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Alaskan hare
Alaskan hare
Alaskan hare
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Alaskan hare
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Lagomorpha
Family: Leporidae
Genus: Lepus
Species:
L. othus
Binomial name
Lepus othus
Merriam, 1900
Alaskan hare skeleton on display at the Museum of Osteology.

The Alaskan hare (Lepus othus), also known as the tundra hare, is a species of mammal in the family Leporidae.[2] They do not dig burrows and are found in the open tundra of western Alaska and the Alaska Peninsula in the United States. They are solitary for most of the year except during mating season, when they produce a single litter of up to eight young. Predators include birds of prey (such as the snowy owl), lynx, mustelids and wolves, among other animals, as well as humans (typically hunted for food).

Description

[edit]

The Alaskan, or tundra, hare (Lepus othos) is one of the largest species of hares.[3][4] They are one of two species of hares native to the state of Alaska, the other being the more widespread snowshoe hare (Lepus americanus).[4] Both male and female adult Alaskan hares normally measure between 50–70 centimetres (20–28 in) in length, with the tail measuring up to an additional 8 centimetres (3.1 in). Their hind feet are 20 centimetres (7.9 in) long, which is thought to allow them to move easily in snowy conditions. It has also been reported that they utilize their feet for defense against predators, notably birds of prey, which attack from overhead. Lepus othos typically weighs between 2.9 to 7.2 kg (6.4 to 15.9 lb), with an average of 4.8 kg (11 lb), thus making it one of the largest lagomorphs, alongside the similarly-sized Eurasian brown hare (L. europaeus), Arctic hare (L. arcticus) and the Asian desert hare (L. tibetanus).[5] The Alaskan hare's ears are fairly short, compared to other hares.[3] This is thought to be an evolutionary adaptation in order to conserve heat throughout the colder months. A hare's ears play an important role in thermoregulation. In the summer, Alaskan hares have a brown fur coat with white underparts. In the winter, they grow a white fur coat with black-tipped ears.[3][5] Alaskan hares are known to be carriers of Francisella tularensis, a bacterium that causes an infectious disease known as tularemia, which can be transmitted to pets and humans. Tularemia symptoms include infectious or weepy sores, swollen lymph nodes, and fever or flu-like symptoms.[6]

Breeding habits

[edit]

The Alaskan hare is mostly solitary, and the species usually only congregates in groups during mating season in April and May.[5] They will normally have one litter per year of between four and eight leverets, with the young born during June and July. The leverets are active shortly after birth, and are born with full coats and open eyes.[5][3]

Taxonomy

[edit]

The closest relatives of the Alaskan hare are the Arctic hare, Lepus arcticus, of northern Canada and Greenland, and the mountain hare, Lepus timidus, of northern Eurasia,[2] from which the Alaskan hare is geographically isolated.[1]

Habitat and diet

[edit]

They do not live in burrows, but instead nest in open sites. They are most commonly found in upland tundra or in rocky or brushy areas which provide camouflage and protection from predators.[5] Their range includes western and southwestern Alaska, including the Alaska Peninsula.[1][4] They are herbivores, eating a variety of foliage and fruits, with foraging taking place primarily at dawn and dusk.[5] Alaskan hares also feed on green plants in the summer, and bark and twigs in the winter.[3] Predators include foxes, polar bears, wolverines, weasels, and birds of prey.[5] They are taken opportunistically by humans for food or for their fur.[7] Their fur can be and is used to line shoes and robes in Alaska.[3]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Alaskan hare

