Monday, August 22, 2016

THE WATER DEER

The water deer (Hydropotes inermis) is a small deer superficially more similar to a musk deer than a true deer. Native to China and Korea, there are two subspecies: the Chinese water deer (Hydropotes inermis inermis) and the Korean water deer (Hydropotes inermis argyropus). Despite its lack of antlers and certain other anatomical anomalies—including a pair of prominent tusks (downward-pointing canine teeth), it is classified as a cervid. Its unique anatomical characteristics have caused it to be classified in its own genus (Hydropotes) as well as its own subfamily (Hydropotinae).[2] However, a study of mitochondrial cytochrome b sequences placed it near Capreolus within an Old World section of the subfamily Capreolinae.[3] Its prominent tusks (elongated canines), similar to those of musk deer, have led to both being colloquially named vampire deer in English-speaking areas to which they have been imported. The species is listed as Vulnerable by the IUCN.

Habitat and distribution

 



Water deer are indigenous to the lower reaches of the Yangtze River, coastal Jiangsu province (Yancheng Coastal Wetlands), and islands of Zhejiang of east-central China, and in Korea, where the demilitarized zone has provided a protected habitat for a large number. They inhabit the land alongside rivers, where they are protected from sight by the tall reeds and rushes. They are also seen on mountains, swamps, grasslands, and even open cultivated fields. Water deer are proficient swimmers, and can swim several miles to reach remote river islands. Chinese Water Deer are now located in United Kingdom, France and Argentina, and even some in the United States.[4][5]

Britain


Chinese water deer (Hydropotes inermis inermis) at the Whipsnade Zoo
Chinese water deer were first introduced into Great Britain in the 1870s. The animals were kept in the London Zoo until 1896, when Herbrand Russell oversaw their transferral to Woburn Abbey, Bedfordshire. More of the animals were imported and added to the herd over the next three decades. In 1929 and 1930, 32 deer were transferred from Woburn to Whipsnade, also in Bedfordshire, and released into the park. The current population of Chinese water deer at Whipsnade is currently estimated to be more than 600, while the population at Woburn is probably in excess of 250.[citation needed]
The majority of the current population of Chinese water deer in Britain derives from escapees, with the remainder being descended from a number of deliberate releases. Most of these animals still reside close to Woburn Abbey. It appears that the deer’s strong preference for a particular habitat – tall reed and grass areas in rich alluvial deltas - has restricted its potential to colonize further afield. The main area of distribution is from Woburn, east into Cambridgeshire, Norfolk, Suffolk and North Essex, and south towards Whipsnade. There have been small colonies reported in other areas.[citation needed]
The British Deer Society coordinated a survey of wild deer in the United Kingdom between 2005 and 2007 and noted the Chinese water deer as "notably increasing its range" since the last census in 2000.[6]

France

A small population existed in France originating from animals which had escaped an enclosure in 1960 in western France (Haute-Vienne, near Poitiers). The population was reinforced in 1965 and 1970 and species is protected since 1974. Despite efforts to locate the animals with the help of local hunters, there have been no records since the year 2000, and the population is assumed to be extinct.[7]

United States

The species is not native, but a few small deer farms in the southeastern United States have successfully bred water deer.[citation needed]

 Shammy.jpg

 Physical attributes

Body Length Shoulder Height Tail Length Weight
75–100 cm 45–55 cm 6-7.5 cm 9–14 kg
2.5-3.3 ft 18-22 in 2.4-3 in 20-31 lbs
The water deer has narrow pectoral and pelvic girdles, long legs, and a long, graceful neck. The powerful hind legs are longer than the front legs, so that the haunches are carried higher than the shoulders. They run with rabbit-like jumps. In the groin of each leg is an inguinal gland used for scent marking; this deer is the only member of the Cervidae to possess such glands. The short tail is no more than 5–10 cm / 1.9–3.8 in. in length and is almost invisible, except when it is held raised by the male during the rut. The ears are short and very rounded, and both sexes lack antlers.[citation needed]
The coat is an overall golden brown color, and may be interspersed with black hairs, while the undersides are white. The strongly tapered face is reddish brown or gray in color, and the chin and upper throat are cream colored. The hair is longest on the flanks and rump. In the fall, the summer coat is gradually replaced by a thicker, coarse-haired winter coat that varies from light brown to grayish brown. Neither the head nor the tail poles are well differentiated as in gregarious deer; consequently, this deer's coat is little differentiated. Young are born dark brown with white stripes and spots along their upper torso.[citation needed]

Teeth


A stuffed specimen of H. inermis at the National Museum of Nature and Science, Tokyo, Japan.
The water deer have developed long canine teeth which protrude from the upper jaw like the canines of musk deer. The canines are fairly large in the bucks, ranging in length from 5.5 cm / 2.1 in. on average to as long as 8 cm / 3.2 in. Does, in comparison, have tiny canines that are on an average of 0.5 cm / 0.2 in. in length.[8]
The teeth usually erupt in the autumn of the deer’s first year at approximately 6–7 months of age. By early spring the recently erupted tusks reach approximately 50% of their final length. As the tusks develop, the root remains open until the deer is about eighteen months to two years old. When fully grown, only about 60% of the tusk is visible below the gum.[citation needed]
These canines are held loosely in their sockets, with their movement controlled by facial muscles. The buck can draw them backwards out of the way when eating. In aggressive encounters, he thrusts his canines out and draws in his lower lip to pull his teeth closer together. He then presents an impressive two-pronged weapon to rival males. It is due to these teeth that this animal is often referred to as a "vampire deer."[9]

Behavior

Apart from mating during the rutting season, water deer are solitary animals, and males are highly territorial. Each buck marks out his territory with urine and feces. Sometimes a small pit is dug and it is possible that in digging, the male releases scent from the interdigital glands on its feet. The male also scent-marks by holding a thin tree in his mouth behind the upper canines and rubbing his preorbital glands against it. Males may also bite off vegetation to delineate territorial boundaries.[citation needed]
Water deer use their tusks for territorial fights and are not related to carnivores. Confrontations between males begin with the animals walking slowly and stiffly towards each other, before turning to walk in parallel 10–20 m / 32–64 ft. apart, to assess one another. At this point, one male may succeed in chasing off his rival, making clicking noises during the pursuit. However, if the conflict is not resolved at the early stage, the bucks will fight. Each would try to wound the other on the head, shoulders, or back, by stabbing or tearing with his upper canines. The fight is ended by the loser, who either lays his head and neck flat on the ground, or turns tail and is chased out of the territory. Numerous long scars and torn ears seen on males indicate that fighting is frequent. The fights are seldom fatal but may leave the loser considerably debilitated. Tufts of hair are most commonly found on the ground in November and December, showing that encounters are heavily concentrated around the rut.[citation needed]
Females do not seem to be territorial outside the breeding season and can be seen in small groups, although individual deer do not appear to be associated; they will disperse separately at any sign of danger. Females show aggression towards each other immediately before and after the birth of their young and will chase other females from their birth territories.[citation needed]

