Temporal range: Mid-Pleistocene–Recent
|European red fox (V. v. crucigera), British Wildlife Centre, Surrey|
|Distribution of the red fox (green - native, violet - introduced, orange - presence uncertain).|
Canis vulpes Linnaeus, 1758
The red fox (Vulpes vulpes) is the largest of the true foxes and the most abundant member of the Carnivora, being distributed across the entire Northern Hemisphere from the Arctic Circle to North Africa, Central America and Asia. Its range has increased alongside human expansion, having been introduced to Australia, where it is considered harmful to native mammals and bird populations. Because of these factors, it is listed as Least Concern by the IUCN. Due to its presence in Australia, it is included among the list of the "world's 100 worst invasive species".
The red fox originated from smaller-sized ancestors from Eurasia during the Middle Villafranchian period, and colonised North America shortly after the Wisconsin glaciation. Among the true foxes, the red fox represents a more progressive form in the direction of carnivory. Apart from its large size, the red fox is distinguished from other fox species by its ability to adapt quickly to new environments. Despite its name, the species often produces individuals with other colourings, including albinos and melanists. Forty-five subspecies are currently recognised, which are divided into two categories: the large northern foxes, and the small, basal southern foxes of Asia and the Middle East.
Red foxes are usually together in pairs or small groups consisting of families, such as a mated pair and their young, or a male with several females having kinship ties. The young of the mated pair remain with their parents to assist in caring for new kits. The species primarily feeds on small rodents, though it may also target rabbits, game birds, reptiles, invertebrates and young ungulates. Fruit and vegetable matter is also eaten sometimes. Although the red fox tends to kill smaller predators, including other fox species, it is vulnerable to attack from larger predators, such as wolves, coyotes, golden jackals and medium- and large-sized felines.
The species has a long history of association with humans, having been extensively hunted as a pest and furbearer for centuries, as well as being represented in human folklore and mythology. Because of its widespread distribution and large population, the red fox is one of the most important furbearing animals harvested for the fur trade.
- 1 Evolution
- 2 Description
- 3 Behaviour
- 4 Communication
- 5 Ecology
- 6 Range
- 7 Diseases and parasites
- 8 Relationships with humans
- 9 Notes
- 10 References
- 11 External links
The red fox is considered a more specialised form of Vulpes than the Afghan, corsac and Bengal foxes in the direction of size and adaptation to carnivory; the skull displays much fewer neotenous traits than in other species, and its facial area is more developed. It is, however, not as adapted for a purely carnivorous diet as the Tibetan fox.
The species is Eurasian in origin, and may have evolved from either Vulpes alopecoides or the related Chinese V. chikushanensis, both of which lived during the Middle Villafranchian. The earliest fossil specimens of V. vulpes were uncovered in Barany, Hungary dating from between 3.4 and 1.8 million years ago. The ancestral species was likely smaller than the current one, as the earliest red fox fossils are smaller than modern populations. The earliest fossil remains of the modern species date back to the mid-Pleistocene in association with the refuse of early human settlements. This has led to the theory that the red fox was hunted by primitive humans as both a source of food and pelts.
Colonisation of North America
Red foxes colonised the North American continent in two waves: during or before the Illinoian glaciation, and during the Wisconsinan glaciation. In the far north, red fox fossils have been found in Sangamonian deposits in the Fairbanks District and Medicine Hat. Fossils dating from the Wisconsian are present in 25 sites in Arkansas, California, Colorado, Idaho, Missouri, New Mexico, Tennessee, Texas, Virginia and Wyoming. Although they ranged far south during the Wisconsinan, the onset of warm conditions shrank their range toward the north, and have only recently reclaimed their former American ranges because of human-induced environmental changes. Genetic testing indicates two distinct red fox refugia exist in North America, which have been separated since the Wisconsinan. The northern (or boreal) refugium occurs in Alaska and western Canada, and consists of the large subspecies V. v. alascensis, V. v. abietorum, V. v. regalis and V. v. rubricosa. The southern (or montane) refugium occurs in the subalpine parklands and alpine meadows of the Rocky Mountains, the Cascade Range and Sierra Nevada. It encompasses the subspecies V. v. macroura, V. v. cascadensis and V. v. necator. The latter clade has been separated from all other red fox populations since the last glacial maximum, and may possess unique ecological or physiological adaptations.
Substantial gene pool mixing between different subspecies is known; British red foxes have crossbred extensively with foxes imported from Germany, France, Belgium, Sardinia, and possibly Siberia and Scandinavia. European foxes were introduced to portions of the USA in the 18th century, thus crossbreeding with local North American populations. Also, introduced eastern red foxes in California may be interbreeding with local V. v. necator populations. Red fox subspecies are divided into two categories:
- Northern foxes are large and brightly coloured.
- Southern grey desert foxes include the Asian subspecies V. v. griffithi, V. v. pusilla and V. v. flavescens. These foxes display transitional features between northern red foxes and smaller fox species; their skulls possess more primitive, neotenous traits than the northern forms, and are much smaller; the maximum sizes attained by southern foxes are invariably less than the average sizes of northern foxes. Their limbs are also longer, and their ears larger.
Red foxes living in Middle Asia show physical traits intermediate to the northern and southern forms.
|Scandinavian red fox
V. v. vulpes
|(Linnaeus, 1758)||A large subspecies measuring 70–90 cm in length and weighing 5–10 kg, the maximum length of the skull for males is 163.2 mm. The fur is bright red with a strongly developed whitish and yellow ripple on the lower back.||Scandinavia and the northern and middle (forest) districts of the European part of the former Soviet Union, southwards to forest-steppe and eastwards approximately to the Urals, and probably Central and Western Europe||alopex (Linnaeus, 1758)
communis (Burnett, 1829)
|British Columbian fox
V. v. abietorum
|Merriam, 1900||Generally similar to V. v. alascensis, but with a lighter, longer and more slender skull||Interior of British Columbia and probably southeastern Alaska, USA||sitkaensis (Brass, 1911)|
|Northern Alaskan fox
V. v. alascensis
|Merriam, 1900||A large, long tailed, small eared form with golden-fulvous fur||Andreafsky Wilderness, Alaska, USA|
|Eastern trans-Caucasian fox
V. v. alpherakyi
|Satunin, 1906||A small subspecies weighing 4 kg, its maximum skull length is 132–39 mm in males and 121–26 mm in females. The fur is rusty grey or rusty brown, with a brighter rusty stripe along the spine. The coat is short, coarse and sparse.||Geok Tepe, Aralsk, Kazakhstan|
V. v. anatolica
|Thomas, 1920||Izmir, Aegean Region, Turkey|
V. v. arabica
|Thomas, 1920||Dhofar and the Hajar Mountains, Oman|
V. v. atlantica
|(Wagner, 1841)||Atlas Mountains, Mila Province, Algeria||algeriensis (Loche, 1858)|
V. v. bangsi
|Merriam, 1900||Similar to V. v. fulva, but with smaller ears and less pronounced black markings on the ears and legs||L'Anse au Loup, Strait of Belle Isle, Labrador, Canada|
V. v. barbara
|(Shaw, 1800)||Barbary Coast, northwestern Africa||acaab (Cabrera, 1916)|
V. v. beringiana
|(Middendorff, 1875)||A large subspecies, it is the most brightly coloured of Old World red foxes, the fur being saturated bright-reddish and almost lacking the bright ripple along the back and flanks. The coat is fluffy and soft.||Shore of the Bering Strait, north-eastern Siberia||anadyrensis (J. A. Allen, 1903)
beringensis (Merriam, 1902)
|Cascade Mountain fox
V. v. cascadensis
|Merriam, 1900||A short tailed, small toothed fox with yellow rather than fulvous fur, it is the most common form producing "cross" varieties.||Cascade Mountains, Skamania County, Washington, USA|
|North Caucasian fox
V. v. caucasica