View on Grokipedia
from Grokipedia
The Alaskan hare (Lepus othus), also known as the hare, is a large species of lagomorph endemic to , measuring 50–70 cm in total length and weighing 2.7–5.4 kg, with a pelage that shifts from grayish-brown above and white below in summer to entirely white in winter, except for blackish ear tips, aiding in its snowy environment. Its short ears relative to other hares and large, fur-covered hind feet are adaptations for and efficient movement over snow. As one of the largest s in , it is distinguished from the sympatric (Lepus americanus) by its greater size and more restricted range. Primarily inhabiting windswept rocky slopes, upland , and open areas such as alluvial plains, coastal lowlands, thickets, sedge flats, and wet meadows in western , while generally avoiding forested regions. Its distribution spans the , the western coast from the Yukon-Kuskokwim Delta to Kotzebue , and sporadically along the coast and north of the , covering approximately 230,000 square kilometers, though populations appear to be decreasing. An , it consumes green and willow shoots in summer, shifting to woody shrubs and crowberry fruits in winter and spring to sustain itself in the harsh . The Alaskan hare is largely solitary and crepuscular, active at dawn and dusk, using natural depressions or brush for shelter rather than digging burrows. It breeds once annually in late winter or early spring (conception typically in April), with a gestation period of about 46 days yielding litters of 5–7 young, which are precocial and weaned within 5–9 weeks. Non-migratory, it forms loose groups of up to 20 or more individuals only during the mating season. Although hunted for food and fur by Indigenous communities, it faces low overall threats including minor habitat alteration, potential competition from snowshoe hares, and climate change impacts on tundra ecosystems; its conservation status is rated as apparently secure (G4) globally and in Alaska (as of May 2025).

Taxonomy

Classification

The Alaskan hare (Lepus othus) belongs to the kingdom Animalia, phylum Chordata, class Mammalia, order , family , genus Lepus, and species Lepus othus Merriam, 1900.
Taxonomic RankNameAuthority
KingdomAnimalia
PhylumChordata
ClassMammaliaLinnaeus, 1758
OrderBrandt, 1855
FamilyFischer, 1817
GenusLepusLinnaeus, 1758
SpeciesLepus othusMerriam, 1900
The binomial name Lepus othus was established by American zoologist in 1900, based on specimens collected from the type locality at St. Michaels on , . The species has two recognized subspecies: the nominate Lepus othus othus (Merriam, 1900) and Lepus othus poadromus (Merriam, 1900), though earlier accounts considered it monotypic due to clinal variation in size that was deemed insufficient for subspecific division. Although currently recognized as a distinct , its taxonomy remains in dispute, with some sources suggesting close relation or potential conspecificity with the (Lepus arcticus) and (Lepus timidus).

Evolutionary relationships

The Alaskan hare, formally classified as Lepus othus, shares close phylogenetic ties with the (Lepus arcticus) and the mountain hare (Lepus timidus), reflecting a common ancestry among northern leporids adapted to high-latitude environments. Phylogenetic analyses of the mitochondrial control region demonstrate that L. othus forms a single, well-supported monophyletic with low , positioned closely to the two clades of L. arcticus, while L. timidus haplotypes appear polyphyletically across the tree. This genetic pattern underscores shared evolutionary origins in Pleistocene refugia, where these species developed adaptations for conditions, such as tolerance for extreme cold and sparse vegetation. Divergence of L. othus from other North American hares traces to the Pleistocene epoch, with the species persisting in isolated refugia like and the High Canadian during glacial maxima, promoting lineage-specific amid fluctuating ice ages. Mitochondrial cytochrome b sequences further support this timeline, showing minimal differentiation among these northern Lepus taxa compared to southern congeners. Post-glacial isolation in Alaskan populations is evident from genetic studies revealing restricted , with L. othus exhibiting diversity of 0.0050 and no signs of demographic expansion, consistent with barriers like the limiting interbreeding after ice sheet retreat.

Physical characteristics

Size and morphology

The Alaskan hare (Lepus othus) is one of the largest hare species in , with adults typically measuring 50–70 cm in head-body length, a up to 8 cm long, and hind feet around 20 cm in length. There is no in overall size. Adults weigh 2.7–5.4 kg on average, with reported masses up to 7.2 kg in some individuals and an overall mean of 4.8 kg. Morphologically, the species exhibits a robust build adapted for environments, featuring short ears that aid in heat retention and large, strong hind legs and feet suited for efficient locomotion over . The is robust with strongly recurved upper incisors, and the claws are stout, facilitating digging in .

