Lizard

For other uses, see Lizard (disambiguation).

Lizards are a widespread group of squamate reptiles, with over 7,000 species,^[1] ranging across all continents except Antarctica, as well as most oceanic island chains. The group is paraphyletic since it excludes the snakes and Amphisbaenia although some lizards are more closely related to these two excluded groups than they are to other lizards. Lizards range in size from chameleons and geckos a few centimeters long to the 3-meter-long Komodo dragon.

Lizards Temporal range: Late Triassic – Holocene, 202–0 Ma PreꞒ Ꞓ O S D C P T J K Pg N
Clockwise from top left: veiled chameleon (Chamaeleo calyptratus), rock monitor (Varanus albigularis), common blue-tongued skink (Tiliqua scincoides), Italian wall lizard (Podarcis sicula), giant leaf-tailed gecko (Uroplatus fimbriatus), and legless lizard (Anelytropsis papillosus)
Scientific classification
Kingdom:	Animalia
Phylum:	Chordata
Class:	Reptilia
Superorder:	Lepidosauria
Order:	Squamata
Groups included
Anguimorpha Dibamidae Gekkota Iguania Lacertoidea Scincomorpha
Range of the lizards, all species.
Cladistically included but traditionally excluded taxa
Serpentes Amphisbaenia †Mosasauroidea
Synonyms
Sauria Macartney, 1802

Most lizards are quadrupedal, running with a strong side-to-side motion. Some lineages (known as "legless lizards"), have secondarily lost their legs, and have long snake-like bodies. Some such as the forest-dwelling Draco lizards are able to glide. They are often territorial, the males fighting off other males and signalling, often with bright colours, to attract mates and to intimidate rivals. Lizards are mainly carnivorous, often being sit-and-wait predators; many smaller species eat insects, while the Komodo eats mammals as big as water buffalo.

Lizards make use of a variety of antipredator adaptations, including venom, camouflage, reflex bleeding, and the ability to sacrifice and regrow their tails.

Anatomy

Largest and smallest

The adult length of species within the suborder ranges from a few centimeters for chameleons such as Brookesia micra and geckos such as Sphaerodactylus ariasae^[2] to nearly 3 m (10 ft) in the case of the largest living varanid lizard, the Komodo dragon.^[3] Most lizards are fairly small animals.

Distinguishing features

 

Skin of Lacerta agilis, showing overlapping scales made of keratin

 

A young Mediterranean house gecko in the process of moulting.

Lizards typically have rounded torsos, elevated heads on short necks, four limbs and long tails, although some are legless.^[4] Lizards and snakes share a movable quadrate bone, distinguishing them from the rhynchocephalians, which have more rigid diapsid skulls.^[5] Some lizards such as chameleons have prehensile tails, assisting them in climbing among vegetation.^[6]

As in other reptiles, the skin of lizards is covered in overlapping scales made of keratin. This provides protection from the environment and reduces water loss through evaporation. This adaptation enables lizards to thrive in some of the driest deserts on earth. The skin is tough and leathery, and is shed (sloughed) as the animal grows. Unlike snakes which shed the skin in a single piece, lizards slough their skin in several pieces. The scales may be modified into spines for display or protection, and some species have bone osteoderms underneath the scales.^[6][7]

 

Red tegu (Tupinambis rufescens) skull, showing teeth of differing types

The dentitions of lizards reflect their wide range of diets, including carnivorous, insectivorous, omnivorous, herbivorous, nectivorous, and molluscivorous. Species typically have uniform teeth suited to their diet, but several species have variable teeth, such as cutting teeth in the front of the jaws and crushing teeth in the rear. Most species are pleurodont, though agamids and chameleons are acrodont.^[8][6]

The tongue can be extended outside the mouth, and is often long. In the beaded lizards, whiptails and monitor lizards, the tongue is forked and used mainly or exclusively to sense the environment, continually flicking out to sample the environment, and back to transfer molecules to the vomeronasal organ responsible for chemosensation, analogous to but different from smell or taste. In geckos, the tongue is used to lick the eyes clean: they have no eyelids. Chameleons have very long sticky tongues which can be extended rapidly to catch their insect prey.^[6]

Three lineages, the geckos, anoles, and chameleons, have modified the scales under their toes to form adhesive pads, highly prominent in the first two groups. The pads are composed of millions of tiny setae (hair-like structures) which fit closely to the substrate to adhere using van der Waals forces; no liquid adhesive is needed.^[9] In addition, the toes of chameleons are divided into two opposed groups on each foot (zygodactyly), enabling them to perch on branches as birds do.^[a][6]

Physiology

Locomotion

 

Adhesive pads enable geckos to climb vertically.

Aside from legless lizards, most lizards are quadrupedal and move using gaits with alternating movement of the right and left limbs with substantial body bending. This body bending prevents significant respiration during movement, limiting their endurance, in a mechanism called Carrier's constraint. Several species can run bipedally,^[10] and a few can prop themselves up on their hindlimbs and tail while stationary. Several small species such as those in the genus Draco can glide: some can attain a distance of 60 metres (200 feet), losing 10 metres (33 feet) in height.^[11] Some species, like geckos and chameleons, adhere to vertical surfaces including glass and ceilings.^[9] Some species, like the common basilisk, can run across water.^[12]

Senses

Lizards make use of their senses of sight, touch, olfaction and hearing like other vertebrates. The balance of these varies with the habitat of different species; for instance, skinks that live largely covered by loose soil rely heavily on olfaction and touch, while geckos depend largely on acute vision for their ability to hunt and to evaluate the distance to their prey before striking. Monitor lizards have acute vision, hearing, and olfactory senses. Some lizards make unusual use of their sense organs: chameleons can steer their eyes in different directions, sometimes providing non-overlapping fields of view, such as forwards and backwards at once. Lizards lack external ears, having instead a circular opening in which the tympanic membrane (eardrum) can be seen. Many species rely on hearing for early warning of predators, and flee at the slightest sound.^[13]

 

Nile monitor using its tongue for smell

As in snakes and many mammals, all lizards have a specialised olfactory system, the vomeronasal organ, used to detect pheromones. Monitor lizards transfer scent from the tip of their tongue to the organ; the tongue is used only for this information-gathering purpose, and is not involved in manipulating food.^[14][13]

 

Skeleton of bearded dragon (pogona sp.) on display at the Museum of Osteology.

