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Lifespan, longevity, and ageing

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Maximum longevity: 11.2 years (captivity)
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Trophic Strategy

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The diet of Bengal monitors is almost strictly carnivorous. They consume almost anything that is smaller than themselves and that they can easily overpower. They are known to scavenge carcasses of previously felled animals. Their documented observed prey species list is considerable, containing roughly 200 species. Common prey include: annelids, insects, amphibians, smaller reptiles, birds, small mammals, and eggs. Cannibalism of eggs, hatchlings, and even adults has been noted, although predation on adults is rare. As with most varanids, they swallow prey whole but are also capable of ripping and tearing flesh from larger animals and carcasses. At smaller body sizes for Bengal monitors, various beetles species represent the largest portion of their diet, averaging 52.8%. The second largest component of their diet is made up of orthopteran insects at 9.5%. The remainder of their diet is made up of other insects, crabs, rodents, reptiles, spiders, birds and almost any other animal they can reasonably consume.

Animal Foods: birds; mammals; amphibians; reptiles; carrion ; insects; terrestrial non-insect arthropods

Primary Diet: carnivore (Eats terrestrial vertebrates, Insectivore , Eats non-insect arthropods, Scavenger )

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Eric Wright, Radford University
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Christine Small, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Associations

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Predation on V. bengalensis does occur despite the fact that they themselves large predators. Species that prey upon V. bengalensis include other Bengal monitors, pythons and other large snakes, eagles, mongooses, wild and domesticated dogs, feral cats, and even humans. Most predation occurs early in life as eggs, hatchlings, and juveniles, while only a small portion of predation involves fully grown adults.

Known Predators:

  • Bengal monitors (Varanus bengalensis)
  • python species (Python)
  • birds of prey (Accipitridae)
  • mongooses (Herpestidae)
  • feral dogs (Canis lupus familiaris)
  • feral cats (Felis domesticus)
  • humans (Homo sapiens)
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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Morphology

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Adult Bengal monitors are generally grey or greenish-grey in color, with a ventral pattern of grey to black crossbars from the chin to the tail. These markings are generally darkest in the western parts and lightest in the eastern parts of the geographic range. These ventral markings typically become lighter, and the ground color darker, with age. Thus, adults display a less pronounced, less contrasting pattern than younger Bengal monitors.

In the wild, the heaviest recorded male Bengal monitor weighed 7.18 kg, though captive individuals have been reported to reach 10.2 kg. In the wild, males generally weigh 42% more than females. Males of the same snout to vent length (SVL) as females are typically 9.2% heavier. Young Bengal monitors, on average, weigh 0.078 kg.

Range mass: 7.18 (high) kg.

Range length: 61 to 175 cm.

Other Physical Features: heterothermic

Sexual Dimorphism: male larger

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Life Expectancy

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Like many other large predators, V. bengalensis is relatively long-lived. This species is relatively unaffected by drought or daily variations in rainfall, so population sizes remains fairly stable from season to season. Mortality rates are highest for neonates, due to predation, with only about half surviving past the age of two and reaching sexual maturity. For captive individuals, the longest recorded life span was about 22 years.

Age estimates in reptiles are obtained by counting bone layers. Reptiles, including V. bengalensis have annual cyclic bone growth that can be estimated by staining methods.

Average lifespan
Status: captivity:
22 years.

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Habitat

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Unlike other varanid lizards, Bengal monitors have the ability to cope with a broad range of environments, from deserts to rainforests to habitats having seasonally snowy winters. However, generally they are found in areas with continuously warm climates, with mean annual air temperatures of approximately 24 C. Most of southern Asia experiences seasonal monsoons and wind patterns influenced by neighboring seas and mountains. Thus, precipitation across much of the range for Bengal monitors is highly variable. Some habitat areas are relatively arid, with mean precipitation less than 200 mm per year. Other habitats are considerably more humid, with annual rainfall reaching 2,200 mm per year. The most common tropical forest habitats for Bengal monitors are deciduous, semi-deciduous, evergreen tropical forests, and thornbrush.

