BULLETIN FLORIDA MUSEUM NATURAL HISTORY VOL. 38, PT. 11(6) RESULTS Activity and Movement Opossums were strictly nocturnal (Figs. 1, 2). Figure 1 shows the distribution of the onset and end of nightly activity from August to December in relation to sunset and sunrise and minimum nightly temperatures. Usually opossums emerged about one hour after sunset and were active for a varying period of time before reentering a den. However, some animals became active only later at night. Leaving the den late was more common in cool nights. Minimum temperature at nights when opossums emerged from dens after 2200 h averaged 8.0C (n=12) compared to 13.2C of all considered nights. The time activity ended varied more strongly than the time of the onset of activity. The scatter increased in November and December as average nightly temperatures declined and the variation in temperature increased. Average nightly activity ( S.D.) from August to December was 8.01 h ( 1.67), 8.81 h ( 1.47), 8.54 h ( 1.24), 7.85 h ( 3.13) and 8.22 h ( 3.66) and did not differ significantly among months (Kruskal-Wallis test, df=4, H=4.28, p=0.37). Maximum activity is reached between 2000 h and 0200 h (Fig. 2), when on average up to 97.4% of the monitored animals were active (cold nights excluded). Individual nightly activity varied greatly in duration and tended to be slightly, but not significantly longer in females than in males (Table 1, t145=0.97, ns). Activity was neither correlated with home range size (r=0.01, n=147) nor with age (r=-0.03) or body size (r=-0.04), but was clearly influenced by temperature (Fig. 3). Activity increased linearly with temperature up to about 80C (y=2.561+0.828x, n=33, r2=0.571, p<0.0001). Above this threshold activity was less temperature-dependent, but tended to decrease with increasing temperature (y=11.053-0.136x, n=114, r2=0.129, p<0.0001). Based on the former equation, activity is predicted to cease altogether at nightly minimum temperatures of -3C. Nightly inactivity was recorded in only one case (minimum temperature 0C), but several additional cases occurred during the mating season in January at nightly lows of -7 to +6C. Distances moved per hour and per night varied widely, but were significantly greater in males than in females (t140=3.90 and 2.53, respectively, p<0.01 and <0.05, Table 1). Maximum recorded movements within an hour reached 950 m in males and 790 m in females. Maximum distance traveled per night was nearly 4 km in females and 4.7 km in males. A partial correlation analysis showed that distance moved per hour in males was positively associated with home range size and minimum nightly temperature, whereas in females only body size exerted a significant positive effect (Table 2). Distance traveled per night is a function of the duration of activity and of average distances moved per hour and is therefore influenced by the same factors that influence activity and average hourly movement (Table 2). Thus males with large home ranges tended to move farther than males with small home ranges and