dcsimg

Lifespan, longevity, and ageing

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Maximum longevity: 23.2 years (captivity) Observations: In zoos, these animals can live up to 23.2 years (Richard Weigl 2005).
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Associations

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Muntiacus reevesi is predated upon by a number of larger mammals and reptiles in southeast China. These natural enemies include leopards, tigers, dholes, jackals, crocodiles and pythons. In the introduced populations in England, the only potential predator is the fox. Behavioral differences may be noted between the English populations and those of China as the lack of predators leads M. reevesi to be much less vigilent in England and is therefore considered to be comfortable with the presence of man and human-altered surroundings.

When alarmed, Chinese muntjacs will bark for up to one hour. This distress call, however, does not appear to be meant to warn others but may simply be a vocalized expression of internal anxiety. This is mainly evidenced by the fact that muntjac barks tend to be emitted within a frequency range that would not carry through the dense vegetation that they inhabit.

Known Predators:

  • leopards (Panthera pardus)
  • tigers (Panthera tigris)
  • jackals (Canis)
  • foxes (Canidae)
  • dholes (Cuon alpinus)
  • crocodiles (Crocodylus)
  • pythons (Boidae)
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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Morphology

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Muntiacus reevesi has a chestnut-colored coat with a 4-inch tail that is black above and white below. It has been reported that the females tend to be slightly lighter in color than males, but these observations were mainly made on captive and feral M. reevesi in England and have not been corroborated with observations of M. reevesi in its native China. Chinese muntjacs stand 43 to 45 cm in height at the shoulder.

Sexual dimorphism in M. reevesi leads to larger, heavier males that have short antlers (125 to 150 mm) that grow from their pedicles and that have long, tusk-like canines (1 to 2 inches long). The canines are not entirely fixed to the premaxilla so they are less likely to be broken off during a fight. Both the male and female Chinese muntjacs have bony ridges on their faces that are lined with black hair along the inside. These ridges extend into hair-covered pedicles from which antlers (male) or black tufts of hair (females) project. Both the male and female Chinese muntjacs also have preorbital glands that produce a creamy liquid used for chemical communication.

As with all Muntiacus species, M. reevesi has only the upper parts of the 2nd and 5th digit metacarpals present, a physiology known as plesiometacarpalia. However, unlike other deer species that have 2 hooves of the same size and shape, M. reevesi has one hoof that is smaller than the other and that is lined with hairs that are visible in its footprints.

Range mass: 11 to 28 kg.

Average mass: 18 kg.

Range length: 700 to 1130 mm.

Average length: 800 mm.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: male larger; sexes colored or patterned differently; ornamentation

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Life Expectancy

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Little is known about the lifespan of M. reevesi in the wild. Anecdotal evidence would indicate that Chinese muntjacs, which are described as a duiker-like (for example, Cepalophus niger) organism due to its rapid development and its generalist tendencies, would probably have a similar life expectancy: 10 to 12 years. In England, with a lack of predators and abundant food sources, it may be expected that Chinese muntjacs may live even longer.

Range lifespan
Status: wild:
unknown (low) hours.

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

Average lifespan
Status: wild:
10-12 years.

Average lifespan
Status: captivity:
23.2 years.

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Habitat

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Muntiacus reevesi is a forest creature in its native country of China. It creates paths through the subtropical rainforests at moderate elevations, which is why it has been termed by some as a bush hugger. It was observed that muntjacs in general tend to prefer habitats near streams, but evidence of this preference is not strongly demonstrated in the literature for this particular species of muntjac. Chinese muntjacs will fight to defend a fairly specific territory, but males have been shown to tolerate the presence of a subordinate male in their territory so long as that male is not in rut.

In England, M. reevesi exhibits slightly different preferences for habitat. It appears that the feral muntjacs of Britain are equally happy in habitats with and without cover; that is, muntjacs have been found in deciduous and coniferous forests as well as agricultural land, and even suburban and urban areas. In some respects, it is difficult to consider habitat preferences when a number of the metapopulations within the British population were specifically released into certain environments, so their presence in some habitats may not actually be an indication of a preference.

