dcsimg

Lifespan, longevity, and ageing

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Maximum longevity: 12.5 years (captivity) Observations: One wild born specimen was 12-13 years old when it died in captivity (Richard Weigl 2005).
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Conservation Status

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Ermine are not considered threatened or endangered, although hunting pressure in some areas may impact populations severely.

US Federal List: no special status

CITES: no special status

State of Michigan List: no special status

IUCN Red List of Threatened Species: least concern

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Heather Loso, University of Michigan-Ann Arbor
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Associations

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Ermine are fierce and aggressive, although diminutive, animals. Potential predators are larger carnivores including red fox, gray fox, martens, fishers, badgers, raptors, and occasionally domestic cats.

Known Predators:

  • red foxes (Vulpes vulpes)
  • gray foxes (Urocyon cinereoargenteus)
  • American martens (Martes americana)
  • fishers (Martes pennanti)
  • American badgers (Taxidea taxus)
  • raptors (Accipitridae)
  • domestic cats (Felis silvestris)
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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Heather Loso, University of Michigan-Ann Arbor
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Morphology

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At full adult size total body length from head to rump is 170 mm to 330 mm. Males are generally twice as large as females, with males weighing from 67 to 116 grams and females from 25 to 80 grams. The tail length is about 35% of the total body length, ranging from 42 mm to 120 mm. Ermine have the typical weasel form: long body, short legs, long neck supporting a triangular head, slightly protruding round ears, bright black eyes, and long whiskers. Their short, moderately fine fur is white in the winter and the tip of the tail is black. In the summer, the dorsal fur is chocolate brown while the ventral fur extending to the upper lip is yellowish white.

Range mass: 25 to 116 g.

Range length: 170 to 330 mm.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: male larger

Average basal metabolic rate: 1.276 W.

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Heather Loso, University of Michigan-Ann Arbor
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Life Expectancy

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The average life span of an ermine is 1 to 2 years; the maximum is 7 years.

Range lifespan
Status: wild:
7 (high) years.

Typical lifespan
Status: wild:
1 to 2 years.

Average lifespan
Status: wild:
1-2 years.

Range lifespan
Status: captivity:
12.5 (high) years.

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Habitat

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Ermine prefer riparian woodlands, marshes, shrubby fencerows, and open areas adjacent to forests or shrub borders. Although ermine are primarily terrestrial, they climb trees and swim well. Tree roots, hollow logs, stone walls, and rodent burrows are used as dens. Dens are usually around 300 mm below ground. Ermine line their nests with dry vegetation, and fur and feathers from prey. Side cavities of burrows are used as food caches and latrines.

Habitat Regions: temperate ; terrestrial

Terrestrial Biomes: tundra ; taiga ; savanna or grassland ; forest ; scrub forest ; mountains

Other Habitat Features: riparian

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Distribution

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Ermine have a circumpolar distribution. They are found in the north temperate regions of Eurasia and North America. In the New World, they range from east to west in a broad belt from the Arctic Ocean and adjacent islands of the Canadian Archipelago southward into the northern United States. Ermine are absent from the Great Plains.

Biogeographic Regions: nearctic (Native ); palearctic (Native )

Other Geographic Terms: holarctic

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Trophic Strategy

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Ermine are carnivores that hunt primarily at night. They are specialist predators on small, warm-blooded vertebrates, preferably mammals of rabbit size and smaller. When mammalian prey is scarce, ermine eat birds, eggs, frogs, fish, and insects. In severe climates, ermine frequently hunt under snow and survive entirely on small rodents and lemmings. Daily meals are essential to meet the ermine's exhorbitant energy and heat production demands. Ermine cache leftover meals as a way of dealing with these demands.

Once a potential prey is identified, the ermine approaches as closely as possible. With incredible speed it grasps the back of the victim's head and neck with sharp teeth, and wraps its body and feet around the victim. The victim dies from repeated bites to the base of the skull. Ermine have keen senses that help them locate prey. Hares and rodents are mainly followed by scent, insects by sound, and fish by sight.

Animal Foods: birds; mammals; amphibians; fish; eggs; insects

Foraging Behavior: stores or caches food

Primary Diet: carnivore (Eats terrestrial vertebrates)

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Heather Loso, University of Michigan-Ann Arbor
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Allison Poor, University of Michigan-Ann Arbor
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Associations

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Ermine are important predators on small mammal communities in the ecosystems in which they live.

Many ermine die from a parasitic nematode (Skrjabingylus nasicola) that infects the nasal passage, distorting the sinuses. Eventually the skull is perforated and pressure is exerted on the brain, causing death. Shrews are believed to be the carrier hosts of this parasite.

Commensal/Parasitic Species:

  • nematode worms
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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Benefits

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Humans trap thousands of ermine each season, but the demand for pelts has recently decreased. The white winter fur has long been used in trimming coats and making stoles. Ermine are excellent mousers, which makes them valuable to humans.

