Peromyscus trueipinyon mouse

Ge­o­graphic Range

Pinyon mice can be found as far east as the pan­han­dle of north Texas and as far west as the Pa­cific coast. The north­ern limit of their range is cen­tral Ore­gon, and the south­ern limit is south­ern Mex­ico. (Hoffmeis­ter, et al., 1981; Wil­son and Ruff, 1999)

Habi­tat

Pinyon mice are ter­res­trial mam­mals that can be found at al­ti­tudes rang­ing from sea level to el­e­va­tions of greater than 2300 me­ters. They fre­quent arid or semi-arid cli­mates, pre­fer­ring brush­land and desert, and are typ­i­cally found near pinyon ju­nipers, hence their com­mon name. How­ever, pinyon mice can also be found in open, grassy habi­tats, as well as land­scapes in­clud­ing canyons, red­woods, yel­low pine belts, sage­brush, scrub oak, boul­ders, cacti, and rocky slopes. Pinyon mice are able to en­dure warm, dry sum­mers in ad­di­tion to snowy win­ters. They make dens under rock ledges, out­crops, stone shelves and slabs, and in live or dead trees. (Hall and Mor­ri­son, 1997; Hoffmeis­ter, et al., 1981; King, 1968; Wil­son and Ruff, 1999)

  • Range elevation
    0 to greater than 2300 m
    0.00 to ft

Phys­i­cal De­scrip­tion

Pinyon mice have long, silky fur that ranges from yel­low-brown to dark gray on the back and fades to white on the under parts and feet. They may or may not have a pec­toral spot. The tail is tipped with long hairs and has a dark dor­sal stripe run­ning down its length. The hind feet are large, and are typ­i­cally 22 mm or more in length. Ju­ve­niles have gray pelage that changes with a se­ries of molts, start­ing at 7 weeks and fin­ish­ing at 10 to 11 weeks of age. Coat color matches the habi­tat re­gion­ally, al­low­ing these mice to blend into veg­e­ta­tion and hide from preda­tors. Males and fe­males are sim­i­lar in size, the av­er­age weight is about 20 g, and the head and body length ranges be­tween 171 to 231 mm. Tail length varies from 76 to 123 mm. The size of pinyon mice often varies with lo­ca­tion; pinyon mice in the west­ern parts of their range tend to have a longer tail, smaller body size, smaller ears, and smaller hind feet than their coun­ter­parts in the east. (Hoffmeis­ter, et al., 1981; King, 1968; Wil­son and Ruff, 1999)

  • Sexual Dimorphism
  • sexes alike
  • Average mass
    20 g
    0.70 oz
  • Average mass
    25 g
    0.88 oz
    AnAge
  • Range length
    171 to 231 mm
    6.73 to 9.09 in
  • Average basal metabolic rate
    0.307 W
    AnAge

Re­pro­duc­tion

Pinyon mice have a promis­cu­ous mat­ing sys­tem in which fe­males nest in small ter­ri­to­ries and males seek mat­ing op­por­tu­ni­ties with nearby fe­males. (Rib­ble and Stan­ley, 1998)

Al­though mat­ing can occur in all sea­sons, pinyon mice breed pri­mar­ily from mid-Feb­ru­ary to mid-No­vem­ber with a peak be­tween April and June. Fe­males give birth to a lit­ter of three to six pups after a ges­ta­tion pe­riod of ap­prox­i­mately 26 days, though ges­ta­tion may be as long as 40 days if the fe­male is lac­tat­ing. Fe­males first come into es­trus at ap­prox­i­mately 50 days of age, and males are ca­pa­ble of in­sem­i­nat­ing fe­males at ap­prox­i­mately 9 weeks of age. (Hoffmeis­ter, et al., 1981; King, 1968; Scheibe and O'Far­rell, 1995; Scheibe, 1984; Wil­son and Ruff, 1999)

  • Breeding interval
    Pinyon mice breed at intervals as frequent as once monthly.
  • Breeding season
    Pinyon mice will breed at any time between February and mid-November with a peak between April and June.
  • Range number of offspring
    3 to 6
  • Average number of offspring
    3.4
    AnAge
  • Range gestation period
    40 (high) days
  • Average gestation period
    26 days
  • Range weaning age
    3 to 4 weeks
  • Range time to independence
    3 to 4 weeks
  • Average age at sexual or reproductive maturity (female)
    50 days
  • Average age at sexual or reproductive maturity (female)
    Sex: female
    50 days
    AnAge
  • Average age at sexual or reproductive maturity (male)
    9 weeks

New­born pinyon mice weigh around 2.3 grams at birth, and they are born com­pletely hair­less with their ears and eyes folded shut. The pups are ca­pa­ble of squeak­ing at one week of age, and their bod­ies are cov­ered in hair by day 14. The pups nurse for three to four weeks, at which point they be­come in­de­pen­dent. Fe­males ex­clu­sively care for their young in a nest until they are weaned. (Wil­son and Ruff, 1999)