Reliable information on elevation preferences could not be found for the British population of M. reevesi, but in its native environment, it appears that M. reevesi prefers moderate elevations (moderate was not defined).

Habitat Regions: temperate ; tropical

Terrestrial Biomes: forest ; rainforest ; scrub forest

Other Habitat Features: urban ; suburban ; agricultural

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Distribution

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Muntiacus reevesi has a native range that extends throughout the subtropical forests of southeastern China and Taiwan. It has also become established in England after being introduced at Woburn, England (located in the middle of Bedfordshire county) around 1900. Feral populations may also exist in France, where introduced individuals escaped gardens and zoos.

Biogeographic Regions: palearctic (Introduced ); oriental (Native )

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Untitled

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Muntiacus reevesi and other members of the Cervinae subfamily are interesting to geneticists due to their strange genetic history. It appears that while M. reevesi is 2n=46, M. feae is 2n=14 F/13 M, M. crinifrons and M. gongshanenis are 2n=8 F/9 M, and M. muntjak is 2n=6 F/7 M, the smallest known chromosome number for any mammal. It is also noted that evolution from the more primitive to more derived Muntiacus species was rapid, with the fastest evolution occurring in M. feae, where two different karyotypes emerged in only 0.5 Myr. Taxonomists recently added a potential new genus Megamuntjacus to the subfamily Cervinae, although it is still being disputed whether or not this new species should be its own genus or should fall under the genus Muntiacus.

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Behavior

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Muntiacus reevesi, as a member of the Muntiacus genus, is often known as a barking deer, yet the function of barking may be overestimated by casual observers. While it was originally thought that muntjacs used their barks to communicate with other muntjacs to communicate danger or location information, it appears that the barks of muntjacs have a more limited function than expected. Barks are primarily used in two circumstances; when predators are suspected in the environment and during social encounters when subordinate and dominant animals come into contact. The hypothesis that barks are used as a part of reproductive processes has not been substantiated. Likewise, expectations that barks were used to communicate danger to other muntjacs could not be corroborated in studies. The frequency of the barks of muntjacs prevents them from traveling any substantial distance, particularly in dense vegetation, so it is unlikely that barks evolved as a warning response. It has been hypothesized that the barking of muntjacs is actually a vocalization of inner anxiety that accompanies being hunted by predators or challenged by a dominant individual and that it has little to do with mating, defending territory, food procurement or identification of individuals. Evidence supporting this hypothesis is found in the observations of increased barking by the muntjac at dawn and dusk and in environments that have decreased visibility, such as very dense grassland environments.

Chinese muntjacs send signals to others about their identity, their territory and their sexual state using a combination of non-bark vocalizations and chemicals. The non-bark vocalizations that may be emitted by Muntiacus reevesi are used in reproductive situations where the male makes a buzzing sound and a female that is willing will make a cat-like whine. A main form of communication in M. reevesi comes through chemicals emitted by the preorbital gland. These chemicals are used as scent markers to define territories and to advertise presence of an individual. Studies have shown that the chemical composition of these secretions would permit muntjacs to identify an individual’s age, sex and population of origin, but the mere presence of these capabilities within the chemical does not mean that the muntjac are using chemical communication in that way.

Communication Channels: acoustic ; chemical

Other Communication Modes: pheromones ; scent marks

Perception Channels: tactile ; acoustic ; chemical

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Conservation Status

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Muntiacus reevesi is common in southeast China, therefore it is not listed as a threatened or endangered species. It appears not to have been studied by many conservation organizations, which most likely indicates that it is not a species of concern for those involved in protecting biodiversity.