Range elevation: 0 to 1500 m.

Habitat Regions: tropical ; terrestrial

Terrestrial Biomes: savanna or grassland ; forest ; rainforest ; scrub forest

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Distribution

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Bengal monitors or common Indian monitors (Varanus bengalensis) occur across much of southern Asia. Compared to other varanid lizards, Bengal monitors have a much larger geographic range, where they are considered less restricted both geographically and environmentally. This species is widely distributed from Afghanistan to Java, including southeastern Iraq, Iran, and Afghanistan, Pakistan and India, southern Nepal, Bhutan, and China, North and South Vietnam, Laos, and islands in the Strait of Malacca and the Greater Sunda Islands. In Iran they are generally restricted to southeastern regions in close proximity to rivers that drain into marshes or shallow lakes, rather than seas, they are particularly common along the River Gartatab. In Afghanistan, Bengal monitors are limited to the Kabul River Valley in the extreme southeastern part of the country.

Biogeographic Regions: oriental (Native )

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Eric Wright, Radford University
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Christine Small, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Associations

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Bengal monitors are primary predators of many smaller animals in the ecosystems they inhabits. Juveniles are preyed upon by larger predators, including other monitors. There are four tick species known to infect Bengal monitors, including: Aponommon gervaisi, A. varanensis, A. laeve, and Amblyomma helvolum. In addition, trematodes, cestode worms, nematodes, filarial worms, and sporozoan protozoans are known to infect these monitors.

Commensal/Parasitic Species:

  • Aponommon gervaisi
  • Aponommon varanensis
  • Aponommon laeve
  • Amblyomma helvolum
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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Benefits

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Bengal monitor population declines for this species are largely due to the commercial exploitation of their skins for leather products. In addition, various parts of their bodies are used in some village medicines. Monitors in general, also are eaten by human populations in some parts of Asia, Africa, and Australia.

Positive Impacts: food ; body parts are source of valuable material; source of medicine or drug ; controls pest population

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Eric Wright, Radford University
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Benefits

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There are no noted negative impacts of Varanus bengalensis on humans. Bengal monitors are not large enough to attack any livestock nor do they eat any human cultivated crops. They may eat any small mammals that they can easily catch, so may pose a threat to small domestic animals.

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Eric Wright, Radford University
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Christine Small, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Life Cycle

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Development in Bengal monitors begins with a variable length incubation period. Laboratory investigations have shown this incubation period to range from 70 to 327 days. The length of incubation depends largely on mean egg temperature. However, even within a single brood, there can be variations of up to 105 days from first to last hatching. High incubation temperatures typically lead to shorter development times, but also may skew sex ratios or cause developmental defects.

Bengal monitors are relatively long-lived varanids. As such, this species does not reach sexual maturity until 2.5 to 3 years. Most produce one clutch of offspring each year for the remainder of their lives. Environmental influences play an important role in body size and overall length in Bengal monitors. In general, longer individuals are found in areas with greater soil moisture, such as marsh environments, whereas shorter individuals often occur in surrounding forests. In addition, those found on the small islands in both the South China Sea and the Gulf of Thailand have been found to become sexually mature at a much smaller size than those from the nearby mainland, reaching reproductive maturing with SVLs as low as 23.3 cm.

Development - Life Cycle: temperature sex determination

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Eric Wright, Radford University
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Christine Small, Radford University
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Conservation Status

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According to the IUCN Red List of Threatened Species, V. bengalensis is a species of Least Concern. This is based on its wide geographic range. However, there are increasing pressures on the species. They are hunted for their meat, skins, and for use in medicine. Due to expanding human habitation and urbanization, the range threats to their population are likely to increase in the future.

