|Carolina anole (above),
Crested anole (below)
1–8, see text
Dactyloidae are a family of lizards commonly known as anoles (US: // ( listen)) and native to warmer parts of the Americas, ranging from southeastern United States to Paraguay. Instead of treating it as a family, some authorities prefer to treat it as a subfamily, Dactyloinae, of the family Iguanidae. In the past they were included in the family Polychrotidae together with Polychrus (bush anoles), but the latter genus is not closely related to the true anoles.
Anoles are small to fairly large lizards, typically green or brownish, but their color varies depending on species and many can also change it. In most species at least the male has a dewlap, an often brightly colored flap of skin that extents from the throat/neck and is used in displays. Anoles share several characteristics with geckos, including details of the foot structure (for climbing) and the ability to voluntarily break off the tail (to escape predators), but they are only very distantly related, anoles being part of Iguania.
Anoles are active during the day and feed mostly on small animals such as insects, but some will also take fruits, flowers and nectar. They are fiercely territorial. After mating the female lays an egg (occasionally two) and in many species she may repeat this every few days or weeks. The egg is typically placed on the ground, but in some species it is placed at higher levels.
Anoles are widely studied in fields such as ecology, behavior and evolution, and some species are commonly kept in captivity as pets. Anoles can function as a biological pest control by eating insects that may harm humans or plants, but represent a serious risk to small native animals and ecosystems if introduced to regions outside their home range.
- 1 Distribution and habitat
- 2 Appearance and behavior
- 3 Evolution
- 4 Relationship with humans
- 5 References
- 6 External links
Distribution and habitat
Anoles are a very diverse and plentiful group of lizards. They are native to tropical and subtropical South America, Central America, Mexico, the offshore East Pacific Cocos, Gorgona and Malpelo Islands, the West Indies and southeastern United States.
A particularly high species richness exists in Cuba (more than 60 species), Hispaniola (more than 55), Mexico (more than 50), Central America, Colombia (more than 75), and Ecuador (at least 40). Fewer live in eastern and central South America (for example, less than 20 species are known from huge Brazil), Contiguous United States (1 native species), and the Lesser Antilles (about 25 species). However, the Lesser Antilles are relatively rich compared to their very small land area and their species are all highly localized endemics, each only found on one or a few diminutive islands. In South America, the diversity is considerably higher west of the Andes (Tumbes-Chocó-Magdalena region) than east (Amazon basin), as well illustrated in Ecuador where about 2⁄3 of the anole species live in the former region and 1⁄3 in the latter.
The only species native to the contiguous United States is the Carolina (or green) anole, which ranges as far west as central Texas, and north to Oklahoma, Tennessee and Virginia. Its northern limit is likely related to cold winter temperatures. Several anole species have been introduced to the contiguous US, mostly Florida, but also other Gulf Coast states and California. The most prevalent of these introductions is the brown anole. In contrast to the contiguous United States, Puerto Rico and the Virgin Islands are home to 16 native species, all endemic.
Anoles inhabit a wide range of habitats, from highlands (up to at least 2,600 m or 8,500 ft above sea level) to the coast, and rainforest to desert scrub. A few live in limestone karst habitats and at least two of these, the Cuban cave anole and Mexican cave anole, will enter caves, sometimes occurring as much as 20 m (65 ft) from the entrance. Some species live close to humans and may use fences or walls of building as perches, even inhabiting gardens or trees along roads in large cities like Miami. Most anoles are arboreal or semi-arboreal, but there are also terrestrial and semi-aquatic species. They are often, especially in the Caribbean, grouped into six ecomorphs—crown giant, trunk crown, trunk, trunk ground, twig, and grass bush—that inhabit specific niches. Other less widely used groups are ground, ground bush, twig giant, saxicolous, and riparian (alternatively semi-aquatic). However, the species within each ecomorph group are not entirely alike and there are variations in the details of their niches, including both widespread generalists and more restricted specialists. The niche differentiation allows several anoles to inhabit the same locality, with up to 15 species at a single site.
Appearance and behavior
Anoles vary in size. Males generally reach a larger size than females, but in a few species it is the other way around. Adults of most anoles are between 4 and 8 cm (1.5–3 in) in snout-to-vent length, and between 10 and 20 cm (4–8 in) in total length, including the tail. In the smallest, the five-striped grass anole, the snout-to-vent length is about 3 and 3.5 cm (1.2 and 1.4 in) in females and males respectively, but it is a relatively long-tailed species. There are several large species that are more than 10 cm (4 in) in snout-to-vent length. Males of the largest, the knight anole, reach up to about 19 cm (7.5 in) in snout-to-vent length, 50 cm (20 in) in total length, and 84 g (3 oz) in weight.
The tail of anoles is typically longer than the snout-to-vent, ranging from nearly the same to about three times the length. In a few species it is generally slightly shorter than the snout-to-vent. The Caribbean twig ecomorph anoles, proboscis anole and "Phenacosaurus" anoles have a prehensile tail. Semi-aquatic anoles tend to have relatively tall, vertically flattened tails that aid in swimming.
Underneath an anole's toes are pads that have several to a dozen flaps of skin (adhesive lamellae) going horizontally and covered in microscopic hairlike protrusions (setae) that allow them to cling to many different surfaces, similar to but not quite as efficient as a gecko. Despite this similarity, they are very distantly related and the adaptions are the result of convergent evolution in the two groups. The extent of these structures and clinging ability varies, being more developed in anole species that live high in the tree canopy than ones living at lower levels. In one extreme are anoles that easily can run up windows. In the opposite end of the spectrum is the bulky anole of arid coastal Venezuela and adjacent Colombia, which is the only species completely lacking the specialized toe pad structures. The relative length of the limbs vary, mainly between different species, but to some extent also between different populations of a single species. This depends on things like the preferred perch size and whether there are ground-living predators in a habitat.
Their primary sense is sight, which is excellent and in color. Their pupils are round or nearly round. The Guantanamo anole and Cuban cave anole have a transparent "window" in their lower eyelid, allowing them to see even with closed eyes, but why they have this adaption is unclear. Anoles have a good directional hearing, which is able to detect relatively low intensity sounds like the click of a camera and frequencies between 1000 and 7000 Hz.
Anoles are diurnal—active during the daytime—but can also be active during bright moonlit nights and may forage near artificial lights. Many species frequently bask in the sun to increase their temperature, but others are shade-living and do not.
Most anoles are brownish or green, but there are extensive variations depending on the exact species. The majority can change their color depending on things like emotions (for example, aggression or stress), activity level, levels of light and as a social signal (for example, displaying dominance), but evidence showing that they do it in response to the color of the background (camouflage) is lacking. Whether they do it in response to temperature (thermoregulation) is less clear, with studies supporting it and contradicting it. The extent and variations of this color changing ability differ widely throughout the individual species. For example, the Carolina (or green) anole can change its color from a bright, leafy green to a dull brown color, while the brown anole can only change its shade, ranging from pale gray-brown to very dark brown. Even the distinct green-to-brown change in the Carolina anole can happen in only a few minutes. The colors are the result of their skin pigment cells, the chromatophores, of which they have three main types, but the change occurs only in the melanophores. When triggered by melanophore-stimulating hormone and other hormones, the melanosomes of the melanophores partially cover the other skin pigment cells, giving the anole a darker or browner color. In most cases stress results in a darker/browner color, but in the aquatic anole, a species that is dark brown with a barred pattern and light brown stripes on the sides of its body and head, stress results in paler brown upperparts and the stripes turn pale blue-green.
Their colors during the night when sleeping often differ distinctly from their colors during the day where awake. Among these are some species that otherwise do not drastically change their colors, including certain anoles that generally are brown during the day changing to greenish or whitish when sleeping at night, and certain anoles that generally are green during the day changing to brown when sleeping at night.
Disregarding color change, minor individual variations in the basic color and pattern, mostly related to sex or age, are common. In some anole species this variation is more pronounced and not only related to sex and age. An example of this is the basic color of the Cayman blue-throated anole, which varies geographically, roughly matching the main habitat at a location. In others it occurs at the same location. This includes the extensive individual variations in the Guadeloupean anole, which however also shows some geographic variations, but possibly not consistent enough (due in part to clines) to make the typically recognized subspecies valid. In the Puerto Rican giant anole, a species only able to perform minor color changes (essentially lightness/darkness), juveniles are gray-brown and adults typically green, but an uncommon morph maintains a gray-brown color into adulthood. Similarly, rare morphs of the usually green Carolina anole lack certain pigment cells, giving them a mainly turquoise-blue or yellow color.
Most—but not all—anole species have dewlaps, made of erectile cartilage (modified from the hyoid) and covered in skin, that extend from their throat areas. When not in use and closed it lies inconspicuously along the throat and chest. The size, shape, color and pattern of the dewlap vary extensively depending on species, and often it differs between the sexes, being smaller (in some absent) and/or less colorful in females. In a few species, including the Carolina, bark, Cochran's gianthead and slender anoles, it varies in color depending on subspecies on location. Very locally distinct dewlap variations in a single species (not just between sexes) may occur together. In addition to colors that are visible to humans, dewlaps can have ultraviolet reflectance, which is visible to anoles. The striped anole is the only species where it is asymmetrically colored, being brighter on one side than the other. In some species even juveniles have a dewlap. The West Cuban and Cuban stream anoles are the only where both sexes lack a dewlap, but it is reduced and diminutive in about a dozen other species.
The dewlap serves as a signal for attracting partners, territoriality, deterring predators and communicating condition. When several anoles live together the species almost always differ in their dewlap, indicating that it plays a role in species recognition. Studies however reveal a more complex pattern: The bark anole and shortnosed anole species complex (which includes the Webster's and Cochran's gianthead anoles) are closely related and both vary in their dewlap color. In places where their ranges overlap their dewlaps often differ and there is little hybridization, but in some location their dewlaps are alike. Where alike there can be higher levels of hybridization (indicating that they are more likely to confuse each other) or levels can be as low as regions where they differ (indicating that something else allows them to separate each other). Another example is the red-fanned stout and large-headed anoles, which are sister species that overlap in range and are very similar except for their dewlap color. They are highly aggressive to individuals of their own species, but not the other. When one species has its dewlap color modified to resemble the other, only a relatively minor or no increase in aggression occurs, indicating that they still can separate each other.