US Federal List: no special status

CITES: no special status

IUCN Red List of Threatened Species: least concern

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Benefits

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Muntiacus reevesi does not have any reported negative impacts in its native habitat because its populations are controlled by predator species and because it tends to live in forest environments. In England, however, M. reevesi, unchecked by predators, has become the most widely distributed deer and has been found to inhabit urban and suburban areas, as well as forests. They may be a nuisance to farmers and foresters due to their browsing on vegetation, particularly coppice.

Negative Impacts: crop pest

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Benefits

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Muntiacus reevesi has positive impacts for humans in both China and western European feral populations. In both environments, M. reevesi is hunted for meat (and in Britain, for sport). They have also been appreciated in their native environments for warning humans in the woods of the presence of a predator animal, such as a tiger or leopard, with their barks.

Positive Impacts: food

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Associations

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The alarm barks of Chinese muntjacs are excellent warnings for other small mammals that a predator, such as a tiger or leopard, is in the area. In China, the behavior and distribution of M. reevesi is interdependent with the behavior and distribution of other Cervinae species, especially M. crinifrons, M. muntjak and Elaphodus cephalophus. As the most generalized in its food habits of the muntjacs, M. reevesi has the widest range, preferring subtropical forest areas and tending to occur near water. The other Cervinae species have become distributed in either higher elevations, drier, open environments, or wetter, denser environments. These habitat types have led the other Cervinae to become more specialized in their diet and behavior than M. reevesi.

The impacts of muntjacs and other deer on plant diversity and woodland invertebrates in England have been studied and it appears that with natural deer populations, vegetation browsing may create more habitats for invertebrates and the presence of dung may allow for an increased diversity of invertebrates. This is contrasted with high-density deer populations, where deer will overbrowse an area and leave minimal plant diversity and reduce remaining plant quality for invertebrates. Similar impacts have been observed on small mammal populations, where muntjacs may act as direct competitors for resources or act as habitat modifiers. Just as with the invertebrate study, observations made about Chinese muntjacs’ impact on small mammals are density-dependent. Essentially, at high densities, the competition for resources and habitat modification through loss of cover will cause a decline in the populations of small mammals (such as Apodemus sylvaticus, Micromys minutus, Sorex anareus, Sorex minutus, Myodes glareolus, Apodemus flavicollis, Muscardinus avellanarius) that ripples through the food chain, especially affecting the predators of small mammals: Mustela nivalis, Mustela erminea and Vulpes vulpes.

Ecosystem Impact: creates habitat; keystone species

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Trophic Strategy

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Muntiacus reevesi is surprisingly omnivorous. It eats bamboo, seeds, bark, fruit and foliage, as most other deer species, but it has also been found to eat eggs and carrion and is reported to be able to hunt small mammals and ground-nesting birds. It is reported to eat hunters' snared pheasants in China. In China, M. reevesi tends to be aggressively defensive of its territory because while food is available year-round, it is not plentiful.

Animal Foods: birds; mammals; eggs; carrion

Plant Foods: leaves; wood, bark, or stems; seeds, grains, and nuts; fruit; flowers

Other Foods: fungus

Primary Diet: omnivore

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Reproduction

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Males gain access to females by defending territory that overlaps that of females. The males will fight with the tusk-like canines for access to females in estrous. The males do not use their antlers in offensive moves while fighting like the white-tailed deer Odocoileus virginianus, but they spar extensively while still young, and use the horns in defensive moves while fighting.

Mating System: polygynous

Muntiacus reevesi has year round breeding in its natural habitat in China. In England, Chinese muntjacs appear to have a more seasonal breeding cycle that occurs between late October and early March. Both sexes of M. reevesi develop rapidly so that they may reach their reproductive threshold weights (12 kg for bucks, 10 kg for does) within a few months of birth (36 weeks for bucks, 24 weeks for does). It is unlikely that very young males will be able to gain access to a doe in estrus, but younger males tend to be more reproductively successful than older males due to the quality of their canines.

