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Species
Cervus nippon Temminck, 1838
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NCBI
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Sika deer were long considered sacred animals in Japan. The fossil record of this species indicates that the Pleistocene deer of Asia - especially those of Japan - strongly resembled C. nippon (Feldhamer 1980).
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The sika was distributed across east Asia, from central China in the west to Japan and Korea in the east, and from the extreme eastern tip of Russia in the north to southern China and Viet Nam. Specifically, it was originally found in China (formerly from Manchuria south to Guangxi, and Sichuan to Anhui), North and South Korea (including Cheju Island) (but now probably extinct in both countries), Japan, Russia (a few places in Primorsky in the Far East), Taiwan (extinct in 1969, but subsequently re-introduced), and Viet Nam (probably now extinct). Wild populations are now very localized in China. In Japan, the species ranges widely from Hokkaido, Honshu, Shikoku and Kyushu, islands in the Seto Inland Sea (Awaji, Shodo, and others), Goto Islands, Ika, Yakushima, Mageshima, Kuchinoerabu-shima, Tsushima, and the Kerama Islands (introduced) (Okinawa Prefecture) (Abe, 2005).
In China, C. n. mandarinus probably ranged across much of northeastern China, but by the mid-1930s its range had contracted to northeastern Jilin (IUCN 1972, Guo 1992), and is now believed to be extinct (Hu 1998, Smith and Xie 2008). C. n. grassianus ranged throughout western Shanxi Province, China (Ohtaishi and Gao 1990, Guo 1992), and is now believed to be extinct (Hu 1998, Smith and Xie 2008).C. n. kopschi ranged from the Yangtze River Basin eastward to the coast, and south as far as northern Guangdong Province (IUCN 1972); it remains in small numbers in southern China. C. e. taiouanus was widely distributed throughout Taiwan (Green 1989). Free ranging populations were extirpated in 1969, but captive individuals were re-introduced in 1989 (Smith and Xie 2008). C. n. pseudaxis was recorded from Cao Bang, Quang Ninh, Thanh Hoa, Hanoi, and Nghe Tinh provinces in Viet Nam (Dang Huy Huynh et al. 1990), but is probably now extinct in the wild (captive animals remain).
The species has been widely introduced. In the Philippines it was anciently introduced to Solo Island, with questions remaining as to its continued existence there. It was introduced in 17th century to Kerama Islands (Ryukyu Islands, Japan); and introduced in 19th-20th centuries to British Isles, mainland Europe (Armenia, Austria, Azerbaijan, Czech Republic, Denmark, Finland, France, Germany, Lithuania, Poland, western Russia, and Ukraine), New Zealand, USA, and small islands off Japan (Whitehead 1993; Wemmer 1998; Grubb, 2005). It is also widely farmed in Asia, particularly in China (Green et al, 2007; Smith and Xie 2008). Ony the native, extant range is included in the distribution map.
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Sika Deer (Cervus nippon) are native to eastern Asia, mainly Japan and China, but were introduced in ancient times to the Sulu Archipelago (Philippines) and in the 19th and 20th centuries to the British Isles, mainland Europe (Austria, Czech Republic, Denmark, Finland, France, Germany, Poland, western Russia, and Ukraine), Armenia, Azerbaijan, Madagascar, New Zealand, and the United States. Sika Deer have a long relationship with humans, having been farmed, selectively bred, and moved around the globe over centuries.
Sika Deer are typically associated with woodlands with dense undergrowth and adjacent open areas. They can occur up to 3000 m above sea level, but are sensitive to snow depth: more than 40 cm of snow is limiting. Peak activity is around dawn and dusk. Sika Deer are moderately social, living in small groups or alone, with males and females strongly segregated.
Sika Deer routinely jump lengths of 3 to 4 m (8 m maximum) and 1.7 m in height. Normal maximum lifespan for Sika Deer is 15 to 16 years, but maximum longevity in captivity is 25 years.