|Dinnik, 1914||A large subspecies, its coat is variable in colour, ranging from reddish to red-grey and nearly grey. The fur is short and coarse. This form could be a hybrid of mixing V. v. stepensis and V. v. karagan populations.||Near Vladikavkaz, Caucasus, Russia|
V. v. crucigera
|(Bechstein, 1789)||A medium-sized subspecies, its yellowish-fulvous or reddish-brown pelt lacks the whitish shading on the upper back. The tail is not grey, as in most other subspecies. It is primarily distinguished from V. v. vulpes by its slightly smaller size, distinctly smaller teeth and widely spaced premolars. Red foxes present in Britain (and therefore Australia) are usually ascribed to this subspecies, though many populations there display a great degree of tooth compaction not present in continental European populations.||All Europe, except Scandinavia, Spain and some islands of the Mediterranean Sea, introduced to Australia and Virginia||alba (Borkhausen, 1797)
cinera (Bechstein, 1801)
V. v. daurica
|Ognev, 1931||A large subspecies, the colour along its spine is light, dull yellowish-reddish with a strongly developed white ripple and greyish longitudinal stripes on the anterior side of the limbs. The coat is coarse but fluffy.||Kharangoi, 45 km west of Troizkosavsk, Siberia||ussuriensis (Dybowski, 1922)|
V. v. deletrix
|Bangs, 1898||A very pale-coloured form, its light, straw-yellow fur deepens to golden yellow or buff-fulvous in some places. The tail lacks the usual black basal spot. The hind feet and claws are very large.||St. George's Bay, Newfoundland, Canada|
V. v. dolichocrania
|Ognev, 1926||Sidemi, southern Ussuri, southeastern Siberia||ognevi (Yudin, 1986)|
|V. v. dorsalis||(J. E. Gray, 1838)|
V. v. flavescens
|J. E. Gray, 1838||A small subspecies, with an infantile skull and an overall grey coloured coat, its body length is 49–57.5 cm, and it weighs 2.2–3.2 kg.||Northern Iran||cinerascens (Birula, 1913)
splendens (Thomas, 1902)
|American red fox
V. v. fulvus
|(Desmarest, 1820)||This is a smaller subspecies than V. v. vulpes, with a smaller, sharper face, a shorter tail and a lighter pelt more profusely mixed with whitish, and darker limbs.||Eastern Canada and eastern USA||pennsylvanicus (Rhoads, 1894)|
|Afghan red fox
V. v. griffithi
|Blyth, 1854||Slightly smaller than V. vulpes montana, it has a more extensively hoary and silvered pelt.||Kandahar, Afghanistan||flavescens (Hutton, 1845)|
V. v. harrimani
|Merriam, 1900||This large subspecies has an enormous tail and coarse, wolf-like fur on the tail and lower back. The hairs on the neck and shoulders are greatly elongated and form a ruff.||Kodiak Island, Alaska, USA|
|Southern Chinese fox
V. v. hoole
|Swinhoe, 1870||||Near Amoy, Fukien, southern China||aurantioluteus (Matschie, 1907)
lineiventer (Swinhoe, 1871)
V. v. ichnusae
|Miller, 1907||A small subspecies with proportionately small ears||Sarrabus, Sardinia, Italy, may have been introduced to the English Midlands|
V. v. indutus
|Miller, 1907||Cape Pyla, Cyprus|
V. v. jakutensis
|Ognev, 1923||This subspecies is large, but smaller than V. v. beringiana. The back, neck and shoulders are brownish rusty, while the flanks are bright ocherous reddish-yellow.||Taiga, south of Yakutsk, eastern Siberia||sibiricus (Dybowski, 1922)|
|Japanese fox||Ognev, 1923||Japan|
|Karaganka fox||(Erxleben, 1777)||A smaller subspecies than V. v. vulpes, its fur is short, coarse and is of a light sandy-yellow or yellowish grey colour.||Kirghiz Steppes, Khirgizia, Russia||ferganensis (Ognev, 1926)
melanotus (Pallas, 1811)
|Kenai Peninsula fox
V. v. kenaiensis
|Merriam, 1900||One of the largest North American subspecies, it has softer fur than V. v. nbsp;harrimani.||Kenai Peninsula, Alaska, USA|
|Trans-Caucasian montane fox
V. v. kurdistanica
|Satunin, 1906||A form intermediate in size between V. v. alpheryaki and V. v. caucasica, its fur is pale yellow or light grey, sometimes brownish-reddish and is fluffier and denser than that of other Caucasian subspecies.||Northeastern Turkey||alticola (Ognev, 1926)|
|Wasatch Mountain fox
V. v. macroura
|Baird, 1852||This fox is similar to V. v. fulva, but with a much longer tail, larger hind feet and has more extensive blackening of the limbs||Named for the Wasatch Mountains, near Great Salt Lake, Utah. Found in the Rocky Mountains from Colorado and Utah, western Wyoming and Montana through Idaho up to southern Alberta.|
V. v. montana
|(Pearson, 1836)||This subspecies is distinguished from V. v. vulpes by its smaller size, proportionately smaller skull and teeth, and coarser fur. The hairs on the sole of the feet are copiously mixed with softer, woolly hairs.||Himalaya||alopex (Blanford, 1888)
himalaicus (Ogilby, 1837)
|Sierra Nevada red fox or High Sierra fox
V. v. necator
|Merriam, 1900||Externally similar to V. v. fulvus, it has a short tail, but cranially more like V. v. macroura.||High Sierra, California|
V. v. niloticus
|(E. Geoffroy Saint-Hilaire, 1803)||A small subspecies, it measures 76.7–105.3 cm in body length, 30.2–40.1 cm in tail length and weighs 1.8–3.8 kg. It is ruddy to grey-brown above and darker on the back of the neck. The flanks are greyer and tinged with buff. It is larger than V. v. arabica and V. v. palaestina.||Egypt||aegyptiacus (Sonnini, 1816)
anubis (Hemprich and Ehrenberg, 1833)
V. v. ochroxantha
|Ognev, 1926||Aksai, Semirechye, eastern Russian Turkestan, Kirgizia|
V. v. palaestina
|Thomas, 1920||Ramleh, near Jaffa, Israel|
V. v. peculiosa
|Kishida, 1924||Korea||kiyomassai (Kishida and Mori, 1929)|
V. v. pusilla
|Blyth, 1854||Slightly smaller than V. v. griffithii, it closely resembles V. bengalensis in size, but is distinguished by its longer tail and hind feet.||Salt Range, Punjab, Pakistan||leucopus (Blyth, 1854)
persicus (Blanford, 1875)
|Northern plains fox
V. v. regalis
|Merriam, 1900||The largest North American red fox subspecies, it has very large and broad ears and a very long tail. It is of a golden yellow colour with pure black feet.||Elk River, Sherburne County, Minnesota, USA|
|Nova Scotia fox
V. v. rubricosa
|Bangs, 1898||A large sized subspecies with a large, broad tail and larger teeth and rostrum than V. vulpes fulva, it is the deepest-coloured form.||Digby, Nova Scotia, Canada||bangsi (Merriam, 1900)
deletrix (Bangs, 1898)
V. v. schrencki
|Kishida, 1924||Sakhalin, Russia|
V. v. silacea
|Miller, 1907||Though equal in size to V. v. vulpes, it has smaller teeth and more widely spaced premolars. The fur is dull buff, without any yellowish or reddish tints. The hindquarters are frosted with white and the tail is clear grey in colour.||Iberian Peninsula|
|Kurile Island fox
V. v. splendidissima
|Kishida, 1924||North and central Kurile Islands, Russia|
V. v. stepensis
|Brauner, 1914||This subspecies is slightly smaller and more lightly coloured than V. v. crucigera, with shorter, coarser fur. Specimens from the Crimean mountains have brighter, fluffier and denser fur.||Steppes near Kherson, Russia||krymeamontana (Brauner, 1914)
crymensis (Brauner, 1914)
V. v. tobolica
|Ognev, 1926||This large subspecies has yellowish-rusty or dirty-reddish fur with a well-developed cross, and often a black area on the belly. The coat is long and fluffy.||Obdorsk, Tobolsk, Russia|
|Northern Chinese fox
V. v. tschiliensis
|Matschie, 1907||Slightly larger than V. v. hoole, but unlike other Chinese red foxes, it closely approaches V. v. vulpes in size.||Peiping, Chihli, northeastern China||huli (Sowerby, 1923)|
The red fox has an elongated body and relatively short limbs. The tail is longer than half the body length (70% of head and body length), is fluffy and reaches the ground when in a standing position. Their pupils are oval and vertically oriented. Nictitating membranes are present, but move only when the eyes are closed. The forepaws have five digits, while the hind feet have only four and lack dewclaws. They are very agile, being capable of jumping over 2-metre (6 ft 7 in) high fences, and swim well. Vixens normally have four pairs of teats, though vixens with seven, nine or ten teats are not uncommon. The testes of males are smaller than those of Arctic foxes.
Their skulls are fairly narrow and elongated, with small braincases. Their canine teeth are relatively long. Sexual dimorphism of the skull is more pronounced than in corsac foxes, with female red foxes tending to have smaller skulls than males, with wider nasal regions and hard palates, as well as having larger canines. Their skulls are distinguished from those of dogs by their narrower muzzles, less crowded premolars, more slender canine teeth and their concave rather than convex profiles.