Unlike other antlered deer, muntjacs use tusk-like canines to defend territory and gain access to females. When a doe in estrus is located, the male will make a buzzing sound and the female will respond by lying flat, weaving her head and emitting a cat-like whine that is a sign of submission. After copulation, male are no longer involved with the females and once the rut is over, males lose their antlers. Males may grow antlers in a period as rapid as 103 days, which is useful for a species that can breed year-round.

Breeding interval: The mean inter-birth interval is approximately 233 days.

Breeding season: Breeding can occur year round in the subtropics, but in England, the breeding tends to be somewhat seasonal, occuring between late October and early March.

Range number of offspring: 1 to 2.

Average number of offspring: 1.

Range gestation period: 6.97 to 7.33 months.

Average gestation period: 7 months.

Average weaning age: 2 months.

Average time to independence: 6 months.

Range age at sexual or reproductive maturity (female): 24 (low) weeks.

Range age at sexual or reproductive maturity (male): 36 to 59 weeks.

Key Reproductive Features: iteroparous ; year-round breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous ; post-partum estrous

Average birth mass: 1050 g.

Average number of offspring: 1.

Parental investment is minimal in M. reevesi. The young develop extremely rapidly and are weaned early enough so that by the time that the caloric needs of the young really begin to escalate, they have begun to eat solid foods and are no longer dependent on their mother’s milk. Lactation generally occurs for only the first 17 weeks. Because the young become independent so early, there is no extra cost to a female to produce males (which would generally cost more in nutritional needs from a mother). By the age of 6 months, adulthood is reached and the young must leave the mother's territory.

Parental Investment: precocial ; pre-weaning/fledging (Provisioning: Female, Protecting: Female); pre-independence (Protecting: Female)

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Deuling, S. 2004. "Muntiacus reevesi" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Muntiacus_reevesi.html
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Sara Deuling, University of Michigan-Ann Arbor
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Phil Myers, Museum of Zoology, University of Michigan-Ann Arbor
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Matthew Wund, University of Michigan-Ann Arbor
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Biology

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Reeve's muntjac is active throughout the day and night, with peaks of activity at dawn and dusk (2). They feed on bramble, ferns, ivy, grasses and tree shoots, and unfortunately have a penchant for plants with a high conservation status such as bluebells and primulas (2), causing serious conflict in conservation areas (2). This deer is a solitary species; although individuals may occur in the same area (6). Unlike many deer species, Reeve's muntjac does not have a fixed breeding season, but reproduces throughout the year; correspondingly bucks are always territorial (6). They defend their territory by scent marking, depositing heaps of dung and aggressively repelling intruders using their canine teeth and/ or antlers (6). Females produce a single fawn at intervals of about 7 months (3), at 7 months of age, the fawns reach sexual maturity; females tend to remain close to their mothers' range, but males disperse further afield (3). This deer often barks for a number of reasons, which has earned the species the alternative common name of 'barking deer' (5). Both the Latin and common name refer to John Reeves, Assistant Inspector of Tea for the East India Company in 1812 (6).
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Conservation

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No conservation action.
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Description

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This small, stocky (2) introduced species has a shiny reddish coat which turns brownish-grey in winter, and the chin, throat, the area between the hind legs and underside of the long tail are paler (4). Both sexes have a rounded back, and large scent glands below the eye used for scent marking (6). Females are slightly smaller than males; other differences include males possessing antlers, which grow to 7cm in length, and obvious canine teeth that grow up to 3cm long (4). Furthermore, males have a dark 'V' pattern on the forehead (4), whereas females have a diamond shape (5). For the first 8 or so weeks of life, fawns have a light coloured coat with lines of spots around a dark stripe passing along the back (6).
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Habitat

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This secretive deer (5) inhabits dense scrub and woodland as well as quiet gardens (3). It is fairly versatile with regards to habitat, and this has helped it to colonise diverse areas, including Salisbury Plain, which consists of open grassland and scrub (6).
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Range