Some lizards, particularly iguanas, have retained a photosensory organ on the top of their heads called the parietal eye, a basal ("primitive") feature also present in the tuatara. This "eye" has only a rudimentary retina and lens and cannot form images, but is sensitive to changes in light and dark and can detect movement. This helps them detect predators stalking it from above.^[15]

Venom

 

Some lizards including the gila monster are venomous.

Further information: Evolution of snake venom

Until 2006 it was thought that the Gila monster and the Mexican beaded lizard were the only venomous lizards. However, several species of monitor lizards, including the Komodo dragon, produce powerful venom in their oral glands. Lace monitor venom, for instance, causes swift loss of consciousness and extensive bleeding through its pharmacological effects, both lowering blood pressure and preventing blood clotting. Nine classes of toxin known from snakes are produced by lizards. The range of actions provides the potential for new medicinal drugs based on lizard venom proteins.^[16][17]

Genes associated with venom toxins have been found in the salivary glands on a wide range of lizards, including species traditionally thought of as non-venomous, such as iguanas and bearded dragons. This suggests that these genes evolved in the common ancestor of lizards and snakes, some 200 million years ago (forming a single clade, the Toxicofera).^[16] However, most of these putative venom genes were "housekeeping genes" found in all cells and tissues, including skin and cloacal scent glands. The genes in question may thus be evolutionary precursors of venom genes.^[18]

Respiration

Recent studies (2013 and 2014) on the lung anatomy of the savannah monitor and green iguana found them to have a unidirectional airflow system, which involves the air moving in a loop through the lungs when breathing. This was previously thought to only exist in the archosaurs (crocodilians and birds). This may be evidence that unidirectional airflow is an ancestral trait in diapsids.^[19][20]

Reproduction and lifecycle

 

Trachylepis maculilabris skinks mating

As with all amniotes, lizards rely on internal fertilisation and copulation involves the male inserting one of his hemipenes into the female's cloaca.^[21] The majority of species are oviparous (egg laying). The female deposits the eggs in a protective structure like a nest or crevice or simply on the ground.^[22] Depending on the species, clutch size can vary from 4–5 percent of the females body weight to 40–50 percent and clutches range from one or a few large eggs to dozens of small ones.^[23]

 

Two pictures of an eastern fence lizard egg layered onto one image.

In most lizards, the eggs have leathery shells to allow for the exchange of water, although more arid-living species have calcified shells to retain water. Inside the eggs, the embryos use nutrients from the yolk. Parental care is uncommon and the female usually abandons the eggs after laying them. Brooding and protection of eggs does occur in some species. The female prairie skink uses respiratory water loss to maintain the humidity of the eggs which facilitates embryonic development. In lace monitors, the young hatch close to 300 days, and the female returns to help them escape the termite mound where the eggs were laid.^[22]

Around 20 percent of lizard species reproduce via viviparity (live birth). This is particularly common in Anguimorphs. Viviparous species give birth to relatively developed young which look like miniature adults. Embryos are nourished via a placenta-like structure.^[24] A minority of lizards have parthenogenesis (reproduction from unfertilised eggs). These species consist of all females who reproduce asexually with no need for males. This is known in occur in various species of whiptail lizards.^[25] Parthenogenesis was also recorded in species that normally reproduce sexually. A captive female Komodo dragon produced a clutch of eggs, despite being separated from males for over two years.^[26]

Sex determination in lizards can be temperature-dependent. The temperature of the eggs' micro-environment can determine the sex of the hatched young: low temperature incubation produces more females while higher temperatures produce more males. However, some lizards have sex chromosomes and both male heterogamety (XY and XXY) and female heterogamety (ZW) occur.^[25]

Behaviour

Diurnality and thermoregulation

The majority of lizard species are active during the day,^[27] though some are active at night, notably geckos. As ectotherms, lizards have a limited ability to regulate their body temperature, and must seek out and bask in sunlight to gain enough heat to become fully active.^[28] Thermoregulation behavior can be beneficial in the short term for lizards as it allows the ability to buffer environmental variation and endure climate warming.^[29]

In high altitudes, the Podarcis hispaniscus responds to higher temperature with a darker dorsal coloration to prevent UV-radiation and background matching. Their thermoregulatory mechanisms also allow the lizard to maintain their ideal body temperature for optimal mobility.^[30]

Territoriality

 

Fighting male sand lizards

Most social interactions among lizards are between breeding individuals.^[27] Territoriality is common and is correlated with species that use sit-and-wait hunting strategies. Males establish and maintain territories that contain resources which attract females and which they defend from other males. Important resources include basking, feeding, and nesting sites as well as refuges from predators. The habitat of a species affects the structure of territories, for example, rock lizards have territories atop rocky outcrops.^[31] Some species may aggregate in groups, enhancing vigilance and lessening the risk of predation for individuals, particularly for juveniles.^[32] Agonistic behaviour typically occurs between sexually mature males over territory or mates and may involve displays, posturing, chasing, grappling and biting.^[31]

Communication

Main article: Lizard communication

 

