Monitor lizard explained

Monitor lizards are lizards in the genus Varanus, the only extant genus in the family Varanidae. They are native to Africa, Asia, and Oceania, and one species is also found in the Americas as an invasive species.[1] About 80 species are recognized.

Monitor lizards have long necks, powerful tails and claws, and well-developed limbs. The adult length of extant species ranges from 20cm (10inches) in some species such as Varanus sparnus, to over 3abbr=onNaNabbr=on in the case of the Komodo dragon, though the extinct megalania (Varanus priscus) may have reached lengths of more than 7abbr=onNaNabbr=on. Most monitor species are terrestrial, but many are also arboreal or semiaquatic. While most monitor lizards are carnivorous, eating smaller reptiles, fish, birds, insects, small mammals, and eggs, a few species also eat fruit and vegetation.[2]

Etymology

The generic name Varanus is derived from the Arabic word Arabic: ورل waral [Standard Arabic] / Arabic: ورر warar [colloquially] / Arabic: ورن waran [colloquially], from a common Semitic root ouran, waran, warar or waral, meaning "lizard beast".[3]

In English, they are known as "monitors" or "monitor lizards". The earlier term "monitory lizard" became rare by about 1920.[4] The name may have been suggested by the occasional habit of varanids to stand on their two hind legs and to appear to "monitor",[3] or perhaps from their supposed habit of "warning people of the approach of venomous animals".[5] But all of these explanations for the name "monitor" postdate Linnaeus giving the scientific name Lacerta monitor to the Nile monitor in 1758, which may have been based on a mistaken idea by Linnaeus that the German word Waran (borrowed from Arabic) was connected to warnen (to warn), leading him to incorrectly Latinize it as monitor ('warner', 'adviser').[6]

Austronesian languages spoken across Southeast Asia, where varanids are common, have a large number of slightly related local names for them. They are usually known as biawak (Malay, including Indonesian standard variety), bayawak (Filipino), binjawak or minjawak or nyambik (Javanese), or variations thereof.[7] Other names include hokai (Solomon Islands); bwo, puo, or soa (Maluku); halo (Cebu); galuf or kaluf (Micronesia and the Caroline Islands); batua or butaan (Luzon); alu (Bali); hora or ghora (Komodo group of islands); phut (Burmese); and guibang (Manobo).[8] [9]

In South Asia, they are known as in Meitei, mwpou in Boro, घोरपड in Marathi, உடும்பு in Tamil and udumbu ഉടുമ്പ് in Malayalam, in Bhojpuri, gohi (गोहि) in Maithili, in Sinhala as තලගොයා / කබරගොයා, in Telugu as uḍumu (ఉడుము), in Kannada as (ಉಡ), in Punjabi and Magahi as गोह (goh), in Assamese as gui xaap, in Odia as ଗୋଧି (godhi), and in Bengali as গোসাপ or গুইসাপ, and गोह (goh) in Hindi.

The West African Nile monitor is known by several names in Yoruba, including,, and . In Wolof it is known as mbossé or bar, and is the traditional totem of the city of Kaolack.[10]

Due to confusion with the large New World lizards of the family Iguanidae, the lizards became known as "goannas" in Australia. Similarly, in South African English, they are referred to as leguaans, or likkewaans, from the Dutch term for the Iguanidae, leguanen.

Distribution

The various species cover a vast area, occurring through Africa, the Indian subcontinent, to China, the Ryukyu Islands in southern Japan, south to Southeast Asia to Thailand, Malaysia, Brunei, Indonesia, the Philippines, New Guinea, Australia, and islands of the Indian Ocean and the South China Sea. They have also been introduced outside of their natural range, for instance, the West African Nile monitor is now found in South Florida.[11] Monitor lizards also occurred widely in Europe in the Neogene, with the last known remains in the region dating to the Middle Pleistocene.[12]

Habits and diet

Most monitor lizards are almost entirely carnivorous,[13] consuming prey as varied as insects, crustaceans, arachnids, myriapods, molluscs, fish, amphibians, reptiles, birds, and mammals. Most species feed on invertebrates as juveniles and shift to feeding on vertebrates as adults. Deer make up about 50% of the diet of adult Komodo dragons, the largest monitor species.[14] In contrast, three arboreal species from the Philippines, Varanus bitatawa, mabitang, and olivaceus, are primarily fruit eaters.[15] [16] [17]