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Reeve's muntjac is native to China and Taiwan, and was introduced to the UK in 1894 to Woburn Park (3). Following escapes and deliberate movements, including a release from Whipsnade in 1921 (6), this species now has a wide distribution, which is concentrated in central England (3). There are also a few records from north Wales and northern England (3). Numbers are increasing rapidly at present (3).
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Status

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Introduced to the UK (3). Under Schedule 9, Section 14 of the Wildlife and Countryside Act 1981, it is illegal to release into or grow this species in the wild (4). Listed under Appendix III of the Berne Convention (7).
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Threats

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Road deaths are common (3), and predation of fawns by foxes is a serious cause of mortality (3). Due to the problems this species causes, particularly in highly sensitive conservation areas, this species is controlled by shooting (3), although due to the year-round reproduction there is no close-season in which shooting is restricted (3).
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Associations

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Animal / parasite / ectoparasite
Damalinia indica ectoparasitises Muntiacus reevesi

Foodplant / feeds on
Muntiacus reevesi feeds on Hyacinthoides non-scripta

Foodplant / feeds on
Muntiacus reevesi feeds on Mercurialis perennis

Foodplant / feeds on
Muntiacus reevesi feeds on Orchis mascula

Foodplant / feeds on
Muntiacus reevesi feeds on Dactylorhiza fuchsii

Foodplant / feeds on
Muntiacus reevesi feeds on Anemone nemorosa

Foodplant / feeds on
Muntiacus reevesi feeds on Cardamine pratensis

Foodplant / feeds on
Muntiacus reevesi feeds on Arum maculatum

Animal / parasite / ectoparasite / blood sucker
Solenopotes muntiacus sucks the blood of Muntiacus reevesi

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Reeves's muntjac

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Reeves's muntjac (Muntiacus reevesi; Chinese: 山羌), also known as the Chinese muntjac,[2] is a muntjac species found widely in southeastern China (from Gansu to Yunnan) and Taiwan.[3] It has also been introduced in the United Kingdom, Ireland, the Netherlands, Belgium, and Japan. It takes its name from John Reeves,[4] a naturalist employed by the British East India Company in the 19th century.

Description

Reeves's muntjac grows to 0.5 m (1 ft 8 in) high at the shoulder[5] and 0.95 m (3 ft 1 in) in length, plus a short tail up to 4 in (10 cm) long. It weighs between 10 and 18 kg (22 and 40 lb) when fully grown. It is reddish-brown in appearance with striped markings on its face.[5] The belly is creamy-white, with lighter fur extending to the neck, chin, and the underside of the tail. The males have short antlers,[5] usually 4 in (10 cm) or less, and long upper canines (tusks), usually about 2 in (5.1 cm) long. Females have bony lumps on their foreheads and localized black spots. The Taiwanese subspecies (M. r. micrurus), commonly known as the Formosan Reeves's muntjac, is darker than other subspecies.

Behavior

Reeves's muntjac feeds on herbs, blossoms, succulent shoots, fungi, berries, grasses, and nuts, and has also been reported to eat tree bark. Eggs and carrion are eaten opportunistically.[6] It is also called the barking deer due to its distinctive barking sound,[7] though this name is also used for other species of muntjacs. The barking sound is common during mating or when provoked. Its preferred habitats are forest and shrubland. It is a solitary and crepuscular animal. Both males and females defend small territories that they mark with preorbital gland secretions that are thought to be pheromonal in nature.[8] When fighting, males first use their antlers to push enemies off balance so they can wound them with their 2 in (5.1 cm) upper canine teeth.

Reproduction

Female, Prague Zoo
Female, Prague Zoo

Female muntjacs (known as "does"[7]) become sexually mature within the first year of life.[9] Mating occurs throughout the year. Their gestation period lasts from 209 to 220 days.[10] Females limit the number of mating bouts, though time between successive bouts is determined by males[11] (known as "bucks"[7]).