In some anoles the sexes are very similar and difficult to separated under normal viewing conditions, but most species exhibit clear sexual dimorphism, which allows one to fairly easily discern between adult males and females. In a few species the female is slightly larger than the male, but in others the sexes are about the same size. However, in most the males are larger, in some more than three times the mass of females. This size difference can results in differences in the microhabitat (for example, males using larger branches than females) and feeding (males on average eating large prey) between the sexes of a single species. The males of many species are overall more brightly colored, while females are duller, more cryptic, and sometimes their upperparts have striped or lined patterns that serve to break up the outline of the anole. In general, the juvenile colors and pattern resemble those of the adult female. The dewlap tends to be distinctly larger and more colorful in males; in some species only the male has a dewlap. Anoles of some species have a crest on the nape, back and/or tail, which can be voluntarily raised and is larger in the males. In a few there are differences in the shape of the nose, but this is only known to be prominent in the proboscis and leaf-nosed anoles, which both have long-nosed males and more normal looking females (it is likely that something similar can be seen in smooth anole, but the female of that species is still unknown). A less obvious difference between anole sexes is the enlarged post-cloacal scales in males.
Territoriality and breeding
Anoles are highly territorial, and will fan their dewlap, bob their head, perform "push-ups" and a wide range of other behaviors to scare away potential competitors. If this does not scare off the intruder, a fight proceeds in which the two anoles attempt to bite each other. During fights some species of anoles are known to vocalize. In addition to the behaviors indicating dominance, anoles may move their head up and down in a head-nod display (not to be confused with the head-bob display where entire frontal part of body is moved through "push-ups"), which is a submissive sign. Females maintain a feeding territory. Males maintain a larger breeding territory, which overlaps with the feeding territory of one or several females. The home range is generally larger in males than in females, and larger in large anole species than in smaller. If removed from its territory an anole will usually be able to find its way back home in a relatively short time, but exactly how they do this is unclear. Being highly solitary animals, anoles will only infrequently congregate, but in colder regions individuals may rest adjacent to each other in groups during the winter.
In addition to differences in the appearance of the dewlap, the frequency of the dewlap opening/closing and the frequency and amplitude of the head bobbing differ between species, allowing them to separate each other. Territoriality is typically aimed at other individuals of the same species, but in a few cases it is also directed towards other anoles, as can be seen between the crested and Cook's anoles. Unlike most anoles with widely overlapping ranges, these two inhabit very similar niches and directly compete for resources.
The breeding period varies. In species or populations living in highly seasonal regions it is generally relatively short, typically during the wet season. It is prolonged, often even year-round, in species or populations living in regions with less distinct seasons. In some species where it is year-round the egg production is however higher during the rainy season than the dry season, and in many where it is prolonged but not year-round, it begins in the spring and ends in the fall.
Males attract and court females by performing a range of behaviors, often mirroring those used to scare away competitors, including extending their dewlap and bobbing their heads. During mating the male inserts one of his hemipenes into the female's cloaca, fertilizing the egg inside the oviduct. The female may mate with multiple males, but is also able to store sperm inside her body for fertilization of eggs several months after mating. A female anole produces an egg in each ovary, meaning that when one is maturing in one of her follicles the yolk of another is forming in the other. The white shell only forms when the egg has been fertilized and females will sometimes lay infertile, unshelled yellowish eggs known as "slugs". The female lays one (occasionally two) eggs per time, which typically is placed casually on the ground among leaf-litter, under debris, logs or rocks, or in a small hole. In some species it is placed at higher levels in a bromeliad, tree hole or rock crevice. A small number of species lay their eggs together, forming a communal nest. Among these is the unusual Cuban cave anole where as many as 25 eggs may be glued together in a small cavity on the side of a cave wall. A nest that contained eggs from the bay anole and the geckos Sphaerodactylus armasi and Tarentola crombiei represents the only known multi-species communal nest for an anole and the only known communal nest involving more than one family of lizard. Although typically only laying a single egg per time (clutch), females of many anole species can lay an egg every five days to four weeks. Some only have a single clutch per year, while other species may have as many as 20 on average. Depending on species, anole eggs hatch after about 30–70 days.
Anoles are opportunistic feeders, and may attempt to eat any attractive meal that is of the right size. They primarily feed on insects like flies, grasshoppers, crickets, caterpillars, moths, butterflies, beetles and ants, and arachnids like spiders. Several species will also eat small vertebrates such as mice, small birds (including nestlings), lizards (including other anole species and cannibalism of their own) and frogs. The slow-moving Cuban false chameleon anoles ("Chamaeleolis") are specialized snail-eaters, and a few semi-aquatic species like the Cuban stream anole may catch prey in water such as shrimp and fish. In some species the average prey-size varies with the individual anole's size, age and sex, with juvenile anoles eating the smallest prey, adult females taking intermediate-sized prey and adult males the largest prey. In other species there are no clear differences in the preferred prey size, regardless of an individual's size and sex. Hunting is done by sight. Many will chase down or sneak up to a potential prey item, while others are sit-and-wait predators that pounce on prey when it gets close to the anole. Anoles have numerous small, sharp and pointed teeth that allow them to effeciently grab their prey. They are heterodonts with each tooth in the frontal half of the jaw having a single tip (unicuspid) and each in a rear half having three tips (tricuspid); one in the middle and a smaller behind and in front of it. Unusually, the Cuban false chameleon anoles have enlarged and blunt, molar-like teeth in the rear part of their jaw, allowing them to crush the shells of their snail prey.
In addition to animal prey, many anole species will take plant material, notably fruits, flowers and nectar, and overall they are best described as omnivorous. Some fruit-eating species, like the knight anole, may function as seed dispersers. Anoles have been recorded drinking sweetened water from hummingbird feeders. Anoles are vulnerable to drying out and generally need access to water for drinking, like dew or rain on leaves, although some species are less susceptible to water loss than others and are able to live in relatively arid places.
Predator avoidance and deterrence
A wide range of animals will eat anoles, such as large spiders, centipedes, predatory katydids, snakes, large frogs, lizards, birds, monkeys and carnivoran mammals. At least in part of their range, snakes may be the most significant predator of anoles. For example, the Caribbean Alsophis and Borikenophis racers feed mostly on lizards like anoles. On some Caribbean Islands anoles make up as much as 40–75% of the diet of American kestrels. Large anoles may eat smaller individuals of other anole species and cannibalism—eating smaller individuals of their own species—is also widespread. There is a documented case of a small anole being captured and killed by an outside potted Venus flytrap plant.
Anoles mainly detect potential enemies by sight, but their hearing range also closely matches the typical vocal range of birds. If hearing a predatory bird, like a ketrel or hawk, they increase their vigilance. When hearing a non-predatory bird little or no change happens. Most anole species will try to escape from a predator by rapidly running or climbing away, but some will move to the opposite side of a tree trunk (facing away from the would-be attacker), jump to the ground from their perch or will freeze when disturbed, hoping the adversary does not spot it. Some anole species will show their fitness by displaying their dewlap when encountering a predator; the greater the endurance of the anole, the greater the display. Conversely, when suddenly forced to share their habitat with an effecient anole predator like the northern curly-tailed lizard (for example, if it is introduced to a place where formerly not present), the anoles may decrease the amplitude of their head bobbing, making them less conspicuous, and may become slower to emerge from hiding (less willing to take a risk) after having been scared by a predator. Slow-moving anoles, like the twig ecomorphs of the Caribbean and many Dactyloa species of mainland Central and South America, are generally cryptically colored and often coordinate their movements with the wind, resembling the surrounding vegetation. A few semi-aquatic species will attempt to escape from predators by diving into water or running bipedally across it, similar to basilisks. However, the anoles lack the specialized toe fringes that helps basilisks when doing this.
Anole tails often have the ability to break off at special segments, which is known as autotomy. The tail continues to wriggle for some minutes after detaching, attracting the attention of the predator and commonly allowing the anole to escape. The tail is regenerated, but it takes more than two months to complete this process. About two dozen anoles, including almost all members of the latifrons species group, all in the chamaeleonides species group and the La Palma anole, do not have the ability to autotomize the tail.
If caught or cornered, anoles will bite in self-defense. This can be relatively effective against some predators. When fighting back and biting, sometimes for as much as 20 minutes, Puerto Rican crested anoles escape from more than 1⁄3 of all attacks by Puerto Rican racer snakes. Some species of anoles will vocalize (typically rowls, chirps or squeals) when caught.
The evolution of anoles has been widely studied, and they have been described as a "textbook example of adaptive radiation and convergent evolution". Especially the widespread convergent evolution seen in anoles living in the Greater Antilles has attracted the attention of scientists, and resulted in comparisons with the Darwin's finches of the Galápagos Islands, lemurs of Madagascar and cichlid fish in the African Great Lakes.
