Table 13—Food Present in 114 Coyote Scats Collected at Mesa Verde National Park each Month from September 1963 through August 1964.

Food Item Number of occurrences Percentage of total items
Sylvilagus sp. 32 12.65
Spermophilus variegatus 5 1.97
Eutamias sp. 12 4.74
Reithrodontomys megalotis 4 1.58
Peromyscus boylei 2 0.79
Peromyscus maniculatus 3 1.18
Peromyscus truei 7 2.76
Neotoma cinerea 2 0.79
Neotoma mexicana 9 3.56
Neotoma albigula 5 1.97
Neotoma sp. 3 1.18
Microtus longicaudus 1 0.39
Microtus mexicanus 11 4.34
Microtus montanus 1 0.39
Microtus sp. 1 0.39
Odocoileus hemionus 59 23.32
Grass 34 13.44
Juniper berries 23 9.09
Pinyon needles 14 5.53
Pinyon nuts 1 0.39
Arthropods 7 2.76
Juniper needles 3 1.18
Rodent or Lagomorph bones 5 1.97
Sceloporus sp. 1 0.39
Unidentified fruit 2 0.79
Rocks 3 1.18
Paper 4 1.58
Soil 3 1.18
Feathers 5 1.97

Total

253

Hawks, owls and eagles live in the park. Red-tailed hawks were seen frequently in the burned area on the northern end of Wetherill Mesa. Both hawks and owls probably prey upon Peromyscus in Mesa Verde, for they are well-known predators upon mice and small rodents in other areas. I tried to find owl and hawk nests that were occupied, but located only nests that were abandoned or impossible to reach.

Captive gopher snakes, Pituophis melanoleucus, ate adults of both species of Peromyscus. Gopher snakes probably are the most abundant snake in the park; they feed mostly on mice and other rodents. Fur of Peromyscus was found in the stomach of a striped whipsnake, Masticophis taeniatus (Douglas, 1966:734).

Discussion

Five species of Peromyscus inhabit Mesa Verde National Park (Anderson, 1961). Two of these species, P. crinitus and P. difficilis are rare, and none was taken in more than 14,000 trap nights. Several individuals of P. boylei were taken in live traps, but this species could not be regarded as common. The two remaining species, P. truei and P. maniculatus, are the most abundant species in the park. Comparison of the habitats and life-cycles of these two forms and analyses of their interrelationships have been the objectives of this study.

The distribution of P. truei in the park is regulated by the presence of living pinyon-juniper woodland where logs and hollow trees of Juniperus osteosperma provide nesting and hiding places, and where seeds of juniper trees and nuts of pinyon trees provide food. Several other investigators have reported P. truei to be associated with trees, but apparently these findings have not assumed the importance they warrant in understanding the ecology of this species. Bailey (1931:152) observed an individual of P. truei nesting in a tree on Conchas Creek, New Mexico, and thought that this species might be more arboreal than was generally supposed. The type specimen of P. t. truei was taken by Shufeldt from a "nest protruding from an opening in the dead and hollow trunk of a small pinon, at least 2 feet above the ground#8230. The nest, composed of the fine fibers of the inner bark of the pinon, was soon pulled out, and its owner dislodged...." (Shufeldt, 1885:403). Individuals of P. truei usually build nests in trees, or in hollow logs, and are therefore more abundant in pinyon-juniper woodland where there are many such nesting sites.

Rocks and stones are not necessary in the habitat of P. truei, although this species was most abundant where there was stony soil. The coincidence of rock or stones and a high density of P. truei is thought to be explainable in terms of vegetation. Stony soils support mixed shrubs as well as pinyon and juniper trees; the additional cover and source of food probably allow a greater abundance of P. truei than would be possible without the shrubs. Secondarily, the rock provides nesting sites for more mice.

Stands of mixed shrubs, lacking a pinyon-juniper canopy, do not support P. truei. Its absence was noteworthy on Navajo Hill and on the northern end of Wetherill Mesa where only P. maniculatus lived among the mixed shrubs and grassland. On the Mesa Verde, pinyon and juniper trees must be present in order for P. truei to live in an area; and, these trees must be alive. Dead pinyons and junipers still stand in the burned part of Morfield Ridge, but no P. truei were found there.

Although a few individuals of P. truei were taken in stands of sagebrush adjacent to pinyon-juniper woodlands, this species does not ordinarily venture far from the forest.