In their native range, Sika Deer are secure in Japan, but populations across much of their historical range on continental Asia are extinct or endangered due to hunting (for meat, hides, antler velvet, blood, and organs) and habitat loss.
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Cervus nippon is a small to medium-sized deer with a head and body length of approximately 950-1,800 mm, a tail length of about 75-130 mm, and a height (measured at the shoulder) of 640-1090 mm (Feldhamer 1980, Nowak 1991). On average, males grow until they are 7-10 years old, while females stop growing at age 4-6 years (Nowak 1991). This results in the sexual dimorphism of males averaging 8.7% larger than females (Feldhamer 1980 and Nowak 1991). The pelage of C. nippon ranges from chestnut-brown to reddish-olive and exhibits a great deal of variation resulting in colors such as yellow-brown, gray-brown, tan, black, or gray depending on the subspecies (Feldhamer 1980, Flerov 1952, Nowak 1991, Putman 1988, and Whitehead 1972). In addition, the coats of these animals are mottled with white spots arranged in seven or eight rows on the upper sides of the back (Feldhamer 1980, http://www.assateague.com/sika.html 1997, Nowak 1991). Moreover, the mid-dorsal area of C. nippon is darker than the rest of its coat, and this forms a line from head to rear, terminating at a large, white, erectile rump patch often used as a distinguishing characteristic of these animals (Feldhamer 1980, http://www.assateague.com/sika.html 1997, Nowak 1991). The metatarsals of these deer are surrounded by tufts of grayish-tan hairs, and the hooves of adult males average 60 mm in length and 40 mm in width (those of females are slightly smaller) (Feldhamer 1980). The winter coat of sika deer is very dense with 50-70 mm long hairs, while its summer pelage is composed of much finer, straighter, and shorter (30 mm) hairs (Feldhamer 1980 and Putman 1988). The chin, throat, and belly of sika deer have an off-white or gray hue (Feldhamer 1980 and Nowak 1991). Finally, both sexes have a shaggy neck mane that darkens in the winter (Feldhamer 1980 and Nowak 1991).
Two molts occur annually in sika deer (Feldhamer 1980). In northern temperate climates the molt into winter pelage takes place over a 2-4 week period beginning in September, while the summer molt requires approximately 3 months and begins in March (Feldhamer 1980). Interestingly and for unknown reasons, it is the older deer that molt first (Feldhamer 1980).
Antlers are only found among the males of this species (Nowak 1991). In the Northern Hemisphere, males are in velvet antlers from May until August, but hard antlers predominate by early September, just in time for intrasexual selection activities like fraying (Feldhamer 1980). The growth phase of antlers is about 130 days beginning immediately in May when they are generally shed (Feldhamer 1980 and Flerov 1952). It should be noted that older males shed their antlers before their younger counterparts (Feldhamer 1980 and Flerov 1952). The antlers of sika deer are narrow, erect, and directed slightly posteriorly (Brown 1983, Feldhamer 1980, and Nowak 1991). Each is fairly short - measuring about 300-660 mm in length depending on the subspecies and local conditions - and has 2-5 tines (prongs) (Brown 1983, Feldhamer 1980, Nowak 1991, and Putman 1988). A 25 mm diameter at the base of each antler is common, while a spread of 400-500 mm is the maximum observed length (Feldhamer 1980). An upswept brow tine arises approximately 25 mm above the coronet (burr), while a bay tine is absent (Brown 1983 and Feldhamer 1980). Also, a forked, or sometimes palmated, tine surmounts the tray tine and faces forward (Brown 1983 and Feldhamer 1980). Finally, experimentation with antler growth and development have revealed that these processes can be entrained in deer previously sensitized to decreasing day lengths by increasing day lengths (Brown 1983 and Feldhamer 1980).