Communication

Water deer are capable of emitting a number of sounds. The main call is a bark, and this has more of a growl tone when compared with the sharper yap of a muntjac. The bark is used as an alarm, and water deer will bark repeatedly at people and at each other for reasons unknown. If challenged during the rut, a buck will emit a clicking sound. It is uncertain how this unique sound is generated, although it is possibly by using its molar teeth. During the rut a buck following a doe will make a weak whistle or squeak. The does emit a soft pheep to call to their fawns, whilst an injured deer will emit a screaming wail.[citation needed]

Reproduction

Gestation Period Young per Birth Sexual Maturity Life Span
180–210 days 1-7 Does: 7–8 months 10–12 years

Commonly 2-5 Bucks: 5–6 months
During the annual rut in November and December, the male will seek out and follow females, giving soft squeaking contact calls and checking for signs of estrus by lowering his neck and rotating his head with ears flapping. Scent plays an important part in courtship, with both animals sniffing each other. Mating among water deer is polygynous, with most females being mated inside the buck's own territory. After repeated mountings, copulation is brief.[citation needed]
Water deer have been known to produce up to seven young, but two to three is normal for this species, the most prolific of all deer.[citation needed] The doe often gives birth to her spotted young in the open, but they are quickly taken to concealing vegetation, where they will remain most of the time for up to a month. During these first few weeks, fawns come out to play. Once driven from the natal territory in late summer, young deer sometimes continue to associate with each other, later separating to begin their solitary existence.[citation needed]

THE GERENUK

The gerenuk Somali: garanuug (pronounced /\ˈger-ə-ˌnu̇k, gə-ˈre-nək\/) (Litocranius walleri), also known as the giraffe gazelle, is a long-necked antelope found in the Horn of Africa and the African Great Lakes region. The sole member of the genus Litocranius, the gerenuk was first described by Anglo-Irish naturalist Victor Brooke in 1878. It is characterised by its long, slender neck and limbs. The antelope is 80–105 centimetres (31–41 in) tall, and weighs between 28 and 52 kilograms (62 and 115 lb). Two types of colouration are clearly visible on the smooth coat: the reddish brown back or the "saddle", and the lighter flanks, fawn to buff. The horns, present only on males, are lyre-shaped. Curving backward then slightly forward, these measure 25–44 centimetres (9.8–17.3 in).

 Taxonomy








Gazella


Blackbuck




Eudorcas


Nanger





Gerenuk


Springbok




Saiga



Oribi



Phylogenetic relationships of the gerenuk (Bärmann et.al. 2013)
The scientific name of the gerenuk is Litocranius walleri. The gerenuk is the sole member of the genus Litocranius, and is placed in the family Bovidae. The species was first described by Anglo-Irish naturalist Victor Brooke in 1878.[2] In 1997, Colin Groves had proposed that Litocranius is a sister taxon of Ammodorcas, but reverted from this in 2000.[2] The vernacular name "gerenuk" (pronounced /\ˈger-ə-ˌnu̇k, gə-ˈre-nək\/) comes from the Somali word gáránúug , meaning "giraffe-necked".[3] It is also known as the "giraffe gazelle" due to its resemblance to the giraffe.[4]
In 1999, a phylogenetic study based on cytochrome b and cytochrome c oxidase subunit III analysis showed that the tribe Antilopini, to which the gerenuk belongs, is monophyletic.[5] In 2013, Eva Verena Bärmann (of the University of Cambridge) and colleagues revised the phylogeny of Antilopini on the basis of nuclear and mitochondrial data. The cladogram prepared by them showed that the springbok (Antidorcas marsupialis) forms a clade with the gerenuk; this clade is sister to the saiga (Saiga tatarica, tribe Saigini) and the genera Antilope (blackbuck), Eudorcas, Gazella and Nanger (of Antilopini).[6]
Two subspecies are identified,[2][7] which are sometimes considered to be independent species:[8][9]
  • L. w. sclateri (Northern gerenuk) Neumann, 1988 : Known as Sclater's gazelle. Its range extends from northwestern Somalia (Berbera District) westward to touch the Egyptian border and Djibouti.
  • L. w. walleri (Southern gerenuk) (Brooke, 1878): Known as Waller's gazelle. Its range extends through northeastern Tanzania through Kenya to Galcaio (Somalia). The range lies north of the Shebelle River and near Juba River.

Lightmatter gerenuk.jpg

 Description

Close-up view of a male. Note the white facial markings and the lyre-shaped horns.
The gerenuk is a notably tall, slender antelope that resembles gazelles. It is characterised by its long, slender neck and limbs, the flat, wedge-like head and the large, round ears. Males are nearly 89–105 centimetres (35–41 in) tall, and the shorter females 80–100 centimetres (31–39 in); the head-and-body length is typically between 140 and 160 centimetres (55 and 63 in). Males weigh between 31 and 52 kilograms (68 and 115 lb); females are lighter, weighing 28–45 kilograms (62–99 lb). The species is sexually dimorphic. The tail, that ends in a black tuft, measures 25–35 centimetres (9.8–13.8 in).[8][10]
Two types of colouration are clearly visible on the smooth coat: the reddish brown dorsal parts (the back or the "saddle"), and the lighter flanks, fawn to buff. The underbelly and insides of the legs are cream in colour. The eyes and the mouth are surrounded by white fur. Females have a dark patch on the crown. The horns, present only on males, are lyre-like ("S"-shaped). Curving backward then slightly forward, these measure 25–44 centimetres (9.8–17.3 in).[8][10]
The gerenuk resembles the dibatag, with which it is sympatric in eastern and central Somalia and southeastern Ethiopia. Both are brachyodonts and share several facial and cranial features, along with a two-tone colouration of the coat and strong thick horns (only in males).[11] However, there are also some features distinguishing it from the gerenuk, including major morphological differences in horns, horn cores, tail, postorbital area and basioccipital processes. The gerenuk has a longer, heavier neck and a shorter tail.[8] A finer point of difference is the absence of an inward-curving lobe in the lower edge of the ear (near its tip) in the gerenuk.[11] The subspecies of the gerenuk are similar in colouration; the southern gerenuk is the smaller of the two.[8]