Positive Impacts: body parts are source of valuable material; controls pest population

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Heather Loso, University of Michigan-Ann Arbor
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Benefits

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Ermine, and other Mustela species can take domestic fowl when they can gain access to them.

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Heather Loso, University of Michigan-Ann Arbor
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Behavior

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Ermine have keen senses of smell, vision, hearing, and touch that help them to locate prey. Most mustelids are fairly quiet animals, but some vocalizations may be used in intra-specific communication. Chemical cues are probably the main means of communicating reproductive readiness to potential mates.

Communication Channels: visual ; tactile ; acoustic ; chemical

Other Communication Modes: scent marks

Perception Channels: visual ; tactile ; acoustic ; chemical

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Heather Loso, University of Michigan-Ann Arbor
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Untitled

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There are 16 Palearctic and 10 Nearctic subspecies recognized.

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Heather Loso, University of Michigan-Ann Arbor
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Reproduction

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Ermine are a polygynous-promiscuous species, with males and females mating opportunistically.

Mating System: polygynandrous (promiscuous)

Ermine mate in late spring to early summer. Females are polyestrous, but produce only 1 litter per year. Young are born in April or May after an average gestation period of 280 days, which includes an 8 to 9 month period of developmental delay. Longer days beginning in March trigger the resumption of fetal development. Litter size ranges from 3 to 18 offspring and averages 4 to 9. The sex ratio is unequal. Young are blind and helpless. They are covered with fine white hair, and a prominent dark mane of dense fur develops around the neck by the third week (function unknown). The young grow quickly and are able to hunt with their mother by their eighth week. Although females do not reach adult size until a least 6 weeks after birth, they are able to mate when they are 60 to 70 days old, often before they are weaned. Males do not breed or gain adult dimensions until their second summer.

Females in nature may survive for at least 2 breeding seasons, while males generally do not survive this long. Reproductive success is highly dependent on food availability.

Breeding interval: Ermine generally breed once yearly.

Breeding season: Ermine mate in late spring to early summer.

Range number of offspring: 3 to 18.

Average number of offspring: 4-9.

Average gestation period: 280 days.

Average weaning age: 8-10 weeks.

Average age at sexual or reproductive maturity (female): 60-70 days.

Average age at sexual or reproductive maturity (male): 2 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization ; viviparous ; delayed implantation ; embryonic diapause

Average birth mass: 2.3 g.

Average gestation period: 43 days.

Average number of offspring: 6.77.

Average age at sexual or reproductive maturity (male)
Sex: male:
365 days.

Average age at sexual or reproductive maturity (female)
Sex: female:
95 days.

Females exclusively care for their offspring, nursing and protecting them until they become independent. The young are born blind and helpless.

Parental Investment: no parental involvement; altricial ; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female); pre-independence (Provisioning: Female, Protecting: Female)

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Loso, H. 1999. "Mustela erminea" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Mustela_erminea.html
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Heather Loso, University of Michigan-Ann Arbor
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Allison Poor, University of Michigan-Ann Arbor
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Biology

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The stoat is a carnivore, and a very skillful predator (1), typically feeding on birds and small mammals, particularly rabbits and small rodents, even taking prey as large as rats and grey squirrels (5). They hunt in a zigzag pattern, making use of features such as walls and hedgerows to provide cover, probing crevices and holes, and often standing alert on the hind legs to look around (1). Their exceptionally keen senses help them to locate prey; they try to get as close as possible to their target, before rushing in and dispatching it with a swift bite to the back of the neck (1). Males (dogs, bucks, jacks or hobs) (4) and females (bitches, does, or jills) (4) live in separate territories, which they defend against individuals of the same sex (2). In spring, males set off to search for females (2). Mating occurs in early summer, but births do not occur until the spring of the following year, as development of the fertilised egg is delayed (2) for 8 to 9 months (1). Between 6 and 12 blind, helpless kits are born per litter (2), after about 8 weeks the young stoats begin to hunt alongside their mother (1). Females are able to mate before they are fully weaned at just 60 to 70 days of age, whereas males are unable to breed until they reach at least 2 years of age (1). Females typically stay within or close to the area of birth, and males disperse and establish large territories that overlap several female ranges (1). Predators of stoats include owls, larger carnivores and hawks (2). The average life expectancy of a stoat is just 1.5 years (3).
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Conservation

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Research is currently being carried out to determine whether the populations of weasels and stoats, our smallest carnivores are in decline (4).
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Description

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Stoats are elusive predators, with long, slender bodies and short legs (2). The pelage is reddish to ginger in colour with white or cream underparts (2). Some individuals turn either partially or fully white in winter (2). The tail has a black tip, a feature that allows stoats to be distinguished from weasels (2). The head, which is supported by a fairly long neck, is triangular in shape, and features bright black eyes, long whiskers and round ears (1). Male stoats are much larger than females (1). At birth the kits are covered with fine white hair, and a dark 'mane' of fur forms around the neck after the third week (1).
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Habitat

