Geographic Range
Crested anoles are native to neotropical areas, such as Puerto Rico (including the
islands of Vieques, Culebra) and islands in the Caribbean (Anegada, Tortola, Virgin
Gorda, Jost Van Dyke, St. John, and St. Thomas). They are also considered to be an
introduced species in Florida, the Dominican Republic, and Costa Rica. It is uncertain
exactly when this species was introduced into these areas, although there is some
consensus that the crested anole was introduced into La Romana (Dominican Republic)
before 1920.
- Biogeographic Regions
- nearctic
- neotropical
Habitat
This is a perching species that is common in arboreal habitats. Males especially will
use the trunks of trees as a way of displaying to other animals. Because they tend
to remain close to the ground, they have been called a trunk-ground species. They
may also perch on walls and fences, which are usually in more open areas and give
a better vantage point for spotting prey or being seen by intruders in their territory.
For this reason, crested anoles are commonly found in urban and suburban areas.
- Habitat Regions
- tropical
- terrestrial
- Terrestrial Biomes
- savanna or grassland
- forest
Physical Description
Crested anoles are known to reach lengths of 10 to 20.5 cm (4 to 8 in). Because this
species has such a long tail, the SVL (snout-vent length) is usually just 7.5 cm for
males and 5.7 cm for females. Females are much smaller than males. Hatchlings of this
species are about 5.08 cm (2 in). Males can can vary from a grayish to a light brown
color, and may have a crest on their tails. Males also have a dewlap, a flap of skin
located under the neck that is able to be extended for use in communication. Dewlaps
vary in color from yellow to red and may be lighter or darker depending on habitat
moisture conditions. Females are drab and colored similarly to the ground, with a
dark-bordered light stripe on their backs. Young males also have this dorsal stripe
until they reach maturity. Females lack a tail crest and dewlap. This species has
the ability to change color depending on its environment, lighting or mood.
- Other Physical Features
- heterothermic
- Sexual Dimorphism
- male larger
- sexes colored or patterned differently
- ornamentation
Development
Little is known about the specific development of crested anoles. Males tend to grow
faster than females in most
Anolis
species. As individuals reach adulthood, this growth rate difference leads to sexual
dimorphism. As juveniles, male crested anoles resemble females and their dewlap is
not developed. This structure, and the dorsal crest, develops in males over time.
- Development - Life Cycle
- indeterminate growth
Reproduction
Males will regularly mate with females within their territory. In order to attract
a mate, male anoles will approach females and perform a series of displays. These
include bobbing the head, pushups, and displaying the dewlap. If the female acknowledges
the male's display, she will bob her head in response. When the male mounts the female,
she will arch her neck and the male will bite it. He then brings his tail closer to
the female's and inserts his hemipene into the female's cloaca. However, females may
reject the mating advances of a male before this point and if so, will flee instead
of arching their neck.
- Mating System
- polygynous
Egg production in crested anoles is seasonal, with activity dropping in colder months
and during the dry season. Crested anole females lay one or two eggs under logs and
rock piles at two-week intervals. In general, when a female anole finds a spot to
lay her eggs, she will nudge this spot with her snout. This behavior is then followed
by digging with her forelegs. When the has been laid in the hole, the female will
push it in further and then cover it with dirt. This species also participates in
communal egg-laying, in which multiple females will use the same nest site to lay
their eggs. The incubation period is 50 days, on average.
- Key Reproductive Features
- iteroparous
- year-round breeding
- sexual
- fertilization
- oviparous
With the exception of the nutrients present in the egg and digging a hole in which
to lay them, crested anoles do not contribute further to the success of their offspring.
- Parental Investment
- no parental involvement
-
pre-fertilization
- provisioning
-
protecting
- female
Lifespan/Longevity
Little is known about the lifespan of crested anoles in the wild or in captivity.
Several other
Anolis
species, however, have been reported to have average lifespans of about 7 years in
captivity. It has been determined that the lifespan of an anole is strongly linked
to the number of predators who share their habitat.
Behavior
Crested anoles are diurnal lizards that use perching as a means of warding off other
males, attracting females, and foraging for foods such as insects, fruit, frogs, and
even other lizards. Generally, crested anoles perch parallel to the tree with their
head facing the ground. Although, they can climb higher than 3m, they tend to prefer
areas where sunlight is more plentiful, such as fence posts, tree trunks, or the walls
of buildings. Males will climb to the top of the trees at night to sleep, while females
and younger males stay lower.
This species is extremely territorial. It uses threat displays that resemble pushups
and extensions of the dewlap. Head-bobbing is also common in these displays. In most
cases the male will make these threat displays from a perching position in their territory.
This will alert any other males in the area of their ownership of that territory.
These behaviors are also very similar to mating and anti-predator displays. If these
displays fail to chase away other males, they will typically fight with each other
over territories and access to females.
