Common collared lizard

Last updated

Common collared lizard
Common Collared Lizard.jpg
A male common collared lizard in
Taum Sauk Mountain State Park, Missouri
Crotaphytus collaris-female basking.jpg
Female in Petrified Forest National Park, Arizona
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Squamata
Suborder: Iguania
Family: Crotaphytidae
Genus: Crotaphytus
Species:
C. collaris
Binomial name
Crotaphytus collaris
(Say, 1823)
Synonyms [2]
A male common collared lizard (Crotaphytus collaris) near Hatch Point, Utah Collared Lizard near Hatch Point.jpg
A male common collared lizard (Crotaphytus collaris) near Hatch Point, Utah

The common collared lizard (Crotaphytus collaris), also commonly called eastern collared lizard, [3] Oklahoma collared lizard, yellow-headed collared lizard, and collared lizard, is a North American species of lizard in the family Crotaphytidae. The common name "collared lizard" comes from the lizard's distinct coloration, which includes bands of black around the neck and shoulders that look like a collar. Males can be very colorful, with blue green bodies, yellow stripes on the tail and back, and yellow orange throats. There are five recognized subspecies.

Contents

Etymology

The subspecific name, baileyi, is in honor of American mammalogist Vernon Orlando Bailey. [4]

Subspecies

Five subspecies are recognized as being valid, including the nominotypical subspecies. [2]

Nota bene : A trinomial authority in parentheses indicates that the subspecies was originally described in a genus other than Crotaphytus.

Description

C. collaris can grow up to 8–15 in (20–38 cm) in total length (including the tail), with a large head and powerful jaws. Males have a blue-green body with a light brown head. Females have a light brown head and body. C. collaris exhibit a wide range of physical characteristics, particularly in coloration and spotting patterns, and this phenotypic variability may be attributed to a combination of differences in population, social organizations, or habitat. [5] They are a sexually dichromatic lizard species with the adult males being more vivid and colorful than the females. Male dorsal and head color tend to range from green to tan and yellow to orange respectively, while females, overall, possess more muted body pigmentations, varying from brown to gray. However, when reproductively active during breeding seasons, females undergo a rapid color change, in which faint orange spots on their heads increase in brightness; this orange spotting reaches a maximum during egg maturation but gradually fades again after expulsion from the female's oviduct as she lays her eggs. [6] Both males and females have two distinct black bands around their neck, providing additional context to their name, the common collared lizards.

Similar to adult females, juveniles also exhibit dull body colorations compared to adult males, but a key distinction is that the young have pronounced, dark brown markings that eventually fade as they grow and mature. [7] Consequently, juvenile collared lizards lose this sharp cross-band pattern, and their features drastically change to resemble those of either adult males or females. [7]

Moderate in size, C. collaris have disproportionately large heads and long hind limbs. It can reach a length of 14 inches, including the tail, with males being larger than females. Hence, they are sexually dimorphic, and adult males exhibit larger and more muscular heads than females, which tend to vary in size. Used as a weapon during male combat, the head dimensions play a key role in determining dominance, territoriality, fitness, as well as mating success. In general, bigger heads are associated with greater jaw strength and thus, bite force.

Bipedal locomotion

C. collaris are known for their bipedal locomotion–the ability to run on their two hind legs–and can sprint at incredible speeds of up to 24 kilometers per hour; this behavior is usually observed when trying to escape predators. [8]

Like many other lizards, including the frilled lizard and basilisk, the collared lizard can run on its hind legs, and is a relatively fast sprinter. Record speeds have been around 16 miles per hour (26 km/h), much slower than the world record for lizards (21.5 mph or 34.6 km/h) attained by the larger-bodied Costa Rican spiny-tailed iguana, Ctenosaura similis .

Geographic range and habitat

C. collaris is chiefly found in dry, open regions of Mexico and the south-central United States including Arizona, Arkansas, Colorado, Kansas, Missouri, New Mexico, Oklahoma, and Texas. The full extent of its habitat in the United States ranges from the Ozark Mountains to Western Arizona.

C. collaris is distributed across the Southwestern United States and extend to Northern Mexico as well. Individuals occupy a range of different habitats from rocky desert landscapes to grasslands, but they often prefer to inhabit mountainous regions with high environmental temperatures for optimal thermoregulation. [9] In addition, the hilly topography allows these keen and highly alert lizards to stay hidden between rocks, despite their flamboyant features, and look out for potential predators or territory intruders from the top of elevated platforms.