Ecomorphs and origin
On each major Greater Antillean Island (Cuba, Hispaniola, Puerto Rico and Jamaica), there are anole species that have adapted to specific niches and are referred to as ecomorphs: crown giant, trunk crown, trunk, trunk ground, twig and grass bush (a few additional, less widely used ecomorphs also exist). However, even within the Greater Antilles there are differences depending on island size and the amount of available habitats. The largest, Cuba and Hispaniola, have all six primary ecomorphs, while the smaller Puerto Rico and Jamaica have five and four respectively. Species living in a specific niche on each island tend to resemble each other in both appearance and behavior. For example, the Escambray twig anole of Cuba closely resembles the Puerto Rican twig and Jamaican twig anoles, as well as several species of twig ecomorphs from Hispaniola. Despite this they are not closely related and have adapted to their specific niche independently of each other. At least four of the six primary ecomorphs are of ancient origin as they have been documented in amber fossils from Hispaniola that are about 15–20 million years old (the two missing ecomorphs are crown giant and grass bush). Otherwise there are few known fossils, but early phylogenetic and immunological studies indicate that anoles originated 40–66 million years ago, first inhabitant Central or South America, and then coming to the Caribbean (initially likely Cuba or Hispaniola). A more recent phylogenetic study, published in 2012, indicated that anoles originated in South America and diverged from other reptiles far earlier, about 95 million years ago. While a South American origin has been generally accepted, the very high age has been controversial and other studies published in 2011–2014 arrived at a lower age, estimating that anoles diverged from other reptiles 23–75, 53–72 or 81–83 million years ago, while a comprehensive study from 2017 estimated about 46–65 million years ago. This indicates that early anoles arrived on the Greater Antillean Islands in the Caribbean from the mainland of the Americas via rafting rather than overland via ancient (now submerged) land bridges. After arriving in the Caribbean they diversified into several new groups and one of these, the Norops lineage, later made its way back to mainland of the Americas.
Species and adaptability
Species level evolution in anoles can be very slow. Martinique originally consisted of four tiny islands, which then merged into a single as a result of uplifting. Anoles lived on each of the tiny ancient islands and were isolated six to eight million years ago. Despite this long separation, they did not experience allopatric speciation, as mixed couples of the different Martinique anole populations can successfully reproduce and remain part of a single species. The Barbados anole is part of the same group, but Barbados remains a separate, isolated island. The genetic divergence between the different Martinique anole populations is similar to that between other Lesser Antillean anoles consistently recognized as separate species. Another Lesser Antillean species, the Guadeloupean anole, has several distinct populations that generally are recognized as subspecies. However, Guadeloupean anoles exhibit high individual variability and the populations widely intergrade, something that possibly has been enhanced by habitats changes by humans (allowing populations to easier come into contact with each other) and translocations of individuals. This indicates that the subspecies are invalid today. Genetic studies confirm that strong assortative mating between the different Guadeloupean anole populations does not exist, despite their distinct differences in appearance and them having separated about 650,000 years ago (confidence interval starting at 351,000 years). Hybridization between different anole species has rarely been documented.
In contrast to this, anoles can change rapidly in response to changes and they are one of the few known examples if "visible evolution" (i.e., where changes happen at a speed where they can be observed within a human lifetime), together with groups like stickleback fish, guppies and Peromyscus beach mice. In studies of brown anoles introduced to Florida it has been seen that they can become longer-legger in a single generation when living with the predatory, ground-living northern curly-tailed lizard (shorter-legger anoles are slower and easier to catch for the curly-tailed lizard). Over a longer period, however, their legs become shorter, which are better suited for perching on smaller branches higher off the ground, out of reach for the curly-tailed lizard. When brown anoles are introduced to small islands with low vegetation, their legs become shorter, better suited for rapidly moving among the shrunken shrubbery to catch insects and avoid predatory birds. Furthermore, in a study where brown anoles were introduced to seven small, anole-free Bahaman islands (anoles had disappeared because of Hurricane Frances), it was seen that—although all populations became shorter-legged within a few years—this was proportional to the leg-size of the founders. In other words: The few founder brown anoles introduced to one island were shorter-legged than the few introduced to another. Both populations became shorter-legged over time, but the first remained shorter-legged than the second. This is an example of the founder effect. Similarly, when brown anoles were introduced to Florida, the native Carolina (or green) anoles moved to higher perches and gained larger toe pads better suited for those perches. This adaptation occurred in just 20 generations. Anoles are also adapting to life with humans: Puerto Rican crested anoles living in cities have developed more adhesive lamellae on their toe pads than ones living in forests, reflecting the need for being able to climb very smooth surfaces like windows in the former habitat. In contrast to these fast changes, anole's adaptability to temperature changes have traditionally been considered relatively minor. Nevertheless, when Puerto Rican crested anoles in Florida (where introduced in the 1970s) were compared to the original, native population in Puerto Rico, it was discovered that the former had become adapted to colder temperatures, by about 3 °C (5.4 °F). An even faster adaption was observed in Carolina anoles from Texas during the unusually cold winter of 2013–2014. Carolina anoles living in central Texas and further north were already adapted to relatively cold temperatures, but those of southern Texas were not. However, after the winter of 2013–2014, the cold tolerance of the southern Texan populations had increased by as much as 1.5 °C (2.7 °F) and their genomic profiles had changed to more closely resemble the more northerly living Carolina anoles.
The name for this group of lizards originates from the Carib anoli. It was modified and used in French Creole, and then transferred to English via the genus name Anolis, coined by French zoologist François Marie Daudin in 1802.
Several family names have been used for the anoles in recent decades. Initially they were placed in Iguanidae. This family, then comprising several very different groups, was split into eight families in 1989, with anoles being part of Polychrotidae together with Polychrus (bush anoles). However, genetic studies have shown that Polychrus is closer to Hoplocercidae than the true anoles. The true anoles are closer to Corytophanidae (basilisks and relatives). The true anoles have therefore been transferred to their own family Dactyloidae, alternatively listed as subfamily Dactyloinae of family Iguanidae. The name Anolidae (Cope, 1864) has sometimes been used, but it is a junior synonym of Dactyloidae (Fitzinger, 1843).
More than 425 species of true anoles are known. New species are regularly described, including 12 in 2016 alone. Most of the recent discoveries have been from the mainland of the Americas, with fewer new anoles described from the comparably better-known Caribbean Islands.
Traditionally, all the true anoles were included in the genus Anolis and some continue to use this treatment, in which case it is the largest genus of reptile. An attempt of dividing this huge genus was already made in 1959–1960, when they were placed in two major groups, the so-called "alpha anoles" (comprising most anole subgroups) and "beta anoles" (equalling today's Norops). In the following decades other changes were recommended. This included a proposal to recognize four genera, Anolis, Chamaeleolis, Chamaelinorops and Phenacosaurus, in 1976. In 1986, it was proposed that eight should be recognized: the four from 1976, and Ctenonotus, Dactyloa, Norops and Semiurus (the last was later replaced by its senior synonym Xiphosurus). These changes were adopted by some and rejected by others, who continued placing all in Anolis. In 1998–1999, the first comprehensive molecular studies of the anoles were published, confirming the earlier suspicion that the so-called "beta anoles" are a monophyletic group, but the "alpha anoles" are not. Furthermore, the genus splits proposed in 1976 and 1986 caused problems, as the narrowly defined Anolis was not monophyletic. In 2004, a major review based on several types of data (both molecular and morphological) revealed several groups and partially confirmed the genetic results from 1998–1999. No major changes were proposed and all anoles were maintained in a broadly defined Anolis. Two recent studies, primarily genetic and published in 2012 and 2017, confirmed several of the groups found in earlier studies, but rejected others. They found that the anoles fall into eight primary clades. Some of these can be further subdivided: For example, Chamaeleolis (from Cuba) is one of two subclades within Xiphosurus and it is sometimes considered a valid genus (in which case Xiphosurus is restricted to Hispaniola, Puerto Rico and nearby smaller islands). In contrast, the earlier proposed genus Phenacosaurus (from the Andes and tepui highlands in northwestern South America) is now included in Dactyloa. The phylogenetic position of most species is clear, but in a few the available evidence is conflicting and/or labelled with considerable statistic uncertainty.
The relationship of Dactyloidae can be described with a cladogram. Whether the eight groups are best recognized as separate genera or only as clades within a single genus, Anolis, is disputed. A few families between Polychrotidae and Corytophanidae+Dactyloidae are not shown:
|The eight proposed genera in Dactyloidae|
Relationship with humans
Anoles are model organisms often studied in fields such as ecology, behavior, physiology and evolution. The Carolina (or green) anole is the most-studied anole species, with the earliest dedicated studies being more than 100 years old, from the late 1800s. The Carolina anole was the first reptile where the entire genome was sequenced.
Anoles are harmless to humans, but if caught or cornered they will bite in self-defense. As typical of animals, the bite force is strongly correlated to the size of the anole. It causes little pain in the smaller anoles which usually do not break the skin. Large species have relatively strong jaws lined with small, sharp teeth, and their bite can be painful and result in a superficual wound, but it is still essentially harmlesss.
Some anole species are commonly kept in captivity as pets and especially the Carolina (or green) anole is often described as a good "beginner's reptile", but it too requires specialized care.
Anoles can function as a biological pest control by eating pest insects that may harm humans or plants. Anole abundances can be considerably higher in diversified agroecosystems (multiple different plant types) than high-intensity agroecosystems (typically only one or very few plant types, and regular use of agrochemicals), making the former particularly suitable for this type of pest control. However, because of their potential of becoming invasive species, releasing anoles outside their native range is strongly discouraged and often illegal, even if the species occurs elsewhere in a country (for example, it is illegal to release Carolina anoles to California, as its native range is in Southeastern United States).