Coloration and seasonal adaptations

The Alaskan hare (Lepus othus) exhibits a distinctive summer pelage characterized by a dusky dorsal coat grizzled with gray, which is darker on the head, contrasting with white underparts; the ears are dusky gray with black tips, and a white ring encircles the dark eyes. This coloration provides effective against the tundra's earthy tones during the snow-free months. In winter, the hare undergoes a dramatic transformation to a predominantly pelage, except for the black tips on the ears, which remain visible for identification. This coat enhances in snowy landscapes, reducing detection by predators such as foxes and through improved background matching in and environments. The seasonal pelage change involves biannual molting, with the transition to winter beginning in mid-; molting initiates on the ears, which become fully by late except for the tips, then progresses across the body. The spring molt reverses this process, restoring the brown summer coat. These molts are primarily triggered by changes in photoperiod, the length of daylight, which cues physiological responses in seasonal coat color (SCC) mammals like the Alaskan hare, though temperature and cover can modulate the rate. Additionally, the winter is denser and longer than the summer pelage, providing enhanced insulation against extreme cold through increased air-trapping capacity in the underfur and guard hairs.

Distribution and habitat

Geographic range

The Alaskan hare (Lepus othus) is endemic to the tundra of western , with its current distribution spanning approximately 230,000 square kilometers, including primary areas south of the along the coastal margins from Kotzebue Sound to the southern tip of the near Cold Bay, including the lowlands, and sporadic occurrences along the coast and on the north slope of the . Within this area, the species occurs in coastal and extends inland up to about 150 kilometers, as evidenced by records near St. Mary’s, with additional confirmed populations on islands such as Unimak, Hagemeister, and Little Diomede. It is absent from eastern and the broader North American mainland beyond , though with only sporadic and possibly historical presence on the North Slope. Historically, the Alaskan hare's range was likely more extensive during the cooler glacial periods of the Pleistocene, when it persisted in the Beringian refugium encompassing parts of and eastern , but postglacial warming and habitat shifts have confined it to its present Alaskan distribution. A specimen from near Point Barrow dating to the late 1800s indicates possible historical presence on the North Slope, though no modern records support ongoing occurrence there.

Habitat preferences

The Alaskan hare (Lepus othus) primarily inhabits windswept rocky slopes, upland , open , rocky outcrops, and brushy areas characterized by low vegetation cover, including open areas such as alluvial plains, coastal lowlands, thickets, and sedge flats, which provide suitable cover and foraging opportunities while avoiding dense forests and low-lying or areas. For nesting, Alaskan hares utilize shallow, unlined depressions known as forms in open sites or under the shelter of thick or brush, rather than digging burrows; in winter, they rely on cover for and protection. These forms are typically above ground and offer minimal structural modification by the hare. The species occupies an altitudinal range from lowlands to subalpine zones across its Alaskan distribution, selecting habitats that support its adaptations to open, non-forested landscapes.

Behavior

Activity patterns

The Alaskan hare (Lepus othus) displays crepuscular activity patterns, with peak periods of movement and foraging occurring at dawn and dusk. During these times, individuals emerge from cover to traverse , relying on their acute senses to navigate while minimizing exposure. Midday hours are dedicated to rest, during which the hare seeks refuge in shallow scrapes called forms or amid dense willow and alder thickets to avoid diurnal predators and conserve energy. These resting sites provide concealment in the otherwise exposed landscape. Activity exhibits seasonal variation, with heightened mobility in summer to exploit abundant vegetation across larger areas. In winter, movements diminish amid deep snow, though the hare's oversized, fur-covered hind feet—measuring up to 20 cm—facilitate efficient locomotion over snowpack. The species remains non-migratory, undertaking only local displacements responsive to food distribution and weather fluctuations. Outside of the breeding season, it maintains a solitary lifestyle.

