Eighty-three individuals in a population of S. undulatus garmani were either parietalectomized (n = 41) or sham-operated (n = 42). Subsequently their daily activity, cloacal temperature, vegetation density preference and distance traveled were recorded. Six of the lizards from the field study were used in outdoor enclosure and light gradient experiments. The parietal eye in lizards has been shown to be a photoreceptor (Clausen and Mofshin, 1939; Eakin and Westfall, 1959; Eakin, 1960; Miller and Wolbarsht, 1962; Engbretson and Lent, 1974). Stebbins and Eakin (1958) found that parietalectomy (destruction of the parietal eye) and shielding of the parietal eye in Sceloporus occidentalis, S. virgatus, Uta stansburiana and Uma inornata increased exposure to light, presence on the surface, and locomotor activity, and caused a decrease in the inclination to retreat when approached. Parietalectomy in Xantusia vigilis resulted in increased locomotor activity (Glaser, 1958; LaPointe, 1966). In S. virgatus and S. occidentalis it increased exposure time to high intensity light (Stebbins, 1963; Stebbins and Cohen, 1973). Stebbins and Eakin concluded that the parietal eye functioned as a register of solar radiation (Eakin, 1973) to help inhibit activity levels that are directly dependent on solar radiation. Not all studies have supported Stebbins and Eakin's conclusions. Francis and Brooks (1970) found that parietalectomy in S. occidentalis did not increase metabolic or ventilatory rates as expected. In parietalectomized Callisaurus draconoides, only males increased their exposure to sunlight (Packard and Packard, 1972), and parietalectomized Tropidurus albemarlensis showed no difference in locomotor activities or exposure times (Lowenstein and Stebbins, 1969). Removal of the parietal eye has also caused an increase in the activity of I Present address: Department of Zoology, University of Nairobi, P.O. Box 30197, Nairobi, Kenya. This content downloaded from 157.55.39.25 on Tue, 02 Aug 2016 04:40:48 UTC All use subject to http://about.jstor.org/terms 72 TRANSACTIONS OF THE KANSAS ACADEMY OF SCIENCE reproductive organs in several lizards (Clausen and Poris, 1937; Stebbins, 1970; Stebbins and Cohen, 1973), and of the thyroid gland (Stebbins and Eakin, 1958; Eakin et al., 1959; Stebbins and Cohen, 1973). Licht and Pearson (197 1) did not find any difference in the testicular cycle of parietalectomized Anolis carolinensis when compared to controls. Several investigators have suggested that the parietal eye helps synchronize daily and seasonal cyclic activity by controlling the amount of exposure to light (e.g., Stebbins and Wolhoft, 1966). The parietal eye may play a direct role in thermal regulation. After parietalectomy S. occidentalis emerged earlier and retreated later than did controls (Stebbins and Eakin, 1958), and S. virgatus had lower body temperatures at the time of burial (Stebbins, 1963). Parietalectomized A. carolinensis had lower thermal tolerance (Kosh and Hutchison, 1972) and when placed in a thermal gradient chose higher body temperatures (Hutchison and Kosh, 1974). The present study tested the hypothesis proposed by Stebbins and Eakin (1958) regarding the role of the parietal eye as a register of solar radiation. The northern prairie lizard, S. u. garmani, was the subject of this study because much of its ecology is well known (Ballinger et al., 1981), yet no work on the parietal eye has been carried out on a population living so far north. MATERIALS AND METHODS Field study. Between 12 June and 20 August 1974 a population of S. u. garmani was studied in Lacreek National Wildlife Refuge, Bennett County, South Dakota. The 2 hectare study site was located within the Nebraska sandhills which make up the southwestern portion of the Refuge (Section 27 R37W T36N). Each lizard, when first caught, was placed in ice, the parietal scale removed, then either the parietal eye destroyed or the tissue posterior to the parietal eye scarred (sham-operated). The parietal scale was replaced and covered with Parlodion (Mallinckrodt Chemicals) in ethyl ether alcohol and the lizard released. The parietalectomized and sham-operated lizards were similar with respect to sex, SVL and group size. Each individual was given a distinct insignia following Tinkle (1967). When a lizard was captured ambient (AT), substrate (ST) and cloacal (CT) temperatures, SVL, and sex were recorded. A marker was placed at the site of capture. The position of the lizard with regard to vegetation density, and whether in the sun, shade or both, was noted. Eighty-three (41, 42) individuals were caught: 41 (20, 21) were parietalectomized (P-lizards) and 42 (21, 21) were sham-operated (S-lizards). Vegetation density was categorized as sparse, moderate and heavy, based on the sampling of 2 representative sites of each type. For each sample the This content downloaded from 157.55.39.25 on Tue, 02 Aug 2016 04:40:48 UTC All use subject to http://about.jstor.org/terms VOLUME 91, NUMBERS 3-4 73 Table 1. Vegetation density of the three types of areas categorized in the study site. Vegetation density (cm/m) Vegetation type Sparse Moderate Heavy Herbaceous 0.35 ? 0.16 1.93 ? 0.14 2.78 ? 0.28 Yucca 0.57 ? 0.28 1.09 ? 0.26 1.64 ? 0.4 basal length intercept of the herbaceous vegetation and yucca plants were measured along a 30 meter transect (Table 1). Outdoor enclosure and light gradient experiments. Two experiments were conducted using 6 lizards caught in August near the field site. The lizards were kept indoors between 25 August and 9 September at room temperature and were exposed to normal sun light. On 10 September the lizards were placed in a 212 cm long by 92 cm wide by 37 cm high outdoor enclosure. The bottom of the enclosure was covered with 0.5 cm of sand and 2 wooden shelters, 31 cm square, were placed at each end of the enclosure which was oriented along the north-south axis. The lizards were fed once daily with a variety of local insects and meal worms. Water was available at all times in a petri dish. Normal basking behavior was recorded hourly from 0700 to 1900 hours between 10 and 17 September. The following positions were distinguished: 1. in deep shade 2. only head exposed to direct sunlight 3. entire body in weak shade 4. entire body exposed to direct sunlight. On 18 September the lizards were either parietalectomized or sham-operated, and from 24 September to 31 October observations were continued. Each day CT, AT and ST were taken of one animal from each group every hour they were active. After this experiment, the lizards were kept in a cold temperature unit in simulated hibernation conditions (60C) from 15 November 1974 to 6 January 1975. In a second experiment AT was held constant while the lizards were exposed to a light gradient in order to determine the relative importance of light as sensory stimulus for the parietal eye. A copper trough, 139 cm long by 16 cm wide by 15 cm high was used as the experimental runway. The bottom was covered with 5 cm of sand and 2 feeding dishes were placed equally distant from a water dish in the center of the runway. A light gradient was established by placing 2 fluorescent bulbs close to the surface of the sand at one end of the runway and having it angle upward. The gradient ranged from 14 to 280 foot candles. The lizards were observed This content downloaded from 157.55.39.25 on Tue, 02 Aug 2016 04:40:48 UTC All use subject to http://about.jstor.org/terms 74 TRANSACTIONS OF THE KANSAS ACADEMY OF SCIENCE