Pronghorn

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Pronghorn
Temporal range: 2.5–0  Ma
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Early Pleistocene – Recent
Antilocapra americana.jpg
Adult male pronghorn in Oregon
Antilocapra americana female (Wyoming, 2012).jpg
Adult female pronghorn in Wyoming
CITES Appendix I (CITES) [2] [note 1]
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Artiodactyla
Family: Antilocapridae
Subfamily: Antilocaprinae
Tribe: Antilocaprini
Genus: Antilocapra
Species:
A. americana [3]
Binomial name
Antilocapra americana [3]
(Ord, 1815)
Subspecies

A. a. americana
A. a. mexicana
A. a. oregona
A. a. peninsularis
A. a. sonoriensis

PronghornRange.png
Range of the pronghorn

The pronghorn ( UK: /ˈprɒŋhɔːrn/ , US: /ˈprɔːŋ-/ ) [4] (Antilocapra americana) is a species of artiodactyl (even-toed, hoofed) mammal indigenous to interior western and central North America. Though not an antelope, it is known colloquially in North America as the American antelope, prong buck, pronghorn antelope and prairie antelope, [5] because it closely resembles the antelopes of the Old World and fills a similar ecological niche due to parallel evolution. [6] It is the only surviving member of the family Antilocapridae. [7]

During the Pleistocene epoch, about 11 other antilocaprid species existed in North America, many with long or spectacularly-twisted horns. [8] Three other genera ( Capromeryx , [9] [10] Stockoceros [11] [12] and Tetrameryx [13] ) existed when humans entered North America but are now extinct.

The pronghorn's closest living relatives are the giraffe and okapi. [14] The Antilocaprids are part of the infraorder Pecora, making them distant relatives of deer, bovids, and moschids.

The pronghorn is the fastest land mammal in the Americas, with running speeds of up to 88.5 km/h (55 mph). It is the symbol of the American Society of Mammalogists. [15]

Etymology

The animal gets its name from its horn sheaths that branch and have a forward-pointing tine, unlike the horns of species from the ox family Bovidae. [16]

European discovery

Pronghorns were first seen and described by Spanish explorers in the 16th century, the species was not formally recorded or scrutinized until the expedition in 1804-06 by Captain Meriwether Lewis and Second Lieutenant William Clark. [17] Following the discovery of a few subspecies of the sharp-tailed grouse, Lewis and Clark came across the pronghorn near the mouth of the Niobrara River, in present-day Nebraska. Clark was among the first Euro-Americans to publish the experience of killing a pronghorn, and described his experience as follows: [18]

I walked on shore to find an old Vulcanoe [the Ionia Volcano?] ... in my walk I killed a Buck Goat of this Countrey, about the height of the Grown Deer, its body Shorter the horns which is not very hard and forks 23 up one prong Short the other round & Sharp arched, and is immediately above its Eyes the Color is a light gray with black behind its ears down the neck, and its face white round its neck, its Sides and its rump round its tail which is Short & white; Verry actively made, has only a pair of hoofs to each foot, his brains on the back of his head, his Nostrals large, his eyes like a Sheep he is more like the Antilope or Gazelle of Africa than any other Species of Goat.

The pronghorn was first officially described by American ornithologist George Ord in 1815. [19]

Description

Profile of an adult male Antilocapra americana male (Wyoming, 2012).jpg
Profile of an adult male

Pronghorns have distinct white fur on their rumps, sides, breasts, bellies, and across their throats. 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 (2 ft 8 in – 3 ft 5 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). [8] [20] [16] [21]

Head of an adult male Pronghorn Nebraska 1.jpg
Head of an adult male

They have very large eyes with a 320° field of vision. [22] Their orbits (eye sockets) are prominent and set high on the skull. Their teeth are hypsodont, and their dental formula is 0.0.3.33.1.3.3. Unlike deer, pronghorns possess a gallbladder. [22]