Ecology and behaviour

The gerenuk is a diurnal animal (active mainly during the day), though it typically stands or rests in shade during the noon. Foraging and feeding is the major activity throughout the day; females appear to spend longer time in feeding. The gerenuk may expose itself to rain, probably to cool its body.[12] The social structure consists of small herds of two to six members. Herds typically comprise members of a single sex, though female herds additionally have juveniles. Some males lead a solitary life.[8]
Fighting and travel are uncommon, possibly as a strategy to save energy for foraging.[4] Both sexes maintain home ranges 3–6 square kilometres (1.2–2.3 sq mi) large, and might overlap. Those of males are scent-marked with preorbital gland secretions and guarded - hence these may be termed territories. The sedentary tendency of the antelope appears to increase with age.[9]

Diet

Gerenuks feeding
Primarily a browser, the gerenuk feed on foliage of bushes as well as trees, shoots, herbs, flowers and fruits. It can reach higher branches and twigs better than other gazelles and antelopes by standing erect on its hindlegs and elongating its neck; this helps it reach nearly 2 metres (6.6 ft) above the ground.[13] Acacia species are eaten whenever available,[9] while evergreen vegetation forms the diet during droughts.[10] The pointed mouth assists in extracting leaves from thorny vegetation.[9] The gerenuk does not drink water regularly. Major predators of the antelope include Cape hunting dogs, cheetah, hyenas, lions and leopards.[8]

 

 Reproduction




Gerenuk reproduce throughout the year. Females reach sexual maturity at around one year, and males reach sexual maturity at 1.5 years, although in the wild they may only be successful after acquiring a territory (perhaps 3.5 years).[13] The gestation period is about seven months. They are born one at a time, weighing about 3 kg (6.6 lb) at birth. Offspring were produced through artificial insemination for the first time in 2010 at White Oak Conservation in Yulee, Florida. Four female calves were born, and one of the four was later inseminated successfully by White Oak and SEZARC (South-East Zoo Alliance for Reproduction & Conservation), creating a second generation of calves born from artificial insemination.[14] Gerenuk can live 13 years or more in captivity, and at least eight years in the wild.[13]


 

THE WATER MONITOR

Varanus salvator, commonly known as the water monitor, is a large lizard native to South and Southeast Asia. Water monitors are one of the most common monitor lizards found throughout Asia, and range from Sri Lanka and India to Indochina, the Malay Peninsula, and various islands of Indonesia, living in areas close to water.
The species is known as Malayan water monitor, Asian water monitor, common water monitor, two-banded monitor, and as rice lizard, ring lizard, plain lizard and no-mark lizard, as well as simply "water monitor".[2]



Varanus salvator - 01.jpg

Description

The water monitor is a large species of monitor lizard. Breeding maturity is attained for males when they are a relatively modest 40 cm (16 in) long and weigh 1 kg (2.2 lb), and for females at 50 cm (20 in). However, they grow much larger throughout life, with males being larger than females.[3] Adults rarely exceed 1.5–2 m (4.9–6.6 ft) in length,[4] but the largest specimen on record, from Sri Lanka, measured 3.21 m (10.5 ft). A common mature weight of V. salvator can be 19.5 kg (43 lb).[3][5] However, 80 males killed for the leather trade in Sumatra averaged only 3.42 kg (7.5 lb) and 56.6 cm (22.3 in) snout-to-vent and 142 cm (56 in) in total length; 42 females averaged only 3.52 kg (7.8 lb) and 59 cm (23 in) snout-to-vent and 149.6 cm (58.9 in) in total length,[6] although unskinned outsized specimens weighed 16 to 20 kg (35 to 44 lb). Another study from the same area by the same authors similarly estimated mean body mass for mature specimens at 20 kg (44 lb)[7] while yet another study found a series of adults to weigh 7.6 kg (17 lb).[8] The maximum weight of the species is over 50 kg (110 lb).[9] In exceptional cases, the species has been reported to attain 75 to 90 kg (165 to 198 lb), though most such reports are unverified and may be unreliable. They are the world's second-heaviest lizard, after the Komodo dragon.[6][10] Their bodies are muscular, with long, powerful, laterally compressed tails.
Water monitor (V. s. macromaculatus) showing split tongue (Sunderbans National Park, West Bengal, India)

Etymology

The generic name Varanus is derived from the Arabic waral (ورل), which translates as "monitor". The specific name is the Latin word for "saviour", denoting a possible religious connotation.[11] The water monitor is occasionally confused with the crocodile monitor (V. salvadorii) because of their similar scientific names.[12]
In Thailand, the local word for a water monitor, hia (เหี้ย), is used as an insulting word for bad and evil things, including bad persons. The word is also thought to bring bad luck, so some people prefer to call the animals 'silver-and-gold' (ตัวเงินตัวทอง) to avoid the jinx.
The origin of this offensive meaning can be traced back to a time when more people lived in rural areas in close proximity to monitor lizards. Traditionally, Thai villagers lived in two-story houses; the top floor was for living, while the ground floor was designed to be a space for domestic animals such as pigs, chickens, and dogs. Water monitors would enter the ground floor and eat or maim the domestic animals, also hence the other name dtua gin gai (ตัวกินไก่ ‘chicken eater’).[13]
In Indonesian and Malay, the water monitor is called biawak air,[14] to differentiate it from the biawak pasir ("sand lizard"), Leiolepis belliana.[15]
Water monitor at Kandy Lake, Sri Lanka

Subspecies

  • The Asian water monitor, V. s. salvator, the nominate subspecies, is now restricted to Sri Lanka, where it is known as the kabaragoya (කබරගොයා) in Sinhala and kalawathan in Tamil.
  • The Andaman Islands water monitor, V. s. andamanensis, is found on the Andaman Islands; the type locality is Port Blair, Andaman Islands.
  • The two-striped water monitor, V. s. bivittatus, is common to Java, Bali, Lombok, Sumbawa, Flores, Ombai (Alor), Wetar, and some neighbouring islands within the Sunda arch, Indonesia; the type locality is Java (designated by Mertens 1959).
  • The black water monitor, V. s. komaini, from Thailand (type locality: Amphoe La-ngu, Satun Prov., Thailand, and Thai-Malaysian border area), was formerly a subspecies, but now is regarded as a synonym of V. s. macromaculatus.[16] It is known as the "black dragon" or "black water monitor" (มังกรดำ, เหี้ยดำ) in Thai[17]
  • The Southeast Asian water monitor, V. s. macromaculatus (type locality: Siam [Thailand]), is found in mainland Southeast Asia, Singapore, Sumatra, Borneo, and smaller associated offshore islands.[16]
  • Ziegler's water monitor, V. s. ziegleri, is from Obi Island.
  • Varanus cumingi, Varanus marmoratus, and Varanus nuchalis were classified as subspecies until 2007, when they were elevated to full species.[16][18]

