Abstract. Sin Nombre virus (SNV), hosted by the deer mouse (Peromyscus maniculatus), is the primary etiologic agent of Hantavirus pulmonary syndrome (HPS) in North America. To improve our understanding of the epidemiology of HPS in the western United States, we conducted studies of population dynamics and SNV antibody prevalence in deer mouse populations for 6 years on 12 mark-recapture grids in Montana. Monthly numbers of deer mice ranged from zero to over 170 on 1-hectare grids. SNV antibody prevalence was higher than observed in studies in other parts of the United States, averaging 13% (0% to 50%), and peaking in May or June each year. Antibody-positive mice were older (heavier) (78% of positives were adults versus 52% of negatives) and more likely to be males (61% of positives versus 53.4% of negatives). A higher proportion of antibody-positive deer mice of all age-mass classes had scars than did antibody-negative mice. Month-to-month survivorship of antibody-positive adult mice was similar to that of antibody-negative mice, but survival of young antibody-positive deer mice was lower than antibody-negative deer mice. This is the first study to clearly suggest a detrimental effect of SNV infection on deer mice.

A structural model is proposed for bulk amorphous alloys based on the pair distribution functions (PDFs) measured using neutron scattering at ambient and cryogenic temperatures and different structural states. Reverse Monte Carlo (RMC) simulations were performed, in which icosahedral and cubic structures were used as the initial structures for the PDF refinement. The combined PDF and RMC studies show that strongly bonded clusters, with atomic-bond lengths shorter than their crystalline counterpart structures, are randomly distributed and strongly connected in the amorphous matrix. An attempt has also been made to identify the relationship between amorphous structures and their mechanical properties.

Handling mortality and recapture rates of wild rodents that were bled from the retroorbital capillary plexus without anesthesia were assessed. In 9,670 captures of seven species of rodents from 1994 through 1998, we found no difference in handling mortality in bled mice compared to those from trapping grids where mice were not bled. Recapture rates of rodents on control (non-bleeding grids) and rodents on bleeding grids was not significantly different for any species. We conclude that bleeding in the absence of anesthesia does not affect immediate mortality or subsequent recapture.

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