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Inhabits a range of habitats including open moor, woodland, farmland and marsh (3).
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Range

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Widespread and common throughout mainland Britain and Ireland (3), and occurs on a number of the larger islands around the UK (3). It is found throughout north temperate and cold parts of Eurasia and North America (1).
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Status

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Listed under Appendix III of the Bern Convention, and classified as a species of conservation concern under the UK Biodiversity Action Plan, but not a priority species (6).
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Threats

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Stoats are controlled by gamekeepers because they prey on gamebirds (3). Historically they were trapped extensively for their winter fur (ermine). At present, competition with foxes, declines of farmland bird populations, habitat loss (3) and the effects of rodenticides (5) may all be affecting stoats (3). Although the current status of stoats in the UK is unclear, it is apparent that the population has not shown an increase following the post-myxamatosis recovery of rabbit populations (4). This fact is cause for concern regarding the conservation status of this species (4).
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Brief Summary

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Stoats are found in wooded banks and forests as well as along ditches, marshes and in the dunes. They find places to hide in old rat and rabbit holes, under tree roots and in piles of wood, niches and tree hollows. If the opening is smaller than five centimeters, stoats cannot enter. They eat mainly (water) voles, but also like rabbits, birds and their eggs. Stoats appear brown in the summer and pure white in the winter. However, in the Netherlands, the animals are often only partially white. The tip of the stoat's tail is always black.
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Stoat

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The stoat (Mustela erminea), also known as the Eurasian ermine, Beringian ermine and ermine, is a mustelid native to Eurasia and the northern portions of North America. Because of its wide circumpolar distribution, it is listed as Least Concern on the IUCN Red List.[1] It is distinct from the long-tailed weasel (Neogale frenata), also known as the "masked ermine", or "big stoat"; the two species are visually similar, especially the black tail tip.

The name ermine (/ˈɜːrmɪn/) is used for species in the genus Mustela, especially the stoat, in its pure white winter coat, or the fur thereof.[2] Introduced into New Zealand in the late 19th century to control rabbits, the stoat has had a devastating effect on native bird populations. It was nominated as one of the world's top 100 "worst invaders".[3] Ermine fur was used in the 15th century by Catholic monarchs, who sometimes used it as the mozzetta cape. It has long been used on the ceremonial robes of members of the United Kingdom House of Lords. It was also used in capes on images such as the Infant Jesus of Prague.

Etymology

Skull of a stoat

The root word for "stoat" is likely either the Dutch word stout ("bold")[4] or the Gothic word 𐍃𐍄𐌰𐌿𐍄𐌰𐌽 (stautan, "to push").[5] According to John Guillim, in his Display of Heraldrie, the word "ermine" is likely derived from Armenia, the nation where it was thought the species originated,[4] though other authors have linked it to the Norman French from the Teutonic harmin (Anglo-Saxon hearma). This seems to come from the Lithuanian word šarmu.[5] In Ireland (where the least weasel does not occur), the stoat is referred to as a weasel, while in North America it is called a short-tailed weasel. A male stoat is called a dog, hob, or jack, while a female is called a jill. The collective noun for stoats is either gang or pack.[6]

Taxonomy

Formerly considered a single species with a very wide circumpolar range, a 2021 study split M. erminea into 3 species: M. erminea sensu stricto (Eurasia and northern North America), M. richardsonii (most of North America), and M. haidarum (several islands off the Pacific Northwest coast).[7][8][9]

Subspecies

As of 2021, 21 subspecies are recognized.[7]

Evolution

The stoat's direct ancestor was Mustela palerminea, a common carnivore in central and eastern Europe during the Middle Pleistocene,[18] that spread to North America during the late Blancan or early Irvingtonian.[19] The stoat is the product of a process that began 5–7 million years ago, when northern forests were replaced by open grassland, thus prompting an explosive evolution of small, burrowing rodents. The stoat's ancestors were larger than the current form, and underwent a reduction in size as they exploited the new food source. The stoat first arose in Eurasia, shortly after the long-tailed weasel, which is in a different genus (Neogale), arose as its mirror image in North America 2 million years ago. The stoat thrived during the Ice Age, as its small size and long body allowed it to easily operate beneath snow, as well as hunt in burrows. The stoat and the long-tailed weasel remained separated until 500,000 years ago, when falling sea levels exposed the Bering land bridge.[20]

Combined phylogenetic analyses indicate the stoat's closest living relatives are the American ermine (M. richardsonii) and Haida ermine (M. haidarum), the latter of which partially descends from M. erminea.[7] It is basal to most other members of Mustela, with only the yellow-bellied (M. kathia), Malayan (M. katiah), and back-striped (M. strigidorsa) weasels being more basal.[21] The mountain weasel (Mustela altaica) was formerly considered its closest relative although more recent analyses have found it to be significantly more derived. It was also previously thought to be allied with members of the genus Neogale such as the long-tailed weasel, but as those species have since been separated into a new genus, this is likely not the case.[22]

