Fig. 14: Diagram of hygrothermograph traces showing daily progressions of air temperatures and relative humidities at each of four microclimatic stations, from the morning of July 1 through the morning of July 8, 1964. Slanting vertical lines on each chart designate midnight (2400 Hrs.) of each day.

Nights of high trapping success usually were associated with days having solar insolation below the average. Insolation was measured with a recording pyrheliometer at a regional weather station (M-2) on the middle of Chapin Mesa, at an elevation of 7,150 feet (Erdman, Douglas, and Marr, in press). This station was approximately one mile south of the trapping grid; isolation at this site would have been essentially the same as that received by the trapping grid. Below-average isolation for one day indicates cloudy conditions, which are accompanied by increased humidity, but may or may not be accompanied by precipitation. Trapping on nights preceded and followed by days of average or above average isolation with average humidities—indicative of clear days and clear moonlit nights—did not yield appreciably higher catches of mice than other nights. Hence there was no evidence that mice tended to avoid, or to seek out, traps on clear moonlit nights.

On cold, humid nights in autumn numerous mice caught in Sherman live traps succumbed from exposure, even though nesting material (kapok or cotton) and food were in the traps. Occasionally mice succumbed to heat when traps were inadvertently exposed to too much sunlight. Apparently little heat is required to kill individuals of either species. Traps in which animals died due to excessive heat usually were not hot to the touch; in most instances the traps were checked before 9:00 A. M., several hours before the sun caused maximum heating. Such individuals may have licked the fur of their chests in an attempt to lower their body temperatures. Although mice characteristically salivate before succumbing from heat, these individuals had moist fur over the entire chest and upper parts of the front legs, indicating licking. Mice killed by exposure to heat or cold usually were juveniles or young; subadult and adult individuals of both species were more tolerant. Older animals would be expected to have better homeostatic controls than younger individuals.

Habitat Preference

In Mesa Verde P. truei and P. maniculatus occur together only at the fringes of the pinyon-juniper woodland, where ecotonal areas provide less than optimum habitats for both species. Almost all individuals of P. truei occur only in pinyon-juniper woodland, whereas P. maniculatus occurs only in more open habitats, such as grassy meadows and stands of sagebrush.

Pinyon mice were abundant in a variety of associations within the pinyon-juniper woodland. The highest population densities were in pinyon-juniper woodland having an understory of mixed shrubs. In such an association, Poa fendleriana usually is the dominant grass in the ground cover. P. truei was especially abundant along brushy slopes where mixed shrubs (Amelanchier, Cercocarpos and Fendlera) were codominant with pinyon pines and Utah junipers. The pinyon-juniper-mixed shrub area west of Far View Ruins was almost optimum habitat for P. truei.

P. truei was abundant on the rocky ridge of Wetherill Mesa near Mug House; the pinyon-juniper woodland here has a Cercocarpos understory, and appears to provide close to optimum conditions for this species.