Towards uncertainty estimates in global operational forecasts of trace gases in the Copernicus Atmosphere Monitoring System

Science.gov (United States)

Huijnen, V.; Bouarar, I.; Chabrillat, S. H.; Christophe, Y.; Thierno, D.; Karydis, V.; Marecal, V.; Pozzer, A.; Flemming, J.

2017-12-01

Operational atmospheric composition analyses and forecasts such as developed in the Copernicus Atmosphere Monitoring Service (CAMS) rely on modules describing emissions, chemical conversion, transport and removal processing, as well as data assimilation methods. The CAMS forecasts can be used to drive regional air quality models across the world. Critical analyses of uncertainties in any of these processes are continuously needed to advance the quality of such systems on a global scale, ranging from the surface up to the stratosphere. With regard to the atmospheric chemistry to describe the fate of trace gases, the operational system currently relies on a modified version of the CB05 chemistry scheme for the troposphere combined with the Cariolle scheme to describe stratospheric ozone, as integrated in ECMWF's Integrated Forecasting System (IFS). It is further constrained by assimilation of satellite observations of CO, O3 and NO2. As part of CAMS we have recently developed three fully independent schemes to describe the chemical conversion throughout the atmosphere. These parameterizations originate from parent model codes in MOZART, MOCAGE and a combination of TM5/BASCOE. In this contribution we evaluate the correspondence and elemental differences in the performance of the three schemes in an otherwise identical model configuration (excluding data-assimilation) against a large range of in-situ and satellite-based observations of ozone, CO, VOC's and chlorine-containing trace gases for both troposphere and stratosphere. This analysis aims to provide a measure of model uncertainty in the operational system for tracers that are not, or poorly, constrained by data assimilation. It aims also to provide guidance on the directions for further model improvement with regard to the chemical conversion module.

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.

Trace gases and other potential perturbations to global climate

International Nuclear Information System (INIS)

Wang, W.; Wuebbles, D.J.; Washington, W.M.; Isaacs, R.G.; Molnar, G.

1986-01-01

We review the various natural and anthropogenic factors that may affect the climate. The purpose is to summarize our understanding of these factors and their potential future climatic effects so that CO 2 -induced climate change can be viewed in a proper context. The factors we discuss include trace gases, anthropogenic and volcanic aerosols, variation of solar constant, change of surface characteristics, and releases of waste heat. We discuss the origins of the various natural and anthropogenic perturbations, the physical and chemical processes and their interactions, model sensitivity calculations, and model projections of their potential future climatic effects. The discussions center on trace gases because of their potentially large climatic effects. It appears that the increases of atmospheric trace gases of other kinds in addition to CO 2 could have important climatic effects. The model calculations suggest that the combined effect of these other trace gases, and the associated change of atmospheric ozone and water vapor distributions, could potentially warm the climate by an amount comparable in magnitude to the effect of doubling the CO 2 . Aerosols of anthropogenic origins may have substantial effects on regional climate, while the volcanic aerosols may have an effect on large-scale climate for up to a few years after injection. Changes of surface characteristics and releases of waste heat may also have substantial effects on the regional climate, but these effects are most likely to be small when compared with the effect of CO 2 increase. Changes of solar constant could have an effect on the global scale, but the time scale is much longer. There is much more that needs to be learned with regard to the above mentioned natural and anthropogenic factors that may affect the climate. A brief summary of those needs is presented

Climate-chemical interactions and effects of changing atmospheric trace gases

Science.gov (United States)

Ramanathan, V.; Callis, L.; Cess, R.; Hansen, J.; Isaksen, I.

1987-01-01

The paper considers trace gas-climate effects including the greenhouse effect of polyatomic trace gases, the nature of the radiative-chemical interactions, and radiative-dynamical interactions in the stratosphere, and the role of these effects in governing stratospheric climate change. Special consideration is given to recent developments in the investigations of the role of oceans in governing the transient climate responses, and a time-dependent estimate of the potential trace gas warming from the preindustrial era to the early 21st century. The importance of interacting modeling and observational efforts is emphasized. One of the problems remaining on the observational front is the lack of certainty in current estimates of the rate of growth of CO, O3, and NOx; the primary challenge is the design of a strategy that will minimize the sampling errors.

Soil-atmosphere trace gas exchange in semiarid and arid zones.

Science.gov (United States)

Galbally, Ian E; Kirstine, Wayne V; Meyer, C P Mick; Wang, Ying Ping

2008-01-01

A review is presented on trace gas exchange of CH4, CO, N2O, and NOx arising from agriculture and natural sources in the world's semiarid and arid zones due to soil processes. These gases are important contributors to the radiative forcing and the chemistry of the atmosphere. Quantitative information is summarized from the available studies. Between 5 and 40% of the global soil-atmosphere exchange for these gases (CH4, CO, N2O, and NOx) may occur in semiarid and arid zones, but for each of these gases there are fewer than a dozen studies to support the individual estimates, and these are from a limited number of locations. Significant differences in the biophysical and chemical processes controlling these trace gas exchanges are identified through the comparison of semiarid and arid zones with the moist temperate or wet/dry savanna land regions. Therefore, there is a poorly quantified understanding of the contribution of these regions to the global trace gas cycles and atmospheric chemistry. More importantly, there is a poor understanding of the feedback between these exchanges, global change, and regional land use and air pollution issues. A set of research issues is presented.

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

International Nuclear Information System (INIS)

Cushman, R.M.; Stoss, F.W.; Univ. of Tennessee, Knoxville, TN

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 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

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.

Ultrasensitive detection of atmospheric trace gases using frequency modulation spectroscopy

Science.gov (United States)

Cooper, David E.

1986-01-01

Frequency modulation (FM) spectroscopy is a new technique that promises to significantly extend the state-of-the-art in point detection of atmospheric trace gases. FM spectroscopy is essentially a balanced bridge optical heterodyne approach in which a small optical absorption or dispersion from an atomic or molecular species of interest generates an easily detected radio frequency (RF) signal. This signal can be monitored using standard RF signal processing techniques and is, in principle, limited only by the shot noise generated in the photodetector by the laser source employed. The use of very high modulation frequencies which exceed the spectral width of the probed absorption line distinguishes this technique from the well-known derivative spectroscopy which makes use of low (kHz) modulation frequencies. FM spectroscopy was recently extended to the 10 micron infrared (IR) spectral region where numerous polyatomic molecules exhibit characteristic vibrational-rotational bands. In conjunction with tunable semiconductor diode lasers, the quantum-noise-limited sensitivity of the technique should allow for the detection of absorptions as small as .00000001 in the IR spectral region. This sensitivity would allow for the detection of H2O2 at concentrations as low as 1 pptv with an integration time of 10 seconds.

Applications of stable isotope analysis to atmospheric trace gas budgets

Directory of Open Access Journals (Sweden)

Brenninkmeijer C. A.M.

2009-02-01

Full Text Available Stable isotope analysis has become established as a useful method for tracing the budgets of atmospheric trace gases and even atmospheric oxygen. Several new developments are briefly discussed in a systematic way to give a practical guide to the scope of recent work. Emphasis is on applications and not on instrumental developments. Processes and reactions are less considered than applications to resolve trace gas budgets. Several new developments are promising and applications hitherto not considered to be possible may allow new uses.

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.

History of chemically and radiatively important atmospheric gases from the Advanced Global Atmospheric Gases Experiment (AGAGE

Directory of Open Access Journals (Sweden)

R. G. Prinn

2018-06-01

�to determine the average concentrations and trends of tropospheric hydroxyl radicals (OH from the rates of destruction of atmospheric trichloroethane (CH3CCl3, HFCs, and HCFCs and estimates of their emissions; (5 to determine from atmospheric observations and estimates of their destruction rates the magnitudes and distributions by region of surface sources and sinks of all measured gases; (6 to provide accurate data on the global accumulation of many of these trace gases that are used to test the synoptic-, regional-, and global-scale circulations predicted by three-dimensional models; and (7 to provide global and regional measurements of methane, carbon monoxide, and molecular hydrogen and estimates of hydroxyl levels to test primary atmospheric oxidation pathways at midlatitudes and the tropics. Network Information and Data Repository: http://agage.mit.edu/data or http://cdiac.ess-dive.lbl.gov/ndps/alegage.html (https://doi.org/10.3334/CDIAC/atg.db1001.

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.

Measurement of Selected Organic Trace Gases During TRACE-P

Science.gov (United States)

Atlas, Elliot

2004-01-01

Major goals of the TRACE-P mission were: 1) to investigate the chemical composition of radiatively important gases, aerosols, and their precursors in the Asian outflow over the western Pacific, and 2) to describe and understand the chemical evolution of the Asian outflow as it is transported and mixed into the global troposphere. The research performed as part of this proposal addressed these major goals with a study of the organic chemical composition of gases in the TRACE-P region. This work was a close collaboration with the Blake/Rowland research group at UC-Irvine, and they have provided a separate report for their funded effort.

Human activities affecting trace gases and climate

International Nuclear Information System (INIS)

Braatz, B.; Ebert, C.

1990-01-01

The Earth's climate has been in a constant state of change throughout geologic time due to natural perturbations in the global geobiosphere. However, various human activities have the potential to cause future global warming over a relatively short amount of time. These activities, which affect the Earth's climate by altering the concentrations of trace gases in the atmosphere, include energy consumption, particularly fossil-fuel consumption; industrial processes (production and use of chlorofluorocarbons, halons, and chlorocarbons, landfilling of wastes, and cement manufacture); changes in land use patterns, particularly deforestation and biomass burning; and agricultural practices (waste burning, fertilizer usage, rice production, and animal husbandry). Population growth is an important underlying factor affecting the level of growth in each activity. This paper describes how the human activities listed above contribute to atmospheric change, the current pattern of each activity, and how levels of each activity have changed since the early part of this century

Tracking Oxidation During Transport of Trace Gases in Air from the Northern to Southern Hemisphere

Science.gov (United States)

Montzka, S. A.; Moore, F. L.; Atlas, E. L.; Parrish, D. D.; Miller, B. R.; Sweeney, C.; McKain, K.; Hall, B. D.; Siso, C.; Crotwell, M.; Hintsa, E. J.; Elkins, J. W.; Blake, D. R.; Barletta, B.; Meinardi, S.; Claxton, T.; Hossaini, R.

2017-12-01

Trace gas mole fractions contain the imprint of recent influences on an air mass such as sources, transport, and oxidation. Covariations among the many gases measured from flasks during ATom and HIPPO, and from the ongoing NOAA cooperative air sampling program enable recent influences to be identified from a wide range of sources including industrial activity, biomass burning, emissions from wetlands, and uptake by terrestrial ecosystems. In this work we explore the evolution of trace gas concentrations owing to atmospheric oxidation as air masses pass through the tropics, the atmospheric region with the highest concentrations of the hydroxyl radical. Variations in C2-C5 hydrocarbon concentrations downwind of source regions provide a measure of photochemical ageing in an air mass since emission, but they become less useful when tracking photochemical ageing as air is transported from the NH into the SH owing to their low mixing ratios, lifetimes that are very short relative to transport times, non-industrial sources in the tropics (e.g., biomass burning), and southern hemispheric sources. Instead, we consider a range of trace gases and trace gas pairs that provide a measure of photochemical processing as air transits the tropics. To be useful in this analysis, these trace gases would have lifetimes comparable to interhemispheric transport times, emissions arising from only the NH at constant relative magnitudes, and concentrations sufficient to allow precise and accurate measurements in both hemispheres. Some anthropogenically-emitted chlorinated hydrocarbons meet these requirements and have been measured during ATom, HIPPO, and from NOAA's ongoing surface sampling efforts. Consideration of these results and their implications for tracking photochemical processing in air as it is transported across the tropics will be presented.

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

Isotope aided studies of atmospheric carbon dioxide and other greenhouse gases. Phase II

Energy Technology Data Exchange (ETDEWEB)

NONE

2002-01-01

The substantial increase in atmospheric greenhouse gas concentrations and their role in global warming have become major concerns of world governments. Application of isotope techniques to label sources and sinks of CO{sub 2} and other greenhouse gases has emerged as a potentially powerful method for reducing uncertainties in the global CO{sub 2} budgets and for tracing pathways and interaction of terrestrial, oceanic, and atmospheric pools of carbon. As with CO{sub 2} concentration measurements, meaningful integration of isotopes in global models requires careful attention to quality assurance, quality control and inter-comparability of measurements made by a number of networks and laboratories. To support improvements in isotope measurement capabilities, the IAEA began implementing Co-ordinated Research Projects (CRPs) in 1992. The first project, entitled Isotope Variations of Carbon Dioxide and other Trace Gases in the Atmosphere, was implemented from 1992 to 1994. A significant contribution was made towards a better understanding of the global carbon cycle and especially of the sources and sinks of carbon with data on the {sup 14}C and {sup 13}C content of atmospheric CO{sub 2}, pointing to a better understanding of the problem of the 'missing sink' in the global carbon cycle. Important methodological developments in the field of high precision stable isotope mass spectrometry and improved data acquisition procedures emerged from work carried out within the framework of this programme. The development of pressurized gas standards and planning for an associated interlaboratory calibration were initiated. Due to the good progress and long standing nature of the required work a second CRP was initiated and implemented from 1996 to 1999. It was entitled Isotope aided Studies of Atmospheric Carbon Dioxide and Other Trace Gases - Phase II, to document the close relationship of both programmes. This publication provides an overview of the scientific outcomes of the

Isotope aided studies of atmospheric carbon dioxide and other greenhouse gases. Phase II

International Nuclear Information System (INIS)

2002-01-01

The substantial increase in atmospheric greenhouse gas concentrations and their role in global warming have become major concerns of world governments. Application of isotope techniques to label sources and sinks of CO 2 and other greenhouse gases has emerged as a potentially powerful method for reducing uncertainties in the global CO 2 budgets and for tracing pathways and interaction of terrestrial, oceanic, and atmospheric pools of carbon. As with CO 2 concentration measurements, meaningful integration of isotopes in global models requires careful attention to quality assurance, quality control and inter-comparability of measurements made by a number of networks and laboratories. To support improvements in isotope measurement capabilities, the IAEA began implementing Co-ordinated Research Projects (CRPs) in 1992. The first project, entitled Isotope Variations of Carbon Dioxide and other Trace Gases in the Atmosphere, was implemented from 1992 to 1994. A significant contribution was made towards a better understanding of the global carbon cycle and especially of the sources and sinks of carbon with data on the 14 C and 13 C content of atmospheric CO 2 , pointing to a better understanding of the problem of the 'missing sink' in the global carbon cycle. Important methodological developments in the field of high precision stable isotope mass spectrometry and improved data acquisition procedures emerged from work carried out within the framework of this programme. The development of pressurized gas standards and planning for an associated interlaboratory calibration were initiated. Due to the good progress and long standing nature of the required work a second CRP was initiated and implemented from 1996 to 1999. It was entitled Isotope aided Studies of Atmospheric Carbon Dioxide and Other Trace Gases - Phase II, to document the close relationship of both programmes. This publication provides an overview of the scientific outcomes of the studies conducted within Phase

Adsorption of trace gases to ice surfaces: surface, bulk and co-adsorbate effects

Science.gov (United States)

Kerbrat, Michael; Bartels-Rausch, Thorsten; Huthwelker, Thomas; Schneebeli, Martin; Pinzer, Bernd; Ammann, Markus

2010-05-01

Atmospheric ices frequently interact with trace gases and aerosol making them an important storage, transport or reaction medium in the global ecosystem. Further, this also alters the physical properties of the ice particles with potential consequences for the global irradiation balance and for the relative humidity of surrounding air masses. We present recent results from a set of laboratory experiments of atmospheric relevance to investigate the nature of the uptake processes. The focus of this talk will be placed on the partitioning of acidic acid and nitrous acid on ice surfaces.The presented results span from very simple reversible adsorption experiments of a single trace gas onto ice surfaces to more complex, but well controlled, experimental procedures that successfully allowed us to - Disentangle surface adsorption and uptake into the ice matrix using radioactive labelled trace gases. - Show that simultaneous adsorption of acetic acid and nitrous acid to an ice surface is consistent with the Langmuir co-adsorption model. The experiments were done in a packed ice bed flow tube at atmospheric pressure and at temperatures between 213 and 253 K. The HONO gas phase mixing ratio was between 0.4 and 137 ppbv, the mixing ratio of acetic acid between 5 and 160 ppbv . The use of the radioactive labelled nitrous acid molecules for these experiments enabled in situ monitoring of the migration of trace gas in the flow tube. The measurements showed that the interactions do not only occur through adsorption but also via diffusion into polycrystalline ice. A method is suggested to disentangle the bulk and the surface processes. The co-adsorption of acetic and nitrous acids was also investigated. The measurements are well reproduced by a competitive Langmuir adsorption model.

Long Term Association of Tropospheric Trace gases over Pakistan by exploiting satellite observations and development of Econometric Regression based Model

Science.gov (United States)

Zeb, Naila; Fahim Khokhar, Muhammad; Khan, Saud Ahmed; Noreen, Asma; Murtaza, Rabbia

2017-04-01

Air pollution is the expected key environmental issue of Pakistan as it is ranked among top polluted countries in the region. Ongoing rapid economic growth without any adequate measures is leading to worst air quality over time. The study aims to monitor long term atmospheric composition and association of trace gases over Pakistan. Tropospheric concentrations of CO, TOC, NO2 and HCHO derived from multiple satellite instruments are used for study from year 2005 to 2014. The study will provide first database for tropospheric trace gases over Pakistan. Spatio-temporal assessment identified hotspots and possible sources of trace gases over the Pakistan. High concentrations of trace gases are mainly observed over Punjab region, which may be attributed to its metropolitan importance. It is the major agricultural, industrialized and urbanized (nearly 60 % of the Pakistan's population) sector of the country. The expected sources are the agricultural fires, biomass/fossil fuel burning for heating purposes, urbanization, industrialization and meteorological variations. Seasonal variability is observed to explore seasonal patterns over the decade. Well defined seasonal cycles of trace gases are observed over the whole study period. The observed seasonal patterns also showed some noteworthy association among trace gases, which is further explored by different statistical tests. Seasonal Mann Kendall test is applied to test the significance of trend in series whereas correlation is carried out to measure the strength of association among trace gases. Strong correlation is observed for trace gases especially between CO and TOC. Partial Mann Kendall test is used to ideally identify the impact of each covariate on long term trend of CO and TOC by partialling out each correlating trace gas (covariate). It is observed that TOC, NO2 and HCHO has significant impact on long term trend of CO whereas, TOC critically depends on NO2 concentrations for long term increase over the region

Trace gases and CO sub(2) isotope records from Cabo de Rama, India

Digital Repository Service at National Institute of Oceanography (India)

Bhattacharya, S.K.; Borole, D.V.; Francey, R.J.; Allison, C.E.; Steele, L.P.; Krummel, P.; Langenfelds, R.; Masarie, K.A.; Tiwari, Y.K.; Patra, P.K.

to avoid dan- gerous climate change due to GHG forced warming. Con- centrations of CO 2 , CH 4 and N 2 O have increased at alarming rates, from preindustrial values of 280 ppm, 715 ppb and 270 ppb (circa. 1750) to 379 ppm, 1732 ppb and 319 ppb... an important effect on the con- centration and isotopic composition of atmospheric CO 2 , and the concentrations of other trace gases. Air sampling at CRI contributes to the global atmospheric composition study 10,11 . Given the potential for global impacts...

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

Sensitivity of RF-driven Plasma Filaments to Trace Gases

Science.gov (United States)

Burin, M. J.; Czarnocki, C. J.; Czarnocki, K.; Zweben, S. J.; Zwicker, A.

2011-10-01

Filamentary structures have been observed in many types of plasma discharges in both natural (e.g. lightning) and industrial systems (e.g. dielectric barrier discharges). Recent progress has been made in characterizing these structures, though various aspects of their essential physics remain unclear. A common example of this phenomenon can be found within a toy plasma globe (or plasma ball), wherein a primarily neon gas mixture near atmospheric pressure clearly and aesthetically displays filamentation. Recent work has provided the first characterization of these plasma globe filaments [Campanell et al., Physics of Plasmas 2010], where it was noticed that discharges of pure gases tend not to produce filaments. We have extended this initial work to investigate in greater detail the dependence of trace gases on filamentation within a primarily Neon discharge. Our preliminary results using a custom globe apparatus will be presented, along with some discussion of voltage dependencies. Newly supported by the NSF/DOE Partnership in Basic Plasma Science and Engineering.

First results of the observations of trace gases in the Martian atmosphere by the Planetary Fourier Spectrometer onboard the Mars Express

Science.gov (United States)

Titov, D. V.; Ignatiev, N.; Formisano, V.; Grassi, D.; Giuranna, M.; Maturilli, A.; Piccioni, G.; Moroz, V. I.; Lellouch, E.; Encrenaz, T.; Pfs Team

High spectral resolution observations of Mars by the PFS/Mars Express provide new insight into the atmospheric composition. Spectral features of atmospheric CO2 and its isotopes at 15, 4.3, 2.7, 1.4 μ m, CO at 4.7 and 2.35 μ m, and H2O at 40, 2.56, and 1.38 μ m as well as solar spectral features are clearly identified in the PFS spectra. HDO spectral details at 3.7 μ m were also tentatively detected. The paper will present qualitative and quantitative analysis of the PFS spectra in the regions of spectral bands of trace gases. Abundance of minor constituents will be determined using complete radiative transfer modeling including possible non-LTE effects. We will also present results of search for other minor species with emphasis on the limb observations that provide higher air mass factor.

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

Techniques for the measurement of trace moisture in high-purity electronic specialty gases

International Nuclear Information System (INIS)

Funke, Hans H.; Grissom, Brad L.; McGrew, Clark E.; Raynor, Mark W.

2003-01-01

The control of water vapor (moisture) contamination in process gases is critical to the successful manufacture of semiconductor devices. As specified moisture levels have become more stringent, there is a growing demand for more sensitive analytical methods. Instrumental methods currently being used or in development for measuring trace moisture at ppbv levels include Fourier transform infrared spectroscopy, tunable diode laser absorption spectroscopy, cavity ringdown spectroscopy, intracavity laser spectroscopy, electron impact ionization mass spectrometry, and atmospheric pressure ionization mass spectrometry. In addition, sensor-based technologies such as oscillating quartz crystal microbalances, and chilled mirror-, capacitor-, and electrolytic-based hygrometers operate in this regime. These approaches are presented and reviewed. As the success of each trace moisture method is dependent on the degree to which the different process gases interfere with the measurement process, important process gas applications of the techniques are highlighted. Advantages and disadvantages as well as future developments and trends are also presented

A fiber optic sensor with a metal organic framework as a sensing material for trace levels of water in industrial gases.

Science.gov (United States)

Ohira, Shin-Ichi; Miki, Yusuke; Matsuzaki, Toru; Nakamura, Nao; Sato, Yu-ki; Hirose, Yasuo; Toda, Kei

2015-07-30

Industrial gases such as nitrogen, oxygen, argon, and helium are easily contaminated with water during production, transfer and use, because there is a high volume fraction of water in the atmosphere (approximately 1.2% estimated with the average annual atmospheric temperature and relative humidity). Even trace water (industrial gases can cause quality problems in the process such as production of semiconductors. Therefore, it is important to monitor and to control trace water levels in industrial gases at each supplying step, and especially during their use. In the present study, a fiber optic gas sensor was investigated for monitoring trace water levels in industrial gases. The sensor consists of a film containing a metal organic framework (MOF). MOFs are made of metals coordinated to organic ligands, and have mesoscale pores that adsorb gas molecules. When the MOF, copper benzene-1,3,5-tricarboxylate (Cu-BTC), was used as a sensing material, we investigated the color of Cu-BTC with water adsorption changed both in depth and tone. Cu-BTC crystals appeared deep blue in dry gases, and then changed to light blue in wet gases. An optical gas sensor with the Cu-BTC film was developed using a light emitting diode as the light source and a photodiode as the light intensity detector. The sensor showed a reversible response to trace water, did not require heating to remove the adsorbed water molecules. The sample gas flow rate did not affect the sensitivity. The obtained limit of detection was 40 parts per billion by volume (ppbv). The response time for sample gas containing 2.5 ppmvH2O was 23 s. The standard deviation obtained for daily analysis of 1.0 ppmvH2O standard gas over 20 days was 9%. Furthermore, the type of industrial gas did not affect the sensitivity. These properties mean the sensor will be applicable to trace water detection in various industrial gases. Copyright © 2015 Elsevier B.V. All rights reserved.

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.

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.

EVALUATION OF SIGNIFICANT ANTHROPOGENIC SOURCES OF RADIATIVELY IMPORTANT TRACE GASES

Science.gov (United States)

The report is an initial evaluation of significant anthropogenic sources of radiatively important trace gases. missions of greenhouse gases from human activities--including fossil fuel combustion, industrial/agricultural activities, and transportation--contribute to the increasin...

LIDAR technology for measuring trace gases on Mars and Earth

Science.gov (United States)

Riris, H.; Abshire, J. B.; Graham, Allan; Hasselbrack, William; Rodriguez, Mike; Sun, Xiaoli; Weaver, Clark; Mao, Jianping; Kawa, Randy; Li, Steve; Numata, Kenji; Wu, Stewart

2017-11-01

Trace gases and their isotopic ratios in planetary atmospheres offer important but subtle clues as to the origins of a planet's atmosphere, hydrology, geology, and potential for biology. An orbiting laser remote sensing instrument is capable of measuring trace gases on a global scale with unprecedented accuracy, and higher spatial resolution that can be obtained by passive instruments. For Earth we have developed laser technique for the remote measurement of the tropospheric CO2, O2, and CH4 concentrations from space. Our goal is to develop a space instrument and mission approach for active CO2 measurements. Our technique uses several on and off-line wavelengths tuned to the CO2 and O2 absorption lines. This exploits the atmospheric pressure broadening of the gas lines to weigh the measurement sensitivity to the atmospheric column below 5 km and maximizes sensitivity to CO2 changes in the boundary layer where variations caused by surface sources and sinks are largest. Simultaneous measurements of O2 column use a selected region in the Oxygen A-band. Laser altimetry and atmospheric backscatter can also be measured simultaneously, which permits determining the surface height and measurements made to thick cloud tops and through aerosol layers. We use the same technique but with a different transmitter at 1.65 um to measure methane concentrations. Methane is also a very important trace gas on earth, and a stronger greenhouse gas than CO2 on a per molecule basis. Accurate, global observations are needed in order to better understand climate change and reduce the uncertainty in the carbon budget. Although carbon dioxide is currently the primary greenhouse gas of interest, methane can have a much larger impact on climate change. Methane levels have remained relatively constant over the last decade but recent observations in the Arctic have indicated that levels may be on the rise due to permafrost thawing. NASA's Decadal Survey underscored the importance of Methane as a

The broad-band overlap problem in atmospheric trace gases

International Nuclear Information System (INIS)

Subasilar, B.

1991-01-01

In relation to a better understanding of climate change and the related greenhouse problem, one way of projecting for the next decades is through general circulation models (GCMs). The only input as a driving force in the changing atmospheric and oceanic circulation patterns is the amount of heat perturbation either due to natural or man-caused activities. Among these, CO 2 concentrations resulting from the latter has been observed to be accelerating at alarmingly high rates especially after the advent of the industrialization which just began in the last century. In addition to that, collective effects of other greenhouse gases (freons, SO 2 , H 2 O, CH 4 , etc.) are as important as CO 2 . Hence, it is evident from the above considerations that, in the predictions of climate models, the heat input which triggers changes in the atmospheric patterns, should be formulated accurately. In order to realize this objective, in this research, beginning with the available line parameter data, the problems of absorption have been investigated and attacked in the frame known as the broad band modeling since that is the only best and fastest manageable representation for GCMs. The first step was the construction of a full broad band (intra band overlap) model that was also flexible enough to accommodate the individual peculiarities of the bands. Before, the well known and very useful Ramanathan model had a limited applicability in the concentration scale, and it was also not systematically or successfully incorporated into an inter band overlap picture. Then, the established ideas that served as bases up to present, have been employed but found to have a limited practical applicability when it came to predict the inter band overlaps

Adsorption and Detection of Hazardous Trace Gases by Metal-Organic Frameworks.

Science.gov (United States)

Woellner, Michelle; Hausdorf, Steffen; Klein, Nicole; Mueller, Philipp; Smith, Martin W; Kaskel, Stefan

2018-06-19

The quest for advanced designer adsorbents for air filtration and monitoring hazardous trace gases has recently been more and more driven by the need to ensure clean air in indoor, outdoor, and industrial environments. How to increase safety with regard to personal protection in the event of hazardous gas exposure is a critical question for an ever-growing population spending most of their lifetime indoors, but is also crucial for the chemical industry in order to protect future generations of employees from potential hazards. Metal-organic frameworks (MOFs) are already quite advanced and promising in terms of capacity and specific affinity to overcome limitations of current adsorbent materials for trace and toxic gas adsorption. Due to their advantageous features (e.g., high specific surface area, catalytic activity, tailorable pore sizes, structural diversity, and range of chemical and physical properties), MOFs offer a high potential as adsorbents for air filtration and monitoring of hazardous trace gases. Three advanced topics are considered here, in applying MOFs for selective adsorption: (i) toxic gas adsorption toward filtration for respiratory protection as well as indoor and cabin air, (ii) enrichment of hazardous gases using MOFs, and (iii) MOFs as sensors for toxic trace gases and explosives. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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.

An investigation of the sub-grid variability of trace gases and aerosols for global climate modeling

Directory of Open Access Journals (Sweden)

Y. Qian

2010-07-01

Full Text Available One fundamental property and limitation of grid based models is their inability to identify spatial details smaller than the grid cell size. While decades of work have gone into developing sub-grid treatments for clouds and land surface processes in climate models, the quantitative understanding of sub-grid processes and variability for aerosols and their precursors is much poorer. In this study, WRF-Chem is used to simulate the trace gases and aerosols over central Mexico during the 2006 MILAGRO field campaign, with multiple spatial resolutions and emission/terrain scenarios. Our analysis focuses on quantifying the sub-grid variability (SGV of trace gases and aerosols within a typical global climate model grid cell, i.e. 75×75 km².

Our results suggest that a simulation with 3-km horizontal grid spacing adequately reproduces the overall transport and mixing of trace gases and aerosols downwind of Mexico City, while 75-km horizontal grid spacing is insufficient to represent local emission and terrain-induced flows along the mountain ridge, subsequently affecting the transport and mixing of plumes from nearby sources. Therefore, the coarse model grid cell average may not correctly represent aerosol properties measured over polluted areas. Probability density functions (PDFs for trace gases and aerosols show that secondary trace gases and aerosols, such as O₃, sulfate, ammonium, and nitrate, are more likely to have a relatively uniform probability distribution (i.e. smaller SGV over a narrow range of concentration values. Mostly inert and long-lived trace gases and aerosols, such as CO and BC, are more likely to have broad and skewed distributions (i.e. larger SGV over polluted regions. Over remote areas, all trace gases and aerosols are more uniformly distributed compared to polluted areas. Both CO and O₃ SGV vertical profiles are nearly constant within the PBL during daytime, indicating that trace gases

Recent trends in the variability of halogenated trace gases over the United States

Science.gov (United States)

Hurst, Dale F.; Bakwin, Peter S.; Elkins, James W.

1998-10-01

Recent trends in the atmospheric variability of seven halogenated trace gases are determined from three years (November 1994 through October 1997) of hourly gas chromatographic measurements at a 610 m tower in North Carolina and 17 months (June 1996 through October 1997) of similar measurements at a 450 m tower in Wisconsin. Production of five of these gases, CCl3F (CFC-11), CCl2F2 (CFC-12), CCl2FCClF2 (CFC-113), CH3CCl3 (methyl chloroform), and CCl4 (carbon tetrachloride), is now strictly regulated in the United States and other developed countries under international legislation. C2Cl4 (tetrachloroethene) and SF6 (sulfur hexafluoride) are currently produced without restriction, but requests for voluntary cutbacks in C2Cl4 emissions have been made, at least in the United States. Atmospheric variability of these gases is examined at several sampling heights on the towers, but trends are deduced using only nighttime data at the top sampling level of each tower to minimize variability driven by local emissions and the diurnal cycle of the planetary boundary layer, leaving regional emissions as the main source of day-to-day variability. Significant downward trends are determined for CFC-12, CFC-113, CH3CCl3, and C2Cl4 variability at both towers, reflecting decreased emissions of these gases in two regions of the United States. Trends in CFC-11, CCl4, and SF6 variability at both towers are not significantly different from zero.

BIOSIGNATURE GASES IN H{sub 2}-DOMINATED ATMOSPHERES ON ROCKY EXOPLANETS

Energy Technology Data Exchange (ETDEWEB)

Seager, S.; Bains, W.; Hu, R. [Department of Earth, Atmospheric, and Planetary Sciences, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139 (United States)

2013-11-10

Super-Earth exoplanets are being discovered with increasing frequency and some will be able to retain stable H{sub 2}-dominated atmospheres. We study biosignature gases on exoplanets with thin H{sub 2} atmospheres and habitable surface temperatures, using a model atmosphere with photochemistry and a biomass estimate framework for evaluating the plausibility of a range of biosignature gas candidates. We find that photochemically produced H atoms are the most abundant reactive species in H{sub 2} atmospheres. In atmospheres with high CO{sub 2} 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 accumulate detectable biosignature gases in an H{sub 2} atmosphere is closely analogous to the case of oxidized atmospheres, where photochemically produced OH is the major destructive species. Most potential biosignature gases, such as dimethylsulfide and CH{sub 3}Cl, are therefore more favorable in low-UV, as compared with solar-like UV, environments. A few promising biosignature gas candidates, including NH{sub 3} and N{sub 2}O, are favorable even in solar-like UV environments, as these gases are destroyed directly by photolysis and not by H (or O). A more subtle finding is that most gases produced by life that are fully hydrogenated forms of an element, such as CH{sub 4} and H{sub 2}S, are not effective signs of life in an H{sub 2}-rich atmosphere because the dominant atmospheric chemistry will generate such gases abiologically, through photochemistry or geochemistry. Suitable biosignature gases in H{sub 2}-rich atmospheres for super-Earth exoplanets transiting M stars could potentially be detected in transmission

Remote sensing FTIR-system for emission monitoring and ambient air control of atmospheric trace gases and air pollutants; Remote sensing FTIR-System zur Emissions- und Immissionsmessung atmosphaerischer Spurengasse und Luftschadstoffe

Energy Technology Data Exchange (ETDEWEB)

Eisenmann, T; Mosebach, H; Bittner, H [Kayser-Threde GmbH, Muenchen (Germany)

1994-01-01

The Fourier Transform Infrared spectrometer K300, based on the double-pendulum interferometer, is due to its optical design particularly suitable for high resolution remote sensing emission and transmission (long path monitoring) measurements of air pollutants and atmospheric trace gases in the field. The applications encompass direct emission measurements of hot flue gases and aircraft engine exhaust as well as surveillance of industrial complexes and waste disposal sites and ambient air control of e.g. traffic polluted sites. For direct emission measurements the infrared radiation of hot gases is utilized. Monitoring of cold diffuse emissions (e.g. at waste disposal sites) and ambient air control is carried out applying a bistatic transmission configuration with an artificial infrared source (glowbar) facing the instrument from a distance up to several hundred meters (long-path monitoring). Following a short introduction of the measurement technique and system, results from the above mentioned applications, obtained during several field studies are depicted and discussed. 19 refs., 8 figs., 12 tabs.

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)

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.

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

Measurements of Long-Lived Trace Gases from Commercial Aircraft Platforms: Development of Instrumentation

Science.gov (United States)

2002-01-01

The upper troposphere (6-12 km altitude) is a poorly understood and highly vulnerable region of the atmosphere. It is important because many trace species, including ozone, have their greatest impact as greenhouse (infrared-absorbing) gases in this region. The addition of relatively small amounts of anthropogenic chemicals, such as nitrogen oxides, can have a dramatic effect on the abundance of ozone. Some of these pollutants are deposited directly, e.g., by aircraft, while others are transported in. The primary goal of this project was to measure several chemical compounds in the upper troposphere that will help us to understand how air is to transported to that part of the atmosphere; that is, does it come down from the stratosphere, does it rise from the surface via convection, and so on. To obtain adequate sampling to accomplish this goal, we proposed to make measurements from revenue aircraft during normal flight operations.

Global Observations of Inorganic Gases in the Remote Atmosphere - First Observations from the Atmospheric Tomography Mission (ATom)

Science.gov (United States)

Veres, P. R.; Neuman, J. A.

2017-12-01

The Atmospheric Tomography Mission (ATom) is a NASA field program that investigates the impact of human emissions on air quality and climate in remote regions of the atmosphere. NASA DC-8 flights during the ATom sampled the atmosphere over the Pacific and Atlantic Oceans, up to 12 km altitude and nearly from pole to pole. New observations of key species (e.g. N2O5, reactive halogens, nitrous acid) in these regions are provided during the third deployment of the NASA DC-8 research aircraft (October, 2017) by the NOAA iodide ion time-of-flight chemical ionization mass spectrometer (iCIMS). In this study, we will present the first observations of inorganic gas-phase species using iCIMS from the ATom 3 deployment. Laboratory results detailing the instrument performance including inlet response times, background characterization and sensitivity will be presented. We will show vertical profiles of newly measured trace gases derived from in-situ observations, and discuss the potential impact on the NOx, NOy and reactive halogen budgets.

Diffusive retention of atmospheric gases in chert

Science.gov (United States)

Pettitt, E.; Cherniak, D. J.; Watson, E. B.; Schaller, M. F.

2016-12-01

Throughout Earth's history, the volatile contents (N2, CO2, Ar) of both deep and shallow terrestrial reservoirs has been dynamic. Volatiles are important chemical constituents because they play a significant role in regulating Earth's climate, mediating the evolution of complex life, and controlling the properties of minerals and rocks. Estimating levels of atmospheric volatiles in the deep geological past requires interrogation of materials that have acquired and retained a chemical memory from that time. Cherts have the potential to trap atmospheric components during formation and later release those gases for analysis in the laboratory. However, cherts have been underexploited in this regard, partly because their ability to retain a record of volatile components has not been adequately evaluated. Before cherts can be reliably used as indicators of past levels of major atmospheric gases, it is crucial that we understand the diffusive retentiveness of these cryptocrystalline silica phases. As the first step toward quantifying the diffusivity and solubility of carbon dioxide and nitrogen in chert, we have performed 1-atmosphere diffusive-uptake experiments at temperatures up to 450°C. Depth profiles of in-diffusing gases are measured by nuclear reaction analysis (NRA) to help us understand the molecular-scale transport of volatiles and thus the validity of using chert-bound volatiles to record information about Earth history. Data collected to date suggest that at least some cherts are ideal storage containers and can retain volatiles for a geologically long time. In addition to these diffusion experiments, preliminary online-crush fast-scan measurements using a quadrupole mass spectrometer indicate that atmospheric volatiles are released upon crushing various chert samples. By coupling such volatile-release measurements made by mass spectrometry with diffusion experiments, we are uniquely able to address the storage and fidelity of volatiles bound in crustal

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.

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

International Nuclear Information System (INIS)

Lee, Kyung Won; Cheong, Ae Ju; Shin, Andong; Suh, Nam Duk

2015-01-01

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

Change in the atmospheric concentration of greenhouse gases

International Nuclear Information System (INIS)

GARREC, Jean-Pierre

2000-01-01

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

Influence of 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.)

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

Science.gov (United States)

Zhang, Tianhao; Zhu, Zhongmin; Gong, Wei; Xiang, Hao; Fang, Ruimin

2016-01-01

Atmospheric fine particles (diameter 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 industrial cities of developing countries. PMID:27517948

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.

Characterization of atmospheric trace gases and particulate matter in Hangzhou, China

Science.gov (United States)

Zhang, Gen; Xu, Honghui; Qi, Bing; Du, Rongguang; Gui, Ke; Wang, Hongli; Jiang, Wanting; Liang, Linlin; Xu, Wanyun

2018-02-01

The Yangtze River Delta (YRD) is one of the most densely populated regions in China with severe air quality issues that have not been fully understood. Thus, in this study, based on 1-year (2013) continuous measurement at a National Reference Climatological Station (NRCS, 30.22° N, 120.17° E; 41.7 m a.s.l.) in the center of Hangzhou in the YRD, we investigated the seasonal characteristics, interspecies relationships, and the local emissions and the regional potential source contributions of trace gases (including O3, NOx, NOy, SO2, and CO) and particulate matter (PM2.5 and PM10). Results revealed that severe two-tier air pollution (photochemical and haze pollution) occurred in this region, with frequent exceedances in O3 (38 days) and PM2.5 (62 days). O3 and PM2.5 both exhibited distinct seasonal variations with reversed patterns: O3 reaching a maximum in warm seasons (May and July) but PM2.5 reaching a maximum in cold seasons (November to January). The overall results from interspecies correlation indicated a strong local photochemistry favoring the O3 production under a volatile organic compound (VOC)-limited regime, whereas it moved towards an optimum O3 production zone during warm seasons, accompanied by the formation of secondary fine particulates under high O3. The emission maps of PM2.5, CO, NOx, and SO2 demonstrated that local emissions were significant for these species on a seasonal scale. The contributions from the regional transport among inland cities (Zhejiang, Jiangsu, Anhui, and Jiangxi Province) on a seasonal scale were further confirmed to be crucial to air pollution at the NRCS site by using backward trajectory simulations. Air masses transported from the offshore areas of the Yellow Sea, East Sea, and South Sea were also found to be highly relevant to the elevated O3 at the NRCS site through the analysis of potential source contribution function (PSCF). Case studies of photochemical pollution (O3) and haze (PM2.5) episodes both suggested the

Characterization of atmospheric trace gases and particulate matter in Hangzhou, China

Directory of Open Access Journals (Sweden)

G. Zhang

2018-02-01

Full Text Available The Yangtze River Delta (YRD is one of the most densely populated regions in China with severe air quality issues that have not been fully understood. Thus, in this study, based on 1-year (2013 continuous measurement at a National Reference Climatological Station (NRCS, 30.22° N, 120.17° E; 41.7 m a.s.l. in the center of Hangzhou in the YRD, we investigated the seasonal characteristics, interspecies relationships, and the local emissions and the regional potential source contributions of trace gases (including O3, NOx, NOy, SO2, and CO and particulate matter (PM2.5 and PM10. Results revealed that severe two-tier air pollution (photochemical and haze pollution occurred in this region, with frequent exceedances in O3 (38 days and PM2.5 (62 days. O3 and PM2.5 both exhibited distinct seasonal variations with reversed patterns: O3 reaching a maximum in warm seasons (May and July but PM2.5 reaching a maximum in cold seasons (November to January. The overall results from interspecies correlation indicated a strong local photochemistry favoring the O3 production under a volatile organic compound (VOC-limited regime, whereas it moved towards an optimum O3 production zone during warm seasons, accompanied by the formation of secondary fine particulates under high O3. The emission maps of PM2.5, CO, NOx, and SO2 demonstrated that local emissions were significant for these species on a seasonal scale. The contributions from the regional transport among inland cities (Zhejiang, Jiangsu, Anhui, and Jiangxi Province on a seasonal scale were further confirmed to be crucial to air pollution at the NRCS site by using backward trajectory simulations. Air masses transported from the offshore areas of the Yellow Sea, East Sea, and South Sea were also found to be highly relevant to the elevated O3 at the NRCS site through the analysis of potential source contribution function (PSCF. Case studies of photochemical pollution (O3 and haze (PM2.5 episodes both

Atmospheric noble gases in Mid-Ocean Ridge Basalts: Identification of atmospheric contamination processes

Science.gov (United States)

Roubinet, Claire; Moreira, Manuel A.

2018-02-01

Noble gases in oceanic basalts always show the presence in variable proportions of a component having elemental and isotopic compositions that are similar to those of the atmosphere and distinct from the mantle composition. Although this component could be mantle-derived (e.g. subduction of air or seawater-derived noble gases trapped in altered oceanic crust and sediments), it is most often suggested that this air component is added after sample collection and probably during storage at ambient air, although the mechanism remains unknown. In an attempt to reduce this atmospheric component observed in MORBs, four experimental protocols have been followed in this study. These protocols are based on the hypothesis that air can be removed from the samples, as it appears to be sheltered in distinct vesicles compared to those filled with mantle gases. All of the protocols involve a glove box filled with nitrogen, and in certain cases, the samples are stored under primary vacuum (lower than 10-2 mbar) to pump air out or, alternatively, under high pressure of N2 to expel atmospheric noble gases. In all protocols, three components are observed: atmospheric, fractionated atmospheric and magmatic. The fractionated air component seems to be derived from the non-vitreous part of the pillow-lava, which has cooled more slowly. This component is enriched in Ne relative to Ar, reflecting a diffusive process. This contaminant has already been observed in other studies and thus seems to be relatively common. Although it is less visible, unfractionated air has also been detected in some crushing steps, which tends to indicate that despite the experiments, air is still present in the vesicles. This result is surprising, since studies have demonstrated that atmospheric contamination could be limited if samples were stored under nitrogen quickly after their recovery from the seafloor. Thus, the failure of the protocols could be explained by the insufficient duration of these protocols or

Source apportionment of particulate matter and trace gases near a major refinery near the Houston Ship Channel

Science.gov (United States)

Wallace, Henry W.; Sanchez, Nancy P.; Flynn, James H.; Erickson, Mathew H.; Lefer, Barry L.; Griffin, Robert J.

2018-01-01

From February 7 to 27, 2015, a mobile air quality laboratory was deployed to a location proximate to a major refinery, the Port of Houston, and several neighborhoods to conduct measurements of atmospheric trace gases and particulate matter. Two statistical models were utilized to apportion the sources of pollution impacting this site and the denizens of the nearby neighborhoods. Positive matrix factorization (PMF) was performed on the organic signal of the aerosol mass spectra, resulting in five factors totaling an average of 4.1 μg/m3 of the organic aerosol: hydrocarbon-like (0.67 μg/m3), cooking (0.35 μg/m3) biomass burning (1.14 μg/m3), low-volatility oxidized (1.15 μg/m3), and semi-volatile oxidized (0.78 μg/m3). Principal component analysis was performed on daytime and nighttime data, including concentrations from PMF output, of other PM1 components, and of trace gases. This generated five daytime and five nighttime factors that explained 74.5% and 73.0% of the variance, respectively. The most important factors impacting this site were from mobile source exhaust and petrochemical aromatic compound emissions. Together these two factors also constitute most of the observed carcinogens.

Pilot Institute on Global Change on Trace Gases and the Biosphere, 1988

Science.gov (United States)

Eddy, J. A.; Moore, B.

1998-01-01

Table of Contents: Summary; Background; General Framework for a Series of Institutes on Global Change; The 1988 Pilot Institute on Global Changes: Trace Gases and the Biosphere; Budget; List of Acronyms; and Attachments.

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.

Overview of the physical-chemical properties of the noble gases

International Nuclear Information System (INIS)

McKinley, C.