The willingness of many anoles of living close to humans in heavily altered habitats have made them common. Some anoles can occur in very high densities, as illustrated by the Saint Vincent bush, Puerto Rican bush and spotted anoles where it has been estimated that there locally are almost 28,000 individuals per hectare (11,500 per acre) in the first species and at least 20,000–21,000 per hectare (8,000–8,500 per acre) in the last two. However, in most species the density is lower and in rare anoles it is can be well below 100 individuals per hectare (40 per acre). Some are restricted to specific habitats such as primary rainforest, making them more vulnerable. In a review in 2017, it was found that more than 50 anole species had a known total range that covered 100 km2 (40 sq mi) or less around their type locality. As of April 2018[update], only 90 anoles, equalling less than one-quarter of the total number of recognized species, had been rated by the IUCN. Most of these are either least concern (not threatened) or data deficient (limited available data prevents an assessment), but 7 are considered vulnerable, 14 endangered and 1 critically endangered. Typical threats to these are habitat loss from both humans and extreme weather, or competition/predation by introduced species. For example, the Finca Ceres anole, a critically endangered species only known from a single unprotected location in Matanzas Province, Cuba, has suffered habitat loss both due to hurricanes and expanding agricultural land. A. amplisquamosus, an endangered species only known from highland forest in the Cusuco National Park region of Honduras, was common in the early 2000s, but by 2006 it had experienced a drastic decline and was only infrequently encountered. A clear explanation for this is lacking, although it may be related to habitat loss due to human development and agriculture. Similarly, A. landestoyi, which only was described in 2016 and has not been rated by the IUCN, is restricted to the Loma Charco Azul reserve in Hispaniola, but it is seriously threatened by continuing illegal habitat destruction by slash-and-burn agriculture, livestock grazing and production of wood charcoal. Another example of a species that has not been rated by the IUCN is the strikingly colored blue anole from Colombia's Gorgona Island. It is threatened from deforestation and predation by the introduced western basilisks. Certain highly localized species can be threatened by other anoles. The Cook's anole, found only in southwestern Puerto Rico and considered endangered by the Puerto Rico Department of Natural and Environmental Resources, faces habitat loss and fragmentation from human development, predation by introduced species (especially cats and rats) and direct competition from a more widespread native, the Puerto Rican crested anole. The Puerto Rican crested anole has also been introduced to Dominica where it locally is outcompeting the endemic Dominican anole, having already largely displaced the South Caribbean ecotype (traditionally subspecies Anolis o. oculatus), which possibly may require a captive breeding program to ensure its survival.
Nevertheless, anoles overall do not appear to have experienced the widespread extinctions and extirpations prevalent among larger Caribbean reptiles. The Culebra Island giant anole is the only anole considered possibly extinct in recent history (other extinct anoles are prehistoric and only known from fossil remains that are millions of years old). Locals reported sighting of the Culebra Island giant anole as recent as the 1980s, but this likely involved misidentifications of young green iguanas. Others, at least the Morne Constant anole, do not grow as large today as they once did.
Species restricted to a specific habitat in relatively remote regions, infrequently visited by biologists looking for reptiles, are often virtually unknown and rarely recorded. In a review in 2017, it was found that 15 anole species only were known from their holotype. These may truly be rare and seriously threatened, as the proboscis anole, a species that only was known from a single specimen collected in 1953 until it was rediscovered in cloud forests of Ecuador in 2004. In others with few records, like the Neblina anole, this is not the case. It was initially known from six 1980s specimens from the remote Neblina highlands in Venezuela, but when the Brazilian part of these highlands were visited in 2017 it was discovered that the species was locally abundant. Some species are easily overlooked, even if common. For example, if searching for Orces' Andes anole during the night when asleep they can be fairly easy to find, but if visiting the same location during the day it can be very difficult to find any.
As introduced species
When introduced to regions outside their native range by humans, anoles may become invasive and represent a serious threat to small local animals. Such introductions may happen by mistake (for example, as "stowaways" on garden plants) or deliberately (as predators introduced to combat insects or release of pet anoles people no longer want).
In the contiguous United States, the Carolina anole has been introduced to California, the brown anole has been introduced to the Gulf Coast states and California, and the knight, Jamaican giant, bark, large-headed, Puerto Rican crested, Cuban green and Hispaniolan green anoles have been introduced to Florida. The Barbados and Morne Constant anoles have also been recorded in Florida, but do not appear to have become established. There are indications that the invasive brown anole is displacing the native Carolina anole in Florida and Texas by outcompeting it and eating its young. In the most disturbed habitats the Carolina anole may disappear entirely, but in less disturbed habitats where there is more cover (allowing young to avoid predation) it may remain fairly common, although it is forced to occur higher in trees where less visible to humans. Regardless, the Carolina anole is common and widespread overall, and it has itself been introduced to several regions outside its native range, including California, Hawaii, Guam, Palau, the Bahamas, Cayman Islands, Tamaulipas in Mexico, isolated locations in Spain, and Japan's Okinawa and Ogasawara (Bonin) Islands. In Japan's Ogasawara Islands, the introduced Carolina anoles have caused declines in native lizards and diurnal insects, including the near-extinction of the endemic Celastrina ogasawaraensis butterfly and five dragonfly species. This may be due to the ecological naïvete of the insects (before the introduction, there were no diurnal, highly arboreal lizards) and a very high anole density on these Japanese islands, as similar insect declines have not been reported from the Bahamas (which already had diurnal, arboreal lizards), or Guam, Saipan and Hawaii (where the anole density is lower). In addition to Florida, the Cuban green anole has been introduced to the Dominican Republic, São Paulo (Brazil) and Tenerife (Spain). In Florida and the Dominican Republic it competes with native anoles (Carolina anole and Hispaniolan green anole, respectively) and it is feared that something similar may happen in São Paulo. The same pattern can be seen in Dominica where the introduced Puerto Rican crested anole locally has displaced the endemic Dominican anole. The brown anole and Graham's anole have both been introduced to Bermuda where they threaten the very rare Bermuda skink. In the Cayman Islands the endemic Cayman blue-throated anole has moved to higher perched in places where the introduced brown anole is present (similar to the Carolina anole in places where brown anoles are present). Outside the Americas, the brown anole has been introduced to Hawaii, Tenerife, Singapore and Taiwan, and it is able to change ant communities on the last of these islands.
- Conant, R.; J.T. Collins (1998). A Field Guide to the Reptiles and Amphibians of Eastern and Central North America (3 ed.). pp. 208–215. ISBN 978-0395904527.
- Kristen A. Nicholson; Brian I. Crother; Craig Guyer; Jay M. Savage (10 September 2012). "It is time for a new classification of anoles (Squamata: Dactyloidae)" (PDF). Zootaxa. 3477: 1–108. Retrieved 19 May 2013.
- Poe; Nieto-Montes de Oca; Torres-Carvajal; Queiroz; Velasco; Truett; Gray; Ryan; Köhler; Ayala-Varela; Latella (2017). "A Phylogenetic, Biogeographic, and Taxonomic study of all Extant Species of Anolis (Squamata; Iguanidae)". Systematic Biology. 66 (5): 663–697. doi:10.1093/sysbio/syx029.
- Torres-Carvajal; Ayala-Varela; Lobos; Poe; Narváez (2017). "Two new Andean species of Anolis lizard (Iguanidae: Dactyloinae) from southern Ecuador". Journal of Natural History. 8: 1–23. doi:10.1080/00222933.2017.1391343.
- Losos, J. (5 June 2013). Lizard Super-Phylogeny Contains 4,000+ Species. Anole Annals. Retrieved 18 March 2018.
- Townsend; Mulcahy; Noonan; Sites Jr; Kuczynski; Wiens; Reeder (2011). "Phylogeny of iguanian lizards inferred from 29 nuclear loci, and a comparison of concatenated and species-tree approaches for an ancient, rapid radiation". Molecular Phylogenetics and Evolution. 61 (2): 363–380. doi:10.1016/j.ympev.2011.07.008.
- Losos, J.B. (2011). Lizards in an Evolutionary Tree: Ecology and Adaptive Radiation of Anoles. University of California Press. ISBN 978-0-520-26984-2.
- Savage, J.M. (2002). "The Amphibians and Reptiles of Costa Rica". University of Chicago Press: 444–480. ISBN 0-226-73537-0.
- Naish, D. (5 May 2011). "Lamellae, scansor pads, setae and adhesion… and the secondary loss of all of these things (gekkotans part IV)". Retrieved 21 March 2018.
- Kirsten Tyler; Winchell; Revell (2016). "Tails of the City: Caudal Autotomy in the Tropical Lizard, Anolis cristatellus, in Urban and Natural Areas of Puerto Rico". Journal of Herpetology. 50 (3): 435–441.
- Pyron; Burbrink; Wiens (2013). "A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes". BMC Evolutionary Biology. 13: 93. doi:10.1186/1471-2148-13-93.
- 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.
- "Nonnatives - Cuban Green Anole". Florida Fish and Wildlife Conservation Commission. Retrieved 20 March 2018.
- Ríos-López, N.; Alicea-Ortíz, J.D.; Burgos-Apont, E. (2016). "Natural History Observations in the Puerto Rican Dwarf Anole, Anolis occultus Williams and Rivero 1965 (Squamata: Dactyloidae): Nectar-Feeding, Bird Predation, and a Review of the Species' Natural History with Implications for Its Conservation". Life: The Excitement of Biology. 4 (2): 100–113. doi:10.9784/LEB4(2)Rios.01.
- Durso, A. (27 June 2013). Fill In The Blank: Obscure Anole Life History Traits. Anole Annals. Retrieved 22 March 2018.
- Domínguez, M.; Sanz, A.; Chávez, J.; Almaguer, N. (2010). "Cyclical Reproduction in Females of the Cuban Lizard Anolis lucius (Polychrotidae)". Herpetologica. 66 (4): 443–450.
- Herrel, and Holáňová (2008). Cranial morphology and bite force in Chamaeleolis lizards – Adaptations to molluscivory? Zoology 111: 467–475.
- Bartlett, R.D.; P. P. Bartlett (2008). Anoles, Basilisks, and Water Dragons. ISBN 978-0764137754.
- Monagan Jr.; Morris; Davis Rabosky; Perfecto; Vandermeer (2017). "Anolis lizards as biocontrol agents in mainland and island agroecosystems". Ecology and Evolution. 7: 7. doi:10.1002/ece3.2806.
- Suzuki-Ohno; Morita; Nagata; Abe; Makino; Kawata (2017). "Factors restricting the range expansion of the invasive green anole Anolis carolinensis on Okinawa Island, Japan". Ecol Evol. 7: 4357–4366. doi:10.1002/ece3.3002.
- Stroud; Giery; Outerbridge (2017). "Establishment of Anolis sagrei on Bermuda represents a novel ecological threat to Critically Endangered Bermuda skinks (Plestiodon longirostris)". Biological Invasions. 19 (6): 1723–1731.
- Hedges, B. (30 May 2017). "Cuba". CaribHerp. Retrieved 20 March 2018.