A green anole (Anolis carolinensis) signalling with its extended dewlap

Lizards signal both to attract mates and to intimidate rivals. Visual displays include body postures and inflation, push-ups, bright colours, mouth gapings and tail waggings. Male anoles and iguanas have dewlaps or skin flaps which come in various sizes, colours and patterns and the expansion of the dewlap as well as head-bobs and body movements add to the visual signals.^[33][6] Some species have deep blue dewlaps and communicate with ultraviolet signals.^[27] Blue-tongued skinks will flash their tongues as a threat display.^[34] Chameleons are known to change their complex colour patterns when communicating, particularly during agonistic encounters. They tend to show brighter colours when displaying aggression^[35] and darker colours when they submit or "give up".^[36]

Several gecko species are brightly coloured; some species tilt their bodies to display their coloration. In certain species, brightly coloured males turn dull when not in the presence of rivals or females. While it is usually males that display, in some species females also use such communication. In the bronze anole, head-bobs are a common form of communication among females, the speed and frequency varying with age and territorial status. Chemical cues or pheromones are also important in communication. Males typically direct signals at rivals, while females direct them at potential mates. Lizards may be able to recognise individuals of the same species by their scent.^[33]

 

Tokay gecko mating call

Mating call of a male Tokay gecko

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Acoustic communication is less common in lizards. Hissing, a typical reptilian sound, is mostly produced by larger species as part of a threat display, accompanying gaping jaws. Some groups, particularly geckos, snake-lizards, and some iguanids, can produce more complex sounds and vocal apparatuses have independently evolved in different groups. These sounds are used for courtship, territorial defense and in distress, and include clicks, squeaks, barks and growls. The mating call of the male tokay gecko is heard as "tokay-tokay!".^[34][33][37] Tactile communication involves individuals rubbing against each other, either in courtship or in aggression.^[33] Some chameleon species communicate with one another by vibrating the substrate that they are standing on, such as a tree branch or leaf.^[38]

Ecology

 

Lizard in tree. Many species are tree-dwelling

 

A lizard from Thar desert

Distribution and habitat

Lizards are found worldwide, excluding the far north and Antarctica, and some islands. They can be found in elevations from sea level to 5,000 m (16,000 ft). They prefer warmer, tropical climates but are adaptable and can live in all but the most extreme environments. Lizards also exploit a number of habitats; most primarily live on the ground, but others may live in rocks, on trees, underground and even in water. The marine iguana is adapted for life in the sea.^[6]

Diet

 

Western green lizard ambushes its grasshopper prey.

The majority of lizard species are predatory and the most common prey items are small, terrestrial invertebrates, particularly insects.^[6][39] Many species are sit-and-wait predators though others may be more active foragers.^[40] Chameleons prey on numerous insect species, such as beetles, grasshoppers and winged termites as well as spiders. They rely on persistence and ambush to capture these prey. An individual perches on a branch and stays perfectly still, with only its eyes moving. When an insect lands, the chameleon focuses its eyes on the target and slowly moves towards it before projecting its long sticky tongue which, when hauled back, brings the attach prey with it. Geckos feed on crickets, beetles, termites and moths.^[6][39]

Termites are an important part of the diets of some species of Autarchoglossa, since, as social insects, they can be found in large numbers in one spot. Ants may form a prominent part of the diet of some lizards, particularly among the lacertas.^[6][39] Horned lizards are also well known for specializing on ants. Due to their small size and indigestible chitin, ants must be consumed in large amounts, and ant-eating lizards have larger stomachs than even herbivorous ones.^[41] Species of skink and alligator lizards eat snails and their power jaws and molar-like teeth are adapted for breaking the shells.^[6][39]

 

Young Komodo dragon feeding on a water buffalo carcass

 

Marine iguana foraging under water at Galápagos Islands, Ecuador.

Larger species, such as monitor lizards, can feed on larger prey including fish, frogs, birds, mammals and other reptiles. Prey may be swallowed whole and torn into smaller pieces. Both bird and reptile eggs may also be consumed as well. Gila monsters and beaded lizards climb trees to reach both the eggs and young of birds. Despite being venomous, these species rely on their strong jaws to kill prey. Mammalian prey typically consists of rodents and leporids; the Komodo dragon can kill prey as large as water buffalo. Dragons are prolific scavengers, and a single decaying carcass can attract several from 2 km (1.2 mi) away. A 50 kg (110 lb) dragon is capable of consuming a 31 kg (68 lb) carcass in 17 minutes.^[39]

Around 2 percent of lizard species, including many iguanids, are herbivores. Adults of these species eat plant parts like flowers, leaves, stems and fruit, while juveniles eat more insects. Plant parts can be hard to digest, and, as they get closer to adulthood, juvenile iguanas eat faeces from adults to acquire the microflora necessary for their transition to a plant-based diet. Perhaps the most herbivorous species is the marine iguana which dives 15 m (49 ft) to forage for algae, kelp and other marine plants. Some non-herbivorous species supplement their insect diet with fruit, which is easily digested.^[6][39]

Antipredator adaptations

 

The frilled-neck lizard with fully extended frill. The frilled serves to make it look bigger than it actually is.

Main article: Antipredator adaptation

Lizards have a variety of antipredator adaptations, including running and climbing, venom, camouflage, tail autotomy, and reflex bleeding.

Camouflage

 

The flat-tail horned lizard's body is flattened and fringed to minimise its shadow.