Each horn of the pronghorn is composed of a slender, laterally flattened blade of bone which is thought to grow from the frontal bones of the skull, or from the subcutaneous tissues of the scalp, forming a permanent core. [23] As in the Giraffidae, skin covers the bony cores, but in the pronghorn, it develops into a keratinous sheath which is shed and regrown annually. Males have a horn sheath about 12.5–43 cm (5–17 in) (average 25 cm or 10 in) long with a prong. Females have smaller horns that range from 3–15 cm (1–6 in) (average 12 cm or 4+12 in) and sometimes barely visible; they are straight and very rarely pronged. [16]

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 on the sides of the head. [8] The major chemical component in this gland's secretion is the highly odoriferous compound, 2-ethyl-3-methylpyrazine. This compound is also the major volatile component found on the animal's back in the male's medial gland. [24]

Pronghorns have well developed glands on each hoof. Like many ungulates, these interdigital (hoof) glands of pronghorn contain chemical compounds that are known to have antimicrobial activity against soil and mammalian pathogens. [25]

Movement

The pronghorn is the fastest land mammal in the Western Hemisphere, being built for maximum predator evasion through running. The top speed is dependent upon the length of time over which it is measured. It can run 56 km/h (35 mph) for 6.5 km (4 mi), 68 km/h (42 mph) for 1.5 km (1 mi), and 88.5 km/h (55 mph) for 800 m (12 mi). [20] [26] Although it is slower than the African cheetah, [27] it can sustain top speeds much longer than cheetahs. [7] The pronghorn may have evolved its running ability to escape from now-extinct predators such as the American cheetah, since its speed greatly exceeds that of all extant North American predators. [7] [28] :318 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. [29] They also have an extremely light bone structure and hollow hair.

Pronghorns are built for speed, not for jumping. Since their ranges are sometimes affected by sheep ranchers' fences, 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. [30]

The pronghorn has been observed to have at least 13 distinct gaits, including one reaching nearly 7.3 m (23 ft 11 in) per stride. [7]

When a pronghorn sees something that alarms it, the white hair on the rump flairs open and exposes two highly odoriferous glands that releases a compound described as having an odour "reminiscent of buttered popcorn." This sends a message to other pronghorns by both sight and smell about a present danger. This scent has been observed by humans 20 to 30 meters downwind from alarmed animals. The major odour compound identified from this gland is 2-pyrrolidinone. [31]

Range and ecology

Pronghorns in Fort Rock, Oregon Antelope1.jpg
Pronghorns in Fort Rock, Oregon

Prior to the arrival of Europeans, the pronghorn was particularly abundant in the regions west of the Mississippi River (still its primary range today). Pronghorn herds filled a vital ecological niche of the prairie habitat, as well as other climatic zones. The amount of wildlife was considered to be so vast at one time that the prehistoric American Prairie—and as recently as 200 to 300 years ago—has been dubbed the "American Serengeti", due to the once-millions-strong herds of bison, elk, hundreds of thousands of pronghorn, as well as other now-extinct megafauna.

The present-day range of the pronghorn is generally west of the Mississippi, extending from southern Saskatchewan and Alberta, Canada south into the western US, primarily in the states of Arizona, Colorado, Idaho, Kansas, Montana, Nebraska, Nevada, New Mexico, North Dakota, Oklahoma, Oregon, South Dakota, Texas, Utah, Washington and Wyoming. In extreme Northern California, pronghorn can be found in inland counties, ranging from neighboring Nevada and Oregon, as well as the central coastal grasslands, further south. [32] [33] In Mexico, the Sonoran pronghorn (A. a. sonoriensis) subspecies may be found from the state of Baja California Sur east through Sonora to San Luis Potosí, in north-central regions of the country, albeit in gradually diminishing populations. [8] [34] They have been extirpated from Iowa and Minnesota in the United States, and from Manitoba in Canada. [35]

Other regional subspecies include the Rocky Mountain pronghorn (A. a. americana), 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 250–400 mm (10–15+12 in) of rainfall per year. They eat a wide variety of plant foods, often including plants unpalatable or toxic to domestic livestock, though they also compete with them for food. [20] In one study, forbs comprised 62% of their diet, shrubs 23%, and grasses 15%, [20] while in another, cacti comprised 40%, grass 22%, forbs 20%, and shrubs 18%. [16] Pronghorns also chew and eat (ruminate) cud.