P. maniculatus lives almost everywhere in Mesa Verde; the preferred habitats are open and grassy with an overstory of mixed shrubs. Individuals of P. maniculatus venture into ecotonal areas lying between grasslands and pinyon-juniper forest, or between sagebrush and pinyon-juniper forest. P. maniculatus is found also in disturbed areas and in stands of sagebrush that occur in clearings of the pinyon-juniper woodland. In such areas, P. maniculatus and P. truei are sympatric; their home ranges overlap and any inter-specific competition that might occur would be expected in these places.

The ability of P. maniculatus to live in many different habitats is correlated in part with its ability to build nests in a variety of sites. Whereas P. truei usually builds nests only in dead branches or logs, P. maniculatus builds nests in such varied places as spaces under rocks, at the bases of rotten trees, and in abandoned tunnels of pocket gophers. This adaptability is advantageous for the dispersal of young individuals and the movement of adults into new areas.

Nesting sites have important bearing on survival of the young. In Mesa Verde the rainy season occurs in July and August, while both species of Peromyscus are reproducing. It is reasonable to assume that young animals that remain dry survive better than those that become wet and chilled. The nestling young of P. truei are in a more favorable position to remain dry and warm than are nestling young of P. maniculatus.

Captives of each species differed in the amounts of water consumed per gram of body weight. Individuals of P. truei consumed more water per gram of body weight than individuals of P. maniculatus. Animals may drink more water than they require when allowed to drink ad libitum, but Lindeborg (1952) has shown that species which consume less water when it is not restricted also fare better on a reduced ration. P. maniculatus appears to be better adapted to aridity than P. truei. The preferred habitats of each species are in accord with these findings.

Within the trapping grid, the most moderate microenvironment, in terms of temperature and humidity, was in the pinyon-juniper forest, where P. truei lives. The temperature extremes were wider in the microenvironments of a thicket of oak brush and of two different stands of sagebrush, where P. maniculatus lives, than in the forest. P. maniculatus tends to live in the harsher, more arid parts of Mesa Verde. Because of its propensity to build nests under things, or in the ground, and because of its ability to use less water per gram of body weight, P. maniculatus is better adapted to withstand harsh environments than is P. truei.

P. truei may be restricted to the pinyon-juniper woodland because of its need for more mesic conditions. Still, Mesa Verde is semi-arid and there are few permanent sources of water available for animals. The primary source of moisture for rodents must be their food. Analysis of the percentages of moisture contained in the three most common plants in the trapping grid showed that P. truei could obtain the required moisture by eating about ten grams of these plants daily; individuals of P. maniculatus would need to eat less in order to satisfy their water needs.

Individuals of P. truei died more frequently in warm live-traps than did individuals of P. maniculatus. This indicates that P. truei can tolerate less desiccation, or a narrower range of temperatures, than can P. maniculatus.

Both species of mice eat some of the same plants, but these plants occur widely. P. truei seems to rely more upon the nuts of pinyons and the seeds of junipers than does P. maniculatus. Mounds of discarded juniper seeds were associated with all nesting sites of P. truei. Bailey (1931:153) also noticed the fondness of this species for pine nuts and juniper seeds. Apparently, the availability of these foods is one of the major factors affecting the distribution of P. truei. However, this is not the only factor, as is shown by the presence of P. maniculatus but lack of P. truei in a juniper-pinyon association with an understory of bitterbrush. This habitat was seemingly too arid for P. truei.

Factors Affecting Population Densities

The production of young, and success in rearing them, is essential to continuity of any population. P. maniculatus is favored in this respect, because the females produce more young and wean them sooner than do females of P. truei. In addition, lactating females of P. maniculatus require significantly less water than do females of P. truei. Since young mice of both species require no more water per gram of body weight than do adults, the young can disperse into any area that is habitable by their species. P. maniculatus probably is affected less by prolonged drought than is P. truei. Since lactating females require the most water of any animal in the population, they are the weakest link in the system. Females of Peromyscus are known to reabsorb embryos when conditions are unfavorable for continued pregnancy. If prolonged drought occurred in the reproductive season, and desiccated the vegetation upon which the mice depend for moisture, the populations should diminish the following year. Lactating females of P. truei would be affected more seriously by a shortage of water than would lactating females of P. maniculatus.

Of two species, the one producing the more young probably would be subjected to more parasitism and predation than the species producing fewer young. A favorable season for botflies, Cuterebra sp., revealed that P. maniculatus has a higher incidence of parasitism by these flies than has P. truei; possibly the adult flies concentrate in the open, grassy areas where P. maniculatus is more abundant, rather than in the woodlands where P. truei lives. Perhaps the lower parasitism of P. truei by warbles is related to the physiology of this species of mouse. Near Boulder, Colorado, the incidence of infection by warbles is lower in P. difficilis, a species closely related to P. truei, than in P. maniculatus (V. Keen, personal communication).