Lizards exploit a variety of different camouflage methods. Many lizards are disruptively patterned. In some species, such as Aegean wall lizards, individuals vary in colour, and select rocks which best match their own colour to minimise the risk of being detected by predators.^[42] The Moorish gecko is able to change colour for camouflage: when a light-coloured gecko is placed on a dark surface, it darkens within an hour to match the environment.^[43] The chameleons in general use their ability to change their coloration for signalling rather than camouflage, but some species such as Smith's dwarf chameleon do use active colour change for camouflage purposes.^[44]

The flat-tail horned lizard's body is coloured like its desert background, and is flattened and fringed with white scales to minimise its shadow.^[45]

Autotomy

A skink tail continuing to move after autotomy

Many lizards, including geckos and skinks, are capable of shedding their tails (autotomy). The detached tail, sometimes brilliantly coloured, continues to writhe after detaching, distracting the predator's attention from the fleeing prey. Lizards partially regenerate their tails over a period of weeks. Some 326 genes are involved in regenerating lizard tails.^[46] The fish-scale gecko Geckolepis megalepis sheds patches of skin and scales if grabbed.^[47]

Escape, playing dead, reflex bleeding

Many lizards attempt to escape from danger by running to a place of safety;^[48][b] for example, wall lizards can run up walls and hide in holes or cracks.^[9] Horned lizards adopt differing defences for specific predators. They may play dead to deceive a predator that has caught them; attempt to outrun the rattlesnake, which does not pursue prey; but stay still, relying on their cryptic coloration, for Masticophis whip snakes which can catch even swift prey. If caught, some species such as the greater short-horned lizard puff themselves up, making their bodies hard for a narrow-mouthed predator like a whip snake to swallow. Finally, horned lizards can squirt blood at cat and dog predators from a pouch beneath its eyes, to a distance of about two metres (6.6 feet); the blood tastes foul to these attackers.^[50]

Evolution

Fossil history

 

Fossil lizard Dalinghosaurus longidigitus, Early Cretaceous, China

The closest living relatives of lizards are rhynchocephalians, a once diverse order of reptiles, of which is there is now only one living species, the tuatara of New Zealand. Some reptiles from the Early and Middle Triassic, like Sophineta and Megachirella, are suggested to be stem-group squamates, more closely related to modern lizards than rhynchocephalians, however, their position is disputed, with some studies recovering them as less closely related to squamates than rhynchocephalians are.^[51] In 2022 Cryptovaranoides from the Late Triassic was described and was suggested to the oldest known crown group lizard by 35 million years, as previously described undisputed lizards are unknown until the Middle Jurassic.^[52] Middle Jurassic lizards include representatives of modern clades like Scincomorpha.^[53] Lizard morphological and ecological diversity substantially increased over the course of the Cretaceous.^[54]

Mosasaurs likely evolved from an extinct group of aquatic lizards^[55] known as aigialosaurs in the Early Cretaceous. Dolichosauridae is a family of Late Cretaceous aquatic varanoid lizards closely related to the mosasaurs.^[56][57]

Phylogeny

External

The position of the lizards and other Squamata among the reptiles was studied using fossil evidence by Rainer Schoch and Hans-Dieter Sues in 2015. Lizards form about 60% of the extant non-avian reptiles.^[58]

Archelosauria	Archosauromorpha   Lepidosauromorpha †Kuehneosauridae  Lepidosauria Squamata  Rhynchocephalia  Pantestudines

Internal

Both the snakes and the Amphisbaenia (worm lizards) are clades deep within the Squamata (the smallest clade that contains all the lizards), so "lizard" is paraphyletic.^[59] The cladogram is based on genomic analysis by Wiens and colleagues in 2012 and 2016.^[60][61] Excluded taxa are shown in upper case on the cladogram.

Squamata

Dibamia Dibamidae Bifurcata Gekkota Pygopodomorpha Diplodactylidae   Pygopodidae   Carphodactylidae Gekkomorpha Eublepharidae Gekkonoidea Sphaerodactylidae Phyllodactylidae   Gekkonidae   Unidentata Scinciformata Scincomorpha Scincidae   Cordylomorpha Xantusiidae Gerrhosauridae   Cordylidae   Episquamata Laterata Teiformata Gymnophthalmidae   Teiidae   Lacertibaenia Lacertiformata Lacertidae   AMPHISBAENIA (worm lizards, not usually considered "true lizards")   Toxicofera Anguimorpha Palaeoanguimorpha Shinisauria Shinisauridae Varanoidea Lanthanotidae Varanidae   Neoanguimorpha Helodermatoidea Helodermatidae   Xenosauroidea Xenosauridae Anguioidea Diploglossidae Anniellidae Anguidae   Iguania Acrodonta Chamaeleonidae   Agamidae   Pleurodonta Leiocephalidae Iguanidae   Hoplocercidae Crotaphytidae Corytophanidae   Tropiduridae Phrynosomatidae Dactyloidae Polychrotidae Liolaemidae Leiosauridae Opluridae SERPENTES (snakes, not considered to be lizards)

Taxonomy

Main article: List of Lacertilia families

 

Artistic restoration of a mosasaur, Prognathodon

In the 13th century, lizards were recognized in Europe as part of a broad category of reptiles that consisted of a miscellany of egg-laying creatures, including "snakes, various fantastic monsters, […], assorted amphibians, and worms", as recorded by Vincent of Beauvais in his Mirror of Nature.^[62] The seventeenth century saw changes in this loose description. The name Sauria was coined by James Macartney (1802);^[63] it was the Latinisation of the French name Sauriens, coined by Alexandre Brongniart (1800) for an order of reptiles in the classification proposed by the author, containing lizards and crocodilians,^[64] later discovered not to be each other's closest relatives. Later authors used the term "Sauria" in a more restricted sense, i.e. as a synonym of Lacertilia, a suborder of Squamata that includes all lizards but excludes snakes. This classification is rarely used today because Sauria so-defined is a paraphyletic group. It was defined as a clade by Jacques Gauthier, Arnold G. Kluge and Timothy Rowe (1988) as the group containing the most recent common ancestor of archosaurs and lepidosaurs (the groups containing crocodiles and lizards, as per Mcartney's original definition) and all its descendants.^[65] A different definition was formulated by Michael deBraga and Olivier Rieppel (1997), who defined Sauria as the clade containing the most recent common ancestor of Choristodera, Archosauromorpha, Lepidosauromorpha and all their descendants.^[66] However, these uses have not gained wide acceptance among specialists.

