Cnemidophorus uniparensDesert Grassland Whiptail

Geographic Range

Desert grassland whiptail lizards, Cnemidophorus uniparens, are a southwest American and Mexican species. Their geographic range extends into Arizona, stopping just south of Grand Canyon National Park and west of Tanto National Forest. In New Mexico, their range extends north to the city of Albuquerque while staying relatively close to the western border of the state. In Texas, their range only includes the very tip of the western border near the city of El Paso. In Mexico, their range extends southward to Chihuahua, staying northeast of the Sierra Madre Occidental. This range is continuous across these state and country borders. (Degenhardt, et al., 2005; Hammerson and Santos-Barrera, 2007; Painter, et al., 2017; Sullivan, et al., 2018)


Desert grassland whiptail lizards are found in desert and grassland habitats. Their habitats range in elevation from 1120 meters to 2100 meters. These lizards often reside in arid areas with sparse vegetation. They can also be found living in dense shrubbery or small valleys. These areas vary greatly in composition, switching between grasslands, dense mesquite such as brittlebush (Encelia farinosa), and arid desert. These lizards spend much of their time under rocks and dense shrubbery to escape heat. They also escape heat with a burrow, where they spend their time at night and lay eggs. (Brennan and Holycross, 2006; Degenhardt, et al., 2005; Hammerson and Santos-Barrera, 2007; McClaran and Van Devender, 1997)

  • Range elevation
    1120 to 2100 m
    3674.54 to 6889.76 ft

Physical Description

Desert grassland whiptails are an all-female species with an olive-brown to black base color. They have six cream colored stripes that run longitudinal along their bodies from head to tail, separated from each other by about 4 to 8 scales. When these lizards are hatchlings, their tails are bright blue. This color fades into olive-brown to black as they become adults. Their ventral surfaces are white and sometimes the adults have some light blue tinting on their throat and chin. Some of these lizards also have the beginnings of a seventh stripe near their head. There are a few populations of desert grassland whiptails near Chihuahua, Mexico that have more vividly colored stripes, likely due to allopatric congeners. They have granular dorsal scales numbering in the range of 59 to 78 rows around the mid-body. Wright (1968) reports that average snout-vent length (SVL) is 52.8 mm and weight is 4.1 g (N=1117).

Desert grassland whiptails co-occur with two similar-looking species. Little striped whiptails (Cnemidophorus inornatus) are smaller on average, more blue-colored throughout their ventral surface as well as their tail even as adults, and they have a full set of seven longitudinal stripes. Plateau striped whiptails (Cnemidophorus velox) are larger on average, have a complete set of seven longitudinal stripes, and often times have spots on the olive-brown areas covering their bodies. (Brennan and Holycross, 2006; Degenhardt, et al., 2005; Walker, et al., 2018)

  • Average mass
    4.1 g
    0.14 oz
  • Average length
    52.8 (SVL, not total) mm


When desert grassland whiptail lizards' eggs are laid, they weigh about 0.4 g, on average. Desert grassland whiptails are triploid, meaning that they have three sets of homologous chromosomes. These lizards are parthenogenic, meaning that they develop from an unfertilized egg. They are genetic clones of the female that laid the egg. Once hatched, the hatchling lizards grow at a rate of 0.012 g per day, on average, for the first 30 days of life. Like all other lizards, they have indeterminate growth, meaning that they grow for the rest of their lives. These lizards are fully developed sexually after an average of seven months. (Allen, 1988; Bateman, et al., 2010; Walker, et al., 2018)


Desert grassland whiptail lizards are parthenogenic, meaning that they are all females and they do not mate to reproduce. Even though they do not mate sexually, they often display pseudocopulatory behavior. The female-like pseudocopulatory behavior consists of allowing dominance by another desert grassland whiptail, that is displaying male-like behavior. The male-like pseudocopulatory behavior consists of general aggression, biting, and mounting. Sometimes there is even an alignment of the cloacae as though mating will occur but it does not. They most often display female-like behavior while they are producing their clutches of eggs. They most often display male-like behaviors before and after laying their eggs and before their next production of eggs. (Crews and Fitzgerald, 1980; Crews and Moore, 1993; Crews, et al., 1986; Degenhardt, et al., 2005; Lemos-Espinal, et al., 2017)