Diet

As obligate carnivores, they consume insects and small vertebrates as their main diet. [10] While they may occasionally ingest plant materials, it is not preferred. They feed on a variety of large insects, including crickets, grasshoppers, spiders, moths, beetles, and cicadas, along with other small lizards and even snakes. [11] As plants do not provide enough nutrients for constant body weight maintenance, C. collaris cannot survive solely on an herbivorous diet. [10] Their stomachs are too small to accommodate the amount of flowers, shrubs, herbs, etc. that would be needed to maintain a constant body weight. [10] Thus, they are considered obligate carnivores, requiring nutrients from arthropods or other small reptiles.

Diet can also vary depending on age, sex, as well as seasonal changes. In the case of younger lizards, they consume the same kinds of foods, specifically insect species, that adults do, but since younger lizards and adults differ in body size and weight, the amount of food intake tends to vary. [11] On the other hand, male and female adults are similar in terms of their sizes and the amounts of food ingested but exhibit drastic differences in the kinds of foods that they eat. [11] From an evolutionary standpoint, these sexual differences in diet may act to reduce intra-species competition for resources, whereby females and males do not need to fight for the same type of food. [11] Moreover, changes in season can drastically affect their diets as well.

Cultural impact

The collared lizard is the state reptile of Oklahoma, where it is known as the mountain boomer. The origin of the name "mountain boomer" is not clear, but it may be traceable to settlers traveling west during the Gold Rush. One theory is that settlers mistook the sound of wind in canyons for the call of an animal in an area where the collared lizard was abundant. In reality, collared lizards are silent.[ citation needed ]

Behavior

Collared lizards are diurnal; [12] they are active during the day, and spend most of their time basking on top of elevated rocks or boulders. As a highly territorial species, [13] they remain hyper-vigilant, scanning for predators or intruders, ready to sprint or fight when necessary. Generally, males are more active than females, as the former engage in more chase, fight, display, and courtship behaviors while the latter exhibit basking and foraging behaviors. The collared lizard in the wild has been the subject of a number of studies of sexual selection; in captivity if two males are placed in the same cage they will fight to the death. Females, on the other hand, do not demonstrate aggressive behaviors as frequently as males, experiencing less intra-species competition with other females. [13]

Social behavior

In an effort to monopolize as many female mates as they can, male C. collaris viciously defend their exclusive territories through aggression, patrolling activities, and displays. [13] [14] These territories provide ample resources and shelter the harem of females claimed and protected by the male territory owners. However, when agonistic interactions between male rivals escalate to violent fights, both lizards must expend substantial amounts of energy and risk getting seriously injured. [15] Thus, though males do actively exclude other males from territories, they do so without resorting to physical and unfavorable conflict. Instead, they partake in social displays, either at a distance or proximally from their competitors to advertise their superiority. Surprisingly, both types of social encounters, in which males perform push ups and compressions and elevations of the trunk with the dewlap extended, [13] rarely lead to arduous and violent fights; rather, distant displays barely evoke a response while proximal confrontations may lead to chasing at most. [15]

Furthermore, C. collaris territory owners exhibit differential behaviors in response to neighbors and strangers, in which residents reduce the cost of territorial defense by demonstrating less aggression for spatial neighbors. [16] Thus, when nearby residents approach an owner's shared territorial boundaries, the owner will recognize this individual and only engage in aggressive behaviors, usually in the form of a costly fight, if a threat to its territory is perceived. [16] However, in the case of a stranger, the owner will exhibit intense hostility towards the intruder without hesitation. [16] In relation, male territorial behaviors also vary within the reproductive season, decreasing in June due to the higher prevalence of reproductively active females and instead, engaging in more courtship behaviors. [14] This cost-benefit strategy demonstrates the complex social behaviors and decision making processes exhibited by the male collared lizards.

Reproduction

The reproductive season starts in mid-March to early April and concludes in mid-July. [14] Females and smaller individuals emerge first from hibernation with males following around two weeks later. Though lizards are considered mature and may breed following their first hibernation, those that are two years and older exhibit greater reproductive success due to their larger size. [14] In late May, courtship occurs between adult males and females. Subsequently, mature females, typically two years and older, produce their first clutches and lay them in a burrow or under a rock about two weeks after copulation. They may then go on to produce second and sometimes even third clutches throughout June until mid-July. The eggs are incubated in a temperature dependent manner, and the incubation period may vary from 50 to 100 days. On average, clutch size can range from 4 to 6 eggs, but larger, older females can produce more. By August, adults begin to hibernate again, and juveniles do the same after hatching. The earliest of the clutches can hatch in mid-July and later ones follow until mid-October. Upon hatching, juveniles are fully developed and behave independently of their parents, as the C. collaris do not exhibit any parental care in offspring.