1973-01-01

This paper lists the concentrations of noble gases in the atmosphere and the relative abundance of the stable isotopes. Selected physical properties are tabulated; solubilities of noble gases in water and other liquids, and liquid-vapor equilibria data for binary systems containing a noble gas are presented. Adsorption data are tabulated for illustrative conventional adsorbents and are also presented by a Polanyi correlation. Clathration, biochemical effects, and chemical reactivity are highlighted. Analytical procedures are briefly described. Other relatively non-reactive gases present in the atmosphere in trace quantities are mentioned: methane, carbon tetrafluoride, and sulfur hexafluoride.

GREENHOUSE GASES AND MEANS OF PREVENTION

Directory of Open Access Journals (Sweden)

Dušica Stojanović

2013-09-01

Full Text Available The greenhouse effect can be defined as the consequence of increased heating of the Earth's surface, as well as the lower atmosphere by carbon dioxide, water vapor, and other trace amounts gases. It is well-known that human industrial activities have released large amounts of greenhouse gases in the atmosphere, about 900 billion tons of carbon dioxide, and it is estimated that up to 450 billion are still in the atmosphere. In comparison to greenhouse gases water vapor is one of the greatest contributors to the greenhouse effect on Earth. Many projects, as does the PURGE project, have tendences to build on the already conducted research and to quantify the positive and negative impacts on health and wellbeing of the population with greenhouse gas reduction strategies that are curently being implemented and should be increasingly applied in various sectors and urban areas, having offices in Europe, China and India.

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

Radioactive rare gases emission at underground nuclear explosions

International Nuclear Information System (INIS)

Dubasov, Yu.V.

2016-01-01

The examples of radioactive rare gases emission at underground nuclear explosions conducted in the USSR on the Novaya Zemlya and Semipalatinsk test sites are considered. It is pointed out that in the case of evasive explosion in vertical wells without apparent radioactive gases emission the samples of subsurface gas must contain the traces of radioactive rare gases. Under the inspection of evasive explosion in horizontal workings of rock massif, one should guided by the analysis of atmospheric air samples in the inspected area [ru

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 NO_x, 36 ppb for O₃ and 105 ppb for CO. The corresponding PM₁, PM_2.5 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 NO_x concentrations. Of gases, NO_x and CO had a clear annual, and SO₂, NO_x 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.

Loess as an environmental archive of atmospheric trace element deposition

Science.gov (United States)

Blazina, T.; Winkel, L. H.

2013-12-01

Environmental archives such as ice cores, lake sediment cores, and peat cores have been used extensively to reconstruct past atmospheric deposition of trace elements. These records have provided information about how anthropogenic activities such as mining and fossil fuel combustion have disturbed the natural cycles of various atmospherically transported trace elements (e.g. Pb, Hg and Se). While these records are invaluable for tracing human impacts on such trace elements, they often provide limited information about the long term natural cycles of these elements. An assumption of these records is that the observed variations in trace element input, prior to any assumed anthropogenic perturbations, represent the full range of natural variations. However, records such as those mentioned above which extend back to a maximum of ~400kyr may not capture the potentially large variations of trace element input occurring over millions of years. Windblown loess sediments, often representing atmospheric deposition over time scales >1Ma, are the most widely distributed terrestrial sediments on Earth. These deposits have been used extensively to reconstruct continental climate variability throughout the Quaternary and late Neogene periods. In addition to being a valuable record of continental climate change, loess deposits may represent a long term environmental archive of atmospheric trace element deposition and may be combined with paleoclimate records to elucidate how fluctuations in climate have impacted the natural cycle of such elements. Our research uses the loess-paleosol deposits on the Chinese Loess Plateau (CLP) to quantify how atmospheric deposition of trace elements has fluctuated in central China over the past 6.8Ma. The CLP has been used extensively to reconstruct past changes of East Asian monsoon system (EAM). We present a suite of trace element concentration records (e.g. Pb, Hg, and Se) from the CLP which exemplifies how loess deposits can be used as an

Trapping, chemistry, and export of trace gases in the South Asian summer monsoon observed during CARIBIC flights in 2008

Directory of Open Access Journals (Sweden)

A. Rauthe-Schöch

2016-03-01

Full Text Available The CARIBIC (Civil Aircraft for the Regular Investigation of the Atmosphere Based on an Instrument Container passenger aircraft observatory performed in situ measurements at 10–12 km altitude in the South Asian summer monsoon anticyclone between June and September 2008. These measurements enable us to investigate this atmospheric region (which so far has mostly been observed from satellites using the broad suite of trace gases and aerosol particles measured by CARIBIC. Elevated levels of a variety of atmospheric pollutants (e.g. carbon monoxide, total reactive nitrogen oxides, aerosol particles, and several volatile organic compounds were recorded. The measurements provide detailed information about the chemical composition of air in different parts of the monsoon anticyclone, particularly of ozone precursors. While covering a range of 3500 km inside the monsoon anticyclone, CARIBIC observations show remarkable consistency, i.e. with distinct latitudinal patterns of trace gases during the entire monsoon period. Using the CARIBIC trace gas and aerosol particle measurements in combination with the Lagrangian particle dispersion model FLEXPART, we investigated the characteristics of monsoon outflow and the chemical evolution of air masses during transport. The trajectory calculations indicate that these air masses originated mainly from South Asia and mainland Southeast Asia. Estimated photochemical ages of the air were found to agree well with transport times from a source region east of 90–95° E. The photochemical ages of the air in the southern part of the monsoon anticyclone were systematically younger (less than 7 days and the air masses were mostly in an ozone-forming chemical mode. In its northern part the air masses were older (up to 13 days and had unclear ozone formation or destruction potential. Based on analysis of forward trajectories, several receptor regions were identified. In addition to predominantly westward

Emission rates of sulfur dioxide, trace gases and metals from Mount Erebus, Antartica

Energy Technology Data Exchange (ETDEWEB)

Kyle, P.R.; Meeker, K. (New Mexico Institute of Mining and Technology, Socorro (USA)); Finnegan, D. (Los Alamos National Lab., NM (USA))

1990-11-01

SO{sub 2} emission rates have been measured annually since 1983 at Mount Erebus, Antarctica by correlation spectrometer (COSPEC V). Following a 4 month period of sustained strombolian activity in late 1984, SO{sub 2} emissions declined from 230 Mg/day in 1983 to 25 Mg/day and then slowly increased from 16 Mg/day in 1985 to 51 Mg/day in 1987. Nine sets of filter packs containing partcle and {sup 7}LiOH treated filters were collected in the plume in 1986 and analyzed by neutron activation. Using the COSPEC data and measured element/S ratios on the filters, emission rates have been determined for trace gases and metals. The authors infer HCl and HF emissions in 1983 to be about 1200 and 500 Mg/day, respectively. Mt Erebus has therefore been an important source of halogens to the Anarctic atmosphere and could be responsible for excess Cl found in Central Antarctica snow.

Problems in global atmospheric chemistry

Science.gov (United States)

Crutzen, Paul J.

1993-02-01

The chemistry of the atmosphere is substantially influenced by a wide range of chemical processes which are primarily driven by the action of ultraviolet radiation of wavelengths shorter than 320 nm (UV-B) on ozone and water vapor. This leads to the formation of hydroxyl (OH) radicals which, despite very low tropospheric concentrations, remove most gases that are emitted into the atmosphere by natural and anthropogenic processes. Therefore, although only about 10% of all atmospheric ozone is located in the troposphere, through the formation of OH, it determines the oxidation efficiency of the atmosphere and is, therefore, of the utmost importance for maintaining its chemical composition. Due to a variety of human activities, especially through increasing emissions of CH4, CO, and NOx, the concentrations of tropospheric ozone and hydroxyl are expected to be increasing in polluted and decreasing in clean tropospheric environments. Altogether, this may be leading to an overall decrease in the oxidation efficiency of the atmosphere, contributing to a gradual buildup of several longlived trace gases that are primarily removed by reaction with OH. In the stratosphere, especially due to catalytic reactions of chlorine-containing gases of industrial origin, ozone is being depleted, most drastically noted during the early spring months over Antarctica. Because ozone is the only atmospheric constituent that can significantly absorb solar radiation in the wavelength region 240 - 320 nm, this loss of ozone enhances the penetration of biologically harmful UV-B radiation to the earth's surface with ensuing negative consequences for the biosphere. Several of the aforementioned chemically active trace gases with growing trends in the atmosphere are also efficient greenhouse gases. Together they can exert a warming effect on the earth's climate about equal to that of carbon dioxide.

A new numerical model of the middle atmosphere. I - Dynamics and transport of tropospheric source gases

Science.gov (United States)

Garcia, Rolando R.; Stordal, Frode; Solomon, Susan; Kiehl, Jeffrey T.

1992-01-01

Attention is given to a new model of the middle atmosphere which includes, in addition to the equations governing the zonal mean state, a potential vorticity equation for a single planetary-scale Rossby wave, and an IR radiative transfer code for the stratosphere and lower mesosphere, which replaces the Newtonian cooling parameterization used previously. It is shown that explicit computation of the planetary-scale wave field yields a more realistic representation of the zonal mean dynamics and the distribution of trace chemical species. Wave breaking produces a well-mixed 'surf zone' equatorward of the polar night vortex and drives a meridional circulation with downwelling on the poleward side of the vortex. This combination of mixing and downwelling produces shallow meridional gradients of trace gases in the subtropics and middle latitudes, and very steep gradients at the edge of the polar vortex. Computed distributions of methane and nitrous oxide are shown to agree well with observations.

Greenhouse gases regional fluxes estimated from atmospheric measurements

International Nuclear Information System (INIS)

Messager, C.

2007-07-01

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

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

Directory of Open Access Journals (Sweden)

K. Sellegri

2005-01-01

Full Text Available Biogenic VOCs are important in the growth and possibly also in the early stages of 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 68amu (candidate=isoprene, monoterpenes, methyl vinyl ketone (MVK and methacrolein (MaCR and monoterpene oxidation products (MTOP. For all of them except for the amines, we present daily variations during different classes of nucleation events, and non-event days. BVOC oxidation products (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. Moreover, BVOC oxidation products are found to show significant correlations with the condensational sink (CS on nucleation event days, which indicates that they are representative of less volatile organic compounds that contribute to the growth of the nucleated particles and generally secondary organic aerosol formation. Behaviors of BVOC on event and non event days are compared to the behavior of CO.

Natural and human-related sources of ozone-forming trace gases in southern Africa

CSIR Research Space (South Africa)

Scholes, RJ

1998-09-01

Full Text Available or vehicular pollution. The cloud of tropospheric ozone which forms over southern Africa every spring probably has its main origin in natural emissions of the ozone-forming trace gases, including CO from vegetation fires, emissions of NO from soils...

Photoacoustic absorption spectra of atmospheric gases near 7603 cm-1

International Nuclear Information System (INIS)

Lawton, S.A.; Bragg, S.L.

1984-01-01

Absorption spectra of carbon monoxide, water vapor, memane, and ammonia are presented as part of an effort to determine absolute absorption cross sections for some atmospheric gases at the iodine laser wavelength

ARTEAM - Advanced ray tracing with earth atmospheric models

NARCIS (Netherlands)

Kunz, G.J.; Moerman, M.M.; Eijk, A.M.J. van

2002-01-01

The Advanced Ray Tracing with Earth Atmospheric Models (ARTEAM) aims at a description of the electro-optical propagation environment in the marine atmospheric surface layer. For given meteorological conditions, the model evaluates height- and range-resolved transmission losses, refraction and

Trace water vapor determination in nitrogen and corrosive gases using infrared spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Espinoza, L.H.; Niemczyk, T.M. [Univ. of New Mexico, Albuquerque, NM (United States). Dept. of Chemistry; Stallard, B.R.; Garcia, M.J. [Sandia National Labs., Albuquerque, NM (United States)

1997-06-01

The generation of particles in gas handling systems as a result of corrosion is a major concern in the microelectronics industry. The corrosion can be caused by the presence of trace quantities of water in corrosive gases such as HCl or HBr. FTIR spectroscopy has been shown to be a method that can be made compatible with corrosive gases and is capable of detecting low ppb levels of water vapor. In this report, the application of FTIR spectroscopy combined with classical least squares multivariate calibration to detect trace H{sub 2}O in N{sub 2}, HCl and HBr is discussed. Chapter 2 discusses the gas handling system and instrumentation required to handle corrosive gases. A method of generating a background spectrum useful to the measurements discussed in this report, as well as in other application areas such as gas phase environmental monitoring, is discussed in Chapter 3. Experimental results obtained with the first system are presented in Chapter 4. Those results made it possible to optimize the design options for the construction of a dedicate system for low ppb water vapor determination. These designs options are discussed in Chapter 5. An FTIR prototype accessory was built. In addition, a commercially available evacuable FTIR system was obtained for evaluation. Test results obtained with both systems are discussed in Chapter 6. Experiments dealing with the interaction between H{sub 2}O-HCl and potential improvements to the detection system are discussed in Chapter 7.

The Atmospheric Chemistry Suite (ACS) of Three Spectrometers for the ExoMars 2016 Trace Gas Orbiter

Science.gov (United States)

Korablev, O.; Montmessin, F.; Trokhimovskiy, A.; Fedorova, A. A.; Shakun, A. V.; Grigoriev, A. V.; Moshkin, B. E.; Ignatiev, N. I.; Forget, F.; Lefèvre, F.; Anufreychik, K.; Dzuban, I.; Ivanov, Y. S.; Kalinnikov, Y. K.; Kozlova, T. O.; Kungurov, A.; Makarov, V.; Martynovich, F.; Maslov, I.; Merzlyakov, D.; Moiseev, P. P.; Nikolskiy, Y.; Patrakeev, A.; Patsaev, D.; Santos-Skripko, A.; Sazonov, O.; Semena, N.; Semenov, A.; Shashkin, V.; Sidorov, A.; Stepanov, A. V.; Stupin, I.; Timonin, D.; Titov, A. Y.; Viktorov, A.; Zharkov, A.; Altieri, F.; Arnold, G.; Belyaev, D. A.; Bertaux, J. L.; Betsis, D. S.; Duxbury, N.; Encrenaz, T.; Fouchet, T.; Gérard, J.-C.; Grassi, D.; Guerlet, S.; Hartogh, P.; Kasaba, Y.; Khatuntsev, I.; Krasnopolsky, V. A.; Kuzmin, R. O.; Lellouch, E.; Lopez-Valverde, M. A.; Luginin, M.; Määttänen, A.; Marcq, E.; Martin Torres, J.; Medvedev, A. S.; Millour, E.; Olsen, K. S.; Patel, M. R.; Quantin-Nataf, C.; Rodin, A. V.; Shematovich, V. I.; Thomas, I.; Thomas, N.; Vazquez, L.; Vincendon, M.; Wilquet, V.; Wilson, C. F.; Zasova, L. V.; Zelenyi, L. M.; Zorzano, M. P.

2018-02-01

The Atmospheric Chemistry Suite (ACS) package is an element of the Russian contribution to the ESA-Roscosmos ExoMars 2016 Trace Gas Orbiter (TGO) mission. ACS consists of three separate infrared spectrometers, sharing common mechanical, electrical, and thermal interfaces. This ensemble of spectrometers has been designed and developed in response to the Trace Gas Orbiter mission objectives that specifically address the requirement of high sensitivity instruments to enable the unambiguous detection of trace gases of potential geophysical or biological interest. For this reason, ACS embarks a set of instruments achieving simultaneously very high accuracy (ppt level), very high resolving power (>10,000) and large spectral coverage (0.7 to 17 μm—the visible to thermal infrared range). The near-infrared (NIR) channel is a versatile spectrometer covering the 0.7-1.6 μm spectral range with a resolving power of ˜20,000. NIR employs the combination of an echelle grating with an AOTF (Acousto-Optical Tunable Filter) as diffraction order selector. This channel will be mainly operated in solar occultation and nadir, and can also perform limb observations. The scientific goals of NIR are the measurements of water vapor, aerosols, and dayside or night side airglows. The mid-infrared (MIR) channel is a cross-dispersion echelle instrument dedicated to solar occultation measurements in the 2.2-4.4 μm range. MIR achieves a resolving power of >50,000. It has been designed to accomplish the most sensitive measurements ever of the trace gases present in the Martian atmosphere. The thermal-infrared channel (TIRVIM) is a 2-inch double pendulum Fourier-transform spectrometer encompassing the spectral range of 1.7-17 μm with apodized resolution varying from 0.2 to 1.3 cm-1. TIRVIM is primarily dedicated to profiling temperature from the surface up to ˜60 km and to monitor aerosol abundance in nadir. TIRVIM also has a limb and solar occultation capability. The technical concept of

The effects of anthropogenous on atmosphere and climate. Anthropogene Beeinflussung des Klimas

Energy Technology Data Exchange (ETDEWEB)

Grassl, H [Max-Planck-Institut fuer Meteorologie, Hamburg (Germany, F.R.) Hamburg Univ. (Germany, F.R.). Meteorologisches Inst.

1989-11-01

The mostly uncontrolled emission of trace gases varies the composition of the atmosphere. Since some of the trace gases are emitted belong to the group of greenhouse gases and many of them are quite stable, and thus spread world wide, a global change to the radiation balance is inevitable. The present state of knowledge can be summarized by presenting the basic physical effects, the growth rates of the gases and their sources, the relative proportion of additional greenhouse effects and climatic variations calculated using models of the climate. (orig.).

Application of the FTIR system K300 for the emission and immission measurement of atmospheric trace gases and harmful substances in the air: examples of cases and results. Anwendung des FTIR-Systems K300 zur Emissions- und Immissionsmessung atmosphaerischer Spurengase und Luftschadstoffe: Fallbeispiele und Ergebnisse

Energy Technology Data Exchange (ETDEWEB)

Eisenmann, T [Kayser-Threde GmbH, Muenchen (Germany); Mosebach, H [Kayser-Threde GmbH, Muenchen (Germany); Bittner, H [Kayser-Threde GmbH, Muenchen (Germany)

1993-01-01

The K300 double oscillation interferometer used for the investigations is a Fourier transform infrared (FTIR) spectrometer which, due to its special optical design, is very suitable for high resolution remote sensing emission and immission (long-path monitoring) measurements of harmful substances in the air and atmospheric trace gases, when used in the field. The spectrum of applications extends from the direct measurement of hot chimney waste gases and of engine exhaust gases via the monitoring of industrial plants or waste dumps (diffuse emission) to the immission measurement of sites with heavy traffic. For direct emission measurements, the infrared characteristic radiation of hot waste gases is used; for the measurement of cold diffuse emission or immission, one measures against an artificial infrared source of radiation, which can be erected at a distance of several hundred metres from the equipment (bistatic configuration, socalled long-path monitoring). The results of different applications, which were obtained in the context of various campaigns of measurements, are shown after a short introduction of the system. (orig./BBR)

Optical remote sensing of properties and concentrations of atmospheric trace constituents

Science.gov (United States)

Vladutescu, Daniela Viviana

application is the detection of water vapor in the atmosphere. Water vapor is an important greenhouse gas due to its high concentration in the atmosphere (parts per thousand), among the trace constituents, and its interaction with tropospheric aerosols particles. The upward convection of water vapor and aerosols due to intense heating of the ground lead to aggregation of water particles or ice on aerosols in the air forming different types of clouds at various altitudes. In this regard a reliable method of retrieving atmospheric water vapor profiles is presented in the third part of the paper. The proposed technique here is the Raman lidar procedure that is calibrated afterwards. The accuracy of the water vapor measurements is obtained by calibration techniques based on different techniques that where compared and validated. The calibration method is based on data fusion from different sources like: GPS (global positioning system) sunphotometer, radiosonde. The condensation of water vapor on aerosols is affecting their size, shape, refractive index and chemical composition. The warming or cooling effect of the clouds hence formed are both possible depending on the cloud location, cover, composition and structure. The effect of these clouds on radiative global forcing and therefore on the short and long term global climate is of high interest in the scientific world. In an effort to understand the hygroscopic properties of aerosols, a major interest is manifested in obtaining accurate vertical water vapor profiles simultaneously with aerosol extinction and backscatter profiles. A reliable method of retrieving atmospheric water vapor profiles and aerosols backscatter and extinction in the same atmospheric volume is presented in the fourth chapter of the paper. As mentioned above the determination of greenhouse gases and other molecular pollutants is important in process control as well as environmental monitoring. Since many molecular vibrational modes are in the infrared

A research program on radiative, chemical, and dynamical feedback progresses influencing the carbon dioxide and trace gases climate effects

International Nuclear Information System (INIS)

1989-07-01

This report summarizes the up-to-date progress. The program includes two tasks: atmospheric radiation and climatic effects and their objective is to link quantitatively the radiation forcing changes and the climate responses caused by increasing greenhouse gases. Here, the objective and approach are described. We investigate the combined atmospheric radiation characteristics of the greenhouse gases (H 2 O, CO 2 , CH 4 , N 2 O, CFCs, and O 3 ), aerosols and clouds. Since the climatic effect of increasing atmospheric greenhouse gases is initiated by perturabtion to the longwave thermal radiation, it is critical to understand better the radiation characteristics of the greenhouse gases and their relationship to radiatively-important aerosols and clouds; the latter reflect solar radiation (a cooling of the surface) and provide a greenhouse effect (a warming to the surface). Therefore, aerosol and cloud particles are an integral part of the radiation field in the atmosphere. 9 refs

Effects of land use on surface–atmosphere exchanges of trace gases and energy in Borneo: comparing fluxes over oil palm plantations and a rainforest

Science.gov (United States)

Fowler, David; Nemitz, Eiko; Misztal, Pawel; Di Marco, Chiara; Skiba, Ute; Ryder, James; Helfter, Carole; Cape, J. Neil; Owen, Sue; Dorsey, James; Gallagher, Martin W.; Coyle, Mhairi; Phillips, Gavin; Davison, Brian; Langford, Ben; MacKenzie, Rob; Muller, Jennifer; Siong, Jambery; Dari-Salisburgo, Cesare; Di Carlo, Piero; Aruffo, Eleonora; Giammaria, Franco; Pyle, John A.; Hewitt, C. Nicholas

2011-01-01

This paper reports measurements of land–atmosphere fluxes of sensible and latent heat, momentum, CO2, volatile organic compounds (VOCs), NO, NO2, N2O and O3 over a 30 m high rainforest canopy and a 12 m high oil palm plantation in the same region of Sabah in Borneo between April and July 2008. The daytime maximum CO2 flux to the two canopies differs by approximately a factor of 2, 1200 mg C m−2 h−1 for the oil palm and 700 mg C m−2 h−1 for the rainforest, with the oil palm plantation showing a substantially greater quantum efficiency. Total VOC emissions are also larger over the oil palm than over the rainforest by a factor of 3. Emissions of isoprene from the oil palm canopy represented 80 per cent of the VOC emissions and exceeded those over the rainforest in similar light and temperature conditions by on average a factor of 5. Substantial emissions of estragole (1-allyl-4-methoxybenzene) from the oil palm plantation were detected and no trace of this VOC was detected in or above the rainforest. Deposition velocities for O3 to the rainforest were a factor of 2 larger than over oil palm. Emissions of nitrous oxide were larger from the soils of the oil palm plantation than from the soils of the rainforest by approximately 25 per cent. It is clear from the measurements that the large change in the species composition generated by replacing rainforest with oil palm leads to profound changes in the net exchange of most of the trace gases measured, and thus on the chemical composition of the boundary layer over these surfaces. PMID:22006962

Investigation of size-fractionated urban aerosol and trace gases in Budapest by nuclear-related and other analytical techniques

International Nuclear Information System (INIS)

Salma, I.; Maenhaut, W.; Zemplen-Papp, E.; Bobvos, J.

1998-01-01

An air pollution study was conducted at two urban residential sites in Budapest (one representing the downtown, the other representing a wooded suburb) from 9 April till 17 May 1996. Size-fractionated aerosol samples were simultaneously collected on a daily basis, and meteorological conditions were recorded at both sampling sites. Stacked filter units (SFUs) with an upper size inlet cut-off were used as sampling device separating the urban aerosol into a coarse (about 10-2 μm equivalent aerodynamic diameter, EAD) and a fine ( 2 , SO 2 , CO and the total mass of the suspended particulate matter were measured every half hour at one of the sampling sites by commercial equipment. The SFU filters were analyzed by gravimetry for the total particle mass, by a light reflectance technique for black carbon, by particle-induced X-ray emission analysis and instrumental neutron activation analysis for elemental composition (in combination for up to 40-45 elements). The analytical results were used for characterizing the levels and the multi-elemental composition of the urban aerosol at both sampling sites and for both size fractions, for investigating the atmospheric concentrations and diurnal variation of some criteria pollutants, and for comparing the time-trends of aerosols and trace gases. Identification of the major source types of the aerosol fractions and trace gases, and assessment of the relative contribution from these sources are to be accomplished by multivariate receptor modeling. The present paper reports on the status of the air pollution study, and gives a discussion of the results

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

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.

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.

Characteristics of aerosol particles and trace gases in ship exhaust plumes

Science.gov (United States)

Drewnick, F.; Diesch, J.; Borrmann, S.

2011-12-01

Gaseous and particulate matter from marine vessels gain increasing attention due to their significant contribution to the anthropogenic burden of the atmosphere, implying the change of the atmospheric composition and the impact on local and regional air quality and climate (Eyring et al., 2010). As ship emissions significantly affect air quality of onshore regions, this study deals with various aspects of gas and particulate plumes from marine traffic measured near the Elbe river mouth in northern Germany. In addition to a detailed investigation of the chemical and physical particle properties from different types of commercial marine vessels, we will focus on the chemistry of ship plumes and their changes while undergoing atmospheric processing. Measurements of the ambient aerosol, various trace gases and meteorological parameters using a mobile laboratory (MoLa) were performed on the banks of the Lower Elbe which is passed on average, daily by 30 ocean-going vessels reaching the port of Hamburg, the second largest freight port of Europe. During 5 days of sampling from April 25-30, 2011 170 commercial marine vessels were probed at a distance of about 1.5-2 km with high temporal resolution. Mass concentrations in PM1, PM2.5 and PM10 and number as well as PAH and black carbon (BC) concentrations in PM1 were measured; size distribution instruments covered the size range from 6 nm up to 32 μm. The chemical composition of the non-refractory aerosol in the submicron range was measured by means of an Aerosol Mass Spectrometer (Aerodyne HR-ToF-AMS). Gas phase species analyzers monitored various trace gas concentrations in the air and a weather station provided meteorological parameters. Additionally, a wide spectrum of ship information for each vessel including speed, size, vessel type, fuel type, gross tonnage and engine power was recorded via Automatic Identification System (AIS) broadcasts. Although commercial marine vessels powered by diesel engines consume high

EDDY RESOLVING NUTRIENT ECODYNAMICS IN THE GLOBAL PARALLEL OCEAN PROGRAM AND CONNECTIONS WITH TRACE GASES IN THE SULFUR, HALOGEN AND NMHC CYCLES

Energy Technology Data Exchange (ETDEWEB)

S. CHU; S. ELLIOTT

2000-08-01

Ecodynamics and the sea-air transfer of climate relevant trace gases are intimately coupled in the oceanic mixed layer. Ventilation of species such as dimethyl sulfide and methyl bromide constitutes a key linkage within the earth system. We are creating a research tool for the study of marine trace gas distributions by implementing coupled ecology-gas chemistry in the high resolution Parallel Ocean Program (POP). The fundamental circulation model is eddy resolving, with cell sizes averaging 0.15 degree (lat/long). Here we describe ecochemistry integration. Density dependent mortality and iron geochemistry have enhanced agreement with chlorophyll measurements. Indications are that dimethyl sulfide production rates must be adjusted for latitude dependence to match recent compilations. This may reflect the need for phytoplankton to conserve nitrogen by favoring sulfurous osmolytes. Global simulations are also available for carbonyl sulfide, the methyl halides and for nonmethane hydrocarbons. We discuss future applications including interaction with atmospheric chemistry models, high resolution biogeochemical snapshots and the study of open ocean fertilization.

Advective transport of CO2 in permeable media induced by atmospheric pressure fluctuations: 1. An analytical model

Science.gov (United States)

W. J. Massman

2006-01-01

Advective flows within soils and snowpacks caused by pressure fluctuations at the upper surface of either medium can significantly influence the exchange rate of many trace gases from the underlying substrate to the atmosphere. Given the importance of many of these trace gases in understanding biogeochemical cycling and global change, it is crucial to quantify (as much...

A Nanoparticulate Photocatalytic Filter for Removal of Trace Contaminant Gases, Phase I

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...

Tracing the Atmospheric Source of Desert Nitrates Using Δ 17O

Science.gov (United States)

Michalski, G. M.; Holve, M.; Feldmeier, J.; Bao, H.; Reheis, M.; Bockheim, J. G.; Thiemens, M. H.

2001-05-01

Mineral, caliche, and soil nitrates are found throughout the worlds deserts, including the cold dry Wright Valley of Antarctica, the Atacama desert in Chile and the Mojave desert in the southwest United States. Several authors have suggested biologic sources of these nitrates while others have postulated atmospheric deposition. A recent study utilizing 18O indicated that 30%, and perhaps 100%, of nitrates found in the Atacama and Mojave were of atmospheric origin [1]. A more quantitative assessment of the source strength of atmospheric nitrates was impossible because of the high variability of δ 18 18O of atmospheric nitrates and uncertainties in conditions of biologic production. Mass independently fractionated (MIF) processes are defined and quantified by the equation Δ 17O = δ 17O - .52x δ 18O. MIF processes are associated with the photochemistry of trace gases in the atmosphere and have been found in O3, N2O, CO, and sulfate aerosols . A large MIF (Δ 17O ~ 28 ‰ ) in nitrate aerosols collected in polluted regions was recently reported [2]. Here we extend measurements of MIF in nitrate to the dry deposition of nitrate in less polluted areas (Mojave desert). In addition we trace the MIF signal as it accumulates in the regolith as nitrate salts and minerals and is mixed with biologically produced nitrate (nitrification). Also examined were the isotopic composition of soil nitrates from Antarctic dry valleys. Dust samples were collected as part of the NADP program and soils were collected throughout the Mojave and Death Valley regions of California. Isotope analysis was done in addition to soluble ion content (Cl, NO3, SO4). Dust samples collected by dry deposition samplers showed a large MIF > 20‰ approaching values measured in urban nitrate aerosol. Soils collected throughout the region showed large variations in Δ 17O from ~ 0 to 18 ‰ . The low Δ 17O values are nitrates dominated by biologic nitrification and higher values are nitrates derived by

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

Trace Gas Quantification with Small Unmanned Aerial Systems

Science.gov (United States)

Schuyler, T. J.; Guzman, M. I.; Bailey, S.; Jacob, J.

2017-12-01

Measurements of atmospheric composition are generally performed with advanced instrumentation from ground stations using tall towers and weather balloons or with manned aircraft. Unmanned aerial systems (UAS) are a promising technology for atmospheric monitoring of trace atmospheric gases as they can bridge the gap between the regions of the atmospheric boundary layer measured by ground stations and aircraft. However, in general, the sophisticated instrumentation required for these measurements are heavy, preventing its deployment with small UAS. In order to successfully detect and quantify these gases, sensor packages aboard UAS must be lightweight, have low-power consumption, and possess limits of detection on the ppm scale or below with reasonably fast response times. Thus, a new generation of portable instrument is being developed in this work to meet these requirements employing new sensing packages. The cross sensitivity of these sensors to several gases is examined through laboratory testing of the instrument under variable environmental conditions prior to performing field measurements. Datasets include timestamps with position, temperature, relative humidity, pressure, along with variable mixing ratio values of important greenhouse gases. The work will present an analysis of the results gathered during authorized flights performed during the second CLOUD-MAP§ field campaign held in June 2017. §CLOUD-MAP: Collaboration Leading Operational UAS Development for Meteorology and Atmospheric Physics, a 4-year NSF funded effort.

Molecular line parameters for the atmospheric trace molecule spectroscopy experiment

Science.gov (United States)

Brown, L. R.; Farmer, C. B.; Toth, R. A.; Rinsland, Curtis P.

1987-01-01

During its first mission in 1985 onboard Spacelab 3, the ATMOS (atmospheric trace molecule spectroscopy) instrument, a high speed Fourier transform spectrometer, produced a large number of high resolution infrared solar absorption spectra recorded in the occultation mode. The analysis and interpretation of these data in terms of composition, chemistry, and dynamics of the earth's upper atmosphere required good knowledge of the molecular line parameters for those species giving rise to the absorptions in the atmospheric spectra. This paper describes the spectroscopic line parameter database compiled for the ATMOS experiment and referenced in other papers describing ATMOS results. With over 400,000 entries, the linelist catalogs parameters of 46 minor and trace species in the 1-10,000/cm region.

Atmospheric observations and inverse modelling for quantifying emissions of point-source synthetic greenhouse gases in East Asia

Science.gov (United States)

Arnold, Tim; Manning, Alistair; Li, Shanlan; Kim, Jooil; Park, Sunyoung; Muhle, Jens; Weiss, Ray

2017-04-01

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-replacements that are emitted from fugitive and mobile emission sources, these gases are mostly emitted from large single point sources - semiconductor manufacturing facilities (all three), aluminium smelting plants (CF4) and chlorodifluoromethane (HCFC-22) factories (HFC-23). In this work we show that atmospheric measurements can serve as a basis to calculate emissions of these gases and to highlight emission 'hotspots'. We use measurements from one Advanced Global Atmospheric Gases Experiment (AGAGE) long term monitoring sites at Gosan on Jeju Island in the Republic of Korea. This site measures 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 seven years between 2008 and 2015. We show that our 'top-down' emission estimates for NF3 and CF4 are significantly larger than 'bottom-up' estimates in the EDGAR emissions inventory (edgar.jrc.ec.europa.eu). For example we calculate South Korean emissions of CF4 in 2010 to be 0.29±0.04 Gg/yr, which is significantly larger than the Edgar prior emissions of 0.07 Gg/yr. Further, inversions for several separate years indicate that emission hotspots can be found without prior spatial information. At present these gases make a small contribution to global radiative forcing, however, given

Photoionization of atmospheric gases studied by time-resolved terahertz spectroscopy

Czech Academy of Sciences Publication Activity Database

Mics, Zoltan; Kužel, Petr; Jungwirth, Pavel; Bradforth, S. E.

2008-01-01

Roč. 465, 1-3 (2008), s. 20-24 ISSN 0009-2614 R&D Projects: GA MŠk LC512; GA ČR(CZ) GA202/06/0286 Institutional research plan: CEZ:AV0Z10100520; CEZ:AV0Z40550506 Keywords : terahertz * pump -probe * atmospheric gases * photoionization * plasma Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.169, year: 2008

Linking genes to ecosystem trace gas fluxes in a large-scale model system

Science.gov (United States)

Meredith, L. K.; Cueva, A.; Volkmann, T. H. M.; Sengupta, A.; Troch, P. A.

2017-12-01

Soil microorganisms mediate biogeochemical cycles through biosphere-atmosphere gas exchange with significant impact on atmospheric trace gas composition. Improving process-based understanding of these microbial populations and linking their genomic potential to the ecosystem-scale is a challenge, particularly in soil systems, which are heterogeneous in biodiversity, chemistry, and structure. In oligotrophic systems, such as the Landscape Evolution Observatory (LEO) at Biosphere 2, atmospheric trace gas scavenging may supply critical metabolic needs to microbial communities, thereby promoting tight linkages between microbial genomics and trace gas utilization. This large-scale model system of three initially homogenous and highly instrumented hillslopes facilitates high temporal resolution characterization of subsurface trace gas fluxes at hundreds of sampling points, making LEO an ideal location to study microbe-mediated trace gas fluxes from the gene to ecosystem scales. Specifically, we focus on the metabolism of ubiquitous atmospheric reduced trace gases hydrogen (H2), carbon monoxide (CO), and methane (CH4), which may have wide-reaching impacts on microbial community establishment, survival, and function. Additionally, microbial activity on LEO may facilitate weathering of the basalt matrix, which can be studied with trace gas measurements of carbonyl sulfide (COS/OCS) and carbon dioxide (O-isotopes in CO2), and presents an additional opportunity for gene to ecosystem study. This work will present initial measurements of this suite of trace gases to characterize soil microbial metabolic activity, as well as links between spatial and temporal variability of microbe-mediated trace gas fluxes in LEO and their relation to genomic-based characterization of microbial community structure (phylogenetic amplicons) and genetic potential (metagenomics). Results from the LEO model system will help build understanding of the importance of atmospheric inputs to

Trace gases over Northern Eurasia: background level and disturbing factors

Science.gov (United States)

Skorokhod, A.; Shumsky, R.; Pankratova, N.; Moiseenko, K.; Vasileva, A.; Berezina, E.; Elansky, N.

2012-04-01

Atmospheric air composition over the vast and low inhabited areas of Northern Eurasia is still poorly studied because of lack of the precise direct measurements. This harms to accuracy of both global and regional models which simulate climatological and ecosystem changes in that highly important region. In this work background trace gases (such as O3, NO, NO2, CO) concentrations and their variability are considered on base of results of continuous measurements at ZOTTO station in the middle of Siberia which have been carried out since March, 2007. Also factors implying background regime (like long-range transport, wild fires emissions) are analyzed. To compliment study data of TROICA train-based campaigns which have been regularly provided across Russia for many years (1995-2010) are used. The concentration of ozone has a pronounced seasonal variation with a clear peak in spring (40-45 ppbv in average and up to 80 ppbv in extreme cases) and minimum in winter. Average ozone level is about 20 ppbv that corresponds to the background conditions. Enhanced concentration in March-July is due to increased stratospheric-tropospheric exchange. In autumn and winter distribution of ozone is close to uniform. Photochemical processes under low light and air temperature does not cause the generation of ozone. Sink on the snow surface is very small, and therefore the diurnal variations are absent. In general, seasonal variations correspond to the average seasonal course, which is typical for Russia. The analysis of diurnal ozone variations in Zotino in different seasons showed that the maximum rate of ozone formation is observed in summer from 9 to 15 h local time and is 1-2 ppbv/hour. It correlates well with the data on the isoprene emissions and others biogenic VOC reacting with OH- radical. Thus they are biogenic VOC emissions that seem to be the main factor of the lower troposphere oxidation power in summer. In other seasons it is significantly lower. NOx concentration does

Effect of ''outer'' sources and dissipative processes on abundance of inert gases in atmospheres of the Earth group planets

International Nuclear Information System (INIS)

Pavlov, A.K.

1981-01-01

The problem of abundance of inert gases in atmospheres of the Earth group planets is discussed. It is shown that introduction of He, Ne and 36 Ar into the Mars and Mercury atmospheres with interplanetary dust and from other external sources require the presence of special mechanisms of losses for these gases. For the Mars atmosphere dissipation on atmosphere interaction with solar wind during the periods of anomalously low temperatures is a probable mechanisms of Ne and 36 Ar losses. For the Mercury thermal dissipation for He and polar wind for other inert gases are possible. For all the planets of the Earth group dissipation on interaction with solar wind and introduction with interplanetary dust could play an important role at the early stages of evolution of planets [ru

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.

Ultrafast-Laser-Induced Backward Stimulated Raman Scattering for Tracing Atmospheric Gases

Directory of Open Access Journals (Sweden)

Zheltiko A.

2013-03-01

Full Text Available By combining tunable broadband pulse generation with nonlinear spectral compression, we demonstrate a prototype scheme for highly selective coherent standoff sensing of air molecules and discuss its coupling to the recently demonstrated backward atmospheric lasing.

Trace elements controlling the atmospheric circulation. Atmospheric environmental research as part of future FhG research

Energy Technology Data Exchange (ETDEWEB)

1986-11-01

Atmospheric trace substances such as methane (CH/sub 4/), ozone and nitrogen oxides (NO/sub x/) essentially influence the biosphere. FhG research work will be consisting in the long-term measurement of trace substance concentrations in different places (e.g. South Africa, Italy, Thailand or China). An air container packed with measuring instruments and data storage equipment was sent to South America with scientists on board measuring the distribution of trace substances over the northern and southern hemisphere.

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.)

Freeze dried samples of volcanic gases - a new method for the determination of trace elements by NAA

International Nuclear Information System (INIS)

Bichler, M.; Sortino, F.

1997-01-01

A new routine technique for the determination of trace elements in volcanic gases by NAA is presented. For time and money saving reasons this method is applicable to samples, collected by the conventional method. This technique uses evacuated glass bottles, partly filled with NaOH solution to absorb acidic gas components and CO 2 , which is the main constituent of the incondensable gas fraction at ambient conditions. The application of NAA to samples collected by this method shows two main sources of difficulties: drying of NaOH without loosing volatile elements of interest (in particular Hg and Se) and the high activities of 24 Na after neutron irradiation. The first can be avoided by liquid irradiation, thereby limiting the irradiation time, the second excludes the determination of short and medium lived nuclides because of the high γ-background due to 24 Na. A new freeze drying technique enables the application of long irradiation times and therefore the use of long-lived activation products for analysis. The samples of volcanic gases were collected at the fumarole fields of La Fossa volcano on the island Vulcano. Southern Italy. This technique allows very sensitive determinations of trace elements in volcanic gases and adds highly valuable information to the understanding and modeling of volcanic gas sources. (orig.)

PHOTOCHEMISTRY IN TERRESTRIAL EXOPLANET ATMOSPHERES. I. PHOTOCHEMISTRY MODEL AND BENCHMARK CASES

Energy Technology Data Exchange (ETDEWEB)

Hu Renyu; Seager, Sara; Bains, William, E-mail: hury@mit.edu [Department of Earth, Atmospheric and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139 (United States)

2012-12-20

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., CH{sub 4} and CO{sub 2}) 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 CO{sub 2}-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

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

International Nuclear Information System (INIS)

Shah, M.H.; Shaheen, N.

2009-01-01

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

Trace substances in landfill gases. Evaluation and meaningful analysis. Spurenstoffe in Deponiegasen. Bewertung und sinnvolle Analyse

Energy Technology Data Exchange (ETDEWEB)

Eisenmann, R [Karlsruhe Univ. (T.H.) (Germany, F.R.). Engler-Bunte-Institut

1989-06-01

Many of the innumerable substances which may occur in landfill gases are to be considered as possibly dangerous; they lead to environmental problems due to their malodour or noxious combustion products. With respect to the evaluation of the traces of substances there is great unsecurity and often extreme requirements as to volume and quality of gas analyses have to be met. Generally it can be noticed that there are hazards emanating from landfill gases, but in comparison to other risks they are not excessive. The contribution shall help to clarify questions and furnish a basis for the practice-oriented and appropriate landfill gas analytics. (orig.).

NUCAPS: NOAA Unique Combined Atmospheric Processing System Environmental Data Record (EDR) Products

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — This dataset consists of numerous retrieved estimates of hydrological variables and trace gases as Environmental Data Record (EDR) products from the NOAA Unique...

Noble gases in Mars atmosphere: new precise analysis with Paloma

Science.gov (United States)

Sarda, Ph.; Paloma Team

2003-04-01

The Viking mission embarked a mass spectrometer designed by Alfred O. Nier that yielded the first determination of the elemental and isotopic composition of noble gases in Mars atmosphere. For example, the 40Ar/36Ar ratio in martian air is roughly 10 fold that in terrestrial air. This extraordinary accomplishment, however, has furnished only partial results with large analytical uncertainties. For example, we do not know the isotopic composition of helium, and only very poorly that of Ne, Kr and Xe. In planetary science, it is fundamental to have a good knowledge of the atmosphere because this serves as a reference for all further studies of volatiles. In addition, part of our present knowledge of Mars atmosphere is based on the SNC meteorites, and again points to important differences between the atmospheres of Earth and Mars. For example the 129Xe/132Xe ratio of martian atmosphere would be twice that of terrestrial air and the 36Ar/38Ar ratio strongly different from the terrestrial or solar value. There is a need for confirming that the atmospheric components found in SNC meteorites actually represents the atmosphere of Mars, or to determine how different they are. Paloma is an instrument designed to generate elemental and isotopic data for He, Ne, Ar, Kr and Xe (and other gases) using a mass spectrometer with a purification and separation line. Gas purification and separation did not exist on the Vicking instrument. Because Paloma includes purification and separation, we expect strong improvement in precision. Ne, Ar and Xe isotope ratios should be obtained with an accuracy of better than 1%. Determination of the presently unknown ^3He/^4He ratio is also awaited from this experiment. Knowledge of noble gas isotopes in Mars atmosphere will allow some insight into major planetary processes such as degassing (^3He/^4He, 40Ar/36Ar, 129Xe/130Xe, 136Xe/130Xe), gravitational escape to space (^3He/^4He, 20Ne/22Ne), hydrodynamic escape and/or impact erosion of the

Influence of atmospheric 14CO2 on determination of the ratio of biogenic carbon to fossil one in exhaust gases using accelerator mass spectrometry. Experimental evaluation for industrial flue gases

International Nuclear Information System (INIS)

Yunoki, Shunji; Saito, Masaaki; Nagakawa, Yoshiyasu

2012-01-01

The influence of atmospheric 14 CO 2 was evaluated on the determination of biogenic carbon ratios in industrial flue gases using accelerated mass spectrometry(AMS). Bioethanol, n-hexane, and their mixtures were combusted with a four-stroke engine, and 14 CO 2 in exhaust gases was analyzed by AMS. The experimental biogenic carbon ratio determined by ASTM D6866 method was 1.2 times higher than the theoretical value of mixed fuel containing 3.18% biogenic carbons. In general, the influence of atmospheric 14 CO 2 taken in combustion gases is neglected. It seems that the error cannot be neglected under international trading of emission allowances, where a large amount of carbons in the fuel were evaluated. The experimental value became to be the theoretical value by subtracting the amount of atmospheric 14 C from that of the samples. As the contents of biofuel increased, the experimental biogenic carbon ratios reached the theoretical values and the influence of atmospheric 14 CO 2 decreased. We recommend that the influence of atmospheric 14 CO 2 should be corrected when fuel samples contain low amounts of 14 C. (author)

Trace elements in the atmosphere over South Africa

International Nuclear Information System (INIS)

Wells, R.B.; Van As, D.

