A pika ( , ) is a small, mountain-dwelling mammal native to Asia and North America. With short limbs, a very round body, an even coat of fur, and no external tail, they resemble their close relative the rabbit, but with short, rounded ears. The large-eared pika of the Himalayas and nearby mountains lives at elevations of more than .
The name pika appears to be derived from the Tungusic piika, and the scientific name Ochotona is derived from the Mongolian word ogotno (оготно), which means 'pika'. General pika information . twycrosszoo.org It is used for any member of the Ochotonidae (), a family within the order of Lagomorpha, the order which also includes the Leporidae (rabbits and ). They are the smallest animal in the lagomorph group. Only one genus, Ochotona ( ), is extant within the family, covering 37 species, though many fossil genera are known. Another species, the Sardinian pika, belonging to the separate genus Prolagus, has become extinct within the last 2,000 years owing to human activity.
Pikas prefer rocky slopes and graze on a range of plants, primarily grasses, flowers, and young stems. In the autumn, they pull hay, soft twigs, and other stores of food under rocks to eat during the long, cold winter. The pika is also known as the whistling hare because of its high-pitched alarm call it gives when alarmed. The two species found in North America are the American pika, found primarily in the mountains of the western United States and far southwestern Canada, and the collared pika of northern British Columbia, the Yukon, western Northwest Territories and Alaska.
These animals are and feed on a wide variety of plant matter, including , Poaceae, Cyperaceae, shrub twigs, moss and lichens. Easily digestible food is processed in the gastrointestinal tract and expelled as regular feces. But in order to get nutrients out of hard to digest fiber, pika ferment fiber in the cecum (in the GI tract) and then expel the contents as soft pellets, or , which are reingested. This process is known as cecotrophy, and is a common behavior among all lagomorphs. The cecotropes are absorbed in the small intestine after consumption to utilize the nutrients.
Collared pikas have been known to store dead birds in their burrows for food during winter and eat the feces of other animals.
As with other lagomorphs, pikas have gnawing and no canines, although they have fewer molars than rabbits. They have a dentition of = 26. Another similarity that pikas share with other lagomorphs is that the bottom of their paws are covered with fur and lack paw pads.
Rock-dwelling pikas have small litters of fewer than five young, whilst the burrowing species tend to give birth to more young and to breed more frequently, possibly owing to a greater availability of resources in their native habitats. The young are born altricial (eyes and ears closed, no fur) after a gestation period of between 25 and 30 days.
The impact of human activity on the tundra ecosystems where pikas live has been recorded dating back to the 1970s.Brown, R. W., R. S. Johnston, and K. Van Cleve. "Rehabilitation problems of Arctic and alpine regions." Reclamation of drastically disturbed lands (1978): 23-44. Rather than hibernate during winter, pikas forage for grasses and other forms of plant matter and stash these findings in protected dens in a process called "haying". They eat the dried plants during the winter.Dearing, M. Denise. "The function of haypiles of pikas ( Ochotona princeps)." Journal of Mammalogy 78.4 (1997): 1156-1163. APA When pikas mistake humans as predators, they may respond to humans as they do to other species that do prey on pikas. Such interactions with humans have been linked to pikas having reduced amounts of foraging time, consequentially limiting the amount of food they can stockpile for winter months. Pikas prefer foraging in temperatures below , so they generally spend their time in shaded regions and out of direct sunlight when temperatures are high. A link has also been found between temperature increases and lost foraging time, where for every increase of to the ambient temperature in alpine landscapes home to pikas, those pikas lose 3% of their foraging time.
Eurasian pikas commonly live in family groups and share duties of gathering food and keeping watch. Some species are territorial. North American pikas ( American pika and O. collaris) are , leading solitary lives outside the breeding season.
Paleontologists have also described multiple forms of pika not referred to specific species ( Ochotona indet.) or not certainly identified ( O. cf. antiqua, O. cf. cansus, O. cf. daurica, O. cf. eximia, O. cf. gromovi, O. cf. intermedia, O. cf. koslowi, O. cf. lagrelii, O. cf. nihewanica). The statuses of Ochotona ( Proochotona) kirgisica and O. spelaeus are uncertain. The " pusilla" group of pikas is characterized by archaic (Symplesiomorphy) cheek teeth and small size. Pikas on the whole have been described as "one of the most complex and problematic groups in mammalian systematics".
The North American species migrated from Eurasia. They invaded the New World twice:
Ochotona cf. whartoni and small pikas of the O. pusilla group are also known from Siberia. The extant, endemic North American species appeared in the Pleistocene. The North American collared pika ( O. collaris) and American pika ( O. princeps) have been suggested to have descended from the same ancestor as the steppe pika ( O. pusilla).
The range of Ochotona was larger in the past, with both extinct and extant species inhabiting Western Europe and Eastern North America, areas that are currently free of pikas. Pleistocene fossils of the extant steppe pika O. pusilla currently native to Asia have been found also in many countries of Europe from the United Kingdom to Russia and from Italy to Poland, and the Asiatic extant northern pika O. hyperborea in one location in the middle Pleistocene United States.
While Ochotona is the only currently living genus of Ochotonidae, extinct Genus of ochotonids include † Albertona, † Alloptox, † Amphilagus, † Australagomys, † Austrolagomys, † Bellatona, † Bellatonoides, † Bohlinotona, † Cuyamalagus, † Desmatolagus, † Eurolagus, † Gripholagomys, † Gymnesicolagus, † Hesperolagomys, † Heterolagus, † Kenyalagomys, † Lagopsis, † Marcuinomys, † Ochotonoides, † Ochotonoma, † Oklahomalagus, † Oreolagus, † Paludotona, † Piezodus, † Plicalagus, † Pliolagomys, † Prolagus, † Proochotona (syn. Ochotona), † Pseudobellatona, † Ptychoprolagus, † Russellagus, † Sinolagomys, † Titanomys and † Tonomochota. The earliest one is Desmatolagus (middle Eocene to Miocene, 42.5–14.8 Ma), usually included in the Ochotonidae, sometimes in Leporidae or in neither ochotonid nor leporid stem-Lagomorpha.
Ochotonids appeared in Asia between the late Eocene and the early Oligocene, and continued to develop along with increased distribution of C3 grasses in previously forest dominated areas under the "climatic optimum" from the late Oligocene to middle Miocene. They thrived in Eurasia, North America, and even Africa. The peak of their diversity occurred during the period from the early Miocene to middle Miocene. Most of them became extinct during the transition from the Miocene to Pliocene, which was accompanied by an increase in diversity of the Leporidae. It has been proposed that this switch between ochotonids and larger leporids was caused by expansion of C4 plants (particularly the Poaceae) related to global cooling in the late Miocene, since extant pikas reveal a strong preference for C3 plants (Asteraceae, Rosaceae, and Fabaceae, many of them C3). Replacement of large areas of forests by open grassland first started probably in North America and is called sometimes "nature's green revolution".
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Extinct species
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Additional references of the Paleobiology Database
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