultural methane and nitrous oxide emissions, particularly in Southern Asia, may help mitigate climate change.

  20. Production of stable, non-thermal atmospheric pressure rf capacitive plasmas using gases other than helium or neon

    Science.gov (United States)

    Park, Jaeyoung; Henins, Ivars

    2005-06-21

    The present invention enables the production of stable, steady state, non-thermal atmospheric pressure rf capacitive .alpha.-mode plasmas using gases other than helium and neon. In particular, the current invention generates and maintains stable, steady-state, non-thermal atmospheric pressure rf .alpha.-mode plasmas using pure argon or argon with reactive gas mixtures, pure oxygen or air. By replacing rare and expensive helium with more readily available gases, this invention makes it more economical to use atmospheric pressure rf .alpha.-mode plasmas for various materials processing applications.

  1. Atmospheric observations for quantifying emissions of point-source synthetic greenhouse gases (CF4, NF3 and HFC-23)

    Science.gov (United States)

    Arnold, Tim; Manning, Alistair J.; Li, Shanlan; Kim, Jooil; Park, Sunyoung; Fraser, Paul J.; Mitrevski, Blagoj; Steele, L. Paul; Krummel, Paul B.; Mühle, Jens; Weiss, Ray F.

    2016-04-01

    The fluorinated species carbon tetrafluoride (CF4; PFC-14), nitrogen trifluoride (NF3) and trifluoromethane (CHF3; HFC-23) are potent greenhouse gases with 100-year global warming potentials of 6,630, 16,100 and 12,400, respectively. Unlike the majority of CFC-replacement compounds that are emitted from fugitive and mobile emission sources, these gases are largely emitted from large single point sources - semiconductor manufacturing facilities (all three), aluminium smelting plants (CF4) and chlorodifluoromethane factories (HFC-23). In this work we show the potential for atmospheric measurements to understand regional sources of these gases and to highlight emission 'hotspots'. We target our analysis on measurements from two Advanced Global Atmospheric Gases Experiment (AGAGE) long term monitoring sites that are particularly sensitive to regional emissions of these gases: Gosan on Jeju Island in the Republic of Korea and Cape Grim on Tasmania in Australia. These sites measure CF4, NF3 and HFC-23 alongside a suite of greenhouse and stratospheric ozone depleting gases every two hours using automated in situ gas-chromatography mass-spectrometry instrumentation. We couple each measurement to an analysis of air history using the regional atmospheric transport model NAME (Numerical Atmospheric dispersion Modelling Environment) driven by 3D meteorology from the Met Office's Unified Model, and use a Bayesian inverse method (InTEM - Inversion Technique for Emission Modelling) to calculate yearly emission changes over a decade (2005-2015) at high spatial resolution. At present these gases make a small contribution to global radiative forcing, however, given that their impact could rise significantly and that point sources of such gases can be mitigated, atmospheric monitoring could be an important tool for aiding emissions reduction policy.

  2. Characteristics of Ultrafine Particles and Their Relationships with Meteorological Factors and Trace Gases in Wuhan, Central China

    Directory of Open Access Journals (Sweden)

    Tianhao Zhang

    2016-07-01

    Full Text Available Ultrafine particles with a diameter below 1 μm are strongly linked to traffic and industrial emissions, causing a growing global health concern. In order to reveal the characteristics of ultrafine particles in central China, which makes up the sparse research in industrial cities of a developing country, particle number concentrations (PNC together with meteorological parameters and concentrations of trace gases were measured over one year in Wuhan. The number concentration of ultrafine particles peaked in winter and was the lowest in summer across the entire size range monitored. Further, particles with a diameter smaller than 30 nm increased dramatically in concentration with decreasing diameter. The monthly averaged number concentrations of particles discriminated in three size ranges formed a near- inverse parabolic distribution peaking in January. This trend is supported by a negative correlation between PNC and precipitation, temperature, and mixing layer height, which emphasizes the effect of these meteorological parameters on scouring, convection, and diffusion of particles. However, since wind not only disperses particulate matter but also brings in exogenous particles, wind speed plays an equivocal role in particle number concentrations. The diurnal analysis indicates that hourly measurements of trace gases concentrations could be used as a proxy for dense industrial activities and to reveal some complex chemical reactions. The results of this study offer reasonable estimations of particle impacts and provide references for policymaking of emission control in the industrial cities of developing countries.

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

    Energy Technology Data Exchange (ETDEWEB)

    Angulo-Brown, F.; Sanchez-Salas, N. [Departamento de Fisica, Escuela Superior de Fisica y Matematicas, del IPN Edif. 9, U.P. Zacatenco, 07738 Mexico, D.F. (Mexico); Barranco-Jimenez, M.A. [Departamento de Ciencias Basicas, Escuela Superior de Computo, del IPN Av., Miguel Bernard s/n., Esq. Juan de Dios Batiz, U.P. Zacatenco, 07738 Mexico, D.F. (Mexico); Rosales, M.A. [Departamento de Fisica y Matematicas, Universidad de las Americas Puebla, Exhacienda Sta., Catarina Martir, Cholula 72820, Puebla (Mexico)

    2009-11-15

    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{sub 2}. The atmospheric concentration of CO{sub 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{sub 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{sub 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{sub 2} concentration, for instance, drastically diminishes. A simple qualitative criterion to design ecological taxes is also suggested. (author)

  4. A comparative summary on streamers of positive corona discharges in water and atmospheric pressure gases

    Science.gov (United States)

    Tachibana, Kunihide; Motomura, Hideki

    2015-07-01

    From an intention of summarizing present understandings of positive corona discharges in water and atmospheric pressure gases, we tried to observe streamers in those media by reproducing and complementing previously reported results under a common experimental setup. We used a point-to-plane electrode configuration with different combinations of electrode gap (7 and 19 mm length) and pulsed power sources (0.25 and 2.5 ɛs duration). The general features of streamers were similar and the streamer-to-spark transition was also observed in both the media. However, in the details large differences were observed due to inherent nature of the media. The measured propagation speed of streamers in water of 0.035 × 106 ms-1 was much smaller than the speed in gases (air, N2 and Ar) from 0.4 to 1.1 × 106 ms-1 depending on species. In He the discharge looked glow-like and no streamer was observed. The other characteristics of streamers in gases, such as inception voltage, number of branches and thickness did also depend on the species. The thickness and the length of streamers in water were smaller than those in gases. From the volumetric expansion of a streamer in water after the discharge, the molecular density within the streamer medium was estimated to be rarefied from the density of water by about an order of magnitude in the active discharge phase. We derived also the electron density from the analysis of Stark broadened spectral lines of H and O atoms on the order of 1025 m-3 at the earlier time of the streamer propagation. The analyzed background blackbody radiation, rotational temperature of OH band emission and population density of Cu atomic lines yielded a consistent temperature of the streamer medium between 7000 and 10 000 K. Using the present data with a combination of the analysis of static electric field and previously reported results, we discuss the reason for the relatively low streamer inception voltage in water as compared to the large difference in the

  5. Organic Nitrates: A Complex Family of Atmospheric Trace Constituents

    Science.gov (United States)

    Ballschmiter, K.; Fischer, R. G.; Grünert, A.; Kastler, J.; Schneider, M.; Woidich, S.

    2003-04-01

    Biogenic and geogenic hydrocarbons are the precursors of organic nitrates that are formed as tropospheric photo-oxidation products in the presence of NOx. Air chemistry leads to a very complex pattern of nitric acid esters: alkyl nitrates, aryl-alkyl nitrates, and bifunctional nitrates like alkyl dinitrates, hydroxy alkyl nitrates and carbonyl alkyl nitrates. We have analyzed the pattern of organic nitrates in air samples after adsorption/thermal desorption (low volume sampling-LVS) or adsorption/solvent desorption (high volume sampling-HVS) by capillary gas chromatography with electron capture (ECD) and mass spectrometric detection (MSD) using air aliquotes of 100 up to 3000 liters on column. The complexity of the organic nitrates found in air requires a group pre-separation by normal phase liquid chromatography. A detection limit per compound of 0.005 ppt(v) is achieved by our approach. We have synthesized a broad spectrum of organic nitrates as reference compounds. Air samples were taken from central Europe, the US West (Utah, Nevada, California), and the North- and South Atlantic including Antarctica. Levels and patterns of the regional and global occurrence of the various groups of C1-C12 organic nitrates including dinitrates and hydroxy nitrates and nitrates of isoprene (2-methylbutadiene) are presented. Werner G., J. Kastler, R. Looser, K. Ballschmiter: "Organic nitrates of isoprene as atmospheric trace compounds" Angewandte Chemie - International Edition (1999) 38: 1634-1637. Woidich S., O. Froescheis, O. Luxenhofer, K. Ballschmiter: "EI- and NCI-mass spectrometry of arylalkyl nitrates and their occurrence in urban air" Fresenius J. Anal. Chem. (1999) 364 : 91-99. Kastler, J; Jarman, W; Ballschmiter, K.: "Multifunctional organic nitrates as constituents in European and US urban photo-smog" Fresenius J. Anal. Chem. (2000) 368:244-249. Schneider M., K. Ballschmiter: "C3-C14 alkyl nitrates in remote South Atlantic air" Chemosphere (1999) 38: 233-244. Fischer

  6. Continuous and immediate method for the detection of SF/sub 6/ and other tracer gases by electron capture in atmospheric diffusion experiments

    Energy Technology Data Exchange (ETDEWEB)

    Thomsen, E.L. (Aerosol Lab., Risoe, Denmark); Lovelock, J.E.

    1976-01-01

    In many atmospheric diffusion experiments using tracer gases continuous tracer recording is of decisive importance. The main obstacle to continuous electron capture detection of tracer gases in the atmosphere is presented by the oxygen, which is an electron capturer. A method for removing this difficulty is described. Its practical use in an airborne atmospheric plume diffusion experiment is demonstrated.

  7. Trace Atmospheric Gas Analyzer (TAGA) Dispersant Data for BP Spil/Deepwater Horizon - August 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  8. Increased soil emissions of potent greenhouse gases under increased atmospheric CO2.

    Science.gov (United States)

    van Groenigen, Kees Jan; Osenberg, Craig W; Hungate, Bruce A

    2011-07-13

    Increasing concentrations of atmospheric carbon dioxide (CO(2)) can affect biotic and abiotic conditions in soil, such as microbial activity and water content. In turn, these changes might be expected to alter the production and consumption of the important greenhouse gases nitrous oxide (N(2)O) and methane (CH(4)) (refs 2, 3). However, studies on fluxes of N(2)O and CH(4) from soil under increased atmospheric CO(2) have not been quantitatively synthesized. Here we show, using meta-analysis, that increased CO(2) (ranging from 463 to 780 parts per million by volume) stimulates both N(2)O emissions from upland soils and CH(4) emissions from rice paddies and natural wetlands. Because enhanced greenhouse-gas emissions add to the radiative forcing of terrestrial ecosystems, these emissions are expected to negate at least 16.6 per cent of the climate change mitigation potential previously predicted from an increase in the terrestrial carbon sink under increased atmospheric CO(2) concentrations. Our results therefore suggest that the capacity of land ecosystems to slow climate warming has been overestimated.

  9. Atmosphere Resource Recovery and Environmental Monitoring Trace Contaminant Control Through FY 2012

    Science.gov (United States)

    Perry, J. L.; Pruitt, M. W.; Wheeler, R. M.; Monje, O.

    2013-01-01

    Trace contaminant control has been a concern of spacecraft designers and operators from early in the progression of manned spaceflight. Significant technological advancement has occurred since the first designs were implemented in the 1960s, culminating in the trace contaminant control system currently in use aboard the International Space Station as part of the atmosphere revitalization system.

  10. Real-time measurements of ammonia, acidic trace gases and water-soluble inorganic aerosol species at a rural site in the Amazon Basin

    Directory of Open Access Journals (Sweden)

    I. Trebs

    2004-01-01

    Full Text Available We measured the mixing ratios of ammonia (NH3, nitric acid (HNO3, nitrous acid (HONO, hydrochloric acid (HCl, sulfur dioxide (SO2 and the corresponding water-soluble inorganic aerosol species, ammonium (NH4+, nitrate (NO3-, nitrite (NO2-, chloride (Cl- and sulfate (SO42-, and their diel and seasonal variations at a pasture site in the Amazon Basin (Rondônia, Brazil. This study was conducted within the framework of LBA-SMOCC (Large Scale Biosphere Atmosphere Experiment in Amazonia - Smoke Aerosols, Clouds, Rainfall and Climate: Aerosols from Biomass Burning Perturb Global and Regional Climate. Sampling was performed from 12 September to 14 November 2002, extending from the dry season (extensive biomass burning activity, through the transition period to the wet season (background conditions. Measurements were made continuously using a wet-annular denuder (WAD in combination with a Steam-Jet Aerosol Collector (SJAC followed by suitable on-line analysis. A detailed description and verification of the inlet system for simultaneous sampling of soluble gases and aerosol compounds is presented. Overall measurement uncertainties of the ambient mixing ratios usually remained below 15%. The limit of detection (LOD was determined for each single data point measured during the field experiment. Median LOD values (3σ-definition were ≤0.015ppb for acidic trace gases and aerosol anions and ≤0.118ppb for NH3 and aerosol NH4+. Mixing ratios of acidic trace gases remained below 1ppb throughout the measurement period, while NH3 levels were an order of magnitude higher. Accordingly, mixing ratios of NH4+ exceeded those of other inorganic aerosol contributors by a factor of 4 to 10. During the wet season, mixing ratios decreased by nearly a factor of 3 for all compounds compared to those observed when intensive biomass burning took place. Additionally, N-containing gas and aerosol species featured pronounced diel variations. This is attributed to strong

  11. Real-time measurements of ammonia, acidic trace gases and water-soluble inorganic aerosol species at a rural site in the Amazon Basin

    Directory of Open Access Journals (Sweden)

    I. Trebs

    2004-02-01

    Full Text Available We measured the mixing ratios of ammonia (NH3, nitric acid (HNO3, nitrous acid (HONO, hydrochloric acid (HCl, sulfur dioxide (SO2 and the corresponding water-soluble inorganic aerosol species, ammonium (NH4+, nitrate (NO3, nitrite (NO2, chloride (Cl and sulfate (SO42−, and their diel and seasonal variations at a pasture site in the Amazon Basin (Rondônia, Brazil. This study was conducted within the framework of LBA-SMOCC (Large Scale Biosphere Atmosphere Experiment in Amazonia Smoke Aerosols, Clouds, Rainfall and Climate. Sampling was performed from 12 September to 14 November 2002, extending from the dry season (extensive biomass burning activity, through the transition period to the wet season (background conditions. Measurements were made continuously using a wet-annular denuder in combination with a Steam-Jet Aerosol Collector (SJAC followed by suitable on-line analysis. A detailed description and verification of the inlet system for simultaneous sampling of soluble gases and aerosol compounds is presented. Overall measurement uncertainties of the ambient mixing ratios usually remained below 15%. The limit of detection (LOD was determined for each single data point measured during the field experiment. Median LOD values (3σ-definition were ≤0.015 ppb for acidic trace gases and aerosol anions and ≤0.118 ppb for NH3 and aerosol NH4+. Mixing ratios of acidic trace gases remained below 1ppb throughout the measurement period, while NH3 levels were an order of magnitude higher. Accordingly, mixing ratios of NH4+ exceeded those of other inorganic aerosol contributors by a factor of 4 to 10. During the wet season, mixing ratios decreased by nearly a factor of 3 for all compounds compared to those observed when intensive biomass burning

  12. Global warming: Experimental study about the effect of accumulation of greenhouse gases in the atmosphere

    Science.gov (United States)

    Molto, Carlos; Mas, Miquel

    2010-05-01

    The project presented here was developed by fifteen year old students of the Institut Sabadell (Sabadell Secondary School. Spain). The objective of this project was to raise the students awareness' about the problem of climate change, mainly caused by the accumulation of greenhouse gases in the atmosphere. It is also intended that students use the scientific method as an effective system of troubleshooting and that they use the ICTs (Information and Communication Technologies) to elicit data and process information. To develop this project, four lessons of sixty minutes each were needed. The first lesson sets out the role of the atmosphere as an Earth's temperature regulator, highlighting the importance of keeping the levels of carbon dioxide, methane and water steam in balance. The second lesson is focused on the experimental activity that students will develop in the following lesson. In lesson two, students will present and justify their hypothesis about the experiment. Some theoretical concepts, necessary to carry out the experiment, will also be explained. The third lesson involves the core of the project, that is the experiment in the laboratory. The experiment consists on performing the atmosphere heating on a little scale. Four different atmospheres are created inside four plastic boxes heated by an infrared lamp. Students work in groups (one group for each atmosphere) and have to monitor the evolution of temperature by means of a temperature sensor (Multilog software). The first group has to observe the relationship between temperature and carbon dioxide levels increase, mainly caused by the widespread practice of burning fossil fuels by growing human populations. The task of this group is to measure simultaneously the temperature of an empty box (without CO2) and the temperature of a box with high carbon dioxide concentration. The carbon dioxide concentration is the result of the chemical reaction when sodium carbonate mixes with hydrochloric acid. The

  13. The state of greenhouse gases in the atmosphere using global observations through 2013

    Science.gov (United States)

    Tarasova, Oksana; Koide, Hiroshi; Dlugokencky, Ed; Montzka, Stephen A.; Keeling, Ralph; Tanhua, Toste; Lorenzoni, Laura

    2015-04-01

    We present results from the tenth annual Greenhouse Gas Bulletin (http://www.wmo.int/pages/prog/arep/gaw/ ghg/GHGbulletin.html) of the World Meteorological Organization (WMO). The results are based on research and observations performed by laboratories contributing to the WMO Global Atmosphere Watch (GAW) Programme (www.wmo.int/gaw). The Bulletin presents results of global analyses of observational data collected according to GAW recommended practices and submitted to the World Data Center for Greenhouse Gases (WDCGG), and for the first time, it includes a summary of ocean acidification. Bulletins are prepared by the WMO/GAW Scientific Advisory Group for Greenhouse Gases (http://www.wmo.int/pages/prog/arep/gaw/ScientificAdvisoryGroups.html) in collaboration with WDCGG. The summary of ocean acidification and trends in ocean pCO2 was jointly produced by the International Ocean Carbon Coordination Project (IOCCP) of the Intergovernmental Oceanographic Commission of UNESCO (IOC-UNESCO), the Scientific Committee on Oceanic Research (SCOR), and the Ocean Acidification International Coordination Centre (OA-ICC) of the International Atomic Energy Agency (IAEA). The tenth Bulletin included a special edition published prior to the United Nations Climate Summit in September 2014. The scope of this edition was to demonstrate the level of emission reduction necessary to stabilize radiative forcing by long-lived greenhouse gases. It shows in particular that a reduction in radiative forcing from its current level (2.92 W m-2 in 2013) requires significant reductions in anthropogenic emissions of all major greenhouse gases. Observations used for global analysis are collected at more than 100 marine and terrestrial sites worldwide for CO2 and CH4 and at a smaller number of sites for other greenhouse gases. Globally averaged dry-air mole fractions of carbon dioxide, methane and nitrous oxide derived from this network reached new highs in 2013, with CO2 at 396.0 ± 0.1 ppm, CH4 at

  14. Monte Carlo Ray Tracing Based Sensitivity Analysis of the Atmospheric and the Ocean Parameters on Top of the Atmosphere Radiance

    Directory of Open Access Journals (Sweden)

    Kohei Arai

    2013-01-01

    Full Text Available Monte Carlo Ray Tracing: MCRT based sensitivity analysis of the geophysical parameters (the atmosphere and the ocean on Top of the Atmosphere: TOA radiance in visible to near infrared wavelength regions is conducted. As the results, it is confirmed that the influence due to the atmosphere is greater than that of the ocean. Scattering and absorption due to aerosol particles and molecules in the atmosphere is major contribution followed by water vapor and ozone while scattering due to suspended solid is dominant contribution for the ocean parameters.

  15. Emissions of Trace Gases and Particles from Two Ships in the Southern Atlantic Ocean

    Science.gov (United States)

    Sinha, Parikhit; Hobbs, Peter V.; Yokelson, Robert J.; Christian, Ted J.; Kirchstetter, Thomas W.; Bruintjes, Roelof

    2003-01-01

    Measurements were made of the emissions of particles and gases from two diesel-powered ships in the southern Atlantic Ocean off the coast of Namibia. The measurements are used to derive emission factors from ships of three species not reported previously, namely, black carbon, accumulation-mode particles, and cloud condensation nuclei (CCN), as well as for carbon dioxide, carbon monoxide (CO), methane (CH4), non-methane hydrocarbons, sulfur dioxide (SO2), nitrogen oxides (NOx), and condensation nuclei. The effects of fuel grade and engine power on ship emissions are discussed. The emission factors are combined with fuel usage data to obtain estimates of global annual emissions of various particles and gases from ocean-going ships. Global emissions of black carbon, accumulation- mode particles, and CCN from ocean-going ships are estimated to be 19-26 Gg yr(sup -1), (4.4-6.1) x 10(exp 26) particles yr(sup -1), and (1.0-1.5) x l0(exp 26) particles yr(sup -1), respectively. Black carbon emissions from ocean-going ships are approximately 0.2% of total anthropogenic emissions. Emissions of NOx and SO2 from ocean-going ships are approximately 10-14% and approximately 3-4%, respectively, of the total emissions of these species from the burning of fossil fuels, and approximately 40% and approximately 70%, respectively, of the total emissions of these species from the burning of biomass. Global annual emissions of CO and CH4 from ocean-going ships are approximately 2% and approximately 2-5%, respectively, of natural oceanic emissions of these species.

  16. Potential Trace Metal–Organic Complexation in the Atmosphere

    Directory of Open Access Journals (Sweden)

    Hiroshi Okochi

    2002-01-01

    Full Text Available It is possible that metal–organic complexation enhances the uptake of gaseous organic compounds and the solubility of metals in aerosols and atmospheric water. We investigated potential atmospheric organic ligands and the enhanced uptake of hydroxy-, oxo-, and dicarboxylic acids as well as dicarbonyls into atmospheric aqueous aerosol. We examined complexation with transition metals (iron, manganese, nickel, copper, zinc and lead on the basis of available references and our experimental data. Humic-like substances are most likely ligands in the atmosphere, although this is a poorly characterized material. A number of polycarboxylic acids and hydroxy forms (e.g., citric and tartronic acids effectively complex metals such as copper in atmospheric aerosols. The simple equilibrium model calculations show that the effect of the complexation on the gas–aqueous phase partition of gaseous atmospheric ligands is quite small for the ligands with the high physical Henry’s law constants, e.g., dicarboxylic acids represented by oxalic acid, even if they have high affinity with metal ions. The lower Henry’s law constants of the α-dicarbonyls, such as glyoxal and methylglyoxal, mean that the complexation could lead to profound increases in their partition into the aqueous phase. Despite quantum mechanical arguments for copper–glyoxal complexes, experiments showed no evidence of complexation between either hydrated or unhydrated α-dicarbonyls and the cupric ion. By contrast the β-dicarbonyl, malondialdehyde, has properties that would allow it to partition into atmospheric water via the complexation with metal ions under some conditions.

  17. Field measurements of trace gases and aerosols emitted by peat fires in Central Kalimantan, Indonesia, during the 2015 El Niño

    Science.gov (United States)

    Stockwell, Chelsea E.; Jayarathne, Thilina; Cochrane, Mark A.; Ryan, Kevin C.; Putra, Erianto I.; Saharjo, Bambang H.; Nurhayati, Ati D.; Albar, Israr; Blake, Donald R.; Simpson, Isobel J.; Stone, Elizabeth A.; Yokelson, Robert J.

    2016-09-01

    Peat fires in Southeast Asia have become a major annual source of trace gases and particles to the regional-global atmosphere. The assessment of their influence on atmospheric chemistry, climate, air quality, and health has been uncertain partly due to a lack of field measurements of the smoke characteristics. During the strong 2015 El Niño event we deployed a mobile smoke sampling team in the Indonesian province of Central Kalimantan on the island of Borneo and made the first, or rare, field measurements of trace gases, aerosol optical properties, and aerosol mass emissions for authentic peat fires burning at various depths in different peat types. This paper reports the trace gas and aerosol measurements obtained by Fourier transform infrared spectroscopy, whole air sampling, photoacoustic extinctiometers (405 and 870 nm), and a small subset of the data from analyses of particulate filters. The trace gas measurements provide emission factors (EFs; grams of a compound per kilogram biomass burned) for up to ˜ 90 gases, including CO2, CO, CH4, non-methane hydrocarbons up to C10, 15 oxygenated organic compounds, NH3, HCN, NOx, OCS, HCl, etc. The modified combustion efficiency (MCE) of the smoke sources ranged from 0.693 to 0.835 with an average of 0.772 ± 0.053 (n = 35), indicating essentially pure smoldering combustion, and the emissions were not initially strongly lofted. The major trace gas emissions by mass (EF as g kg-1) were carbon dioxide (1564 ± 77), carbon monoxide (291 ± 49), methane (9.51 ± 4.74), hydrogen cyanide (5.75 ± 1.60), acetic acid (3.89 ± 1.65), ammonia (2.86 ± 1.00), methanol (2.14 ± 1.22), ethane (1.52 ± 0.66), dihydrogen (1.22 ± 1.01), propylene (1.07 ± 0.53), propane (0.989 ± 0.644), ethylene (0.961 ± 0.528), benzene (0.954 ± 0.394), formaldehyde (0.867 ± 0.479), hydroxyacetone (0.860 ± 0.433), furan (0.772 ± 0.035), acetaldehyde (0.697 ± 0.460), and acetone (0.691 ± 0.356). These field data support significant revision

  18. Evolution of Trace Gases and Particles Emitted by a Chaparral Fire in California

    Science.gov (United States)

    2012-02-07

    resolution aerosol mass spectrometry, J. Geophys. Res., 112, D22305, doi:10.1029/2007JD008614, 2007. Bertschi, I. T., Yokelson, R. J., Ward, D. E., Babbitt ...10.1016/j.foreco.2003.11.006, 2004. Chakrabarty, R. K., Moosmuller, H., Garro, M. A., Arnott, W. P., Walker, J., Susott, R. A., Babbitt , R. E., Wold, C. E...transformation and growth in the atmosphere, J. Appl. Meteorol., 33, 792–796, 1994b. Trent, A., Davies, M. A., Fisher, R., Thistle, H., and Babbitt , R

  19. Global analysis of the relation between aerosols and short-lived trace gases

    Directory of Open Access Journals (Sweden)

    J. P. Veefkind

    2010-08-01

    Full Text Available The spatial and temporal correlations between concurrent satellite observations of aerosol optical thickness (AOT from the Moderate Resolution Imaging Spectroradiometer (MODIS and tropospheric columns of nitrogen dioxide, sulfur dioxide, and formaldehyde from the Ozone Monitoring Instrument (OMI are used to infer information on the global composition of aerosol particles. When averaging the satellite data over large regions and longer time periods, we find significant correlation between MODIS AOT and OMI trace gas columns for various regions in the world. This suggests that enhanced aerosol and trace gas concentrations originate from common sources, such as fossil fuel combustion, biomass burning, and organic compounds released from the biosphere. This leads us to propose that satellite-inferred AOT to NO2 ratios for regions with comparable photochemical regimes can be used as indicators for the relative (local efficiency of combustion processes. Indeed, satellites observe low AOT to NO2 ratios over the eastern United States and western Europe, and high AOT to NO2 ratios over comparably industrialized regions in eastern Europe and China. Emission databases and OMI SO2 observations over these regions suggest a much stronger sulfur contribution to aerosol formation than over the well-regulated areas of the eastern United States and western Europe. Furthermore, satellite observations show AOT to NO2 ratios are a factor 100 higher over biomass burning regions than over industrialized areas, reflecting the unregulated burning practices with strong primary particle emissions in the tropics compared to the heavily controlled combustion processes in the industrialized Northern Hemisphere. Simulations with a global chemistry transport model (GEOS-Chem capture most of these differences, providing some confidence in our understanding of aerosol sources, formation mechanisms, and sinks. Wintertime

  20. Flux measurements of energy and trace gases in urban Houston, Texas

    Science.gov (United States)

    Boedeker, I.; Schade, G. W.; Adams, S.; Park, C.

    2008-12-01

    We describe the setup and some first year results of a new flux measurements tower in an urban area. An existing radio communications tower 4 km north of downtown Houston was equipped with micrometeorological instrumentation and trace gas sampling lines in spring 2007. Wind speed, temperature and relative humidity are recorded at five levels between 12 and 60 m above ground; 3-D wind speed measurements, solar and net radiances, and trace gas sampling are established from the 60 m level. A closed path IRGA is used for CO2 and water vapor fluxes, and independent instrumentation for criteria pollutant and VOC fluxes. Two CSI data loggers and software control the measurements, and EdiRe software is used to analyze turbulence data and compute fluxes. A project description is provided at http://atmo.tamu.edu/yellowcabtower. Surface properties as calculated from the gradient measurements show the site to be surprisingly uniform, with displacement heights between 5 and 9 m and roughness lengths between 0.4 and 0.7 m, despite urban heterogeneity. The latter is investigated through visible/near IR orthoimagery and LIDAR data, which are incorporated into a local GIS. Net radiation was also only marginally affected by surface heterogeneity. At this urban location it is balanced by roughly equal amounts of sensible heat, latent heat, and storage fluxes. Latent heat flux, however, is smaller outside the growing season, with an equivalent increase in winter storage fluxes, as expected. Significant differences are also observed with direction during summer, showing decreased Bowen ratios and lower CO2 emissions from sectors with a larger urban tree canopy cover in the footprint. The largely mature, dominantly oak urban canopy cover alleviates approximately 100 W m- 2 during typical summer days. On the other hand, anthropogenic CO2 emissions dominate over photosynthetic uptake all year round. Measured carbon fluxes peak during morning rush-hour traffic, especially when increasing

  1. Herschel/PACS spectroscopy of trace gases of the stratosphere of Titan

    CERN Document Server

    Rengel, Miriam; Hartogh, Paul; Lellouch, Emmanuel; Feuchtgruber, Helmut; Moreno, Raphael; Jarchow, Christopher; Courtin, Regis; Cernicharo, Jose; Lara, Luisa

    2014-01-01

    Aims: We investigate the composition of Titan's stratosphere from new medium-resolution far-infrared observations performed with the full range of Herschel's Photodetector Array Camera and Spectrometer (PACS) (51-220 $\\mu$m at a resolution $\\lambda$/$\\Delta \\lambda$ ranging from 950 to 5500 depending on wavelength and grating order). Methods: Using PACS, we obtained the spectral emission of several features of the Titan's stratosphere. We used a line-by-line radiative transfer code and the least-squares fitting technique to infer the abundances of the trace constituents. Results: Numerous spectral features attributable to CH$_4$, CO, HCN, and H$_2$O are present. From the flux density spectrum measured and by a detailed comparison with synthetic spectra, we constrain the stratospheric abundance of CH4, which is assumed to be constant with altitude, to be 1.29 $\\pm$ 0.03%. Similarly, we constrain the abundance of CO to be 50 $\\pm$ 2 ppm, and the HCN vertical distribution consistent with an increase from 40 ppb ...

  2. Applications of broadband cavity enhanced spectroscopy for measurements of trace gases and aerosols

    Science.gov (United States)

    Washenfelder, R. A.; Attwood, A. R.; Brock, C. A.; Brown, S. S.; Dube, W. P.; Flores, J. M.; Langford, A. O.; Min, K. E.; Rudich, Y.; Stutz, J.; Wagner, N.; Young, C.; Zarzana, K. J.

    2015-12-01

    Broadband cavity enhanced spectroscopy (BBCES) uses a broadband light source, optical cavity, and multichannel detector to measure light extinction with high sensitivity. This method differs from cavity ringdown spectroscopy, because it uses an inexpensive, incoherent light source and allows optical extinction to be determined simultaneously across a broad wavelength region.Spectral fitting methods can be used to retrieve multiple absorbers across the observed wavelength region. We have successfully used this method to measure glyoxal (CHOCHO), nitrous acid (HONO), and nitrogen dioxide (NO2) from ground-based and aircraft-based sampling platforms. The detection limit (2-sigma) in 5 s for retrievals of CHOCHO, HONO and NO2 is 32, 250 and 80 parts per trillion (pptv).Alternatively, gas-phase absorbers can be chemically removed to allow the accurate determination of aerosol extinction. In the laboratory, we have used the aerosol extinction measurements to determine scattering and absorption as a function of wavelength. We have deployed a ground-based field instrument to measure aerosol extinction, with a detection limit of approximately 0.2 Mm-1 in 1 min.BBCES methods are most widely used in the near-ultraviolet and visible spectral region. Recently, we have demonstrated measurements at 315-350 nm for formaldehyde (CH2O) and NO2. Extending the technique further into the ultraviolet spectral region will allow important additional measurements of trace gas species and aerosol extinction.

  3. Bioindication of atmospheric trace metals - With special references to megacities

    Energy Technology Data Exchange (ETDEWEB)

    Markert, Bernd, E-mail: markert@schlundmail.de [Fliederweg 17, D-49733 Haren/Erika (Germany); Wuenschmann, Simone [Fliederweg 17, D-49733 Haren/Erika (Germany); Fraenzle, Stefan [International Graduate School Zittau, D-02763 Zittau (Germany); Graciana Figueiredo, Ana Maria; Ribeiro, Andreza P. [Instituto de Pesquisas Energeticas e Nucleares, IPEN-CNEN/SP, Av. Prof. Linea Prestes 2242, CEP 05508-090, Sao Paulo (Brazil); Wang Meie [State Key Laboratory of Urban and Regional Ecology, Research Centre for Eco-environmental Sciences, Beijing 110016 (China)

    2011-08-15

    After considering the particular problems of atmospheric pollution in megacities, i.e. agglomerations larger than 5 mio. inhabitants, with urbanization of World's population going on steadily, possibilities of active biomonitoring by means of green plants are discussed. Based on specific definitions of active and passive bioindication the chances of monitoring heavy metals in Sao Paulo megacity were demonstrated (first results published before). This is to show that there is need for increased use of bioindication to tackle the particular problems of megacities concerning environmental 'health', the data to be processed according to the Multi-Markered-Bioindication-Concept (MMBC). Comparison to other work shows this approach to be reasonable. - Highlights: > Chemical Pollution. > Bioindication. > Multi-Markered-Bioindication-Concept (MMBC). > Mega cities. - Bioindication is a relevant technique for observing the atmospheric deposition of chemical elements of the environment in megacities.

  4. Temporal and latitudinal variations of stratospheric trace gases - A critical comparison between theory and experiment

    Science.gov (United States)

    Wofsy, S. C.

    1978-01-01

    Global calculations of stratospheric HOx, Clx, and NOx are presented which include the effects of planetary albedo and diurnal and seasonal variations of the insolation. Comparisons are made with a wide range of atmospheric measurements at different latitudes and altitudes. Agreement between theory and observations is generally within a factor of 2. The theory appears to explain adequately the major features of latitude and seasonal distributions of NO2 and HNO3. The results indicate that mesospheric OH makes an appreciable contribution to the total OH column abundance and strongly suggest that nitrogen oxides exist principally in the form of HNO3 at high latitudes in winter. There are difficulties in reconciling OH, ClO, and O3 observations in the upper stratosphere.

  5. Trans-Pacific transport and evolution of aerosols and trace gases from Asia during the INTEX-B field campaign

    Directory of Open Access Journals (Sweden)

    B. Adhikary

    2009-08-01

    Full Text Available The Sulfur Transport and dEposition Model (STEM developed at the University of Iowa is applied to the analysis of observations obtained during the Intercontinental Chemical Transport Experiment-Phase B (INTEX-B, conducted over the Pacific Ocean during the 2006 North American spring season. This paper reports on the model performance of meteorological parameters, trace gases, aerosols and photolysis rate (J-values predictions with the NASA DC-8 and NSF/NCAR C-130 airborne measurements along with observations from three surface sites Mt. Bachelor, Trinidad Head and Kathmandu, Nepal. In general the model shows appreciable skill in predicting many of the important aspects of the observed distributions. The major meteorological parameters driving long range transport are accurately predicted by the WRF simulations used in this study. Furthermore, the STEM model predicts aerosols and trace gases concentrations within a standard deviation of most of the observed mean values. The results also point towards areas where model improvements are needed; e.g., the STEM model underestimates CO (15% for the DC8 and 6% for the C-130, whereas it overpredicts PAN (by a factor of two for both aircraft. The errors in the model calculations are attributed to uncertainty in emissions estimates and uncertainty in the top and lateral boundary conditions. Results from a series of sensitivity simulations examining the impact of the growth of emissions in Asia from 2000 to 2006, the importance of biomass burning, the effect of using boundary conditions from different global models, and the role of heterogeneous chemistry on the predictions are also presented. The impacts of heterogeneous reactions at specific times during dust transport episodes can be significant, and in the presence of dust both sulfate and nitrate aerosol production is increased and gas phase nitric acid levels are reduced appreciably (~50%. The aging of the air masses during the long range

  6. Atmospheric Deposition of Trace Elements in Ombrotrophic Peat as a Result of Anthropic Activities

    Science.gov (United States)

    Fabio Lourençato, Lucio; Cabral Teixeira, Daniel; Vieira Silva-Filho, Emmanoel

    2014-05-01

    Ombrotrophic peat can be defined as a soil rich in organic matter, formed from the partial decomposition of vegetable organic material in a humid and anoxic environment, where the accumulation of material is necessarily faster than the decomposition. From the physical-chemical point of view, it is a porous and highly polar material with high adsorption capacity and cation exchange. The high ability of trace elements to undergo complexation by humic substances happens due to the presence of large amounts of oxygenated functional groups in these substances. Since the beginning of industrialization human activities have scattered a large amount of trace elements in the environment. Soil contamination by atmospheric deposition can be expressed as a sum of site contamination by past/present human activities and atmospheric long-range transport of trace elements. Ombrotrophic peat records can provide valuable information about the entries of trace metals into the atmosphere and that are subsequently deposited on the soil. These trace elements are toxic, non-biodegradable and accumulate in the food chain, even in relatively low quantities. Thus studies on the increase of trace elements in the environment due to human activities are necessary, particularly in the southern hemisphere, where these data are scarce. The aims of this study is to evaluate the concentrations of mercury in ombrotrophic peat altomontanas coming from atmospheric deposition. The study is conducted in the Itatiaia National Park, Brazilian conservation unit, situated between the southeastern state of Rio de Janeiro, São Paulo and Minas Gerais. An ombrotrophic peat core is being sampled in altitude (1980m), to measure the trace elements concentrations of this material. As it is conservation area, the trace elements found in the samples is mainly from atmospheric deposition, since in Brazil don't exist significant lithology of trace elements. The samples are characterized by organic matter content which

  7. Bifunctional alkyl nitrates - trace constituents of the atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Kastler, J. [Department of Analytical and Environmental Chemistry, University of Ulm (Germany); Ballschmiter, K. [Center of Technology Assessment in Baden-Wuerttemberg, Stuttgart (Germany)

    1998-04-01

    Mono- and multifunctional esters of nitric acid (alkyl nitrates or organonitrates) form very complex mixtures of organic trace constituents in air. An analytical method was developed which combines selectivity in separation and detection in order to simplify this complexity in analytical terms. Mononitrates, dinitrates, keto nitrates, hydroxy nitrates of alkanes and alkenes, respecitvely, and bifunctional terpene nitrates were synthesized as reference substances. A specially developed new HPLC stationary phase (organonitrate phase) allows a group separation of mono-, di-, and hydroxy nitrates. After the HPLC preseparation the single components were finally separated by capillary HRGC-ECD and HRGC-MSD on polar and non-polar stationary phases. Mass spectrometric detection in the selected-ion-mode using the highly selective NO{sub 2}{sup +} fragment (m/z = 46 amu) led to very good selectivities for the nitric acid ester moiety. The analysis of a 100 m{sup 3} ambient air sample using this new analytical protocol allowed the identification of seven hydroxy nitrates and 24 dinitrates ranging from C2 to C7, 22 of them for the first time ever. (orig.) With 3 figs., 3 tabs., 20 refs.

  8. Can Positive Matrix Factorization identify sources of organic trace gases at the continental GAW site Hohenpeissenberg?

    Directory of Open Access Journals (Sweden)

    M. Leuchner

    2014-03-01

    Full Text Available From the rural Global Atmosphere Watch (GAW site Hohenpeissenberg in the pre-alpine area of Southern Germany, a dataset of 24 C2–C8 non-methane hydrocarbons over a period of seven years was analyzed. Receptor modeling was performed by Positive Matrix Factorization (PMF and the resulting factors were compared to literature source profiles. Photochemical aging during transport to the relatively remote site violates the PMF prerequisite of mass conservation from source to receptor. However, previous studies showed plausible results with this method at remote sites; the applicability and restrictions of the PMF model to such a remote dataset and the influence of photochemical processing on the interpretability of the results are discussed. A six factor solution showed a high stability and the most plausible results. In addition to biogenic sources and remote sources of very stable compounds – reflecting the continental background – four additional anthropogenic factors were resolved that could be divided into two short- and two long-lived patterns from evaporative sources and incomplete combustion processes, respectively. A method to increase the uncertainty for each individual compound by including photochemical reactivity did not improve the results, but decreased the stability of the model output. The contribution of the different source categories at the site over the entire period was, in decreasing order: remote sources, long-lived evaporative sources, residential heating and long-lived combustion sources, short-lived evaporative sources, short-lived combustion sources, and biogenic sources. Despite a low overall impact, biogenic sources played an important role during summer, in particular in terms of reactivity.

  9. Laser Atmospheric Transmitter Receiver-Network (LAnTeRN): A new approach for active measurement of atmospheric greenhouse gases

    Science.gov (United States)

    Dobler, J. T.; Braun, M.; Zaccheo, T.

    2012-12-01

    The Laser Atmospheric Transmitter Receiver-Network (LAnTeRN) is a new measurement concept that will enable local, regional and continental determination of key greenhouse gases, with unparalleled accuracy and precision. This new approach will offer the ability to make low bias, high precision, quasi-continuous, measurements to the accuracies required for separating anthropogenic and biogenic sources and sinks. In 2004 ITT Exelis developed an airborne demonstration unit, based on an intensity modulated continuous wave (IM-CW) lidar approach, for actively measuring atmospheric CO2 and O2. The multi-functional fiber laser lidar (MFLL) system relies on low peak power, high reliability, and efficient telecom laser components to implement this unique measurement approach. While evaluating methods for discriminating against thin clouds for the MFLL instrument, a new measurement concept was conceived. LAnTeRN has several fundamental characteristics in common with the MFLL instrument, but is a fundamentally different implementation and capability. The key difference is that LAnTeRN operates in transmission rather than in the traditional backscatter lidar configuration, which has several distinct advantages. Operating as a forward scatter, bistatic lidar system, LAnTeRN enables consideration of continuous monitoring from a geostationary orbit to multiple locations on the ground. Having the receivers on the ground significantly lowers cost and risk compared to an all space based mission, and allows the transmitter subsystem to be implemented, near term, as a hosted payload. Furthermore, the LAnTeRN measurement approach is also applicable for ground to ground measurements where high precision measurements over a long open path is required, such as facilities monitoring, or monitoring of passive volcanoes and fault lines. Using narrow linewidth laser sources allows flexibility to select the position on the absorption feature being probed. This feature allows for weighting the

  10. Millimeter wavelength spectroscopy of trace atmospheric constituents from the Five College Radio Astronomy Observatory

    Science.gov (United States)

    Huguenin, G. R.; Irvine, W. M.

    1978-01-01

    The Five College Radio Astronomy Observatory system, located in western Massachusetts, is described. It is suggested that high sensitivity in the three-millimeter wavelength band facilitates detection and monitoring of a number of trace molecules in the earth's atmosphere as well as astonomical observation at radio wavelengths. Line formation and radiative transfer in the earth's atmosphere are discussed, and the receiver sensitivity is considered.

  11. Online technique for isotope and mixing ratios of CH4, N2O, Xe and mixing ratios of organic trace gases on a single ice core sample

    Directory of Open Access Journals (Sweden)

    J. Schmitt

    2014-03-01

    Full Text Available Polar ice cores enclosing trace gas species offer a unique archive to study changes in the past atmosphere and in terrestrial/marine source regions. Here we present a new online technique for ice core and air samples to measure a suite of isotope ratios and mixing ratios of trace gas species on a single small sample. Isotope ratios are determined on methane, nitrous oxide and xenon with reproducibilities for ice core samples of 0.15‰ for δ13C-CH4, 0.22‰ for δ15N-N2O, 0.34 ‰ for δ18O-N2O, and 0.05‰ for δ136Xe. Mixing ratios are determined on methane, nitrous oxide, xenon, ethane, propane, methyl chloride and dichloro-difluoromethane with reproducibilities of 7 ppb for CH4, 3 ppb for N2O, 50 ppt for 136Xe, 70 ppt for C2H6, 70 ppt for C3H8, 20 ppt for CH3Cl, and 2 ppt for CCl2F2. The system consists of a vacuum extraction device, a preconcentration unit and a gas chromatograph coupled to an isotope ratio mass spectrometer. CH4 is combusted to CO2 prior to detection while we bypassed the oven for all other species. The highly automated system uses only ~160 g ice, equivalent to ~16 mL air, which is less than previous methods. This large suite of parameters on a single ice sample is new and helpful to study phase relationships of parameters which are usually not measured together. A multi-parameter dataset is also key to understand in situ production processes of organic species in the ice, a critical issue observable in many organic trace gases. Novel is the determination of xenon isotope ratios using doubly charged Xe ions. The attained precision for δ136Xe is suitable to correct the isotopic ratios and mixing ratios for gravitational firn effects, with the benefit that this information is derived from the same sample. Lastly, anomalies in the Xe mixing ratio, δXe/air, can be used to detect melt layers.

  12. Refraction in planetary atmospheres: improved analytical expressions and comparison with a new ray-tracing algorithm

    CERN Document Server

    Betremieux, Yan

    2015-01-01

    Atmospheric refraction affects to various degrees exoplanet transit, lunar eclipse, as well as stellar occultation observations. Exoplanet retrieval algorithms often use analytical expressions for the column abundance along a ray traversing the atmosphere as well as for the deflection of that ray, which are first order approximations valid for low densities in a spherically symmetric homogeneous isothermal atmosphere. We derive new analytical formulae for both of these quantities, which are valid for higher densities, and use them to refine and validate a new ray tracing algorithm which can be used for arbitrary atmospheric temperature-pressure profiles. We illustrate with simple isothermal atmospheric profiles the consequences of our model for different planets: temperate Earth-like and Jovian-like planets, as well as HD189733b, and GJ1214b. We find that, for both hot exoplanets, our treatment of refraction does not make much of a difference to pressures as high as 10 atmosphere, but that it is important to ...

  13. Ray-Tracing studies in a perturbed atmosphere I- The initial value problem

    CERN Document Server

    Tannous, C

    2001-01-01

    We report the development of a new ray-tracing simulation tool having the potential of the full characterization of a radio link through the accurate study of the propagation path of the signal from the transmitting to the receiving antennas across a perturbed atmosphere. The ray-tracing equations are solved, with controlled accuracy, in three dimensions (3D) and the propagation characteristics are obtained using various refractive index models. The launching of the rays, the atmospheric medium and its disturbances are characterized in 3D. The novelty in the approach stems from the use of special numerical techniques dealing with so called stiff differential equations without which no solution of the ray-tracing equations is possible. Starting with a given launching angle, the solution consists of the ray trajectory, the propagation time information at each point of the path, the beam spreading, the transmitted (resp. received) power taking account of the radiation pattern and orientation of the antennas and ...

  14. Miniaturized Sensors for Monitoring of Atmospheric Trace Gases using Multiple Deployment Platforms Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Daylight Solutions proposes a miniaturized sensor package based on ECqcLTM and QEPAS technology that were independently developed by Daylight Solutions (San Diego,...

  15. Russian contribution to ExoMars Trace Gas Orbiter: Atmospheric Chemistry Suite (ACS)

    Science.gov (United States)

    Shakun, Alexey; Korablev, Oleg; Trokhimovskiy, Alexander; Grigoriev, Alexey; Anufreychik, Konstantin; Fedorova, Anna; Ignatiev, Nikolay; Ivanov, Yuriy; Moshkin, Boris; Kalinnikov, Yuriy; Montmessin, Franck

    2016-04-01

    . The MIR channel is a novel, high-aperture cross-dispersion spectrometer working in 2.3-4.2 μm spectral range, with resolving power of 50000, and covering simultaneously up to 300 nm per measurement. Targeting very high spectral resolution the MIR channel will operate in solar occultation only with a narrow FOV. MCT detector array with cryo-cooler is applied. The main science goal of MIR channel is to do record-breaking measurements and detections of minor gaseous species (CH4, C2H2, H2S, HCl and others), some yet undetected, some possibly related to volcanic or biologic activity. For the methane we predicting ~20 ppt sensitivity. The spectral range of MIR includes several CO2 absorption bands allowing doing measurements of density and temperature. D/H and its vertical profile in the Martian atmosphere will be measured for the first time. The short-wavelength side of MIR's spectral range is extended to cover almost the whole carbon monoxide band. TIRVIM is a 2-inch double pendulum Fourier-transform spectrometer covering in one interferometric channel the spectral range of 2-17 μm. Instrument has maximal optical path difference of 6 cm so its apodized spectral resolution is 0.2 cm-1. Single element PV-MCT detector with Stirling cooler is applied. To calibrate TIRVIM data onboard, internal black body and one-coordinate scanner are implemented. Scanning mirror provides possibility of observation in both nadir and solar occultation modes. FOV of the TIRVIM is 2.5deg. Main science goals of TIRVIM are detection of trace gases (solar occultation) and measurement of thermal profiles using 15μm-CO2 band (nadir). Martian aerosol properties and profiles can be also retrieved. Trace gases NO and N2O can be detected.

