Ecological half-lives (Te's) were estimated for 137Cs in largemouth bass, sunfishes, and bullheads from two reservoirs and three streams on the Savannah River Site, a nuclear weapons material production facility in South Carolina. Ecological half-life is the time required for a given contaminant concentration to decrease by 50% as a result of physical, chemical, and/or biological processes that remove it from an ecosystem or render it biologically unavailable. Te's were estimated from whole-fish 137Cs concentrations in samples collected during 1972-1996, following radionuclide releases that occurred primarily during the 1960's and early 1970's. Te's ranged from 3.2 to 16.7 y, and all were shorter than expected from the half-life for radioactive decay (Tp = 30.2 y) alone. Fish taxa from the same locations differed in mean 137Cs concentrations (highest in largemouth bass and lowest in sunfishes) but, in most cases, exhibited similar 137Cs Te's. Rates of 137Cs removal in fishes were strongly correlated with rates of 137Cs removal in water. The shortest Te's occurred in the upper portions of the streams. Te's in lower portions of the streams were longer, as were Te's in one of the reservoirs. Te's in the second reservoir, which had a much shorter water residence time, were nearly comparable to those in the upper portions of the streams until 1991. At that time, 137Cs concentrations in fishes began to increase following drainage and refilling of the reservoir, which apparently resuspended 137Cs buried in the sediments.

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Protozoan parasites of Leishmania spp. invade macrophages as promastigotes and differentiate into replicative amastigotes within parasitophorous vacuoles. Infection of inbred strains of mice with Leishmania major is a well-studied model of the mammalian immune response to Leishmania species, but the ultrastructure and biochemical properties of the parasitophorous vacuole occupied by this parasite have been best characterized for other species of Leishmania. We examined the parasitophorous vacuole occupied by L. major in lymph nodes of infected mice and in bone marrow-derived macrophages infected in vitro. At all time points after infection, single L. major amastigotes were wrapped tightly by host membrane, suggesting that amastigotes segregate into separate vacuoles during replication. This small, individual vacuole contrasts sharply with the large, communal vacuoles occupied by Leishmania amazonensis. An extensive survey of the literature revealed that the single vacuoles occupied by L. major are characteristic of those formed by Old World species of Leishmania, while New World species of Leishmania form large vacuoles occupied by many amastigotes.

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