Distribution

It is found widely in southeastern China (from Gansu to Yunnan) and Taiwan.[3] It has also been introduced in several other regions.

Continental Europe

It has been introduced in Belgium and seen in the Netherlands.[12]

In Europe, this species is included since 2016 in the list of Invasive Alien Species of Union concern (the Union list).[13] This implies that this species cannot be imported, bred, transported, commercialized, or intentionally released into the environment in the whole of the European Union.[14]

Great Britain

Reeves's muntjacs were first introduced to the UK in the early 19th century.[15]

In the late 19th century, the then Duke of Bedford brought some to Woburn Abbey in Bedfordshire, then in 1901 released them into the surrounding woods.[15]: 96  A few more probably escaped from the nearby Whipsnade Zoo. During the mid-20th century, Woburn conducted several deliberate releases in distant locations throughout England.[15]: 97  It is suspected that there were also other unrecorded releases or escapes from private collections. These releases later caused misperception that muntjacs spread very rapidly.[15]: 98  The estimated population of Reeves's muntjacs in England was 52,000 in 1995,[2] and 104,000 in 2008.[15]: 100 

Under the Wildlife and Countryside Act 1981 it was illegal to release the species except where already established, and the Invasive Alien Species (Enforcement and Permitting) Order 2019 has subsequently prohibited the capture and re-release of muntjac in all cases.[16] As of 2017, colonies exist throughout England south of the Humber, and the population continues to grow.[17]

Ireland

It has been introduced in the Republic of Ireland.[18]

Sightings in 2008 caused the government, concerned at the risk of the species becoming established, to quickly introduce a year-round hunting season.[19]

Japanese archipelago

In the 1960s, several specimens escaped from an exhibition zoo in the Bōsō Peninsula in eastern Japan. By 2017, their numbers had reached at least 60,000. It is considered a harmful invasive species[20] and has inflicted severe damage to ashitaba plantations. Also, Reeves's muntjac escaped a zoo on Izu Ōshima in 1970 when a fence fell due to a typhoon. A muntjac eradication effort on Izu Ōshima was undertaken in 2007–2014 but failed, and as of 2014, at least 11,000 individuals exist and have a yearly population growth rate of 15%. This failure has been blamed on inadequate survey methods.[21]

Conservation

In Hong Kong, Reeve's muntjac is a protected species under the Wild Animals Protection Ordinance Cap 170. It is listed as least concern by the IUCN due to being generally common and widespread.[1]

Economic significance

The tanned skin of Reeves's muntjac is notable for its softness and is occasionally used in beauty-care products, musical instruments, lenses, and antique items packaging. Low-fat muntjac meat is also noted for its culinary qualities.[22]