Behavior and diet

Water monitors robbing eggs from a nest. Illustration by P.J. Smit from Richard Lydekker's The Royal Natural History, 1893–1896
Water monitors defend themselves using their tails, claws, and jaws. They are excellent swimmers, using the raised fin on their tails to steer through water. They are carnivores, and consume a wide range of prey. They are known to eat fish, frogs, rodents, birds, crabs, and snakes.[11] They have also been known to eat turtles, as well as young crocodiles and crocodile eggs.[19] Like the Komodo dragon, they will often eat carrion.[11] Water monitors have been observed eating catfish in a fashion similar to a mammalian carnivore, tearing off chunks of meat with their sharp teeth while holding it with their front legs and then separating different parts of the fish for sequential consumption.[20]

Conservation

In Nepal's Chitwan National Park it is a protected species under the Wild Animals Protection Act of 2002. In Hong Kong, it is a protected species under Wild Animals Protection Ordinance Cap 170. In Malaysia, this species is one of the most common wild animals, with numbers comparable to the population of macaques there. Although many fall victim to humans via roadkill and animal cruelty, they still thrive in most states of Malaysia, especially in the shrubs of the east coast states such as Pahang and Terengganu. In the east coast states of Malaysia, this species is very common in roadkill. In Thailand, all monitor lizards are protected species.[21] This monitor is exploited by the pet trade.[21]
They are hunted (often illegally) for their skins, with as many as 1.5 million skins being exported each year to Europe, the U.S., and Japan for use in fashion accessories such as shoes, belts and handbags. In some places they are even consumed by humans. Loss of habitat and hunting has exterminated water monitors from most of mainland India. In other areas they survive despite being hunted, due in part to the fact that larger ones, including large females that breed large numbers of eggs, have tough skins that are not desirable.[2]
In Sri Lanka, they are protected by locals who value their predation of "crabs that would otherwise undermine the banks of rice fields".[2]

Gallery

Closeup of the head
Closeup of split tongue
Resting on tree limb
A hatchling

References

THE BANDED MONGOOSE

The banded mongoose (Mungos mungo) is a mongoose commonly found in the central and eastern parts of Africa. It lives in savannas, open forests and grasslands and feeds primarily on beetles and millipedes. Mongooses use various types of dens for shelter including termite mounds. While most mongoose species live solitary lives, the banded mongoose live in colonies with a complex social structure.

 Banded Mongoose on a log.jpg

 Physical characteristics

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The banded mongoose is a sturdy mongoose with a large head, small ears, short, muscular limbs and a long tail, almost as long as the rest of the body. Animals of wetter areas are larger and darker colored than animals of dryer regions. The abdominal part of the body is higher and rounder than the breast area. The rough fur is grayish brown, and there are several dark brown to black horizontal bars across the back. The limbs and snout are darker, while the underparts are lighter than the rest of the body. Banded mongooses have long strong claws that allow them to dig in the soil.
An adult animal can reach a length of 30 to 45 cm and a weight of 1.5 to 2.25 kg. The tail is 15 to 30 cm long.

 Image result for banded mongoose

Range and ecology


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The banded mongoose is found in a large part of East, Southeast and South-Central Africa. There are also populations in the northern savannas of West Africa. The banded mongoose lives in savannas, open forests and grassland, especially near water, but also in dry, thorny bushland but not deserts. The species uses various types of dens for shelter, most commonly termite mounds.[2] They will also live in rock shelters, thickets, gullies, and warrens under bushes. Mongooses prefer multi-entranced termitaria with open thicket, averaging 4 m from the nearest shelter, located in semi-closed woodland.[3] In contrast to the den of the dwarf mongoose, banded mongoose dens are less dependent on vegetation cover and have more entrances.[3] Banded mongooses live in larger groups than dwarf mongooses and this more entrances means more members have access to the den and ventilation.[3] The development of agriculture in the continent has had a positive influence on the number of banded mongooses. The crops of the farmland serve as an extra food source.
Mongoose looking out a burrow entrance

Food and foraging

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Banded mongoose feed primarily on insects, myriapods, small reptiles, and birds. Millipedes and beetles made of most of their diet,[2] but they also commonly eat ants, crickets, termites, grasshoppers, caterpillars and earwigs.[4][5] Other prey items of the mongoose includes frogs, lizards, small snakes, ground bird and the eggs of both birds and reptiles. On some occasions, mongooses will drink water from rain pools and lake shores.[4]
Banded mongoose forage in groups but each member searches for food alone.[4] They forage in the morning for several hours and then rest in the shade. They will usually forage again in the late afternoon. Mongooses use their sense of smell to locate their prey and dig them out with their long claws, both in holes in the ground and holes in trees. Mongoose will also frequent near the dung of large herbivores since they attract beetles.[4] Low grunts are produced every few seconds for communication. Mongoose also feed individually and are not cooperative feeders. When hunting prey that secrete toxins, mongooses will roll them on the ground. Durable prey is thrown on hard surfaces.[6]

Social behavior

 Image result for banded mongoose


Banded mongooses live in mixed-sex groups of 7–40 individuals (average around 20).[7] Groups sleep together at night in underground dens, often abandoned termite mounds, and change dens frequently (every 2–3 days). When no refuge is available and hard-pressed by predators such as wild dogs, the group will form a compact arrangement in which they lie on each other with heads facing outwards and upwards.
Banded mongoose Mungos mungo
There is generally no strict hierarchy in mongoose groups and aggression is low. Sometimes, mongoose may squabble over food. However, typically, the one who claims the food first wins. Most aggression and hierarchical behavior occurs between males when females are in oestrus. Female are usually not aggressive but do live in hierarchies based on age. The older females have earlier estrous periods and have larger litters.[7] When groups get too large, some females are forced out of the group by either older females or males. These females may form new groups with subordinate males.[8]
Banded mongoose, Mungos mungo subsp. grisonax, photographed at Ingwelala, Umbabat Nature Reserve, Mpumalanga, South Africa.
Relations between groups are highly aggressive and mongooses are sometimes killed and injured during intergroup encounters. Nevertheless, breeding females will often mate with males from a rival groups during fights.[9] Mongooses establish their territories with scent markings that may also serve as communication between those in the same group.[10] In the society of the banded mongoose there is a clear separation between mating rivals and territorial rivals. Individuals within groups are rivals for mates while those from neighboring groups are competitors for food and resources.[10]