Healthy pronghorn populations tend to stay within 5.0–6.5 km (3–4 mi) of a water source. The majority are found within 5 mi (8 km) of a water source. [36]

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 260 km (160 mi). [37] 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 the 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." [38]

Cougars (Puma concolor), wolves (Canis lupus), coyotes (Canis latrans), grizzly bears (Ursus arctos horribilis) and bobcats (Lynx rufus) are major predators of pronghorns. [39] Golden eagles (Aquila chrysaetos) have been reported to prey on fawns and adults. [39] [40] Jaguars (Panthera onca) also likely prey on pronghorns in their native range in the southwestern United States and in northern Mexico. In the Pleistocene, jaguars would likely be dangerous to pronghorns as a short-range ambush predator. [41]

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 harems, and adult males living solitarily. [28] 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. [42] 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. [28] :228 Where precipitation is high, adult males tend to be territorial and maintain their territories with scent marking, vocalizing, and challenging intruders. [43] In these systems, territorial males have access to better resources than bachelor males. [43] 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 estrous approaches. "Inciting" females behave as samplers until estrous, and then incite conflicts between males, watching and then mating with the winners. [44] Before fighting, males try to intimidate each other. If intimidation fails, they lock horns and try to injure each other. [16] "Quiet" females remain with a single male in an isolated area throughout estrous. [44] Females continue this mating behavior for two to three weeks. [16]

When courting an estrous female, a male pronghorn approaches her while softly vocalizing [45] [28] and waving his head side to side, displaying his cheek patches. [46] The scent glands on the pronghorn are on either side of the jaw, between the hooves, and on the rump. [16] A receptive female remains motionless, sniffs his scent gland, and then allows the male to mount her. [28]

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. The gestation period is around six weeks longer than that of the white-tailed deer. Females usually bear within a few days of each other. [20] Twin fawns are common. [29] Newborn pronghorns weigh 2–4 kg (4–9 lb), most commonly 3 kg (7 lb). In their first 21–26 days, fawns spend time hiding in vegetation. [43] Fawns interact with their mothers for 20–25 minutes a day; this continues even when the fawn joins a nursery. [43] The females nurse, groom, and lead their young to food and water, as well as keep predators away from them. [43] Females usually nurse the young about three times a day. [20] Males are weaned 2–3 weeks earlier than females. [43] 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. [20] [16] [21]

Relationship with humans

In regions inhabited by the Plains Indians tribes, as well as the Northwest Plateau, pronghorn was hunted as a principal food source by the local people. [47] The pronghorn has also featured prominently in Native American mythology and oral history.[ further explanation needed ] [48] [ page needed ]

Merriwether Lewis and William Clark made several other observations on the behavior of the pronghorn and how the local tribes hunted them. They described the animal, which they referred to as the "Antelope" or the "Goat", as follows: [19]

Of all the animals we have seen the Antelope seems to possess the most wonderful fleetness. Shy and timorous they generally repose only on the ridges, which command a view of all the approaches of an enemy ... When they first see the hunters they run with great velocity ... The Indians near the Rocky Mountains hunt these animals on horseback, and shoot them with arrows. The Mandans' mode of hunting them is to form a large, strong pen or fold, from which a fence made of bushes gradually widens on each side. The animals are surrounded by the hunters, and gently driven towards this pen, in which they imperceptibly find themselves enclosed, and are then at the mercy of the hunters.

