Gray wolves are all Canis lupus subspecies except two, domestic dog and dingo. The gray wolf, often known as wolf, is the largest extant wild member of the Canidae family. Though once abundant over much of Eurasia, North Africa and North America, the gray wolf inhabits a reduced portion of its former range due to widespread destruction of its territory, human encroachment, and the resulting human-wolf encounters that sparked broad extirpation. Even so, the gray wolf is regarded as being of least concern for extinction by the International Union for Conservation of Nature, when the entire gray wolf population is considered as a whole. Today, wolves are protected in some areas, hunted for sport in others, or may be subject to population control or extermination as threats to livestock, people, and pets.
Gray wolves are social predators that live in nuclear families consisting of a mated pair, their offspring and, occasionally, adopted immature wolves. They primarily feed on ungulates, which they hunt by wearing them down in short chases. Gray wolves are typically apex predators throughout their range, with only humans and tigers posing significant threats to them.
Genetic studies reaffirm that the gray wolf is the ancestor of the domestic dog. A number of other Canis lupus subspecies have been identified, though the actual number of subspecies is still open to discussion.
In areas where human cultures and wolves both occur, wolves frequently feature in the folklore and mythology of those cultures, both positively and negatively.
This primitive wolf closely resembled the modern southern wolf populations of the Arabian Peninsula and South Asia, which were once distributed in Europe in the early Quaternary glaciation until about 500,000 years ago (see Subspecies). C. mosbachensis evolved in the direction of Canis lupus, and recolonised North America in the late Rancholabrean era. There, a larger canid species called Canis dirus was already established, but it became extinct 8,000 years ago after the large prey it relied on was wiped out. Competition with the newly arrived gray wolves for the smaller and swifter prey that survived may have contributed to its decline. With the extinction of dire wolves, gray wolves became the only large and widespread canid species left.
The North American recolonisation likely occurred in several waves, with the most distinctive populations occurring in the periphery of the range. These populations (C. l. arctos on the high arctic islands, C. l. lycaon in the eastern forests, C. l. baileyi in the far south and C. l. rufus at the continental corner opposite the point of invasion) may represent survivors of early migrations from Eurasia. C. l. baileyi, C. l. lycaon and C. l. rufus display some primitive traits and systematic affinity to one another. Fossil remains from the late Pleistocene of large bodied wolves similar to C. l. arctos and C. l. albus occur in coastal southern California, indicating that large North American gray wolf subspecies were once widespread, and may have been driven southward by glaciation, though wolves no longer reside there. Fossils of small bodied wolves similar to C. l. baileyi have been found in a range encompassing Kansas and southern California. This indicates a late Pleistocene population flux, in which large, Arctic forms of wolf moved farther south, with smaller, warmth adapted wolves expanding as the climate moderated.
The now extinct Japanese wolves were descended from large Siberian wolves which colonised the Korean Peninsula and Japan, before it separated from mainland Asia, 20,000 years ago during the Pleistocene. During the Holocene, the Tsugaru Strait widened and isolated Honshu from Hokkaidō, thus causing climactic changes leading to the extinction of most large bodied ungulates inhabiting the archipelago. Japanese wolves likely underwent a process of island dwarfism 7,000–13,000 years ago in response to these climatological and ecological pressures. C. l. hattai (formerly native to Hokkaidō) was significantly larger than it southern cousin C. l. hodophilax, as it inhabited higher elevations and had access to larger prey, as well as a continuing genetic interaction with dispersing wolves from Siberia.
"Northern wolves": large-sized, large-brained wolves with strong carnassials which inhabit North America, Europe and northern Asia.
(Canis lupus arabs), an example of the "southern" wolf clade]] "Southern wolves": native to North Africa, the Arabian Peninsula and South Asia. They are characterised by their short fur, small brains and weak carnassials. They may represent a relict population of early wolves, as they closely resemble fossil European wolves, and the rate of changes observed in their DNA sequences date them to about 800,000 years, as opposed to the American and European lineages which stretch back only 150,000. The vocalisations of southern wolves have a higher proportion of short, sharp barking, and they seldom howl. It is likely that dogs and dingoes stem from this group.
