The geographic range of Texas kangaroo rats, (Carter, et al., 1985; Davis and Schmidly, 1994; Martin and Matocha, 1972; Martin and Matocha, 1991; Moss and Mehlhop-Cifelli, 1990; North American Rodents: Status Survey and Conservation Action Plan, 2004), is very limited, and the species is often referred to as a remnant or relict population. Because of human modification of the landscape, its range is now restricted to the north-central portion of Texas, but historically it was likely much greater. Texas kangaroo rats have been recorded in recent history in Motley, Cottle, Hardeman, Foard, Wilbarger, Baylor, Wichita, Archer, Clay and Montague counties in Texas, and Comanche county in Oklahoma. However, it has not been recorded in Oklahoma since 1905 and the Texas range now appears to be restricted to Motley, Hardeman, Wilbarger, and Wichita counties, and potentially Foard and Archer counties. These counties are estimated to contain 6,520 square km of potential habitat, but reliable information indicates the actual area to be much less.
One reason for the highly truncated geographic range of Prosopis glandulosa) or on sand. The mesquite grassland cover-type has been greatly reduced by agricultural modification. This practice has caused the wholesale removal of the ecosystem and promoted the invasion of exotic species on remaining patches. Mesquite grassland cover has also been limited by the extirpation of bison, black-tailed prairie dogs, and fire; these would have historically rejuvenated old patches on the landscape. Disturbance seems to be a key component for with its recent extirpation from sites where cattle-grazing was discontinued. The species also appears to need mounds for its burrows; historically these were mesquite root-balls, but bulldozer scrapes, road-cuts, and other earthworks seem acceptable. (Carter, et al., 1985; Davis and Schmidly, 1994; Martin and Matocha, 1972; Martin and Matocha, 1991; Moss and Mehlhop-Cifelli, 1990; Packard and Roberts, 1973; Roberts and Packard, 1973; Stangl, et al., 1992)is its requisite habitat. Texas kangaroo rats are found in association with mesquite grasslands with bare-ground areas and clay soil; it does not live more than 0.8 km from mesquite (
As with all kangaroo rats, is characterized by a tail longer than its body. Unlike most other kangaroo rats, has a white tuft on the end of its tail. Additionally, it has one of the thickest tails per body length and one of the larger bodies of the genus. Mass ranges between 50 and 102 g. The tail length ranges from 135 mm to 205 mm with total body length from 260 mm to 345 mm. The tail length is generally 160% of the head plus body length. In addition to the white tuft, the tail has a dorsal and ventral stripe; both are a paler color than the buff-colored tail. The hind feet are also very long (42 mm to 49 mm), have four toes, and stand out next to the white thigh patches.
Pelage is somewhat variable from juvenile to adult, but generally consistent among adults. Juveniles sometimes have darker flanks, mid-dorsal areas, and hair tips. Additionally, individual hairs are thinner and do not grow as densely, especially on the belly. Adults are generally a buff color with blackish guard-hairs and a white belly.
The coat is replaced annually, with adults molting in the summer and non-adults molting in the fall. Molt begins at the nose and between the shoulders and proceeds in all directions from there.
D. ordii, and Merriam’s kangaroo rats, D. merriami, but neither occurs within the range of . (Baumgardner and Kennedy, 1994; Best, 1987; Carter, et al., 1985; Davis and Schmidly, 1994; Webster and Jones, 1985)has large eyes and small ears that are nearly hairless. Males are generally heavier than females and have larger skulls, but the sexes are otherwise externally indistinguishable. Average individual size varies geographically, with greater sexual dimorphism on the periphery than in the heart of the range. Texas kangaroo rats are very similar in appearance to Ord’s kangaroo rats,
The baculum of (Jannett, 1976)is nondescript in comparison to other mammals. Its average measurements are: total length, 13.13 mm; dorsovetral diameter at midshaft, 0.69 mm; dorsoventral diameter of base, 1.51 mm; lateral diameter at base, 1.47 mm. The baculum is generally straight, but may have a slight curve. It is round in cross-section, and has a distal end that is square to laterally expanded.