  16. Atmospherically deposited trace metals from bulk mineral concentrate port operations.

    Science.gov (United States)

    Taylor, Mark Patrick

    2015-05-15

    Although metal exposures in the environment have declined over the last two decades, certain activities and locations still present a risk of harm to human health. This study examines environmental dust metal and metalloid hazards (arsenic, cadmium, lead and nickel) associated with bulk mineral transport, loading and unloading port operations in public locations and children's playgrounds in the inner city of Townsville, northern Queensland. The mean increase in lead on post-play hand wipes (965 μg/m(2)/day) across all sites was more than 10-times the mean pre-play loadings (95 μg/m(2)/day). Maximum loading values after a 10-minute play period were 3012 μg/m(2), more than seven times the goal of 400 μg/m(2) used by the Government of Western Australia (2011). Maximum daily nickel post-play hand loadings (404 μg/m(2)) were more than 26 times above the German Federal Immission Control Act 2002 annual benchmark of 15 μg/m(2)/day. Repeat sampling over the 5-day study period showed that hands and surfaces were re-contaminated daily from the deposition of metal-rich atmospheric dusts. Lead isotopic composition analysis of dust wipes ((208)Pb/(207)Pb and (206)Pb/(207)Pb) showed that surface dust lead was similar to Mount Isa type ores, which are exported through the Port of Townsville. While dust metal contaminant loadings are lower than other mining and smelting towns in Australia, they exceeded national and international benchmarks for environmental quality. The lessons from this study are clear - even where operations are considered acceptable by managing authorities, targeted assessment and monitoring can be used to evaluate whether current management practices are truly best practice. Reassessment can identify opportunities for improvement and maximum environmental and human health protection.

  17. Atmospherically deposited trace metals from bulk mineral concentrate port operations

    Energy Technology Data Exchange (ETDEWEB)

    Taylor, Mark Patrick, E-mail: mark.taylor@mq.edu.au

    2015-05-15

    Although metal exposures in the environment have declined over the last two decades, certain activities and locations still present a risk of harm to human health. This study examines environmental dust metal and metalloid hazards (arsenic, cadmium, lead and nickel) associated with bulk mineral transport, loading and unloading port operations in public locations and children's playgrounds in the inner city of Townsville, northern Queensland. The mean increase in lead on post-play hand wipes (965 μg/m{sup 2}/day) across all sites was more than 10-times the mean pre-play loadings (95 μg/m{sup 2}/day). Maximum loading values after a 10-minute play period were 3012 μg/m{sup 2}, more than seven times the goal of 400 μg/m{sup 2} used by the Government of Western Australia (2011). Maximum daily nickel post-play hand loadings (404 μg/m{sup 2}) were more than 26 times above the German Federal Immission Control Act 2002 annual benchmark of 15 μg/m{sup 2}/day. Repeat sampling over the 5-day study period showed that hands and surfaces were re-contaminated daily from the deposition of metal-rich atmospheric dusts. Lead isotopic composition analysis of dust wipes ({sup 208}Pb/{sup 207}Pb and {sup 206}Pb/{sup 207}Pb) showed that surface dust lead was similar to Mount Isa type ores, which are exported through the Port of Townsville. While dust metal contaminant loadings are lower than other mining and smelting towns in Australia, they exceeded national and international benchmarks for environmental quality. The lessons from this study are clear — even where operations are considered acceptable by managing authorities, targeted assessment and monitoring can be used to evaluate whether current management practices are truly best practice. Reassessment can identify opportunities for improvement and maximum environmental and human health protection. - Graphical abstract: Post-play hand wipe, Headland Park, Townsville, Australia. - Highlights: • Bulk mineral port

  18. Measurements of reactive trace gases and variable O3 formation rates in some South Carolina biomass burning plumes

    Directory of Open Access Journals (Sweden)

    D. W. T. Griffith

    2013-02-01

    Full Text Available In October–November 2011 we measured trace gas emission factors from seven prescribed fires in South Carolina (SC, US, using two Fourier transform infrared spectrometer (FTIR systems and whole air sampling (WAS into canisters followed by gas-chromatographic analysis. A total of 97 trace gas species were quantified from both airborne and ground-based sampling platforms, making this one of the most detailed field studies of fire emissions to date. The measurements include the first emission factors for a suite of monoterpenes produced by heating vegetative fuels during field fires. The first quantitative FTIR observations of limonene in smoke are reported along with an expanded suite of monoterpenes measured by WAS including α-pinene, β-pinene, limonene, camphene, 4-carene, and myrcene. The known chemistry of the monoterpenes and their measured abundance of 0.4–27.9% of non-methane organic compounds (NMOCs and ~ 21% of organic aerosol (mass basis suggests that they impacted secondary formation of ozone (O3, aerosols, and small organic trace gases such as methanol and formaldehyde in the sampled plumes in the first few hours after emission. The variability in the initial terpene emissions in the SC fire plumes was high and, in general, the speciation of the initially emitted gas-phase NMOCs was 13–195% different from that observed in a similar study in nominally similar pine forests in North Carolina ~ 20 months earlier. It is likely that differences in stand structure and environmental conditions contributed to the high variability observed within and between these studies. Similar factors may explain much of the variability in initial emissions in the literature. The ΔHCN/ΔCO emission ratio, however, was found to be fairly consistent with previous airborne fire measurements in other coniferous-dominated ecosystems, with the mean for these studies being 0.90 ± 0.06%, further confirming the value of HCN as a biomass burning tracer. The

  19. Measurements of reactive trace gases and variable O3 formation rates in some South Carolina biomass burning plumes

    Directory of Open Access Journals (Sweden)

    D. W. T. Griffith

    2012-09-01

    Full Text Available In October–November 2011 we measured trace gas emission factors from seven prescribed fires in South Carolina (SC, US, using two Fourier transform infrared spectrometer (FTIR systems and whole air sampling (WAS into canisters followed by gas-chromatographic analysis. A total of 97 trace gas species were quantified from both airborne and ground-based sampling platforms, making this one of the most detailed field studies of fire emissions to date. The measurements include the first emission factors for a suite of monoterpenes produced by heating vegetative fuels during field fires. The first quantitative FTIR observations of limonene in smoke are reported along with an expanded suite of monoterpenes measured by WAS including α-pinene, β-pinene, limonene, camphene, 4-carene, and myrcene. The known chemistry of the monoterpenes and their measured abundance of 0.4–27.9% of non-methane organic compounds (NMOCs and ~21% of organic aerosol (mass basis suggests that they impacted secondary formation of ozone (O3, aerosols, and small organic trace gases such as methanol and formaldehyde in the sampled plumes in first few hours after emission. The variability in the initial terpene emissions in the SC fire plumes was high and, in general, the speciation of the initially emitted gas-phase NMOCs was 13–195% different from that observed in a similar study in nominally similar pine forests in North Carolina ~20 months earlier. It is likely that differences in stand structure and environmental conditions contributed to the high variability observed within and between these studies. Similar factors may explain much of the variability in initial emissions in the literature. The ΔHCN/ΔCO emission ratio, however, was found to be fairly consistent with previous airborne fire measurements in other coniferous-dominated ecosystems, with the mean for these studies being 0.90 ± 0.06%, further confirming the value of HCN as a biomass burning tracer. The SC

  20. Agricultural fires in the southeastern U.S. during SEAC4RS: Emissions of trace gases and particles and evolution of ozone, reactive nitrogen, and organic aerosol

    Science.gov (United States)

    Liu, Xiaoxi; Zhang, Y.; Huey, L. G.; Yokelson, R. J.; Wang, Y.; Jimenez, J. L.; Campuzano-Jost, P.; Beyersdorf, A. J.; Blake, D. R.; Choi, Y.; St. Clair, J. M.; Crounse, J. D.; Day, D. A.; Diskin, G. S.; Fried, A.; Hall, S. R.; Hanisco, T. F.; King, L. E.; Meinardi, S.; Mikoviny, T.; Palm, B. B.; Peischl, J.; Perring, A. E.; Pollack, I. B.; Ryerson, T. B.; Sachse, G.; Schwarz, J. P.; Simpson, I. J.; Tanner, D. J.; Thornhill, K. L.; Ullmann, K.; Weber, R. J.; Wennberg, P. O.; Wisthaler, A.; Wolfe, G. M.; Ziemba, L. D.

    2016-06-01

    Emissions from 15 agricultural fires in the southeastern U.S. were measured from the NASA DC-8 research aircraft during the summer 2013 Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys (SEAC4RS) campaign. This study reports a detailed set of emission factors (EFs) for 25 trace gases and 6 fine particle species. The chemical evolution of the primary emissions in seven plumes was examined in detail for ~1.2 h. A Lagrangian plume cross-section model was used to simulate the evolution of ozone (O3), reactive nitrogen species, and organic aerosol (OA). Observed EFs are generally consistent with previous measurements of crop residue burning, but the fires studied here emitted high amounts of SO2 and fine particles, especially primary OA and chloride. Filter-based measurements of aerosol light absorption implied that brown carbon (BrC) was ubiquitous in the plumes. In aged plumes, rapid production of O3, peroxyacetyl nitrate (PAN), and nitrate was observed with ΔO3/ΔCO, ΔPAN/ΔNOy, and Δnitrate/ΔNOy reaching ~0.1, ~0.3, and ~0.3. For five selected cases, the model reasonably simulated O3 formation but underestimated PAN formation. No significant evolution of OA mass or BrC absorption was observed. However, a consistent increase in oxygen-to-carbon (O/C) ratios of OA indicated that OA oxidation in the agricultural fire plumes was much faster than in urban and forest fire plumes. Finally, total annual SO2, NOx, and CO emissions from agricultural fires in Arkansas, Louisiana, Mississippi, and Missouri were estimated (within a factor of ~2) to be equivalent to ~2% SO2 from coal combustion and ~1% NOx and ~9% CO from mobile sources.

  1. The ExoMars Trace Gas Orbiter NOMAD Spectrometer Suite for Nadir and Solar Occultation Observations of Mars' Atmosphere

    Science.gov (United States)

    Thomas, Ian; Carine Vandaele, Ann; López-Moreno, José Juan; Patel, Manish; Bellucci, Giancarlo; Drummond, Rachel; Neefs, Eduard; Depiesse, Cedric; Daerden, Frank; Rodriguez-Gómez, Julio; Neary, Lori; Robert, Séverine; Willame, Yannick; Mahieux, Arnaud

    2015-04-01

    NOMAD (Nadir and Occultation for MArs Discovery) is one of four instruments on board the ExoMars Trace Gas Orbiter, scheduled for launch in January 2016 and to begin nominal science mission around Mars in late 2017. It consists of a suite of three high-resolution spectrometers - Solar Occultation (SO), LNO (Limb Nadir and Occultation) and UVIS (Ultraviolet-Visible) - which will generate a huge dataset of Martian atmospheric observations during the mission, across a wide spectral range. Specifically, the SO spectrometer channel will perform occultation measurements, operating between 2.2-4.3μm at a resolution of 0.15cm-1, with 180-1000m vertical spatial resolution and an SNR of 1500-3000. LNO will perform limb scanning, nadir and occultation measurements, operating between 2.2-3.8μm at a resolution of 0.3cm-1. In nadir, global coverage will extend between ±74O latitude with an IFOV of 0.5x17km on the surface. This channel can also make occultation measurements should the SO channel fail. UVIS will make limb, nadir and occultation measurements between 200-650nm, at a resolution of 1nm. It will have 300-1000m vertical resolution during occultation and 5x60km ground resolution during 15s nadir observations. An order-of-magnitude increase in spectral resolution over previous instruments will allow NOMAD to map previously unresolvable gas species, such as important trace gases and isotopes. CO, CO2, H2O, C2H2, C2H4, C2H6, H2CO, CH4, SO2, H2S, HCl, O3 and several isotopologues of methane and water will be detectable, providing crucial measurements of the Martian D/H and methane isotope ratios. It will also be possible to map the sources and sinks of these gases, such as regions of surface volcanism/outgassing and atmospheric production, over the course of an entire Martian year, to further constrain atmospheric dynamics and climatology. NOMAD will also continue to monitor the Martian water, carbon, ozone and dust cycles, extending existing datasets made by successive

  2. Measurement of the Residual Gases O2 and CO2 in Meat Products Packed in Modified Atmosphere

    Directory of Open Access Journals (Sweden)

    Jozef Čapla

    2013-02-01

    Full Text Available Nowadays, consumers have increased demand for quality and food safety and also rising demand for natural foods without chemical additives. There are many ways to presserve freshness of these products, one of them is modified atmosphere packaging, which can mean elimination and/or replacement surrounding the product before closing it in package with a mixture of gases other than the original ambient air atmosphere. for replacement of atmosphere are generally used three types of gases such as carbon dioxide, oxygen and nitrogen. this type of packaging is often used for meat and meat products, which belongs to foods that are under normal conditions perishable and for increasing the shelf life of meat products are also used various other preservation methods or their combinations. Packaging of meat and meat products in modified atmosphere is usually made with a high content of carbon dioxide, which has good bacteriostatic and fungistatic effect and is also an effective mean for increasing the shelf life of packaged products during storage and sale.

  3. Volcano emissions of trace metals, atmospheric deposition, and supply to biogeochemical cycles

    Science.gov (United States)

    Hinkley, T.; Thornber, C. R.; Matsumoto, A.

    2003-12-01

    Quiescently degassing (not exploding) volcanoes inject into the troposphere plumes that have remarkably high concentrations of ordinarily-rare, volatile trace metals. In pre-industrial times, these emissions appear to have accounted for the strong "enrichments" (relative to concentrations in crustal material or in ocean solute) of many such trace metals in the material deposited from the atmosphere. This has been shown by measuring the source strength of the emissions of metals from volcanoes, and comparing that to the amounts of the metals (excess over amounts accounted for by rock dust and sea salt) deposited onto high-latitude ice sheets: volcano degassing outputs of metals and deposition masses of metals to ice are comparable, on the basis of the masses (fluxes) and proportions of the metals, and from the proportions of lead (Pb) isotopes. There is indication that in modern industrial times the elevated trace metal fractions in the atmospheric material that has small particle size and long atmospheric residence time is still more strongly influenced by volcano emissions than by industrial emissions. Throughout earth's history it is likely that volcano emissions were a major control on the environmental background levels of trace elements, in which plants and animals evolved their tolerances to these mostly-poisonous substances.

  4. Phytochemical, spectroscopic and density functional theory study of Diospyrin, and non-bonding interactions of Diospyrin with atmospheric gases.

    Science.gov (United States)

    Fazl-i-Sattar; Ullah, Zakir; Ata-ur-Rahman; Rauf, Abdur; Tariq, Muhammad; Tahir, Asif Ali; Ayub, Khurshid; Ullah, Habib

    2015-04-15

    Density functional theory (DFT) and phytochemical study of a natural product, Diospyrin (DO) have been carried out. A suitable level of theory was developed, based on correlating the experimental and theoretical data. Hybrid DFT method at B3LYP/6-31G (d,p) level of theory is employed for obtaining the electronic, spectroscopic, inter-molecular interaction and thermodynamic properties of DO. The exact structure of DO is confirmed from the nice validation of the theory and experiment. Non-covalent interactions of DO with different atmospheric gases such as NH3, CO2, CO, and H2O were studied to find out its electroactive nature. The experimental and predicted geometrical parameters, IR and UV-vis spectra (B3LYP/6-31+G (d,p) level of theory) show excellent correlation. Inter-molecular non-bonding interaction of DO with atmospheric gases is investigated through geometrical parameters, electronic properties, charge analysis, and thermodynamic parameters. Electronic properties include, ionization potential (I.P.), electron affinities (E.A.), electrostatic potential (ESP), density of states (DOS), HOMO, LUMO, and band gap. All these characterizations have corroborated each other and confirmed the presence of non-covalent nature in DO with the mentioned gases.

  5. Robust IR Remote Sensing Technique of the Total Column of Trace Gases Including Carbon Dioxide and Methane

    Science.gov (United States)

    Georgieva, E. M.; Heaps, W. S.

    2011-01-01

    Progress on the development of a differential radiometer based upon the Fabry-Perot interferometer (FPI) for methane (CH4) and carbon dioxide (C02) detection in the atmosphere is presented. Methane measurements are becoming increasingly important as a component of NASA's programs to understand the global carbon cycle and quantifY the threat of global warming. Methane is the third most important greenhouse gas in the Earth's radiation budget (after water vapor and carbon dioxide) and the second most important anthropogenic contributor to global warming. The importance of global warming and air quality to society caused the National Research Council to recommend that NASA develop the following missions [1]: ASCENDS (Active Sensing of C02 Emissions over Nights, Days, and Seasons), GEOCAPE (Geostationary Coastal and Air Pollution Events), and GACM (Global Atmosphere Composition Mission). Though methane measurements are not specifically called out in these missions, ongoing environmental changes have raised the importance of understanding the methane budget. In the decadal survey is stated that "to close the carbon budget, we would also address methane, but the required technology is not obvious at this time. If appropriate and cost-effective methane technology becomes available, we strongly recommend adding a methane capability". In its 2007 report the International Panel on Climate Change identified methane as a key uncertainty in our understanding saying that the causes of recent changes in the growth rate of atmospheric CH4 are not well understood. What we do know is that methane arises from a number of natural sources including wet lands and the oceans plus man made sources from agriculture, as well as coal and petroleum production and distribution. It has recently been pointed out that large amount of methane are frozen in the permafrost of Canada and Siberia. There is a fear that melting of this permafrost driven by global warming may release large amounts of

  6. The Influence of Urban Emissions on Background Aerosols and Trace Gases in Amazonia as Seen in the GoAmazon2014/2015 Experiment.

    Science.gov (United States)

    Artaxo, P.; Martin, S. T.; Barbosa, H. M.; Brito, J.; Carbone, S.; Rizzo, L. V.; Andreae, M. O.; Pöhlker, C.; Souza, R. A. F. D.

    2015-12-01

    As part of the GoAmazon2014/2015 experiment, several aerosol and trace gas monitoring stations are being operated for two years before and after the Manaus urban plume in Central Amazonia. Three sites are being operated in pristine conditions, with atmospheric properties under natural biogenic conditions. These three sites named T0 are ATTO (Amazon Tall Tower Observatory), ZF2 and EMBRAPA. After the air masses are exposed to the Manaus plume, one site (called T2) is being operated under the direct influence of the Manaus plume at 5 Km downwind. Finally, at about 150 Km downwind of Manaus is the T3 Manacapuru site. Aerosol chemical composition is being analysed using filters for fine (PM2.5) and coarse mode aerosol as well as three Aerodyne ACSM (Aerosol Chemical Speciation Monitors) instruments. Optical properties were measured with several AE33 aethalometers and MAAP, and multi wavelengths nephelometers. Aerosol size distribution is determined using scanning mobility particle sizers. The aerosol column is measures using AERONET sunphotometers before and after the Manaus plume, as well as several Lidar systems. The three sites before the Manaus plume show remarkable similar variability in aerosol concentrations and optical properties. This pattern is very different at the T2 site, with large aerosol concentrations enhancing aerosol absorption and scattering significantly as a result of the Manaus pollution plume. The aerosol is very oxidized before being exposed to the Manaus plume, and this pattern changes significantly for T2 and T3 sites, with a much higher presence of less oxidized aerosol. Typical ozone concentrations at mid-day before Manaus plume is a low 10-12 ppb, value that changes to 50-70 ppb for air masses suffering the influence of Manaus plume. Aerosol size distribution also change significantly, with stronger presence of nucleation mode particles. A detailed comparison of aerosol characteristics and composition for the several sites will be

  7. Greenhouse Gases

    Science.gov (United States)

    ... life. Governments all around the world ban and control production and use of several industrial gases that destroy atmospheric ozone and create a hole in the ozone layer . At lower elevations of the atmosphere (the troposphere), ozone is harmful to ... for Future Emissions FAQs How much carbon dioxide is produced when ...

  8. Development of proton-transfer reaction mass spectrometry techniques : detection of trace gases in biology and medicine

    NARCIS (Netherlands)

    Steeghs, Marco Matheus Louis

    2007-01-01

    The measurement of small quantities of gases and volatiles in air is used nowadays in many different fields of science, such as chemistry, physics, biology, food science and medicine. The study of these minute quantities of gases requires highly sensitive detectors. Using such detectors to monitor t

  9. The spectroscopic search for the trace aerosols in the planetary atmospheres - the results of numerical simulations

    Science.gov (United States)

    Blecka, Maria I.

    2010-05-01

    The passive remote spectrometric methods are important in examinations the atmospheres of planets. The radiance spectra inform us about values of thermodynamical parameters and composition of the atmospheres and surfaces. The spectral technology can be useful in detection of the trace aerosols like biological substances (if present) in the environments of the planets. We discuss here some of the aspects related to the spectroscopic search for the aerosols and dust in planetary atmospheres. Possibility of detection and identifications of biological aerosols with a passive InfraRed spectrometer in an open-air environment is discussed. We present numerically simulated, based on radiative transfer theory, spectroscopic observations of the Earth atmosphere. Laboratory measurements of transmittance of various kinds of aerosols, pollens and bacterias were used in modeling.

  10. System and Method for Providing Vertical Profile Measurements of Atmospheric Gases

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — A system and method for using an air collection device to collect a continuous air sample as the device descends through the atmosphere are provided. The air...

  11. Characteristic emission enhancement in the atmosphere with Rn trace using metal assisted LIBS

    Energy Technology Data Exchange (ETDEWEB)

    Hashemi, M. M. [Physics Department, Doctorate Technical Center of PNU, P.O. Box 19536-33511, Tehran (Iran, Islamic Republic of); Parvin, P., E-mail: parvin@aut.ac.ir; Moosakhani, A. [Physics Department, Amirkabir University of Technology, P.O. Box 15875-4413, Tehran (Iran, Islamic Republic of); Mortazavi, S. Z.; Reyhani, A. [Physics Department, Imam Khomeini International University, P.O. Box 34149-16818, Qazvin (Iran, Islamic Republic of); Majdabadi, A. [Laser and Optics Research School, NSTRI, P.O. Box 11155-3486, Tehran (Iran, Islamic Republic of); Abachi, S. [Physics Department, University of California, Irvin, CA 92697 (United States)

    2014-06-15

    Several characteristic emission lines from the metal targets (Cu, Zn and Pb) were investigated in trace presence of radon gas in the atmospheric air, using Q-SW Nd:YAG laser induced plasma inside a control chamber. The emission lines of metal species are noticeably enhanced in (Rn+air), relative to those in the synthetic air alone. Similar spectra were also taken in various sub-atmospheric environments in order to determine the optimum pressure for enhancement. Solid-state nuclear track detectors were also employed to count the tracks due to alpha particles for the activity assessment.

  12. Characteristic emission enhancement in the atmosphere with Rn trace using metal assisted LIBS

    Directory of Open Access Journals (Sweden)

    M. M. Hashemi

    2014-06-01

    Full Text Available Several characteristic emission lines from the metal targets (Cu, Zn and Pb were investigated in trace presence of radon gas in the atmospheric air, using Q-SW Nd:YAG laser induced plasma inside a control chamber. The emission lines of metal species are noticeably enhanced in (Rn+air, relative to those in the synthetic air alone. Similar spectra were also taken in various sub-atmospheric environments in order to determine the optimum pressure for enhancement. Solid-state nuclear track detectors were also employed to count the tracks due to alpha particles for the activity assessment.

  13. Delonix regia and Casuarina equisetifolia as passive biomonitors and as bioaccumulators of atmospheric trace metals.

    Science.gov (United States)

    Ukpebor, Emmanuel Ehiabhi; Ukpebor, Justina Ebehirieme; Aigbokhan, Emmanuel; Goji, Idris; Onojeghuo, Alex Okiemute; Okonkwo, Anthony Chinedum

    2010-01-01

    The suitability of two common and ubiquitously distributed and exotic ornamental plant species in Nigeria-Delonix regia and Casuarina equisetifolia as biomonitors and as effective bioaccumulators of atmospheric trace metals (Cd, Pb, Zn and Cu) has been evaluated. Bark and leaf samples from these plant species were collected in June and July 2006 at five locations in Benin City. Four of the sampling sites were in areas of high traffic density and commercial activities, the fifth site is a remote site, selected to act as a control and also to provide background information for the metals. The plant samples were collected and processed using standard procedures and trace metals were determined using atomic absorption spectrometer. The bark of the plants was able to bioaccumulate the trace metals, especially Pb which originates from anthropogenic contributions in the city. The Pb range of 20.00-70.00 microg/g measured for the bark samples of D. regia, exceeded the normal plant Pb concentration of 0.2-20.0 microg/g and most Pb data available in literature. The bark of the plants was observed to accumulate more metals compared to the leave, while D. regia was found to be slightly better than C. equisetifolia in trace metal uptake efficiency. Spatial variations in the distributions of Pb and Zn were significant (p < 0.05), and the continuous use of leaded fuel in Nigeria was identified as the predominant source of Pb in the atmosphere.

  14. Biomass burning emissions of trace gases and particles in marine air at Cape Grim, Tasmania, 41° S

    Science.gov (United States)

    Lawson, S. J.; Keywood, M. D.; Galbally, I. E.; Gras, J. L.; Cainey, J. M.; Cope, M. E.; Krummel, P. B.; Fraser, P. J.; Steele, L. P.; Bentley, S. T.; Meyer, C. P.; Ristovski, Z.; Goldstein, A. H.

    2015-07-01

    with a large CO enhancement, an increase of the NMOC / CO emission ratio (ER) by a factor of 2-4 and a halving of the BC / CO ratio. Rainfall on Robbins Island was observed by radar during this period which likely resulted in a lower fire combustion efficiency, and higher emission of compounds associated with smouldering. This highlights the importance of relatively minor meterological events on BB emissions. Emission factors (EF) were derived for a range of trace gases, some never before reported for Australian conditions, (including hydrogen, phenol and toluene) using a calculated ER to CO and a published CO EF. The EF derived for most species are comparable to other temperate Australian studies but lower than Northern Hemisphere temperate studies. This work demonstrates the substantial impact that BB plumes have on the composition of marine air, and the significant changes that can occur as the plume is diluted and interacts with other emission sources. We also provide new trace gas and particle EF for temperate southern Australia.

  15. Biomass burning emissions of trace gases and particles in marine air at Cape Grim, Tasmania, 41° S

    Directory of Open Access Journals (Sweden)

    S. J. Lawson

    2015-07-01

    corresponded with a large CO enhancement, an increase of the NMOC / CO emission ratio (ER by a factor of 2–4 and a halving of the BC / CO ratio. Rainfall on Robbins Island was observed by radar during this period which likely resulted in a lower fire combustion efficiency, and higher emission of compounds associated with smouldering. This highlights the importance of relatively minor meterological events on BB emissions. Emission factors (EF were derived for a range of trace gases, some never before reported for Australian conditions, (including hydrogen, phenol and toluene using a calculated ER to CO and a published CO EF. The EF derived for most species are comparable to other temperate Australian studies but lower than Northern Hemisphere temperate studies. This work demonstrates the substantial impact that BB plumes have on the composition of marine air, and the significant changes that can occur as the plume is diluted and interacts with other emission sources. We also provide new trace gas and particle EF for temperate southern Australia.

  16. Dating of young groundwater using four anthropogenic trace gases (SF6, SF5CF3, CFC-12 and Halon-1301): methodology and first results.

    Science.gov (United States)

    Bartyzel, Jakub; Rozanski, Kazimierz

    2016-01-01

    A dedicated, GC-based analytical system is presented which allows detection of four anthropogenic trace gases (SF6, SF5CF3, CFC-12 and Halon-1301) in a single water sample, with detection limits and measurement uncertainties sufficiently low to employ them as quantitative indicators of groundwater age. The gases dissolved in water are extracted in the field using the method based on a dynamic head-space concept. In the laboratory, the investigated gases are cryogenically enriched, separated and measured using an electron capture detector. Reproducibility of the analyses is in the order of 2-5 %. The investigated tracers were measured in several production wells located in the recharge area of an intensively exploited aquifer in southern Poland. While the piston-flow ages of groundwater in the investigated wells revealed internal consistency, they appeared to be generally smaller than the ages derived from time series of tritium content in those wells, interpreted by lumped-parameter models. This difference stems mainly from significantly longer travel times of tritium through the unsaturated zone, when compared to the gaseous tracers being used. The results of this study highlight the benefits of using multiple tracing in quantifying timescales of groundwater flow in shallow aquifer systems.

  17. Laser photoacoustic trace detection of C2H4 revealing adverse environmental effects of atmospheric pollution on plant material

    Science.gov (United States)

    Harren, Frans J. M.; Petruzzelli, Luciana

    1993-03-01

    The photoacoustic detection method for trace gases in the atmosphere is well developed towards very low limits of detection, in the last years. Due to the combination of a sensitive photoacoustic cell placed intracavity in an infrared CO2 laser we were able to detect C2H4 at ultralow (hormone which seems to play an important role throughout all the life stages of a plant, including seed germination. In addition, various types of stress have been reported to promote ethylene production from different plant tissues. As part of our ongoing research on the role of ethylene in seed germination, we have compared our laser photoacoustic set-up to a gaschromatograph for measuring C2H4 produced by germinating Pisum sativum L. seeds within the first days of imbibition. C2H4 evolution by intact seeds shows a maximum at about 25 hours of germination. Thereafter, the rate of ethylene measured by gaschromatograph continues to decrease while that measured by the laser-driven photoacoustic system shows further increases. Most of the ethylene produced by seeds is found in isolated embryonic axes. The fumigation with ozone affects the growth of seedlings and their ethylene evolution.

  18. Contribution to the chromatography of atmospheric gases (1963); Contribution a la chromatographie des gaz de l'air (1963)

    Energy Technology Data Exchange (ETDEWEB)

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

    1963-06-15

    In the first part, the author studies the gas-phase chromatographic separation of the atmospheric rare gases, of hydrogen, and of some gaseous compounds of carbon (CO, CO{sub 2}, CH{sub 4}) using inactive gases to obtain the most favourable operational conditions far this separation. In the second part, the optimum conditions for detecting non-active gases using an ionisation chamber and a {sup 239}Pu radioactive source emitting 5.15 MeV {alpha} particles are determined. (author) [French] Dans une premiere partie, l'auteur etudie la separation par chromatographie en phase gazeuse des gaz rares de l'air, de l'hydrogene, et de quelques composes gazeux du carbone (CO, CO{sub 2}, CH{sub 4}) en utilisant des gaz inactifs an vue d'obtenir les conditions experimenales les plus favorables en vue de cette separation. Dans une deuxieme partie, les conditions optimales de detection de gaz non actifs a l'aide d'une chambre d'ionisation, en utilisant comme source radioactive du {sup 239}Pu qui emet des particules {alpha} de 5,15 MeV, sont determinees. (auteur)

  19. Horizonal and Vertical Spatial Patterns of Radon and Other Soil-gases Across the El Pilar Fault Trace at Guaraphiche, Edo. Surce (Venezuela)

    Science.gov (United States)

    LaBrecque, J. J.

    2002-05-01

    Soil-gases (radon, thoron, carbon dioxide and hydrogen) were measured at 63-cm depths along a transect perpendicular to the rupture (fault trace) from the 1997 Caricao earthquake (Mw=6.9) at Guarapiche, state of Sucre (Venezuela). The transect was about 40 meters long with ten sampling points with the spacings was smaller near the rupture. The shapes of the horizontal spatial patterns for radon (Rn-222), thoron (Rn-220) and total radon (Rn-222+Rn-220) were similar; the gas concentrations increased from both ends of the transect toward the rupture where a dip (valley) occurred. Both carbon dioxide and hydrogen gases showed anomalous values at the same sampling points. Twin peaks (anomalies) had been previously reported and suggested that they were due to blockage in the rupture. We have also determined soil-gases from 25-cm to 155-cm depths near the rupture and at the ends of the transect. The results showed that the soil-gas concentrations were not only higher in the upper levels (less than 65-cm) near the fault trace but were similar or greater than the lower levels. Thus, producing the twin peaks when soil-gas sampling was performed at the 65-cm depth. When the sampling was performed at only 45-cm depth the dip over the rupture was much less and the patterns looked more like a broad doublet peak. In conclusion, one can clearly see that not only positive soil-gas anomalies can occur over a fault trace but also negative ones too. 1) This work was partially funded by a research contract from the Venezuelan National Science Foundation (CONICIT Proyecto S1-95000448). 2) Mailing Address: Centro de Quimica, 8424 NW 56th Street, Suite 00204,Miami, Fl 33166 (USA). E-mail jjlabrec@ivic.ve FAX: +58-212-504-1214

  20. Trace Atmospheric Gas Analyzer (TAGA) Volatile Organic Compound (VOC) Data for BP Spill/Deepwater Horizon - May 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  1. Trace Atmospheric Gas Analyzer (TAGA) Volatile Organic Compound (VOC) Data for BP Spill/Deepwater Horizon - August 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  2. Trace Atmospheric Gas Analyzer (TAGA) Volatile Organic Compound (VOC) Data for BP Spill/Deepwater Horizon - July 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  3. Trace Atmospheric Gas Analyzer (TAGA) Volatile Organic Compound (VOC) Data for BP Spill/Deepwater Horizon - June 2010

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Trace Atmospheric Gas Analyzer (TAGA) buses are self-contained mobile laboratories that conduct instant-result monitoring of air quality at particular locations....

  4. Coupling field and laboratory measurements to estimate the emission factors of identified and unidentified trace gases for prescribed fires

    Directory of Open Access Journals (Sweden)

    R. J. Yokelson

    2012-08-01

    Full Text Available An extensive program of experiments focused on biomass burning emissions began with a laboratory phase in which vegetative fuels commonly consumed in prescribed fires were collected in the southeastern and southwestern US and burned in a series of 71 fires at the US Forest Service Fire Sciences Laboratory in Missoula, Montana. The particulate matter (PM2.5 emissions were measured by gravimetric filter sampling with subsequent analysis for elemental carbon (EC, organic carbon (OC, and 38 elements. The trace gas emissions were measured by an open-path Fourier transform infrared (OP-FTIR spectrometer, proton-transfer-reaction mass spectrometry (PTR-MS, proton-transfer ion-trap mass spectrometry (PIT-MS, negative-ion proton-transfer chemical-ionization mass spectrometry (NI-PT-CIMS, and gas chromatography with MS detection (GC-MS. 204 trace gas species (mostly non-methane organic compounds – NMOC were identified and quantified with the above instruments. Many of the 182 species quantified by the GC-MS have rarely, if ever, been measured in smoke before. An additional 153 significant peaks in the unit mass resolution mass spectra were quantified, but either could not be identified or most of the signal at that molecular mass was unaccounted for by identifiable species.

    In a second, "field" phase of this program, airborne and ground-based measurements were made of the emissions from prescribed fires that were mostly located in the same land management units where the fuels for the lab fires were collected. A broad variety, but smaller number of species (21 trace gas species and PM2.5 was measured on 14 fires in chaparral and oak savanna in the southwestern US, as well as pine forest understory in the southeastern US and Sierra Nevada mountains of California. The field measurements of emission factors (EF are useful both for modeling and to examine the representativeness of our lab fire EF. The lab EF/field EF ratio for

  5. Coupling field and laboratory measurements to estimate the emission factors of identified and unidentified trace gases for prescribed fires

    Directory of Open Access Journals (Sweden)

    R. J. Yokelson

    2013-01-01

    Full Text Available An extensive program of experiments focused on biomass burning emissions began with a laboratory phase in which vegetative fuels commonly consumed in prescribed fires were collected in the southeastern and southwestern US and burned in a series of 71 fires at the US Forest Service Fire Sciences Laboratory in Missoula, Montana. The particulate matter (PM2.5 emissions were measured by gravimetric filter sampling with subsequent analysis for elemental carbon (EC, organic carbon (OC, and 38 elements. The trace gas emissions were measured by an open-path Fourier transform infrared (OP-FTIR spectrometer, proton-transfer-reaction mass spectrometry (PTR-MS, proton-transfer ion-trap mass spectrometry (PIT-MS, negative-ion proton-transfer chemical-ionization mass spectrometry (NI-PT-CIMS, and gas chromatography with MS detection (GC-MS. 204 trace gas species (mostly non-methane organic compounds (NMOC were identified and quantified with the above instruments. Many of the 182 species quantified by the GC-MS have rarely, if ever, been measured in smoke before. An additional 153 significant peaks in the unit mass resolution mass spectra were quantified, but either could not be identified or most of the signal at that molecular mass was unaccounted for by identifiable species.

    In a second, "field" phase of this program, airborne and ground-based measurements were made of the emissions from prescribed fires that were mostly located in the same land management units where the fuels for the lab fires were collected. A broad variety, but smaller number of species (21 trace gas species and PM2.5 was measured on 14 fires in chaparral and oak savanna in the southwestern US, as well as pine forest understory in the southeastern US and Sierra Nevada mountains of California. The field measurements of emission factors (EF are useful both for modeling and to examine the representativeness of our lab fire EF. The lab EF/field EF ratio for

  6. Coupling field and laboratory measurements to estimate the emission factors of identified and unidentified trace gases for prescribed fires

    Energy Technology Data Exchange (ETDEWEB)

    Yokelson, R. J.; Burling, I. R.; Gilman, J. B.; Warneke, C.; Stockwell, C. E.; de Gouw, J.; Akagi, S. K.; Urbanski, S. P.; Veres, P.; Roberts, J. M.; Kuster, W. C.; Reardon, J.; Griffith, D. W. T.; Johnson, T. J.; Hosseini, S.; Miller, J. W.; Cocker III, D. R.; Jung, H.; Weise, D. R.

    2013-01-01

    Vegetative fuels commonly consumed in prescribed fires were collected from five locations in the southeastern and southwestern U.S. and burned in a series of 77 fires at the U.S. Forest Service Fire Sciences Laboratory in Missoula, Montana. The particulate matter (PM2.5) emissions were measured by gravimetric filter sampling with subsequent analysis for elemental carbon (EC), organic carbon (OC), and 38 elements. The trace gas emissions were measured with a large suite of state-of-the-art instrumentation including an open-path Fourier transform infrared (OP FTIR) spectrometer, proton-transfer-reaction mass spectrometry (PTR-MS), proton-transfer ion-trap mass spectrometry (PIT-MS), negative-ion proton-transfer chemical-ionization mass spectrometry (NI-PT-CIMS), and gas chromatography with MS detection (GC-MS). 204 trace gas species (mostly non-methane organic compounds (NMOC)) were identified and quantified with the above instruments. An additional 152 significant peaks in the unit mass resolution mass spectra were quantified, but either could not be identified or most of the signal at that molecular mass was unaccounted for by identifiable species. As phase II of this study, we conducted airborne and ground-based sampling of the emissions from real prescribed fires mostly in the same land management units where the fuels for the lab fires were collected. A broad variety, but smaller number of species (21 trace gas species and PM2.5) was measured on 14 fires in chaparral and oak savanna in the southwestern US, as well as pine forest understory in the southeastern US and Sierra Nevada mountains of California. These extensive field measurements of emission factors (EF) for temperate biomass burning are useful both for modeling and to examine the representativeness of our lab fire EF. The lab/field EF ratio for the pine understory fuels was not statistically different from one, on average. However, our lab EF for “smoldering compounds” emitted by burning the semi

  7. Fractionation of trace elements in total atmospheric deposition by filtrating-bulk passive sampling.

    Science.gov (United States)

    Rueda-Holgado, F; Palomo-Marín, M R; Calvo-Blázquez, L; Cereceda-Balic, F; Pinilla-Gil, E

    2014-07-01

    We have developed and validated a new simple and effective methodology for fractionation of soluble and insoluble forms of trace elements in total atmospheric deposition. The proposed methodology is based on the modification of a standard total deposition passive sampler by integrating a quartz fiber filter that retains the insoluble material, allowing the soluble fraction to pass through and flow to a receiving bottle. The quartz filter containing the insoluble fraction and the liquid containing the soluble fraction are then separately assayed by standardized ICP-MS protocols. The proposed atmospheric elemental fractionation sampler (AEFS) was validated by analyzing a Coal Fly Ash reference material with proper recoveries, and tested for field fractionation of a set of 10 key trace elements in total atmospheric deposition at the industrial area of Puchuncaví-Ventanas, Chile. The AEFS was proven useful for pollution assessment and also to identify variability of the soluble and insoluble fractions of the selected elements within the study area, improving the analytical information attainable by standard passive samplers for total deposition without the need of using sophisticated and high cost wet-only/dry only collectors.

  8. Trace gas retrievals from Airborne Compact Atmospheric Mapper (ACAM) observations during the 2011 DISCOVER-AQ flight campaign

    Science.gov (United States)

    Liu, X.; Kowalewski, M. G.; Janz, S. J.; Bhartia, P. K.; Chance, K.; Krotkov, N. A.; Pickering, K. E.; Crawford, J. H.

    2011-12-01

    The DISCOVER-AQ (Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality) mission has just finished its first flight campaign in the Baltimore-Washington D.C. area in July 2011. The ACAM, flown on board the NASA UC-12 aircraft, includes two spectrographs covering the spectral region 304-900 nm and a high-definition video camera, and is expected to provide column measurements of several important air quality trace gases and aerosols for the DISCOVER-AQ mission. The quick look results for NO2 have been shown to very useful in capturing the strong spatiotemporal variability of NO2. Preliminary fitting of UV/Visible spectra has shown that ACAM measurements have adequate signal to noise ratio to measure the trace gases O2, NO2, HCHO, and maybe SO2 and CHOCHO, at individual pixel resolution, although a great deal of effort is needed to improve the instrument calibration and derive proper reference spectrum for retrieving absolute trace gas column densities. In this study, we present analysis of ACAM instrument calibration including slit function, wavelength registration, and radiometric calibration for both nadir-viewing and zenith-sky measurements. Based on this analysis, an irradiance reference spectrum at ACAM resolution will be derived from a high-resolution reference spectrum with additional correction to account for instrument calibration. Using the derived reference spectrum and/or the measured zenith sky measurements, we will perform non-linear least squares fitting to investigate the retrievals of slant column densities of these trace gases from ACAM measurements, and also use an optimal estimation based algorithm including full radiative transfer calculations to derive the vertical column densities of these trace gases. The initial results will be compared with available in-situ and ground-based measurements taken during the DISCOVER-AQ campaign.

  9. 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

  10. Nighttime chemical evolution of aerosol and trace gases in a power plant plume: Implications for secondary organic nitrate and organosulfate aerosol formation, NO₃ radical chemistry, and N₂O₅ heterogeneous hydrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Zaveri, Rahul A.; Berkowitz, Carl M.; Brechtel, Fred J.; Gilles, Marry K.; Hubbe, John M.; Jayne, J. T.; Kleinman, Lawrence I.; Laskin, Alexander; Madronich, Sasha; Onasch, Timothy B.; Pekour, Mikhail S.; Springston, Stephen R.; Thornton, Joel A.; Tivanski, Alexei V.; Worsnop, Douglas R.

    2010-06-22

    Chemical evolution of aerosols and trace gases in the Salem Harbor power plant plume was monitored with the DOE G-1 aircraft on the night of July 30-31, 2002. Quasi-Lagrangian sampling in the plume at increasing downwind distances/processing times was guided by a constant-volume tetroon that was released near the power plant at sunset. While no evidence of fly ash particles was found, concentrations of particulate organics, sulfate, and nitrate were higher in the plume than in the nearby background air. These species were internally mixed and the particles were acidic, suggesting that particulate nitrate was in the form of organic nitrate. The enhanced particulate organic and nitrate masses in the plume were inferred to be as secondary organic aerosol, possibly formed from the NO3 radical-initiated oxidation of isoprene and other trace organic gases in the presence of acidic sulfate particles. The enhanced particulate sulfate concentrations observed in the plume were attributed to direct emissions of gaseous SO3/H2SO4 from the power plant. Furthermore, concentration of nucleation mode particles was significantly higher in the plume than in background air, suggesting that some of the emitted H2SO4 had nucleated to form new particles. Spectromicroscopic analyses of particle samples suggested that some sulfate was likely in the form of organosulfates. Constrained Lagrangian model analysis of the aircraft and tetroon observations showed that heterogeneous hydrolysis of N2O5 was negligibly slow. These results have significant implications for several scientific and regulatory issues related to the impacts of power plant emissions on atmospheric chemistry, air quality, visibility, and climate.

  11. DAVINCI: Deep Atmosphere Venus Investigation of Noble gases, Chemistry, and Imaging

    Science.gov (United States)

    Glaze, Lori S.; Garvin, James B.; Robertson, Brent; Johnson, Natasha M.; Amato, Michael J.; Thompson, Jessica; Goodloe, Colby; Everette, Dave

    2017-01-01

    DAVINCI is one of five Discovery-class missions selected by NASA in October 2015 for Phase A studies. Launching in November 2021 and arriving at Venus in June of 2023, DAVINCI would be the first U.S. entry probe to target Venus atmosphere in 45 years. DAVINCI is designed to study the chemical and isotopic composition of a complete cross-section of Venus atmosphere at a level of detail that has not been possible on earlier missions and to image the surface at optical wavelengths and process-relevant scales.

  12. Multipass optical absorption spectroscopy: a fast-scanning laser spectrometer for the in situ determination of atmospheric trace-gas components, in particular OH.

    Science.gov (United States)

    Armerding, W; Spiekermann, M; Walter, J; Comes, F J

    1996-07-20

    The optical design of an absorption spectrometer for in situ measurements of atmospheric trace gases is reported. The light source is a rapidly tuned and power-stabilized dye-ring laser, which is frequency doubled by an intracavity BBO crystal. The second harmonic and the fundamental are used simultaneously for measurement of OH, SO(2), CH(2)O, and naphthalene in the UV and of NO(2) in the visible. The 1.2-km absorption path is folded within a 6-m White-cell-type multiple-reflection system with an open-path setup. The absorption sensitivity of the spectrometer is better than 1 part in 10(-5) under tropospheric conditions (integration time 1 min., signal-to-noise ratio 1).

  13. PREP-CHEM-SRC – 1.0: a preprocessor of trace gas and aerosol emission fields for regional and global atmospheric chemistry models

    Directory of Open Access Journals (Sweden)

    S. R. Freitas

    2011-05-01

    Full Text Available The preprocessor PREP-CHEM-SRC presented in the paper is a comprehensive tool aiming at preparing emission fields of trace gases and aerosols for use in atmospheric-chemistry transport models. The considered emissions are from the most recent databases of urban/industrial, biogenic, biomass burning, volcanic, biofuel use and burning from agricultural waste sources. For biomass burning, emissions can be also estimated directly from satellite fire detections using a fire emission model included in the tool. The preprocessor provides emission fields interpolated onto the transport model grid. Several map projections can be chosen. The inclusion of these emissions in transport models is also presented. The preprocessor is coded using Fortran90 and C and is driven by a namelist allowing the user to choose the type of emissions and the databases.

  14. Atmospheric inverse modeling with known physical bounds: an example from trace gas emissions

    Directory of Open Access Journals (Sweden)

    S. M. Miller

    2013-09-01

    Full Text Available Many inverse problems in the atmospheric sciences involve parameters with known physical constraints. Examples include non-negativity (e.g., emissions of some urban air pollutants or upward limits implied by reaction or solubility constants. However, probabilistic inverse modeling approaches based on Gaussian assumptions cannot incorporate such bounds and thus often produce unrealistic results. The atmospheric literature lacks consensus on the best means to overcome this problem, and existing atmospheric studies rely on a limited number of the possible methods with little examination of the relative merits of each. This paper investigates the applicability of several approaches to bounded inverse problems and is also the first application of Markov chain Monte Carlo (MCMC to estimation of atmospheric trace gas fluxes. The approaches discussed here are broadly applicable. A common method of data transformations is found to unrealistically skew estimates for the examined example application. The method of Lagrange multipliers and two MCMC methods yield more realistic and accurate results. In general, the examined MCMC approaches produce the most realistic result but can require substantial computational time. Lagrange multipliers offer an appealing alternative for large, computationally intensive problems when exact uncertainty bounds are less central to the analysis. A synthetic data inversion of US anthropogenic methane emissions illustrates the strengths and weaknesses of each approach.

  15. Atmospheric dry deposition fluxes of trace elements measured in Queretaro City, Mexico

    Science.gov (United States)

    Garcia, R.; Hernandez, R.; Solis, S.; Perez, R.; Hernandez, G.; Morton, O.; Hernandez, E.; Torres, M. C.; Baez, A.

    2012-04-01

    Sampling was made in the southern section of downtown Mexico City. Samples were collected with an Mini-Vol PM10 . Eight different sources were identified for PM10 aerosols: secondary sulfate, wood combustion, fireworks, road traffic, mineral dust, de-icing salt, industrial and local anthropogenic activities. The ions SO42-, NO3-, Cl-, Na+, K+, Ca2+, Mg2+ and NH4+,were analyzed by ion chromatography and the trace metals using an atomic absorption spectrometer. The result indicated that SO42- was the most abundant ion and with respect to trace metal. All the trace elements except Mn and V show statistically significant differences between monitoring sites. The Pearson's correlation applied to all data, showed a high correlation among SO42-, NO3- and NH4+, indicating a common anthropogenic origin. In addition the correlation found between Ca2+ and Al indicated a crustal origin. On the other hand, in considering the total sampling period for particles as well as for all the metals, it is appreciable the significant differences between sites and meteorological seasons. The cluster analysis of air back-trajectories employed in the paper is a technique widely used to identify transport patterns and potential sources of both anthropogenic pollution and natural constituents of the atmosphere, including atmospheric aerosols. It is also used to determine how aerosol optical properties observed over the station differ depending on source region and transport pathways In order to gain a better insight into the origin of trace metal and major inorganic ions, a Principal Component Analysis was applied to the results for 6 elements and 8 ions, from the years 2009 and 2010. Further, the statistical analysis demonstrated the adequate selection of the monitoring areas, confirming that main emission source of these atmospheric pollutants is anthropogenic origin. Evidence suggests that the organic and inorganic species are not always internally mixed, especially in the small modes. The

  16. Atmospheric electrification in dusty, reactive gases in the solar system and beyond

    CERN Document Server

    Helling, Ch; Honary, F; Diver, D A; Aplin, K; Dobbs-Dixon, I; Ebert, U; Inutsuka, S; Gordillo-Vazquez, F J; Littlefair, S

    2016-01-01

    Detailed observations of the solar system planets reveal a wide variety of local atmospheric conditions. Astronomical observations have revealed a variety of extrasolar planets none of which resembles any of the solar system planets in full. Instead, the most massive amongst the extrasolar planets, the gas giants, appear very similar to the class of (young) Brown Dwarfs which are amongst the oldest objects in the universe. Despite of this diversity, solar system planets, extrasolar planets and Brown Dwarfs have broadly similar global temperatures between 300K and 2500K. In consequence, clouds of different chemical species form in their atmospheres. While the details of these clouds differ, the fundamental physical processes are the same. Further to this, all these objects were observed to produce radio and X-ray emission. While both kinds of radiation are well studied on Earth and to a lesser extent on the solar system planets, the occurrence of emission that potentially originate from accelerated electrons o...