Wolves in Central and East Asia are intermediate in form and size to northern and southern wolves. Differences in brain size are well defined in different wolf populations, with wolves in northern Eurasia having the highest values, North American wolves having slightly smaller brains, and the southern wolves having the smallest. Southern wolves have brains 5–10% smaller than northern wolves. Though different in behaviour and morphology, northern and southern wolves can still interbreed: the Zoological Gardens of London for example once successfully managed to mate a male European wolf to an Indian female, resulting in a cub bearing an almost exact likeness to its sire.
The actual domestication process is a source of debate. Although it is popularly assumed that dogs are the result of artificial selection, the general intractability of adult wolves to human handling has led certain experts to theorise that the domestication process occurred through natural selection when Mesolithic human communities began building permanent settlements in which a new ecological niche (middens and landfills) was opened to wolves. These wolves would have formed a commensal relationship with humans, feeding on their waste over many generations, with natural selection favouring assertive wolves with shorter flight distances in human presence, and causing physical changes related to the redundancy of features adapted for hunting big game.
Although dogs are the most closely related canids to gray wolves (the sequence divergence between gray wolves and dogs is only 1.8%, as opposed to over 4% between gray wolves, Ethiopian wolves and coyotes), there are a number of physical and behavioural differences. Comparative studies on dog and wolf behaviour and anatomy have shown that dog physiology and most dog behaviours are comparable to those of young wolves, an example of neoteny and pedomorphism.
The tympanic bullae are large, convex and almost spherical in wolves, in contrast to dogs whose bullae are smaller, compressed and slightly crumpled. Compared to equally sized dogs, wolves tend to have 20% larger skulls and 10% bigger brains. The reduction lies in the parts of the brain that deal with sense impressions. The teeth of wolves are also proportionately larger than those of dogs; premolars and molars of wolves are much less crowded, and have more complex cusp patterns. Dogs lack a pre-caudal gland, and enter estrus twice yearly, unlike wolves which only do so once annually.
The forelegs of wolves are closer to each other than those of dogs, with the former's tracks being further apart. Their tails hang straight or in a slight curve toward the body when neutral, whereas dogs carry their tails in a slight curl. Wolf paws are generally larger than dog paws, though it is almost impossible to distinguish similarly sized wolf and dog prints with certainty, though most dogs tend to have rounder paw prints than wolves.
Wolves' heads are large and heavy, with wide foreheads, strong jaws and long, blunt muzzles. The ears are relatively small and triangular. Wolves usually carry their heads at the same level as their backs, raising their heads only when alert. The sagittal and lambdoid crests are well developed, the former dividing just in front of the bregma into two ridges curving outward to form posterior border of postorbital processes. The interorbital region is moderately elevated and well defined, with distinct longitudinal concavity between raised and thickened postorbital processes. The dental formula is: at The Museum of Zoology, St. Petersburg. Note the wolf's larger size and broader muzzle.]] The teeth are heavy and large, being better suited to bone crushing than those of other extant canids, though not as specialised as those found in hyenas. The canine teeth are robust and relatively short (26 mm). The animal can develop a crushing pressure of perhaps 1,500 lbf/in2 compared to 750 lbf/in2 for a German shepherd. This force is sufficient to break open most bones, as well as cut through half inch lassos with one snap.
They generally resemble German shepherds or huskies in bodily configuration, but are distinguishable from them by their orbital angle of 40°–45° rather than 53°–60°, and the greater size of their heads and teeth (see Domestication). Compared to coyotes, wolves are larger and have broader snouts, shorter ears, and a proportionately smaller brain case and lack sweat glands on their pawpads. Compared to golden jackals, wolves are larger and heavier, and have proportionately longer legs, shorter torsos and longer tails. The teeth are overall less trenchant than the jackal's, particularly in the upper molars, which have lower cusps, are broader, and are more .
Females in any given wolf population typically weigh 5–10 lbs less than males. Wolves weighing over 54 kg (120 lbs) are uncommon, though exceptionally large individuals have been recorded in Alaska, Canada, and the former Soviet Union. The heaviest recorded gray wolf in North America was killed on 70 Mile River in east-central Alaska on July 12, 1939 and weighed , while the heaviest recorded wolf in Eurasia was killed after World War II in the Kobelyakski Area of the Poltavskij Region, Ukrainian SSR, and weighed .