US Federal List: endangered

CITES: appendix i

State of Michigan List: no special status

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Eric Wright, Radford University
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Christine Small, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Behavior

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Like most varanids, Bengal monitors use primarily scent as their main method of communication and perception. They “taste” the environment around them by constantly flicking their highly sensitive tongues while moving their head from side to side. This is useful in tracking prey and mates and in signaling between monitors of the same species. It has been documented in the wild that V. bengalensis spends large amounts of time examining the droppings of other Bengal monitors that have passed through their territory. Even though they are solitary creatures, scent messages in feces are said to be important in communication. The scent perceived by one monitor from another can inform of hostile intentions or to stay away from the particular territory.

There is a diverse range of intraspecific communication exhibited by V. bengalensis through touching, biting, clawing and wrestling. Being solitary predators, roughly three quarters of encounters begin as purely investigatory and the remaining quarter are for the purpose of sex and courtship. Conflict between males, whether over food or mating, usually results in an initial investigation through acquiring each others scents and their intent. Conflict typically involves vocalization which is usually a hissing noise accompanied by the monitor inflating its upper body to appear larger. Tail-slapping and whipping is also common behavior between males and sometimes females to establish dominance. Encounters between males can lead to wrestling in which case both males stand on their hind legs and embrace each other while thrashing their heads and upper bodies. Occasionally biting and clawing can occur during wrestling but it is usually collateral damage rather than intentional.

Communication Channels: chemical

Other Communication Modes: scent marks

Perception Channels: visual ; chemical

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Eric Wright, Radford University
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Christine Small, Radford University
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Tanya Dewey, University of Michigan-Ann Arbor
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Reproduction

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Chemical cues play an important role in the ability of males to recognize receptive females. These chemical cues are produced by the female, from glands located in skin of the abdomen. In captivity, females show the greatest chances of successful copulation by mating with only one or two individual males in successive years, though they still may be courted by several other males.

Mating System: polygynandrous (promiscuous)

In females, the reproductive cycle is annual. Follicles mature only during one part of the year, shortly before ovulation. Follicles and ovaries reach their largest size during the months of July and August for those individuals in the western part of the species range, and from October to December for those in more southern areas such as India and Sri Lanka. Yolk deposition in an egg has no correlation with the ovulatory phase in females, but it does correlate with fat accumulation.

There are three major phases in the reproductive cycle of female V. bengalensis: previtellogenesis, recrudescence, and ovulation. During the previtellogenesis phase, the ovaries are small and inactive. This stage usually occurs during the fall months, usually September through March. Females forage less during this time for individuals in more southern regions, while those in more northern regions do not forage at all. A return to foraging in the spring initiates oogenesis. This phase is also characterized by regressed oviducts and nonsecretory epithelial and gland cells, which are used to attract mates. In the second phase of the reproductive cycle, called recrudescence (or true vitellogenesis), the ovarian follicles will fully mature with the completion of yolk deposition. This phase occurs in the premonsoon period, from April to June. In a short time, the ovaries increase in size and change from a pearly white to a deep yellow color. A mature preovulatory ova has a mean diameter of 17.8 mm. The oviducts will also increase in width and secretions will start to flow into the oviductal lumen. The last phase of the reproductive cycle, ovulation, is characterized by the movement of the egg from the upper part of the oviduct to the lower portion after fertilization has occurred. Once the egg reaches the lower portion of the oviduct, a shell will form around each egg. Ovulation begins in June, but reaches full force in July. The most successful copulation occurs slightly before or after ovulation has reached its peak. Egg laying will occur two weeks after copulation, usually during the months of July, August, and early September. By the last week of October, both sexes are largely inactive with size and sperm production heavily reduced in the male and new follicles for the next year appearing in the ovaries of the female.