  17. The role of atmospheric greenhouse gases, orbital parameters, and southern ocean gateways: an idealized model study

    CERN Document Server

    Hertwig, Eileen; Fraedrich, Klaus

    2016-01-01

    A set of idealized experiments are performed to analyze the competing effects of declining atmospheric CO2 concentrations, the opening of an ocean gateway, and varying orbital parameters. These forcing mechanisms, which influence the global mean climate state, may have played a role for triggering climate transitions of the past (for example during the Eocene-Oligocene climate transition and the build-up of the Antarctic Ice Sheet). Sensitivity simulations with a coupled atmosphere-ocean general circulation model are conducted to test these three forcings and their roles for the global climate. The simulations are carried out under idealized conditions to focus on the essentials. The combination of all three forcings triggers a climate transition which resembles the onset of the Antarctic glaciation. In particular, the temperatures in the southern high latitudes decrease and snow accumulates constantly. Moreover, the relative importance of each possible forcing is explored. All three of the mechanisms (atmosp...

  18. Abundance and isotopic composition of gases in the martian atmosphere from the Curiosity rover

    NARCIS (Netherlands)

    Mahaffy, P.R.; Webster, C.R.; Atreya, S.K.; Franz, H.; Wong, M.; Conrad, P.G.; Harpold, D.; Jones, J.J.; Leshin, L.A.; Manning, H.; Owen, T.; Pepin, R.O.; Squyres, S.; Trainer, M.; MSL Science Team, the

    2013-01-01

    Volume mixing and isotope ratios secured with repeated atmospheric measurements taken with the Sample Analysis at Mars instrument suite on the Curiosity rover are: carbon dioxide (CO2), 0.960(±0.007); argon-40 (40Ar), 0.0193(±0.0001); nitrogen (N2), 0.0189(±0.0003); oxygen, 1.45(±0.09) × 10−3; carbo

  19. [Errors Analysis and Correction in Atmospheric Methane Retrieval Based on Greenhouse Gases Observing Satellite Data].

    Science.gov (United States)

    Bu, Ting-ting; Wang, Xian-hua; Ye, Han-han; Jiang, Xin-hua

    2016-01-01

    High precision retrieval of atmospheric CH4 is influenced by a variety of factors. The uncertainties of ground properties and atmospheric conditions are important factors, such as surface reflectance, temperature profile, humidity profile and pressure profile. Surface reflectance is affected by many factors so that it is difficult to get the precise value. The uncertainty of surface reflectance will cause large error to retrieval result. The uncertainties of temperature profile, humidity profile and pressure profile are also important sources of retrieval error and they will cause unavoidable systematic error. This error is hard to eliminate only using CH4 band. In this paper, ratio spectrometry method and CO2 band correction method are proposed to reduce the error caused by these factors. Ratio spectrometry method can decrease the effect of surface reflectance in CH4 retrieval by converting absolute radiance spectrometry into ratio spectrometry. CO2 band correction method converts column amounts of CH4 into column averaged mixing ratio by using CO2 1.61 μm band and it can correct the systematic error caused by temperature profile, humidity profile and pressure profile. The combination of these two correction methods will decrease the effect caused by surface reflectance, temperature profile, humidity profile and pressure profile at the same time and reduce the retrieval error. GOSAT data were used to retrieve atmospheric CH4 to test and validate the two correction methods. The results showed that CH4 column averaged mixing ratio retrieved after correction was close to GOSAT Level2 product and the retrieval precision was up to -0.24%. The studies suggest that the error of CH4 retrieval caused by the uncertainties of ground properties and atmospheric conditions can be significantly reduced and the retrieval precision can be highly improved by using ratio spectrometry method and CO2 hand correction method.

  20. Effect of atmospheric gases, surface albedo and cloud overlap on the absorbed solar radiation

    Directory of Open Access Journals (Sweden)

    Ashok Sinha

    Full Text Available Recent studies have provided new evidence that models may systematically underestimate cloud solar absorption compared to observations. This study extends previous work on this "absorption anomaly'' by using observational data together with solar radiative transfer parameterisations to calculate fs (the ratio of surface and top of the atmosphere net cloud forcings and its latitudinal variation for a range of cloud types. Principally, it is found that (a the zonal mean behaviour of fs varies substantially with cloud type, with the highest values obtained for low clouds; (b gaseous absorption and scattering can radically alter the pattern of the variation of fs with latitude, but gaseous effects cannot in general raise fs to the level of around 1.5 as recently determined; (c the importance of the gaseous contribution to the atmospheric ASR is such that whilst fs rises with surface albedo, the net cloud contribution to the atmospheric ASR falls; (d the assumed form of the degree of cloud overlap in the model can substantially affect the cloud contribution to the atmospheric ASR whilst leaving the parameter fs largely unaffected; (e even large uncertainties in the observed optical depths alone cannot account for discrepancies apparent between modelled and newly observed cloud solar absorption. It is concluded that the main source of the anomaly may derive from the considerable uncertainties regarding impure droplet microphysics rather than, or together with, uncertainties in macroscopic quantities. Further, variable surface albedos and gaseous effects may limit the use of contemporaneous satellite and ground-based measurements to infer the cloud solar absorption from the parameter fs.

  1. A comparison of minor trace gas retrievals from the Tropospheric Emission Spectrometer (TES) and the Infrared Atmospheric Sounding Interferometer (IASI)

    Science.gov (United States)

    Cady-Pereira, K. E.; Shephard, M. W.; Henze, D. K.; Millet, D. B.; Gombos, D.; Van Damme, M.; Clarisse, L.; Coheur, P. F.; Pommier, M.; Clerbaux, C.

    2014-12-01

    The advent of hyperspectral infrared instruments orbiting the Earth has allowed for detecting and measuring numerous trace gas species that play important roles in atmospheric chemistry and impact air quality, but for which there is a dearth of information on their distribution and temporal variability. Here we will present global and regional comparisons of measurements from the NASA TES and the European MetOp IASI instruments of three of these gases: ammonia (NH3), formic acid (HCOOH) and methanol (CH3OH). Ammonia is highly reactive and thus very variable in space and time, while the sources and sinks of methanol and formic acid are poorly quantified: thus space-based measurements have the potential of significantly increasing our knowledge of the emissions and distributions of these gases. IASI and TES have many similarities but some significant differences. TES has significantly higher spectral resolution (0.06 cm-1), and its equator crossing times are ~1:30 am and 1:30 pm, local time, while IASI has lower resolution (0.5 cm-1) and an earlier equator crossing time (9:30 am and 9:30 pm), which leads to lower thermal contrast; however IASI provides much greater temporal and spatial coverage due to its cross-track scanning. Added to the instrumental differences are the differences in retrieval algorithms. The IASI team uses simple but efficient methods to estimate total column amounts of the species above, while the TES team performs full optimal estimation retrievals. We will compare IASI and TES total column measurements averaged on a 2.5x2.5 degree global grid for each month in 2009, and we will examine the seasonal cycle in some regions of interest, such as South America, eastern China, and the Midwest and the Central Valley in the US. In regions where both datasets are in agreement this analysis will provide confidence that the results are robust and reliable. In regions where there is disagreement we will look for the causes of the discrepancies, which will

  2. Critical Masses for Various Terrestrial Planet Atmospheric Gases and Water in/on Mars

    Directory of Open Access Journals (Sweden)

    Lin-gun Liu

    2014-01-01

    Full Text Available The lower critical mass boundaries (CM for various atmospheric gas species on terrestrial planets are estimated. The CM is different for different gas molecules. Except for He, the observed atmospheric compositions of the terrestrial planets are consistent with these estimates. The lower CM boundary for gaseous H2O is calculated as 8.06 × 1026 g, which is significantly greater than the Martian mass (6.419 × 1026 g. Thus, Mars is not capable of retaining H2O in its atmosphere. If the speculated ocean on Mars and the claimed H2O ice in the Martian soil are true, both the ocean and ice had to be derived earlier from H2O degassed from the Martian interior after the surface temperature cooled much below 100°C. These watery bodies cannot be sustained for long durations because evaporation and sublimation would turn them into gaseous H2O, which would be lost to outer-space. It is concluded that H2O in/on Mars is inherent and that the primordial planetesimals that formed Mars must have contained appreciable amounts of hydrous minerals, if the oceans and/or H2O ice on Mars are true.

  3. An Experimental Study on Atmospheric Pressure Glow Discharge in Different Gases

    Institute of Scientific and Technical Information of China (English)

    刘鹏; 詹如娟; 等

    2002-01-01

    Usually,the electrical breakdown of dielectric barrier discharge(DBD) at atmospheric pressure leads to a filamentary non-homogeneous discharge,However,it is also possible to obtain a diffuse DBD in homogeneous form,called atmospheric pressure glow discharge(APGD).We obtained a uniform APGD in helium and in the mixture of argon with alcohol,and studied the electrical characteristics of helium APGD.It if found that the relationship between discharge current and source frequency is different depending on the difference in gas gap when the applied voltage is kept constant.The discharge current shows an increasing trend with the increased frequency when gas gap is 0.8cm ,but the discharge current tends to decrease with the increased frequency when the gas gap increases.The discharge current always increases with the increased applied voltage when the source frequency is kept constant.We also observed a glow-like discharge in nitrogen at atmospheric pressure.

  4. Critical Masses for Various Terrestrial Planet Atmospheric Gases and Water in/on Mars

    Directory of Open Access Journals (Sweden)

    Lin-gun Liu

    2014-01-01

    Full Text Available The lower critical mass boundaries (CM for various atmospheric gas species on terrestrial planets are estimated. The CM is different for different gas molecules. Except for He, the observed atmospheric compositions of the terrestrial planets are consistent with these estimates. The lower CM boundary for gaseous H2O is calculated as 8.06 ×× 1026 g, which is significantly greater than the Martian mass (6.419 ×× 1026 g. Thus, Mars is not capable of retaining H2O in its atmosphere. If the speculated ocean on Mars and the claimed H2O ice in the Martian soil are true, both the ocean and ice had to be derived earlier from H2O degassed from the Martian interior after the surface temperature cooled much below 100°C.100°C. These watery bodies cannot be sustained for long durations because evaporation and sublimation would turn them into gaseous H2O, which would be lost to outer-space. It is concluded that H2O in/on Mars is inherent and that the primordial planetesimals that formed Mars must have contained appreciable amounts of hydrous minerals, if the oceans and/or H2O ice on Mars are true.

  5. Spatial and temporal variation in domestic biofuel consumption rates and patterns in Zimbabwe: implications for atmospheric trace gas emission

    Energy Technology Data Exchange (ETDEWEB)

    Ludwig, J.; Andreae, M.O.; Helas, G. [Max Planck Institute for Chemistry, Mainz (Germany). Dept. of Biogeochemistry; Marufu, L. [Max Planck Institute for Chemistry, Mainz (Germany). Dept. of Biogeochemistry; University of Utrecht, (Netherlands). Institute for Marine and Atmospheric Research Utrecht; Lelieveld, J. [University of Utrecht, (Netherlands). Institute for Marine and Atmospheric Research Utrecht

    1999-05-01

    An ecologically nationwide and all-year-round domestic biofuel consumption study was conducted in Zimbabwe from January 1996 to March 1997. The study aimed at (a) establishing the determinants and magnitudes of spatial and temporal variations in biofuel consumption rates, (b) estimating the overall mean national rural and urban consumption rates, and (c) estimating the contribution of domestic biomass burning in Zimbabwe to the emission of atmospheric trace gases. The main source of spatial variation in biofuel consumption rates was found to be settlement type (rural or urban). Within a settlement type, per capita consumption rates varied in time and space with household size, ambient temperature, and physical availability. In rural areas wood and agricultural residues were consumed at national average rates of 1.3{+-}0.2 and 0.07{+-}0.01 tonnes capita{sup -1} year{sup -1}, respectively. In urban centres wood was consumed at an average rate of 0.4{+-}0.26 tonnes capita{sup -1} year{sup -1}. These consumption rates translate into emission outputs from Zimbabwe of 4.6 Tg CO{sub 2}-C year{sup -1}, 0.4 Tg CO-C year{sup -1}, 5.3 Gg NO-N year{sup -1}, 14.5 Gg CH{sub 4}-C year{sup -1}, 24.2 Gg NMHC-C year{sup -1}, 2.9 Gg organic acid-C year{sup -1} (formic and acetic acids) and 48.4 Gg aerosol-C year{sup -1}. For CO{sub 2}, CO, and NO, these domestic biofuel emissions represent 41{+-}6%, 67{+-}6%, and 8{+-}1%, respectively, of the total output of all sources evaluated and documented in Zimbabwe to date. This means that of the studied sources, domestic biomass burning is the major source of CO{sub 2} and CO emission in Zimbabwe.

  6. Reusable In Situ AirCore System for CO2 and Trace Gas Measurements Project

    Data.gov (United States)

    National Aeronautics and Space Administration — A novel design for an in situ atmospheric sensor for CO2 and trace gases is proposed. The sensor, named AirCore, provides the advantages of existing in situ sensors...

  7. Barometric pumping of burial trench soil gases into the atmosphere at the 740-G Sanitary Landfill

    Energy Technology Data Exchange (ETDEWEB)

    Wyatt, D.E.; Pirkle, R.J.; Masdea, D.J.

    1992-12-01

    In 1991, a soil gas survey was performed at the Savannah River Site Sanitary Landfill as part of the characterization efforts required under the integrated Resource Conservation and Recovery Act (RCRA) Facility Investigation and Comprehensive Environmental Resource Conservation and Recovery Act (CERCLA) Remedial Investigation (RFI/RI) program. This report details the findings of this survey, which identified several areas of the landfill that were releasing volatile organic compounds to the atmosphere at levels exceeding regulatory standards. Knowledge of the rates of VOC outgassing is necessary to protect site workers, provide input into the human health and environmental risk assessment documents and provide input into the remedial design scenario.

  8. Detection of trace gases from fermentation processes using photoacoustic spectroscopy and proton-transfer-reaction mass spectrometry

    NARCIS (Netherlands)

    Boamfă-Ivan, Elena Iuliana

    2005-01-01

    This thesis presents novel interdisciplinary Physics - Biology research work that employed Photoacoustic Spectroscopy and Proton-Transfer-Reaction Mass Spectrometry. Both techniques were used in biological studies of trace gasses emitted by crop plants and fruit under stress situations. The findings

  9. Atmospheric trace element concentrations in total suspended particles near Paris, France

    Science.gov (United States)

    Ayrault, Sophie; Senhou, Abderrahmane; Moskura, Mélanie; Gaudry, André

    2010-09-01

    To evaluate today's trace element atmospheric concentrations in large urban areas, an atmospheric survey was carried out for 18 months, from March 2002 to September 2003, in Saclay, nearby Paris. The total suspended particulate matter (TSP) was collected continuously on quartz fibre filters. The TSP contents were determined for 36 elements (including Ag, Bi, Mo and Sb) using two analytical methods: Instrumental Neutron Activation Analysis (INAA) and Inductively Coupled Plasma Mass Spectrometry (ICP-MS). The measured concentrations were in agreement within the uncertainties with the certified values for the polycarbonate reference material filter SRM-2783 (National Institute for Standard Technology NIST, USA). The measured concentrations were significantly lower than the recommended atmospheric concentrations. In 2003, the Pb atmospheric level at Saclay was 15 ng/m 3, compared to the 500 ng/m 3 guideline level and to the 200 ng/m 3 observed value in 1994. The typical urban background TSP values of 1-2, 0.2-1, 4-6, 10-30 and 3-5 ng/m 3 for As, Co, Cr, Cu and Sb, respectively, were inferred from this study and were compared with the literature data. The typical urban background TSP concentrations could not be realised for Cd, Pb and Zn, since these air concentrations are highly influenced by local features. The Zn concentrations and Zn/Pb ratio observed in Saclay represented a characteristic fingerprint of the exceptionally large extent of zinc-made roofs in Paris and its suburbs. The traffic-related origin of Ba, Cr, Cu, Pb and Sb was demonstrated, while the atmospheric source(s) of Ag was not identified.

  10. Dynamics of submarine groundwater discharge and associated fluxes of dissolved nutrients, carbon, and trace gases to the coastal zone (Okatee River estuary, South Carolina)

    Science.gov (United States)

    Porubsky, W.P.; Weston, N.B.; Moore, W.S.; Ruppel, C.; Joye, S.B.

    2014-01-01

    Multiple techniques, including thermal infrared aerial remote sensing, geophysical and geological data, geochemical characterization and radium isotopes, were used to evaluate the role of groundwater as a source of dissolved nutrients, carbon, and trace gases to the Okatee River estuary, South Carolina. Thermal infrared aerial remote sensing surveys illustrated the presence of multiple submarine groundwater discharge sites in Okatee headwaters. Significant relationships were observed between groundwater geochemical constituents and 226Ra activity in groundwater with higher 226Ra activity correlated to higher concentrations of organics, dissolved inorganic carbon, nutrients, and trace gases to the Okatee system. A system-level radium mass balance confirmed a substantial submarine groundwater discharge contribution of these constituents to the Okatee River. Diffusive benthic flux measurements and potential denitrification rate assays tracked the fate of constituents in creek bank sediments. Diffusive benthic fluxes were substantially lower than calculated radium-based submarine groundwater discharge inputs, showing that advection of groundwater-derived nutrients dominated fluxes in the system. While a considerable potential for denitrification in tidal creek bank sediments was noted, in situ denitrification rates were nitrate-limited, making intertidal sediments an inefficient nitrogen sink in this system. Groundwater geochemical data indicated significant differences in groundwater chemical composition and radium activity ratios between the eastern and western sides of the river; these likely arose from the distinct hydrological regimes observed in each area. Groundwater from the western side of the Okatee headwaters was characterized by higher concentrations of dissolved organic and inorganic carbon, dissolved organic nitrogen, inorganic nutrients and reduced metabolites and trace gases, i.e. methane and nitrous oxide, than groundwater from the eastern side

  11. Atmospheric Electrification in Dusty, Reactive Gases in the Solar System and Beyond

    Science.gov (United States)

    Helling, Christiane; Harrison, R. Giles; Honary, Farideh; Diver, Declan A.; Aplin, Karen; Dobbs-Dixon, Ian; Ebert, Ute; Inutsuka, Shu-ichiro; Gordillo-Vazquez, Francisco J.; Littlefair, Stuart

    2016-07-01

    Detailed observations of the solar system planets reveal a wide variety of local atmospheric conditions. Astronomical observations have revealed a variety of extrasolar planets none of which resembles any of the solar system planets in full. Instead, the most massive amongst the extrasolar planets, the gas giants, appear very similar to the class of (young) brown dwarfs which are amongst the oldest objects in the Universe. Despite this diversity, solar system planets, extrasolar planets and brown dwarfs have broadly similar global temperatures between 300 and 2500 K. In consequence, clouds of different chemical species form in their atmospheres. While the details of these clouds differ, the fundamental physical processes are the same. Further to this, all these objects were observed to produce radio and X-ray emissions. While both kinds of radiation are well studied on Earth and to a lesser extent on the solar system planets, the occurrence of emissions that potentially originate from accelerated electrons on brown dwarfs, extrasolar planets and protoplanetary disks is not well understood yet. This paper offers an interdisciplinary view on electrification processes and their feedback on their hosting environment in meteorology, volcanology, planetology and research on extrasolar planets and planet formation.

  12. Influence of Biomass Burning on Temporal and Diurnal Variations of Acidic Gases, Particulate Nitrate, and Sulfate in a Tropical Urban Atmosphere

    OpenAIRE

    Sailesh N. Behera; Rajasekhar Balasubramanian

    2014-01-01

    The present study investigated the temporal and diurnal distributions of atmospheric acidic gases (sulphur dioxide (SO2), nitrous acid (HONO), and nitric acid (HNO3)) and those of particulate nitrate (NO3-) and sulfate (SO42-) through a comprehensive field campaign during the largest smoke haze episode in Singapore, a representative country in Southeast Asia (SEA). To identify the atmospheric behavior of these pollutants during the smoke haze period, the data generated from the measurement ca...

  13. On the marine atmospheric boundary layer characteristics over Bay of Bengal and Arabian Sea during the Integrated Campaign for Aerosols, gases and Radiation Budget (ICARB)

    Indian Academy of Sciences (India)

    Denny P Alappattu; D Bala Subrahamanyam; P K Kunhikrishnan; K M Somayaji; G S Bhat; R Venkatesan; C B S Dutt; A Bagavath Singh; V K Soni; A S Tripathi

    2008-07-01

    Detailed measurements were carried out in the Marine Atmospheric Boundary Layer (MABL) during the Integrated Campaign for Aerosols, gases and Radiation Budget (ICARB) which covered both Arabian Sea and Bay of Bengal during March to May 2006. In this paper, we present the meteorological observations made during this campaign. The latitudinal variation of the surface layer turbulent fluxes is also described in detail.

  14. Gases Working Group: Why is it important to study Air-Sea Gas Exchange?

    NARCIS (Netherlands)

    Liss, P.; Grimalt, J.O.; Hov, O.; Johannessen, T.; Larsen, S.E.; Oost, W.A.; Leeuw, G. de

    1998-01-01

    Exchange of trace gases between the oceans and the atmosphere affects the atrnospheric content and cycling of a range of chemical trace species which are related to climate change, ozone layer depletion, acid deposition, eutrophication amospheric pafticle formation, photo-oxidants, heavy metals and

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

    Science.gov (United States)

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

    2015-01-01

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

  16. Note: A dual temperature closed loop batch reactor for determining the partitioning of trace gases within CO{sub 2}-water systems

    Energy Technology Data Exchange (ETDEWEB)

    Warr, Oliver, E-mail: oliver.warr@earth.ox.ac.uk; Ballentine, Christopher J. [Department of Earth Sciences, University of Oxford, South Parks Road, Oxford OX1 3AN (United Kingdom); Rochelle, Christopher A. [British Geological Survey, Environmental Science Centre, Nicker Hill, Keyworth, Nottingham NG12 5GG (United Kingdom); Masters, Andrew J. [School of Chemical Engineering and Analytical Science, University of Manchester, Manchester M13 9PL (United Kingdom)

    2016-01-15

    An experimental approach is presented which can be used to determine partitioning of trace gases within CO{sub 2}-water systems. The key advantages of this system are (1) The system can be isolated with no external exchange, making it ideal for experiments with conservative tracers. (2) Both phases can be sampled concurrently to give an accurate composition at each phase at any given time. (3) Use of a lower temperature flow loop outside of the reactor removes contamination and facilitates sampling. (4) Rapid equilibration at given pressure/temperature conditions is significantly aided by stirring and circulating the water phase using a magnetic stirrer and high-pressure liquid chromatography pump, respectively.

  17. Atmospheric greenhouse gases retrieved from SCIAMACHY: comparison to ground-based FTS measurements and model results

    Directory of Open Access Journals (Sweden)

    O. Schneising

    2012-02-01

    Full Text Available SCIAMACHY onboard ENVISAT (launched in 2002 enables the retrieval of global long-term column-averaged dry air mole fractions of the two most important anthropogenic greenhouse gases carbon dioxide and methane (denoted XCO2 and XCH4. In order to assess the quality of the greenhouse gas data obtained with the recently introduced v2 of the scientific retrieval algorithm WFM-DOAS, we present validations with ground-based Fourier Transform Spectrometer (FTS measurements and comparisons with model results at eight Total Carbon Column Observing Network (TCCON sites providing realistic error estimates of the satellite data. Such validation is a prerequisite to assess the suitability of data sets for their use in inverse modelling.

    It is shown that there are generally no significant differences between the carbon dioxide annual increases of SCIAMACHY and the assimilation system CarbonTracker (2.00 ± 0.16 ppm yr−1 compared to 1.94 ± 0.03 ppm yr−1 on global average. The XCO2 seasonal cycle amplitudes derived from SCIAMACHY are typically larger than those from TCCON which are in turn larger than those from CarbonTracker. The absolute values of the northern hemispheric TCCON seasonal cycle amplitudes are closer to SCIAMACHY than to CarbonTracker and the corresponding differences are not significant when compared with SCIAMACHY, whereas they can be significant for a subset of the analysed TCCON sites when compared with CarbonTracker. At Darwin we find discrepancies of the seasonal cycle derived from SCIAMACHY compared to the other data sets which can probably be ascribed to occurrences of undetected thin clouds. Based on the comparison with the reference data, we conclude that the carbon dioxide data set can be characterised by a regional relative precision (mean standard deviation of the differences of about 2.2 ppm and a relative accuracy (standard deviation of the mean differences

  18. Simulation of ion motion at atmospheric pressure: particle tracing versus electrokinetic flow.

    Science.gov (United States)

    Wissdorf, Walter; Pohler, Larissa; Klee, Sonja; Müller, David; Benter, Thorsten

    2012-02-01

    Results obtained with two computational approaches for the simulation of ion motion at elevated pressure are compared with experimentally derived ion current data. The computational approaches used are charged particle tracings with the software package SIMION ver. 8 and finite element based calculations using the software package Comsol Multiphysics ver. 4.0/4.0a. The experimental setup consisted of a tubular corona discharge ion source coupled to a cylindrical measurement chamber held at atmospheric pressure. Generated ions are flown into the chamber at essentially subsonic laminar isothermal conditions. In the simulations, strictly stationary conditions were assumed. The results show very good agreement between the SIMION/SDS model and experimental data. For the Comsol model, only qualitative agreement is observed.

  19. Predicting the thermal/structural performance of the atmospheric trace molecules spectroscopy /ATMOS/ Fourier transform spectrometer

    Science.gov (United States)

    Miller, J. M.

    1980-01-01

    ATMOS is a Fourier transform spectrometer to measure atmospheric trace molecules over a spectral range of 2-16 microns. Assessment of the system performance of ATMOS includes evaluations of optical system errors induced by thermal and structural effects. In order to assess the optical system errors induced from thermal and structural effects, error budgets are assembled during system engineering tasks and line of sight and wavefront deformations predictions (using operational thermal and vibration environments and computer models) are subsequently compared to the error budgets. This paper discusses the thermal/structural error budgets, modelling and analysis methods used to predict thermal/structural induced errors and the comparisons that show that predictions are within the error budgets.

  20. Tracing atmospheric nitrate in groundwater using triple oxygen isotopes: evaluation based on bottled drinking water

    Directory of Open Access Journals (Sweden)

    F. Nakagawa

    2013-06-01

    Full Text Available The stable isotopic compositions of nitrate dissolved in 49 brands of bottled drinking water collected worldwide were measured, to trace the fate of atmospheric nitrate (NO3− atm that had been deposited into subaerial ecosystems, using the 17O anomalies (Δ17O of nitrate as tracers. The use of bottled water enables collection of groundwater recharged at natural, background watersheds. The nitrate in groundwater had small Δ17O values ranging from −0.2‰ to +4.5‰ n = 49. The average Δ17O value and average mixing ratio of atmospheric nitrate to total nitrate in the groundwater samples were estimated to be 0.8‰ and 3.1%, respectively. These findings indicated that the majority of atmospheric nitrate had undergone biological processing before being exported from the surface ecosystem to the groundwater. Moreover, the concentrations of atmospheric nitrate were estimated to range from less than 0.1 μmol L−1 to 8.5 μmol L−1 with higher NO3−atm concentrations being obtained for those recharged in rocky, arid or elevated areas with little vegetation and lower NO3−atm concentrations being obtained for those recharged in forested areas with high levels of vegetation. Additionally, many of the NO3−atm-depleted samples were characterized by elevated δ15N values of more than +10‰. Uptake by plants and/or microbes in forested soils subsequent to deposition and the progress of denitrification within groundwater likely plays a significant role in the removal of NO3−atm.

  1. Evidence for multiple magma ocean outgassing and atmospheric loss episodes from mantle noble gases

    CERN Document Server

    Tucker, Jonathan M

    2014-01-01

    The energy associated with giant impacts is large enough to generate global magma oceans during Earth's accretion. However, geochemical evidence requiring a terrestrial magma ocean is scarce. Here we present evidence for at least two separate magma ocean outgassing episodes on Earth based on the ratio of primordial 3He to 22Ne in the present-day mantle. We demonstrate that the depleted mantle 3He/22Ne ratio is at least 10 while a more primitive mantle reservoir has a 3He/22Ne ratio of 2.3 to 3. The 3He/22Ne ratios of the mantle reservoirs are higher than possible sources of terrestrial volatiles, including the solar nebula ratio of 1.5. Therefore, a planetary process must have raised the mantle's 3He/22Ne ratio. We show that long-term plate tectonic cycling is incapable of raising the mantle 3He/22Ne ratio and may even lower it. However, ingassing of a gravitationally accreted nebular atmosphere into a magma ocean on the proto-Earth explains the 3He/22Ne and 20Ne/22Ne ratios of the primitive mantle reservoir....

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2005-02-01

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

  3. Canopy influence on trace metal atmospheric inputs on forest ecosystems: Speciation in throughfall

    Science.gov (United States)

    Gandois, L.; Tipping, E.; Dumat, C.; Probst, A.

    2010-02-01

    Atmospheric inputs of selected Trace Metals (TM: Cd, Cu, Ni, Pb, Sb, Zn, as well as Al, Fe and Mn) were studied on six forested sites in France. In order to evaluate canopy interaction with atmospheric inputs, TM were measured in both Open Field Bulk Deposition (BD) and Throughfall (TF). Anthropogenic contribution to BD composition is high for Zn, Cd and Sb, reflecting actual TM emissions trends. Canopy greatly influences precipitation composition, through different processes, including assimilation and leaching by canopy, complexation as well as accumulation/dissolution of dry deposition. TM and Dissolved Organic Carbon (DOC) physical fractionation between colloidal and truly dissolved phases was performed with ultrafiltration. Al, Fe, Pb and Cu are found in the colloidal fraction whereas Cd, Ni, Zn and Sb are mostly in the truly dissolved fraction. Chemical speciation predicted with WHAM-VI shows that in throughfall, Al, Fe, Pb and Cu are almost entirely complexed by DOC, whereas Ni, Cd and Zn are present in average 30% in the free metal ion form. TM present in labile forms (Cd, Ni, Zn) interact with the canopy, are cycled in the ecosystem, and their concentration is either slightly increased or even decreased in throughfall. Sb, Pb and Cu concentration are increased through canopy, as a consequence of dry deposition accumulation.

  4. Atmospheric pollution in an urban environment by tree bark biomonitoring--part I: trace element analysis.

    Science.gov (United States)

    Guéguen, Florence; Stille, Peter; Lahd Geagea, Majdi; Boutin, René

    2012-03-01

    Tree bark has been shown to be a useful biomonitor of past air quality because it accumulates atmospheric particulate matter (PM) in its outermost structure. Trace element concentrations of tree bark of more than 73 trees allow to elucidate the impact of past atmospheric pollution on the urban environment of the cities of Strasbourg and Kehl in the Rhine Valley. Compared to the upper continental crust (UCC) tree barks are strongly enriched in Mn, Ni, Cu, Zn, Cd and Pb. To assess the degree of pollution of the different sites in the cities, a geoaccumulation index I(geo) was applied. Global pollution by V, Ni, Cr, Sb, Sn and Pb was observed in barks sampled close to traffic axes. Cr, Mo, Cd pollution principally occurred in the industrial area. A total geoaccumulation index I(GEO-tot) was defined; it is based on the total of the investigated elements and allows to evaluate the global pollution of the studied environment by assembling the I(geo) indices on a pollution map.

  5. Impact features tracing hypervelocity airbursts on earth from the atmosphere to the ground

    Science.gov (United States)

    Courty, M. M.

    2012-12-01

    In the absence of deep craters, impact features have been debated to possibly tracing proximal ejecta from yet undetected structure or airburst debris from a meteorite collision with the terrestrial atmosphere or lithosphere. We examine the possibility for impact features to have originated from the shock layer formed ahead of a hypervelocity collider in the earth atmosphere. This hypothesis is approached by comparing impact features from controlled materials to puzzling geological ones: (1) debris collected at the ground from a high altitude meteor airburst recorded on 2011 August 2nd in Southern France; (2) laboratory experiments performed for defense purposes at the CEA Gramat Center (France) with the Persephone hypervelocity light gas gun; (3) the Zhamanshin impact breccia, the Lybian glass, the Egyptian Dakhleh glass, the Tasmanian Darwin glass, the Australasian tektite strewnfield and the Australian Henbury crater field. The Persephone experiments include collisions from 4.1 to 7.9 km/s by a steel projectile embedded into a polycarbonate holder with a polystyrene separator on to a 40 mm thick aluminum target. The impact features been characterized by coupling Environmental SEM with EDS, Raman micro-spectrometry, XRD, TEM, Tof-SIMS, ICP-MS and isotope analyses. Similar carbonaceous polymorphs that are closely imbricated at meso to nano-scales to the crystallized components (including the metal blebs) and to the glass phases (spherules or matrix) are present in all the impact features studied. They dominantly consist of aliphatic polymers, rare aromatic compounds, with graphite-lonsdaleite inclusions. The Persephone experiments help relating the graphite-lonsdaleite couple to transformed organic residues by the transient high pressure shock (a few tens MPa) and the transient heating (ca 100°C) and the aliphatic polymers to new hydrocarbons that formed from the pulverized polycarbonate and polystyrene. The Persephone experiments provide the controlled situation

  6. Sources of Sahelian-Sudan moisture: Insights from a moisture-tracing atmospheric model

    Science.gov (United States)

    Salih, Abubakr A. M.; Zhang, Qiong; Pausata, Francesco S. R.; Tjernström, Michael

    2016-07-01

    The summer rainfall across Sahelian-Sudan is one of the main sources of water for agriculture, human, and animal needs. However, the rainfall is characterized by large interannual variability, which has attracted extensive scientific efforts to understand it. This study attempts to identify the source regions that contribute to the Sahelian-Sudan moisture budget during July through September. We have used an atmospheric general circulation model with an embedded moisture-tracing module (Community Atmosphere Model version 3), forced by observed (1979-2013) sea-surface temperatures. The result suggests that about 40% of the moisture comes with the moisture flow associated with the seasonal migration of the Intertropical Convergence Zone (ITCZ) and originates from Guinea Coast, central Africa, and the Western Sahel. The Mediterranean Sea, Arabian Peninsula, and South Indian Ocean regions account for 10.2%, 8.1%, and 6.4%, respectively. Local evaporation and the rest of the globe supply the region with 20.3% and 13.2%, respectively. We also compared the result from this study to a previous analysis that used the Lagrangian model FLEXPART forced by ERA-Interim. The two approaches differ when comparing individual regions, but are in better agreement when neighboring regions of similar atmospheric flow features are grouped together. Interannual variability with the rainfall over the region is highly correlated with contributions from regions that are associated with the ITCZ movement, which is in turn linked to the Atlantic Multidecadal Oscillation. Our result is expected to provide insights for the effort on seasonal forecasting of the rainy season over Sahelian Sudan.

  7. Water soluble inorganic trace gases and related aerosol compounds in the tropical boundary layer. An analysis based on real time measurements at a pasture site in the Amazon Basin

    NARCIS (Netherlands)

    Trebs, I.

    2005-01-01

    This dissertation investigates the behavior of water-soluble inorganic trace gases and related aerosol species in the tropical boundary layer. Mixing ratios of ammonia (NH3), nitric acid (HNO3), nitrous acid (HONO), hydrochloric acid (HCl), sulfur dioxide (SO;,) and the corresponding water-soluble a

  8. Estimation of the atmosphere-ocean fluxes of greenhouse gases and aerosols at the finer resolution of the coastal ocean.

    Science.gov (United States)

    Vieira, Vasco; Sahlée, Erik; Jurus, Pavel; Clementi, Emanuela; Pettersson, Heidi; Mateus, Marcos

    2016-04-01

    The balances and fluxes of greenhouse gases and aerosols between atmosphere and ocean are fundamental for Earth's heat budget. Hence, the scientific community needs to know and simulate them with accuracy in order to monitor climate change from Earth-Observation satellites and to produce reliable estimates of climate change using Earth-System Models (ESM). So far, ESM have represented earth's surface with coarser resolutions so that each cell of the marine domain is dominated by the open ocean. In such case it is enough to use simple algorithms considering the wind speed 10m above sea-surface (u10) as sole driver of the gas transfer velocity. The formulation by Wanninkhof (1992) is broadly accepted as the best. However, the ESM community is becoming increasingly aware of the need to model with finer resolutions. Then, it is no longer enough to only consider u10 when modelling gas transfer velocities across the coastal oceans' surfaces. More comprehensive formulations are required that adjust better to local conditions by also accounting for the effects of sea-surface agitation, wave breaking, atmospheric stability of the Surface Boundary Layer, current drag with the bottom, surfactants and rain. Accurate algorithms are also fundamental to monitor atmosphere and ocean greenhouse gas concentrations using satellite data and reverse modelling. Past satellite missions ERS, Envisat, Jason-2, Aqua, Terra and Metop, have already been remotely sensing the ocean's surface at much finer resolutions than ESM using instruments like MERIS, MODIS, AMR, AATSR, MIPAS, Poseidon-3, SCIAMACHY, SeaWiFS, and IASI. The planned new satellite missions Sentinel-3, OCO-2 and GOSAT will further increase the resolutions. We developed a framework to congregate competing formulations for the estimation of the solubility and transfer velocity of virtually any gas on the biosphere taking into consideration the atmosphere and ocean fundamental variables and their derived geophysical processes

  9. Rare earths and trace elements contents in leaves: A new indicator of the composition of atmospheric dust.

    Science.gov (United States)

    Censi, P; Cibella, F; Falcone, E E; Cuttitta, G; Saiano, F; Inguaggiato, C; Latteo, V

    2017-02-01

    The relationship between the trace element distribution in atmospheric particles and leaves of some exposed plants in the environment was recently demonstrated. This indication would suggest that the trace element analysis of leaves in these plants could provide information about the composition, nature and origin of the atmospheric dust dispersed in the environment. In order to corroborate this hypothesis, the distribution of trace elements and Rare Earths were studied in leaves of some endemic plants, in the atmospheric fallout and in soils of rural, urban and industrial ecosystems in Sicily. These elements have been chosen to discriminate the source and nature of different source on atmospheric dust and the larger capability of the composition of the latter materials to influence the metal ion distribution in leaves of studied plants rather than the soil composition. These evidences are related to the recognition both of positive La anomaly and trace element enrichments in studied leaves and to their particular V/Th and Co/Ni signature. On the other hand, some particular normalised REE features recognised in leaves suggest that a limited contribution to the REE budget in studied leaves is provided by the REE migration from roots.

  10. Trend and variability of atmospheric ozone over middle Indo-Gangetic Plain: impacts of seasonality and precursor gases.

    Science.gov (United States)

    Shukla, K; Srivastava, Prashant K; Banerjee, T; Aneja, Viney P

    2017-01-01

    Ozone dynamics in two urban background atmospheres over middle Indo-Gangetic Plain (IGP) were studied in two contexts: total columnar and ground-level ozone. In terms of total columnar ozone (TCO), emphases were made to compare satellite-based retrieval with ground-based observation and existing trend in decadal and seasonal variation was also identified. Both satellite-retrieved (Aura Ozone Monitoring Instrument-Differential Optical Absorption Spectroscopy (OMI-DOAS)) and ground-based observations (IMD-O3) revealed satisfying agreement with OMI-DOAS observation over predicting TCO with a positive bias of 7.24 % under all-sky conditions. Minor variation between daily daytime (r = 0.54; R (2) = 29 %; n = 275) and satellite overpass time-averaged TCO (r = 0.58; R (2) = 34 %; n = 208) was also recognized. A consistent and clear seasonal trend in columnar ozone (2005-2015) was noted with summertime (March-June) maxima (Varanasi, 290.9 ± 8.8; Lucknow, 295.6 ± 9.5 DU) and wintertime (December-February) minima (Varanasi, 257.4 ± 10.1; Lucknow, 258.8 ± 8.8 DU). Seasonal trend decomposition based on locally weighted regression smoothing technique identified marginally decreasing trend (Varanasi, 0.0084; Lucknow, 0.0096 DU year(-1)) especially due to reduction in monsoon time minima and summertime maxima. In continuation to TCO, variation in ground-level ozone in terms of seasonality and precursor gases were also analysed from September 2014 to August 2015. Both stations registered similar pattern of variation with Lucknow representing slightly higher annual mean (44.3 ± 30.6; range, 1.5-309.1 μg/m(3)) over Varanasi (38.5 ± 17.7; range, 4.9-104.2 μg/m(3)). Variation in ground-level ozone was further explained in terms water vapour, atmospheric boundary layer height and solar radiation. Ambient water vapour content was found to associate negatively (r = -0.28, n = 284) with ground-level ozone with considerable seasonal variation in

  11. Field measurement of acid gases and soluble anions in atmospheric particulate matter using a parallel plate wet denuder and an alternating filter-based automated analysis system.

    Science.gov (United States)

    Boring, C Bradley; Al-Horr, Rida; Genfa, Zhang; Dasgupta, Pumendu K; Martin, Michael W; Smith, William F

    2002-03-15

    We present a new fully automated instrument for the measurement of acid gases and soluble anionic constituents of atmospheric particulate matter. The instrument operates in two independent parallel channels. In one channel, a wet denuder collects soluble acid gases; these are analyzed by anion chromatography (IC). In a second channel, a cyclone removes large particles and the aerosol stream is then processed by another wet denuder to remove potentially interfering gases. The particles are then collected by one of two glass fiber filters which are alternately sampled, washed, and dried. The washings are preconcentrated and analyzed by IC. Detection limits of low to subnanogram per cubic meter concentrations of most gaseous and particulate constituents can be readily attained. The instrument has been extensively field-tested; some field data are presented. Results of attempts to decipher the total anionic constitution of urban ambient aerosol by IC-MS analysis are also presented.

  12. Atmospheric trace elements at Enewetak Atoll: 2. Transport to the ocean by wet and dry deposition

    Science.gov (United States)

    Arimoto, R.; Duce, R. A.; Ray, B. J.; Unni, C. K.

    1985-02-01

    The concentrations of trace elements in precipitation and dry deposition are presented for samples collected at Enewetak Atoll (11°N, 162° E) during SEAREX experiments in 1979. The concentrations of Al, Sc, Mn, Fe, Co, and Th in rain are dominated by crustal material, and for these elements, wet deposition evidently exceeds dry deposition. For most of these elements the present rates of atmospheric deposition at Enewetak are similar to their mean rate of accumulation in sediments over the past 5-10,000 years, suggesting that the air-to-sea exchange of particles is closely tied to the sedimentary cycle of the mid-Pacific. Noncrustal sources govern the concentrations of Pb, Zn, Cu, Se, and Cd in wet and dry deposition samples. Analyses of dry deposition collected from a flat plastic plate indicate that the amount of material recycled from the sea surface varies markedly between samples, and even though these estimates do not necessarily reflect the dry deposition to the ocean surface, the results suggest that recycled sea spray often amounts to more than 50% of the total dry deposition of the enriched elements. Recycled sea spray also makes up a significant fraction of the total wet deposition of the enriched elements. The net deposition rates of elements such as Cu and Zn are greater than or equal to their inputs from vertical mixing, but the net deposition of Pb clearly exceeds the input from upwelling. The current net deposition rates of the enriched elements are also similar to their rates of removal to sediments. These results indicate that air-sea exchange processes may significantly affect the chemistry of trace metals in the open ocean.

  13. Atmospheric input of N, P, Fe and trace metals to north Indian Ocean

    Science.gov (United States)

    Sarin, Manmohan; Srinivas, Bikkina

    2016-04-01

    The air-sea deposition of chemical constituents to the north Indian Ocean is influenced by seasonal continental outflow during the late NE-monsoon (December-April). Our recent studies have focused on deposition of mineral dust, nutrients (N, P and Fe) and toxic trace metals to the Arabian Sea (ARS) and Bay of Bengal (BoB), two important limbs of the north Indian Ocean. The chemical composition of PM2.5 in the continental outflow to the marine atmospheric boundary layer reveals dominance of nss-SO42- (as high as 25 μg m-3) and abundance of dust varies from 3 to 20 μg m-3. A striking similarity in the temporal variability of total inorganic acidity (TIA = NO3- + nss-SO42-) and fractional solubility of aerosol-Fe (FeTot: 60 - 1145 ng m-3) provides evidence for chemical processing of mineral dust during atmospheric transport. The enhanced solubility of Fe has implications to further increase in the deposition of this micro-nutrient to ocean surface. The mass ratio of nutrients (NInorg/NTot, Norg/NTot and PInorg/nss-Ca2+) also suggests further increase in their air-sea deposition to the surface BoB. The dry-deposition flux of PInorgto BoB varies by one order of magnitude (0.5 - 5.0 μmol-P m-2 d-1; Av: 0.02 Tg P yr-1). Based on atmospheric deposition of P and Fe, C-fixation in BoB (˜1 Pg yr-1) is dominated by anthropogenic sources and that in ARS (0.3 Pg yr-1) is limited by P and Fe. This is attributed to poor fractional solubility (˜1%) of mineral dust over the Arabian Sea. However, N-fixation by diazotrophs in the two oceanic regions is somewhat similar (0.03 Pg yr-1). Our estimate of N-deposition (0.2 Tg yr-1) to the northern Indian Ocean is significantly lower than the model results (˜800 - 1200 mg-N m-2 yr-1 ≈ 5.7 - 8.6 Tg yr-1 by Duce et al. (2008); ˜4.1 Tg yr-1 by Okin et al. (2011); and ˜0.8 Tg yr-1 by Kanakidou et al. (2012). The increase in aerosol toxicity is also evident from high enrichment factors of anthropogenic trace metal (Pb, Cd, Cr, Cu and

  14. Tracing atmospheric nitrate in groundwater using triple oxygen isotopes: evaluation based on bottled drinking water

    Directory of Open Access Journals (Sweden)

    U. Tsunogai

    2012-11-01

    Full Text Available The stable isotopic compositions of nitrate dissolved in 49 types of bottled drinking water collected worldwide were determined, to trace the fate of atmospheric nitrate (NO3atm that had been deposited into subaerial ecosystems, using the 17O anomalies (Δ17O of nitrate as tracers. The use of bottled water enables collection of groundwater recharged at natural, background watersheds. The nitrate in groundwater had small Δ17O values ranging from −0.2‰ to +4.5‰ (n = 49. The average Δ17O value and average mixing ratio of atmospheric nitrate to total nitrate in the groundwater samples were estimated to be 0.8‰ and 3.1%, respectively. These findings indicated that the majority of atmospheric nitrate had undergone biological processing before being exported from the surface ecosystem to the groundwater. Moreover, the concentrations of atmospheric nitrate were estimated to range from less than 0.1 μmol l−1 to 8.5 μmol l−1, with higher NO3atm concentrations being obtained for those recharged in rocky, arid or elevated areas with little vegetation and lower NO3atm concentrations being obtained for those recharged in forested areas with high levels of vegetation. Additionally, many of the NO3atm-depleted samples were characterized by elevated δ15N values of more than +10‰. Uptake by plants and/or microbes in forested soils subsequent to deposition and the progress of denitrification within groundwater likely plays a significant role in the removal of NO3atm.

  15. Relationship between trace gases and aerosols from biomass burning in Southeast Asia using satellite and emission data

    Science.gov (United States)

    Azuma, Yoshimi; Nakamura, Maya; Kuji, Makoto

    2012-11-01

    Southeast Asia is one of the biggest regions of biomass burning with forest fires and slash-and-burn farming. From the fire events, a large amount of air pollutants are emitted such as carbon monoxide (CO), nitrogen oxide (NOx) and aerosol (black carbon; BC). Biomass burning generally causes not only local, but also transboundary air pollution, and influences the atmospheric environment in the world accordingly. However, impact of air pollutants' emissions from large-scale fire in Southeast Asia is not well investigated compared to other regions such as South America and Africa. In this study, characteristics of the atmospheric environment were investigated with correlative analyses among several satellite data (MOPITT, OMI, and MODIS) and emission inventory (GFEDv3) in Southeast Asia from October 2004 to June 2008 on a monthly basis. As a result, it is suggested that the transboundary air pollution from the biomass burning regions occurred over Southeast Asia, which caused specifically higher air pollutants' concentration at Hanoi, Vietnam in spring dry season.