The winter fur is highly resistant to cold; wolves in northern climates can rest comfortably in open areas at −40° by placing their muzzles between the rear legs and covering their faces with their tail. Wolf fur provides better insulation than dog fur, and, as with wolverines, it does not collect ice when warm breath is condensed against it. In warm climates, the fur is coarser and scarcer than in northern wolves.
Female wolves tend to have smoother furred limbs than males, and generally develop the smoothest overall coats as they age. Older wolves generally have more white hairs in the tip of the tail, along the nose and on the forehead. The winter fur is retained longest in lactating females, though with some hair loss around their nipples. Hair length on the middle of the back is 60–70 mm. Hair length of the guard hairs on the shoulders generally does not exceed 90 mm, but can reach 110–130 mm.
Coat colour ranges from almost pure white through various shades of blond, cream, and ochre to grays, browns, and blacks. Differences in coat colour between sexes are largely absent, though females may have redder tones. Fur colour does not seem to serve any camouflage purpose, with some scientists concluding that the blended colors have more to do with emphasizing certain gestures during interaction. Black coloured wolves (which occur through wolf-dog hybridisation) rarely occur in Eurasia, where interactions with domestic dogs has been reduced over the past thousand years due to the depletion of wild wolf populations. They are more common in North America; about half of the wolves in the reintroduced wolf population in Wyoming's Yellowstone National Park are black. In southern Canada and Minnesota the black phase is more common than the white, though gray coloured wolves predominate.
In popular literature, wolf packs are often portrayed as strictly hierarchical social structures with a breeding "alpha" pair which climbs the social ladder through fighting, followed by subordinate "beta" wolves and a low ranking "omega" which bears the brunt of the pack's aggression. This terminology is based heavily on the behaviour of captive wolf packs composed of unrelated animals, which will fight and compete against each other for status. Also, as dispersal is impossible in captive situations, fights become more frequent than in natural settings. In the wild, wolf packs are little more than nuclear families whose basic social unit consists of a mated pair, followed by its offspring. Northern wolf packs tend not to be as compact or unified as those of African wild dogs and spotted hyenas, though they are not as unstable as those of coyotes. Southern wolves are more similar in social behaviour to coyotes and dingoes, living largely alone or in pairs. The average pack consists of 5–11 animals; 1–2 adults, 3–6 juveniles and 1–3 yearlings, though exceptionally large packs consisting of 42 wolves are known. Wolf packs rarely adopt other wolves into their fold, and typically kill them. In the rare cases where strange wolves are adopted, the adoptee is almost invariably a young animal of 1–3 years of age, while killed wolves are mostly fully grown. The adoption of a new member can be a lengthy process, and can consist of weeks of exploratory, non-fatal attacks in order to establish whether or not the newcomer is trustworthy. During times of ungulate abundance (migration, calving etc.), different wolf packs may temporarily join forces. Wolves as young as five months and as old as five years have been recorded to leave their packs to start their own families, though the average age is 11–24 months. Triggers for dispersal include the onset of sexual maturity and competition within the pack for food and breeding.
Estrus typically occurs in late winter, with older, multiparous females entering estrus 2–3 weeks earlier than younger females. Before the rut ensues, wolf packs will temporarily dissolve until the end of the mating season. When receptive, females will avert the base of their tails to one side, exposing the vulva. During mating, the pair is locked into a copulatory tie which may last 5–36 minutes. Because estrus in wolves only lasts a month, the males do not abandon their mates to find other females to inseminate as dogs do. During pregnancy, female wolves will remain in a den located away from the peripheral zone of their territories, where violent encounters with other packs are more likely. Old females usually whelp in the den of their previous litter, while younger females typically den near their birthplace. The gestation period lasts 62–75 days, with pups usually being born in the summer period. The average litter consists of 5–6 pups. Litters of 14–17 occur 1% of the time. Litter sizes tend to increase in areas where prey is abundant. Wolves bear relatively large pups in small litters compared to other canid species. Pups are born blind and deaf, and are covered in short soft grayish-brown fur. They weigh 300–500 grams at birth, and begin to see after 9–12 days. The milk canines erupt after one month. Pups first leave the den after 3 weeks. At 1.5 months of age, they are agile enough to flee from danger. Mother wolves do not leave the den for the first few weeks, relying on the fathers to provide food for them and their young. Unlike wolf mothers, the fathers do not regurgitate the pups' food, but carry them pieces from a kill. If the mother dies prior to the pups' weaning period, they are suckled by the pack's other females. Pups begin to eat solid food at the age of 3–4 weeks. Pups have a fast growth rate during their first four months of life: during this period: a pup's weight can increase nearly 30 times.