Reproduction

Group in Botswana
Unlike most other social mongoose species, all females in a banded mongoose group can breed.[7] They all enter oestrus around 10 days after giving birth, and are guarded and mated by 1–3 dominant males.[7] The dominant males monitor the females and aggressively defend them from subordinates. While these males do most of the mating, the females often try to escape from them and mate with other males in the group. A dominant male will spend 2–3 days guarding each female.[7] A guarding male will snap at, lunge at or pounce on any males that come near.[7] A non-guarding male may follow a guarding male and his female and may face this aggression. Non-guarding males mate in a more secretive way.[7] This kind of "sneaking" behavior is similar to what subordinate males of the fish species Neolamprologus pulcher do; they also try to mate with females that are guarded by the dominant males.
Gestation is 60–70 days. In most breeding attempts, all females give birth either on the same day[7][11] or within a few days. Litters range 2–6 pups and average 4. For their first four weeks of life, pups stay in the dens. At this time they are guarded at the den by 1–3 babysitters while the other group member go on their foraging trips.[12] After four weeks, the pups are able to go foraging themselves. Each pup is cared for by a single adult "escort" who helps the pup to find food and protects it from danger.[13] Pups become nutritionally independent at three months of age.

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Inbreeding avoidance

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Inbreeding depression is largely caused by the homozygous expression of deleterious recessive alleles.[14] Inbreeding depression appears to occur in banded mongooses as indicated by a decline in progeny body mass with increasing inbreeding coefficient.[15] This finding suggests that avoiding breeding with close relatives would be beneficial. Successfully breeding pairs were found to be less related than expected under random mating.[15] This mating bias appears to be driven by both male mate choice and female control of paternity. Both sexes of banded mongoose likely use kin discrimination to avoid inbreeding.[15]

Interspecies relations

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In some locations (e.g., Kenya) banded mongooses have been found in close relationship with baboons.[citation needed] They forage together and probably enjoy greater security as a large group because of more eyes on the lookout for predators. The mongooses are handled by baboons of all ages and show no fear of such contact.
Banded mongooses have been observed removing ticks and other parasites from warthogs in Kenya[16] and Uganda.[17] The mongooses get food, while the warthogs get cleaned.

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 Status and abundance



 Banded Mongoose area.png

Banded mongooses lives in many of Africa's protected areas.[1] The Serengeti of Tanzania, has a density of around 3 mongooses per km2.[18] In southern KwaZulu-Natal, South Africa, mongoose numbers are at a similar density at 2.4 km2.[19] Queen Elizabeth National Park has much higher mongoose densities at 18/km 2.[20] Overall the banded mongoose tends to be more abundant in the eastern and south-eastern areas of its range than in more western areas.

THE KOMODO DRAGON

The Komodo dragon[4] (Varanus komodoensis), also known as the Komodo monitor, is a large species of lizard found in the Indonesian islands of Komodo, Rinca, Flores, Gili Motang, and Padar.[5] A member of the monitor lizard family Varanidae, it is the largest living species of lizard, growing to a maximum length of 3 metres (10 ft) in rare cases and weighing up to approximately 70 kilograms (150 lb).[5]
Their unusually large size has been attributed to island gigantism, since no other carnivorous animals fill the niche on the islands where they live.[6][7] However, recent research suggests the large size of Komodo dragons may be better understood as representative of a relict population of very large varanid lizards that once lived across Indonesia and Australia, most of which, along with other megafauna,[1] died out after the Pleistocene. Fossils very similar to V. komodoensis have been found in Australia dating to greater than 3.8 million years ago, and its body size remained stable on Flores, one of the handful of Indonesian islands where it is currently found, over the last 900,000 years, "a time marked by major faunal turnovers, extinction of the island's megafauna, and the arrival of early hominids by 880 ka [kiloannums]."[1]
As a result of their size, these lizards dominate the ecosystems in which they live.[8] Komodo dragons hunt and ambush prey including invertebrates, birds, and mammals. It has been claimed that they have a venomous bite; there are two glands in the lower jaw which secrete several toxic proteins. The biological significance of these proteins is disputed, but the glands have been shown to secrete an anticoagulant. Komodo dragon group behaviour in hunting is exceptional in the reptile world. The diet of big Komodo dragons mainly consists of deer, though they also eat considerable amounts of carrion.[5] Komodo dragons also occasionally attack humans in the area of West Manggarai Regency where they live in Indonesia.[9]
Mating begins between May and August, and the eggs are laid in September. About 20 eggs are deposited in abandoned megapode nests or in a self-dug nesting hole.[5] The eggs are incubated for seven to eight months, hatching in April, when insects are most plentiful. Young Komodo dragons are vulnerable and therefore dwell in trees, safe from predators and cannibalistic adults. They take 8 to 9 years to mature, and are estimated to live up to 30 years.[5]
Komodo dragons were first recorded by Western scientists in 1910.[10] Their large size and fearsome reputation make them popular zoo exhibits. In the wild, their range has contracted due to human activities, and they are listed as vulnerable by the IUCN.[2] They are protected under Indonesian law, and a national park, Komodo National Park, was founded to aid protection efforts.

 

 Komodo dragon (Varanus komodoensis) 3.jpgEtymology

The Komodo dragon is also known as the Komodo monitor or the Komodo Island monitor in scientific literature,[4] although this is not very common. To the natives of Komodo Island, it is referred to as ora, buaya darat (land crocodile), or biawak raksasa (giant monitor).[11][12]

Evolutionary history

The evolutionary development of the Komodo dragon started with the Varanus genus, which originated in Asia about 40 million years ago and migrated to Australia. Around 15 million years ago, a collision between Australia and Southeast Asia allowed the varanids to move into what is now the Indonesian archipelago, extending their range as far east as the island of Timor. The Komodo dragon was believed to have differentiated from its Australian ancestors 4 million years ago. However, recent fossil evidence from Queensland suggests the Komodo dragon evolved in Australia before spreading to Indonesia.[1][13] Dramatic lowering of sea level during the last glacial period uncovered extensive stretches of continental shelf that the Komodo dragon colonised, becoming isolated in their present island range as sea levels rose afterwards.[1][12]

Description


Closeup of the head and fore-quarters

Closeup of the skin
In the wild, an adult Komodo dragon usually weighs around 70 kg (150 lb), although captive specimens often weigh more.[14] According to the Guinness Book of World Records, an average adult male will weigh 79 to 91 kg (174 to 201 lb) and measure 2.59 m (8.5 ft), while an average female will weigh 68 to 73 kg (150 to 161 lb) and measure 2.29 m (7.5 ft).[15] The largest verified wild specimen was 3.13 m (10.3 ft) long and weighed 166 kg (366 lb), including undigested food.[12] The Komodo dragon has a tail as long as its body, as well as about 60 frequently replaced, serrated teeth that can measure up to 2.5 cm (1 in) in length. Its saliva is frequently blood-tinged, because its teeth are almost completely covered by gingival tissue that is naturally lacerated during feeding.[16] It also has a long, yellow, deeply forked tongue.[12] Komodo dragon skin is reinforced by armoured scales, which contain tiny bones called osteoderms that function as a sort of natural chain-mail.[17][18] This rugged hide makes Komodo dragon skin poorly suited for making into leather.