- Key Behaviors
- arboreal
- scansorial
- diurnal
- territorial
Home Range
Adult crested anoles typically defend territories on trees, walls, or shrubs. The
adult males usually occupy territories until death. However, young anoles usually
move from territory to territory. Adult females occupy much smaller territories and
will usually overlap with a male's. Crested anoles show weak orientation skills and
will have a difficult time returning to their territory if they are placed outside
their realm of familiarity. Though both males and females have homing capabilities,
they are much weaker in females.
Communication and Perception
Crested anoles rely heavily on visual cues in order to communicate with one another.
Generally, males who defend territories exhibit this behavior. These displays include
pushups, extensions of the dewlap, head bobbing, biting, and tail lashing. These behaviors
convey one of two meanings, either telling a potential mate that the male is interested,
or warning other males that they are intruding into their territory. The dewlap is
a very important part of anole species' intraspecific and interspecific communication,
as it varies in color across species. This visual cue is very important when defending
a territory from a potential threat.
- Communication Channels
- visual
- Perception Channels
- visual
- tactile
- acoustic
- vibrations
- chemical
Food Habits
Crested anoles are primarily insectivores, eating prey that range in size from ants
to large roaches. They also feed on small fruits, frogs, and even other lizards (including
the young of their own species). Crested anoles are foragers and typically scan their
environment for food from a perching position on the trunks of trees or the sides
of buildings.
- Primary Diet
- carnivore
- Animal Foods
- amphibians
- reptiles
- insects
- terrestrial non-insect arthropods
- Plant Foods
- fruit
Predation
In Puerto Rico, crested anoles are primarily eaten by birds, mongoosex, and snakes,
including Puerto Rican racers (
Alsophis portoricensis
). However, coqui frogs (
Eleutherodactylus coqui
) and other lizards (
Ameiva exsul
) have also been known to eat anoles in Puerto Rico. In the Lesser Antilles (St. John,
Virgin Gorda, Jost Van Dyke, Tortola, and St. Thomas), American kestrels (
Falco sparverius
) and early-eyed thrashers (
Margarops fuscatus
) are the most important bird predators of anoles.
Crested anoles exhibit several different behaviors when confronted by predators. These
include expression of the dewlap, body thrashing, biting, tail lashing, head-bobbing,
and pushups. These can be used separately or in combination to escape predation.
- Anti-predator Adaptations
- cryptic
Ecosystem Roles
Crested anoles serve as predators of insects and other small animals and prey to larger
carnivorous organisms. In locations where they have been introduced, they have negatively
impacted other anoles that were already present in the ecosystem. For example, in
La Romana (Dominican Republic),
Anolis chlorocyanus
are now confined to trees that are slippery, to avoid predation by larger, non-native
crested anoles. Cat liver flukes (
Platynosomum concinnum
) use crested anoles as a secondary intermediate host after it has already infected
the snail species
Subulina octona
.
- Plasmodium azurophilum (Order Haemosporida, Phylum Apicomplexa)
- cat liver flukes ( Platynosomum concinnum )
- Mesocoelium danforthi (Subclass Digenea, Phylum Platyhelminthes)
- Ascarops sp. (Family Spiruridae, Phylum Nematoda)
- Physocephalus sp. (Family Thelaziidae, Phylum Nematoda)
- Parapharyngodon cubensis (Family Pharyngodonidae, Phylum Nematoda)
- Skrjabinoptera leiocephalorum (Family Physalopteridae, Phylum Nematoda)
- Centrorhynchus sp. (Order Polymorphida, Phylum Acanthocephala)
Economic Importance for Humans: Positive
Because crested anoles are mostly insectivores, they are important factors in controlling
pest populations in the areas where they coexist with humans. Crested anoles are also
becoming more popular as pets.
As an invasive species in many areas, crested anoles have been subject to different
types of habitats. Because introduction in a new habitat can lead to the natural selection
of traits that may not have been selected for in their native habitat (for example
dewlap design), crested anoles have become a popular model organism in evolutionary
studies.
- Positive Impacts
- pet trade
- research and education
- controls pest population
Economic Importance for Humans: Negative
There are no known adverse effects of crested anoles on humans.
Conservation Status
At this time, crested anoles have no special conservation status.
Additional Links
Contributors
Dylan McDaniel (author), Radford University, Karen Powers (editor), Radford University, Kiersten Newtoff (editor), Radford University, Melissa Whistleman (editor), Radford University, Jeremy Wright (editor), University of Michigan-Ann Arbor.
- Nearctic
-
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
- introduced
-
referring to animal species that have been transported to and established populations in regions outside of their natural range, usually through human action.
- Neotropical
-
living in the southern part of the New World. In other words, Central and South America.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- tropical
-
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
- terrestrial
-
Living on the ground.
- tropical savanna and grassland
-
A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.
- savanna
-
A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.
- temperate grassland
-
A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- urban
-
living in cities and large towns, landscapes dominated by human structures and activity.
- suburban
-
living in residential areas on the outskirts of large cities or towns.
- heterothermic
-
having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.
- sexual ornamentation
-
one of the sexes (usually males) has special physical structures used in courting the other sex or fighting the same sex. For example: antlers, elongated tails, special spurs.
- indeterminate growth
-
Animals with indeterminate growth continue to grow throughout their lives.
