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Safety_Series_041_1975 - gnssn - International Atomic Energy ...

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54 APPENDIX II<br />

stable counterpart in the receiving water m ass, due to differences<br />

in physico-chem ical states, which require time and therefore distance<br />

to resolve.<br />

Ultimately, this approach offers the possibility, at least so far<br />

as food-chain problem s in relation to sea disposal are concerned,<br />

of setting maximum perm issible concentrations for the water. We<br />

are some way yet from being able to attain this objective because<br />

many more data are required on trace element concentrations in<br />

seawater and on their variability in time and space, on the central<br />

problems of relative biological availability, and on the role of<br />

particulate matter and organic com plexes in the cycling of trace<br />

elements and their artificial radionuclides. Indeed, it is appropriate<br />

to sound a note of caution since recent evidence in relation to 55Fe,<br />

60Co and 65Zn, introduced to the marine environment from weapon-test<br />

fall-out, suggests that rather large differences in specific activity<br />

between the water and some elements of the biota can occur.<br />

However, this was foreseen, in the original consideration of this<br />

system , by the Isaacs Committee who allowed a reduction factor<br />

of 10 in permitted concentrations to account for preferential uptake<br />

of such complexed metal radionuclides. Even so, the factors<br />

suggested by the recent findings would need to be m ore of the order<br />

of 1 0 0- 1 0 0 0.<br />

N evertheless, this method does seem to offer perhaps the only<br />

sensible approach to the problem s encountered in assessing the<br />

marine contamination consequences of a project such as the use of<br />

nuclear explosives in the excavation of an A tlantic-Pacific interoceanic<br />

canal. Here, many neutron-induced and fission-product<br />

radionuclides can be shown to be below maximum perm issible<br />

specific activity prior to the time of release, due to very thorough<br />

mixing with stable nuclides from the geological matrix in which the<br />

explosion takes place. Since these will also presumably be in the<br />

same physico-chem ical states after such intimate mixing, their<br />

biological availability and ultimate reconcentration in foods and<br />

humans should be governed by the specific activity model.<br />

The consequences of this system for marine monitoring requirements,<br />

so far as they were considered by the Isaacs Committee at<br />

the time, involved the sampling of all marine foodstuffs and organisms<br />

of com m ercial importance and their analysis for radionuclides and<br />

stable nuclides to provide data on both the curie quantities and the<br />

specific activity. Thus, although only an initial requirement in<br />

that once the validity of the specific activity model for the particular<br />

situation had been demonstrated it could be considerably relaxed,

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