Abstract

Evaluation of the results of radioactivity monitoring in the southern North Sea between 1977 and 1987 has shown that in the water of the German Bight three areas stand out due to their different ratios between salinity and concentration of dissolved Cs-137 and tritium. While salinity steadily increases with greater distance from the coast, the Cs-137 concentration above 34 PSU (Practical Salinity Unit) increases sharply and shows how far water from the western and central North Sea, contaminated by nuclear reprocessing in Sellafield (Irish Sea), reaches into the German Bight. In the 34 to 32.5 PSU range, the influence can be seen of water contaminated by tritium originating in the rivers Rhein, Maas and Schelde, precipitation and the nuclear reprocessing plant at La Hague (Channel). Below 32.5 PSU, the influence of the influx from the rivers Elbe, Weser and Ems becomes apparent. These rivers are less contaminated with tritium. Assuming that Cs-137 and tritium, like the salinity of sea water, behave conservatively and that the decay-time of these two isotopes is long compared with the time-scale of water exchange in the southern North Sea, the concentration values measured are used to calculate the structure of the water masses in the three areas of the German Bight mentioned above using the mixing principle. Evaporation is taken into account. Results show that beyond 34 PSU, about half the sea water originates in the western central North Sea while the other half comes from the Channel. Below 34 PSU, the first mentioned share amounts only to a few per cent. Results also show that fresh water from the Rhein delta and precipitation, increasing with a decrease in salinity from 34 to 32.5 PSU, accounts for a maximum of 5% each. The fresh water influx into the German Bight via the rivers Elbe, Weser and Ems amounts to app. 11% when the PSU value reaches 29. The calculated portions are the mean values for the observation period. The number of measurements available makes it impossible to distinguish more exactly between the temporal and spatial variability of the amounts of the individual components. The quantity of each calculated portion of sea water also represents the “transfer factor of concentration” between the nuclide concentration in the source (e. g. the Rhein) and the concentration in the German Bight. In addition, these factors are used to calculate the “transfer factors of discharge” using the annual drainage rates of the sources. Thus a radioactive discharge rate of 1015 Bq per year into the Rhein would produce a mean activity concentration of 0.34 Bq/l in the German Bight (at a salinity of 33.5 PSU). To verify the calculated transfer factors, tritium concentrations in the German Bight are derived from existing environmental tritium data and the results are compared with the values actually measured.

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