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  • 1980-1984  (5)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 302 (1983), S. 380-380 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] CHLOROFLUOROMETHANES (CFMs), the gases used in refrigerators and aerosol cans, have recently acquired a bad reputation for the effect they may have on the ozone layer of the upper atmosphere. Harmful or not, their use does provide a scientific bonus; they make it possible to trace quantitatively ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 36 (1980), S. 1017-1025 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The fate of fossil fuel CO2 in the ocean is discussed and a comparison is made with the natural oceanic cycle of carbon. The oceanic share of fossil fuel carbon, pressently about 40%, will decrease in the future. Much of the fossil fuel carbon will remain in the atmosphere, and will stay there for many centuries. In the long run, however, the ocean will bring to an end the fossil fuel excursion of atmospheric CO2-firstly by dissolution as bicarbonate and ultimately by burial in ocean sediments.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Boundary layer meteorology 27 (1983), S. 97-103 
    ISSN: 1573-1472
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract In order to obtain field data of ocean-atmosphere gas transfer coefficients, it is preferable to measure the interfacial gas flux in the air rather than in the water. This approach has been reported in the literature for CO2. However, it is shown here that 222Rn and methyliodide, CH3I, may be more suitable gases for air-side flux measurements.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 2022-06-24
    Description: 14C concentrations, as weil as 13C, hydrographic and nutrient data are reported for 5 hydrographic stations that form a transatlantic section near 40° N ("Meteor" cruise no. 23, 1971). Precision (for 14C ± 0.3% or better) and comparability with literature data are specified. A planned intercomparison with the US GEOSECS program within the Newfoundland Basin deep water failed because of variability of water characteristics. The observed 14C values decrease from about Δ 14C = + 80‰ at the surface to -70‰ at 2000 m depth. Deeper down, the values west of the Midatlantic Ridge remain similar, whereas those east of the ridge decrease further, to about -110‰. It is shown that bomb-14C is prominent down to about 1500 m depth. Beyond this depth the bomb 14C component is small and is negligible in the eastern basin below 2800 m. On the basis of the 14C-tritium correlation, the distribution of natural 14C below about 1500 m depth is derived from the observations. In the deep and bottom water east of the ridge the 14C-salinity relationship seemingly is non-linear. Contrary to expectation, the 14C concentration in the bottom water is not lower than found on an US GEOSECS station near 10° N. Apparently, lateral concentration differences in the Northeast Atlantic bottom water as well as nonlinearity of the 14C-salinity relationship at 40°N do not exceed 10‰ in Δ 14C.
    Type: Article , PeerReviewed
    Format: text
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  • 5
    Publication Date: 2022-06-27
    Description: We present field measurements of air-sea gas exchange by the radon deficit method that were carried out during JASIN 1978 (NE Atlantic) and FGGE 1979 (Equatorial Atlantic). Both experiments comprised repeated deficit measurements at mixed position over periods of days or longer, using a previously described precise and fast-acquisition, automatic radon measuring system. The deficit time series exhibit variations that only partly reflect the expected changes in gas transfer. By evaluating averages over each time series we deduce the following average gas transfer velocities (average wind velocity and water temperature in parentheses): JASIN phase 1: 1.6 ± 0.8 mid (at -6 mis, 13 °C) JASIN phase 2: 4.3 ± 1.2 mid (at -8 mis, 13 °C) FGGE: 1.2 ± 0.4 mid (at -5 mis, 28 °C) 0.9 ± 0.4 mid (at -7 mis, 28 °C) 1.5 ± 0.4 mid (at -7 mis, 28 °C) The large difference between the JASIN phase 2 and FGGE values despite quite similar average wind velocity becomes even larger when the values are corrected to a common temperature. Both values are, however, fully compatible with the range of gas transfer velocities observed in laboratory experiments and the conclusion is suggested that their difference is caused by the highly different wind variability in JASIN and FGGE. We conclude that in gas exchange parameterization it is not sufficient to consider wind velocity only. A comparison of our observations with laboratory results outlines the range of variation of air-sea gas transfer velocities with wind velocity and sea state. We also reformulate the radon deficit method, in the light of our observed deficit variations, to account explicitely for non-stationarity and horizontal inhomogeneity in the near-surface radon deficit layer (i.e., mixed-layer and upper thermocline). We show that neglection of non-stationarity and horizontal inhomogeneity in previous radon work introduces considerable uncertainty in deduced gas transfer velocities. We furthermore discuss the observational requirements that have to be met for an adequate exploitation of the radon deficit method, of which an observation area of minimum horizontal inhomogeneity and monitoring of the remaining inhomogeneities are thought to be the most stringent ones.
    Type: Article , PeerReviewed
    Format: text
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