|Adult male in Oregon|
|Adult female in Wyoming|
The pronghorn, Antilocapra americana, is a species of artiodactyl mammal indigenous to interior western and central North America. Though not an antelope, it is often known colloquially in North America as the prong buck, pronghorn antelope, cabri (native American), or simply antelope because it closely resembles the true antelopes of the Old World and fills a similar ecological niche due to convergent evolution.
It is the only surviving member of the family Antilocapridae. During the Pleistocene period, 12 antilocaprid species existed in North America. About five existed when humans entered North America, but all except A. americana are now extinct.
Pronghorns have distinct white fur on their rumps, sides, breasts, bellies, and across their throats. They have a highly developed sense of curiosity compared to related animals. Adult males are 1.3–1.5 m (4 ft 3 in–4 ft 11 in) long from nose to tail, stand 81–104 cm (32–41 in) high at the shoulder, and weigh 40–65 kg (88–143 lb). The females are the same height as males, but weigh 34–48 kg (75–106 lb). The feet have two hooves, with no dewclaws. Their body temperature is 38°C (100°F).
Each "horn" of the pronghorn is composed of a slender, laterally flattened blade of bone that grows from the frontal bones of the skull, forming a permanent core. As in the Giraffidae, skin covers the bony cores, but in the pronghorn, it develops into a keratinous sheath which is shed and regrown on an annual basis. Unlike the horns of the family Bovidae, the horn sheaths of the pronghorn are branched, each sheath possessing a forward-pointing tine (hence the name pronghorn). Males have a horn sheath about 12.5–43 cm (4.9–16.9 in) (average 25 cm (9.8 in)) long with a prong. Females have smaller horns that range from 2.5–15.2 cm (1–6 in) (average 12 centimetres (4.7 in)) and sometimes barely visible; they are straight and very rarely pronged. Males are further differentiated from females in having a small patch of black hair at the angle of the mandible. Pronghorns have a distinct, musky odor. Males mark territory with a preorbital scent gland which is located on the sides of the head. They also have very large eyes with a 320° field of vision. Unlike deer, pronghorns possess a gallbladder.
The pronghorn is the fastest land mammal in the Western Hemisphere, being built for maximum predator evasion through running. The top speed is very hard to measure accurately and varies between individuals; it can run 35 mph for 4 mi (56 km/h for 6 km), 42 mph for 1 mi (67 km/h for 1.6 km); and 55 mph for 0.5 mi (88.5 km/h for .8 km). It is often cited as the second-fastest land animal, second only to the cheetah. It can, however, sustain high speeds longer than cheetahs. University of Idaho zoologist John Byers has suggested the pronghorn evolved its running ability to escape from extinct predators such as the American cheetah, since its speed greatly exceeds that of extant North American predators. Compared to its body size, the pronghorn has a large windpipe, heart, and lungs to allow it to take in large amounts of air when running. Additionally, pronghorn hooves have two long, cushioned, pointed toes which help absorb shock when running at high speeds. They also have an extremely light bone structure and hollow hair. Pronghorns are built for speed, not for jumping. Their ranges are sometimes affected by sheep ranchers' fences. However, they can be seen going under fences, sometimes at high speed. For this reason, the Arizona Antelope Foundation and others are in the process of removing the bottom barbed wire from the fences, and/or installing a barbless bottom wire.
Range and ecology
Pronghorns were brought to scientific notice by the Lewis and Clark Expedition, which found them in what is now South Dakota. Their range extends from southern Saskatchewan and Alberta in Canada south through the United States (southwestern Minnesota and central Texas west to coastal southern California and northern Baja California Sur, to Sonora and San Luis Potosí in northern Mexico.
The subspecies known as the Sonoran pronghorn (A. a. sonoriensis) occurs in Arizona and Mexico. Other subspecies include the Mexican pronghorn (A. a. mexicana), the Oregon pronghorn (A. a. oregona), and the critically endangered Baja California pronghorn (A. a. peninsularis).
Pronghorns prefer open, expansive terrain at elevations varying between 900 and 1,800 m (3,000 and 5,900 ft), with the densest populations in areas receiving around 25–40 cm (9.8–15.7 in) of rainfall per year. They eat a wide variety of plant foods, often including plants unpalatable or toxic to domestic livestock (sheep and cattle), though they also compete with them for food. In one study, forbs comprised 62% of their diet, shrubs 23%, and grasses 15%, while in another, cacti comprised 40%, grass 22%, forbs 20%, and shrubs 18%. Pronghorns also chew and eat (ruminate) cud, which is their own partially digested food. Healthy pronghorn populations tend to stay within 5.0–6.5 km (3.1–4.0 mi) of water. An ongoing study by the Lava Lake Institute for Science and Conservation and the Wildlife Conservation Society shows an overland migration route that covers more than 160 mi (260 km). The migrating pronghorn start travel from the foothills of the Pioneer Mountains through Craters of the Moon National Monument to the Continental Divide. Dr. Scott Bergen of Wildlife Conservation Society says, "This study shows that pronghorn are the true marathoners of the American West. With these new findings, we can confirm that Idaho supports a major overland mammal migration - an increasingly rare phenomenon in the U.S. and worldwide."