Suborder Lacertilia (Sauria) – (lizards)

• Family †Bavarisauridae
• Family †Eichstaettisauridae
• Infraorder Iguania
  • Family †Arretosauridae
  • Family †Euposauridae
  • Family Corytophanidae (casquehead lizards)
  • Family Iguanidae (iguanas and spinytail iguanas)
  • Family Phrynosomatidae (earless, spiny, tree, side-blotched and horned lizards)
  • Family Polychrotidae (anoles)
    • Family Leiosauridae (see Polychrotinae)
  • Family Tropiduridae (neotropical ground lizards)
    • Family Liolaemidae (see Tropidurinae)
    • Family Leiocephalidae (see Tropidurinae)
  • Family Crotaphytidae (collared and leopard lizards)
  • Family Opluridae (Madagascar iguanids)
  • Family Hoplocercidae (wood lizards, clubtails)
  • Family †Priscagamidae
  • Family †Isodontosauridae
  • Family Agamidae (agamas, frilled lizards)
  • Family Chamaeleonidae (chameleons)
• Infraorder Gekkota
  • Family Gekkonidae (geckos)
  • Family Pygopodidae (legless geckos)
  • Family Dibamidae (blind lizards)

• Infraorder Scincomorpha
  • Family †Paramacellodidae
  • Family †Slavoiidae
  • Family Scincidae (skinks)
  • Family Cordylidae (spinytail lizards)
  • Family Gerrhosauridae (plated lizards)
  • Family Xantusiidae (night lizards)
  • Family Lacertidae (wall lizards or true lizards)
  • Family †Mongolochamopidae
  • Family †Adamisauridae
  • Family Teiidae (tegus and whiptails)
  • Family Gymnophthalmidae (spectacled lizards)
• Infraorder Diploglossa
  • Family Anguidae (slowworms, glass lizards)
  • Family Anniellidae (American legless lizards)
  • Family Xenosauridae (knob-scaled lizards)
• Infraorder Platynota (Varanoidea)
  • Family Varanidae (monitor lizards)
  • Family Lanthanotidae (earless monitor lizards)
  • Family Helodermatidae (Gila monsters and beaded lizards)
  • Family †Mosasauridae (marine lizards)

 

The slowworms, Anguis, are among over twenty groups of lizards that have convergently evolved a legless body plan.^[67]

Convergence

Lizards have frequently evolved convergently, with multiple groups independently developing similar morphology and ecological niches. Anolis ecomorphs have become a model system in evolutionary biology for studying convergence.^[68] Limbs have been lost or reduced independently over two dozen times across lizard evolution, including in the Anniellidae, Anguidae, Cordylidae, Dibamidae, Gymnophthalmidae, Pygopodidae, and Scincidae; snakes are just the most famous and species-rich group of Squamata to have followed this path.^[67]

Relationship with humans

Interactions and uses by humans

Most lizard species are harmless to humans. Only the largest lizard species, the Komodo dragon, which reaches 3.3 m (11 ft) in length and weighs up to 166 kg (366 lb), has been known to stalk, attack, and, on occasion, kill humans. An eight-year-old Indonesian boy died from blood loss after an attack in 2007.^[69]

 

Green iguanas (Iguana iguana), are popular pets.

Numerous species of lizard are kept as pets, including bearded dragons,^[70] iguanas, anoles,^[71] and geckos (such as the popular leopard gecko).^[70]Monitor lizards such as the savannah monitor and tegus such as the Argentine tegu and red tegu are also kept.

Green iguanas are eaten in Central America, where they are sometimes referred to as "chicken of the tree" after their habit of resting in trees and their supposedly chicken-like taste,^[72] while spiny-tailed lizards are eaten in Africa. In North Africa, Uromastyx species are considered dhaab or 'fish of the desert' and eaten by nomadic tribes.^[73]

 

Red tegu drinking water out of a dispenser.

Lizards such as the Gila monster produce toxins with medical applications. Gila toxin reduces plasma glucose; the substance is now synthesized for use in the anti-diabetes drug exenatide (Byetta).^[17] Another toxin from Gila monster saliva has been studied for use as an anti-Alzheimer's drug.^[74]

In culture

Lizards appear in myths and folktales around the world. In Australian Aboriginal mythology, Tarrotarro, the lizard god, split the human race into male and female, and gave people the ability to express themselves in art. A lizard king named Mo'o features in Hawaii and other cultures in Polynesia. In the Amazon, the lizard is the king of beasts, while among the Bantu of Africa, the god UNkulunkulu sent a chameleon to tell humans they would live forever, but the chameleon was held up, and another lizard brought a different message, that the time of humanity was limited.^[75] A popular legend in Maharashtra tells the tale of how a common Indian monitor, with ropes attached, was used to scale the walls of the fort in the Battle of Sinhagad.^[76] In the Bhojpuri speaking region of India and Nepal, there is a belief among children that, on touching skink's tail three (or five) time with the shortest finger gives money.

Lizards in many cultures share the symbolism of snakes, especially as an emblem of resurrection. This may have derived from their regular molting. The motif of lizards on Christian candle holders probably alludes to the same symbolism. According to Jack Tresidder, in Egypt and the Classical world they were beneficial emblems, linked with wisdom. In African, Aboriginal and Melanesian folklore they are linked to cultural heroes or ancestral figures.^[77]

Notes

1. Chameleon forefeet have groups composed of 3 inner and 2 outer digits; the hindfeet have groups of 2 inner and 3 outer digits.^[6]
2. The BBC's 2016 Planet Earth II showed a sequence of newly-hatched marine iguanas running to the sea past a waiting crowd of racer snakes. It was edited for dramatic effect but the sections were all genuine.^[49]