Senses

As with other varanids, Komodo dragons have only a single ear bone, the stapes, for transferring vibrations from the tympanic membrane to the cochlea. This arrangement means they are likely restricted to sounds in the 400 to 2,000 hertz range, compared to humans who hear between 20 and 20,000 hertz.[12][19] It was formerly thought to be deaf when a study reported no agitation in wild Komodo dragons in response to whispers, raised voices, or shouts. This was disputed when London Zoological Garden employee Joan Proctor trained a captive specimen to come out to feed at the sound of her voice, even when she could not be seen.[20]
The Komodo dragon can see objects as far away as 300 m (980 ft), but because its retinas only contain cones, it is thought to have poor night vision. The Komodo dragon is able to see in colour, but has poor visual discrimination of stationary objects.[21]
Komodo dragon using their tongue to sample the air
The Komodo dragon uses its tongue to detect, taste, and smell stimuli, as with many other reptiles, with the vomeronasal sense using the Jacobson's organ, rather than using the nostrils.[22] With the help of a favorable wind and its habit of swinging its head from side to side as it walks, a Komodo dragon may be able to detect carrion from 4–9.5 km (2.5–5.9 mi) away.[21] It only has a few taste buds in the back of its throat.[22] Its scales, some of which are reinforced with bone, have sensory plaques connected to nerves to facilitate its sense of touch. The scales around the ears, lips, chin, and soles of the feet may have three or more sensory plaques.[16]

Behaviour and ecology


Foot and tail
The Komodo dragon prefers hot and dry places, and typically lives in dry, open grassland, savanna, and tropical forest at low elevations. As an ectotherm, it is most active in the day, although it exhibits some nocturnal activity. Komodo dragons are solitary, coming together only to breed and eat. They are capable of running rapidly in brief sprints up to 20 km/h (12 mph), diving up to 4.5 m (15 ft), and climbing trees proficiently when young through use of their strong claws.[14] To catch out-of-reach prey, the Komodo dragon may stand on its hind legs and use its tail as a support.[20] As it matures, its claws are used primarily as weapons, as its great size makes climbing impractical.[16]
For shelter, the Komodo dragon digs holes that can measure from 1 to 3 m (3.3 to 9.8 ft) wide with its powerful forelimbs and claws.[23] Because of its large size and habit of sleeping in these burrows, it is able to conserve body heat throughout the night and minimise its basking period the morning after.[24] The Komodo dragon hunts in the afternoon, but stays in the shade during the hottest part of the day.[25] These special resting places, usually located on ridges with cool sea breezes, are marked with droppings and are cleared of vegetation. They serve as strategic locations from which to ambush deer.[26]

Diet


Komodo dragons feeding on a banded pig
Komodo dragons are carnivores. Although they eat mostly carrion,[6] they will also ambush live prey with a stealthy approach. When suitable prey arrives near a dragon's ambush site, it will suddenly charge at the animal and go for the underside or the throat.[16] It is able to locate its prey using its keen sense of smell, which can locate a dead or dying animal from a range of up to 9.5 km (5.9 mi). Komodo dragons have been observed knocking down large pigs and deer with their strong tails.[27][28]
Komodo dragons eat by tearing large chunks of flesh and swallowing them whole while holding the carcass down with their forelegs. For smaller prey up to the size of a goat, their loosely articulated jaws, flexible skulls, and expandable stomachs allow them to swallow prey whole. The vegetable contents of the stomach and intestines are typically avoided.[26] Copious amounts of red saliva the Komodo dragons produce help to lubricate the food, but swallowing is still a long process (15–20 minutes to swallow a goat). A Komodo dragon may attempt to speed up the process by ramming the carcass against a tree to force it down its throat, sometimes ramming so forcefully, the tree is knocked down.[26] A small tube under the tongue that connects to the lungs allows it to breathe while swallowing.[16] After eating up to 80% of its body weight in one meal,[8] it drags itself to a sunny location to speed digestion, as the food could rot and poison the dragon if left undigested for too long. Because of their slow metabolism, large dragons can survive on as few as 12 meals a year.[16] After digestion, the Komodo dragon regurgitates a mass of horns, hair, and teeth known as the gastric pellet, which is covered in malodorous mucus. After regurgitating the gastric pellet, it rubs its face in the dirt or on bushes to get rid of the mucus, suggesting it does not relish the scent of its own excretions.[16]

Young Komodo dragon feeding on a water buffalo carcass
The largest animals eat first, while the smaller ones follow a hierarchy. The largest male asserts his dominance and the smaller males show their submission by use of body language and rumbling hisses. Dragons of equal size may resort to "wrestling". Losers usually retreat, though they have been known to be killed and eaten by victors.[29]

Komodo excrement has a dark portion, which is stool, and a whitish portion which is urate, the nitrogenous end-product of their digestion process.
[30]
The Komodo dragon's diet is wide-ranging, and includes invertebrates, other reptiles (including smaller Komodo dragons), birds, bird eggs, small mammals, monkeys, wild boar, goats, deer, horses, and water buffalo.[31] Young Komodos will eat insects, eggs, geckos, and small mammals.[6] Occasionally, they attack and bite humans (see first paragraphs of this article). Sometimes they consume human corpses, digging up bodies from shallow graves.[20] This habit of raiding graves caused the villagers of Komodo to move their graves from sandy to clay ground and pile rocks on top of them to deter the lizards.[26] The Komodo dragon may have evolved to feed on the extinct dwarf elephant Stegodon that once lived on Flores, according to evolutionary biologist Jared Diamond.[32]
The Komodo dragon drinks by sucking water into its mouth via buccal pumping (a process also used for respiration), lifting its head, and letting the water run down its throat.[28]

