Yellow-spotted monitor

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Yellow-spotted monitor
Varanus panoptes panoptes, Middleton QLD 4735, Australia imported from iNaturalist photo 87988921.jpg
V. p. panoptes in Queensland, Australia
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Squamata
Family: Varanidae
Genus: Varanus
Subgenus: Varanus
Species:
V. panoptes
Binomial name
Varanus panoptes
Storr, 1980
Subspecies
  • V. p. panoptes
  • V. p. rubidus
  • V. p. horni

The yellow-spotted monitor [1] [2] [3] (Varanus panoptes), also known as the Argus monitor, [4] is a monitor lizard found in northern and western regions of Australia and southern New Guinea. [1] [2]

Contents

Taxonomy

V. p. rubidus, Western Australia Western Argus Monitor, Karijini WA 6751, Australia imported from iNaturalist photo 149135082 (cropped).jpg
V. p. rubidus, Western Australia

The first description of the species was provided in a revision of the varanids of Western Australia, where the family is represented by diverse taxa in a wide variety of habitats. Early collections and descriptions of the region's species have historically been uncertain, leading the ICZN to issue an opinion that related to this taxon. [5] A third subspecies was published in 1988, based on specimens from southern New Guinea. The describing author discovered that the specimen selected as the type of Varanus gouldii was in fact assignable to this species, recently described by reptile specialist Glenn Storr. By issuing an opinion on the various taxonomic considerations, the voting members conserved the name published with John Edward Gray's description and stabilised the nomenclature of this species name. [6]

The epithet panoptes was inspired by a mythological figure with one hundred eyes, the protector of Princess Io named Argus Panoptes. [7] The species may be referred to as the floodplains goanna in the northern regions of Australia. [6]

Subspecies

Three subspecies are recognised by the Australian Faunal Directory [3] and the Reptile Database: [2]

Description

Varanus panoptes (15848624016) 2.jpg
Juvenile V. p. panoptes
Varanus panoptes panoptes 300544375.jpg
Adult V. p. panoptes
Yellow-spotted monitor (left), lace monitor (right) Argus Monitor and Lace Monitor.jpg
Yellow-spotted monitor (left), lace monitor (right)

This ground dwelling monitor species, somewhat resembles the widespread sand goanna (Varanus gouldii). Large, dark spots appear in rows along its back, becoming especially distinct at the center of the back where they are interspersed with smaller and paler spots. Bands of color occur toward the tip of the tail. The overall coloration is brownish in the nominate subspecies, V. panoptes panoptes, and reddish in V. panoptes rubidus. [7]

The Argus monitor displays great sexual dimorphism, with the female reaching an average total length of three feet (90 cm), while the male reaches an average of 4–5 feet (120–150 cm). [9] The largest specimens can have a length in 1.6 m (5 ft 3 in) and a mass in 7 kg (15 lb). [10] [11] It is the third largest lizard in Australia, after perentie and lace monitor. The larger subspecies is V. panoptes panoptes and the smaller one is V. panoptes horni. It is a reasonably lean monitor and does not put on the bulk that other monitors in Africa and Asia do. Most Argus monitors are yellow in colour, with a background of brown or dark tan, but their colour often varies on an individual basis or on their place of origin.[ citation needed ]

Life cycle and reproduction

Argus monitors have an unusually "fast" life cycle compared to other monitors. Large-bodied monitors usually take 2 or more years to mature, but Argus monitors may mature in less than 1 year (though this varies among populations). Males grow faster than females and also live longer; in the Kimberley, male monitors have a mean age of 465 days versus 263 days for females. [12]

In Arnhem Land, they lay 6 to 13 eggs between January and February. [8] Due to similar genetic structures, the Argus monitor is able to naturally hybridise with the Gould's monitor with a stable hybrid zone.[ citation needed ]

Behavior

Yellow-spotted monitor "tripod" stance Monitor1.jpg
Yellow-spotted monitor "tripod" stance