The dental formula of Texas kangaroo rats is the same as all Heteromyidae; it exhibits an I 1/1, C 0/0, P 1/1, M 3/3 pattern for a total of 20 teeth. However, the cusp pattern of the P4 is unique in this species and highly differentiated from any other described tooth within the genus Dipodomys. The P4 consists of a double-cusped protoloph with accessory styles (protostyles), and a transverse valley that extends across the entire tooth. (Carrasco, 2000; Carter, et al., 1985; Dalquest, et al., 1992)
D. phillipsii and diverged from it approximately 3,050,000 years ago. Intraspecific genetic examination indicates that differentiation has been occurring between disjunct populations which is likely the result of recent habitat reduction. Such habitat reduction has impeded migration, and reproductively isolated these disjunct populations. (Carter, et al., 1985; Hamilton, et al., 1987; Mantooth, et al., 2000)has 36 chromosomes (35 autosomal chromosomes, plus sex chromosomes) with a diploid number of 72. Molecular systematics indicate that is most closely related to
- Sexual Dimorphism
- male larger
- Range mass
- 50 to 102.2 g
- 1.76 to 3.60 oz
- Average mass
- 80.7 g
- 2.84 oz
- Range length
- 260 to 345 mm
- 10.24 to 13.58 in
- Average length
- 303 mm
- 11.93 in
There is currently no information on the mating system of Texas kangaroo rats. It is generally asocial and females are known to be antagonistic towards males when housed together in captivity. (Packard and Roberts, 1973)
Although data on reproduction in Dipodomys, and many parameters are remarkably consistent between species. In general, the estrus cycle is between 5 and 13 days. Gestation lasts 29 to 36 days, with longer gestations occuring after a postpartum estrus. At birth, neonates are naked and helpless, and weigh between 3 and 6 g. Weaning takes place between 18 and 29 days of age. Young may remain in their natal nest for 4 to 5 weeks. It is likely that given the consistency of these parameters within the genus, is similar. (Nowak, 1999)are scant, much is known about reproduction within the genus
- Key Reproductive Features
- year-round breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- post-partum estrous
- Breeding interval
- The breeding interval is unknown, but is likely variable and environmentally dependent
- Breeding season
- Breeding appears to spike in spring and again in early summer through fall.
- Average number of offspring
Beyond the investment by the female in gestation and lactation there is no information on parental investment in offspring. It is likely that there is little parental investment beyond this. Given the solitary nature of these animals, it is likely that only the female provides parental care.
is generally solitary; the only time it has been found in groups is when young have been found in the burrow together. It is also very quiet; the only sounds noted have been squeaks from marking (toe-clipping) and a thumping noise made upon entering a burrow.
is nocturnal, and does not become active until complete darkness. Its greatest period of activity occurs approximately two to three hours after nightfall. Weather and moonlight do not seem to affect activity levels; it has been observed under the full moon and has been active during a snowfall of 10 cm.
Texas kangaroo rats are very active stockpilers of food. In one instance, a single individual transported several bushels of wheat from the shed where it was stored to its burrow under the floorboards.
normally does not place its burrows near human habitation. Burrow systems are complex warrens with numerous opening and interwoven tunnels. The openings are generally bounded by the roots of a mesquite bush (or other imbedded object), are 5 to 10 cm in diameter, and though generally left open may sometimes be plugged (temporarily) by the resident. Tunnel systems average 2.5 m in total length, 46 cm under the surface, and have several dead-end chambers. There is typically a single nest chamber located near the bottom of the warren, and several food storage chambers. Tunnel diameter is typcially 5 cm to 12.5 cm, but may be as small as 2.5 cm with interwoven tunnels walls as little as 1 cm apart. Burrows maintain a very constant temperature of 15.5 ºC to 18 ºC even when surface temperatures range from 8 ºC to 36 ºC.