  16. On the role of atmosphere-ocean interactions in the expected long-term changes of the Earth's ozone layer caused by greenhouse gases

    Science.gov (United States)

    Zadorozhny, Alexander; Dyominov, Igor

    It is well known that anthropogenic emissions of greenhouse gases into the atmosphere produce a global warming of the troposphere and a global cooling of the stratosphere. The expected stratospheric cooling essentially influences the ozone layer via increased polar stratospheric cloud formation and via temperature dependences of the gas phase reaction rates. One more mechanism of how greenhouse gases influences the ozone layer is enhanced water evaporation from the oceans into the atmosphere because of increasing temperatures of the ocean surface due to greenhouse effect. The subject of this paper is a study of the influence of anthropogenic pollution of the atmosphere by the greenhouse gases CO2, CH4, N2O and ozone-depleting chlorine and bromine compounds on the expected long-term changes of the ozone layer with taking into account an increase of water vapour content in the atmosphere due to greenhouse effect. The study based on 2-D zonally averaged interactive dynamical radiative-photochemical model of the troposphere and stratosphere. The model allows to self-consistently calculating diabatic circulation, temperature, gaseous composition of the troposphere and stratosphere at latitudes from the South to North Poles, as well as distribution of sulphate aerosol particles and polar stratospheric clouds of two types. It was supposed in the model that an increase of the ocean surface temperature caused by greenhouse effect is similar to calculated increase of atmospheric surface temperature. Evaporation rate from the ocean surface was computed in dependence of latitude. The model time-dependent runs were made for the period from 1975 to 2100 using two IPCC scenarios depicting maximum and average expected increases of greenhouse gases in the atmosphere. The model calculations show that anthropogenic increasing of water vapour abundance in the atmosphere due to heating of the ocean surface caused by greenhouse effect gives a sensible contribution to the expected ozone

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

    CERN Document Server

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

    2005-01-01

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

  18. Physical and chemical properties of the regional mixed layer of Mexico's Megapolis – Part 2: Evaluation of measured and modeled trace gases and particle size distributions

    Directory of Open Access Journals (Sweden)

    C. Ochoa

    2012-04-01

    Full Text Available This study extends the work of Baumgardner et al. (2009 in which measurements of trace gases and particles, at a remote, high altitude mountain site, 60 km from Mexico City were analyzed with respect to the origin of the air masses. In the current evaluation, the temperature, water vapor, ozone (O3, carbon monoxide (CO, acyl peroxy nitrate (APN and particle size distributions (PSDs of the mass concentrations of sulfate, nitrate, ammonium and organic mass (OM were simulated with the WRF-Chem chemical transport model and compared with the measurements at the mountain site. The model predictions of the diurnal trends of the gases were well correlated with the measurements before the regional mixed layer (RML reached the measurement site but underestimated the concentration after that time. The differences are caused by an over rapid growth of the boundary layer by the model and too much dilution. There also is more O3 being actually produced by photochemical production downwind of the emission sources than predicted by the model.

    The measured and modeled PSDs compare very well with respect to their general shape and diameter of the peak concentrations. The spectra are lognormal with most of the mass in the accumulation mode and the geometric diameter centered at 200±20 nm, showing little observed or predicted change with respect to the time when the RML is above the Altzomoni research station. Only the total mass changed with time and air mass origin. The invariability of average diameter of the accumulation mode suggests that there is very little growth of the particles by condensation or coagulation past about six hours of aging downwind of the major sources of anthropogenic emissions in Mexico's Megapolis. This could greatly simplify parameterization in climate models although it is not known at this time if this invariance can be extended to other megacity regions.

  19. Simulations of atmospheric pressure discharge in a high-voltage nanosecond pulse using the particle-in-cell Monte Carlo collision model in noble gases

    Science.gov (United States)

    Shi, Feng; Wang, Dezhen; Ren, Chunsheng

    2008-06-01

    Atmospheric pressure discharge nonequilibrium plasmas have been applied to plasma processing with modern technology. Simulations of discharge in pure Ar and pure He gases at one atmospheric pressure by a high voltage trapezoidal nanosecond pulse have been performed using a one-dimensional particle-in-cell Monte Carlo collision (PIC-MCC) model coupled with a renormalization and weighting procedure (mapping algorithm). Numerical results show that the characteristics of discharge in both inert gases are very similar. There exist the effects of local reverse field and double-peak distributions of charged particles' density. The electron and ion energy distribution functions are also observed, and the discharge is concluded in the view of ionization avalanche in number. Furthermore, the independence of total current density is a function of time, but not of position.

  20. Atmospheric trace elements in aerosols observed over the Southern Ocean and coastal East Antarctica

    Directory of Open Access Journals (Sweden)

    Guojie Xu

    2014-11-01

    Full Text Available Atmospheric aerosol samples were collected over the Southern Ocean (SO and coastal East Antarctica (CEA during the austral summer of 2010/11. Samples were analysed for trace elements, including Na, Mg, K, Al, Fe, Mn, Ni, Cd and Se, by inductively coupled plasma mass spectrometry (ICP-MS. The mean atmospheric concentrations over the SO were 1100 ng m−3 for Na, 190 ng m−3 for Mg, 150 ng m−3 for Al, 14 ng m−3 for Fe, 0.46 ng m−3 for Mn and 0.25 ng m−3 for Se. Over CEA, the mean concentrations were 990 ng m−3 for Na, 180 ng m−3 for Mg, 190 ng m−3 for Al, 26 ng m−3 for Fe, 0.70 ng m−3 for Mn and 0.29 ng m−3 for Se. Particle size distributions, enrichment factors (EFs and correlation analysis indicate that Na, Mg and K mainly came from the marine source, while Al, Fe and Mn were mainly from the crustal source, which also contributed to Mg and K over CEA. High EFs were associated with Ni, Cd and Se, suggesting likely contributions from mixed sources from the Antarctic continent, long-range transport, marine biogenic emissions and anthropogenic emissions. Sea-salt elements (Na, Mg, K were mainly accumulated in the coarse mode, and crustal elements (Al, Fe, Mn presented a bimodal size distribution pattern. Bioactive elements (Fe, Ni, Cd were enriched in the fine mode, especially with samples collected over the SO, possibly affecting biogeochemical cycles in this oceanic region.

  1. Physical and chemical properties of the regional mixed layer of Mexico's Megapolis Part II: evaluation of measured and modeled trace gases and particle size distributions

    Directory of Open Access Journals (Sweden)

    C. Ochoa

    2012-11-01

    Full Text Available This study extends the work of Baumgardner et al. (2009 in which measurements of trace gases and particles, at a remote, high altitude mountain site, 60 km from Mexico City were analyzed with respect to the origin of the air masses. In the current evaluation, the temperature, water vapor mixing ratio (WMR, ozone (O3, carbon monoxide (CO, sulfur dioxide (SO2 and acyl peroxy nitrate (APN are simulated with the WRF-Chem chemical transport model and compared with the measurements at the mountain site. Comparisons between the model and measurements are also evaluated for particle size distributions (PSDs of the mass concentrations of sulfate, nitrate, ammonium and organic mass (OM. The model predictions of the diurnal trends in temperature, WMR and trace gases were generally well correlated; 13 of the 18 correlations were significant at a confidence level of <0.01. Less satisfactory were the average hourly differences between model and measurements that showed predicted values within expected, natural variation for only 10 of the 18 comparisons. The model performed best when comparing with the measurements during periods when the air originated from the east. In that case all six of the parameters being compared had average differences between the model and measurements less than the expected standard deviation. For the cases when the air masses are from the southwest or west northwest, only two of the comparisons from each case showed differences less than the expected standard deviation. The differences appear to be a result of an overly rapid growth of the boundary layer predicted by the model and too much dilution. There also is more O3 being produced, most likely by photochemical production, downwind of the emission sources than is predicted by the model.

    The measured and modeled PSD compare very well with respect to their general shape and the diameter of the peak concentrations. The spectra are log

  2. Emission factors of fine particles, carbonaceous aerosols and traces gases from road vehicles: Recent tests in an urban tunnel in the Pearl River Delta, China

    Science.gov (United States)

    Zhang, Yanli; Wang, Xinming; Li, Guanghui; Yang, Weiqiang; Huang, Zhonghui; Zhang, Zhou; Huang, Xinyu; Deng, Wei; Liu, Tengyu; Huang, Zuzhao; Zhang, Zhanyi

    2015-12-01

    Motor vehicles contribute primarily and secondarily to air quality problems due to fine particle (PM2.5) and ozone (O3) pollution in China's megacities. Characterizing vehicle emission with the rapid change of vehicle numbers and fleet compositions is vital for both bottom-up emission survey and top-down source apportioning. To obtain emission factors (EFs) of PM2.5, carbonaceous aerosols and trace gases for road vehicles, in urban Guangzhou we conducted a field campaign in 2014 in the Zhujiang Tunnel, a heavily burdened tunnel with about 40,000 motor vehicles passing through each of its two separated bores per day. PM2.5 and volatile organic compounds (VOCs) were sampled for offline analysis while trace gases including SO2, NOx and CO were measured online and in situ. An eddy covariance system with an integrated 3-D sonic anemometer was also adopted to measure CO2 and winds inside the tunnel. We recorded an average fleet composition of 61% light-duty gasoline vehicles (LDVs) + 12% heavy-duty diesel vehicles (HDVs) + 27% liquefied petroleum gas vehicles (LPGVs), and EFs of 82.7 ± 28.3, 19.3 ± 4.7 and 13.3 ± 3.3 mg veh-1 km-1, respectively, for PM2.5, organic carbon (OC) and elemental carbon (EC). These EFs were respectively 23.4%, 18.3% and 72.3% lower when compared to that measured in the same tunnel in 2004. EFs of PM2.5, OC and EC were higher at night time (148 ± 126, 29 ± 24 and 21 ± 18 mg veh-1 km-1, respectively) due to significantly elevated fractions of HDVs in the traffic fleets. An average ratio of OC to EC 1.45 from this tunnel study was much higher than that of ∼0.5 in previous tunnel studies. The EFs of SO2, NOx, CO, CO2 and NMHCs for road traffic were also obtained from our tunnel tests, and they were 20.7 ± 2.9, (1.29 ± 0.2)E+03, (3.10 ± 0.68)E+03, (3.90 ± 0.49)E+05, and 448 ± 39 mg veh-1 km-1, respectively.

  3. Dissociation against oxidation kinetics for the conversion of VOCs in non-thermal plasmas of atmospheric gases

    Science.gov (United States)

    Pasquiers, Stéphane; Blin-Simiand, Nicole; Magne, Lionel

    2016-08-01

    The kinetics of four volatile organic compounds (VOCs) (propene, propane, acetaldehyde, acetone) were studied in plasmas of atmospheric gases using a photo-triggered discharge (homogeneous plasma) or a dielectric barrier discharge (filamentary plasma). It was shown for the homogeneous plasma that quenchings of nitrogen metastable states, A3Ʃ+u and the group of singlets a' 1Ʃ-u, a 1Πg and w 1∆u, are important processes for the decomposition of such molecules. Recent measurements of the H2 concentration produced in the N2/C3H6 mixture emphasize that the hydrogen molecule can be an exit route for propene dissociation. It is also found that H2 and CO molecules are efficiently produced following the dissociation of CH3COCH3 and the subsequent chemical reactivity induced by radicals coming from acetone. Addition of oxygen to a N2/VOC mixture can change drastically the kinetics. However, the quenching processes of N2 metastables by the VOC are always present and compete with oxidation reactions for the conversion of the pollutant. At low temperature, oxidations by O or by OH are not always sufficiently effective to induce an increase of the molecule decomposition when oxygen is added to the mixture. In particular, the presence of O2 has a detrimental effect on the acetone removal. Also, as evidenced for acetaldehyde and propane, some kinetic analogies appear between filamentary and homogeneous plasmas. Contribution to the topical issue "6th Central European Symposium on Plasma Chemistry (CESPC-6)", edited by Nicolas Gherardi, Ester Marotta and Cristina Paradisi

  4. Toward reconciling the influence of atmospheric aerosols and greenhouse gases on light precipitation changes in Eastern China: AEROSOLS AND GREENHOUSE GASES

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Yuan [Jet Propulsion Laboratory, California Institute of Technology, Pasadena California USA; Ma, Po-Lun [Pacific Northwest National Laboratory, Richland Washington USA; Jiang, Jonathan H. [Jet Propulsion Laboratory, California Institute of Technology, Pasadena California USA; Su, Hui [Jet Propulsion Laboratory, California Institute of Technology, Pasadena California USA; Rasch, Philip J. [Pacific Northwest National Laboratory, Richland Washington USA

    2016-05-21

    The attribution of the widely observed shifted precipitation extremes to different forcing agents represents a critical issue for understanding of changes in the hydrological cycle. To compare aerosol and greenhouse-gas effects on the historical trends of precipitation intensity, we performed AMIP-style NCAR/DOE CAM5 model simulations from 1950-2005 with and without anthropogenic aerosol forcings. Precipitation rates at every time step in CAM5 are used to construct precipitation probability distribution functions. By contrasting the two sets of experiments, we found that the global warming induced by the accumulating greenhouse gases is responsible for the changes in precipitation intensity at the global scale. However, regionally over the Eastern China, the drastic increase in anthropogenic aerosols primarily accounts for the observed light precipitation suppression since the 1950s. Compared with aerosol radiative effects, aerosol microphysical effect has a predominant role in determining the historical trends of precipitation intensity in Eastern China.

  5. Tree species influence soil-atmosphere fluxes of the greenhouse gases CO2, CH4 and N2O

    Science.gov (United States)

    Steffens, Christina; Vesterdal, Lars; Pfeiffer, Eva-Maria

    2016-04-01

    In the temperate zone, forests are the greatest terrestrial sink for atmospheric CO2, and tree species affect soil C stocks and soil CO2 emissions. When considering the total greenhouse gas (GHG) balance of the forest soil, the relevant GHGs CH4 and N2O should also be considered as they have a higher global warming potential than CO2. The presented data are first results from a field study in a common garden site in Denmark where tree species with ectomycorrhizal colonization (beech - Fagus sylvatica, oak - Quercus robur) and with arbuscular mycorrhizal colonization (maple - Acer pseudoplatanus, ash - Fraxinus excelsior) have been planted in monocultures in adjacent blocks of about 0.25 ha in the year 1973 on former arable land. The soil-atmosphere fluxes of all three gases were measured every second week since August 2015. The hypothesis is that the total GHG efflux from forest soil would differ between species, and that these differences could be related to the type of mycorrhizal association and leaf litter quality. Preliminary results (August to December 2015) indicate that tree species influence the fluxes (converted to CO2-eq) of the three GHGs. Total soil CO2 efflux was in the low end of the range reported for temperate broadleaved forests but similar to the measurements at the same site approximately ten years ago. It was highest under oak (9.6±2.4 g CO2 m-2 d-1) and lowest under maple (5.2±1.6 g CO2 m-2 d-1). In contrast, soil under oak was a small but significant sink for CH4(-0.005±0.003 g CO2-eq m-2 d-1), while there were almost no detectable CH4 fluxes in maple. Emissions of N2O were highest under beech (0.6±0.6 g CO2-eq m-2 d-1) and oak (0.2±0.09 g CO2-eq m-2 d-1) and lowest under ash (0.03±0.04 g CO2-eq m-2 d-1). In the total GHG balance, soil CH4 uptake was negligible (≤0.1% of total emissions). Emissions of N2O (converted to CO2-eq) contributed mycorrhiza and produce leaf litter with a lower lignin:N ratio.

  6. Variability of atmospheric greenhouse gases as a biogeochemical processing signal at regional scale in a karstic ecosystem

    Science.gov (United States)

    Borràs, Sílvia; Vazquez, Eusebi; Morguí, Josep-Anton; Àgueda, Alba; Batet, Oscar; Cañas, Lídia; Curcoll, Roger; Grossi, Claudia; Nofuentes, Manel; Occhipinti, Paola; Rodó, Xavier

    2015-04-01

    The South-eastern area of the Iberian Peninsula is an area where climatic conditions reach extreme climatic conditions during the year, and is also heavily affected by the ENSO and NAO. The Natural Park of Cazorla, Segura de la Sierra and Las Villas is located in this region, and it is the largest protected natural area in Spain (209920 Ha). This area is characterized by important climatic and hydrologic contrasts: although the mean annual precipitation is 770 nm, the karstic soils are the main cause for water scarcity during the summer months, while on the other hand it is in this area where the two main rivers of Southern Spain, the Segura and the Guadalquivir, are born. The protected area comprises many forested landscapes, karstic areas and reservoirs like Tranco de Beas. The temperatures during summer are high, with over 40°C heatwaves occurring each year. But during the winter months, the land surface can be covered by snow for periods of time up until 30 days. The ENSO and NAO influences cause also an important inter annual climatic variability in this area. Under the ENSO, autumnal periods are more humid while the following spring is drier. In this area vegetal Mediterranean communities are dominant. But there are also a high number of endemic species and derelict species typical of temperate climate. Therefore it is a protected area with high specific diversity. Additionally, there is an important agricultural activity in the fringe areas of the Natural Park, mainly for olive production, while inside the Park this activity is focused on mountain wheat production. Therefore the diverse vegetal communities and landscapes can easily be under extreme climatic pressures, affecting in turn the biogeochemical processes at the regional scale. The constant, high-frequency monitoring of greenhouse gases (GHG) (CO2 and CH4) integrates the biogeochemical signal of changes in this area related to the carbon cycle at the regional scale, capturing the high diversity of

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

    Directory of Open Access Journals (Sweden)

    W. M. Landing

    2009-12-01

    Full Text Available To understand and quantify the impact of local, regional, and distant atmospheric mercury sources to rainfall mercury deposition in the Pensacola, Florida watershed, a program of event-based rainfall sampling was started in late 2004. Modified Aerochem-Metrics wet/dry rainfall samplers were deployed at three sites in the region around the Crist coal-fired power plant and event-based samples were collected continuously for three years. Samples were analyzed for total mercury, volatile elements As, Se, and Sn, and a suite of trace elements including Al, Bi, Cd, Ce, Co, Cr, Cs, Cu, Dy, Er, Eu, Fe, Ho, Ga, Gd, La, Li, Lu, Mg, Mn, Na, Nb, Nd, Ni, P, Pb, Pr, Rb, Sb, Sc, Si, Sm, Sr, Tb, Th, Ti, Tm, U, V, Y, Yb, and Zn. Nutrients and major ions were also measured on each sample.

    Multivariate statistical methods are used to sort these tracers into factors that represent potential source components that contribute to the rainfall chemistry. Hg, As, Se, Sn, Sb, and non sea-salt sulfate were all significantly correlated with one anthropogenic factor. Using various Hg/element ratios, we can estimate that 22–33% of the rainfall mercury in the region results from coal combustion.

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

    Directory of Open Access Journals (Sweden)

    W. M. Landing

    2010-05-01

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

  9. Heavy Metals and Trace Elements Atmospheric Deposition Studies in Tula Region Using Moss Biomonitors Technique

    CERN Document Server

    Ermakova, E V; Steinnes, E

    2002-01-01

    For the first time the moss biomonitors technique was used in air pollution studies in Tula Region (Central Russia), applying NAA, AAS. Moss samples were collected at 83 sites in accordance with the sampling strategy adopted in European projects on biomonitoring atmospheric deposition. A wide set of trace elements in mosses was determined. The method of epithermal neutron activation at IBR-2 reactor of FLNP JINR has made it possible to identify 33 elements (Na, Mg, Al, Cl, K, Ca, Sc, V, Cr, Mn, Fe, Co, Ni, Zn, As, Br, Rb, Sr, Mo, Sb, I, Cs, Ba, La, Ce, Sm, Tb, Yb, Hf, Ta, W, Th, U) in the large-scale concentration range - from 10000 ppm for K to 0,001 ppm for Tb and Ta. Cu, Cd and Pb were determined by the flame AAS in the Norwegian Institute of Science and Technology. Using the graphical technique and principal component analysis allowed to separate plant, crustal and general pollution components in the moss. The obtained data will be used for constructing coloured maps of the distribution of elements over t...

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

    Science.gov (United States)

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

    2014-11-01

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

  11. Marine Primary Productivity as a Potential Indirect Source of Selenium and Other Trace Elements in Atmospheric Deposition.

    Science.gov (United States)

    Blazina, Tim; Läderach, Alexander; Jones, Gerrad D; Sodemann, Harald; Wernli, Heini; Kirchner, James W; Winkel, Lenny H E

    2017-01-03

    Atmospheric processes play an important role in the supply of the trace element selenium (Se) as well as other essential trace elements to terrestrial environments, mainly via wet deposition. Here we investigate whether the marine biosphere can be identified as a source of Se and of other trace elements in precipitation samples. We used artificial neural network (ANN) modeling and other statistical methods to analyze relationships between a high-resolution atmospheric deposition chemistry time series (March 2007-January 2009) from Plynlimon (UK) and exposure of air masses to marine chlorophyll a and to other source proxies. Using ANN sensitivity analyses, we found that higher air mass exposure to marine productivity leads to higher concentrations of dissolved organic carbon (DOC) in rainfall. Furthermore, marine productivity was found to be an important but indirect factor in controlling Se as well as vanadium (V), cobalt (Co), nickel (Ni), zinc (Zn), and aluminum (Al) concentrations in atmospheric deposition, likely via scavenging by organic compounds derived from marine organisms. Marine organisms may thus play an indirect but important role in the delivery of trace elements to terrestrial environments and food chains.

  12. Carbon monoxide and related trace gases and aerosols over the Amazon Basin during the wet and dry seasons

    Directory of Open Access Journals (Sweden)

    M. O. Andreae

    2012-07-01

    Full Text Available We present the results of airborne measurements of carbon monoxide (CO and aerosol particle number concentration (CN made during the Balanço Atmosférico Regional de Carbono na Amazônia (BARCA program. The primary goal of BARCA is to address the question of basin-scale sources and sinks of CO2 and other atmospheric carbon species, a central issue of the Large-scale Biosphere-Atmosphere (LBA program. The experiment consisted of two aircraft campaigns during November–December 2008 (BARCA-A and May–June 2009 (BARCA-B, which covered the altitude range from the surface up to about 4500 m, and spanned most of the Amazon Basin.

    Based on meteorological analysis and measurements of the tracer, SF6, we found that airmasses over the Amazon Basin during the late dry season (BARCA-A, November 2008 originated predominantly from the Southern Hemisphere, while during the late wet season (BARCA-B, May 2009 low-level airmasses were dominated by northern-hemispheric inflow and mid-tropospheric airmasses were of mixed origin. In BARCA-A we found strong influence of biomass burning emissions on the composition of the atmosphere over much of the Amazon Basin, with CO enhancements up to 300 ppb and CN concentrations approaching 10 000 cm−3; the highest values were in the southern part of the Basin at altitudes of 1–3 km. The ΔCN/ΔCO ratios were diagnostic for biomass burning emissions, and were lower in aged than in fresh smoke. Fresh emissions indicated CO/CO2 and CN/CO emission ratios in good agreement with previous work, but our results also highlight the need to consider the residual smoldering combustion that takes place after the active flaming phase of deforestation fires.

    During the late wet season, in contrast, there was little evidence for a significant presence of biomass smoke. Low CN concentrations (300–500 cm−3 prevailed basinwide, and CO mixing ratios were enhanced

  13. 载人航天器密封舱微量有害气体质谱检测方法%Mass spectrometric detection of harmful trace gases in manned spacecraft capsule

    Institute of Scientific and Technical Information of China (English)

    陈联; 邱家稳; 王丽红; 张晓曦

    2011-01-01

    Detection of multi -component harmful trace gases in manned spacecraft capsule by miniature vacuum mass spectrometer was introduced. Online monitoring of a variety of harmful trace gases in the capsule was realized through detecting the gas concentration. Experimental data of relative sensitivity of some gases such as toluene, dimethylbenzene, dichloromethane, methane and acetone were given and the experiment also verified that the minimum detectable concentration of before -mentioned gases can reach lppm. The results indicated that monitoring of harmful trace gas concentration by miniature vacuum mass spectrometer in manned spacecraft capsule is feasible.%介绍了采用小型真空质谱计进行载人航天器密封舱内多组分微量有害气体的检测方法.通过测量微量气体浓度,实现密封舱内多种微量有害气体在线监测.给出了甲苯、二甲苯、二氯甲烷、甲烷、丙酮等5种气体的相对灵敏度试验数据,验证了现有小型真空质谱计最小可检浓度可以达到1ppm要求.研究结果表明,采用小型真空质谱计进行舱内微量有害气体浓度监测是可行的.

  14. Turbulent fluxes and transfer of trace gases from ship-based measurements during TexAQS 2006

    Science.gov (United States)

    Grachev, Andrey A.; Bariteau, Ludovic; Fairall, Christopher W.; Hare, Jeffrey E.; Helmig, Detlev; Hueber, Jacques; Lang, E. Kathrin

    2011-07-01

    Air-sea/land turbulent fluxes of momentum, sensible heat, water vapor, carbon dioxide, and ozone are discussed on the basis of eddy covariance measurements made aboard the NOAA R/V Ronald H. Brown during the Texas Air Quality Study (TexAQS) in August-September 2006. The TexAQS 2006 field campaign focused on air pollution meteorology associated primarily with ozone and aerosol transport in the Houston/Galveston region and the nearby coastal zone. The ship-based complement of instrumentation was used for the boundary layer measurements over water (the Gulf of Mexico and various harbors/bay areas) and "over land" (specifically, 80 km inside the Houston Ship Channel). In this study we focus on direct comparisons of TexAQS 2006 flux observations with the Coupled Ocean-Atmosphere Response Experiment (COARE) bulk flux algorithm to investigate possible coastal and urban area influences. It is found that the average neutral drag coefficient can be about an order of magnitude larger over very rough urban areas than over the sea surface. However, a similar effect was not observed for the scalar transfer; that is, the neutral Stanton and Dalton numbers do not change significantly over different footprint surfaces. Our data suggest that the TexAQS 2006 region was generally a sink for surface ozone whether over water or over land. The turbulent flux of carbon dioxide was mostly negative (uptake by the surface) for measurements over waters of the Gulf of Mexico and some bays, but the flux becomes positive (release to the air) for inland regions. Both ozone and carbon dioxide turbulent fluxes above land were larger in magnitude compared to the over water measurements.

  15. Identifying the origin of atmospheric inputs of trace elements in the Prades Mountains (Catalonia) with bryophytes, lichens, and soil monitoring.

    Science.gov (United States)

    Achotegui-Castells, Ander; Sardans, Jordi; Ribas, Àngela; Peñuelas, Josep

    2013-01-01

    The biomonitors Hypnum cupressiforme and Xanthoria parietina were used to assess the deposition of trace elements and their possible origin in the Prades Mountains, a protected Mediterranean forest area of NE Spain with several pollution sources nearby. Al, As, Cd, Co, Cu, Cr, Ni, Pb, Sb, Ti, V, and Zn were determined in 16 locations within this protected area. Soil trace element concentrations were also ascertained to calculate enrichment factors (EF) and use them to distinguish airborne from soilborne trace element inputs. In addition, lichen richness was measured to further assess atmospheric pollution. EF demonstrated to be useful not only for the moss but also for the lichen. Cd, Cr, Cu, Ni, and Zn presented values higher than three in both biomonitors. These trace elements were also the main ones emitted by the potential sources of pollutants. The distance between sampling locations and potential pollution sources was correlated with the concentrations of Cu, Sb, and Zn in the moss and with Cr, Ni, and Sb in the lichen. Lichen richness was negatively correlated with lichen Cu, Pb, and V concentrations on dry weight basis. The study reflected the remarkable influence that the pollution sources have on the presence of trace elements and on lichen species community composition in this natural area. The study highlights the value of combining the use of biomonitors, enrichment factors, and lichen diversity for pollution assessment to reach a better overview of both trace elements' impact and the localization of their sources.

  16. Emission of greenhouse gases in the atmosphere of the Manaus city due to burning of fossil fuels; Emissao de gases poluentes na atmosfera urbana da cidade de Manaus devida a queima de combustiveis fosseis

    Energy Technology Data Exchange (ETDEWEB)

    Valois, I.M. [Universidade Federal do Amazonas (UFAM), Manaus, AM (Brazil). Fac. de Tecnologia], E-mail: ivalois@ufam.edu.br; Cartaxo, E.F. [Universidade Federal do Amazonas (NIEMA/UFAM), Manaus, AM (Brazil). Fac. de Tecnologia. Nucleo de Energia, Meio Ambiente e Agua], E-mail: ecartaxo@ufam.edu.br; Chaar, Jamal da Silva [Universidade Federal do Amazonas (ICE/UFAM), Manaus, AM (Brazil). Inst. de Ciencias Exatas

    2009-07-01

    This paper intends to think over the impacts of pollutants gases in the atmosphere of the city of Manaus, caused by the thermal, the main electricity source in the State of Amazonas. The focus of the study is the urban atmosphere where physical and chemical phenomenon accelerate the effects of increased concentration of some components and secondary pollutants, which are produced due to human activities. It is based on two studies: monitoring the exhaust gas applied at a factory in the district of Aparecida, located in the urban area, and monitoring conducted by the energy operating company, about the influence of exhaust gas around the district of Mauazinho, also in urban area. It is a preliminary research that seeks to demonstrate the inconsistency of some studies and the need to make progress in search for more efficient methods and techniques. This is an important step toward a policy of environmental management that will complement future studies about air pollution in the city. (author)

  17. Trace element content of sedimentary pyrite as a new proxy for deep-time ocean-atmosphere evolution

    Science.gov (United States)

    Large, Ross R.; Halpin, Jacqueline A.; Danyushevsky, Leonid V.; Maslennikov, Valeriy V.; Bull, Stuart W.; Long, John A.; Gregory, Daniel D.; Lounejeva, Elena; Lyons, Timothy W.; Sack, Patrick J.; McGoldrick, Peter J.; Calver, Clive R.

    2014-03-01

    Sedimentary pyrite formed in the water column, or during diagenesis in organic muds, provides an accessible proxy for seawater chemistry in the marine rock record. Except for Mo, U, Ni and Cr, surprisingly little is known about trace element trends in the deep time oceans, even though they are critical to developing better models for the evolution of the Earth's atmosphere and evolutionary pathways of life. Here we introduce a novel approach to simultaneously quantify a suite of trace elements in sedimentary pyrite from marine black shales. These trace element concentrations, at least in a first-order sense, track the primary elemental abundances in coeval seawater. In general, the trace element patterns show significant variation of several orders of magnitude in the Archaean and Phanerozoic, but less variation on longer wavelengths in the Proterozoic. Certain trace elements (e.g., Ni, Co, As, Cr) have generally decreased in the oceans through the Precambrian, other elements (e.g., Mo, Zn, Mn) have generally increased, and a further group initially increased and then decreased (e.g., Se and U). These changes appear to be controlled by many factors, in particular: 1) oxygenation cycles of the Earth's ocean-atmosphere system, 2) the composition of exposed crustal rocks, 3) long term rates of continental erosion, and 4) cycles of ocean anoxia. We show that Ni and Co content of seawater is affected by global Large Igneous Province events, whereas redox sensitive trace elements such as Se and Mo are affected by atmosphere oxygenation. Positive jumps in Mo and Se concentrations prior to the Great Oxidation Event (GOE1, c. 2500 Ma) suggest pulses of oxygenation may have occurred as early as 2950 Ma. A flat to declining pattern of many biologically important nutrient elements through the mid to late Proterozoic may relate to declining atmosphere O2, and supports previous models of nutrient deficiency inhibiting marine evolution during this period. These trace elements (Mo

  18. Carbon Dioxide Analysis Center and World Data Center-A for Atmospheric Trace Gases fiscal year 1997 annual report

    Energy Technology Data Exchange (ETDEWEB)

    Burtis, M.D. [comp.; Cushman, R.M.; Boden, T.A.; Jones, S.B.; Kaiser, D.P.; Nelson, T.R.

    1998-03-01

    Fiscal year (FY) 1997 was another exciting and productive one for the Carbon Dioxide Information Analysis Center (CDIAC) at the Oak Ridge National Laboratory. During FY 1997, CDIAC launched the Quality Systems Science Center for the North American Research Strategy for Tropospheric Ozone (NARSTO). The purpose of NARSTO--a US-Canada-Mexico initiative of government agencies, industry, and the academic research community--is to improve the understanding of the formation and transport of tropospheric ozone.

  19. Features of motivation of the crewmembers in an enclosed space at atmospheric pressure changes during breathing inert gases.

    Science.gov (United States)

    Komarevcev, Sergey

    Since the 1960s, our psychologists are working on experimenting with small groups in isolation .It was associated with the beginning of spaceflight and necessity to study of human behaviors in ways different from the natural habitat of man .Those, who study human behavior especially in isolation, know- that the behavior in isolation markedly different from that in the natural situаtions. It associated with the development of new, more adaptive behaviors (1) What are the differences ? First of all , isolation is achieved by the fact ,that the group is in a closed space. How experiments show - the crew members have changed the basic personality traits, such as motivation Statement of the problem and methods. In our experimentation we were interested in changing the features of human motivation (strength, stability and direction of motivation) in terms of a closed group in the modified atmosphere pressure and breathing inert gases. Also, we were interested in particular external and internal motivation of the individual in the circumstances. To conduct experimentation , we used an experimental barocomplex GVK -250 , which placed a group of six mаns. A task was to spend fifteen days in isolation on barokomplex when breathing oxigen - xenon mixture of fifteen days in isolation on the same complex when breathing oxygen- helium mixture and fifteen days of isolation on the same complex when breathing normal air All this time, the subjects were isolated under conditions of atmospheric pressure changes , closer to what you normally deal divers. We assumed that breathing inert mixtures can change the strength and stability , and with it , the direction and stability of motivation. To check our results, we planned on using the battery of psychological techniques : 1. Schwartz technique that measures personal values and behavior in society, DORS procedure ( measurement of fatigue , monotony , satiety and stress ) and riffs that give the test once a week. Our assumption is

  20. Evaluation of trace elemental composition of aerosols in the atmosphere of Rawalpindi and Islamabad using radio analytical methods

    Energy Technology Data Exchange (ETDEWEB)

    Qadir, Muhammad Abdul, E-mail: mabdulqadir@gmail.com [Institute of Chemistry, University of the Punjab, Lahore-54590 (Pakistan); Zaidi, Jamshaid Hussain [Pakistan Institute of Nuclear Science and Technology, Nilore, Islamabad Capital Territory (Pakistan); Ahmad, Shaikh Asrar; Gulzar, Asad [Division of Science and Technology, University of Education, Township, Lahore (Pakistan); Yaseen, Muhammad [Department of Chemistry, Gugrat University, Gugrat (Pakistan); Atta, Sadia; Tufail, Asma [Institute of Chemistry, University of the Punjab, Lahore-54590 (Pakistan)

    2012-05-15

    Geological and anthropogenic contributions to air pollution were monitored by analyzing aerosol particulates present in the atmosphere of Rawalpindi and Islamabad, Pakistan, using instrumental neutron activation for trace elemental analysis. A scanning electron microscope was used to study particulate size distribution and morphology. Twenty two elements were analyzed and their likely sources were identified. It was found that 69% of the suspended particulate matter in the atmosphere of Islamabad, and 52% in Rawalpindi, were of a diameter less than 3 {mu}m. The presence of Yb, Cs, Sc, Rb, Co, Eu, La, Ba, Zn and Hf indicates that a major portion of the trace elements in the aerosol particulates was due to the geological nature of the land, while Sc was considered to be arising from coal burning. The presence of Cr, Fe, Ce, Pb and Cd was attributed to anthropogenic activities at Rawalpindi and Islamabad. Unusually high concentrations of Mo and Nb were found in the atmosphere of Islamabad, based on soil derived aerosols. - Highlights: Black-Right-Pointing-Pointer Discussion is made on Total suspended Particulate (TSP) matter in the atmosphere. Black-Right-Pointing-Pointer Measurement of Radio active elements in the TSP by using SSNTD which was found non significant. Black-Right-Pointing-Pointer 23 Trace element analysis of the TSPs in the atmosphere of twin cities i.e. Rawalpindi and Islamabad and their relation to their sources by using Neutron activation analysis. Black-Right-Pointing-Pointer The mountain of Islamabad has some unique and important deposits of Nb and Gd , this paper will help the Geological survey of Pakistan to explore their deposits. Black-Right-Pointing-Pointer There is high level of TSPs>10 um, which is a great threat to the peoples of Islamabad.

  1. Properties and Developments of Combustion and Gasification of Coal and Char in a CO2-Rich and Recycled Flue Gases Atmosphere by Rapid Heating

    Directory of Open Access Journals (Sweden)

    Zhigang Li

    2012-01-01

    Full Text Available Combustion and gasification properties of pulverized coal and char have been investigated experimentally under the conditions of high temperature gradient of order 200°C·s−1 by a CO2 gas laser beam and CO2-rich atmospheres with 5% and 10% O2. The laser heating makes a more ideal experimental condition compared with previous studies with a TG-DTA, because it is able to minimize effects of coal oxidation and combustion by rapid heating process like radiative heat transfer condition. The experimental results indicated that coal weight reduction ratio to gases followed the Arrhenius equation with increasing coal temperature; further which were increased around 5% with adding H2O in CO2-rich atmosphere. In addition, coal-water mixtures with different water/coal mass ratio were used in order to investigate roles of water vapor in the process of coal gasification and combustion. Furthermore, char-water mixtures with different water/char mass ratio were also measured in order to discuss the generation ratio of CO/CO2, and specified that the source of Hydrocarbons is volatile matter from coal. Moreover, it was confirmed that generations of CO and Hydrocarbons gases are mainly dependent on coal temperature and O2 concentration, and they are stimulated at temperature over 1000°C in the CO2-rich atmosphere.

  2. Study of Atmospheric Trace Gas Amounts at the Stara Zagora Ground-Based Station

    Science.gov (United States)

    Werner, R.; Valev, D.; Kostadinov, I.; Atanassov, At.; Giovanelli, G.; Petritoli, A.; Bortoli, D.; Ravegnani, F.

    2006-03-01

    Since the end of August 1999 twilight daily measurements of scattered zenith sky radiation have been carried out at Stara Zagora for determination of trace gas amounts, deploying GASCOD instrument. It was developed at the Institute of Atmospheric Science and Climate, Bologna. Reference spectra are obtained at midday. The instrument, appearing a UV-VIS spectrometer, registers the zenith sky spectra automatically and 410 nm to 460 nm spectral interval is used to retrieve NO2 and O3 slant column amounts (SCA) by application of the DOAS methodology. The spectral analysis uses minimum least squares fitting of the cross sections at the expected absorbers to a logarithm of the twilight spectrum and a reference spectrum. The accumulated time series show the well-known typical seasonal variations, caused by the solar insulation. The residual time series of the removed semi-annual seasonal cycles from the measured original series show many different variations, with short periods up to inter-annual variations. Single spikes of SCA are detected and we consider them a result of over-passing weather fronts and/or lightning. Variations of SCA with time scale up to about 10 days are the consequence of weather cyclones. Some short-term variations of NO2 and O3 SCA are a result of intensive stratospheric-tropospheric exchange. Other residual time series periods are caused by Rossby waves, by over-passing of the polar vortex filaments. The inter-annual variations can be affected by QBO and NAO. Applying wavelet analysis of the obtained NO2 slant column amount data series, and the total O3 amount obtained by the GOME instrument, during the 23-rd solar cycle maximum, time intervals are found with periods of 27 days on the time scale. The applied cross-correlation analysis demonstrates a phase lag of some days of the NO2 and O3 response to the 27-days solar cycle. The calculated vertical column amounts of NO2 are used for validation of the satellite measurements, e.g. SCIAMACHY NO2

  3. Detailed history of atmospheric trace elements from the Quelccaya ice core (Southern Peru) during the last 1200 years

    Science.gov (United States)

    Uglietti, C.; Gabrielli, P.; Thompson, L. G.

    2013-12-01

    The recent increase in trace element concentrations, for example Cr, Cu, Zn, Ag, Pb, Bi, and U, in polar snow and ice has provided compelling evidence of a hemispheric change in atmospheric composition since the nineteenth century. This change has been concomitant with the expansion of the Industrial Revolution and points towards an anthropogenic source of trace elements in the atmosphere. There are very few low latitude trace element ice core records and these are believed to be sensitive to perturbations of regional significance. To date, these records have not been used to document a preindustrial anthropogenic impact on atmospheric composition at low latitudes. Ice cores retrieved from the tropical Andes are particularly interesting because they have the potential to reveal detailed information about the evolution and environmental consequences of mineral exploitation related to the Pre Inca Civilizations, the Inca Empire (1438-1533 AD) and the subsequent Spanish invasion and dominance (1532-1833 AD). The chemical record preserved in the ice of the Quelccaya ice cap (southern Peruvian Andes) offers the exceptional opportunity to geochemically constrain the composition of the tropical atmosphere at high resolution over the last ~1200 years. Quantification of twenty trace elements (Ag, Al, As, Bi, Cd, Co, Cr, Cu, Fe, Mn, Mo, Pb, Rb, Sb, Sn, Ti, Tl, U, V, and Zn) was performed by ICP-SFMS over 105 m of the Quelccaya North Dome core (5600 m asl, 128.57 m) by analyzing 2450 samples. This provides the first atmospheric trace element record in South America spanning continuously and at high resolution for the time period between 1990 and 790 AD. Ag, As, Bi, Cd, Cr, Co, Cu, Mn, Mo, Sb, Sn, Pb and Zn show increases in concentration and crustal enrichment factor starting at different times between 1450 and 1550 AD, in concomitance with the expansions of the Inca Empire and, subsequently, the Spanish Empire well before the inception of the Industrial Revolution. This

  4. Atmospheric concentrations and dry deposition fluxes of particulate trace metals in Salvador, Bahia, Brazil

    Science.gov (United States)

    de P. Pereira, Pedro A.; Lopes, Wilson A.; Carvalho, Luiz S.; da Rocha, Gisele O.; de Carvalho Bahia, Nei; Loyola, Josiane; Quiterio, Simone L.; Escaleira, Viviane; Arbilla, Graciela; de Andrade, Jailson B.

    Respiratory system is the major route of entry for airborne particulates, being the effect on the human organism dependent on chemical composition of the particles, exposure time and individual susceptibility. Airborne particulate trace metals are considered to represent a health hazard since they may be absorbed into human lung tissues during breathing. Fossil fuel and wood combustion, as well as waste incineration and industrial processes, are the main anthropic sources of metals to the atmosphere. In urban areas, vehicular emissions—and dust resuspension associated to road traffic—become the most important manmade source. This work investigated the atmospheric concentrations of TSP, PM 10 and elements such as iron, manganese, copper and zinc, from three different sites around Salvador Region (Bahia, Brazil), namely: (i) Lapa Bus Station, strongly impacted by heavy-duty diesel vehicles; (ii) Aratu harbor, impacted by an intense movement of goods, including metal ores and concentrates and near industrial centers and; (iii) Bananeira Village located on Maré Island, a non-vehicle-influenced site, with activities such as handcraft work and fishery, although placed near the port. Results have pointed out that TSP concentrations ranged between 16.9 (Bananeira) and 354.0 μg m -3 (Aratu#1), while for PM 10 they ranged between 30.9 and 393.0 μg m -3, both in the Lapa Bus Station. Iron was the major element in both Lapa Station and Aratu (#1 and #2), with average concentrations in the PM 10 samples of 148.9, 79.6 and 205.0 ng m -3, respectively. Zinc, on the other hand, was predominant in samples from Bananeira, with an average concentration of 145.0 ng m -3 in TSP samples, since no PM 10 sample was taken from this site. The main sources of iron in the Lapa Station and Aratu harbor were, respectively, soil resuspension by buses and discharge of solid granaries, as fertilizers and metal ores. On the other hand, zinc and copper in the bus station were mainly from

  5. Measurements of reactive trace gases and variable O3 formation rates in some South Carolina biomass burning plumes

    Energy Technology Data Exchange (ETDEWEB)

    Akagi, S. K.; Yokelson, R. J.; Burling, I. R.; Meinardi, S.; Simpson, I.; Blake, D. R.; McMeeking, G. R.; Sullivan, A.; Lee, T.; Kreidenweis, S.; Urbanski, S.; Reardon, J.; Griffith, D. W. T.; Johnson, T. J.; Weise, D. R.

    2013-02-01

    In October-November 2011 we measured the trace gas emission factors from 7 prescribed fires in South Carolina, U.S. using two Fourier transform infrared spectrometer (FTIR) systems and whole air sampling (WAS) into canisters followed by gas-chromatographic analyses. The fires were intended to emulate high-intensity burns as they were lit during the dry season and in most cases represented stands that had not been treated with prescribed burns in 10+ years, if at all. A total of 97 trace gas species are reported here from both airborne and ground-based platforms making this one of the most detailed field studies of fire emissions to date. The measurements included the first data for a suite of monoterpene compounds emitted via distillation of plant tissues during real fires. The known chemistry of the monoterpenes and their measured abundance of ~0.40% of CO (molar basis), ~3.9% of NMOC (molar basis), and ~21% of organic aerosol (mass basis), suggests that they impacted post-emission formation of ozone, aerosol, and small organic trace gases such as methanol and formaldehyde in the sampled plumes. The variability in the terpene emissions in South Carolina (SC) fire plumes was high and, in general, the speciation of the emitted gas-phase non-methane organic compounds was surprisingly different from that observed in a similar study in nominally similar pine forests in North Carolina ~20 months earlier. It is likely that the slightly different ecosystems, time of year and the precursor variability all contributed to the variability in plume chemistry observed in this study and in the literature. The ΔHCN/ΔCO emission ratio, however, is fairly consistent at 0.9 ± 0.06 % for airborne fire measurements in coniferous-dominated ecosystems further confirming the value of HCN as a good biomass burning indicator/tracer. The SC results also support an earlier finding that C3-C4 alkynes may be of use as biomass burning indicators on the time-scale of

  6. Estimated total emissions of trace gases from the Canberra Wildfires of 2003: a new method using satellite measurements of aerosol optical depth & the MOZART chemical transport model

    Directory of Open Access Journals (Sweden)

    C. Paton-Walsh

    2010-06-01

    Full Text Available In this paper we describe a new method for estimating trace gas emissions from large vegetation fires using satellite measurements of aerosol optical depth (AOD at 550 nm, combined with an atmospheric chemical transport model. The method uses a threshold value to screen out normal levels of AOD that may be caused by raised dust, sea salt aerosols or diffuse smoke transported from distant fires. Using this method we infer an estimated total emission of 15±5 Tg of carbon monoxide, 0.05±0.02 Tg of hydrogen cyanide, 0.11±0.03 Tg of ammonia, 0.25±0.07 Tg of formaldehyde, 0.03±0.01 of acetylene, 0.10±0.03 Tg of ethylene, 0.03±0.01 Tg of ethane, 0.21±0.06 Tg of formic acid and 0.28±0.09 Tg of methanol released to the atmosphere from the Canberra fires of 2003. An assessment of the uncertainties in the new method is made and we show that our estimate agrees (within expected uncertainties with estimates made using current conventional methods of multiplying together factors for the area burned, fuel load, the combustion efficiency and the emission factor for carbon monoxide. A simpler estimate derived directly from the satellite AOD measurements is also shown to be in agreement with conventional estimates, suggesting that the method may, under certain meteorological conditions, be applied without the complication of using a chemical transport model. The new method is suitable for estimating emissions from distinct large fire episodes and although it has some significant uncertainties, these are largely independent of the uncertainties inherent in conventional techniques. Thus we conclude that the new method is a useful additional tool for characterising emissions from vegetation fires.

  7. Comparison of the characteristics of atmospheric pressure plasma jets using different working gases and applications to plasma-cancer cell interactions

    Directory of Open Access Journals (Sweden)

    Hea Min Joh

    2013-09-01

    Full Text Available Atmospheric pressure plasma jets employing nitrogen, helium, or argon gases driven by low-frequency (several tens of kilohertz ac voltage and pulsed dc voltage were fabricated and characterized. The changes in discharge current, optical emission intensities from reactive radicals, gas temperature, and plume length of plasma jets with the control parameters were measured and compared. The control parameters include applied voltage, working gas, and gas flow rate. As an application to plasma-cancer cell interactions, the effects of atmospheric pressure plasma jet on the morphology and intracellular reactive oxygen species (ROS level of human lung adenocarcinoma cell (A549 and human bladder cancer cell (EJ were explored. The experimental results show that the plasma can effectively control the intracellular concentrations of ROS. Although there exist slight differences in the production of ROS, helium, argon, or nitrogen plasma jets are found to be useful in enhancing the intracellular ROS concentrations in cancer cells.

