76

THE SHORTER-TERM BIOLOGICAL HAZARDS QF A FALLOUT FIELD

terest has been discussed [1], and can be sum-

marized briefly. The available data are conflicting; however, it appears that such an energy
dependence mayexist in mice over the range of
250 to 2,000 KVP, and that 1,000 and 2,000

KVP X-rays may beless effective by a factor of
0.8 or 0.9 (in terms of tissue dose). There are
several pieces of evidence that Co” gamma may
be even less effective—perhaps 0.7. Part of
these differences may be dosimetric in origin;
however, they appear to be real as doses are
measured at present. With large animals, dogs
and swine, there appears to be no such dependence of effect over the range of 250 to 2,000
KVP. Undegraded gamma radiation (Co)
appears to be less effective in the dog (Table I),
as with mice. It would appear that intrinsic
energy dependence over the range of energies of
interest is at. most of the order of 10 or 15 percent, a factor much smaller than other sources

of uncertainty.

In considering the effect of distribution of dose
as it affects degree of response, the concern is
mainly in comparing one type of unilateral exposure to another, and unilateral to bilateral
exposures. It is obvious by now that with iden-

tical depth-dose patterns, the same degree of
effect, within a few percent, will result from the
same dose. In comparing one typeof unilateral
irradiation to another, it is of course known that
the shallower the curve, the /ess the effect for a

given entrance or midline tissue dose. This can

be easily seen from the data of Potter [27] and

Ellinger [28], and that of Tullis in swine (Table
TI). Little difference is noted for dogs irradiated unilaterally with 250 and 2,000 KVP
X-rays (Table 1); however, the beams were

filtered such that the depth-dose patterns were
not greatly different [29]. It is thus clear that

differences do exist; however, the data are not

sufficiently good to allow quantitative treatment,

As for a means of predicting effects with a
given unilateral pattern, some data obtained
with small animals indicate that the erit tissue
dose may be a normalizing quantity [27, 28].
The data in large animals are insufficient to
evaluate this point. Integral dose or gram

GEOMETRICAL, ENERGY FACTORS--BFFECT OF RADIATIONS ON MAN

roentgens has been proposed as a normalizing
quantity. Grahn and Sacher [18] have shown
that with different types of “total body” irradiation, integral dose is of no value in this regard and the concept does not apply in predicting mortality with partial-bodyirradiation
(30]. Evenif integral dose were the normalizing
factor, the computations involved are so com-

Thus inverse square fall off is appreciable,
unlike the fallout field. Also with large
animals placed in a standing position among

tion.

With the cooperation of Col. Trum, additional

plex and lengthly that this parameter would
have no practical usefulness in hazard evalua-

Some additional points will be mentioned in
regard to the large animal data in Tables I
and II. Looking first at the btlateral data for
dogs and swine, it is seen that the air dose
LDw’s vary considerably among investigators,
but that the LDy’s in terms of midline tissue
dose are remarkably constant for X-rays with
8 variety of energies and experimental conditions. The discrepancy between air dose and
midline dose is muchlarger for swine than for
dogs, which would be expected from the larger

swine.

This indicates that such data, to be

quantitative for man, must be obtained on
man-sized animals. Data from dogs or
monkeys do not apply directly. It is apparent
that the usually quoted LD» values for large
animals, in terms of air dose, are much too
high, and that there is no true energy dependence of effect over the range of 250 to
2,000 KVP. The LD,»for dogs and swine are
approximately equal and considerably below
the LDfor mice or rats. No biological data
are available for large animals exposed to fallout gammaradiations; however, the LD» in
terms of midline tissue dose would be expected
to equal those in the tables to a few percent.

With regard to the Co” gamma data in

Tables I and II, the bigher LDy values may

reflect in part the apparent intrinsic energy
dependence that has been noted for mice.
With the swine exposed to Co® in the multisource field at Oak Ridge, however, additional
factors enter. It can be easily shown that

approximately 65 percent of the radiation
received at any point in air at the “center” of
any unit of 3 of the total of 19 sources comes
from a distance of approximately 1.5 meters.

the sources, a large percentage of the radiation
traverses the long axis of the animal, rather
than a transverse (shorter) diameter as with

animals exposed to bilateral X-irradiation or
with man upright in the fallout field. Thus
the midline dose would be expected to be
relatively quite low compared to the air dose.

depth-dose curves were obtained in the Co®
field, which indicate that the midline dese in a

swine phantom is less than half of the entrance
dose. The LD» value (Table ID) is corre-

spondingly low in terms of midline tissue dose.

From Tables I and IT, it can be seen that in
the laboratory, more radiation dose (entrance
air or tissue dose) is required to produce a given

effect with unilateral than with bilateral exposure. With “unilateral” exposure to the immediate bomb gamma radiation in the field,

however, the LD values are lower than for
unilateral irradiation in the laboratory, and

approximately.equal to bilateral irradiation in
the laboratory. This could indicate uncertainties in the field data—the LDy values were
obtained in a single determination with 10
animals per point, and the swine used were

smaller than those used in the laboratory. It
could also mean that the relatively flat curve

for bomb immediate gamma resembles in effect
bilateral, more than unilateral irradiation.

The considerations outlined must be taken

into account in hazard evaluation.

The prob-

lem is analogous to the RBE problem, which
gave rise to the dose unit “rem” to more closely
estimate hazard than is possible with the
roentgen or rad. The dose in rem is equal to
the dose in r multiplied by an experimentally
determined RBE factor. It would appear that
another factor should be introduced, a geometry
or g factor, which must be experimentally
determined for each situation as is the RBE
factor. It is seen from the present paper, that
under many circumstances the g factor may

greatly exceed in magnitude the RBE factor.

The problem of accurate hazard evaluation

77

in large animals and man is seen to be particu-

larly complex. It is not possible to use a single
quantity such as “r” or “rem” alone to predict,
hazard under a variety of circumstances—

additional factors to describe the situation considered must be introduced. No one would
ask for the “hazard” from a given dose of any
common toxic agent such as arsenic without

describing the situation farther-—-howthe drug
is to be given, the chemical form, part of the

bodyreceiving it, time over which it was administered, size of individual, ole. Yet it is

frequently expected that a “dose” of radiation
in “ry”? or “rem’’ will describe the hazard under
all situations. And the difficulties cannot be

circumvented by changing a name—introducing, as has been suggested, some arbitrary type

of “hazard” unit that supposeldy will indicate
what effect can be expected in man. No one
unit can ever describe the hazard; other
quantities are necessary. Substitution of a
“hazard�� unit represents a regression to the

“skin erythema dose” days, that nullifies the

very great advance made with the introduction
of the roentgen unit. The roentgen (or rep or
rad) is as good as any presently available single

quantity to allow a very general estimate of

hazard. Hf greater accuracy of prediction is
desired, then the situation must be recognized
and treated as a complex one. This is done in
other disciplines, and personnel are trained to

handle the problem.

Quantities in addition

to the instrumentreading in r or rads (where
dose is measured, type of exposure, type of
radiation (RBE), type of biological response of
interest, dose rate, body region exposed, etc.)

must be taken into account.

These factors

could be incorporated into one, or a series of
nomograms; however they cannot be incorporated into a single “hazard” unit or into a
single instrument reading. Perhaps most dangerous in attempts to devise a hazard unit is

that it will involve combinations of several
factors in unknown proportions. Thus one
trained and conversant will not he able to sort
out the important quantities that would allow
accurate evaluation of the hazard.
LD for man.—The consideration of the

Select target paragraph3