Social structure and defense

The Alaskan hare (Lepus othus) exhibits a predominantly solitary throughout most of the year, with individuals interacting minimally outside of reproductive periods. During the brief breeding season in April and May, however, temporary aggregations of up to 20 or more individuals may form, though these groups disperse quickly after mating. Such limited aligns with the ' adaptation to open environments, where dense groupings could increase visibility to predators. For defense, Alaskan hares primarily rely on cryptic coloration for camouflage against the tundra landscape, blending seamlessly with snow in winter and vegetation in summer to evade detection. They also employ high-speed bursts, capable of reaching up to 60 km/h during short escapes, leveraging their powerful hind legs for rapid acceleration and erratic zigzagging maneuvers. When cornered, individuals may deliver forceful kicks with their hind legs to deter close-range threats, particularly avian predators attacking from above. Major predators include raptors such as gyrfalcons (Falco rusticolus), rough-legged hawks (Buteo lagopus), and snowy owls (Bubo scandiacus), as well as mammalian carnivores like arctic foxes (Vulpes lagopus), red foxes (Vulpes vulpes), weasels (Mustela spp.), wolverines (Gulo gulo), gray wolves (Canis lupus), and polar bears (Ursus maritimus); humans also hunt them for food and fur. Their crepuscular activity patterns further aid evasion by aligning peak movement with low-light conditions that reduce predator visibility.

Diet

Food sources

The Alaskan hare (Lepus othus) maintains a strictly herbivorous diet composed primarily of materials, with distinct seasonal shifts to accommodate available resources in its environment. During the , it consumes high-protein green vegetation such as grasses, forbs, sedges, leaves, berries, and flowers, which provide essential nutrients for growth and reproduction. Specific examples include leaves of crowberry (), blueberries (), (Ledum palustre), and dwarf birch (). In winter and early spring, when snow cover limits access to fresh greens, the diet transitions to lignified tissues including bark, twigs, shoots, and buds of shrubs, particularly willow species (Salix spp., such as S. alaxensis), which can comprise up to 66% of the intake during April and May. This woody forage supports survival in nutrient-scarce conditions but is lower in protein compared to summer foods. The Alaskan hare's high-fiber diet is adapted to fermentation in the and colon, where microbial activity breaks down for energy extraction, enabling efficient processing of tough plant matter typical of vegetation. This digestive strategy, common to lagomorphs, allows the hare to derive sustenance from fibrous materials that would otherwise be indigestible; lagomorphs produce nutrient-rich cecotropes in the , which are re-ingested through coprophagy to maximize absorption of proteins, vitamins, and other nutrients.

Foraging behavior

The Alaskan hare employs a selective strategy in open habitats, methodically selecting tender shoots, leaves, and bark from available woody to maximize nutritional intake while minimizing energy expenditure. This approach allows it to efficiently exploit sparse vegetation in its coastal Alaskan range, often focusing on accessible growth in upland areas. During winter, when snow cover buries much of the , the hare digs craters through the snow using its stout claws to reach buried lichens, sedges, and roots, enabling sustained access to despite harsh conditions. To mitigate predation risks in exposed environments, the Alaskan hare maintains high vigilance during , frequently pausing to scan the horizon with its large ears and eyes while cropping vegetation. It preferentially forages along the edges of brushy cover or melting snow patches, positions that provide proximity to escape routes without fully venturing into dense thickets. This risk-averse behavior balances nutritional needs against threats from predators such as foxes and , with individuals often feeding solitarily to reduce detection. The hare's daily food intake typically ranges from 5 to 10% of its body weight, a volume adjusted downward during periods of scarcity to conserve energy while still meeting metabolic demands in the variable . hares browse on willows and ericaceous shrubs, which can influence local vegetation through pressure.