Description

Build

Stoat (left) and least weasel (right) pelts—note the stoat's larger size and black tail-tip

The stoat is similar to the least weasel in general proportions, manner of posture, and movement, though the tail is relatively longer, always exceeding a third of the body length,[23] though it is shorter than that of the long-tailed weasel. The stoat has an elongated neck, the head being set exceptionally far in front of the shoulders. The trunk is nearly cylindrical, and does not bulge at the abdomen. The greatest circumference of body is little more than half its length.[24] The skull, although very similar to that of the least weasel, is relatively longer, with a narrower braincase. The projections of the skull and teeth are weakly developed, but stronger than those of the least weasel.[25] The eyes are round, black and protrude slightly. The whiskers are brown or white in colour, and very long. The ears are short, rounded and lie almost flattened against the skull. The claws are not retractable, and are large in proportion to the digits. Each foot has five toes. The male stoat has a curved baculum with a proximal knob that increases in weight as it ages.[26] Fat is deposited primarily along the spine and kidneys, then on gut mesenteries, under the limbs and around the shoulders. The stoat has four pairs of nipples, though they are visible only in females.[26]

Skeleton

The dimensions of the stoat are variable, but not as significantly as the least weasel's.[27] Unusual among the Carnivora, the size of stoats tends to decrease proportionally with latitude, in contradiction to Bergmann's rule.[18] Sexual dimorphism in size is pronounced, with males being roughly 25% larger than females and 1.5-2.0 times their weight.[14] On average, males measure 187–325 mm (7.4–12.8 in) in body length, while females measure 170–270 mm (6.7–10.6 in). The tail measures 75–120 mm (3.0–4.7 in) in males and 65–106 mm (2.6–4.2 in) in females. In males, the hind foot measures 40.0–48.2 mm (1.57–1.90 in), while in females it is 37.0–47.6 mm (1.46–1.87 in). The height of the ear measures 18.0–23.2 mm (0.71–0.91 in) in males and 14.0–23.3 mm (0.55–0.92 in). The skulls of males measure 39.3–52.2 mm (1.55–2.06 in) in length, while those of females measure 35.7–45.8 mm (1.41–1.80 in). Males average 258 g (9.1 oz) in weight, while females weigh less than 180 g (6.3 oz).[27]

The stoat has large anal scent glands measuring 8.5 mm × 5 mm (0.33 in × 0.20 in) in males and smaller in females. Scent glands are also present on the cheeks, belly and flanks.[26] Epidermal secretions, which are deposited during body rubbing, are chemically distinct from the products of the anal scent glands, which contain a higher proportion of volatile chemicals. When attacked or being aggressive, the stoat secretes the contents of its anal glands, giving rise to a strong, musky odour produced by several sulphuric compounds. The odour is distinct from that of least weasels.[28]

Fur

A stoat in winter fur

The winter fur is very dense and silky, but quite closely lying and short, while the summer fur is rougher, shorter and sparse.[23] In summer, the fur is sandy-brown on the back and head and a white below. The division between the dark back and the light belly is usually straight, though this trait is only present in 13.5% of Irish stoats. The stoat moults twice a year. In spring, the moult is slow, starting from the forehead, across the back, toward the belly. In autumn, the moult is quicker, progressing in the reverse direction. The moult, initiated by photoperiod, starts earlier in autumn and later in spring at higher latitudes. In the stoat's northern range, it adopts a completely white coat (save for the black tail-tip) during the winter period.[26] Differences in the winter and summer coats are less apparent in southern forms of the species.[29] In the species' southern range, the coat remains brown, but is denser and sometimes paler than in summer.[26]

Distribution and habitat

The stoat has a circumboreal range throughout North America, Europe, and Asia. The stoat in Europe is found as far south as 41ºN in Portugal, and inhabits most islands with the exception of Iceland, Svalbard, the Mediterranean islands and some small North Atlantic islands. In Japan, it is present in central mountains (northern and central Japan Alps) to northern part of Honshu (primarily above 1,200 m) and Hokkaido. Its vertical range is from sea level to 3,000 m (9,800 ft).[1] In North America, it is found throughout Alaska and western Yukon to most of Arctic Canada east to Greenland. Throughout the rest of North America, as well as parts of Nunavut including Baffin Island and some islands in southeast Alaska, it is replaced by M. richardsonii.[7]

Introduction to New Zealand

Stoats were introduced into New Zealand during the late 19th century to control rabbits and hares, but are now a major threat to native bird populations. The introduction of stoats was opposed by scientists in New Zealand and Britain, including the New Zealand ornithologist Walter Buller. The warnings were ignored and stoats began to be introduced from Britain in the 1880s, resulting in a noticeable decline in bird populations within six years.[30] Stoats are a serious threat to ground- and hole-nesting birds, since the latter have very few means of escaping predation. The highest rates of stoat predation occur after seasonal gluts in southern beechmast (beechnuts), which enable the reproduction of rodents on which stoats also feed, enabling stoats to increase their own numbers.[31] For instance, the endangered South Island takahē's wild population dropped by a third between 2006 and 2007, after a stoat plague triggered by the 2005–06 mast wiped out more than half the takahē in untrapped areas.[32]