The skull of C. nippon is relatively short, with a rounded frontal-parietal region (Feldhamer 1980). The nasal bone does not extend beyond the maxilla, the lacrimal vacuity is fairly shallow, and the paroccipital processes extend below the occipital condyle (Feldhamer 1980). Overall, the cranial measurements of adult males averaged 8.9% larger than those of females (Feldhamer 1980). The dental formula of this species is 0/3, 1/1, 3/3, and 3/3 (Feldhamer 1980). The upper canines of sika deer protrude from the maxilla anteriorly, while the lower canines are incisiform (Feldhamer 1980). The molariform teeth are hypsodont and selenodont (Feldhamer 1980).
Range mass: 4.5 to 80 kg.
Range length: 950 to 1800 mm.
Other Physical Features: endothermic ; homoiothermic; bilateral symmetry
Sexual Dimorphism: male larger; ornamentation
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Source | http://animaldiversity.ummz.umich.edu/accounts/Cervus_nippon/ |
In Maryland and Virginia: onset of sexual maturity in females occurs as early as age 6 months, but most females probably first breed as yearlings (study in Japan found parturition only in females 3-12 years old) (Mullan et al. 1988). Seasonally reproductive in Texas (Howery et al. 1989).
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The sika deer (Cervus nippon) also known as the spotted deer or the Japanese deer, is a species of deer native to much of East Asia, and introduced to various other parts of the world. Previously found from northern Vietnam in the south to the Russian Far East in the north,[1] it is now uncommon in these areas, excluding Japan, where the species is overabundant.[2] Its name comes from shika (鹿?), the Japanese word for "deer"; in Japan the species is known as the nihonjika (ニホンジカ(日本鹿)?, lit. "Japan deer").
Contents
§Taxonomy[edit]
The sika deer is a member of the genus Cervus, a group of deer also known as the "true deer".[citation needed] Formerly, sika were grouped together in this genus with nine other species. Now, only the sika and red deer remain, the latter being divided into three separate species European red deer, central Asian red deer and American elk (though this remains controversial).[3] Recent DNA evidence indicates these deer are not as closely related as previously thought, resulting in the creation of new species and genera. The genera Rucervus, Rusa, and Przewalskium are where most of the former Cervus species now belong. The ancestor of all Cervus species probably originated in central Asia and resembled sika deer.[4] All Cervus species can crossbreed and produce hybrids in areas where they coexist (for example, introduced sika hybridize with native red deer in the Scottish Highlands, where this is a serious threat to the gene pool of the red deer population).
§Subspecies[edit]
Serious genetic pollution has occurred in many populations, especially in China. Therefore, the status of many subspecies remains unclear.[1] The status of C. n. hortulorum is particularly uncertain and might in fact be of mixed origin, hence it is not listed here.
- C. n. aplodontus, northern Honshu
- C. n. grassianus, Shanxi, China
- C. n. keramae, Kerama Islands of the Ryukyu Islands, Japan
- C. n. kopschi, southern China
- C. n. mandarinus, northern and northeastern China
- C. n. mantchuricus, northeastern China, Korea, and Russian Far East.
- C. n. nippon, southern Honshu, Shikoku, and Kyushu
- C. n. pseudaxis, northern Vietnam
- C. n. pulchellus, Tsushima Island
- C. n. sichuanicus, western China
- C. n. soloensis, Southern Philippines (Anciently introduced in Jolo island (unknown subspecies origin), probably extinct DD)[5]
- C. n. taioanus, Taiwan
- C. n. yesoensis, Hokkaido
§Description[edit]
The sika deer is one of the few deer species that does not lose its spots upon reaching maturity. Spot patterns vary with region. The mainland subspecies have larger and more obvious spots, in contrast to the Taiwanese and Japanese subspecies, whose spots are nearly invisible. Many introduced populations are from Japan, so also lack significant spots.