- polygynous
-
having more than one female as a mate at one time
- iteroparous
-
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
- year-round breeding
-
breeding takes place throughout the year
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- fertilization
-
union of egg and spermatozoan
- oviparous
-
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
- arboreal
-
Referring to an animal that lives in trees; tree-climbing.
- diurnal
-
- active during the day, 2. lasting for one day.
- territorial
-
defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement
- visual
-
uses sight to communicate
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- vibrations
-
movements of a hard surface that are produced by animals as signals to others
- chemical
-
uses smells or other chemicals to communicate
- cryptic
-
having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.
- pet trade
-
the business of buying and selling animals for people to keep in their homes as pets.
- carnivore
-
an animal that mainly eats meat
- insectivore
-
An animal that eats mainly insects or spiders.
References
Bartlett, P., R. Bartlett. 1997. Anoles, Basilisks, and Water Dragons . Hauppauge, NY: Barron's Educational Series.
Bartlett, R., P. Bartlett. 2006. Guide and Reference to the Crocodilians, Turtles, and Lizards of Eastern and Central North America (North of Mexico) . Gainesville, FL: The University Press of Florida.
Behler, J., W. King. 1979. The Audubon Society Field Guide to North American Reptiles and Amphibians . New York: Alfred A. Knipf, Inc..
Brandley, M., K. de Queiroz. 2004. Phylogeny, ecomorphological evolution, and historical biogeography of the Anolis cristatellus series. Herpetological Monographs , 18/1: 90-126.
Collins, J., R. Conant. 1998. A Field Guide to Reptiles and Amphibians of Eastern and Central North America . New York, NY: Houghtton Mifflin Company.
Dyer, W., L. Bunkley-Williams, E. Williams Jr.. 2001. Some helminth parasites of Anolis stratulus and Anolis cristatellus (Sauria: Polychrotidae) in Puerto Rico. Transactions of the Illinois State Academy of Science , 94/3: 161-165.
Fitch, H., R. Henderson, H. Guarisco. 1989. Aspects of the ecology of an introduced anole: Anolis cristatellus in the Dominican Republic. Amphibia-Reptilia , 10/3: 307-320.
Glor, R., J. Michele, A. Larson. 2007. Polymorphic microsatellite loci for the Puerto Rican crested anole (Anolis cristatellus) and their amplification in related Puerto Rican species. Conservation Genetics , 8/6: 1491-1493.
Goldberg, S., C. Bursey, H. Cheam. 1998. Helminths of Six Species of Anolis Lizards (Polychrotidae) from Hispaniola, West Indies. Journal of Parasitology , 84/6: 1291-1295.
Gorman, G., P. Licht. 1974. Seasonality in ovarian cycles among tropical anolis lizards. Ecology , 55/2: 360-369.
Griffiths, H. 1978. A Handbook of Veterinary Parasitology: Domestic Animals of North America . Minneapolis, MN: University of Minnesota Press.
Jenssen, T. 2002. Spatial awareness by the lizard Anolis cristatellus: Why should a non-ranging species demonstrate homing behavior?. Herpetologica , 58/3: 364-371.
Leal, M., L. Fleishman. 2004. Differences in visual signal design and detectability between allopatric populations of anolis lizards. The American Naturalist , 163/1: 26-39.
Leal, M., J. Rodriguez-Robles. 1995. Antipredator responses of Anolis cristatellus. Copeia , 1995/1: 155-161.
Lever, C. 2003. Naturalized Reptiles and Amphibians of the World . New York, NY: Oxford University Press.
Losos, J. 2009. Lizards in an Evolutionary Tree: Ecology and Adaptive Radiation in Anoles . Berkeley and Los Angeles, California: University of California Press.
MacLean, W. 1982. Reptiles and Amphibians of the Virgin Islands . London and Basingstoke: Macmillan Education Limited.
Nicholson, K., L. Harmon, J. Losos. 2007. Evolution of Anolis lizard dewlap diversity. PLoS ONE , 2/3: e274.
Perry, G., K. Levering, I. Girard, T. Garland. 2004. Locomotor performance and social dominance in male Anolis cristatellus. Animal Behavior , 67: 37-47.
Philibosian, R. 1975. Territorial behavior and population regulation in the lizards, Anolis acutus and A. cristatellus. Copeia , 3: 428-444.
Rand, S. 1967. Egg laying in anoline lizards. Herpetoligica , 23/3: 227-230.
Rivero, J. 1998. Los Anfibios y Reptiles de Puerto Rico . Puerto Rico: University of Puerto Rico.
Roughgarden, J. 1995. Anolis Lizards of the Caribbean: Ecology, Evolution, and Plate Tectonics . New York, NY: Oxford University Press.
Schall, J., S. Vogt. 1993. Distribution of malaria in Anolis lizards of the Luquillo forest, Puerto Rico: Implications for host community ecology. Biotropica , 25/2: 229-235.
de Magalhaes, J., J. Costa. 2009. A database of vertebrate longevity records and their relation to other life-history traits. Journal of Evolutionary Biology , 22/8: 1770-1774.