Usually, mature females of V. bengalensis will produce only one clutch annually. However, in some areas where the environment experiences two monsoon seasons, some females may lay two clutches annually. If two clutches are laid, there are 23 to 30 days between the first egg laying and breeding for the second clutch. Data also suggests that those females from more mesic environments have a higher proportion of pregnancies than those from xeric areas. This may be due to the longer breeding periods in more mesic environments as well as higher food abundance, which has an effect on fat production. In captive species, day length also had an effect on courtship and breeding patterns. When day length was artificially lengthened, combat among males occurred as early as April and courtship initiation and breeding began earlier. The average number of eggs laid per year is 20, of which about 80% typically hatch. This results in about 16 young per female per year. Additionally, because V. bengalensis has a large clutch size relative to most tropical lizards, neonates are subject to relatively high predation rates. Because of predation, roughly half of the offspring do not live past the age of two.

Both males and females become sexually mature at approximately 2.5 to 3 years of age, both in the wild and in captivity. In both sexes, the onset of sexual maturity is linked to a body mass greater than 0.4 kg. In female Bengal monitors, reproductive efforts occur throughout most of their life span. After reaching sexual maturity, females remain reproductively active for the remainder of their lives, which may extend to 27 years.

Breeding interval: Female Bengal monitors that live in environments that experience two monsoon seasons may lay two clutches annually while those in one monsoon areas lay just one clutch annually.

Breeding season: Individuals mate in June, July, and early August and the shelled eggs are laid any time from July through early September. The incubation period is from 4 to 8 months.

Average number of offspring: 20.

Range gestation period: 4 to 8 months.

Range age at sexual or reproductive maturity (female): 2.5 to 3 years.

Range age at sexual or reproductive maturity (male): 2.5 to 3 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; sexual ; fertilization ; oviparous

In varanid species, the bulk of parental investment occurs through the materials and energy supplied prior to hatching. This includes resources provided for egg, embryonic, and initial post-hatching development. For example, during embryonic development the yolk supplies the fetus with nutrients required for growth. Females typically create and spend a large amount of time in the nest. She devotes energy to ensuring eggs are protected from predators, such as other monitors, and have proper incubation conditions in order to increase the offsprings' chances of survival. After their lengthy incubation period, however, neonates have very little yolk remaining when they hatch from the egg. This means that new hatchlings must locate food resources quickly and independently. It is interesting to note that females in captivity will frequently retain the eggs longer, spending additional time searching for an appropriate nesting medium. This makes the egg shells thicker than usual. Thicker shells require greater movement and strength on the part of the offspring to break out of the egg. Thus, small yolk food reserves also affect hatchling success. There are no reports showing sufficient evidence that female varanids provide additional care for offspring after laying eggs and hiding them in the nest. In fact, both males and females often eat eggs of other monitors. There also is evidence that females sometimes eat their own eggs. Data suggest that mean egg size and hatchling size are reduced in xeric habitats.

Parental Investment: no parental involvement; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female)

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Farmer, K. and E. Wright 2012. "Varanus bengalensis" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Varanus_bengalensis.html
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Kathleen Farmer, Radford University
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Distribution

provided by ReptileDB
Continent: Near-East Asia
Distribution: SE Iran, Afghanistan, Pakistan, N India, Bhutan, Nepal, Sri Lanka, Bangladesh, Myanmar (= Burma), Thailand (incl. Phuket), N Vietnam, Laos, Cambodia, W Malaysia, Pulau Tioman, Indonesia (Java), China (Yunnan) irrawadicus: S China (Yunnan).
Type locality: Wanding Valley, Yunnan Prov., southern China. vietnamensis: NW Vietnam (based on information from a dealer where the specimens were obtained).
Type locality: see comment.
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Bengal monitor

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The Bengal monitor (Varanus bengalensis), also called the common Indian monitor, is a monitor lizard distributed widely in the Indian Subcontinent, as well as parts of Southeast Asia and West Asia. This large lizard is mainly a terrestrial animal, and its length ranges from about 61 to 175 cm (24 to 69 in) from the tip of the snout to the end of the tail. Young monitors may be more arboreal, but adults mainly hunt on the ground, preying mainly on arthropods, but also taking small terrestrial vertebrates, ground birds, eggs and fish. Although large Bengal monitors have few predators apart from humans who hunt them for meat, younger individuals are hunted by many predators.

