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  • 1
    Publication Date: 2012-06-08
    Description: Based on a case-study of the nickel smelter in Norilsk (Siberia), the retrieval of trace gas fluxes using airborne remote sensing is discussed. A DOAS system onboard an Airbus 340 detected large amounts of SO2 and NO2 near Norilsk during a regular passenger flight within the CARIBIC project. The remote sensing data were combined with ECMWF wind data to estimate the SO2 output of the Norilsk industrial complex to be around 1 Mt per year, which is in agreement with independent estimates. This value is compared to results using data from satellite remote sensing (GOME, OMI). The validity of the assumptions underlying our estimate is discussed, including the adaptation of this method to other gases and sources like the NO2 emissions of large industries or cities.
    Print ISSN: 0148-0227
    Topics: Geosciences , Physics
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 2
    Publication Date: 2011-01-05
    Description: A measurement intensive was carried out in Barrow, Alaska, in spring 2009 as part of the Ocean-Atmosphere-Sea-Ice–Snowpack (OASIS) program. The central focus of this campaign was the role of halogen chemistry in the Arctic. A chemical ionization mass spectrometer (CIMS) performed in situ bromine oxide (BrO) measurements. In addition, a long path-differential optical absorption spectrometer (LP-DOAS) measured the average concentration of BrO along light paths of either 7.2 or 2.1 km. A comparison of the 1 min observations from both instruments is presented in this work. The two measurements were highly correlated and agreed within their uncertainties (R2 = 0.74, slope = 1.10, and intercept = −0.15 pptv). Better correlation was found (R2 = 0.85, slope = 1.04, and intercept = −0.11 pptv) for BrO observations at moderate wind speeds (〉3 m s−1 and
    Print ISSN: 0148-0227
    Topics: Geosciences , Physics
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 3
    Publication Date: 2011-09-27
    Description: We present results from multiaxis differential optical absorption spectroscopy (MAX-DOAS) and long-path DOAS (LP-DOAS) measurements performed at the North Slope of Alaska from February to April 2009 as part of the Ocean-Atmosphere-Sea Ice-Snowpack Barrow 2009 campaign. For the first time, vertical profiles of aerosol extinction and BrO in the boundary layer were retrieved simultaneously from MAX-DOAS measurements using the method of optimal estimation. Even at very low visibility, retrieved extinction profiles and aerosol optical thickness are in good agreement with colocated ceilometer and Sun photometer measurements, respectively. BrO surface concentrations measured by MAX-DOAS and LP-DOAS are in very good agreement, and it has been found that useful information on the BrO vertical distribution can be retrieved from MAX-DOAS even in cases when blowing snow strongly reduces visibility. The retrieved BrO and extinction vertical profiles allow for a thorough characterization of the vertical structure of the boundary layer during numerous ozone depletion events observed during Barrow 2009. High BrO concentrations are usually present during the onset of ozone depletion events, and BrO disappears as ozone concentrations approach zero. The finding that elevated BrO concentrations occur mainly in the presence of high extinction near the surface strongly suggests that release of reactive bromine from airborne aerosols and/or ice particles at high wind speed plays an important role. Back trajectory calculations indicate that the particles were transported from the frozen ocean to the measurement site and that the release of reactive bromine from sea ice and/or frost flowers occurs when low temperatures (
    Print ISSN: 0148-0227
    Topics: Geosciences , Physics
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 4
    Publication Date: 1999
    Description: Episodes of elevated bromine oxide (BrO) concentration are known to occur at high latitudes in the Arctic boundary layer and to lead to catalytic destruction of ozone at those latitudes; these events have not been observed at lower latitudes. With the use of differential optical absorption spectroscopy (DOAS), locally high BrO concentrations were observed at mid-latitudes at the Dead Sea, Israel, during spring 1997. Mixing ratios peaked daily at around 80 parts per trillion around noon and were correlated with low boundary-layer ozone mixing ratios.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hebestreit -- Stutz -- Rosen -- Matveiv V -- Peleg -- Luria -- Platt -- New York, N.Y. -- Science. 1999 Jan 1;283(5398):55-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉K. Hebestreit, J. Stutz, U. Platt, Institut fur Umweltphysik, Ruprecht-Karls-Universitat Heidelberg, Im Neuenheimer Feld 366, D-69120 Heidelberg, Germany. D. Rosen, V. Matveiv, M. Peleg, M. Luria, Environmental Science, School of Applie.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9872738" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2005-03-19
    Description: In the past two centuries, atmospheric methane has more than doubled and now constitutes 20% of the anthropogenic climate forcing by greenhouse gases. Yet its sources are not well quantified, introducing uncertainties in its global budget. We retrieved the global methane distribution by using spaceborne near-infrared absorption spectroscopy. In addition to the expected latitudinal gradient, we detected large-scale patterns of anthropogenic and natural methane emissions. Furthermore, we observed unexpectedly high methane concentrations over tropical rainforests, revealing that emission inventories considerably underestimated methane sources in these regions during the time period of investigation (August through November 2003).〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Frankenberg, C -- Meirink, J F -- van Weele, M -- Platt, U -- Wagner, T -- New York, N.Y. -- Science. 2005 May 13;308(5724):1010-4. Epub 2005 Mar 17.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Environmental Physics, University of Heidelberg, INF 229, 69120 Heidelberg, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15774724" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2011-09-24