The reproductive season of desert grassland whiptail lizards extends from the beginning of May through July. These lizards reach sexual maturity at the minimum size of 60 mm (SVL) during the first reproductive season after they hatch, which is on average seven months old. These lizards are parthenogenic, meaning they develop in unfertilized eggs. They are also clones of their single parent, and so are siblings genetically. Each sexually mature individual produces 2 to 3 clutches per year with 21 to 28 days between each clutch. Clutches range from 1 to 4 eggs with an average of 2.77. The amount of eggs per clutch correlates strongly with the size of the lizard. Females of SVL length smaller than 65 mm are reported to have an average of 2 eggs per clutch. Females with SVLs ranging 65 to 70 mm averaged 3 eggs per clutch. Females larger than 70 mm averaged 4 eggs per clutch. Desert grassland whiptail eggs, freshly laid, are cream-colored, oval shaped, and on average 0.4 g. Eggs hatch after approximately 2-3 months. When desert grassland whiptails hatch they weigh, on average, 0.56 g with a range of 0.53 to 0.58 g. Lizard hatchlings are immediately independent from their parent. (Allen, 1988; Crews and Fitzgerald, 1980; Crews and Moore, 1993; Crews, et al., 1986; Degenhardt, et al., 2005; Lemos-Espinal, et al., 2017; Leuck, 1985; Ramírez-Bautista, et al., 2000; Walker, et al., 2018)

  • Breeding interval
    During reproductive season, 2-3 clutches 21-28 days apart.
  • Breeding season
    May through July
  • Range number of offspring
    1 egg per clutch to 4 eggs per clutch
  • Average number of offspring
    2.77 eggs per clutch
  • Average time to independence
    0 minutes
  • Average age at sexual or reproductive maturity (female)
    7 months

These lizards are precocial, meaning they are well developed when hatched. There is no parental investment beyond the act of egg-laying. (Allen, 1988; Congdon, et al., 1978)

  • Parental Investment
  • no parental involvement
  • precocial


There is very limited information detailing lifespans of desert grassland whiptail lizards. There is no information concerning the longevity of captive desert grassland whiptail lizards because they are not kept in captivity. However, research on another species of whiptail lizards suggests that they have a minimal annual survival in adults of 54-60% and average lifespans of at least seven years in the wild. These data are based on western whiptails (Cnemidophorus tigris), and suggests a similar lifespan but does not confirm one. According to Carey and Judge (2002), the longest known lifespan of a western whiptail in captivity is 7.8 years. (Carey and Judge, 2002; Turner, et al., 1969)


Desert grassland whiptail lizards are not a very social species. Most of their time during the day is spent foraging for food and basking in sunlight. Most interactions between desert grassland whiptails are not aggressive. This lack of aggressive behavior compared to other lizard species is likely because they are all female and have no need to compete for mates or establish dominance in most settings. Most interactions between lizards occur during their reproductive season. At nighttime, desert grassland whiptail lizards retreat into their burrows within their home ranges, until dawn when they come out and resume foraging. These lizards are active during overcast days, but activity ceases during rainfall. (Degenhardt, et al., 2005; Eifler and Eifler, 1998; Eifler, et al., 2007; Leuck, 1985; McClaran and Van Devender, 1997)

Home Range

According to Eifler and Eifler (1998), desert grassland whiptails' median home ranges are 1080 square meters. This is the area that they use primarily for foraging and they spend an average of 50% of their time in one-tenth of this range. These lizards are not territorial. (Degenhardt, et al., 2005; Eifler and Eifler, 1998)

Communication and Perception

Desert grassland whiptail lizards use their visual, tactile, and olfactory senses to perceive their environment. They have eyes to see their surroundings and they can use their limbs and bodies to feel their surroundings. Lizards hear their surroundings using an organ called the cochlea. Lizards have a Jacobson's organ, a specialized olfactory organ that allows them to use their tongues to smell their surroundings. Using this organ, they perceive chemical signals that tell them when prey is near. Desert grassland whiptail lizards use several means of communication, even though they are not very social lizards. They sometimes use touch to communicate through mounting and biting. They also use pheromones to communicate their intentions to other lizards about mating and homestead range. (Cooper, 1995; Crews and Fitzgerald, 1980; Ferguson, 1977)

Food Habits

Desert grassland whiptail lizards are insectivores. Eifler and Eifler (1998) found that their diets consisted of both fossorial and surface insects, 42.5% of which were termites. A second study reported that these termites were arid land subterranean termites, Reticulitermes tibialis. About 6.7% of their diet consisted of queen ants (Formica perpilosa), 0.6% beetles, 5.4% grasshoppers, 2.0% butterflies, and 42.5% unknown insects. When foraging for prey, desert grassland whiptails will use a series of movements and intermittent sessions of digging and searching. They also use their tongues to smell the surrounding area and locate prey. When predators are nearby, desert grassland whiptails search for prey far less often. This is likely because digging attracts the attention of said predators. (Degenhardt, et al., 2005; Eifler and Eifler, 1998; Eifler, et al., 2007)