References

1. "The Reptile Database". Reptile-database.reptarium.cz. Retrieved on 2022-06-13
2. Muir, Hazel (3 December 2001). "Minute gecko matches smallest reptile record". New Scientist.
3. "The world's top 10 reptiles – in pictures". The Guardian. 5 May 2016.
4. McDiarmid, Roy W. (2012). "Reptile Diversity and Natural History: An Overview". In McDiarmid, Roy W.; et al. (eds.). Reptile Biodiversity: Standard Methods for Inventory and Monitoring. p. 13. ISBN 978-0520266711.
5. Jones; et al. (2011). "Hard tissue anatomy of the cranial joints in Sphenodon (Rhynchocephalia): sutures, kinesis, and skull mechanics". Palaeontologia Electronica. 14(2, 17A): 1–92.
6. Bauer, A. M.; Kluge, A. G.; Schuett, G. (2002). "Lizards". In Halliday, T.; Adler, K. (eds.). The Firefly Encyclopedia of Reptiles and Amphibians. Firefly Books. pp. 139–169. ISBN 978-1-55297-613-5.
7. Starr, C.; Taggart, R.; Evers, C. (2012). Biology: The Unity and Diversity of Life. Cengage Learning. p. 429. ISBN 978-1111425692.
8. Pough; et al. (2002) [1992]. Herpetology (Third ed.). Pearson Prentice Hall.
9. Spinner, Marlene; et al. (2014). "Subdigital setae of chameleon feet: Friction-enhancing microstructures for a wide range of substrate roughness". Scientific Reports. 4: 5481. Bibcode:2014NatSR...4E5481S. doi:10.1038/srep05481. PMC 4073164. PMID 24970387.
10. Irschick, D. J.; Jayne, B. C. (1 May 1999). "Comparative three-dimensional kinematics of the hindlimb for high-speed bipedal and quadrupedal locomotion of lizards". Journal of Experimental Biology. 202 (9): 1047–1065. doi:10.1242/jeb.202.9.1047. PMID 10101105 – via jeb.biologists.org.
11. Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
12. Pianka and Vitt, 23–24
13. Wilson, Steve (2012). Australian Lizards: A Natural History. Csiro Publishing. pp. 65–74. ISBN 978-0-643-10642-0.
14. Frasnelli, J.; et al. (2011). "The vomeronasal organ is not involved in the perception of endogenous odors". Hum. Brain Mapp. 32 (3): 450–60. doi:10.1002/hbm.21035. PMC 3607301. PMID 20578170.
15. Brames, Henry (2007), "Aspects of Light and Reptile Immunity" (PDF), Iguana: Conservation, Natural History, and Husbandry of Reptiles, 14 (1): 19–23^{[permanent dead link]}
16. Fry, Bryan G.; et al. (16 November 2005). "Early evolution of the venom system in lizards and snakes". Nature. 439 (7076): 584–588. Bibcode:2006Natur.439..584F. doi:10.1038/nature04328. PMID 16292255. S2CID 4386245.
17. Casey, Constance (26 April 2013). "Don't Call It a Monster". Slate.
18. Hargreaves, Adam D.; et al. (2014). "Testing the Toxicofera: Comparative transcriptomics casts doubt on the single, early evolution of the reptile venom system". Toxicon. 92: 140–156. doi:10.1016/j.toxicon.2014.10.004. PMID 25449103.
19. Schachner, Emma R.; Cieri, Robert L.; Butler, James P.; Farmer, C. G. (2014). "Unidirectional pulmonary airflow patterns in the savannah monitor lizard". Nature. 506 (7488): 367–370. Bibcode:2014Natur.506..367S. doi:10.1038/nature12871. PMID 24336209. S2CID 4456381.
20. Robert L.; Craven, Brent A.; Schachner, Emma R.; Farmer, C. G. (2014). "New insight into the evolution of the vertebrate respiratory system and the discovery of unidirectional airflow in iguana lungs". PNAS. 111 (48): 17218–17223. Bibcode:2014PNAS..11117218C. doi:10.1073/pnas.1405088111. PMC 4260542. PMID 25404314.
21. Pianka and Vitt, pp. 108.
22. Pianka and Vitt, pp. 115–116.
23. Pianka and Vitt, pp. 110–111.
24. Pianka and Vitt, pp. 117–118.
25. Pianka and Vitt, pp. 119.
26. Morales, Alex (20 December 2006). "Komodo Dragons, World's Largest Lizards, Have Virgin Births". Bloomberg Television. Retrieved 28 March 2008.
27. Pianka and Vitt, pp. 86.
28. Pianka and Vitt, pp. 32–37.
29. Buckley, Lauren B.; Ehrenberger, Joseph C.; Angilletta, Michael J. (2015). "Thermoregulatory behaviour limits local adaptation of thermal niches and confers sensitivity to climate change". Functional Ecology. 29 (8): 1038–1047. doi:10.1111/1365-2435.12406. ISSN 0269-8463. JSTOR 48577009.
30. Ortega, Jesús; Martín, José; Crochet, Pierre-André; López, Pilar; Clobert, Jean (2019-03-15). "Seasonal and interpopulational phenotypic variation in morphology and sexual signals of Podarcis liolepis lizards". PLOS ONE. 14 (3): e0211686. Bibcode:2019PLoSO..1411686O. doi:10.1371/journal.pone.0211686. ISSN 1932-6203. PMC 6419997. PMID 30875384.
31. Pianka and Vitt, pp. 94–106.
32. Lanham, E. J.; Bull. M. C. (2004). "Enhanced vigilance in groups in Egernia stokesii, a lizard with stable social aggregations". Journal of Zoology. 263 (1): 95–99. doi:10.1017/S0952836904004923.
33. Pianka and Vitt, pp. 87–94.
34. Langley, L. (24 October 2015). "Are Lizards as Silent as They Seem?". news.nationalgeographic.com. Retrieved 9 July 2017.
35. Ligon, Russell A.; McGraw, Kevin J. (2013). "Chameleons communicate with complex colour changes during contests: different body regions convey different information". Biology Letters. 9 (6): 20130892. doi:10.1098/rsbl.2013.0892. PMC 3871380. PMID 24335271.
36. Ligon, Russell A (2014). "Defeated chameleons darken dynamically during dyadic disputes to decrease danger from dominants". Behavioral Ecology and Sociobiology. 68 (6): 1007–1017. doi:10.1007/s00265-014-1713-z. S2CID 18606633.
37. Frankenberg, E.; Werner, Y. L. (1992). "Vocal communication in the Reptilia–facts and questions". 41. Acta Zoologica: 45–62. {{cite journal}}: Cite journal requires |journal= (help)
38. Barnett, K. E.; Cocroft, R. B.; Fleishman, L. J. (1999). "Possible communication by substrate vibration in a chameleon" (PDF). Copeia. 1999 (1): 225–228. doi:10.2307/1447408. JSTOR 1447408.
39. Pianka and Vitt, pp. 41–51.
40. Pianka and Vitt, pp. 53–55.
41. Pianka and Vitt, pp. 162.
42. Marshall, Kate; Philpot, Kate E.; Stevens, Martin (25 January 2016). "Microhabitat choice in island lizards enhances camouflage against avian predators". Scientific Reports. 6: 19815. Bibcode:2016NatSR...619815M. doi:10.1038/srep19815. PMC 4726299. PMID 26804463.
43. Yong, Ed (16 July 2014). "Lizard 'Sees' With Its Skin For Automatic Camouflage". National Geographic.
44. Stuart-Fox, Devi; Moussalli, Adnan; Whiting, Martin J. (23 August 2008). "Predator-specific camouflage in chameleons". Biology Letters. 4 (4): 326–329. doi:10.1098/rsbl.2008.0173. PMC 2610148. PMID 18492645.