1976-01-01

Natural sources of trace elements in the atmosphere are suspended soil particles, the evaporation of sea spray and smoke from veld fires. In urban and industrialised areas the main sources are fossil-fuel power plants, metallurgical smelters, blast furnaces, incinerators, automobiles, fossil-fueled locomotives and open fires in the Black townships. Often a source can be recognised by the relative concentrations of particular trace elements. A monitoring programme was established in 1974 by the Air Pollution Research Group of the CSIR and the Isotope and Radiation Division of the Atomic Energy Board in order to study the levels of trace elements in urban areas such as Johannesburg, Cape Town, and Durban, to measure the effects of industrialisation on trace elements levels in developing areas such as Richards Bay and Saldanha Bay and also to determine baseline values in rural areas. Extremely sensitive analytical techniques, e.g. neutron activation and atomic absorption were used for the analyses of filter samples. Methods of sampling and analysis are discussed and the preliminary results of this programme are presented

Mobile Instruments Measure Atmospheric Pollutants

Science.gov (United States)

2009-01-01

As a part of NASA's active research of the Earth s atmosphere, which has included missions such as the Atmospheric Laboratory of Applications and Science (ATLAS, launched in 1992) and the Total Ozone Mapping Spectrometer (TOMS, launched on the Earth Probe satellite in 1996), the Agency also performs ground-based air pollution research. The ability to measure trace amounts of airborne pollutants precisely and quickly is important for determining natural patterns and human effects on global warming and air pollution, but until recent advances in field-grade spectroscopic instrumentation, this rapid, accurate data collection was limited and extremely difficult. In order to understand causes of climate change and airborne pollution, NASA has supported the development of compact, low power, rapid response instruments operating in the mid-infrared "molecular fingerprint" portion of the electromagnetic spectrum. These instruments, which measure atmospheric trace gases and airborne particles, can be deployed in mobile laboratories - customized ground vehicles, typically - to map distributions of pollutants in real time. The instruments must be rugged enough to operate rapidly and accurately, despite frequent jostling that can misalign, damage, or disconnect sensitive components. By measuring quickly while moving through an environment, a mobile laboratory can correlate data and geographic points, revealing patterns in the environment s pollutants. Rapid pollutant measurements also enable direct determination of pollutant sources and sinks (mechanisms that remove greenhouse gases and pollutants), providing information critical to understanding and managing atmospheric greenhouse gas and air pollutant concentrations.

Biogenic and pyrogenic emissions from Africa and their impact on the global atmosphere

International Nuclear Information System (INIS)

Scholes, Mary; Andreae, M.O.

2000-01-01

Tropical regions, with their high biological activity, have the potential to emit large amounts of trace gases and aerosols to the atmosphere. This can take the form of trace gas fluxes from soils and vegetation, where gaseous species are produced and consumed by living organisms, or of smoke emissions from vegetation fires. In the last decade, considerable scientific effort has gone into quantifying these fluxes from the African continent. We find that both biogenic and pyrogenic emissions have a powerful impact on regional and global atmospheric chemistry, particularly on photooxidation processes and tropospheric ozone. The emissions of radiatively active gases and aerosols from the African continent are likely to have a significant climatic effect, but presently available data are not sufficient for reliable quantitative estimates of this effect

Variations of trace gases over the Bay of Bengal during the summer monsoon

Science.gov (United States)

Girach, I. A.; Ojha, Narendra; Nair, Prabha R.; Tiwari, Yogesh K.; Kumar, K. Ravi

2018-02-01

In situ measurements of near-surface ozone (O3), carbon monoxide (CO), and methane (CH4) were carried out over the Bay of Bengal (BoB) as a part of the Continental Tropical Convergence Zone (CTCZ) campaign during the summer monsoon season of 2009. O3, CO and CH4 mixing ratios varied in the ranges of 8-54 ppbv, 50-200 ppbv and 1.57-2.15 ppmv, respectively during 16 July-17 August 2009. The spatial distribution of mean tropospheric O3 from satellite retrievals is found to be similar to that in surface O3 observations, with higher levels over coastal and northern BoB as compared to central BoB. The comparison of in situ measurements with the Monitoring Atmospheric Composition & Climate (MACC) global reanalysis shows that MACC simulations reproduce the observations with small mean biases of 1.6 ppbv, -2.6 ppbv and 0.07 ppmv for O3, CO and CH4, respectively. The analysis of diurnal variation of O3 based on observations and the simulations from Weather Research and Forecasting coupled with Chemistry (WRF-Chem) at a stationary point over the BoB did not show a net photochemical build up during daytime. Satellite retrievals show limitations in capturing CH4 variations as measured by in situ sample analysis highlighting the need of more shipborne in situ measurements of trace gases over this region during monsoon.

Facilitating breakdown in noble gases at near-atmospheric pressure using antennas

Energy Technology Data Exchange (ETDEWEB)

Sobota, A; Van Veldhuizen, E M; Haverlag, M [Eindhoven University of Technology, Department of Applied Physics, Postbus 513, 5600MB Eindhoven (Netherlands); Gendre, M F; Manders, F, E-mail: a.sobota@tue.nl [Philips Lighting, Mathildelaan 1, 5600JM Eindhoven (Netherlands)

2011-04-20

Electrical breakdown in near-atmospheric pressure noble gases requires voltages that are quite high, which is undesirable for a large number of possible applications. Metallic structures (antennas) were used on the outer side of the lamp burner to enhance the electric field locally while keeping the same potential difference across the electrodes. Optical and electrical measurements were performed in an argon or xenon atmosphere at 0.3 or 0.7 bar, with 4 or 7 mm between the electrode tips. We used rod-shaped tungsten electrodes of 0.6 mm in diameter. We found that both active and passive antennas facilitate breakdown, and we demonstrated the differences between the two types and their effects on the breakdown process.

Facilitating breakdown in noble gases at near-atmospheric pressure using antennas

International Nuclear Information System (INIS)

Sobota, A; Van Veldhuizen, E M; Haverlag, M; Gendre, M F; Manders, F

2011-01-01

Electrical breakdown in near-atmospheric pressure noble gases requires voltages that are quite high, which is undesirable for a large number of possible applications. Metallic structures (antennas) were used on the outer side of the lamp burner to enhance the electric field locally while keeping the same potential difference across the electrodes. Optical and electrical measurements were performed in an argon or xenon atmosphere at 0.3 or 0.7 bar, with 4 or 7 mm between the electrode tips. We used rod-shaped tungsten electrodes of 0.6 mm in diameter. We found that both active and passive antennas facilitate breakdown, and we demonstrated the differences between the two types and their effects on the breakdown process.

CARBON TRACE GASES IN LAKE AND BEAVER POND ICE NEAR THOMPSON, MANITOBA, CANADA

Science.gov (United States)

Concentrations of CO2, CO, and CH4 were measured in beaver pond and lake ice in April 1996 near Thompson, Manitoba to derive information on possible impacts of ice melting on corresponding atmospheric trace gas concentrations. CH4 concentrations in beaver pond and lake ice ranged...

Noble Gases in Lakes and Ground Waters

OpenAIRE

Kipfer, Rolf; Aeschbach-Hertig, Werner; Peeters, Frank; Stute, Marvin

2002-01-01

In contrast to most other fields of noble gas geochemistry that mostly regard atmospheric noble gases as 'contamination,' air-derived noble gases make up the far largest and hence most important contribution to the noble gas abundance in meteoric waters, such as lakes and ground waters. Atmospheric noble gases enter the meteoric water cycle by gas partitioning during air / water exchange with the atmosphere. In lakes and oceans noble gases are exchanged with the free atmosphere at the surface...

Airborne measurements of reactive organic trace gases in the atmosphere - with a focus on PTR-MS measurements onboard NASA's flying laboratories

Science.gov (United States)

Wisthaler, Armin; Mikoviny, Tomas; Müller, Markus; Schiller, Sven Arne; Feil, Stefan; Hanel, Gernot; Jordan, Alfons; Mutschlechner, Paul; Crawford, James H.; Singh, Hanwant B.; Millet, Dylan

2017-04-01

Reactive organic gases (ROGs) play an important role in atmospheric chemistry as they affect the rates of ozone production, particle formation and growth, and oxidant consumption. Measurements of ROGs are analytically challenging because of their large variety and low concentrations in the Earth's atmosphere, and because they are easily affected by measurement artefacts. On aircraft, ROGs are typically measured by canister sampling followed by off-line analysis in the laboratory, fast online gas chromatography or online chemical ionization mass spectrometry. In this work, we will briefly sum up the state-of-the-art in this field before focusing on proton-transfer-reaction mass spectrometry (PTR-MS) and its deployment onboard NASA's airborne science laboratories. We will show how airborne PTR-MS was successfully used in NASA missions for characterizing emissions of ROGs from point sources, for following the photochemical evolution of ROGs in a biomass burning plume, for determining biosphere-atmosphere fluxes of selected ROGs and for validating satellite data. We will also present the airborne PTR-MS instrument in its most recent evolution which includes a radiofrequency ion funnel and ion guide combined with a compact time-of-flight mass spectrometer and discuss its superior performance characteristics. The development of the airborne PTR-MS instrument was supported by the Austrian Federal Ministry for Transport, Innovation and Technology (bmvit) through the Austrian Space Applications Programme (ASAP) of the Austrian Research Promotion Agency (FFG) (grants #833451, #847967). This work was also partly supported by NASA under grant #NNX14AP89G.

On the "well-mixed" assumption and numerical 2-D tracing of atmospheric moisture

Directory of Open Access Journals (Sweden)

H. F. Goessling

2013-06-01

Full Text Available Atmospheric water vapour tracers (WVTs are an elegant tool to determine source–sink relations of moisture "online" in atmospheric general circulation models (AGCMs. However, it is sometimes desirable to establish such relations "offline" based on already existing atmospheric data (e.g. reanalysis data. One simple and frequently applied offline method is 2-D moisture tracing. It makes use of the "well-mixed" assumption, which allows for treating the vertical dimension integratively. Here we scrutinise the "well-mixed" assumption and 2-D moisture tracing by means of analytical considerations in combination with AGCM-WVT simulations. We find that vertically well-mixed conditions are seldom met. Due to the presence of vertical inhomogeneities, 2-D moisture tracing (i neglects a significant degree of fast-recycling, and (ii results in erroneous advection where the direction of the horizontal winds varies vertically. The latter is not so much the case in the extratropics, but in the tropics this can lead to large errors. For example, computed by 2-D moisture tracing, the fraction of precipitation in the western Sahel that originates from beyond the Sahara is ~40%, whereas the fraction that originates from the tropical and Southern Atlantic is only ~4%. According to full (i.e. 3-D moisture tracing, however, both regions contribute roughly equally, showing that the errors introduced by the 2-D approximation can be substantial.

Effects of vegetation burning on the atmospheric chemistry of the Venezuelan savanna

International Nuclear Information System (INIS)

Sanhueza, E.

1991-01-01

Biomass burning in tropical savanna and rainforest regions is an important factor in the chemical composition of the atmosphere. On the global scale, burning of savanna grass procedures three to four times greater emission of trace gases than deforestation processes of tropical rainforest. As part of a comprehensive study of the Venezuelan savanna atmosphere, measurements of gases and particles, chemical composition of rain, and biogenic soil emission were made during burning and nonburning periods at several rural savanna sites. A review of the most significant findings is presented in this chapter, and their regional and global implications are discussed

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.

Combustion's impact on the global atmosphere

International Nuclear Information System (INIS)

Prather, M.J.; Logan, J.A.

1994-01-01

The combustion of a hydrocarbon fuel removes molecular oxygen (O 2 ) from the atmosphere and releases equivalent amounts of water (H 2 ) and carbon dioxide (CO 2 ), almost always with trace amounts of numerous other compounds including hydrocarbon (CH 4 , C 2 H 2 , C 2 H 4 , C 2 H 6 , C 3 H 8 , C 6 H 6 , CH 3 CHO, etc.), carbon monoxide (CO), nitrogen oxides (NO, N 2 O) and reduced nitrogen (NH 3 and HCN), sulfur gases (SO 2 , OCS, CS 2 ), halocarbons (CH 3 Al and CH 3 Br), and particles. A review of the atmospheric budgets of these gases shows that burning of fossil fuels and recent biomass has led to global alterations in the composition of the atmosphere. Combustion is clearly responsible for most of the enhanced greenhouse forcing to date (through CO 2 , tropospheric O 3 , soot) and also some counteracting effects (through SO 2 ). It has had minimal impact on stratospheric O 3 (through CH 3 Cl, CH 3 Br, CH 4 ), but has likely changed the tropospheric oxidant levels (through CO, NO x , NMHC), at least over the northern hemisphere. Most of the important greenhouse gases and tropospheric oxidant gases have significant natural sources, which are not well defined today and may be changing; and thus, quantifying the role of combustion is difficult. 113 refs

Preparation and analysis of zero gases for the measurement of trace VOCs in air monitoring

Science.gov (United States)

Englert, Jennifer; Claude, Anja; Demichelis, Alessia; Persijn, Stefan; Baldan, Annarita; Li, Jianrong; Plass-Duelmer, Christian; Michl, Katja; Tensing, Erasmus; Wortman, Rina; Ghorafi, Yousra; Lecuna, Maricarmen; Sassi, Guido; Sassi, Maria Paola; Kubistin, Dagmar

2018-06-01

Air quality observations are performed globally to monitor the status of the atmosphere and its level of pollution and to assess mitigation strategies. Regulations of air quality monitoring programmes in various countries demand high-precision measurements for harmful substances often at low trace concentrations. These requirements can only be achieved by using high-quality calibration gases including high-purity zero gas. For volatile organic compound (VOC) observations, zero gas is defined as being hydrocarbon-free and can be, for example, purified air, nitrogen or helium. It is essential for the characterisation of the measurement devices and procedures, for instrument operation as well as for calibrations. Two commercial and one self-built gas purifiers were tested for their VOC removal efficiency following a standardised procedure. The tested gas purifiers included one adsorption cartridge with an inorganic media and two types of metal catalysts. A large range of VOCs were investigated, including the most abundant species typically measured at air monitoring stations. Both catalysts were able to remove a large range of VOCs whilst the tested adsorption cartridge was not suitable to remove light compounds up to C4. Memory effects occurred for the adsorption cartridge when exposed to higher concentration. This study emphasises the importance of explicitly examining a gas purifier for its intended application before applying it in the field.

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.

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

Determination of traces of fluorine and hydrofluoric acid in the atmosphere

International Nuclear Information System (INIS)

Francois, H.; Grand-Clement, A.M.; Faltot, G.

1963-01-01

As some publications highlighted hazards related to the presence of dispersed fluorine and hydrofluoric acid in the atmosphere, the authors, after a brief recall of some measurement devices presented in some publications, present an experimental set-up which aims at measuring traces of these compounds in the atmosphere. They notably describe the preparation of a controlled fluorine atmosphere, discuss the efficiency of the absorption-based trap, report the study of the electrolytic analysis cell, discuss its calibration. They also report the study of the influence of temperature and of the presence of disturbing ions

On the Role of Dissolved Gases in the Atmosphere Retention of Low-mass Low-density Planets

Science.gov (United States)

Chachan, Yayaati; Stevenson, David J.

2018-02-01

Low-mass low-density planets discovered by Kepler in the super-Earth mass regime typically have large radii for their inferred masses, implying the presence of H2–He atmospheres. These planets are vulnerable to atmospheric mass loss due to heating by the parent star’s XUV flux. Models coupling atmospheric mass loss with thermal evolution predicted a bimodal distribution of planetary radii, which has gained observational support. However, a key component that has been ignored in previous studies is the dissolution of these gases into the molten core of rock and iron that constitute most of their mass. Such planets have high temperatures (>2000 K) and pressures (∼kbars) at the core-envelope boundary, ensuring a molten surface and a subsurface reservoir of hydrogen that can be 5–10 times larger than the atmosphere. This study bridges this gap by coupling the thermal evolution of the planet and the mass loss of the atmosphere with the thermodynamic equilibrium between the dissolved H2 and the atmospheric H2 (Henry’s law). Dissolution in the interior allows a planet to build a larger hydrogen repository during the planet formation stage. We show that the dissolved hydrogen outgasses to buffer atmospheric mass loss. The slow cooling of the planet also leads to outgassing because solubility decreases with decreasing temperature. Dissolution of hydrogen in the interior therefore increases the atmosphere retention ability of super-Earths. The study highlights the importance of including the temperature- and pressure-dependent solubility of gases in magma oceans and coupling outgassing to planetary evolution models.

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.

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

Assessment of Burned Area and Atmospheric Gases from Multi- temporal MODIS Images (2000- 2017) in Nainital District, Uttarakhand

Science.gov (United States)

Aggarwal, R.; K V, S. B.; Dhakate, P. M.

2017-12-01

Recent times have observed a significant rate of deforestation and forest degradation. One of the major causes of forest degradation is forest fires. Forest fires though have shaped the current forest ecosystem but also have continued to degrade the system by causing loss of flora and fauna. In addition to that, forest fire leads to emission of carbon and other trace gases which contributes to global warming. The hill states in India, particularly Uttarakhand witnesses annual forest fires; which are primarily anthropogenic caused, occurring from March to June. Nainital one of the thirteen districts in Uttarakhand, has been selected as the study site. The region has diverse endemic species of vegetation, ranging from Alpine in North to moist deciduous in South. The increasing forest fire incidents in the region and limited studies on the subject, calls for landscape assessment of the complex Human Environment System (HES). It is in this context, that a greater need for monitoring forest fire incidents has been felt. Remote Sensing and GIS which are robust tool, provides continuous information of an area at various spatial and temporal resolutions. The goal of this study is to map burned area, burned severity and estimate atmospheric gas emissions in forested areas of Nainital by utilizing cloud free MODIS images from 2000- 2017. Multiple spectral indices were generated from pre and post burn dataset of MODIS to conclude the most sensitive band combination. Inter- comparison of results obtained from different spectral indices and the global MODIS MCD45A1 was carried out using linear regression analysis. Additionally, burned area estimation from satellite was compared to figures reported by forest department. There were considerable differences amongst the two which could be primarily due to differences in spatial resolution, and timings of forest fire occurrence and image acquisition. Further, estimation of various atmospheric gases was carried out based on the IPCC

Time resolved IR-LIGS experiments for gas-phase trace detection and temperature measurements

Energy Technology Data Exchange (ETDEWEB)

Fantoni, R.; Giorgi, M. [ENEA, Centro Ricerche Frascati, Rome (Italy). Dip. Innovazione; Snels, M. [CNR, Tito Scalo, Potenza (Italy). Istituto per i Materiali Speciali; Latzel, H.

1997-01-01

Time resolved Laser Induced Grating Spectroscopy (LIGS) has been performed to detect different gases in mixtures at atmospheric pressure or higher. The possibility of trace detection of minor species and of temperature measurements has been demonstrated for various molecular species either of environmental interest or involved in combustion processes. In view of the application of tracing unburned hydrocarbons in combustion chambers, the coupling of the IR-LIGS technique with imaging detection has been considered and preliminary results obtained in small size ethylene/air flames are shown.

Estimation of the Atmosphere-Ocean Fluxes of Greenhouse Gases and Aerosols at the Finer Resolution of the Coastal Ocean

Czech Academy of Sciences Publication Activity Database

Vieira, V.; Sahlée, E.; Juruš, Pavel; Clementi, E.; Pettersson, H.; Mateus, M.

2016-01-01

Roč. 18 (2016), EGU2016-1990-1 ISSN 1607-7962. [EGU General Assembly 2016. 17.04.2016-22.04.2016, Vienna] Institutional support: RVO:67985807 Keywords : greenhouse gases * carbon cycle * atmosphere- ocean interaction * atmosphere modelling * ocean modelling Subject RIV: DG - Athmosphere Sciences, Meteorology

Future Applications in Quantitative Isotopic Tracing using Homogeneously Carbon-13 Labelled Plant Material

International Nuclear Information System (INIS)

Slaets, Johanna I.F.; Chen, Janet; Resch, Christian; Mayr, Leopold; Weltin, Georg; Heiling, Maria; Gruber, Roman; Dercon, Gerd

2017-01-01

Carbon-13 ("1"3C) and nitrogen-15 ("1"5N) labelled plant material is increasingly being used to trace the fate of plant-derived C and N into the atmosphere, soil, water and organisms in many studies, including those investigating the potential of soils to store greenhouse gases belowground. Storage of C in soils can offset and even reduce atmospheric levels of the greenhouse gas, CO_2, and interest in such studies is growing due to problems associated with anthropogenic greenhouse gas emissions impacting climate change. Reduction of N loss in soils is also of great interest, as it reduces release of the greenhouse gas, N_2O, into the atmosphere. However, accurate quantitative tracing of plant-derived C and N in such research is only possible if plant material is labelled both homogeneously and in sufficient quantities.

Quantification of trace elements and speciation of iron in atmospheric particulate matter

Science.gov (United States)

Upadhyay, Nabin

Trace metal species play important roles in atmospheric redox processes and in the generation of oxidants in cloud systems. The chemical impact of these elements on atmospheric and cloud chemistry is dependent on their occurrence, solubility and speciation. First, analytical protocols have been developed to determine trace elements in particulate matter samples collected for carbonaceous analysis. The validated novel protocols were applied to the determination of trace elements in particulate samples collected in the remote marine atmosphere and urban areas in Arizona to study air pollution issues. The second part of this work investigates on solubility and speciation in environmental samples. A detailed study on the impact of the nature and strength of buffer solutions on solubility and speciation of iron lead to a robust protocol, allowing for comparative measurements in matrices representative of cloud water conditions. Application of this protocol to samples from different environments showed low iron solubility (less than 1%) in dust-impacted events and higher solubility (5%) in anthropogenically impacted urban samples. In most cases, Fe(II) was the dominant oxidation state in the soluble fraction of iron. The analytical protocol was then applied to investigate iron processing by fogs. Field observations showed that only a small fraction (1%) of iron was scavenged by fog droplets for which each of the soluble and insoluble fraction were similar. A coarse time resolution limited detailed insights into redox cycling within fog system. Overall results suggested that the major iron species in the droplets was Fe(1I) (80% of soluble iron). Finally, the occurrence and sources of emerging organic pollutants in the urban atmosphere were investigated. Synthetic musk species are ubiquitous in the urban environment (less than 5 ng m-3) and investigations at wastewater treatment plants showed that wastewater aeration basins emit a substantial amount of these species to

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...

Tracing enhanced oil recovery signatures in casing gases from the Lost Hills oil field using noble gases

Science.gov (United States)

Barry, Peter H.; Kulongoski, Justin; Landon, Matthew K.; Tyne, R.L.; Gillespie, Janice; Stephens, Michael; Hillegonds, D.J.; Byrne, D.J.; Ballentine, C.J.

2018-01-01

Enhanced oil recovery (EOR) and hydraulic fracturing practices are commonly used methods to improve hydrocarbon extraction efficiency; however the environmental impacts of such practices remain poorly understood. EOR is particularly prevalent in oil fields throughout California where water resources are in high demand and disposal of high volumes of produced water may affect groundwater quality. Consequently, it is essential to better understand the fate of injected (EOR) fluids in California and other subsurface petroleum systems, as well as any potential effect on nearby aquifer systems. Noble gases can be used as tracers to understand hydrocarbon generation, migration, and storage conditions, as well as the relative proportions of oil and water present in the subsurface. In addition, a noble gas signature diagnostic of injected (EOR) fluids can be readily identified. We report noble gas isotope and concentration data in casing gases from oil production wells in the Lost Hills oil field, northwest of Bakersfield, California, and injectate gas data from the Fruitvale oil field, located within the city of Bakersfield. Casing and injectate gas data are used to: 1) establish pristine hydrocarbon noble-gas signatures and the processes controlling noble gas distributions, 2) characterize the noble gas signature of injectate fluids, 3) trace injectate fluids in the subsurface, and 4) construct a model to estimate EOR efficiency. Noble gas results range from pristine to significantly modified by EOR, and can be best explained using a solubility exchange model between oil and connate/formation fluids, followed by gas exsolution upon production. This model is sensitive to oil-water interaction during hydrocarbon expulsion, migration, and storage at reservoir conditions, as well as any subsequent modification by EOR.

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

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.

Observation of Atmospheric Constituents From Space

Science.gov (United States)

Burrows, J. P.

Remote sensing of the atmosphere from space is a growing research field. Surprisingly but for good physical reasons, the mesosphere and stratosphere are easier to probe from space than the troposphere. GOME (Global Ozone Monitoring Experiment) and SCIAMACHY (Scanning Imaging absorption spectroMeter for Atmospheric CHartographY) are related European instruments, which were proposed and been designed to measure atmospheric constituents (gases, aerosols and clouds) by passive remote sensing of the up-welling solar radiation leaving atmosphere. GOME is a smaller version of SCIAMACHY and was launched as part of the core payload of the second European research satellite (ERS-2) on the 20th April 1995. GOME comprises four spectral channels and measures simultaneously the earthshine radiance or solar extra terrestrial irradiance between 240 and 790 nm. Inversion of GOME measurements using the DOAS (Differential Optical Absorption Spectroscopy) yields the total column of trace gases (e.g. O3, NO2, HCHO, BrO and OClO). Application of the FURM (Full Retrieval Method) enables the profiles of O3 to be retrieved. One of the important achievements of GOME has been the separation of tropopsheirc columns of trace gases using TEM (Tropospheric Excess Method). SCIAMACHY has been developed as Germa n, Dutch and Belgian contribution to ENVISAT. It has significantly enhanced capability compared to GOME, measuring a larger spectral range, 220-2380 nm, and observing in alternate nadir and limb modes as well as solar and lunar occultation. ENVISAT is to be launched into a sun synchronous polar orbit, having an equator crossing time of 10.00 a.m. at the beginning of March 2002. SCIAMACHY is thereby able to measure many more species and vertical profiles than GOME. This facilitates improved tropospheric retrievals. Finally GeoTROPE (Geostationary TROPospheric Explorer) is a new mission, which is proposed for launch within the ESA Earth Explorer Opportunity Mission. It comprises two national

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.

GreenNet: A Global Ground-Based Network of Instruments Measuring Greenhouse Gases in the Atmosphere

Science.gov (United States)

Floyd, M.; Grunberg, M.; Wilson, E. L.

2017-12-01

Climate change is the most important crisis of our lifetime. For policy makers to take action to combat the effects of climate change, they will need definitive proof that it is occurring globally. We have developed a low-cost ground instrument - a portable miniaturized laser heterodyne radiometer (mini-LHR) - capable of measuring concentrations of two of the most potent anthropogenic greenhouse gases, CO2 and methane, in columns in the atmosphere. They work by combining sunlight that has undergone absorption by gases with light from a laser. This combined light is detected by a photoreciever and a radio frequency beat signal is produced. From this beat signal, concentrations of these gases throughout the atmospheric column can be determined. A network of mini-LHR instruments in locations around the world will give us the data necessary to significantly reduce uncertainty in greenhouse gas sinks and sources contributing to climate change. Each instrument takes one reading per minute while the sun is up. With a goal to establish up to 500 instrument sites, the estimated total data per day will likely exceed 1GB. Every piece of data must be sorted as it comes in to determine whether it is a good or bad reading. The goal of the citizen science project is to collaborate with citizen scientists enrolled with Zooniverse.org to cycle through our data and help sort it, while also learning about the mini-LHR, greenhouse gases and climate change. This data will be used to construct an algorithm to automatically sort data that relies on statistical analyses of the previously sorted data.

Mars Atmospheric Capture and Gas Separation

Science.gov (United States)

Muscatello, Anthony; Santiago-Maldonado, Edgardo; Gibson, Tracy; Devor, Robert; Captain, James

2011-01-01

The Mars atmospheric capture and gas separation project is selecting, developing, and demonstrating techniques to capture and purify Martian atmospheric gases for their utilization for the production of hydrocarbons, oxygen, and water in ISRU systems. Trace gases will be required to be separated from Martian atmospheric gases to provide pure C02 to processing elements. In addition, other Martian gases, such as nitrogen and argon, occur in concentrations high enough to be useful as buffer gas and should be captured as welL To achieve these goals, highly efficient gas separation processes will be required. These gas separation techniques are also required across various areas within the ISRU project to support various consumable production processes. The development of innovative gas separation techniques will evaluate the current state-of-the-art for the gas separation required, with the objective to demonstrate and develop light-weight, low-power methods for gas separation. Gas separation requirements include, but are not limited to the selective separation of: (1) methane and water from un-reacted carbon oxides (C02- CO) and hydrogen typical of a Sabatier-type process, (2) carbon oxides and water from unreacted hydrogen from a Reverse Water-Gas Shift process, (3) carbon oxides from oxygen from a trash/waste processing reaction, and (4) helium from hydrogen or oxygen from a propellant scavenging process. Potential technologies for the separations include freezers, selective membranes, selective solvents, polymeric sorbents, zeolites, and new technologies. This paper and presentation will summarize the results of an extensive literature review and laboratory evaluations of candidate technologies for the capture and separation of C02 and other relevant gases.

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

International Nuclear Information System (INIS)

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

2009-01-01

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

Greenhouse Gases Concentrations in the Atmosphere Along ...

African Journals Online (AJOL)

This study investigated effect of vehicular emission on greenhouse gases concentrations along selected roads of different traffic densities in Abeokuta, Ogun State, Nigeria. Nine roads comprised highway, commercial and residential were selected. Greenhouse Gases (GHGs) were determined from both sides of the roads by ...

Influence of local emissions on concentration and isotopic composition of trace gases (CO2 and CH4) under strong anthropopression: A case study from Krakow, southern Poland

International Nuclear Information System (INIS)

Florkowski, T.; Korus, A.; Kuc, T.; Lasa, J.; Necki, J.M.; Zimnoch, M.

2002-01-01

Full text: Measurements of the isotopic composition of carbon dioxide and methane together with their concentrations in the atmosphere, yield useful information on the contribution of anthropogenic sources to regional budgets of these gases and their seasonal changes. Observed correlation between isotopic composition and inverse concentration of these gases is used for estimation of mean isotopic composition of the local source. Monitoring of atmospheric CO 2 has been initiated in Krakow in 1982. The sampling point is located in a polluted urban area with strong contribution of anthropogenic gases originating both from local sources (coal burning, car traffic, leakages from city gas network, landfills) and large distant emitters - industrial district located ca. 80 km to the west from Krakow (Silesia district). Quasi-continuous measurements of CO 2 , and CH 4 concentrations in the low atmosphere are performed using gas chromatographic method. For isotope measurements, the atmospheric CO 2 is continuously sampled by sorption on molecular sieve in be-weekly intervals and radiocarbon concentration is measured by liquid scintillation spectrometer, while δ 13 C is determined by isotope ratio mass spectrometer. Measurement error (1σ for single measurement) is in the order of 0.1 ppm for CO 2 concentration, ±8 per mille for δ 14 C, and ± 0.1 per mille for δ 13 C. In 1994, a new station for regular observations of greenhouse gases in lower atmosphere was set up in the High Tatra mountains, at Kasprowy Wierch (49 deg. N, 20 deg. E, 1980 m a.s.l., 300 m above the tree line). Kasprowy Wierch, with only small influences from local sources of trace gases can be considered as a reference station for this region of Poland. The record of CO 2 and CH 4 concentration and their isotope composition obtained at Kasprowy Wierch is considered as a background level for Krakow observations. The presented study was aimed at better characterisation and quantification of the local

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.

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

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.

The laser absorption spectrometer - A new remote sensing instrument for atmospheric pollution monitoring

Science.gov (United States)

Shumate, M. S.

1974-01-01

An instrument capable of remotely monitoring trace atmospheric constituents is described. The instrument, called a laser absorption spectrometer, can be operated from an aircraft or spacecraft to measure the concentration of selected gases in three dimensions. This device will be particularly useful for rapid determination of pollutant levels in urban areas.

Use of mosses as biomonitors of atmospheric deposition of trace elements

International Nuclear Information System (INIS)

Steinnes, E.

2000-01-01

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

Average rainwater pH, concepts of atmospheric acidity, and buffering in open systems

Energy Technology Data Exchange (ETDEWEB)

Liljestrand, H.M.

1985-01-01

The system of water equilibrated with a constant partial pressure of CO/sub 2/, as a reference point for pH acidity-alkalinity relationships, has nonvolatile acidity and alkalinity components as conservative quantities, but not (H/sup +/). Simple algorithms are presented for the determination of the average pH for combinations of samples both above and below pH 5.6. Averaging the nonconservative quantity (H/sup +/) yields erroneously low mean pH values. To extend the open CO/sub 2/ system to include other volatile atmospheric acids and bases distributed among the gas, liquid and particulate matter phases, a theoretical framework for atmospheric acidity is presented. Within certain oxidation-reduction limitations, the total atmospheric acidity (but not free acidity) is a conservative quantity. The concept of atmospheric acidity is applied to air-water systems approximating aerosols, fogwater, cloudwater and rainwater. The buffer intensity in hydrometers is described as a function of net strong acidity, partial pressures of acid and base gases and the water to air ratio. For high liquid to air volume ratios, the equilibrium partial pressures of trace acid and base gases are set by the pH or net acidity controlled by the nonvolatile acid and base concentrations. For low water to air volume ratios as well as stationary state systems such as precipitation scavenging with continuous emissions, the partial pressures of trace gases (NH/sub 3/, HCl, NHO/sub 3/, SO/sub 2/, and CH/sub 3/COOH) appear to be of greater or equal importance as carbonate species as buffers in the aqueous phase.

Average rainwater pH, concepts of atmospheric acidity, and buffering in open systems

Science.gov (United States)

Liljestrand, Howard M.

The system of water equilibrated with a constant partial pressure of CO 2, as a reference point for pH acidity-alkalinity relationships, has nonvolatile acidity and alkalinity components as conservative quantities, but not [H +]. Simple algorithms are presented for the determination of the average pH for combinations of samples both above and below pH 5.6. Averaging the nonconservative quantity [H +] yields erroneously low mean pH values. To extend the open CO 2 system to include other volatile atmospheric acids and bases distributed among the gas, liquid and particulate matter phases, a theoretical framework for atmospheric acidity is presented. Within certain oxidation-reduction limitations, the total atmospheric acidity (but not free acidity) is a conservative quantity. The concept of atmospheric acidity is applied to air-water systems approximating aerosols, fogwater, cloudwater and rainwater. The buffer intensity in hydrometeors is described as a function of net strong acidity, partial pressures of acid and base gases and the water to air ratio. For high liquid to air volume ratios, the equilibrium partial pressures of trace acid and base gases are set by the pH or net acidity controlled by the nonvolatile acid and base concentrations. For low water to air volume ratios as well as stationary state systems such as precipitation scavenging with continuous emissions, the partial pressures of trace gases (NH 3, HCl, HNO 3, SO 2 and CH 3COOH) appear to be of greater or equal importance as carbonate species as buffers in the aqueous phase.

Laser Spectroscopy for Atmospheric and Environmental Sensing

Directory of Open Access Journals (Sweden)

Solomon Bililign

2009-12-01

Full Text Available Lasers and laser spectroscopic techniques have been extensively used in several applications since their advent, and the subject has been reviewed extensively in the last several decades. This review is focused on three areas of laser spectroscopic applications in atmospheric and environmental sensing; namely laser-induced fluorescence (LIF, cavity ring-down spectroscopy (CRDS, and photoluminescence (PL techniques used in the detection of solids, liquids, aerosols, trace gases, and volatile organic compounds (VOCs.

Noble gases, nitrogen, and methane from the deep interior to the atmosphere of Titan

Science.gov (United States)

Glein, Christopher R.

2015-04-01

Titan's thick N2-CH4 atmosphere is unlike any in the Solar System, and its origin has been shrouded in mystery for over half a century. Here, I perform a detailed analysis of chemical and isotopic data from the Cassini-Huygens mission to develop the hypothesis that Titan's (non-photochemical) atmospheric gases came from deep within. It is suggested that Titan's CH4, N2, and noble gases originated in a rocky core buried inside the giant satellite, and hydrothermal and cryovolcanic processes were critical to the creation of Titan's atmosphere. Mass balance and chemical equilibrium calculations demonstrate that all aspects of this hypothesis can be considered geochemically plausible with respect to contemporary observational, experimental, and theoretical knowledge. Specifically, I show that a rocky core with a bulk noble gas content similar to that in CI carbonaceous meteorites would contain sufficient 36Ar and 22Ne to explain their reported abundances. I also show that Henry's law constants for noble gases in relevant condensed phases can be correlated with the size of their atoms, which leads to expected mixing ratios for 84Kr (∼0.2 ppbv) and 132Xe (∼0.01 ppbv) that can explain why these species have yet to be detected (Huygens upper limit serpentinization). I show that sufficient CH4 can be produced to replenish Titan's atmosphere many times over in the face of irreversible photolysis and escape of CH4, which is consistent with the favored model of episodic cryovolcanic outgassing. There should also have been enough NH3 inside Titan so that its thermal decomposition in a hot rocky core can generate the observed atmospheric N2, and if correct this model would imply that Titan's interior has experienced vigorous hydrothermal processing. The similarity in 14N/15N between cometary NH3 and Titan's N2 is consistent with this picture. As for the isotopes in CH4, I show that their observed relative abundances can be explained by low-temperature (∼20 °C) equilibria

Chemical kinetic studies of atmospheric reactions using tunable diode laser spectroscopy

Science.gov (United States)

Worsnop, Douglas R.; Nelson, David D.; Zahniser, Mark S.

1993-01-01

IR absorption using tunable diode laser spectroscopy provides a sensitive and quantitative detection method for laboratory kinetic studies of atmospheric trace gases. Improvements in multipass cell design, real time signal processing, and computer controlled data acquisition and analysis have extended the applicability of the technique. We have developed several optical systems using off-axis resonator mirror designs which maximize path length while minimizing both the sample volume and the interference fringes inherent in conventional 'White' cells. Computerized signal processing using rapid scan (300 kHz), sweep integration with 100 percent duty cycle allows substantial noise reduction while retaining the advantages of using direct absorption for absolute absorbance measurements and simultaneous detection of multiple species. Peak heights and areas are determined by curve fitting using nonlinear least square methods. We have applied these techniques to measurements of: (1) heterogeneous uptake chemistry of atmospheric trace gases (HCl, H2O2, and N2O5) on aqueous and sulfuric acid droplets; (2) vapor pressure measurements of nitric acid and water over prototypical stratospheric aerosol (nitric acid trihydrate) surfaces; and (3) discharge flow tube kinetic studies of the HO2 radical using isotopic labeling for product channel and mechanistic analysis. Results from each of these areas demonstrate the versatility of TDL absorption spectroscopy for atmospheric chemistry applications.

OH reactivity and potential SOA yields from volatile organic compounds and other trace gases measured in controlled laboratory biomass burns

Science.gov (United States)

J. B. Gilman; C. Warneke; W. C. Kuster; P. D. Goldan; P. R. Veres; J. M. Roberts; J. A. de Gouw; I. R. Burling; R. J. Yokelson

2010-01-01

A comprehensive suite of instruments were used to characterize volatile organic compounds (VOCs) and other trace gases (e.g., CO, CH4, NO2, etc.) emitted from controlled burns of various fuel types common to the Southeastern and Southwestern United States. These laboratory-based measurements were conducted in February 2009 at the U.S. Department of Agriculture’s Fire...

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

Science.gov (United States)

Thiagarajan, Nivedita; Aeolus Lee, Cin-Ty

2004-07-01

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

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.

ACS experiment for atmospheric studies on "ExoMars-2016" Orbiter

Science.gov (United States)

Korablev, O. I.; Montmessin, F.; Fedorova, A. A.; Ignatiev, N. I.; Shakun, A. V.; Trokhimovskiy, A. V.; Grigoriev, A. V.; Anufreichik, K. A.; Kozlova, T. O.

2015-12-01

ACS is a set of spectrometers for atmospheric studies (Atmospheric Chemistry Suite). It is one of the Russian instruments for the Trace Gas Orbiter (TGO) of the Russian-European "ExoMars" program. The purpose of the experiment is to study the Martian atmosphere by means of two observations regimes: sensitive trace gases measurements in solar occultations and by monitoring the atmospheric state during nadir observations. The experiment will allow us to approach global problems of Mars research such as current volcanism, and the modern climate status and its evolution. Also, the experiment is intended to solve the mystery of methane presence in the Martian atmosphere. Spectrometers of the ACS set cover the spectral range from the near IR-range (0.7 μm) to the thermal IR-range (17 μm) with spectral resolution λ/Δλ reaching 50000. The ACS instrument consists of three independent IR spectrometers and an electronics module, all integrated in a single unit with common mechanical, electrical and thermal interfaces. The article gives an overview of scientific tasks and presents the concept of the experiment.

Trace-Element Evidence for an Aqueous Atmospheric Origin of Desert Varnish: implications for the aqueous atmospheric input flux into the ocean

Science.gov (United States)

Thiagarajan, N.; Lee, C.

2003-12-01

Desert varnish is a slow-growing dark patina commonly found on rock surfaces in arid environments. Varnishes consist of about 30% Mn and Fe oxides accompanied by oxides of Si, Al, Mg, K and Ca, which occur primarily in the form of clays. Although it is generally agreed that varnishes have an atmospheric origin, their exact formation mechanism remains highly debated. Two endmember hypotheses are gradual accumulation of wind-blown dust followed by diagenesis, and direct chemical precipitation of dissolved elements from atmospheric aerosols. To rule out one of these hypotheses, we investigated the trace-element systematics of varnishes, in particular, focusing on those elements that have contrasting solubilities in aqueous environments. If our trace element analyses are consistent with the varnishes being derived from dissolved atmospheric constituents then the data can be used to quantify the paleofluxes of the soluble fraction of atmospheric aerosols to various depositional environments. For example, this will have implications for the transport of metals to the ocean that are immediately biologically available. We collected varnishes deposited on smooth basaltic lava flow surfaces in the Cima Volcanic Field (Mojave Desert) and in Death Valley, California. The chosen lava flows retain original flow surface structure and are topographical highs; the effects of erosion are hence minimal. Varnishes were scraped off with a quartz rod to minimize trace element contamination and the trace element compositions were then determined by ICP-MS using an external synthetic standard for calibration. Our analyses show that the rare-earth elements (REEs), Co, Ni, and Pb are enriched 1.5 to 10 times relative to the upper continental crust (UCC) and that Nb, Ti, Ta, Hf, Th, Rb and Cs are depleted to varying degrees relative to UCC and the REEs. These fractionations can be explained by their differing chemical behaviors in aqueous environments. The extreme depletion in Rb and Cs

Process of radioactive waste gases

International Nuclear Information System (INIS)

Queiser, H.; Schwarz, H.; Schroter, H.J.

1975-01-01

A method is described in which the radiation level of waste gases from nuclear power plants containing both activation and fission gases is controlled at or below limits permitted by applicable standards by passing such gases, prior to release to the atmosphere, through an adsorptive delay path including a body of activated carbon having the relation to the throughput and character of such gases. (U.S.)

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.

Correlation of trace element content in air particulates with solar meteorological data in the atmosphere of Athens

International Nuclear Information System (INIS)

Kanias, G.D.; Grimanis, A.P.; Viras, L.G.

2003-01-01

Relation between the trace element content in air particulates and solar meteorological data in the atmospheric environment of Athens, Greece, was studied. For this purpose, Sm, Br, As, Na, K, La, Ce, Cr, Ag, Sc, Fe, Zn, Co, Sb, Th were determined by INAA in respirable aerosols collected during winter 1993-1994. The results showed that the average cloudiness, sunshine, and the total solar radiation (sun and sky) on a horizontal surface, (3 variables) have no relation with trace element variation. However, diffuse solar radiation (sun and sky) on a horizontal surface seems to have statistically significant relationship with some of the trace element variation. It forms a single component with some trace elements after the application of the factor analysis. The increase of the same solar variable in the Athens City center, is one of the factors which cannot permit the emission of trace elements in the atmospheric environment from dust soil and car tires. (author)

Spectroscopic technique for measuring atmospheric CO2

International Nuclear Information System (INIS)

Stokes, G.M.; Stokes, R.A.

1979-01-01

As part of a continuing effort to identify areas in which astronomical techniques and data may be profitably applied to atmospheric problems, both new and archival solar spectra have been collected to prepare for an analysis of their use for studying the changes of the atmospheric CO 2 burden. This analysis has resulted in the initiation of an observing program using the Fourier Transform Spectrometer (FTS) of the McMath Solar Telescope at Kitt Peak National Observatory (KPNO). This program is generating spectra, the quality of which should not only aid the archival CO 2 study but also lead to analyses of other trace gases

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.

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

Weekly cycle of minor air gases in Moscow

Science.gov (United States)

Lokoshchenko, Mikhail A.; Elansky, Nikolay F.; Trifanova, Alexandra V.

2017-04-01

The weekly cycle of the surface concentrations of five trace atmospheric gases in Moscow has been analyzed based on continuous automatic once-a-minute measurements. The data of joint ecological station of the Institute of Atmospheric Physics and Moscow State University for nine years (2002-2010) were used. This station operated in conditions of comparatively clear park zone of the University on the South-Western periphery of the city at a distance of 8 km from the city centre. Fortunately, none of the great sources of the air pollution - neither point sources, nor linear ones - are present in the vicinity of the station so that the measurements there are quite representative. Results of spectral analysis demonstrate statistically significant maximum of spectral density close to 7 days. Any clear periodicity of around seven days may be a consequence of either natural synoptic period or weekly cycle. The fact that the influence of human activity on urban air composition changes with a weekly periodicity is confirmed by statistically significant difference between concentrations of trace gases on working days and on Sunday (when emissions from both the traffic and the industrial sources are minimal). On average, both primary pollutants (nitrogen oxide and carbon oxide) and the secondary ones (NO2) show the lowest concentrations of the week on Sunday whereas ozone, by contrast, peaks on this day. Besides, usual diurnal cycle of air pollutants is transformed on Sunday - e.g., secondary nocturnal maximum of ozone in the city is absent on Sunday like at rural area. On Saturday concentrations of trace gases are in between working days and Sunday; this 'Saturday effect' is a result of a gradual clearing of the urban air. An additional effect is that in the first half of Monday (before noon) surface concentrations of NO and NO2 are generally less, whereas the concentration of O3 is, on the contrary, a bit higher than at the same time on the rest of working days. The 'Monday

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....

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.

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

Dissolved atmospheric gas in xylem sap measured with membrane inlet mass spectrometry.

Science.gov (United States)

Schenk, H Jochen; Espino, Susana; Visser, Ate; Esser, Bradley K

2016-04-01

A new method is described for measuring dissolved gas concentrations in small volumes of xylem sap using membrane inlet mass spectrometry. The technique can be used to determine concentrations of atmospheric gases, such as argon, as reported here, or for any dissolved gases and their isotopes for a variety of applications, such as rapid detection of trace gases from groundwater only hours after they were taken up by trees and rooting depth estimation. Atmospheric gas content in xylem sap directly affects the conditions and mechanisms that allow for gas removal from xylem embolisms, because gas can dissolve into saturated or supersaturated sap only under gas pressure that is above atmospheric pressure. The method was tested for red trumpet vine, Distictis buccinatoria (Bignoniaceae), by measuring atmospheric gas concentrations in sap collected at times of minimum and maximum daily temperature and during temperature increase and decline. Mean argon concentration in xylem sap did not differ significantly from saturation levels for the temperature and pressure conditions at any time of collection, but more than 40% of all samples were supersaturated, especially during the warm parts of day. There was no significant diurnal pattern, due to high variability between samples. © 2015 John Wiley & Sons Ltd.