  • Parental Investment
  • altricial
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

The lifes­pan of pinyon mice and other mice in the genus Per­omyscus has not been stud­ied in de­tail. An in­di­vid­ual Per­omyscus man­ic­u­la­tus lived to be eight years old in cap­tiv­ity, but stud­ies have shown that mice in this genus rarely live more than a year in the wild. Only 20% of the young in each nest will sur­vive their first year of life, and only 2-3% of adults live long enough to breed in con­sec­u­tive sea­sons. (Hoffmeis­ter, et al., 1981; King, 1968)

  • Average lifespan
    Status: wild
    1 years
  • Average lifespan
    Status: captivity
    5.4 years
    AnAge

Be­hav­ior

Pinyon mice are noc­tur­nal ro­dents that sleep pe­ri­od­i­cally through­out the day. They are ex­cel­lent climbers, fre­quently using their long tails for bal­ance. Stud­ies have shown that pinyon mice are more ac­tive for­agers when am­bi­ent tem­per­a­tures are higher. Pinyon mice are less ac­tive on moon­lit nights, most likely be­cause there is an in­creased risk of pre­da­tion when it is brighter out­side. In times of se­vere drought, pinyon mice can in­crease urine con­cen­tra­tion, re­duce the mois­ture con­tent of their feces, and drop into a di­ur­nal tor­por to save en­ergy. (Hall and Mor­ri­son, 1997; Hoffmeis­ter, et al., 1981; King, 1968; Rib­ble and Stan­ley, 1998; Scheibe and O'Far­rell, 1995; Scheibe, 1984)

Home Range

Pinyon mice fre­quently use mul­ti­ple den sites dur­ing the day. Male dens are typ­i­cally far­ther apart from each other than fe­male dens, but the ter­ri­to­ries of males tend to over­lap each other more than the ter­ri­to­ries of fe­males. In gen­eral, male ter­ri­to­ries are larger, while fe­male ter­ri­to­ries are smaller be­cause fe­males are con­strained to their dens dur­ing breed­ing. This re­pro­duc­tive con­straint is the basis for their promis­cu­ous mat­ing sys­tem in which males must search for fe­males. (Hall and Mor­ri­son, 1997; Hoffmeis­ter, et al., 1981; King, 1968; Rib­ble and Stan­ley, 1998; Scheibe and O'Far­rell, 1995; Scheibe, 1984)

Com­mu­ni­ca­tion and Per­cep­tion

Com­mu­ni­ca­tion in pinyon mice hasn't been well-stud­ied. They are likely to use vi­sual, au­di­tory, chem­i­cal, and tac­tile modes of com­mu­ni­ca­tion.

Per­omyscus species are known for their acute senses of hear­ing and smell, which they use to nav­i­gate, find food, and es­cape pre­da­tion at night. Their en­larged eyes sug­gest they have a well-de­vel­oped sense of vi­sion in low light con­di­tions. Their long whiskers are used for tac­tile per­cep­tion.

Food Habits

Pinyon mice are pri­mar­ily fru­giv­o­rous and graniv­o­rous, al­though they will also read­ily eat in­sects, spi­ders, and other in­ver­te­brates. Adults typ­i­cally feed on ju­niper seeds (Ju­nipe­rus) and berries in the win­ter and acorn mast (Quer­cus) in the sum­mer. Pinyon mice are no­to­ri­ous at caching their food sup­ply; they fre­quently dig holes and bury their food in var­i­ous places around their ter­ri­tory, par­tic­u­larly around den sites. These cache net­works may be­come quite ex­ten­sive. Fi­nally, pinyon mice are ca­pa­ble of sur­viv­ing on a very lim­ited water sup­ply, which is cru­cial to their sur­vival in the arid habi­tats they oc­cupy. (Hoffmeis­ter, et al., 1981; King, 1968; Wil­son and Ruff, 1999)

  • Animal Foods
  • insects
  • terrestrial non-insect arthropods
  • Plant Foods
  • leaves
  • seeds, grains, and nuts
  • fruit

Pre­da­tion

Pre­da­tion on pinyon mice has not been well stud­ied, al­though pre­da­tion most likely plays a role in the high mor­tal­ity rate of these ro­dents. Their pri­mary preda­tors are owls, di­ur­nal birds of prey, and snakes, es­pe­cially rat­tlesnakes. They es­cape pre­da­tion by re­main­ing in­ac­tive dur­ing the day in dens, by their cryp­tic col­oration, and by their acute senses at night. (King, 1968)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Pinyon mice are al­most al­ways found near pinyon ju­nipers, hence their com­mon name. Ju­niper seeds are the main food source of pinon mice, mak­ing them, like other mem­bers of the genus Per­omyscus, sig­nif­i­cant preda­tors of conifer seeds. Thus they im­pact their com­mu­ni­ties by im­pact­ing the com­po­si­tion of the plant com­mu­nity. Their seed caching be­hav­ior may also re­sult in ger­mi­na­tion of seeds. Pinyon mice are also an im­por­tant and abun­dant source of prey for many avian and mam­malian preda­tors. (King, 1968)