45. Sherbrooke, WC (2003). Introduction to horned lizards of North America. University of California Press. pp. 117–118. ISBN 978-0-520-22825-2.
46. Scientists discover how lizards regrow tails, The Independent, August 20, 2014
47. Scherz, Mark D.; et al. (2017). "Off the scale: a new species of fish-scale gecko (Squamata: Gekkonidae: Geckolepis) with exceptionally large scales". PeerJ. 5: e2955. doi:10.7717/peerj.2955. PMC 5299998. PMID 28194313.
48. Cooper, William E. Jr. (2010). "Initiation of Escape Behavior by the Texas Horned Lizard (Phrynosoma cornutum)". Herpetologica. 66 (1): 23–30. doi:10.1655/08-075.1. S2CID 84653226.
49. "From Planet Earth II, a baby iguana is chased by snakes". BBC. 15 November 2016.
50. Hewitt, Sarah (5 November 2015). "If it has to, a horned lizard can shoot blood from its eyes". BBC.
51. Tałanda, Mateusz; Fernandez, Vincent; Panciroli, Elsa; Evans, Susan E.; Benson, Roger J. (2022-11-03). "Synchrotron tomography of a stem lizard elucidates early squamate anatomy". Nature. 611 (7934): 99–104. doi:10.1038/s41586-022-05332-6. ISSN 0028-0836. PMID 36289329. S2CID 253160713.
52. Whiteside, David I.; Chambi-Trowell, Sofía A. V.; Benton, Michael J. (2022-12-02). "A Triassic crown squamate". Science Advances. 8 (48): eabq8274. doi:10.1126/sciadv.abq8274. ISSN 2375-2548. S2CID 254180027.
53. Evans, S. E. (1998). "Crown group lizards (Reptilia, Squamata) from the Middle Jurassic of the British Isles". Palaeontographica, Abteilung A. 250 (4–6): 123–154. doi:10.1127/pala/250/1998/123. S2CID 246932992.
54. Herrera-Flores, Jorge A.; Stubbs, Thomas L.; Benton, Michael J. (March 2021). "Ecomorphological diversification of squamates in the Cretaceous". Royal Society Open Science. 8 (3): rsos.201961, 201961. doi:10.1098/rsos.201961. ISSN 2054-5703. PMC 8074880. PMID 33959350.
55. Dash, Sean (2008). . United States: Workaholic Productions / History Channel. Archived from the original on 2016-01-27. Retrieved December 18, 2015.
56. Ilaria Paparella; Alessandro Palci; Umberto Nicosia; Michael W. Caldwell (2018). "A new fossil marine lizard with soft tissues from the Late Cretaceous of southern Italy". Royal Society Open Science. 5 (6): 172411. Bibcode:2018RSOS....572411P. doi:10.1098/rsos.172411. PMC 6030324. PMID 30110414.
57. Caldwell, M. (1999-01-01). "Squamate phylogeny and the relationships of snakes and mosasauroids". Zoological Journal of the Linnean Society. 125 (1): 115–147. doi:10.1006/zjls.1997.0144. ISSN 0024-4082.
58. Schoch, Rainer R.; Sues, Hans-Dieter (24 June 2015). "A Middle Triassic stem-turtle and the evolution of the turtle body plan". Nature. 523 (7562): 584–587. Bibcode:2015Natur.523..584S. doi:10.1038/nature14472. PMID 26106865. S2CID 205243837.
59. Reeder, Tod W.; Townsend, Ted M.; Mulcahy, Daniel G.; Noonan, Brice P.; Wood, Perry L.; Sites, Jack W.; Wiens, John J. (2015). "Integrated Analyses Resolve Conflicts over Squamate Reptile Phylogeny and Reveal Unexpected Placements for Fossil Taxa". PLOS ONE. 10 (3): e0118199. Bibcode:2015PLoSO..1018199R. doi:10.1371/journal.pone.0118199. PMC 4372529. PMID 25803280.
60. Wiens, J. J.; Hutter, C. R.; Mulcahy, D. G.; Noonan, B. P.; Townsend, T. M.; Sites, J. W.; Reeder, T. W. (2012). "Resolving the phylogeny of lizards and snakes (Squamata) with extensive sampling of genes and species". Biology Letters. 8 (6): 1043–1046. doi:10.1098/rsbl.2012.0703. PMC 3497141. PMID 22993238.
61. Zheng, Yuchi; Wiens, John J. (2016). "Combining phylogenomic and supermatrix approaches, and a time-calibrated phylogeny for squamate reptiles (lizards and snakes) based on 52 genes and 4162 species". Molecular Phylogenetics and Evolution. 94 (Pt B): 537–547. doi:10.1016/j.ympev.2015.10.009. PMID 26475614.
62. Franklin-Brown, Mary (2012). Reading the world : encyclopedic writing in the scholastic age. Chicago London: The University of Chicago Press. p. 223;377. ISBN 9780226260709.
63. James Macartney: Table III in: George Cuvier (1802) "Lectures on Comparative Anatomy" (translated by William Ross under the inspection of James Macartney). Vol I. London, Oriental Press, Wilson and Co.
64. Alexandre Brongniart (1800) "Essai d'une classification naturelle des reptiles. 1ère partie: Etablissement des ordres." Bulletin de la Science. Société Philomathique de Paris 2 (35): 81–82
65. Gauthier, J. A.; Kluge, A. G.; Rowe, T. (June 1988). "Amniote phylogeny and the importance of fossils" (PDF). Cladistics. 4 (2): 105–209. doi:10.1111/j.1096-0031.1988.tb00514.x. hdl:2027.42/73857. PMID 34949076. S2CID 83502693.
66. Debraga, M. & Rieppel, O. (1997). "Reptile phylogeny and the interrelationships of turtles". Zoological Journal of the Linnean Society. 120 (3): 281–354. doi:10.1111/j.1096-3642.1997.tb01280.x.
67. Brandley, Matthew C.; et al. (August 2008). "Rates And Patterns In The Evolution Of Snake-Like Body Form In Squamate Reptiles: Evidence For Repeated Re-Evolution Of Lost Digits And Long-Term Persistence Of Intermediate Body Forms". Evolution. 62 (8): 2042–2064. doi:10.1111/j.1558-5646.2008.00430.x. PMID 18507743. S2CID 518045.
68. Losos, Jonathan B. (1992). "The Evolution of Convergent Structure in Caribbean Anolis Communities". Systematic Biology. 41 (4): 403–420. doi:10.1093/sysbio/41.4.403.
69. "Komodo dragon kills boy in Indonesia". NBC News. 2007-06-04. Retrieved 2011-11-07.
70. Virata, John B. . Reptiles Magazine. Archived from the original on 17 May 2017. Retrieved 28 May 2017.
71. McLeod, Lianne. "An Introduction to Green Anoles as Pets". The Spruce. Retrieved 28 May 2017.
72. . Archived from the original on 2016-10-26. Retrieved 2018-11-25.
73. Grzimek, Bernhard. Grzimek's Animal Life Encyclopedia (Second Edition) Vol 7 – Reptiles. (2003) Thomson – Gale. Farmington Hills, Minnesota. Vol Editor – Neil Schlager. ISBN 0-7876-5783-2 (for vol.7). p. 48
74. "Alzheimer's research seeks out lizards". BBC. 5 April 2002.
75. Greenberg, Daniel A. (2004). Lizards. Marshall Cavendish. pp. 15–16. ISBN 978-0-7614-1580-0.
76. Auffenberg, Walter (1994). The Bengal Monitor. University Press of Florida. p. 494. ISBN 978-0-8130-1295-7.
77. Tresidder, Jack (1997). the Hutchinson Dictionary of Symbols. London: Helicon. p. 125. ISBN 978-1-85986-059-5.