The reproductive behaviour of introduced wolf packs in Yellowstone is unusual, as they often have multiple breeding females who mate with lone male wolves that encroach upon the pack territories during the mating season. These so called "Casanova wolves" are young males that, having failed to procure mates or territories after leaving their natal pack, mate with the daughters of already established breeding pairs from other packs. Unlike males from established packs, Casanova wolves do not form pair bonds with the females they mate with. Because of the great abundance of prey in Yellowstone, female wolves there can bear multiple litters in this fashion.
Wolves defend their territories from other packs through a combination of scent marking, direct attacks and howling (see Communication). Scent marking is used for territorial advertisement, and involves urination, defecation and ground scratching. Scent marks are generally left every 240 metres throughout the territory on regular travelways and junctions. Such markers can last for 2–3 weeks, and are typically placed near rocks, boulders, trees or the skeletons of large animals. When scent marking and howling fail to deter strange wolf packs from entering another's territory, violent interactions can ensue. Territorial fights are among the principal causes of wolf mortality: one study on wolf mortality in Minnesota and the Denali National Park and Preserve concluded that 14–65% of wolf deaths were due to predation by other wolves. In fact, 91% of wolf fatalities occur within of the borders between neighboring territories. Because the consequences of trespassing can be fatal, such incursions are thought to be largely due to desperation or deliberate aggressiveness.
The breeding pair typically monopolizes food in order to continue producing pups. When food is scarce, this is done at the expense of other family members, especially non-pups. This is in marked contrast to the feeding behaviours of dholes and African wild dogs, who give priority to their pups when feeding. The breeding pair typically eats first, though as it is they who usually work the hardest in killing prey, they may rest after a long hunt and allow the rest of the family to eat unmolested. Once the breeding pair has finished eating, the rest of the family will tear off pieces of the carcass and transport them to secluded areas where they can eat in peace. Wolves typically commence feeding by consuming the larger internal organs of their prey, such as the heart, liver, lungs and stomach lining. The kidneys and spleen are eaten once they are exposed, followed by the muscles.
Two forms of submissive behaviour are recognised: passive and active. Passive submission usually occurs as a reaction to the approach of a dominant animal, and consists of the submissive wolf lying partly on its back and allowing the dominant wolf to sniff its anogenital area. Active submission occurs often as a form of greeting, and involves the submissive wolf approaching another in a low posture, and licking the other wolf's face. When wolves are together, they commonly endulge in behaviours such as nose pushing, jaw wrestling, cheek rubbing and facial licking. The mouthing of each other's muzzles is a friendly gesture, while clamping on the muzzle with bared teeth is a dominance display. Dominant wolves may assert themselves by straddling over a subordinate family member. At a kill, wolves will protect the carcass from afar from other wolves by flattening their ears outwardly, thus indicating that they are covering something belonging to them.
Wolf howls are generally indistinguishable from those of large dogs. Male wolves give voice through an octave, passing to a deep bass with a stress on "O", while females produce a modulated nasal baritone with stress on "U". Pups almost never howl, while yearling wolves produce howls ending in a series of dog-like yelps. Howls used for calling pack mates to a kill are long, smooth sounds similar to the beginning of the cry of a horned owl. When pursuing prey, they emit a higher pitched howl, vibrating on two notes. When closing in on their prey, they emit a combination of a short bark and a howl. When howling together, wolves harmonize rather than chorus on the same note, thus creating the illusion of there being more wolves than there actually are. Lone wolves typically avoid howling in areas where other packs are present. Wolves do not respond to howls in rainy weather and when satiated.