  8. Iterative maximum a posteriori (IMAP-DOAS for retrieval of strongly absorbing trace gases: Model studies for CH4 and CO2 retrieval from near infrared spectra of SCIAMACHY onboard ENVISAT

    Directory of Open Access Journals (Sweden)

    C. Frankenberg

    2005-01-01

    Full Text Available In the past, differential optical absorption spectroscopy (DOAS has mostly been employed for atmospheric trace gas retrieval in the UV/Vis spectral region. New spectrometers such as SCIAMACHY onboard ENVISAT also provide near infrared channels and thus allow for the detection of greenhouse gases like CH4, CO2, or N2O. However, modifications of the classical DOAS algorithm are necessary to account for the idiosyncrasies of this spectral region, i.e. the temperature and pressure dependence of the high resolution absorption lines. Furthermore, understanding the sensitivity of the measurement of these high resolution, strong absorption lines by means of a non-ideal device, i.e. having finite spectral resolution, is of special importance. This applies not only in the NIR, but can also prove to be an issue for the UV/Vis spectral region. This paper presents a modified iterative maximum a posteriori-DOAS (IMAP-DOAS algorithm based on optimal estimation theory introduced to the remote sensing community by rodgers76. This method directly iterates the vertical column densities of the absorbers of interest until the modeled total optical density fits the measurement. Although the discussion in this paper lays emphasis on satellite retrieval, the basic principles of the algorithm also hold for arbitrary measurement geometries. This new approach is applied to modeled spectra based on a comprehensive set of atmospheric temperature and pressure profiles. This analysis reveals that the sensitivity of measurement strongly depends on the prevailing pressure-height. The IMAP-DOAS algorithm properly accounts for the sensitivity of measurement on pressure due to pressure broadening of the absorption lines. Thus, biases in the retrieved vertical columns that would arise in classical algorithms, are obviated. Here, we analyse and quantify these systematic biases as well as errors due to variations in the temperature and pressure profiles, which is indispensable for

  9. The dynamic chamber method: trace gas exchange fluxes (NO, NO2, O3 between plants and the atmosphere in the laboratory and in the field

    Directory of Open Access Journals (Sweden)

    F. X. Meixner

    2012-05-01

    Full Text Available We describe a dynamic chamber system to determine reactive trace gas exchange fluxes between plants and the atmosphere under laboratory and, with small modifications, also under field conditions. The system allows measurements of the flux density of the reactive NO-NO2-O3 triad and additionally of the non-reactive trace gases CO2 and H2O. The chambers are made of transparent and chemically inert wall material and do not disturb plant physiology. For NO2 detection we used a highly NO2 specific blue light converter coupled to chemiluminescence detection of the photolysis product, NO. Exchange flux densities derived from dynamic chamber measurements are based on very small concentration differences of NO2 (NO, O3 between inlet and outlet of the chamber. High accuracy and precision measurements are therefore required, and high instrument sensitivity (limit of detection and the statistical significance of concentration differences are important for the determination of corresponding exchange flux densities, compensation point concentrations, and deposition velocities. The determination of NO2 concentrations at sub-ppb levels (2 analyzer with a lower detection limit (3σ-definition of 0.3 ppb or better. Deposition velocities and compensation point concentrations were determined by bi-variate weighted linear least-squares fitting regression analysis of the trace gas concentrations, measured at the inlet and outlet of the chamber. Performances of the dynamic chamber system and data analysis are demonstrated by studies of Picea abies L. (Norway Spruce under field and laboratory conditions. Our laboratory data show that the quality selection criterion based on the use of only significant NO2 concentration differences has a considerable impact on the resulting compensation point concentrations yielding values closer to zero. The results of field experiments demonstrate the need to consider photo-chemical reactions of NO, NO2, and O3 inside the chamber for

  10. Greenhouse gases regional fluxes estimated from atmospheric measurements; Estimation des flux de gaz a effet de serre a l'echelle regionale a partir de mesures atmospheriques

    Energy Technology Data Exchange (ETDEWEB)

    Messager, C

    2007-07-15

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

  11. Combining moving inlets for measuring gradients of reactive trace gases and thoron measurements for the determination of near surface fluxes -first results from the Amazon rain forest-

    Science.gov (United States)

    Sörgel, Matthias; Artaxo, Paulo; Kesselmeier, Jürgen; Quesada, Carlos Alberto; Ferreira de Souza, Rodrigo Augusto; Trebs, Ivonne; Vega, Oscar; Yañez-Serrano, Ana Maria

    2016-04-01

    For many compounds of interest no fast response sensors for the determination of eddy covariance fluxes are available. Therefore, flux-gradient relationships are used. The most common are the aerodynamic gradient method and the modified Bowen ratio method. For those approaches some assumptions have to be made which restrict their use. An alternative approach to calculate these fluxes might be given by the "thoron clock" method. The radon isotope Thoron (220Rn) is exhaled from the soil and has a half life time of 56 seconds. Therefore, it exists in measureable amounts only close to the ground and is hardly advected. Its only source is the radioactive decay of Thorium in soil. As it is a noble gas Thoron is not influenced by biochemical processes in air. Consequently, its concentration profile only depends on vertical mixing and the radioactive decay which is a physical constant. According to Lehmann et al. (1999) and Plake and Trebs (2013) a transport-time can be directly calculated from two heights thoron concentration/activity for the layer in-between without further assumptions. From this transport time the transfer velocity is derived which is then applied to calculate the fluxes of other (reactive) trace gases. A major advantage of the method is that the transport-time is known and using the measured concentration profile the chemical loss of a compound can be directly calculated and corrected for. We have applied this method for a first time in the Amazon rainforest during a field campaign at the ATTO site 150 km North East of Manaus in the dry season of 2014. We measured gradients of NO, NO2, O3, HONO and VOCs by using a movable inlet on a lift system close to the forest floor (0.19 m, 0.52 m and 1.59 m). A Thoron profile was measure in parallel at the lower two heights. First results of the gradients, the transport times and some preliminary flux values will be presented. References: Lehmann, B.E., Lehmann, M., Neftel, A .: 220 Radon calibration of near

  12. Modeling ionospheric disturbance features in quasi-vertically incident ionograms using 3-D magnetoionic ray tracing and atmospheric gravity waves

    Science.gov (United States)

    Cervera, M. A.; Harris, T. J.

    2014-01-01

    The Defence Science and Technology Organisation (DSTO) has initiated an experimental program, Spatial Ionospheric Correlation Experiment, utilizing state-of-the-art DSTO-designed high frequency digital receivers. This program seeks to understand ionospheric disturbances at scales employ a 3-D magnetoionic Hamiltonian ray tracing engine, developed by DSTO, to (1) model the various disturbance features observed on both the O and X polarization modes in our QVI data and (2) understand how they are produced. The ionospheric disturbances which produce the observed features were modeled by perturbing the ionosphere with atmospheric gravity waves.

  13. Annual input fluxes and source identification of trace elements in atmospheric deposition in Shanxi Basin: the largest coal base in China.

    Science.gov (United States)

    Zhong, Cong; Yang, Zhongfang; Jiang, Wei; Yu, Tao; Hou, Qingye; Li, Desheng; Wang, Jianwu

    2014-11-01

    Industrialization and urbanization have led to a great deterioration of air quality and provoked some serious environmental concerns. One hundred and five samples of atmospheric deposition were analyzed for their concentrations of 13 trace elements (As, Cd, Cu, Fe, Al, Co, Cr, Hg, Mn, Mo, Pb, Se, and Zn) in Shanxi Basin, which includes six isolate basins. The input fluxes of the trace elements in atmospheric deposition were observed and evaluated. Geostatistical analysis (EF, PCA, and CA ) were conducted to determine the spatial distribution, possible sources, and enrichment degrees of trace elements in atmospheric deposition. Fe/Al and K/Al also contribute to identify the sources of atmospheric deposition. The distribution of trace elements in atmospheric deposition was proved to be geographically restricted. The results show that As, Cd, Pb, Zn, and Se mainly come from coal combustion. Fe, Cu, Mn, Hg, and Co originate mainly from interactions between local polluted soils and blowing dust from other places, while the main source of Al, Cr, and Mo are the soil parent materials without pollution. This work provides baseline information to develop policies to control and reduce trace elements, especially toxic elements, from atmospheric deposition. Some exploratory analytical methods applied in this work are also worth considering in similar researches.

  14. Tracing the fate of carbon and the atmospheric evolution of Mars

    CERN Document Server

    Hu, Renyu; Ehlmann, Bethany L; Yung, Yuk L

    2015-01-01

    The climate of Mars likely evolved from a warmer, wetter early state to the cold, arid current state. However, no solutions for this evolution have previously been found to satisfy the observed geological features and isotopic measurements of the atmosphere. Here we show that a family of solutions exist, invoking no missing reservoirs or loss processes. Escape of carbon via CO photodissociation and sputtering enriches heavy carbon (13C) in the Martian atmosphere, partially compensated by moderate carbonate precipitation. The current atmospheric 13C/12C and rock and soil carbonate measurements indicate an early atmosphere with a surface pressure <1 bar. Only scenarios with large amounts of carbonate formation in open lakes permit higher values up to 1.8 bar. The evolutionary scenarios are fully testable with data from the MAVEN mission and further studies of the isotopic composition of carbonate in the Martian rock record through time.

  15. A new laboratory facility to study the interactions of aerosols, cloud droplets/ice crystals, and trace gases in a turbulent environment: The Π Chamber

    Science.gov (United States)

    Cantrell, W. H., II; Chang, K.; Ciochetto, D.; Niedermeier, D.; Bench, J.; Shaw, R. A.

    2014-12-01

    A detailed understanding of gas-aerosol-cloud interaction within the turbulent atmosphere is of prime importance for an accurate understanding of Earth's climate system. As one example: While every cloud droplet began as an aerosol particle, not every aerosol particle becomes a cloud droplet. The particle to droplet transformation requires that the particle be exposed to some critical concentration of water vapor, which differs for different combinations of particle size and chemical composition. Similarly, the formation of ice particles in mixed phase clouds is also catalyzed by aerosol particles. Even in the simplest scenarios it is challenging to gain a full understanding of the aerosol activation and ice nucleation processes. At least two other factors contribute significantly to the complexity observed in the atmosphere. First, aerosols and cloud particles are not static entities, but are continuously interacting with their chemical environment, and therefore changing in their properties. Second, clouds are ubiquitously turbulent, so thermodynamic and compositional variables, such as water vapor or other trace gas concentrations, fluctuate in space and time. Indeed, the coupling between turbulence and microphysical processes is one of the major research challenges in cloud physics. We have developed a multiphase, turbulent reaction chamber, (dubbed the Π Chamber, after the internal volume of 3.14 cubic meters) designed to address the problems outlined above. It is capable of pressures ranging from sea level to ~ 100 mbar, and can sustain temperatures of +40 to -55 ºC. We can independently control the temperatures on the surfaces of three heat transfer zones. This allows us to establish a temperature gradient between the floor and ceiling inducing Rayleigh-Benard convection and inducing a turbulent environment. Interior surfaces are electropolished stainless steel to facilitate cleaning before and after chemistry experiments. At present, supporting

  16. A comparative study between the fluxes of trace elements in bulk atmospheric deposition at industrial, urban, traffic, and rural sites.

    Science.gov (United States)

    Fernández-Olmo, I; Puente, M; Irabien, A

    2015-09-01

    The input of trace elements via atmospheric deposition towards industrial, urban, traffic, and rural areas is quite different and depends on the intensity of the anthropogenic activity. A comparative study between the element deposition fluxes in four sampling sites (industrial, urban, traffic, and rural) of the Cantabria region (northern Spain) has been performed. Sampling was carried out monthly using a bulk (funnel bottle) sampler. The trace elements, As, Cd, Cr, Cu, Mn, Mo, Ni, Pb, Ti, Zn, and V, were determined in the water soluble and insoluble fractions of bulk deposition samples. The element deposition fluxes at the rural, urban, and traffic sites followed a similar order (Zn > Mn> > Cu ≈ Ti > Pb > V ≈ Cr > Ni> > As ≈ Mo > Cd). The most enriched elements were Cd, Zn, and Cu, while V, Ni, and Cr were less enriched. An extremely high deposition of Mn was found at the industrial site, leading to high enrichment factor values, resulting from the presence of a ferro-manganese/silico-manganese production plant in the vicinity of the sampling site. Important differences were found in the element solubilities in the studied sites; the element solubilities were higher at the traffic and rural sites, and lower at the urban and industrial sites. For all sites, Zn and Cd were the most soluble elements, whereas Cr and Ti were less soluble. The inter-site correlation coefficients for each element were calculated to assess the differences between the sites. The rural and traffic sites showed some similarities in the sources of trace elements; however, the sources of these elements at the industrial and rural sites were quite different. Additionally, the element fluxes measured in the insoluble fraction of the bulk atmospheric deposition exhibited a good correlation with the daily traffic volume at the traffic site.

  17. Trace elements associated with atmospheric particulate matter in the Upper Hunter Valley, NSW, Australia

    Energy Technology Data Exchange (ETDEWEB)

    Farhana, Biswas Karabi [Bangladesh Institute of Research and Rehabilitation in Diabetes, Endcrine and Metabolic Disorders (BIRDEM), Research Division, Dhaka (Bangladesh); Bridgman, Howard [University of Newcastle, Dept. of Geography and Environmental Science (Australia); McOrist, Gordon [Australian Nuclear Science and Technology Organization (ANSTO), Environment Division, Menai (Australia)

    2002-05-01

    Airbone particulate matter, both total suspended particulate (TSP) and PM{sub 10}, and soil samples from four sampling sites were collected in the Upper Hunter Valley in NSW, Australia in early 1999. This study aimed to measure relative amounts of particulates during this period, and identify associated trace elements and their potential sources. Particulates were analyzed for trace elements using Neutron Activation Analysis technique. Total concentrations ({mu}g m{sup -3}) of TSP and PM{sub 10} varied within 7-135 and 4-19, respectively, among sampling sites. Mean concentrations (ng m{sup -3}) of iron, barium, zinc, lanthanum, bromine, chromium, rubidium, neodymium, cobalt, hafnium, cerium, thorium, uranium, scandium and cesium varied within 2042-2867, 529-1500, 28-40, 5.45-11.44, 5.3-20.6, 10.4-12.7, 4.14-11.56, 5.4-8.1, 1.16-1.98, 1.76-2.17, 0.71-3.9, 0.21-0.50, 0.29-0.84, 0.28-1.23, and 0.18-0.30, respectively. Significant correlation between sites for many elements suggested some common source(s) of some elements. The enrichment levels of the trace elements identified some crustal materials as a predominant source of particulate matter. (author)

  18. A new method based on low background instrumental neutron activation analysis for major, trace and ultra-trace element determination in atmospheric mineral dust from polar ice cores

    Energy Technology Data Exchange (ETDEWEB)

    Baccolo, Giovanni, E-mail: giovanni.baccolo@mib.infn.it [Graduate School in Polar Sciences, University of Siena, Via Laterina 8, 53100, Siena (Italy); Department of Environmental Sciences, University of Milano-Bicocca, P.zza della Scienza 1, 20126, Milano (Italy); INFN, Section of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Clemenza, Massimiliano [INFN, Section of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Department of Physics, University of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Delmonte, Barbara [Department of Environmental Sciences, University of Milano-Bicocca, P.zza della Scienza 1, 20126, Milano (Italy); Maffezzoli, Niccolò [Centre for Ice and Climate, Niels Bohr Institute, Juliane Maries Vej, 30, 2100, Copenhagen (Denmark); Nastasi, Massimiliano; Previtali, Ezio [INFN, Section of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Department of Physics, University of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Prata, Michele; Salvini, Andrea [LENA, University of Pavia, Pavia (Italy); Maggi, Valter [Department of Environmental Sciences, University of Milano-Bicocca, P.zza della Scienza 1, 20126, Milano (Italy); INFN, Section of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy)

    2016-05-30

    Dust found in polar ice core samples present extremely low concentrations, in addition the availability of such samples is usually strictly limited. For these reasons the chemical and physical analysis of polar ice cores is an analytical challenge. In this work a new method based on low background instrumental neutron activation analysis (LB-INAA) for the multi-elemental characterization of the insoluble fraction of dust from polar ice cores is presented. Thanks to an accurate selection of the most proper materials and procedures it was possible to reach unprecedented analytical performances, suitable for ice core analyses. The method was applied to Antarctic ice core samples. Five samples of atmospheric dust (μg size) from ice sections of the Antarctic Talos Dome ice core were prepared and analyzed. A set of 37 elements was quantified, spanning from all the major elements (Na, Mg, Al, Si, K, Ca, Ti, Mn and Fe) to trace ones, including 10 (La, Ce, Nd, Sm, Eu, Tb, Ho, Tm, Yb and Lu) of the 14 natural occurring lanthanides. The detection limits are in the range of 10{sup −13}–10{sup −6} g, improving previous results of 1–3 orders of magnitude depending on the element; uncertainties lies between 4% and 60%. - Highlights: • A new method based on neutron activation for the multi-elemental characterization of atmospheric dust entrapped in polar ice cores is proposed. • 37 elements were quantified in μg size dust samples with detection limits ranging from 10{sup −13} to 10{sup −6} g. • A low background approach and a clean analytical protocol improved INAA performances to unprecedented levels for multi-elemental analyses.

  19. A new method based on low background instrumental neutron activation analysis for major, trace and ultra-trace element determination in atmospheric mineral dust from polar ice cores.

    Science.gov (United States)

    Baccolo, Giovanni; Clemenza, Massimiliano; Delmonte, Barbara; Maffezzoli, Niccolò; Nastasi, Massimiliano; Previtali, Ezio; Prata, Michele; Salvini, Andrea; Maggi, Valter

    2016-05-30

    Dust found in polar ice core samples present extremely low concentrations, in addition the availability of such samples is usually strictly limited. For these reasons the chemical and physical analysis of polar ice cores is an analytical challenge. In this work a new method based on low background instrumental neutron activation analysis (LB-INAA) for the multi-elemental characterization of the insoluble fraction of dust from polar ice cores is presented. Thanks to an accurate selection of the most proper materials and procedures it was possible to reach unprecedented analytical performances, suitable for ice core analyses. The method was applied to Antarctic ice core samples. Five samples of atmospheric dust (μg size) from ice sections of the Antarctic Talos Dome ice core were prepared and analyzed. A set of 37 elements was quantified, spanning from all the major elements (Na, Mg, Al, Si, K, Ca, Ti, Mn and Fe) to trace ones, including 10 (La, Ce, Nd, Sm, Eu, Tb, Ho, Tm, Yb and Lu) of the 14 natural occurring lanthanides. The detection limits are in the range of 10(-13)-10(-6) g, improving previous results of 1-3 orders of magnitude depending on the element; uncertainties lies between 4% and 60%.

  20. Trace analysis of organics in air by corona discharge atmospheric pressure ionization using an electrospray ionization interface.

    Science.gov (United States)

    Nikolaev, Eugene; Riter, Leah S; Laughlin, Brian C; Handberg, Eric; Cooks, R Graham

    2004-01-01

    A corona discharge ion source operating at atmospheric pressure in the point-to-plane configuration was constructed by reconfiguring the ion source of a commercial electrospray ionization (ESI) quadrupole mass spectrometer. This new source allows direct air analysis without modification to the mass spectrometer. Detection and quantitation of semi-volatile compounds in air is demonstrated. The analytical performance of the system was established using the chemical warfare agent simulants methyl salicylate and dimethyl methylphosphonate. Limits of detection are 60 pptr in the negative-ion mode and 800 pptr in the positive-ion mode for methyl salicylate and 800 pptr in the negative-ion mode and 3.6 ppb in the positive-ion mode for dimethyl methylphosphonate. A linear response was observed from 60 pptr to 8 ppb for methyl salicylate in air in the negative-ionization mode. Cluster ion formation versus production of analyte ions was investigated and it was found that dry air or an elevated capillary interface temperature (130 degrees C) was needed to avoid extensive clustering, mostly of water. Reagent gases are not needed as proton sources, as is usually the case for atmospheric pressure chemical ionization, and this, together with the simplicity, sensitivity and speed of the technique, makes it promising for miniaturization and future field studies.

  1. Trace metals in atmospheric particulates characterized of aerosol emitted by industrial and urban sources

    Energy Technology Data Exchange (ETDEWEB)

    Del Borghi, A.; Solisio, C.; Zilli, M.; Del Borghi, M. [Genoa University, Genoa (Italy). Chemical and Process Engineering Institute G.B. Bonino

    1998-12-31

    The results of a year`s study in the Savona area (Italy) for dust deposition have been analyzed in order to characterize the emission sources. The contribution of the major pollutant sources has been determined by tracer metals and their enrichment factors. The selected metals were Cd, Cu, Pb, An, Cr, and Ni. The obtained results show four types of emission sources responsible for airborne trace metals; traffic, industrial plants a large oil and coal fired power station, resuspension of soil particles and residential heating. 9 refs., 9 figs., 1 tab.

  2. The dynamic chamber method: trace gas exchange fluxes (NO, NO2, O3) between plants and the atmosphere in the laboratory and in the field

    Science.gov (United States)

    Breuninger, C.; Oswald, R.; Kesselmeier, J.; Meixner, F. X.

    2012-05-01

    We describe a dynamic chamber system to determine reactive trace gas exchange fluxes between plants and the atmosphere under laboratory and, with small modifications, also under field conditions. The system allows measurements of the flux density of the reactive NO-NO2-O3 triad and additionally of the non-reactive trace gases CO2 and H2O. The chambers are made of transparent and chemically inert wall material and do not disturb plant physiology. For NO2 detection we used a highly NO2 specific blue light converter coupled to chemiluminescence detection of the photolysis product, NO. Exchange flux densities derived from dynamic chamber measurements are based on very small concentration differences of NO2 (NO, O3) between inlet and outlet of the chamber. High accuracy and precision measurements are therefore required, and high instrument sensitivity (limit of detection) and the statistical significance of concentration differences are important for the determination of corresponding exchange flux densities, compensation point concentrations, and deposition velocities. The determination of NO2 concentrations at sub-ppb levels (data analysis are demonstrated by studies of Picea abies L. (Norway Spruce) under field and laboratory conditions. Our laboratory data show that the quality selection criterion based on the use of only significant NO2 concentration differences has a considerable impact on the resulting compensation point concentrations yielding values closer to zero. The results of field experiments demonstrate the need to consider photo-chemical reactions of NO, NO2, and O3 inside the chamber for the correct determination of the exchange flux densities, deposition velocities, as well as compensation point concentrations. Under our field conditions NO2 deposition velocities would have been overestimated up to 80%, if NO2 photolysis has not been considered. We also quantified the photolysis component for some previous NO2 flux measurements. Neglecting photo

  3. Abundance and Isotopic Composition of Gases in the Martian Atmosphere: First Results from the Mars Curiosity Rover

    Science.gov (United States)

    Mahaffy, Paul; Webster, Chris R.; Atreya, Sushil K.; Franz, Heather; Wong, Michael; Conrad, Pamela G.; Harpold, Dan; Jones, John J.; Leshin, Laurie, A.; Manning, Heidi; Owen, Tobias; Pepin, Robert O.; Squyres, Steven; Trainer, Melissa

    2013-01-01

    Repeated measurements of the composition of the Mars atmosphere from Curiosity Rover yield a (40)Ar/N2 ratio 1.7 times greater and the (40)Ar/(36)Ar ratio 1.6 times smaller than the Viking Lander values in 1976. The unexpected change in (40)Ar/N2 ratio probably results from different instrument characteristics although we cannot yet rule out some unknown atmospheric process. The new (40)Ar/(36)Ar ratio is more aligned with Martian meteoritic values. Besides Ar and N2 the Sample Analysis at Mars instrument suite on the Curiosity Rover has measured the other principal components of the atmosphere and the isotopes. The resulting volume mixing ratios are: CO2 0.960(+/- 0.007); (40)Ar 0.0193(+/- 0.0001); N2 0.0189(+/- 0.0003); O2 1.45(+/- 0.09) x 10(exp -3); and CO 5.45(+/- 3.62) x 10(exp 4); and the isotopes (40)Ar/(36)Ar 1.9(+/- 0.3) x 10(exp 3), and delta (13)C and delta (18)O from CO2 that are both several tens of per mil more positive than the terrestrial averages. Heavy isotope enrichments support the hypothesis of large atmospheric loss. Moreover, the data are consistent with values measured in Martian meteorites, providing additional strong support for a Martian origin for these rocks.

  4. Tracing changes in atmospheric sources of lead contamination using lead isotopic compositions in Australian red wine.

    Science.gov (United States)

    Kristensen, Louise Jane; Taylor, Mark Patrick; Evans, Andrew James

    2016-07-01

    Air quality data detailing changes to atmospheric composition from Australia's leaded petrol consumption is spatially and temporally limited. In order to address this data gap, wine was investigated as a potential proxy for atmospheric lead conditions. Wine spanning sixty years was collected from two wine regions proximal to the South Australian capital city, Adelaide, and analysed for lead concentration and lead and strontium isotopic composition for source apportionment. Maximum wine lead concentrations (328 μg/L) occur prior to the lead-in-air monitoring in South Australia in the later 1970s. Wine lead concentrations mirror available lead-in-air measurements and show a declining trend reflecting parallel reductions in leaded petrol emissions. Lead from petrol dominated the lead in wine ((206)Pb/(207)Pb: 1.086; (208)Pb/(207)Pb: 2.360) until the introduction of unleaded petrol, which resulted in a shift in the wine lead isotopic composition closer to vineyard soil ((206)Pb/(207)Pb: 1.137; (208)Pb/(207)Pb: 2.421). Current mining activities or vinification processes appear to have no impact with recent wine samples containing less than 4 μg/L of lead. This study demonstrates wine can be used to chronicle changes in environmental lead emissions and is an effective proxy for atmospherically sourced depositions of lead in the absence of air quality data.

  5. Bioindication of atmospheric trace metals--with special references to megacities.

    Science.gov (United States)

    Markert, Bernd; Wuenschmann, Simone; Fraenzle, Stefan; Graciana Figueiredo, Ana Maria; Ribeiro, Andreza P; Wang, Meie

    2011-01-01

    After considering the particular problems of atmospheric pollution in megacities, i.e. agglomerations larger than 5 mio. inhabitants, with urbanization of World's population going on steadily, possibilities of active biomonitoring by means of green plants are discussed. Based on specific definitions of active and passive bioindication the chances of monitoring heavy metals in Sao Paulo megacity were demonstrated (first results published before). This is to show that there is need for increased use of bioindication to tackle the particular problems of megacities concerning environmental "health", the data to be processed according to the Multi-Markered-Bioindication-Concept (MMBC). Comparison to other work shows this approach to be reasonable.

  6. Influence of Biomass Burning on Temporal and Diurnal Variations of Acidic Gases, Particulate Nitrate, and Sulfate in a Tropical Urban Atmosphere

    Directory of Open Access Journals (Sweden)

    Sailesh N. Behera

    2014-01-01

    Full Text Available The present study investigated the temporal and diurnal distributions of atmospheric acidic gases (sulphur dioxide (SO2, nitrous acid (HONO, and nitric acid (HNO3 and those of particulate nitrate (NO3- and sulfate (SO42- through a comprehensive field campaign during the largest smoke haze episode in Singapore, a representative country in Southeast Asia (SEA. To identify the atmospheric behavior of these pollutants during the smoke haze period, the data generated from the measurement campaign were divided into three distinct periods: prehaze, during haze, and posthaze periods. The 24 hr average data indicated that ambient SO2, HONO, and HNO3 during the smoke haze episodes increased by a factor ranging from 1.2 to 2.6 compared to those during the prehaze and posthaze periods. Similarly, in the case of particulates SO42- and NO3-, the factor ranged from 2.3 to 4.2. Backward air trajectories were constructed and used to find the sources of biomass burning to the recurring smoke haze in this region. The air trajectory analysis showed that the smoke haze episodes experienced in Singapore were influenced by transboundary air pollution, caused by severe biomass burning events in the islands of Indonesia.

  7. A comparison of sulfur-free and ambient air enclosure techniques for measuring the exchange of reduced sulfur gases between soils and the atmosphere

    Science.gov (United States)

    Castro, Mark S.; Galloway, James N.

    1991-08-01

    The exchange of reduced sulfur gases between the atmosphere and forest soils in the Shaver Hollow watershed (Shenandoah National Park, Virginia) were measured with sulfur-free and ambient air enclosures at least twice a month from March through November 1989. Soils within sulfur-free enslosures were sources of carbonyl sulfide (COS) and carbon disulfide (CS2). Atmospheric fluxes of COS and CS2 ranged from 0.77 to 13.03 ng COS-S/sq m-min and from 2.04 to 15.74 ng CS2-S/sq m-min. In contrast, soils within ambient air enclosures were sinks for COS and CS2. Uptake rates of COS and CS2 ranged from 2.78 to 16.20 ng COS-S/sq m-min and from 3.42 to 26.62 ng CS2-S/sq m-min. The discrepancy in the direction of these fluxes was caused by the flux-measurement techniques.

  8. Acidic gases and nitrate and sulfate particles in the atmosphere in the city of Guadalajara, México.

    Science.gov (United States)

    Saldarriaga-Noreña, Hugo; Waliszewski, Stefan; Murillo-Tovar, Mario; Hernández-Mena, Leonel; de la Garza-Rodríguez, Iliana; Colunga-Urbina, Edith; Cuevas-Ordaz, Rosalva

    2012-05-01

    Atmospheric concentrations of nitrous acid, nitric acid, nitrate and sulfate particles were obtained in this study from April to June 2008 in the center of the city of Guadalajara, while concentrations of ozone, sulfur dioxide, nitrogen dioxide and meteorological parameters (temperature and relative humidity), were acquired by the Secretaría del Medio Ambiente para el Desarrollo Sustentable del Estado de Jalisco (SEMADES). The results showed that nitric acid (2.7 μg m(-3)) was 2.7 times higher than nitrous acid (1.0 μg m(-3)). The sulfur dioxide (SO(2)) concentration indicated an opposite trend to sulfate (SO(4) (2-)), with the average concentration of SO(2) (6.9 μg m(-3)) higher in almost the entire period of study. The sulfur conversion ratio (Fs, 24.9%) and nitrogen conversion ratio (Fn, 6.2%), were revealed to be similar to that reported in other urban areas during warm seasons. It is also noted that ozone is not the main oxidizer of nitrogen dioxide and sulfur dioxide. This determination was made by taking into account the slightly positively correlation determined for Fn (r(2) = 0.084) and Fs (r(2) = 0.092) with ozone that perhaps suggests there are other oxidizing species such as the radical OH, which are playing an important role in the processes of atmospheric oxidation in this area.

  9. Atmospheric trace elements at Enewetak Atoll. I Concentrations, sources, and temporal variability

    Science.gov (United States)

    Duce, R. A.; Arimoto, R.; Ray, B. J.; Unni, C. K.; Harder, P. J.

    1983-06-01

    The concentrations of 29 elements in aerosol particles collected in 1979 during Searex (Sea/Air Exchange) experiments at Enewetak Atoll (11 deg N, 162 deg E), in the tropical North Pacific, are measured. The concentrations of Na, Mg, Cl, K, Ca, and Br are dominated by marine sources; the elements have similar mass-size distributions, and their atmospheric concentration ratios (normalized to Na) are similar to the corresponding ratios in bulk seawater. Atmospheric inputs of aluminosilicate particles from crustal weathering are found to control the aerosol particle concentration of Al, Sc, Mn, Fe, Co, Cs, Ba, Ce, Eu, Hf, Ta, and Th. The mean concentrations of these crustally derived elements decrease by an average of 91 percent (+ or - 4.1 percent) from the local dry season (April to May) to the wet season (July to August); this general decrease is attributed to the abatement of dust storms in Asia. At times, the influx of dust from Asia dominates the concentrations of V, Cr, Rb, and Cu in aerosol particles, but when dust concentrations decrease, noncrustal sources for these elements manifest themselves.

  10. Urban and industrial contribution to trace elements in the atmosphere as measured in holm oak bark

    Science.gov (United States)

    Drava, Giuliana; Brignole, Daniele; Giordani, Paolo; Minganti, Vincenzo

    2016-11-01

    The concentrations of As, Cd, Co, Cu, Fe, Mn, Ni, Pb, V and Zn were measured by ICP-OES in samples of bark of the holm oak (Quercus ilex L.) collected from trees in different urban environments (residential and mixed residential/industrial). The use of tree bark as a bioindicator makes it easy to create maps that can provide detailed data on the levels and on the spatial distribution of each trace element. For most of the elements considered (As, Co, Fe, Mn, Ni, V and Zn), the concentrations in the industrial sites are about twice (from 1.9 to 2.8 times higher) of those in the residential area. Arsenic, Fe and Zn show the highest concentrations near a steel plant (operational until 2005), but for the other elements it is not possible to identify any localized source, as evident from the maps. In areas where urban pollution is summed up by the impact of industrial activities, the population is exposed to significantly higher amounts of some metals than people living in residential areas.

  11. Comparative study of the suitability of two lichen species for trace element atmospheric monitoring

    Energy Technology Data Exchange (ETDEWEB)

    Saiki, Mitiko; Alves, Edson R.; Genezini, Frederico A., E-mail: mitiko@ipen.br, E-mail: eralves@ipen.br, E-mail: fredzini@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN-CNEN-SP), Sao Paulo, SP (Brazil); Saldiva, Paulo H.N., E-mail: pepino@usp.br [Universidade de Sao Paulo (USP), Sao Paulo, SP (Brazil). Faculdade de Medicina

    2013-07-01

    Lichens have been widely used in monitoring studies. Consequently, it is very useful to study the suitability of lichen species to monitor pollutants allowing in this way the best choice. The aim of this study was to compare the accumulation of trace elements by two epiphytic lichen species Canoparmelia texana (Tuck) Elix and Hale and Usnea amblyoclada (Mull. Arg.) Zahlbr. Five samples of each species were collected during the period from November 2010 in a same site far from downtown Sao Paulo city. Lichens collected from tree barks were cleaned, freeze-dried, ground and analyzed by neutron activation analysis. Aliquots of lichen samples and synthetic elemental standards were irradiated at the IEA-R1 nuclear research reactor. The induced gamma activities were measured using a hyperpure Ge detector coupled to a digital spectrum analyzer. Concentrations of As, Ba, Cd, Cr, Cs, Fe, Mg, Mn, Na, Rb, V and Zn were determined in both lichen species. The results demonstrated that both species can be used for evaluating air quality. The element concentrations showed difference between lichen species and also among their sampling periods. These differences may be attributed to the distinct mechanisms of element absorption by lichens as well as various other factors that affect their element accumulation. The comparative evaluation made calculating the ratios between C. texana species sample and that in Usnea amblyoclada for elemental concentrations indicated that, in general, foliose C. texana present similar or higher concentrations than those presented by fruticose Usnea. (author)

  12. Trace determination of the flame retardant tetrabromobisphenol A in the atmosphere by gas chromatography-mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Xie Zhiyong [GKSS Research Centre, Institute for Coastal Research, Department of Environmental Chemistry, Max-Planck-Str. 1, D-21502 Geesthacht (Germany) and Johann Wolfgang Goethe-University Frankfurt at Main, Institute of Atmospheric and Environmental Sciences, Department of Analytical Environmental Chemistry, Georg-Voigt-Str. 14, 60054 Frankfurt (Germany)]. E-mail: zhiyong.xie@gkss.de; Ebinghaus, Ralf [GKSS Research Centre, Institute for Coastal Research, Department of Environmental Chemistry, Max-Planck-Str. 1, D-21502 Geesthacht (Germany); Lohmann, Rainer [Graduate School of Oceanography, University of Rhode Island, Narragansett, RI 02882-1197 (United States); Heemken, Olaf [LAVES, Philosophenweg 36/38, D-26121 Oldenburg (Germany); Caba, Armando [GKSS Research Centre, Institute for Coastal Research, Department of Environmental Chemistry, Max-Planck-Str. 1, D-21502 Geesthacht (Germany); Puettmann, Wilhelm [Johann Wolfgang Goethe-University Frankfurt at Main, Institute of Atmospheric and Environmental Sciences, Department of Analytical Environmental Chemistry, Georg-Voigt-Str. 14, 60054 Frankfurt (Germany)

    2007-02-19

    A simple and effective method has been developed for analysis of the flame retardant tetrabromobisphenol A (TBBPA) in environmental samples by using modified soxhlet extraction in combination with silica gel clean-up, derivatization with silylation reagent and gas chromatography-mass spectrometry (GC-MS) in selected ion monitoring mode (SIM). Satisfactory recoveries were achieved for the large volume sampling, soxhlet extraction and silica gel clean-up. The overall recovery is 79 {+-} 1%. The derivatization procedure is simple and fast, and produces stable TBBPA derivative. GC-MS with electronic impact (EI) ionization mode shows better detection power than using negative chemical ionization (NCI) mode. EI gives a method detection limit of 0.04 pg m{sup -3} and enables to determine trace TBBPA in ambient air in remote area. The method was successfully applied to the determination of TBBPA in atmospheric samples collected over land and coastal regions. The concentrations of TBBPA ranged from below the method detection limit (0.04 pg m{sup -3}) to 0.85 pg m{sup -3}. A declining trend with increasing latitude was present from the Wadden Sea to the Arctic. The atmospheric occurrence of TBBPA in the Arctic is significant and might imply that TBBPA has long-range transport potential.

  13. Laboratory studies of reactions of atmospheric gases with components of mineral dust aerosol and research in chemical education

    Science.gov (United States)

    Schuttlefield, Jennifer Dianne

    Mineral dust aerosol surfaces provide a medium in the atmosphere for heterogeneous chemistry to occur, which can alter the chemical balance of the Earth's atmosphere. It is becoming increasingly clear that the heterogeneous chemistry of these aerosols is a function of relative humidity (RH), as water on the surface of these particles can enhance or inhibit reactivity depending on the reaction. In this thesis, the uptake of water on clays and oxides was investigated, as well as phase transitions for atmospherically relevant salts. Reactions of carbon dioxide and nitric acid on oxide particles in the presence and absence of water were also examined. Following the reaction of HNO 3 on an alumina surface, photoirradiation experiments were preformed to determine the effect of irradiation on the adsorbed nitrate. The results presented in this thesis provide insight into the heterogeneous reactivity of mineral dust aerosol in the presence and absence of co-adsorbed water, as well as a fundamental understanding of water uptake on soluble and insoluble aerosols. A new method, using a quartz crystal microbalance, was developed to attempt to obtain a better fundamental understanding of different mineral dust components. In addition to the laboratory research, research in chemical education is also presented in this thesis. Two different types of work being done in the area of chemical education are shown. First a new experiment was implemented into an undergraduate physical chemistry course. The technique, ATR-FTIR spectroscopy, was chosen for its ability to expose students to a technique that is commonly used in laboratory research as well as the ease for which high quality results can be obtained. Students used ATR-FTIR spectroscopy to monitor sulfate, SO 42-, adsorption on TiO2 thin films. Second, the role of cognitive load and problem difficulty was accessed with data acquired while students completed an introductory-level chemistry word problem using a web-based tool

  14. Atmospheric Pressure Ionization Mass Spectrometry and Its Application in Ultra High Purity Gases Analysis:A Review%大气压电离质谱及其用于超高纯气体分析研究进展

    Institute of Scientific and Technical Information of China (English)

    张体强; 胡树国; 韩桥

    2014-01-01

    Ultra high purity (UHP)gases are very important in the manufacturing industry.As an example,in the semiconductor industry,the quality of electron gas directly affects the performance of semiconductor devices;a few parts per million of trace impurities in gases can reduce component store information in integrated circuits.Thus, challenges to the sensitivity of the analytical instruments and the analysis methods arise for detection of ultra-trace impurities.Atmospheric Pressure Ionization Mass Spectrometry (APIMS),which could ionize impurities under the atmospheric pressure conditions with high efficiency of ionization and sensitivity,becomes the most important instrument for the purity analysis of the UHP gases.APIMS is especially suitable for the analysis of trace impurities with a concentration below 1 0 -9 mol/mol or even 1 0 -1 2 mol/mol.Two ionization sources based on corona discharge and 63 Ni have been developed for APIMS,where the former is more commonly equipped.Quadruple rod is usually used as the mass filter.A sampling and dilution system,in which the components in standard gas can be diluted to far lower concentrations for calibration,is utilized in APIMS for analysis of UHP gases.The detection sensitivity of impurities by APIMS is quite relevant to the ionization modes.One of the main modes is charge transfer reaction, which is applicable to matrix and impurities with large different ionization energy.For example,most impurities in Ar and N2 can be determined by this mode due to the high ionization energy of Ar and N2 .And by adding H2 , APIMS is also used for detecting N2 in Ar.The third mode is the reaction of forming cluster ions,for which few applications have been reported.The mode could enhance the detection sensitivity of H2 O in matrix O2 by detecting the ion of O2 +·H2 O.Based on these ionization modes,various detecting methods for different impurities can be designed to effectively detect trace or ultra-trace impurities.The sensitivity of

  15. The Berkeley Atmospheric CO2 Observation Network (BEACON): Measuring Greenhouse Gases and Criteria Pollutants within the Urban Dome

    Science.gov (United States)

    Teige, V. E.; Weichsel, K.; Hooker, A.; Wooldridge, P. J.; Cohen, R. C.

    2012-12-01

    Efforts to curb greenhouse gas emissions, while global in their impacts, often focus on local and regional scales for execution and are dependent on the actions of communities and individuals. Evaluating the effectiveness of local policies requires observations with much higher spatial resolution than are currently available---kilometer scale. The Berkeley Atmospheric CO2 Observation Network (BEACON):, launched at the end of 2011, aims to provide measurements of urban-scale concentrations of CO2, temperature, pressure, relative humidity, O3, CO, and NO2 with sufficient spatial and temporal resolution to characterize the sources of CO2 within cities. Our initial deployment in Oakland, California uses ~40 sensor packages at a roughly 2 km spacing throughout the city. We will present an initial analysis of the vertical gradients and other spatial patterns observed to date.

  16. Poster 6: Influence of traces elements in the organic chemistry of upper atmosphere of Titan

    Science.gov (United States)

    Mathe, Christophe; Carrasco, Nathalie; Trainer, Melissa G.; Gautier, Thomas; Gavilan, Lisseth; Dubois, David; Li, Xiang

    2016-06-01

    In the upper atmosphere of Titan, complex chemistry leads to the formation of organic aerosols. Since the work of Khare et al. in 1984, several experiments investigated the formation of Titan aerosols, so called tholins, in the laboratory. It has been suggested that nitrogen-containing compounds may contribute significantly to the aerosols formation process. In this study, we focused on the influence of pyridine, the simplest nitrogenous aromatic hydrocarbon, on the chemistry of Titan's atmosphere and on aerosol formation. To assess the effect of pyridine on aerosol formation chemistry, we used two different experimental setups : a capacitively coupled radio-frequency (electronic impact), and a VUV Deuterium lamp (photochemistry) in a collaboration between LATMOS (Guyancourt) and NASA-GSFC (Greenbelt), respectively. Aerosols produced with both setups were first analyzed using a FTIR-ATR (Fourier Transform Infrared spectroscopy - Attenuated Total Reflection) with a spectral range of 4000-800 cm-1 to characterize their optical properties. Next the samples were analysed using a Bruker Autoflex Speed MALDI mass spectrometer with a m/z range up to 2000 Da in order to infer their composition. Infrared spectroscopy analysis showed that tholins produced with a nitrogen-methane gas mixture (95:5) and nitrogenpyridine gas mixture (99:250ppm) present very similar spectra features. Tholins produced with a mixture of nitrogenmethane-pyridine (99:1:250ppm) do not present aliphatic CH2 or CH3 vibrational signatures. This could indicate a cyclic polymerization by a pyridine skeleton. Mass spectrometry is still in progress to confirm this.

  17. High-sensitivity remote detection of atmospheric pollutants and greenhouse gases at low ppm levels using near-infrared tunable diode lasers

    Science.gov (United States)

    Roy, Anirban; Upadhyay, Abhishek; Chakraborty, Arup Lal

    2016-05-01

    The concentration of atmospheric pollutants and greenhouse gases needs to be precisely monitored for sustainable industrial development and to predict the climate shifts caused by global warming. Such measurements are made on a continuous basis in ecologically sensitive and urban areas in the advanced countries. Tunable diode laser spectroscopy (TDLS) is the most versatile non-destructive technology currently available for remote measurements of multiple gases with very high selectivity (low cross-sensitivity), very high sensitivity (on the order of ppm and ppb) and under hazardous conditions. We demonstrate absolute measurements of acetylene, methane and carbon dioxide using a fielddeployable fully automated TDLS system that uses calibration-free 2f wavelength modulation spectroscopy (2f WMS) techniques with sensitivities of low ppm levels. A 40 mW, 1531.52 nm distributed feedback (DFB) diode laser, a 10 mW, 1650 nm DFB laser and a 1 mW, 2004 nm vertical cavity surface emitting laser (VCSEL) are used in the experiments to probe the P9 transition of acetylene, R4 transition of methane and R16 transition of carbon dioxide respectively. Data acquisition and on-board analysis comprises a Raspberry Pi-based embedded system that is controllable over a wireless connection. Gas concentration and pressure are simultaneously extracted by fitting the experimental signals to 2f WMS signals simulated using spectroscopic parameters obtained from the HITRAN database. The lowest detected concentration is 11 ppm for acetylene, 275 ppm for methane and 285 ppm for carbon dioxide using a 28 cm long single-pass gas cell.

  18. Sulfur Isotope of Epilithic Mosses to Trace Variation of Atmospheric Sulfur Sources

    Directory of Open Access Journals (Sweden)

    HU Fei-fei1,2;PAN Jia-yong1,3;ZHANG Liang1,2;XIE Shu-rong3;CHEN Yi-ping3;XIA Fei1,3

    2016-08-01

    Full Text Available 全文: PDF (5099 KB HTML (1 KB 输出: BibTeX | EndNote (RIS 摘要 为探讨石生苔藓硫同位素组成特征对区域性大气硫源的指示作用,连续两年采集鄱阳湖生态经济区内的石生苔藓样品,测定δ34S值;并结合已有的雨水、煤的硫同位素值等相关研究数据进行对比分析。样品δ34S值均偏正,平均为+4.9‰,取值范围为+1.9‰~+9.6‰;石生苔藓δ34S值与空气中SO2浓度呈负相关关系;南昌、抚州两市苔藓δ34S值的取值范围与其对应城市大气降水δ34S值的变化区间相接近;研究区内土壤相对富集重硫,且土壤中可溶性硫主要受大气硫沉降影响。结果表明,石生苔藓的硫同位素组成对区域性大气硫源具有指示意义,鄱阳湖生态经济区大气硫沉降的硫源主要来自人为成因硫和生物成因硫,可能还有远距离传输硫等其他硫源的影响。 服务 把本文推荐给朋友 加入我的书架 加入引用管理器 E-mail Alert RSS 作者相关文章 胡菲菲 潘家永 张良 谢淑容 陈益平 夏菲 关键词 : 石生苔藓, 硫同位素, 大气硫源 Abstract: The variation of atmospheric sulfur sources in Poyang Lake Eco-economic Region was explored by sulfur isotopes in epilithic mosses which collected from the research area during 2012 to 2013, and then compared it with the existing research δ34S values of rain and coal. The results showed that all of the δ34S values of epilithic mosses performed as positive value at a range of 1.9‰ to 9.6‰, the average was 4.9‰. It was found a significant negative correlation existed between the δ34S values of epilithic mosses (x and atmospheric SO2 concentration (y (y=-82.61x+7.63, R2=0.85. The δ34S values of epilithic mosses in Nanchang and Fuzhou were close to the δ34S values of its corresponding city’s atmospheric precipitation. The δ34S values of soil total sulfur were higher than that of epilithic mosses

  19. Heavy metals and trace elements in atmospheric fall-out: Their relationship with topsoil and wheat element composition

    Energy Technology Data Exchange (ETDEWEB)

    Bermudez, Gonzalo M.A., E-mail: gbermudez@com.uncor.edu [Instituto Multidisciplinario de Biologia Vegetal (IMBIV), CONICET (Argentina); Catedra de Quimica General, FCEFyN, Universidad Nacional de Cordoba, Avda. Velez Sarsfield 1611, Ciudad Universitaria (X5016 GCA), Cordoba (Argentina); Jasan, Raquel; Pla, Rita [Tecnicas Analiticas Nucleares, Comision Nacional de Energia Atomica (CAE), Presbitero Gonzalez y Aragon N Degree-Sign 15 (B1802AYA), Ezeiza (Argentina); Pignata, Maria L. [Instituto Multidisciplinario de Biologia Vegetal (IMBIV), CONICET (Argentina); Catedra de Quimica General, FCEFyN, Universidad Nacional de Cordoba, Avda. Velez Sarsfield 1611, Ciudad Universitaria (X5016 GCA), Cordoba (Argentina)

    2012-04-30

    Highlights: Black-Right-Pointing-Pointer Metal and trace element deposition rates and concentrations in bulk samples. Black-Right-Pointing-Pointer Anthropogenic vs. natural sources were identified using enrichment factors and PCA. Black-Right-Pointing-Pointer Anthropogenic sources for Ca, Cd, Cu, Fe, Mn, Ni, Pb, Sb, U, Zn and lanthanides. Black-Right-Pointing-Pointer Main sources were a cement plant, chemical-mechanical industries, cities and mining. Black-Right-Pointing-Pointer Metals in wheat grain were predicted by soil and bulk deposition composition. - Abstract: The objectives of this study were to determine the average concentrations and deposition rates of 28 elements in atmospheric bulk deposition and to elucidate associations among topsoil, bulk deposition and wheat element composition. The fluxes of arsenic (As), copper (Cu), lead (Pb) and zinc (Zn) deposition in Cordoba were higher than in other agro-ecosystems, which reflects both natural (geochemistry and topsoil removal) and anthropogenic sources. High lanthanide, uranium (U) and thorium (Th) concentrations revealed the impact of an open cast uranium mine. The highest enrichment factors (EF) were those of Cu, Pb, Zn and nickel (Ni), with calcium (Ca) being the most prominent in the surroundings of a cement plant. Industries and the transport of airborne urban pollutants were the main anthropogenic sources for Ca, Cu, Ni, Pb, Zn, cadmium (Cd), iron (Fe), manganese (Mn) and antimony (Sb). The concentrations of metals in wheat grain were predicted using the topsoil and atmospheric fall-out composition with R{sup 2} = 0.90, with the latter being the best explanatory variable. The present study highlights the potential health hazards of wheat consumption (Environmental Protection Agency) by the assessment of heavy metals in bulk atmospheric deposition.

  20. The Relation of Stratospheric Aerosols with Trace Gases and Temperature%平流层气溶胶与多种微量气体以及温度的关系

    Institute of Scientific and Technical Information of China (English)

    蔡宏珂; 郭静超; 周任君; 刘鹏兵; 傅云飞

    2011-01-01

    The HALOE (Halogen Occultation Experiment) dataset is used to study the relation of stratospheric aerosols with trace gases (O3, H2O, HC1, NOX, CH4, and HF) and temperature in a period of relative volcanic quiescence. The lag-correlation analysis shows trace gases and temperature are significantly related to aerosol surface area density. Characteristics of the relevance vary with different components. Temperature is negatively correlated with aerosol for 70 - 20 hPa over low-and mid-latitudes. Standardized multiple linear regression demonstrates that greenhouse gases are the primary direct contributor for temperature change, and the direct contribution of aerosols is much less. The impact of aerosols on the stratosphere is simulated with the two-dimensional model SOCRATES (Simulation of Chemistry, Radiation, and Transport of Environmentally important Species). The response of trace gases and temperature coincides with the analysis of the HALOE. The rangeability of temperature is much less than that of aerosols. The result suggests that the stratospheric heterogeneous processes on aerosol surfaces are important for the relation between aerosols and trace gases in the aerosol-enriched layers. The radiation effect of aerosolsis cooling in the period of relative volcanic quiescence, which is different from the warming effect after volcanic eruptions. The phenomenon depends on the aerosol contents. The indirect radiation effect via heterogeneous processes is stronger than the direct effect of aerosols themselves, but the total radiation effect makes little impact on temperature.%本文采用卤素掩星试验(Halogen Occultation Experiment,HALOE)资料探讨了火山活动相对平静期平流层气溶胶与O3、H2O、HC1、NOx、CH4、HF等微量气体以及温度的关系.滞后相关分析显示气溶胶与微量气体和温度有显著关系,不同成分的相关性特征有所差异,中低纬度上空70~20 hPa高度上气溶胶与温度旱负相关.标准化多

  1. Atmospheric trace metals in the snow layers deposited at the South Pole from 1928 to 1977

    Energy Technology Data Exchange (ETDEWEB)

    Boutron, C.