Mating behavior and rituals

C. collaris are polygamous, which leads to intense territorial behaviors that include male to male competition for females partners. [14] This triggers aggressive behaviors in males and induces fierce competition for mating. With regards to female selection of male mates, females not only prefer males who are bright and conspicuous in body coloration but also consider the resources such as food and territory that males may be able to provide in order to ensure reproductive success. [14] Moreover, as males often must compete with other males for potential mates, their body and head size play a significant role in determining mating success. [17] The variability in head size gives rise to differential jaw strength and bite force in males, which ultimately results in intra-species selection against smaller headed males. [17] For example, if an instance of male-to-male conflict escalates into a violent fight between two males, the larger male with a substantial larger body mass and head size will overpower its weaker and smaller counterpart. Consequently, successful males may, more often than not, possess vibrant body coloration and patterns and may be bigger in size, specifically having larger head proportions. [18]

During courtship rituals, a male or a female lizard approaches the opposite sex within 1 body length and subsequently engages in various behavioral patterns, which include either individual superimposing its limbs, torso, or tail over its partner, mounting the dorsum of the other lizard, males nudging females with their snouts or grasping them with their jaws, and mutual displays. [15] These mutual displays involve a complex set of movements and behaviors, unique to each sex. Males flex their forearms up and down and extend their dewlaps while females also extend their dewlaps and raise the base of their tails to signal receptivity. [15] Ultimately, at the end of this courting process, both sexes walk in circles, making sure to remain within 1 body length of one another throughout. [15]

Related Research Articles

<span class="mw-page-title-main">Sexual dimorphism</span> Condition where males and females exhibit different characteristics

Sexual dimorphism is the condition where sexes of the same species exhibit different morphological characteristics, particularly characteristics not directly involved in reproduction. The condition occurs in most dioecious species, which consist of most animals and some plants. Differences may include secondary sex characteristics, size, weight, color, markings, or behavioral or cognitive traits. Male-male reproductive competition has evolved a diverse array of sexually dimorphic traits. Aggressive utility traits such as "battle" teeth and blunt heads reinforced as battering rams are used as weapons in aggressive interactions between rivals. Passive displays such as ornamental feathering or song-calling have also evolved mainly through sexual selection. These differences may be subtle or exaggerated and may be subjected to sexual selection and natural selection. The opposite of dimorphism is monomorphism, when both biological sexes are phenotypically indistinguishable from each other.

<i>Anolis carolinensis</i> Species of reptile

Anolis carolinensis or green anole is a tree-dwelling species of anole lizard native to the southeastern United States and introduced to islands in the Pacific and Caribbean. A small to medium-sized lizard, the green anole is a trunk-crown ecomorph and can change its color to several shades from brown to green.

<span class="mw-page-title-main">Sand lizard</span> Species of lizard

The sand lizard is a lacertid lizard distributed across most of Europe from France and across the continent to Lake Baikal in Russia. It does not occur in European Turkey. Its distribution is often patchy. In the northern extremes of the sand lizard's distribution, such as along the southern English coast of Great Britain, it can only survive by inhabiting seaside heathlands, where the ground temperature is sufficiently elevated from the Sun's rays; the warmth is also critical to the lizard being able to successfully incubate their eggs, which are laid in sand.

<span class="mw-page-title-main">Viviparous lizard</span> Species of lizard

The viviparous lizard, or common lizard, is a Eurasian lizard. It lives farther north than any other species of non-marine reptile, and is named for the fact that it is viviparous, meaning it gives birth to live young. Both "Zootoca" and "vivipara" mean "live birth", in (Latinized) Greek and Latin respectively. It was called Lacerta vivipara until the genus Lacerta was split into nine genera in 2007 by Arnold, Arribas & Carranza.

<span class="mw-page-title-main">Common side-blotched lizard</span> Species of lizard

The common side-blotched lizard is a species of side-blotched lizard in the family Phrynosomatidae. The species is native to dry regions of the western United States and northern Mexico. It is notable for having a unique form of polymorphism wherein each of the three different male morphs utilizes a different strategy in acquiring mates. The three morphs compete against each other following a pattern of rock paper scissors, where one morph has advantages over another but is outcompeted by the third.