Red foxes are the largest species of the genus Vulpes. However, relative to dimensions, red foxes are much lighter than similarly sized dogs of the genus Canis. Their limb bones, for example, weigh 30% less per unit area of bone than expected for similarly sized dogs. They display significant individual, sexual, age and geographical variation in size. On average, adults measure 35–50 cm (14–20 in) high at the shoulder and 45 to 90 cm (18 to 35 in) in body length with tails measuring 32 to 53 cm (13 to 21 in). The ears measure 7.7–12.5 cm (3–5 in) and the hind feet 12–18.5 cm (5–7 in). They weigh 2.2 to 14 kg (4.9 to 30.9 lb), with vixens typically weighing 15–20% less than males. Adult red foxes have skulls measuring 129–167 mm (5.1–6.6 in), while those of vixens measure 128–159 mm (5.0–6.3 in). The forefoot print measures 60 mm (2.4 in) in length and 45 mm (1.8 in) in width, while the hind foot print measures 55 mm (2.2 in) long and 38 mm (1.5 in) wide. They trot at a speed of 6–13 km/h, and have a maximum running speed of 50 km/h. They have a stride of 25–35 cm (9.8–13.8 in) when walking at a normal pace. North American red foxes are generally lightly built, with comparatively long bodies for their mass and have a high degree of sexual dimorphism. British red foxes are heavily built, but short, while continental European red foxes are closer to the general average among red fox populations. The largest red fox on record in Great Britain was a 17.2 kg (38.1 lbs), 1.4-metre (4 ft 7 in) long male, killed in Aberdeenshire, Scotland in early 2012.
The winter fur is dense, soft, silky and relatively long. For the northern foxes, the fur is very long, dense and fluffy, but is shorter, sparser and coarser in southern forms. Among northern foxes, the North American varieties generally have the silkiest guard hairs, while most Eurasian red foxes have coarser fur. There are three main colour morphs; red, silver/black and cross (see Mutations). In the typical red morph, their coats are generally bright reddish-rusty with yellowish tints. A stripe of weak, diffuse patterns of many brown-reddish-chestnut hairs occurs along the spine. Two additional stripes pass down the shoulder blades which, together with the spinal stripe, form a cross. The lower back is often a mottled silvery colour. The flanks are lighter coloured than the back, while the chin, lower lips, throat and front of the chest are white. The remaining lower surface of the body is dark, brown or reddish. During lactation, the belly fur of vixens may turn brick red. The upper parts of the limbs are rusty reddish, while the paws are black. The frontal part of the face and upper neck is bright brownish-rusty red, while the upper lips are white. The backs of the ears are black or brownish-reddish, while the inner surface is whitish. The top of the tail is brownish-reddish, but lighter in colour than the back and flanks. The underside of the tail is pale grey with a straw-coloured tint. A black spot, the location of the supracaudal gland, is usually present at the base of the tail. The tip of the tail is white.
|Red||The typical colouration. See Fur|
|Grey||The rump and spine is brown or grey with light yellowish bands on the guard hairs. The cross on the shoulders is brown, rusty brown or brownish-reddish. The limbs are brown|
|Cross||The fur has a darker colouration to the former. The rump and lower back are dark brown or dark grey, with varying degrees of silver on the guard hairs. The cross on the shoulders is black or brown, sometimes with light silvery fur. The feet and head are brown|
|Blackish-brown||The melanistic form of the Eurasian red fox. Has blackish-brown or black skin with a light-brownish tint. The skin usually has an admixture of various amounts of silver. Reddish hairs are either completely absent or in small quantities|
|Silver||The melanistic form of the North American red fox, but introduced to the Old World by the fur trade. Characterised by pure black colour with a variable admixture of silver (covering 25–100% of the skin area)|
|Platinum||Distinguished from the silver morph by its late pale, almost silver-white fur with a bluish cast|
|Samson||Distinguished by its woolly pelt which lacks guard hairs|
Red foxes have binocular vision, but their sight reacts mainly to movement. Their auditory perception is acute, being able to hear black grouses changing roosts at 600 paces, the flight of crows at 0.25–0.5 kilometres (0.16–0.31 mi) and the squeaking of mice at about 100 metres (330 ft). They are capable of locating sounds to within one degree at 700–3,000 Hz, though less accurately at higher frequencies. Their sense of smell is good, but weaker than that of specialised dogs.
Red foxes have a pair of anal sacs lined by sebaceous glands, both of which open through a single duct. The anal sacs act as fermentation chambers in which aerobic and anaerobic bacteria convert sebum into odorous compounds, including aliphatic acids. The oval-shaped caudal gland is 25 mm (1.0 in) long and 13 mm (0.51 in) wide, and reportedly smells of violets. The presence of foot glands is equivocal. The interdigital cavities are deep, with a reddish tinge and smell strongly. Sebaceous glands are present on the angle of the jaw and mandible.
Social and territorial behaviour
Red foxes either establish stable home ranges within particular areas or are itinerant with no fixed abode. They use their urine to mark their territories. A male fox raises one hind leg and his urine is sprayed forward in front of him, whereas a female fox squats down so that the urine is sprayed in the ground between the hind legs. Urine is also used to mark empty cache sites, used to store found food, as reminders not to waste time investigating them. The use of up to 12 different urination postures allows them to precisely control the position of the scent mark. Red foxes live in family groups sharing a joint territory. In favourable habitats and/or areas with low hunting pressure, subordinate foxes may be present in a range. Subordinate foxes may number 1 or 2, sometimes up to 8 in one territory. These subordinates could be formerly dominant animals, but are mostly young from the previous year, who act as helpers in rearing the breeding vixen's kits. Alternatively, their presence has been explained as being in response to temporary surpluses of food unrelated to assisting reproductive success. Non-breeding vixens will guard, play, groom, provision and retrieve kits, an example of kin selection. Red foxes may leave their families once they reach adulthood if the chances of winning a territory of their own are high. If not, they will stay with their parents, at the cost of postponing their own reproduction.
Reproduction and development
Red foxes reproduce once a year in spring. Two months prior to oestrus (typically December), the reproductive organs of vixens change shape and size. By the time they enter their oestrus period, their uterine horns double in size, and their ovaries grow 1.5–2 times larger. Sperm formation in males begins in August–September, with the testicles attaining their greatest weight in December–February. The vixen's oestrus period lasts three weeks, during which the dog-foxes mate with the vixens for several days, often in burrows. Copulation is accompanied by a copulatory tie which may last for more than an hour. The copulatory tie occurs when the bulbus glandis at the base of the male fox's penis enlarges. The gestation period lasts 49–58 days. Though foxes are largely monogamous, DNA evidence from one population indicated large levels of polygyny, incest and mixed paternity litters. Subordinate vixens may become pregnant, but usually fail to whelp, or have their kits killed postpartum by either the dominant female or other subordinates.
The average litter size consists of four to six kits, though litters of up to 13 kits have occurred. Large litters are typical in areas where fox mortality is high. Kits are born blind, deaf and toothless, with dark brown fluffy fur. At birth, they weigh 56–110 g (2.0–3.9 oz) and measure 14.5 cm (5.7 in) in body length and 7.5 cm (3.0 in) in tail length. At birth, they are short-legged, large-headed and have broad chests. Mothers remain with the kits for 2–3 weeks, as they are unable to thermoregulate. During this period, the fathers or barren vixens feed the mothers. Vixens are very protective of their kits, and have been known to even fight off terriers in their defence. If the mother dies before the kits are independent, the father takes over as their provider. The kit's eyes open after 13–15 days, during which time their ear canals open and their upper teeth erupt, with the lower teeth emerging 3–4 days later. Their eyes are initially blue, but change to amber at 4–5 weeks. Coat colour begins to change at 3 weeks of age, when the black eye streak appears. By one month, red and white patches are apparent on their faces. During this time, their ears erect and their muzzles elongate. Kits begin to leave their dens and experiment with solid food brought by their parents at the age of 3–4 weeks. The lactation period lasts 6–7 weeks. Their woolly coats begin to be coated by shiny guard hairs after 8 weeks. By the age of 3–4 months, the kits are long-legged, narrow-chested and sinewy. They reach adult proportions at the age of 6–7 months. Some vixens may reach sexual maturity at the age of 9–10 months, thus bearing their first litters at one year of age. In captivity, their longevity can be as long as 15 years, though in the wild they typically do not survive past 5 years of age.
