Jökull

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Jökull - 01.12.1962, Qupperneq 53

Jökull - 01.12.1962, Qupperneq 53
A/V£fí VAfíMA x(2> s (re) f/VFRAG£fíO/ R£YKJA V/fíf Afí£A Fig. 2. Location of samples from the Reykjavik area. heavy isotope concentration as the latitude varies from equatorial to polar. This refiects a continuous loss of vapour from the poleward moving air masses. As a consequence of this the precipitation has a latitude label. In general, the D-concentration in fresh water varies by about 30%, ranging from 3% higher to 27% lower than in average ocean water. The 018-concentration varies by only 4%, ranging from 0,6% higher to 3,4% lower than average ocean water. On the other hand, it must be emphasized that the dependance on the latitude is often quite complex and depending on the local meteorological conditions. Dansgaard (1961) has shown tliat there are substantial time-variations in the 018-concentration of the local precipita- tion. In experimental work it is necessary to mea- sure the D-concentration with an accuracy of 0,1% and the 018-concentration with an ac- curacy of 0,1 to 0,2%. The radioactive isotope tritium. The third isotope of importance is tritium or H8. It is radioactive with a half-life of 12,5 years and decays to He8. It is found in a very low con- centration in natural waters. The pattern of distribution has not been studied in detail and the experimental work lias been highly com- plicated by the H-bomb tests. Libby has carried out pioneering work in this field. The pre- bomb ratio T/H may for average rain water have amounted to 5xl0-18. Natural water derives tritium from the atmos- phere. It is believed to be produced at high altitudes by the action of cosmic radiation. Therefore, tritium is not produced in surface or ground water. Its concentration in ground water will consequently decrease as a result of JÖKULL 51
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