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]
Varanus panoptes rubidus Storr, 1980.[7] The holotype of this subspecies was obtained near Cue, Western Australia, at the midwest of the continent, and the population is endemic to the north and west of that state.[6] (rubidus referring to its reddish coloration)
Varanus panoptes horni, Böhme, 1988. A population that discovered in southern New Guinea that was recognised as having a close affinity to the description of this species.[6] It is also known as Horn's monitor.[1]
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]
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's 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.
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, it 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]
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.[12]
Recent studies suggest that the infestation of cane toads, a novel and toxic species, has severely damaged the population structure of Argus monitors within the Top End. It is estimated that numbers have dropped by as much as 90% in many areas.[13] 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.[14]
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.
^ abAustralian 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.
Akeret, B. 2006. Bau einer Großterrarienanlage für Warane und Hornvipern. Draco 7 (26): 38-
Anonymous 2000. Hydrosaurus gouldii Gray, 1838 (currently Varanus gouldii) and Varanus panoptes Storr, 1980 (Reptilia, Squamata): specific names conserved by the designation of a neotype for H. gouldii. Bull. Zool. Nomenclature 57 (1): 63-65
Böhme, W. 1988. Der Arguswaran (Varanus panoptes, Storr 1980) auf Neuguinea: Varanus panoptes horni spp. n. Salamandra 24 (2/3): 87-101.
Böhme,W. 2003. Checklist of the living monitor lizards of the world (family Varanidae). Zool. Verhand., Leiden 341: 6-43
Böhme,W. & T. ZIEGLER 1998. Comments 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 (Case 3042; see BZN 54: 95-99, 249-250; 55: 106-111). Bull. Zool. Nomenclature 55 (3): 173-174.
Cogger, H.G. (2000). Reptiles and Amphibians of Australia, 6th ed. Ralph Curtis Publishing, Sanibel Island, 808 pp.
Lenk, P.; Eidenmueller, B.; Staudter, H.; Wicker, R.; Wink, M. 2005. A parthenogenetic Varanus. Amphibia-Reptilia 26 (4): 507-514
Packard, Gary C. and THOMAS J. BOARDMAN 2009. Bias in interspecic allometry: examples from morphological scaling in varanid lizards. Biological Journal of the Linnean Society, (2009), 96, 296–305.
Schardt, M. (2000). Aktuelle Übersicht zur Nomenklatur der australischen "Gouldswarane" sowie Angaben zur Haltung und Nachzucht von Varanus panoptes panoptes Storr, (1980). Herpetofauna 22 (129): 22-32
Sprackland R G.; Smith H M. & Strimple P D. 1997. Hydrosaurus gouldii Gray, 1838 (currently Varanus gouldii) and Varanus panoptes Storr, 1980 (Reptilia, Squamata): Proposed conservation of the specific names by the designation of a neotype for H. gouldii. Bulletin of Zoological Nomenclature 54 (2): 95-99.