Outside the breeding season, most red foxes favour living in the open, in densely vegetated areas, though they may enter burrows to escape bad weather. Their burrows are often dug on hill or mountain slopes, ravines, bluffs, steep banks of water bodies, ditches, depressions, gutters, in rock clefts and neglected human environments. Red foxes prefer to dig their burrows on well drained soils. Dens built among tree roots can last for decades, while those dug on the steppes last only several years. They may permanently abandon their dens during mange outbreaks, possibly as a defence mechanism against the spread of disease. In the Eurasian desert regions, foxes may use the burrows of wolves, porcupines and other large mammals, as well as those dug by gerbil colonies. Compared to burrows constructed by Arctic foxes, badgers, marmots and corsac foxes, red fox dens are not overly complex. Red fox burrows are divided into a den and temporary burrows, which consist only of a small passage or cave for concealment. The main entrance of the burrow leads downwards (40–45°) and broadens into a den, from which numerous side tunnels branch. Burrow depth ranges from 0.5–2.5 metres (1 ft 8 in–8 ft 2 in), rarely extending to ground water. The main passage can reach 17 m (56 ft) in length, standing an average of 5–7 m (16–23 ft). In spring, red foxes clear their dens of excess soil through rapid movements, first with the forepaws then with kicking motions with their hind legs, throwing the discarded soil over 2 m (6 ft 7 in) from the burrow. When kits are born, the discarded debris is trampled, thus forming a spot where the kits can play and receive food. They may share their dens with woodchucks or badgers. Unlike badgers, which fastidiously clean their earths and defecate in latrines, red foxes habitually leave pieces of prey around their dens. The average sleep time of a captive red fox is 9.8 hours per day.
Red fox body language consists of movements of the ears, tail and postures, with their body markings emphasising certain gestures. Postures can be divided into aggressive/dominant and fearful/submissive categories. Some postures may blend the two together.
Inquisitive foxes will rotate and flick their ears whilst sniffing. Playful individuals will perk their ears and rise on their hind legs. Male foxes courting females, or after successfully evicting intruders, will turn their ears outwardly, and raise their tails in a horizontal position, with the tips raised upward. When afraid, red foxes grin in submission, arching their backs, curving their bodies, crouching their legs and lashing their tails back and forth with their ears pointing backwards and pressed against their skulls. When merely expressing submission to a dominant animal, the posture is similar, but without arching the back or curving the body. Submissive foxes will approach dominant animals in a low posture, so that their muzzles reach up in greeting. When two evenly matched foxes confront each other over food, they approach each other sideways and push against each other's flanks, betraying a mixture of fear and aggression through lashing tails and arched backs without crouching and pulling their ears back without flattening them against their skulls. When launching an assertive attack, red foxes approach directly rather than sideways, with their tails aloft and their ears rotated sideways. During such fights, red foxes will stand on each other's upper bodies with their forelegs, using open mouthed threats. Such fights typically only occur among juveniles or adults of the same sex.
Red foxes have a wide vocal range, and produce different sounds spanning five octaves, which grade into each other. Recent analyses identify 12 different sounds produced by adults and 8 by kits. The majority of sounds can be divided into "contact" and "interaction" calls. The former vary according to the distance between individuals, while the latter vary according to the level of aggression.
- Contact calls: The most commonly heard contact call is a 3–5 syllable barking "wow wow wow" sound, which is often made by two foxes approaching one another. This call is most frequently heard from December to February (when they can be confused with the territorial calls of tawny owls). The "wow wow wow" call varies according to individual; captive foxes have been recorded to answer pre-recorded calls of their pen-mates, but not those of strangers. Kits begin emitting the "wow wow wow" call at the age of 19 days, when craving attention. When red foxes draw close together, they emit trisyllabic greeting warbles similar to the clucking of chickens. Adults greet their kits with gruff huffing noises.
- Interaction calls: When greeting one another, red foxes emit high pitched whines, particularly submissive animals. A submissive fox approached by a dominant animal will emit a ululating siren-like shriek. During aggressive encounters with conspecifics, they emit a throaty rattling sound, similar to a ratchet, called "gekkering". Gekkering occurs mostly during the courting season from rival males or vixens rejecting advances.
Another call which does not fit into the two categories is a long, drawn out, monosyllabic "waaaaah" sound. As it is commonly heard during the breeding season, it is thought to be emitted by vixens summoning males. When danger is detected, foxes emit a monosyllabic bark. At close quarters, it is a muffled cough, while at long distances it is sharper. Kits make warbling whimpers when nursing, these calls being especially loud when they are dissatisfied.
Diet, hunting and feeding behaviour
Red foxes are omnivores with a highly varied diet. In the former Soviet Union, up to 300 animal and a few dozen plant species are known to be consumed by them. They primarily feed on small, mouse-like rodents like voles, mice, ground squirrels, hamsters, gerbils, woodchucks, pocket gophers and deer mice. Secondary prey species include birds (with passeriformes, galliformes and waterfowl predominating), leporids, porcupines, raccoons, opossums, reptiles, insects, other invertebrates and flotsam (marine mammals, fish and echinoderms). On very rare occasions, they may attack young or small ungulates. They typically target mammals up to about 3.5 kg (7.7 lb) in weight, and require 500 grams (18 oz) of food daily. Red foxes readily eat plant material and in some areas, fruit can amount to 100% of their diet in autumn. Commonly consumed fruits include blueberries, blackberries, raspberries, cherries, persimmons, mulberries, apples, plums, grapes and acorns. Other plant material includes grasses, sedges and tubers.
Red foxes prefer to hunt in the early morning hours before sunrise and late evening. Although they typically forage alone, they may aggregate in resource-rich environments. When hunting mouse-like prey, they first pinpoint their prey's location by sound, then leap, sailing high above their quarry, steering in mid-air with their tails, before landing on target up to 5 metres (16 ft) away. They typically only feed on carrion in the late evening hours and at night. They are extremely possessive of their food, and will defend their catches from even dominant animals. Red foxes may occasionally commit acts of surplus killing; during one breeding season, four foxes were recorded to have killed circa 200 black-headed gulls each, with peaks during dark, windy hours when flying conditions were unfavourable. Losses to poultry and penned game birds can be substantial because of this. Red foxes seem to dislike the taste of moles, but will nonetheless catch them alive and present them to their kits as playthings.
A 2008-2010 study of 84 Red foxes in the Czech Republic and Germany found that successful hunting in long vegetation or under snow appeared to involve an alignment of the fox with the Earth's magnetic field.
Enemies and competitors
Red foxes typically dominate other fox species. Arctic foxes generally escape competition from red foxes by living farther north, where food is too scarce to support the larger-bodied red species. Although the red species' northern limit is linked to the availability of food, the Arctic species' southern range is limited by the presence of the former. Red and Arctic foxes were both introduced to almost every island from the Aleutian Islands to the Alexander Archipelago during the 1830s–1930s by fur companies. The red foxes invariably displaced the Arctic foxes, with one male red fox having been reported to have killed off all resident Arctic foxes on a small island in 1866. Where they are sympatric, Arctic foxes may also escape competition by feeding on lemmings and flotsam, rather than voles, as favoured by red foxes. Both species will kill each other's kits, given the opportunity. Red foxes are serious competitors of corsac foxes, as they hunt the same prey all year. The red species is also stronger, is better adapted to hunting in snow deeper than 10 cm (4 in) and is more effective in hunting and catching medium to large-sized rodents. Corsac foxes seem to only outcompete red foxes in semi-desert and steppe areas. In Israel, Blanford's foxes escape competition with red foxes by restricting themselves to rocky cliffs and actively avoiding the open plains inhabited by red foxes. Red foxes dominate kit and swift foxes. Kit foxes usually avoid competition with their larger cousins by living in more arid environments, though red foxes have been increasing in ranges formerly occupied by kit foxes due to human-induced environmental changes. Red foxes will kill both species, and compete for food and den sites. Grey foxes are exceptional, as they dominate red foxes wherever their ranges meet. Historically, interactions between the two species were rare, as grey foxes favoured heavily wooded or semiarid habitats as opposed to the open and mesic ones preferred by red foxes. However, interactions have become more frequent due to deforestation allowing red foxes to colonise grey fox-inhabited areas.
Wolves may kill and eat red foxes in disputes over carcasses. In areas in North America where red fox and coyote populations are sympatric, fox ranges tend to be located outside coyote territories. The principal cause of this separation is believed to be active avoidance of coyotes by the foxes. Interactions between the two species vary in nature, ranging from active antagonism to indifference. The majority of aggressive encounters are initiated by coyotes, and there are few reports of red foxes acting aggressively toward coyotes except when attacked or when their kits were approached. Foxes and coyotes have sometimes been seen feeding together. In Israel, red foxes share their habitat with golden jackals. Where their ranges meet, the two canids compete due to near identical diets. Foxes ignore jackal scents or tracks in their territories, and avoid close physical proximity with jackals themselves. In areas where jackals become very abundant, the population of foxes decreases significantly, apparently because of competitive exclusion.
Red foxes dominate raccoon dogs, sometimes killing their kits or biting adults to death. Cases are known of foxes killing raccoon dogs entering their dens. Both species compete for mouse-like prey. This competition reaches a peak during early spring, when food is scarce. In Tartaria, red fox predation accounted for 11.1% of deaths among 54 raccoon dogs, and amounted to 14.3% of 186 raccoon dog deaths in north-western Russia.