Growling has a fundamental frequency of 380–450 Hz, and is usually emitted during food challenges. Pups commonly growl when playing. One variation of the howl is accompanied by a high pitched whine, which precedes a lunging attack. Whining is associated with situations of anxiety, curiosity, inquiry and intimacy such as greeting, feeding pups and playing.
In Eurasia, many wolf populations are forced to subsist largely on livestock and garbage in areas with dense human activity, though wild ungulates such as moose, red deer, roe deer and wild boar are still important food sources in Russia and the more mountainous regions of Eastern Europe. Other prey species include reindeer, mouflon, wisent, saiga, ibex, chamois, wild goats, fallow deer and musk deer. The prey animals of North American wolves have largely continued to occupy suitable habitats with low human density, and cases of wolves subsisting largely on garbage or livestock are exceptional. Animals commonly preyed on by North American wolves include moose, white-tailed deer, elk, mule deer, mountain sheep and caribou. In North Africa, wolves feed on various cultivated crops and vegetables and domestic animals.
Brown bears are encountered by wolves in both Eurasia and North America. Generally, the outcome of such encounters depends on context: brown bears typically prevail against wolves in disputes over carcasses, while wolves mostly prevail against bears when defending their den sites. Both species will kill each other's young. Wolves will eat the brown bears they kill, while brown bears seem to only eat young wolves. American black bears occur solely in the Americas. Wolf interactions with black bears are much rarer than with brown bears, due to differences in habitat preferences. The majority of black bear encounters with wolves occur in the species' northern range, with no interactions being recorded in Mexico. Wolves have been recorded on numerous occasions to actively seek out black bears in their dens and kill them without eating them. Unlike brown bears, black bears frequently lose against wolves in disputes over kills. While encounters with brown and black bears appear to be common, polar bears are rarely encountered by wolves, though there are two records of wolf packs killing polar bear cubs. Wolves will also kill the cubs of Asian black bears. When attacking bears in daylight, wolf packs have been known to harry their quarry and wait till nightfall before making the final assault, as wolves have better night vision than bears.
Wolves may encounter striped hyenas in Israel and Central Asia, usually in disputes over carcasses. Hyenas feed extensively on wolf-killed carcasses in areas where the two species interact. On a one-to-one basis, hyenas dominate wolves, though wolf packs can drive off single hyenas.
Large wolf populations limit the numbers of small to medium sized felines. Wolves encounter cougars along portions of the Rocky Mountains and adjacent mountain ranges. Wolves and cougars typically avoid encountering each other by hunting on different elevations. In winter however, when snow accumulation forces their prey into valleys, interactions between the two species become more likely. Although they rarely interact, wolves and cougars will kill each other, with packs of the former sometimes usurping the latter's kills. They hunt steppe cats, and may pose a threat to snow leopards. Wolves may reduce Eurasian lynx populations.
Other than humans, tigers appear to be the only serious predators of wolves. In areas where wolves and tigers share ranges, such as the Russian Far East, the two species typically display a great deal of dietary overlap, resulting in intense competition. Wolf and tiger interactions are well documented in Sikhote-Alin, which until the beginning of the 20th century, held very few wolves. It is thought by certain experts that wolf numbers increased in the region after tigers were largely eliminated during the Russian colonization in the late 19th and early 20th centuries. This is corroborated by native inhabitants of the region claiming that they had no memory of wolves inhabiting Sikohte-Alin until the 1930s, when tiger numbers decreased. Tigers depress wolf numbers, either to the point of localized extinction or to such low numbers as to make them a functionally insignificant component of the ecosystem. Wolves appear capable of escaping competitive exclusion from tigers only when human persecution decreases the latter's numbers. Today wolves are considered scarce in tiger inhabited areas, being found in scattered pockets, and usually seen traveling as loners or in small groups. First hand accounts on interactions between the two species indicate that tigers occasionally chase wolves from their kills, while wolves will scavenge from tiger kills. Tigers are not known to prey on wolves, though there are four records of tigers killing wolves without consuming them. This competitive exclusion of wolves by tigers has been used by Russian conservationists to convince hunters in the Far East to tolerate the big cats, as they limit ungulate populations less than wolves, and are effective in controlling the latter's numbers.