Population and conservation

Pronghorns in Montana Pronghorn antelope.jpg
Pronghorns in Montana

At the turn of the 20th century, members of the wildlife conservation group Boone and Crockett Club had determined that the extinction of the pronghorn was likely. 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. [7] Boone and Crockett Club member Charles Alexander 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 Oklahoma, the National Bison Range in Montana, and the 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 Alexander Sheldon Antelope Refuge in northern Nevada. About 2900 acres of land were jointly purchased by the two organizations and subsequently turned over to the Biological Survey as a pronghorn refuge. This donation was contingent upon the government's adding 30,000 acres of surrounding public lands. On June 20, 1929, United States President Herbert 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. On December 31, 1936, President Franklin Roosevelt signed an executive order creating a 222,000-hectare (549,000-acre) tract; this was the true beginning for pronghorn recovery in North America. [49]

Male adult pronghorn in Yellowstone National Park 2015-06-10 Pronghorn in Yellowstone National Park, USA 7862.jpg
Male adult pronghorn in Yellowstone National Park

The protection of habitat and hunting restrictions have allowed pronghorn numbers to recover to an estimated population between 500,000 and 1,000,000 since the 1930s. [1] Some recent decline has occurred in a few localized populations, [20] due to bluetongue disease which is spread from sheep, but the overall trend has been positive.

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. [50]

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 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. [1]

Three subspecies are considered endangered in all (A. a. sonoriensis, A. a. peninsularis), or part of their ranges (A. a. mexicana). The Sonoran pronghorn has an estimated population of fewer than 300 in the United States and 200–500 in Mexico, while there are approximately 200 Peninsula pronghorn in Baja California. [1] 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. [1] 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 hunt pronghorns. [1]

Explanatory notes

  1. Only populations of Mexico.

Related Research Articles

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<span class="mw-page-title-main">Springbok</span> Antelope of southwest and south Africa

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<span class="mw-page-title-main">Wildebeest</span> Genus of antelope

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<span class="mw-page-title-main">Antilocapridae</span> Family of mammals belonging to even-toed ungulates

The Antilocapridae are a family of ruminant artiodactyls endemic to North America. Their closest extant relatives are the giraffids. Only one species, the pronghorn, is living today; all other members of the family are extinct. The living pronghorn is a small ruminant mammal resembling an antelope.

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<i>Stockoceros</i> Extinct genus of mammals

Stockoceros is an extinct genus of the North American artiodactyl family Antilocapridae (pronghorns), known from what is now Mexico and the southwestern United States. The genus survived until about 12,000 years ago, and was present when Paleo-Indians reached North America.

<span class="mw-page-title-main">Heuglin's gazelle</span> Species of mammal

Heuglin's gazelle, also known as the Eritrean gazelle, is a species of gazelle found east of the Nile River in Eritrea, Ethiopia and Sudan. It was considered a subspecies of the red-fronted gazelle or conspecific with Thomson's gazelle and Mongalla gazelle by some authors in the past. This small gazelle stands nearly 67 cm (26 in) at the shoulder and weighs between 15 and 35 kg. The coat is dark reddish brown with a dark reddish stripe on the flanks, except for the underparts and the rump which are white. Horns, present in both sexes, measure 15 to 35 cm in length.