Description

Juveniles are patterned and more colourful

The Bengal monitor can reach 175 cm with a snout-to-vent length (SVL) of 75 cm and a tail of 100 cm. Males are generally larger than females. Heavy individuals may weigh nearly 7.2 kg.[2] The populations of monitors in India and Sri Lanka differ in the scalation from those of Myanmar; these populations were once considered subspecies of the Bengal monitor, but are now considered two species within the V. bengalensis species complex.[3] What was once the nominate subspecies, V. bengalensis, is found west of Myanmar, while the clouded monitor (V. nebulosus) is found to the east. Clouded monitors can be differentiated by the presence of a series of enlarged scales in the supraocular region. The number of ventral scales varies, decreasing from 108 in the west to 75 in the east (Java).[4]

Showing forked tongue
Eating egg
Climbing tree

Young monitor lizards are more colourful than adults. Young have a series of dark crossbars on the neck, throat and back. The belly is white, banded with dark crossbars and are spotted with grey or yellow (particularly in the eastern part of the range). On the dorsal surface of young monitors, there are a series of yellow spots with dark transverse bars connecting them. As they mature, the ground colour becomes light brown or grey, and dark spots give them a speckled appearance. Clouded monitor hatchlings by comparison tend to have a series of backward-pointing, V-shaped bands on their necks.[5]

Bengal monitors have external nostril openings (nares) that is slit-like and oriented near horizontal, and positions between the eye and the tip of the snout. The nares can be closed at will, especially to keep away debris or water.[6] The scales of the skin are rougher in patches and on the sides, they have minute pits, especially well distributed in males.[7] These scales with micropores have glandular structures in the underlying dermal tissue and produce a secretion which may be a pheromone-like substance. Like other monitors, Bengal monitors have a forked tongue similar to snakes. The function is mainly sensory, and is not very involved in the transport of food down the throat. Bengal monitors have fat deposits in the tail and body that serve them in conditions when prey are not easily available.

The lungs have spongy tissue unlike the sacs of other saurians. This allows for a greater rate of gas exchange and allows a faster metabolic rate and higher activity levels. Like all monitors, they have subpleurodont teeth, meaning the teeth are fused to the inside of the jaw bones.[8] The teeth are placed one behind another, and there are replacement teeth behind and between each functional tooth (polyphyodont). The maxillary and dentary teeth are laterally compressed, sometimes with a slightly serrate cutting edge, while the premaxillary teeth are conical. There are 78 premaxillary teeth, 10 maxillary and 13 dentary teeth. Replacement teeth move forward and about four replacements happens each year for a tooth.[9] While monitor lizards are venomous, there are no reports of the effects of venom in Bengal monitors other than a very controversial case report of fatal renal failure as a result of envenomation from this species.[10]

Distribution and habitat

The species ranges from Iran to Java, among the most widely distributed of monitor lizards as they are eurytopic and adaptable to a range of habitats.[11] It is found in river valleys in eastern Iran, Afghanistan, India, Nepal, Sri Lanka, Pakistan, Bangladesh and Burma. The closely related species, the clouded monitor, occurs in southern Myanmar, Vietnam, Cambodia, Thailand, Malaysia, Sumatra, Java and the Sunda Islands. They have not been confirmed on Sumatra, and have been found to be absent from the Andaman Islands.[12]

The species is mainly distributed through lower elevations below an altitude of 1500 metres, and is found both in dry semiarid desert habitats to moist forest. They are often found in agricultural areas.[13][1]

Ecology and behaviour

Bengal monitors are usually solitary and usually found on the ground, although the young are often seen on trees. Clouded monitors by contrast have a greater propensity for tree climbing. Bengal and yellow monitors are sympatric but are partially separated by their habitat as Bengal monitors prefers forest over agricultural areas.[14] Bengal monitors shelter in burrows they dig or crevices in rocks and buildings, whilst clouded monitors prefer tree hollows. Both species will make use of abandoned termite mounds. Bengal monitors are diurnal like other monitors, becoming active around 6 AM and bask in the morning sun.[15] During winter in the colder parts of their range, they may take shelter and go through a period of reduced metabolic activity.[16] They are not territorial, and may change their range seasonally in response to food availability.[17]