<i>Gambelia sila</i> Species of lizard

Gambelia sila, commonly known as the blunt-nosed leopard lizard, is a species of lizard in the family Crotaphytidae. The species is endemic to southern California.

<i>Urosaurus ornatus</i> Species of lizard

Urosaurus ornatus, commonly known as the ornate tree lizard, is a species of lizard in the family Phrynosomatidae. The species is native to the southwestern United States and northwestern Mexico. The species, which was formerly called simply the "tree lizard", has been used to study physiological changes during the fight-or-flight response as related to stress and aggressive competition. Its life history and costs of reproduction have been documented in field populations in New Mexico and Arizona. This species has been fairly well studied because of its interesting variation in throat color in males that can correlate with different reproductive strategies,

<span class="mw-page-title-main">Great Basin collared lizard</span> Species of lizard

The Great Basin collared lizard, also known commonly as the desert collared lizard or the Mojave black-collared lizard, is a species of lizard in the family Crotaphytidae. The species is endemic to the Western United States.

<span class="mw-page-title-main">Eastern fence lizard</span> Species of lizard

The eastern fence lizard is a medium-sized species of lizard in the family Phrynosomatidae. The species is found along forest edges, rock piles, and rotting logs or stumps in the eastern United States. It is sometimes referred to as the prairie lizard, fence swift, gray lizard, gravid lizard, northern fence lizard or pine lizard. It is also referred to colloquially as the horn-billed lizard. One of its most notable behaviors is that of its escape behavior when encountering fire ants.

<i>Acanthodactylus erythrurus</i> Species of lizard

Acanthodactylus erythrurus, commonly known as the spiny-footed lizard, is a species of lizard in the family Lacertidae. The species is endemic to northwestern Africa and the Iberian Peninsula. It is considered to be the fastest member of the family Lacertidae. Its common name refers to the spines that are arranged like a comb on the toes of its hind legs.

<i>Podarcis hispanicus</i> Species of lizard

Podarcis hispanicus, also known as Iberian wall lizard, is a small wall lizard species of the genus Podarcis. It is found in the Iberian peninsula, in northwestern Africa and in coastal districts in Languedoc-Roussillon in France. In Spanish, this lizard is commonly called lagartija Ibérica.

<span class="mw-page-title-main">Robust skink</span> Species of reptile

Oligosoma alani,, also known as the robust skink is the largest endemic skink to New Zealand. The robust skink is in the family Scincidae and found in the protected nature reserves of the Mercury Islands in the North Island of New Zealand. The robust skink has an at risk - recovering conservation status.

<i>Iberolacerta cyreni</i> Species of lizard

Iberolacerta cyreni, commonly known as the Cyren's rock lizard, is a species of lizard in the family Lacertidae. The species is endemic to central Spain and is currently listed as endangered by the IUCN due to global warming. I. cyreni has evolved to exhibit key behavioral characteristics, namely individual recognition, in which a lizard is able to identify another organism of the same species, as well as thermoregulation.

<span class="mw-page-title-main">Collared brown lemur</span> Species of lemur

The collared brown lemur, also known as the red-collared brown lemur or red-collared lemur, is a medium-sized strepsirrhine primate and one of twelve species of brown lemur in the family Lemuridae. It is only found in south-eastern Madagascar. Like most species of lemur, it is arboreal, moving quadrupedally and occasionally leaping from tree to tree. Like other brown lemurs, this species is cathemeral, lives in social groups, primarily eats fruit, exhibits sexual dichromatism, and does not demonstrate female dominance. The species is listed as Endangered by the International Union for Conservation of Nature (IUCN) and is threatened primarily by habitat loss.

<span class="mw-page-title-main">Sexual dimorphism in non-human primates</span>

Sexual dimorphism describes the morphological, physiological, and behavioral differences between males and females of the same species. Most primates are sexually dimorphic for different biological characteristics, such as body size, canine tooth size, craniofacial structure, skeletal dimensions, pelage color and markings, and vocalization. However, such sex differences are primarily limited to the anthropoid primates; most of the strepsirrhine primates and tarsiers are monomorphic.

<i>Uracentron flaviceps</i> Species of lizard

Uracentron flaviceps, the tropical thornytail iguana or Amazon thornytail iguana is an elusive species of medium-sized arboreal lizard found in the tropical lowlands of the Amazon Rainforest. The species was described by French zoologist Alphone Guichenot in 1855. They are considered to be ant specialists and exhibit communal nesting and a harem-style breeding system in which one male mates with and attends to multiple females. Study of this species has been impeded by difficulties collecting and observing them.