Red foxes may kill small mustelids like weasels, stone martens, pine martens, stoats, kolonoks, polecats and young sables. Eurasian badgers may live alongside red foxes in isolated sections of large burrows. It is possible that the two species tolerate each other out of commensalism; foxes provide badgers with food scraps, while badgers maintain the shared burrow's cleanliness. However, cases are known of badgers driving vixens from their dens and destroying their litters without eating them. Wolverines may kill red foxes, often while the latter are sleeping or near carrion. Foxes in turn may kill unattended young wolverines.
Red foxes may compete with striped hyenas on large carcasses. Red foxes may give way to hyenas on unopened carcasses, as the latter's stronger jaws can easily tear open flesh that is too tough for foxes. Foxes may harass hyenas, using their smaller size and greater speed to avoid the hyena's attacks. Sometimes, foxes seem to deliberately torment hyenas even when there is no food at stake. Some foxes may mistime their attacks, and are killed. Fox remains are often found in hyena dens, and hyenas may steal foxes from traps.
In Eurasia, red foxes may be preyed upon by leopards, caracals and Eurasian lynxes. The lynxes chase red foxes into deep snow, where their longer legs and larger paws give them an advantage over foxes, especially when the depth of the snow exceeds one metre. In the Velikoluki district in Russia, red foxes are absent or are seen only occasionally where lynxes establish permanent territories. Researchers consider lynxes to represent considerably less danger to red foxes than wolves do. North American felid predators of red foxes include cougars, Canadian lynxes and bobcats. Occasionally, large raptors such as Eurasian eagle owls will prey on young foxes, while golden eagles have been known to kill adults.
Red foxes are wide ranging animals, whose range covers nearly 70 million km2 (27 million mi2). They are distributed across the entire Northern Hemisphere from the Arctic Circle to North Africa, Central America, and Asia. They are absent in Iceland, the Arctic islands, some parts of Siberia, and in extreme deserts.
In Australia, 2012 estimates indicate that there are more than 7.2 million red foxes with a range extending throughout most of the continental mainland. The species became established in Australia through successive introductions by settlers in 1830s in the British colonies of Van Diemen's Land (as early as 1833) and the Port Phillip District of New South Wales (as early as 1845) for the purpose of the traditional English sport of fox hunting. A permanent fox population was not established on the island of Tasmania and it is widely held that they were outcompeted by the Tasmanian Devil. On the mainland, however, the species was successful as an apex predator. It is generally less common in areas where the dingo is more prevalent, however it has, primarily through its burrowing behaviour, achieved niche differentiation with both the feral dog and the feral cat. As such it has become one of the continent's most invasive species. The red fox has been implicated in the extinction and decline of several native Australian species, particularly those of the Potoroidae family including the Desert rat-kangaroo. The spread of red foxes across the southern part of the continent has coincided with the spread of rabbits in Australia and corresponds with declines in the distribution of several medium-sized ground-dwelling mammals, including brush-tailed bettongs, burrowing bettongs, rufous bettongs, bilbys, numbats, bridled nailtail wallabys and quokkas. Most of these species are now limited areas (such as islands) where red foxes are absent or rare. Local eradication programs exist, although eradication has proven difficult due to the denning behaviour and nocturnal hunting, so the focus is on management with the introduction of state bounties. According to the Tasmanian government, red foxes were introduced to the previously fox-free island of Tasmania in 1999 or 2000, posing a significant threat to native wildlife including the Eastern Bettong, and an eradication program conducted by the Tasmanian Department of Primary Industries and Water has been established.
The origin of the Sardinian ichnusae subspecies is uncertain, as it is absent from Pleistocene deposits in their current homeland. It is possible it originated during the Neolithic following its introduction to the island by humans. It is likely then that Sardinian fox populations stem from repeated introductions of animals from different localities in the Mediterranean. This latter theory may explain the subspecies' phenotypic diversity.
Diseases and parasites
Red foxes are the most important rabies vector in Europe. In London, arthritis is not uncommon in foxes, being particularly frequent in the spine. Foxes may be infected with leptospirosis and tularemia, though they are not overly susceptible to the latter. They may also fall ill from listeriosis and spirochetosis, as well as acting as vectors in spreading erysipelas, brucellosis and tick-born encephalitis. A mysterious fatal disease near Lake Sartlan in the Novosibirsk Oblast was noted among local red foxes, but the cause was undetermined. The possibility was considered that it was caused by an acute form of encephalomyelitis, which was first observed in captive bred silver foxes. Individual cases of foxes infected with Yersinia pestis are known.
Red foxes are not readily prone to infestation with fleas. Species like Spilopsyllus cuniculi are probably only caught from the fox's prey species, while others like Archaeopsylla erinacei are caught whilst travelling. Fleas that feed on red foxes include Pulex irritans, Ctenocephalides canis and Paraceras melis. Ticks such as Ixodes ricinus and I. hexagonus are not uncommon in foxes, and are typically found on nursing vixens and kits still in their earths. The louse Trichodectes vulpis specifically targets foxes, but is found infrequently. The mite Sarcoptes scabiei is the most important cause of mange in red foxes. It causes extensive hair loss, starting from the base of the tail and hindfeet, then the rump before moving on to the rest of the body. In the final stages of the condition, foxes can lose most of their fur, 50% of their body weight and may gnaw at infected extremities. In the epizootic phase of the disease, it usually takes foxes four months to die after infection. Other endoparasites include Demodex folliculorum, Notoderes, Otodectes cynotis (which is frequently found in the ear canal), Linguatula serrata (which infects the nasal passages) and ringworms.
Up to 60 helminth species are known to infect foxes in fur farms, while 20 are known in the wild. Several coccidian species of the genera Isospora and Eimeria are also known to infect them. The most common nematode species found in fox guts are Toxocara canis and Uncinaria stenocephala, Capillaria aerophila  and Crenosoma vulpis, the latter two infect their lungs. Capillaria plica infect the fox's bladder. Trichinella spiralis rarely affects them. The most common tapeworm species in foxes are Taenia spiralis and T. pisiformis. Others include Echinococcus granulosus and E. multilocularis. Eleven trematode species infect red foxes.
Relationships with humans
In folklore and mythology
Red foxes feature prominently in the folklore and mythology of human cultures with which they are sympatric. In Greek mythology, the Teumessian fox or Cadmean vixen, was a gigantic fox that was destined never to be caught. The fox was one of the children of Echidna.
In Celtic mythology, the red fox is a symbolic animal. In the Cotswolds, witches were thought to take the shape of foxes in order to steal butter from their neighbours. In later European folklore, the figure of Reynard the Fox symbolises trickery and deceit. He originally appeared (then under the name of "Reinardus") as a secondary character in the 1150 poem Ysengrimus. He reappeared in 1175 in Pierre Saint Cloud's Le Roman de Renart, and made his debut in England in Geoffrey Chaucer's The Nun's Priest's Tale. Many of Reynard's adventures may stem from actual observations on fox behaviour ; he is an enemy of the wolf and has a fondness for blackberries and grapes.
Chinese folk tales tell of fox-spirits called huli jing that may have up to nine tails, orkumiho as they are known in Korea. In Japanese mythology, the kitsune are fox-like spirits possessing magical abilities that increase with their age and wisdom. Foremost among these is the ability to assume human form. While some folktales speak of kitsune employing this ability to trick others, other stories portray them as faithful guardians, friends, lovers, and wives. In Arab folklore, the fox is considered a cowardly, weak, deceitful and cunning animal, said to feign death by filling its abdomen with air in order to appear bloated, then lies on its side, awaiting the approach of unwitting prey. The animal's cunning was noted by the authors of the Bible, and applied the word "fox" to false prophets (Ezekiel 13:4) and the hypocrisy of Herod Antipas (Luke 13:32).
The cunning Fox is commonly found in Native American mythology, where it is portrayed as an almost constant companion to coyote. Fox, however, is a deceitful companion who often steals Coyote's food. In the Achomawi creation myth, Fox and Coyote are the co-creators of the world, who leave just before the arrival of humans. The Yurok tribe believed that Fox, in anger, captured the sun, and tied him to a hill, causing him to burn a great hole in the ground. An Inuit story tells of how Fox, portrayed as a beautiful woman, tricks a hunter into marrying her, only to resume her true form and leave after he offends her. A Menominee story tells of how Fox is an untrustworthy friend to the Wolf.