    1982-01-01

    Forty-seven successive dated snow samples, covering a 50 y continuous time sequence between 1928 and 1977 with a time resolution of approximately one sample per year, have been collected using stringent contamination-free techniques from a 10 m deep pit in the clean sector at the geographic South Pole, Antarctica. They have been analyzed for Na, Mg, K, Ca, Fe, Al, Mn, Pb, Cd, Cu, Zn and Ag in clean room conditions by flameless atomic absorption after preconcentration. For all the elements, the concentrations observed in the most recent snow layers are comparable to the ones in the 50 y old snow layers, except for Pb, for which an increase (x4) is observed after 1960 approximately. These data therefore confirm that the influence of global atmospheric pollution is probably still negligible in the remote areas of the southern hemisphere for the 12 measured elements except possibly for Pb after 1960. For this last element, however, an alternative explanation of the post-1960 increase could be that the post-1960 snow layers have been contaminated by operations at Amundsen Scott station, which has been occupied since 1957.

  2. Degradation and emission of carbonyl sulfide, an atmospheric trace gas, by fungi isolated from forest soil.

    Science.gov (United States)

    Masaki, Yoshihito; Ozawa, Rie; Kageyama, Kei; Katayama, Yoko

    2016-09-01

    Soil is thought to be important both as a source and a sink of carbonyl sulfide (COS) in the troposphere, but the mechanism affecting COS uptake, especially for fungi, remains uncertain. Fungal isolates that were collected randomly from forest soil showed COS-degrading ability at high frequencies: 38 out of 43 isolates grown on potato dextrose agar showed degradation of 30 ppmv COS within 24 h. Of these isolates, eight degraded 30 ppmv of COS to below the detection limit within 2 h. These isolates also showed an ability to degrade COS included in ambient air (around 500 pptv) and highly concentrated (12 500 ppmv) level, even though the latter is higher than the lethal level for mammals. COS-degrading activity was estimated by using ergosterol as a biomass index for fungi. Trichoderma sp. THIF08 had the highest COS-degrading activity of all the isolates. Interestingly, Umbelopsis/Mortierella spp. THIF09 and THIF13 were unable to degrade 30 ppmv COS within 24 h, and actually emitted COS during the cultivation in ambient air. These results indicate a fungal contribution to the flux of COS between the terrestrial and atmospheric environments.

  3. Technical Note: A trace gas climatology derived from the Atmospheric Chemistry Experiment Fourier Transform Spectrometer dataset

    Directory of Open Access Journals (Sweden)

    A. Jones

    2011-11-01

    Full Text Available The Atmospheric Chemistry Experiment-Fourier Transform Spectrometer (ACE-FTS aboard the Canadian satellite SCISAT (launched in August 2003 was designed to investigate the composition of the upper troposphere, stratosphere, and mesosphere. ACE-FTS utilizes solar occultation to measure temperature and pressure as well as vertical profiles of over thirty chemical species including O3, H2O, CH4, N2O, CO, NO, NO2, N2O5, HNO3, HCl, ClONO2, CCl3F, CCl2F2, and HF. Global coverage for each species is obtained approximately over a three month period and measurements are made with a vertical resolution of typically 3–4 km. A quality-controlled climatology has been created for each of these 14 baseline species, where individual profiles are averaged over the period of February 2004 to February 2009. Measurements used are from the ACE-FTS version 2.2 data set including updates for O3 and N2O5. The climatological fields are provided on a monthly and three-monthly basis (DJF, MAM, JJA, SON at 5 degree latitude and equivalent latitude spacing and on 28 pressure surfaces (26 of which are defined by the Stratospheric Processes And their Role in Climate (SPARC Chemistry Climate Model validation activity. The ACE-FTS climatological dataset is available through the ACE website.

  4. Parameterization of the Absorption of the H2O Continuum, CO2, O2, and Other Trace Gases in the Fu-Liou Solar Radiation Program

    Institute of Scientific and Technical Information of China (English)

    ZHANG Feng; ZENG Qingcun; Y.GU; K.N.LIOU

    2005-01-01

    The absorption properties of the water vapor continuum and a number of weak bands for H2O, O2, CO2,CO, N2O, CH4, and O3 in the solar spectrum are incorporated into the Fu-Liou radiation parameterization program by using the correlated k-distribution method (CKD) for the sorting of absorption lines. The overlap absorption of the H2O lines and the H2O continuum (2500-14500 cm-1) are treated by taking the two gases as a single-mixture gas in transmittance calculations. Furthermore, in order to optimize the computation efforts, CO2 and CH4 in the spectral region 2850-5250 cm-1 are taken as a new singlemixture gas as well. For overlap involving other absorption lines in the Fu-Liou spectral bands, the authors adopt the multiplication rule for transmittance computations under which the absorption spectra for two gases are assumed to be uncorrelated. Compared to the line-by-line (LBL) computation, it is shown that the errors in fluxes introduced by these two approaches within the context of the CKD method are small and less than 0.48% for the H2O line and continuum in the 2500-14500 cm-1 solar spectral region, ~1% for H2O (line)+H2O (continuum)+CO2+CH4 in the spectral region 2850-5250 cm-1, and ~1.5% for H2O (line)+H2O (continuum)+O2 in the 7700-14500 cm-1 spectral region. Analysis also demonstrates that the multiplication rule over a spectral interval as wide as 6800 cm-1 can produce acceptable errors with a maximum percentage value of about 2% in reference to the LBL calculation. Addition of the preceding gases increases the absorption of solar radiation under all sky conditions. For clear sky, the increase in instantaneous solar absorption is about 9%-13% (~12 W m-2) among which the H2O continuum produces the largest increase, while the contributions from O2 and CO2 rank second and third, respectively. In cloudy sky, the addition of absorption amounts to about 6-9 W m-2. The new, improved program with the incorporation of the preceding gases produces a smaller

  5. Biomass burning emissions and potential air quality impacts of volatile organic compounds and other trace gases from fuels common in the US

    Science.gov (United States)

    Gilman, J. B.; Lerner, B. M.; Kuster, W. C.; Goldan, P. D.; Warneke, C.; Veres, P. R.; Roberts, J. M.; de Gouw, J. A.; Burling, I. R.; Yokelson, R. J.

    2015-12-01

    A comprehensive suite of instruments was used to quantify the emissions of over 200 organic gases, including methane and volatile organic compounds (VOCs), and 9 inorganic gases from 56 laboratory burns of 18 different biomass fuel types common in the southeastern, southwestern, or northern US. A gas chromatograph-mass spectrometry (GC-MS) instrument provided extensive chemical detail of discrete air samples collected during a laboratory burn and was complemented by real-time measurements of organic and inorganic species via an open-path Fourier transform infrared spectroscopy (OP-FTIR) instrument and three different chemical ionization-mass spectrometers. These measurements were conducted in February 2009 at the US Department of Agriculture's Fire Sciences Laboratory in Missoula, Montana and were used as the basis for a number of emission factors reported by Yokelson et al. (2013). The relative magnitude and composition of the gases emitted varied by individual fuel type and, more broadly, by the three geographic fuel regions being simulated. Discrete emission ratios relative to carbon monoxide (CO) were used to characterize the composition of gases emitted by mass; reactivity with the hydroxyl radical, OH; and potential secondary organic aerosol (SOA) precursors for the 3 different US fuel regions presented here. VOCs contributed less than 0.78 % ± 0.12 % of emissions by mole and less than 0.95 % × 0.07 % of emissions by mass (on average) due to the predominance of CO2, CO, CH4, and NOx emissions; however, VOCs contributed 70-90 (±16) % to OH reactivity and were the only measured gas-phase source of SOA precursors from combustion of biomass. Over 82 % of the VOC emissions by mole were unsaturated compounds including highly reactive alkenes and aromatics and photolabile oxygenated VOCs (OVOCs) such as formaldehyde. OVOCs contributed 57-68 % of the VOC mass emitted, 41-54 % of VOC-OH reactivity, and aromatic-OVOCs such as benzenediols, phenols, and benzaldehyde

  6. Observations of ambient trace gas and PM10 concentrations at Patna, Central Ganga Basin during 2013-2014: The influence of meteorological variables on atmospheric pollutants

    Science.gov (United States)

    Tiwari, S.; Tunved, P.; Hopke, Philip K.; Srivastava, A. K.; Bisht, D. S.; Pandey, A. K.

    2016-11-01

    Atmospheric pollutants including ozone (O3), sulfur dioxide (SO2), oxides of nitrogen (NOx), carbon monoxide (CO), and inhalable particulate matter (PM10) were measured in the central Indo-Gangetic Basin (IGB) at Patna, India, from 1st March 2013 to 31st December 2014, and significant variability was observed in the temporal patterns of these pollutant concentrations. The mean O3, SO2, NO, NO2, CO (trace gases: TG), and PM10 (PM) concentrations were 14.5 ± 4.8, 5.9 ± 4.8, 23.1 ± 22, 20.6 ± 14.6 ppb, 1.5 ± 0.7 ppm, and 192.0 ± 132.8 μg/m3, respectively, over the study period. The highest concentrations of these species were during the post-monsoon and winter seasons except O3 and SO2 that showed the highest concentrations during the pre-monsoon. The lowest concentrations of TG and PM were observed during the monsoon season as a result of scavenging by rain. NO and NO2 along with PM concentrations decreased by ~ 76, 19, and 63% when the wind speed (WS) was > 0.5 m/s. However, for O3, an opposite trend was observed with ~ 14% higher concentrations. The WS was negatively correlated with PM during the winter (- 0.48) and post-monsoon (- 0.32) seasons. In order to investigate the source region of TG and PM, 5-day air mass back trajectories were computed. The dominance of the air masses (92, 53, and 49%) were from the IGB is highly polluted during the winter, pre-monsoon, and post-monsoon, respectively. The TG and PM were observed much higher during these periods. During the biomass burning period (post-monsoon), the trajectory analysis showed that the TG and PM concentrations were around three-fold higher (flow from the IGB) than the other seasons. To improve air quality over IGB, the mitigation measures should be designed to reduce emissions from both local and regional sources.

  7. Are coarse particles unexpected common reservoirs for some atmospheric anthropogenic trace elements? A case study

    Science.gov (United States)

    Catinon, Mickaël; Ayrault, Sophie; Boudouma, Omar; Bordier, Louise; Agnello, Gregory; Reynaud, Stéphane; Tissut, Michel

    2013-08-01

    Without specific experimental equipment, it is very difficult to sample long-term atmospheric deposits on a pure state. That is why the composition of air-transferred solid material accumulated for 40 years in the 2 m-high walls, pierced with numerous holes of an outdoor public shelter, Grenoble city, France, was studied. An appropriate fractionation procedure allowed to obtain several fractions which were i) a sand fraction (8.3%) (fraction A), ii) a large mass of organic matter corresponding mostly to large fragments (>250 μm) of plant origin (66.7%) (fraction B) or to pollen fraction C (0.4%), iii) a slowly depositing organo-clay fraction (20%) (fractions D1 and D2) and iv) a solution mixed with non-settable particles (4.3%) (fraction E). The composition of each fraction was determined for 20 elements. The sand fraction showed very high concentrations specifically in Cu, Pb and Fe corresponding respectively to 81.5, 48.2 and 35.2% of the samples content in these elements. In contrast, Cd and Zn were mainly accumulated in the fraction B (67.5 and 62.2%, respectively). The scanning electron microscopy coupled to energy dispersive X-ray analysis (SEM-EDX) study of the fraction A showed the presence of large particles bearing Pb and Fe, particles rich in Cu and typical fly ashes originating mostly from iron industry. Most of these particles had a crystalline shape suggesting that they were formed after emission at a high temperature. The Pb-Fe-Cu deposit seen in fraction A likely originates from the neighbouring road surface contaminated by car traffic for several decades. The 206Pb/207Pb ratio (1.146 ± 0.004) showed that in the coarse sandy fraction A, Pb was represented at 65% by non-gasoline lead and 35% by "gasoline" lead emitted before 1999. The fraction A particles can only be transported on a limited distance by high magnitude events. They constitute a large reservoir for Cu and Pb and may play a major role in the long-term contamination of urban soils.

  8. Study on the effect of atmospheric gases adsorbed in MnFe2O4/MCM-41 nanocomposite on ortho-positronium annihilation

    Directory of Open Access Journals (Sweden)

    Wiertel Marek

    2015-12-01

    Full Text Available In this paper, results of positron annihilation lifetime spectroscopy (PALS studies of MnFe2O4/MCM-41 nanocomposites in N2 and O2 atmosphere have been presented. In particular, the influence of manganese ferrite loading and gas filling on pick-off ortho-positronium (o-Ps annihilation processes in the investigated samples was a point of interest. Disappearance of the longest-lived o-Ps component with τ5 present in the PAL spectrum of initial MCM-41 mesoporous material in the PAL spectra of MnFe2O4-impregnated MCM-41 measured in vacuum is a result of either a strong chemical o-Ps quenching or the Ps inhibition effects. The intensity I4 of the medium-lived component initially increases, reaching a maximum value for the sample with minimum manganese ferrite content, and then decreases monotonically. Analogous dependence for the intensity I3 of the shortest-lived component shows a maximum at higher MnFe2O4 content. Filling of open pores present in the studied nanocomposites by N2 or O2 at ambient pressure causes partial reappearance of the τ4 and τ5 components, except a sample with maximum ferrite content. The lifetimes of these components measured in O2 are shortened in comparison to that observed in N2 because of paramagnetic quenching. Anti-inhibition and anti-quenching effects of atmospheric gases observed in the MnFe2O4/MCM-41 samples are a result of neutralization of some surface active centers acting as inhibitors and weakening of pick-off annihilation mechanism, respectively.

  9. Measurements of several atmospheric gases above the South Pole in December 1986 from high-resolution 3- to 4-micron solar spectra

    Science.gov (United States)

    Goldman, Aaron; Murcray, Frank J.; Murcray, Frank H.; Murcray, David G.; Rinsland, Curtis P.

    1988-01-01

    This paper reports the quantitative analysis of absorption features of a number of atmospheric gases in 0.02/cm resolution 3- to 4-micron solar spectra recorded at the Amundsen-Scott South Pole Station. The measurements were obtained shortly after the austral spring ozone minimum and define, for the first time, the ambient levels of the species immediately following the breakup of the polar vortex. The retrieved total vertical column amounts in molecules per sq cm are: 2.4 + or - 0.4 x 10 to the 21st for H2(O-16), 4.5 + or - 0.5 x 10 to the 18th for H2(O-18), 3.9 + or - 0.4 x 10 to the 17th for HDO, 2.1 + or - 0.2 x 10 to the 19th for CH4, 5.1 + or - 0.5 x 10 to the 21st for CO2, 3.9 + or - 0.4 x 10 to the 18th for N2O, and 3.7 + or - 0.5 x 10 to the 15th for C2H6. Identification of (C-12)H3D absorption features and a search for H2CO absorption in the spectral data are also described.

  10. Effects of ploughing on land-atmosphere exchange of greenhouse gases in a managed temperate grassland in central Scotland

    Science.gov (United States)

    Helfter, Carole; Drewer, Julia; Anderson, Margaret; Scholtes, Bob; Rees, Bob; Skiba, Ute

    2015-04-01

    Grasslands are important ecosystems covering > 20% and > 30% of EU and Scotland's land area respectively. Management practices such as grazing, fertilisation and ploughing can have significant short- and long-term effects on greenhouse gas exchange. Here we report on two separate ploughing events two years apart in adjacent grasslands under common management. The Easter Bush grassland, located 10 km south of Edinburgh (55° 52'N, 3° 2'W), comprises two fields separated by a fence and is used for grazing by sheep and cattle. The vegetation is predominantly Lolium perenne (> 90%) growing on poorly drained clay loam. The fields receive several applications of mineral fertiliser a year in spring and summer. Net ecosystem exchange (NEE) of carbon dioxide (CO2) has been monitored continuously by eddy-covariance (EC) since 2002 which has demonstrated that the site is a consistent yet variable sink of atmospheric CO2. The EC system comprises a LI-COR 7000 closed-path analyser and a Gill Instruments Windmaster Pro ultrasonic anemometer mounted atop a 2.5 m mast located along the fence line separating the fields. In addition, fluxes of nitrous oxide (N2O), methane (CH4)and CO2were measured with static chambers installed along transects in each field. Gas samples collected from the chambers were analysed by gas chromatography and fluxes calculated for each 60-minute sampling period. The ploughing events in 2012 and 2014 exhibited multiple similarities in terms of NEE. The light response (i.e. relationship between CO2 flux, and photosynthetically active radiation, PAR) of the NF and SF during the month preceding each ploughing event was of comparable magnitude in both years. Following ploughing, CO2 uptake ceased in the ploughed field for approximately one month and full recovery of the photosynthetic potential was observed after ca. 2 months. During the month following the 2014 ploughing event, the ploughed NF released on average 333 ± 17 mg CO2-C m-2 h-1. In contrast, the

  11. The impact of atmospheric dust deposition and trace elements levels on the villages surrounding the former mining areas in a semi-arid environment (SE Spain)

    Science.gov (United States)

    Sánchez Bisquert, David; Matías Peñas Castejón, José; García Fernández, Gregorio

    2017-03-01

    It is understood that particulate matter in the atmosphere from metallic mining waste has adverse health effects on populations living nearby. Atmospheric deposition is a process connecting the mining wasteswith nearby ecosystems. Unfortunately, very limited information is available about atmospheric deposition surrounding rural metallic mining areas. This article will focus on the deposition from mining areas, combined with its impact on nearby rural built areas and populations. Particle samples were collected between June 2011 and March 2013. They were collected according to Spanish legislation in ten specialised dust collectors. They were located near populations close to a former Mediterranean mining area, plus a control, to assess the impact of mining waste on these villages. This article and its results have been made through an analysis of atmospheric deposition of these trace elements (Mn, Zn, As, Cd and Pb). It also includes an analysis of total dust flux. Within this analysis it has considered the spatial variations of atmospheric deposition flux in these locations. The average annual level of total bulk deposition registered was 42.0 g m-2 per year. This was higher than most of the areas affected by a Mediterranean climate or in semi-arid conditions around the world. Regarding the overall analysis of trace elements, the annual bulk deposition fluxes of total Zn far exceeded the values of other areas. While Mn, Cd and Pb showed similar or lower values, and in part much lower than those described in other Mediterranean mining areas. This study confirmed some spatial variability of dust and trace elements, contained within the atmospheric deposition. From both an environmental and a public health perspective, environmental managers must take into account the cumulative effect of the deposition of trace elements on the soil and air quality around and within the villages surrounding metallic mining areas.

  12. Nighttime chemical evolution of aerosol and trace gases in a power plant plume: Implications for secondary organic nitrate and organosulfate aerosol formation, NO3 radical chemistry, and N2O5 heterogeneous hydrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Zaveri, R.A.; Kleinman, L.; Berkowitz, C. M.; Brechtel, F. J.; Gilles, M. K.; Hubbe, J. M.; Jayne, J. T.; Laskin, A.; Madronich, S.; Onasch, T. B.; Pekour, M. S.; Springston, S. R.; Thornton, J. A.; Tivanski, A. V.; Worsnop, D. R.

    2010-06-01

    Nighttime chemical evolution of aerosol and trace gases in a coal-fired power plant plume was monitored with the Department of Energy Grumman Gulfstream-1 aircraft during the 2002 New England Air Quality Study field campaign. Quasi-Lagrangian sampling in the plume at increasing downwind distances and processing times was guided by a constant-volume balloon that was released near the power plant at sunset. While no evidence of fly ash particles was found, concentrations of particulate organics, sulfate, and nitrate were higher in the plume than in the background air. The enhanced sulfate concentrations were attributed to direct emissions of gaseous H{sub 2}SO{sub 4}, some of which had formed new particles as evidenced by enhanced concentrations of nucleation-mode particles in the plume. The aerosol species were internally mixed and the particles were acidic, suggesting that particulate nitrate was in the form of organic nitrate. The enhanced particulate organic and nitrate masses in the plume were inferred as secondary organic aerosol, which was possibly formed from NO{sub 3} radical-initiated oxidation of isoprene and other trace organic gases in the presence of acidic sulfate particles. Microspectroscopic analysis of particle samples suggested that some sulfate was in the form of organosulfates. Microspectroscopy also revealed the presence of sp{sup 2} hybridized C = C bonds, which decreased with increasing processing time in the plume, possibly because of heterogeneous chemistry on particulate organics. Constrained plume modeling analysis of the aircraft and tetroon observations showed that heterogeneous hydrolysis of N{sub 2}O{sub 5} was negligibly slow. These results have significant implications for several issues related to the impacts of power plant emissions on air quality and climate.

  13. Atmospheric dry deposition of mineral dust to the Gulf of Aqaba, Red Sea: rate and trace elements.

    Science.gov (United States)

    Al-Taani, Ahmed A; Rashdan, Maen; Khashashneh, Safaa

    2015-03-15

    Atmospheric dry deposition to the Gulf of Aqaba (GoA) is particularly a significant source of trace elements. Amid desert regions, the Gulf receives high fluxes of mineral dust with an average rate of 34.68 g/m(2)/year measured in 2012. Patterns of dry deposition showed seasonal fluxes with highest rates observed in summer and lowest in winter. The observed variations were attributed to wind direction, timing of deposition and sources of dust. The average dry fluxes of Al, Fe, Mn, Cr, Cd, Cu, Pb and Zn were 551, 440, 10.29, 1.42, 0.04, 0.68, 1.42 and 4.02 mg/m(2)/year, respectively. While the dry deposition fluxes were enriched in Cd, Cu, Pb and Zn indicating their dominant anthropogenic sources, they appeared to be less influenced compared to the neighboring Mediterranean area and other industrial countries, but were similar to or slightly higher than those in remote areas. The enrichment values for Fe and Mn were low, consistent with their crustal origin. The fluxes of all elements suggested the impacts of both crustal (due to climate change) and anthropogenic sources became stronger in this region. The Sahara dust was probably a minor contributor to dry deposition in the GoA.

  14. Assessment of atmospheric trace element concentrations by lichen-bag near an oil/gas pre-treatment plant in the Agri Valley (southern Italy

    Directory of Open Access Journals (Sweden)

    R. Caggiano

    2014-10-01

    Full Text Available The atmospheric concentrations of 17 trace elements (Al, Ca, Cd, Cr, Cu, Fe, K, Li, Mg, Mn, Na, Ni, P, Pb, S, Ti and Zn were measured by means of the "lichen-bag" technique in the Agri Valley (southern Italy. The lichen samples were collected from an unpolluted site located in Rifreddo forest (southern Italy. The bags were exposed to ambient air for 6 and 12 months. The exposed-to-control (EC ratio values highlighted that the used lichen species were suitable for biomonitoring investigations. The results showed that the concentrations of almost all the examined trace elements increased with respect to the control after 6–12 month exposures. Furthermore, Ca, Al, Fe, K, Mg and S were the most abundant trace elements both in the 6 and 12 month-exposed samples. Moreover, principal component analysis (PCA results highlighted that the major sources of the measured atmospheric trace elements were related both to anthropogenic contributions due to traffic, combustion processes, agricultural practices, construction and quarrying activities, and to natural contributions mainly represented by the re-suspension of local soil and road dusts. In addition, the contribution both of secondary atmospheric reactions involving Centro Olio Val d'Agri (COVA plant emissions and the African dust long-range transport were also identified.

  15. Assessment of atmospheric trace element concentrations by lichen-bag near an oil/gas pre-treatment plant in the Agri Valley (southern Italy)

    Science.gov (United States)

    Caggiano, R.; Trippetta, S.; Sabia, S.

    2015-02-01

    The atmospheric concentrations of 17 trace elements (Al, Ca, Cd, Cr, Cu, Fe, K, Li, Mg, Mn, Na, Ni, P, Pb, S, Ti and Zn) were measured by means of the "lichen-bag" technique in the Agri Valley (southern Italy). The lichen samples were collected from an unpolluted site located in Rifreddo forest (southern Italy), about 30 km away from the study area along the north direction. The bags were exposed to ambient air for 6 and 12 months. The exposed-to-control (EC) ratio values highlighted that the used lichen species were suitable for biomonitoring investigations. The results showed that the concentrations of almost all the examined trace elements increased with respect to the control after 6-12-month exposures. Furthermore, Ca, Al, Fe, K, Mg and S were the most abundant trace elements both in the 6-month and 12-month-exposed samples. Moreover, principal component analysis (PCA) results highlighted that the major sources of the measured atmospheric trace elements were related both to anthropogenic contributions due to traffic, combustion processes agricultural practices, construction and quarrying activities, and to natural contributions mainly represented by the re-suspension of local soil and road dusts. In addition, the contribution both of secondary atmospheric reactions involving Centro Olio Val d'Agri (COVA) plant emissions and the African dust long-range transport were also identified.

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

    Science.gov (United States)

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

    2016-02-01

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

  17. Impact of western Siberia heat wave 2012 on greenhouse gases and trace metal concentration in thaw lakes of discontinuous permafrost zone

    Directory of Open Access Journals (Sweden)

    O. S. Pokrovsky

    2013-08-01

    Full Text Available During the anomalously hot summer in 2012, surface air temperatures in Western Siberia were 5 to 15 °C higher than those observed during the previous period of > 30 yr. This unusual climate phenomenon provided an opportunity to examine the effects of short-term natural heating of water in thermokarst ponds and lakes in discontinuous permafrost zones and compare these observations to previous field results obtained when the temperature was normal during the summer of 2010 in the same region. In 2012, thermokarst bodies of water shrank significantly, water levels dropped approximately 50 cm in large lakes and small (2 ponds, and shallow soil depressions disappeared. Based on samples from ~ 40 bodies of water collected previously and in 2012, first-order features of changes in chemical composition in response to increased water temperatures (from 14.1 ± 2.2 to 23.8 ± 2.3 °C in 2010 and 2012, respectively were established. In these thermokarst bodies of water that covered a full range of surface areas, the average conductivity and pH were almost unchanged, whereas dissolved organic carbon (DOC, Cl- and SO42- concentrations were higher by a factor of ~ 2 during summer 2012 compared to periods with normal temperatures. Similarly, most divalent metals and insoluble trivalent and tetravalent elements were more concentrated by a factor of 1.7–2.4 in the summer of 2012 than normal periods. The average concentrations of dissolved CO2 and CH4 during the hot summer of 2012 increased by factors of 1.4 and 4.9, respectively. For most of the trace elements bound to colloids, the degree of colloidal binding decreased by a factor of 1.44 ± 0.33 (for an average of 40 elements during the hot summer of 2012 compared to normal periods. Increases in CO2 and CH4 concentrations with the decreasing size of the body of water were well-pronounced during the hot summer of 2012. The concentrations of CO2 and CH4 rose by factors of 5 and 150, respectively, in small (

  18. Stratospheric and mesospheric pressure-temperature profiles from rotational analysis of CO2 lines in atmospheric trace molecule spectroscopy/ATLAS 1 infrared solar occultation spectra

    Science.gov (United States)

    Stiller, G. P.; Gunson, M. R.; Lowes, L. L.; Abrams, M. C.; Raper, O. F.; Farmer, C. B.; Zander, R.; Rinsland, C. P.

    1995-01-01

    A simple, classical, and expedient method for the retrieval of atmospheric pressure-temperature profiles has been applied to the high-resolution infrared solar absorption spectra obtained with the atmospheric trace molecule spectroscopy (ATMOS) instrument. The basis for this method is a rotational analysis of retrieved apparent abundances from CO2 rovibrational absorption lines, employing existing constituent concentration retrieval software used in the analysis of data returned by ATMOS. Pressure-temperature profiles derived from spectra acquired during the ATLAS 1 space shuttle mission of March-April 1992 are quantitatively evaluated and compared with climatological and meteorological data as a means of assessing the validity of this approach.

  19. Microbial production and consumption of greenhouse gases: methane, nitrogen oxides, and halomethanes

    Energy Technology Data Exchange (ETDEWEB)

    Rogers, J.E.; Whitman, W.B.

    1991-01-01

    The aim is to provide an overview of the biological processes that contribute to the increase in trace gases (CH[sub 4], N[sub 2]O, NO[sub x] and halocarbons) in the atmosphere. Physical and chemical processes are discussed as they relate to biological processes. It is an introduction to biological processes that contribute to changes in global climate and processes that can be influenced by biofeedback mechanisms as climate changes occur.

  20. On-line, real time monitoring of exhaled trace gases by SIFT-MS in the perioperative setting: a feasibility study.

    Science.gov (United States)

    Boshier, Piers R; Cushnir, Julia R; Mistry, Vikash; Knaggs, Alison; Španěl, Patrik; Smith, David; Hanna, George B

    2011-08-21

    A study is described of the first on line, real time analyses of the exhaled breath of five anaesthetized patients during the complete perioperative periods of laparoscopic surgery. These breath analyses were achieved using a selected ion flow tube, SIFT-MS, instrument, located in the operating theatre at an acceptable distance from the operating table, and coupled to the endotracheal tube in the ventilation circuit via a 5 metre long capillary tube. Thus, inhalation/exhalation breathing cycles, set to be at a frequency of 10 per minute, were sampled continuously for water vapour, the metabolites acetone and isoprene and the propofol used to induce anaesthesia for each operating period that ranged from 20 min (shortest) to 80 min (longest). Whilst there was some loss of water vapour along the long sampling line, the concentrations of the other trace compounds were not diminished. The breath acetone was essentially at a constant level for each patient, but increased somewhat over the longest operating period due to the onset of lipolysis. Most interesting is the clear increase of breath isoprene following abdomen inflation with carbon dioxide. The vapour of the intravenously injected propofol was detected in the exhaled breath and remained essentially constant during the perioperative period. These analyses were performed totally non-invasively and the data were immediately and constantly available to the anaesthetist and surgeon. Exploitation of this development could influence decision making and potentially improve patient safety within the perioperative setting.

  1. Real-time profiling of organic trace gases in the planetary boundary layer by PTR-MS using a tethered balloon

    Directory of Open Access Journals (Sweden)

    R. Schnitzhofer

    2009-12-01

    Full Text Available A method for real-time profiling of volatile organic compounds (VOCs was developed combining the advantages of a tethered balloon as a research platform and of proton transfer reaction mass spectrometry (PTR-MS as an analytical technique for fast and highly sensitive VOC measurements. A 200 m Teflon tube was used to draw sampling air from a tethered aerodynamic balloon to the PTR-MS instrument. Positive and negative artefacts (i.e. formation and loss of VOCs in the tube were characterised in the laboratory and in the field by a set of 11 atmospherically relevant VOCs including both pure and oxygenated hydrocarbons. The only two compounds that increased or decreased when sampled through the tube were acetone (+7% and xylene (-6%. The method was successfully deployed during a winter field campaign to determine the small scale spatial and temporal patterns of air pollutants under winter inversion conditions.

  2. Transport and build-up of tropospheric trace gases during the MINOS campaign: comparision of GOME, in situ aircraft measurements and MATCH-MPIC-data

    Directory of Open Access Journals (Sweden)

    A. Ladstätter-Weißenmayer

    2003-01-01

    Full Text Available The MINOS (Mediterranean INtensive Oxidant Study campaign was an international, multi-platform field campaign to measure long-range transport of air-pollution and aerosols from South East Asia and Europe towards the Mediterranean basin during August 2001. High pollution events were observed during this campaign. For the Mediterranean region enhanced tropospheric nitrogen dioxide (NO2 and formaldehyde (HCHO, which are precursors of tropospheric ozone (O3, were detected by the satellite based GOME (Global Ozone Monitoring Experiment instrument and compared with airborne in situ measurements as well as with the output from the global 3D photochemistry-transport model MATCH-MPIC (Model of Atmospheric Transport and CHemistry - Max Planck Institute for Chemistry. The increase of pollution in that region leads to severe air quality degradation with regional and global implications.

  3. Atmospheric composition

    Science.gov (United States)

    Daniels, G. E.

    1973-01-01

    The earth's atmosphere is made up of a number of gases in different relative amounts. Near sea level and up to about 90 km, the amount of these atmospheric gases in clean, relatively dry air is practically constant. Four of these gases, nitrogen, oxygen, argon, and carbon dioxide, make up 99.99 percent by volume of the atmosphere. Two gases, ozone and water vapor, change in relative amounts, but the total amount of these two is very small compared to the amount of the other gases. The atmospheric composition shown in a table can be considered valid up to 90 km geometric altitude. Above 90 km, mainly because of molecular dissociation and diffusive separation, the composition changes.

  4. Role of climate feedback on methane and ozone studied with a coupled ocean-atmosphere-chemistry model.

    OpenAIRE

    Johnson, C E; D. S. Stevenson; Collins, W. J.; R. G. Derwent

    2001-01-01

    We present results from two experiments carried out with a coupled ocean-atmosphere-tropospheric chemistry model run continously over the period 1990 to 2100. In the control experiment, climate is unforced, but emissions of trace gases to the chemical model increase in line with an illustrative scenario for future trace gas emissions with medium high growth. In the climate change experiment trace gas emissions are identical to the control, but climate is also forced using greenhouse gas conce...

  5. Irritant gases

    NARCIS (Netherlands)

    Meulenbelt, J

    2016-01-01

    Acute inhalation injury can result from the use of household cleaning agents (e.g. chlorine, ammonia), industrial or combustion gases (e.g. sulfur dioxide, nitrogen oxides) or bioterrorism. The severity of the injury is to a great extent determined by the circumstances of exposure. If exposure was i

  6. Field measurements of trace gases emitted by prescribed fires in southeastern US pine forests using an open-path FTIR system

    Directory of Open Access Journals (Sweden)

    S. K. Akagi

    2013-07-01

    Full Text Available We report trace-gas emission factors from three pine-understory prescribed fires in South Carolina, US measured during the fall of 2011. The fires were more intense than many prescribed burns because the fuels included mature pine stands not subjected to prescribed fire in decades that were lit following an extended drought. The emission factors were measured with a fixed open-path Fourier transform infrared (OP-FTIR system that was deployed on the fire control lines. We compare these emission factors to those measured with a roving, point sampling, land-based FTIR and an airborne FTIR that were deployed on the same fires. We also compare to emission factors measured by a similar OP-FTIR system deployed on savanna fires in Africa. The data suggest that the method used to sample smoke can strongly influence the relative abundance of the emissions that are observed. The majority of the fire emissions were lofted in the convection column and they were sampled by the airborne FTIR along with the downwind chemistry. The roving, ground-based, point sampling FTIR measured the contribution of actively located individual residual smoldering combustion fuel elements scattered throughout the burn site. The OP-FTIR provided a ~30 m path-integrated sample of emissions transported to the fixed path via complex ground-level circulation. The OP-FTIR typically probed two distinct combustion regimes, "flaming-like" (immediately after adjacent ignition and before the adjacent plume achieved significant vertical development and "smoldering-like." These two regimes are denoted "early" and "late", respectively. The emission factors from all three systems were plotted versus modified combustion efficiency and for some species (e.g. CH4 and CH3OH they fit a single trend suggesting that the different emission factors for these species were mainly due to the specific mix of flaming and smoldering that each system sampled. For other species, the different fuels sampled

  7. Determination of trace rare earth elements in coal fly ash and atmospheric particulates by electrothermal vaporization inductively coupled plasma mass spectrometry with slurry sampling

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Yuefei [Department of Chemistry, Wuhan University, Wuhan, Hubei Province 430072 (China); Jiang Zucheng [Department of Chemistry, Wuhan University, Wuhan, Hubei Province 430072 (China); He Man [Department of Chemistry, Wuhan University, Wuhan, Hubei Province 430072 (China); Hu Bin [Department of Chemistry, Wuhan University, Wuhan, Hubei Province 430072 (China)]. E-mail: binhu@whu.edu.cn

    2007-07-15

    A method of fluorination assisted electrothermal vaporization (FETV)-ICP-MS with polytetrafluoroethylene as fluorinating reagent was developed for the direct determination of trace rare earth elements (REEs) in coal fly ash and atmospheric particulates. Under the optimal conditions, the detection limits for REEs were 0.1 pg m{sup -3}(Eu) to 6.7 pg m{sup -3}(Nd) with the precisions of 4.1%(Yb) to 10%(La) (c = 1 {mu}g L{sup -1}, n = 9). The proposed method was applied to determine trace REEs in coal fly ash, airborne particulates and NIES SRM No. 8 Vehicle Exhaust Particulates. It was found that the determined values for Y, La, Pr and Nd obtained by slurry sampling FETV-ICP-MS with external calibration coincided with that obtained by pneumatic nebulization (PN)-ICP-MS and slurry sampling FETV-ICP-MS with standard addition. However, the determined values for Ce and Sm obtained by slurry sampling FETV-ICP-MS with external calibration were lower than that obtained by PN-ICP-MS and slurry sampling FETV-ICP-MS with standard addition. - A new method for direct determination of trace rare earth elements in coal fly ash and atmospheric particulates by fluorination ETV-ICP-MS with slurry sampling.

  8. Design and application of a mobile ground-based observatory for continuous measurements of atmospheric trace gas and criteria pollutant species

    Science.gov (United States)

    Bush, S. E.; Hopkins, F. M.; Randerson, J. T.; Lai, C.-T.; Ehleringer, J. R.

    2015-08-01

    Ground-based measurements of atmospheric trace gas species and criteria pollutants are essential for understanding emissions dynamics across space and time. Gas composition in the lower 50 m of the atmosphere has the greatest direct impacts on human health as well as ecosystem processes; hence data at this level are necessary for addressing carbon-cycle- and public-health-related questions. However, such surface data are generally associated with stationary measurement towers, where spatial representation is limited due to the high cost of establishing and maintaining an extensive network of measurement stations. We describe here a compact mobile laboratory equipped to provide high-precision, high-frequency, continuous, on-road synchronous measurements of CO2, CO, CH4, H2O, NOx, O3, aerosol, meteorological, and geospatial position data. The mobile laboratory has been deployed across the western USA. In addition to describing the vehicle and its capacity, we present data that illustrate the use of the laboratory as a powerful tool for investigating the spatial structure of urban trace gas emissions and criteria pollutants at spatial scales ranging from single streets to whole ecosystem and regional scales. We assess the magnitude of known point sources of CH4 and also identify fugitive urban CH4 emissions. We illustrate how such a mobile laboratory can be used to better understand emissions dynamics and quantify emissions ratios associated with trace gas emissions from wildfire incidents. Lastly, we discuss additional mobile laboratory applications in health and urban metabolism.

  9. Field measurements of trace gases emitted by prescribed fires in southeastern U.S. pine forests using an open-path FTIR system

    Energy Technology Data Exchange (ETDEWEB)

    Akagi, Sheryl; Burling, Ian R.; Mendoza, Albert; Johnson, Timothy J.; Cameron, Melanie; Griffith, David WT; Paton-Walsh, C.; Weise, David; Reardon, James; Yokelson, Robert J.

    2014-01-08

    We report trace-gas emission factors from three pine-understory prescribed fires in South Carolina, U.S. measured during the fall of 2011. The fires were an attempt to simulate high-intensity burns and the fuels included mature pine stands not frequently subjected to prescribed fire that were lit following a sustained period of drought. In this work we focus on the emission factor measurements made using a fixed open-path gas analyzer Fourier transform infrared (FTIR) system. We compare these emission factors with those measured using a roving, point sampling, land-based FTIR and an airborne FTIR that were deployed on the same fires. We also compare to emission factors measured by a similar open-path FTIR system deployed on savanna fires in Africa. The data suggest that the method in which the smoke is sampled can strongly influence the relative abundance of the emissions that are observed. The airborne FTIR probed the bulk of the emissions, which were lofted in the convection column and the downwind chemistry while the roving ground-based point sampling FTIR measured the contribution of individual residual smoldering combustion fuel elements scattered throughout the burn site. The open-path FTIR provided a fixed path-integrated sample of emissions produced directly upwind mixed with emissions that were redirected by wind gusts, or right after ignition and before the adjacent plume achieved significant vertical development. It typically probed two distinct combustion regimes, “flaming-like” (immediately after adjacent ignition) and “smoldering-like”, denoted “early” and “late”, respectively. The calculated emission factors from open-path measurements were closer to the airborne than to the point measurements, but this could vary depending on the calculation method or from fire to fire given the changing MCE and dynamics over the duration of a typical burn. The emission factors for species whose emissions are not highly fuel dependent (e.g. CH4 and

  10. Investigation of trace gas to aerosol relationships over biomass burning areas using daily satellite observations

    Science.gov (United States)

    Wagner, Thomas; Penning de Vries, Marloes; Zörner, Jan; Beirle, Steffen

    2014-05-01

    The quantification and characterization of aerosols from space is a great challenge. Especially in the presence of clouds and over land surfaces, it is often difficult to distinguish the signals of aerosol scattering from scattering by cloud particles or surface reflection. Instead of deriving aerosol properties directly, satellite observations of tropospheric trace gases, emitted by the same emission sources as the aerosols, can be used to derive additional information on the aerosols. Such observations have two potential advantages: First, from the composition of trace gases, information on the aerosol type can be derived. Second, such observations are possible in the presence of clouds (although usually with reduced sensitivity if the trace gases are located below the cloud). In this feasibility study we investigate the relationship between satellite observations of trace gases (CO, NO2, HCHO, CHOCHO) and AOD (measured from satellite or ground). We also include in our comparison satellite observations of the so called UV aerosol index (UVAI), which is an indicator of the aerosol absorption. Like the trace gas observations, also the UVAI can be retrieved in the presence of clouds. We investigate aerosol-trace gas relationships over biomass burning regions. Depending on their optical properties and altitude distribution such aerosols can have a strong impact on the atmospheric energy budget through direct and indirect effects. We perform correlation analyses for selected AERONET stations and also for larger biomass burning areas by also taking into account satellite observations of fire counts.

  11. Quantification of fluorine traces in solid samples using CaF molecular emission bands in atmospheric air Laser-Induced Breakdown Spectroscopy

    Science.gov (United States)

    Alvarez-Llamas, C.; Pisonero, J.; Bordel, N.

    2016-09-01

    Direct solid determination of trace amounts of fluorine using Laser-Induced Breakdown Spectroscopy (LIBS) is a challenging task due to the low excitation efficiency of this element. Several strategies have been developed to improve the detection capabilities, including the use of LIBS in a He atmosphere to enhance the signal to background ratios of F atomic emission lines. An alternative method is based on the detection of the molecular compounds that are formed with fluorine in the LIBS plasma. In this work, the detection of CaF molecular emission bands is investigated to improve the analytical capabilities of atmospheric air LIBS for the determination of fluorine traces in solid samples. In particular, Cu matrix samples containing different fluorine concentration (between 50 and 600 μg/g), and variable amounts of Ca, are used to demonstrate the linear relationships between CaF emission signal and F concentration. Limits of detection for fluorine are improved by more than 1 order of magnitude using CaF emission bands versus F atomic lines, in atmospheric-air LIBS. Furthermore, a toothpaste powder sample is used to validate this analytical method. Good agreement is observed between the nominal and the predicted fluorine mass-content.

  12. The supply of trace elements from the atmosphere recorded in a natural archive by the example of the Ilas ombrotrophic bog in the White Sea drainage basin

    Science.gov (United States)

    Shevchenko, V. P.; Kusnetsov, O. L.; Politova, N. V.; Zaretskaya, N. E.; Kutenkov, S. A.; Lisitzin, A. P.; Pokrovsky, O. S.

    2015-12-01

    The results of studies are presented for the elemental composition of peat from the Ilas ombrotrophic bog (White Sea drainage basin). The calculations of enrichment factors of trace elements over the section of the bog peat relatively to the average composition of the Earth's continental crust showed that the concentrations of most of chemical elements is determined by the contributions of lithogenic and biogenic sources, and the content of trace elements is equal to the background level. Enrichment growth since the beginning of intense development of European industry until the early 21th century was revealed only for Zn, Sb, Pb, and Cd. These elements were supplied to the bog resulting from long-range air transport and precipitation from the atmosphere. No pronounced heavy-metal contamination caused by the Arkhangelsk agglomeration was revealed for the peat in the Ilas bog.

  13. Noble Gases

    Science.gov (United States)

    Podosek, F. A.

    2003-12-01

    The noble gases are the group of elements - helium, neon, argon, krypton, xenon - in the rightmost column of the periodic table of the elements, those which have "filled" outermost shells of electrons (two for helium, eight for the others). This configuration of electrons results in a neutral atom that has relatively low electron affinity and relatively high ionization energy. In consequence, in most natural circumstances these elements do not form chemical compounds, whence they are called "noble." Similarly, much more so than other elements in most circumstances, they partition strongly into a gas phase (as monatomic gas), so that they are called the "noble gases" (also, "inert gases"). (It should be noted, of course, that there is a sixth noble gas, radon, but all isotopes of radon are radioactive, with maximum half-life a few days, so that radon occurs in nature only because of recent production in the U-Th decay chains. The factors that govern the distribution of radon isotopes are thus quite different from those for the five gases cited. There are interesting stories about radon, but they are very different from those about the first five noble gases, and are thus outside the scope of this chapter.)In the nuclear fires in which the elements are forged, the creation and destruction of a given nuclear species depends on its nuclear properties, not on whether it will have a filled outermost shell when things cool off and nuclei begin to gather electrons. The numerology of nuclear physics is different from that of chemistry, so that in the cosmos at large there is nothing systematically special about the abundances of the noble gases as compared to other elements. We live in a very nonrepresentative part of the cosmos, however. As is discussed elsewhere in this volume, the outstanding generalization about the geo-/cosmochemistry of the terrestrial planets is that at some point thermodynamic conditions dictated phase separation of solids from gases, and that the

  14. "Atmospheric Measurements by Ultra-Light SpEctrometer" (AMULSE) dedicated to vertical profile measurements of greenhouse gases (CO2, CH4) under stratospheric balloons: instrumental development and field application.

    Science.gov (United States)

    Maamary, Rabih; Joly, Lilian; Decarpenterie, Thomas; Cousin, Julien; Dumelié, Nicolas; Grouiez, Bruno; Albora, Grégory; Chauvin, Nicolas; Miftah-El-Khair, Zineb; Legain, Dominique; Tzanos, Diane; Barrié, Joel; Moulin, Eric; Ramonet, Michel; Bréon, François-Marie; Durry, Georges

    2016-04-01

    Human activities disrupt natural biogeochemical cycles such as the carbon and contribute to an increase in the concentrations of the greenhouse gases (carbone dioxide and methane) in the atmosphere. The current atmospheric transport modeling (the vertical trade) still represents an important source of uncertainty in the determination of regional flows of greenhouse gases, which means that a good knowledge of the vertical distribution of CO2 is necessary to (1) make the link between the ground measurements and spatial measurements that consider an integrated concentration over the entire column of the atmosphere, (2) validate and if possible improve CO2 transport model to make the link between surface emissions and observed concentration. The aim of this work is to develop a lightweight instrument (based on mid-infrared laser spectrometry principles) for in-situ measuring at high temporal/spatial resolution (5 Hz) the vertical profiles of the CO2 and the CH4 using balloons (meteorological and BSO at high precision levels (logistics flights. These laser spectrometers are built on recent instrumental developments. Several flights were successfully done in the region Champagne-Ardenne and in Canada recently. Aknowledgments: The authors acknowledge financial supports from CNES, CNRS défi instrumental and the region Champagne-Ardenne.

  15. Ultrapure Gases — From the Production Plant to the Laboratory

    Science.gov (United States)

    Simgen, H.; Zuzel, G.

    2007-03-01

    Radioactive noble gas isotopes are a potential source of background in low-level physics experiments, since they are present in the atmosphere and also in widely used gases produced from the atmosphere. We have studied the 39Ar, 85Kr and 222Rn contamination of commercially available nitrogen using low background proportional counters and a rare gas mass spectrometer. It was found that air separation plants are very effective in removing traces of radioactive noble gases and that the available purity can be significantly higher than commercial specifications. On the other hand the gas handling processes which are necessary to deliver gases from the production plant to the customer are a possible source of re-contaminations and determine in most cases the achievable purity. By simulating these processes under realistic conditions we have establish together with the Italian company `SOL group' a well controlled delivery path which can hold the purity. For the short-lived 222Rn the initial contamination is less critical, because it decays away. Instead the emanation rate of the cryogenic tank was found to determine the achievable purity, since it permanently delivers new 222Rn.

  16. Thermal dissociation atmospheric chemical ionization ion trap mass spectrometry with a miniature source for selective trace detection of dimethoate in fruit juices.