Argus monitors are versatile predators and inhabits a large variety of biomes and habitats. They are primarily terrestrial, meaning they spend a great deal of time on the ground. This species is an avid digger and will dig large burrows or take over an already existing burrow, where they spend a sizable portion of their time. Despite this, they will eagerly forage in trees and in the water. These large lizards are quite fast and will run up to 100 meters (330 ft) away to the nearest tree or burrow when they are chased. They are riparian in habits and as such, can usually be found around a permanent source of water. Argus monitors will often "tripod", raising up on their hind legs and supporting themselves with their tail. This unusual behavior is used to spot potential prey or enemies from a distance or when they are threatened. They exhibit this behavior regularly in captivity as well. This habit provides them a unique characteristic that separates them from most other monitors.[ citation needed ]

V. p. panoptes feeding on a road-killed kangaroo. Eastern Argus Monitor, Corfield QLD 4733, Australia imported from iNaturalist photo 87993092.jpg
V. p. panoptes feeding on a road-killed kangaroo.

Its prey consists of almost anything that it can overpower. This includes fish, crabs, small birds, rodents, insects and even other monitors. They hunt for prey by keying in on movement, chasing it down and overpowering it. In captivity, this monitor has been observed swinging rodent prey around rapidly by the tail in what appears to be an attempt to stun the animal, before biting at the prey's neck. Argus monitors frequently prey on the dwarf monitors that it shares its range with. Spiny-tailed goannas and Kimberley rock monitors are eaten regularly. Argus monitors have great senses, with smell being the most acute. Like all monitors, they have a forked tongue and a vomeronasal organ in the roof of its mouth. It uses this organ in the same manner as snakes and other monitor species do and can often be seen flicking their tongues in search of a meal.[ citation needed ]

Argus monitors have also been recorded diving underwater to forage for freshwater Velesunio mussels, during the dry season when terrestrial food is scarce. [13]

Recent studies suggest that the infestation of cane toads, a novel and toxic species, has severely damaged the population structure of yellow-spotted monitors within the Top End. It is estimated that numbers have dropped by as much as 90% in many areas. [14] Yellow-spotted monitors are more vulnerable to cane toads than similar-sized lace monitors, because the former are "risky" foragers that more readily consume novel prey such as cane toads. [12] It appears they can be taught to avoid cane toads if exposed to toads that are too young to be lethal if ingested. In experimental areas where 200,000 total cane toad eggs, tadpoles, and metamorphs were introduced ahead of an inevitable invasion front, substantial populations of monitors persisted following invasion by wild toads. In control areas where "teacher toads" were not introduced, yellow-spotted monitor populations crashed. [15]

Ecology

V. p. panoptes climbing a tree Varanus panoptes panoptes 327589086.jpg
V. p. panoptes climbing a tree

Varanus panoptes is an ecosystem engineer. The high abundance, high feeding rate and generalist diet of this species make it an important predator in the ecosystem. [12] The species consumes more prey than co-occurring predators such as dingoes or black kites, because while these predators consume more on an individual basis, monitor population densities are far higher (25 monitors/km2, versus 0.15 dingoes/km2 or 0.2 kites/km2). [12] Toad-induced declines in Argus monitor populations result in increases in populations of their prey, such as common tree snakes ( Dendrelaphis punctulatus ) becoming 26–46 times more abundant (though this may include toad impacts on other monitor species as well). [16] Additionally, the burrows dug by these monitors are used by other species of animals. [12]

Argus monitors are themselves preyed on by black-headed pythons (Aspidites melanocephalus) and olive pythons (Lialis olivaceus). [12]

In captivity

At the Cincinnati Zoo ArgusMonitorCincinnati.jpg
At the Cincinnati Zoo

Many individuals of this species are captive bred as a conservation effort against poisoning from the cane toad infestation of the species’ native range and as exotic pets. Argus monitors are fed insects, fish and mice. Argus monitors are husky lizards that can be a challenge to physically handle, do not like to be restrained, and can use their sharp claws in their attempts to squirm free. If left to wander freely on open ground, their ability to suddenly flee makes escape likely. [4] Argus monitors prefer to bask each morning and return to bask as needed to maintain optimal body temperatures at 80 to 90 °F (26.7 to 32.2 °C). Night-time temperatures may drop 20 °F (11.1 °C) or more if the opportunity to warm up the next day exists.