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

Directory of Open Access Journals (Sweden)

C. E. Stockwell

2016-09-01

Full Text Available 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

Seasonal and spatial changes in trace gases over megacities from Aura TES observations: two case studies

Directory of Open Access Journals (Sweden)

K. E. Cady-Pereira

2017-08-01

Full Text Available The Aura Tropospheric Emission Spectrometer (TES is collecting closely spaced observations over 19 megacities. The objective is to obtain measurements that will lead to better understanding of the processes affecting air quality in and around these cities, and to better estimates of the seasonal and interannual variability. We explore the TES measurements of ozone, ammonia, methanol and formic acid collected around the Mexico City metropolitan area (MCMA and in the vicinity of Lagos (Nigeria. The TES data exhibit seasonal signals that are correlated with Atmospheric Infrared Sounder (AIRS CO and Moderate Resolution Imaging Spectroradiometer (MODIS aerosol optical depth (AOD, with in situ measurements in the MCMA and with Goddard Earth Observing System (GEOS-Chem model output in the Lagos area. TES was able to detect an extreme pollution event in the MCMA on 9 April 2013, which is also evident in the in situ data. TES data also show that biomass burning has a greater impact south of the city than in the caldera where Mexico City is located. TES measured enhanced values of the four species over the Gulf of Guinea south of Lagos. Since it observes many cities from the same platform with the same instrument and applies the same retrieval algorithms, TES data provide a very useful tool for easily comparing air quality measures of two or more cities. We compare the data from the MCMA and Lagos, and show that, while the MCMA has occasional extreme pollution events, Lagos consistently has higher levels of these trace gases.

Chemical composition measurements of the atmosphere of Jupiter with the Galileo Probe mass spectrometer

Science.gov (United States)

Niemann, H. B.; Atreya, S. K.; Carignan, G. R.; Donahue, T. M.; Haberman, J. A.; Harpold, D. N.; Hartle, R. E.; Hunten, D. M.; Kasprzak, W. T.; Mahaffy, P. R.;

Airborne Measurements and Emission Estimates of Greenhouse Gases and Other Trace Constituents From the 2013 California Yosemite Rim Wildfire

Science.gov (United States)

Yates, E. L.; Iraci, L. T.; Singh, H. B.; Tanaka, T.; Roby, M. C.; Hamill, P.; Clements, C. B.; Lareau, N.; Contezac, J.; Blake, D. R.;

Detection of benzene and toluene gases using a midinfrared continuous-wave external cavity quantum cascade laser at atmospheric pressure.

Science.gov (United States)

Sydoryk, Ihor; Lim, Alan; Jäger, Wolfgang; Tulip, John; Parsons, Matthew T

2010-02-20

We demonstrate the application of a commercially available widely tunable continuous-wave external cavity quantum cascade laser as a spectroscopic source for the simultaneous detection of multiple gases. We measured broad absorption features of benzene and toluene between 1012 and 1063 cm(-1) (9.88 and 9.41 microm) at atmospheric pressure using an astigmatic Herriott multipass cell. Our results show experimental detection limits of 0.26 and 0.41 ppm for benzene and toluene, respectively, with a 100 m path length for these two gases.

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.

The benefit of limb cloud imaging for infrared limb sounding of tropospheric trace gases

OpenAIRE

G. Heinemann; P. Preusse; R. Spang; S. Adams

2009-01-01

Advances in detector technology enable a new generation of infrared limb sounders to measure 2-D images of the atmosphere. A proposed limb cloud imager (LCI) mode will detect clouds with a spatial resolution unprecedented for limb sounding. For the inference of temperature and trace gas distributions, detector pixels of the LCI have to be combined into super-pixels which provide the required signal-to-noise and information content for the retrievals. This study examines the extent to which tr...

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.

MIRAGE: Model description and evaluation of aerosols and trace gases

Science.gov (United States)

Easter, Richard C.; Ghan, Steven J.; Zhang, Yang; Saylor, Rick D.; Chapman, Elaine G.; Laulainen, Nels S.; Abdul-Razzak, Hayder; Leung, L. Ruby; Bian, Xindi; Zaveri, Rahul A.

2004-10-01

The Model for Integrated Research on Atmospheric Global Exchanges (MIRAGE) modeling system, designed to study the impacts of anthropogenic aerosols on the global environment, is described. MIRAGE consists of a chemical transport model coupled online with a global climate model. The chemical transport model simulates trace gases, aerosol number, and aerosol chemical component mass (sulfate, methane sulfonic acid (MSA), organic matter, black carbon (BC), sea salt, and mineral dust) for four aerosol modes (Aitken, accumulation, coarse sea salt, and coarse mineral dust) using the modal aerosol dynamics approach. Cloud-phase and interstitial aerosol are predicted separately. The climate model, based on Community Climate Model, Version 2 (CCM2), has physically based treatments of aerosol direct and indirect forcing. Stratiform cloud water and droplet number are simulated using a bulk microphysics parameterization that includes aerosol activation. Aerosol and trace gas species simulated by MIRAGE are presented and evaluated using surface and aircraft measurements. Surface-level SO2 in North American and European source regions is higher than observed. SO2 above the boundary layer is in better agreement with observations, and surface-level SO2 at marine locations is somewhat lower than observed. Comparison with other models suggests insufficient SO2 dry deposition; increasing the deposition velocity improves simulated SO2. Surface-level sulfate in North American and European source regions is in good agreement with observations, although the seasonal cycle in Europe is stronger than observed. Surface-level sulfate at high-latitude and marine locations, and sulfate above the boundary layer, are higher than observed. This is attributed primarily to insufficient wet removal; increasing the wet removal improves simulated sulfate at remote locations and aloft. Because of the high sulfate bias, radiative forcing estimates for anthropogenic sulfur given in 2001 by S. J. Ghan and

Long open-path measurements of greenhouse gases in air using near-infrared Fourier transform spectroscopy

Science.gov (United States)

Griffith, David W. T.; Pöhler, Denis; Schmitt, Stefan; Hammer, Samuel; Vardag, Sanam N.; Platt, Ulrich

2018-03-01

In complex and urban environments, atmospheric trace gas composition is highly variable in time and space. Point measurement techniques for trace gases with in situ instruments are well established and accurate, but do not provide spatial averaging to compare against developing high-resolution atmospheric models of composition and meteorology with resolutions of the order of a kilometre. Open-path measurement techniques provide path average concentrations and spatial averaging which, if sufficiently accurate, may be better suited to assessment and interpretation with such models. Open-path Fourier transform spectroscopy (FTS) in the mid-infrared region, and differential optical absorption spectroscopy (DOAS) in the UV and visible, have been used for many years for open-path spectroscopic measurements of selected species in both clean air and in polluted environments. Near infrared instrumentation allows measurements over longer paths than mid-infrared FTS for species such as greenhouse gases which are not easily accessible to DOAS.In this pilot study we present the first open-path near-infrared (4000-10 000 cm-1, 1.0-2.5 µm) FTS measurements of CO2, CH4, O2, H2O and HDO over a 1.5 km path in urban Heidelberg, Germany. We describe the construction of the open-path FTS system, the analysis of the collected spectra, several measures of precision and accuracy of the measurements, and the results a four-month trial measurement period in July-November 2014. The open-path measurements are compared to calibrated in situ measurements made at one end of the open path. We observe significant differences of the order of a few ppm for CO2 and a few tens of ppb for CH4 between the open-path and point measurements which are 2 to 4 times the measurement repeatability, but we cannot unequivocally assign the differences to specific local sources or sinks. We conclude that open-path FTS may provide a valuable new tool for investigations of atmospheric trace gas composition in

Airborne mapping of Seoul's atmosphere: Trace gas measurements from GeoTASO during KORUS-AQ

Science.gov (United States)

Nowlan, C. R.; Al-Saadi, J. A.; Castellanos, P.; Chance, K.; Gonzalez Abad, G.; Janz, S. J.; Judd, L.; Kowalewski, M. G.; Liu, X.

2017-12-01

The Geostationary Trace gas and Aerosol Sensor Optimization (GeoTASO) instrument is a pushbroom airborne remote sensing instrument capable of making measurements of air quality and ocean color using backscattered UV and visible light. GeoTASO is an airborne test-bed for the upcoming Tropospheric Emissions: Monitoring of Pollution (TEMPO) and Geostationary Environment Monitoring Spectrometer (GEMS) geostationary satellite missions, which will measure air quality over North America and Asia, respectively. GeoTASO also acts as a satellite analogue during field campaigns. GeoTASO flew on the NASA Langley Research Center UC-12 aircraft during the Korea-United States Air Quality Study in May-June 2016, collecting spectra over South Korea during 30 flights over 19 flight days. These observations can be used to derive 2-D maps of tropospheric trace gases including ozone, nitrogen dioxide, sulfur dioxide, formaldehyde, nitrous acid and glyoxal below the aircraft at spatial resolutions between 250 m x 250 m and 1 km x 1 km, depending on the gas. We present spatially resolved trace gas retrievals over Seoul and its surrounding industrial regions, and comparisons with correlative satellite and campaign data.

Impact of Convection and Long Range Transport on Short-Lived Trace Gases in the UT/LS

Science.gov (United States)

Atlas, E. L.; Schauffler, S.; Navarro, M. A.; Lueb, R.; Hendershot, R.; Ueyama, R.

2017-12-01

Chemical composition of the air in the upper troposphere/lower stratosphere is controlled by a balance of transport, photochemistry, and physical processes, such as interactions with clouds, ice, and aerosol. The chemistry of the air masses that reach the upper troposphere can potentially have profound impacts on the chemistry in the near tropopause region. For example, the transport of reactive organic halogens and their transformation to inorganic halogen species, e.g., Br, BrO, etc., can have a significant impact on ozone budgets in this region and even deeper the stratosphere. Trace gas measurements in the region near the tropopause can also indicate potential sources of surface emissions that are transported to high altitudes. Measurement of trace gases, including such compounds as non-methane hydrocarbons, hydrochlorofluorocarbons, halogenated solvents, methyl halides, etc., can be used to characterize source emissions from industrial, urban, biomass burning, or marine origins. Recent airborne research campaigns have been conducted to better characterize the chemical composition and variations in the UT/LS region. This presentation will discuss these measurements, with a special emphasis on the role of convection and transport in modifying the chemical composition of the UT/LS.

Trace elements partitioning during coal combustion in fluidized bed under O{sub 2}/CO{sub 2} atmosphere

Energy Technology Data Exchange (ETDEWEB)

Li, Haixin; Zhao, Changsui; Liang, Cai; Duan, Lunbo; Chen, Huichao [Southeast Univ., Nanjing (China). School of Energy and Environment

2013-07-01

Experiments were conducted to investigate the effects of temperature and O{sub 2}/CO{sub 2} atmosphere on trace elements (Cr, Mn, Co, Ni, Cd, Pb, Hg, As, Se) partitioning during combustion of Xuzhou bituminous coal in a 6 kWth fluidized bed. Inductively coupled plasma mass spectrometry (ICP-MS) and atomic fluorescence spectrometry (AFS) were used to determine trace elements contents in raw coal, bottom ash, fly ash and flue gas. The results indicate that with bed temperature increase, the relative enrichment of all the trace elements except Cr in bottom ash decreases suggesting that their volatility is enhanced. The relative enrichments of hardly volatile elements, like Cr and Mn in fly ash increase with bed temperature increase while those of partially volatile and highly volatile elements in fly ash are opposite. The relative enrichments of trace elements except Cr and Mn in fly ash are higher than those in bottom ash. Increasing bed temperature promotes elements like As, Se and Hg to migrate to vapor phase, Mn to migrate to fly ash and Cr to migrate to both bottom ash and fly ash. 21%O{sub 2}/79%CO{sub 2} atmosphere improves the volatility of Cr, Mn, Co, Se and their migration to fly ash, while restrains the volatility of As, Ni, Pb. It has little effect on the volatility of Hg but improves its migration to fly ash. Mass balance ratio was also calculated to observe trace elements distribution in bottom ash, fly ash and flue gas. There is no much difference in trace elements distribution between the two atmospheres. It can be seen that the trace elements proportion in fly ash is much greater, and more than 40% of Hg is distributed in the gas phase. Most of Hg and Se volatilize during combustion. The mass balance ratios are 87 {proportional_to} 129% which is considered acceptable.

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.

Atmospheric trace metal pollution in the Naples urban area based on results from moss and lichen bags

International Nuclear Information System (INIS)

Giordano, S.; Adamo, P.; Sorbo, S.; Vingiani, S.

2005-01-01

The results of trace element content analysed in Sphagnum capillifolium and Pseudevernia furfuracea exposed in bags in 1999 are reconsidered to evaluate the reliability of moss and lichen transplants to detect urban trace element atmospheric pollution, using Naples as a case example. After 4 months' exposure, trace element concentrations were at least twice as high as the pre-exposure values and in general higher in Sphagnum than in Pseudevernia. Moss samples were enriched in the following order: As = Cu > Mo > Pb > V > Co > Cr > Zn; lichen samples in the order: Mo > Cu > As = Co = Ni > V > Pb. Based on the calculation of a cumulative load factor, all sites located along the coast had higher trace element loads compared to sites in the hilly inland area. Complementary SEM, TEM and EDS observations showed, despite significant damage to tissue and cell integrity, the recurrent presence of particulate matter in moss and lichen, indicating the considerable presence of dust in the urban atmosphere which, according to chemical composition, may be due both to anthropogenic and natural sources such as volcanic rock and soil and sea salts. - Despite significant damage to tissue and cell integrity, moss and lichen in bags efficiently intercept airborne trace elements

Photochemistry of Planetary Atmospheres

Science.gov (United States)

Yung, Y. L.

2005-12-01

The Space Age started half a century ago. Today, with the completion of a fairly detailed study of the planets of the Solar System, we have begun studying exoplanets (or extrasolar planets). The overriding question in is to ask whether an exoplanet is habitable and harbors life, and if so, what the biosignatures ought to be. This forces us to confront the fundamental question of what controls the composition of an atmosphere. The composition of a planetary atmosphere reflects a balance between thermodynamic equilibrium chemistry (as in the interior of giant planets) and photochemistry (as in the atmosphere of Mars). The terrestrial atmosphere has additional influence from life (biochemistry). The bulk of photochemistry in planetary atmospheres is driven by UV radiation. Photosynthesis may be considered an extension of photochemistry by inventing a molecule (chlorophyll) that can harvest visible light. Perhaps the most remarkable feature of photochemistry is catalytic chemistry, the ability of trace amounts of gases to profoundly affect the composition of the atmosphere. Notable examples include HOx (H, OH and HO2) chemistry on Mars and chlorine chemistry on Earth and Venus. Another remarkable feature of photochemistry is organic synthesis in the outer solar system. The best example is the atmosphere of Titan. Photolysis of methane results in the synthesis of more complex hydrocarbons. The hydrocarbon chemistry inevitably leads to the formation of high molecular weight products, giving rise to aerosols when the ambient atmosphere is cool enough for them to condense. These results are supported by the findings of the recent Cassini mission. Lastly, photochemistry leaves a distinctive isotopic signature that can be used to trace back the evolutionary history of the atmosphere. Examples include nitrogen isotopes on Mars and sulfur isotopes on Earth. Returning to the question of biosignatures on an exoplanet, our Solar System experience tells us to look for speciation

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

International Nuclear Information System (INIS)

Punjabi, Sangeeta B.; Joshi, N. K.; Mangalvedekar, H. A.; Lande, B. K.; Das, A. K.; Kothari, D. C.

2012-01-01

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 (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.

Stratospheric measurements of ozone-depleting substances and greenhouse gases using AirCores

Science.gov (United States)

Laube, Johannes; Leedham Elvidge, Emma; Kaiser, Jan; Sturges, Bill; Heikkinen, Pauli; Laurila, Tuomas; Hatakka, Juha; Kivi, Rigel; Chen, Huilin; Fraser, Paul; van der Veen, Carina; Röckmann, Thomas

2017-04-01

Retrieving air samples from the stratosphere has previously required aircraft or large balloons, both of which are expensive to operate. The novel "AirCore" technique (Karion et al., 2010) enables stratospheric sampling using weather balloons, which is much more cost effective. AirCores are long (up to 200 m) stainless steel tubes which are placed as a payload on a small balloon, can ascend to over 30 km and fill upon descent, collecting a vertical profile of the atmosphere. Retrieved volumes are much smaller though, which presents a challenge for trace gas analysis. To date, only the more abundant trace gases such as carnon dioxide (CO2) and methane (CH4) have been quantified in AirCores. Halogenated trace gases are also important greenhouse gases and many also deplete stratospheric ozone. Their concentrations are however much lower i.e. typically in the part per trillion (ppt) molar range. We here present the first stratospheric measurements of halocarbons in AirCores obtained using UEA's highly sensitive (detection limits of 0.01-0.1 ppt in 10 ml of air) gas chromatography mass spectrometry system. The analysed air originates from a Stratospheric Air Sub-sampler (Mrozek et al., 2016) which collects AirCore segments after the non-destructive CO2 and CH4 analysis. Successfully measured species include CFC-11, CFC-12, CFC-113, CFC-115, H-1211, H-1301, HCFC-22, HCFC-141b, HCFC-142b, HCFC-133a, and sulphur hexafluoride (SF6). We compare the observed mixing ratios and precisions with data obtained from samples collected during various high-altitude aircraft campaigns between 2009 and 2016 as well as with southern hemisphere tropospheric long-term trends. As part of the ERC-funded EXC3ITE (EXploring stratospheric Composition, Chemistry and Circulation with Innovative Techniques) project more than 40 AirCore flights are planned in the next 3 years with an expanded range of up to 30 gases in order to explore seasonal and interannual variability in the stratosphere

Civil Aircraft for the regular investigation of the atmosphere based on an instrumented container: The new CARIBIC system

Directory of Open Access Journals (Sweden)

C. A. M. Brenninkmeijer

2007-09-01

Full Text Available An airfreight container with automated instruments for measurement of atmospheric gases and trace compounds was operated on a monthly basis onboard a Boeing 767-300 ER of LTU International Airways during long-distance flights from 1997 to 2002 (CARIBIC, Civil Aircraft for Regular Investigation of the Atmosphere Based on an Instrument Container, atmospheric.com">http://www.caribic-atmospheric.com. Subsequently a more advanced system has been developed, using a larger capacity container with additional equipment and an improved inlet system. CARIBIC phase #2 was implemented on a new long-range aircraft type Airbus A340-600 of the Lufthansa German Airlines (Star Alliance in December 2004, creating a powerful flying observatory. The instrument package comprises detectors for the measurement of O₃, total and gaseous H₂O, NO and NO_y, CO, CO₂, O₂, Hg, and number concentrations of sub-micrometer particles (>4 nm, >12 nm, and >18 nm diameter. Furthermore, an optical particle counter (OPC and a proton transfer mass spectrometer (PTR-MS are incorporated. Aerosol samples are collected for analysis of elemental composition and particle morphology after flight. Air samples are taken in glass containers for laboratory analyses of hydrocarbons, halocarbons and greenhouse gases (including isotopic composition of CO₂ in several laboratories. Absorption tubes collect oxygenated volatile organic compounds. Three differential optical absorption spectrometers (DOAS with their telescopes mounted in the inlet system measure atmospheric trace gases such as BrO, HONO, and NO₂. A video camera mounted in the inlet provides information about clouds along the flight track. The flying observatory, its equipment and examples of measurement results are reported.

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

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.

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

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

Science.gov (United States)

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

2013-08-01

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

Rare gases in Samoan xenoliths

Science.gov (United States)

Poreda, R. J.; Farley, K. A.

1992-09-01

The rare gas isotopic compositions of residual harzburgite xenoliths from Savai'i (SAV locality) and an unnamed seamount south of the Samoan chain (PPT locality) provide important constraints on the rare gas evolution of the mantle and atmosphere. Despite heterogeneous trace element compositions, the rare gas characteristics of the xenoliths from each of the two localities are strikingly similar. SAV and PPT xenoliths have 3He/ 4He ratios of11.1 ± 0.5 R A and21.6 ± 1 R A, respectively; this range is comparable to the 3He/ 4He ratios in Samoan lavas and clearly demonstrates that they have trapped gases from a relatively undegassed reservoir. The neon results are not consistent with mixing between MORB and a plume source with an atmospheric signature. Rather, the neon isotopes reflect either a variably degassed mantle (with a relative order of degassing of Loihi Honda et al. that the 20Ne/ 22Ne ratio in the mantle more closely resembles the solar ratio than the atmospheric one. 40Ar/ 36Ar ratios in the least contaminated samples range from 4,000 to 12,000 with the highest values in the 22 RA PPT xenoliths. There is no evidence for atmospheric 40Ar/ 36Ar ratios in the mantle source of these samples, which indicates that the lower mantle may have 40Ar/ 36Ar ratios in excess of 5,000. Xenon isotopic anomalies in 129Xe and 136Xe are as high as 6%, or about half of the maximum MORB excess and are consistent with the less degassed nature of the Samoan mantle source. These results contradict previous suggestions that the high 3He/ 4He mantle has a near-atmospheric heavy rare gas isotopic composition.

Lightning, atmospheric electricity and climate change

International Nuclear Information System (INIS)

Price, C.

1993-10-01

Temperature records indicate that a global warming of 0.5-0.7 degrees C has occurred over the past century (Hansen and Lebedeff, 1987). Whether this trend is a result of increased trace gas concentrations in the atmosphere, or simply a result of natural variability; is still not known. These temperature trends are derived from thousands of observations worldwide. However, these observations are concentrated largely over continental areas, and then mainly in the northern hemisphere's populated regions. This northern hemisphere continental bias results in large uncertainties in estimates of global temperature trends. Due to the increasing evidence that the present buildup of greenhouse gases in the atmosphere may result in an additional global warming of 1-5 degrees C by the year 2050 (IPCC, 1990), it is increasingly important to find afternative methods to monitor fluctuations in global surface temperatures. As shown by two recent studies (Williams, 1992; Price, 1993), the global atmospheric electric circuit may provide a promising afternative for monitoring future climate change

The trace-elements of the atmospheric aerosol of the Amazon basin

International Nuclear Information System (INIS)

Orsini, C.M.Q.; Artaxo Netto, P.E.; Tabacniks, M.H.

1981-05-01

The distribution of the trace-elements AL, Si, P, S, CL, K, Ca, Ti, Fe and V in the atmospheric aerosol of the Amazon Basin was determined by means of samples collected between August 23 and September 2 of 1980, at a remote place located in the Amazon Forest, about 30 Km NE of the city of Manaus, Brazil. 33 samples were succesfully analyzed by the PIXE method (Particle Induced X-Ray Emission) by using α-particle beam of the Pelletron Accelerator of the University of Sao Paulo, and the results revealed that the trace-elements S and K have a large predominance, mainly as fine particle size relative to the others; this fact is consistent with the statement that the natural cycles of these two elements are critically involved in the biophysical processes responsible for the life of the tropical rain forest of the Amazon. (Author) [pt

Warming Early Mars by Impact Degassing of Reduced Greenhouse Gases

Science.gov (United States)

Haberle, R. M.; Zahnle, K.; Barlow, N. G.

2018-01-01

Reducing greenhouse gases are once again the latest trend in finding solutions to the early Mars climate dilemma. In its current form collision induced absorptions (CIA) involving H2 and/or CH4 provide enough extra greenhouse power in a predominately CO2 atmosphere to raise global mean surface temperatures to the melting point of water provided the atmosphere is thick enough and the reduced gases are abundant enough. Surface pressures must be at least 500 mb and H2 and/or CH4 concentrations must be at or above the several percent level for CIA to be effective. Atmospheres with 1-2 bars of CO2 and 2- 10% H2 can sustain surface environments favorable for liquid water. Smaller concentrations of H2 are sufficient if CH4 is also present. If thick CO2 atmospheres with percent level concentrations of reduced gases are the solution to the faint young Sun paradox for Mars, then plausible mechanisms must be found to generate and sustain the gases. Possible sources of reducing gases include volcanic outgassing, serpentinization, and impact delivery; sinks include photolyis, oxidation, and escape to space. The viability of the reduced greenhouse hypothesis depends, therefore, on the strength of these sources and sinks. In this paper we focus on impact delivered reduced gases.

The Atmospheric Distribution of Molecular Hydrogen (H2) and Related Species During HIPPO and Other Recent Airborne Missions

Science.gov (United States)

Hintsa, E. J.; Moore, F. L.; Dutton, G. S.; Hall, B. D.; Nance, J. D.; Hurst, D. F.; Novelli, P. C.; Elkins, J. W.; Daube, B.; Kort, E. A.; Pittman, J. V.; Santoni, G. W.; Wofsy, S. C.; Jaegle, L.

2012-12-01

The goal of the HIAPER Pole-to-Pole Observations (HIPPO) of Carbon Cycle and Greenhouse Gases Study was to measure a large set of trace gases and aerosols as a function of altitude and latitude in different seasons in order to better understand their sources, sinks, and atmospheric transport, and to use these measurements to compare with a variety of chemical transport models, ultimately leading to improvements in the models. The NSF/NCAR Gulfstream V (GV) aircraft (formerly known as HIAPER) was equipped with instruments for trace gases, aerosols, and meteorological parameters, and flew a set of five transects in 2009-2011 from Colorado, to Anchorage, AK, to near the North Pole, then south to Christchurch, NZ, toward the edge of Antarctica, and back to the northern hemisphere high latitudes, with intermediate stops at different locations in the Pacific Ocean. On each leg of the journey, the GV carried out a series of profiles from the marine (or continental) boundary layer to the stratosphere, generating a set of altitude/latitude slices of the atmosphere in different seasons (January 2009, October-November 2009, March-April 2010, June-July 2011, and August-September 2011). While HIPPO was in progress, data were also obtained at higher altitudes in the stratosphere over the Pacific Ocean from the NASA Global Hawk aircraft during the GloPac (Global Hawk Pacific; March-April 2010) and ATTREX (Airborne Tropical Tropopause Experiment; October-November 2011) missions, respectively. In this presentation, results are shown that were obtained from the UCATS and PANTHER instruments and other sensors on board the GV and the Global Hawk. UCATS (the UAS Chromatograph for Atmospheric Trace Species) flew on both platforms and was configured to measure N2O, SF6, H2, CH4, CO, water vapor, and ozone. PANTHER (PAN and other Trace Hydrohalocarbon ExpeRiment) measures an even larger set of trace gases with gas chromatography and a mass spectrometer, and flew on every leg of HIPPO. The

Effect of human activities on the Earth's atmosphere and future trends

Energy Technology Data Exchange (ETDEWEB)

Junge, C

1977-01-01

Measurements showing the global increase in atmospheric carbon dioxide concentration are discussed in terms of estimates of the future increase in coal and oil consumption. The problems of predicting the scale of any warming of the earth's surface due to increasing atmospheric carbon dioxide are analysed. It is concluded that direct thermal energy input is of secondary importance, accounting for less than one tenth of that due to carbon dioxide. The problem of the increasing atmospheric concentrations of chlorofluoromethanes due to their continued use as cooling liquids and spray can propellants is outlined: stratospheric ozone depletion and its implications for the incidence of skin cancer. Other man-made trace gases are not considered hazardous. Basic research on natural climate is recommended.

Central Tibetan Plateau atmospheric trace metals contamination: a 500-year record from the Puruogangri ice core

Science.gov (United States)

Beaudon, E.; Gabrielli, P.; Sierra Hernandez, R.; Wegner, A.; Thompson, L. G.

2017-12-01

Since the 1980s, Asia has experienced enormous industrial development from rapid population growth, industrialization and consequent large-scale environmental changes. The inherent generated atmospheric pollution currently contributes to half of all Earth's anthropogenic trace metals emissions. Asian trace metal aerosols, when deposited on glaciers of the surrounding mountains of the Tibetan Plateau (TP), leave a characteristic chemical fingerprint. Interpreting trace element (TE) records from glaciers implies a thorough comprehension of their provenance and temporal variability. It is then essential to discriminate the TEs' natural background components from their anthropogenic components. Here we present 500-year TE records from the Puruogangri ice core (Tibet, China) that provide a highly resolved account of the impact of past atmospheric influences, environmental processes and human activities on the central TP. A decreasing aeolian dust input to the ice cap allowed the detection of an atmospheric pollution signal. The anthropogenic pollution contribution emerges in the record since the early 1900s and increases substantially after 1935. The metallurgy (Zn, Pb and steel smelting) emission products from the former Soviet Union and especially from central Asia likely enhanced the anthropogenic deposition to the Puruogangri ice cap between 1935 and 1980, suggesting that the westerlies served as a conveyor of atmospheric pollution to central Tibet. The impact of this industrial pollution cumulated with that of the hemispheric coal and gasoline combustion which are respectively traced by Sb and Pb enrichment in the ice. The Chinese steel production accompanying the Great Leap Forward (1958-1961) and the Chinese Cultural Revolution (1966-1976) is proposed as a secondary but proximal source of Pb pollution affecting the ice cap between 1958 and 1976. The most recent decade (1980-1992) of the enrichment time series suggests that Puruogangri ice cap recorded the early

Diffusion model of solid particles in a gaseous atmosphere. Pt. 1

International Nuclear Information System (INIS)

Fernandez Ruiz, J.L.

1987-01-01

Starting from Voinov and Garipov's lagrangian statements on the problem of dynamic evolution of bubbles in liquids, this work is trying to determine some diffusion equations of solid particles in little dense matter like gases or liquids, aiming at applying it to the tracing of matter in atmospheric diffusion and the tracing of corpuscles in liquids. All the resulting equations lead to a solution given as a tensor θ ij related to the velocity states v i defined as v i = , and to the potential from which derive. One has had in mind the factor of mutual correlation between the diffusing particles. This increases the scope of application of these equations to Chemistry and to Biomedical Sciences. (author)

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

International Nuclear Information System (INIS)

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

2005-01-01

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

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....

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....

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....

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....

Trace element contents in atmospheric suspended particles: inferences from instrumental neutron activation analysis

International Nuclear Information System (INIS)

Querol, X.; Alastuey, A.; Lopez-Soler, A.; Boix, A.; Sanfeliu, T.; Martynov, V.V.; Piven, P.I.; Kabina, L.P.; Souschov, P.A.

1997-01-01

This study focuses on the determination of trace element concentrations in total suspended particles by instrumental neutron activation analysis (INAA) in two different areas in Northeastern Spain (a rural area influenced by the emissions of a large coal-fired power station, and the urban and industrial areas of Castellon). Total suspended particles were sampled by means of standard MCV high- and medium-volume captors, using cellulose membrane filters of 0.8 and 0.45 μm pore size. Preliminary research was performed on the homogeneous distribution of elements in the sample filters and on the study of blank filters for the calculations of the background average element contents. The results obtained allowed to distinguish different major anthropogenic sources of trace elements in the atmosphere at the sampling sites: (a) Zr, Hf, Sc, U and Th are related to atmospheric pollution derived from the ceramic industry of the Castellon area; (b) As, Cr, Cs, Rb, Sb, Se, Zn are related to traffic and other industrial emission in the Castellon area, and As, Cr, Sb and Zn to power generation emissions in the rural area. (orig.). With 3 figs., 5 tabs

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

Monsoon signatures in trace gas records from Cape Rama, India

International Nuclear Information System (INIS)

Bhattacharya, S.K.; Jani, R.A.; Borole, D.V.; Francey, R.J.; Allison, C.E.; Masarie, K.A.

2002-01-01

Concentrations of trace gases CO 2 , CH 4 , CO, N 2 O and H 2 , and the stable carbon and oxygen isotopic composition of CO 2 have been measured in air samples collected from Cape Rama, a coastal station on the west coast of India, since 1993. The data show clear signatures of continental and oceanic air mass resulting in complex seasonal variation of trace gas characteristics. The regional atmospheric circulation in the Indian Ocean and Arabian Sea undergoes biannual reversal in low-level winds associated with the yearly migration of the inter-tropical convergence zone (ITCZ). From June to September, the wind is from the equatorial Indian Ocean to the Indian subcontinent (southwest monsoon) and brings in pristine marine air. From December to February, dry continental winds blow from the northeast and transport continental emissions to the ocean (northeast monsoon). Detailed transport and chemical modelling will be necessary to interpret these records, however the potential to identify and constrain the regional trace gas emissions appears to be high. (author)

Infrasonic ray tracing applied to mesoscale atmospheric structures: refraction by hurricanes.

Science.gov (United States)

Bedard, Alfred J; Jones, R Michael

2013-11-01

A ray-tracing program is used to estimate the refraction of infrasound by the temperature structure of the atmosphere and by hurricanes represented by a Rankine-combined vortex wind plus a temperature perturbation. Refraction by the hurricane winds is significant, giving rise to regions of focusing, defocusing, and virtual sources. The refraction of infrasound by the temperature anomaly associated with a hurricane is small, probably no larger than that from uncertainties in the wind field. The results are pertinent to interpreting ocean wave generated infrasound in the vicinities of tropical cyclones.

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)

Long open-path measurements of greenhouse gases in air using near-infrared Fourier transform spectroscopy

Directory of Open Access Journals (Sweden)

D. W. T. Griffith

2018-03-01

Full Text Available In complex and urban environments, atmospheric trace gas composition is highly variable in time and space. Point measurement techniques for trace gases with in situ instruments are well established and accurate, but do not provide spatial averaging to compare against developing high-resolution atmospheric models of composition and meteorology with resolutions of the order of a kilometre. Open-path measurement techniques provide path average concentrations and spatial averaging which, if sufficiently accurate, may be better suited to assessment and interpretation with such models. Open-path Fourier transform spectroscopy (FTS in the mid-infrared region, and differential optical absorption spectroscopy (DOAS in the UV and visible, have been used for many years for open-path spectroscopic measurements of selected species in both clean air and in polluted environments. Near infrared instrumentation allows measurements over longer paths than mid-infrared FTS for species such as greenhouse gases which are not easily accessible to DOAS.In this pilot study we present the first open-path near-infrared (4000–10 000 cm−1, 1.0–2.5 µm FTS measurements of CO2, CH4, O2, H2O and HDO over a 1.5 km path in urban Heidelberg, Germany. We describe the construction of the open-path FTS system, the analysis of the collected spectra, several measures of precision and accuracy of the measurements, and the results a four-month trial measurement period in July–November 2014. The open-path measurements are compared to calibrated in situ measurements made at one end of the open path. We observe significant differences of the order of a few ppm for CO2 and a few tens of ppb for CH4 between the open-path and point measurements which are 2 to 4 times the measurement repeatability, but we cannot unequivocally assign the differences to specific local sources or sinks. We conclude that open-path FTS may provide a valuable new tool for investigations of

Assessing the ability to derive rates of polar middle-atmospheric descent using trace gas measurements from remote sensors

Science.gov (United States)

Ryan, Niall J.; Kinnison, Douglas E.; Garcia, Rolando R.; Hoffmann, Christoph G.; Palm, Mathias; Raffalski, Uwe; Notholt, Justus

2018-02-01

We investigate the reliability of using trace gas measurements from remote sensing instruments to infer polar atmospheric descent rates during winter within 46-86 km altitude. Using output from the Specified Dynamics Whole Atmosphere Community Climate Model (SD-WACCM) between 2008 and 2014, tendencies of carbon monoxide (CO) volume mixing ratios (VMRs) are used to assess a common assumption of dominant vertical advection of tracers during polar winter. The results show that dynamical processes other than vertical advection are not negligible, meaning that the transport rates derived from trace gas measurements do not represent the mean descent of the atmosphere. The relative importance of vertical advection is lessened, and exceeded by other processes, during periods directly before and after a sudden stratospheric warming, mainly due to an increase in eddy transport. It was also found that CO chemistry cannot be ignored in the mesosphere due to the night-time layer of OH at approximately 80 km altitude. CO VMR profiles from the Kiruna Microwave Radiometer and the Microwave Limb Sounder were compared to SD-WACCM output, and show good agreement on daily and seasonal timescales. SD-WACCM CO profiles are combined with the CO tendencies to estimate errors involved in calculating the mean descent of the atmosphere from remote sensing measurements. The results indicate errors on the same scale as the calculated descent rates, and that the method is prone to a misinterpretation of the direction of air motion. The true rate of atmospheric descent is seen to be masked by processes, other than vertical advection, that affect CO. We suggest an alternative definition of the rate calculated using remote sensing measurements: not as the mean descent of the atmosphere, but as an effective rate of vertical transport for the trace gas under observation.

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.

Trace Gas Emissions in Temperate Forests and Impact of Forest Conversion

Science.gov (United States)

Butterbach-Bahl, K.; Papen, H.

2003-12-01

Temperate forest ecosystems play a significant role as sources and sinks for primarily and secondarily active trace gases such as N2O, NO and CH4. In recent decades the magnitude of the biosphere-atmosphere exchange of these trace gases has been substantially altered due to direct and indirect anthropogenic activities. E.g. measurements at different forest sites across Europe exposed to different loads of atmospheric N-deposition clearly show, that N-oxides emissions are positively correlated to N-deposition, whereas CH4 uptake rates are negatively affected. Furthermore, stand properties such as tree species composition as well as stand age have also been demonstrated to strongly affect the exchange of these trace gases. Results of continuous measurements of N-oxide emissions at the Hoglwald Forest site, Germany, show that e.g. NO-emissions from a spruce site are approx. 6 fold higher (5-7 kg NO-N ha-1 yr-1) than N2O emissions (0.5-1 kg N2O-N ha-1 yr-1), whereas at an adjacent beech site -stocking on a comparable soil- N2O-emissions are 3-5 kg N2O-N ha-1 yr-1 and NO emissions are 2-2.5 kg NO-N ha-1 yr-1. These results are further supported by microbiological process studies, which show that the forest type can alter the magnitude of the key microbial processes mineralization and nitrification by its effect on soil moisture conditions and substrate quality. However, estimates of trace gas exchange between temperate forest soils and the atmosphere remain fragmentary if the effect of direct anthropogenic management activities such as clear cutting and reforestation are neglected. Therefore, in 1999 we started a multi-year experiment at the H”glwald Forest, Bavaria, in which we investigated the effect of the conversion of a spruce forest into a beech forest either by clear cutting or selected cutting on N2O, NO and CH4 emission/ deposition. The results of this study show, that clear cutting strongly enhanced N2O emissions from approx. 0.5 kg N2O-N ha-1 yr-1 to >5 kg

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 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

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

International Nuclear Information System (INIS)

Qadir, Muhammad Abdul; Zaidi, Jamshaid Hussain; Ahmad, Shaikh Asrar; Gulzar, Asad; Yaseen, Muhammad; Atta, Sadia; Tufail, Asma

2012-01-01

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 μm. 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: ► Discussion is made on Total suspended Particulate (TSP) matter in the atmosphere. ► Measurement of Radio active elements in the TSP by using SSNTD which was found non significant. ► 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. ► 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. ► There is high level of TSPs>10 um, which is a great threat to the peoples of Islamabad.

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.

Characterization of atmospheric trace elements in the Puruogangri ice core: a preliminary account of Tibetan Plateau environmental and contamination histories

Science.gov (United States)

Beaudon, E.; Gabrielli, P.; Sierra Hernandez, R.; Wegner, A.; Thompson, L. G.

2014-12-01

Asia is facing enormous challenges including large-scale environmental changes, rapid population growth and industrialization. The inherent generated pollution contributes to half of all Earth's anthropogenic trace metals emissions that, when deposited to glaciers of the surrounding mountains of the Third Pole region, leave a characteristic chemical fingerprint. Records of past atmospheric deposition preserved in snow and ice from Third Pole glaciers provide unique insights into changes of the chemical composition of the atmosphere and into the nature and intensity of the regional atmospheric circulation systems. The determination of the elemental composition of aeolian dust stored in Himalayan and Tibetan Plateau glaciers can help to qualify the potential contamination of glacial meltwater as a part of the greater fresh Asian water source. The 215 m long Puruogangri ice core retrieved in 2000 at 6500 m a.s.l. in central Tibetan Plateau (Western Tanggula Shan, China) provides one of the first multi-millennium-long environmental archives (spanning the last 7000 years and annually resolved for the last 400 years) obtained from the Tibetan Plateau region. The Puruogangri's area is climatologically of particular interest because of its location at the boundary between the monsoon (wet) and the westerly (dry) dominated atmospheric circulation. The major objective of this study is to determine the concentration of trace and ultra-trace elements in the Puruogangri ice core between 1600 and 2000 AD in order to characterize the atmospheric aerosols entrapped in the ice. Particular attention is given to assess the amount of trace elements originating from anthropogenic sources during both the pre-industrial and industrial periods. The distinction between the anthropogenic contribution and the crustal background may rely on the precise decoupling of the dry and wet seasons signals, the former being largely influenced by dust contribution.

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 ...

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

Energy Technology Data Exchange (ETDEWEB)

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

1996-12-31

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

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

Energy Technology Data Exchange (ETDEWEB)

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

1995-12-31

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

The role of neutron activation analysis for trace elements characterization, analysis and certification in atmospheric particulates

International Nuclear Information System (INIS)

Rizzio, Enrico; Gallorini, Mario

2002-01-01

The Neutron Activation Analysis (NAA) owns these requirements and is universally accepted as one of the most reliable analytical tools for trace and ultratrace elements determination. Its use in trace elements atmospheric pollution related studies has been and is still extensive as can be demonstrate by several specific works and detailed reviews. In this work, the application of this nuclear technique, in solving a series of different analytical problems related to trace elements in air pollution processes is reported. Examples and results are given on the following topics: characterization of urban and rural airborne particulate samples; particles size distribution in the different inhalable and respirable fractions (PM10 and PM 2.5); certification of related Standard Reference Materials for data quality assurance. (author)

A survey of atmospheric trace elements in the U.K

International Nuclear Information System (INIS)

Cawse, P.A.

1976-08-01

Concentrations of some 36 trace and major elements were measured in air particulate, rainwater and dry deposition samples collected each month at seven non-urban sites in the U.K. from January to December 1975. The samples were bulked for analysis each quarter year, and the majority were analysed by instrumental neutron activation analysis. The main objectives were to provide information on concentrations of elements in air to compare with urban measurements, to study the longer term trends in atmospheric concentrations, and to record the deposition inventory to the ground. Continuity of data from the sampling station network has been maintained since January 1972, but at the Wraymires site in north-west England operations began one year earlier. (author)

Is climate influenced by biogenic atmospheric sulfur compounds. Beeinflussen biogene atmosphaerische Schwefelverbindungen das Klima

Energy Technology Data Exchange (ETDEWEB)

Georgii, H W

1990-01-01

About 10 years ago, traces of gaseous sulfur compounds were detected in the atmosphere which are of mainly biogenic origin and are formed in large areas in the oceans by phytoplankton. Continental sources, too, are important. These gases - dimethyl sulfide, carbon bisulfide and carbonyl sulfide - provide an important, if not the main, part to the natural sulfur budget of the atmosphere. While dimethyl sulfide and carbon bisulfide are quickly oxidized in the lower atmosphere forming sulfate particles in the process, carbonyl sulfide is an inert gas which is oxidized only after reaching the stratosphere. Lately, the relevance of these trace components to climate is being discussed. Conceivably, they might influence the radiation budget of the earth via the formation of aerosol particles: While, in the case of dimethyl sulfide, these would change the microphysical parameters of maritime clouds, an increase in the production of carbonyl sulfide would entail a strengthening of the stratospheric sulfate particle layer. Both processes might have a stabilizing effect on the climate as they act in opposite direction to the much discussed greenhouse effect. (orig.).

Active moss biomonitoring of trace elements with Sphagnum girgensohnii moss bags in relation to atmospheric bulk deposition in Belgrade, Serbia

International Nuclear Information System (INIS)

Anicic, M.; Tasic, M.; Frontasyeva, M.V.; Tomasevic, M.; Rajsic, S.; Mijic, Z.; Popovic, A.

2009-01-01

Active biomonitoring with wet and dry moss bags was used to examine trace element atmospheric deposition in the urban area of Belgrade. The element accumulation capability of Sphagnum girgensohnii Russow was tested in relation to atmospheric bulk deposition. Moss bags were mounted for five 3-month periods (July 2005-October 2006) at three representative urban sites. For the same period monthly bulk atmospheric deposition samples were collected. The concentrations of Al, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Cd, and Pb were determined by instrumental neutron activation analyses and atomic absorption spectrometry. Significant accumulation of most elements occurred in the exposed moss bags compared with the initial moss content. High correlations between the elements in moss and bulk deposits were found for V, Cu, As, and Ni. The enrichment factors of the elements for both types of monitor followed the same pattern at the corresponding sites. - Accumulated trace elements in the moss Sphagnum girgensohnii reflect atmospheric deposition

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

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.

Biomass burning - Combustion emissions, satellite imagery, and biogenic emissions

Science.gov (United States)

Levine, Joel S.; Cofer, Wesley R., III; Winstead, Edward L.; Rhinehart, Robert P.; Cahoon, Donald R., Jr.; Sebacher, Daniel I.; Sebacher, Shirley; Stocks, Brian J.

1991-01-01

After detailing a technique for the estimation of the instantaneous emission of trace gases produced by biomass burning, using satellite imagery, attention is given to the recent discovery that burning results in significant enhancement of biogenic emissions of N2O, NO, and CH4. Biomass burning accordingly has an immediate and long-term impact on the production of atmospheric trace gases. It is presently demonstrated that satellite imagery of fires may be used to estimate combustion emissions, and could be used to estimate long-term postburn biogenic emission of trace gases to the atmosphere.

Note: A dual temperature closed loop batch reactor for determining the partitioning of trace gases within CO2-water systems.

Science.gov (United States)

Warr, Oliver; Rochelle, Christopher A; Masters, Andrew J; Ballentine, Christopher J

2016-01-01

An experimental approach is presented which can be used to determine partitioning of trace gases within CO2-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.

Method for storing radioactive rare gases

International Nuclear Information System (INIS)

Watabe, Atsushi; Nagao, Hiroyuki; Takiguchi, Yukio; Kanazawa, Toshio; Soya, Masataka.

1975-01-01

Object: To safely and securely store radioactive rare gases for a long period of time. Structure: The waste gases produced in nuclear power plant are cooled by a cooler and then introduced into a low temperature adsorbing device so that the gases are adsorbed by adsorbents, and then discharged into atmosphere through the purifying gas discharge line. When the radioactive rare gases reach a level of saturation in the amount of adsorption, they are heated and extracted by a suction pump and heated by a heater. The gases are then introduced into an oxygen-impurity removing device and the purified rare gases containing no oxygen and impurities are cooled by a cooler and fed into a gas holder. When the amount of radioactive rare gases stored within the gas holder reaches a given level, they are compressed and sealed by a compressure into a storing cylinder and residual gases in the piping are sucked and recovered into the gas holder, after which the cylinder is removed and stored in a fixed room. (Kamimura, M.)

Global Atmosphere Watch Workshop on Measurement-Model ...