Saliva

Although previous studies proposed that Komodo dragon saliva contains a variety of highly septic bacteria that would help to bring down prey, [29][33] research in 2013 suggested that the bacteria in the mouths of Komodo dragons are ordinary and similar to those found in other carnivores. They actually have surprisingly good mouth hygiene. As Bryan Fry put it: "After they are done feeding, they will spend 10 to 15 minutes lip-licking and rubbing their head in the leaves to clean their mouth... Unlike people have been led to believe, they do not have chunks of rotting flesh from their meals on their teeth, cultivating bacteria." The observation of prey dying of sepsis would then be explained by the natural instinct of water buffalos, who are not native to the islands where the Komodo dragon lives, to run into water when attacked. The warm, faeces-filled water would then cause the infections.[34] The study used samples from 16 captive dragons (10 adults and six neonates) from three U.S. zoos.[35]

Venom

In late 2005, researchers at the University of Melbourne speculated the perentie (Varanus giganteus), other species of monitors, and agamids may be somewhat venomous. The team believes the immediate effects of bites from these lizards were caused by mild envenomation. Bites on human digits by a lace monitor (V. varius), a Komodo dragon, and a spotted tree monitor (V. scalaris) all produced similar effects: rapid swelling, localised disruption of blood clotting, and shooting pain up to the elbow, with some symptoms lasting for several hours.[36]
In 2009, the same researchers published further evidence demonstrating Komodo dragons possess a venomous bite. MRI scans of a preserved skull showed the presence of two glands in the lower jaw. The researchers extracted one of these glands from the head of a terminally ill dragon in the Singapore Zoological Gardens, and found it secreted several different toxic proteins. The known functions of these proteins include inhibition of blood clotting, lowering of blood pressure, muscle paralysis, and the induction of hypothermia, leading to shock and loss of consciousness in envenomated prey.[37][38] As a result of the discovery, the previous theory that bacteria were responsible for the deaths of Komodo victims was disputed.[39]
Kurt Schwenk, an evolutionary biologist at the University of Connecticut, finds the discovery of these glands intriguing, but considers most of the evidence for venom in the study to be "meaningless, irrelevant, incorrect or falsely misleading". Even if the lizards have venom-like proteins in their mouths, Schwenk argues, they may be using them for a different function, and he doubts venom is necessary to explain the effect of a Komodo dragon bite, arguing that shock and blood loss are the primary factors.[40][41]
Other scientists have stated that this allegation of venom glands "has had the effect of underestimating the variety of complex roles played by oral secretions in the biology of reptiles, produced a very narrow view of oral secretions and resulted in misinterpretation of reptilian evolution". According to these scientists "reptilian oral secretions contribute to many biological roles other than to quickly dispatch prey". These researchers concluded that, "Calling all in this clade venomous implies an overall potential danger that does not exist, misleads in the assessment of medical risks, and confuses the biological assessment of squamate biochemical systems".[42]

Reproduction


Komodo dragons mating
Mating occurs between May and August, with the eggs laid in September.[12] During this period, males fight over females and territory by grappling with one another upon their hind legs, with the loser eventually being pinned to the ground. These males may vomit or defecate when preparing for the fight.[20] The winner of the fight will then flick his long tongue at the female to gain information about her receptivity.[8] Females are antagonistic and resist with their claws and teeth during the early phases of courtship. Therefore, the male must fully restrain the female during coitus to avoid being hurt. Other courtship displays include males rubbing their chins on the female, hard scratches to the back, and licking.[43] Copulation occurs when the male inserts one of his hemipenes into the female's cloaca.[21] Komodo dragons may be monogamous and form "pair bonds", a rare behavior for lizards.[20]

Komodo dragon with its long tail and claws fully visible
Female Komodos lay their eggs from August to September and may use several types of locality; in one study, 60% laid their eggs in the nests of orange-footed scrubfowl (a moundbuilder or megapode), 20% on ground level and 20% in hilly areas.[44] The females make many camouflage nests/holes to prevent other dragons from eating the eggs.[45] Clutches contain an average of 20 eggs, which have an incubation period of 7–8 months.[20] Hatching is an exhausting effort for the neonates, which break out of their eggshells with an egg tooth that falls off soon after. After cutting themselves out, the hatchlings may lie in their eggshells for hours before starting to dig out of the nest. They are born quite defenseless and are vulnerable to predation.[29] Sixteen youngsters from a single nest were on average 46.5 cm long and weighed 105.1 grams.[44]
Young Komodo dragons spend much of their first few years in trees, where they are relatively safe from predators, including cannibalistic adults, as juvenile dragons make up 10% of their diets.[20] The habit of cannibalism may be advantageous in sustaining the large size of adults, as medium-sized prey on the islands is rare.[27] When the young approach a kill, they roll around in faecal matter and rest in the intestines of eviscerated animals to deter these hungry adults.[20] Komodo dragons take approximately 8 to 9 years to mature, and may live for up to 30 years.[5]

Parthenogenesis

Main article: Parthenogenesis

Parthenogenetic baby Komodo dragon, Chester Zoo, England
A Komodo dragon at London Zoo named Sungai laid a clutch of eggs in late 2005 after being separated from male company for more than two years. Scientists initially assumed she had been able to store sperm from her earlier encounter with a male, an adaptation known as superfecundation.[46] On 20 December 2006, it was reported that Flora, a captive Komodo dragon living in the Chester Zoo in England, was the second known Komodo dragon to have laid unfertilised eggs: she laid 11 eggs, and seven of them hatched, all of them male.[47] Scientists at Liverpool University in England performed genetic tests on three eggs that collapsed after being moved to an incubator, and verified Flora had never been in physical contact with a male dragon. After Flora's eggs' condition had been discovered, testing showed Sungai's eggs were also produced without outside fertilization.[48] On 31 January 2008, the Sedgwick County Zoo in Wichita, Kansas, became the first zoo in the Americas to document parthenogenesis in Komodo dragons. The zoo has two adult female Komodo dragons, one of which laid about 17 eggs on 19–20 May 2007. Only two eggs were incubated and hatched due to space issues; the first hatched on 31 January 2008, while the second hatched on 1 February. Both hatchlings were males.[49][50]
Komodo dragons have the ZW chromosomal sex-determination system, as opposed to the mammalian XY system. Male progeny prove Flora's unfertilised eggs were haploid (n) and doubled their chromosomes later to become diploid (2n) (by being fertilised by a polar body, or by chromosome duplication without cell division), rather than by her laying diploid eggs by one of the meiosis reduction-divisions in her ovaries failing. When a female Komodo dragon (with ZW sex chromosomes) reproduces in this manner, she provides her progeny with only one chromosome from each of her pairs of chromosomes, including only one of her two sex chromosomes. This single set of chromosomes is duplicated in the egg, which develops parthenogenetically. Eggs receiving a Z chromosome become ZZ (male); those receiving a W chromosome become WW and fail to develop,[51][52] meaning that only males are produced by parthenogenesis in this species.
It has been hypothesised that this reproductive adaptation allows a single female to enter an isolated ecological niche (such as an island) and by parthenogenesis produce male offspring, thereby establishing a sexually reproducing population (via reproduction with her offspring that can result in both male and female young).[51] Despite the advantages of such an adaptation, zoos are cautioned that parthenogenesis may be detrimental to genetic diversity.[53]

