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  • 1
    ISSN: 1573-0662
    Keywords: active nitrogen ; ozone ; radicals ; snow chemistry ; Arctic ; surface layer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Measurements of NOx (NO +NO2) and the sum of reactive nitrogenconstituents, NOy, were made near the surface atAlert (82.5°N), Canada during March and April1998. In early March when solar insolation was absentor very low, NOx mixing ratios were frequentlynear zero. After polar sunrise when the sun was abovethe horizon for much or all of the day a diurnalvariation in NOx and NOy was observed withamplitudes as large as 30–40 pptv. The source ofactive nitrogen is attributed to release from the snowsurface by a process that is apparently sensitized bysunlight. If the source from the snowpack is a largescale feature of the Arctic then the diurnal trendsalso require a competing process for removal to thesurface. From the diurnal change in the NO/NO2ratio, mid-April mixing ratios for the sum of peroxyand halogen oxide radicals of ≤10 pptv werederived for periods when ozone mixing ratios were inthe normal range of 30–50 ppbv. Mid-day ozoneproduction and loss rates with the active nitrogensource were estimated to be ∼1–2 ppbv/day and in nearbalance. NOy mixing ratios which averaged only295±66 pptv do not support a large accumulation inthe high Arctic surface layer in the winter and springof 1998. The small abundance of NOy relative tothe elevated mixing ratios of other long-livedanthropogenic constituents requires that reactivenitrogen be removed to the surface during transport toor during residence within the high Arctic.
    Type of Medium: Electronic Resource
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  • 2
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    AGU (American Geophysical Union)
    In:  Geophysical Research Letters, 31 (23). L23S05.
    Publication Date: 2018-02-27
    Description: Oceanic bromoform (CHBr3) is the major source of organic Br to the atmosphere and may be significant for ozone depletion through the contribution of reactive bromine to the upper troposphere and lower stratosphere of the midlatitudes and tropics. We report the first analyses of boundary layer air, surface and deep ocean waters from the tropical Atlantic. The data provide evidence of a source of CHBr3 throughout the tropical open ocean associated with the deep chlorophyll maximum within the tropical thermocline. Equatorial upwelling carries the CHBr3 to the surface, adding to increased concentrations in the equatorial mixed layer and driving oceanic emissions that support locally elevated atmospheric concentrations. In air masses that had crossed the coastal upwelling region off NW Africa even higher atmospheric mixing ratios were measured. The observations suggest a link between climate, wind-driven upwelling, and the supply of Br to the upper atmosphere of the tropics.
    Type: Article , PeerReviewed
    Format: text
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  • 3
    Publication Date: 2014-07-30
    Description: The central detector in the MuSun experiment is a pad-plane time projection ionization chamber that operates without gas amplification in deuterium at 31 K; it is used to measure the rate of the muon capture process μ − + d → n + n +ν μ . A new charge-sensitive preamplifier, operated at 140 K, has been developed for this detector. It achieved a resolution of 4.5 keV(D 2 ) or 120 e − RMS with zero detector capacitance at 1.1 μ s integration time in laboratory tests. In the experimental environment, the electronic resolution is 10 keV(D 2 ) or 250 e − RMS at a 0.5 μ s integration time. The excellent energy resolution of this amplifier has enabled discrimination between signals from muon-catalyzed fusion and muon capture on chemical impurities, which will precisely determine systematic corrections due to these processes. It is also expected to improve the muon tracking and determination of the...
    Electronic ISSN: 1748-0221
    Topics: Physics
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