Behaviour and ecology

Reproduction and development

Young stoat

In the Northern Hemisphere, mating occurs in the April–July period. In spring, the male's testes are enlarged, a process accompanied by an increase of testosterone concentration in the plasma. Spermatogenesis occurs in December, and the males are fertile from May to August, after which the testes regress.[33] Female stoats are usually only in heat for a brief period, which is triggered by changes in day length.[34] Copulation can last as long as 1 hour.[35] Stoats are not monogamous, with litters often being of mixed paternity. Stoats undergo embryonic diapause, meaning that the embryo does not immediately implant in the uterus after fertilization, but rather lies dormant for a period of nine to ten months.[36] The gestation period is therefore variable but typically around 300 days, and after mating in the summer, the offspring will not be born until the following spring – adult female stoats spend almost all their lives either pregnant or in heat.[34] Females can reabsorb embryos and in the event of a severe winter they may reabsorb their entire litter.[37] Males play no part in rearing the young, which are born blind, deaf, toothless and covered in fine white or pinkish down. The milk teeth erupt after three weeks, and solid food is eaten after four weeks. The eyes open after five to six weeks, with the black tail-tip appearing a week later. Lactation ends after 12 weeks. Prior to the age of five to seven weeks, kits have poor thermoregulation, so they huddle for warmth when the mother is absent. Males become sexually mature at 10–11 months, while females are sexually mature at the age of 2–3 weeks whilst still blind, deaf and hairless, and are usually mated with adult males before being weaned.[38]

Territorial and sheltering behaviour

Stoat nesting in a hollow tree.

Stoat territoriality has a generally mustelid spacing pattern, with male territories encompassing smaller female territories, which they defend from other males. The size of the territory and the ranging behaviour of its occupants varies seasonally, depending on the abundance of food and mates. During the breeding season, the ranges of females remain unchanged, while males either become roamers, strayers or transients. Dominant older males have territories 50 times larger than those of younger, socially inferior males. Both sexes mark their territories with urine, faeces and two types of scent marks; anal drags are meant to convey territorial occupancy, and body rubbing is associated with agonistic encounters.[28]

The stoat does not dig its own burrows, instead using the burrows and nest chambers of the rodents it kills. The skins and underfur of rodent prey are used to line the nest chamber. The nest chamber is sometimes located in seemingly unsuitable places, such as among logs piled against the walls of houses. The stoat also inhabits old and rotting stumps, under tree roots, in heaps of brushwood, haystacks, in bog hummocks, in the cracks of vacant mud buildings, in rock piles, rock clefts, and even in magpie nests. Males and females typically live apart, but close to each other.[39] Each stoat has several dens dispersed within its range. A single den has several galleries, mainly within 30 cm (12 in) of the surface.[40]

Diet

As with the least weasel, mouse-like rodents predominate in the stoat's diet. However, unlike the least weasel, which almost exclusively feeds on small voles, the stoat regularly preys on larger rodent and lagomorph species, and will take down individuals far larger than itself. In Russia, its prey includes rodents and lagomorphs such as European water voles, common hamsters, pikas, and others, which it overpowers in their burrows. Prey species of secondary importance include small birds, fish, and shrews and, more rarely, amphibians, lizards, and insects.[41] In Great Britain, European rabbits are an important food source, with the frequency in which stoats prey on them having increased between the 1960s and mid 1990s since the end of the myxomatosis epidemic. Typically, male stoats prey on rabbits more frequently than females do, which depend to a greater extent on smaller rodent species. British stoats rarely kill shrews, rats, squirrels and water voles, though rats may be an important food source locally. In Ireland, shrews and rats are frequently eaten. In mainland Europe, water voles make up a large portion of the stoat's diet. Hares are sometimes taken, but are usually young specimens.[42] In New Zealand, the stoat feeds principally on birds, including the rare kiwi, kaka, mohua, yellow-crowned parakeet, and New Zealand dotterel.[42] Cases are known of stoats preying on young muskrats. The stoat typically eats about 50 g (1.8 oz) of food a day, which is equivalent to 25% of the animal's live weight.[43]