Texas kangaroo rats seem to have a very good knowledge of the location of both their own and surrounding burrow entrances. Upon release after trapping, individuals of this species have been noted to hop directly to the nearest burrow opening. There is evidence of interspecific antagonistic behavior between Sigmodon hispidus, but seems to otherwise avoid interspecific contact.and
Texas kangaroo rats are bipedal and move by hopping (saltatorial). They are very agile and fast. Movement is facilitated by the paths individuals clear through their territory to help them move from point to point.
Texas kangaroo rats also maintain several small, cleared, and inconspicuous patches of dust near burrow openings that are used for dust-bathing. This habit helps to remove ectoparasites without the necessity of water. (Bailey, 1905; Davis and Schmidly, 1994; Moss and Mehlhop-Cifelli, 1990; Packard and Roberts, 1973; Roberts and Packard, 1973; Stangl, et al., 1992; Webster and Jones, 1985)
- Range territory size
- 100 to 1900 m^2
- Average territory size
- 800 m^2
Texas kangaroo rats have a large home range when compared to other kangaroo rats. Home ranges varied in size from 0.01 ha to 0.19 ha with an average size of 0.08 ha. Population densities are high for this habitat type, with between 8.6 and 24.7 individuals per hectare. also travels long distances; it has traveled up to 108 meters between traps and up to 300 m along roadsides and field terraces. (Roberts and Packard, 1973)
Communication and Perception
Since (Packard and Roberts, 1973)is uncommon, nocturnal, and asocial, little is known about how it communicates. It is known to make a thumping noise upon entering a burrow, but the purpose of this is unknown. Nothing is known about scent marking or other means of territory delineation. It is known to have excellent vision and hearing and these likely facilitate communication. Also, tactile commmunication is likely in territorial conflicts, between mates, and between mothers and their offspring.
Avena sativa, Sorghum halepense, and Cenchrus sp. are the major component of the grass portion; the florets and foliage of Erodium circutarium are the major component of the forb portion; and the seeds of Opentia sp. are the major component of the perennial portion of the diet. Texas kangaroo rats store large amounts of food to help themselves overwinter and they is not known to hibernate. During the spring and early summer, the green parts of several forbs are cached; in the late summer and fall, seeds are cached. Diet changes seasonally to take advantage of the available resources. These kangaroo rats continue to forage during the winter. (Bailey, 1905; Carter, et al., 1985; Chapman, 1972; Davis and Schmidly, 1994)feeds mainly on grasses and annual forbs. It also supplements its diet with perennial plants and a few insects. The seeds of
- Plant Foods
- seeds, grains, and nuts
- Foraging Behavior
- stores or caches food
There is only one recorded instance of a Texas kangaroo rat killed by an animal other than a human; that was by a rattlesnake. This is likely indicative of the animals that feed on D. elator. Any nocturnal predator large enough to take a 100 g rodent by surprise would have to be considered potential predators. This would include owls, canines, cats, weasels, and snakes. (Bailey, 1905)
- Known Predators
- rattlesnakes (Crotalus)
has two main ecosystem roles. The first is to aerate the soil, which its digging does. This is very important in clay soils that are prone to poor oxygen and water absorption properties. The second is as a prey item. The mesquite grasslands in which it lives do not support high animal densities given the lack of standing water and food. An auxiliary role may be as a seed disperser, but this would only occur when an individual dies and seeds are left uneaten in its burrow.
