pocket mouse, any of 36 species of American rodents having fur-lined external cheek pouches that open alongside the mouth. The pouches are used for storing food, particularly seeds, as the animal forages. Like “true” mice and rats (family Muridae), pocket mice travel on all four limbs along the ground, as opposed to hopping like their relative, the kangaroo mouse. Pocket mice are nocturnal and usually solitary. They eat seeds, succulent plant parts, and nuts, carrying food (mainly seeds) in their cheek pouches to hoard in burrows. Most are active all year, even some of those living at northern latitudes. Others remain in burrows during winter or on hot days in summer; they may become torpid but do not hibernate.

Natural history

The nine species of silky pocket mice (genus Perognathus) are very small, weighing from 5 to 30 grams (0.2 to 1.1 ounces) and having a body length of 6 to 9 cm (2.4 to 3.5 inches) and hairy tails 5 to 10 cm long. Silky pocket mice have soft fur ranging from yellowish to gray on the upperparts and white to buff on the underparts; soles of the hind feet are furry, but in all other pocket mice the soles are hairless.

The 15 species of coarse-haired pocket mice (genus Chaetodipus) are larger on average, weighing 15 to 47 grams and having a body length of 8 to 13 cm and hairy, tufted tails as long as or much longer than the body (up to 15 cm). Coarse-haired pocket mice are similar in colour to silky pocket mice, but the fur is harsh and the rump has spiny bristles. Silky and coarse-haired pocket mice range from western Canada and the United States into southern Mexico, where they inhabit open desert country.

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The five species of spiny pocket mice (genus Liomys) are found in extreme southern Texas, but they live mostly in Mexico southward to Panama in semiarid brushy and rocky habitats. These pocket mice weigh 34 to 50 grams and have a body length of 10 to 14 cm and long tails of up to 16 cm.

The seven species of forest spiny pocket mice (genus Heteromys) are the largest, weighing from 37 to 85 grams and having 11- to 18-cm bodies and long scantily haired tails. Forest pocket mice range from southern Mexico to northern South America, where they live from sea level upward into mountains. All the spiny pocket mice have harsh fur made up of stiff, bristly hairs that may be gray, reddish brown, dark brown, or glossy black. In some species a rust-coloured strip separates upperparts and underparts.

Classification and paleontology

Pocket mice are classified in the family Heteromyidae, meaning “different mouse,” or “other mouse,” in Greek. This family also includes kangaroo rats and kangaroo mice. Within Heteromyidae, the silky and coarse-haired pocket mice constitute the subfamily Perognathinae, and the spiny pocket mice constitute the subfamily Heteromyinae. Spiny pocket mice are more ratlike and probably bear a closer structural resemblance to the family’s extinct fossil ancestors than do any other living members.

  • Subfamily Perognathinae
    24 in 2 genera.
    • Genus Chaetodipus (coarse-haired pocket mice)
      15 species.
    • Genus Perognathus (silky pocket mice)
      9 species.
  • Subfamily Heteromyinae
    12 species in 2 genera.
    • Genus Heteromys (forest spiny pocket mice)
      7 species.
    • Genus Liomys (spiny pocket mice)
      5 species.
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desert, any large, extremely dry area of land with sparse vegetation. It is one of Earth’s major types of ecosystems, supporting a community of distinctive plants and animals specially adapted to the harsh environment. For a list of selected deserts of the world, see below.

Desert environments are so dry that they support only extremely sparse vegetation; trees are usually absent and, under normal climatic conditions, shrubs or herbaceous plants provide only very incomplete ground cover. Extreme aridity renders some deserts virtually devoid of plants; however, this barrenness is believed to be due in part to the effects of human disturbance, such as heavy grazing of cattle, on an already stressed environment.

According to some definitions, any environment that is almost completely free of plants is considered desert, including regions too cold to support vegetation—i.e., “frigid deserts.” Other definitions use the term to apply only to hot and temperate deserts, a restriction followed in this account.

Origin

The desert environments of the present are, in geologic terms, relatively recent in origin. They represent the most extreme result of the progressive cooling and consequent aridification of global climates during the Cenozoic Era (65.5 million years ago to the present), which also led to the development of savannas and scrublands in the less arid regions near the tropical and temperate margins of the developing deserts. It has been suggested that many typical modern desert plant families, particularly those with an Asian centre of diversity such as the chenopod and tamarisk families, first appeared in the Miocene (23 to 5.3 million years ago), evolving in the salty, drying environment of the disappearing Tethys Sea along what is now the Mediterranean–Central Asian axis.

Deserts also probably existed much earlier, during former periods of global arid climate in the lee of mountain ranges that sheltered them from rain or in the centre of extensive continental regions. However, this would have been primarily before the evolution of angiosperms (flowering plants, the group to which most present-day plants, including those of deserts, belong). Only a few primitive plants, which may have been part of the ancient desert vegetation, occur in present-day deserts. One example is the bizarre conifer relative welwitschia in the Namib Desert of southwestern Africa. Welwitschia has only two leaves, which are leathery, straplike organs that emanate from the middle of a massive, mainly subterranean woody stem. These leaves grow perpetually from their bases and erode progressively at their ends. This desert also harbours several other plants and animals peculiarly adapted to the arid environment, suggesting that it might have a longer continuous history of arid conditions than most other deserts.

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Ecosystems

Desert floras and faunas initially evolved from ancestors in moister habitats, an evolution that occurred independently on each continent. However, a significant degree of commonality exists among the plant families that dominate different desert vegetations. This is due in part to intrinsic physiologic characteristics in some widespread desert families that preadapt the plants to an arid environment; it also is a result of plant migration occurring through chance seed dispersal among desert regions.

Such migration was particularly easy between northern and southern desert regions in Africa and in the Americas during intervals of drier climate that have occurred in the past two million years. This migration is reflected in close floristic similarities currently observed in these places. For example, the creosote bush (Larrea tridentata), although now widespread and common in North American hot deserts, was probably a natural immigrant from South America as recently as the end of the last Ice Age about 11,700 years ago.

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Migration between discrete desert regions also has been relatively easier for those plants adapted to survival in saline soils because such conditions occur not only in deserts but also in coastal habitats. Coasts can therefore provide migration corridors for salt-tolerant plants, and in some cases the drifting of buoyant seeds in ocean currents can provide a transport mechanism between coasts. For example, it is thought that the saltbush or chenopod family of plants reached Australia in this way, initially colonizing coastal habitats and later spreading into the inland deserts.

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