Interpretation of the records is difficult because of the paucity of direct observations on the behavior and movements of skinks under natural conditions. Often when one is alarmed, it will run as much as 30 feet, in a fairly direct course, to a tree or bush or rock where it can find refuge. Undisturbed individuals move about slowly and circuitously. It is difficult to keep one under observation for any length of time because of the secretive habits causing it to keep under cover, as much as possible while moving about, and to hide in response to any slight disturbance.
It is obvious that individuals shift their activities from time to time, occupying new areas either abruptly or by gradual stages. Even though a successful skink has a life span of several or many years, the populations on the small study areas were found to be much altered from one year to the next. Presumably this change was brought about largely by shifts in home ranges. Several shifts of hundreds of feet were recorded, but the chances of recovering marked individuals that moved so far were relatively poor because their movements generally took them beyond the limits of the study area to locations where recapture was unlikely. Skinks often were caught at their hiding places beneath rocks or other sheltering objects. In many of these instances it was evident from the position, temperature and state of activity of the lizard that it had been in the open but had become alarmed as the collector drew near and had retreated unnoticed to its shelter just before capture, whereas in other instances it was obviously at rest in its chosen shelter. Except for females in their nest burrows individuals were not ordinarily recaptured regularly at the same hiding places. They may seek new hiding places after each period of activity.
However many of the skinks captured were taken again, after long intervals, near the same places. Time elapsed between successive captures for different individuals ranged from one day to 47 months. Of the total of 323 recaptured by September, 1952, approximately half, 162, were taken after intervals including one or more hibernation periods. In appraising home ranges and detecting the occasional shifts over a relatively long time span, chronology of the records needs to be taken into account. Records clustering about the same center seem to indicate continued occupancy of an established home range. However, when one or more early records are well separated from one or more later records, a shift in range seems probable. In some instances successive records were progressively farther from the starting point suggesting two or more shifts in the same direction from an original home range.
Although recorded movements varied from a few inches to hundreds of yards, the most noteworthy feature in general was the short distance between points of capture (considered in relation to the potential mobility of the lizards) after days, weeks, months or years. In many instances no movement was demonstrable, even though successive points of capture were not exactly the same. Named natural landmarks, mostly trees, boulders and logs, well distributed over the study area, were used as a basis for locating points on the map. Direction and distance in feet to the nearest landmark was recorded for each site of capture, but for distances of more than 25 feet estimates were made to the nearest ten feet. Usually at least one landmark was available within a 50-foot radius from any point where a capture was made. Occasional estimates made for distances of more than 50 feet, or even more than 100 feet, in the absence of suitable landmarks nearby, were sources of inaccuracy. For such estimates errors of up to ten feet were common, and some errors of greater magnitude were made.
For most individuals successive sites of capture tended to cluster within a small area, but the occasional outlying capture sites indicate that each individual does range outside the area in which its activities are concentrated. These occasional excursions cannot be consistently attributed to any one ecologic requirement, nor are they limited to any particular time within the season of activity. Adult males, however, tend to make longer movements in the brief period of concentrated sexual activity, thereby increasing their chances of finding mates. Similarly, adult females may wander beyond their usual ranges in search of suitable nesting sites. The home range may be thought of as consisting of a small central portion where activities are largely concentrated, and an outer area several times as large, familiar to the animal but used to a lesser extent by it. The activities gradually become more diffuse farther from the central part of the home range. In the five-lined skink, home ranges are unlikely to approximate the circular shape because they are molded with respect to environmental features that are not uniformly distributed. A rotting log, an old tree with decayed hollow base and nearby fallen slabs of bark and dead limbs, a rock outcrop with numerous deep holes and crevices, or a group of flat rocks in a forest glade fulfill requirements not met in the surrounding habitat with the result that home ranges are built around them. Consequently a home range may be long and narrow, with maximum diameter several times the minimum diameter.
The usual concept of home range, as a finite area with well defined boundaries is not entirely satisfactory for an animal with the habits of the five-lined skink. The skink spends much of its time in inactivity underground or otherwise concealed and sheltered, and when it does move about it takes advantage of natural travel-ways over rock surfaces, tree trunks, and logs. If a log happens to be the home range center, the skink may travel the length of the log many times without making a comparable trip at right angles to this axis of travel, although it may make short side dashes to secure food. On more extended forays, the directional sequence of movements is largely controlled by the distribution of suitable cover and travel routes, as the skink avoids both open areas and dense vegetation. Outlying portions of the home range probably are not uniformly covered but are reached only occasionally as the lizard is led along some natural travel route, or after it has visited, in succession, a series of locations attractive in providing shelter or food.
Marked skinks were recaptured at distances up to 680 feet from points of original capture. Considering only the most remote points of capture for those individuals recaptured more than once, the average recorded movement for the entire group of 323 recaptured skinks was 58 feet. This figure provides a basis for comparing vagility of this species with others. Eliminating some individuals of indefinite status, the average movement for 75 adult males was 69 feet; for 102 adult females, 45 feet; and for 112 young, 61 feet. For the adult females, home range data are biased by the fact that many were caught repeatedly at or near their nests. It is not clear whether females that do not have nests range less widely than males.
Only 15 individuals, less than five per cent, had moved more than 250 feet. These longest movements were: 680 feet, adult female, 26 months; 680 feet, adult female, 10 months; 680 feet, subadult male, one year; 650 feet, young to adult male, 22 months; 640 feet, subadult to adult female, two years; 535 feet, young male, 11 months; 510 feet, adult male, 11 months; 490 feet, young (sex undetermined), 10 months; 450 feet, young male, 13 months; 350 feet, young (sex undetermined), 101⁄2 months; 335 feet, adult female 131⁄2 months; 275 feet, adult male, 35 months; 275 feet, adult male, 24 months; 270 feet, young to adult male, 121⁄2 months.
For those skinks caught on only two occasions, at different places, the single movement record provides some clue as to the location and size of the home range. No evidence was obtained to indicate that the activities of these lizards center at fixed home bases. It may be assumed that any two successive captures of the same individual separated by a substantial time interval, will be distributed at random to each other within the area to which the animal’s activities are confined. The varied techniques of capture, by hand and with different types of traps, would help to secure random distribution of capture sites. If the home range were covered uniformly by the animal in the course of its activities, any two random capture sites would be on the average separated by a distance equal to half the home range diameter. If the animal tends to concentrate its activities in the central part of the home range, as seems to be the case, the capture sites will be correspondingly closer together. For the 196 skinks that were caught on only two occasions, average movement was 62 feet. Within this group the 42 adult males that were recaptured only once had averaged movements of 58 feet. One had made an exceptionally long movement of 510 feet, which obviously was not entirely within its home range. Excluding this one long movement, the remaining 41 had moved on the average, approximately 47 feet ([Table 15]). Among the other skinks caught only twice one of 61 females and 8 of 93 young had likewise made such long shifts that it seemed inadvisable to include them in computing the size of the home range.
Distance between points of capture showed little correlation with elapsed time. For 24 of the adult males that were recaptured in the same year they were originally marked, the average distance was 49 feet, whereas in the 17 others recaptured after one or more hibernations the average movement was 45 feet. For adult females, the corresponding figures were, respectively, 22 feet and 29 feet; and for young, 33 feet and 66 feet.