Science.gov (United States)

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

Improved mapping of tropospheric air quality gases based on the Copernicus Sentinel 5 Precursor/TROPOMI mission

Science.gov (United States)

Van Roozendael, Michel; De Smedt, Isabelle; Theys, Nicolas; Danckaert, Thomas; Yu, Huan; Lerot, Christophe; van Gent, Jeroen; Vlietinck, Jonas

2017-04-01

Scheduled for launch in summer 2017, the Sentinel 5 Precursor (S5P) mission having onboard the TROPOMI payload will fly on a sun-synchronous polar orbit and provide daily global early-afternoon observations of a number of key atmospheric trace gases at the unprecedented spatial resolution of 7x3.5 km2. By the early 2020's, S5P will be complemented by geostationary observations from the Sentinel 4 UVN instrument to be delivered at hourly resolution over Europe, and by mid-morning global observations from the low-earth orbiting Sentinel 5 mission. Altogether these missions will form a constellation serving the needs of the Copernicus Atmospheric Monitoring Services (CAMS). Owing to their unprecedented spatial resolution and spectral performance, TROPOMI/S5P and the subsequent Sentinel 4 and 5 missions will significantly push forward monitoring capabilities addressing anthropogenic and natural emissions of air quality-related trace gases. They will also extend the long-term datasets from past and existing UV-Vis sensors (GOME, SCIAMACHY, OMI, GOME-2, OMPS). In this presentation, we explore the potential of S5P to improve on several aspects of the monitoring of tropospheric pollutants, with a focus on the short-lived species NO2, SO2 and HCHO. Based on algorithms designed at BIRA as part of TROPOMI/S5P and S4/S5 level-2 development projects, and their application to the current OMI and GOME-2 sensors, we illustrate and discuss the expected ability of the new sensors to detect smaller scale point sources with better accuracy and selectivity. The retrieval challenges associated with higher resolution measurements are also addressed.

Sources of atmospheric acidity

International Nuclear Information System (INIS)

Clarke, A.G.

1992-01-01

The emissions of acid gases from anthropogenic sources and their impact on the environment are the main concern of this book. However, that impact can only be assessed if all the naturally occurring sources of these gases are also known and can be quantified. Given the widely dispersed nature of the natural sources and the problems of measurement of trace species at low concentrations, often in remote regions, the quantification is a very difficult task. Nevertheless, considerable progress has been made over the last decade. In this chapter both man-made and natural sources of atmospheric acidity will be reviewed, but the emphasis will be placed not so much on the global balances as on the scale of the natural sources in relation to the man-made sources. This requires that the very uneven geographical distribution of emissions and the lifetime of individual chemical species be taken into account. The emissions considered are sulphur compounds, nitrogen compounds, chlorine compounds and organic acids. The anthropogenic sources discussed are the combustion of fossil fuels and certain industrial processes. Emissions data for anthropogenic sources are given for the United Kingdom, Europe, USA and globally. A list of 95 references is given. (Author)

Biomonitoring of atmospheric pollution (with emphasis on trace elements) - BioMAP. Proceedings of an international workshop

International Nuclear Information System (INIS)

2000-06-01

Some organisms accumulate atmospheric contaminants over certain periods of time and concentrate them, thus allowing reliable analytical measurements if the organisms are suitably chosen. Measurements of contaminants accumulated by such organisms (biomonitors) provide information on the integrated exposure over an extended period of time. They may also be present in remote areas, and no expensive technical equipment is involved in collecting them. Therefore, biomonitoring can be an effective tool for pollutant mapping and trend monitoring by real time and retrospective analysis. The IAEA is making concerted efforts to promote the practical use of nuclear and related analytical techniques in studies of non-radioactive environmental pollutants that may impact human health, and one of the main emphases is on studying air contaminants. The idea of organizing a workshop on biomonitoring atmospheric pollution arose during an IAEA Technical Co-operation Project on Monitoring of Trace Element Air Pollution, carried out at the Instituto Tecnologico e Nuclear (ITN), Portugal, with substantial technical support by the Interfaculty Reactor Institute (IRI) of the Delft University of Technology (TUDelft), Netherlands. The International Workshop on Biomonitoring of Atmospheric Pollution (With Emphasis on Trace Elements) - BioMAP, was held in Lisbon, Portugal, from 21 to 24 September 1997. The meeting was organized in co-operation with the Instituto Tecnologico e Nuclear

Biomonitoring of atmospheric pollution (with emphasis on trace elements) - BioMAP. Proceedings of an international workshop

Energy Technology Data Exchange (ETDEWEB)

NONE

2000-06-01

Some organisms accumulate atmospheric contaminants over certain periods of time and concentrate them, thus allowing reliable analytical measurements if the organisms are suitably chosen. Measurements of contaminants accumulated by such organisms (biomonitors) provide information on the integrated exposure over an extended period of time. They may also be present in remote areas, and no expensive technical equipment is involved in collecting them. Therefore, biomonitoring can be an effective tool for pollutant mapping and trend monitoring by real time and retrospective analysis. The IAEA is making concerted efforts to promote the practicaluse of nuclear and related analytical techniques in studies of non-radioactive environmental pollutants that may impact human health, and one of the main emphases is on studying air contaminants. The idea of organizing a workshop on biomonitoring atmospheric pollution arose during an IAEA Technical Co-operation Project on Monitoring of Trace Element Air Pollution, carried out at the Instituto Tecnologico e Nuclear (ITN), Portugal, with substantial technical support by the Interfaculty Reactor Institute (IRI) of the Delft University of Technology (TUDelft), Netherlands. The International Workshop on Biomonitoring of Atmospheric Pollution (With Emphasis on Trace Elements) - BioMAP, was held in Lisbon, Portugal, from 21 to 24 September 1997. The meeting was organized in co-operation with the Instituto Tecnologico e Nuclear.

Direct observations of reactive atmospheric gases at ZOTTO station in the middle of Siberia as a base for large-scale modeling of atmospheric chemistry over Northern Eurasia

Science.gov (United States)

Skorokhod, Andrey; Belikov, Igor; Shtabkin, Yury; Moiseenko, Konstantin; Pankratova, Natalia; Vasileva, Anastasia; Rakitin, Vadim; Heimann, Martin

2015-04-01

Direct observations of atmospheric air composition are very important for a comprehensive understanding of atmospheric chemistry over Northern Eurasia and its variability and trends driven by abrupt climatic and ecosystem changes and anthropogenic pressure. Atmospheric air composition (including greenhouse gases and aerosols), its trends and variability is still insufficiently known for most of the nearly uninhabited areas of Northern Eurasia. This limits the accuracy of both global and regional models, which simulate climatological and ecosystem changes in this highly important region. From that point of view, the Zotino Tall Tower Observatory (ZOTTO) in the middle of Siberia (near 60N, 90E), launched in 2006 and governed by a scientific international consortium plays an important role providing unique information about concentrations of greenhouse and reactive trace gases, as well as aerosols. Simulations of surface concentrations of O3, NOx and CO performed by global chemical-transport model GEOS-Chem using up-to-date anthropogenic and biogenic emissions databases show very good agreement with values observed at ZOTTO in 2007-2012. Observed concentration of ozone has a pronounced seasonal variation with a clear peak in spring (40-45 ppbv in average and up to 80 ppbv in extreme cases) and minimum in winter. Average ozone level is about 20 ppbv that corresponds to the background conditions. Enhanced concentration in March-July is due to increased stratospheric-tropospheric exchange. In autumn and winter distribution of ozone is close to uniform. NOx concentration does not exceed 1 ppb that is typical for background areas but may vary by order and some more in few hours. Higher surface NOx(=NO+NO2) concentrations during day time generally correspond to higher ozone when NO/NO2 ratio indicates on clean or slightly polluted conditions. CO surface concentration has a vivid seasonal course and varies from about 100 ppb in summer till 150 ppb in winter. But during

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

Directory of Open Access Journals (Sweden)

F. Obersteiner

2016-10-01

Full Text Available 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 �

Measurements of trace contaminants in closed-type plant cultivation chambers

Science.gov (United States)

Tani, A.; Kiyota, M.; Aiga, I.; Nitta, K.; Tako, Y.; Ashida, A.; Otsubo, K.; Saito, T.

Trace contaminants generated in closed facilities can cause abnormal plant growth. We present measurement data of trace contaminants released from soils, plants, and construction materials. We mainly used two closed chambers, a Closed-type Plant and Mushroom Cultivation Chamber (PMCC) and Closed-type Plant Cultivation Equipment (CPCE). Although trace gas budgets from soils obtained in this experiment are only one example, the results indicate that the budgets of trace gases, as well as CO_2 and O_2, change greatly with the degree of soil maturation and are dependent on the kind of substances in the soil. Both in the PMCC and in the CPCE, trace gases such as dioctyl phthalate (DOP), dibutyl phthalate (DBP), toluene and xylene were detected. These gases seemed to be released from various materials used in the construction of these chambers. The degree of increase in these trace gas levels was dependent on the relationship between chamber capacity and plant quantity. Results of trace gas measurement in the PMCC, in which lettuce and shiitake mushroom were cultivated, showed that ethylene was released both from lettuce and from the mushroom culture bed. The release rates were about 90 ng bed^-1 h^-1 for the shiitake mushroom culture bed (volume is 1700 cm^3) and 4.1 ~ 17.3 ng dm^-2h^-1 (leaf area basis) for lettuce. Higher ethylene release rates per plant and per unit leaf area were observed in mature plants than in young plants.

The influence of water vapor on atmospheric exchange measurements with an ICOS* based Laser absorption analyzer

Science.gov (United States)

Bunk, Rüdiger; Quan, Zhi; Wandel, Matthias; Yi, Zhigang; Bozem, Heiko; Kesselmeier, Jürgen

2014-05-01

Carbonyl sulfide and carbon monoxide are both atmospheric trace gases of high interest. Recent advances in the field of spectroscopy have enabled instruments that measure the concentration of the above and other trace gases very fast and with good precision. Increasing the effective path length by reflecting the light between two mirrors in a cavity, these instruments reach impressive sensitivities. Often it is possible to measure the concentration of more than one trace gas at the same time. The OCS/CO2 Analyzer by LGR (Los Gatos Research, Inc.) measures the concentration of water vapor [H2O], carbonyl sulfide [COS], carbon dioxide [CO2] and carbon monoxide [CO] simultaneously. For that the cavity is saturated with light, than the attenuation of light is measured as in standard absorption spectroscopy. The instrument proved to be very fast with good precision and to be able to detect even very low concentrations, especially for COS (as low as 30ppt in the case of COS). However, we observed a rather strong cross sensitivity to water vapor. Altering the water vapor content of the sampled air with two different methods led to a change in the perceived concentration of COS, CO and CO2. This proved especially problematic for enclosure (cuvette) measurements, where the concentrations of one of the above species in an empty cuvette are compared to the concentration of another cuvette containing a plant whose exchange of trace gases with the atmosphere is of interest. There, the plants transpiration leads to a large difference in water vapor content between the cuvettes and that in turn produces artifacts in the concentration differences between the cuvettes for the other above mentioned trace gases. For CO, simultaneous measurement with a UV-Emission Analyzer (AL 5002, Aerolaser) and the COS/CO Analyzer showed good agreement of perceived concentrations as long as the sample gas was dry and an increasing difference in perceived concentration when the sample gas was

Sensitive Multi-Species Emissions Monitoring: Infrared Laser-Based Detection of Trace-Level Contaminants

Energy Technology Data Exchange (ETDEWEB)

Steill, Jeffrey D. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Huang, Haifeng [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Hoops, Alexandra A. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Patterson, Brian D. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Birtola, Salvatore R. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Jaska, Mark [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Strecker, Kevin E. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Chandler, David W. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Bisson, Soott [Sandia National Lab. (SNL-CA), Livermore, CA (United States)

2014-09-01

This report summarizes our development of spectroscopic chemical analysis techniques and spectral modeling for trace-gas measurements of highly-regulated low-concentration species present in flue gas emissions from utility coal boilers such as HCl under conditions of high humidity. Detailed spectral modeling of the spectroscopy of HCl and other important combustion and atmospheric species such as H 2 O, CO 2 , N 2 O, NO 2 , SO 2 , and CH 4 demonstrates that IR-laser spectroscopy is a sensitive multi-component analysis strategy. Experimental measurements from techniques based on IR laser spectroscopy are presented that demonstrate sub-ppm sensitivity levels to these species. Photoacoustic infrared spectroscopy is used to detect and quantify HCl at ppm levels with extremely high signal-to-noise even under conditions of high relative humidity. Additionally, cavity ring-down IR spectroscopy is used to achieve an extremely high sensitivity to combustion trace gases in this spectral region; ppm level CH 4 is one demonstrated example. The importance of spectral resolution in the sensitivity of a trace-gas measurement is examined by spectral modeling in the mid- and near-IR, and efforts to improve measurement resolution through novel instrument development are described. While previous project reports focused on benefits and complexities of the dual-etalon cavity ring-down infrared spectrometer, here details on steps taken to implement this unique and potentially revolutionary instrument are described. This report also illustrates and critiques the general strategy of IR- laser photodetection of trace gases leading to the conclusion that mid-IR laser spectroscopy techniques provide a promising basis for further instrument development and implementation that will enable cost-effective sensitive detection of multiple key contaminant species simultaneously.

The bark of the branches of holm oak (Quercus ilex L.) for a retrospective study of trace elements in the atmosphere

International Nuclear Information System (INIS)

Drava, Giuliana; Brignole, Daniele; Giordani, Paolo; Minganti, Vincenzo

2017-01-01

Tree bark has proved to be a useful bioindicator for trace elements in the atmosphere, however it reflects an exposure occurring during an unidentified period of time, so it provides spatial information about the distribution of contaminants in a certain area, but it cannot be used to detect temporal changes or trends, which is an important achievement in environmental studies. In order to obtain information about a known period of time, the bark collected from the annual segments of tree branches can be used, allowing analyses going back 10–15 years with annual resolution. In the present study, the concentrations of As, Cd, Co, Cu, Fe, Mn, Ni, Pb, V and Zn were measured by atomic emission spectrometry in a series of samples covering the period from 2001 to 2013 in an urban environment. Downward time trends were significant for Cd, Pb and Zn. The only trace element showing an upward time trend was V. The concentrations of the remaining six trace elements were constant over time, showing that their presence in bark is not simply proportional to the duration of exposure. This approach, which is simple, reliable and widely applicable at a low cost, allows the “a posteriori” reconstruction of atmospheric trace element deposition when or where no monitoring programme is in progress and no other natural archives are available. - Highlights: • Branch bark allows the historical reconstruction of atmospheric trace elements. • This approach is simple, reliable, widely applicable and “a posteriori”. • Downward time trends were found for Cd, Pb and Zn; upward trend for V.

The bark of the branches of holm oak (Quercus ilex L.) for a retrospective study of trace elements in the atmosphere

Energy Technology Data Exchange (ETDEWEB)

Drava, Giuliana, E-mail: drava@difar.unige.it; Brignole, Daniele; Giordani, Paolo; Minganti, Vincenzo

2017-04-15

Tree bark has proved to be a useful bioindicator for trace elements in the atmosphere, however it reflects an exposure occurring during an unidentified period of time, so it provides spatial information about the distribution of contaminants in a certain area, but it cannot be used to detect temporal changes or trends, which is an important achievement in environmental studies. In order to obtain information about a known period of time, the bark collected from the annual segments of tree branches can be used, allowing analyses going back 10–15 years with annual resolution. In the present study, the concentrations of As, Cd, Co, Cu, Fe, Mn, Ni, Pb, V and Zn were measured by atomic emission spectrometry in a series of samples covering the period from 2001 to 2013 in an urban environment. Downward time trends were significant for Cd, Pb and Zn. The only trace element showing an upward time trend was V. The concentrations of the remaining six trace elements were constant over time, showing that their presence in bark is not simply proportional to the duration of exposure. This approach, which is simple, reliable and widely applicable at a low cost, allows the “a posteriori” reconstruction of atmospheric trace element deposition when or where no monitoring programme is in progress and no other natural archives are available. - Highlights: • Branch bark allows the historical reconstruction of atmospheric trace elements. • This approach is simple, reliable, widely applicable and “a posteriori”. • Downward time trends were found for Cd, Pb and Zn; upward trend for V.

Detecting Methane From Leaking Pipelines and as Greenhouse Gas in the Atmosphere

Science.gov (United States)

Riris, Haris; Numata, Kenji; Li, Steven; Wu, Stewart; Ramanathan, Anand; Dawsey, Martha

2012-01-01

Laser remote sensing measurements of trace gases from orbit can provide unprecedented information about important planetary science and answer critical questions about planetary atmospheres. Methane (CH4) is the second most important anthropogenically produced greenhouse gas. Though its atmospheric abundance is much less than that of CO2 (1.78 ppm vs. 380 ppm), it has much larger greenhouse heating potential. CH4 also contributes to pollution in the lower atmosphere through chemical reactions, leading to ozone production. Atmospheric CH4 concentrations have been increasing as a result of increased fossil fuel production, rice farming, livestock, and landfills. Natural sources of CH4 include wetlands, wild fires, and termites, and perhaps other unknown sources. Important sinks for CH4 include non-saturated soils and oxidation by hydroxyl radicals in the atmosphere. Remotely measuring CH4 and other biogenic molecules (such as ethane and formaldehyde) on Mars also has important implications on the existence of life on Mars. Measuring CH4 at very low (ppb) concentrations from orbit will dramatically improve the sensitivity and spatial resolution in the search for CH4 vents and sub-surface life on other planets. A capability has been developed using lasers and spectroscopic detection techniques for the remote measurements of trace gases in open paths. Detection of CH4, CO2, H2O, and CO in absorption cells and in open paths, both in the mid- IR and near-IR region, has been demonstrated using an Optical Parametric Amplifier laser transmitter developed at GSFC. With this transmitter, it would be possible to develop a remote sensing methane instrument. CH4 detection also has very important commercial applications. Pipeline leak detection from an aircraft or a helicopter can significantly reduce cost, response time, and pinpoint the location. The main advantage is the ability to rapidly detect CH4 leaks remotely. This is extremely important for the petrochemical industry

Biogeochemical linkage between atmosphere and ocean in the eastern equatorial Pacific Ocean: Results from the EqPOS research cruise

Science.gov (United States)

Furutani, H.; Inai, Y.; Aoki, S.; Honda, H.; Omori, Y.; Tanimoto, H.; Iwata, T.; Ueda, S.; Miura, K.; Uematsu, M.

2012-12-01

Eastern equatorial Pacific Ocean is a unique oceanic region from several biogeochemical points of view. It is a remote open ocean with relatively high marine biological activity, which would result in limited influence of human activity but enhanced effect of marine natural processes on atmospheric composition. It is also characterized as high nutrient low chlorophyll (HNLC) ocean, in which availability of trace metals such as iron and zinc limits marine primary production and thus atmospheric deposition of these trace elements to the ocean surface is expected to play an important role in regulating marine primary production and defining unique microbial community. High sea surface temperature in the region generates strong vertical air convection which efficiently brings tropospheric atmospheric composition into stratosphere. In this unique eastern equatorial Pacific Ocean, EqPOS (Equatorial Pacific Ocean and Stratospheric/Tropospheric Atmospheric Study) research cruise was organized as a part of SOLAS Japan activity to understand biogeochemical ocean-atmospheric interaction in the region. Coordinated atmospheric, oceanic, and marine biological observations including sampling/characterization of thin air-sea interfacial layer (sea surface microlayer: SML) and launching large stratospheric air sampling balloons were carried out on-board R/V Hakuho Maru starting from 29 January for 39 days. Biogeochemically important trace/long-lived gases such as CO2, dimethyl sulfide (DMS), and some volatile organic carbons (VOCs) both in the atmosphere and seawater were continuously monitored and their air-sea fluxes were also observed using gradient and eddy-covariance techniques. Atmospheric gas measurement of CO2, CH4, N2O, SF6, CO, H2, Ar and isotopic composition of selected gases were further extended to stratospheric air by balloon-born sampling in addition to a vertical profiling of O3, CO2, and H2O with sounding sondes. Physical and chemical properties of marine

Trace Gas Emissions From the Production and Use of Biofuels in the African Tropics

Science.gov (United States)

Bertschi, I.; Yokelson, R. J.; Ward, D. E.; Christian, T. J.; Hao, W. M.

2001-12-01

Biomass burning is an important source of many atmospheric trace gases and particles that play a significant role in regional-global, tropospheric and stratospheric chemical processes, and in the global climate. About 80% of biomass burning is thought to occur in the tropics in association with traditional land management practices and domestic biofuel use. More than 220 Tg (1 Tg = 1 x 1012 g) of fuel-wood and 11 Tg of charcoal are consumed annually for domestic heating and cooking in tropical Africa alone. Approximately 90% of the fuel-wood is consumed in open fires in rural areas. Previously, the emissions for fuel-wood fires and charcoal use and production in the tropics were known for only a limited number of chemical species. During SAFARI-2000 we conducted field experiments in remote Zambian villages and observed most of the major trace gases emitted from the production and use of biofuels using open-path Fourier transform infrared (OP-FTIR) spectroscopy, which provides an artifact-free overview of the trace gases present above several ppbv. Our OP-FTIR was deployed for several spot measurements over the course of an earthen kiln charcoal-making process and of several open wood and charcoal fires, all of which were built and tended by local inhabitants. We quantified the emissions of carbon dioxide (CO2), carbon monoxide (CO), methane (CH4), nitrogen oxides (NOx), ammonia (NH3), non-methane hydrocarbons (NMHC), and oxygenated volatile organic compounds (OVOC). Our results also show much higher emission factors for methanol (CH3OH), acetic acid (CH3COOH), and formaldehyde (CH2O) from domestic biofuel production and use than from savanna fires in southern Africa. Thus, these year-round OVOC emissions will play an important role in the photochemistry of the troposphere and in the acidity of aerosols and precipitation especially in tropical regions.

Distribution of trace gases and aerosols in the Siberian air shed during wildfires of summer 2012

Science.gov (United States)

Belan, Boris D.; Paris, Jean-Daiel; Nedelec, Philippe; Antokhin, Pavel N.; Arshinova, Victoriya; Arshinov, Mikhail Yu.; Belan, Sergey B.; Davydov, Denis K.; Ivlev, Georgii A.; Fofonov, Alexandre V.; Kozlov, Artem V.; Rasskazchikova, Tatyana M.; Savkin, Denis E.; Simonenkov, Denis V.; Sklyadneva, Tatyana K.; Tolmachev, Gennadii N.

2017-04-01

During the last two decades, three strong biomass burning events have been observed in Russia: two of them in 2002 and 2010 in the European part of Russia, and another one in 2012 in West and East Siberia. In this paper we present results of the extensive airborne study of the vertical distribution of trace gases and aerosols carried out during strong wildfire event happened in summer 2012 in Siberia. For this purpose, the Optik TU-134 aircraft laboratory was used as a research platform. A large-scale airborne campaign has been undertaken along the route Novosibirsk-Mirny-Yakutsk-Bratsk-Novosibirsk on 31st of July and 1st of August, 2012. Flight pattern consisted of a number of ascents and descents between close to the ground and 8 km altitude that enabled 20 vertical profiles to be obtained. Campaign was conducted under the weather conditions of low-gradient baric field that determined the low speed transport of air masses, as well as the accumulation of biomass burning emissions in the region under study. Highest concentrations of CO2, CH4 and CO over wildfire spots reached 432 ppm, 2367 ppb, and 4036 ppb, correspondingly. If we exclude from the analysis the data obtained when crossing smoke plumes, we can find a difference between background concentrations measured in the atmosphere over regions affected by biomass burning and clean areas. Enhancement of CO2 over the wildfire areas changed with altitude. On average, it was 10.5 ppm in the atmospheric boundary layer (ABL) and 5-6 ppm in the free troposphere. Maximum CO2 enhancements reached 27 ppm and 24 ppm, correspondingly. The averaged CH4 enhancement varied from 75 ppb in the boundary layer to 30 ppb in the upper troposphere, and a little bit lower than 30 ppb in the middle troposphere. Maximum CH4 enhancements reached 202 ppb, 108 ppb, and 50-60 ppb, correspondingly. The averaged and maximum enhancements of CO differed by an order of magnitude. Thus, in the ABL the maximum difference in concentration between

Towards a List of Molecules as Potential Biosignature Gases for the Search for Life on Exoplanets

Science.gov (United States)

Seager, Sara; Bains, William; Petkowski, Janusz

2015-12-01

Thousands of exoplanets are known to orbit nearby stars. Plans for the next generation of space-based and ground-based telescopes are fueling the anticipation that a precious few habitable planets can be identified in the coming decade. Even more highly anticipated is the chance to find signs of life on these habitable planets by way of biosignature gases. But which gases should we search for? We expand on the search of possible biosignature gases and go beyond those studied so far, which include O2, O3, N2O, and CH4, as well as secondary metabolites: methanethiol (CH3SH), dimethyl sulfide ((CH3)2S), methyl chloride (CH3Cl), and carbonyl sulfide (CSO).We present the results of a project to map the chemical space of life’s metabolic products. We have constructed a systematic survey of all possible stable volatile molecules (up to N=6 non-H atoms), and identified those made by life on Earth. Some (such as methyl chloride) are made by Earth life in sufficiently substantial quantities to be candidate biosignatures in an Earth-like exoplanet’s atmosphere; some, such as stibine (SbH3), are produced only in trace amounts. Some entire categories of molecules are not made by Earth life (such as the silanes); these and other absences from the list of biogenic volatiles point to functional patterns in biochemical space. Such patterns may be different for different biochemistry, and so we cannot rule out any small, stable molecule as a candidate biosignature gas. Our goal is for the community to use the list to study the chemicals that might be potential biosignature gases on exoplanets with atmospheres and surface environments different from Earth’s.

The effects of Southeast Asia fire activities on tropospheric ozone, trace gases and aerosols at a remote site over the Tibetan Plateau of Southwest China

International Nuclear Information System (INIS)

Chan, C.Y.; Wong, K.H.; Li, Y.S.; Chan, L.Y.

2006-01-01

Tropospheric ozone (O 3 ), carbon monoxide (CO), total reactive nitrogen (NO y ) and aerosols (PM 2.5 and PM 10 ) were measured on the southeastern Tibetan Plateau at Tengchong (25.01 deg N, 98.3 deg E, 1960 m a.s.l.) in Southwest China, where observational data is scarce, during a field campaign of the TAPTO-China (Transport of Air Pollutants and Tropospheric O 3 over China) in the spring of 2004. Fire maps derived from satellite data and backward air trajectories were used to trace the source regions and transport pathways of pollution. Ozone, CO, NO y , PM 10 and PM 2.5 had average concentrations of 26 ± 8 ppb, 179 ± 91 ppb, 2.7 ± 1.2 ppb and 34 ± 23 and 28 ± 19 μg/m 3 , respectively. The measured O 3 level is low when compared with those reported for similar longitudinal sites in Southeast (SE) Asia and northeastern Tibetan Plateau in Northwest China suggesting that there exist complex O 3 variations in the Tibetan Plateau and its neighbouring SE Asian region. High levels of pollution with hourly averages of O 3 , CO, NO y , PM 10 and PM 2.5 concentrations up to 59, 678 and 7.7 ppb and 158 and 137 μg/m 3 , respectively, were observed. The increase of pollutants in the lower troposphere was caused by regional built-up and transport of pollution from active fire regions of the SE Asia subcontinent and from northern South Asia. Our results showed that pollution transport from SE Asia and South Asia had relatively stronger impacts than that from Central and South China on the abundance of O 3 , trace gases and aerosols in the background atmosphere of the Tibetan Plateau of Southwest China

Integrated method for the measurement of trace nitrogenous atmospheric bases

Directory of Open Access Journals (Sweden)

D. Key

2011-12-01

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, gaseous 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 (e.g., methylamine, 1 pptv; ethylamine, 2 pptv; morpholine, 1 pptv; aniline, 1 pptv; hydrazine, 0.1 pptv; methylhydrazine, 2 pptv, as supported by field measurements in an urban park and in the exhaust of on-road vehicles.

Ozone-Depleting Gases in the Atmosphere: Results From 28 Years of Measurements by the NOAA Climate Monitoring and Diagnostics Laboratory (CMDL)

Science.gov (United States)

Hurst, D. F.; Elkins, J. W.; Montzka, S. A.; Butler, J. H.; Dutton, G. S.; Hall, B. D.; Mondeel, D. J.; Moore, F. L.; Nance, J. D.; Romashkin, P. A.; Thompson, T. M.

2005-12-01

Back in 1978, NOAA/CMDL initiated the weekly filling of flasks at CMDL observatories in Alaska, Hawaii, American Samoa, and Antarctica for analyses of CFC-11, CFC-12 and N2O in the home laboratory. A decade later, each observatory was outfitted with an automated gas chromatograph to make routine, in situ measurements of these three source gases plus methyl chloroform and carbon tetrachloride. Both measurement programs are ongoing, having expanded over the years to include methyl halides and substitutes for regulated halocarbons, to presently account for 95% of the total burden of long-lived Cl and Br believed to enter the stratosphere. These long-term monitoring data have been assimilated into temporal records of the global tropospheric burdens of ozone-depleting chlorine and bromine which are critical input to models that predict future trends in stratospheric ozone. Other information pivotal to ozone projections, such as the atmospheric lifetimes of source gases, stratospheric entry values for total chlorine and total bromine, and identification of the stratospheric sink regions for long-lived source gases, has been gained from in situ measurements by NOAA/CMDL instruments aboard NASA high-altitude aircraft (ER-2 and WB-57) and balloons since 1991. Though CMDL's routine monitoring activities provide important historical records of halogenated source gases in the atmosphere, significant inaccuracies in ozone projections may propagate from the uncertain estimates of impending emissions of ozone-depleting gases. Scenarios of future halocarbon emissions require substantial assumptions about past and pending compliance with the Montreal Protocol, and the sizes and release rates of existing global reservoirs (banks) of halocarbons. Recent work by CMDL has focused on quantifying halocarbon bank emission rates in Russia, the USA, and Canada through geographically extensive measurements aboard trains and low-altitude aircraft. The USA and Canada results indicate that

Greenhouse gases and their impact on climate change: case of Pakistan

International Nuclear Information System (INIS)

Ghauri, B.; Lodhi, A.

1997-01-01

Changes in climate caused by human activities will have far-reaching environmental impacts. Of particular concern are the possibilities of major changes in regional water quantity and quality. An increase in average monthly temperature of 4 deg. C decreases spring runoff over 50% while increasing winter runoff nearly 35%; summer Soil moisture decreases over 30%. Changes in precipitation, whether positive or negative may have been greater consequences for the timing and magnitude of runoff and may contribute significantly to the possibility and consequences of flooding and drought. Global Climatic Changes caused by increasing atmospheric concentration of CO/sub 2/ from fuel combustion and other trace gases are likely to appear within the next few decades. One of the most important of such environmental changes will be alternations in regional hydrologic characteristics such as surface runoff and soil moisture. (author)

Trace metal emissions from the Estonian oil shale fired power

DEFF Research Database (Denmark)

Aunela-Tapola, Leena A.; Frandsen, Flemming; Häsänen, Erkki K.

1998-01-01

Emission levels of selected trace metals from the Estonian oil shale fired power plant were studied. The plant is the largest single power plant in Estonia with an electricity production capacity of 1170 MWe (1995). Trace metals were sampled from the flue gases by a manual method incorporating...... in the flue gases of the studied oil shale plant contribute, however, to clearly higher total trace metal emission levels compared to modern coal fired power plants. Although the old electrostatic precipitators in the plant have been partly replaced by state-of-the-art electrostatic precipitators...... a two-fraction particle sampling and subsequent absorption of the gaseous fraction. The analyses were principally performed with ICP-MS techniques. The trace metal contents of Estonian oil shale were found to be in the same order of magnitude as of coal on average. The high total particle concentrations...

Developing Tighter Constraints on Exoplanet Biosignatures by Modeling Atmospheric Haze

Science.gov (United States)

Felton, Ryan; Neveu, Marc; Domagal-Goldman, Shawn David; Desch, Steven; Arney, Giada

2018-01-01

As we increase our capacity to resolve the atmospheric composition of exoplanets, we must continue to refine our ability to distinguish true biosignatures from false positives in order to ultimately distinguish a life-bearing from a lifeless planet. Of the possible true and false biosignatures, methane (CH4) and carbon dioxide (CO2) are of interest, because on Earth geological and biological processes can produce them on large scales. To identify a biotic, Earth-like exoplanet, we must understand how these biosignatures shape their atmospheres. High atmospheric abundances of CH4 produce photochemical organic haze, which dramatically alters the photochemistry, climate, and spectrum of a planet. Arney et al. (2017) have suggested that haze-bearing atmospheres rich in CO2 may be a type of biosignature because the CH4 flux required to produce the haze is similar to the amount of biogenic CH4 on modern Earth. Atmospheric CH4 and CO2 both affect haze-formation photochemistry, and the potential for hazes to form in Earth-like atmospheres at abiotic concentrations of these gases has not been well studied. We will explore a wide range of parameter space of abiotic concentration levels of these gases to determine what spectral signatures are possible from abiotic environments and look for measurable differences between abiotic and biotic atmospheres. We use a 1D photochemical model with an upgraded haze production mechanism to compare Archean and modern Earth atmospheres to abiotic versions while varying atmospheric CH4 and CO2 levels and atmospheric pressure. We will vary CO2 from a trace gas to an amount such that it dominates atmospheric chemistry. For CH4, there is uncertainty regarding the amount of abiotic CH4 that comes from serpentinizing systems. To address this uncertainty, we will model three cases: 1) assume all CH4 comes from photochemistry; 2) use estimates of modern-day serpentinizing fluxes, assuming they are purely abiotic; and 3) assume serpentinizing

HARPA: A versatile three-dimensional Hamiltonian ray-tracing program for acoustic waves in the atmosphere above irregular terrain

Science.gov (United States)

Jones, R. M.; Riley, J. P.; Georges, T. M.

1986-08-01

The modular FORTRAN 77 computer program traces the three-dimensional paths of acoustic rays through continuous model atmospheres by numerically integrating Hamilton's equations (a differential expression of Fermat's principle). The user specifies an atmospheric model by writing closed-form formulas for its three-dimensional wind and temperature (or sound speed) distribution, and by defining the height of the reflecting terrain vs. geographic latitude and longitude. Some general-purpose models are provided, or users can readily design their own. In addition to computing the geometry of each raypath, HARPA can calculate pulse travel time, phase time, Doppler shift (if the medium varies in time), absorption, and geometrical path length. The program prints a step-by-step account of a ray's progress. The 410-page documentation describes the ray-tracing equations and the structure of the program, and provides complete instructions, illustrated by a sample case.

Thermal Oxidation of Tail Gases from the Production of Oil-furnace Carbon Black

Directory of Open Access Journals (Sweden)

Bosak, Z.

2009-01-01

Full Text Available This paper describes the production technology of oil-furnace carbon black, as well as the selected solution for preventing the emissions of this process from contaminating the environment.The products of industrial oil-furnace carbon black production are different grades of carbon black and process tail gases. The qualitative composition of these tail gases during the production of oil-furnace carbon black are: carbon(IV oxide, carbon(II oxide, hydrogen, methane, hydrogen sulfide, nitrogen, oxygen, and water vapor.The quantitative composition and lower caloric value of process tail gases change depending on the type of feedstock used in the production, as well as the type of process. The lower caloric value of process tail gases is relatively small with values ranging between 1500 and 2300 kJ m–3.In the conventional production of oil-furnace carbon black, process tail gases purified from carbon black dust are freely released into the atmosphere untreated. In this manner, the process tail gases pollute the air in the town of Kutina, because their quantitative values are much higher than the prescribed emissions limits for hydrogen sulfide and carbon(II oxide. A logical solution for the prevention of such air pollution is combustion of the process tail gases, i. e. their thermal oxidation. For this purpose, a specially designed flare system has been developed. Consuming minimum amounts of natural gas needed for oxidation, the flare system is designed to combust low caloric process tail gases with 99 % efficiency. Thus, the toxic and flammable components of the tail gases (hydrogen sulfide, hydrogen, carbon(II oxide, methane and other trace hydrocarbons would be transformed into environmentally acceptable components (sulfur(IV oxide, water, carbon(IV oxide and nitrogen(IV oxide, which are in compliance with the emissions limit values prescribed by law.Proper operation of this flare system in the production of oil-furnace carbon black would solve

Greenhouse gases - observed tendencies contra scenarios

International Nuclear Information System (INIS)

Groenaas, Sigbjoern

2006-01-01

The article presents a study of the increase in greenhouse gases and concludes that it will be necessary to substantially reduce the CO2 concentrations in the atmosphere in order to avoid serious climatic changes

Tropospheric effects of energy conversion

International Nuclear Information System (INIS)

Derwent, R.G.

1992-01-01

The tropospheric concentrations of a number of trace gases are increasing due to man's activities. For some trace gases, their atmospheric life cycles are not fully understood and it is difficult to be certain about the role of man's activities. Emissions from the energy industries and energy conversion processes represent an important subset of source terms in these life cycles, along with agriculture, deforestation, cement manufacture, biomass burning, process industries and natural biospheric processes. Global Warming Potentials (GWPs) allow the tropospheric effects of a range of climate forcing trace gases to be assessed on a comparable basis. If a short term view of the commitment to global warming is adopted then the contribution from other trace gases may approach and exceed that of carbon dioxide, itself. Over longer time horizons, the long atmospheric lifetime of carbon dioxide shows through as a major influence and the contributions from the other trace gases appear to be much smaller, representing an additional 13-18% contribution on top of that from CO 2 itself

Potential use of the non-random distribution of N2 and N2O mole masses in the atmosphere as a tool for tracing atmospheric mixing and isotope fractionation processes

International Nuclear Information System (INIS)

Well, R.; Langel, R.; Reineking, A.

2002-01-01

The variation in the natural abundance of 15 N in atmospheric gas species is often used to determine the mixing of trace gases from different sources. With conventional budget calculations one unknown quantity can be determined if the remaining quantities are known. From 15 N tracer studies in soils with highly enriched 15 N-nitrate a procedure is known to calculate the mixing of atmospheric and soil derived N 2 based on the measurement of the 30/28 and 29/28 ratios in gas samples collected from soil covers. Because of the non-random distribution of the mole masses 30 N 2 , 29 N 2 and 28 N 2 in the mixing gas it is possible to calculate two quantities simultaneously, i.e. the mixing ratio of atmospheric and soil derived N 2 , and the isotopic signature of the soil derived N 2 . Routine standard measurements of laboratory air had suggested a non-random distribution of N 2 -mole masses. The objective of this study was to investigate and explain the existence of non-random distributions of 15 N 15 N, 14 N 15 N and 14 N 14 N in N 2 and N 2 O in environmental samples. The calculation of theoretical isotope data resulting from hypothetical mixing of two sources differing in 15 N natural abundance demonstrated, that the deviation from an ideal random distribution of mole masses is not detectable with the current precision of mass spectrometry. 15 N-analysis of N 2 or N 2 O was conducted with randomised and non-randomised replicate samples of different origin. 15 N abundance as calculated from 29/28 ratios were generally higher in randomised samples. The differences between the treatments ranged between 0.05 and 0.17 δper mille 15 N. It was concluded that the observed randomisation effect is probably caused by 15 N 15 N fractionation during environmental processes. (author)

Climate aspects of radioactive trace gases, especially krypton-85

International Nuclear Information System (INIS)

Kollert, R.; Butzin, M.

1990-01-01

The amount of krypton 85 currently present in the atmosphere is 3.300 Peta Bq. This atmospheric krypton contamination stems from atom bomb tests of the past and from nuclear power plants as well as spent fuel reprocessing plants. The paper investigates the air-electric and air-chemical impact of Kr-85 on the atmosphere and makes a forecast of the future Kr-85 contamination. (DG) [de

Trajectory mapping of middle atmospheric water vapor by a mini network of NDACC instruments

Directory of Open Access Journals (Sweden)

M. Lainer

2015-08-01

Full Text Available The important task to observe the global coverage of middle atmospheric trace gases like water vapor or ozone usually is accomplished by satellites. Climate and atmospheric studies rely upon the knowledge of trace gas distributions throughout the stratosphere and mesosphere. Many of these gases are currently measured from satellites, but it is not clear whether this capability will be maintained in the future. This could lead to a significant knowledge gap of the state of the atmosphere. We explore the possibilities of mapping middle atmospheric water vapor in the Northern Hemisphere by using Lagrangian trajectory calculations and water vapor profile data from a small network of five ground-based microwave radiometers. Four of them are operated within the frame of NDACC (Network for the Detection of Atmospheric Composition Change. Keeping in mind that the instruments are based on different hardware and calibration setups, a height-dependent bias of the retrieved water vapor profiles has to be expected among the microwave radiometers. In order to correct and harmonize the different data sets, the Microwave Limb Sounder (MLS on the Aura satellite is used to serve as a kind of traveling standard. A domain-averaging TM (trajectory mapping method is applied which simplifies the subsequent validation of the quality of the trajectory-mapped water vapor distribution towards direct satellite observations. Trajectories are calculated forwards and backwards in time for up to 10 days using 6 hourly meteorological wind analysis fields. Overall, a total of four case studies of trajectory mapping in different meteorological regimes are discussed. One of the case studies takes place during a major sudden stratospheric warming (SSW accompanied by the polar vortex breakdown; a second takes place after the reformation of stable circulation system. TM cases close to the fall equinox and June solstice event from the year 2012 complete the study, showing the high

Distribution of trace species in power plant streams: A European perspective

International Nuclear Information System (INIS)

Meij, R.

1994-01-01

In the Netherlands only pulverized coal-fired dry bottom boilers are installed. The flue gases are cleaned by high-efficiency cold-side electrostatic precipitators (ESPs) and in all large coal-fired power plants by flue-gas desulfurization (FGD) installations of the lime(stone)/gypsum process. KEMA has performed a large research program on the fate of (trace) elements at coal-fired power plants. A great deal of attention has been paid to the concentrations and distribution of trace elements in coal, in ash and in the vapor phase in the flue gases. Sixteen balance studies of coal-fired power plants, where coal imported from various countries is fired, have been performed. With the information provided by these studies the enrichment factors for the trace elements in ash and the vaporization percentage of the minor and trace elements in the flue gases have been calculated. Using these enrichment factors and vaporization percentages combined with data on the concentration in the coal, the concentrations in the ash and in the vapor phase in the flue gases can be predicted. The emission into the air of trace elements occurs in the solid state (fly ash) and in the gaseous state. The emissions in the solid state are low due to the high degree of removal in the ESPs. The emissions in the gaseous phase are, relatively speaking, more important. In an FGD both emissions are further diminished. In the next section the behavior of elements in the boiler and ESP will be discussed. The influence of the electrostatic precipitators will be reviewed the section thereafter, followed by the fate of gaseous minor and trace elements. And finally the behavior of elements in the FGD will be treated in the last section

Zeppelin NT - Measurement Platform for the Exploration of Atmospheric Chemistry and Dynamics in the Planetary Boundary Layer

Science.gov (United States)

Hofzumahaus, Andreas; Holland, Frank; Oebel, Andreas; Rohrer, Franz; Mentel, Thomas; Kiendler-Scharr, Astrid; Wahner, Andreas; Brauchle, Artur; Steinlein, Klaus; Gritzbach, Robert

2014-05-01

The planetary boundary layer (PBL) is the chemically most active and complex part of the atmosphere where freshly emitted reactive trace gases, tropospheric radicals, atmospheric oxidation products and aerosols exhibit a large variability and spatial gradients. In order to investigate the chemical degradation of trace gases and the formation of secondary pollutants in the PBL, a commercial Zeppelin NT was modified to be used as an airborne measurement platform for chemical and physical observations with high spatial resolution. The Zeppelin NT was developed by Zeppelin Luftschifftechnik (ZLT) and is operated by Deutsche Zeppelin Reederei (DZR) in Friedrichshafen, Germany. The modification was performed in cooperation between Forschungszentrum Jülich and ZLT. The airship has a length of 75 m, can lift about 1 ton of scientific payload and can be manoeuvered with high precision by propeller engines. The modified Zeppelin can carry measurement instruments mounted on a platform on top of the Zeppelin, or inside the gondola beneath the airship. Three different instrument packages were developed to investigate a. gas-phase oxidation processes involving free radicals (OH, HO2) b. formation of secondary organic aerosols (SOA) c. new particle formation (nucleation) The presentation will describe the modified airship and provide an overview of its technical performance. Examples of its application during the recent PEGASOS flight campaigns in Europe will be given.

Atmospheric reaction systems as null-models to identify structural traces of evolution in metabolism.

Directory of Open Access Journals (Sweden)

Petter Holme

Full Text Available The metabolism is the motor behind the biological complexity of an organism. One problem of characterizing its large-scale structure is that it is hard to know what to compare it to. All chemical reaction systems are shaped by the same physics that gives molecules their stability and affinity to react. These fundamental factors cannot be captured by standard null-models based on randomization. The unique property of organismal metabolism is that it is controlled, to some extent, by an enzymatic machinery that is subject to evolution. In this paper, we explore the possibility that reaction systems of planetary atmospheres can serve as a null-model against which we can define metabolic structure and trace the influence of evolution. We find that the two types of data can be distinguished by their respective degree distributions. This is especially clear when looking at the degree distribution of the reaction network (of reaction connected to each other if they involve the same molecular species. For the Earth's atmospheric network and the human metabolic network, we look into more detail for an underlying explanation of this deviation. However, we cannot pinpoint a single cause of the difference, rather there are several concurrent factors. By examining quantities relating to the modular-functional organization of the metabolism, we confirm that metabolic networks have a more complex modular organization than the atmospheric networks, but not much more. We interpret the more variegated modular arrangement of metabolism as a trace of evolved functionality. On the other hand, it is quite remarkable how similar the structures of these two types of networks are, which emphasizes that the constraints from the chemical properties of the molecules has a larger influence in shaping the reaction system than does natural selection.

Atmospheric pollution for trace elements in the remote high-altitude atmosphere in central Asia as recorded in snow from Mt. Qomolangma (Everest) of the Himalayas.

Science.gov (United States)

Lee, Khanghyun; Hur, Soon Do; Hou, Shugui; Hong, Sungmin; Qin, Xiang; Ren, Jiawen; Liu, Yapping; Rosman, Kevin J R; Barbante, Carlo; Boutron, Claude F

2008-10-01

A series of 42 snow samples covering over a one-year period from the fall of 2004 to the summer of 2005 were collected from a 2.1-m snow pit at a high-altitude site on the northeastern slope of Mt. Everest. These samples were analyzed for Al, V, Cr, Mn, Co, Ni, Cu, Zn, As, Rb, Sr, Cd, Sb, Pb, and Bi in order to characterize the relative contributions from anthropogenic and natural sources to the fallout of these elements in central Himalayas. Our data were also considered in the context of monsoon versus non-monsoon seasons. The mean concentrations of the majority of the elements were determined to be at the pg g(-1) level with a strong variation in concentration with snow depth. While the mean concentrations of most of the elements were significantly higher during the non-monsoon season than during the monsoon season, considerable variability in the trace element inputs to the snow was observed during both periods. Cu, Zn, As, Cd, Sb, and Bi displayed high crustal enrichment factors (EFc) in most samples, while Cr, Ni, Rb, and Pb show high EFc values in some of the samples. Our data indicate that anthropogenic inputs are potentially important for these elements in the remote high-altitude atmosphere in the central Himalayas. The relationship between the EFc of each element and the Al concentration indicates that a dominant input of anthropogenic trace elements occurs during both the monsoon and non-monsoon seasons, when crustal contribution is relatively minor. Finally, a comparison of the trace element fallout fluxes calculated in our samples with those recently obtained at Mont Blanc, Greenland, and Antarctica provides direct evidence for a geographical gradient of the atmospheric pollution with trace elements on a global scale.