    Science.gov (United States)

    Ouyang, Yongzhong; Zhang, Xinglei; Han, Jing; Guo, Xiali; Zhu, Zhiqiang; Chen, Huanwen; Luo, Liping

    2013-01-21

    A miniature thermal dissociation atmospheric chemical ionization (TDCI) source, coupled with LTQ-MS, has been developed for rapid trace detection of pesticide residues such as dimethoate in highly viscous fruit juice samples. Instead of toxic organic solvents and the high electric field used in the conventional ionizations, an ionic liquid, a "green solvent", was employed to directly generate reagent ions in the TDCI process, followed by the proton or charge transfer with the analytes prior to the LTQ instrument for mass analysis. Trace amounts of dimethoate in fresh orange juices have been quantitatively detected, without any sample pretreatment or aid of high-pressure gas. A low limit of detection (LOD = 8.76 × 10(-11) g mL(-1)), acceptable relative standard deviation (RSD = 3.1-10.0%), and reasonable recoveries (91.2-102.8%) were achieved with this method for direct detection of dimethoate in highly viscous orange juice samples. The average analysis time for each single sample was less than 30 seconds. These experimental results showed that the miniature TDCI developed here is a powerful tool for the fast trace detection of pesticide residues in complex viscous fruit juices, with the advantage of high sensitivity, high speed, and high-throughput, ease of operation, and so on. Because of no chemical contamination and high voltage damage to the analytes and the environment, the technique has promising applications for online quality monitoring in the area of food safety.

  17. Design and application of a mobile ground-based observatory for continuous measurements of atmospheric trace-gas and criteria pollutant species

    Directory of Open Access Journals (Sweden)

    S. E. Bush

    2015-01-01

    Full Text Available Ground-based measurements of atmospheric trace gas species and criteria pollutants are essential for understanding emissions dynamics across space and time. Gas composition in the surface 50 m has the greatest direct impacts on human health as well as ecosystem processes, hence data at this level is necessary for addressing carbon cycle and public health related questions. However, such surface data are generally associated with stationary measurement towers, where spatial representation is limited due to the high cost of establishing and maintaining an extensive network of measurement stations. We describe here a compact mobile laboratory equipped to provide high-precision, high-frequency, continuous, on-road synchronous measurements of CO2, CO, CH4, H2O, NOx, O3, aerosol, meteorological, and geospatial position data. The mobile laboratory has been deployed across the western USA. In addition to describing the vehicle and its capacity, we present data that illustrate the use of the laboratory as a powerful tool for investigating the spatial structure of urban trace gas emissions and criteria pollutants at spatial scales ranging from single streets to whole ecosystem and regional scales. We identify fugitive urban CH4 emissions and assess the magnitude of CH4 emissions from known point sources. We illustrate how such a mobile laboratory can be used to better understand emissions dynamics and quantify emissions ratios associated with trace gas emissions from wildfire incidents. Lastly, we discuss additional mobile laboratory applications in health and urban metabolism.

  18. Design and application of a mobile ground-based observatory for continuous measurements of atmospheric trace-gas and criteria pollutant species

    Science.gov (United States)

    Bush, S. E.; Hopkins, F. M.; Randerson, J. T.; Lai, C.-T.; Ehleringer, J. R.

    2015-01-01

    Ground-based measurements of atmospheric trace gas species and criteria pollutants are essential for understanding emissions dynamics across space and time. Gas composition in the surface 50 m has the greatest direct impacts on human health as well as ecosystem processes, hence data at this level is necessary for addressing carbon cycle and public health related questions. However, such surface data are generally associated with stationary measurement towers, where spatial representation is limited due to the high cost of establishing and maintaining an extensive network of measurement stations. We describe here a compact mobile laboratory equipped to provide high-precision, high-frequency, continuous, on-road synchronous measurements of CO2, CO, CH4, H2O, NOx, O3, aerosol, meteorological, and geospatial position data. The mobile laboratory has been deployed across the western USA. In addition to describing the vehicle and its capacity, we present data that illustrate the use of the laboratory as a powerful tool for investigating the spatial structure of urban trace gas emissions and criteria pollutants at spatial scales ranging from single streets to whole ecosystem and regional scales. We identify fugitive urban CH4 emissions and assess the magnitude of CH4 emissions from known point sources. We illustrate how such a mobile laboratory can be used to better understand emissions dynamics and quantify emissions ratios associated with trace gas emissions from wildfire incidents. Lastly, we discuss additional mobile laboratory applications in health and urban metabolism.

  19. Development and characterization of the superconducting integrated receiver channel of the TELIS atmospheric sounder

    NARCIS (Netherlands)

    De Lange, Gert; Birk, Manfred; Boersma, Dick; Dercksen, Johannes; Dmitriev, Pavel; Ermakov, Andrey B.; Filippenko, Lyudmila V.; Golstein, Hans; Hoogeveen, Ruud W. M.; de Jong, Leo; Khudchenko, Andrey V.; Kinev, Nickolay V.; Kiselev, Oleg S.; van Kuik, Bart; de Lange, Arno; van Rantwijk, Joris; Selig, Avri M.; Sobolev, Alexander S.; Torgashin, Mikhail Yu; de Vries, Ed; Wagner, Georg; Yagoubov, Pavel A.; Koshelets, Valery P.

    2010-01-01

    The balloon-borne instrument TELIS (TErahertz and submillimetre LImb Sounder) is a three-channel superconducting heterodyne spectrometer for atmospheric research use. It detects spectral emission lines of stratospheric trace gases that have their rotational transitions at THz frequencies. One of the

  20. Quantitative sampling and analysis of trace elements in atmospheric aerosols: impactor characterization and Synchrotron-XRF mass calibration

    Directory of Open Access Journals (Sweden)

    A. Richard

    2010-10-01

    Full Text Available Identification of trace elements in ambient air can add substantial information to pollution source apportionment studies, although they do not contribute significantly to emissions in terms of mass. A method for quantitative size and time-resolved trace element evaluation in ambient aerosols with a rotating drum impactor and synchrotron radiation based X-ray fluorescence is presented. The impactor collection efficiency curves and size segregation characteristics were investigated in an experiment with oil and salt particles. Cutoff diameters were determined through the ratio of size distributions measured with two particle sizers. Furthermore, an external calibration technique to empirically link fluorescence intensities to ambient concentrations was developed. Solutions of elemental standards were applied with an ink-jet printer on thin films and area concentrations were subsequently evaluated with external wet chemical methods. These customized and reusable reference standards enable quantification of different data sets analyzed under varying experimental conditions.

  1. Tomographic LP-DOAS measurements of 2D trace gas distributions above the city of Heidelberg, Germany

    Energy Technology Data Exchange (ETDEWEB)

    Poehler, Denis; Hartl, Andreas; Platt, Ulrich [Institute of Environmental Physics, University of Heidelberg (Germany)

    2007-07-01

    LP-DOAS (Long Path-Differential Optical Absorption Spectroscopy) is a well known remote sensing technique for measuring the average concentration of tropospheric trace gases along extended light paths in the open atmosphere. In order to retrieve information of the spatial trace gas distribution tomographic LP-DOAS measurements are useful. They combine the measurement along several intersecting light paths with tomographic inversion techniques and allow 2 and 3 dimensional retrieval of trace gas distributions. In a campaign in Heidelberg, Germany, a measurement set-up encompassing a total of 18 horizontal light paths by using three, Multibeam, LP-DOAS instruments is being tested. In the wavelength range from 285 nm to 365 nm the average concentrations of the trace gases NO{sub 2}, SO{sub 2}, O{sub 3}, HCHO and HONO along each light path could be retrieved with a temporal resolution below 15 minutes. The first evaluated data from winter 2005/06 show high accuracy for NO{sub 2} and SO{sub 2} mean concentrations. They allow deriving for these trace gases twodimensional distributions above the city. Different emission sources varying strongly in space and time can be identified. The results demonstrate that tomographic DOAS measurements can be used to study emissions and transport of trace gases and can be used to evaluate models predicting the air quality.

  2. Worldwide trend of atmospheric mercury since 1995

    Directory of Open Access Journals (Sweden)

    F. Slemr

    2011-01-01

    Full Text Available Concern about the adverse effects of mercury on human health and ecosystems has led to tightening emission controls since the mid 1980s. But the resulting mercury emissions reductions in many parts of the world are believed to be offset or even surpassed by the increasing emissions in rapidly industrializing countries. Consequently, concentrations of atmospheric mercury are expected to remain roughly constant. Here we show that the worldwide atmospheric mercury concentration have decreased by about 20 to 38% since 1996 as indicated by long term monitoring at stations in the Southern and Northern Hemispheres combined with intermittent measurements of latitudinal distribution over the Atlantic Ocean. The total reduction of the atmospheric mercury burden of this magnitude within 14 yrs is unprecedented among most of atmospheric trace gases and is at odds with the current mercury emission inventories with nearly constant emissions over the period. It suggests a major shift in the biogeochemical cycle of mercury including oceans and soil reservoirs. Decreasing reemissions from the legacy of historical mercury emissions are the most likely explanation for this decline since the hypothesis of an accelerated oxidation rate of elemental mercury in the atmosphere is not supported by the observed trends of other trace gases. Consequently, models of the atmospheric mercury cycle have to include soil and ocean mercury pools and their dynamics to be able to make projections of future trends.

  3. Rationale and Methods for Archival Sampling and Analysis of Atmospheric Trace Chemical Contaminants On Board Mir and Recommendations for the International Space Station

    Science.gov (United States)

    Perry, J. L.; James, J. T.; Cole, H. E.; Limero, T. F.; Beck, S. W.

    1997-01-01

    Collection and analysis of spacecraft cabin air samples are necessary to assess the cabin air quality with respect to crew health. Both toxicology and engineering disciplines work together to achieve an acceptably clean cabin atmosphere. Toxicology is concerned with limiting the risk to crew health from chemical sources, setting exposure limits, and analyzing air samples to determine how well these limits are met. Engineering provides the means for minimizing the contribution of the various contaminant generating sources by providing active contamination control equipment on board spacecraft and adhering to a rigorous material selection and control program during the design and construction of the spacecraft. A review of the rationale and objectives for sampling spacecraft cabin atmospheres is provided. The presently-available sampling equipment and methods are reviewed along with the analytical chemistry methods employed to determine trace contaminant concentrations. These methods are compared and assessed with respect to actual cabin air quality monitoring needs. Recommendations are presented with respect to the basic sampling program necessary to ensure an acceptably clean spacecraft cabin atmosphere. Also, rationale and recommendations for expanding the scope of the basic monitoring program are discussed.

  4. Continuous on-line calibration of diffusive soil-atmosphere trace gas transport using vertical {sup 220}Rn- and {sup 222}Rn-activity profiles

    Energy Technology Data Exchange (ETDEWEB)

    Lehmann, B.E. [Bern Univ. (Switzerland). Physics Inst.; Neftel, A. [Inst. of Environmental Protection and Agriculture, Bern (Switzerland); Tarakanov, S.V. [Inst. of Silicate Chemistry, St. Petersburg (Russian Federation)

    2001-07-01

    Continuous monitoring of {sup 220}Rn- and {sup 222}Rn-activities above and below the soil surface combined with sporadic direct {sup 222}Rn-flux measurements is used to quantify diffusive trace gas transport in the air-filled pore space of soil, through the soil-atmosphere interface and in the lowest layers of the atmosphere. In a calm night, {sup 222}Rn-activities above the surface first build-up near the ground (z < 10 cm) and subsequently with a delay of 2-3 hours at higher altitudes (z < 5 m). Knowing (1) the {sup 222}Rn-flux from activity profiles measured in soil gas, (2) from direct flux determinations and (3) using information about atmospheric diffusion parameters from {sup 220}Rn-activities measured near the surface it is possible to model the temporal evolution of the vertical {sup 222}Rn-profiles in a night with stable weather and constant soil conditions. The system operates automatically for extended periods of time in the field enabling a better understanding of transport processes in response to changing environmental conditions (wind, rain, soil humidity). (orig.)

  5. Nepal Ambient Monitoring and Source Testing Experiment (NAMaSTE): emissions of trace gases and light-absorbing carbon from wood and dung cooking fires, garbage and crop residue burning, brick kilns, and other sources

    Science.gov (United States)

    Stockwell, Chelsea E.; Christian, Ted J.; Goetz, J. Douglas; Jayarathne, Thilina; Bhave, Prakash V.; Praveen, Puppala S.; Adhikari, Sagar; Maharjan, Rashmi; DeCarlo, Peter F.; Stone, Elizabeth A.; Saikawa, Eri; Blake, Donald R.; Simpson, Isobel J.; Yokelson, Robert J.; Panday, Arnico K.

    2016-09-01

    The Nepal Ambient Monitoring and Source Testing Experiment (NAMaSTE) campaign took place in and around the Kathmandu Valley and in the Indo-Gangetic Plain (IGP) of southern Nepal during April 2015. The source characterization phase targeted numerous important but undersampled (and often inefficient) combustion sources that are widespread in the developing world such as cooking with a variety of stoves and solid fuels, brick kilns, open burning of municipal solid waste (a.k.a. trash or garbage burning), crop residue burning, generators, irrigation pumps, and motorcycles. NAMaSTE produced the first, or rare, measurements of aerosol optical properties, aerosol mass, and detailed trace gas chemistry for the emissions from many of the sources. This paper reports the trace gas and aerosol measurements obtained by Fourier transform infrared (FTIR) spectroscopy, whole-air sampling (WAS), and photoacoustic extinctiometers (PAX; 405 and 870 nm) based on field work with a moveable lab sampling authentic sources. The primary aerosol optical properties reported include emission factors (EFs) for scattering and absorption coefficients (EF Bscat, EF Babs, in m2 kg-1 fuel burned), single scattering albedos (SSAs), and absorption Ångström exponents (AAEs). From these data we estimate black and brown carbon (BC, BrC) emission factors (g kg-1 fuel burned). The trace gas measurements provide EFs (g kg-1) for CO2, CO, CH4, selected non-methane hydrocarbons up to C10, a large suite of oxygenated organic compounds, NH3, HCN, NOx, SO2, HCl, HF, etc. (up to ˜ 80 gases in all). The emissions varied significantly by source, and light absorption by both BrC and BC was important for many sources. The AAE for dung-fuel cooking fires (4.63 ± 0.68) was significantly higher than for wood-fuel cooking fires (3.01 ± 0.10). Dung-fuel cooking fires also emitted high levels of NH3 (3.00 ± 1.33 g kg-1), organic acids (7.66 ± 6.90 g kg-1), and HCN (2.01 ± 1.25 g kg-1), where the latter could

  6. Evolution of the atmosphere.

    Science.gov (United States)

    Nunn, J F

    1998-01-01

    Planetary atmospheres depend fundamentally upon their geochemical inventory, temperature and the ability of their gravitational field to retain gases. In the case of Earth and other inner planets, early outgassing released mainly carbon dioxide and water vapour. The secondary veneer of comets and meteorites added further volatiles. Photodissociation caused secondary changes, including the production of traces of oxygen from water. Earth's gravity cannot retain light gases, including hydrogen. but retains oxygen. Water vapour generally does not pass the cold trap at the stratopause. In the archaean, early evolution of life, probably in hydrothermal vents, and the subsequent development of photosynthesis in surface waters, produced oxygen, at 3500 Ma or even earlier, becoming a significant component of the atmosphere from about 2000 Ma. Thereafter banded iron formations became rare, and iron was deposited in oxidized red beds. Atmospheric levels of carbon dioxide and oxygen have varied during the Phanerozoic: major changes may have caused extinctions. particularly the Permian/Triassic. The declining greenhouse effect due to the long-term decrease in carbon dioxide has largely offset increasing solar luminosity, and changes in carbon dioxide levels relate strongly to cycles of glaciation.

  7. Cell Model of In-cloud Scavenging of Highly Soluble Gases

    Science.gov (United States)

    Baklanov, A.; Elperin, T.; Fominykh, A.; Krasovitov, B.

    2012-04-01

    Transport of soluble gases in clouds is an integral part of the atmospheric transport of gases and is important for understanding the global distribution pattern of soluble trace gases. In the present study we investigated mass transfer during absorption of highly soluble gases such as hydrogen peroxide H2O2 and nitric acid HNO3 by stagnant cloud droplets in the presence of inert admixtures. Diffusion interactions between droplets, caused by the overlap of depleted of soluble gas regions around the neighboring droplets, are taken into account in the approximation of a cellular model of a gas-droplet suspension whereby a suspension is viewed as a periodic structure consisting of the identical spherical cells with periodic boundary conditions at the cell boundary. Using this model we determined temporal and spatial dependencies of the concentration of the soluble trace gas in a gaseous phase and in a droplet and calculated the dependence of the scavenging coefficient on time. It is shown that scavenging of highly soluble gases by cloud droplets leads to essential decrease of soluble trace gas concentration in the interstitial air. We found that scavenging coefficient for gas absorption by cloud droplets remains constant and sharply decreases only at the final stage of absorption. This assertion implies the exponential time decay of the average concentration of the soluble trace gas in the gaseous phase and can be used for the parameterization of gas scavenging by cloud droplets in the atmospheric transport modeling. In the calculations we employed gamma size distribution of cloud droplets. It was shown that despite of the comparable values of Henry's law constants for the hydrogen peroxide and the nitric acid, the nitric acid is scavenged more effectively by cloud than the hydrogen peroxide due to a major affect of the dissociation reaction on nitric acid scavenging. We obtained also the analytical expressions for the "equilibrium values" of concentration of the

  8. 微弱气体光声光谱监测光声信号影响因素分析%Influential factors analysis on photoacoustic signal of photoacoustic spectroscopy monitoring trace gases

    Institute of Scientific and Technical Information of China (English)

    陈伟根; 刘冰洁; 胡金星; 周恒逸; 李剑

    2011-01-01

    气体光声光谱检测技术灵敏度高,不消耗被测气体,能很好地应用于变压器油中溶解微弱气体的在线监测.检测中,微音器输出的光声信号是进行气体浓度分析的唯一特征量.基于光声光谱技术的基本原理,构建了一种便携式、可调谐的光声光谱装置.在分析气体光声信号激发机理的基础上,结合实验深入探讨了影响气体光声信号的多种因素,获得气体光声信号与压力、温度、激光功率、气体浓度、背景气体、斩波频率及谐振频率漂移之间的关系曲线,理论及实验结果为进一步完善油中气体光声光谱在线监测系统提供了技术参照和支撑.%Photoacoustic spectroscopy (PAS) is a highly sensitive gas analyzing method without the shortcoming of gas consumption, which can be used in transformer oil trace gases dissolved in on line monitoring. The photoacoustic signal is detected with a microphone, which is the only feature in gas concentration analysis. A portable and tunable experimental setup has been developed based on the photoacoustic spectroscopy fundamental. Through the photoacoustic signal stimulate mechanism analysis, this paper thoroughly discusses the influences of gas pressure, temperature, laser power, gas concentration, background gas, chopped frequency and the resonant frequency drift on the gas photoacoustic signal. The theoretical and experimental results supply reference and technical support for further improvements in oil gas photoacoustic spectroscopy of on-line monitoring system.

  9. Chemical and isotopical characterisation of atmospheric pollution from urban and rural environments of the Rhine Valley (PCBs, trace elements and Sr-, Nd- and Pb- isotope determinations)

    Science.gov (United States)

    Guéguen, F.; Stille, P.; Millet, M.; Dietze, V.; Gieré, R.

    2010-05-01

    Atmosheric samples (gas and particulate matter (PM)) have been collected in the urban environment of the cities of Strasbourg and Kehl and in the rural environment of the Vosges mountains. For sampling of gas phase pollutants and particles two different passive sampler devices have been applied (PAS and Sigma-2, respectively). The PAS has been used for gas phase Polychlorinated Biphenyls (PCBs) sampling and is based on the passive adsorption of gas phase pollutants onto XAD-2 resin. The Sigma-2 sampler is based on the sedimentation principle (Stoke's law), collects particles in the size range 2.5-100 μm and allows the calculation of ambient air concentration. The sampler is mainly used for routine air quality measurements in German health and recreation resorts and in this field study the first time for collection of samples for subsequent trace element and isotope analysis. The collection time for the Sigma-2 and PAS are four and two weeks, respectively. Major and trace elements have been analyzed by ICP-MS and the Sr, Nd and Pb isotope ratios by a sector field MC-ICP-MS (Neptune) while PCBs were ASE extracted and analysed by GC-ECD. The aerosol data are compared with those from tree barks which have previously been used successfully as biomonitors of atmospheric pollution (Lahd Geagea et al. 2008)1. The outer 1 mm thick part of the bark has been analyzed corresponding to about 2 to 8 years of accumulation. Some of the trace elements (Cr, Ni and Mo) of the aerosol samples are strongly (up to 1000 times) enriched compared to average 'upper continental crust (UCC)'. Normalization to a « natural » sample with an atmospheric baseline composition allows to identify industrial contributions: transition metals (Cr, Mn, Fe, Co, Ni, Zn, Mo, Cd), Ba and Pb appear to be important elements in steel plant and incinerator (chemical waste) emissions. Similarly enrichment in light rare earth elements (La, Pr, Nd) is observable. The enrichments increase with decreasing distance

  10. On Modeling the Upper Atmosphere and Ionosphere Response to Global Change

    Science.gov (United States)

    Roble, R. G.; Solomon, S. C.

    2005-05-01

    Ice core records indicate that the temperature and composition of the atmosphere can change significantly over geologic times. These changes occur naturally, however, recently the releases of trace gases from human activity have been recognized to have a potential for causing a significant change in the climate of the Earth. Most of the effort in investigating the global response to these trace gases has been directed toward the troposphere and stratosphere. Studies have shown that the troposphere will warm and the stratosphere will cool as trace gas concentrations increase in the 21st century. Studies have also been made that suggest that the mesosphere and thermosphere could also cool and affect the compositional structure of the upper atmosphere and ionosphere. We first review previous studies of the upper atmosphere and ionosphere response to trace gas increases. We then use both a global average model and the NCAR Thermosphere - Ionosphere - Mesosphere - Electrodynamics General Circulation Model (TIME-GCM) to investigate the atmospheric response to various scenarios of trace gas increases and compare the modeling results to the present day upper atmosphere and ionosphere structure. We will also discuss the key aeronomic processes that control the structure of the upper atmosphere as well as the extent to which these processes are known.

  11. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2-C10 volatile organic compounds (VOCs), CO2, CH4, CO, NO, NO2, NOy, O3 and SO2

    Science.gov (United States)

    Simpson, I. J.; Blake, N. J.; Barletta, B.; Diskin, G. S.; Fuelberg, H. E.; Gorham, K.; Huey, L. G.; Meinardi, S.; Rowland, F. S.; Vay, S. A.; Weinheimer, A. J.; Yang, M.; Blake, D. R.

    2010-12-01

    ). Prominent in the second group, SO2 and NO were remarkably enhanced over the oil sands, with maximum mixing ratios of 38.7 ppbv and 5.0 ppbv, or 383× and 319× the local background, respectively. These SO2 levels are comparable to maximum values measured in heavily polluted megacities such as Mexico City and are attributed to coke combustion. By contrast, relatively poor correlations between CH4, ethane and propane suggest low levels of natural gas leakage despite its heavy use at the surface mining sites. Instead the elevated CH4 levels are attributed to methanogenic tailings pond emissions. In addition to the emission of many trace gases, the natural drawdown of OCS by vegetation was absent above the surface mining operations, presumably because of the widespread land disturbance. Unexpectedly, the mixing ratios of α-pinene and β-pinene were much greater over the oil sands (up to 217 pptv and 610 pptv, respectively) than over vegetation in the background boundary layer (20±7 pptv and 84±24 pptv, respectively), and the pinenes correlated well with several industrial tracers that were elevated in the oil sands plumes. Because so few independent measurements from the oil sands mining industry exist, this study provides an important initial characterization of trace gas emissions from oil sands surface mining operations.

  12. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2–C10 volatile organic compounds (VOCs, CO2, CH4, CO, NO, NO2, NOy, O3 and SO2

    Directory of Open Access Journals (Sweden)

    A. J. Weinheimer

    2010-08-01

    remarkably enhanced over the oil sands, with maximum enhancements of 38.7 and 5.0 ppbv, or 383 and 319× the local background, respectively. The SO2 enhancements are comparable to maximum values measured in heavily polluted megacities such as Mexico City and are attributed to coke combustion. By contrast, relatively poor correlations between CH4 ethane and propane suggest low natural gas leakage despite its heavy use at the surface mining sites. In addition to the emission of many trace gases, the natural drawdown of OCS by vegetation was absent above the surface mining operations, presumably because of the widespread land disturbance. Unexpectedly, the mixing ratios of α- and β-pinene were much higher over the oil sands (up to 217 and 610 pptv, respectively than over vegetation in the background boundary layer (20±7 and 84±24 pptv, respectively, and the pinenes correlated well with several industrial tracers that were elevated in the oil sands plumes. Because so few independent measurements from the oil sands mining industry exist, this study provides an important initial characterization of trace gas emissions from oil sands surface mining operations.

  13. Fractionated (Martian) Noble Gases — EFA, Experiments and Meteorites

    Science.gov (United States)

    Schwenzer, S. P.; Barnes, G.; Bridges, J. C.; Bullock, M. A.; Chavez, C. L.; Filiberto, J.; Herrmann, S.; Hicks, L. J.; Kelley, S. P.; Miller, M. A.; Moore, J. M.; Ott, U.; Smith, H. D.; Steer, E. D.; Swindle, T. D.; Treiman, A. H.

    2016-08-01

    Noble gases are tracers for physical processes, including adsorption, dissolution and secondary mineral formation. We examine the Martian fractionated atmosphere through literature, terrestrial analogs and experiments.

  14. New perspectives for noble gases in oceanography

    Science.gov (United States)

    Aeschbach, Werner

    2016-08-01

    Conditions prevailing in regions of deep water formation imprint their signature in the concentrations of dissolved noble gases, which are conserved in the deep ocean. Such "recharge conditions" including temperature, salinity, and interactions with sea ice are important in view of ocean-atmosphere CO2 partitioning. Noble gases, especially the temperature sensitive Kr and Xe, are well-established tracers to reconstruct groundwater recharge conditions. In contrast, tracer oceanography has traditionally focused on He isotopes and the light noble gases Ne and Ar, which could be analyzed at the required high precision. Recent developments of analytical and data interpretation methods now provide fresh perspectives for noble gases in oceanography.

  15. Determination of trace rare earth elements in coal fly ash and atmospheric particulates by electrothermal vaporization inductively coupled plasma mass spectrometry with slurry sampling

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Y.F.; Jiang, Z.C.; He, M.; Hu, B. [Wuhan University, Wuhan (China). Dept. of Chemistry

    2007-07-15

    A method of fluorination assisted electrothermal vaporization (FETV)-ICP-MS with polytetrafluoroethylene as fluorinating reagent was developed for the direct determination of trace rare earth elements (REEs) in coal fly ash and atmospheric particulates. Under the optimal conditions, the detection limits for REEs were 0.1 pg m{sup -3} (Eu) to 6.7 Pg m{sup -3} (Nd) with the precisions of 4.1% (Yb) to 10% (La) = 1 {mu} g L{sup -1}, n = 9). The proposed method was applied to determine trace REEs in coal fly ash, airborne particulates and NIES SRM No. 8 Vehicle Exhaust Particulates. It was found that the determined values for Y, La, Pr and Nd obtained by slurry sampling FETV-ICP-MS with external calibration coincided with that obtained by pneumatic nebulization (PN)-ICP-MS and slurry sampling FETV-ICP-MS with standard addition. However, the determined values for Ce and Sm obtained by slurry sampling FETV-ICP-MS with external calibration were lower than that obtained by PN-ICP-MS and slurry sampling FETV-ICP-MS with standard addition.

  16. Determination of trace rare earth elements in coal fly ash and atmospheric particulates by electrothermal vaporization inductively coupled plasma mass spectrometry with slurry sampling.

    Science.gov (United States)

    Zhang, Yuefei; Jiang, Zucheng; He, Man; Hu, Bin

    2007-07-01

    A method of fluorination assisted electrothermal vaporization (FETV)-ICP-MS with polytetrafluoroethylene as fluorinating reagent was developed for the direct determination of trace rare earth elements (REEs) in coal fly ash and atmospheric particulates. Under the optimal conditions, the detection limits for REEs were 0.1 pg m(-3)(Eu) to 6.7 pg m(-3)(Nd) with the precisions of 4.1%(Yb) to 10%(La) (c=1 microg L(-1), n=9). The proposed method was applied to determine trace REEs in coal fly ash, airborne particulates and NIES SRM No. 8 Vehicle Exhaust Particulates. It was found that the determined values for Y, La, Pr and Nd obtained by slurry sampling FETV-ICP-MS with external calibration coincided with that obtained by pneumatic nebulization (PN)-ICP-MS and slurry sampling FETV-ICP-MS with standard addition. However, the determined values for Ce and Sm obtained by slurry sampling FETV-ICP-MS with external calibration were lower than that obtained by PN-ICP-MS and slurry sampling FETV-ICP-MS with standard addition.

  17. The role of trace gas flux networks in biogeosciences

    Energy Technology Data Exchange (ETDEWEB)

    Baldocch, Dennis [Univ. of California, Berkeley, CA (United States); Reichstein, Markus [Max Planck Institute for Biogeochemistry. Jena (Germany); Papale, D. [Univ. of Tuscia, Viterbo (Italy); Koteen, Laurie [Univ. of California, Berkeley, CA (United States); Vargas, Rodrigo [Ensenada Center for Scientific Research and Higher Education. (CICESE), Ensenada (Mexico); Agarwal, D. A. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Cook, Robert B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2012-01-01

    Vast networks of meteorological sensors ring the globe, providing continuous measurements of an array of atmospheric state variables such as temperature, humidity, rainfall, and the concentration of carbon dioxide [New etal., 1999; Tans etal., 1996]. These measurements provide input to weather and climate models and are key to detecting trends in climate, greenhouse gases, and air pollution. Yet to understand how and why these atmospheric state variables vary in time and space, biogeoscientists need to know where, when, and at what rates important gases are flowing between the land and the atmosphere. Tracking trace gas fluxes provides information on plant or microbial metabolism and climate-ecosystem interactions. The existence of trace gas flux networks is a relatively new phenomenon, dating back to research in 1984. The first gas flux measurement networks were regional in scope and were designed to track pollutant gases such as sulfur dioxide, ozone, nitric acid, and nitrogen dioxide. Atmospheric observations and model simulations were used to infer the depositional rates of these hazardous chemicals [Fowler etal., 2009; Meyers etal., 1991]. In the late 1990s, two additional trace gas flux measurement networks emerged. One, the United States Trace Gas Network (TRAGNET), was a short-lived effort that measured trace gas emissions from the soil and plants with chambers distributed throughout the country [Ojima etal., 2000]. The other, FLUXNET, was an international endeavor that brought many regional networks together to measure the fluxes of carbon dioxide, water vapor, and sensible heat exchange with the eddy covariance technique [Baldocchi etal., 2001]. FLUXNET, which remains active today, currently includes more than 400 tower sites, dispersed across most of the world's climatic zones and biomes, with sites in North and South America, Europe, Asia, Africa, and Australia. More recently, several specialized networks have emerged, including networks dedicated

  18. Photochemistry in Terrestrial Exoplanet Atmospheres. I. Photochemistry Model and Benchmark Cases

    Science.gov (United States)

    Hu, Renyu; Seager, Sara; Bains, William

    2012-12-01

    We present a comprehensive photochemistry model for exploration of the chemical composition of terrestrial exoplanet atmospheres. The photochemistry model is designed from the ground up to have the capacity to treat all types of terrestrial planet atmospheres, ranging from oxidizing through reducing, which makes the code suitable for applications for the wide range of anticipated terrestrial exoplanet compositions. The one-dimensional chemical transport model treats up to 800 chemical reactions, photochemical processes, dry and wet deposition, surface emission, and thermal escape of O, H, C, N, and S bearing species, as well as formation and deposition of elemental sulfur and sulfuric acid aerosols. We validate the model by computing the atmospheric composition of current Earth and Mars and find agreement with observations of major trace gases in Earth's and Mars' atmospheres. We simulate several plausible atmospheric scenarios of terrestrial exoplanets and choose three benchmark cases for atmospheres from reducing to oxidizing. The most interesting finding is that atomic hydrogen is always a more abundant reactive radical than the hydroxyl radical in anoxic atmospheres. Whether atomic hydrogen is the most important removal path for a molecule of interest also depends on the relevant reaction rates. We also find that volcanic carbon compounds (i.e., CH4 and CO2) are chemically long-lived and tend to be well mixed in both reducing and oxidizing atmospheres, and their dry deposition velocities to the surface control the atmospheric oxidation states. Furthermore, we revisit whether photochemically produced oxygen can cause false positives for detecting oxygenic photosynthesis, and find that in 1 bar CO2-rich atmospheres oxygen and ozone may build up to levels that have conventionally been accepted as signatures of life, if there is no surface emission of reducing gases. The atmospheric scenarios presented in this paper can serve as the benchmark atmospheres for

  19. The microwave limb sounder for the Upper Atmosphere Research Satellite

    Science.gov (United States)

    Waters, J. W.; Peckham, G. E.; Suttie, R. A.; Curtis, P. D.; Maddison, B. J.; Harwood, R. S.

    1988-01-01

    The Microwave Limb Sounder was designed to map the concentrations of trace gases from the stratosphere to the lower thermosphere, to improve understanding of the photochemical reactions which take place in this part of the atmosphere. The instrument will measure the intensity of thermal radiation from molecules in the atmosphere at frequencies corresponding to rotational absorption bands of chlorine monoxide, ozone, and water vapor. Molecular concentration profiles will be determined over a height range of 15 to 80 km (20 to 45 km for C10). The 57 deg inclination orbit proposed for the Upper Atmosphere Research Satellite will allow global coverage.

  20. Permeation tubes. Their use in the preparation of controlled gas atmospheres; Tubos de permeacion. su empleo en la preparaciond e atmosferas contoladas de gases

    Energy Technology Data Exchange (ETDEWEB)

    Galianos, J. A.; Palomares, F.

    1981-07-01

    In this paper, the state of the art on the nature, construction and properties of the permeation tubes Is reviewed; after describing the main calibration procedures In use, examples of their application in the area of the atmospheric pollution are given, especially in the case of sulfur dioxides. (Author) 38 refs.

  1. Atmospheric Fossil Fuel CO2 Traced by Δ(14)C in Beijing and Xiamen, China: Temporal Variations, Inland/Coastal Differences and Influencing Factors.

    Science.gov (United States)

    Niu, Zhenchuan; Zhou, Weijian; Wu, Shugang; Cheng, Peng; Lu, Xuefeng; Xiong, Xiaohu; Du, Hua; Fu, Yunchong; Wang, Gehui

    2016-06-07

    One year of atmospheric Δ(14)CO2 were observed in 2014 in the inland city of Beijing and coastal city of Xiamen, China, to trace temporal CO2ff variations and to determine the factors influencing them. The average CO2ff concentrations at the sampling sites in Beijing and Xiamen were 39.7 ± 36.1 ppm and 13.6 ± 12.3 ppm, respectively. These contributed 75.2 ± 14.6% and 59.1 ± 26.8% to their respective annual ΔCO2 offsets over background CO2 concentrations. Significantly (p < 0.05) high CO2ff values were observed in winter in Beijing. We did not find any significant differences in CO2ff values between weekdays and weekends. Diurnal CO2ff variations were plainly evident, with high values between midnight and 4:00, and during morning and afternoon rush hours. The sampling site in the inland city of Beijing displayed much higher CO2ff inputs and overall temporal variations than the site in the coastal city of Xiamen. The variations of CO2ff at both sites were controlled by a combination of emission sources, topography, and atmospheric dispersion. In particular, diurnal observations at the urban site in Beijing showed that CO2ff was easily accumulated under the southeast wind conditions.

  2. Atmospheric background trace elements deposition in Tierra del Fuego region (Patagonia, Argentina), using transplanted Usnea barbata lichens.

    Science.gov (United States)

    Conti, Marcelo Enrique; Finoia, Maria Grazia; Bocca, Beatrice; Mele, Giustino; Alimonti, Alessandro; Pino, Anna

    2012-01-01

    Lichen, Usnea barbata, transplants taken from Tierra del Fuego (south Patagonia, Argentina) were tested as potential biomonitors of atmospheric airborne deposition in an apparently pristine environment. In 2005, lichens were sampled in a reference site (n = 31) and transplanted in the northern Region of Tierra del Fuego. After, respectively, 1 month and 1 year of exposure, we collected them. The aim of the study was to determine the bioaccumulation of 26 elements in order to evaluate the background levels in the selected area. Samples were analyzed by the sector field inductively coupled plasma mass spectrometry. Discriminant analysis on principal component analysis factors was applied in order to explore the relationship among the different elements as far as time and spatial variation in transplants regards. The analysis was tested by Monte Carlo test based on 999 replicates. The most important contamination source resulted to be the atmospheric soil particle deposition. Furthermore, the results were compared with those obtained from the lichens collected in central and southern Tierra del Fuego. This study confirms the ability of U. barbata to reflect the background levels of the 26 elements in that environment. Compared with other background sites in the world, we did confirm that Tierra del Fuego lichens have a low content of the studied elements. Tierra del Fuego turned out not to be a pristine environment as supposed, but it can be considered as a reference basal ecosystem for useful comparisons among different geographical areas. These findings can be very relevant and useful for environmental conservation programs.

  3. Trace determination of 13 haloacetamides in drinking water using liquid chromatography triple quadrupole mass spectrometry with atmospheric pressure chemical ionization.

    Science.gov (United States)

    Chu, Wenhai; Gao, Naiyun; Yin, Daqiang; Krasner, Stuart W; Templeton, Michael R

    2012-04-27

    The haloacetamides (HAcAms) are disinfection by-products (DBPs) in drinking water which are currently receiving increased scientific attention due to their elevated toxicity relative to regulated disinfection by-products. A simultaneous determination method of 13 HAcAms, combining solid-phase extraction (SPE) enrichment, liquid chromatographic (LC) separation, and triple quadrupole mass spectrometry (tqMS) detection with atmospheric pressure chemical ionization (APCI) using selective reaction monitoring in positive mode, was developed to measure HAcAms, including chlorinated, brominated, and iodinated analogs. Ammonium chloride and Oasis HLB were selected as the dechlorinating reagent and polymeric SPE sorbent of HAcAm samples. The used tqMS apparatus showed higher sensitivity for the studied HAcAms in the APCI mode than electrospray ionization. 13 HAcAms were separated by LC in 9.0 min, and the detection limits ranged from 7.6 to 19.7 ng/L. The SPE-LC/tqMS method was successfully applied to quantify 13 HAcAms in drinking water samples for the first time, and first indentified tribromoacetamide and chloroiodoacetamide as DBPs in drinking water.

  4. Generation and release of radioactive gases in LLW disposal facilities

    Energy Technology Data Exchange (ETDEWEB)

    Yim, M.S. [Harvard School Public Health, Boston, MA (United States); Simonson, S.A. [Massachusetts Institute of Technology, Cambridge, MA (United States)

    1995-02-01

    The atmospheric release of radioactive gases from a generic engineered LLW disposal facility and its radiological impacts were examined. To quantify the generation of radioactive gases, detailed characterization of source inventory for carbon-14, tritium, iodine-129, krypton-85, and radon-222, was performed in terms of their activity concentrations; their distribution within different waste classes, waste forms and containers; and their subsequent availability for release in volatile or gaseous form. The generation of gases was investigated for the processes of microbial activity, radiolysis, and corrosion of waste containers and metallic components in wastes. The release of radionuclides within these gases to the atmosphere was analyzed under the influence of atmospheric pressure changes.

  5. Technical Note: A trace gas climatology derived from the Atmospheric Chemistry Experiment Fourier Transform Spectrometer (ACE-FTS data set

    Directory of Open Access Journals (Sweden)

    A. Jones

    2012-06-01

    Full Text Available The Atmospheric Chemistry Experiment-Fourier Transform Spectrometer (ACE-FTS aboard the Canadian satellite SCISAT (launched in August 2003 was designed to investigate the composition of the upper troposphere, stratosphere, and mesosphere. ACE-FTS utilizes solar occultation to measure temperature and pressure as well as vertical profiles of over thirty chemical species including O3, H2O, CH4, N2O, CO, NO, NO2, N2O5, HNO3, HCl, ClONO2, CCl3F, CCl2F2, and HF. Global coverage for each species is obtained approximately over a three month period and measurements are made with a vertical resolution of typically 3–4 km. A quality-controlled climatology has been created for each of these 14 baseline species, where individual profiles are averaged over the period of February 2004 to February 2009. Measurements used are from the ACE-FTS version 2.2 data set including updates for O3 and N2O5. The climatological fields are provided on a monthly and three-monthly basis (DJF, MAM, JJA, SON at 5 degree latitude and equivalent latitude spacing and on 28 pressure surfaces (26 of which are defined by the Stratospheric Processes And their Role in Climate (SPARC Chemistry-Climate Model Validation Activity. The ACE-FTS climatological data set is available through the ACE website.

  6. Global warming and greenhouse gases

    OpenAIRE

    Belić Dragoljub S.

    2006-01-01

    Global warming or Climate change refers to long-term fluctuations in temperature, precipitation, wind, and other elements of the Earth's climate system. Natural processes such as solar-irradiance variations, variations in the Earth's orbital parameters, and volcanic activity can produce variations in climate. The climate system can also be influenced by changes in the concentration of various gases in the atmosphere, which affect the Earth's absorption of radiation.

  7. Heterogeneous reactions on the surface of fine particles in the atmosphere

    Institute of Scientific and Technical Information of China (English)

    DING Jie; ZHU Tong

    2003-01-01

    Fine particles play an important role in the atmosphere. Research on heterogeneous reactions on the surface of fine particles is one of the frontier areas of atmospheric science. In this paper, physical and chemical characteristics of fine particles in the atmosphere and the interactions between trace gases and fine particles are described, methods used in heterogeneous reactions research are discussed in detail, progress in the study of heterogeneous reactions on the surface of fine particles in the atmosphere is summarized, existing importantquestions are pointed out and future research directions are suggested.

  8. Atmospheric energy for subsurface life on Mars?

    Science.gov (United States)

    Weiss, B. P.; Yung, Y. L.; Nealson, K. H.

    2000-01-01

    The location and density of biologically useful energy sources on Mars will limit the biomass, spatial distribution, and organism size of any biota. Subsurface Martian organisms could be supplied with a large energy flux from the oxidation of photochemically produced atmospheric H(2) and CO diffusing into the regolith. However, surface abundance measurements of these gases demonstrate that no more than a few percent of this available flux is actually being consumed, suggesting that biological activity driven by atmospheric H(2) and CO is limited in the top few hundred meters of the subsurface. This is significant because the available but unused energy is extremely large: for organisms at 30-m depth, it is 2,000 times previous estimates of hydrothermal and chemical weathering energy and far exceeds the energy derivable from other atmospheric gases. This also implies that the apparent scarcity of life on Mars is not attributable to lack of energy. Instead, the availability of liquid water may be a more important factor limiting biological activity because the photochemical energy flux can only penetrate to 100- to 1,000-m depth, where most H(2)O is probably frozen. Because both atmospheric and Viking lander soil data provide little evidence for biological activity, the detection of short-lived trace gases will probably be a better indicator of any extant Martian life.

  9. Spectrometers for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR) Upgrade to Full Sun-Sky-Cloud-Trace Gas Spectrometry Capability for Airborne Science

    Science.gov (United States)

    Dunagan, S. E.; Flynn, C. J.; Johnson, R. R.; Kacenelenbogen, M. S.; Knobelspiesse, K. D.; LeBlanc, S. E.; Livingston, J. M.; Redemann, J.; Russell, P. B.; Schmid, B.; Segal-Rosenhaimer, M.; Shinozuka, Y.

    2014-12-01

    The Spectrometers for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR) instrument has been developed at NASA Ames in collaboration with Pacific Northwest National Laboratory (PNNL) and NASA Goddard, supported substantially since 2009 by NASA's Radiation Science Program and Earth Science Technology Office. It combines grating spectrometers with fiber optic links to a tracking, scanning head to enable sun tracking, sky scanning, and zenith viewing. 4STAR builds on the long and productive heritage of the NASA Ames Airborne Tracking Sunphotometers (AATS-6 and -14), which have yielded more than 100 peer-reviewed publications and extensive archived data sets in many NASA Airborne Science campaigns from 1986 to the present. The baseline 4STAR instrument has provided extensive data supporting the TCAP (Two Column Aerosol Project, July 2012 & Feb. 2013), SEAC4RS (Studies of Emissions, Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys, 2013), and ARISE (Arctic Radiation - IceBridge Sea and Ice Experiment, 2014), field campaigns.This poster presents plans and progress for an upgrade to the 4STAR instrument to achieve full science capability, including (1) direct-beam sun tracking measurements to derive aerosol optical depth spectra, (2) sky radiance measurements to retrieve aerosol absorption and type (via complex refractive index and mode-resolved size distribution), (3) cloud properties via zenith radiance, and (4) trace gas spectrometry. Technical progress in context with the governing physics is reported on several upgrades directed at improved light collection and usage, particularly as related to spectrally and radiometrically stable propagation through the collection light path. In addition, improvements to field calibration and verification, and flight operability and reliability are addressed.

  10. ROLE OF CANOPY-SCALE PHOTOCHEMISTRY IN MODIFYING BIOGENIC-ATMOSPHERE EXCHANGE OF REACTIVE TERPENE SPECIES: RESULTS FROM THE CELTIC FIELD STUDY

    Science.gov (United States)

    A one-dimensional canopy model was used to quantify the impact of photochemistry in modifying biosphere-atmosphere exchange of trace gases. Canopy escape efficiencies, defined as the fraction of emission that escapes into the well-mixed boundary layer, were calculated for reactiv...

  11. A single gas chromatograph for accurate atmospheric mixing ratio measurements of CO2, CH4, N2O, SF6 and CO

    NARCIS (Netherlands)

    van der Laan, S.; Neubert, R. E. M.; Meijer, H. A. J.; Simpson, W.R.

    2009-01-01

    We present an adapted gas chromatograph capable of measuring simultaneously and semi-continuously the atmospheric mixing ratios of the greenhouse gases CO2, CH4, N2O and SF6 and the trace gas CO with high precision and long-term stability. The novelty of our design is that all species are measured w

  12. PRELIMINARY RESULTS OF ATMOSPHERIC DEPOSITION OF MAJOR AND TRACE ELEMENTS IN THE GREATER AND LESSER CAUCASUS MOUNTAINS STUDIED BY THE MOSS TECHNIQUE AND NEUTRON ACTIVATION ANALYSIS

    Directory of Open Access Journals (Sweden)

    S. Shetekauri

    2015-05-01

    Full Text Available The method of moss biomonitoring of atmospheric deposition of trace elements was applied for the first time in the western Caucasus Mountains to assess the environmental situation in this region. The sixteen moss samples have been collected in 2014 summer growth period along altitudinal gradients in the range of altitudes from 600 m to 2665 m. Concentrations of Na, Mg, Al, Cl, K, Ca, Ti, V, Mn, Fe, Zn, As, Br, Rb, Mo, Cd, I, Sb, Ba, La, Sm, W, Au, and U determined by neutron activation analysis in the moss samples are reported. A comparison with the data for moss collected in Norway (pristine area was carried out.  Multivariate statistical analysis of the results was used for assessment pollution sources in the studied part of the Caucasus. The increase in concentrations of most of elements with rising altitude due to gradually disappearing vegetation cover and wind erosion of soil was observed. A comparison with the available data for moss collected in the Alps at the same altitude (~ 2500 m was performed.

  13. Summer fluxes of atmospheric greenhouse gases N{sub 2}O, CH{sub 4} and CO{sub 2} from mangrove soil in South China

    Energy Technology Data Exchange (ETDEWEB)

    Chen, G.C. [Department of Biology and Chemistry, City University of Hong Kong, Hong Kong SAR (China); Tam, N.F.Y., E-mail: bhntam@cityu.edu.hk [Department of Biology and Chemistry, City University of Hong Kong, Hong Kong SAR (China); Ye, Y. [State Key Laboratory of Marine Environmental Science, Xiamen University, Xiamen, Fujian (China)

    2010-06-01

    The atmospheric fluxes of N{sub 2}O, CH{sub 4} and CO{sub 2} from the soil in four mangrove swamps in Shenzhen and Hong Kong, South China were investigated in the summer of 2008. The fluxes ranged from 0.14 to 23.83 {mu}mol m{sup -2} h{sup -1}, 11.9 to 5168.6 {mu}mol m{sup -2} h{sup -1} and 0.69 to 20.56 mmol m{sup -2} h{sup -1} for N{sub 2}O, CH{sub 4} and CO{sub 2}, respectively. Futian mangrove swamp in Shenzhen had the highest greenhouse gas fluxes, followed by Mai Po mangrove in Hong Kong. Sha Kong Tsuen and Yung Shue O mangroves in Hong Kong had similar, low fluxes. The differences in both N{sub 2}O and CH{sub 4} fluxes among different tidal positions, the landward, seaward and bare mudflat, in each swamp were insignificant. The N{sub 2}O and CO{sub 2} fluxes were positively correlated with the soil organic carbon, total nitrogen, total phosphate, total iron and NH{sub 4}{sup +}-N contents, as well as the soil porosity. However, only soil NH{sub 4}{sup +}-N concentration had significant effects on CH{sub 4} fluxes.

  14. Isotope modeling of nitric acid formation in the atmosphere using ISO-RACM: testing the importance of NO oxidation, heterogeneous reactions, and trace gas chemistry

    Directory of Open Access Journals (Sweden)

    G. Michalski

    2010-03-01

    Full Text Available Here we present ISO-RACM, an isotope mass balance model that utilizes the Regional Atmospheric Chemistry Mechanism to predict Δ17O values in atmospheric nitrate. A large number of simulations were carried out that varied atmospheric parameters that are important in altering the magnitude and range of Δ17O values generated in photochemically produce nitrate. These parameters included temperature, relative humidity, actinic flux, aerosol surface area and chemical speciation, and three different N2O5 uptake parameterizations. Trace gas mixing ratios were also varied including CH4, CO, NOx, O3, volatile organic compounds and biogenic organic compounds. The model predicts that there are seasonal, latitudinal and diurnal variations in Δ17O values due to changes in actinic flux with lower values corresponding to higher actinic fluxes. There was also a minor positive correlation between higher Δ17O values and increased temperature. There were distinct differences in Δ17O depending on which N2O5 parameterization was used, mostly the result of changing relative humidity being a factor in two of the parameterization schemes. Changing CO and CH4 mixing ratios had negligible impact on Δ17O values but significant variation in magnitude and range were predicted with NOx, O3, and organic loading. High NOx and O3 generated high Δ17O with a narrow (10 ‰ range, while high organics led to low Δ17O values and a wider range of possible values. Implications for using Δ17O to evaluate NOx-NOy chemistry and aerosol formation processes are discussed, as is needed future research.