  • Ecosystem Impact
  • disperses seeds

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

It is not known whether pinyon mice have pos­i­tive af­fects on human pop­u­la­tions, aside from their im­por­tant ecosys­tem roles.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Pinyon mice serve as an im­por­tant reser­voir for sev­eral types of par­a­sites. Some have spec­u­lated that they are ca­pa­ble of car­ry­ing plague-in­fested fleas, but this has not been well doc­u­mented. Mem­bers of the genus Per­omyscus are ca­pa­ble of car­ry­ing chig­gers, a com­mon pest, as well as the ticks that trans­mit Rocky Moun­tain Spot­ted Fever and Lyme dis­ease to hu­mans. Per­omyscus species are also im­por­tant reser­voirs for han­taviruses. (King, 1968)

  • Negative Impacts
  • injures humans
    • carries human disease

Con­ser­va­tion Sta­tus

Pinyon mice are not cur­rently threat­ened through­out much of their range. How­ever, since pinyon ju­nipers are a cru­cial part of their habi­tat, de­struc­tion of such habi­tats can im­peril these mice. The sub­species Per­omyscus truei co­manche, found in the pand­han­dle of north­west­ern Texas, is con­sid­ered near threat­ened by the IUCN. (King, 1968)

Con­trib­u­tors

Tanya Dewey (ed­i­tor), An­i­mal Di­ver­sity Web.

Jen­nifer Gumas (au­thor), Michi­gan State Uni­ver­sity, Bar­bara Lun­dri­gan (ed­i­tor), Michi­gan State Uni­ver­sity.

Glossary

Nearctic

living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.

World Map

Neotropical

living in the southern part of the New World. In other words, Central and South America.

World Map

acoustic

uses sound to communicate

altricial

young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

chemical

uses smells or other chemicals to communicate

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

desert or dunes

in deserts low (less than 30 cm per year) and unpredictable rainfall results in landscapes dominated by plants and animals adapted to aridity. Vegetation is typically sparse, though spectacular blooms may occur following rain. Deserts can be cold or warm and daily temperates typically fluctuate. In dune areas vegetation is also sparse and conditions are dry. This is because sand does not hold water well so little is available to plants. In dunes near seas and oceans this is compounded by the influence of salt in the air and soil. Salt limits the ability of plants to take up water through their roots.

endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

granivore

an animal that mainly eats seeds

herbivore

An animal that eats mainly plants or parts of plants.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

motile

having the capacity to move from one place to another.

mountains

This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.

native range

the area in which the animal is naturally found, the region in which it is endemic.

nocturnal

active during the night

polygynandrous

the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.

scrub forest

scrub forests develop in areas that experience dry seasons.

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

solitary

lives alone

stores or caches food

places a food item in a special place to be eaten later. Also called "hoarding"

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

terrestrial

Living on the ground.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

tropical savanna and grassland

A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.

savanna

A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.

temperate grassland

A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.

visual

uses sight to communicate

viviparous

reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.

Ref­er­ences

Hall, L., M. Mor­ri­son. 1997. Den and Re­lo­ca­tion Site Char­ac­ter­is­tics and Home Ranges of <<Per­omyscus truei>> in the White Moun­tains of Cal­i­for­nia. Great Basin Nat­u­ral­ist, 57 (2): 124-130.

Hoffmeis­ter, D., D. Williams, S. An­der­son, T. Lawlor. 1981. Mam­malian Species #161: <<Per­omyscus truei>>. Pp. 1-5 in Mam­malian Species, Vol. 151-200. The Amer­i­can So­ci­ety of Mam­mal­o­gists.

King, J. 1968. Bi­ol­ogy of <<Per­omyscus>> (Ro­den­tia). The United States of Amer­ica: The Amer­i­can So­ci­ety of Mam­mal­o­gists.

Rib­ble, D., S. Stan­ley. 1998. Home Ranges and So­cial Or­ga­ni­za­tion of Syn­topic <<Per­omyscus boylii>> and <<P. truei>>. Jour­nal of Mam­mal­ogy, 79 (3): 932-941.

Scheibe, J. 1984. The Ef­fects of Weather, Sex, and Sea­son on the Noc­tur­nal Ac­tiv­ity of <<Per­omyscus truei>> (Ro­den­tia). The South­west­ern Nat­u­ral­ist, 29 (1): 1-4.

Scheibe, J., M. O'Far­rell. 1995. Habi­tat Dy­nam­ics in <<Per­omyscus truei>>: Eclec­tic Fe­males, Den­sity De­pen­dence, or Re­pro­duc­tive Con­straints?. Jour­nal of Mam­mal­ogy, 76 (2): 368-375.

Wil­son, D., S. Ruff. 1999. The Smith­son­ian Book of North Amer­i­can Mam­mals. Wash­ing­ton and Lon­don: Smith­son­ian In­sti­tu­tion Press.