The earliest historical records of fox hunting come from the 4th century BC; Alexander the Great is known to have hunted foxes and a seal dated from 350 BC depicts a Persian horseman in the process of spearing a fox. Xenophon, who viewed hunting as part of a cultured man's education, advocated the killing of foxes as pests, as they distracted hounds from hares. The Romans were hunting foxes by 80 AD. During the Dark Ages in Europe, foxes were considered secondary quarries, but gradually grew in importance. Cnut the Great reclassed foxes as Beasts of the Chase, a lower category of quarry than Beasts of Venery. Foxes were gradually hunted less as vermin and more as Beasts of the Chase, to the point that by the late 13th century, Edward I had a royal pack of foxhounds and a specialised fox huntsman. In this period, foxes were increasingly hunted above ground with hounds, rather than underground with terriers. Edward, Second Duke of York assisted the climb of foxes as more prestigious quarries in his The Master of Game. By the Renaissance, fox hunting became a traditional sport of the nobility. After the English Civil War saw a drop in deer populations, fox hunting grew in popularity. By the mid-17th century, Britain was divided into fox hunting territories, with the first fox hunting clubs being formed (the first was the Charlton Hunt Club in 1737). The popularity of fox hunting in Britain reached a peak during the 18th century. Although already native to North America, red foxes from England were imported for sporting purposes to Virginia and Maryland in 1730 by prosperous tobacco planters. These American fox hunters considered the red species more sporting than grey species.
The grays furnished more fun, the reds more excitement. The grays did not run so far, but usually kept near home, going in a circuit of six or eight miles. 'An old red,' generally so called irrespective of age, as a tribute to his prowess, might lead the dogs all day, and end by losing them as evening fell, after taking them a dead stretch for thirty miles. The capture of a gray was what men boasted of ; a chase after 'an old red' was what they 'yarned' about.
Red foxes are still widely persecuted as pests, with human-caused deaths among the highest causes of mortality in the species. Annual fox kills are: UK 21,500–25,000 (2000); Germany 600,000 (2000–2001); Austria 58,000 (2000–2001); Sweden 58,000 (1999–2000); Finland 56,000 (2000–2001); Denmark 50,000 (1976–1977); Switzerland 34,832 (2001); Norway 17,000 (2000–2001); Saskatchewan (Canada) 2,000 (2000–2001); Nova Scotia (Canada) 491 (2000–2001); New Mexico (USA) 69 (1999–2000).
Red foxes are among the most important furbearing animals harvested by the fur trade. Their pelts are used for trimmings, scarfs, muffs, jackets and coats. They are principally used as trimming for both cloth coats and fur garments, including evening wraps. The pelts of silver-morph foxes are popular as capes, while cross foxes are mostly used for scarfs and rarely for trimming. The number of sold fox scarfs exceeds the total number of scarfs made from other furbearers. However, this amount is overshadowed by the total number of fox pelts used for trimming purposes. The silver morphs are the most valued by furriers, followed by the cross and red morphs respectively. In the early 20th century, over 1,000 American fox skins were imported to Britain annually, while 500,000 were exported annually from Germany and Russia. The total worldwide trade of wild red foxes in 1985–86 was 1,543,995 pelts. Foxes amounted to 45% of US wild-caught pelts worth $50 million. Pelt prices are increasing, with 2012 North American wholesale auction prices averaging $39, and 2013 prices averaging $65.78.
North American red foxes, particularly those of northern Alaska, are the most valued for their fur, as they have guard hairs of a silky texture which, after dressing, allow the wearer unrestricted mobility. Red foxes living in southern Alaska's coastal areas and the Aleutian Islands are an exception, as they have extremely coarse pelts that rarely exceed one-third of the price of their northern Alaskan cousins. Most European peltries have coarse-textured fur compared to North American varieties. The only exceptions are the Nordic and Far Eastern Russian peltries, but they are still inferior to North American peltries in terms of silkiness.
Livestock, game and pet predation
Red foxes are implicated in the destruction of game and song birds, hares, rabbits, muskrats and young ungulates, particularly in preserves, reserves, and hunting farms where ground nesting birds are protected and raised, as well as in poultry farms. Foxes may on occasions prey on lambs. Usually, lambs targeted by foxes tend to be physically weakened specimens, but not invariably. Lambs belonging to small breeds, such as blackface, are more vulnerable than larger breeds such as merino. Twins may be more vulnerable to foxes than singlets, as ewes cannot effectively defend both simultaneously. Crossbreeding small, upland ewes with larger, lowland rams can cause difficult and prolonged labour for ewes due to the heaviness of the resulting offspring, thus making the lambs more at risk to fox predation. Lambs born from gimmers (ewes breeding for the first time) are more often killed by foxes than those of experienced mothers, who stick closer to their young. It is often the case that the extent of game and livestock predation by red foxes is exaggerated, since the degree of fox damage is usually determined by the remains of food found at their burrows.
Red foxes may prey on domestic rabbits and guinea pigs if they are kept in open runs or are allowed to range freely in gardens. This problem is usually averted by housing them in robust hutches and runs. Urban foxes frequently encounter cats and may feed alongside them. In physical confrontations, the cats usually have the upper hand. Authenticated cases of foxes killing cats usually involve kittens. Although most foxes do not prey on cats, some may do so, and may treat them more as competitors rather than food.
Taming and domestication
In their unmodified wild state, red foxes are generally unsuitable as pets. Many supposedly abandoned kits are adopted by well-meaning people during the spring period, though it is unlikely that vixens would abandon their young. Actual orphans are rare, and the ones that are adopted are likely kits that simply strayed from their den site. Kits require almost constant supervision; when still suckling, they require milk at four-hour intervals day and night. Once weaned, they may become destructive to leather objects, furniture and electric cables. Though generally friendly toward people when young, captive red foxes become fearful of humans, save for their handlers, once they reach 10 weeks of age. They maintain their wild counterpart's strong instinct of concealment, and may pose a threat to domestic birds, even when well fed. Although suspicious of strangers, they can form bonds with cats and dogs, even ones bred for fox hunting. Practical uses for tame foxes are few, though they can be encouraged to kill rats and mice in granaries. Tame foxes were once used to draw ducks close to hunting blinds.
A strain of truly domesticated red foxes was introduced by Russian geneticist Dmitry Konstantinovich Belyaev who, over a 40-year period, bred several generations of silver morph foxes on fur farms, selecting only those individuals that showed the least fear of humans. Eventually, Belyaev's team selected only those that showed the most positive response to humans, thus resulting in a population of foxes whose behaviour and appearance was significantly changed. After about ten generations of controlled breeding, these foxes no longer showed any fear of humans, and often wagged their tails and licked their human caretakers to show affection. These behavioural changes were accompanied by physical alterations, which included piebald coats, floppy ears in pups, and curled tails, similar to traits that distinguish domestic dogs from wolves.
Red foxes thrive particularly well in urban environments. Throughout the twentieth century, they established themselves in many Australian, European, Japanese, and North American cities. The species first colonised British cities during the 1930s, entering Bristol and London during the 1940s, and later established themselves in Cambridge and Norwich. In Australia, red foxes were recorded in Melbourne as early as the 1930s, while in Zurich, Switzerland, they only starting appearing in the 1980s. Urban red foxes are most common in residential suburbs consisting of privately owned, low-density housing, but are rare in areas where industry, commerce or council-rented houses predominate.
In 2006 it was estimated that there were 10,000 foxes in London. City-dwelling foxes may have the potential to consistently grow larger than their rural counterparts, as a result of abundant scraps and a relative dearth of predators. While foxes will scavenge successfully in the city (and the foxes tend to eat anything that the humans eat) some urban residents will deliberately leave food out for the animals, finding them endearing.
The urban fox has become quite a problem for some people. Disrupting rubbish bins, stealing chickens and wrecking gardens, the urban fox causes a nuisance. In the UK, hunting foxes in urban areas is banned, and shooting them in an urban environment is not suitable. One alternative to hunting urban foxes has been to trap them, which appears to be an effective method.
Relationship between urban and rural foxes
In January 2014 it was reported that "Fleet", a relatively tame urban fox tracked as part of a wider study by the University of Brighton in partnership with the BBC's Winterwatch, had unexpectedly travelled 195 miles in 21 days from his neighbourhood in Hove, West Sussex, across rural countryside as far as Rye, East Sussex. He was still continuing his journey when the GPS collar stopped transmitting, due to suspected water damage. Along with setting a record for the longest journey undertaken by a tracked fox in the country, his travels have highlighted the fluidity of movement between rural and urban fox populations.
- Macdonald, D.W.; Reynolds, J.C. (2008). 'Vulpes vulpes'. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 20 September 2013. Database entry includes justification for why this species is of least concern
- Linnæus, Carl (1758). Systema naturæ per regna tria naturæ, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I (in Latin) (10 ed.). Holmiæ (Stockholm): Laurentius Salvius. p. 40.
- "100 of the World's Worst Invasive Alien Species". Invasive Species Specialist Group.