They are usually shy and avoid humans. They have keen eyesight and can detect human movement nearly 250 m away. When caught, a few individuals may bite, but rarely do so.[18]

Although they are found on agricultural land, they prefer forests with large trees.[14] Generally, high ground cover with large trees are favorable areas.[19]

Captives have been known to live for nearly 22 years.[20] Predators of adults include pythons, mammalian predators and birds. A number of ectoparasites and endoparasites are recorded.

Breeding

Females may be able to retain sperm, and females held in confinement have been able to lay fertile eggs.[21] Some species of monitor lizards such as the Nile monitor have additionally demonstrated to be capable of parthenogenesis. The main breeding season is June to September, but males begin to show combat behaviour by April. Females dig a nest hole in level ground or a vertical bank and lay the eggs inside, filling it up and using their snouts to compact the soil. The females often dig false nests nearby and shovel soil around the area. They sometimes make use of a termite mound to nest. A single clutch of about 20 eggs are laid. The eggs hatch in 168 to nearly as long as 254 days.[22] About 40-80% of the eggs may hatch.

Locomotion

They are capable of rapid movement on the ground. Small individuals may climb trees to escape, but larger ones prefer to escape on the ground. They can climb well. On the ground, they sometimes stand on the hind legs to get a better view or when males fight other males.[23] They can also swim well and can stay submerged for at least 17 minutes.[24] They can use both trees and bushes for shelter.[19]

Feeding

Bengal monitors tend to remain active the whole day. Large adults may ascend vertical tree trunks, where they sometimes stalk and capture roosting bats. The species is a generalist, and feeds on a varied diet of invertebrates and vertebrates. Invertebrate prey mostly consists of beetles and their larvae followed by orthopterans, but also maggots, caterpillars, centipedes, scorpions, crabs, crayfish, snails, termites, ants, and earwigs. Larger individuals in addition to invertebrates also eat a large amount of vertebrate prey, including toads and frogs and their eggs, fish, lizards, snakes, rats, squirrels, hares, musk shrews, and birds. Hares and rodents such as Indian bandicoot rats are often caught by digging them out of their nests. Diet may differ based on season and locality, for example, they often forage for fish and aquatic insects in streams during the summer, and individuals in Andhra Pradesh eat mostly frogs and toads. Bengal monitors will also scavenge carrion, and sometimes congregate when feeding on large carcasses such as that of deer.[11][25] In areas where livestock are common, they often seek out dung to forage for beetles and other insects.[26][27]

In culture

Comparison to water monitor (Varanus salvator)

The lizard is known as bis-cobra in western India, Goyra in Rajasthan, guishaap or goshaap in Bangladesh and West Bengal, goh in Punjab and Bihar, as ghorpad in Maharashtra and as Thalagoya[28] in Sri Lanka. Folk mythology across the region includes the idea that these lizards, though actually harmless, are venomous, and in Rajasthan, the locals believe that the lizards become venomous only during the rainy season.[29] Monitor lizards are hunted, and their body fat, extracted by boiling, is used in a wide range of folk remedies.[30]

In Sri Lanka, the water monitor (Kabaragoya) is considered venomous and dangerous when confronted, while the Bengal monitor (Thalagoya) is considered harmless and rather defenseless. Land monitor meat is considered edible (especially by indigenous Veddah and Rodiya people) while water monitor meat is not. Killing a land monitor is usually considered a cowardly act, and is frequently referred to folklore along with other harmless reptiles such as rat snakes (Garandiya).[31][32]

A clan in Maharashtra called Ghorpade claims that the name is derived from a legendary founder Tanaji Malusare who supposedly scaled a fort wall using a monitor lizard tied to a rope.[33]