Biology

Monitor lizards are considered unique among animals in that its members are relatively morphologically conservative, yet show a very large size range.[18] However, finer morphological features such as the shape of the skull and limbs do vary, and are strongly related to the ecology of each species.[19] [20]

Monitor lizards maintain large territories and employ active-pursuit hunting techniques that are reminiscent of similar-sized mammals.[21] The active nature of monitor lizards has led to numerous studies on the metabolic capacities of these lizards. The general consensus is that monitor lizards have the highest standard metabolic rates of all extant reptiles.[22]

Like snakes, monitor lizards have highly forked tongues that act as part of the "smell" sense, where the tips of the tongue carry molecules from the environment to sensory organs in the skull. The forked apparatus allows for these lizards to sense boundaries in the molecules they collect, almost smelling in "stereo".[23]

Monitor lizards have a high aerobic scope[24] that is afforded, in part, by their heart anatomy. Whereas most reptiles are considered to have three-chambered hearts, the hearts of monitor lizards – as with those of boas and pythons – have a well developed ventricular septum that completely separates the pulmonary and systemic sides of the circulatory system during systole.[25] This allows monitor lizards to create mammalian-equivalent pressure differentials between the pulmonary and systemic circuits, which in turn ensure that oxygenated blood is quickly distributed to the body without also flooding the lungs with high-pressure blood.

Monitor lizards are oviparous, laying from seven to 38 eggs,[26] which they often cover with soil or protect in a hollow tree stump. Some species, including the Komodo dragon, are capable of parthenogenesis.[27]

Venom

Anatomical and molecular studies indicate that all varanids (and possibly all lizards) are venomous.[28] [29] Unlike snakes, monitor lizard venom glands are situated in their lower jaw.[30] The venom of monitor lizards is diverse and complex, as a result of the diverse ecological niches monitor lizards occupy.[31]

For example, many species have anticoagulant venom, disrupting clotting through a combination of fibrinogenolysis and blocking platelet aggregation. Amongst them, arboreal species, such as the tree monitors and the banded monitor, have by far the strongest fibrinogenolytic venom. As a result, wounds from monitor lizard bites often bleed more than they would if they were simply lacerations. Venom may also cause hypotension.[32]

In some species such as the Komodo dragon and the desert monitor, venom also induces a powerful neurotoxic effect. In the latter species for instance, envenomation causes immediate paralysis in rodents (but not birds) and lesser effects of the same nature in humans.[33]

Intelligence

See also: Animal cognition.

At least some species of monitors are known to be able to count; studies feeding rock monitors varying numbers of snails showed that they can distinguish numbers up to six.[34] [35] Nile monitors have been observed to cooperate when foraging; one animal lures the female crocodile away from her nest, while the other opens the nest to feed on the eggs. The decoy then returns to also feed on the eggs.[34] [35] Komodo dragons at the National Zoo in Washington, DC, recognize their keepers and seem to have distinct personalities.[35] Blue and green tree monitors in British zoos have been observed shredding leaves, apparently as a form of play.[36]

Exploitation

As pets

Monitor lizards have become a staple in the reptile pet trade. The most commonly kept monitors are the savannah monitor and Ackie dwarf monitor, due to their relatively small size, low cost, and relatively calm dispositions with regular handling.[3] Among others, black-throated, Timor, Asian water, Nile, mangrove, emerald tree, black tree, roughneck, Dumeril's, peach-throated, crocodile, and Argus monitors have been kept in captivity.[3]

Traditional medicines

Monitor lizards are poached in some South- and Southeast Asian countries, as their organs and fat are used in some traditional medicines, although there is no scientific evidence as to their effectiveness.[37] [38]

Monitor lizard meat, particularly the tongue and liver, is eaten in parts of India and Malaysia and is supposed to be an aphrodisiac.[39] [40]

In parts of Pakistan and southern India, as well in Northeastern India, particularly Assam, the different parts of monitor lizards are traditionally used for treating rheumatic pain, skin infections and hemorrhoids, and the oil is used as an aphrodisiac lubricant (sande ka tel).[41]

Consuming raw blood and flesh of monitor lizards has been reported to cause eosinophilic meningoencephalitis, as some monitors are hosts for the parasite Angiostrongylus cantonensis.

