Tamias rufusHopi chipmunk

Ge­o­graphic Range

Hopi chip­munks are found only in west­ern North Amer­ica from north-cen­tral Ari­zona to Mon­u­ment Val­ley as well as into east­ern Utah, east­ern Idaho, west­ern Col­orado (re­stricted to Yampa River south­ward), and into the Rocky Moun­tain Range to­wards Canada. (Burt and Best, 1994; Good, et al., 2003; Saldaña-DeLeon and Jones, 1998)

Habi­tat

Hopi chip­munks pre­fer bare or veg­e­tated rocky sub­strate that con­tains ju­niper and pinyon pine. In west­ern Col­orado, they oc­cupy two mi­cro­hab­i­tats: sage patches and ju­niper/pine patches. Hopi chip­munks live at el­e­va­tions of 1,290 to 2,700 me­ters. (Burt and Best, 1994; Root, et al., 2001)

  • Range elevation
    1,290 to 2,700 m
    to ft

Phys­i­cal De­scrip­tion

Hopi chip­munks are small, mono­typic chip­munks in the sub­genus Neo­tamias. They weigh 47.9 to 59.3 grams de­pend­ing on the sea­son. Their ex­ter­nal length mea­sures 197 to 235 mm. Fe­males are gen­er­ally slightly larger than males but have no other dis­tinct dif­fer­ences in mor­phol­ogy. The col­or­ing is buffy and gray patch­work. Up­per­parts have black stripes high­lighted with tones of or­ange-red run­ning in an an­te­rior to pos­te­rior di­rec­tion down its back. Hopi chip­munks also have pale fa­cial white and "ru­fous" fa­cial stripes with the lower stripe ex­tend­ing under the ears. The tail is mixed black and chest­nut dor­sally and chest­nut with faint black stripes ven­trally. There are two an­nual molts: one in the spring and one in early au­tumn. The den­tal for­mula is I 1/1, C 0/0, P 2/1, M 3/3, to­tal­ing 22 teeth. The skull has a long and nar­row brain­case, short nasals, a nar­row in­teror­bital re­gion, and rather large au­di­tory bul­lae. (Burt and Best, 1994; Hall, 1981; Hoffmeis­ter and Ellis, 1979; Lev­en­son, et al., 1985; Nowak, 1999; Saldaña-DeLeon and Jones, 1998; Wil­son and Reeder, 2005)

  • Sexual Dimorphism
  • female larger
  • Range mass
    47.9 to 59.3 g
    1.69 to 2.09 oz
  • Range length
    197 to 235 mm
    7.76 to 9.25 in

Re­pro­duc­tion

The mat­ing be­hav­ior of Hopi chip­munks is un­known. In other Neo­tamias species such as Mer­riam's chip­munks (Tamias mer­ri­ami), sev­eral males con­gre­gate in areas where there are many fe­males. Males run around if an es­trous fe­male is nearby. It is un­known if males chase the fe­male until one cor­ners her for cop­u­la­tion (such as in the East­ern chip­munk) or if males per­form a dis­play. When a male ap­proaches a fe­male, he rubs his body and face against hers. This may be a form of scent-mark­ing, and pre­cedes cop­u­la­tion. Pre-cop­u­la­tion vo­cals and mat­ing calls have been noted in other Neo­tamias chip­munks and are most likely uti­lized by Hopi chip­munks. (Comp­ton and Calla­han, 1995; Nowak, 1999; Yah­ner, 1978)

The breed­ing sea­son of Hopi chim­punks is from Feb­ru­ary until mid-April. Males pre­pare for the breed­ing sea­son by be­com­ing sex­u­ally ac­tive through en­large­ment of testes about a week after emerg­ing from their win­ter dens. Fe­males are pre­pared for mat­ing im­me­di­ately after ex­it­ing their win­ter dens. Fe­males give birth to one lit­ter after a ges­ta­tion pe­riod of 30 to 33 days. Young chip­munks weigh an av­er­age of 3 grams at birth. The heads of the young are larger than bod­ies and they have no hair. The young are cold to the touch until they are a week old. They have a fairly uni­form growth rate and gain 0.50 g per day on av­er­age. By 2 weeks, the color of the adult fa­cial pat­terns be­comes vis­i­ble, the in­cisors have erupted, the toes have begun to sep­a­rate, and the young can drag them­selves using their front legs. By 3 weeks, the hair be­comes smooth and more adult-like, the toes are fully sep­a­rated, and the young can move more ef­fi­ciently. At 5 weeks, the young be­come ac­tive out­side and the cheek-teeth have erupted. At 6 weeks, they are con­sum­ing solid foods. Wean­ing is a slow process and usu­ally oc­curs when the young are 6 to 7 weeks old and by then are fully in­de­pen­dent. Sex­ual ma­tu­rity usu­ally oc­curs at 10 to 12 months with most fe­males hav­ing their first lit­ter in their first year. (Burt and Best, 1994; Hoffmeis­ter and Ellis, 1979; Nowak, 1999; Root, et al., 2001)