The Bengal monitor's belly skin has traditionally been used in making the drum head for the kanjira (known as Dimadi in Maharashtra), a South Indian percussion instrument.[34]

Conservation

While it is assessed LC (Least Concern) by the IUCN 2009, the assessment currently requires updating. The Bengal monitor is listed as Appendix I of CITES and Schedule I of the 1972 Wildlife Protection Act. The wild population is decreasing as it is hunted for both consumption and medicinal purposes as well as for the skin. As it is adaptable to a range of habitats, the threat of habitat degradation is relatively less prominent and is superseded by the threat of agricultural pollution, as pesticides reduce the availability of prey. In Iran, it is also sometimes killed due to being seen as a dangerous threat.[1]

Notes

  1. ^ a b c d Cota, M.; Stuart, B.L.; Grismer, L.; Quah, E.; Panitvong, N.; Neang, T.; Nguyen, N.S.; Wogan, G.; Lwin, K.; Srinivasulu, C.; Srinivasulu, B.; Vijayakumar, S.P.; Ramesh, M.; Ganesan, S.R.; Madala, M.; Sreekar, R.; Rao, D.-Q.; Thakur, S.; Mohapatra, P. & Vyas, R. (2021). "Varanus bengalensis". IUCN Red List of Threatened Species. 2021: e.T164579A1058949. doi:10.2305/IUCN.UK.2021-2.RLTS.T164579A1058949.en. Retrieved 22 January 2022.
  2. ^ Auffenberg (1994):14-15
  3. ^ Böhme, Wolfgang (2003-01-01). "Checklist of the living lizards of the world (family Varanidae)". BMC Evolutionary Biology - BMC EVOL BIOL. 341 – via ResearchGate.
  4. ^ Auffenberg (1994):24
  5. ^ Auffenberg (1994):39
  6. ^ Auffenberg (1994):22
  7. ^ Auffenberg (1994):36
  8. ^ Auffenberg (1994):50
  9. ^ Auffenberg (1994):51
  10. ^ White, Julian; Weinstein, Scott A. (2015-04-21). "Reply to Vikrant and Verma about "Monitor Lizard Envenoming"". Renal Failure. 37 (4): 740–741. doi:10.3109/0886022X.2015.1006116. ISSN 0886-022X. PMID 25835553. S2CID 34375062.
  11. ^ a b Losos, Jonathan B.; Greene, Harry W. (1988-12-01). "Ecological and evolutionary implications of diet in monitor lizards". Biological Journal of the Linnean Society. 35 (4): 379–407. doi:10.1111/j.1095-8312.1988.tb00477.x. ISSN 0024-4066.
  12. ^ Auffenberg (1994):86
  13. ^ Auffenberg (1994):103-118
  14. ^ a b Ghimire, H. R., & Shah, K. B. (2014). Status and habitat ecology of the Yellow Monitor, Varanus flavescens, in the Southeastern part of Kanchanpur District, Nepal. Herpetological Conservation and Biology, 9(2), 387-393. http://www.herpconbio.org/Volume_9/Issue_2/Ghimire_Shah_2014.pdf
  15. ^ Auffenberg (1994):138-145
  16. ^ Auffenberg (1994):147
  17. ^ Auffenberg (1994):175
  18. ^ Auffenberg (1994):182
  19. ^ a b Ghimire, H. R.; Phuyal, S. (2013). "Impacts of community forestry on the Bengal monitor, Varanus bengalensis (Daudin, 1802): an empirical study from Nepal" (PDF). Biawak. 7 (1): 11–17.
  20. ^ Auffenberg (1994):180
  21. ^ Auffenberg (1994):221
  22. ^ Auffenberg (1994):230-247
  23. ^ Auffenberg (1994):183
  24. ^ Auffenberg (1994):185
  25. ^ Auffenberg (1994):267
  26. ^ Auffenberg (1994):349
  27. ^ Rahman K. M. M.; Rakhimov I. I. (2015). "Habitat preference and feeding ecology of the Bengal monitor (Varanus bengalensis) in Natore, Bangladesh". International Research Journal. 11 (42 Part 3): 96–98. doi:10.18454/IRJ.2015.42.212.
  28. ^ Abayaratna, M.G.T.H; Mahaulpatha, W.A. Dharshani (2006). "Activity budgets and habitat preference of land monitor, Thalagoya Varanus bengalensis in a residential area" (PDF). Vidyodaya Journal of Science. 13: 127. Archived from the original (PDF) on 3 April 2015. Retrieved 27 January 2015.
  29. ^ Auffenberg (1994):58
  30. ^ Auffenberg (1994):appendix
  31. ^ Sri Lankan Lizards: kabaragoyas & Thalagoyas The concise guide to the Anglo-Sri Lankan lexicon by Richard Boyle, at http://www.lankalibrary.com/wlife/kabara.htm (Accessed: 29.10.2016.)
  32. ^ Thalagoya Vs. Kabaragoya by Maryam Azwer, at http://roar.lk/environment-wildlife/thalagoya-vs-kabaragoya/ (Accessed 29.10.2016)
  33. ^ Vidal, G. W. (1888). "The Bis Cobra". Journal of the Bombay Natural History Society. 3 (2): 71–82.
  34. ^ Khati, Anand S. (1998). National parks of India. Pelican Creations International. p. 323. ISBN 978-81-86738-00-9. Retrieved 30 December 2012.