Resonant photoacoustic detection of NO2 traces with a Q-switched green laser

Science.gov (United States)

Slezak, Verónica; Codnia, Jorge; Peuriot, Alejandro L.; Santiago, Guillermo

2003-01-01

Resonant photoacoustic detection of NO2 traces by means of a high repetition pulsed green laser is presented. The resonator is a cylindrical Pyrex glass cell with a measured Q factor 380 for the first radial mode in air at atmospheric pressure. The system is calibrated with known mixtures in dry air and a minimum detectable volume concentration of 50 parts in 109 is obtained (S/N=1). Its sensitivity allows one to detect and quantify NO2 traces in the exhaust gases of cars. Previously, the analysis of gas adsorption and desorption on the walls and of changes in the sample composition is carried out in order to minimize errors in the determination of NO2 content upon application of the extractive method. The efficiency of catalytic converters of several models of automobiles is studied and the NO2 concentration in samples from exhausts of different types of engine (gasoline, diesel, and methane gas) at idling operation are measured.

Investigation of the influence of atmospheric stability and turbulence on land-atmosphere exchange

Science.gov (United States)

Osibanjo, O.; Holmes, H.

2015-12-01

Surface energy fluxes are exchanged between the surface of the earth and the atmosphere and impact weather, climate, and air quality. The radiation from the sun triggers the surface-atmosphere interaction during the day as heat is transmitted to the surface and the surface heats the air directly above generating wind (i.e., thermal turbulence) that transports heat, moisture, and momentum in the atmospheric boundary layer (ABL). This process is impacted by greenhouse gasses (i.e., water vapor, carbon dioxide and other trace gases) that absorb heat emitted by the earth's surface. The concentrations of atmospheric greenhouse gasses are increasing leading to changes in ABL dynamics as a result of the changing surface energy balance. The ABL processes are important to characterize because they are difficult to parameterize in global and regional scale atmospheric models. Empirical data can be collected using eddy covariance micrometeorological methods to measure turbulent fluxes (e.g., sensible heat, moisture, and CO2) and quantify the exchange between the surface and the atmosphere. The objective of this work is to calculate surface fluxes using observational data collected during one week in September 2014 from a monitoring site in Echo, Oregon. The site is located in the Columbia Basin with rolling terrain, irrigated farmland, and over 100 wind turbines. The 10m tower was placed in a small valley depression to isolate nighttime cold air pools. This work will present observations of momentum, sensible heat, moisture, and carbon dioxide fluxes from data collected at a sampling frequency of 10Hz at four heights. Atmospheric stability is determined using Monin-Obukov length and flux Richardson number, and the impact of stability on surface-atmosphere exchange is investigated. This work will provide a better understanding of surface fluxes and mixing, particularly during stable ABL periods, and the results can be used to compare with numerical models.

Application of microwave air plasma in the destruction of trichloroethylene and carbon tetrachloride at atmospheric pressure

Energy Technology Data Exchange (ETDEWEB)

Rubio, S.J., E-mail: f62rugas@uco.es [Departamento de Fisica, Campus de Rabanales, Edificio Einstein, Planta Baja, Universidad de Cordoba (Spain); Quintero, M.C.; Rodero, A. [Departamento de Fisica, Campus de Rabanales, Edificio Einstein, Planta Baja, Universidad de Cordoba (Spain)

2011-02-15

In this study, the destruction rate of a volatile waste destruction system based on a microwave plasma torch operating at atmospheric pressure was investigated. Atmospheric air was used to maintain the plasma and was introduced by a compressor, which resulted in lower operating costs compared to other gases such as argon and helium. To isolate the output gases and control the plasma discharge atmosphere, the plasma was coupled to a reactor. The effect of the gas flow rate, microwave power and initial concentration of compound on the destruction efficiency of the system was evaluated. In this study, trichloroethylene and carbon tetrachloride were used as representative volatile organic compounds to determine the destruction rate of the system. Based on the experimental results, at an applied microwave power less than 1000 W, the proposed system can reduce input concentrations in the ppmv range to output concentrations at the ppbv level. High air flow rates and initial concentrations produced energy efficiency values greater than 1000 g/kW h. The output gases and species present in the plasma were analysed by gas chromatography and optical emission spectroscopy, respectively, and negligible amounts of halogenated compounds resulting from the cleavage of C{sub 2}HCl{sub 3} and CCl{sub 4} were observed. The gaseous byproducts of decomposition consisted mainly of CO{sub 2}, NO and N{sub 2}O, as well as trace amounts of Cl{sub 2} and solid CuCl.

Application of microwave air plasma in the destruction of trichloroethylene and carbon tetrachloride at atmospheric pressure.

Science.gov (United States)

Rubio, S J; Quintero, M C; Rodero, A

2011-02-15

In this study, the destruction rate of a volatile waste destruction system based on a microwave plasma torch operating at atmospheric pressure was investigated. Atmospheric air was used to maintain the plasma and was introduced by a compressor, which resulted in lower operating costs compared to other gases such as argon and helium. To isolate the output gases and control the plasma discharge atmosphere, the plasma was coupled to a reactor. The effect of the gas flow rate, microwave power and initial concentration of compound on the destruction efficiency of the system was evaluated. In this study, trichloroethylene and carbon tetrachloride were used as representative volatile organic compounds to determine the destruction rate of the system. Based on the experimental results, at an applied microwave power less than 1000 W, the proposed system can reduce input concentrations in the ppmv range to output concentrations at the ppbv level. High air flow rates and initial concentrations produced energy efficiency values greater than 1000 g/kW h. The output gases and species present in the plasma were analysed by gas chromatography and optical emission spectroscopy, respectively, and negligible amounts of halogenated compounds resulting from the cleavage of C(2)HCl(3) and CCl(4) were observed. The gaseous byproducts of decomposition consisted mainly of CO(2), NO and N(2)O, as well as trace amounts of Cl(2) and solid CuCl. Copyright © 2010 Elsevier B.V. All rights reserved.

Seasonal patterns of ascorbate in the needles of Scots Pine (Pinus sylvestris L.) trees: Correlation analyses with atmospheric O3 and NO2 gas mixing ratios and meteorological parameters

International Nuclear Information System (INIS)

Haberer, Kristine; Jaeger, Lutz; Rennenberg, Heinz

2006-01-01

In the present field study the role of ascorbate in scavenging the harmful atmospheric trace gases O 3 and NO 2 was examined. For this purpose ascorbate contents were determined in needles of adult Scots pine trees (Pinus sylvestris L.) during three consecutive years. Ascorbate contents were correlated with ambient tropospheric O 3 and NO 2 concentrations and with meteorological parameters. The results showed a strong correlation of atmospheric O 3 but not of atmospheric NO 2 concentrations with the apoplastic content of ascorbate during the seasonal course. Ascorbate contents in needle extracts did not correlate with ambient trace gas concentrations. In the apoplastic space, but not in needle extracts ascorbate contents correlate highly significantly with global radiation. From these results it is assumed that apoplastic ascorbate in Scots pine needles is adapted to the actual atmospheric O 3 concentration to mediate immediate detoxification of O 3 , while the atmospheric O 3 concentration itself is largely dependent on light intensity. - Contents of apoplastic but not symplastic ascorbate correlate significantly with atmospheric ozone concentrations

Influence of water vapour and permanent gases on the atmospheric optical depths and transmittance

Science.gov (United States)

Badescu, V.

1991-05-01

The influence of the atmospheric state on the extinction of direct solar radiation has been studied by using a four layer atmospheric model. Simple analytical formulae are established for the spectral optical depths of permanent gases and water vapour. These formulae use the ground level values of air pressure, temperature and relative huniidity. An additional parameter, related to the vertical distribution of the hunmidity content, is used for a better estimation of the water vapour optical depth. Good agreement between theory and measurements is found. The paper shows the dependence of the atmospheric spectral transmittance on the above mentioned parameters. L'influence de l'état atmosphérique sur l'extinction de la radiation solaire directe a été étudiée à l'aide d'un modèle atmosphérique développé antérieurement par l'auteur. Des formules simples ont été établies pour l'épaisseur optique spectrale des gaz et de la vapeur d'eau. Ces formules utilisent les valeurs de la pression atmosphérique, de la température et de l'humidité relative, mesurées au niveau du sol. Un paramètre supplémentaire, lié à la distribution verticale du contenu d'humidité, est utilisé pour calculer l'épaisseur optique due à la vapeur d'eau. La théorie est en bon accord avec les résultats des mesures. Le travail montre la dépendance de la transmittance atmosphérique spectrale en fonction des paramètres spécifiés ci-dessus.

Climate Change, Greenhouse Gases and Aerosols

Indian Academy of Sciences (India)

user

their radiative properties are similar to the glass used in a green- house. Greenhouse gases in the Earth's atmosphere absorb 90% of the radiation emitted .... and wind speed and direction in each box is calculated using the physical laws gov-.

Isotopic studies of rare gases in terrestrial samples and in natural nucleosynthesis

International Nuclear Information System (INIS)

Reynolds, J.H.

1988-08-01

This project is concerned with research in rare gas mass spectrometry. The broad objective is to read the natural record that isotopes of the rare gases comprise as trace constituents of natural gases, rocks, and meteorites. In past years, these interests have led to the study of such diverse problems as the dating of rocks, the early chronology and isotopic structure of the solar system as revealed by extinct radioactivities, and the elemental and isotopic composition of trapped primordial rare gases in meteorites. In recent years, the project has focused progressively more on terrestrial problems

Isotopic studies of rare gases in terrestrial samples and in natural nucleosynthesis

International Nuclear Information System (INIS)

1987-07-01

This project is concerned with research in rare gas mass spectrometry. The broad objective is to read the natural record that isotopes of the rare gases comprise as trace constituents of natural gases, rocks, and meteorites. In past years, these interests have led to the study of such diverse problems as the dating of rocks, the early chronology and isotopic structure of the solar system as revealed by extinct radioactivities, and the elemental and isotopic composition of trapped primordial rare gases in meteorites. In recent years, the project has focused progressively more on terrestrial problems

Biosphere-Atmosphere Exchange of NOx, CH4, and O3 in Central Amazon

Science.gov (United States)

Wiedemann, K. T.; Munger, J. W.; Wofsy, S. C.; Budney, J.; Rizzo, L. V.; Campos, K.; Rocha, H.; Freitas, H.

2016-12-01

Oxidation by OH is the dominant pathway for removing important trace gases such as CH4, CO, CH3Br, and HCFCs. The primary source of atmospheric OH is the photolysis of O3 in the presence of water vapor, and NOx are the main precursors of O3 and OH. Thus, in NOx-rich environments that have both high humidity and high solar radiation, OH concentrations are enhanced, and therefore, tropical forests dominate global oxidation of long-lived gases. The Amazon rain forest has a unique combination of vegetation with diverse characteristics, climate, and a dynamic land use, factors that altogether govern the emission and fate of trace-gases and control particle formation and atmospheric chemistry. Understanding the interactions among the mechanisms that govern local precursor emissions will lead to a better description of the local atmospheric chemistry, which have global impacts. As part of the GoAmazon project, an array of complementary measurements was conducted in a research site in central Amazon, southeast of Santarem (PA, Brazil), situated inside the Tapajos National Forest. The site where the measurements were taken is surrounded by intact rain forest in a 6 km radius, and a 45 m closed canopy. In the east side out of this radius (upwind), some settlements are distributed in a stripe along a road, which were cleared for agriculture and are sparsely populated. The 67 m tower was assembled in the site in 2001 for flux measurements (CO2 and H2O), and included CO in order to assess local and regional biomass burning. In mid 2014 additional instrumentation were added, measuring NOx, O3, CH4, and SO2 fluxes and profiles. The SO2 measurements (until early 2015) showed concentrations up to 0.1 ppb during the peak of the dry season, and a small vertical gradient, suggesting the predominance of biogenic sources. Preliminary results show no significant seasonality in the daytime and nighttime O3 vertical profiles. Occasionally, nighttime profiles showed high concentrations for

Solar radiation transfer in the inhomogeneous atmosphere; Solarer Strahlungstransport in der inhomogenen Atmosphaere

Energy Technology Data Exchange (ETDEWEB)

Scheirer, R.

2001-07-01

A most profound knowledge about the radiative characteristics of clouds is required for the development of realistic atmospheric circulation models and cloud remote sensing algorithms. At present, cloud fields are treated extremely simplified in both application areas. Cloud radiative flux parameterizations in atmospheric circulation models as well as the correlation between radiance and cloud properties as required for remote sensing algorithm are usually based on the assumption of plane-parallel homogeneous (PPHOM) clouds. Compared to realistically 3D cloud fields, this simplification leads to large systematic errors. In order to quantify these errors a Monte Carlo radiative transfer model has been developed and applied to 3D cloud fields. The latter origin from the non-hydrostatic 3D atmospheric model GESIMA. Absorption and scattering properties of the cloud particles have been calculated by means of Mie-theory for spherical water droplets and a ray-tracing code for non-spherical ice, rain, and snow particles. Line by line calculations have been used to obtain the absorption properties of the relevant atmospheric gases. (orig.) [German] Die Erstellung realistischer Zirkulationsmodelle der Atmosphaere erfordert unter Anderem eine moeglichst genaue Kenntnis der Strahlungseigenschaften von Wolken. Auch fuer Ableitung und Korrektur von Fernerkundungsalgorithmen sind die Einfluesse der Wolken auf die zu messenden Strahldichten von grosser Bedeutung. In den beiden genannten Anwendungen werden Wolkenfelder zur Zeit nur in stark vereinfachter Weise beruecksichtigt. Parameterisierungen der Strahlungsfluesse bei bewoelkter Atmosphaere in atmosphaerischen Zirkulationsmodellen, sowie die Ableitung der Zusammenhaenge zwischen Strahldichten und optischen Wolkeneigenschaften basieren auf der Annahme von planparallelen und horizontal homogenen Wolken (PPHOM). Diese Approximation kann gegenueber der dreidimensionalen Strahlungstransportberechnung (3D) zu erheblichen Fehlern

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

International Nuclear Information System (INIS)

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

2005-01-01

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

Investigation of different types of filters for atmospheric trace elements analysis by three analytical techniques

International Nuclear Information System (INIS)

Ali, A.E.; Bacso, J.

1996-01-01

Different atmospheric aerosol samples were collected on three types of filters. Disks of both loaded and clean areas of each kind of filter were investigated by XRF, PIXE and Scanning Electron Microscope (SEM) methods. The blank concentration values of the elements Al, Si, P, S, Cl, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Br and Pb in the three types of filters are discussed. It is found that for trace elemental analysis, the Nuclepore membrane filters are the most suitable for sampling. These have much lower blank element concentration values than the glass fibres and ash free filters. It was found also that the PIXE method is a more reliable analytical technique for atmospheric aerosol particles than the other methods. (author). 20 refs., 3 figs., 3 tabs

Anesthetic gases and global warming: Potentials, prevention and future of anesthesia.

Science.gov (United States)

Gadani, Hina; Vyas, Arun

2011-01-01

Global warming refers to an average increase in the earth's temperature, which in turn causes changes in climate. A warmer earth may lead to changes in rainfall patterns, a rise in sea level, and a wide range of impacts on plants, wildlife, and humans. Greenhouse gases make the earth warmer by trapping energy inside the atmosphere. Greenhouse gases are any gas that absorbs infrared radiation in the atmosphere and include: water vapor, carbon dioxide (CO2), methane (CH4), nitrous oxide (N2O), halogenated fluorocarbons (HCFCs), ozone (O3), perfluorinated carbons (PFCs), and hydrofluorocarbons (HFCs). Hazardous chemicals enter the air we breathe as a result of dozens of activities carried out during a typical day at a healthcare facility like processing lab samples, burning fossil fuels etc. We sometimes forget that anesthetic agents are also greenhouse gases (GHGs). Anesthetic agents used today are volatile halogenated ethers and the common carrier gas nitrous oxide known to be aggressive GHGs. With less than 5% of the total delivered halogenated anesthetic being metabolized by the patient, the vast majority of the anesthetic is routinely vented to the atmosphere through the operating room scavenging system. The global warming potential (GWP) of a halogenated anesthetic is up to 2,000 times greater than CO2. Global warming potentials are used to compare the strength of different GHGs to trap heat in the atmosphere relative to that of CO2. Here we discuss about the GWP of anesthetic gases, preventive measures to decrease the global warming effects of anesthetic gases and Xenon, a newer anesthetic gas for the future of anesthesia.

The impact of vibrational Raman scattering of air on DOAS measurements of atmospheric trace gases

Science.gov (United States)

Lampel, J.; Frieß, U.; Platt, U.

2015-09-01

In remote sensing applications, such as differential optical absorption spectroscopy (DOAS), atmospheric scattering processes need to be considered. After inelastic scattering on N2 and O2 molecules, the scattered photons occur as additional intensity at a different wavelength, effectively leading to "filling-in" of both solar Fraunhofer lines and absorptions of atmospheric constituents, if the inelastic scattering happens after the absorption. Measured spectra in passive DOAS applications are typically corrected for rotational Raman scattering (RRS), also called Ring effect, which represents the main contribution to inelastic scattering. Inelastic scattering can also occur in liquid water, and its influence on DOAS measurements has been observed over clear ocean water. In contrast to that, vibrational Raman scattering (VRS) of N2 and O2 has often been thought to be negligible, but it also contributes. Consequences of VRS are red-shifted Fraunhofer structures in scattered light spectra and filling-in of Fraunhofer lines, additional to RRS. At 393 nm, the spectral shift is 25 and 40 nm for VRS of O2 and N2, respectively. We describe how to calculate VRS correction spectra according to the Ring spectrum. We use the VRS correction spectra in the spectral range of 420-440 nm to determine the relative magnitude of the cross-sections of VRS of O2 and N2 and RRS of air. The effect of VRS is shown for the first time in spectral evaluations of Multi-Axis DOAS data from the SOPRAN M91 campaign and the MAD-CAT MAX-DOAS intercomparison campaign. The measurements yield in agreement with calculated scattering cross-sections that the observed VRS(N2) cross-section at 393 nm amounts to 2.3 ± 0.4 % of the cross-section of RRS at 433 nm under tropospheric conditions. The contribution of VRS(O2) is also found to be in agreement with calculated scattering cross-sections. It is concluded, that this phenomenon has to be included in the spectral evaluation of weak absorbers as it

Late Impacts and the Origins of the Atmospheres on the Terrestrial Planets

Science.gov (United States)

Mukhopadhyay, S.; Stewart, S. T.; Lock, S. J.; Parai, R.; Tucker, J. M.

2014-12-01

Models for the origin of terrestrial atmospheres typically require an intricate sequence of events, including hydrodynamic escape, outgassing of mantle volatiles and late delivery. Here we discuss the origin of the atmospheres on the terrestrial planets in light of new ideas about the formation of the Moon, giant impact induced atmospheric loss and recent noble gas measurements. Our new measurements indicate that noble gases in the Earth's atmosphere cannot be derived from any combination of fractionation of a nebular-derived atmosphere followed by outgassing of deep or shallow mantle volatiles. While Ne in the mantle retains a nebular component, the present-day atmosphere has no memory of nebular gases. Rather, atmospheric noble gases have a close affinity to chondrites. On the other hand, Venus's atmosphere has 20 and 70 times higher abundance of 20Ne and 36Ar, respectively, and a 20Ne/22Ne ratio closer to the solar value than Earth's atmosphere. While the present atmosphere of Mars is significantly fractionated in the lighter noble gases due to long term atmospheric escape, the Kr isotopic ratios in Martian atmosphere are identical to solar. Thus, while Earth's atmosphere has no memory of accretion of nebular gases, atmospheres on both Venus and Mars preserve at least a component of nebular gases. To explain the above observations, we propose that a common set of processes operated on the terrestrial planets, and that their subsequent evolutionary divergence is simply explained by planetary size and the stochastic nature of giant impacts. We present geochemical observations and simulations of giant impacts to show that most of Earth's mantle was degassed and the outgassed volatiles were largely lost during the final sequence of giant impacts onto Earth. Earth's noble gases were therefore dominantly derived from late-accreting planetesimals. In contrast, Venus did not suffer substantial atmospheric loss by a late giant impact and retains a higher abundance of

Development of monitoring and control technology based on trace gas monitoring. Final report

Energy Technology Data Exchange (ETDEWEB)

Liebowitz, B.

1997-07-01

Trace gases are generated by many biological reactions. During anaerobic decomposition, trace levels of hydrogen (H{sub 2}) and carbon monoxide (CO) gases are produced. It was shown previously that these trace gases are intrinsically related to the biochemical reactions occurring and, therefore, offer promise for on-line process monitoring and control. This work was designed to test how effectively hydrogen and CO could be to monitor high-rate anaerobic systems that has significant mass transfer and complex hydraulics. An experimental program was designed to examine the behavior of an upflow anaerobic sludge blanket (UASB) reactor system under steady state and in response to organic loading perturbations. The responses of trace gases CO and H{sub 2} were tracked using an on-line, real-time gas-monitoring system linked to a computer-controlled data acquisition package. Data on conventional process parameters such as pH, chemical oxygen demand (COD), volatile fatty acids (VFAs) were concurrently collected. Monitoring of conventional process indicators (i.e., pH, VFA, gas production) and trace gas (H{sub 2} and CO) indicators was conducted using a matrix of nine different steady-state OLRs (4-23 kg COD/m{sup 3} -d) and system HRTs (0.5 to 2.5 days) was performed to determine any correlation among the indicators. Of OLR, HRT, and influent COD, only OLR had any significant influence on the process indicators examined. All parameters except methane increased with increases in OLR; methane decreased with increased OLR. The OLR and gas production rate (GP) were observed to be linearly correlated.

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.

Pre-LBA TRACE-A Data

Data.gov (United States)

National Aeronautics and Space Administration — This data set contains atmospheric chemistry and meteorological data from the NASA Transport and Atmospheric Chemistry near the Equator-Atlantic (TRACE-A) field...

Robust extraction of baseline signal of atmospheric trace species using local regression

Science.gov (United States)

Ruckstuhl, A. F.; Henne, S.; Reimann, S.; Steinbacher, M.; Vollmer, M. K.; O'Doherty, S.; Buchmann, B.; Hueglin, C.

2012-11-01

The identification of atmospheric trace species measurements that are representative of well-mixed background air masses is required for monitoring atmospheric composition change at background sites. We present a statistical method based on robust local regression that is well suited for the selection of background measurements and the estimation of associated baseline curves. The bootstrap technique is applied to calculate the uncertainty in the resulting baseline curve. The non-parametric nature of the proposed approach makes it a very flexible data filtering method. Application to carbon monoxide (CO) measured from 1996 to 2009 at the high-alpine site Jungfraujoch (Switzerland, 3580 m a.s.l.), and to measurements of 1,1-difluoroethane (HFC-152a) from Jungfraujoch (2000 to 2009) and Mace Head (Ireland, 1995 to 2009) demonstrates the feasibility and usefulness of the proposed approach. The determined average annual change of CO at Jungfraujoch for the 1996 to 2009 period as estimated from filtered annual mean CO concentrations is -2.2 ± 1.1 ppb yr-1. For comparison, the linear trend of unfiltered CO measurements at Jungfraujoch for this time period is -2.9 ± 1.3 ppb yr-1.

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…

Paloma: an instrument to measure the molecular, elemental and isotopic composition of the mars atmosphere from a landed platform (MSL 09, EXOMARS)

Energy Technology Data Exchange (ETDEWEB)

Sabroux, J.Ch

2003-07-01

An instrument to analyze the molecular, elemental and isotopic composition of Mars atmosphere from a landed platform is being developed under CNES funding. This instrument, called PALOMA (Payload for Local Observation of Mars Atmosphere), will be proposed in response to the AO for the instrumentation of the NASA Mars Smart Lander mission, planned to be launched in 2009. It might be part as well of the EXOMARS mission presently studied at ESA in the frame of the Aurora program. Noble gases (He, Ne, Ar, Xr, Xe) and stable isotopes (C, H, O, N) will be analyzed by using a system of gas purification and separation, coupled with a mass spectrometer. The heaviest, radioactive, noble gas (Rn) and its short-lived daughters will be measured using a small additional device (alpha particle detector). Detailed search for trace constituents of astro-biological interest, like CH{sub 4}, H{sub 2}CO, N{sub 2}O, H{sub 2}S (abundances, isotopic ratios, time variability) will be done on a regular temporal basis during one Martian year. Isotopic ratios will be measured with an accuracy of about 1 ppm, or better, in order to provide a clear diagnosis of possible life signatures, to allow a detailed comparison of Earth and Mars atmospheric fractionation patterns and, finally, to accurately disentangle escape, climatic, geochemical and hypothesized biological effects. High sensitivity is required for elemental and isotopic compositions of trace gases of interest. Such an accurate monitoring of Mars atmosphere volatile composition is expected to provide the necessary reference for future composition studies of minerals, soils, bio-markers, polar cap material, either by in-situ measurement, or from laboratory analyses of returned samples. (author)

Paloma: an instrument to measure the molecular, elemental and isotopic composition of the mars atmosphere from a landed platform (MSL 09, EXOMARS)

International Nuclear Information System (INIS)

Sabroux, J.Ch.

2003-01-01

An instrument to analyze the molecular, elemental and isotopic composition of Mars atmosphere from a landed platform is being developed under CNES funding. This instrument, called PALOMA (Payload for Local Observation of Mars Atmosphere), will be proposed in response to the AO for the instrumentation of the NASA Mars Smart Lander mission, planned to be launched in 2009. It might be part as well of the EXOMARS mission presently studied at ESA in the frame of the Aurora program. Noble gases (He, Ne, Ar, Xr, Xe) and stable isotopes (C, H, O, N) will be analyzed by using a system of gas purification and separation, coupled with a mass spectrometer. The heaviest, radioactive, noble gas (Rn) and its short-lived daughters will be measured using a small additional device (alpha particle detector). Detailed search for trace constituents of astro-biological interest, like CH 4 , H 2 CO, N 2 O, H 2 S (abundances, isotopic ratios, time variability) will be done on a regular temporal basis during one Martian year. Isotopic ratios will be measured with an accuracy of about 1 ppm, or better, in order to provide a clear diagnosis of possible life signatures, to allow a detailed comparison of Earth and Mars atmospheric fractionation patterns and, finally, to accurately disentangle escape, climatic, geochemical and hypothesized biological effects. High sensitivity is required for elemental and isotopic compositions of trace gases of interest. Such an accurate monitoring of Mars atmosphere volatile composition is expected to provide the necessary reference for future composition studies of minerals, soils, bio-markers, polar cap material, either by in-situ measurement, or from laboratory analyses of returned samples. (author)

Aspects of airborne particles and radiation in the atmosphere

International Nuclear Information System (INIS)

Hidy, G.M.

1975-01-01

There are two major ways that thermal radiation may interact with airborne particles in the Earth's atmosphere. The first is a classical problem in which the radiation balance is influenced by scattering and absorption from haze or aerosol layers in the atmosphere. Absorption is generally believed to have a minor effect on attenuation of radiation compared with scattering. In the visible and infrared, scattering by submicron sized particles can have a substantial influence on the balance of radiation in the atmosphere. Considerable interest in this question has developed recently with the assessment of the global impact of air pollution in the lower atmosphere and of exhaust emissions from aircraft flying in the stratosphere. In the first part of this review, the physics of atmospheric aerosol scattering is summarized, and the current status of observational knowledge is examined to identify areas of greatest uncertainty. The second way the radiation is involved in aerosols lies in the production in the atmosphere. Until recently, evidence for airborne particle production by atmospheric photochemistry was quite ambiguous. However, with the advent of results from several new field experiments the role of photochemistry in the generation of aerosol precursors from traces of such gases as sulfur dioxide, nitrogen oxides, and olefinic hydrocarbons is much better understood. The remaining part of this paper is devoted to the discussion of several new observations that indicate the complicated nature of photochemical aerosol formation in the polluted and non-polluted atmosphere

Atmospheric greenhouse effect - simple model; Atmosfaerens drivhuseffekt - enkel modell

Energy Technology Data Exchange (ETDEWEB)

Kanestroem, Ingolf; Henriksen, Thormod

2011-07-01

The article shows a simple model for the atmospheric greenhouse effect based on consideration of both the sun and earth as 'black bodies', so that the physical laws that apply to them, may be used. Furthermore, explained why some gases are greenhouse gases, but other gases in the atmosphere has no greenhouse effect. But first, some important concepts and physical laws encountered in the article, are repeated. (AG)

Greenhouse gases and global warming

International Nuclear Information System (INIS)

1995-01-01

From previous articles we have learned about the complexities of our environment, its atmosphere and its climate system. we have also learned that climate change and, therefore global warm and cool periods are naturally occurring phenomena. Moreover, all scientific evidence suggests that global warming, are likely to occur again naturally in the future. However, we have not yet considered the role of the rates of climate change in affecting the biosphere. It appears that how quickly the climate changes may be more important than the change itself. In light of this concern, let us now consider the possibility that, is due to human activity. We may over the next century experience global warming at rates and magnitudes unparalleled in recent geologic history. The following questions are answered; What can we learn from past climates? What do we know about global climates over the past 100 years? What causes temperature change? What are the greenhouse gases? How much have concentration of greenhouse gases increased in recent years? Why are increases in concentrations of greenhouse of concern? What is the e nhanced greenhouse effect ? How can human activity impact the global climate? What are some reasons for increased concentrations of greenhouse gases? What are fossil fuel and how do they transform into greenhouse gases? Who are the biggest emitters of greenhouse gases? Why are canada per capita emissions of greenhouse gases relatively high? (Author)

Origin of the atmospheres of the earth and the planets

Energy Technology Data Exchange (ETDEWEB)

Chen, Z M

1978-06-01

From a systematic analysis of the whole history of the protoplanetary cloud and the observational facts of the earth's atmosphere, new theory is proposed on the origin of the atmospheres of the earth and the planets. For the earth-like planets, there were profound primordial atmospheres originated from the protoplanetary cloud by the accretion of the embryoes of planets. These primordial atmospheres has existed in a time scale of 10/sup 3/ to 10/sup 7/ years and were composed of chemically reducing gases. The presence of such a reducing atmosphere may be of great significance to the theories of cosmogony and the origin of life. The contents are as follows: the escape of the nebulae and the planetary atmospheres, the blowing-off of the atmospheres and the disspiation of gases driven by the solar wind, the accretion of gases by the planetary embryoes, the primordial atmospheres.

Using biogenic sulfur gases as remotely detectable biosignatures on anoxic planets.

Science.gov (United States)

Domagal-Goldman, Shawn D; Meadows, Victoria S; Claire, Mark W; Kasting, James F

2011-06-01

We used one-dimensional photochemical and radiative transfer models to study the potential of organic sulfur compounds (CS(2), OCS, CH(3)SH, CH(3)SCH(3), and CH(3)S(2)CH(3)) to act as remotely detectable biosignatures in anoxic exoplanetary atmospheres. Concentrations of organic sulfur gases were predicted for various biogenic sulfur fluxes into anoxic atmospheres and were found to increase with decreasing UV fluxes. Dimethyl sulfide (CH(3)SCH(3), or DMS) and dimethyl disulfide (CH(3)S(2)CH(3), or DMDS) concentrations could increase to remotely detectable levels, but only in cases of extremely low UV fluxes, which may occur in the habitable zone of an inactive M dwarf. The most detectable feature of organic sulfur gases is an indirect one that results from an increase in ethane (C(2)H(6)) over that which would be predicted based on the planet's methane (CH(4)) concentration. Thus, a characterization mission could detect these organic sulfur gases-and therefore the life that produces them-if it could sufficiently quantify the ethane and methane in the exoplanet's atmosphere.

Laser Fluence Recognition Using Computationally Intelligent Pulsed Photoacoustics Within the Trace Gases Analysis

Science.gov (United States)

Lukić, M.; Ćojbašić, Ž.; Rabasović, M. D.; Markushev, D. D.; Todorović, D. M.

2017-11-01

In this paper, the possibilities of computational intelligence applications for trace gas monitoring are discussed. For this, pulsed infrared photoacoustics is used to investigate SF6-Ar mixtures in a multiphoton regime, assisted by artificial neural networks. Feedforward multilayer perceptron networks are applied in order to recognize both the spatial characteristics of the laser beam and the values of laser fluence Φ from the given photoacoustic signal and prevent changes. Neural networks are trained in an offline batch training regime to simultaneously estimate four parameters from theoretical or experimental photoacoustic signals: the laser beam spatial profile R(r), vibrational-to-translational relaxation time τ _{V-T} , distance from the laser beam to the absorption molecules in the photoacoustic cell r* and laser fluence Φ . The results presented in this paper show that neural networks can estimate an unknown laser beam spatial profile and the parameters of photoacoustic signals in real time and with high precision. Real-time operation, high accuracy and the possibility of application for higher intensities of radiation for a wide range of laser fluencies are factors that classify the computational intelligence approach as efficient and powerful for the in situ measurement of atmospheric pollutants.

Field Measurements of Trace Gases and Aerosols Emitted by Undersampled Combustion Sources Including Wood and Dung Cooking Fires, Garbage and Crop Residue Burning, and Indonesian Peat Fires

Science.gov (United States)

Stockwell, C.; Jayarathne, T. S.; Goetz, D.; Simpson, I. J.; Selimovic, V.; Bhave, P.; Blake, D. R.; Cochrane, M. A.; Ryan, K. C.; Putra, E. I.; Saharjo, B.; Stone, E. A.; DeCarlo, P. F.; Yokelson, R. J.

2017-12-01

Field measurements were conducted in Nepal and in the Indonesian province of Central Kalimantan to improve characterization of trace gases and aerosols emitted by undersampled combustion sources. The sources targeted included cooking with a variety of stoves, garbage burning, crop residue burning, and authentic peat fires. Trace gas and aerosol emissions were studied using a land-based Fourier transform infrared spectrometer, whole air sampling, photoacoustic extinctiometers (405 and 870nm), and filter samples that were analyzed off-line. These measurements were used to calculate fuel-based emission factors (EFs) for up to 90 gases, PM2.5, and PM2.5 constituents. The aerosol optical data measured included EFs for the scattering and absorption coefficients, the single scattering albedo (at 870 and 405 nm), as well as the absorption Ångström exponent. The emissions varied significantly by source, although light absorption by both brown and black carbon (BrC and BC, respectively) was important for all non-peat sources. For authentic peat combustion, the emissions of BC were negligible and absorption was dominated by organic aerosol. The field results from peat burning were in reasonable agreement with recent lab measurements of smoldering Kalimantan peat and compare well to the limited data available from other field studies. The EFs can be used with estimates of fuel consumption to improve regional emissions inventories and assessments of the climate and health impacts of these undersampled sources.

A Miniaturized Laser Heterodyne Radiometer for Greenhouse Gas Measurements in the Atmospheric Column

Science.gov (United States)

Steel, Emily Wilson

2015-01-01

Laser Heterodyne Radiometry is a technique adapted from radio receiver technology has been used to measure trace gases in the atmosphere since the 1960s.By leveraging advances in the telecommunications industry, it has been possible to miniaturize this technology.The mini-LHR (Miniaturized Laser Heterodyne Radiometer) has been under development at NASA Goddard Space flight Center since 2009. This sun-viewing instrument measures carbon dioxide and methane in the atmospheric column and operates in tandem with an AERONET sun photometer producing a simultaneous measure of aerosols. The mini-LHR has been extensively field tested in a range of locations ranging in the continental US as well as Alaska and Hawaii and now operates autonomously with sensitivities of approximately 0.2 ppmv and approximately10 ppbv, for carbon dioxide and methane respectively, for 10 averaged scans under clear sky conditions.

Mitigation of greenhouse gases emissions impact and their influence on terrestrial ecosystem.

Science.gov (United States)

Wójcik Oliveira, K.; Niedbała, G.

2018-05-01

Nowadays, one of the most important challenges faced by the humanity in the current century is the increasing temperature on Earth, caused by a growing emission of greenhouse gases into the atmosphere. Terrestrial ecosystems, as an important component of the carbon cycle, play an important role in the sequestration of carbon, which is a chance to improve the balance of greenhouse gases. Increasing CO2 absorption by terrestrial ecosystems is one way to reduce the atmospheric CO2 emissions. Sequestration of CO2 by terrestrial ecosystems is not yet fully utilized method of mitigating CO2 emission to the atmosphere. Terrestrial ecosystems, especially forests, are essential for the regulation of CO2 content in the atmosphere and more attention should be paid to seeking the natural processes of CO2 sequestration.

A Portable FTIR Analyser for Field Measurements of Trace Gases and their Isotopologues: CO2, CH4, N2O, CO, del13C in CO2 and delD in water vapour

Science.gov (United States)

Griffith, D. W.; Bryant, G. R.; Deutscher, N. M.; Wilson, S. R.; Kettlewell, G.; Riggenbach, M.

2007-12-01

We describe a portable Fourier Transform InfraRed (FTIR) analyser capable of simultaneous high precision analysis of CO2, CH4, N2O and CO in air, as well as δ13C in CO2 and δD in water vapour. The instrument is based on a commercial 1 cm-1 resolution FTIR spectrometer fitted with a mid-IR globar source, 26 m multipass White cell and thermoelectrically-cooled MCT detector operating between 2000 and 7500 cm-1. Air is passed through the cell and analysed in real time without any pre-treatment except for (optional) drying. An inlet selection manifold allows automated sequential analysis of samples from one or more inlet lines, with typical measurement times of 1-10 minutes per sample. The spectrometer, inlet sampling sequence, real-time quantitative spectrum analysis, data logging and display are all under the control of a single program running on a laptop PC, and can be left unattended for continuous measurements over periods of weeks to months. Selected spectral regions of typically 100-200 cm-1 width are analysed by a least squares fitting technique to retrieve concentrations of trace gases, 13CO2 and HDO. Typical precision is better than 0.1% without the need for calibration gases. Accuracy is similar if measurements are referenced to calibration standard gases. δ13C precision is typically around 0.1‰, and for δD it is 1‰. Applications of the analyser include clean and polluted air monitoring, tower-based flux measurements such as flux gradient or integrated horizontal flux measurements, automated soil chambers, and field-based measurements of isotopic fractionation in soil-plant-atmosphere systems. The simultaneous multi-component advantages can be exploited in tracer-type emission measurements, for example of CH4 from livestock using a co-released tracer gas and downwind measurement. We have also developed an open path variant especially suited to tracer release studies and measurements of NH3 emissions from agricultural sources. An illustrative

Use of Spanish Moss as an atmospheric monitor for trace elements

International Nuclear Information System (INIS)

Padaki, P.M.; McWilliams, E.L.; James, W.D

1992-01-01

Samples of Spanish Moss (Tillandsia usneoides L.) were analyzed by neutron activation analysis (NAA) and inductively coupled argon plasma emission spectrometry (ICP) for trace elements as atmospheric environmental monitors. The plant material was collected at a single location in east Texas, then deployed along a 6*6 matrix gridwork in the extreme northeastern corner of the state. The study area includes several possible pollution sources including fossil fuel fired power plants. Two separate study periods were conducted, one during the summer months of 1989 and the other the following winter. Concentrations of about 35 elements were determined and contour plots for each element were prepared for each study period. Concentration ranges were found to be somewhat lower than those reported in other studies using epihytic plants as environmental indicators. Initial correlations between elements and the possible relationships to pollution sources are discussed. (author) 10 refs.; 3 figs.; 1 tab

Method and apparatus for removing radioactive gases from a nuclear reactor

International Nuclear Information System (INIS)

Frumerman, R.; Brown, W.W.

1975-01-01

A description is given of a method for removing radioactive gases from a nuclear reactor including the steps of draining coolant from a nuclear reactor to a level just below the coolant inlet and outlet nozzles to form a vapor space and then charging the space with an inert gas, circulating coolant through the reactor to assist the release of radioactive gases from the coolant into the vapor space, withdrawing the radioactive gases from the vapor space by a vacuum pump which then condenses and separates water from gases carried forward by the vacuum pump, discharging the water to a storage tank and supplying the separated gases to a gas compressor which pumps the gases to gas decay tanks. After the gases in the decay tanks lose their radioactive characteristics, the gases may be discharged to the atmosphere or returned to the reactor for further use

Atmospheric Chemistry in a Changing World

Science.gov (United States)

Brune, William H.

The world is changing,and the atmosphere's composition is changing with it. Human activity is responsible for much of this. Global population growth and migration to urban centers, extensive biomass burning, the spread of fertilizer-intensive agribusiness, globalization of business and industry, rising standards of living in the developing world, and increased energy use fuels atmospheric change. If current practices continue, atmospheric increases are likely for the greenhouse gases carbon dioxide, methane, nitrous oxide; and for the chemically active gases nitric oxide, sulfur dioxide,and ammonia. Increases in global tropospheric ozone and aerosols are a distinct possibility.

A new multi-gas constrained model of trace gas non-homogeneous transport in firn: evaluation and behaviour at eleven polar sites

Directory of Open Access Journals (Sweden)

E. Witrant

2012-12-01

Full Text Available Insoluble trace gases are trapped in polar ice at the firn-ice transition, at approximately 50 to 100 m below the surface, depending primarily on the site temperature and snow accumulation. Models of trace gas transport in polar firn are used to relate firn air and ice core records of trace gases to their atmospheric history. We propose a new model based on the following contributions. First, the firn air transport model is revised in a poromechanics framework with emphasis on the non-homogeneous properties and the treatment of gravitational settling. We then derive a nonlinear least square multi-gas optimisation scheme to calculate the effective firn diffusivity (automatic diffusivity tuning. The improvements gained by the multi-gas approach are investigated (up to ten gases for a single site are included in the optimisation process. We apply the model to four Arctic (Devon Island, NEEM, North GRIP, Summit and seven Antarctic (DE08, Berkner Island, Siple Dome, Dronning Maud Land, South Pole, Dome C, Vostok sites and calculate their respective depth-dependent diffusivity profiles. Among these different sites, a relationship is inferred between the snow accumulation rate and an increasing thickness of the lock-in zone defined from the isotopic composition of molecular nitrogen in firn air (denoted δ¹⁵N. It is associated with a reduced diffusivity value and an increased ratio of advective to diffusive flux in deep firn, which is particularly important at high accumulation rate sites. This has implications for the understanding of δ¹⁵N of N₂ records in ice cores, in relation with past variations of the snow accumulation rate. As the snow accumulation rate is clearly a primary control on the thickness of the lock-in zone, our new approach that allows for the estimation of the lock-in zone width as a function of accumulation may lead to a better constraint on the age difference between the ice and entrapped gases.

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.

Monitoring Of The Middle Atmosphere: Grille Spectrometer Experiment Results On Board SPACELAB 1 And Scientific Program Of ATLAS 1 Mission

Science.gov (United States)

Papineau, N.; Camy-Peyret, C.; Ackerman, Marcel E.

1989-10-01

Measurements of atmospheric trace gases have been performed during the first Spacelab mission on board the Space Shuttle. The principle of the observations is infrared absorption spectroscopy using the solar occultation technique. Infrared absorption spectra of NO, CO, CO2, NO2, N20, CH4 and H2O have been recorded using the Grille spectrometer developped by ONERA and IASB. From the observed spectra, vertical profiles for these molecules have been derived. The present paper summarizes the main results and compares them with computed vertical profiles from a zonally averaged model of the middle atmosphere. The scientific objectives of the second mission, Atlas 1, planned for 1990 are also presented.

Modulation of capillary condensation by trace component

Directory of Open Access Journals (Sweden)

Shiqi Zhou

2011-06-01

Full Text Available Impact of trace component on capillary condensation (CC is investigated systematically using a classical density functional theory. It is discovered that (i presence of the trace component makes the CC to occur at much lower condensation pressure than when its absence; (ii Lennard-Jones potential parameters like size parameter and energy parameter of the trace component, and its concentration in the bulk adsorption system, show their effects the most remarkably within a particular range beyond which the effects eventually become insignificant. The present discoveries have implications in low pressure storage of gases, separation and enrichment of low concentration component, and easy control of CC transition, etc.

Robust extraction of baseline signal of atmospheric trace species using local regression

Directory of Open Access Journals (Sweden)

A. F. Ruckstuhl

2012-11-01

Full Text Available The identification of atmospheric trace species measurements that are representative of well-mixed background air masses is required for monitoring atmospheric composition change at background sites. We present a statistical method based on robust local regression that is well suited for the selection of background measurements and the estimation of associated baseline curves. The bootstrap technique is applied to calculate the uncertainty in the resulting baseline curve. The non-parametric nature of the proposed approach makes it a very flexible data filtering method. Application to carbon monoxide (CO measured from 1996 to 2009 at the high-alpine site Jungfraujoch (Switzerland, 3580 m a.s.l., and to measurements of 1,1-difluoroethane (HFC-152a from Jungfraujoch (2000 to 2009 and Mace Head (Ireland, 1995 to 2009 demonstrates the feasibility and usefulness of the proposed approach.

The determined average annual change of CO at Jungfraujoch for the 1996 to 2009 period as estimated from filtered annual mean CO concentrations is −2.2 ± 1.1 ppb yr⁻¹. For comparison, the linear trend of unfiltered CO measurements at Jungfraujoch for this time period is −2.9 ± 1.3 ppb yr⁻¹.

Improvement and validation of trace gas retrieval from ACAM aircraft observation

Science.gov (United States)

Liu, C.; Liu, X.; Kowalewski, M. G.; Janz, S. J.; Gonzalez Abad, G.; Pickering, K. E.; Chance, K.; Lamsal, L. N.

2014-12-01

The ACAM (Airborne Compact Atmospheric Mapper) instrument, flown on board the NASA UC-12 aircraft during the DISCOVER-AQ (Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality) campaigns, was designed to provide remote sensing observations of tropospheric and boundary layer pollutants and help understand some of the most important pollutants that directly affect the health of the population. In this study, slant column densities (SCD) of trace gases (O3, NO2, HCHO) are retrieved from ACAM measurements during the Baltimore-Washington D.C. 2011 campaign by the Basic Optical Absorption Spectroscopy (BOAS) trace gas fitting algorithm using a nonlinear least-squares (NLLS) inversion technique, and then are converted to vertical column densities (VCDs) using the Air Mass Factors (AMF) calculated with the VLIDORT (Vector Linearized Discrete Ordinate Radiative Transfer) model and CMAQ (Community Multi-scale Air Quality) model simulations of trace gas profiles. For surface treatment in the AMF, we use high-resolution MODIS climatological BRDF product (Bidirectional Reflectance Distribution Function) at 470 nm for NO2, and use high-resolution surface albedo derived by combining MODIS and OMI albedo databases for HCHO and O3. We validate ACAM results with coincident ground-based PANDORA, aircraft (P3B) spiral and satellite (OMI) measurements and find out generally good agreement especially for NO2 and O3

Impact of aircraft exhaust on the atmosphere. Box model studies and 3-D mesoscale numerical case studies of seasonal differences

Energy Technology Data Exchange (ETDEWEB)

Petry, H; Ebel, A; Franzkowiak, V; Hendricks, J; Lippert, E; Moellhoff, M [Koeln Univ. (Germany). Inst. fuer Geophysik und Meteorologie

1998-12-31

The impact of aircraft emissions released in the tropopause region on atmospheric trace gases as O{sub 3} or HNO{sub 3} is investigated by means of model studies. Special emphasis is drawn on seasonal effects. A box model is applied as well as a 3-D mesoscale chemistry transport model. These model studies show that the impact of aircraft emissions on ozone in the tropopause region is much stronger in summer than in late autumn with a difference of one order of magnitude. (author) 14 refs.