    Description: Megacities are immense sources of air pollutants, with large impacts on air quality and climate. However, emission inventories in many of them still are highly uncertain, particularly in developing countries. Satellite observations allow top-down estimates of emissions to be made for nitrogen oxides (NO(x) = NO + NO(2)), but require poorly quantified a priori information on the NO(x) lifetime. We present a method for the simultaneous determination of megacity NO(x) emissions and lifetimes from satellite measurements by analyzing the downwind patterns of NO(2) separately for different wind conditions. Daytime lifetimes are ~4 hours at low and mid-latitudes, but ~8 hours in wintertime for Moscow. The derived NO(x) emissions are generally in good agreement with existing emission inventories, but are higher by a factor of 3 for the Saudi Arabian capital Riyadh.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Beirle, Steffen -- Boersma, K Folkert -- Platt, Ulrich -- Lawrence, Mark G -- Wagner, Thomas -- New York, N.Y. -- Science. 2011 Sep 23;333(6050):1737-9. doi: 10.1126/science.1207824.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max-Planck-Institut fur Chemie, Joh.-Joachim-Becherweg 27, 55128 Mainz, Germany. steffen.beirle@mpic.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21940891" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
    Publication Date: 2014-06-07
    Description: In-situ measurements have been the basis for monitoring volcanic gas emissions for many years and - being complemented by remote sensing techniques - still play an important role to date. Concerning in-situ techniques for sampling a dilute plume, an increase in accuracy and a reduction of detection limits are still necessary for most gases (e.g. CO 2 , SO 2 , HCl, HF, HBr, HI). In this work the Raschig-Tube technique (RT) is modified and utilized for application on volcanic plumes. The theoretical and experimental absorption properties of the RT and the Drechsel bottle (DB) set-ups are characterized and both are applied simultaneously to the well-established Filter packs technique (FP) in the field (on Stromboli Island and Mount Etna). The comparison points out that FPs are the most practical to apply but the results are error-prone compared to RT and DB, whereas the RT results in up to 13-times higher analyte concentrations than the DB in the same sampling time. An optimization of the analytical procedure, including sample pre-treatment and analysis by titration, Ion Chromatography, and Inductively Coupled Plasma Mass Spectrometry, led to a comprehensive data set covering a wide range of compounds. In particular, less abundant species were quantified more accurately and iodine was detected for the first time in Stromboli's plume. Simultaneously applying Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) the chemical transformation of emitted bromide into bromine monoxide (BrO) from Stromboli and Etna was determined to 3-6% and 7%, respectively, within less than 5 minutes after the gas release from the active vents.
    Electronic ISSN: 1525-2027
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 8
    Publication Date: 2023-07-20
    Description: Volatiles released from magma can form bubbles and leave the magma body to eventually mix with atmospheric air. The composition of those volatiles, as derived from measurements made after their emission, is used to draw conclusions on processes in the Earth's interior or their influences on Earth's atmosphere. So far, the discussion of the influence of high‐temperature mixing with atmospheric air (in particular oxygen) on the measured volcanic gas composition is almost exclusively based on thermodynamic equilibrium (TE) considerations. By modeling the combined effects of C‐H‐O‐S reaction kinetics, turbulent mixing, and associated cooling during the first seconds after magmatic gas release into the atmosphere we show that the resulting gas compositions generally do not represent TE states, with individual species (e.g., CO, H2, H2S, OCS, SO3, HO2, H2O2) deviating by orders of magnitude from equilibrium levels. Besides revealing the chemical details of high‐temperature emission processes, our results question common interpretations of volcanic gas studies, particularly affecting the present understanding of auto‐catalytic conversion of volcanic halogen species in the atmosphere and redox state determination from volcanic plume gas measurements.
    Description: Plain Language Summary: A major fraction of magmatic gas emissions are released into the atmosphere from open vents. The emission processes are characterized by fast turbulent mixing with atmospheric air (within seconds) and associated rapid cooling. Hardly anything is known about the chemical kinetics within this brief mixing and cooling period. We simulate the chemical kinetics during the first seconds of hot magmatic gases in the atmosphere and find severe deviation to common interpretations and central thermodynamic equilibrium assumptions prevailing in volcanic gas geochemistry.
    Description: Key Points: We model the chemical kinetics of high‐temperature volcanic gas emissions within the first seconds of mixing with atmospheric air. We identify key chemical processes within the magma‐atmosphere interface and quantify influences on the volcanic plume composition. Our results question common assumptions prevailing in volcanic gas geochemistry and refine interpretations of gas emissions from open vents.
    Description: German Research Foundation
    Keywords: ddc:551.9 ; volcanic gas emissions ; kinetic chemistry modeling ; atmospheric chemistry ; magmatic redox states ; reactive halogen chemistry
    Language: English
    Type: doc-type:article
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 285 (1980), S. 312-314 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Nitrous acid was detected and monitored using the long path differential UV absorption technique described by Platt et al6. The optical system in the present experiments used a 0.3m McPherson spectrograph with a 600 grooves mm-1 grating blazed at 500 nm (giving a dispersion of 5.3nm per mm). A ...
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillan Magazines Ltd.
    Nature 395 (1998), S. 486-490 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Reactive bromine species contribute significantly to the destruction of ozone in the polar stratosphere. Reactive halogen compounds can have a strong effect not only on the chemistry of the stratosphere but also on that of the underlying troposphere. For example, severe ozone depletion events ...
    Type of Medium: Electronic Resource
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