Stoat killing a European rabbit

The stoat is an opportunistic predator that moves rapidly and checks every available burrow or crevice for food. Because of their larger size, male stoats are less successful than females in pursuing rodents far into tunnels. Stoats regularly climb trees to gain access to birds' nests, and are common raiders of nest boxes, particularly those of large species. The stoat reputedly mesmerises prey such as rabbits by a "dance" (sometimes called the weasel war dance), though this behaviour could be linked to Skrjabingylus infections.[42] The stoat seeks to immobilize large prey such as rabbits with a bite to the spine at the back of the neck. The stoat may surplus kill when the opportunity arises, though excess prey is usually cached and eaten later to avoid obesity, as overweight stoats tend to be at a disadvantage when pursuing prey into their burrows.[44] Small prey typically die instantly from a bite to the back of the neck, while larger prey, such as rabbits, typically die of shock, as the stoat's canine teeth are too short to reach the spinal column or major arteries.[42]

Communication

The stoat is a usually silent animal, but can produce a range of sounds similar to those of the least weasel. Kits produce a fine chirping noise. Adults trill excitedly before mating, and indicate submission through quiet trilling, whining and squealing. When nervous, the stoat hisses, and will intersperse this with sharp barks or shrieks and prolonged screeching when aggressive.[28]

Aggressive behavior in stoats is categorized in these forms:[28]

  • Noncontact approach, which is sometimes accompanied by a threat display and vocalization from the approached animal
  • Forward thrust, accompanied by a sharp shriek, which is usually done by stoats defending a nest or retreat site
  • Nest occupation, when a stoat appropriates the nesting site of a weaker individual
  • Kleptoparasitism, in which a dominant stoat appropriates the killing of a weaker one, usually after a fight.

Submissive stoats express their status by avoiding higher-ranking animals, fleeing from them or making whining or squealing sounds.[28]

Predators

Larger mammalian predators such as red foxes (Vulpes vulpes) and sables (Martes zibellina) are known to prey on stoats.[45] Additionally, a wide range of birds of prey can take stoats, from small northern hawk-owls (Surnia ulula) and short-eared owls (Asio flammeus) to various buzzards, kites, goshawks, and even Eurasian eagle-owls (Bubo bubo) and golden eagles (Aquila chrysaetos).[46] Although not classified as birds of prey, grey herons (Ardea cinerea) are known to prey on stoats.[47]

Diseases and parasites

Tuberculosis has been recorded in stoats inhabiting the former Soviet Union and New Zealand. They are largely resistant to tularemia, but are reputed to suffer from canine distemper in captivity. Symptoms of mange have also been recorded.[48]

Stoats are vulnerable to ectoparasites associated with their prey and the nests of other animals on which they do not prey. The louse Trichodectes erminea is recorded in stoats living in Canada, Ireland and New Zealand. In continental Europe, 26 flea species are recorded to infest stoats, including Rhadinospylla pentacantha, Megabothris rectangulatus, Orchopeas howardi, Spilopsyllus ciniculus, Ctenophthalamus nobilis, Dasypsyllus gallinulae, Nosopsyllus fasciatus, Leptospylla segnis, Ceratophyllus gallinae, Parapsyllus n. nestoris, Amphipsylla kuznetzovi and Ctenopsyllus bidentatus. Tick species known to infest stoats are Ixodes canisuga, I. hexagonus, and I. ricinus and Haemaphysalis longicornis. Louse species known to infest stoats include Mysidea picae and Polyplax spinulosa. Mite species known to infest stoats include Neotrombicula autumnalis, Demodex erminae, Eulaelaps stabulans, Gymnolaelaps annectans, Hypoaspis nidicorva, and Listrophorus mustelae.[48]

The nematode Skrjabingylus nasicola is particularly threatening to stoats, as it erodes the bones of the nasal sinuses and decreases fertility. Other nematode species known to infect stoats include Capillaria putorii, Molineus patens and Strongyloides martes. Cestode species known to infect stoats include Taenia tenuicollis, Mesocestoides lineatus and rarely Acanthocephala.[48]

In culture

Folklore and mythology

In Irish mythology, stoats were viewed anthropomorphically as animals with families, which held rituals for their dead. They were also viewed as noxious animals prone to thieving, and their saliva was said to be able to poison a grown man. To encounter a stoat when setting out for a journey was considered bad luck, but one could avert this by greeting the stoat as a neighbour.[49] Stoats were also supposed to hold the souls of infants who died before baptism.[50] In the folklore of the Komi people of the Urals, stoats are symbolic of beautiful and coveted young women.[51] In the Zoroastrian religion, the stoat is considered a sacred animal, as its white winter coat represented purity. Similarly, Mary Magdalene was depicted as wearing a white stoat pelt as a sign of her reformed character. One popular European legend had it that a white stoat would die before allowing its pure white coat to be besmirched. When it was being chased by hunters, it would supposedly turn around and give itself up to the hunters rather than risk soiling itself.[52] The former nation (now province) of Brittany in France uses a stylized ermine-fur pattern in forming the Coat of Arms and Flag of Brittany. Gilles Servat's song La Blanche Hermine ("The White Ermine") became an anthem for Bretons (and is popular among French people in general).

In the 16th century Chinese novel Investiture of the Gods, Erlang Shen transforms into an ermine to demonstrate his shapeshifting abilities.