Although predation by carnivores would be expected to be higher on P. maniculatus, because this species does not climb, my data show that more individuals of P. truei were taken by coyotes. I lack confidence in these findings, suspecting that another sample might indicate the reverse. Birds of prey probably catch more individuals of P. maniculatus, because this species lives in more open habitats. My data do not warrant firm conclusions regarding predation.

The length of time females must care for their young influences the rate at which individuals can be added to the population. Females of P. truei nurse their young longer and keep them in the nest longer than do females of P. maniculatus. Although this may enhance the chances of survival of young of P. truei, it also reduces the number of litters that each female can have in each breeding season. Females of P. maniculatus can produce more young per litter, and each female probably can produce more litters per year than females of P. truei.

Captives of P. truei were tolerant of other individuals of the same species, even when kept in close confinement. However, when there was slight shortage of food or water they killed their litter mates, or females killed their young. Only a short period of time was necessary for one mouse to dispatch all others in the litter. The attacked mice were bitten through the head before being eaten; the brains and viscera were the first parts consumed. The population might be decimated rapidly if drought forced this species to cannibalism. When the supply of food or water was restored, the captive mice resumed their tolerant nature.

In captivity, P. maniculatus is amazingly tolerant of close confinement with members of the same species; individuals did not tend to kill their litter mates, or their young, even during shortage of food and water. This tolerance, especially under stressful conditions, probably enables P. maniculatus to persist in relatively unfavorable areas.

Adaptations to Environment

Each of the two species of Peromyscus illustrates one or more adaptations to its environment. P. truei is adapted to climbing by possession of long toes, a long tail, and large hind feet. The tail is used as a counterbalance when climbing (Horner, 1954). When frightened, individuals of P. truei often ran across the ground in a semi-saltatorial fashion, bounding over clumps of grass that were as much as 18 inches high. Such individuals usually ran to the nearest tree and climbed to branches 10 to 20 feet above the ground.

Large eyes are characteristic of the truei group of mice, and may be an adaptation to a semi-arboreal mode of life. A similar adaptation is shared by some other arboreal mammals, and of arboreal snakes. The large eyes of P. truei in comparison to those of P. maniculatus, probably increase the field of vision, and permit the animal to look downward as well as in other directions.

The above-mentioned adaptations of P. truei permit these graceful mice to use their environment effectively. By climbing, this species can nest above-ground in the hollow branches of trees, and can rear its young in a comparatively safe setting. The ability to climb also permits vertical as well as horizontal use of a limited habitat. Because of the three-dimensional nature of the home range of truei, its range is actually larger than that of maniculatus although the standard trapping procedures makes the home range of the two appear to be about the same size. Finally, trees may offer safety from predators, and a source of food that probably is the winter staple of this species.

Peromyscus maniculatus has adapted differently to its environment. Small size of body and appendages permit this species to use a variety of nesting sites and hiding places even though it is restricted, by its anatomy, to life on the ground. The tail and hind feet are shorter than in P. truei, and P. maniculatus is an inefficient climber. I have placed individuals in bushes, and found that many walk off into space from a height of several feet. Perhaps the relative smallness of their eyes accounts for their seeming lack of awareness of how high they are above the ground.

When frightened, individuals of P. maniculatus ran rapidly in a zig-zag path and dove into the nearest cover. Mice, released from live traps, often stuck their heads under leaves, leaving their bodies exposed. This species tends to hide as rapidly as possible, and remain motionless. This tactic would not be of much value as an escape from carnivores, but it could be effective against birds of prey.

In Mesa Verde, P. maniculatus inhabits the more arid, open areas. When the population is dense, individuals of this species are found also in pinyon-juniper woodland. Apparently P. maniculatus prefers the grassy areas and the thickets of oak brush. Although such habitats have harsh climatic conditions, they offer innumerable hiding places, and thus have great advantage for a species confined to the ground.

The low requirements of water per gram of body weight, the ability to eat diversified foods, the use of varied habitats, the high fecundity, and the ability to use any nook for retreat or nesting make P. maniculatus a successful inhabitant of most parts of Mesa Verde, and indeed, of most of North America.