References

  1. 1 2 3 4 Shea, G.; Allison, A.; Parker, F.; Tallowin, O.; Doughty, P. (2018). "Varanus panoptes". IUCN Red List of Threatened Species . 2018: e.T42485740A42485745. doi: 10.2305/IUCN.UK.2018-1.RLTS.T42485740A42485745.en . Retrieved 19 November 2021.
  2. 1 2 3 Varanus panoptes at the Reptarium.cz Reptile Database. Accessed 8 December 2020.
  3. 1 2 Australian Biological Resources Study (16 August 2012). "Subspecies Varanus panoptes Storr, 1980". Australian Faunal Directory. Canberra, Australian Capital Territory: Department of the Environment, Water, Heritage and the Arts, Australian Government. Retrieved 11 July 2019.
  4. 1 2 Burokas, Justin (14 March 2012). "An Owner's Guide To The Argus Monitor". Reptiles Magazine. Retrieved 3 September 2017.
  5. Shea, G.M.; Cogger, H.G. (1998). "Comment On The Proposed Conservation Of The Names Hydrosaurus gouldii Gray, 1838 and Varanus panoptes Storr, 1980 (Reptilia, Squamata) By The Designation Of A Neotype For Hydrosaurus gouldii". The Bulletin of Zoological Nomenclature. 55: 106–111. doi: 10.5962/bhl.part.159 .
  6. 1 2 3 4 5 Pianka, E.R.; King, D.; King, R.A. (2004). Varanoid Lizards of the World. Indiana University Press. pp. 423, 428. ISBN   9780253343666.
  7. 1 2 3 4 Storr, G.M. (1980). "The monitor lizards (genus Varanus Merrem, 1820) of Western Australia". Records of the Western Australian Museum. 8 (2): 237–293.
  8. 1 2 Ehmann, Harald. (1992). Encyclopedia of Australian Animals: Reptiles, p. 152. Angus&Robertson. Pymble, Sydney, Australia. ISBN   0-207-17379-6
  9. "Argus Monitor". Reptile Range. Retrieved 11 August 2022.
  10. "Visual Identification Guide for the Monitor Lizard Species of the World (Genus Varanus)" (PDF). Bfn.de.
  11. Pianka, E.; King, D.; King, R.A., eds. (2004). Varanoid Lizards of the World. Indiana University Press. ISBN   9780253343666.
  12. 1 2 3 4 5 6 Ward-Fear, Georgia; Brown, Gregory P.; Pettit, Lachlan; Rollins, Lee-Ann; Shine, Richard (2024). "Live Fast, Die Young: Life History Traits of an Apex Predator Exacerbate the Ecological Impact of a Toxic Invader". Ecology and Evolution. 14 (12): e70625. doi:10.1002/ece3.70625. ISSN   2045-7758. PMC   11606729 . PMID   39619789.
  13. Shannon, Rod; Mendyk, Robert (2009). "Aquatic Foraging Behavior and Freshwater Mussel (Velesunio sp.) Predation by Varanus panoptes panoptes in Central-Western Queensland". BIAWAK. 3 (3): 85–87.
  14. "Reptile watch". Australian Broadcasting Corporation . 2010-10-15.
  15. Ward-Fear, Georgia; Rangers, Bunuba; Bruny, Miles; Everitt, Corrin; Shine, Richard (2024-04-08). "Teacher toads: Buffering apex predators from toxic invaders in a remote tropical landscape". Conservation Letters. doi: 10.1111/conl.13012 . ISSN   1755-263X.
  16. Doody, J. Sean; Castellano, Christina M.; Rhind, David; Green, Brian (2013). "Indirect facilitation of a native mesopredator by an invasive species: are cane toads re-shaping tropical riparian communities?". Biological Invasions. 15 (3): 559–568. doi:10.1007/s10530-012-0308-8. ISSN   1387-3547.

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