  • Breeding interval
    Hopi chipmunks breed once a year between February and April.
  • Breeding season
    Breeding season of Hopi chipmunks runs from February to April.
  • Range number of offspring
    4 to 7
  • Average number of offspring
    5
  • Range gestation period
    30 to 33 days
  • Average gestation period
    31 days
  • Range weaning age
    6 to 7 weeks
  • Average weaning age
    6 weeks
  • Range time to independence
    6 to 7 weeks
  • Average time to independence
    6 weeks
  • Range age at sexual or reproductive maturity (female)
    10 to 12 months
  • Average age at sexual or reproductive maturity (female)
    10 months
  • Range age at sexual or reproductive maturity (male)
    10 to 12 months
  • Average age at sexual or reproductive maturity (male)
    10 months

The mother cares for the young ex­ten­sively until they are ca­pa­ble of being in­de­pen­dent. Wean­ing is a grad­ual process. Males con­tribute no parental care to­wards the young. (Burt and Best, 1994)

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

Lifes­pan/Longevity

Exact lifes­pan of Hopi chimp­munks is un­known. The max­i­mum lifes­pan of other Tamias chip­munks in cap­tiv­ity is roughly 9.5 years, but their lifestyle tends to lower their life ex­pectancy con­sid­er­ably. The longest ex­pected lifes­pan in the wild is 8 years, but most in­di­vid­u­als sur­vive only 2 to 3 years, and only 10% of in­di­vid­u­als sur­vive their first 64 months of life. (Bergstrom and Hoff­mann, 1991; Gor­bunova, et al., 2008; Nowak, 1999)

  • Range lifespan
    Status: wild
    8 (high) years
  • Range lifespan
    Status: captivity
    5 to 9.5 years
  • Typical lifespan
    Status: wild
    2 to 8 years
  • Average lifespan
    Status: wild
    2-3 years

Be­hav­ior

Hopi chip­munks are di­ur­nal and ac­tive dur­ing the early morn­ing hours, es­pe­cially fol­low­ing rain­storms or thun­der­show­ers. They are also hi­ber­na­tors, usu­ally de­creas­ing ac­tiv­ity just be­fore the breed­ing sea­son from No­vem­ber to April. Hopi chip­munks do not hi­ber­nate for great lengths of time, es­pe­cially since the species can be ac­tive until late No­vem­ber and pe­ri­od­i­cally leave their dens dur­ing the win­ter. Hopi chip­munks often in­ter­act with other species of chip­munks in west­ern North Amer­ica, cre­at­ing a very dis­tinct eco­log­i­cal com­mu­nity that is based on their en­vi­ron­men­tal pref­er­ence. This cre­ates a mo­saic of dif­fer­ent mi­cro­hab­i­tats in which the Hopi chip­munks oc­cupy higher el­e­va­tions while species such as yel­low-pine chip­munks (Tamias amoenus) oc­cupy the lower re­gions. This sug­gests that Hopi chip­munk in­ter­ac­tions with other Tamias species are lim­ited by habi­tat pref­er­ence and ge­o­log­i­cal iso­la­tion and do not in­clude hy­bridiza­tion be­tween species. Knowl­edge of in­ter­ac­tions be­tween species is lim­ited, but com­par­ing with other Tamias species, it can be as­sumed that Hopi chip­munks share sim­i­lar char­ac­ter­is­tics of soli­tary liv­ing and tend to dis­play dom­i­nance and soli­tary be­hav­ior when other chip­munks enter their ter­ri­tory. (Burt and Best, 1994; Good, et al., 2003; Nowak, 1999; Yah­ner, 1978)

  • Range territory size
    0.005 to 0.0128 km^2

Home Range

Home range is hard to cal­cu­late in a two-di­men­sional space be­cause Hopi chip­munks are avid climbers whose home range may in­clude trees and sand­stone cliffs. Pro­jected ter­ri­tory size varies among males, fe­males, and ju­ve­niles. Ter­ri­tory size is 1.28 ha for adult males and 1.04 ha for adult fe­males. Ter­ri­tory size of ju­ve­niles is no larger than 0.50 ha. (Burt and Best, 1994)