Literature Cited
Anderson, S.
1961. Mammals of Mesa Verde National Park, Colorado. Univ. Kansas Publ., Mus. Nat. Hist., 14:29-67, 2 pls., 3 figs.
Arrhenius, G., and E. Bonatti
1965. The Mesa Verde loess, pp. 92-100, in Contributions of the Wetherill Mesa Archeological Project, Memoirs Soc. Amer. Archeol., 19; American Antiquity, 31, No. 2, Pt. 2.
Asdell, S. A.
1964. Patterns of mammalian reproduction. Comstock Publ. Co., Ithaca, viii + 1-670 pp.
Bailey, V.
1931. Mammals of New Mexico. N. Amer. Fauna, 53:1-412, 22 pls., 58 figs.
Beidleman, R. G.
1954. October breeding of Peromyscus in north central Colorado. Jour. Mamm., 35:118.
Brusven, M. A., and G. B. Mulkern
1960. The use of epidermal characteristics for the identification of plants recovered in fragmentary condition from the crops of grasshoppers. North Dakota Agricultural Exp. Sta., Fargo, Research Rept., 3:3-11.
Burt, W. H.
1940. Territorial behavior and populations of some small mammals in southern Michigan. Misc. Publ. Mus. Zool., Univ. Michigan, 45: 1-58, 2 pls.
Calhoun, J. B., ed.
1948-1956. Annual reports of the North American census of small mammals. Distributed by the editor, National Institutes of Health, Bethesda 14, Maryland.
1959. Population dynamics of vertebrates release No. 10, Revised sampling procedure for the North American census of small mammals (NACSM). pp. 1-12, Distributed by the editor, Nat. Inst. Health, Bethesda 14, Maryland.
Chew, R. M.
1951. The water exchanges of some small mammals. Ecological Monographs, 21:215-225.
1965. Water metabolism of mammals, pp. 43-178, in Physiological Mammology Vol. II Mammalian reactions to stressful environments, Mayer, W. V., and R. G. Van Gelder, eds., Academic Press, New York, xii + 1-326 pp.
Cogshall, A. S.
1928. Food habits of deer mice of the genus Peromyscus in captivity. Jour. Mamm., 9:217-221.
Collins, H. H.
1918. Studies of normal molt and of artificially induced regeneration of pelage in Peromyscus. Jour. Exptl. Zool., 27:73-99.
Dice, L. R.
1922. Some factors affecting the distribution of the prairie vole, forest deer mouse, and prairie deer mouse. Ecology, 3:29-47.
1934. An improved Peromyscus ration. Jour. Mamm., 15:160-161.
Douglas, C. L.
1965. Biological techniques in archeology, pp. 193-201, in Contributions of the Wetherill Mesa Archeological Project, Memoirs Soc. Amer. Archeol., 19; American Antiquity, 31, No. 2, Pt. 2.
1966. Amphibians and reptiles of Mesa Verde National Park, Colorado. Univ. Kansas Publ. Mus. Nat. Hist., 15:711-744, 2 pls., 6 figs.
Dusi, J. L.
1949. Methods for the determination of food habits by plant microtechnique and histology and their application to cottontail rabbit food habits. Jour. Wildlife Mgt., 13:295-298
Erdman, J. A.
1962. Ecology of the pinyon-juniper woodland of Wetherill Mesa, Mesa Verde National Park, Colorado. Unpublished M. A. thesis, Univ. Colorado.
Erdman, J. A., C. L. Douglas, and J. W. Marr
1968. The environment of Mesa Verde, Mesa Verde National Park, Colorado. Archeol. Res. Series, No. 7-D. Nat. Park Serv., Washington, D. C., in press.
Esau, K.
1960. Anatomy of Seed Plants. John Wiley and Sons, New York, xvi + 1-376 pp.
Geiger, R.
1965. The climate near the ground. Harvard Univ. Press, Cambridge, Mass., xiv + 1-611 pp.
Hall, E. R.
1928. Note on the life history of the woodland deer mouse. Jour. Mamm., 9:255-256
Hamilton, W. J., Jr.
1941. The food of small forest mammals in eastern United States. Jour. Mamm., 22:250-263
Hayne, D. W.
1949. Calculation of size of home range. Jour. Mamm., 30:1-18.
Hoffmeister, D. F.
1951. A taxonomic and evolutionary study of the pinon mouse, Peromyscus truei. Illinois Biol. Monographs, Vol. 21, No. 4, ix + 1-104 pp.
Horner, B. E.
1954. Arboreal adaptations of Peromyscus with special reference to use of the tail. Cont. Lab. Vert. Biol., Univ. Michigan, 61:1-85.
Howard, W. E.
1950. Winter fecundity of caged male white-footed mice in Michigan. Jour. Mamm., 31:319-321.
Jameson, E. W., Jr.
1952. Food of deer mice Peromyscus maniculatus and P. boylei in the northern Sierra Nevada, California. Jour. Mamm., 33:50-60.
1953. Reproduction of deer mice (Peromyscus maniculatus and P. boylei) in the Sierra Nevada, California. Jour. Mamm., 34:44-58.
Johnson, D. R.
1962. Effects of habitat change on the food habits of rodents. Abstract of Ph. D. dissertation, Colorado State Univ., Ft. Collins.