- Malhotra, A.; R.S. Thorpe (1999). Reptiles & Amphibians of the Eastern Caribbean. Macmillan Caribbean. ISBN 978-0333691410.
- Hedges, B. (30 May 2017). "Hispaniola". CaribHerp. Retrieved 20 March 2018.
- Gray; Meza-Lázaro; Poe; Nieto-Montes de Oca (2016). "A new species of semiaquatic Anolis (Squamata: Dactyloidae) from Oaxaca and Veracruz, Mexico". Herpetological Journal. 26: 253–262.
- Köhler, G. (2000). Reptilien und Amphibien Mittelamerikas. 2. Herpeton Verlag. pp. 57–71. ISBN 3-9806214-0-5.
- Salvador Mendoza, J. (29 February 2012). A View Of The Anole Diversity Of The Colombian Caribbean Coast. Anole Annals. Retrieved 20 March 2018.
- Antonio de Freitas; Coutinho Machado; Mendes Venâncio; Pereira; de França; Veríssimo (2013). "First record for Brazil of the Odd Anole lizard, Anolis dissimilis Williams, 1965 (Squamata: Polychrotidae) with notes on coloration". Herpetology Notes. 6: 383–385.
- Hedges, B. (30 May 2017). "Lesser Antilles". CaribHerp. Retrieved 20 March 2018.
- Ayala-Varela; Troya-Rodríguez; Talero-Rodríguez; Torres-Carvajal (2014). "A new Andean anole species of the Dactyloa clade (Squamata: Iguanidae) from western Ecuador". Amphibian & Reptile Conservation. 8 (1): 8–24.
- Hedges, B. (30 May 2017). "Puerto Rico–Virgin Islands". CaribHerp. Retrieved 20 March 2018.
- "Green Anole". New Hampshire PBS. 2017. Retrieved 20 April 2018.
- Distler; Dorcas; Gibbons; Kandl; Russel (1998). "Winter Mortality in the Green Anole, Anolis carolinensis (Lacertilia: Polychridae)". Brimleyana. 25: 140–143.
- "Nonnatives - Brown Anole". Florida Fish and Wildlife Conservation Commission. Retrieved 18 March 2018.
- "Brown Anole - Anolis sagrei". California Herps. Retrieved 18 March 2018.
- Losos, J. (29 July 2011). In Quest of Phenacosaurus. Anole Annals. Retrieved 30 March 2018.
- Scarpetta; Gray; Nieto-Montes de Oca; Castañeda; Herrel; Losos; Luna-Reyes; Jiménez Lang; Poe (2015). "Morphology and ecology of the Mexican cave anole Anolis alvarezdeltoroi". Mesoamerican Herpetology. 2: 260–268.
- Crother, B.I. (1999). Caribbean Amphibians and Reptiles. Academic Press. p. xxiv. ISBN 978-0121979553.
- Howard; Forester; Ruder; Parmerlee, Jr.; Powell (1999). "Natural History of a Terrestrial Hispaniolan Anole: Anolis barbouri". Journal of Herpetology. 33 (4): 702–706.
- Losos, J.B. (1992). "The Evolution of Convergent Structure in Caribbean Anolis Communities". Systematic Biology. 41 (4): 403–420. doi:10.1093/sysbio/41.4.403.
- Mahler; Ingram; Revell; Losos (2013). "Exceptional Convergence on the Macroevolutionary Landscape in Island Lizard Radiations". Science. 341 (6143): 292–295. doi:10.1126/science.12323923.
- Mahler; Lambert; Geneva; Ng; Hedges; Losos; Glor (2016). "Discovery of a Giant Chameleon-Like Lizard (Anolis) on Hispaniola and Its Significance to Understanding Replicated Adaptive Radiations". Am. Nat. 188 (3): 357–364. doi:10.1086/687566.
- Kahrl; Ivonov; Valero; Johnson (2018). "Ecomorphological Variation in Three Species of Cybotoid Anoles". Herpetologica. 74 (1): 29–37. doi:10.1655/Herpetologica-D-17-00040.
- Losos, J. (12 March 2013). "Scientists at Work: Quest for a little-known suburban lizard". New York Times. Retrieved 28 March 2018.
- Vitti, L.J.; Caldwell, J.P. (2009). Herpetology: An Introductory Biology of Amphibians and Reptiles (3 ed.). Elsevier. p. 524. ISBN 978-0-12-374346-6.
- Bleisch, M. "Anolis ophiolepis" (in German). saumfinger.de. Retrieved 18 April 2018.
- Scharf, I.; Meiri, S. (2013). "Sexual dimorphism of heads and abdomens: Different approaches to 'being large' in female and male lizards". Biological Journal of the Linnean Society. 110 (3): 665–673. doi:10.1111/bij.12147.
- Camposano; Krysko; Enge; Donlan; Granatosky (2008). "The Knight Anole (Anolis equestris) in Florida". Iguana. 15 (4): 212–219.
- Lotzkat; Hertz; Bienentreu; Köhler (2013). "Distribution and variation of the giant alpha anoles (Squamata: Dactyloidae) of the genus Dactyloa in the highlands of western Panama, with the description of a new species formerly referred to as D. microtus". Zootaxa. 3626 (1): 1–54. doi:10.11646/zootaxa.3626.1.1.
- Bradley K. (2011). "Alien Lizard – Care for the cryptic Cuban false chameleon". Reptiles. 2011 (April): 32–41.
- Hedges; Thomas (1989). "A new species of Anolis (Sauria: Iguanidae) from Sierra de Neiba, Hispaniola". Herpetologica. 45 (3): 330–336.
- Poe; Ayala; Latella; Kennedy; Christensen; Gray; Blea; Armijo; Schaad (2012). "Morphology, Phylogeny, and Behavior of Anolis proboscis". Breviora. 530: 1–11. doi:10.3099/530.1.
- Torres-Carvajal; Ayala; Carvajal-Campos (2010). "Reptilia, Squamata, Iguanidae, Anolis heterodermus Duméril, 1851: Distribution extension, first record for Ecuador and notes on color variation". Check List. 6 (1): 189–190. doi:10.15560/6.1.189.
- Leal, Manuel; Knox, Alison K. & Losos, Jonathan B. (2002). "Lack of convergence in aquatic Anolis lizards". Evolution. 56 (4): 785–791. doi:10.1554/0014-3820(2002)056[0785:lociaa]2.0.co;2.
- Hagey; Harte; Vickers; Harmon; Schwarzkopf (2017). "There's more than one way to climb a tree: Limb length and microhabitat use in lizards with toe pads". PLoS One. 12 (9): e0184641. doi:10.1371/journal.pone.0184641.
- Elstrott, J.; D.J. Irschick (2004). "Evolutionary correlations among morphology, habitat use and clinging performance in Caribbean Anolis lizards". Biological Journal of the Linnean Society. 83 (3): 389–398. doi:10.1111/j.1095-8312.2004.00402.x.
- Macrini; Irschick; Losos (2003). "Ecomorphological Differences in Toepad Characteristics between Mainland and Island Anoles". Journal of Herpetology. 37 (1): 52–58. doi:10.1670/0022-1511(2003)037[0052:EDITCB]2.0.CO;2.
- Beans, C. (26 April 2016). "Lizard gets to grips with city life by evolving stickier feet". New Scientist. Retrieved 30 March 2018.
- Nicholson; Mijares-Urrutia; Larson (2006). "Molecular phylogenetics of the Anolis onca series: a case history in retrograde evolution revisited". Journal of Experimental Zoology Part B Molecular and Developmental Evolution. 305 (5): 450–459. doi:10.1002/jez.b.21098.
- Losos, J. (2 April 2013). Anole Beach Party In Venezuela. Anole Annals. Retrieved 28 March 2018.
- Munoz, Martha (November 16, 2012). "Physiological Adaptation On Ecological Timescales – New Research by Alex Gunderson and Manuel Leal". Anole Annals. Retrieved November 18, 2012.
- Rothblum; Watkins; Jenssen (1979). "A Learning Paradigm and the Behavioral Demonstration of Audition for the Lizard Anolis grahami". Copeia. 1979 (3): 490–494.
- Kolbe; Feeley; Battles; Stroud, Field Identification Guide for the Anole Lizards of Miami (PDF), retrieved 19 April 2018
- Campbell, J.A. (1998). Amphibians and Reptiles of Northern Guatemala, the Yucatan, and Belize. University of Oklahoma Press. pp. 131–141. ISBN 0-8061-3064-4.
- Lambert, S. (11 April 2014). Spotlight on Cuban Anoles, Part II: Anolis lucius. Anole Annals. Retrieved 19 April 2018.
- Cantwell, L.R.; Forrest, T.G. (2013). "Response of Anolis sagrei to Acoustic Calls from Predatory and Nonpredatory Birds". Journal of Herpetology. 47 (2): 293–298.
- Huang; Lubarsky; Teng; Blumstein (2011). "Take only pictures, leave only...fear? The effects of photography on the West Indian anole Anolis cristatellus". Current Zoology. 57 (1): 77−82.
- Losos, J. (7 December 2017). Night Time Activity by the Brown Anole in Guatemala. Anole Annals. Retrieved 15 March 2018.
- Kamath, A. (25 June 2016). Nocturnal Behavior in the Green Anole. Anole Annals. Retrieved 15 March 2018.
- Macedonia; Echternacht; Walguarnery (2003). "Color Variation, Habitat Light, and Background Contrast in Anolis carolinensis along a Geographical Transect in Florida". Journal of Herpetology. 37 (3): 467–478.
- Boyer, J.F.F.; L. Swierk (2017). "Rapid body color brightening is associated with exposure to a stressor in an Anolis lizard". Canadian Journal of Zoology. 95 (3): 213–219. doi:10.1139/cjz-2016-0200.
- Jenssen; Greenberg; Hovde (1995). "Behavioral profile of free-ranging male Anolis carolinensis across breeding and post-breeding seasons". Herpetol. Monographs. 9: 41–62.