Com­mu­ni­ca­tion and Per­cep­tion

Com­mu­ni­ca­tion and per­cep­tion strate­gies of Hopi chip­munks are likely sim­i­lar to other Neo­tamias species. These an­i­mals pro­duce two main cat­e­gories of calls: alarm calls and ag­o­nis­tic (courtship) sounds. Alarms calls vary and may in­clude a chip, chuck, or "chip­per­ing" sound. Trills and whis­tles have also been recorded. Courtship sounds were sim­i­lar, but tended to be much harsher. (Nowak, 1999)

Food Habits

The diet of Hopi chip­munks con­sists largely of the berries and seeds of its local re­gion. The va­ri­ety and type avail­able for con­sump­tion is af­fected by the sea­son and ge­o­graph­i­cal range. In Utah, Hopi chip­munks feed pri­mar­ily on the berries of the one-seeded ju­niper (Ju­nipe­rus monosperma). In other areas, in­di­vid­u­als feed on cliff rose, squaw­berry (Rhus trilo­bata), moun­tain ma­hogany, and seeds and nuts from Russ­ian this­tle, pinyon pine, and the Gam­bel and waxy leaf oaks. In late spring and sum­mer, Hopi chip­munks feed on green veg­e­ta­tion. In the fall, their diet changes to favor nuts as they be­come avail­able. The species also has been seen caching food in rocky ledges and uti­lizes its large cheek pouches to carry food to caches. Hopi chip­munks do not typ­i­cally eat leaves or stems in the wild al­though in cap­tiv­ity, they are known to eat parts of dan­de­lions. They need con­stant ac­cess to water, and can die of thirst if de­prived of water for only 2 days. (Burt and Best, 1994; Nowak, 1999)

  • Plant Foods
  • leaves
  • roots and tubers
  • wood, bark, or stems
  • seeds, grains, and nuts
  • flowers

Pre­da­tion

Hopi chip­munks are eaten by snakes, birds, and pos­si­bly mam­mals. Bull­snakes (Pituophis catenifer sayi) have been known to eat ju­ve­nile chip­munks. Other preda­tors in­clude coy­otes (Canis la­trans), Swain­son's hawks (Buteo swain­soni), and long-tailed weasels (Mustela fre­nata). The exact mor­tal­ity of the chip­munks by these preda­tors is not known. (Burt and Best, 1994)

Ecosys­tem Roles

Mites and fleas are com­mon par­a­sites that in­fect Hopi chip­munks. In one case, bot­fly larva (likely Cutere­bra) was found under the skin of an in­di­vid­ual, but it is not known whether this lar­vae typ­i­cally uses the Hopi chip­munk as a host. Hopi chip­munks dis­plays caching be­hav­ior, so it can be as­sumed that it may also dis­perse seeds. The species also in­ter­acts with a large num­ber of west­ern chip­munks in North Amer­ica, but due to its habi­tat pref­er­ence, it is thought that there are not a lot of in­ter­spe­cific in­ter­ac­tions in the ecosys­tem. (Burt and Best, 1994; Nowak, 1999)

  • Ecosystem Impact
  • disperses seeds
Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

The pos­i­tive im­pact of the Hopi chip­munk on hu­mans is un­known, but most likely min­i­mal. Some chip­munks of the sub­genus Neo­tamias are killed for their skins in the fur trade, al­though it is not cer­tain if Hopi chip­munks are in­cluded in this trade. (Nowak, 1999)

  • Positive Impacts
  • body parts are source of valuable material

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There have been sug­ges­tions that Hopi chip­munks dam­age crops (as some Neo­tamias live close to agri­cul­tural areas) but the species rarely oc­curs in large enough con­cen­tra­tions to cause much dam­age. (Nowak, 1999)

  • Negative Impacts
  • crop pest

Con­ser­va­tion Sta­tus

Hopi chip­munks are con­sid­ered sta­ble and not en­dan­gered. There has been some con­cern that habi­tat loss due to agri­cul­tural and urban ex­pan­sion may ad­versely af­fect Neo­tamias species in the fu­ture. (Nowak, 1999; Wil­son and Reeder, 2005)

Other Com­ments

The species has been called by dif­fer­ent names, which in­clude the 1905 clas­si­fi­ca­tion of Eu­tamias hopi­en­sis. The species has also been called Eu­tamias quadrivit­ta­tus rufus, sug­gest­ing it to be a sub­species of Col­orado chip­munks (Eu­tamias quadrivit­ta­tus), but there has been con­sid­er­able de­bate con­cern­ing the arrange­ment of Neo­tamias and Eu­tamias and where Tamias falls under as a sub­genus. Stud­ies such as the size of the skull and bac­u­lum, as well as body shape and col­or­ing, have sought to see if T. quadrivit­ta­tus and T. rufus are sub­species or sep­a­rate species. As of now, Hopi chip­munks are clas­si­fied as Tamias rufus, sep­a­rate from Eu­tamias quadrivit­ta­tus. (Hoffmeis­ter and Ellis, 1979; Nowak, 1999; Pat­ter­son, 1984; Wil­son and Reeder, 2005)

Con­trib­u­tors

Jes­sica Mor­ris (au­thor), Uni­ver­sity of Alaska Fair­banks, Laura Prugh (ed­i­tor), Uni­ver­sity of Wash­ing­ton.