Lang, H.
1925. How squirrels and other rodents carry their young. Jour. Mamm., 6:18-24.
Lindeborg, R. G.
1950. An adaptation of breeding Peromyscus maniculatus bairdii females to available water, and observations on changes in body weight. Jour. Mamm., 31:74-78.
1952. Water requirements of certain rodents from xeric and mesic habitats. Cont. Lab. Vert. Biol., Univ. Michigan, 58:1-32.
McCabe, T. T., and B. D. Blanchard
1950. Three species of Peromyscus. Rood Associates, Santa Barbara, California, v + 1-136 pp.
Metcalfe, C. R., and L. Chalk
1950. Anatomy of the dicotyledons I and II. Clarendon Press, Oxford, 1500 pp.
Mohr, C. O., and W. A. Stumpf
1966. Comparison of methods for calculating areas of animal activity. Jour. Wildlife Mgt., 30:293-304.
Osgood, W. H.
1909. Revision of the mice of the American genus Peromyscus. N. Amer. Fauna, 28:1-285, 8 pls., 12 figs.
Redman, J. P., and J. A. Sealander
1958. Home ranges of deer mice in southern Arkansas. Jour. Mamm., 39:390-395.
Ross, L. G.
1930. A comparative study of daily water-intake among certain taxonomic and geographic groups within the genus Peromyscus. Biol. Bull., 59:326-338.
Sanderson, G. C.
1966. The study of mammal movements—a review. Jour. Wildlife Mtg., 30:215-235.
Schmidt-Nielsen, K.
1964. Desert animals: physiological problems of heat and water. Oxford Univ. Press, London, xv + 1-277 pp.
Schmidt-Nielsen, K., B. Schmidt-Nielsen, and A. Brokaw
1948. Urea excretion in desert rodents exposed to high protein diets. Jour. Cell. Comp. Physiol., 32:361-379.
Scott, T. G., and E. Snead
1942. Warbles in Peromyscus leucopus noveboracensis. Jour. Mamm., 23:94-95.
Sealander, J. A.
1961. Hematological values in deer mice in relation to botfly infection. Jour. Mamm., 42:57-60.
Seton, E. T.
1920. Notes on the breeding habits of captive deer mice. Jour. Mamm., 1:134-138.
Shufeldt, R. W.
1885. Description of Hesperomys truei, a new species belonging to the subfamily Murinae. Proc. U. S. Nat. Mus., 8:403-408, 21 pls.
Stickel, L. F.
1954. A comparison of certain methods of measuring ranges of small mammals. Jour. Mamm., 35:1-15.

Svihla, A.
1932. A comparative life history study of the mice of the genus Peromyscus. Univ. Michigan Mus. Zool., Misc. Publ., 24:1-39.
Test, F. H., and A. R. Test
1943. Incidence of dipteran parasitosis in populations of small mammals. Jour. Mamm., 24:506-508.
Welsh, S. L., and J. A. Erdman
1964. Annotated checklist of the plants of Mesa Verde, Colorado. Brigham Young Univ. Sci. Bull., Biol. Ser., 4(2):1-32.
Williams, O.
1955. The food of mice and shrews in a Colorado montane forest. Univ. Colorado Studies, Ser. in Biol., 3:109-114.
1959a. Food habits of the deer mouse. Jour. Mamm., 40:415-419.
1959b. Water intake in the deer mouse. Jour. Mamm., 40:602-606.
1959c. Modified gum syrup. Turtox News, Vol. 37, No. 10.
Wilson, L. W.
1945. Parasites collected from wood mouse in West Virginia. Jour. Mamm., 26:200.

Transcriber's Notes

All obvious typographic errors corrected. For consistency, the species listings for boylii has been standardised to boylei.

Typographical Corrections

Page    Correction
429    nuaseosus ⇒ nauseosus
430    Orthocarpos ⇒ Orthocarpus
447    unbellata ⇒ umbellata
450    ludovociana ⇒ ludoviciana
456    phrheliometer ⇒ pyrheliometer
480    rudale ⇒ ruderale
481    rates ⇒ rats
482    bases ⇒ basis
499    clumbs ⇒ clumps