  • Animal Foods
  • insects


The known predators of desert grassland whiptail lizards are long-nosed leopard lizards (Gambelia wislizenii), greater roadrunners (Geococcyx californianus), burrowing owls (Speotyto cunicularia), and loggerhead shrikes (Lanius ludovicianus). There is no difference in predators between juveniles and adults. These lizards have been observed to behave differently in the presence of a predator. When a predator is near, foraging lizards keep movement short and infrequent. This is likely in an effort not to attract the attention of predators. Also, when digging for prey, they have a significantly lower likelihood of finding prey, likely because the lizards are distracted by the presence of the predator. (Degenhardt, et al., 2005; Eifler, et al., 2007)

Ecosystem Roles

Desert grassland whiptail lizards act as both predator and prey within their ecosystem. According to Bursey and Goldberg (1992), 26% of desert grassland whiptails in Arizona are infected with cestodes Oochoristica bivitellobata. Mahrt (1979), observed no cases of infection of desert grassland whiptails with hematozoans (Hematozoa). Goldberg and Bursey (1990) reported no indications of desert grassland whiptails being infested with nematodes (Nematoda), but there were infections of acanthocephalans (Acanthocephalus) in the stomachs of 3% of tested lizards. (Bursey and Goldberg, 1992; Degenhardt, et al., 2005; Goldberg and Bursey, 1990; Mahrt, 1979; McAllister, 1990)

Commensal/Parasitic Species
  • Cestode Oochoristica bivitellobata
  • Acanthocephalan Acanthocephalus

Economic Importance for Humans: Positive

Due to the fact that these lizards are insectivores, it is possible they could provide pest control on some insects. However, there is no conclusive evidence to confirm this. (Degenhardt, et al., 2005; Eifler, et al., 2007)

Economic Importance for Humans: Negative

There are no known negative economic impacts of desert grassland whiptail lizards on humans.

Conservation Status

Desert grassland whiptails lizards are listed as a species of "least concern" on the IUCN Red List. These lizards are not listed under any special status on the United States Endangered Species Act list, CITES, or the state of Michigan list.

Because they are parthogenic, desert grassland whiptail lizards are all genetically similar. Therefore, any biological or environmental threats to an individual (e.g. disease, climate change) are a threat to the whole species.

Much of the geographic range of desert grassland whiptail lizards consists of government protected areas; this prevents dramatic loss of habitat. Therefore, there are no conservation efforts in place for these lizards. (Hammerson and Santos-Barrera, 2007)

Other Comments

Desert grassland whiptail lizards were originally scientifically named Cnemidophorus uniparens, but are now called Aspidoscelis uniparens.


Logan Platt (author), Radford University, Lauren Burroughs (editor), Radford University, Layne DiBuono (editor), Radford University, Lindsey Lee (editor), Radford University, Karen Powers (editor), Radford University, Galen Burrell (editor), Special Projects.



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


uses sound to communicate

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.


an animal that mainly eats meat


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.

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

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature


Referring to a burrowing life-style or behavior, specialized for digging or burrowing.

indeterminate growth

Animals with indeterminate growth continue to grow throughout their lives.


An animal that eats mainly insects or spiders.


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.


reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.


development takes place in an unfertilized egg


chemicals released into air or water that are detected by and responded to by other animals of the same species

seasonal breeding

breeding is confined to a particular season


remains in the same area


lives alone


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

young precocial

young are relatively well-developed when born


Allen, B. 1988. Observations on the embryology of the unisexual lizard Cnemidophorus uniparens (Teiidae). Journal of Zoology, 215/1: 55-81.

Bateman, H., H. Snell, A. Chung-MacCoubrey, D. Finch. 2010. Growth, activity, and survivorship from three sympatric parthenogenic whiptails (family Teiidae). Journal of Herpetology, 44/2: 301-306.

Brennan, T., A. Holycross. 2006. A Field Guide to Amphibians and Reptiles in Arizona. Phoenix, AZ: Arizona Game and Fish Department.

Bursey, C., S. Goldberg. 1992. Oochoristica bezyi n. sp. (Cestoda: Linstowiidae) from the desert night lizard, Xantusia vigilis vigilis (Xantusiidae). Transactions of the American Microscopical Society, 111/1: 36-43.

