3. The Sr® activity from each test is added to the accumulated Sr® activity from previous
tests.

4. For each sampling day the Sr®to total fission product activity ratio is calculated.
5. Each day’s measuredbeta activity is converted to Sr™ activity by use of this factor.

This method of calculation would give high strontium values for locations near test sites
on days of high fallout. This is caused by attributing the activity to the total accumulated pool
of fission products rather than to the immediate burst that caused the fallout. This can be
corrected by treating these few cases individually.
The only practical evaluation of the new calculations technique is by comparison with
radiochemical analyses of open samplers. During the period May 1956—June 1957, several
locations had parallel sampling units for at least part of the time. These data are shown in
the following table in which one finds that the gummed film system, together with the above
method of computation, yields estimates of Sr® deposition which tend to be higher than the

estimates derived by radiochemical analyses of pot samples. The mean ratio of Sr®® estimated

from gummed film to pot analyses is 1.45 with a maximum ratio of 1.66 at Salt Lake City and

a minimum of 0.90 in New York City.

COMPARISON OF Sr® ESTIMATES FROM GUMMED FILM
WITH RADIOCHEMICAL ANALYSES OF MONTHLY POT COLLECTIONS
Total

Periodof

Location

observation

Sr", me/sq. mile Film/pot Monthly ratios iin/pot
Film

Pots

ratio

Low

High

mean

New York City
Pittsburgh
Chicago
Salt Lake City

May
May
Dec.
Dec.

1956—June 1957
1956—June 1957
1956-June 1957
1956—June 1957

12.3
12.1
6.3
15.1

13.7
10.6
4.6
9.1

0.90
1.14
1.37
1.66

0.32
0.62
1.0
1.1

2.2
2.5
1.9
3.3

1.1
1.2
1.4
1.8

Los Angeles
Hiroshima

Dec. 1956—June 1957
Oct. 1956—June 1957

3.5
5.6

3.1
3.7

1.13
1.51

0.78
0.82

2.4
3.7

1.4
1.7

Nagasaki

Aug. 1956—June 1957

6.7

5.5

1.22

0.64

5.5

1.6

The calculation of external gamma doseis less sensitive to variations in the source of

fallout. In addition, it appears that the important gamma dose from fission products is from
internal Cs'*" rather than the external gamma from distributed fission products after suitable
allowance for shielding and weathering.

11

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