BULLETIN FLORIDA STATE MUSEUM VOL 34(6) the proportion of non-reproductive individuals nearly tripled in April 1984, in comparison to the preceding March. The onset of the regular breeding season in April is indicated by the sudden appearance of perforate females in that month in all three years (Fig. 10). The female cohort, viewed by themselves during the main breeding season, shows that at any one time most females were either pregnant or lactating (Fig. 11, Table 11). Structure during the main breeding season is very similar for 1982 (Fig. 14) and 1984 (Fig. 16). The sample shown for August 1983 (Fig. 15) reflects the origin of the sample: all P. natalensis examined for that month came from the area in which the mark and release study was done, which showed progressively disparate sex ratios in favor of females in each of the three years (Tang Christensen pers. comm.). This was also the only area on campus from which viral seropositives were obtained. It is tempting to speculate that infection by this virus, which cross reacts with Lassa and Mopeia viruses, caused differential mortality against males. Influence of habitat.-- From July through April, trap success for Praomys natalensis in uncultivated grass areas was approximately half that obtained in fallow fields (Table 12). In Ma and June, however, there was no difference between habitats. Population structure was similar in both habitats when densities were at peak, as shown by the female cohort in October (Fig. 22). In other seasons, though, there were differences which probably reflect the influence of both rainfall and habitat upon reproduction. This is shown by the composition of the female cohort from December 1982 through March 1983 (Fig. 23). In December, a few reproductive females were taken in fallow field. Those taken in January from grass areas (Fig. 25) were either young, non- reproductives or post-reproductive females of the preceding year. In February and March, there were many newly post-reproductive females present in fallow field as well as many newly weaned juveniles, demonstrating production of a litter in January (Fig. 26). The proportion of post-reproductive females had increased in samples from grass in February (Fig. 23), but no juveniles were taken and these females could have been from the preceding year. Even more post-reproductive females were found in fallow field in March (Fig. 23), while there was evidence that reproduction was just beginning in grass habitats. Another contrast appeared between habitats in August 1984 (Fig. 24), when females collected in grass had already completed reproducing, yet in post- harvest maize fields, 20-35 percent were still breeding. Among males from grass only 10 percent showed visible epididymal tubules, in comparison to 29 percent from fallow field. Influence of rainfall upon growth.-- Growth data on P. natalensis were obtained during the capture-mark-release-recapture study (Tang Christensen unpubl.), and will be presented elsewhere. Data obtained from monthly