Lepus alleni, the antelope jackrabbit, is found mostly along the western coast of Mexico, but also in southern Arizona in the United States. In Mexico, antelope jackrabbits inhabit the Mexican states adjacent to the Gulf of California and the Pacific Ocean: Sonora, Sinaloa, and northern Nayarit. In Arizona, antelope jackrabbits inhabit a small southern area, mostly in the Sonoran desert. Lepus alleni is also located on Tiburon, a small island off the coast of the Mexican state of Sonora. (Best and Henry, 1993)
In Arizona, antelope jackrabbits inhabit grassy slopes at moderate elevations. They are most commonly found in areas where grass grows well under desert shrubs that are moderately high and open. They are less common in creosote bush desert and in the low parts of valleys with dense mesquite stands. In Mexico, antelope jackrabbits prefers grasslands that are open and low, as well as foothills with patchy, low bushes and grass. They are most common in the foothills near the coast. (Best and Henry, 1993)
Size is the most distinctive trait of Lepus alleni; it is a large Lepus species, with the head and ears being especially large. Their ears are tall (on average 162mm long) and mostly devoid of hair except for fringes of white hair along the edges and on the tips. The side of the body (limbs, hips, rump) are white haired with black tips. The ventral surface (chin, throat, stomach, insides of limbs) are all white haired as well as the tail. The rest of the body (upper part) is yellow/brown with some black.
Lepus alleni deals with seasonality by adjusting its basal metabolic rate. It increases by 15% during the winter compared to the summer.
Antelope jackrabbits have many ways of dealing with heat. The fur is highly reflective and insulated, which helps to eliminate heat gain from the environment. Antelope jackrabbits can reduce blood flow to their large ears, which reduces heat exchanger. When not able to find shelter, Lepus alleni can tolerate heat stress at high levels better and for a longer time than Lepus californicus. (Best and Henry, 1993; David S. Hinds, 1977; Mearns, 1890; Vorhies and Taylor, 1933)
Only 2 copulations have been observed, so mating behavior is not well known for Lepus alleni. Both copulations were characterized by an aggressive female: one was aggressive afterwards, growling and chasing the male away and the other female growled and fought with the male before mating. (Best and Henry, 1993)
Antelope jackrabbit males will fight by boxing. They stand on their hind feet, using their forelimbs to strike each other repeatedly and rapidly for several seconds. This exchange is usually quiet and the fight ends when the winner chases the loser away. Fights can be serious enough to wound a jackrabbit badly, including torn ears, cuts, and even rare injuries such as one case where a male lost the paw of its forelimb. Male on male fighting is likely to be related to competition for females, but the mating system is not well known. (Best and Henry, 1993; Vorhies and Taylor, 1933)
The gestation period for a female is about 6 weeks, with an average of 2 young per litter. Litter sizes range from 1 to 5 young. Females can have 3 or 4 litters each year. Like most hares (Lepus), antelope jackrabbit young are born well-developed and are weaned and independent just a few days after birth, exact numbers are not given in the literature. By 5 days old the young have well-developed incisors and are covered in short fur. Young are not born with the characteristic white rump, but the rump flash can be displayed at as young as 19 days if the young antelope jackrabbit is alarmed. (Best and Henry, 1993; Vorhies and Taylor, 1933)
It is thought that female antelope jackrabbits scatter their young in different hiding places after birth, and return to feed the young at night. There are no indications of burrows made by mothers for their young, but there are a few instances of well concealed "nests." One nest was concealed under some beargrass, another under a mesquite near sacaton grass and one was even in a hollowed-out barrel cactus shell. Females invest heavily in the development of their young during gestation, giving birth to precocial young that are independent just a few days after their birth. Male antelope jackrabbits do not contribute to the care of their young. (Best and Henry, 1993; Vorhies and Taylor, 1933)
Not much is known about the lifespan of antelope jackrabbits as they are hard to keep alive in captivity and they are difficult to capture and study in the wild.
Lepus alleni is crepuscular and nocturnal, although they may be active during the day on cloudy days. Antelope jackrabbits spend their days in the hot season staying out of the sun in what are called "shelter forms." These are created by backing up under grass, weeds or brush, or just sitting in the shade of a cactus or mesquite trunk; though they preferentially choose mesquite and creosote bush. These forms help with the extreme heat during the day. Since leporids are coprophagic, forms might also help with the re-digestion of pellets, by making it safer to sit and digest. Like other jackrabbits, antelope jackrabbits are solitary. (Best and Henry, 1993; C.F. Brown, 2003; Vorhies and Taylor, 1933)
Home ranges in Lepus alleni have not been documented.