The color of the pelage ranges from mahogany to black, and white individuals are also known. During winter, the coat becomes darker and shaggier and the spots less prominent, and a mane forms on the back of the males' necks.[6] They are medium-sized herbivores, though they show notable size variation across their several subspecies and considerable sexual dimorphism, with males invariably much larger than females. They can vary from 50 to 110 cm (20 to 43 in) tall at the shoulder and from 95 to 180 cm (37 to 71 in) in head-and-body length. The tail measures about 7.5–13 cm (3.0–5.1 in) long. The largest subspecies is the Manchurian sika deer (C. n. mantchuricus), in which males commonly weigh about 68–109 kg (150–240 lb) and females weigh 45–50 kg (99–110 lb), with large stags scaling up to 160 kg (350 lb). On the other end of the size spectrum, in the Japanese sika deer (C. n. nippon), males weigh 40–70 kg (88–154 lb) and females weigh 30–40 kg (66–88 lb).[7][8] All sikas are compact and dainty-legged, with short, trim, wedge-shaped heads and a boisterous disposition. When alarmed, they will often display a distinctive flared rump, much like the American elk.
Sika stags have stout, upright antlers with an extra buttress up from the brow tine and a very thick wall. A forward-facing intermediate tine breaks the line to the top, which is usually forked. Occasionally, sika antlers develop some palmation (flat areas). Females carry a pair of distinctive black bumps on the forehead. Antlers can range from 28 to 45 centimetres (11 to 18 in) to more than 80 centimetres (30 in), depending on the subspecies. Stags also have distinctive manes during the rut.
§Behavior[edit]
The sika deer can be active throughout the day, though in areas with heavy human disturbance, they tend to be nocturnal. Seasonal migration is known to occur in mountainous areas, such as Japan, with winter ranges being up to 700 metres (2,300 ft) lower in elevation than summer ranges.[6] Lifestyles vary between individuals, with some occurring alone while others are found in single-sex groups. Large herds will gather in autumn and winter. The sika deer is a highly vocal species, with over 10 individual sounds, ranging from soft whistles to loud screams.
Sika males are territorial and keep harems of females during the rut, which peaks from early September through October, but may last well into the winter months. Territory size varies with habitat type and size of the buck; strong, prime bucks may hold up to 2 hectares (5 acres). Territories are marked with a series of shallow pits or "scrapes", into which the males urinate and from which emanates a strong, musky odor. Fights between rival males are sometimes fierce and long, and may even be fatal.
In Nara Prefecture, Japan, the deer are also known as "bowing deer", as they bow their heads before being fed special shika senbei (鹿せんべい?, called "deer cookies"). However, deer bow heads to signal that they are about to headbutt. Therefore, when a human 'bows' to a deer, the deer will assume the same stance and may charge and injure the human. Deer headbutt both for play and to assert dominance, as do goats. Sika deer are found throughout the Prefecture, particularly Nara's many parks and temples like Tōdai-ji, as they are considered to be the messengers of the Shinto gods.
§Habitat[edit]
Sika deer are found in the temperate in a warm forest of eastern Asia, preferring areas with dense understory, and where snowfall does not exceed 10–20 cm (3.9–7.9 in). They tend to forage in patchy clearings of forests. Introduced populations are found in areas with similar habitats to their native ranges, including Western and Central Europe, Eastern United States, and New Zealand.
§Population[edit]
The sika deer inhabits temperate and subtropical woodlands, which often occupy areas suitable for farming and other human exploitation. Its range encompasses some of the most densely populated areas in the world, where forests were cleared hundreds of years ago. Their population status varies significantly in different countries. Although the species as a whole is thriving, it is endangered and extinct in many areas.