Fur use

Stoat skins are prized by the fur trade, especially in winter coat, and used to trim coats and stoles. The fur from the winter coat is referred to as ermine and is the traditional ancient symbol of the Duchy of Brittany, forming the earliest flag of that nation. There is also a design called ermine inspired by the winter coat of the stoat and painted onto other furs, such as rabbit.[53] In Europe these furs are a symbol of royalty and high status. The ceremonial robes of members of the United Kingdom House of Lords and the academic hoods of the universities of Oxford and Cambridge are traditionally trimmed with ermine.[53] In practice rabbit or fake fur is now often used due to expense or animal rights concerns. Prelates of the Catholic Church still wear ecclesiastical garments featuring ermine (a sign of their status equal to that of the nobility). Cecilia Gallerani is depicted holding an ermine in her portrait, Lady with an Ermine, by Leonardo da Vinci. Henry Peacham's Emblem 75, which depicts an ermine being pursued by a hunter and two hounds, is entitled "Cui candor morte redemptus" ("Purity Bought with His Own Death"). Peacham goes on to preach that men and women should follow the example of the ermine and keep their minds and consciences as pure as the legendary ermine keeps its fur.[54]

Ermine (both M. erminea and M. richardsonii, both of which inhabited the Tlingit's territory) were also valued by the Tlingit and other indigenous peoples of the Pacific Northwest Coast. They could be attached to traditional regalia and cedar bark hats as status symbols, or they were also made into shirts.[55]

The stoat was a fundamental item in the fur trade of the Soviet Union, with no less than half the global catch coming from within its borders. The Soviet Union also contained the highest grades of stoat pelts, with the best grade North American pelts being comparable only to the 9th grade in the quality criteria of former Soviet stoat standards. Stoat harvesting never became a specialty in any Soviet republic, with most stoats being captured incidentally in traps or near villages. Stoats in the Soviet Union were captured either with dogs or with box-traps or jaw-traps. Guns were rarely used, as they could damage the pelt.[56]