Carey, J., D. Judge. 2002. Longevity Records: Life Spans of Mammals, Birds, Amphibians, Reptiles, and Fish. Odense, Denmark: Odense University Press.

Congdon, J., L. Vitt, N. Hadley. 1978. Parental investment: comparative reproductive energetics in bisexual and unisexual lizards, genus Cnemidophorus. The American Naturalist, 112/985: 509-521.

Cooper, W. 1995. Foraging mode, prey chemical discrimination, and phylogeny in lizards. Animal Behavior, 50/4: 973-985.

Crews, D., K. Fitzgerald. 1980. "Sexual" behavior in parthenogenetic lizards (Cnemidophorus). Proceedings of the National Academy of Sciences, 77/1: 499-502.

Crews, D., M. Grassman, J. Lindzey. 1986. Behavioral facilitation of reproduction in sexual and unisexual whiptail lizards. Proceedings of the National Academy of Sciences, 83/24: 499-502.

Crews, D., M. Moore. 1993. Biology of Whiptail Lizards (Genus Cnemidophorus). Norman, OK: University of Oklahoma Press.

Degenhardt, W., C. Painter, A. Price. 2005. Amphibians and Reptiles of New Mexico. Albuquerque, NM: University of New Mexico Press.

Eifler, D., M. Eifler. 1998. Foraging behavior and spacing patterns of the lizard Cnemidophorus uniparens. Journal of Herpetology, 32/1: 24-33.

Eifler, D., M. Eifler, B. Harris. 2007. Foraging under the risk of predation in desert grassland whiptail lizards (Aspidoscelis uniparens). Journal of Ethology, 26/2: 219-223.

Ferguson, G. 1977. Display and communications in reptiles: an historical perspective. American Zoologist, 17/1: 167-176.

Goldberg, S., C. Bursey. 1990. Helminths of the Arizona little striped whiptail, Cnemidophorus inornatus arizonae, and the desert grassland whiptail, Cnemidophorus uniparens (Sauria: Teiidae), from southeastern Arizona. Journal of the Helminthological Society, 57/1: 83-86.

Hammerson, G., G. Santos-Barrera. 2007. "Aspidoscelis uniparens" (On-line). The IUCN Red List of Threatened Species 2007: e.T64291A12754846. Accessed January 29, 2019 at

Lemos-Espinal, J., J. Walker, H. Smith. 2017. Aspidoscelis uniparens (desert grassland whiptail) reproduction. Herpetological Review, 48/3: 639.

Leuck, B. 1985. Comparative social behavior of bisexual and unisexual whiptail lizards (Cnemidophorus). Journal of Herpetology, 19/4: 492-506.

Mahrt, J. 1979. Hematozoa of lizards from southeastern Arizona and Isla San Pedro Nolasco, Gulf of California, Mexico. The Journal of Parasitology, 65/6: 972-975.

McAllister, C. 1990. Helminth parasites of unisexual and bisexual whiptail lizards (Teiidae) in North America. II. The New Mexico whiptail (Cnemidophorus neomexicanus). Journal of Wildlife Diseases, 26/3: 403-406.

McClaran, M., T. Van Devender. 1997. The Desert Grassland. Tuscon, AZ: University of Arizona Press.

Painter, C., J. Stuart, J. Giermakowski, L. Pierce. 2017. Checklist of the amphibians and reptiles of New Mexico, USA, with notes on taxonomy, status, and distribution. Western Wildlife, 4/29-60: 42.

Ramírez-Bautista, A., C. Balderas-Valdivia, L. Vitt. 2000. Reproductive ecology of the whiptail lizard Cnemidophorus lineatissimus (Squamata: Teiidae) in a tropical dry forest. Copeia, 2000/3: 712-722.

Sullivan, B., K. Sullivan, J. Sullivan, J. Cordes, J. Walker. 2018. Aspidoscelis velox (plateau striped whiptail) and Aspidoscelis uniparens (desert grassland whiptail). Herpetological Review, 49/1: 116.

Turner, F., P. Medica, J. Lannom, G. Hoddenbach. 1969. A demographic analysis of fenced populations of the whiptail lizard, Cnemidophorus tigris, in southern Nevada. The Southwestern Naturalist, 14/2: 189-201.

Walker, J., J. Lemos-Espinal, J. Cordes, H. Smith. 2018. Abundance, color pattern variation, life cycle, and reproduction of the triploid parthenogenetic lizard Aspidoscelis uniparens (Squamata:Teiidae) in Chihuahua, Mexico. Phyllomedusa, 17/1: 83-99.