Leather

"Large-scale exploitation" of monitor lizards is undertaken for their skins, which are described as being "of considerable utility" in the leather industry.[41] In Papua New Guinea, monitor lizard leather is used for membranes in traditional drums (called kundu), and these lizards are referred to as kundu palai or "drum lizard" in Tok Pisin, the main Papuan trade language. Monitor lizard skins are prized in making the resonant part of serjas (Bodo folk sarangis) and dotaras (native strummed string instruments of Assam, Bengal and other eastern states). The leather is also used in making a Carnatic music percussion instrument called the kanjira.

Food

The meat of monitor lizards is eaten by some tribes in India,[42] Nepal,[43] the Philippines, Australia, South Africa and West Africa as a supplemental meat source. Both meat and eggs are also eaten in Southeast Asian countries such as Vietnam and Thailand as a delicacy.[44]

Conservation

According to IUCN Red List of threatened species, most of the monitor lizards species fall in the categories of least concern, but the population is decreasing globally. All but five species of monitor lizards are classified by the Convention on International Trade in Endangered Species of Wild Fauna and Flora under Appendix II, which is loosely defined as species that are not necessarily threatened with extinction but may become so unless trade in such species is subject to strict regulation to avoid use incompatible with the survival of the species in the wild. The remaining five species – the Bengal, yellow, desert, and clouded monitors and the Komodo Dragon– are classified under CITES Appendix I, which outlaws international commercial trade in the species.[45]

The yellow monitor is protected in all countries in its range except Bhutan, Nepal, India, Pakistan, and Bangladesh.[46]

In Kerala, Andhra Pradesh, Karnataka, Telangana and all other parts of South India, catching or killing of monitor lizards is banned under the Protected Species Act.

Evolution

Varanus is the only living genus of the family Varanidae. Varanids last shared a common ancestor with their closest living relatives, earless "monitors", during the Late Cretaceous. The oldest known varanids are from the Late Cretaceous of Mongolia. During the Eocene, the varanid Saniwa occurred in North America. The closest known relative of Varanus is Archaeovaranus from the Eocene of China, suggesting that the genus Varanus is of Asian origin. The oldest fossils of Varanus date to the early Miocene.[47]

Many of the species within the various subgenera also form species complexes with each other:

Euprepriosaurus

Odatria

Varanus

Polydaedalus

Empagusia

Soterosaurus

The tree monitors of the V. prasinus species complex (V. prasinus, V. beccarii, V. boehmei, V. bogerti, V. keithhornei, V. kordensis, V. macraei, V. reisingeri, V. telenesetes) were once in the subgenus Euprepriosaurus, but as of 2016, form their own subgenus Hapturosaurus.[54]

V. jobiensis was once considered to be a member of the V. indicus species complex, but is now considered to represent its own species complex.

Taxonomy

Genus Varanus

Species marked with are extinct

Subgenus Empagusia:

Subgenus Euprepiosaurus:[60]

Subgenus Hapturosaurus:

Subgenus Odatria:

Subgenus Papusaurus

Subgenus Philippinosaurus:

Subgenus Polydaedalus:

Subgenus Psammosaurus:

Subgenus Solomonsaurus:[69]

Subgenus Soterosaurus:

Subgenus Varanus:

References

Further reading

External links

Notes and References

  1. Web site: 2023-05-23 . Monitor lizard Britannica . 2023-06-06 . www.britannica.com . en.
  2. Book: Cogger, H.G. . Zweifel, R.G. . Bauer, Aaron M. . 1998 . Encyclopedia of Reptiles and Amphibians . Academic Press . San Diego . 157–159 . 0-12-178560-2.
  3. Book: Robert George Sprackland . Giant lizards . T.F.H. Publications . Neptune, NJ . 1992 . 61 . 0-86622-634-6.
  4. https://books.google.com/ngrams/graph?content=monitory+lizard%2F%28monitory+lizard%2Bmonitor+lizard%29&year_start=1800&year_end=2000&corpus=15&smoothing=3&share=&direct_url=t1%3B%2C%28monitory%20lizard%20/%20%28monitory%20lizard%20%2B%20monitor%20lizard%29%29%3B%2Cc0 Google ngrams
  5. [Horatio Nelson]
  6. Book: Heinrich Zimmern . Akkadische Fremdwörter als Beweis für babylonischen Kultureinfluss . German . Thesis . Universität Leipzig . 1915 . 52 . 697605207.
  7. Web site:
    • bayawak: monitor lizard, Varanus spp. (esp. V. salvator)
    . Blust. Robert. Trussel. Stephen. Austronesian Comparative Dictionary. 2010. Max Planck Institute for Evolutionary Anthropology. January 30, 2022.
  8. Mark K. Bayless. 2004. The local names of Pacific monitor lizards (Sauria: Varanidae) of Oceania & Indo-Malaysia, excluding Australia. Micronesia. 37. 1. 49–55.
  9. . 1992. Taxonomy and biology of Philippine water monitors (Varanus salvator) . The Philippine Journal of Science. 121. 4. 345–381.
  10. Book: Kesteloot. Lilyan . Veirman. Anja. 1999. Histoire d'Afrique : les enjeux de mémoire. Un lieu de mémoire sans stèle et sans visite guidée : le culte du Mboose à Kaolack (Sénégal). https://archive.org/details/histoiredafrique0000unse/page/83/mode/1up. Paris. Karthala. 83-91. 9782865379040 . French.
  11. Yong . Ed . 20 April 2016 . Florida's Dragon Problem . The Atlantic . .
  12. L. Georgalis Georgios. Andrea. Villa. Massimo. Delfino. 4 March 2017. The last European varanid: demise and extinction of monitor lizards (Squamata, Varanidae) from Europe. Journal of Vertebrate Paleontology. 37. 2. e1301946. 10.1080/02724634.2017.1301946. 2017JVPal..37E1946G . 0272-4634. 2318/1635702. 90865661. free.
  13. Book: Pianka. Eric R.. King. Dennis R. King. Ruth Allen. Varanoid Lizards of the World. 2004. Indiana University Press. Bloomington, Indiana.
  14. Book: Auffenberg. Walter. The Behavioral Ecology of the Komodo Monitor. 1981. University Press of Florida.
  15. Book: Greene, Harry W. . Diet and Arboreality in the Emerald Monitor, Varanus Prasinus, with Comments on the Study of Adaptation . Field Museum of Natural History . Chicago . 1986 . 14915452 . 7155983M .
  16. Welton . L. J. . Siler . C. D. . Bennett . D. . Diesmos . A. . Duya . M. R. . Dugay. R.. Rico. E. L. B. . Van Weerd . M. . Brown. R. M.. A spectacular new Philippine monitor lizard reveals a hidden biogeographic boundary and a novel flagship species for conservation . Biology Letters . 6 . 5 . 2010 . 654–658 . 10.1098/rsbl.2010.0119 . 20375042 . 2936141.
  17. Struck. U. Altenbach. AV. Gaulke. M. F. Glaw. Tracing the diet of the monitor lizard Varanus mabitang by stable isotope analyses (d15N, d13C). Naturwissenschaften. 2002. 89. 10. 470–473. 10.1007/s00114-002-0361-8. 12384723. 12091969.
  18. Pianka, E.R. . Evolution of Body Size: Varanid Lizards as a Model System. The American Naturalist. 146. 3. 398–414. 10.1086/285806. 1995. 85237692.