Despite not being at risk for extinction, local populations of wolves are still threatened. One such threat is genetic bottlenecking caused by population fragmentation. Human populations have isolated small pockets of animals, which then suffer the effects of inbreeding. Studies have shown that the reproduction rate in wolves is strongly related to genetic diversity. Isolated wolf populations are greatly affected by the introduction of the alleles of even a single additional wolf.
With the exception of the Great Britain and Ireland, wolves were widespread in Europe during the 18th century. Wolves were exterminated from all central and northern European countries during the 19th century and the post World War II period. Remnant populations remain in Portugal, Spain, Italy, Greece and Finland, though Eurasian wolves have been recovering naturally in several parts of Europe; recolonising France, Germany, Sweden and Norway. The largest populations now occur in eastern Europe, primarily in Romania, the Balkans and Poland.
Wolf populations generally seem to be stable or increasing in most, but not all, Bern Convention nations. Limiting factors in member nations include a lack of acceptance of wolves (particularly in areas where they have made a comeback) due to concerns on livestock and dog predation and competition with hunters. Although properly regulated wolf harvests and control have been largely accepted as compatible with maintaining wolf numbers to economically acceptable levels, overhunting and poaching are recognised as the main limiting factor in European wolf populations.
With the exception of Israel and Saudi Arabia, there is little information available on wolves in the Middle East. The Arabian Peninsula is home to an estimated 300–600 wolves which, though hunted year round in all Middle Eastern countries except Israel, are relatively stable and protected by the inaccessibility of the northern mountains and central and northern deserts. In India, wolves are classed as endangered, and number an estimated 800-3,000 individuals scattered among several remnant populations. In China and Mongolia, wolves are not protected except in reserves.
Wolves once ranged over much of North America north of Mexico City, save for parts of California. Today, their status varies by country, state and province. Canadian and Alaskan wolves number in thousands and are in excellent biological condition. Wolves have expanded from Canada to the northern Rocky Mountains since the 1970s, establishing themselves southward in Montana, Washington, Idaho and Wyoming. In 1994, wolves from Alberta and British Columbia were captured and introduced into Yellowstone National Park, where they had been extinct since the 1930s. A similar introduction took place in 1998 in the Apache National Forest in Arizona. A small, isolated group of wolves on Isle Royale is believed to be suffering from the effects of reduced genetic variability. In 1991, the population was reduced from 50 to 12 wolves. Studies have shown that this reduction has coincided with a 50% loss of allozyme heterozygosity.
The presence of wolves in Egypt, Libya and Ethiopia was confirmed in 2011, when a comparison was made between the MtDNA sequences of golden jackals, Holarctic wolves (most modern wolves are of this ancestry), the Indian wolf, and the Himalayan wolf (which are considered older lineages than the main Holarctic wolf lineage) revealed that North African wolves are more closely related to Indian and Himalayan wolves than they are to golden jackals, a species which they were associated with in the past.
However, gray wolf populations are remarkably resilient against disease outbreaks. Usually, a wolf displaying the first symptoms of disease will leave its pack, thus preventing the sickness from spreading to its pack mates. Wolves in the former Soviet Union have been recorded to carry over 50 different parasite species. Ticks carried by wolves include Ixodes ricinus and Dermacentor pictus. Although wolves are host to Sarcoptes scabiei (or mange mite) they rarely develop full blown mange, unlike foxes. Other ectoparasites include biting lice, sucking lice and the fleas Pulex irritans and Ctenocephalides canis. Endoparasites include nematodes such as Toxascaris leonina and T. canis. Wolves are also carriers of Trichinella spiralis, the prevalence of which is significantly related to age.
Other endoparasites include cestodes such as Taenia pisiformis, T. hydatigena, Echinococcus granulosus, Mesocestoidea lineatus, Dioctophyme renale and the adult phase of Multiceps multiceps. Wolves may carry Neospora caninum, which is of particular concern to farmers, as the disease can be spread to livestock; infected animals being three to thirteen times more likely to abort than those not infected. Wolves suffering from tapeworms may deliberately forego eating fresh meat in favour of putrified flesh, in order to rid themselves of the parasites.