Texas kangaroo rats also host many ectoparasites. These include: Geomylichus dipodomius, Echinonyssus incomptis, Androlaelaps fahrenholzi, Euschoengastia decipiens, Ixodes sp. larvae, Fahrenholzia pinnata, and Meringis agilis. Texas kangaroo rats also have their own species of nematode. This is Trichuris elatoris and it has not been found within any other species. (Pfaffenberger and Best, 1989; Thomas, et al., 1990)
Vegetative species found in association with Texas kangaroo rats include Prosopis glandulosa, Bothriochloa saccharoides, Aristida purpurea, Bromus unioloides, Chloris verticullata, Panicum halli, Sporobolus cryptandrus, Tridens albescens, Xanthisma texanum, Hoffmanseggia glauca, Convolvulus equitans, Melampodium leucanthum, Monarda citriodora, Teucrium laciniatum, Linum pratense, Physalis viscosa, Solanum dimidiatum, and Tribulus terrestris. (Martin and Matocha, 1991)
Mammals found in association with the Texas kangaroo rat: Didelphis virginiana, Cryptotis parva, Sylvilagus floridanus, Lepus californicus, Spermophilus tridecemlineatus, Geomys bursarius, Chaetodipus hispidus, Perognathus flavus, Perognathus merriami, Reithrodontomys montanus, Peromyscus leucopus, Peromyscus maniculatus, Sigmodon hispidus, Neotoma micropus, Mus musculus, Mephitis mephitis, Taxidea taxus, Canis latrans, Procyon lotor, and Dasypus novemcinctus. (Carter, et al., 1985; Roberts and Packard, 1973; Stangl, et al., 1992)
- Ecosystem Impact
- soil aeration
Economic Importance for Humans: Positive
has no described economic importance. Given its rarity it has potential value for ecotourism, though this has not yet occurred.
Economic Importance for Humans: Negative
Because of its rarity, limited range, and disjunct populationsis of significant conservation concern. Additionally, except for the Copper Breaks State Park, Texas, the entire population resides on private land.
The IUCN Red List listsas vulnerable due to severely fragmented habitat and because this area is continuing to be degraded and reduced. The major source of this degradation is continued agricultural expansion.
The US Fish and Wildlife does not listas either threatened or endangered. It does not appear to be under consideration for listing either.
CITES does not list Texas kangaroo rats. This is likely because it is not used in the pet or medicine trade and is otherwise of no economic value. ("Convention on International Trade in Endangered Species of Wild Fauna and Flora", 2004; "U.S. Fish and Wildlife Service", 2004; North American Rodents: Status Survey and Conservation Action Plan, 2004)
Nancy Shefferly (editor), Animal Diversity Web.
Andrew Strassman (author), University of Michigan-Ann Arbor, Phil Myers (editor, instructor), Museum of Zoology, University of Michigan-Ann Arbor.
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
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.
uses smells or other chemicals to communicate
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
union of egg and spermatozoan
an animal that mainly eats seeds
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.
- native range
the area in which the animal is naturally found, the region in which it is endemic.
active during the night
specialized for leaping or bounding locomotion; jumps or hops.
- scrub forest
scrub forests develop in areas that experience dry seasons.
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- soil aeration
digs and breaks up soil so air and water can get in
- stores or caches food
places a food item in a special place to be eaten later. Also called "hoarding"
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.
- 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.
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.
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.
- year-round breeding
breeding takes place throughout the year
2004. "Convention on International Trade in Endangered Species of Wild Fauna and Flora" (On-line). CITES - Listed Species Database. Accessed March 18, 2004 at http://www.cites.org/eng/resources/species.html.
2004. "U.S. Fish and Wildlife Service" (On-line). Species Information: Threatened and Endangered Animals and Plants. Accessed March 28, 2004 at http://endangered.fws.gov/wildlife.html.
Bailey, V. 1905. North American fauna. no. 25: Biological survey of Texas. Washington, D.C.: Government Printing Office.
Baumgardner, G., M. Kennedy. 1994. Patterns of Interspecific Morphometric Variation in kangaroo rats (Genus Dipodomys). Journal of Mammalogy, 75(1): 203 - 211.