  19. 10.1371/journal.pone.0130625. 26106889. The Relationship between Cranial Structure, Biomechanical Performance and Ecological Diversity in Varanoid Lizards. PLOS ONE. 10. 6. e0130625. 2015. McCurry. Matthew R.. Mahony. Michael. Clausen. Phillip D.. Quayle. Michelle R.. Walmsley. Christopher W.. Jessop. Tim S.. Wroe. Stephen. Richards. Heather. McHenry. Colin R.. 4479569. 2015PLoSO..1030625M. free.
  20. 10.1111/j.1469-7998.2009.00559.x. Evolutionary relationships of sprint speed in Australian varanid lizards. Journal of Zoology. 278. 4. 270–280. 2009. Clemente. C. J.. Thompson. G. G.. Withers. P. C.. free.
  21. King, D., Green, B., Knight, F. (1999). Monitors: The Biology of Varanid Lizards. Florida. Krieger Publishing Company.
  22. Pianka, E.R., Vitt, L.J. (2003). Lizards: Windows to the Evolution of Diversity. California. University of California Press.
  23. Sack . Jeffrey D. . 2022-08-01 . True Facts: Snake and Lizard Tongues . The American Biology Teacher . en . 84 . 6 . 378 . 10.1525/abt.2022.84.6.378 . 251407423 . 0002-7685. free .
  24. Wood SC, Johansen K, Glass ML, ((Maloiy GMO)) . Aerobic Metabolism of the Lizard Varanus exanthematicus: Effects of Activity, Temperature, and Size. Journal of Comparative Physiology B. 127. 4. 331–336. 10.1007/BF00738417. 1978. 19320799.
  25. Wang T, Altimiras J, Klein W, Axelsson M . Ventricular Haemodynamics in Python molurus: Separation of Pulmonary and Systemic Pressures. The Journal of Experimental Biology. 206. Pt 23. 4241–5. 14581594. 2003. 10.1242/jeb.00681 . free.
  26. https://indonesiaindonesia.com/f/37477-sejarah-pulau-komodo/ (in Indonesian)
  27. Smith . Kerri . 2006 . Dragon virgin births startle zoo keepers . Nature . 10.1038/news061218-7 . 191590714 . 2006-12-20 . free.
  28. Fry BG, Wroe S, Teeuwisse W, van Osch JP, Moreno K, Ingle J, McHenry C, Ferrara T, Clausen P, Scheib H, Winter KL, Greisman L, Roelants K, van der Weerd L, Clemente CJ, Giannakis E, Hodgson WC, Luz S, Martelli P, Krishnasamy K, Kochva E, Kwok HF, Scanlon D, Karas J, Citron DM, Goldstein EJ, Mcnaughtan JE, Norman JA . June 2009 . A central role for venom in predation by Varanus komodoensis (Komodo dragon) and the extinct giant Varanus (Megalania) priscus. . PNAS . 106 . 8969–8974 . 10.1073/pnas.0810883106 . 19451641 . 22 . 2690028. 2009PNAS..106.8969F . free .
  29. Fry BG, Vidal N, Norman JA, Vonk FJ, Scheib H, Ramjan SF, Kuruppu S, Fung K, Hedges B, Richardson MK, Hodgson WC, Ignjatovic V, Summerhays R, Kochva E . February 2006 . Early evolution of the venom system in lizards and snakes . Nature . 439 . 584–588 . 10.1038/nature04328 . 16292255 . 7076. 2006Natur.439..584F . 4386245 .
  30. Fry . Bryan G. . Wroe . Stephen . Teeuwisse . Wouter . van Osch . Matthias J. P. . Moreno . Karen . Ingle . Janette . McHenry . Colin . Ferrara . Toni . Clausen . Phillip . Scheib . Holger . Winter . Kelly L. . Greisman . Laura . Roelants . Kim . van der Weerd . Louise . Clemente . Christofer J. . 2009-06-02 . A central role for venom in predation by Varanus komodoensis (Komodo Dragon) and the extinct giant Varanus (Megalania) priscus . Proceedings of the National Academy of Sciences . en . 106 . 22 . 8969–8974 . 10.1073/pnas.0810883106 . 0027-8424 . 2690028 . 19451641 . 2009PNAS..106.8969F . free .
  31. Dobson. James S.. Zdenek. Christina N.. Hay. Chris. Violette. Aude. Fourmy. Rudy. Cochran. Chip. Fry. Bryan G.. May 2019. Varanid Lizard Venoms Disrupt the Clotting Ability of Human Fibrinogen through Destructive Cleavage. Toxins. en. 11. 5. 255. 10.3390/toxins11050255. 31067768. 6563220. free.
