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  • INSTRUMENTATION AND PHOTOGRAPHY  (2)
  • Arctic  (1)
  • 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
    Publication Date: 2011-08-19
    Description: In July of 1983, ambient measurements of nitric oxide (NO) were obtained at Wallops Island, VA, during the NASA GTE/CITE ground-based instrument intercomparison field study. The instrument, which was designed for measurements in the remote troposphere from an aircraft platform, is briefly described. Ten days of ambient air observations showed broadly uniform diurnal behavior, although considerable variability was encountered. Two distinct synoptic meteorological conditions resulted in markedly different levels of nitric oxide abundance. When the local winds were from the north to west sectors, which placed the sampling site within 130 to 300 km of large urban centers, the midday mixing ratios were typically in the range of 200-300 pptv. In contrast, when the air mass sustained a 1- or 2-day period over the Atlantic Ocean, the mixing ratios were substantially lower and in the 50-60 pptv range.
    Keywords: INSTRUMENTATION AND PHOTOGRAPHY
    Type: Journal of Geophysical Research (ISSN 0148-0227); 90; 12
    Format: text
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  • 3
    Publication Date: 2011-08-19
    Description: Results from an intercomparison of techniques to measure tropospheric levels of nitric oxide (NO) are discussed. The intercomparison was part of the National Aeronautics and Space Administration's Global Tropospheric Experiment and was conducted at Wallops Island, VA, in July 1983. Instruments intercompared included a laser-induced fluorescence system and two chemiluminescence instruments. The intercomparisons were performed with ambient air at NO mixing ratios ranging from 10 to 60 pptv and NO-enriched ambient air at mixing ratios from 20 to 170 pptv. All instruments sampled from a common manifold. The techniques exhibited a high degree of correlation among themselves and with changes in the NO mixing ratio. Agreement among the three techniques was placed at approximately + or - 30 percent. Within this level of agreement, no artifacts or species interferences were identified.
    Keywords: INSTRUMENTATION AND PHOTOGRAPHY
    Type: Journal of Geophysical Research (ISSN 0148-0227); 90; 12
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