<span class="mw-page-title-main">Yellow-headed gecko</span> Species of reptile

Gonatodes albogularis, which has been called a number of vernacular names in English, is a smallish species of gecko found in warm parts of Central and South America, Cuba, Hispaniola and Jamaica. They prefer to live in tropical dry forest habitats. It is sexually dimorphic: the male is colourful, while the female is a more drab grey. The fingers do not have lamellar pads for climbing smooth surfaces like many other geckos but instead have normal claws like most lizards. At one time the species had a breeding population in southern Florida, especially Key West, but this population appears to have died out by the early 1990s. They are believed to be able to tell the difference between brightness and hues of conspecifics. Males are incredibly aggressive with territory defense against both other males and potential predators.

<span class="mw-page-title-main">Sexual selection in scaled reptiles</span>

Sexual selection in scaled reptiles studies how sexual selection manifests in snakes and lizards, which constitute the order Squamata of reptiles. Each of the over three thousand snakes use different tactics in acquiring mates. Ritual combat between males for the females they want to mate with includes topping, a behavior exhibited by most viperids in which one male will twist around the vertically elevated fore body of its opponent and forcing it downward. It is common for neck biting to occur while the snakes are entwined.

<i>Diploderma swinhonis</i> Species of lizard

Diploderma swinhonis, also known commonly as the Taiwan japalure, Swinhoe's japalure, Swinhoe's lizard, and Swinhoe's tree lizard, is a species of lizard in the family Agamidae. The species is native to Taiwan. It is considered an invasive alien species in Japan after likely being transported from Taiwan by humans. A foraging ambush predator, this lizard preys primarily on arthropods and thus remains at the bottom of forests perched on trees where sunlight is present. D. swinhonis is not a major threat to humans and is able to adapt to a variety of habitats, including urban environments. The male D. swinhonis is physically distinct from the female, with its body size being much larger and having a yellow stripe. This species sexually reproduces on a seasonal basis and hibernates during the winter time.

<i>Anolis aquaticus</i> Species of reptile

Anolis aquaticus, commonly known as the water anole, is a semi-aquatic species of anole, a lizard in the family Dactyloidae, native to southwestern Costa Rica and far southwestern Panama. The species demonstrates adaptations that allows it to spend periods of time underwater up to approximately a quarter of an hour, forming an air bubble which clings to its head and serves to recycle the animal's air supply while it spends time beneath the surface. Although highly unusual, similar adaptions and behavior are found in other species of semi-aquatic anoles.