<i>Capromeryx</i> Extinct genus of mammals

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References

  1. 1 2 3 4 5 6 IUCN SSC Antelope Specialist Group (2017) [errata version of 2016 assessment]. "Antilocapra americana". IUCN Red List of Threatened Species . 2016: e.T1677A115056938. doi: 10.2305/IUCN.UK.2016-3.RLTS.T1677A50181848.en . Retrieved 31 August 2020.
  2. "Appendices | CITES". cites.org. Retrieved 2022-01-14.
  3. 1 2 Grubb, P. (2005). "Order Artiodactyla". In Wilson, D.E.; Reeder, D.M (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. pp. 671–2. ISBN   978-0-8018-8221-0. OCLC   62265494.
  4. Wells, John C. (2008), Longman Pronunciation Dictionary (3rd ed.), Longman, ISBN   9781405881180
  5. Caton, J. D. (1876). "The American Antelope, or Prong Buck". The American Naturalist. 10 (4): 193–205. doi: 10.1086/271628 . JSTOR   2448724.
  6. Farb, Peter (1970). Ecology. Time Life Books. pp. 126, 136
  7. 1 2 3 4 5 Hawes, Alex (November 2001). "Pronghorns - Survivors of the American Savanna". Zoogoer. Smithsonian. Archived from the original on 2009-07-13. Retrieved 2015-11-21.
  8. 1 2 3 4 Smithsonian Institution. North American Mammals: Pronghorn Antilocapra americana Archived 2016-01-22 at the Wayback Machine
  9. "Capromeryx furcifer Matthew 1902". Paleobiology Database . Retrieved 2015-11-21.
  10. "Capromeryx minor Taylor 1911". Paleobiology Database . Retrieved 2015-11-21.
  11. "Stockoceros conklingi Stock 1930". Paleobiology Database . Retrieved 2015-11-21.
  12. "Stockoceros onusrosagris Roosevelt and Burden 1934". Paleobiology Database . Retrieved 2015-11-23.
  13. "Tetrameryx shuleri Lull 1921". Paleobiology Database . Retrieved 2015-11-21.
  14. Upham, N.S.; Esselstyn, J.A.; Jetz, W. (2019). "Inferring the mammal tree: Species-level sets of phylogenies for questions in ecology, evolution, and conservation". PLOS Biology. 17 (12): e3000494. doi: 10.1371/journal.pbio.3000494 . PMC   6892540 . PMID   31800571. See Fig. S10 in Supplementary Information.
  15. "About ASM | American Society of Mammalogists". www.mammalsociety.org. 2011-03-16. Retrieved 2019-10-31.
  16. 1 2 3 4 5 6 7 8 Antilocapra americana. Animal Diversity Web. Last retrieved 24 October 2013
  17. Woodger, E.; Toporov, B. (2004). Encyclopedia of the Lewis and Clark Expedition. New York, USA: Facts On File. pp. 31–2. ISBN   978-1-4381-1023-3.
  18. Cutright, P.R. (2003). Lewis and Clark: Pioneering Naturalists. Nebraska, USA: University of Nebraska Press. pp. 81–2. ISBN   978-0-8032-6434-2.
  19. 1 2 Guthrie, W.; Ferguson, J. (1815). A New Geographical, Historical, and Commercial Grammar and Present State of the Several Kingdoms of the World. Vol. 2. Philadelphia, USA: Johnson & Warner. p. 308.
  20. 1 2 3 4 5 6 7 8 Mammals of Texas: Pronghorn Archived 2010-06-22 at the Wayback Machine Last retrieved 24 October 2013
  21. 1 2 AnAge: Antilocapra americana
  22. 1 2 Verts, B. J.; Carraway, Leslie N. (1998). Land mammals of Oregon. University of California Press. p. 485. ISBN   978-0-520-21199-5 . Retrieved 17 September 2011.
  23. Nasoori, Alireza (2020). "Formation, structure, and function of extra-skeletal bones in mammals". Biological Reviews. 95 (4): 986–1019. doi:10.1111/brv.12597. PMID   32338826. S2CID   216556342.
  24. Wood, William F. (2011). "2-Ethyl-3-methylpyrazine in the subauricular and median glands of pronghorn, Antilocapra americana". Biochemical Systematics and Ecology. 39 (2): 159–169. Bibcode:2011BioSE..39..159W. doi:10.1016/j.bse.2011.01.015.
  25. Wood, William F. (2001). "Antibacterial compounds in the interdigital glands of pronghorn, Antilocapra americana". Biochemical Systematics and Ecology. 29 (4): 417–419. Bibcode:2001BioSE..29..417W. doi:10.1016/S0305-1978(00)00060-0. PMID   11182489.