- Losos, J. (24 February 2012). New Study on Color Change In Green Anoles. Anole Annals. Retrieved 21 March 2018.
- Claussen, D.L.; Art, G.R. (1981). "Heating and cooling rates in Anolis carolinensis and comparisons with other lizards". Comparative Biochemistry and Physiology Part A: Physiology. 69 (1): 23–29. doi:10.1016/0300-9629(81)90634-4.
- Yabuta, S.; Suzuki-Watanabe, A. (2011). "Function of Body Coloration in Green Anoles (Anolis carolinensis) at the Beginning of the Breeding Season: Advertisement Signaling and Thermoregulation". Current Herpetology. 30 (2): 155–158. doi:10.5358/hsj.30.155.
- Taylor, J.D.; M.E. Hadley (1970). "Chromatophores and Color Change in the Lizard, Anolis carolinensis". Zeitschrift für Zellforschung und Mikroskopische Anatomie. 104 (2): 282–294.
- "Nonnatives - Bark Anole". Florida Fish and Wildlife Conservation Commission. Retrieved 29 March 2018.
- Badger, D.P. (2006). Reptiles. Voyageur Press. p. 100. ISBN 978-0-7603-2579-7.
- Rand, A.S.; Andrews, R. (1975). "Adult color dimorphism and juvenile pattern in Anolis cuvieri". Journal of Herpetology. 9 (2): 257–260.
- Macedonia, J.M. (2001). "Habitat light, colour variation, and ultraviolet reflectance in the Grand Cayman anole, Anolis conspersus". Biological Journal of the Linnean Society. 73 (3): 299–320. doi:10.1006/bijl.2001.0545.
- Legreneur, P. (7 April 2012). The Anoles Of Guadeloupe. Anole Annals. Retrieved 27 March 2018.
- Legreneur, P. (11 September 2013). United Colors Of Guadeloupe Anoles. Anole Annals. Retrieved 16 March 2018.
- "The ever-adaptable anole". Lab Anim (NY). 41 (6): 149. 2012. doi:10.1038/laban0612-149.
- Losos, J. (30 May 2014). Green Anole Color Morphs. Anole Annals. Retrieved 25 March 2018.
- Nicholson; Harmon; Losos (2007). "Evolution of Anolis Lizard Dewlap Diversity". PLoS One. 2 (3): e274. doi:10.1371/journal.pone.0000274.
- Ingram; Harrison; Mahler; Castañeda; Glor; Herrel; Stuart; Losos (2016). "Comparative tests of the role of dewlap size in Anolis lizard speciation". Proc Biol Sci. 283 (1845): 20162199. doi:10.1098/rspb.2016.2199.
- Crawford, C. (2011). "Anolis carolinensis – Green anole". Animal Diversity Web. Retrieved 20 March 2018.
- Schwartz, A. (1968). "Geographic Variation in Anolis distichus Cope (Lacertilia, Iguanidae) in the Bahama Islands and Hispaniola". Bulletin of the Museum of Comparative Zoology at Harvard College. 137: 255–309.
- Lambert; Geneva; Mahler; Glor (2013). "Using genomic data to revisit an early example of reproductive character displacement in Haitian Anolis lizards". Molecular Ecology. 22 (15). doi:10.1111/mec.12292.
- Ng, J.; Geneva, A.J.; Noll, S.; Glor, R.E. (2017). "Signals and Speciation: Anolis Dewlap Color as a Reproductive Barrier". Journal of Herpetology. 51 (3): 437–447. doi:10.1670/16-033.
- Gartner; Gamble; Jaffe; Harrison; Losos (2013). "Left–right dewlap asymmetry and phylogeography of Anolis lineatus on Aruba and Curaçao". Biological Journal of the Linnean Society. 110 (2): 409–426. doi:10.1111/bij.12131.
- Lovern; Holmes; Wade (2004). "The Green Anole (Anolis carolinensis): A Reptilian Model for Laboratory Studies of Reproductive Morphology and Behavior". ILAR Journal. 45 (1): 54–64. doi:10.1093/ilar.45.1.54.
- Landestoy, M. (25 May 2013). A Little Giant’s Dewlap… Why Do They Need One? Anole Annals. Retrieved 27 March 2018.
- Orrell, K.S.; Jenssen, T.A. (1998). "Display Behavior of Anolis bahorucoensis: an Anole with a Diminutive Dewlap". Caribbean Journal of Science. 34 (1): 113–125. doi:10.1093/ilar.45.1.54.
- Tokarz, Richard R. (2005). "Importance of Dewlap Display in Male Mating Success in Free-Ranging Brown Anoles". Bio One.
- Lailvaux, SP & Irschick, D (August 6, 2007). "The evolution of performance-based male fighting ability in Caribbean Anolis lizards". American Naturalist. 170: 573–86. doi:10.1086/521234. PMID 17891736.
- Losos, J.B.; Thorpe, R.S. (2004). Dieckmann; Doebeli; Metz; Tautz, eds. Evolutionary Diversification of Caribbean Anolis Lizards (PDF). Adaptive Speciation. Cambridge University Press. pp. 322–344. ISBN 9781139342179.
- Stapley, J.; Wordley, C.; Slate, J. (2011). "No Evidence of Genetic Differentiation Between Anoles With Different Dewlap Color Patterns". Journal of Heredity. 102 (1): 118–124. doi:10.1093/jhered/esq104.
- Losos, J.B. (1985). "An Experimental Demonstration of the Species-Recognition Role of Anolis Dewlap Color". Copeia. 1985 (4): 905. doi:10.2307/1445240.
- Ord; Klomp; Garcia-Porta; Hagman (2015). "Repeated evolution of exaggerated dewlaps and other throat morphology in lizards". Journal of Evolutionary Biology. 28 (11): 1948–1964. doi:10.1111/jeb.12709.
- Deepak; Giri; Asif; Dutta; Vyas; Zambre; Bhosale; Karanth (2016). "Systematics and phylogeny of Sitana (Reptilia: Agamidae) of Peninsular India, with the description of one new genus and five new species". 67–111. 85 (1): 67–111.
- Yánez-Muñoz, M.H.; M.A. Urgilés; M. Altamirano Benavides; S.R. Cáceres (2010). "Redescripción de Anolis proboscis Peters & Orcés (Reptilia: Polychrotidae), con el descubrimiento de las hembras de la especie y comentarios sobre su distribución y taxonomía". Avances en Ciencias e Ingeniería. 2: 1–14.
- Armstead; Ayala-Varela; Torres-Carvajal; Ryan; Poe (2017). "Systematics and ecology of Anolis biporcatus (Squamata: Iguanidae)". Salamandra. 52 (2): 285–293.
- Butler; Sawyer; Losos (2007). "Sexual dimorphism and adaptive radiation in Anolis lizards". Nature. 447: 202–205. doi:10.1038/nature05774.
- Schoener, T.W. (1967). "The Ecological Significance of Sexual Dimorphism in Size in the Lizard Anolis conspersus". Science. 155 (3761): 474–477. doi:10.1126/science.155.3761.474.
- Bartlett, R.D.; P. P. Bartlett (2001). Anoles. pp. 11–12. ISBN 0-7641-1702-5.
- Rodrigues, M.T.; V. Xavier; G. Skuk; D. Pavan (2002). "New specimens of Anolis phyllorhinus (Squamata, Polychrotidae): the first female of the species and of proboscid anoles". Pap. Avulsos Zool. (São Paulo). 42 (16). doi:10.1590/S0031-10492002001600001.
- Ord, T.J. (2008). "Dawn and Dusk "Chorus" in Visually Communicating Jamaican Anole Lizards". Am. Nat. 172 (4): 585–592. doi:10.1086/590960.
- Greenberg, N. (2003). "Sociality, stress, and the corpus striatum of the green anolis lizard". Physiology & Behavior. 79 (3): 429–440.
- Milton, T.H.; Jenssen, T.A. (1979). "Description and Significance of Vocalizations by Anolis grahami (Sauria: Iguanidae)". Copeia. 1979 (3): 481–489.
- Stamps, J.A.; Barlow, G.W. (1973). "Variation and stereotypy in the displays of Anolis aeneus (Sauria: Iguanidae)". Behaviour. 47 (1/2): 67–94.
- Crews D. (1975). "Inter- and intraindividual variation in display patterns in the lizard, Anolis carolinensis". Herpetologica. 31 (1): 37–47.
- Tokarz, R.R. (1985). "Body size as a factor determining dominance in staged agonistic encounters between male brown anoles (Anolis sagrei)". Anim Behav. 33 (3): 746–753. doi:10.1016/S0003-3472(85)80006-3.
- Richards, P.M.; K.E. Nicholson (2011). "Home-range size and overlap within an introduced population of the Cuban Knight Anole, Anolis equestris (Squamata: Iguanidae)". Phyllomedusa: Journal of Herpetology. 10 (1): 65–73.
- Gorman, J. (6 July 2015). "Mystery of the Lizards That Know the Way Home". New York Times. Retrieved 19 April 2018.
- Marrero, R.; Torres, T.; Rodríguez-Cabrera, T.M. (2016). "Winter aggregation in Anolis equestris and A. lucius (Squamata: Dactyloidae), two territorial species from Cuba". Phyllomedusa. 15 (2): 181–186. doi:10.11606/issn.2316-9079.v15i2p181-186.
- Ord, T.J.; Martins, E.P. (2016). "Tracing the origins of signal diversity in anole lizards: Phylogenetic approaches to inferring the evolution of complex behaviour". Animal Behaviour. 71 (6): 1411–1429. doi:10.1016/j.anbehav.2005.12.003.
- Jenssen; Marcellini; Pague; Jenssen (1984). "Competitive Interference between the Puerto Rican Lizards, Anolis cooki and A. cristatellus". Copeia. 1984 (4): 853–862.
- Muñoz, M. (8 January 2018). SICB 2018: Revisiting the Fitch-Hillis Hypothesis in Mexican Anoles. Anole Annals. Retrieved 16 March 2018.