Antelope jackrabbits uses their long ears to listen for predators and get a sense of their surroundings. Only in rare circumstances do antelope jackrabbits use sound as a form of communication. A pheromone may be used by this species in the form of a rectal gland that secretes a strong musky odor and may be used to scent mark a shelter form. (Vorhies and Taylor, 1933)
Lepus alleni is a folivore (leaf-eater), gramnivore (grass-eater) and succulent plant eater (esp. cacti). They do not actively drink water, but derive it from their diet, especially from eating cacti stems. May and June are the most arid months in their range and the rainy season occurs in July and August. In the dry season they depend mostly on mesquite leaves and cacti, but during the wet season, they switch to grass. Some minerals are derived from geophagy, but this behavior is rare. (Best and Henry, 1993; Vorhies and Taylor, 1933)
Lepus alleni is precocial at birth and ready to flee if a predator finds the mother and young soon after birth. Young are more nocturnal, less likely to leave a shelter, and generally more wary of their surroundings than are adults. Once grown, there are many predator avoidance strategies. One is to sit in a shelter form that is open on three sides, but offers protection from birds of prey. If a terrestrial predator is detected, the antelope jackrabbit can run or conceal itself in a shelter form. If it stays concealed, it will back into the shelter form, lay its ears close to the body, and extend the forelimbs for a quick escape. If it decides to run, it will take to all fours and flash a white area on its rump towards the predator. As it runs away in a zig-zag pattern, it will keep a white area exposed towards the predator, in hopes of confusing it. The antelope jackrabbit will also hop like a kangaroo in tall grasses to be able to see where the predator is. (Best and Henry, 1993; Vorhies and Taylor, 1933)
Through their grazing, antelope jackrabbits can force habitat succession in the direction of the climax stage on a range that is moderately deteriorated. On range that has more weeds than grasses (indicating worse deterioration), their grazing may further degrade the habitat. Antelope jackrabbits are important prey for medium to large terrestrial and avian predators. Their folivory influences the composition and health of their native habitats. (C.F. Brown, 2003; Vorhies and Taylor, 1933)
Antelope jackrabbits are valuable for food and their skin. (Best and Henry, 1993)
Through grazing, Lepus alleni is sometimes said to compete with domestic animals that graze on the same land. However, the impact may not be substantial as rabbits may graze in different ways and on different plants than domestic animals. In terms of quantity 15 antelope jackrabbits consume as much as 1 sheep, and 74 antelope jackrabbits consume as much as 1 domestic cow. (Best and Henry, 1993)
Lepus alleni habitat in southern Arizona is threatened by Lehmann lovegrass (Eragrostis lehmanniana), a non-native grass species which is not edible for antelope jackrabbits. Conversion of wild land for agriculture will lead to a further decline in antelope jackrabbit populations. Human impacts on antelope jackrabbit habitat also include housing developments, livestock grazing, recreational trails, and canal building. (Best and Henry, 1993; C.F. Brown, 2003)
The common name antelope jackrabbit is derived from the white flashing behavior of American pronghorns (Antilocapra americana) when they run. Antelope jackrabbits also flash their white tails when they flee.
Lepus alleni is named after John Asaph Allen who was the Curator of the Department of Mammals and Birds at the American Museum of Natural History.
Tanya Dewey (editor), Animal Diversity Web.
Kristen Rosenblum (author), University of Oregon, Stephen Frost (editor, instructor), University of Oregon.
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.
uses sound to communicate
living in landscapes dominated by human agriculture.
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.
Found in coastal areas between 30 and 40 degrees latitude, in areas with a Mediterranean climate. Vegetation is dominated by stands of dense, spiny shrubs with tough (hard or waxy) evergreen leaves. May be maintained by periodic fire. In South America it includes the scrub ecotone between forest and paramo.
uses smells or other chemicals to communicate
active at dawn and dusk
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.
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.
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.
an animal that mainly eats leaves.
A substance that provides both nutrients and energy to a living thing.
An animal that eats mainly plants or parts of plants.
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).
having the capacity to move from one place to another.
the area in which the animal is naturally found, the region in which it is endemic.
active during the night
generally wanders from place to place, usually within a well-defined range.
chemicals released into air or water that are detected by and responded to by other animals of the same species
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
specialized for leaping or bounding locomotion; jumps or hops.
communicates by producing scents from special gland(s) and placing them on a surface whether others can smell or taste them
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
uses touch to communicate
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).
Living on the ground.
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.
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.
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.
uses sight to communicate
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
breeding takes place throughout the year
young are relatively well-developed when born
Best, T., T. Henry. 1993. Lepus alleni. Mammalian Species, 424: 1-8.
C.F. Brown, P. 2003. Habitat Characteristics of 3 Leproid Species in South-Eastern Arizona. The Journal Of Wildlife Management, 67: 83-89.
David S. Hinds, 1977. Acclimatization of Thermoregulation in Desert-Inhabiting Jackrabbits (Lepus Alleni and Lepus Californicus). Ecology, 58: 246-264.
Mearns, E. 1890. Description of supposed new species and subspecies of mammals from Arizona. Bulletin of the American Museum of Natural History, 2: 27-307.
Vorhies, C., W. Taylor. 1933. The life histories and ecology of jack rabbits, Lepus alleni and Lepus californicus ssp. in relation to grazing in Arizona. University of Arizona, College of Agriculture, Agricultural Experiment Station Technical Bulletin, 49: 471-587.