Best, T. 1987. Sexual dimorphism and morphometric variation in the Texas kangaroo rat (Dipodomys elator Merriam 1894). The Southwestern Naturalist, 32(1): 53 - 59.
Carrasco, M. 2000. Species discrimination and morphological relationships of kangaroo rats (Dipodomys) based on their dentition. Journal of Mammalogy, 81(1): 107 - 122.
Carter, D., W. Webster, J. Jones, C. Jones, R. Suttkus. 1985. Dipodomys elator. Mammalian Species, 232: 1 - 3.
Chapman, B. 1972. Food habits of Loring's kangaroo rat, Dipodomys elator . Journal of Mammalogy, 53(4): 877 - 880.
Dalquest, W., J. Grimes, F. Stangl. 1992. Characters of the upper premolars of five speceis of Dipodomys and evidence for diphyly in the genus. The Southwestern Naturalist, 37(3): 231-246.
Davis, W., D. Schmidly. 1994. The Mammals of Texas. Austin, Texas: University of Texas Press.
Hamilton, M., R. Chesser, T. Best. 1987. Genetic variation in the Texas kangaroo rat, Dipodomys elator Merriam. Journal of Mammalogy, 68(4): 775 - 781.
Jannett, F. 1976. Bacula of Dipodomys ordii compactus and Dipodomys elator . Journal of Mammalogy, 57(2): 382 - 387.
Mantooth, S., C. Jones, R. Bradley. 2000. Molecular systematics of Dipodomys elator (Rodentia: Heteromyidae) and its phylogeographic implication. Journal of Mammalogy, 81(3): 885 - 894.
Martin, R., K. Matocha. 1972. Distributional Status of the kangaroo rat, Dipodomys elator. Journal of Mammalogy, 53(4): 873 - 877.
Martin, R., K. Matocha. 1991. The Texas kangaroo rat, Dipodomys elator, from Motley Co., Texas, with notes on Habitat Attributes. The Southwestern Naturalist, 36(3): 354-356.
Moss, S., P. Mehlhop-Cifelli. 1990. Status of the Texas kangaroo rat, Dipodomys elator (Heteromyidae), in Oklahoma. The Southwestern Naturalist, 35(3): 356-358.
North American Rodents: Status Survey and Conservation Action Plan, 2004. "Dipodomys elator" (On-line). IUCN Red List of Threatened Species. Accessed March 18, 2004 at http://www.redlist.org/search/details.php?species=6675.
Nowak, R. 1999. Walker's Mammals of the World, Sixth Edition. Baltimore and London: The Johns Hopkins University Press.
Packard, R., J. Roberts. 1973. Observations of the Behavior of the Texas kangaroo rat, Dipodomys elator Merriam. Mammalia, 37(4): 680 - 682.
Pfaffenberger, G., T. Best. 1989. Trichuris elatoris sp. n. (Nematoda: Trichuridae) from the Texas kangaroo rat (Dipodomys elator). Proceedings of the Helminthological Society of Washington, 56(1): 76 - 81.
Roberts, J., R. Packard. 1973. Comments on movement, home range and ecology of the Texas kangaroo rat, Dipodomys elator Merriam. Journal of Mammalogy, 54(4): 957 - 962.
Stangl, F., T. Schafer, J. Goetze, W. Pinchak. 1992. Opportunistic use of modified and disturbed habitat by the Texas kangaroo rat (Dipodomys elator). The Texas Journal of Science, 44(1): 25-35.
Thomas, H., J. Whitaker, T. Best. 1990. Ectoparasites of Dipodomys elator form North-central Texas with some data from sympatric Chaetodipus hispidus and Perognathus flavus . The Southwestern Naturalist, 35(2): 111-114.
Webster, W., J. Jones. 1985. Nongeographic variation, reproduction, and demography in the Texas kangaroo rat, Dipodomys elator (Rodentia: Heteromyidae). The Texas Journal of Science, 37(1): 51-61.