Reproduction

Breeding season and mating

The breeding season of the Alaskan hare (Lepus othus) occurs primarily from mid-April to May, coinciding with the onset of spring in its and . This timing aligns with increasing photoperiod, a key environmental cue that initiates reproductive activity in lagomorphs adapted to northern latitudes, similar to patterns observed in closely related species. During this period, typically solitary individuals form temporary aggregations of up to 20 or more, facilitating encounters for . The is characterized by brief male competition within these groups, leading to polygynous pairings where individual males mate with multiple females. Post-mating, females resume a solitary , and no prolonged pair bonds form. Females exhibit induced , a physiological trait common in hares that ensures fertilization efficiency during copulation. Conception typically happens in , followed by a period of approximately 46 days. Due to the harsh environment, with its short summers and severe winters, Alaskan hares produce only one per year, limiting reproductive cycles to this single breeding window to maximize offspring survival chances. This strategy reflects adaptations to resource scarcity and predation pressures in habitats.

Litter size and development

Female Alaskan hares typically produce one litter per year, consisting of 4 to 8 leverets, with an average litter size of 5 to 6.3 young. Following a gestation period of approximately 46 days after breeding in April or May, leverets are born in late May to July, often in an aboveground nest concealed by vegetation such as willow thickets. The young are precocial at birth, emerging fully furred with eyes open and capable of mobility within hours, which allows them to disperse from the nest site shortly after birth to reduce predation risk. Maternal care is minimal beyond , with the female visiting the scattered leverets periodically to provide ; this prolonged nursing period supports rapid growth and enhances early survivorship in the environment. Leverets are weaned at around 5 to 9 weeks of age and achieve full adult size by mid-August or September, marking their independence from the mother. Sexual maturity is reached within the first year, enabling most individuals to breed in their initial spring season. Juvenile survival is low due to high mortality from predation by foxes, raptors, and other carnivores, as well as exposure to harsh weather conditions in the Arctic tundra. The precocial nature and timing of birth after snowmelt help mitigate some risks by aligning with abundant forage and camouflage opportunities.

Conservation

The Alaskan hare (Lepus othus) is classified as Least Concern on the , with the most recent formal assessment dating to 2008, though populations are considered stable overall where data exist. However, the species is locally rare across much of its range in western , reflecting sparse and patchy distribution patterns. Population estimates for the Alaskan hare remain limited due to challenges in surveying remote habitats, but available data indicate low abundances. Surveys as of 2022 in key areas have documented fewer than 100 individuals near Nome, fewer than 20 near Ekuk on the coast, and approximately 10 near Kotzebue, suggesting overall densities on the order of less than 1 individual per km² in suitable habitat. These figures underscore the species' rarity, with total population size suspected to be large but unquantified, potentially numbering in the thousands across its endemic Alaskan range. Trends suggest a potential overall decrease, with possible range contraction from historical extents north of the to current limits south of it, driven in part by , though monitoring indicates stability in core southwestern areas. The Department of Fish and Game reports current abundances well below historical averages in most regions, with little quantitative trend data available due to fluctuating populations and limited long-term studies. Historically, the Alaskan hare was more widespread prior to the , with anecdotal accounts placing it farther north on the North Slope and in broader expanses, but it is now confined to patchy distributions in western and southwestern .