- Kurtén 1968, pp. 115–116
- Kurtén 1980, pp. 96, 174
- Heptner & Naumov 1998, p. 480
- Heptner & Naumov 1998, pp. 475–477
- Wozencraft, W. C. (2005). "Order Carnivora". In Wilson, D. E.; Reeder, D. M. Mammal Species of the World (3rd ed.). Johns Hopkins University Press. ISBN 978-0-8018-8221-0. OCLC 62265494.
- Heptner & Naumov 1998, p. 473
- Harris & Yalden 2008, p. 413
- Heptner & Naumov 1998, pp. 513–24
- Heptner, V. G. (Vladimir Georgievich); Nasimovich, A. A; Bannikov, Andrei Grigorevich; Hoffmann, Robert S, Mammals of the Soviet Union, v. 1 (1988), Washington, D.C. : Smithsonian Institution Libraries and National Science Foundation
- Feldhamer, Thompson & Chapman 2003, p. 529
- Fedriani, J.M.; Palomares, F.; Delibes, M. (1999). "Niche relations among three sympatric Mediterranean carnivores". Oecologia 121: 138–148. doi:10.1007/s004420050915. JSTOR 4222449.
- Bachrach 1953, pp. 229–230
- Heptner & Naumov 1998, p. 482
- Lindblad-Toh, K.; Wade, C.M.; Mikkelsen, T.S.; et al. (2005). "Genome sequence, comparative analysis and haplotype structure of the domestic dog". Nature 438 (7069): 803–819. doi:10.1038/nature04338. PMID 16341006.
- PaleoDatabase collection No. 35369, authorized by Alan Turner, Liverpool John Moores University. Entry by H. O'Regan, 8 December 2003
- Spagnesi & De Marina Marinis 2002, p. 222
- Aubry, Keith B.; Statham, Mark J.; Sacks, Benjamin N.; Perrines, John D.; Wisely, Samantha M. (2009). "Phylogeography of the North American red fox: Vicariance in Pleistocene forest refugia". Molecular Ecology 18 (12): 2668–2686. doi:10.1111/j.1365-294X.2009.04222.x. PMID 19457180.
- Sacks, Benjamin N.; Statham, Mark J.; Perrine, John D.; Wisely, Samantha M.; Aubry, Keith B. (2010). "North American montane red foxes: Expansion, fragmentation, and the origin of the Sacramento Valley red fox". Conservation Genetics 11 (4): 1523–1539. doi:10.1007/s10592-010-0053-4.
- Dale 1906, p. 140
- Feldhamer, Thompson & Chapman 2003, p. 511
- Feldhamer, Thompson & Chapman 2003, p. 514
- Heptner & Naumov 1998, pp. 490–492
- Heptner & Naumov 1998, p. 479
- Heptner & Naumov 1998, p. 496
- Merriam 1900, p. 669
- Merriam 1900, p. 668
- Heptner & Naumov 1998, p. 499
- Merriam 1900, p. 667
- Heptner & Naumov 1998, pp. 499–500
- Merriam 1900, p. 665
- Heptner & Naumov 1998, pp. 497–498
- Spagnesi & De Marina Marinis 2002, p. 221
- Harris & Yalden 2008, p. 411
- Heptner & Naumov 1998, pp. 501–502
- Merriam 1900, p. 663
- Pocock 1941, p. 121
- Merriam 1900, pp. 670–671
- Allen 1938
- Dale 1906, p. 6
- Heptner & Naumov 1998, p. 501
- Merriam 1900, p. 664
- Pocock 1941, p. 111
- Hoath, Richard (2009). A Field Guide to the Mammals of Egypt. American Univ in Cairo Press,. ISBN 977-416-254-4.
- Osborn & Helmy 1980, p. 376
- Pocock 1941, pp. 123–124
- Pocock 1941, p. 129
- Merriam 1900, p. 672
- Merriam 1900, p. 666
- Miller, Gerrit Smith (1912) Catalogue of the mammals of Western Europe (Europe exclusive of Russia) in the collection of the British museum, British Museum (Natural History). Department of Zoology.
- Allen 1938, p. 353
- Heptner & Naumov 1998, p. 472
- Larivière & Pasitschniak-Arts 1996
- Harris & Yalden 2008, p. 409
- Sillero-Zubiri, Hoffman & MacDonald 2004, pp. 132–133
- Heptner & Naumov 1998, p. 341
- Heptner & Naumov 1998, p. 478
- Harris & Yalden 2008, p. 408
- Sillero-Zubiri, Hoffman & MacDonald 2004, p. 129
- Macdonald 1987, pp. 122–123
- Burnie D and Wilson DE (eds.), Animal: The Definitive Visual Guide to the World's Wildlife. DK Adult (2005), ISBN 0789477645
- Macdonald 1987, p. 36
- Sillero-Zubiri, Hoffman & MacDonald 2004, p. 130
- Wilkes, David (5 March 2012). "'Largest fox killed in UK' shot on Aberdeenshire farm". BBC News Online.
- Bachrach 1953, pp. 231–232
- Bachrach 1953, p. 235
- Sillero-Zubiri, Hoffman & MacDonald 2004, p. 131
- Heptner & Naumov 1998, p. 477
- Feldhamer, Thompson & Chapman 2003, p. 516
- Heptner & Naumov 1998, p. 476
- Bachrach 1953, p. 251
- Bachrach 1953, p. 230
- Heptner & Naumov 1998, p. 561
- In a freshly killed animal, this gland, especially in freezing weather, gives off the odor of violet. This odor is not strong and rapidly disappears especially in a dead animal taken into a warm location. This explains why the presence of the "violet" odor is sometimes negated. Heptner & Naumov 1998, p. 474
- Macdonald 1987, p. 117
- Fawcett, John K.; Fawcett, Jeanne M.; Soulsbury, Carl D. (2012). "Seasonal and sex differences in urine marking rates of wild red foxes Vulpes vulpes". Journal of Ethology 31 (1): 41–47. doi:10.1007/s10164-012-0348-7.
- Walters, Martin; Bang, Preben; Dahlstrøm, Preben (2001). Animal tracks and signs. Oxford: Oxford University Press. pp. 202–203. ISBN 0-19-850796-8.
- Macdonald 1987, p. 125
- Henry, J. David (1977). "The use of urine marking in the scavenging behavior of the red fox (Vulpes vulpes)". Behaviour 61 (1/2): 82–106. doi:10.1163/156853977X00496. JSTOR 4533812.
- Andersen, K. F.; Vulpius, T. (1999). "Urinary volatile constituents of the lion, Panthera leo". Chemical Senses 24 (2): 179–189. doi:10.1093/chemse/24.2.179. PMID 10321819.
- Elbroch, Lawrence Mark; Kresky, Michael Raymond; Evans, Jonah Wy (2012). Field Guide to Animal Tracks and Scat of California. University of California Press. p. 189. ISBN 978-0-520-25378-0.
- Macdonald 1987, pp. 140–141
- Heptner & Naumov 1998, p. 537
- Harris & Yalden 2008, p. 417
- Feldhamer, George A.; Thompson, Bruce C.; Chapman, Joseph A. (2003). Wild Mammals of North America: Biology, Management, and Conservation. JHU Press. ISBN 978-0-8018-7416-1.
- Heptner & Naumov 1998, p. 538
- Harris & Yalden 2008, pp. 418–419
- Macdonald 1987, p. 93
- Heptner & Naumov 1998, pp. 542–544
- Dale 1906, pp. 21–22
- Dale 1906, p. 13
- Hunter, L. (2011). Carnivores of the World. Princeton University Press. p. 106. ISBN 978-0-691-15227-1.
- Heptner & Naumov 1998, p. 526
- Feldhamer, Thompson & Chapman 2003, pp. 528–530
- Heptner, V. G. (Vladimir Georgievich), 1901–1975; Nasimovich, A. A; Bannikov, Andrei Grigorevich; Hoffmann, Robert S Mammals of the Soviet Union Volume: v. 2, pt. 1b (2001) Washington, D.C. : Smithsonian Institution Libraries and National Science Foundation
- Dale 1906, pp. 15–17
- Holland, Jennifer S. (July 2011). "40 winks?". National Geographic 220 (1).
- Harris & Yalden 2008, p. 414
- Macdonald 1987, p. 28
- Heptner & Naumov 1998, p. 530
- Heptner & Naumov 1998, p. 531
- Macdonald 1987, p. 58
- Macdonald 1987, p. 164
- Macdonald 1987, p. 41
- Jaroslav Červený, Sabine Begall, Petr Koubek, Petra Nováková and Hynek Burda. (2011) Directional preference may enhance hunting accuracy in foraging foxes. 12 January 2011 doi: 10.1098/rsbl.2010.1145; Biol. Lett. 23 June 2011 vol. 7 no. 3 355-357. http://rsbl.royalsocietypublishing.org/content/7/3/355.full
- Macdonald 1987, pp. 84–85
- Heptner & Naumov 1998, pp. 364–365
- Heptner & Naumov 1998, pp. 453–454
- Feldhamer, Thompson & Chapman 2003, p. 527
- Heptner & Naumov 1998, pp. 357, 455 & 545
- Mech, L. David; Boitani, Luigi (2003). Wolves: Behaviour, Ecology and Conservation. University of Chicago Press. p. 269. ISBN 0-226-51696-2.