Wolves will kill dogs on occasion, with some wolf populations relying on dogs as an important food source. Wolves generally outmatch dogs, even large ones, in physical confrontations, because of their larger heads and teeth and stronger bites. Also, the fighting styles of wolves and dogs differ significantly; while dogs typically limit themselves to attacking the head, neck and shoulder, wolves will make greater use of body blocks, and attack the extremities of their opponents. In Croatia, wolves kill more dogs than sheep, and wolves in Russia appear to limit stray dog populations. Wolves may display unusually bold behaviour when attacking dogs accompanied by people, sometimes ignoring nearby humans. Wolf attacks on dogs may occur both in house yards and in forests. On village outskirts, wolves may set up ambushes for dogs, with one wolf soliciting the dog to follow it and lead it to another wolf. In some areas, livestock guardian dogs are fitted with wolf collars in order to protect themselves from wolf attacks. Wolves however may learn to avoid the spiked collars just as they do the antlers of ungulate prey, and still kill guard dogs. Wolf attacks on hunting dogs are considered a major problem in Scandinavia and Wisconsin. The most frequently killed hunting breeds in Scandinavia are harriers, with older animals being most at risk, likely because they are less timid than younger animals, and react differently to the presence of wolves. Wolf-caused injuries on dogs are often located on the back, thighs and hind legs. The fatal wound is mostly a bite to the back of the neck. Large hunting dogs such as Swedish elkhounds are more likely to survive wolf attacks due to their better ability to defend themselves.
Recorded incidences of rabid wolves in Eurasia go far back as the 13th century. The number of cases of rabid wolves are however low when compared to other species. Wolves do not serve as primary reservoirs of the disease, but can catch it from other animals such as dogs, jackals and foxes. Cases of rabies in wolves are very rare in North America, though numerous in the eastern Mediterranean, Middle East and Central Asia. Wolves apparently develop the "furious" phase of rabies to a very high degree. This, coupled with their size and strength, make rabid wolves perhaps the most dangerous of rabid animals, with bites from rabid wolves being 15 times more dangerous than those of rabid dogs. Rabid wolves usually act alone, travelling large distances and often biting large numbers of people and domestic animals. Most rabid wolf attacks occur in the spring and autumn periods. Unlike with predatory attacks, the victims of rabid wolves are not eaten, and the attack generally only lasts a day. Also, the victims are chosen at random, though the majority of cases involve adult men.
Predatory attacks usually involve single wolves or packs that learn to exploit humans as prey. Such attacks may be preceded by a long period of habituation, in which wolves gradually lose their fear of humans. The victims are generally attacked in a sustained manner around the neck and face, and are then dragged off and consumed, unless the wolves are disturbed. Such attacks tend to cluster in time and space until the offending animals are killed. Predatory attacks can occur at any time of the year, with a peak in the June–August period, when the chances of people entering forested areas (for livestock grazing or berry and mushroom picking) increase, though cases of non-rabid wolf attacks in winter have been recorded in Belarus, the Kirovsk and Irkutsk districts, Karelia and Ukraine. Also, wolves with pups experience greater food stresses during this period. The majority of victims of predatory wolf attacks are children under the age of 18 and, in the rare cases where adults are killed, the victims are almost always women. Non-rabid wolves are able to distinguish between armed and unarmed people, and will typically avoid investigating people who display self confident demeanors typical of being armed.
Wolves may react aggressively in self defense, though such attacks are mostly limited to quick bites on extremities, and the attacks are not pressed.