- Hailey, BA (30 March 2017). "Anolis cristatellus (Puerto Rican crested anole)". animals.mom.me. Retrieved 22 March 2018.
- Kahrl, A. (16 January 2016). SICB 2016: Do Seasonal Changes in Developmental Temperature Have Season-Specific Fitness Consequences?. Anole Annals. Retrieved 16 March 2018.
- Team, Ben. "Anole lizard: How long until the egg hatches?". animals.mom.me. Retrieved 17 March 2018.
- Reinke; Erritouni; Calsbeek (2018). "Maternal allocation of carotenoids to eggs in an Anolis lizard". Comparative biochemistry and physiology. Part A, Molecular & integrative physiology. 218: 56–62. doi:10.1016/j.cbpa.2018.01.014.
- Calsbeek; Bonneaud; Prabhu; Manoukis; Smith (2007). "Multiple paternity and sperm storage lead to increased genetic diversity in Anolis lizards". Evolutionary Ecology Research. 9 (3): 495–503.
- Walls, J.G: Breeding Anoles. Reptile Magazine. Retrieved 16 March 2018.
- Rand, A.S. (1967). "Communal Egg Laying in Anoline Lizards". Herpetologica. 23 (3): 227–230.
- Robinson, C.D.; Kircher, B.K.; Johnson, M.A. (2014). "Communal Nesting in the Cuban Twig Anole (Anolis angusticeps) from South Bimini, Bahamas". IRCF Reptiles & Amphibians. 21 (2): 71–72.
- Alfonso; Charruau; Fajardo; Estrada (2012). "Interspecific communal oviposition and reproduction of three lizard species in Southeastern Cuba". Herpetology Notes. 5: 73–77.
- Holáňová, Rehák, and Frynta (2012). Anolis sierramaestrae sp. nov. (Squamata: Polychrotidae) of the “chamaeleolis” species group from Eastern Cuba. Acta Soc. Zool. Bohem. 76: 45–52.
- Losos, Jonathan (May 10, 2011). "They Don't Eat Butterflies, Do They?". Anole Annals. Retrieved November 19, 2012.
- Tan, H.H.; K.K.P. Lim (2012). "Recent introduction of the brown anole Norops sagrei (Reptilia: Squamata: Dactyloidae) to Singapore". Nature in Singapore. 5: 359–362.
- Vitt; Shepard; Vieira; Caldwell; Colli; Mesquita (2008). "Ecology of Anolis nitens brasiliensis in Cerrado Woodlands of Cantão". Copeia. 2008 (1): 144–153. doi:10.1643/CP-06-251.
- Powell, R.; A. Watkins (2014). "First Report of Cannibalism in the Saba Anole (Anolis sabanus), with a Review of Cannibalism in West Indian Anoles". IRCF Reptiles & Amphibians. 21 (4): 137–137.
- Torres, J.; M. Acosta (2014). "Predation attempt by Anolis porcatus (Sauria, Dactyloidae) on Mus musculus (Rodentia, Muridae)". Herpetology Notes. 7: 525–526.
- Berkovitz, B.K.B.; R.P Shellis (2017). The Teeth of Non-Mammalian Vertebrates. Elsevier. pp. 197–198. ISBN 978-0-12-802850-6.
- Zahradnicek; Buchtova; Dosedelova; Tucker (2014). "The development of complex tooth shape in reptiles". Front Physiol. 5 (74). doi:10.3389/fphys.2014.00074.
- Dalrymple, G.H. (1980). "Comments on the Density and Diet of a Giant Anole Anolis equestris". Journal of Herpetology. 14 (4): 412. doi:10.2307/1563699.
- Giery; Vezzani; Zona; Stroud (2017). "Frugivory and seed dispersal by the invasive knight anole (Anolis equestris) in Florida, USA". Food Webs. 11: 13–16. doi:10.1016/j.fooweb.2017.05.003.
- Purser, P. "Green Anole Care Sheet". Mongabay. Retrieved 22 March 2018.
- Lazell, J. (2005). Island: Fact and Theory in Nature. University of California Press. pp. 151–152. ISBN 0-520-24352-8.
- Losos, J. (19 March 2013). "Scientists at Work: Lizard Olympics". New York Times. Retrieved 28 March 2018.
- Henderson, R.W.; Sajdak, R.A. (1996). Powell, R.; Henderson, R.W., eds. Diets of West Indian racers (Colubridae: Alsophis): Composition and biogeographic implications. Contributions to West Indian Herpetology: A Tribute to Albert Schwartz. 12. Society for the Study of Amphibians and Reptiles, Contributions to Herpetology. pp. 327–338.
- McNeil, J. (2009). "The Venusian Lizard Trap". Carnivorous Plant Newsletter. 38 (2): 54.
- Zani, P. (1996). "Patterns of caudal‐autotomy evolution in lizards". Journal of Zoology. 240 (2): 201–220. doi:10.1111/j.1469-7998.1996.tb05280.x.
- Leal, M. (1999). "Honest signalling during prey–predator interactions in the lizard Anolis cristatellus". Animal Behaviour. 58 (3): 521–526. doi:10.1006/anbe.1999.1181.
- Steinberg; Losos; Schoener; Spiller; Kolbe; Leal (2004). "Predation-associated modulation of movement-based signals by a Bahamian lizard". PNAS. 11 (25): 9187–9192. doi:10.1073/pnas.1407190111.
- Stroud, J.T. (27 June 2017). "Evolution 2017: It Doesn't Pay to Be Risky When Predators Are About". Anole Annals. Retrieved 20 April 2018.
- Bauer; Jackman (2008). "Global diversity of lizards in freshwater (Reptilia: Lacertilia)". Hydrobiologia. 595 (1): 581–586.
- Howard, J. (21 August 2014). "Scientists Have Figured Out How Lizards Regrow Their Tails, And That's Good News For Humans". Huffington Post. Retrieved 16 March 2018.
- Losin, N. (19 September 2011). "Video from the Field: Bite Force!". National Geographic. Retrieved 29 March 2018.
- Leal, M.; Rodríguez-Robles, J.A. (1995). "Antipredator Responses of Anolis cristatellus (Sauria: Polychrotidae)". Copeia. 1995 (1): 155–161.
- del Rosario Castañeda; Sherratt; Losos (2014). "The Mexican amber anole, Anolis electrum, within a phylogenetic context: implications for the origins of Caribbean anoles". Zoological Journal of the Linnean Society. 172 (1): 133–144. doi:10.1111/zoj.12159.
- Yong, E. (18 July 2013). "Lookalike Lizards and the Predictability of Evolution". National Geographic. Retrieved 27 March 2018.
- Pinto; Mahler; Harmon; Losos (2008). "Testing the island effect in adaptive radiation: rates and patterns of morphological diversification in Caribbean and mainland Anolis lizards". Proc Biol Sci. 275 (1652): 2749–2757. doi:10.1098/rspb.2008.0686.
- Losos, J.B (2001). "Evolution: A Lizards Tale". Scientific American. 284: 64–69.
- Barrat, J. (27 July 2015). "Trapped in Amber: Ancient fossils reveal remarkable stability of Caribbean lizard communities". Smithsonian Insider. Retrieved 27 March 2018.
- Sherratt; del Rosario Castañeda; Garwood; Mahler; Sanger; Herrel; de Queiroz; Losos (2015). "Amber fossils demonstrate deep-time stability of Caribbean lizard communities". PNAS. 112 (32): 9961–9966. doi:10.1073/pnas.1506516112.
- Subbaraman, N. (18 July 2013). "Caribbean lizards show that evolution repeats itself". NBC News. Retrieved 28 March 2018.
- Thorpe; Surget-Groba; Johansson (2010). "Genetic Tests for Ecological and Allopatric Speciation in Anoles on an Island Archipelago". PLoS Genet. 6 (4): e1000929. doi:10.1371/journal.pgen.1000929.
- "How Important Is Geographical Isolation in Speciation?". ScienceDaily. 1 May 2010. Retrieved 6 May 2010.
- Legreneur, P. (October 2013), Répartition des anoles de la Guadeloupe I. Basse-Terre, Grande-Terre, ilets Pigeon et ilets à Kahouanne, doi:10.13140/RG.2.2.34621.46569
- Muñoz; Crawford; McGreevy; Messana; Tarvin; Revell; Zandvliet; Hopwood; Mock; Schneider; Schneider (2013). "Divergence in coloration and ecological speciation in the Anolis marmoratus species complex". Mol. Ecol. 22 (10): 2668–2682. doi:10.1111/mec.12295.
- Vastag, B. (4 February 2014). "Castaway lizards put evolution to the test". Washington Post. Retrieved 27 March 2018.
- Kolbe; Leal; Schoener; Spiller; Losos (2012). "Founder Effects Persist Despite Adaptive Differentiation: A Field Experiment with Lizards". Science. 335 (6072): 1086–1089. doi:10.1126/science.1209566.
- Stuart; Campbell; Hohenlohe; Reynolds; Revell; Losos (2014). "Rapid evolution of a native species following invasion by a congener". Science. 346 (6208): 463–466. doi:10.1126/science.1257008.
- Leal, M.; Gunderson, A.R. (2012). "Rapid change in the thermal tolerance of a tropical lizard". Am. Nat. 3180 (6): 815–822. doi:10.1086/668077.
- Campbell-Staton; Cheviron; Rochette; Catchen; Losos; Edwards (2017). "Winter storms drive rapid phenotypic, regulatory, and genomic shifts in the green anole lizard". Science. 357 (6350): 495–498. doi:10.1126/science.aam5512.
- Bolotnikova, M.N. (3 August 2017). "Extreme-weather Evolution". Harvard Magazine. Retrieved 30 March 2018.
- Uetz, P.; Hallermann, J. (2018). "Dactyloidae". The Reptile Database. Retrieved 15 March 2018.
- Harris, M.; N. Vincent, eds. (2003). The Romance Languages. Routledge. p. 467. ISBN 0-415-16417-6.