Japan has by far the largest native sika population in the world. Though the exact population is uncertain, it is likely to be in the hundred thousand range and is still increasing,[citation needed] mainly due to recent conservation efforts and the extinction of its main predator, the wolf, over a century ago. Without its main enemy, the population of sika exploded and it is now overpopulated in many areas, posing a threat to both forests and farmlands. Efforts are now being made to control its population instead of conserving it. None of its subspecies is endangered except the Kerama deer (C. n. keramae) in the tiny Kerama Islands.[2]
China used to have the largest population of sika, but thousands of years of hunting and habitat loss have reduced the population to less than 1,000. Of the five subspecies in China, the North China sika deer (C. n. mandarinus) is believed to be extinct in the wild since the 1930s; the Shanxi sika deer (C. n. grassianus) has not been seen in the wild since the 1980s and is also believed to be extinct in the wild. The status of Manchurian sika deer in China is unclear, though it is believed to be extinct, as well, and the sightings there are actually feral populations. The South China sika deer (C. n. kopschi) and Sichuan sika deer (C. n. sichuanicus) are the only remaining subspecies in the wild. The former exists in fragmented populations of around 300 in southeast China, while the latter is found in a single population of over 400. The feral population is likely to be much higher than the wild, though most of them are descended from domesticated sikas of mixed subspecies. All of the subspecies are present in captivity, but a lack of suitable habitats and government efforts prevent their reintroduction.
The Formosan sika deer (C. n. taioanus) has been extinct for almost two decades before individuals from zoos were introduced to Kenting National Park; the population now numbers 200. Reintroduction programs are also under way in Vietnam, where the Vietnamese sika deer (C. n. pseudaxis) is extinct or nearly so.
Russia has a relatively large and stable population of 9,000 individuals of the Manchurian subspecies, but this is limited to a small area in Primorsky Krai. Small populations might exist in North Korea, but the political situation makes investigation impossible. The species is extinct in South Korea, with no plans for reintroduction.
§Introduced populations[edit]
Sika deer have been introduced into a number of other countries, including Estonia, Latvia, Lithuania, Austria, Belgium, Denmark, France, Germany, Ireland, Netherlands, Norway, Switzerland, Russia, Romania, New Zealand, the Philippines (Jolo Island), Poland, Sweden, Finland, Canada, the United Kingdom, and the United States (Maryland, Oklahoma, Nebraska, Pennsylvania, Wisconsin, Virginia, Indiana, Michigan, Minnesota, Maine, Wyoming, Washington, and Kansas).[9] In many cases, they were originally introduced as ornamental animals in parklands, but have established themselves in the wild. On Spieden Island in the San Juan Islands of Washington, they were introduced as a game animal.
In the UK and Ireland, several distinct feral populations now exist. Some of these are in isolated areas, for example on the island of Lundy, but others are contiguous with populations of the native red deer. Since the two species sometimes hybridise, there is a serious conservation concern.[10] In research which rated the negative impact of introduced mammals in Europe, the sika deer was found to be among the most damaging to the environment and economy, along with the brown rat and muskrat.[11]
In the 1900s, King Edward VII presented a pair of sika deer to John, the second Baron Montagu of Beaulieu. This pair escaped into Sowley Wood and were the basis of the sika to be found in the New Forest today.[citation needed] They were so prolific, culling had to be introduced in the 1930s to control their numbers.[12]
§Hunting[edit]
Across its original range and in many areas to which it has been introduced, the sika is regarded as a particularly prized and elusive sportsman's quarry. In Britain, Ireland, and mainland Europe, sika display very different survival strategies and escape tactics from the indigenous deer. They have a marked tendency to use concealment in circumstances when red deer, for example, would flee, and have been seen to squat and lie belly-flat when danger threatens.
Hunters and control cullers have estimated that the Sika's wariness and "cleverness" makes it three or four times more difficult to bring to bag than a red or fallow deer.[citation needed] In the British Isles, sika are widely regarded as a serious threat to new and established woodlands, and public and private forestry bodies adopt policies of rigorous year-round culling.[13]
§Velvet antler[edit]
Velvet antler (dried immature antlers) is a popular ingredient in traditional Chinese medicine, and sika in China were domesticated long ago for the antler trade, along with several other species. In Taiwan, both Formosan sika deer and Formosan sambar deer (Cervus unicolor swinhoei) have been farmed for velvet antlers. Japan is the only country in eastern Asia where sika deer were not farmed for velvet antlers.
Other deer raised for the antler trade were Thorold's deer (Cervus albirostris), central Asian red deer (Cervus affinis) and American elk (Cervus canadensis).