Impact of aircraft exhaust on the atmosphere. Box model studies and 3-D mesoscale numerical case studies of seasonal differences

Energy Technology Data Exchange (ETDEWEB)

Petry, H.; Ebel, A.; Franzkowiak, V.; Hendricks, J.; Lippert, E.; Moellhoff, M. [Koeln Univ. (Germany). Inst. fuer Geophysik und Meteorologie

1997-12-31

The impact of aircraft emissions released in the tropopause region on atmospheric trace gases as O{sub 3} or HNO{sub 3} is investigated by means of model studies. Special emphasis is drawn on seasonal effects. A box model is applied as well as a 3-D mesoscale chemistry transport model. These model studies show that the impact of aircraft emissions on ozone in the tropopause region is much stronger in summer than in late autumn with a difference of one order of magnitude. (author) 14 refs.

Sorption of atmospheric gases by bulk lithium metal

Energy Technology Data Exchange (ETDEWEB)

Hart, C.A. [Department of Physics, University of Maryland, College Park, MD 20742 (United States); Skinner, C.H., E-mail: cskinner@pppl.gov [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Capece, A.M. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Koel, B.E. [Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544 (United States)

2016-01-15

Lithium conditioning of plasma facing components has enhanced the performance of several fusion devices. Elemental lithium will react with air during maintenance activities and with residual gases (H{sub 2}O, CO, CO{sub 2}) in the vacuum vessel during operations. We have used a mass balance (microgram sensitivity) to measure the mass gain of lithium samples during exposure of a ∼1 cm{sup 2} surface to ambient and dry synthetic air. For ambient air, we found an initial mass gain of several mg/h declining to less than 1 mg/h after an hour and decreasing by an order of magnitude after 24 h. A 9 mg sample achieved a final mass gain corresponding to complete conversion to Li{sub 2}CO{sub 3} after 5 days. Exposure to dry air resulted in a 30 times lower initial rate of mass gain. The results have implications for the chemical state of lithium plasma facing surfaces and for safe handling of lithium coated components. - Highlights: • Li in tokamaks will react with air during maintenance and exposure to residual gases in the vacuum vessel. • The mass gain of Li samples upon exposure to ambient air indicates conversion to Li{sub 2}CO{sub 3.} • Exposure to dry air resulted in a 30 times lower rate of mass gain. • A rule of thumb for lithium passivation at 26 °C and 45% relative humidity is proposed.

Retrieval of Vertical Aerosol and Trace Gas Distributions from Polarization Sensitive Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS)

Science.gov (United States)

Tirpitz, Jan-Lukas; Friess, Udo; Platt, Ulrich

2017-04-01

An accurate knowledge of the vertical distribution of trace gases and aerosols is crucial for our understanding of the chemical and dynamical processes in the lower troposphere. Their accurate determination is typically only possible by means of laborious and expensive airborne in-situ measurements but in the recent decades, numerous promising ground-based remote sensing approaches have been developed. One of them is to infer vertical distributions from "Differential Optical Absorption Spectroscopy" (DOAS) measurements. DOAS is a technique to analyze UV- and visible radiation spectra of direct or scattered sunlight, which delivers information on different atmospheric parameters, integrated over the light path from space to the instrument. An appropriate set of DOAS measurements, recorded under different viewing directions (Multi-Axis DOAS) and thus different light path geometries, provides information on the atmospheric state. The vertical profiles of aerosol properties and trace gas concentrations can be retrieved from such a set by numerical inversion techniques, incorporating radiative transfer models. The information content of measured data is rarely sufficient for a well-constrained retrieval, particularly for atmospheric layers above 1 km. We showed in first simulations that, apart from spectral properties, the polarization state of skylight is likely to provide a significant amount of additional information on the atmospheric state and thus to enhance retrieval quality. We present first simulations, expectations and ideas on how to implement and characterize a polarization sensitive Multi-Axis DOAS instrument and a corresponding profile retrieval algorithm.

Tropospheric chemistry over the lower Great Plains of the United States. 2. Trace gas profiles and distributions

Science.gov (United States)

Luke, Winston T.; Dickerson, Russell R.; Ryan, William F.; Pickering, Kenneth E.; Nunnermacker, Linda J.

1992-12-01

Convective clouds and thunderstorms redistribute air pollutants vertically, and by altering the chemistry and radiative balance of the upper troposphere, these local actions can have global consequences. To study these effects, measurements of trace gases ozone, O3, carbon monoxide, CO, and odd nitrogen were made aboard the NCAR Sabreliner on 18 flights over the southern Great Plains during June 1985. To demonstrate chemical changes induced by vertical motions in the atmosphere and to facilitate comparison with computer model calculations, these data were categorized according to synoptic flow patterns. Part 1 of this two-part paper details the alternating pulses of polar and maritime air masses that dominate the vertical mixing in this region. In this paper, trace gas measurements are presented as altitude profiles (0-12 km) with statistical distributions of mixing ratios for each species in each flow pattern. The polar flow regime is characterized by northwesterly winds, subsiding air, and convective stability. Concentrations of CO and total odd nitrogen (NOy) are relatively high in the shallow planetary boundary layer (PBL) but decrease rapidly with altitude. Ozone, on the other hand, is uniformly distributed, suggesting limited photochemical production; in fact, nitric oxide, NO, mixing ratios fell below 10 ppt (parts per 1012 by volume) in the midtroposphere. The maritime regime is characterized by southerly surface winds, convective instability, and a deep PBL; uniformly high concentrations of trace gases were found up to 4 km on one flight. Severe storms occur in maritime flow, especially when capped by a dry layer, and they transport large amounts of CO, O3, and NOy into the upper troposphere. Median NO levels at high altitude exceeded 300 ppt. Lightning produces spikes of NO (but not CO) with mixing ratios sometimes exceeding 1000 ppt. This flow pattern tends to leave the midtroposphere relatively clean with concentrations of trace gases similar to those

Trace gas emissions from burning Florida wetlands

Science.gov (United States)

Cofer, Wesley R.; Levine, Joel S.; Winstead, Edward L.; Lebel, Peter J.; Koller, Albert M.; Hinkle, C. Ross

1990-02-01

Measurements of biomass burn-produced trace gases are presented that were obtained using a helicopter at low altitudes above burning Florida wetlands on November 9, 1987, and from both helicopter and light-aircraft samplings on November 7, 1988. Carbon dioxide (CO2) normalized emission ratios (ΔX/ΔCO2; V/V; where X is trace gas) for carbon monoxide (CO), hydrogen (H2), methane (CH4), total nonmethane hydrocarbons (TNMHC), and nitrous oxide (N2O) were obtained over burning graminoid wetlands consisting primarily of Spartina bakeri and Juncus roemerianus. Some interspersed scrub oak (Quercus spp) and saw palmetto (Screnoa repens) were also burned. No significant differences were observed in the emission ratios determined for these gases from samples collected over flaming, mixed, and smoldering phases of combustion during the 1987 fire. Combustion-categorized differences in emission ratios were small for the 1988 fire. Combustion efficiency was relatively good (low emission ratios for reduced gases) for both fires. We believe that the consistently low emission ratios were a unique result of graminoid wetlands fires, in which the grasses and rushes (both small-size fuels) burned rapidly down to standing water and were quickly extinguished. Consequently, the efficiency of the combustion was good and the amount and duration of smoldering combustion was greatly diminished.

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)

Santa Lucia (2008) (L6) Chondrite, a Recent Fall: Composition, Noble Gases, Nitrogen and Cosmic Ray Exposure Age

Science.gov (United States)

Mahajan, Ramakant R.; Varela, Maria Eugenia; Joron, Jean Louis

2016-04-01

The Santa Lucia (2008)—one the most recent Argentine meteorite fall, fell in San Juan province, Argentina, on 23 January 2008. Several masses (total ~6 kg) were recovered. Most are totally covered by fusion crust. The exposed interior is of light-grey colour. Chemical data [olivine (Fa24.4) and low-Ca pyroxene (En77.8 Fs20.7 Wo1.6)] indicate that Santa Luica (2008) is a member of the low iron L chondrite group, corresponding to the equilibrated petrologic type 6. The meteorite name was approved by the Nomenclature Committee (NomCom) of the Meteoritical Society (Meteoritic Bulletin, no. 97). We report about the chemical composition of the major mineral phases, its bulk trace element abundance, its noble gas and nitrogen data. The cosmic ray exposure age based on cosmogenic 3He, 21Ne, and 38Ar around 20 Ma is comparable to one peak of L chondrites. The radiogenic K-Ar age of 2.96 Ga, while the young U, Th-He are of 1.2 Ga indicates that Santa Lucia (2008) lost radiogenic 4He more recently. Low cosmogenic (22Ne/21Ne)c and absence of solar wind noble gases are consistent with irradiation in a large body. Heavy noble gases (Ar/Kr/Xe) indicated trapped gases similar to ordinary chondrites. Krypton and neon indicates irradiation in large body, implying large pre-atmospheric meteoroid.

Atmospheric input of trace substances into the North Sea and the Baltic Sea. Stoffeintrag in Nord- und Ostsee ueber die Atmosphaere

Energy Technology Data Exchange (ETDEWEB)

Grassl, H; Eppel, D; Petersen, G; Schneider, B; Weber, H; Gandrass, J; Reinhardt, K H; Wodarg, D; Fliess, J

1989-01-01

The concentrations and deposition of atmospheric trace substances were measured over the Kiel Bight and the Southern North Sea. A European longrange-transport model was used to calculate the atmospheric concentrations of trace metals and their deposition into the North Sea and the Baltic Sea. Natural and anthropogenic emitted element concentrations could be separated definitely by the measurements, and preferred transport directions of anthropogenic contributions could be found. Concentrations measured over the North Sea could be related to the surrounding emission areas by airmass trajectory analyses. The deposition measurements show that the main removal process is due to deposition by precipitation. Calculated and measured concentrations at several receptor points agreed well. The model results confirm the dominating role of wet deposition. It could be shown that extrapolations from measurements at coastal stations to the whole sea area tend to overestimate the total deposition into North Sea and Baltic Sea. (orig.) With 78 refs., 26 tabs., 85 figs.

Spanish Moss as an atmospheric tracer for trace elements from fossil fuel burning power plants

International Nuclear Information System (INIS)

James, W.D.; Padaki, P.; McWilliams, E.L.

1991-01-01

Samples of Spanish Moss (Tillandsia usneoides) were analyzed by neutron activation analysis (NAA), inductively coupled argon plasma emission spectrometry (ICP), and x-ray fluorescence analysis (XRF) for trace elements as atmospheric environmental monitors. In particular, certain elements thought likely to be contributed to the atmosphere by combustion of fossil fuels were studied in samples collected along two transects, an east/west transect from the Louisiana line west to Dallas and a north/south transect from the Limestone electric Generating Station north to Dallas. Plants were sampled during peak electric generating periods in the summer, as well as following planned outages during the winter months. Se, As and several other volatile species known to concentrate in fly ash particles which are likely to escape power plant collection devices were shown to correlate with downwind directions of plant plumes. Attempts to determine levels of sulfur taken up by the plants which can be attributed to fossil fuel combustion through the use of these marker elements have also be made

Modeling Microbial Processes in EPIC to Estimate Greenhouse Gas Emissions from soils

Science.gov (United States)

Schwab, D. E.; Izaurralde, R. C.; McGill, W. B.; Williams, J. R.; Schmid, E.

2009-12-01

Emissions of trace gases (CO2, N2O and CH4) to the atmosphere from managed terrestrial ecosystems have been contributing significantly to the warming of Earth. Trace gas production is dominated by biospheric processes. An improved knowledge of the soil-plant-atmosphere interface is of key importance for understanding trace gas dynamics. In soils, microbial metabolism plays a key role in the release or uptake of trace gases. Here we present work on the biophysical and biogeochemical model EPIC (Environmental Policy/Integrated Climate) to extend its capabilities to simulate CO2 and N2O fluxes in managed and unmanaged ecosystems. Emphasis will be given to recently developed, microbially-based, denitrification and nitrification modules. The soil-atmosphere exchange of trace gases can be measured by using various equipments, but often these measurements exhibit extreme space-time variability. We use hourly time steps to account for the variability induced by small changes in environmental conditions. Soils are often studied as macroscopic systems, although their functions are predominantly controlled at a microscopic level; i.e. the level of the microorganisms. We include these processes to the extent that these are known and can be quantitatively described. We represent soil dynamics mathematically with routines for gas diffusion, Michael Menten processes, electron budgeting and other processes such as uptake and transformations. We hypothesize that maximization of energy capture form scarce substrates using energetic favorable reactions drives evolution and that competitive advantage can result by depriving a competitor from a substrate. This Microbe Model changes concepts of production of N-containing trace gases; it unifies understanding of N oxidation and reduction, predicts production and evolution of trace gases and is consistent with observations of anaerobic ammonium oxidation.

Areal-averaged trace gas emission rates from long-range open-path measurements in stable boundary layer conditions

Directory of Open Access Journals (Sweden)

K. Schäfer

2012-07-01

Full Text Available Measurements of land-surface emission rates of greenhouse and other gases at large spatial scales (10 000 m² are needed to assess the spatial distribution of emissions. This can be readily done using spatial-integrating micro-meteorological methods like flux-gradient methods which were evaluated for determining land-surface emission rates of trace gases under stable boundary layers. Non-intrusive path-integrating measurements are utilized. Successful application of a flux-gradient method requires confidence in the gradients of trace gas concentration and wind, and in the applicability of boundary-layer turbulence theory; consequently the procedures to qualify measurements that can be used to determine the flux is critical. While there is relatively high confidence in flux measurements made under unstable atmospheres with mean winds greater than 1 m s⁻¹, there is greater uncertainty in flux measurements made under free convective or stable conditions. The study of N₂O emissions of flat grassland and NH₃ emissions from a cattle lagoon involves quality-assured determinations of fluxes under low wind, stable or night-time atmospheric conditions when the continuous "steady-state" turbulence of the surface boundary layer breaks down and the layer has intermittent turbulence. Results indicate that following the Monin-Obukhov similarity theory (MOST flux-gradient methods that assume a log-linear profile of the wind speed and concentration gradient incorrectly determine vertical profiles and thus flux in the stable boundary layer. An alternative approach is considered on the basis of turbulent diffusivity, i.e. the measured friction velocity as well as height gradients of horizontal wind speeds and concentrations without MOST correction for stability. It is shown that this is the most accurate of the flux-gradient methods under stable conditions.

Impact Delivery of Reduced Greenhouse Gases on Early Mars

Science.gov (United States)

Haberle, R. M.; Zahnle, K. J.; Barlow, N. G.

2017-12-01

Reducing greenhouse gases are the latest trend in finding solutions to the early Mars climate dilemma. In thick CO2 atmospheres with modest concentrations of H2 and/or CH4, collision induced absorptions can reduce the outgoing long wave radiation enough to provide a significant greenhouse effect. To raise surface temperatures significantly by this process, surface pressures must be at least 500 mb and H2 and/or CH4 concentrations must be at or above the several percent level. Volcanism, serpentinization, and impacts are possible sources for reduced gases. Here we investigate the delivery of such gases by impact degassing from comets and asteroids. We use a time-marching stochastic impactor model that reproduces the observed crater size frequency distribution of Noachian surfaces. Following each impact, reduced gases are added to the atmosphere from a production function based on gas equilibrium calculations for several classes of meteorites and comets at typical post-impact temperatures. Escape and photochemistry then remove the reduced greenhouse gases continuously in time throughout each simulation. We then conduct an ensemble of simulations with this simple model varying the surface pressure, impact history, reduced gas production and escape functions, and mix of impactor types, to determine if this could be a potentially important part of the early Mars story. Our goal is to determine the duration of impact events that elevate reduced gas concentrations to significant levels and the total time of such events throughout the Noachian. Our initial simulations indicate that large impactors can raise H2 concentrations above the 10% level - a level high enough for a very strong greenhouse effect in a 1 bar CO2 atmosphere - for millions of years, and that the total time spent at or above that level can be in the 10's of millions of years range. These are interesting results that we plan to explore more thoroughly for the meeting.

"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 (costs and 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.

Biomonitor-Reflection of Large-Distance Air Mass Transported Trace Elements

NARCIS (Netherlands)

Henriques Vieira, B.J.

2017-01-01

The present thesis’ topic is the biomonitoring of atmospheric trace elements with attention focused on the long-range transported trace elements. The aim was to provide improved understanding of aerosol characteristics under the atmospheric transport dynamics of Central North Atlantic at different

Geochemical monitoring using noble gases and carbon isotopes: study of a natural reservoir

International Nuclear Information System (INIS)

Jeandel, E.

2008-12-01

To limit emissions of greenhouse gases in the atmosphere, CO 2 geological sequestration appears as a solution in the fight against climate change. The development of reliable monitoring tools to ensure the sustainability and the safety of geological storage is a prerequisite for the implementation of such sites. In this framework, a geochemical method using noble gas and carbon isotopes geochemistry has been tested on natural and industrial analogues. The study of natural analogues from different geological settings showed systematic behaviours of the geochemical parameters, depending on the containment sites, and proving the effectiveness of these tools in terms of leak detection and as tracers of the behaviour of CO 2 . Moreover, an experience of geochemical tracing on a natural gas storage has demonstrated that it is possible to identify the physical-chemical processes taking place in the reservoir to a human time scale, increasing interest in the proposed tool and providing general information on its use. (author)

Decomposition of poly(amide-imide) film using atmospheric pressure non-equilibrium plasma generated in a stream of H2O/Ar mixed gases

International Nuclear Information System (INIS)

Ueshima, M.; Aoki, Y.; Suzuki, K.; Kuwasima, S.; Sugiyama, K.

2010-01-01

Atmospheric pressure non-equilibrium Ar-H 2 O plasma was irradiated to exfoliate a thin film of a heat-resistant polymer, poly(amide-imide) coating on enamel copper wire. The plasma was produced by applying microwave power inducted with Ar-H 2 , Ar-O 2 , Ar-H 2 O or Ar-H 2 -O 2 mixed gases. The poly(amide-imide) thin film was exfoliate by those plasma irradiations. The magnitude of exfoliation depended on the distance of the copper wire from the plasma generating material and reached a maximum at a distance around 4 cm for each plasma irradiation. Surface conditions of the copper wire varied depending on the inducted gases. Ar-O 2 plasma irradiation oxidized the copper surface while other plasmas kept the copper surface unchanged. The time it took to exfoliate the poly(amide-imide) depended on the irradiation source, either Ar-O 2 (within 60 s), Ar-H 2 O (within 70 s), Ar-H 2 -O 2 (within 70 s) or Ar-H 2 (within 125 s). The Ar-H 2 O plasma irradiation under non-equilibrium atmospheric pressure was found to be the best method for exfoliating the poly(amide-imide) thin film coating on enamel copper wires rather than the Ar-H 2 -O 2 plasma because of its simplicity and safety.

Use of 222Rn for estimation of greenhouse gases emissions at Russian territory

Science.gov (United States)

Berezina, E. V.; Elansky, N. F.

2009-04-01

It is well known that 222Rn is widely used as a tracer for studying different atmospheric processes including estimations of greenhouse gases emissions. Calculation of 222Rn fluxes from the soil into the atmosphere allows quantitative estimation of greenhouse gases emissions having the soil origin or sources of which are located near the surface. For accurate estimation of 222Rn fluxes detailed investigations of spatial and temporal variations of its concentrations are necessary. 222Rn concentrations data in the atmospheric surface layer over continental Russia from Moscow to Vladivostok obtained during the six TROICA (Transcontinental Observations Into the Chemistry of the Atmosphere) expeditions of the mobile laboratory along the Trans-Siberian railroad are analyzed. Spatial distribution, diurnal and seasonal variations of surface 222Rn concentrations along the Trans-Siberian railroad are investigated. According to the obtained data surface 222Rn concentration values above continental Russia vary from 0.5 to 75 Bq/m3 depending on meteorological conditions and geological features of the territory with the average value being 8.42 ± 0.10 Bq/m3. The average 222Rn concentration is maximum in the autumn expedition and minimum in the spring one. The factors mostly influencing 222Rn concentration variations are studied: surface temperature inversions, geological features of the territory, precipitations. 222Rn accumulation features in the atmospheric surface layer during night temperature inversions are analyzed. It was noted that during night temperature inversions the surface 222Rn concentration is 7 - 8 times more than the one during the nights without temperature inversions. Since atmospheric stratification determines accumulation and diurnal variations of many atmospheric pollutants as well as greenhouse gases its features are analyzed in detail. Surface temperature inversions were mainly observed from 18:00-19:00 to 06:00-07:00 in the warm season and from 16

Emissions from vegetation fires and their influence on atmospheric composition over the Amazon Basin (Invited)

Science.gov (United States)

Andreae, M. O.; Artaxo, P.; Bela, M. M.; de Freitas, S. R.; Gerbig, C.; Longo, K. M.; Wiedemann, K. T.; Wofsy, S. C.

2010-12-01

Over the past decades, several campaigns have been conducted in the Amazon Basin, during which the emissions from biomass burning were characterized. Other campaigns, as well as remote sensing studies, have produced clear evidence that the budget of traces gases (including CO2) and aerosols over the Basin are strongly perturbed by vegetation fires. We will briefly review these studies and present some recent measurements made during the the Balanço Atmosférico Regional de Carbono na Amazônia (BARCA) aircraft measurement program, which consisted of two aircraft campaigns during November-December 2008 (BARCA-A) and May-June 2009 (BARCA-B). The measurements covered the altitude range from the surface up to about 4500 m, and spanned across the Amazon Basin. While our results confirm the importance of biomass burning for the atmospheric composition over the Amazon Basin in general, they also highlight some complexities. One is the influence of transatlantic transport: Amazonia is downwind of massive fire regions in Africa, and depending on season and locality, these can make an important contribution to the trace gas and aerosol burden over the Amazon Basin. Another difficulty arises from the fact that representative emission ratios for CO relative to CO2 are difficult to obtain in the field, owing to the influence of biospheric exchange on the distribution of CO2 concentrations. The consequences of these and other uncertainties for a quantitative assessment of the sources of trace gases over Amazonia and for the estimation of carbon exchange with the biosphere will be discussed.

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)

The benefit of limb cloud imaging for infrared limb sounding of tropospheric trace gases

Directory of Open Access Journals (Sweden)

G. Heinemann

2009-06-01

Full Text Available Advances in detector technology enable a new generation of infrared limb sounders to measure 2-D images of the atmosphere. A proposed limb cloud imager (LCI mode will detect clouds with a spatial resolution unprecedented for limb sounding. For the inference of temperature and trace gas distributions, detector pixels of the LCI have to be combined into super-pixels which provide the required signal-to-noise and information content for the retrievals. This study examines the extent to which tropospheric coverage can be improved in comparison to limb sounding using a fixed field of view with the size of the super-pixels, as in conventional limb sounders. The study is based on cloud topographies derived from (a IR brightness temperatures (BT of geostationary weather satellites in conjunction with ECMWF temperature profiles and (b ice and liquid water content data of the Consortium for Small-scale Modeling-Europe (COSMO-EU of the German Weather Service. Limb cloud images are simulated by matching the cloud topography with the limb sounding line of sight (LOS. The analysis of the BT data shows that the reduction of the spatial sampling along the track has hardly any effect on the gain in information. The comparison between BT and COSMO-EU data identifies the strength of both data sets, which are the representation of the horizontal cloud extent for the BT data and the reproduction of the cloud amount for the COSMO-EU data. The results of the analysis of both data sets show the great advantage of the cloud imager. However, because both cloud data sets do not present the complete fine structure of the real cloud fields in the atmosphere it is assumed that the results tend to underestimate the increase in information. In conclusion, real measurements by such an instrument may result in an even higher benefit for tropospheric limb retrievals.

A generalized ray-tracing procedure for an atmospheric Cherenkov imaging telescope and optical characteristics of the TACTIC light collector

International Nuclear Information System (INIS)

Tickoo, A.K.; Suthar, R.L.; Koul, R.; Sapru, M.L.; Kumar, N.; Kaul, C.L.; Yadav, K.K.; Thoudam, S.; Kaul, S.K.; Venugopal, K.; Kothari, M.; Goyal, H.C.; Chandra, P.; Dhar, V.K.; Rannot, R.C.; Koul, M.K.; Kaul, S.R.

2005-01-01

A generalized ray-tracing procedure has been developed, which facilitates the design of a multimirror-based light collector used in atmospheric Cherenkov telescopes. This procedure has been employed to study the optical characteristics of the 3.5 m diameter light collector of the TACTIC Imaging telescope. Comparison of the measured point-spread function of the light collector with the simulated performance of ideal Davies-Cotton and paraboloid designs has been made to determine an optimum arrangement of the 34 spherical mirror facets used in the telescope to obtain the best possible point-spread function. A description of the ray-tracing subroutine used for processing CORSIKA-generated Cherenkov data, required for carrying out Monte-Carlo simulation studies, is also discussed in the paper

Analysis of Atmospheric Mercury and Associated Trace Gases in Dallas Fort Worth, TX (Barnett Shale area)

Science.gov (United States)

Laine, P. L.; Talbot, R. W.; Lefer, B. L.; Flynn, J. H.

2012-12-01

Throughout the month of June 2011, a variety of air quality measurements were obtained in the Dallas Fort Worth (Barnett Shale) field campaign. Species such as Hg0, O3, CO, NO, NO2, SO2 were monitored continuously along with a variety of volatile organic carbon (VOC) species ranging in size from C2 (ethane) to C9 aromatics to sesquiterpines. Mixed layer boundary heights were also monitored by Ceilometer measurements. At first glance, the mercury data has peaks that reach as high as 750 ppqv (parts per quadrillion by volume) which is approximately a 5 fold increase over the typical background values observed (~ 150 ppqv). The Fort Worth area has underlying Barnett Shale with thousands of natural gas compressor stations scattered throughout the surrounding landscape. We believe that a potential source of the elevated Hg0 is the result of leakage from these stations under the nocturnal boundary layer. A closer look at diurnal variations and backward wind trajectories will yield information pertaining to the types of air masses spanning the area. We will utilize the suite of chemical and meteorological measurements conducted during the campaign to facilitate source identification for specific time periods. Analysis of these data should provide new information on as yet unexplored sources of atmospheric mercury.

Laser absorption spectroscopy - Method for monitoring complex trace gas mixtures

Science.gov (United States)

Green, B. D.; Steinfeld, J. I.

1976-01-01

A frequency stabilized CO2 laser was used for accurate determinations of the absorption coefficients of various gases in the wavelength region from 9 to 11 microns. The gases investigated were representative of the types of contaminants expected to build up in recycled atmospheres. These absorption coefficients were then used in determining the presence and amount of the gases in prepared mixtures. The effect of interferences on the minimum detectable concentration of the gases was measured. The accuracies of various methods of solution were also evaluated.

An advanced open-path atmospheric pollution monitor for large areas

International Nuclear Information System (INIS)

Taylor, L.

1995-01-01

Large amounts of toxic waste materials, generated in manufacturing fuel for nuclear reactors, are stored in tanks buried over large areas at DOE sites. Flammable and hazardous gases are continually generated by chemical reactions in the waste materials. To prevent explosive concentrations of these gases, the gases are automatically vented to the atmosphere when the pressure exceeds a preset value. Real-time monitoring of the atmosphere above the tanks with automatic alarming is needed to prevent exposing workers to unsafe conditions when venting occurs. This project is to design, develop, and test an atmospheric pollution monitor which can measure concentrations of DOE-specified and EPA-specified hazardous gases over ranges as long as 4km. A CO 2 laser to measure absorption spectra and to determine the distance over which the measurements are made, is combined with an acousto-optic tunable filter (AOTF) to measure thermal emission spectra

Electron beam induced purification of dilute off gases from industrial processes and automobile tunnels

International Nuclear Information System (INIS)

Paur, H.-R.; Maetzing, H.

1993-01-01

The electron beam process has proved to be an efficient method for the removal of inorganic pollutants from flue gas. Since it simulates natural processes which occur in the atmospheric photochemistry, it appeared attractive to investigate the potential of the e-beam process to clean off-gases which contain hydrocarbon and inorganic trace components. Such emissions arise from industrial processes and from automobile tunnels. Commercial solvents were vaporized in air and irradiated with energetic electrons (300 keV). CO, CO 2 and aerosol particles were found as products and were determined quantitatively. The aerosol particles can be collected by a gravel bed filter and can be removed by combustion or biological degradation. From experiments and model calculations it was found that the e-beam process is a very economic tool to remove hydrocarbons from large off-gas volumes at initial concentrations of 50-100 mg C/m 3 , and that NO x can be removed very efficiently from tunnel off-gas. (author)

The atmosphere: Global commons to protect

International Nuclear Information System (INIS)

Obasi, G.O.P.

1996-01-01

One of the most important greenhouse gases is CO 2 , whose concentration in the atmosphere has increased from 280 parts per million by volume (ppmv) to 358ppmv in 1994, giving a general increase of over 27 per cent since pre-industrial times. This increase has been attributed largely to fossil fuel combustion. Significant increases have also been observed in atmospheric concentrations of the other greenhouse gases, including methane, nitrous oxide and global tropospheric ozone. Concentrations of methane and nitrous oxide have, for example, grown by 145 per cent and 15 per cent respectively since pre-industrial times. Such increases have been linked to the rapid world population growth, which has resulted in increasing demands for energy, food, water, shelter and other basic needs. Computer models indicate that the continued accumulation of greenhouse gases in the atmosphere could result in global climate change and global warming. As some uncertainties still exists in the model predictions, it may take a few more years to uniquely separate human-induced climate change signals from natural climate variability in global climate trends

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)

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. Copyright © 2011 Elsevier Ltd. All rights reserved.

Atmospheric trace metal concentrations in Suspended Particulate ...

African Journals Online (AJOL)

The air particulate samples were collected from the kitchens, living rooms and outdoor environment of five households in the community. The quantification of the trace metals was done using Atomic Absorption spectrometry method, employing HNO based wet digestion. High baseline concentration of SPMwere obtained ...

Observations of atmospheric ammonia from TANSO-FTS/GOSAT

Science.gov (United States)

Someya, Yu; Imasu, Ryoichi; Saitoh, Naoko; Shiomi, Kei

2017-04-01

Atmospheric ammonia has large impacts on the nitrogen cycles or atmospheric environment such as nucleation of PM2.5 particles. It is reported that ammonia in the atmosphere has been increasing rapidly with the growth of population globally and this trend must continue in the future. Satellite observation is an effective approach to get to know the global perspectives of the gas. Atmospheric ammonia is observable using the thermal infrared (TIR) spectra, and IASI, TES and CrIS had been revealed those distributions. GOSAT also has TIR band including the ammonia absorption bands. GOSAT has the shorter revisit cycle than that of the other hyper-spectral TIR sounders mentioned above, therefore, the shorter time-scale events can be represented. In addition to the importance of the impacts of ammonia itself, the concentration ratio between ammonia and the other trace gases such as CO which is one of the main targets of the GOSAT-2 project is useful as the indicator of their emission sources. In this study, we introduce an algorithm to retrieve the column amount of atmospheric ammonia based on non-linear optimal estimation (Rogers, 2000) from GOSAT spectra in the ammonia absorption band between 960 - 970 cm-1. Temperature and water vapor profiles are estimated in advance of the ammonia retrieval. The preliminary results showed significant high concentrations of ammonia in the Northern India and the Eastern China as pointed out in the previous researches. We will discuss the global distribution of ammonia in the presentation.

Emission and Sink of Greenhouse Gases in Soils of Moscow

Science.gov (United States)

Mozharova, N. V.; Kulachkova, S. A.; Lebed'-Sharlevich, Ya. I.

2018-03-01

The first inventory and zoning of the emission and sink of methane and carbon dioxide in the urban structure of greenhouse gases from soils and surface technogenic formations (STFs) (Technosols) on technogenic, recrementogenic, and natural sediments have been performed with consideration for the global warming potential under conditions of different formation rate of these gases, underflooding, and sealing. From gas geochemical criteria and anthropogenic pedogenesis features, the main sources of greenhouse gases, their intensity, and mass emission were revealed. The mass fractions of emissions from the sectors of waste and land use in the inventories of greenhouse gas emissions have been determined. New sources of gas emission have been revealed in the first sector, the emissions from which add tens of percent to the literature and state reports. In the second sector, emissions exceed the available data in 70 times. Estimation criteria based on the degree of manifestation and chemical composition of soil-geochemical anomalies and barrier capacities have been proposed. The sink of greenhouse gases from the atmosphere and the internal (latent) sink of methane in soils and STFs have been determined. Ecological functions of soils and STFs have been shown, and the share of latent methane sink has been calculated. The bacterial oxidation of methane in soils and STFs exceeds its emission to the atmosphere in almost hundred times.

Natural sources of gaseous pollutants in the atmosphere

Energy Technology Data Exchange (ETDEWEB)

Altshuller, A P

1958-01-01

Various gaseous pollutants including ozone, nitrous oxide, nitric oxide, nitrogen dioxide, methane, hydrogen, formaldehyde, ammonia, hydrogen sulfide, mercaptans, chlorine compounds and free radicals can be formed by natural processes such as ultraviolet photochemical processes in the upper atmosphere and microbiological processes. The modes of formation and destruction of these gases, especially of their concentrations in the atmosphere, and the various reactions in which these gases can participate with each other are discussed in detail. 114 references.

Toward a List of Molecules as Potential Biosignature Gases for the Search for Life on Exoplanets and Applications to Terrestrial Biochemistry.

Science.gov (United States)

Seager, S; Bains, W; Petkowski, J J

2016-06-01

Thousands of exoplanets are known to orbit nearby stars. Plans for the next generation of space-based and ground-based telescopes are fueling the anticipation that a precious few habitable planets can be identified in the coming decade. Even more highly anticipated is the chance to find signs of life on these habitable planets by way of biosignature gases. But which gases should we search for? Although a few biosignature gases are prominent in Earth's atmospheric spectrum (O2, CH4, N2O), others have been considered as being produced at or able to accumulate to higher levels on exo-Earths (e.g., dimethyl sulfide and CH3Cl). Life on Earth produces thousands of different gases (although most in very small quantities). Some might be produced and/or accumulate in an exo-Earth atmosphere to high levels, depending on the exo-Earth ecology and surface and atmospheric chemistry. To maximize our chances of recognizing biosignature gases, we promote the concept that all stable and potentially volatile molecules should initially be considered as viable biosignature gases. We present a new approach to the subject of biosignature gases by systematically constructing lists of volatile molecules in different categories. An exhaustive list up to six non-H atoms is presented, totaling about 14,000 molecules. About 2500 of these are CNOPSH compounds. An approach for extending the list to larger molecules is described. We further show that about one-fourth of CNOPSH molecules (again, up to N = 6 non-H atoms) are known to be produced by life on Earth. The list can be used to study classes of chemicals that might be potential biosignature gases, considering their accumulation and possible false positives on exoplanets with atmospheres and surface environments different from Earth's. The list can also be used for terrestrial biochemistry applications, some examples of which are provided. We provide an online community usage database to serve as a registry for volatile molecules

High-pressure plastic scintillation detector for measuring radiogenic gases in flow systems

Science.gov (United States)

Schell, W. R.; Vives-Batlle, J.; Yoon, S. R.; Tobin, M. J.

1999-02-01

Radioactive gases are emitted into the atmosphere from nuclear electric power and nuclear fuel reprocessing plants, from hospitals discarding xenon used in diagnostic medicine, as well as from nuclear weapons tests. A high-pressure plastic scintillation detector was constructed to measure atmospheric levels of such radioactive gases by detecting the beta and internal conversion (IC) electron decays. Operational tests and calibrations were made that permit integration of the flow detectors into a portable Gas Analysis, Separation and Purification system (GASP). The equipment developed can be used for measuring fission gases released from nuclear reactor sources and/or as part of monitoring equipment for enforcing the Comprehensive Test Ban Treaty. The detector is being used routinely for in-line gas separation efficiency measurements, at the elevated operational pressures used for the high-pressure swing analysis system (2070 kPa) and at flow rates of 5-15 l/min [1, 2]. This paper presents the design features, operational methods, calibration, and detector applications.

High-pressure plastic scintillation detector for measuring radiogenic gases in flow systems

International Nuclear Information System (INIS)

Schell, W.R.; Vives-Batlle, J.; Yoon, S.R; Tobin, M.J.

1999-01-01

Radioactive gases are emitted into the atmosphere from nuclear electric power and nuclear fuel reprocessing plants, from hospitals discarding xenon used in diagnostic medicine, as well as from nuclear weapons tests. A high-pressure plastic scintillation detector was constructed to measure atmospheric levels of such radioactive gases by detecting the beta and internal conversion (IC) electron decays. Operational tests and calibrations were made that permit integration of the flow detectors into a portable Gas Analysis, Separation and Purification system (GASP). The equipment developed can be used for measuring fission gases released from nuclear reactor sources and/or as part of monitoring equipment for enforcing the Comprehensive Test Ban Treaty. The detector is being used routinely for in-line gas separation efficiency measurements, at the elevated operational pressures used for the high-pressure swing analysis system (2070 kPa) and at flow rates of 5-15 l/min . This paper presents the design features, operational methods, calibration, and detector applications

High-pressure plastic scintillation detector for measuring radiogenic gases in flow systems

CERN Document Server

Schell, W R; Yoon, S R; Tobin, M J

1999-01-01

Radioactive gases are emitted into the atmosphere from nuclear electric power and nuclear fuel reprocessing plants, from hospitals discarding xenon used in diagnostic medicine, as well as from nuclear weapons tests. A high-pressure plastic scintillation detector was constructed to measure atmospheric levels of such radioactive gases by detecting the beta and internal conversion (IC) electron decays. Operational tests and calibrations were made that permit integration of the flow detectors into a portable Gas Analysis, Separation and Purification system (GASP). The equipment developed can be used for measuring fission gases released from nuclear reactor sources and/or as part of monitoring equipment for enforcing the Comprehensive Test Ban Treaty. The detector is being used routinely for in-line gas separation efficiency measurements, at the elevated operational pressures used for the high-pressure swing analysis system (2070 kPa) and at flow rates of 5-15 l/min . This paper presents the design features, opera...

Climate Forcing Data

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Records of changes in solar irradiance, volcanic aerosols, atmospheric trace gases, and other properties thought to influence climate in the past. Parameter keywords...

Trace Metals Concentration Assessment in Urban Particulate Matter ...

African Journals Online (AJOL)

ADOWIE PERE

Principal component analysis revealed that major sources of trace metals in ambient air ... contributed by earth crust and windblown soil .... Source Apportionment: To probe the origin of trace .... atmospheric accumulation of heavy metals and.

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

Ecological geochemical assessment and source identification of trace elements in atmospheric deposition of an emerging industrial area: Beibu Gulf economic zone.

Science.gov (United States)

Zhong, Cong; Yang, Zhongfang; Jiang, Wei; Hu, Baoqing; Hou, Qingye; Yu, Tao; Li, Jie

2016-12-15

Industrialization and urbanization have led to a deterioration in air quality and provoked some serious environmental concerns. Fifty-four samples of atmospheric deposition were collected from an emerging industrial area and analyzed to determine the concentrations of 11 trace elements (As, Cd, Cu, Fe, Hg, Mn, Mo, Pb, Se, S and Zn). Multivariate geostatistical analyses were conducted to determine the spatial distribution, possible sources and enrichment degrees of trace elements in atmospheric deposition. Results indicate that As, Fe and Mo mainly originated from soil, their natural parent materials, while the remaining trace elements were strongly influenced by anthropogenic or natural activities, such as coal combustion in coal-fired power plants (Pb, Se and S), manganese ore (Mn, Cd and Hg) and metal smelting (Cu and Zn). The results of ecological geochemical assessment indicate that Cd, Pb and Zn are the elements of priority concern, followed by Mn and Cu, and other heavy metals, which represent little threat to local environment. It was determine that the resuspension of soil particles impacted the behavior of heavy metals by 55.3%; the impact of the coal-fired power plants was 18.9%; and the contribution of the local manganese industry was 9.6%. The comparison of consequences from various statistical methods (principal component analysis (PCA), cluster analysis (CA), enrichment factor (EF) and absolute principle component score (APCS)-multiple linear regression (MLR)) confirmed the credibility of this research. Copyright © 2016 Elsevier B.V. All rights reserved.

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

Science.gov (United States)

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

2015-01-01

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

Atmospheric Sounder Spectrometer for Infrared Spectral Technology (ASSIST) Instrument Handbook

Energy Technology Data Exchange (ETDEWEB)

Flynn, Connor J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Atmospheric Radiation Measurement (ARM) Program

2016-03-01

The Atmospheric Sounder Spectrometer for Infrared Spectral Technology (ASSIST) measures the absolute infrared (IR) spectral radiance (watts per square meter per steradian per wavenumber) of the sky directly above the instrument. More information about the instrument can be found through the manufacturer’s website. The spectral measurement range of the instrument is 3300 to 520 wavenumbers (cm^-1) or 3-19.2 microns for the normal-range instruments and 3300 to 400 cm^-1 or 3-25 microns, for the extended-range polar instruments. Spectral resolution is 1.0 cm^-1. Instrument field-of-view is 1.3 degrees. Calibrated sky radiance spectra are produced on cycle of about 141 seconds with a group of 6 radiance spectra zenith having dwell times of about 14 seconds each interspersed with 55 seconds of calibration and mirror motion. The ASSIST data is comparable to the Atmospheric Emitted Radiance Interferometer (AERI) data and can be used for 1) evaluating line-by-line radiative transport codes, 2) detecting/quantifying cloud effects on ground-based measurements of infrared spectral radiance (and hence is valuable for cloud property retrievals), and 3) calculating vertical atmospheric profiles of temperature and water vapor and the detection of trace gases.

Ice Cores

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Records of past temperature, precipitation, atmospheric trace gases, and other aspects of climate and environment derived from ice cores drilled on glaciers and ice...

Electric discharge for treatment of trace contaminants

Science.gov (United States)

Flamm, D. L.; Wydeven, T. J. (Inventor)

1978-01-01

A radio frequency glow discharge reactor is described for removing trace oxidizable contaminants from an oxygen bearing atmosphere. The reaction chamber is defined by an inner metal electrode facing a dielectric backed by an outer conductive electrode. In one embodiment, a conductive liquid forms the conductor of an outer electrode and cools the dielectric. A resonator coupled to a variable radio frequency source generates the high voltages for creating a glow discharge in the chamber at a predetermined pressure whereby the trace contaminants are oxidized into a few simple non-toxic products that may be easily recovered. The corresponding process for removal of trace contaminants from an oxygen-bearing atmosphere with high efficiency independent of the concentration level is also disclosed.

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

International Nuclear Information System (INIS)

Ludwig, J.; Andreae, M.O.; Helas, G.; Marufu, L.; University of Utrecht; Lelieveld, J.

1999-01-01

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 -1 year -1 , respectively. In urban centres wood was consumed at an average rate of 0.4±0.26 tonnes capita -1 year -1 . These consumption rates translate into emission outputs from Zimbabwe of 4.6 Tg CO 2 -C year -1 , 0.4 Tg CO-C year -1 , 5.3 Gg NO-N year -1 , 14.5 Gg CH 4 -C year -1 , 24.2 Gg NMHC-C year -1 , 2.9 Gg organic acid-C year -1 (formic and acetic acids) and 48.4 Gg aerosol-C year -1 . For CO 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 2 and CO emission in Zimbabwe

Atmospheric and precipitation chemistry over the North Atlantic Ocean: Shipboard results, April-May 1984

Science.gov (United States)

Church, T. M.; Tramontano, J. M.; Whelpdale, D. M.; Andreae, M. O.; Galloway, J. N.; Keene, W. C.; Knap, A. H.; Tokos, J.

1991-10-01

During a North Atlantic cruise from Dakar, Senegal, to Woods Hole, Massachusetts (April 14-May 11, 1984), crossing the area of 14°-48°N; 17°-70°W, we collected atmospheric aerosols (C, N, S species), gases (SO4, HNO3, dimethyl sulfide (DMS), synthetic organic chemicals), and precipitation (major inorganic/organic ions, trace metals). Air masses that had not contacted land for over 5 days had a composition close to that from the remote marine atmosphere. Oxidation of biogenic DMS to SO4= aerosol accounted for most nss-SO4= in these air masses. Air masses that had transected densely populated North America (in the westerlies) or the Mediterranean/North Africa ( in the easterlies) within 2-5 days of being sampled over the North Atlantic were enriched in acid precursor compounds and synthetic hydrocarbons relative to air that had spent longer over the North Atlantic. Strong acids and trace metals were also elevated in precipitation. Air masses that had transected regions of strong emissions within the preceding 2 days had concentrations of atmospheric pollutants approaching those typically found in continental air masses. More frequent storm tracks between the Icelandic low and the Bermuda high favored transport of North American emissions northeasterly, toward Europe. Trajectory analyses suggested that air masses sampled off the northwest African coast had passed over the Mediterranean. Composition of the aerosol and precipitation of these air masses was also indicative of continental emissions, including biomass and petroleum burning. Transport and deposition of continental emissions to the North Atlantic were significantly influencing surface atmospheric and oceanic chemistry of this region.

Assessing the DICE model: uncertainty associated with the emission and retention of greenhouse gases

International Nuclear Information System (INIS)

Kaufmann, R.K.

1997-01-01

Analysis of the DICE model indicates that it contains unsupported assumptions, simple extrapolations, and mis-specifications that cause it to understate the rate at which economic activity emits greenhouse gases and the rate at which the atmosphere retains greenhouse gases. The model assumes a world population that is 2 billion people lower than the 'base case' projected by demographers. The model extrapolates a decline in the quantity of greenhouse gases emitted per unit of economic activity that is possible only if there is a structural break in the economic and engineering factors have determined this ratio over the last century. The model uses a single equation to simulate the rate at which greenhouse gases accumulate in the atmosphere. The forecast for the airborne fraction generated by this equation contradicts forecasts generated by models that represent the physical and chemical processes which determine the movement of carbon from the atmosphere to the ocean. When these unsupported assumptions, simple extrapolations, and misspecifications are remedied with simple fixes, the economic impact of global climate change increases several fold. Similarly, these remedies increase the impact of uncertainty on estimates for the economic impact of global climate change. Together, these results indicate that considerable scientific and economic research is needed before the threat of climate change can be dismissed with any degree of certainty. 23 refs., 3 figs

Determining Atmospheric Pressure Using a Water Barometer

Science.gov (United States)

Lohrengel, C. Frederick, II; Larson, Paul R.

