There are several favorable sites of attachment. The most favored site is in the axilla. There the scales are minute and granular with exposed areas of thin and tender skin, and the chiggers are well protected from dessication and are not likely to be rubbed off as the skink moves about. Other favorite sites of attachment are: about the insertion of the hind limb, about the cloacal opening, on the eyelids and on the toes. Only occasionally are chiggers found attached on the dorsal surface. When attached in protected spots in the tender skin of the axilla or groin, they are often in dense clusters of a dozen or more. Damage to the skin resulting from the attachment of the first chiggers renders conditions more favorable for the attachment of others. At Rat Ledge and at the quarry, many of the larger Sonoran skinks (Eumeces obsoletus) were captured, and individuals were far more heavily infested than were E. fasciatus from the same places. A single Sonoran skink might be found to have hundreds of chiggers, widely distributed over its body with concentrations at the axillae, groins, lateral neck region, and any injured spots where the protective armor of scales was broken. The reasons for the greater susceptibility of E. obsoletus are not entirely clear. It is a larger, less active species with coarser scalation, and is more subterranean in its habits.
The chiggers that attach to skinks seem to occasion but little discomfort. There is no local swelling and inflammation such as occurs in humans. The infestations observed in five-lined skinks were not sufficiently severe to cause debilitation or any noticeable symptoms. There is, however, a possibility that chiggers are vectors of microorganisms causing diseases in reptiles, just as they are for certain mammals (including humans) in some parts of the world.
Bishopp and Trembley (1935:42) record a single kind of tick, Ixodes ricinus scapularis Say, the black-legged tick, as parasitic in its immature stages on Eumeces fasciatus. This tick, however, has been recorded principally from mammals, of which many kinds serve as hosts for its larval, nymphal, and adult stages.
Population
Composition
Population structure obviously differs from place to place and from time to time. Because of the differences in secretiveness and elusiveness between young and adults and between males and females, true sex ratios and age ratios are obscured. In the period of weeks between the emergence from hibernation and the onset of the breeding season, these skinks tend to be less secretive than at other times, and secondary sexual and age differences in behavior are minimized. A sample at this season should be more representative of the true population composition than samples taken at other times of year. In a sample of 308 skinks available for the month of April, including the collections made on the Reservation and on nearby areas, in 1949, 1950, 1951, and 1952, 36.7 per cent were adult males, 28.3 per cent were adult females, and 35.0 per cent were young. That these figures cannot, however, be accepted as an accurate indication of the population composition is shown by the data from the areas where intensive population studies were made. Data are most complete from Skink Woods. For 292 adults taken there over a four year period, the sex ratio was 100:122.6. On this area after the first year of study a substantial proportion of the individuals recorded were repeaters from one year to the next, and in some cases for three or even four successive years. Many could be definitely assigned to a known age group. By analogy the majority of others could be tentatively assigned with some assurance on the basis of measurements, and relatively few were of indeterminate status. By assigning each of these indeterminate individuals to one or another age group, on the basis of greatest probability, the approximate composition of the population could be determined. Of 611 adults, 55 per cent were “two-year olds” (in the season between their second and third hibernations, which was their first breeding season). The percentage was not significantly different in the two sexes.
On the average, a pair of adults produces somewhat more than nine eggs per year. From the time individuals of a brood start their development in the egg until they are breeding adults two years later, they undergo such drastic reduction in numbers that, on the average, approximately only one per brood survives. Most of the mortality probably occurs early, especially before hatching, also in the inexperienced hatchlings, and in the first hibernation. In spring, after emergence from hibernation, young are generally taken in smaller numbers than are adults. Their relative scarcity is only apparent, owing to greater secretiveness, and greater elusiveness when found. In spring, newly matured adults (age class about 21 months) may be taken in somewhat larger numbers than young (age class about 9 months). The latter obviously must be more numerous, in a stable population however, as the 21 month age class necessarily has sustained some loss since it was 9 months old.
Success of the annual brood varies greatly from year to year, depending on the weather and various other factors. In 1949 evidently conditions were near optimum; young hatched early and were especially numerous in late summer. In 1950 these young hatched in 1949 made up 40 per cent of the total catch (excluding hatchlings) in Skink Woods and were relatively more numerous than young of the corresponding age group in other years. In 1951, these young of the 1949 brood, grown to adults, made up 70 per cent of the breeding populations, as against 36 per cent for the corresponding class in 1950 and 58 per cent for the corresponding class in 1952.
Even after attainment of adulthood, any given age group evidently is subject to annual reduction amounting to at least half its numbers. Within six or seven years, at the most, the original numbers would be reduced to an insignificant percentage. At an age of four or five years individuals probably have attained their maximum size, with obscured pattern and changed proportions suggestive of advanced age. Occasional individuals possibly attain much greater age, but certainly few live more than five years. Like most small animals, the five-lined skink has a short life expectancy and a rapid population turnover. As compared with mammals of comparable sizes, the small rodents and insectivores that are this lizard’s community associates and are subject to many of the same hazards, the skink is notably successful, with a much longer life expectancy. For these small mammals the life span is seldom as long as a year. Most kinds of small birds likewise have a life expectancy less than that of the five-lined skink, although somewhat greater than that of small mammals.