§See also[edit]
§References[edit]
- ^ a b c Harris, R.B. (2008). Cervus nippon. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 5 April 2009. Database entry includes a brief justification of why this species is of least concern.
- ^ a b Kaji, Koichi; Takashi Saitoh; Hiroyuki Uno; Hiroyuki Matsuda; Kohji Yamamura. "Adaptive management of sika deer populations in Hokkaido, Japan: theory and practice" (PDF). Retrieved 19 January 2011.
- ^ Ludt, Christian J.; Wolf Schroeder; Oswald Rottmann; Ralph Kuehn. "Mitochondrial DNA phylogeography of red deer (Cervus elaphus)" (PDF). Molecular Phylogenetics and Evolution 31 (2004) 1064–1083. Elsevier. Archived from the original on 27 September 2004. Retrieved 6 October 2006.
- ^ Geist, Valerius (1998). Deer of the World: Their Evolution, Behavior, and Ecology. Mechanicsburg, Pa: Stackpole Books. ISBN 0-8117-0496-3.
- ^ http://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=898543
- ^ a b "Ultimate Ungulate Fact Sheet – Sika Deer". [full citation needed]
- ^ Sika Deer. Bds.org.uk. Retrieved on 2012-08-23.
- ^ Nowak, R. M. 1991. Walker's Mammals of the World. Fifth Edition. Volume Two. Johns Hopkins University Press, Baltimore.
- ^ http://www.scirecordbook.org/sika-deer-north-america-introduced/
- ^ "Cross-breeding 'threat' to deer". BBC. 22 January 2009.
- ^ Rats top invasive mammals table. BBC. 7 May 2010.
- ^ "British Mammals: Sika Deer". BBC. 15 June 2007. Retrieved 8 October 2009.
- ^ http://www.nonnativespecies.org/downloadDocument.cfm?id=355
- "Cervus nippon". Integrated Taxonomic Information System. Retrieved 10 February 2006.
- Igota, H., Sakagura, M., Uno, H., Kaji, K., Maneko, M., Akamatsu, R., & Maekawa, (in press). Seasonal patterns of female sika deer in eastern Hokkaidō, Japan. Ecological Research, 19.
§Further reading[edit]
O'Brien, D.J., Rooney, S.M. and Hayden, T.J. 2009. A differential vulnerability to hunting between the sexes in Sika-type calves. I. Nat. J. 30: 7- 9.
§External links[edit]
Wikimedia Commons has media related to Sika Deer. |
Wikispecies has information related to: Cervus nippon |
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The following is a representative barcode sequence, the centroid of all available sequences for this species.
There are 18 barcode sequences available from BOLD and GenBank.
Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species.
See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
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Comments: See Grubb (in Wilson and Reeder 2005) for a list of the many subspecies and synonyms.
See Cronin (1991) for a phylogeny of the Cervidae based on mitochondrial-DNA data. See Kraus and Miyamoto (1991) for a phylogenetic analysis of pecoran ruminants (Cervidae, Bovidae, Moschidae, Antilocapridae, and Giraffidae) based on mitochondrial DNA data.
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This species is active throughout the 24-hour period, but in areas disturbed by humans they tend to be more active under the cover of darkness (1). They may occur either solitarily, or in single-sex groups where population densities are higher (1), and large herds may gather during autumn and winter (2). Sika deer browse on trees and shrubs, and also feed on grasses, sedges, holly, conifers, fungi, acorns, bark, heather and ivy (2). This species causes a great amount of damage, being a serious pest of woodland and farmland (3). During the breeding season, or 'rut', which occurs between late August and October, males occupy territories and compete for access to females (2). These contests involve vocalisations such as screaming, parallel walking and eventually fighting, which can result in serious injury and even death (1). The successful stags then mate, and hinds (females) give birth, usually to a single calf, in May and June (2). Introduced sika deer crossbreed with native red deer, causing hybridisation where the two species occupy the same range. This poses a threat to the red deer as it dilutes the gene pool (2).
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