References

  1. ^ a b Timmins, J.; Chan, B. (2016). "Muntiacus reevesi". IUCN Red List of Threatened Species. 2016: e.T42191A170905827. doi:10.2305/IUCN.UK.2016-2.RLTS.T42191A170905827.en. Retrieved 12 November 2021.
  2. ^ a b Harris, Stephen; Morris, Pat; Wray, Stephanie; Yalden, Derek (1995). "Chinese muntjac Muntiacus reevesi". A review of British mammals:population estimates and conservation status of British mammals other than cetaceans (Report). Joint Nature Conservation Committee (UK). pp. 101–102. ISBN 1-873701-68-3. Archived from the original on 2011-07-13. Retrieved 2022-08-28.
    • p101: in England around 40,000, in Scotland fewer than 50, in Wales fewer than 250.
    • p102: additional fawn and immature individuals 30% (12,000)
  3. ^ a b Wilson, D. E.; Reeder, D. M., eds. (2005). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. ISBN 978-0-8018-8221-0. OCLC 62265494.
  4. ^ Proceedings of the Zoological Society of London. Vol. 6. 1838. p. 105. Cervus Reevesi
  5. ^ a b c "Muntjac, Muntiacus reevesi". GB Non-native species secretariat. DEFRA.
  6. ^ "Reeve's muntjac videos, photos and facts – Muntiacus reevesi". Arkive. Archived from the original on 2017-10-27. Retrieved 7 April 2018.
  7. ^ a b c "Muntjac (Muntiacus reevesi)". www.bds.org.uk. The British Deer Society. Retrieved 13 March 2014.
  8. ^ Rehorek, Susan J.; Hillenius, Willem J.; Kennaugh, John; Chapman, Norma (2005). "The gland and the sac — the preorbital apparatus of muntjacs". Chemical Signals in Vertebrates 10. pp. 152–158. doi:10.1007/0-387-25160-X_19. ISBN 978-0-387-25159-2.
  9. ^ Chapman, Norma G., M. Furlong, and S. Harris. "Reproductive strategies and the influence of date of birth on growth and sexual development of an aseasonally‐breeding ungulate: Reeves' muntjac (Muntiacus reevesi)". Journal of Zoology 241.3 (1997): 551–570.
  10. ^ Whitehead, Kenneth (1993). The Whitehead Encyclopedia of Deer. Stillwater, MN: Voyager Press. p. 597.
  11. ^ Yahner, Richard (August 1979). "Temporal Patterns in Male Mating Behavior of Captive Reeve's Muntjac (muntiacus Reevesi)". Journal of Mammalogy. 3. 60 (3): 560–567. doi:10.2307/1380097. JSTOR 1380097.
  12. ^ Hollander, Hans. "Reeves' muntjac (Muntiacus reevesi) and sika deer (Cervus nippon) in the Netherlands" (PDF). Dutch Mammal Society. Retrieved 13 December 2022.
  13. ^ "List of Invasive Alien Species of Union concern - Environment - European Commission". ec.europa.eu. Retrieved 2021-07-27.
  14. ^ "REGULATION (EU) No 1143/2014 of the European parliament and of the council of 22 October 2014 on the prevention and management of the introduction and spread of invasive alien species".{{cite web}}: CS1 maint: url-status (link)
  15. ^ a b c d e Lever, Christopher (2009). "Reeves's muntjac". The naturalized animals of Britain and Ireland. London: New Holland Publishers (UK). pp. 95–100. ISBN 9781847734549.
    • cited sources: History and distribution: Chapman 1994, 1995; Population: Harris et al. 1995, Chapman 2008
  16. ^ "Alien Species (Enforcement and Permitting) Order 2019".
  17. ^ "Muntjac Deer". The British Deer Society. Archived from the original on 2022-03-21. Retrieved 2022-08-28.
  18. ^ Sleeman, D. P. and Carlsson, J. Introduction in Sleeman, D. P., Carlsson, J. and Carlsson, J. E. L. (eds) 2014. "Mind the Gap 11.: new insights into the Irish postglacial". Ir Nat J. ISBN 978-0-9569704-8-0
  19. ^ Under Statutory Instrument 346 of 2008
  20. ^ "Reeves's (or Chinese) Muntjac / Invasive Species of Japan". www.nies.go.jp. Retrieved 7 April 2018.
  21. ^ 東京新聞:社会:大島のキョンが猛繁殖 島民より多い1万1000頭 アシタバ被害. TOKYO Web (Tokyo Shimbun) (in Japanese). 2015-09-13. Archived from the original on 27 September 2015. Retrieved 7 April 2018.
  22. ^ Charles Smith, Muntjac: Managing an Alien Species ISBN 978-1904784029

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Reeves's muntjac: Brief Summary

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Reeves's muntjac (Muntiacus reevesi; Chinese: 山羌), also known as the Chinese muntjac, is a muntjac species found widely in southeastern China (from Gansu to Yunnan) and Taiwan. It has also been introduced in the United Kingdom, Ireland, the Netherlands, Belgium, and Japan. It takes its name from John Reeves, a naturalist employed by the British East India Company in the 19th century.

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