Table 5. Estimates of the daily intake of 137Cs
from local foods by age group at Rongelap Atoll.

Adult (2 18 y). The average daily intake of
137Cs for adults is obtained from our diet model.
When imported foods are available, the intake
is 1085 pCi/d (specific data are presented in

Age

Appendix A, Table A-1).

0 to 3 months
4 to 8 months

A summary of the !37Cs intake by age group
is given in Table5.

9 monthsto 1.4 y
15yto3y
4ytolly
12 y to17y
218 y

137Cs intake, pCi/d

424
556
773
517
594
761
1085

Retention of 137Cs and 99Sr
represented by a two-compartment, exponential
model, where for adults the short-term

Cesium-137

compartment has a biological half-life (T!/?) for

Fetus

137Cs of 2d for both males and females, and the

long-term compartment a T!/? of 110d and 85 d

The fetus is assumed to be in dynamic
equilibrium with the mother. Experimental
results indicate that in the first few months of
pregnancy the ratio of the !37Cs concentration in
mothers to that in the fetus is 3:1, changing to

for males and females, respectively (ICRP, 1979;
NCRP, 1977; Richmondet al., 1962).

In some

cases, the loss of !37Csis better represented by a
three-compartment model (Leggett et al., 1984),
but generally the short-term compartmentin the ,
two-compartment model represents an average
of compartments with half-lives the order of a
few hours, a few days, and 1 or 2 weeks. The

about 1:1 in last months (linuma et al., 1969;

Nagai, 1970). Consequently, the dose received
by the fetus should be no more and perhapsless
than that received by the adult mother (linuma

fractional deposition of 137Cs in the model for

et al., 1969; Nagai, 1970).
In addition, the biological half-life of

the short- and long-term compartments for

137Cs is shorter in pregnant women than in
nonpregnant women, leading to lesser body

adults is 0.10 and 0.90, respectively (ICRP, 1979;

NCRP, 1977). These fractional depositions and
half-lives represent a model for an average
adult around which particular individuals will
vary.
The long-term compartment is the most

burdens in pregnant women (Bengtsson et al.,
1964; Zundel et al., 1969; Godfrey and Vennart,

1968). Consequently, the dose to pregnant women
would be less than to nonpregnant women. Based
on data presented by linumaet al. (1969), the
dose to the fetus would be about half that
calculated for an adult.

significant compartment for dose assessment, and

there is abundant evidence in the literature that

showsthe long-term T!/? changes dramatically

with age from birth to adulthood (Lloyd et al.,,

Infants, Children, Adolescents, and Adults

1966, 1970; Wilson and Spiers, 1967; Boni, 1969;

It is assumed that when !3/Cs_ is ingested,
100% of the 13’Cs crosses the gut and enters the
blood, i.e., Fy = 1.0 (NCRP, 1977; ICRP, 1979).
Theloss of 137Cs from the bodyis then generally

T0001 bb

linuma etal., 1969; Weng and Beckner, 1973;
Lloyd, 1973; Cryer, 1972; Karcher et al., 1969;

Richmondetal., 1962). The T'”? for 197Cs ranges

from 10 to 12 d in infants (Wilson and Spiers,
12

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