2012-01-01

The atmosphere is an envelope of compressible gases that surrounds Earth. Because of its compressibility and nonuniform heating by the Sun, it is in constant motion. The atmosphere exerts pressure on Earth's surface, but that pressure is in constant flux. This experiment allows students to directly measure atmospheric pressure by measuring the…

Characterization of Fine Particulate Matter (PM) and Secondary PM Precursor Gases in Mexico City

Energy Technology Data Exchange (ETDEWEB)

Dr. Charles E. Kolb

2008-03-31

This project was one of three collaborating grants designed to understand the atmospheric chemistry and aerosol particle microphysics impacting air quality in the Mexico City Metropolitan Area (MCMA) and its urban plume. The overall effort, titled MCMA- 2006, focused on: 1) the primary emissions of fine particles and precursor gases leading to photochemical production of atmospheric oxidants and secondary aerosol particles and 2) the measurement and analysis of secondary oxidants and secondary fine particular matter (PM) production, with particular emphasis on secondary organic aerosol (SOA). MCAM-2006 pursued it goals through three main activities: 1) performance and publication of detailed analyses of extensive MCMA trace gas and fine PM measurements made by the collaborating groups and others during earlier MCMA field campaigns in 2002 and 2003; 2) deployment and utilization of extensive real-time trace gas and fine PM instrumentation at urban and downwind MCMA sites in support of the MAX-Mex/MILAGRO field measurements in March, 2006; and, 3) analyses of the 2006 MCMA data sets leading to further publications that are based on new data as well as insights from analysis and publication of the 2002/2003 field data. Thirteen archival publications were coauthored with other MCMA-2003 participants. Documented findings included a significantly improved speciated emissions inventory from on-road vehicles, a greatly enhanced understanding of the sources and atmospheric loadings of volatile organic compounds, a unique analysis of the high fraction of ambient formaldehyde from primary emission sources, a much more extensive knowledge of the composition, size distributions and atmospheric mass loadings of both primary and secondary fine PM, including the fact that the rate of MCMA SOA production greatly exceeded that predicted by current atmospheric models, and evaluations of significant errors that can arise from standard air quality monitors for ozone and nitrogen

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

Trace gas concentrations, intertropical convergence, atmospheric fronts, and ocean currents in the tropical Pacific m(Paper 8C1060)

International Nuclear Information System (INIS)

Wilkniss, P.E.; Rodgers, E.B.; Swinnerton, J.W.; Larson, R.E.; Lamontagne, R.A.

1979-01-01

Shipboard measurements of atmospheric 222 Rn, CO, and CH 4 and of dissolved CO in surface waters have been carried out in the equatorial Pacific on a cruise from Ecuador to Hawaii, Tahiti and Panama in March and April of 1974, and during transit from Los Angeles to Antarctica in November and December of 1972. The trace gas results, combined with conventional meteorological data and with satellite images from Nimbus 5 and the defense meteorological satellite project (DMSP), have provided descriptions of the intertropical convergence zones (ITCZ) near 04 0 N, 102 0 W and 03 0 N, 154 0 W in March of 1974, near 04 0 N, 86 0 W in April of 1974, and near 05 0 N, 139 0 W in November of 1972. In all cases the ITCZ seems to be located north of the south equatorial current (SEC) as shown by dissolved CO peaks in surface waters. In April of 1974 a 'second' ITCZ was observed near 01 0 S, 102 0 W just south of the SEC. A stationary front near Hawaii (20 0 N, 147 0 W) in March of 1974 was investigated. The ITCZ was marked by light shifting winds near a zone of heavy cloud cover and precipitation. In the eastern Tropical Pacific atmospheric 222 Rn increases distinctly north of the ITCZ and thus serves as an indicator for the ITCZ. CO and CH 4 do not always increase coincident with atmospheric 222 Rn. The atmospheric features of the stationary front near Hawaii are in many ways similar to those observed for the ITCZ. The front is marked by cloud cover, precipitation zone and light shifting winds. 222 Rn, CO and CH 4 increase signifantly behind the front in subsiding air which was traced back to the Asian continent. The variation of atmospheric 222 Rn, CO and CH 4 with time and geographical area over the equatorial Pacific seems to be a consequence of seasonal variations of the trade wind field and long range transport to the central Pacific from Asia and to the eastern equatorial Pacific from North and Central America

Molecular gas species in the lunar atmosphere

International Nuclear Information System (INIS)

Hoffman, J.H.; Hodges, R.R. Jr.

1975-01-01

There is good evidence for the existence of very small amounts of methane, ammonia and carbon dioxide in the very tenuous lunar atmosphere which consists primarily of the rare gases helium, neon and argon. All of these gases, except 40 Ar, originate from solar wind particles which impinge on the lunar surface and are imbedded in the surface material. Here they may form molecules before being released into the atmosphere, or may be released directly, as is the case for rare gases. Evidence for the existence of the molecular gas species is based on the pre-dawn enhancement of the mass peaks attributable to these compounds in the data from the Apollo 17 Lunar Mass Spectrometer. Methane is the most abundant molecular gas but its concentration is exceedingly low, 1 x 10 3 mol cm -3 , slightly less than 36 Ar, whereas the solar wind flux of carbon is approximately 2000 times that of 36 Ar. Several reasons are advanced for the very low concentration of methane in the lunar atmosphere

Photoacoustic Techniques for Trace Gas Sensing Based on Semiconductor Laser Sources

Directory of Open Access Journals (Sweden)

Vincenzo Spagnolo

2009-12-01

Full Text Available The paper provides an overview on the use of photoacoustic sensors based on semiconductor laser sources for the detection of trace gases. We review the results obtained using standard, differential and quartz enhanced photoacoustic techniques.

Global biomass burning. Atmospheric, climatic, and biospheric implications

International Nuclear Information System (INIS)

Levine, J.S.

1991-01-01

Biomass burning is a significant source of atmospheric gases and, as such, may contribute to global climate changes. Biomass burning includes burning forests and savanna grasslands for land clearing, burning agricultural stubble and waste after harvesting, and burning biomass fuels. The chapters in this volume include the following topics: remote sensing of biomass burning from space;geographical distribution of burning; combustion products of burning in tropical, temperate and boreal ecosystems; burning as a global source of atmospheric gases and particulates; impacts of biomass burning gases and particulates on global climate; and the role of biomass burning on biodiversity and past global extinctions. A total of 1428 references are cited for the 63 chapters. Individual chapters are indexed separately for the data bases

Mechanisms of impact of greenhouse gases on the Earth's ozone layer in the Polar Regions

Science.gov (United States)

Zadorozhny, Alexander; Dyominov, Igor

A numerical 2-D zonally averaged interactive dynamical radiative-photochemical model of the atmosphere including aerosol physics is used to examine the impact of the greenhouse gases CO2, CH4, and N2O on the future long-term changes of the Earth's ozone layer, in particular on its expected recovery after reduction of anthropogenic discharges of chlorine and bromine compounds into the atmosphere. The model allows calculating self-consistently diabatic circu-lation, temperature, gaseous composition of the troposphere and stratosphere at latitudes from the North to South Poles, as well as distribution of sulphate aerosol particles and polar strato-spheric clouds (PSCs) of types I and II. The scenarios of expected changes of the anthropogenic pollutants for the period from 1980 through 2050 are taken from Climate Change 2001. The processes, which determine the influence of anthropogenic growth of atmospheric abun-dance of the greenhouse gases on the long-term changes of the Earth's ozone layer in the Polar Regions, have been studied in details. Expected cooling of the stratosphere caused by increases of greenhouse gases, most importantly CO2, essentially influences the ozone layer by two ways: through temperature dependencies of the gas phase reaction rates and through enhancement of polar ozone depletion via increased PSC formation. The model calculations show that a weak-ness in efficiencies of all gas phase catalytic cycles of the ozone destruction due to cooling of the stratosphere is a dominant mechanism of the impact of the greenhouse gases on the ozone layer in Antarctic as well as at the lower latitudes. This mechanism leads to a significant acceleration of the ozone layer recovery here because of the greenhouse gases growth. On the contrary, the mechanism of the impact of the greenhouse gases on the ozone through PSC modification be-gins to be more effective in Arctic in comparison with the gas phase mechanism in springs after about 2020, which leads to retard

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.

Atmospheric Radiation Measurement Program facilities newsletter, July 2001.; TOPICAL

International Nuclear Information System (INIS)

Holdridge, D. J.

2001-01-01

Global Warming and Methane-Global warming, an increase in Earth's near-surface temperature, is believed to result from the buildup of what scientists refer to as ''greenhouse gases.'' These gases include water vapor, carbon dioxide, methane, nitrous oxide, ozone, perfluorocarbons, hydrofluoro-carbons, and sulfur hexafluoride. Greenhouse gases can absorb outgoing infrared (heat) radiation and re-emit it back to Earth, warming the surface. Thus, these gases act like the glass of a greenhouse enclosure, trapping infrared radiation inside and warming the space. One of the more important greenhouse gases is the naturally occurring hydrocarbon methane. Methane, a primary component of natural gas, is the second most important contributor to the greenhouse effect (after carbon dioxide). Natural sources of methane include wetlands, fossil sources, termites, oceans, fresh-waters, and non-wetland soils. Methane is also produced by human-related (or anthropogenic) activities such as fossil fuel production, coal mining, rice cultivation, biomass burning, water treatment facilities, waste management operations and landfills, and domesticated livestock operations (Figure 1). These anthropogenic activities account for approximately 70% of the methane emissions to the atmosphere. Methane is removed naturally from the atmosphere in three ways. These methods, commonly referred to as sinks, are oxidation by chemical reaction with tropospheric hydroxyl ion, oxidation within the stratosphere, and microbial uptake by soils. In spite of their important role in removing excess methane from the atmosphere, the sinks cannot keep up with global methane production. Methane concentrations in the atmosphere have increased by 145% since 1800. Increases in atmospheric methane roughly parallel world population growth, pointing to anthropogenic sources as the cause (Figure 2). Increases in the methane concentration reduce Earth's natural cooling efficiency by trapping more of the outgoing

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

Science.gov (United States)

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

2016-02-01

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

Biomass burning: Combustion emissions, satellite imagery, and biogenic emissions

International Nuclear Information System (INIS)

Levine, J.S.; Cofer, W.R III; Rhinehart, R.P.; Cahoon, D.R. J.; Winstead, E.L.; Sebacher, S.; Sebacher, D.I.; Stocks, B.J.

1991-01-01

This chapter deals with two different, but related, aspects of biomass burning. The first part of the chapter deals with a technique to estimate the instantaneous emissions of trace gases produced by biomass burning using satellite imagery. The second part of the chapter concerns the recent discovery that burning results in significantly enhanced biogenic emissions of N 2 O, NO, and CH 4 . Hence, biomass burning has both an immediate and long-term impact on the production of trace gases to the atmosphere. The objective of this research is to better assess and quantify the role of this research is to better assess and quantify the role and impact of biomass as a driver for global change. It will be demonstrated that satellite imagery of fires may be used to estimate combustion emissions and may in the future be used to estimate the long-term postburn biogenic emissions of trace gases to the atmosphere

Poisoning of bees with fluorine-containing industrial waste gases in Switzerland

Energy Technology Data Exchange (ETDEWEB)

Maurizio, A; Staub, M

1956-01-01

Mass poisoning of bees in the vicinity of Swiss Al factories was traced to high quantities of F in the waste gases. Plants and pollen in the vicinity contained 10-214 and 0.9-2.8 mg. % F resp., and collected rain water contained 0.1-10.4 mg. F/sg. dm. The dead bees each contained an av. of 15 ..gamma.. F.

The Role of Temporal Evolution in Modeling Atmospheric Emissions from Tropical Fires

Science.gov (United States)

Marlier, Miriam E.; Voulgarakis, Apostolos; Shindell, Drew T.; Faluvegi, Gregory S.; Henry, Candise L.; Randerson, James T.

2014-01-01

Fire emissions associated with tropical land use change and maintenance influence atmospheric composition, air quality, and climate. In this study, we explore the effects of representing fire emissions at daily versus monthly resolution in a global composition-climate model. We find that simulations of aerosols are impacted more by the temporal resolution of fire emissions than trace gases such as carbon monoxide or ozone. Daily-resolved datasets concentrate emissions from fire events over shorter time periods and allow them to more realistically interact with model meteorology, reducing how often emissions are concurrently released with precipitation events and in turn increasing peak aerosol concentrations. The magnitude of this effect varies across tropical ecosystem types, ranging from smaller changes in modeling the low intensity, frequent burning typical of savanna ecosystems to larger differences when modeling the short-term, intense fires that characterize deforestation events. The utility of modeling fire emissions at a daily resolution also depends on the application, such as modeling exceedances of particulate matter concentrations over air quality guidelines or simulating regional atmospheric heating patterns.

Global atmospheric changes.

OpenAIRE

Piver, W T

1991-01-01

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

Noble gases in common rocks and their bearing on noble gas occurrences in the hydrological cycle

International Nuclear Information System (INIS)

Mazor, E.

1978-10-01

The comparison of the noble gases contents in different rocks and in thermal and cold water sources in the French Massif Central was aimed to define the amounts and nature of noble gases contributed by country rocks as opposed to atmospheric noble gases brought in by recharged water. No difference in the noble gas contents was found between waters coming in igneous rocks to those issuing in sedimentary rocks. In both, significant variations in the contents of atmospheric and radiogenic noble gases were found. Radiogenic helium has been found to reveal a positive correlation to the contents of atmospheric Ne, Ar, Kr. This indicates water recharge into the deep part of the systems, mixing with radiogenic He and Ar flushed from igneous and sedimentary rocks and subsequent partial gas loss. Loss of gas is evident from the observed low noble gas contents. These losses have been accompanied by a reversed retention pattern of Ne, Ar, Xc. This reversed retention pattern cannot be an artifact of sampling as well as cannot result by partial steam loss. A similar interpretation for the observed noble gas depletions that agrees with the fact that the observed fractionation patterns are not ''normal'' is given by deuterium and oxygen-18. The stable isotope data seem to exclude partial steam losses

Origins of geothermal gases at Yellowstone

Science.gov (United States)

Lowenstern, Jacob B.; Bergfeld, Deborah; Evans, William C.; Hunt, Andrew G.

2015-01-01

Gas emissions at the Yellowstone Plateau Volcanic Field (YPVF) reflect open-system mixing of gas species originating from diverse rock types, magmas, and crustal fluids, all combined in varying proportions at different thermal areas. Gases are not necessarily in chemical equilibrium with the waters through which they vent, especially in acid sulfate terrain where bubbles stream through stagnant acid water. Gases in adjacent thermal areas often can be differentiated by isotopic and gas ratios, and cannot be tied to one another solely by shallow processes such as boiling-induced fractionation of a parent liquid. Instead, they inherit unique gas ratios (e.g., CH4/He) from the dominant rock reservoirs where they originate, some of which underlie the Quaternary volcanic rocks. Steam/gas ratios (essentially H2O/CO2) of Yellowstone fumaroles correlate with Ar/He and N2/CO2, strongly suggesting that H2O/CO2 is controlled by addition of steam boiled from water rich in atmospheric gases. Moreover, H2O/CO2 varies systematically with geographic location, such that boiling is more enhanced in some areas than others. The δ13C and 3He/CO2 of gases reflect a dominant mantle origin for CO2 in Yellowstone gas. The mantle signature is most evident at Mud Volcano, which hosts gases with the lowest H2O/CO2, lowest CH4 concentrations and highest He isotope ratios (~16Ra), consistent with either a young subsurface intrusion or less input of crustal and meteoric gas than any other location at Yellowstone. Across the YPVF, He isotope ratios (3He/4He) inversely vary with He concentrations, and reflect varied amounts of long- stored, radiogenic He added to the magmatic endmember within the crust. Similarly, addition of CH4 from organic-rich sediments is common in the eastern thermal areas at Yellowstone. Overall, Yellowstone gases reflect addition of deep, high-temperature magmatic gas (CO2-rich), lower-temperatures crustal gases (4He- and CH4-bearing), and those gases (N2, Ne, Ar) added

High-pressure plastic scintillation detector for measuring radiogenic gases in flow systems

International Nuclear Information System (INIS)

Schell, W.R.; Tobin, M.J.; Vives-Batlle, J.; Yoon, S.R.

1999-01-01

Radioactive gases are emitted into the atmosphere from nuclear electric power and nuclear fuel reprocessing plants, from hospitals discarding xenon used in diagnostic medicine, as well as from nuclear weapons tests. A high-pressure plastic scintillation detector was constructed to measure atmospheric levels of such radioactive gases by detecting the beta and internal conversion (IC) electron decays. Operational tests and calibrations were made that permit integration of the flow detectors into a portable Gas Analysis, Separation and Purification system (GASP). The equipment developed can be used for measuring fission gases released from nuclear reactor sources and/or as part of monitoring equipment for enforcing the Comprehensive Test Ban Treaty. The detector is being used routinely for in-line gas separation efficiency measurements, at the elevated operational pressures used for the high-pressure swing analysis system (2070 kPa) and at flow rates of 5-15 l/min. This paper presents the design features, operational methods, calibration, and detector applications. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

Neon and xenon isotopes in MORB: Implications for the earth-atmosphere evolution

International Nuclear Information System (INIS)

Marty, B.

1989-01-01

The isotopic composition of neon and xenon measured in MORB glasses confirm significant deviations from atmospheric values. There are 1. 21 Ne excesses with are attributed to nucleogenic reactions in the mantle; 2. 20 Ne/ 22 Ne ratios higher than the air ratio interpreted as an evidence for the occurrence of solar-type Ne at depth; 3. 129 Xe and 131-136 Xe excesses, attributed to both extinct ( 129 I and 244 Pu) and present ( 238 U) radioactivities. Ne and Xe isotopic signatures in the mantle can hardly be explained in the framework of classical models for the atmospheric evolution (which postulate a mantle origin for atmospheric gases) and appeal for at least two sources of gases. Ne isotopic differences between air and MORB appear too large to be accounted for by any reasonable fractionation process in the mantle. They imply either fractionation of neon during hydrodynamic escape of a primary atmosphere or different degrees of mixing between primordial Ne components, which, in turn imply isolation of the surface reservoir (air) and deep reservoir (mantle) from the accretional period (except for mantle outgassing through volcanism, the contribution of which is 41% at best for 20 Ne). 129 I- 129 Xe, 244 Pu- 238 U- 136 Xe systematics for atmospheric and MORB-type xenon suggest that either atmospheric gases derived from a source whose formation was delayed (≥ 17 Ma) with respect to the mean accretion time of the mantle source and/or atmospheric gases and MORB-type gases derived from chemically distinct sources. These features are consistent with heterogeneous accretion models for the Earth. Volatile degassing was probably contemporaneous to accretional events, following impact degassing, and might have been most efficient during the late stages of Earth formation. (orig.)

Preliminary data on atmospheric aerosol of the Amazon basin

International Nuclear Information System (INIS)

Orsini, C.M.Q.; Artaxo Netto, P.E.; Tabacniks, M.H.

1981-10-01

Preliminary distributions of the trace-elements Al, Si, P, S, Cl, K, Ca, Ti, V and Fe in the atmospheric aerosol of the Amazon Basin have been determined through samples collected from August 23 to September 2 of 1980, at a remote place located in the Amazon Forest, about 30 km NE of the city of Manaus. In all, 10 complete cascade impactors of 6-stage, Battelle model, have been exposed but only with 8 success, thus generating 48 samples. From these, 33 samples have been succesfully analyzed by the PIXE method (Particle Induced X-Ray Emission), using particle beam of the Pelletron Accelerator of the University of Sao Paulo, and the results revealed that the trace-elements S and K have a noticeable predominance, mainly as fine particle size, relative to the others. The high correlation factor found between the fine particle concentrations of S and K (0,96) support the assumption of their common airbone transport on the same particulates, originated from the gas-to-particle conversion of gases exuded by the trees of the forest, their only existing sources. Coarse airborne particles, of a probable soil origin, are also present but in unusually small amounts, as it was revelead by the Al, Si, Ca, Ti and Fe size distribution curves. (Author) [pt

Microwave assisted digestion of atmospheric aerosol samples followed by inductively coupled plasma mass spectrometry determination of trace elements

Energy Technology Data Exchange (ETDEWEB)

Swami, K.; Judd, C.D.; Orsini, J.; Yang, K.X. [New York State Dept. of Health, Albany, NY (United States). Wadsworth Center for Labs. and Research; Husain, L. [New York State Dept. of Health, Albany, NY (United States). Wadsworth Center for Labs. and Research; Dept. of Environmental Health and Toxicology, State Univ. of New York, Albany (United States)

2001-01-01

A microwave digestion method in a closed vessel was developed for the determination of trace metals in atmospheric aerosols using inductively coupled plasma mass spectrometry (ICP-MS). A recovery study for the elements V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Cd, Sb, and Pb was conducted using multi-elemental standard solutions, NIST 1633b Trace Elements in Coal Fly Ash, and NIST 1648 Urban Particulate Matter. A simple digestion method using only HNO{sub 3}/H{sub 2}O{sub 2}gave good recoveries (90%-108%) for all elements except Cr in SRM 1648, but yielded low recoveries for SRM 1633b. A more robust method using HNO {sub 3}/H {sub 2}O {sub 2}/HF/H {sub 3}BO {sub 3} yielded higher recoveries (82%-103%) for the lighter elements (V - Zn) in SRM 1633b, and improved the Cr recovery in SRM 1648, but decreased the Se recovery in both SRMs. A comparative analysis of aerosol samples obtained at a remote mountain location Nathiagali, Pakistan (2.5 km above mean sea level), and Mayville, New York, downwind from the highly industrialized Midwestern United States, was carried out using Instrumental Neutron Activation Analysis (INAA) for the elements Cr, Mn, Fe, Co, Zn, As, Se, and Sb. The simple digestion method yielded excellent agreement for Cr, Fe, Zn, As, Se, and Sb, with slopes of the ICP-MS vs. INAA regressions of 0.90-1.00 and R {sup 2} values of 0.96-1.00. The regressions for Mn and Co had slopes of 0.82 and 0.84 with R {sup 2} values of 0.83 and 0.82, respectively. Addition of HF/H {sub 3}BO {sub 3} did not improve the correlation for any of the elements and degraded the precision somewhat. The technique provides sensitivity and accuracy for trace elements in relatively small aerosol samples used in atmospheric chemistry studies related to SO {sub 2} oxidation in cloud droplets. The ability to determine concentrations of a very large number of elements from a single analysis will permit source apportionment of various trace pollutants and hence strategies to control the

Removal of main exhaust gases of vehicles by a double dielectric barrier discharge

International Nuclear Information System (INIS)

Pacheco, M; Valdivia, R; Pacheco, J; Rivera, C; Alva, E; Santana, A; Huertas, J; Lefort, B; Estrada, N

2012-01-01

Because the health effects and their contribution to climate change, the emissions of toxic gases are becoming more controlled. In order to improve the diminution of toxic gases to the atmosphere, several techniques have been developed; here it will be focus only to automotive emissions. This work deals about the treatment of toxic gases emitted from vehicles by a non-thermal plasma. Several tests were done in a 4-cylinder 2002/Z16SE motor to characterize the vehicle emissions. With these results gas mixture simulating the exhaust gases vehicles, was used in experiments at different conditions employing a double dielectric barrier reactor for their treatment. The removal efficiencies superior to 90% show the competence of the non-thermal plasma reactor to treat these gases. Experimental results are explained with the aid of a simple chemical model that suggests a possible mechanism of degradation of toxic gases. The plasma reactor employed could works at 12V supplied without difficulty by a vehicle battery.

Noble Gas Surface Flux Simulations And Atmospheric Transport

Energy Technology Data Exchange (ETDEWEB)

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

2017-09-30

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

Coupled evolution of the atmospheres and interiors of planets and satellites

International Nuclear Information System (INIS)

Schubert, G.; Turcotte, D.L.; Solomon, S.C.; Sleep, N.H.

1989-01-01

The evolution of a planetary atmosphere can be powerfully influenced by the planetary interior's function as both a source and a sink of atmospheric constituents; the interior can in turn be strongly influenced by the atmosphere because the mechanism of interior heat loss depends on a volatile content for which the atmosphere can serve both as sink and source. The dependence of mantle rheology on volatile content could furnish a feedback mechanism tending to keep regassing/degassing in balance, thereby maintaining a relatively constant atmospheric mass. Consideration of the abundances of radiogenic and nonradiogenic noble gases in the earth's atmosphere, and of the fluxes of these gases from the mantle, support a large degassing event early on, followed by a decrease in degassing efficiency with time and relatively inefficient outgassing over most of geologic time

A laboratory flow reactor with gas particle separation and on-line MS/MS for product identification in atmospherically important reactions

Directory of Open Access Journals (Sweden)

J. F. Bennett

2009-12-01

Full Text Available A system to study the gas and particle phase products from gas phase hydrocarbon oxidation is described. It consists of a gas phase photochemical flow reactor followed by a diffusion membrane denuder to remove gases from the reacted products, or a filter to remove the particles. Chemical analysis is performed by an atmospheric pressure chemical ionization (APCI triple quadrupole mass spectrometer. A diffusion membrane denuder is shown to remove trace gases to below detectable limits so the particle phase can be studied. The system was tested by examining the products of the oxidation of m-xylene initiated by HO radicals. Dimethylphenol was observed in both the gas and particle phases although individual isomers could not be identified. Two furanone isomers, 5-methyl-2(3Hfuranone and 3-methyl-2(5Hfuranone were identified in the particulate phase, but the isobaric product 2,5 furandione was not observed. One isomer of dimethyl-nitrophenol was identified in the particle phase but not in the gas phase.

Analysis of trace gases at ppb levels by proton transfer reaction mass spectrometry (PTR-MS)

International Nuclear Information System (INIS)

Lindinger, W.; Hansel, A.

1996-01-01

A proton transfer reaction mass spectrometry (PTR-MS) system has been developed which allows for on-line measurements of trace gas components with concentrations as low as 1 ppb. The method is based on reactions of H 3 O + ions, which perform non-dissociative proton transfer to most of the common organic trace constituents but do not react with any of the components present in clean air. Examples of medical information obtained by means of breath analysis, of environmental trace analysis, and examples in the field of food chemistry demonstrate the wide applicability of the method. (Authors)

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.

Air pollution, greenhouse gases and climate change : global and regional perspectives

Science.gov (United States)

2009-01-01

Greenhouse gases (GHGs) warm the surface and the atmosphere with significant implications for rainfall, retreat of glaciers and sea ice, sea level, among other factors. What is less recognized than problems with GHGs, however, is a comparably major g...

Prediction of breakdown voltages in novel gases for high voltage insulation

International Nuclear Information System (INIS)

Koch, M.

2015-01-01

This thesis submitted to the Swiss Federal Institute of Technology ETH in Zurich examines the use of sulphur hexafluoride (SF_6) and similar gases as important insulation media for high voltage equipment. Due to its superior insulation properties, SF_6 is widely used in gas-insulated switchgear. However, the gas also has a very high global warming potential and the content of SF_6 in the atmosphere is constantly increasing. The search for new insulation gases using classical breakdown experiments is discussed. A model for SF_6 based on the stepped leader model is described. This calculates the breakdown voltages in arbitrary electrode configurations and under standard voltage waveforms. Thus, the thesis provides a method for the prediction of breakdown voltages of arbitrary field configurations under standard voltage waveforms for gases with electron-attaching properties. With this, further gases can be characterized for usage as high voltage insulation media

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

Energy Technology Data Exchange (ETDEWEB)

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

2007-07-01

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

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

International Nuclear Information System (INIS)

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

2007-01-01

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

ENERGY RELAXATION OF HELIUM ATOMS IN ASTROPHYSICAL GASES

International Nuclear Information System (INIS)

Lewkow, N. R.; Kharchenko, V.; Zhang, P.

2012-01-01

We report accurate parameters describing energy relaxation of He atoms in atomic gases, important for astrophysics and atmospheric science. Collisional energy exchange between helium atoms and atomic constituents of the interstellar gas, heliosphere, and upper planetary atmosphere has been investigated. Energy transfer rates, number of collisions required for thermalization, energy distributions of recoil atoms, and other major parameters of energy relaxation for fast He atoms in thermal H, He, and O gases have been computed in a broad interval of energies from 10 meV to 10 keV. This energy interval is important for astrophysical applications involving the energy deposition of energetic atoms and ions into atmospheres of planets and exoplanets, atmospheric evolution, and analysis of non-equilibrium processes in the interstellar gas and heliosphere. Angular- and energy-dependent cross sections, required for an accurate description of the momentum-energy transfer, are obtained using ab initio interaction potentials and quantum mechanical calculations for scattering processes. Calculation methods used include partial wave analysis for collisional energies below 2 keV and the eikonal approximation at energies higher than 100 eV, keeping a significant energy region of overlap, 0.1-2 keV, between these two methods for their mutual verification. The partial wave method and the eikonal approximation excellently match results obtained with each other as well as experimental data, providing reliable cross sections in the astrophysically important interval of energies from 10 meV to 10 keV. Analytical formulae, interpolating obtained energy- and angular-dependent cross sections, are presented to simplify potential applications of the reported database. Thermalization of fast He atoms in the interstellar gas and energy relaxation of hot He and O atoms in the upper atmosphere of Mars are considered as illustrative examples of potential applications of the new database.

The Fate of Trace Contaminants in a Crewed Spacecraft Cabin Environment

Science.gov (United States)

Perry, Jay L.; Kayatin, Matthew J.

2016-01-01

Trace chemical contaminants produced via equipment offgassing, human metabolic sources, and vehicle operations are removed from the cabin atmosphere by active contamination control equipment and incidental removal by other air quality control equipment. The fate of representative trace contaminants commonly observed in spacecraft cabin atmospheres is explored. Removal mechanisms are described and predictive mass balance techniques are reviewed. Results from the predictive techniques are compared to cabin air quality analysis results. Considerations are discussed for an integrated trace contaminant control architecture suitable for long duration crewed space exploration missions.

Ultra-trace Measurements in the WAIS Divide 06A Ice Core, Version 1

Data.gov (United States)

National Aeronautics and Space Administration — These data contain the results of gas chromatography mass spectrometry (GC-MS) analysis of 207 samples from the WAIS Divide 06A ice core. The trace gases found in...

Factors controlling the solubility of trace metals in atmospheric aerosols over the Eastern Mediterranean

Science.gov (United States)

Nikolaou, Panagiota; Mihalopoulos, Nikolaos; Kanakidou, Maria

2015-04-01

Atmospheric input of aerosols is recognized, as an important source of nutrients, for the oceans. The chemical interactions between aerosols and varying composition of air masses lead to different coating of their surfaces with sulfate, nitrate and organic compounds, increasing their solubility and their role as a carrier of nutrients and pollutants in ecosystems. Recent works have highlighted that atmospheric inputs of nutrients and trace metals can considerably influence the marine ecosystem functioning at semi-enclosed or enclosed water bodies such as the eastern Mediterranean. The current work aims to determine the sources and the factors controlling the variability of nutrients in the eastern Mediterranean. Special focus has been given on trace elements solubility, considered either as key nutrients for phytoplankton growth such as iron (Fe), phosphorus (P) or inhibitors such as copper (Cu). This has been accomplished by analyzing size segregated aerosol samples collected at the background site of Finokalia in Crete for an entire year. Phosphorus concentrations indicate important increases in air masses influenced both by anthropogenic activities in the northeast European countries and by dust outbreaks. The last is confirmed by the correlation observed between total P and dust concentrations and by the air mass backward trajectories computed by running the NOAA Hysplit Model (Hybrid Single - Particle Langrangian Integrated Trajectory (http://www.arl.noaa.gov/ready/hysplit4.html). Overall 73% of total P has been found to be associated with anthropogenic sources. The solubility of P and Fe has been found to be closely related to the acidity (pH) and dust amount in aerosols. The aerosol pH was predicted using thermodynamic modeling (ISORROPIA-II), meteorological observations (RH, T), and gas/particle observations. More specifically P and Fe solubility appears to be inversely related to the crustal elements levels, while it increases in acidic environment. The

Sensitivity of direct global warming potentials to key uncertainties

International Nuclear Information System (INIS)

Weubbles, D.J.; Jain, A.K.; Palten, K.O.; Grant, K.E.

1995-01-01

The concept of global warming potential was developed as a relative measure of the potential effects on climate of a greenhouse gas. In this paper a series of sensitivity studies examines several uncertainties in determination of Global Warming Potentials (GWPs). The original evaluation of GWPs did not attempt to account for the possible sinks of carbon dioxide (CO 2 ) that could balance the carbon cycle and produce atmospheric concentrations of CO 2 that match observations. In this study, a balanced carbon cycle model is applied in calculation of the radiative forcing from CO 2 . Use of the balanced model produces up to 21% enhancement of the GWPs for most trace gases compared with the IPCC (1990) values for time horizons up to 100 years, but a decreasing enhancement with longer time horizons. Uncertainty limits of the fertilization feedback parameter contribute a 20% range in GWP values. Another systematic uncertainty in GWPs is the assumption of an equilibrium atmosphere (one in which the concentration of trace gases remains constant) versus a disequilibrium atmosphere (one in which the concentration of trace gases varies with time). The latter gives GWPs that are 19 to 32% greater than the former for a 100 year time horizons, depending upon the carbon dioxide emission scenario chosen. Five scenarios are employed: constant-concentration, constant-emission past 1990 and the three IPCC (1992) emission scenarios. For the analysis of uncertainties in atmospheric lifetime (tor) of the GWP changes in direct proportion to (tor) for short-lived gases, but to a lesser extent for gases with (tor) greater than the time horizontal for the GWP calculation. 40 refs., 7 figs., 13 tabs

Atmospheric dry deposition fluxes of trace elements measured in Bursa, Turkey

International Nuclear Information System (INIS)

Tasdemir, Yuecel; Kural, Can

2005-01-01

Trace element dry deposition fluxes were measured using a smooth, greased, knife-edge surrogate surface (KSS) holding greased Mylar strips in Bursa, Turkey. Sampling program was conducted between October 2002 and June 2003 and 46 dry deposition samples were collected. The average fluxes of crustal metals (Mg, Ca, and Fe) were one to four orders of magnitude higher than the fluxes of anthropogenic metals. Trace element fluxes ranged from 3 (Cd) to 24 230 (Ca) μg m -2 d -1 . The average trace element dry deposition fluxes measured in this study were similar to those measured in other urban areas. In addition, ambient air samples were also collected simultaneously with flux samples and concentrations of trace elements, collected with a TSP sampler, were between 0.7 and 4900 ng m -3 for Cd and Ca, respectively. The overall trace element dry deposition velocities, calculated by dividing the fluxes to the particle phase concentrations ranged from 2.3±1.7 cm s -1 (Pb) to 11.1±6.4 cm s -1 (Ni). These values are in good agreement with the values calculated using similar techniques. The anthropogenic and crustal contributions were estimated by employing enrichment factors (EFs) calculated relative to the average crustal composition. Low EFs for dry deposition samples were calculated. This is probably due to contamination of local dust and its important contribution to the collected samples. - Mechanical turbulence has an important influence on re-suspension and dry deposition of trace elements in an urban area

Distribution of inert gases in fines from the Cayley-Descartes region

Science.gov (United States)

Walton, J. R.; Lakatos, S.; Heymann, D.

1973-01-01

The inert gases in 14 different fines and in one sample of 2 to 4 mm fines from Apollo 16 were measured by mass spectroscopy with respect to trapped solar wind gases, cosmogenic gases, and 'parentless' Ar-40. Such studies are helpful for the understanding of regolith evolution, of transport of regolith fines, and of the lunar atmosphere. The Apollo 16 soils are unique because they represent, after Luna 20, the second and much more extensive record from the lunar highlands. The landing site presents the problem of materials from the Cayley Formation vs those from the Descartes Formation. There are two large, relatively fresh craters in the area, North Ray and South Ray, whose ejecta patterns may be recognized in the inert-gas record.

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, X.; Zhang, Y.; Huey, L. G.; Yokelson, R. J.; Wang, Y.; Jimenez, J. L.; Campuzano-Jost, P.; Beyersdorf, A. J.; Blake, D. R.; Choi, Y.;

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

GYRO-INTERACTION OF MICROWAVES IN MAGNETO PLASMAS IN ATMOSPHERIC GASES

Energy Technology Data Exchange (ETDEWEB)

Narasinga Rao, K. V.; Goldstein, L.

1963-05-15

Electron cyclotron resonance absorption of microwave energy by the electron gas in decaying magneto plasmas of oxygen and nitrogen gases is investigated. The technique of interaction of microwaves of diffent frequencies is utilized to measure the enhancement in electronic energy caused by resonance absorption. The results of these experiments show that the inelastic collisions of low energy electrons introduce a barrier for rapid heating of the electron gas. The implication of these results to the control of the ionospheric plasma parameters by radio frequency EM waves is discussed. (auth)

Evaluating the suitability of different environmental samples for tracing atmospheric pollution in industrial areas.

Science.gov (United States)

Francová, Anna; Chrastný, Vladislav; Šillerová, Hana; Vítková, Martina; Kocourková, Jana; Komárek, Michael

2017-01-01

Samples of lichens, snow and particulate matter (PM 10 , 24 h) are used for the source identification of air pollution in the heavily industrialized region of Ostrava, Upper Silesia, Czech Republic. An integrated approach that uses different environmental samples for metal concentration and Pb isotope analyses was applied. The broad range of isotope ratios in the samples indicates a combination of different pollution sources, the strongest among them being the metallurgical industry, bituminous coal combustion and traffic. Snow samples are proven as the most relevant indicator for tracing metal(loid)s and recent local contamination in the atmosphere. Lichens can be successfully used as tracers of the long-term activity of local and remote sources of contamination. The combination of PM 10 with snow can provide very useful information for evaluation of current pollution sources. Copyright © 2016 Elsevier Ltd. All rights reserved.

Application of copper sulfate pentahydrate as an ammonia removal reagent for the determination of trace impurities in ammonia by gas chromatography.

Science.gov (United States)

Aomura, Yoko; Kobayashi, Yoshihiko; Miyazawa, Yuzuru; Shimizu, Hideharu

2010-03-12

Rapid analysis of trace permanent gas impurities in high purity ammonia gas for the microelectronics industry is described, using a gas chromatograph equipped with a phtoionization detector. Our system incorporates a reactive precolumn in combination with the analytical column to remove the ammonia matrix peak that otherwise would complicate the measurements due to baseline fluctuations and loss of analytes. The performance of 21 precolumn candidate materials was evaluated. Copper sulfate pentahydrate (CuSO(4).5H(2)O) was shown to selectively react with ammonia at room temperature and atmospheric column pressures, without affecting the hydrogen, oxygen, nitrogen, methane or carbon monoxide peak areas. To prevent loss of trace carbon dioxide, an additional boron trioxide reactant layer was inserted above the copper sulfate pentahydrate bed in the reactive precolumn. Using the combined materials, calibration curves for carbon dioxide proved to be equivalent in both ammonia and helium matrix gases. These curves were equivalent in both matrix gases. The quantitative performance of the system was also evaluated. Peak repeatabilities, based on eight injections, were in the range of 4.1-8.2% relative standard deviation; and detection limits were 6.9 ppb for H(2), 1.8 ppb for O(2), 1.6 ppb for N(2), 6.4 ppb for CH(4), 13 ppb for CO, and 5.4 ppb for CO(2). Copyright (c) 2010 Elsevier B.V. All rights reserved.

Design and alignment of the MIPAS focal plane system

NARCIS (Netherlands)

Smorenburg, C.; Visser, H.; Moddemeijer, K.

1996-01-01

The Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) is selected by ESA for the ENVISAT-mission, scheduled for launch in 1999. The instrument will measure the concentration of atmospheric trace gases in the earth atmosphere in a spectral region from 4.15-14.6 rim. MIPAS consists of

Atmospheric Chemistry Over Southern Africa

Science.gov (United States)

Gatebe, Charles K.; Levy, Robert C.; Thompson, Anne M.

2011-01-01

During the southern African dry season, regional haze from mixed industrial pollution, biomass burning aerosol and gases from domestic and grassland fires, and biogenic sources from plants and soils is worsened by a semi-permanent atmosphere gyre over the subcontinent. These factors were a driver of several major international field campaigns in the 1990s and early 2000s, and attracted many scientists to the region. Some researchers were interested in understanding fundamental processes governing chemistry of the atmosphere and interaction with climate change. Others found favorable conditions for evaluating satellite-derived measurements of atmospheric properties and a changing land surface. With that background in mind a workshop on atmospheric chemistry was held in South Africa. Sponsored by the International Commission for Atmospheric Chemistry and Global Pollution (ICACGP; http://www.icacgp.org/), the workshop received generous support from the South African power utility, Eskom, and the Climatology Research Group of the University of the Witwatersrand, Johannesburg, South Africa. The purpose of the workshop was to review some earlier findings as well as more recent findings on southern African climate vulnerability, chemical changes due to urbanization, land-use modification, and how these factors interact. Originally proposed by John Burrows, president of ICACGP, the workshop was the first ICACGP regional workshop to study the interaction of air pollution with global chemical and climate change. Organized locally by the University of the Witwatersrand, the workshop attracted more than 60 delegates from South Africa, Mozambique, Botswana, Zimbabwe, France, Germany, Canada, and the United States. More than 30 presentations were given, exploring both retrospective and prospective aspects of the science. In several talks, attention was focused on southern African chemistry, atmospheric pollution monitoring, and climate processes as they were studied in the field

Evidence for a link between atmospheric thermonuclear detonations and nitric acid

International Nuclear Information System (INIS)

Holdsworth, G.

1986-01-01

Data are presented for an ice core, which show that during the era of intense atmospheric thermonuclear weapons testing, a significant part of the nitrate content in the snow was modulated by the intensity of the nuclear detonations. The fixation of nitrogen by nuclear fireballs leads to NOsub(x) gases in the atmosphere and ultimately to nitric acid in precipitation. At certain concentrations, these gases and the associated aerosols may perturb the climate. (author)

enrichment factor of atmospheric trace metal using zirconium

African Journals Online (AJOL)

user

Twelve (12) elements (Cl, K, Ca, Ti, V, Fe, Ni, Cu, Zn, Ba, Sr, and Zr ) were detected in total suspended particulate matter (TSP) ..... Ni and V didn't show spatial variation (p>0.05). For K, ..... K.A. Wet deposition of trace metals to a remote.

PALOMA : An instrument to measure the molecular, elemental and isotopic composition of Mars atmosphere from a landed platform (MSL 09, EXOMARS)

Science.gov (United States)

Chassefière, E.; Paloma Team

2003-04-01

An instrument to analyze the molecular, elemental and isotopic composition of Mars atmosphere from a landed platform is being developed under CNES funding. This instrument, called PALOMA (PAyload for Local Observation of Mars Atmosphere), will be proposed in response to the AO for the instrumentation of the NASA Mars Smart Lander mission, planned to be launched in 2009. It might be part as well of the EXOMARS mission presently studied at ESA in the frame of the Aurora program. Noble gases (He, Ne, Ar, Xr, Xe) and stable isotopes (C, H, O, N) will be analyzed by using a system of gas purification and separation, coupled with a mass spectrometer. The heaviest, radioactive, noble gas (Rn) and its short-lived daughters will be measured using a small additional device (alpha particle detector). Detailed search for trace constituents of astrobiological interest, like CH_4, H_2CO, N_2O, H_2S (abundances, isotopic ratios, time variability) will be done on a regular temporal basis during one Martian year. Isotopic ratios will be measured with an accuracy of about 1 ppm, or better, in order to provide a clear diagnosis of possible life signatures, to allow a detailed comparison of Earth and Mars atmospheric fractionation patterns and, finally, to accurately disentangle escape, climatic, geochemical and hypothesized biological effects. High sensitivity is required for elemental and isotopic compositions of trace gases of interest (a small fraction of ppbv). Such an accurate monitoring of Mars atmosphere volatile composition is expected to provide the necessary reference for future composition studies of minerals, soils, bio-markers, polar cap material, either by in-situ measurement, or from laboratory analyses of returned samples. The PALOMA instrument consists of : a gas purification and separation line, using techniques of chemical and cryogenic trapping, and possibly membrane permeation, a mass spectrometer working in static mode, a turbo-molecular pump that provides the

The Significance of Land-Atmosphere Processes in the Earth System

Science.gov (United States)

Suni, T.; Kulmala, M. T.; Guenther, A. B.

2012-12-01

The land-atmosphere interface is where humans primarily operate. Humans modify the land surface in many ways that influence the fluxes of energy and trace gases between land and atmosphere. Their emissions change the chemical composition of the atmosphere and anthropogenic aerosols change the radiative balance of the globe directly by scattering sunlight back to space and indirectly by changing the properties of clouds. Feedback loops among all these processes, land, the atmosphere, and biogeochemical cycles of nutrients and trace gases extend the human influence even further. Over the last decade, the importance of land-atmosphere processes and feedbacks in the Earth System has been shown on many levels and with multiple approaches, and a number of publications have shown the crucial role of the terrestrial ecosystems as regulators of climate [1-6]. Modellers have clearly shown the effect of missing land cover changes and other feedback processes and regional characteristics in current climate models and recommended actions to improve them [7-11]. Unprecedented insights of the long-term net impacts of aerosols on clouds and precipitation have also been provided [12-14]. Land-cover change has been emphasized with model intercomparison projects that showed that realistic land-use representation was essential in land surface modelling [11, 15]. Crucially important tools in this research have been the networks of long-term flux stations and large-scale land-atmosphere observation platforms that are also beginning to combine remote sensing techniques with ground observations [16-20]. Human influence has always been an important part of land-atmosphere science but in order to respond to the new challenges of global sustainability, closer ties with social science and economics groups will be necessary to produce realistic estimates of land use and anthropogenic emissions by analysing future population increase, migration patterns, food production allocation, land

Which climate gases is it the most important to reduce?

International Nuclear Information System (INIS)

Godal, Odd; Fuglestvedt, Jan

2002-01-01

If the Kyoto Protocol had used another method for comparing the various climate gases, Norway might have had to implement more and more expensive measures. The selection of methods may be important for the making of new agreements after Kyoto. Calculations show the importance of the comparison methods for the various climate gases in negotiating new climate agreements. The Kyoto Protocol regulates the total emission of climate gases carbon dioxide (CO 2 ), methane (CH 4 ), laughing gas (N 2 O) and sulphur hexafluoride (SF 6 ), and halo fluoro carbons and perfluoro carbon. It is up to each country to choose which of these gases to concentrate on, and a tool is therefore needed to compare the effects of the various gases. In the Kyoto agreement, this is done by means of the global warming potential (GWP) of each gas over a period of 100 years. But different climate gases have different atmospheric residence times and it is not evident how the gases must be compared. Reducing the emission of methane has a strong and short-term effect while reducing the emission of carbon dioxide has a weaker but more lasting effect. Researchers have suggested other ways of comparison than the one used in the Kyoto Protocol. Among other things one may calculate the global warming potential for another time horizon than 100 years. Researchers at Cicero have investigated the consequences of two other ways of weighing climate gases: GWP(20) with time horizon of 20 years gives more weight to short-lived gases like methane, while GWP(500) with a time horizon of 500 years is more favourable to the long-lived gases. To see how much the selection of comparing method means in practice, the consequences for Norway using GWP(20) or GWP(500), have been calculated

Acceleration of radiative transfer model calculations for the retrieval of trace gases under cloudy conditions