Social behavior and reproduction
Pronghorns form mixed-sex herds in the winter. In early spring, the herds break up, with young males forming bachelor groups, females forming their groups, and adult males living solitarily. Some female bands share the same summer range, and bachelor male bands form between spring and fall. Females form dominance hierarchies with few circular relationships. Dominant females aggressively displace other females from feeding sites.
Adult males either defend a fixed territory that females may enter, or defend a harem of females. A pronghorn may change mating strategies depending on environmental or demographic conditions. Where precipitation is high, adult males tend to be territorial and maintain their territories with scent marking, vocalizing, and challenging intruders. In these systems, territorial males have access to better resources than bachelor males. Females also employ different mating strategies. "Sampling" females visit several males and remain with each for a short time before switching to the next male at an increasing rate as oestrus approaches. "Inciting" females behave as samplers until oestrus and then incite conflicts between males, watching and then mating with the winners. Before fighting, males try to intimidate each other. If intimidation fails, they lock horns and try to injure each other. "Quiet" females remain with a single male in an isolated area throughout oestrus. Females continue this mating behavior for two to three weeks.
When courting an estrous female, a male pronghorn approaches her while softly vocalizing and waving his head side to side, displaying his cheek patches. The scent glands on the pronghorn are on either side of the jaw, between the hooves, and on the rump. A receptive female remains motionless, sniffs his scent gland, and then allows the male to mount her. When mating, the tip of a male pronghorn's penis is often the first part to touch the female pronghorn.
Pronghorns have a gestation period of 7–8 months, which is longer than is typical for North American ungulates. They breed in mid-September, and the doe carries her fawn until late May. This gestation period is around six weeks longer than that of the white-tailed deer. Females usually bear within a few days of each other. Twin fawns are common. Newborn pronghorns weigh 2–4 kg (4.4–8.8 lb), most commonly 3 kg (6.6 lb). In their first 21–26 days, fawns spend time hiding in vegetation. Fawns interact with their mothers for 20–25 minutes a day and this continues even when the fawn joins a nursery. The females nurse, groom, and lead their young to food and water, as well as keep predators away from them. Females usually nurse the young about three times a day. Males are weaned 2–3 weeks earlier than females. Sexual maturity is reached at 15 to 16 months, though males rarely breed until three years old. Their lifespan is typically up to 10 years, rarely 15 years.
Population and conservation
At the turn of the 20th century, members of the wildlife conservation group, Boone and Crockett Club, had determined that extinction of the pronghorn was more of a probability than a possibility. In a letter from George Bird Grinnell, Boone and Crockett Club chairman of the game preservation committee to Walter L. Fisher, Secretary of the Interior, Grinnell stated, "The Club is much concerned about the fate of the pronghorn which appears to be everywhere rapidly diminishing". By the 1920s, hunting pressure had reduced the pronghorn population to about 13,000. Boone and Crockett Club member Charles Sheldon, in a letter to fellow member Grinnell, wrote, "Personally, I think that the antelope are doomed, yet every attempt should be made to save them". Although the Club had begun their efforts to save the pronghorn in 1910 by funding and restocking the Wichita Game Refuge in Kansas, the National Bison Range in Montana, and to Wind Cave National Park, in South Dakota, most of the efforts were doomed since experience demonstrated that after initial increases the pronghorns would die off because of the fenced enclosures. In 1927, Grinnell spearheaded efforts along with the help of T. Gilbert Pearson of Grinnell's National Audubon Society to create the Charles Sheldon Antelope Refuge in northern Nevada. About 2900 acres of land were jointly purchased by the two organizations which was subsequently turned over to the Biological Survey as a pronghorn refuge. This donation was contingent upon the government adding 30,00 acres of surrounding public lands. On June 20, 1929, President Hoover included the required public lands upon request of the Department of Agriculture and the Department of the Interior after learning that the Boone and Crockett Club and the National Audubon Society were underwriting the private land buyout. On January 26, 1931, Hoover signed the executive order for the refuge, and on December 31, 1936, another executive order was signed, creating a 549,000-acre tract. This was the true beginning for pronghorn recovery in North America.
The protection of habitat and hunting restrictions have allowed pronghorn numbers to recover to an estimated population between 500,000 and 1,000,000 (excluding the Sonoran pronghorn, which is down to about 200). Some recent decline has occurred in a few localized populations, due to bluetongue disease, which is spread from sheep, but the overall trend has been positive since conservation measures were put in place.
Pronghorn migration corridors are threatened by habitat fragmentation and the blocking of traditional routes. In a migration study conducted by Lava Lake Institute for Science and Conservation and the Wildlife Conservation Society, at one point, the migration corridor bottlenecks to an area only 200 yards wide.