  32. Dobson . James S. . Zdenek . Christina N. . Hay . Chris . Violette . Aude . Fourmy . Rudy . Cochran . Chip . Fry . Bryan G. . 2019-05-07 . Varanid Lizard Venoms Disrupt the Clotting Ability of Human Fibrinogen through Destructive Cleavage . Toxins . en . 11 . 5 . 255 . 10.3390/toxins11050255 . 2072-6651 . 6563220 . 31067768 . free .
  33. Zima . Yuliya . December 2019 . On the Toxicity of the Bite of the Caspian Gray Monitor Lizard (Varanus griseus caspius) . Biawak . 13 . 2 . 115–118 . ResearchGate.
  34. King, Dennis & Green, Brian. 1999. Goannas: The Biology of Varanid Lizards. University of New South Wales Press., p. 43.
  35. Pianka, E.R.; King, D.R. and King, R.A. (2004). Varanoid Lizards of the World. Indiana University Press.
  36. Play behaviour by captive tree monitors, Varanus macraei and Varanus prasinus . Kane . D . Davis . AC . Michaels . C . Herpetological Bulletin . 149 . 28–31 . 2019 . 10.33256/hb149.2831. free .
  37. Web site: How Lizard Genitalia Became a Black Market Craze. https://web.archive.org/web/20210303205156/https://www.nationalgeographic.com/animals/article/wildlife-watch-india-monitor-lizard-poaching-plant-root-hatha-jodi. dead. March 3, 2021. . 7 July 2017.
  38. Web site: Visakhapatnam: Monsoon activates monitor lizard poaching. 4 July 2017.
  39. Case series of eosinophilic meningoencephalitis from South India . Parameswaran . K . Annals of Indian Academy of Neurology . 9 . 4 . 217–222 . 2006 . 10.4103/0972-2327.29203. free .
  40. http://themalaysianlife.blogspot.com/2009/04/eating-biawak.html Eating Biawak
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  42. News: Meats We Also Eat . https://web.archive.org/web/20180812181533/https://www.telegraphindia.com/1170108/jsp/7days/story_129083.jsp . dead . August 12, 2018 . The Telegraph India . 2017-01-08 . 2018-08-12 . en .
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  44. Web site: Eating a DINOSAUR in Asia!!! RARE Mekong Delta Food you will only find here!. https://ghostarchive.org/varchive/youtube/20211107/XOBq37xAsVc. 2021-11-07 . live. Sonny. Side. 5 June 2019. YouTube.
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  49. Böhme. Wolfgang. 2019-11-23. The Kei Islands Monitor Lizard (Squamata: Varanidae: Varanus: Euprepiosaurus) as a Distinct Morphological, Taxonomic, and Conservation Unit. Russian Journal of Herpetology. 26. 5. 272–280. 10.30906/1026-2296-2019-26-5-272-280. 213867767 .
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  51. Koch. Andre. 2010. Updated checklist of the living monitor lizards of the world (Squamata: Varanidae). Bonn Zoological Bulletin. 57. 127–136.
  52. Koch. Andre. 2010-05-06. Unravelling The Underestimated Diversity Of Philippine Water Monitor Lizards (Squamata: Varanus Salvator Complex), With The Description Of Two New Species And A New Subspecies. Zootaxa. 2446. 1–54. 10.11646/zootaxa.2446.1.1.
  53. Mendyk. Robert. 2018. An Annotated Bibliography of Captive Reproduction in Monitor Lizards (Varanidae: Varanus). Part III. Soterosaurus. Biawak. 12.
  54. Weijola. Valter. 2019-03-14. A molecular phylogeny for the Pacific monitor lizards (Varanus subgenus Euprepiosaurus) reveals a recent and rapid radiation with high levels of cryptic diversity. Zoological Journal of the Linnean Society. 186. 4. 1053–1066. 10.1093/zoolinnean/zlz002.
  55. Brennan. Ian G.. Lemmon. Alan R.. Lemmon. Emily Moriarty. Portik. Daniel M.. Weijola. Valter. Welton. Luke. Donnellan. Stephen C.. Keogh. J. Scott. 2020-02-03. Phylogenomics of monitor lizards and the role of competition in dictating body size disparity. bioRxiv. en. 2020.02.02.931188. 10.1101/2020.02.02.931188. 211297088.
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