References

Citations

  1. ^ a b c Reid, F.; Helgen, K.; Kranz, A. (2016). "Mustela erminea". IUCN Red List of Threatened Species. 2016: e.T29674A45203335. doi:10.2305/IUCN.UK.2016-1.RLTS.T29674A45203335.en. Retrieved 19 November 2021.
  2. ^ Shorter Oxford English dictionary. UK: Oxford University Press. 2007. p. 3804. ISBN 978-0199206872.
  3. ^ "100 of the World's Worst Invasive Species". Invasive Species Specialist Group.
  4. ^ a b Coues 1877, pp. 124–125
  5. ^ a b Johnston 1903, p. 160
  6. ^ Harris & Yalden 2008, p. 456
  7. ^ a b c d Colella, Jocelyn P.; Frederick, Lindsey M.; Talbot, Sandra L.; Cook, Joseph A. (2021). "Extrinsically reinforced hybrid speciation within Holarctic ermine (Mustela spp.) produces an insular endemic". Diversity and Distributions. 27 (4): 747–762. doi:10.1111/ddi.13234.
  8. ^ Fleming, Melissa A.; Cook, Joseph A. (2002). "Phylogeography of endemic ermine (Mustela erminea) in southeast Alaska". Molecular Ecology. 11 (4): 795–807. doi:10.1046/j.1365-294X.2002.01472.x. PMID 11972765. S2CID 18874091.
  9. ^ "Explore the Database". www.mammaldiversity.org. Retrieved 2021-07-12.
  10. ^ a b c Heptner & Sludskii 2002, p. 1010
  11. ^ Merriam 1896, p. 15
  12. ^ Heptner & Sludskii 2002, p. 1014
  13. ^ Kotia, A.; Angmo, K.; Bharti, R. R.; Adhikari, B. S.; Rawat, G. S. (2011). "A record of the little-known Stoat Mustela erminea ferghanae from Ladakh, India". Small Carnivore Conservation. 44: 42–43.
  14. ^ a b c Harris & Yalden 2008, p. 459
  15. ^ a b Heptner & Sludskii 2002, p. 1012
  16. ^ Heptner & Sludskii 2002, p. 1013
  17. ^ Heptner & Sludskii 2002, p. 1011
  18. ^ a b Kurtén 1968, pp. 101–102
  19. ^ Kurtén 1980, p. 150
  20. ^ Macdonald 1992, p. 205
  21. ^ Law, C. J.; Slater, G. J.; Mehta, R. S. (2018-01-01). "Lineage Diversity and Size Disparity in Musteloidea: Testing Patterns of Adaptive Radiation Using Molecular and Fossil-Based Methods". Systematic Biology. 67 (1): 127–144. doi:10.1093/sysbio/syx047. PMID 28472434.
  22. ^ Harris & Yalden 2008, p. 458
  23. ^ a b Heptner & Sludskii 2002, p. 997
  24. ^ Coues 1877, pp. 117–121
  25. ^ Heptner & Sludskii 2002, p. 999
  26. ^ a b c d e Harris & Yalden 2008, p. 457
  27. ^ a b Heptner & Sludskii 2002, p. 1002
  28. ^ a b c d e Harris & Yalden 2008, pp. 460–461
  29. ^ Heptner & Sludskii 2002, p. 998
  30. ^ King, Carolyn (1984). Immigrant Killers. Auckland, NZ: Oxford University Press. ISBN 0-19-558121-0.
  31. ^ Purdey, D. C.; King, C. M.; Lawrence, B. (2004). "Age structure, dispersion and diet of a population of stoats (Mustela erminea) in southern Fiordland during the decline phase of the beechmast cycle" (PDF). New Zealand Journal of Zoology. The Royal Society of New Zealand. 31 (3): 205–225. doi:10.1080/03014223.2004.9518373. S2CID 55061896. Archived (PDF) from the original on 2022-10-09. Retrieved 2009-11-30.
  32. ^ "Stoats decimating takahe in Fiordland". stuff.co.nz. 4 March 2008. Retrieved 23 April 2011.
  33. ^ Gulamhusein, A. P., and W. H. Tam. "Reproduction in the male stoat, Mustela erminea." Reproduction 41.2 (1974): 303-312.
  34. ^ a b King & Powell 2007, pp. 215
  35. ^ Amstislavsky, Sergei, and Yulia Ternovskaya. "Reproduction in mustelids." Animal Reproduction Science 60 (2000): 571-581.
  36. ^ King & Powell 2007, pp. 209–210
  37. ^ King & Powell 2007, pp. 255
  38. ^ Harris & Yalden 2008, pp. 464–465
  39. ^ Heptner & Sludskii 2002, pp. 1021–1022
  40. ^ Harris & Yalden 2008, p. 461
  41. ^ Heptner & Sludskii 2002, p. 1018
  42. ^ a b c d Harris & Yalden 2008, p. 463
  43. ^ Heptner & Sludskii 2002, p. 1020
  44. ^ Verts & Carraway 1998, p. 417
  45. ^ Heptner & Sludskii 2002, p. 1025
  46. ^ Korpimäki, Erkki, and Kai Norrdahl. "Avian predation on mustelids in Europe 1: occurrence and effects on body size variation and life traits." Oikos (1989): 205-215.
  47. ^ SAWARA, Yuji, Muneki SAKUYAMA, and Gen DEMACHI. "Diets and foraging site utilization of the Grey Heron, Ardea cinerea, in the breeding season." Japanese Journal of Ornithology 43.2 (1994): 61-71.
  48. ^ a b c Harris & Yalden 2008, p. 466
  49. ^ Monaghan, Patricia (2004) The encyclopedia of Celtic mythology and folklore: Facts on File library of religion and mythology, page 426, Infobase Publishing, ISBN 0-8160-4524-0
  50. ^ Daniels, Cora Linn & Stevans, C. M. Encyclopedia of Superstitions, Folklore, and the Occult Sciences of the World, Volume 2 (2003), The Minerva Group, Inc., ISBN 1-4102-0915-6
  51. ^ Laakso, Johanna (2005) Our otherness: Finno-Ugrian approaches to women's studies, or vice versa, Volume 2 of Finno-Ugrian studies in Austria, LIT Verlag Münster, ISBN 3-8258-8626-3
  52. ^ Sax, Boria (2001) The mythical zoo: an encyclopedia of animals in world myth, legend, and literature, ABC-CLIO, ISBN 1-57607-612-1
  53. ^ a b "A house of traditions". BBC News. January 19, 1999.
  54. ^ The Minerva Britanna Project Archived 2003-04-18 at the Wayback Machine
  55. ^ "Tlingit Ermine-Skin Shirt (Daa dugu k'oodas')".
  56. ^ Heptner & Sludskii 2002, pp. 1029–1030

Bibliography

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Stoat: Brief Summary

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The stoat (Mustela erminea), also known as the Eurasian ermine, Beringian ermine and ermine, is a mustelid native to Eurasia and the northern portions of North America. Because of its wide circumpolar distribution, it is listed as Least Concern on the IUCN Red List. It is distinct from the long-tailed weasel (Neogale frenata), also known as the "masked ermine", or "big stoat"; the two species are visually similar, especially the black tail tip.

The name ermine (/ˈɜːrmɪn/) is used for species in the genus Mustela, especially the stoat, in its pure white winter coat, or the fur thereof. Introduced into New Zealand in the late 19th century to control rabbits, the stoat has had a devastating effect on native bird populations. It was nominated as one of the world's top 100 "worst invaders". Ermine fur was used in the 15th century by Catholic monarchs, who sometimes used it as the mozzetta cape. It has long been used on the ceremonial robes of members of the United Kingdom House of Lords. It was also used in capes on images such as the Infant Jesus of Prague.

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