History

Discovery by the Western world


Komodo dragon coin, issued by Indonesia

Komodo in the emblem of East Nusa Tenggara province
Komodo dragons were first documented by Europeans in 1910, when rumors of a "land crocodile" reached Lieutenant van Steyn van Hensbroek of the Dutch colonial administration.[54] Widespread notoriety came after 1912, when Peter Ouwens, the director of the Zoological Museum at Bogor, Java, published a paper on the topic after receiving a photo and a skin from the lieutenant, as well as two other specimens from a collector.[3] The first two live Komodo dragons to arrive in Europe were exhibited in the Reptile House at London Zoo when it opened in 1927.[55] Joan Beauchamp Procter made some of the earliest observations of these animals in captivity and she demonstrated the behaviour of one of these animals at a Scientific Meeting of the Zoological Society of London in 1928.[56] The Komodo dragon was the driving factor for an expedition to Komodo Island by W. Douglas Burden in 1926. After returning with 12 preserved specimens and 2 live ones, this expedition provided the inspiration for the 1933 movie King Kong.[57] It was also Burden who coined the common name "Komodo dragon."[25] Three of his specimens were stuffed and are still on display in the American Museum of Natural History.[58]

Studies

The Dutch, realizing the limited number of individuals in the wild, outlawed sport hunting and heavily limited the number of individuals taken for scientific study. Collecting expeditions ground to a halt with the occurrence of World War II, not resuming until the 1950s and 1960s, when studies examined the Komodo dragon's feeding behavior, reproduction, and body temperature. At around this time, an expedition was planned in which a long-term study of the Komodo dragon would be undertaken. This task was given to the Auffenberg family, who stayed on Komodo Island for 11 months in 1969. During their stay, Walter Auffenberg and his assistant Putra Sastrawan captured and tagged more than 50 Komodo dragons.[59] The research from the Auffenberg expedition would prove to be enormously influential in raising Komodo dragons in captivity.[60] Research after that of the Auffenberg family has shed more light on the nature of the Komodo dragon, with biologists such as Claudio Ciofi continuing to study the creatures.[61]

Conservation


Basking Komodo dragon
The Komodo dragon is a vulnerable species and is on the IUCN Red List.[2] The Komodo National Park was founded in 1980 to protect Komodo dragon populations on islands including Komodo, Rinca, and Padar.[62] Later, the Wae Wuul and Wolo Tado Reserves were opened on Flores to aid with Komodo dragon conservation.[61]
Komodo dragons avoid encounters with humans. Juveniles are very shy and will flee quickly into a hideout if a human comes closer than about 100 metres (330 ft). Older animals will also retreat from humans from a shorter distance away. If cornered, they will react aggressively by gaping their mouth, hissing, and swinging their tail. If they are disturbed further, they may start an attack and bite. Although there are anecdotes of unprovoked Komodo dragons attacking or preying on humans, most of these reports are either not reputable or caused by defensive bites. Only a very few cases are truly the result of unprovoked attacks by abnormal individuals, which lost their fear towards humans.[29]
Volcanic activity, earthquakes, loss of habitat, fire,[16][61] loss of prey due to poaching, tourism, and illegal poaching of the dragons themselves have all contributed to the vulnerable status of the Komodo dragon. Under Appendix I of CITES (the Convention on International Trade in Endangered Species), commercial trade of skins or specimens is illegal.[63][64]
In 2013, total population in the wild was assessed as 3,222 individuals, declining to 3,092 in 2014 and 3,014 in 2015. Populations remained relatively stable on the bigger islands (Komodo and Rinca), but decreased on smaller island such as Nusa Kode and Gili Motang, likely due to diminishing prey availability.[65] On Padar, a former population of the Komodo dragon became extinct, of which the last individuals were seen in 1975.[66] It is widely assumed that the Komodo dragon died out on Padar after a strong decline of the populations of large ungulate prey, for which poaching was most likely responsible.[67]

In captivity


Profile showing the external earholes behind the eyes. Komodo dragons hear a smaller range of frequencies compared to humans.

Komodo dragon with keeper
Komodo dragons have long been great zoo attractions, where their size and reputation make them popular exhibits. They are, however, rare in zoos because they are susceptible to infection and parasitic disease if captured from the wild, and do not readily reproduce.[11] As of May 2009, there were 13 European, 2 African, 35 North American, 1 Singaporean, and 2 Australian institutions that kept Komodo dragons.[68]
The first Komodo dragons were displayed at London Zoo in 1927. A Komodo dragon was exhibited in 1934 at the National Zoo in Washington, D.C., but it lived for only two years. More attempts to exhibit Komodo dragons were made, but the lifespan of these animals was very short, averaging five years in the National Zoological Park. Studies done by Walter Auffenberg, which were documented in his book The Behavioral Ecology of the Komodo Monitor, eventually allowed for more successful managing and reproducing of the dragons in captivity.[60]
A variety of behaviors have been observed from captive specimens. Most individuals are relatively tame within a short time,[69][70] and are capable of recognising individual humans and discriminating between familiar keepers.[71] Komodo dragons have also been observed to engage in play with a variety of objects, including shovels, cans, plastic rings, and shoes. This behavior does not seem to be "food-motivated predatory behavior".[8][12][72]
Even seemingly docile dragons may become unpredictably aggressive, especially when the animal's territory is invaded by someone unfamiliar. In June 2001, a Komodo dragon seriously injured Phil Bronstein, the then husband of actress Sharon Stone, when he entered its enclosure at the Los Angeles Zoo after being invited in by its keeper. Bronstein was bitten on his bare foot, as the keeper had told him to take off his white shoes and socks, which the keeper stated could potentially excite the Komodo dragon as they were the same colour as the white rats the zoo fed the dragon.[73][74] Although he escaped, Bronstein needed to have several tendons in his foot reattached surgically.[75]

See also