- Daudin, F.M. (1802). Histoire Naturelle, Générale et Particulière des Reptiles. F. Dufart, Paris.
- Frost, D.R.; R.E. Etheridge (1989). A phylogenetic analysis and taxonomy of iguanian lizards (Reptilia: Squamata). Univ. Kansas Mus. Nat. Hist. Misc. Publ. 81. ISBN 0-89338-033-4.
- Losos, J. (3 August 2011). New Multilocus Phylogeny Confirms that Polychrus is Not Sister to Anolis. Anole Annals. Retrieved 18 March 2018.
- Williams,E.E. (1976). "West Indian Anoles: a taxonomic and evolutionary summary. 1. Introduction and a species list". Breviora. 440: 1–21.
- Williams,E.E. (1976). "South American anoles: the species groups". Papeis Avulsos Zoologia. 29: 259–268.
- Guyer, C.; Savage, J.M. (1986). "Cladistic relationships among anoles (Sauria: Iguanidae)". Systematic Zoology. 35 (4): 509–531.
- Losos; Jackman; Larson; de Queiroz; Rodriguez-Schettino (1998). "Contingency and determinism in replicated adaptive radiations of island lizards". Science. 279 (5359): 2115–2118. doi:10.1126/science.279.5359.2115.
- Jackman; Larson; de Queiroz; Losos (1999). "Phylogenetic relationships and tempo of early diversification of Anolis lizards". Systematic Biology. 48 (2): 254–285.
- Poe, S. (2004). "Phylogeny of Anoles". Herpetological Monographs. 18: 37–89.
- Poe, S. (2013). "1986 Redux: New genera of anoles (Squamata: Dactyloidae) are unwarranted". Zootaxa. 3626 (2): 295–299. doi:10.11646/zootaxa.3626.2.7.
- Nicholson; Crother; Guyer; Savage (2014). "Anole classification: A response to Poe". Zootaxa. 3814 (1): 109–120. doi:10.11646/zootaxa.3814.1.67.
- "Anole Genome Project". Broad Institute. Retrieved 17 March 2018.
- Alföldi, J.; et al. (2011). "The genome of the green anole lizard and a comparative analysis with birds and mammals". Nature. 477: 587–591. doi:10.1038/nature10390.
- Wittorski; Losos; Herrel (2016). "Proximate determinants of bite force in Anolis lizards". Journal of Anatomy. 228 (1): 85–95. doi:10.1111/joa.12394.
- "Cuban Knight Anole". butterflies.heuristron.net. Retrieved 21 April 2018.
- McLeod, L. (18 September 2017). "Do Green Anoles Make Good Pets?". The Spruce. Retrieved 22 March 2018.
- "Green Anole - Anolis carolinensis". California Herps. Retrieved 18 March 2018.
- Kaplan, M. (1997). "Releasing Captive Reptiles and Amphibians". anapsid.org. Retrieved 22 March 2018.
- Butler, T. (7 March 2007). "World's only blue lizard heads toward extinction". Mongabay. Retrieved 20 March 2018.
- "Saban Anole". Dutch Caribbean Nature Alliance. Retrieved 20 March 2018.
- Hite; Rodríguez Gómez; Larimer; Díaz-Lameiro; Powell (2008). "Anoles of St. Vincent (Squamate: Polychrotidae): population densities and structural habitat use". Caribbean Journal of Science. 44 (1): 102–115.
- Meiri; Bauer; Allison; et al. (2017). "Extinct, obscure or imaginary: The lizard species with the smallest ranges". Divers Distrib. 24 (3): 1–12. doi:10.1111/ddi.12678.
- "Anolis". The IUCN Red List of Threatened Species. IUCN. 2018. Retrieved 10 April 2018.
- de Queiroz, K.; Powell, R.; Hedges, S.B. & Mayer, G.C. (2018). "Anolis juangundlachi". The IUCN Red List of Threatened Species. IUCN. 2011: e.T178278A7512731. doi:10.2305/IUCN.UK.2011-1.RLTS.T178278A7512731.en. Retrieved 20 March 2018.
- Townsend; Wilson; Talley; Fraser; Plenderleith; Hughes (2006). "Additions to the herpetofauna of Parque Nacional El Cusuco, Honduras". Herpetological Bulletin. 96: 29–39.
- Mayer, G.C. (2018). "Anolis amplisquamosus". The IUCN Red List of Threatened Species. IUCN. 2011: e.T178363A7531612. doi:10.2305/IUCN.UK.2011-1.RLTS.T178363A7531612.en. Retrieved 20 March 2018.
- Landestoy, M. (6 October 2016). How a Well-Hidden Giant Got Uncovered: the Discovery of a New Anole Species from Hispaniola. Anole Annals. Retrieved 28 March 2018.
- Rodríguez-Robles, J.A.; Jezkova, T.; Leal, M. (2008). "Genetic structuring in the threatened "Lagartijo del Bosque Seco" (Anolis cooki) from Puerto Rico". Mol Phylogenet Evol. 46 (2): 503–514. doi:10.1016/j.ympev.2007.11.006.
- Eales; Thorpe; Malhotra (2008). "Weak founder effect signal in a recent introduction of Caribbean Anolis". Molecular Ecology. 17 (6): 1416–1426. doi:10.1111/j.1365-294X.2007.03684.x.
- Malhotra; Thorpe; Hypolite; Arlington (2007). "A report on the status of the herpetofauna of the Commonwealth of Dominica, West Indies". Appl. Herpetol. 4 (2): 177–194. doi:10.1163/157075407780681365.
- Bochaton, B. (3 July 2017). Subfossil Record Reveals Human Impacts on a Lesser Antillean Endemic Anole. Anole Annals. Retrieved 20 March 2018.
- de Queiroz, K. & Mayer, G.C. (2018). "Anolis roosevelti". The IUCN Red List of Threatened Species. IUCN. 2011: e.T1319A3418702. doi:10.2305/IUCN.UK.2011-1.RLTS.T1319A3418702.en. Retrieved 20 March 2018.
- Gaa Ojeda Kessler, A. (2010). "Status of the Culebra Island giant anole (Anolis roosevelti)" (PDF). Herpetological Conservation and Biology. 5 (2): 223–232.
- Prates, I. (14 May 2017). Legendary Brazilian Anoles Rediscovered. Anole Annals. Retrieved 30 March 2018.
- Almendariz, A. C.; Vogt, C. (2007). "Anolis proboscis (Squamata: Polychrotidae), Una lagartija rara pero no extinta" (PDF). Politécnica. 27 (4): Biología 7 133–135.
- Mayer, G.C. & Poe, S. (2018). "Anolis proboscis". The IUCN Red List of Threatened Species. IUCN. 2013: e.T178727A7604096. Retrieved 30 March 2018.
- Prates, I. (11 December 2017). Notes on the Neblina tepui Anole (Anolis neblininus), Discovered in Brazil. Anole Annals. Retrieved 30 March 2018.
- Losos, J. (6 August 2011). The Principle of Unsympathetic Magic Strikes (Yet) Again II. Anole Annals. Retrieved 30 March 2018.
- Conyers, J. & Wingate, D. (2018). "Plestiodon longirostris ". The IUCN Red List of Threatened Species. IUCN. 1996: e.T8218A12900393. doi:10.2305/IUCN.UK.1996.RLTS.T8218A12900393.en. Retrieved 20 March 2018.
- "Nonnatives - Barbados Anole". Florida Fish and Wildlife Conservation Commission. Retrieved 20 March 2018.
- "Nonnatives - Marie Gallant Sail-tailed Anole". Florida Fish and Wildlife Conservation Commission. Retrieved 20 March 2018.
- Scott, C. (2004). Endangered and Threatened Animals of Florida and Their Habitats. University of Texas Press. p. 14. ISBN 978-0292705296.
- Kamath, A. (15 September 2017). Are Brown Anoles in Florida Really Driving Green Anoles to Extinction III: A Post-Irma Update. Anole Annals. Retrieved 18 March 2018.
- Lomax, J.N. (3 December 2015). "The Green Anole, Your Resident Backyard Lizard, Is Being Pushed Out By Its Uglier Cousin". Texas Monthly. Retrieved 20 March 2018.
- Kraus, F. (2009). Alien Reptiles and Amphibians: a Scientific Compendium and Analysis. Springer. pp. 59–60. ISBN 978-1-4020-8945-9.
- Frost, D.R. & Hammerson, G.A. (2018). "Anolis carolinensis". The IUCN Red List of Threatened Species. IUCN. 2007: e.T64188A12745542. doi:10.2305/IUCN.UK.2007.RLTS.T64188A12745542.en. Retrieved 20 March 2018.
- Okochi; Yoshimura; Abe; Suzuki (2006). "High population densities of an exotic lizard, Anolis carolinensis and its possible role as a pollinator in the Ogasawara Islands". Bulletin of FFPRI. 5 (4): 265–269. doi:10.1007/978-4-431-53859-2_12.
- Powell, Robert; Jolley, Martin L.; Taylor, Carl V.; Parmerlee, John S.; Smith, Donald D. (1990). "Range expansion by an introduced anole: Anolis porcatus in the Dominican Republic". Amphibia-Reptilia. 11 (4): 421–425. doi:10.1163/156853890X00113.
- Prates; Hernandez; Samelo; Carnaval (2016). "Molecular identification and geographic origin of an exotic anole lizard introduced to Brazil, with remarks on its natural history". South American Journal of Herpetology. 11 (3): 220–227. doi:10.1111/j.1365-2311.2008.00995.x.
- Losos; Marks; Schoener (1993). "Habitat use and ecological interactions of an introduced and a native species of Anolis lizard on Grand Cayman, with a review of the outcomes of anole introductions". Oecologia. 95 (4): 525–532.
- Huang; Norval; Tso (2008). "Predation by an exotic lizard, Anolis sagrei, alters the ant community structure in betelnut palm plantations in southern Taiwan". Ecological Entomology. 33 (5): 569–576. doi:10.1111/j.1365-2311.2008.00995.x.
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