In Area 11-C, granivores (D. merriamt, D. miecrops, and P. ltongtmembris) did
not differ significantly (P>.05) from insectivore-omnivores (A. leucurus, 0.

torridus, and lizards) in mean Pu tissue burdens from either Activity Stratum.

Mean Pu tissue burdens of both trophic categories, however, were significantly
greater (P<.01) from the High Activity Stratum where Pu carcass burdens were

approximately 2 x 107! nCi/g ash.

Mean Pu/Am ratios of both pelt/skin and carcasses were more variable in insectivore-omnivores than in granivores from both strata. As shown in Table 3,
however, ratios in GI tracts of both trophic categories were consistent with
soil and vegetation ratios and exhibited relatively low variability. In
contrast, mean ratios in carcasses of insectivore-omnivores were not only more

variable, they were significantly higher (P<.01) than either means of the GI
tract samples or soil and vegetation ratios.

This phenomenon is difficult to

explain in light of the consistent ratios found in GI tracts of rodents. In
addition, Romney et az. (1975) present data which indicate relatively consistent
values for Pu/Am in soil and vegetation samples and suggest consistent Pu/Am
ratios in resuspendable contamination in Area 11-C. The high ratios present
in carcass samples of insectivore-omnivores may indicate that these rodents
are exposed to different environmental conditions than plants which have been
sampled and occupy microhabitats which have not been sampled by current soil
sampling design. In addition, insectivore-omnivores have larger home ranges
than granivores (McNab, 1963; our studies) and, hence, may be exposed to a

wider variety of microhabitats.

A supplemental hypothesis may be that some

food sources of insectivore-ominvores, such as arthropods and possibly small
vertebrates, contain Pu and Am which is more or less soluble, hence, more or

less available for uptake, than that of resuspended contaminants.

It is well known that plants and animals play a significant role in development

and dynamics of soil ecosystems.

ing of rock and soil.

Plants aid in chemical and mechanical weather-

Plant roots help break up large soil aggregates and

rocks and provide avenues of access of air and water to subsurface soil.

Fungi and bacteria excrete metabolic acids which can dissolve rock aggregates,

and possibly can solubilize essentially insoluble soil components, such as
plutonium. When plants die, various soil invertebrates, fungi, and bacteria
convert plant tissue to available food for microinvertebrates, and the resulting
Whereas desert soils are relatively
processes add nutrients to the soil.

sterile, the available nutrients are not uniformly distributed. We believe
that nutrient enrichment associated with burrow systems may be a major link in
nutrient cycling of desert ecosystems.
Animal activity, particularly burrowing activity, has been shown to be a
principal force affecting soil chemistry and structure. Taylor (1935) has
reported that ground squirrels move 30 to 40 tons of soil per acre yearly in
arid midwest areas.

Thorp (1949) estimated that burrow mounds consisted of

7-9 Kg of subsoil for each square meter of surface in semiarid portions of the
United States. Burrowing activity has also been shown to be extensive as far
as depth is concerned.

For example, some ants at Rock Valley, NTS, have been

found at depths of 10 meters. Kangaroo rats (Dtpodomys), the most abundant
rodents of NAEG Study Areas, have been shown to significantly alter soil
chemisty in their burrow systems. Green and Reynard (1932) reported that
kangaroo rats defecated extensively throughout their burrow systems. They

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