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

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

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.

diurnal
  1. active during the day, 2. lasting for one day.
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.

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

folivore

an animal that mainly eats leaves.

granivore

an animal that mainly eats seeds

herbivore

An animal that eats mainly plants or parts of plants.

hibernation

the state that some animals enter during winter in which normal physiological processes are significantly reduced, thus lowering the animal's energy requirements. The act or condition of passing winter in a torpid or resting state, typically involving the abandonment of homoiothermy in mammals.

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.

polygynous

having more than one female as a mate at one time

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

visual

uses sight to communicate

Ref­er­ences

Bergstrom, B., R. Hoff­mann. 1991. Dis­tri­b­u­tion and Di­ag­no­sis of Three Species of Chip­munks (Tamias) in the Front Range of Col­orado. The South­west­ern Nat­u­ral­ist, 36: 14-28.

Burt, S., T. Best. 1994. Mam­malian Species: Tamias Rufus. The Amer­i­can So­ci­ety of Mam­mal­o­gists, 460: 1-6.

Comp­ton, S., J. Calla­han. 1995. RE­PRO­DUC­TIVE BE­HAV­IOR IN MER­RIAM'S CHIP­MUNK ( TAMIAS MER­RI­AMI ). Great Basin Nat­u­ral­ist, 55: 89-91.

Good, J., J. Dem­boski, D. Nagorsen, J. Sul­li­van. 2003. PHY­LO­GEOG­RA­PHY AND IN­TRO­GRES­SIVE HY­BRIDIZA­TION: CHIP­MUNKS (GENUS TAMIAS) IN THE NORTH­ERN ROCKY MOUN­TAINS. Evo­lu­tion, 57: 1900-1916.

Gor­bunova, V., M. Bozzella, A. Selu­anov. 2008. Ro­dents for com­par­a­tive aging stud­ies: from mice to beavers. AGE, 30: 111-119.

Hall, E. 1981. Mam­mals of North Amer­ica Vol­ume 1. New York: John Wiley & Sons.

Hoffmeis­ter, D., L. Ellis. 1979. Ge­o­graphic Vari­a­tion in Eu­tamias quadrivit­ta­tus with Com­ments on the Tax­on­omy of Other Ari­zo­nan Chip­munks. The South­west­ern Nat­u­ral­ist, 24: 655-665.

Lev­en­son, H., R. Hoff­man, C. Nadler, L. Deutsch, S. Free­man. 1985. SYS­TEM­AT­ICS OF THE HO­L­ARC­TIC CHIP­MUNKS (TAMIAS). Jour­nal of Mam­mal­ogy, 66: 219-242.

Nowak, R. 1999. Walker's Mam­mals of the World 6th Edi­tion Vol­ume II. Bal­ti­more and Lon­don: The John Hop­kins Uni­ver­sity Press.

Pat­ter­son, B. 1984. Ge­o­graphic Vari­a­tion and Tax­on­omy of Col­orado and Hopi Chip­munks (Genus Eu­tamias). Jour­nal of Mam­mal­ogy, 65: 442-456.

Root, J., C. Cal­isher, B. Beaty. 2001. MI­CRO­HAB­I­TAT PAR­TI­TION­ING BY TWO CHIP­MUNK SPECIES (TAMIAS) IN WEST­ERN COL­ORADO. West­ern North Amer­i­can Nat­u­ral­ist, 61: 114-118.

Saldaña-DeLeon, J., C. Jones. 1998. An­no­tated check­list of the re­cent mam­mals of Col­orado. Mu­seum of Texas Tech Uni­ver­sity: 1-16.

Wil­son, D., D. Reeder. 2005. Mam­mal Species of the World Vol­ume II. Bal­ti­more and Lon­don: The John Hop­kins Uni­ver­sity Press.

Yah­ner, R. 1978. The Adap­tive Na­ture of the So­cial Sys­tem and Be­hav­ior in the East­ern Chip­munk, Tamias stria­tus. Be­hav­ioral and So­cio­bi­ol­ogy, 3: 397-427.