General sources

• Pianka, E. R.; Vitt, L. J. (2003). Lizards: Windows to the Evolution of Diversity. University of California Press. ISBN 978-0-520-23401-7.

Further reading

• Behler, John L.; King, F. Wayne (1979). The Audubon Society Field Guide to Reptiles and Amphibians of North America. New York: Alfred A. Knopf. p. 581. ISBN 978-0-394-50824-5.
• Capula, Massimo; Behler, John L. (1989). Simon & Schuster's Guide to Reptiles and Amphibians of the World. New York: Simon & Schuster. ISBN 978-0-671-69098-4.
• Cogger, Harold; Zweifel, Richard (1992). Reptiles & Amphibians. Sydney: Weldon Owen. ISBN 978-0-8317-2786-4.
• Conant, Roger; Collins, Joseph (1991). A Field Guide to Reptiles and Amphibians Eastern/Central North America. Boston, Massachusetts: Houghton Mifflin Company. ISBN 978-0-395-58389-0.
• Ditmars, Raymond L (1933). Reptiles of the World: The Crocodilians, Lizards, Snakes, Turtles and Tortoises of the Eastern and Western Hemispheres. New York: Macmillan. p. 321.
• Freiberg, Marcos [in Spanish]; Walls, Jerry (1984). The World of Venomous Animals. New Jersey: TFH Publications. ISBN 978-0-87666-567-1.
• Gibbons, J. Whitfield (1983). Their Blood Runs Cold: Adventures With Reptiles and Amphibians. Alabama: University of Alabama Press. p. 164. ISBN 978-0-8173-0135-4.
• Greenberg, Daniel A. (2004). Lizards. Marshall Cavendish. ISBN 9780761415800.
• Rosenfeld, Arthur (1987). Exotic Pets. New York: Simon & Schuster. p. 293. ISBN 978-0671636906.

External links

 

Wikimedia Commons has media related to Sauria.

•   Data related to Sauria at Wikispecies
• Ernest Ingersoll (1920). "Lizard" . Encyclopedia Americana.