- Sargeant, Alan B; Allen, Stephen H. (1989). "Observed interactions between coyotes and red foxes". Journal of Mammology 70 (3): 631–633. doi:10.2307/1381437. JSTOR 1381437.
- Scheinin, Shani; Yom-Tov, Yoram; Motro, Uzi; Geffen, Eli (2006). "Behavioural responses of red foxes to an increase in the presence of golden jackals: A field experiment" (PDF). Animal Behaviours 71 (3): 577–558. doi:10.1016/j.anbehav.2005.05.022.
- Heptner & Naumov 1998, p. 115
- Sillero-Zubiri, Hoffman & MacDonald 2004, p. 134
- Macdonald 1987, pp. 77–79
- Heptner, V. G. and Sludskii, A. A. 1992. Mammals of the Soviet Union. Vol. II, part 2, Carnivores(Feloidea), Leiden, E. J. Brill. ISBN 90-04-08876-8
- Heptner, V. G. and Sludskii, A. A. 1992. Mammals of the Soviet Union. Vol. II, part 2, Carnivores(Feloidea), Leiden, E. J. Brill. ISBN 90-04-08876-8, pp. 627–628
- Heptner & Naumov 1998, pp. 545
- Eurasian Eagle Owl – Bubo bubo. owlpages.com
- Watson, Jeff (2010). The Golden Eagle (2nd ed.). A&C Black. p. 92. ISBN 978-1-4081-1420-9.
- "Hazardous Substances and New Organisms Act 2003 – Schedule 2 Prohibited new organisms". New Zealand Government. Retrieved 26 January 2012.
- "Impacts of Feral Animals". Game Council of New South Wales. Retrieved 29 May 2012.
- Macdonald 1987, p. 14
- Bostanci, A. (2005). "WILDLIFE BIOLOGY: A Devil of a Disease". Science 307 (5712): 1035–1020. doi:10.1126/science.307.5712.1035. PMID 15718445.
- Short, J. (1998). "The extinction of rat-kangaroos (Marsupialia:Potoroidae) in New South Wales, Australia". Biological Conservation 86 (3): 365–201. doi:10.1016/S0006-3207(98)00026-3.
- (PDF) Threat Abatement Plan for Predation by the Red Fox (Vulpes vulpes) (Report). NSW National Parks and Wildlife Service. 2001. ISBN 0731364244. http://www.environment.nsw.gov.au/resources/pestsweeds/RedfoxApproved.pdf.
- Millen, Tracey (Oct–Nov 2006). "Call for more dingoes to restore native species" (PDF). ECOS 133. (Refers to the book Australia's Mammal Extinctions: a 50,000 year history. Christopher N. Johnson. ISBN 978-0-521-68660-0.)
- "Latest Physical Evidence of Foxes in Tasmania". Department of Primary Industries and Water, Tasmania website. July 18, 2013. Retrieved 20 September 2013.
- Harris & Yalden 2008, pp. 421–422
- Heptner & Naumov 1998, p. 547
- Lalošević, V.; Lalošević, D.; Čapo, I.; Simin, V.; Galfi, A.; Traversa, D. (2013). "High infection rate of zoonotic Eucoleus aerophilus infection in foxes from Serbia". Parasite 20 (3). doi:10.1051/parasite/2012003. PMC 3718516. PMID 23340229.
- Ancient Greek: Τευμησ(σ)ία ἀλώπηξ (Teumēs(s)íā alôpēx),gen.: Τευμησίας ἀλώπεκος, also known as ἀλώπηξ τῆς Τευμησσοῦ "fox of Teumessos"; Teumessos was an ancient city in Boeotia.
- Wallen, Martin (2006). Fox. Reaktion Books. p. 40. ISBN 978-1-86189-297-3.
- Monaghan, Patricia (2004). The Encyclopedia of Celtic Mythology and Folklore. Infobase Publishing. pp. 199–200. ISBN 0-8160-4524-0.
- Macdonald 1987, pp. 32–33
- Goff, Janet (1997). "Foxes in Japanese culture: Beautiful or beastly?" (PDF). Japan Quarterly 44 (2).
- Smyers, Karen Ann (1999). The Fox and the Jewel: Shared and Private Meanings in Contemporary Japanese Inari Worship. University of Hawaii Press. ISBN 0-8248-2102-5.
- Osborn & Helmy 1980, p. 379
- Bright, Michael (2006). Beasts of the Field: The Revealing Natural History of Animals in the Bible. London: Robson Books. pp. 120–127. ISBN 1-86105-831-4.
- Bastian, Dawn Elaine; Mitchell, Judy K. (2004). Handbook of Native American Mythology. ABC-CLIO. pp. 99–100. ISBN 1-85109-533-0.
- Macdonald 1987, p. 21
- Potts 1912, p. 7
- Potts 1912, p. 38
- Bachrach 1953, p. 246
- Bachrach 1953, p. 252
- Dale 1906, p. 207
- Dale 1906, p. 204
- "NAFA February 2013 Fur Auction Results". trappingtoday.com. 22 February 2013. Retrieved 9 July 2013.
- Heptner & Naumov 1998, p. 562
- Macdonald 1987, pp. 166–167
- Macdonald 1987, pp. 180–181
- Macdonald 1987, p. 56
- Macdonald 1987, p. 61
- Dale 1906, p. 122
- Dale 1906, pp. 132–133
- Trut, Lyudmila N. (1999). "Early canid domestication: The farm-fox experiment" (PDF). American Scientist 87: 160–169. doi:10.1511/1999.20.813.
- "Urban foxes: Overview". The fox website. Retrieved 20 September 2013.
- "10,000 Foxes Roam London". News.nationalgeographic.com. 28 October 2010. Retrieved 20 September 2013.
- Lindsay-Smith, Bruce (20 September 2013). "Yes, urban foxes are getting bigger... and more deadly. As a 4ft fox is shot in Kent, a marksman who culls them for a living issues a chilling warning". Daily Mail (London).
- "Fieldsports Britain : How to call in great big bucks". Fieldsportschannel.tv. 24 October 2012.
- "Winterwatch, Urban Fox Diary: Part 2".
- "Fleet the Sussex fox breaks British walking record (BBC News article)".
- Bachrach, Max (1953). Fur: a practical treatise. New York : Prentice-Hall, 3rd edition.
- Dale, Thomas Francis (1906). The fox. Longmans, Green, and Co.
- Feldhamer, George A.; Thompson, Bruce Carlyle; Chapman, Joseph A. (2003). Wild mammals of North America: biology, management, and conservation. JHU Press. ISBN 0-8018-7416-5.
- Harris, Stephen; Yalden, Derek (2008). Mammals of the British Isles. Mammal Society; 4th Revised edition edition. ISBN 0-906282-65-9.
- Heptner, V. G.; Naumov, N. P. (1998). Mammals of the Soviet Union Vol.II Part 1a, SIRENIA AND CARNIVORA (Sea cows; Wolves and Bears). Science Publishers, Inc. USA. ISBN 1-886106-81-9.
- Kurtén, Björn (1968). Pleistocene mammals of Europe. Weidenfeld and Nicolson.
- Kurtén, Björn (1980). Pleistocene mammals of North America. Columbia University Press. ISBN 0-231-03733-3.
- Larivière, Serge; Pasitschniak-Arts, Maria (1996). "Vulpes vulpes". Mammalian Species 537 (537): 1–11. doi:10.2307/3504236.
- Macdonald, David (1987). Running with the Fox. Guild Publishing, London. ISBN 0-8160-1886-3.
- Merriam, Clinton Hart (1900). Preliminary revision of the North American red foxes. Washington Academy of Sciences.
- Osborn, Dale. J.; Helmy, Ibrahim (1980). The contemporary land mammals of Egypt (including Sinai). Field Museum of Natural History.
- Pocock, R. I. (1941). Fauna of British India: Mammals Volume 2. Taylor and Francis.
- Potts, Allen (1912). Fox hunting in America. Washington : The Carnahan Press.
- Sillero-Zubiri, Claudio; Hoffman, Michael; MacDonald, David W. (2004). Canids: Foxes, Wolves, Jackals and Dogs – 2004 Status Survey and Conservation Action Plan. IUCN/SSC Canid Specialist Group. ISBN 2-8317-0786-2.
- Spagnesi, Mario; De Marina Marinis, Maria (2002). Mammiferi d'Italia. Quaderni di Conservazione della Natura. ISSN 1592-2901.
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