  15. Seasonally Varying Reference Atmospheres for East Asia

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Vertical profiles of seasonally varying pressure, temperature, water vapor, and trace gases (O3, N2O, CO,CH4), representing atmospheric conditions up to a height of 100 km over the East Asia region (30°-50°N,110°-150°E) were constructed by using various observation data, model outputs of atmospheric thermodynamic parameters, and gaseous concentrations. Optical characteristics of the obtained East Asia reference atmospheres were compared with those from typical midlatitude summer and winter atmospheres. It was noted that, in the water vapor field, there are major differences between the two model atmospheres during the summer. The resultant impact during the summer of water vapor difference on incoming solar fluxes at the surface and emitted terrestrial fluxes at the top of the atmosphere are 14.3 W m-2 and 6.5 W m-2,respectively. On the other hand, the winter difference between East Asian and midlatitude atmospheres appears to be insignificant. Reference atmospheres for the spring and fall are also available. Utilizing the constructed atmospheric profiles as inputs to the radiative transfer model, it is expected that the constructed seasonally varying reference atmospheres can facilitate better descriptions of optical properties in East Asia.

  16. Mercury, trace elements and organic constituents in atmospheric fine particulate matter, Shenandoah National Park, Virginia, USA: A combined approach to sampling and analysis

    Science.gov (United States)

    Kolker, A.; Engle, M.A.; Orem, W.H.; Bunnell, J.E.; Lerch, H.E.; Krabbenhoft, D.P.; Olson, M.L.; McCord, J.D.

    2008-01-01

    Compliance with U.S. air quality regulatory standards for atmospheric fine particulate matter (PM2.5) is based on meeting average 24 hour (35 ?? m-3) and yearly (15 ??g m-3) mass-per-unit-volume limits, regardless of PM2.5 composition. Whereas this presents a workable regulatory framework, information on particle composition is needed to assess the fate and transport of PM2.5 and determine potential environmental/human health impacts. To address these important non-regulatory issues an integrated approach is generally used that includes (1) field sampling of atmospheric particulate matter on filter media, using a size-limiting cyclone, or with no particle-size limitation; and (2) chemical extraction of exposed filters and analysis of separate particulate-bound fractions for total mercury, trace elements and organic constituents, utilising different USGS laboratories optimised for quantitative analysis of these substances. This combination of sampling and analysis allowed for a more detailed interpretation of PM2.5 sources and potential effects, compared to measurements of PM2.5 abundance alone. Results obtained using this combined approach are presented for a 2006 air sampling campaign in Shenandoah National Park (Virginia, USA) to assess sources of atmospheric contaminants and their potential impact on air quality in the Park. PM2.5 was collected at two sampling sites (Big Meadows and Pinnacles) separated by 13.6 km. At both sites, element concentrations in PM2.5 were low, consistent with remote or rural locations. However, element/Zr crustal abundance enrichment factors greater than 10, indicating anthropogenic input, were found for Hg, Se, S, Sb, Cd, Pb, Mo, Zn and Cu, listed in decreasing order of enrichment. Principal component analysis showed that four element associations accounted for 84% of the PM 2.5 trace element variation; these associations are interpreted to represent: (1) crustal sources (Al, REE); (2) coal combustion (Se, Sb), (3) metal production

  17. Bunsen conference 1999. Atmospheric physical chemistry; Bunsentagung 1999. Physikalische Chemie der Atmosphaere

    Energy Technology Data Exchange (ETDEWEB)

    Crutzen, P.J.; Zellner, R. [comps.

    2000-07-01

    The main subject of the 1999 Bunsen conference was atmospheric physical chemistry. There were lectures and posters on measurement and distribution of atmospheric trace gases, photochemical reactions in the different parts of the atmosphere, natural and anthropogenic emissions resulting from biomass combustion, thermodynamics and microphysics of aerosol, and air pollution abatement. [German] Die Bunsentagung 1999 beschaeftigte sich mit dem Thema Physikalische Chemie der Atmosphaere. Themen der Vortraege und Poster waren u.a. die Messung und Verteilung von Spurengasen in der Atmosphaere, photochemische Reaktionen in den verschiedenen Schichten der Atmosphaere, natuerliche und anthropogene Emissionen durch Verbrennung von Biomasse, Thermodynamik und Microphysik von Aerosolen und Klimaschutz.

  18. Worldwide trend of atmospheric mercury since 1995

    Directory of Open Access Journals (Sweden)

    F. Slemr

    2011-05-01

    Full Text Available Concern about the adverse effects of mercury on human health and ecosystems has led to tightening emission controls since the mid 1980s. But the resulting mercury emissions reductions in many parts of the world are believed to be offset or even surpassed by the increasing emissions in rapidly industrializing countries. Consequently, concentrations of atmospheric mercury are expected to remain roughly constant. Here we show that the worldwide atmospheric mercury concentrations have decreased by about 20 to 38 % since 1996 as indicated by long-term monitoring at stations in the Southern and Northern Hemispheres combined with intermittent measurements of latitudinal distribution over the Atlantic Ocean. The total reduction of the atmospheric mercury burden of this magnitude within 14 years is unusually large among most atmospheric trace gases and is at odds with the current mercury emission inventories with nearly constant anthropogenic emissions over this period. This suggests a major shift in the biogeochemical cycle of mercury including oceans and soil reservoirs. Decreasing reemissions from the legacy of historical mercury emissions are the most likely explanation for this decline since the hypothesis of an accelerated oxidation rate of elemental mercury in the atmosphere is not supported by the observed trends of other trace gases. Acidification of oceans, climate change, excess nutrient input and pollution may also contribute by their impact on the biogeochemistry of ocean and soils. Consequently, models of the atmospheric mercury cycle have to include soil and ocean mercury pools and their dynamics to be able to make projections of future trends.

  19. Dynamic Sampling of Trace Contaminants During the Mission Operations Test of the Deep Space Habitat

    Science.gov (United States)

    Monje, Oscar; Valling, Simo; Cornish, Jim

    2013-01-01

    The atmospheric composition inside spacecraft during long duration space missions is dynamic due to changes in the living and working environment of crew members, crew metabolism and payload operations. A portable FTIR gas analyzer was used to monitor the atmospheric composition within the Deep Space Habitat (DSH) during the Mission Operations Test (MOT) conducted at the Johnson Space Center (JSC). The FTIR monitored up to 20 gases in near- real time. The procedures developed for operating the FTIR were successful and data was collected with the FTIR at 5 minute intervals. Not all the 20 gases sampled were detected in all the modules and it was possible to measure dynamic changes in trace contaminant concentrations that were related to crew activities involving exercise and meal preparation.

  20. SOIR and NOMAD: Characterization of Planetary Atmospheres

    Science.gov (United States)

    Robert, S.; Chamberlain, S.; Mahieux, A.; Thomas, I.; Wilquet, V.; Vandaele, A. C.

    2014-06-01

    The Belgian Institute for Space Aeronomy is involved in the Venus Express mission (VeX), launched in 2006 and in the ExoMars Trace Gas Orbiter mission (TGO), due for launch in 2016. BISA is responsible for one instrument in each mission, SOIR onboard VeX and NOMAD onboard TGO respectively. The SOIR instrument onboard Venus Express allows observations of trace gases in the Venus atmosphere, at the terminator for both the morning and evening sides of the planet and for almost all latitudes. It has been designed to measure spectra in the IR region (2.2 - 4.3 µm) of the Venus atmosphere using the solar occultation technique1. This method derives unique information on the vertical composition and structure of the mesosphere and lower thermosphere2,3,4,5. It is unique in terms of spectral coverage and spectral resolution (0.15 cm-1), and is ideally designed to probe the Venus atmosphere for CO2 as well as trace gases, such as H2O, CO, HCl and HF. SOIR is capable of (1) providing vertical information on a broad series of species, such as CO2, CO, H2O, HCl, HF, SO26 and aerosols 7, covering the so far sparsely known region located above the clouds, (2) contributing to a better understanding of the dynamics and stability of the atmosphere by delivering total density and kinetic temperature profiles at the terminator, an up-to-now still unchartered region, and (3) detecting weak absorption bands of rare CO2 isotopologues8, due to the sensitivity of SOIR, the high concentration of CO2 on Venus and the long absorption paths sounded during solar occultations.

  1. NASA's Upper Atmosphere Research Program (UARP) and Atmospheric Chemistry Modeling and Analysis Program (ACMAP): Research Summaries 1997-1999

    Science.gov (United States)

    Kurylo, M. J.; DeCola, P. L.; Kaye, J. A.

    2000-01-01

    Under the mandate contained in the FY 1976 NASA Authorization Act, the National Aeronautics and Space Administration (NASA) has developed and is implementing a comprehensive program of research, technology development, and monitoring of the Earth's upper atmosphere, with emphasis on the upper troposphere and stratosphere. This program aims at expanding our chemical and physical understanding to permit both the quantitative analysis of current perturbations as well as the assessment of possible future changes in this important region of our environment. It is carried out jointly by the Upper Atmosphere Research Program (UARP) and the Atmospheric Chemistry Modeling and Analysis Program (ACMAP), both managed within the Research Division in the Office of Earth Science at NASA. Significant contributions to this effort have also been provided by the Atmospheric Effects of Aviation Project (AEAP) of NASA's Office of Aero-Space Technology. The long-term objectives of the present program are to perform research to: understand the physics, chemistry, and transport processes of the upper troposphere and the stratosphere and their control on the distribution of atmospheric chemical species such as ozone; assess possible perturbations to the composition of the atmosphere caused by human activities and natural phenomena (with a specific emphasis on trace gas geographical distributions, sources, and sinks and the role of trace gases in defining the chemical composition of the upper atmosphere); understand the processes affecting the distributions of radiatively active species in the atmosphere, and the importance of chemical-radiative-dynamical feedbacks on the meteorology and climatology of the stratosphere and troposphere; and understand ozone production, loss, and recovery in an atmosphere with increasing abundances of greenhouse gases. The current report is composed of two parts. Part 1 summarizes the objectives, status, and accomplishments of the research tasks supported

  2. Gases in molten salts

    CERN Document Server

    Tomkins, RPT

    1991-01-01

    This volume contains tabulated collections and critical evaluations of original data for the solubility of gases in molten salts, gathered from chemical literature through to the end of 1989. Within the volume, material is arranged according to the individual gas. The gases include hydrogen halides, inert gases, oxygen, nitrogen, hydrogen, carbon dioxide, water vapor and halogens. The molten salts consist of single salts, binary mixtures and multicomponent systems. Included also, is a special section on the solubility of gases in molten silicate systems, focussing on slags and fluxes.

  3. Handbook of purified gases

    CERN Document Server

    Schoen, Helmut

    2015-01-01

    Technical gases are used in almost every field of industry, science and medicine and also as a means of control by government authorities and institutions and are regarded as indispensable means of assistance. In this complete handbook of purified gases the physical foundations of purified gases and mixtures as well as their manufacturing, purification, analysis, storage, handling and transport are presented in a comprehensive way. This important reference work is accompanied with a large number of Data Sheets dedicated to the most important purified gases.  

  4. Atmospheric Deposition History of Trace Metals and Metalloids for the Last 200 Years Recorded by Three Peat Cores in Great Hinggan Mountain, Northeast China

    Directory of Open Access Journals (Sweden)

    Kunshan Bao

    2015-03-01

    Full Text Available A large number of studies on trace metals and metalloids (TMs accumulations in peatlands have been reported in Europe and North America. Comparatively little information is available on peat chronological records of atmospheric TMs flux in China. Therefore, the objective of our study was to determine the concentrations and accumulation rates (ARs of TMs in Motianling peatland from Great Hinggan Mountain, northeast China, and to assess these in relation to establish a historical profile of atmospheric metal emissions from anthropogenic sources. To meet these aims we analyzed 14 TMs (As, Ba, Cd, Co, Cr, Cu, Mo, Ni, Pb, Sr, Sb, Tl, and Zn and Pb isotopes (206Pb, 207Pb, 208Pb using ICP-AES and ICP-MS, respectively, in three peat sections dated by 210Pb and 137Cs techniques (approximately spanning the last 200 years. There is a general agreement in the elemental concentration profiles which suggests that all investigated elements were conserved in the Motianling bog. Three principal components were discriminated by principal component analysis (PCA based on Eigen-values >1 and explaining 85% of the total variance of element concentrations: the first component representing Ba, Co, Cr, Mo, Ni, Sr and Tl reflected the lithogenic source; the second component covering As, Cu and Sb, and Cd is associated with an anthropogenic source from ore mining and processing; the third component (Pb isotope, Pb and Zn is affected by anthropogenic Pb pollution from industrial manufacturing and fossil-fuel combustion. The pre-industrial background of typical pollution elements was estimated as the average concentrations of TMs in peat samples prior to 1830 AD and with a 207Pb/206Pb ratio close to 1.9. ARs and enrichment factors (EFs of TMs suggested enhanced metal concentrations near the surface of the peatland (in peat layers dated from the 1980s linked to an increasing trend since the 2000s. This pollution pattern is also fingerprinted by the Pb isotopic composition

  5. Temporal and spatial variation of trace elements in atmospheric deposition around the industrial area of Puchuncaví-Ventanas (Chile) and its influence on exceedances of lead and cadmium critical loads in soils.

    Science.gov (United States)

    Rueda-Holgado, F; Calvo-Blázquez, L; Cereceda-Balic, F; Pinilla-Gil, E

    2016-02-01

    Fractionation of elemental contents in atmospheric samples is useful to evaluate pollution levels for risk assessment and pollution sources assignment. We present here the main results of long-term characterization of atmospheric deposition by using a recently developed atmospheric elemental fractionation sampler (AEFS) for major and trace elements monitoring around an important industrial complex located in Puchuncaví region (Chile). Atmospheric deposition samples were collected during two sampling campaigns (2010 and 2011) at four sampling locations: La Greda (LG), Los Maitenes (LM), Puchuncaví (PU) and Valle Alegre (VA). Sample digestion and ICP-MS gave elements deposition values (Al, As, Ba, Cd, Co, Cu, Fe, K, Mn, Pb, Sb, Ti, V and Zn) in the insoluble fraction of the total atmospheric deposition. Results showed that LG location, the closest location to the industrial complex, was the more polluted sampling site having the highest values for the analyzed elements. PU and LM were the next more polluted and, finally, the lowest elements concentrations were registered at VA. The application of Principal Component Analysis and Cluster Analysis identified industrial, traffic and mineral-crustal factors. We found critical loads exceedances for Pb at all sampling locations in the area affected by the industrial emissions, more significant in LG close to the industrial complex, with a trend to decrease in 2011, whereas no exceedances due to atmospheric deposition were detected for Cd.

  6. On the Incorporation of Greenhouse Gases Emission into the Regulatory Scope of the Atmospheric Pollution Prevention and Control Law%《大气污染防治法》将温室气体 排放纳入控制体系的评析

    Institute of Scientific and Technical Information of China (English)

    赵俊; 孙宋龙

    2016-01-01

    对于温室气体控制是否应纳入《大气污染防治法》的调整范畴,一直都有争议. 不应将温室气体控制纳入《大气污染防治法》的调整范畴,这不仅是由于温室气体不属于大气污染物,也是由我国现阶段所处的国际和国内环境决定的. 温室气体主要来源于能源生产等"上游活动"和公众生活消费等"下游活动". 我们应对其进行上堵下疏:一方面力促清洁生产,另一方面倡导低碳生活,将市场机制与行政手段结合起来,多管齐下共同控制温室气体排放,没有必要将温室气体控制纳入《大气污染防治法》的调整范畴.%It has always been controversial whether or not to incorporate greenhouse gases control into the regulatory scope of Atmospheric Pollution Prevention and Control Law of the People' s Republic of China.Green-house gases control should not be incorporated into the regulatory scope of Atmospheric Pollution Prevention Law, not only because greenhouse gases do not belong to the atmospheric pollutants, but also as a result of Chi-na' s current international and domestic environment.Greenhouse gases are mainly derived from the upstream activities, e.g., energy production;and the downstream activities, e.g., public consumption, etc.We will stop the flow from the upstream and dredge the channel to the downstream by promoting cleaner energy produc-tion and advocating low-carbon life.Multi-pronged methods should be employed to control greenhouse gases by combining market mechanism with administrative means.Thus, there is no necessity to incorporate greenhouse gases control into the regulatory scope of Atmospheric Pollution Prevention Law.

  7. A Simple Experiment to Demonstrate the Effects of Greenhouse Gases

    Science.gov (United States)

    Keating, C. F.

    2007-01-01

    The role of greenhouse gases in our atmosphere is the subject of considerable discussion and debate. Global warming is well-documented, as is the continually increasing amount of greenhouse gases that human activity puts in the air. Is there a relationship between the two? The simple experiment described in this paper provides a good demonstration…

  8. Microbial imprint on soil-atmosphere H2, COS, and CO2 fluxes

    Science.gov (United States)

    Meredith, L. K.; Commane, R.; Munger, J. W.; Wofsy, S. C.; Prinn, R. G.

    2013-12-01

    Microorganisms drive large trace gas fluxes between soil and atmosphere, but the signal can be difficult to detect and quantify in the presence of stronger exchange processes in an ecosystem. Partitioning methods are often needed to estimate trace gas budgets and to develop process-based models to explore the sensitivity of microbe-mediated fluxes. In this study, we test the performance of trace gases with predominantly microbe-mediated soil fluxes as a metric of the soil microbial uptake activity of other trace gases. Using simultaneous, collocated measurements at Harvard Forest, we consider three trace gases with microbe-mediated soil fluxes of various importance relative to their other (mainly plant-mediated) ecosystem fluxes: molecular hydrogen (H2), carbonyl sulfide (COS), and carbon dioxide (CO2). These gases probe different aspects of the soil trace-gas microbiology. Soil H2 uptake is a redox reaction driving the energy metabolism of a portion of the microbial community, while soil CO2 respiration is a partial proxy for the overall soil microbial metabolism. In comparison, very little is understood about the microbiological and environmental drivers of soil COS uptake and emissions. In this study, we find that H2, COS, and CO2 soil uptake rates are often correlated, but the relative soil uptake between gases is not constant, and is influenced by seasonality and local environmental conditions. We also consider how differences in the microbial communities and pathways involved in the soil fluxes may explain differences in the observations. Our results are important for informing previous studies using tracer approaches. For example, H2 has been used to estimate COS soil uptake, which must be accounted for to use COS as a carbon cycle tracer. Furthermore, the global distribution of H2 deposition velocity has been inferred from net primary productivity (CO2). Given that insufficient measurement frequency and spatial distribution exists to partition global net

  9. Experimental Study of Trace Element Migration Characteristics in an O_2/CO_2 Atmosphere%O_2/CO_2气氛下痕量元素迁移特性试验研究

    Institute of Scientific and Technical Information of China (English)

    卢骏营; 陈晓平; 段伦博; 周骛

    2009-01-01

    在管式炉上进行徐州烟煤的燃烧试验,采用电感耦合等离子体光谱质谱联用仪(ICP-MS)对燃烧剩余灰渣进行测定.研究了不同温度和不同燃烧气氛(空气气氛和O_2/CO_2气氛)下痕量元素的迁移特性.结果表明,煤燃烧过程中,痕量元素Cr、Mn、Ni、Zn、Cd、Pb在灰渣中富集,As挥发率达70%以上.随着温度的升高,大部分痕量元素在灰渣中的含量降低,Mn、Ni、Cr在灰渣中的含量相对比较稳定.O_2/CO_2气氛下,各元素随温度的变化趋势并未受到影响,但整体上O_2/CO_2气氛下各痕量元素在灰渣中的含量要大于空气气氛下的,随着温度的升高,O_2/CO_2气氛和空气气氛下痕量元素在灰渣中的含量越来越接近,说明燃烧气氛对痕量元素迁移的影响随温度升高而减弱.%On a tubular boiler,conducted was a combustion test of Xuzhou-originated bituminous coal and determined were the ash slag remnants from combustion by using an inductively coupled plasma-mass spectrometer (ICP-MS).The migration characteristics of trace elements were studied under various temperatures and combustion atmospheres (including air and O_2/CO_2 atmosphere).The research results show that during the coal combustion process,such trace elements as Cr,Mn,Ni,Zn,Cd and Pb become enriched in the ash slag,and the As volatilization rate is over 70%.With an increase of temperature,the contents of the majority of trace elements in the ash slag will decrease.However,the contents of Mn,Ni and Cr in the ash slag are relatively stable.In an O_2/CO_2 atmosphere,the changing tendency of various elements with temperature was not affected.In the O_2/CO_2 atmosphere,as a whole,the contents of various trace elements in the ash slag are greater than those in air atmosphere.With an increase of temperature,the above-mentioned contents in the O_2/CO_2 atmosphere are more and more close to those in the air atmosphere,indicating that the influence of the combustion atmosphere

  10. Photochemistry in Terrestrial Exoplanet Atmospheres I: Photochemistry Model and Benchmark Cases

    CERN Document Server

    Hu, Renyu; Bains, William

    2012-01-01

    We present a comprehensive photochemistry model for exploration of the chemical composition of terrestrial exoplanet atmospheres. The photochemistry model is designed from the ground up to have the capacity to treat all types of terrestrial planet atmospheres, ranging from oxidizing through reducing, which makes the code suitable for applications for the wide range of anticipated terrestrial exoplanet compositions. The one-dimensional chemical transport model treats up to 800 chemical reactions, photochemical processes, dry and wet deposition, surface emission and thermal escape of O, H, C, N and S bearing species, as well as formation and deposition of elemental sulfur and sulfuric acid aerosols. We validate the model by computing the atmospheric composition of current Earth and Mars and find agreement with observations of major trace gases in Earth's and Mars' atmospheres. We simulate several plausible atmospheric scenarios of terrestrial exoplanets, and choose three benchmark cases for atmospheres from red...

  11. Gases, liquids and solids

    CERN Document Server

    Tabor, David

    1969-01-01

    It has been tradional to treat gases, liquids and solids as if they were completely unrelated material. However, this book shows that many of their bulk properties can been explained in terms of intermolecular forces.

  12. Response of the Atlantic Thermohaline Circulation to Changes of Atmospheric Green House Gases%北大西洋热盐环流对温室气体浓度变化的响应

    Institute of Scientific and Technical Information of China (English)

    朱江; 杨海军

    2012-01-01

    The equilibrium response of the thermohaline circulation (THC) to changes of atmospheric Green House Gases is simulated using a fully coupled climate model. The strength of the North Atlantic THC decreases about 20% when the concentration of atmospheric CO2 doubles and increases about 13% when the concentration halves. The response of the THC is divided into two different stages: the transient stage and the equilibrium stage. The transient response is mainly attributable to the changes of local surface heat flux and freshwater flux in the high latitude of North Atlantic, while the equilibrium response is also relevant to the non-local transport of heat and freshwater by THC itself, with the former acting as a positive feedback and the later as a negative feedback. The slow recovery of THC in the doubled CO2 experiment implies the role of the positive feedback overwhelms that of negative feedback, while the equilibrium behavior of THC in the halved CO2 experiment suggests that they cancel each other. In addition, the nonlinear relationship between density and temperature of seawater leads to the nonlinear behavior of the THC responses in doubled and halved CO2 experiments.%利用海-气耦合模式模拟了北大西洋热盐环流对外强迫的平衡响应。大气中CO2浓度加倍后,热盐环流强度将减弱约20%;大气中CO2浓度减半后,热盐环流将增强约13%。研究结果表明,热盐环流对外强迫的响应有两个阶段:瞬变阶段和平衡阶段。瞬变响应主要取决于局地海表热通量和淡水通量的变化,平衡响应还与非局地热量输送和淡水输送过程有关,两个过程作用相互竞争。在CO2加倍实验中,与淡水输送相关联的正反馈作用更强,导致热盐环流略有恢复;在CO2减半实验中,热量输送与淡水输送作用相抵,热盐环流没有明显的恢复。此外,海水密度与其温度的非线性关系导致CO2加倍和减半实验中热盐环

  13. The Origin and Time Dependence of the Amount and Composition of Non-Constituent Gases Present in Crystal Growth Systems

    Science.gov (United States)

    Palosz, Witold

    1998-01-01

    Presence of different, non-constituent gases may be a critical factor in crystal growth systems. In Physical Vapor Transport processes the cras(es) can be used intentionally (to prevent excessively high, unstable growth conditions), or can evolve unintentionally during the course of the process (which may lead to undesired reduction in the -rowth rate). In melt growth, particularly under low gravity conditions (reduced hydrostatic pressure) the gas present in the system may contribute to formation of voids in the growing crystals and even to a separation of the crystal and the liquid phase [1]. On the other hand, some amount of gas may facilitate 'contactless' crystal growth particularly under reduced gravity conditions [2 - 6]. Different non-constituent gases may be present in growth ampoules, and their amount and composition may change during the crystallization process. Some gases can appear even in empty ampoules sealed originally under high vacuum: they may diffuse in from the outside, and/or desorb from the ampoule walls. Residual gases can also be generated by the source materials: even very high purity commercial elements and compounds may contain trace amounts of impurities, particularly oxides. The oxides may have low volatilities themselves but their reaction with other species, particularly carbon and hydrogen, may produce volatile compounds like water or carbon oxides. The non-constituent gases, either added initially to the system or evolved during the material processing, may diffuse out of the ampoule during the course of the experiment. Gases present outside (e.g. as a protective atmosphere or thermal conductor) may diffuse into the ampoule. In either case the growth conditions and the quality of the crystals may be affected. The problem is of a particular importance in sealed systems where the amount of the gases cannot be directly controlled. Therefore a reasonable knowledge and understanding of the origin, composition, magnitude, and change with

  14. Surface-atmosphere exchange of ammonia over peatland using QCL-based eddy-covariance measurements and inferential modeling

    DEFF Research Database (Denmark)

    Zöll, Undine; Brümmer, Christian; Schrader, Frederik;

    2016-01-01

    Recent advances in laser spectrometry offer new opportunities to investigate ecosystem-atmosphere exchange of environmentally relevant trace gases. In this study, we demonstrate the applicability of a quantum cascade laser (QCL) absorption spectrometer to continuously measure ammonia concentratio...... as important additional instruments within long-term monitoring research infrastructures such as ICOS or NEON at sites with strong nearby ammonia sources leading to relatively high mean background concentrations and fluxes....

  15. Simulation of source intensity variations from atmospheric dust for solar occultation Fourier transform infrared spectroscopy at Mars

    Science.gov (United States)

    Olsen, K. S.; Toon, G. C.; Strong, K.

    2016-05-01

    A Fourier transform spectrometer observing in solar occultation mode from orbit is ideally suited to detecting and characterizing vertical profiles of trace gases in the Martian atmosphere. This technique benefits from a long optical path length and high signal strength, and can have high spectral resolution. The Martian atmosphere is often subject to large quantities of suspended dust, which attenuates solar radiation along the line-of-sight. An instrument making solar occultation measurements scans the limb of the atmosphere continuously, and the optical path moves through layers of increasing or decreasing dust levels during a single interferogram acquisition, resulting in time-varying signal intensity. If uncorrected, source intensity variations (SIVs) can affect the relative depth of absorption lines, negatively impacting trace gas retrievals. We have simulated SIVs using synthetic spectra for the Martian atmosphere, and investigated different techniques to mitigate the effects of SIVs. We examined high-pass filters in the wavenumber domain, and smoothing methods in the optical path difference (OPD) domain, and conclude that using a convolution operator in the OPD domain can isolate the SIVs and be used to correct for it. We observe spectral residuals of less than 0.25% in both high- and low-dust conditions, and retrieved volume mixing ratio vertical profile differences on the order of 0.5-3% for several trace gases known to be present in the Martian atmosphere. These differences are smaller than those caused by adding realistic noise to the spectra. This work thus demonstrates that it should be possible to retrieve vertical profiles of trace gases in a dusty Martian atmosphere using solar occultation if the interferograms are corrected for the effects of dust.

  16. The search for active release of volcanic gases on Mars

    Science.gov (United States)

    Khayat, Alain; Villanueva, Geronimo; Mumma, Michael; Tokunaga, Alan

    2015-11-01

    The study of planetary atmospheres by means of spectroscopy is important for understanding their origin and evolution. The presence of short-lived trace gases in the martian atmosphere would imply recent production, for example, by ongoing geologic activity. On Earth, sulfur dioxide (SO2), sulfur monoxide (SO) and hydrogen sulfide (H2S) are the main sulfur-bearing gases released during volcanic outgassing. Carbonyl sulfide (OCS), also released from some volcanoes on Earth (e.g., Erebus and Nyiragongo), could be formed by reactions involving SO2 or H2S inside magma chambers. We carried out the first ground-based, semi-simultaneous, multi-band and multi-species search for such gases above the Tharsis and Syrtis volcanic regions on Mars. The submillimeter search extended between 23 November 2011 and 13 May 2012 which corresponded to Mars’ mid Northern Spring and early Northern Summer seasons (Ls = 34-110°). The strong submillimeter rotational transitions of SO2, SO and H2S were targeted using the high-resolution heterodyne receiver (aka Barney) on the Caltech Submillimeter Observatory. We reached sensitivities sufficient to detect a volcanic release on Mars that is 4% of the SO2 released continuously from Kilauea volcano in Hawaii, or 5% that of the Masaya volcano in Nicaragua. The infrared search covered OCS in its combination band (ν2+ν3) at 3.42 μm at two successive Mars years, during Mars’ late Northern Spring and mid Northern Summer seasons, spanning Ls= 43º and Ls= 147º. The targeted volcanic districts were observed during the two intervals, 14 Dec. 2011 to 6 Jan. 2012 in the first year, and 30 May 2014 to 16 June 2014 in the second year, using the high resolution infrared spectrometer (CSHELL) on NASA’s Infrared Telescope Facility (NASA/IRTF). We will present our results and discuss their implications for current volcanic outgassing activity on the red planet. We gratefully acknowledge support from the NASA Planetary Astronomy Program under NASA

  17. Atmospheric materiality

    DEFF Research Database (Denmark)

    Wieczorek, Izabela

    2016-01-01

    experience and, consequently, to the conceptual and methodological shifts in the production of space, and hence in the way we think about materiality. In this context, architectural space is understood as a contingent construction – a space of engagement that appears to us as a result of continuous...... characteristics of atmosphere as a spatial phenomenon, the aim of this text is to illustrate these associations and draw out design protocols, focusing on ways in which atmosphere can be conditioned architecturally. In other words, the objective is to trace the conceptual contours of ‘atmospheric materiality’....

  18. Validation of aerosols, reactive gases and greenhouse gases in the CAMS forecasts, analyses and reanalyses

    Science.gov (United States)

    Eskes, Henk; Basart, Sara; Blechschmidt, Anne; Chabrillat, Simon; Clark, Hannah; Cuevas, Emilio; Engelen, Richard; Kapsomenakis, John; Katragkou, Eleni; Mantzius Hansen, Kaj; Niemeijer, Sander; Ramonet, Michel; Schulz, Michael; Sudarchikova, Natalia; Wagner, Annette; Warneke, Thorsten

    2016-04-01

    The Atmosphere Monitoring Service of the European Copernicus Programme (CAMS) is an operational service providing analyses, reanalyses and daily forecasts of aerosols, reactive gases and greenhouse gases on a global scale, and air quality forecasts and reanalyses on a regional scale. CAMS is based on the systems developed during the European MACC I-II-III (Monitoring Atmospheric Composition and Climate) research projects. In CAMS data assimilation techniques are applied to combine in-situ and remote sensing observations with global and European-scale models of atmospheric reactive gases, aerosols and greenhouse gases. The global component is based on the Integrated Forecast System of the ECMWF, and the regional component on an ensemble of 7 European air quality models. CAMS is implemented by ECMWF, and the transition from MACC to CAMS is currently being implemented (2015-2016). CAMS has a dedicated validation activity, a partnership of 13 institutes co-ordinated by KNMI, to document the quality of the atmospheric composition products. In our contribution we discuss this validation activity, including the measurement data sets, validation requirements, the operational aspects, the upgrade procedure, the validation reports and scoring methods, and the model configurations and assimilation systems validated. Of special concern are the forecasts of high pollution concentration events (fires, dust storms, air pollution events, volcano ash and SO2). A few interesting validation results will be shown.

  19. Broader perspectives for comparing different greenhouse gases.

    Science.gov (United States)

    Manning, Martin; Reisinger, Andy

    2011-05-28

    Over the last 20 years, different greenhouse gases have been compared, in the context of climate change, primarily through the concept of global warming potentials (GWPs). This considers the climate forcing caused by pulse emissions and integrated over a fixed time horizon. Recent studies have shown that uncertainties in GWP values are significantly larger than previously thought and, while past literature in this area has raised alternative means of comparison, there is not yet any clear alternative. We propose that a broader framework for comparing greenhouse gases has become necessary and that this cannot be addressed by using simple fixed exchange rates. From a policy perspective, the framework needs to be clearly aligned with the goal of climate stabilization, and we show that comparisons between gases can be better addressed in this context by the forcing equivalence index (FEI). From a science perspective, a framework for comparing greenhouse gases should also consider the full range of processes that affect atmospheric composition and how these may alter for climate stabilization at different levels. We cover a basis for a broader approach to comparing greenhouse gases by summarizing the uncertainties in GWPs, linking those to uncertainties in the FEIs consistent with stabilization, and then to a framework for addressing uncertainties in the corresponding biogeochemical processes.

  20. Experimental study on mercury removal by Taixi activated coke under complex atmosphere of flue gases%复杂烟气条件下太西活性焦脱除Hg0的实验研究

    Institute of Scientific and Technical Information of China (English)

    张海茹; 刘浩; 王萌; 吴昊; 杨宏旻

    2012-01-01

    为了解复杂烟气条件下活性焦吸附剂的脱汞特性,利用汞渗透管和主要气体成分模拟复杂烟气,在实验室规模的固态吸附剂汞吸附效能测定系统上,进行了太西活性焦吸附单质汞的实验研究,并采用FT-IR对活性焦表面进行了光谱表征.结果表明,在活性焦表面存在各种含氧官能团;在CO2/N2/O2/SO2/Hg0烟气体系中,当SO2加入量为400、855、1 520 mL/m3时,出口汞浓度分别为36、43、48 μg/m3,SO2对系统吸附Hg0的能力有抑制作用;在CO2/N2/O2/NO/Hg0烟气体系中,较低浓度的NO对Hg0脱除有抑制作用,而高浓度值的NO抑制作用减弱;在CO2/N2/O2/NO/SO2/Hg0烟气体系下,提高NO浓度对Hg2脱除有一定的促进作用,而提高SO2浓度初期促进汞的脱除,后期则表现为抑制作用.%In order to clarify the adsorption characteristic of activated coke under complex atmosphere of flue gases, a series of tests were conducted with a bench-scale fixed bed reactor. The simulated flue gas was prepared by mixing main composition of flue gas with mercury vapors generated through permeation tube. The surface properties were characterized by FT-IR. The results show that the performance of mercury removal is related to the surface chemistry of activated coke, and the oxygen-containing functional groups are the important factor affecting the adsorption and catalysis of Hg°. The adsorption performance of Hg° with activated coke is influenced by SO2 obviously and inhibition is observed in the removal process. With increasing concentration of SO2, from 400, 855 to 1 520 mL/m3, the concentration of Hg° at the outlet of the reactor increased from 36, 43 to 48 μg/m3. The complex impact of NO on the adsorptive capacity of Hg° is found that NO with lower concentration promotes the adsorption of elemental mercury while inhibits it at higher value in CO2/N2/O2/NO/ Hg° system. The increasing concentration of NO with the stationary concentration of SO2 has a

  1. Strongly correlated Bose gases

    Science.gov (United States)

    Chevy, F.; Salomon, C.

    2016-10-01

    The strongly interacting Bose gas is one of the most fundamental paradigms of quantum many-body physics and the subject of many experimental and theoretical investigations. We review recent progress on strongly correlated Bose gases, starting with a description of beyond mean-field corrections. We show that the Efimov effect leads to non universal phenomena and to a metastability of the low temperature Bose gas through three-body recombination to deeply bound molecular states. We outline differences and similarities with ultracold Fermi gases, discuss recent experiments on the unitary Bose gas, and finally present a few perspectives for future research.

  2. Molecular understanding of sulphuric acid-amine particle nucleation in the atmosphere

    CERN Document Server

    Almeida, João; Kürten, Andreas; Ortega, Ismael K; Kupiainen-Määttä, Oona; Praplan, Arnaud P; Adamov, Alexey; Amorim, Antonio; Bianchi, Federico; Breitenlechner, Martin; David, André; Dommen, Josef; Donahue, Neil M; Downard, Andrew; Dunne, Eimear; Duplissy, Jonathan; Ehrhart, Sebastian; Flagan, Richard C; Franchin, Alessandro; Guida, Roberto; Hakala, Jani; Hansel, Armin; Heinritzi, Martin; Henschel, Henning; Jokinen, Tuija; Junninen, Heikki; Kajos, Maija; Kangasluoma, Juha; Keskinen, Helmi; Kupc, Agnieszka; Kurtén, Theo; Kvashin, Alexander N; Laaksonen, Ari; Lehtipalo, Katrianne; Leiminger, Markus; Leppä, Johannes; Loukonen, Ville; Makhmutov, Vladimir; Mathot, Serge; McGrath, Matthew J; Nieminen, Tuomo; Olenius, Tinja; Onnela, Antti; Petäjä, Tuukka; Riccobono, Francesco; Riipinen, Ilona; Rissanen, Matti; Rondo, Linda; Ruuskanen, Taina; Santos, Filipe D; Sarnela, Nina; Schallhart, Simon; Schnitzhofer, Ralf; Seinfeld, John H; Simon, Mario; Sipilä, Mikko; Stozhkov, Yuri; Stratmann, Frank; Tomé, Antonio; Tröstl, Jasmin; Tsagkogeorgas, Georgios; Vaattovaara, Petri; Viisanen, Yrjo; Virtanen, Annele; Vrtala, Aron; Wagner, Paul E; Weingartner, Ernest; Wex, Heike; Williamson, Christina; Wimmer, Daniela; Ye, Penglin; Yli-Juuti, Taina; Carslaw, Kenneth S; Kulmala, Markku; Curtius, Joachim; Baltensperger, Urs; Vehkamaki, Hanna; Kirkby, Jasper

    2013-01-01

    Nucleation of aerosol particles from trace atmospheric vapours is thought to provide up to half of global cloud condensation nuclei. Aerosols can cause a net cooling of climate by scattering sunlight and by leading to smaller but more numerous cloud droplets, which makes clouds brighter and extends their lifetimes. Atmospheric aerosols derived from human activities are thought to have compensated for a large fraction of the warming caused by greenhouse gases. However, despite its importance for climate, atmospheric nucleation is poorly understood. Recently, it has been shown that sulphuric acid and ammonia cannot explain particle formation rates observed in the lower atmosphere. It is thought that amines may enhance nucleation, but until now there has been no direct evidence for amine ternary nucleation under atmospheric conditions. Here we use the CLOUD (Cosmics Leaving OUtdoor Droplets) chamber at CERN and find that dimethylamine above three parts per trillion by volume can enhance particle formation rates ...

  3. Noble Gases in the Chelyabinsk Meteorites

    Science.gov (United States)

    Haba, Makiko K.; Sumino, Hirochika; Nagao, Keisuke; Mikouchi, Takashi; Komatsu, Mutsumi; Zolensky, Michael E.

    2014-01-01

    The Chelyabinsk meteorite fell in Russia on February 15, 2013 and was classified as LL5 chondrite. The diameter before it entered the atmosphere has been estimated to be about 20 m [1]. Up to now, numerous fragments weighing much greater than 100 kg in total have been collected. In this study, all noble gases were measured for 13 fragments to investigate the exposure history of the Chelyabinsk meteorite and the thermal history of its parent asteroid.

  4. Comparision Study of Dielectric Barrier Discharge in Inert Gases at Atmospheric Pressure%大气压不同惰性气体介质阻挡放电特性的比较

    Institute of Scientific and Technical Information of China (English)

    罗海云; 冉俊霞; 王新新

    2012-01-01

    To deeply understand dielectric barrier discharge in inert gases at atmospheric pressure, we investigated the breakdown voltage, the discharge mode, and evolution of DBD in a parallel gap by means of electrical measurements and fast photography in helium, neon, and argon at atmospheric pressure. Homogenous discharges could be easily produced in 2 - 8 mm gaps in helium and neon, and they were attributed to glow discharge. Compared to that in helium or neon, the homogenous DBD often covered only a part of the electrode in 2 mm-argon using the high frequency power. And with a small increase of the applied voltage, it would turn into a pattern mode. When the argon width was no less than 3mm, the DBD always resulted in bright filamentary streamers in which the current density could reach 7. 5 A/cm2. High-speed time-resolved photographs of the homogenous discharge in helium, neon and argon were taken using an ICCD camera. Side-view photographs showed an evolution from Townsend discharge to glow discharge. The end-view photographs exhibited a radial development. The spectroscopic diagnosis showed that the penning ionization between energetic metastabilty and impurities was the most important reason leading to a homogenous discharge. The N+ first negative system(B2∑u+ →X2∑g+ ), existing in helium discharge, could not be observed in the neon or argon, as was due to the lower energy level of metastable neon and argon states. Instead, the emission spectral lines of N2 second positive band system( C3 Пu→B3 Пg) were observed in neon and argon.%为了加深对大气压惰性气体介质阻挡放电的认识,使用电特性测量、高速摄影,发射光谱等手段研究了平板结构大气压惰性气体介质阻挡放电的放电模式、演化过程以及放电机理,并对不同气体的放电特性进行了比较。实验结果表明在2~8mm大气压氦气、氖气中可很容易的实现稳定的均匀放电,并且其放

  5. Active Upper-atmosphere Chemistry and Dynamics from Polar Circulation Reversal on Titan

    Science.gov (United States)

    Teanby, Nicholas A.; Irwin, Patrick Gerard Joseph; Nixon, Conor A.; DeKok, Remco; Vinatier, Sandrine; Coustenis, Athena; Sefton-Nash, Elliot; Calcutt, Simon B.; Flasar, Michael F.

    2012-01-01

    Saturn's moon Titan has a nitrogen atmosphere comparable to Earth's, with a surface pressure of 1.4 bar. Numerical models reproduce the tropospheric conditions very well but have trouble explaining the observed middle-atmosphere temperatures, composition and winds. The top of the middle-atmosphere circulation has been thought to lie at an altitude of 450 to 500 kilometres, where there is a layer of haze that appears to be separated from the main haze deck. This 'detached' haze was previously explained as being due to the colocation of peak haze production and the limit of dynamical transport by the circulation's upper branch. Herewe report a build-up of trace gases over the south pole approximately two years after observing the 2009 post-equinox circulation reversal, from which we conclude that middle-atmosphere circulation must extend to an altitude of at least 600 kilometres. The primary drivers of this circulation are summer-hemisphere heating of haze by absorption of solar radiation and winter-hemisphere cooling due to infrared emission by haze and trace gases; our results therefore imply that these effects are important well into the thermosphere (altitudes higher than 500 kilometres). This requires both active upper-atmosphere chemistry, consistent with the detection of high-complexity molecules and ions at altitudes greater than 950 kilometres, and an alternative explanation for the detached haze, such as a transition in haze particle growth from monomers to fractal structures.

  6. Synthetic gases production

    Energy Technology Data Exchange (ETDEWEB)

    Mazaud, J.P.

    1996-06-01

    The natural gas or naphtha are the main constituents used for the production of synthetic gases. Several production ways of synthetic gases are industrially used as for example the natural gas or naphtha catalytic reforming, the selective oxidation of natural gas or heavy fuels and the coal oxy-vapo-gasification. The aim of this work is to study the different steps of production and treatment of the synthetic gases by the way of catalytic reforming. The first step is the desulfurization of the hydrocarbons feedstocks. The process used in industry is described. Then is realized the catalytic hydrocarbons reforming process. After having recalled some historical data on the catalytic reforming, the author gives the reaction kinetics and thermodynamics. The possible reforming catalysts, industrial equipments and furnaces designs are then exposed. The carbon dioxide is a compound easily obtained during the reforming reactions. It is a wasteful and harmful component which has to be extracted of the gaseous stream. The last step is then the gases de-carbonation. Two examples of natural gas or naphtha reforming reactions are at last given: the carbon monoxide conversion by steam and the carbon oxides reactions with hydrogen (methanization). (O.M.). 8 figs., 6 tabs.

  7. Strongly interacting Fermi gases

    Directory of Open Access Journals (Sweden)

    Bakr W.

    2013-08-01

    Full Text Available Strongly interacting gases of ultracold fermions have become an amazingly rich test-bed for many-body theories of fermionic matter. Here we present our recent experiments on these systems. Firstly, we discuss high-precision measurements on the thermodynamics of a strongly interacting Fermi gas across the superfluid transition. The onset of superfluidity is directly observed in the compressibility, the chemical potential, the entropy, and the heat capacity. Our measurements provide benchmarks for current many-body theories on strongly interacting fermions. Secondly, we have studied the evolution of fermion pairing from three to two dimensions in these gases, relating to the physics of layered superconductors. In the presence of p-wave interactions, Fermi gases are predicted to display toplogical superfluidity carrying Majorana edge states. Two possible avenues in this direction are discussed, our creation and direct observation of spin-orbit coupling in Fermi gases and the creation of fermionic molecules of 23Na 40K that will feature strong dipolar interactions in their absolute ground state.

  8. Atmospheric refraction : a history

    NARCIS (Netherlands)

    Lehn, WH; van der Werf, S

    2005-01-01

    We trace the history of atmospheric refraction from the ancient Greeks up to the time of Kepler. The concept that the atmosphere could refract light entered Western science in the second century B.C. Ptolemy, 300 years later, produced the first clearly defined atmospheric model, containing air of un

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1979-06-01

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

  10. High-resolution spectroscopy of gases for industrial applications

    DEFF Research Database (Denmark)

    Fateev, Alexander; Clausen, Sønnik

    High-resolution spectroscopy of gases is a powerful technique which has various fundamental and practical applications: in situ simultaneous measurements of gas temperature and gas composition, radiative transfer modeling, validation of existing and developing of new databases and etc. Existing...... to, for example, atmospheric research, combustion and gasification. Some high-temperature, high-resolution IR/UV absorption/transmission measurements gases (e.g. CO2, SO2, SO3 and phenol) are presented....

  11. Global Reactive Gases in the MACC project

    Science.gov (United States)

    Schultz, M. G.

    2012-04-01

    In preparation for the planned atmospheric service component of the European Global Monitoring for Environment and Security (GMES) initiative, the EU FP7 project Monitoring of Atmospheric Composition and Climate (MACC) developed a preoperational data assimilation and modelling system for monitoring and forecasting of reactive gases, greenhouse gases and aerosols. The project is coordinated by the European Centre for Medium-Range Weather Forecast (ECMWF) and the system is built on ECMWF's Integrated Forecasting System (IFS) which has been coupled to the chemistry transport models MOZART-3 and TM5. In order to provide daily forecasts of up to 96 hours for global reactive gases, various satellite retrieval products for ozone (total column and profile data), CO, NO2, CH2O and SO2 are either actively assimilated or passively monitored. The MACC system is routinely evaluated with in-situ data from ground-based stations, ozone sondes and aircraft measurements, and with independent satellite retrievals. Global MACC reactive gases forecasts are used in the planning and analysis of large international field campaigns and to provide dynamical chemical boundary conditions to regional air quality models worldwide. Several case studies of outstanding air pollution events have been performed, and they demonstrate the strengths and weaknesses of chemical data assimilation based on current satellite data products. Besides the regular analyses and forecasts of the tropospheric chemical composition, the MACC system is also used to monitor the evolution of stratospheric ozone. A comprehensive reanalysis simulation from 2003 to 2010 provides new insights into the interannual variability of the atmospheric chemical composition.

  12. Trace-gas sensing using the compliance voltage of an external cavity quantum cascade laser

    Energy Technology Data Exchange (ETDEWEB)

    Phillips, Mark C.; Taubman, Matthew S.

    2013-06-04

    Quantum cascade lasers (QCLs) are increasingly being used to detect, identify, and measure levels of trace gases in the air. External cavity QCLs (ECQCLs) provide a broadly-tunable infrared source to measure absorption spectra of chemicals and provide high detection sensitivity and identification confidence. Applications include detecting chemical warfare agents and toxic industrial chemicals, monitoring building air quality, measuring greenhouse gases for atmospheric research, monitoring and controlling industrial processes, analyzing chemicals in exhaled breath for medical diagnostics, and many more. Compact, portable trace gas sensors enable in-field operation in a wide range of platforms, including handheld units for use by first responders, fixed installations for monitoring air quality, and lightweight sensors for deployment in unmanned aerial vehicles (UAVs). We present experimental demonstration of a new chemical sensing technique based on intracavity absorption in an external cavity quantum cascade laser (ECQCL). This new technique eliminates the need for an infrared photodetector and gas cell by detecting the intracavity absorption spectrum in the compliance voltage of the laser device itself. To demonstrate and characterize the technique, we measure infrared absorption spectra of chemicals including water vapor and Freon-134a. Sub-ppm detection limits in one second are achieved, with the potential for increased sensitivity after further optimization. The technique enables development of handheld, high-sensitivity, and high-accuracy trace gas sensors for in-field use.

  13. The greenhouse gases