Pronghorns are now quite numerous, and outnumbered people in Wyoming and parts of northern Colorado until just recently. They are legally hunted in western states for purposes of population control and food. No major range-wide threats exist, although localized declines are taking place, particularly to the Sonoran pronghorn, mainly as a result of, among others, livestock grazing, the construction of roads, fences, and other barriers that prevent access to historical habitat, illegal hunting, insufficient forage and water, and lack of recruitment.
Three subspecies are considered endangered in all (A. a. sonoriensis, A. a. peninsularis), or part of their ranges (A. a. mexicana). Populations of the Sonoran pronghorn in Arizona and Mexico are protected under the Endangered Species Act (since 1967), and a recovery plan for this subspecies has been prepared by U.S. Fish and Wildlife Service. Mexican animals are listed on CITES Appendix I. Pronghorns have game-animal status in all of the western states of the United States, and permits are required to trap or shoot pronghorns.
- Hoffmann, M., Byers, J. & Beckmann, J. (2008). Antilocapra americana. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 10 April 2009. Database entry includes a brief justification of why this species is of least concern.
- Wilson, D. E.; Reeder, D. M., eds. (2005). Mammal Species of the World (3rd ed.). Johns Hopkins University Press. ISBN 978-0-8018-8221-0. OCLC 62265494.
- Caton, J. D. (1876). "The American Antelope, or Prong Buck". The American Naturalist 10 (4): 193–205. doi:10.1086/271628. JSTOR 2448724.
- Farb, Peter (1970). Ecology. Time Life Books. pp. 126, 136
- Smithsonian Institution. North American Mammals: Pronghorn Antilocapra americana
- Hawes, Alex. Pronghorns - Survivors of the American Savanna, Zoogoer, Nov/Dec 2001
- Mammals of Texas: Pronghorn Last retrieved 24 October 2013
- Antilocapra americana. Animal Diversity Web. Last retrieved 24 October 2013
- AnAge: Antilocapra americana
- B. J. Verts; Leslie N. Carraway (15 August 1998). Land mammals of Oregon. University of California Press. pp. 485–. ISBN 978-0-520-21199-5. Retrieved 17 September 2011.
- Carwardine, Mark (2008). Animal Records. New York: Sterling. p. 11. ISBN 9781402756238.
- Klesius, M. (2007). "Losing Ground". National Geographic 211 (1): 22.
- Byers, John (1998). American Pronghorn: Social Adaptations and the Ghosts of Predators Past. Chicago University Press. p. 318. ISBN 978-0-226-08699-6.
- Pronghorn, San Diego Zoo
- Dickens, Glen (December 2012). "Malpai Cooperative Fence Project - Pronghorn 4th Quarter 2012" 18 (4). azantelope.org. p. 5. Retrieved 2013-12-23.
- Frank Stephens (1906). California Mammals. San Diego, California: The West Coast Publishing Company. p. 56. Retrieved 2011-01-30.
- Pedro Font. Expanded Diary of Pedro Font. Retrieved 2011-01-30.
- J. Cancino, R. Rodríguez-Estrella, A. Ortega (1995). "First Aerial Survey of Historical Range for Peninsular Pronghorn of Baja California, Mexico". Journal of the Arizona-Nevada Academy of Science 28 (1): 46–50. JSTOR 40024301.
- "Pronghorn Antelope Migration Route: 160 Miles Plus : Discovery News". News.discovery.com. Retrieved 2010-07-21.
- "Pronghorn migration circuit found in Idaho - NatGeo News Watch". Blogs.nationalgeographic.com. 2009-11-02. Retrieved 2010-07-21.
- John Alexander Byers (1997). American pronghorn: social adaptations & the ghosts of predators past. University of Chicago Press. pp. 228–. ISBN 978-0-226-08698-9. Retrieved 17 September 2011.
- Fairbanks, W.S. (1994). "Dominance, age and aggression among female pronghorn, Antilocapra americana (Family: Antilocapridae)". Ethology 97 (4): 278–293. doi:10.1111/j.1439-0310.1994.tb01047.x.
- "Pronghorn" in The Encyclopedia of Mammals David MacDonald (ed.) Oxford University Press pp. 528-529 ISBN 0816064946.
- Byers, J.A., J.D. Moodie, and N. Hall (1994). "Pronghorn females choose vigorous mates". Animal Behavior 47: 33–43. doi:10.1006/anbe.1994.1005.
- Min, S.E. (1997). "The effect of variation in male sexually dimorphic traits on female behavior in pronghorn (Antilocapra americana)". Ethology 103 (9): 732–743. doi:10.1111/j.1439-0310.1997.tb00182.x.
- American Pronghorn: Social Adaptations and the Ghosts of Predators Past - John A. Byers. Books.google.com. 1997. ISBN 9780226086996. Retrieved 2013-06-22.
- Sheldon, Charles (1955). A History of the Boone and Crockett Club. Boone and Crockett Club.
- Antilocapra americana, International Union for Conservation of Nature and Natural Resources
- New Long Distance Migration Route for Pronghorn Found in Idaho by WCS and Lava Lake Institute, November 2, 2009
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