References

  • Auffenberg, W. (1994). The Bengal Monitor. University Press of Florida. p. 494. ISBN 0-8130-1295-3.
  • Auffenberg, W. (1979). "Intersexual differences in behaviour of captive Varanus bengalensis (Reptilia, Lacertilia, Varanidae)". Journal of Herpetology. 13 (3): 313–315. doi:10.2307/1563325. JSTOR 1563325.
  • Auffenberg, W. 1979 Research on monitor lizards. Tiger Paper 6(4): 20–21.
  • Auffenberg, W. 1981 Combat behaviour in Varanus bengalensis. J.Bombay N.H.S. 78(1):54-72.
  • Auffenberg, W. 1983 The burrows of Varanus bengalensis. Rec. Zool. Surv. India 80:375-385.
  • Auffenberg, W. 1983 Courtship behaviour in Varanus bengalensis. In Advances in Herpetology and Evolutionary Biology: Essays in Honor of Ernest E. Williams (Rhodin & Myata eds.): 535–551.
  • Auffenberg, W. 1983 Notes on feeding behaviour of Varanus bengalensis. J. Bombay N.H.S. 80 (2): 286–302.
  • Auffenberg, W. 1986. The Indian monitor lizard. Sanctuary Asia. 6 (4):327-333.
  • Ghimire, H. R. & Shah, K. B. (2014). Status and habitat ecology of the Yellow Monitor, Varanus flavescens, in the Southeastern part of Kanchanpur District, Nepal. Herpetological Conservation and Biology, 9(2), 387–393. http://www.herpconbio.org/Volume_9/Issue_2/Ghimire_Shah_2014.pdf
  • Mertens, R. 1942. Ein weiterer neuer Warane aus Australien. Zool. Anz. 137: 41-44

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Bengal monitor: Brief Summary

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The Bengal monitor (Varanus bengalensis), also called the common Indian monitor, is a monitor lizard distributed widely in the Indian Subcontinent, as well as parts of Southeast Asia and West Asia. This large lizard is mainly a terrestrial animal, and its length ranges from about 61 to 175 cm (24 to 69 in) from the tip of the snout to the end of the tail. Young monitors may be more arboreal, but adults mainly hunt on the ground, preying mainly on arthropods, but also taking small terrestrial vertebrates, ground birds, eggs and fish. Although large Bengal monitors have few predators apart from humans who hunt them for meat, younger individuals are hunted by many predators.

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