In Medieval Europe, pelts were considered the only practical aspect of wolves, though they were seldom used, due to the skin's foul odour. In Scandinavian folklore, wolf-skin girdles assisted in transforming the wearers into werewolves. Several Native American tribes used wolf pelts for medicinal purposes, though some Inuit tribes favour dog skin over wolf skin, as the latter is thinner, and more prone to tearing when sewn. The Pawnee wore wolf skins as capes when exploring enemy territories. The United States Army used wolf skin for parkas during the later stages of WWII and the Korean War to protect the faces of soldiers from frostbite. In the Soviet Union, between 1976 and 1988, 30,000 wolf pelts were produced annually. Recent statistics from CITES indicate that 6,000–7,000 wolf skins are internationally traded each year, with Canada, the former Soviet Union, Mongolia and China being the largest exporters, and the United States and Great Britain being the largest importers. Overall, the harvesting of wolves for their fur has little impact on their population, as only the northern varieties (whose numbers are stable) are of commercial value. Wolf trapping for fur remains a lucrative source of income for many Native Americans.
Though wolves are trainable, they lack the same degree of tractability seen in dogs. They are generally not as responsive as dogs are to coercive techniques involving fear, aversive stimuli and force. Generally, far more work is required to obtain the same degree of reliability seen in most dogs. Even then, once a certain behavior has been repeated several times, wolves may get bored and ignore subsequent commands. Wolves are most responsive toward positive conditioning and rewards, though simple praise is not sufficient as in most dogs. Unlike dogs, wolves tend to respond more to hand signals than voice.
Gray Wolf Category:Arctic land animals Category:Fauna of the Arctic Category:Mammals of Asia Category:Mammals of Europe Category:Mammals of North America Category:Megafauna of Eurasia Category:Megafauna of North America Category:Fauna of the Rocky Mountains Category:Scavengers Gray Wolf
af:Wolf ang:Ƿulf ab:Абгаду ar:ذئب رمادي an:Canis lupus frp:Lop ast:Llobu az:Adi canavar bn:নেকড়ে zh-min-nan:Lông ba:Бүре be:Воўк be-x-old:Воўк bar:Wuif bo:སྤྱང་ཀི bs:Vuk br:Bleiz gris bg:Вълк bxr:Шоно ca:Llop cv:Кашкăр cs:Vlk obecný co:Lupu cy:Blaidd da:Ulv de:Wolf nv:Mąʼiitsoh et:Hunt el:Λύκος eml:Lauv myv:Верьгиз es:Canis lupus eo:Lupo eu:Otso fa:گرگ fo:Úlvur fr:Loup fy:Wolf fur:Lôf ga:Mac tíre gd:Faol gl:Lobo glk:ورگ got:𐍅𐌿𐌻𐍆𐍃/Wulfs hak:Lòng ko:늑대 hy:Գորշ գայլ hi:भेड़िया hr:Sivi vuk io:Volfo id:Serigala abu-abu ia:Lupo gris iu:Amaruk ik:Amaġuq os:Бирæгъ is:Úlfur it:Canis lupus he:זאב מצוי kl:Amaroq ka:მგელი csb:Tósz kk:Қасқыр ky:Карышкыр kv:Кӧин ht:Lou ku:Gur mrj:Пирӹ ltg:Palākais vylks la:Lupus lv:Pelēkais vilks lb:Wollef lt:Pilkasis vilkas lij:Canis lupus lmo:Canis lupus hu:Szürke farkas mk:Волк ml:ചെന്നായ് mzn:ورگ ms:Serigala mdf:Вьрьгаз mn:Саарал чоно nah:Cuetlāchtli nl:Wolf (dier) cr:ᒪᐦᐃᐦᑲᓐ ne:ब्वाँसो ja:オオカミ ce:Borz no:Ulv nn:Ulv nrm:Loup oc:Canis lupus mhr:Пире koi:Кӧин pl:Wilk pt:Lobo kbd:Дыгъужъ ro:Lup cenușiu qu:Lupu rue:Вовк ru:Волк sah:Бөрө se:Gumpe stq:Wulf sq:Ujku scn:Lupu simple:Grey wolf sk:Vlk dravý cu:Влькъ sl:Sivi volk szl:Wilk so:Yeey sr:Вук sh:Vuk fi:Susi sv:Varg tl:Lobo (hayop) ta:ஓநாய் te:బూడిదరంగు తోడేలు th:หมาป่า tg:Гург chy:Ho'nehe tr:Kurt udm:Кион uk:Вовк vi:Sói xám fiu-vro:Susi wa:Leu bat-smg:Vėlks zh:狼
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