[en] Most of the plutonium entering aquatic and terrestrial ecosystems of the United States originates from nuclear weapons testing and from the burnup of the SNAP-9A satellite power source (Hanson 1975). But in the future, local ecosystems may receive small quantities of Pu released from nuclear facilities such as those at Oak Ridge, Los Alamos and other sites. The purpose of this paper is to compare and contrast the distribution of Pu in two contaminated ecosystems which are representative of humid and semi-arid environments of the United States. Results summarized in terms of inventories for the respective ecosystems several decades after initial contamination are used to anticipate the longer term (i.e., decades or centuries) behavior of Pu in the environment. One important question is whether the availability of this element to plants and other organisms will change after it is subjected to weathering and ecological processes of the environment. It is pointed out that potential radiological toxicity and long physical half-lives of Pu dictate that its behavior in ecosystems be understood