  26. Carwardine, Mark (2008). Animal Records. New York: Sterling. p. 11. ISBN   9781402756238.
  27. Klesius, M. (2007). "Losing Ground". National Geographic. 211 (1): 22.
  28. 1 2 3 4 5 Byers, John A. (1997). American Pronghorn: Social Adaptations and the Ghosts of Predators Past. Chicago University Press. ISBN   978-0-226-08699-6.
  29. 1 2 "Pronghorn | San Diego Zoo Animals & Plants". animals.sandiegozoo.org.
  30. Dickens, Glen (December 2012). "Malpai Cooperative Fence Project - Pronghorn 4th Quarter 2012" (PDF). azantelope.org. p. 5. Archived from the original (PDF) on 2013-12-24. Retrieved 2013-12-23.
  31. Wood, William F. (2002). "2-Pyrrolidinone, a putative alerting pheromone from rump glands of pronghorn, Antilocapra Americana". Biochemical Systematics and Ecology. 30 (4): 361–363. Bibcode:2002BioSE..30..361W. doi:10.1016/S0305-1978(01)00097-7.
  32. Frank Stephens (1906). California Mammals. San Diego, California: The West Coast Publishing Company. p.  56 . Retrieved 2011-01-30.
  33. Pedro Font. Expanded Diary of Pedro Font. Archived from the original on 2011-07-17. Retrieved 2011-01-30.
  34. 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.
  35. "NatureServe Explorer 2.0". explorer.natureserve.org. Retrieved 9 May 2022.
  36. "Appendix K Pronghorn Antelope" (PDF). Texas Parks & Wildlife Department . Retrieved September 1, 2023.
  37. "Pronghorn Antelope Migration Route: 160 Miles Plus : Discovery News". News.discovery.com. Archived from the original on 2012-09-29. Retrieved 2010-07-21.
  38. "Pronghorn migration circuit found in Idaho". NatGeo News Watch. Blogs.nationalgeographic.com. 2009-11-02. Retrieved 2010-07-21.[ dead link ]
  39. 1 2 White, P. J.; Barnowe-Meyer, Kerey K.; Garrott, Robert A.; Byers, John A. Reid, Charissa O. (ed.). Yellowstone Pronghorn: Recovering from the Brink of Extirpation (PDF) (Report). National Park Service. p. 21. Retrieved September 1, 2023.
  40. Switek, Brian (August 25, 2010). "Of Pronghorn and Predators". Wired . Retrieved September 1, 2023.
  41. Byers, John A. (1997). American Pronghorn: Social Adaptations and the Ghosts of Predators Past. The University of Chicago Press. p. 11. ISBN   0-226-08698-4.
  42. Fairbanks, W.S. (1994). "Dominance, age and aggression among female pronghorn, Antilocapra americana (Family: Antilocapridae)". Ethology. 97 (4): 278–293. Bibcode:1994Ethol..97..278F. doi:10.1111/j.1439-0310.1994.tb01047.x.
  43. 1 2 3 4 5 6 "Pronghorn" in The Encyclopedia of Mammals David MacDonald (ed.) Oxford University Press pp. 528-529 ISBN   0816064946.
  44. 1 2 Byers, J.A.; J.D. Moodie; N. Hall (1994). "Pronghorn females choose vigorous mates". Animal Behaviour. 47: 33–43. doi:10.1006/anbe.1994.1005. S2CID   53157415.
  45. Bromley, Peter T., and David W. Kitchen. "Courtship in the pronghorn (Antilocapra americana) [ dead link ]." The behaviour of ungulates and its relationship to management (GEIST, V. & WALTHER, F., eds) (1974): 356-364.
  46. 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. Bibcode:1997Ethol.103..732M. doi:10.1111/j.1439-0310.1997.tb00182.x.
  47. Brunton BB: Kootenai. In: Handbook of North American Indians, Volume 12: Plateau. edn. Edited by Walker DE, Jr. Washington, DC: Smithsonian Institution; 1998: 223-228. ISBN   0-16-049514-8
  48. Bruchac, Joseph (1992). Native American Animal Stories. Fulcrum Publishing. ISBN   978-1555911270.
  49. Sheldon, Charles (1955). A History of the Boone and Crockett Club. Boone and Crockett Club.
  50. New Long Distance Migration Route for Pronghorn Found in Idaho by WCS and Lava Lake Institute Archived 2011-07-13 at the Wayback Machine , November 2, 2009