Threats and management

The Alaskan hare faces several primary threats, including , which is projected to alter vegetation composition and reduce cover duration, potentially disrupting the species' seasonal and . Models indicate uncertain but significant impacts on suitable availability, with some predicting contraction in southern ranges due to warming temperatures and shifting communities. Habitat loss from development, particularly mining activities on the and expansion of communities, fragments landscapes essential for the hare's survival. Additionally, increased predation pressure arises from elevated predator populations, such as foxes and raptors, that follow cyclic peaks in sympatric (Lepus americanus) abundances, as snowshoe hares expand northward into Alaskan hare territory amid climate-driven shrub encroachment. Human activities exacerbate these risks through subsistence hunting, which targets the hare for and , with an estimated harvest of approximately 7,500 individuals in 2013. is regulated by bag limits and seasons, though in 2025 the Alaska Board of closed the season in Game Management Units 9 and 17 to address conservation concerns. The species serves as a potential carrier for diseases like (), which can transmit to humans and other wildlife via contact or vectors, although outbreaks are more commonly associated with in . Interference from expanding populations may further limit resources in overlapping areas. Management of the Alaskan hare is overseen by the Alaska Department of Fish and Game (ADFG), which classifies it as a of greatest conservation need despite its global Least Concern status on the , indicating no immediate need for specific legal protections but emphasizing monitoring. Ongoing research focuses on , distribution, and , including field studies initiated in 2017 to track movements and abundances using radio telemetry. Habitat safeguards exist within protected areas like national parks and wildlife refuges, where development is restricted, though broader regulation of mining and oil extraction is recommended to mitigate fragmentation. Knowledge gaps persist, including the scarcity of long-term population data and systematic surveys, raising concerns about potential uplisting if warming accelerates habitat degradation.

References

  1. https://www.adfg.alaska.gov/static/education/wns/hares.pdf
  2. https://www.adfg.alaska.gov/index.cfm?adfg=alaskahare.main
  3. https://explorer.natureserve.org/Taxon/ELEMENT_GLOBAL.2.105721/Lepus_othus
  4. https://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=552513
  5. https://www.science.smith.edu/departments/Biology/VHAYSSEN/msi/pdf/i0076-3519-458-01-0001.pdf
  6. https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-294X.2005.02625.x
  7. https://pubmed.ncbi.nlm.nih.gov/16101770/
  8. https://web.corral.tacc.utexas.edu/UAF/arctos/2012_01_20/Waltari_and_Cook_2005_Phylogeography_and_historical_demographics_of_Lepus_arcticus_othus_and_timidus.pdf
  9. https://www.adfg.alaska.gov/static/species/speciesinfo/_aknhp/Alaskan_hare_2008.pdf
  10. https://animaldiversity.org/accounts/Lepus_othus/
  11. https://onlinelibrary.wiley.com/doi/10.1111/brv.12405
  12. https://cdnsciencepub.com/doi/10.1139/as-2015-0019
  13. https://spo.nmfs.noaa.gov/sites/default/files/legacy-pdfs/CIRC211.pdf
  14. https://www.auburn.edu/cosam/faculty/biology/best/research/PDFs/1999BestLepusOthus.pdf
  15. https://www.adfg.alaska.gov/index.cfm?adfg=alaskahare.printerfriendly
  16. https://hypertextbook.com/facts/2001/RobertCohen.shtml
  17. https://lafeber.com/vet/adaptations-in-herbivore-nutrition/
  18. https://www.theveterinarynurse.com/content/clinical/small-mammal-herbivores-part-1-digestive-system-adaptations-to-a-herbivorous-diet
  19. https://www.gbif.org/species/2436701
  20. https://www.fs.usda.gov/pnw/pubs/journals/pnw_2010_tape001.pdf
  21. https://www.fws.gov/sites/default/files/documents/2025-09/snowshoe-hare-lepus-americanus-a-technical-conservation-assessment.pdf
  22. https://pubmed.ncbi.nlm.nih.gov/18555621/
  23. https://doi.org/10.2305/IUCN.UK.2008.RLTS.T11795A3308465.en
  24. https://alaskapublic.org/news/2022-02-23/western-alaskas-dwindling-jackrabbit-population-is-being-surveyed-for-the-first-time
  25. https://accs.uaa.alaska.edu/wp-content/uploads/lepus_othus.pdf
  26. https://www.adfg.alaska.gov/static/regulations/wildliferegulations/pdfs/regulations_complete.pdf
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