References

  1. Hammerson, G.A.; Lavin, P.; Vazquez Díaz, J.; Quintero Díaz, G.; Gadsden, H. (2007). "Crotaphytus collaris". IUCN Red List of Threatened Species . 2007: e.T64007A12734318. doi: 10.2305/IUCN.UK.2007.RLTS.T64007A12734318.en . Retrieved 19 November 2021.
  2. 1 2 "Crotaphytus collaris (Say, 1823)". The Reptile Database. Archived from the original on 2014-10-08. Retrieved 2012-02-16.
  3. Stebbins RC (2003). A Field Guide to Western Reptiles and Amphibians, Third Edition. The Peterson Field Guide Series ®. Boston and New York: Houghton Mifflin. xiii + 533 pp. ISBN   0-395-98272-3. (Crotaphytus collaris, pp. 271-272 + Plate 27 + Map 85).
  4. Beolens, Bo; Watkins, Michael; Grayson, Michael (2011). The Eponym Dictionary of Reptiles. Baltimore: Johns Hopkins University Press. xiii + 296 pp. ISBN   978-1-4214-0135-5. (Crotaphytus collaris baileyi, p. 14).
  5. Baird, Troy A.; Fox, Stanely [sic] F.; McCoy, J. Kelly (September 1997). "Population differences in the roles of size and coloration in intra– and intersexual selection in the collared lizard, Crotaphytus collaris: influence of habitat and social organization". Behavioral Ecology. 8 (5): 506–517. doi: 10.1093/beheco/8.5.506 .
  6. Ferguson, Gary W. (1976). "Color Change and Reproductive Cycling in Female Collared Lizards (Crotaphytus collaris)". Copeia. 1976 (3): 491–494. doi:10.2307/1443364. ISSN   0045-8511. JSTOR   1443364.
  7. 1 2 Fitch, Henry S.; Tanner, Wilmer W. (1951). "Remarks concerning the Systematics of the Collared Lizard, (Crotaphytus collaris), with a Description of a New Subspecies". Transactions of the Kansas Academy of Science. 54 (4): 548–559. doi:10.2307/3626220. ISSN   0022-8443. JSTOR   3626220.
  8. Husak, Jerry F.; Fox, Stanley F. (2006). "Field Use of Maximal Sprint Speed by Collared Lizards (Crotaphytus collaris): Compensation and Sexual Selection". Evolution. 60 (9): 1888–1895. doi: 10.1111/j.0014-3820.2006.tb00532.x . ISSN   0014-3820. JSTOR   4095428. PMID   17089973. S2CID   2024684.
  9. Angert, Amy L.; Hutchison, Delbert; Glossip, Danielle; Losos, Jonathan B. (2002). "Microhabitat Use and Thermal Biology of the Collared Lizard (Crotaphytus collaris collaris) and the Fence Lizard (Sceloporus undulatus hyacinthinus) in Missouri Glades". Journal of Herpetology. 36 (1): 23–29. doi:10.2307/1565797. ISSN   0022-1511. JSTOR   1565797.
  10. 1 2 3 Ruppert, Ron M. (1980-01-01). "Comparative assimilation efficiencies of two lizards". Comparative Biochemistry and Physiology Part A: Physiology. 67 (3): 491–496. doi:10.1016/S0300-9629(80)80028-4. ISSN   0300-9629.
  11. 1 2 3 4 Best, Troy L.; Pfaffenberger, Gary S. (1987). "Age and Sexual Variation in the Diet of Collared Lizards (Crotaphytus collaris)". The Southwestern Naturalist. 32 (4): 415–426. doi:10.2307/3671473. ISSN   0038-4909. JSTOR   3671473.
  12. Macedonia, Joseph M.; Brandt, Yoni; Clark, David L. (2002-09-01). "Sexual dichromatism and differential conspicuousness in two populations of the common collared lizard (Crotaphytus collaris) from Utah and New Mexico, USA". Biological Journal of the Linnean Society. 77 (1): 67–85. doi: 10.1046/j.1095-8312.2002.00092.x . ISSN   0024-4066. S2CID   30673864.
  13. 1 2 3 4 Baird, Troy A.; Acree, Mark A.; Sloan, Chris L. (1996). "Age and Gender-Related Differences in the Social Behavior and Mating Success of Free-Living Collared Lizards, Crotaphytus collaris". Copeia. 1996 (2): 336–347. doi:10.2307/1446849. ISSN   0045-8511. JSTOR   1446849.
  14. 1 2 3 4 5 6 Baird, Troy A.; Sloan, Chris L.; Timanus, Dusti K. (2001). "Intra- and Inter-seasonal Variation in the Socio-Spatial Behavior of Adult Male Collared Lizards, Crotaphytus collaris (Reptilia, Crotaphytidae)". Ethology. 107 (1): 15–32. doi:10.1046/j.1439-0310.2001.00628.x. ISSN   1439-0310.
  15. 1 2 3 4 5 Baird, Troy A.; Curtis, Jennifer L. (2010-07-01). "Context-dependent acquisition of territories by male collared lizards: the role of mortality". Behavioral Ecology. 21 (4): 753–758. doi: 10.1093/beheco/arq049 . ISSN   1045-2249.
  16. 1 2 3 Husak, Jerry F; Fox, Stanley F (2003-02-01). "Adult male collared lizards, Crotaphytus collaris, increase aggression towards displaced neighbours". Animal Behaviour. 65 (2): 391–396. doi:10.1006/anbe.2003.2058. ISSN   0003-3472. S2CID   53156904.
  17. 1 2 Lappin, A. Kristopher; Husak, Jerry F. (September 2005). "Weapon Performance, Not Size, Determines Mating Success and Potential Reproductive Output in the Collared Lizard (Crotaphytus collaris)". The American Naturalist. 166 (3): 426–436. doi:10.1086/432564. ISSN   0003-0147. PMID   16224696. S2CID   34094246.
  18. Cabido, Carlos; Galán, Pedro; López, Pilar; Martín, José (March–April 2009). "Conspicuousness-dependent antipredatory behavior may counteract coloration differences in Iberian rock lizards". Behavioral Ecology. 20 (2): 362–370. doi: 10.1093/beheco/arn152 .

Further reading