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Herpetology and Me
Tuesday, June 5, 2012
Mythical Kings and Iguanas
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Saturday, April 7, 2012
Eating invasive iguanas in Florida [VIDEO] | Grist
Eating invasive iguanas in Florida [VIDEO]
Over the course of 30 years, the island of Boca Grande in Florida went from having zero iguanas to over 10,000. This invasive species was making it impossible for native plants and animals to survive, so the island’s residents finally decided to do something about it, and called in George Cera. In this video we go on a trip around the island with Cera that culminates in an impromptu iguana tasting.
Lizard Patrol: Episode 87 of The Perennial Plate from Daniel Klein on Vimeo.
Since March, Daniel has been documenting his culinary, agricultural and hunting adventures on film in a series called The Perennial Plate, featuring long winters, urban gardens, ice fishing, slaughterhouses, foraging for wild edibles, and more.
Follow him on twitter @perennialplate.
Saturday, March 17, 2012
Iguanas Use Mockingbird Calls To Survive
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http://blogs.scientificamerican.com/thoughtful-animal/2012/03/15/eavesdropping-iguanas-use-mockingbird-calls-to-survive/avesdropping
Eavesdropping Iguanas use Mockingbirds' Calls to Survive
By Jason G. Goldman | March 15, 2012
Predator-prey interactions are often viewed as evolutionary arms races; while predators improve their hunting behaviors and their ability to sneak up on their prey, the prey improve upon their abilities to detect and escape from their predators. The problem, of course, is that there is a trade-off between maintaining vigilance – the attention necessary to be consistently aware of others in the environment takes quite a bit of physical and mental energy – and doing all the other things that an animal must do, such as finding its own food. As a result of this trade-off, many social species, especially mammalian and avian species, have developed alarm calls. Alarm calls are specific vocalizations that signal the presence of a danger in the environment to nearby conspecifics, and sometimes contain additional information about the type of threat or predator.
Subsequent to the introduction of predatory birds, howler monkeys on Barro Colorado Island near Panama rapidly developed an alarm call specific for those birds that indicated the presence of an avian predator: something like “danger from above!” They did not merely adapt an already existing alarm call to the new predator, they developed an entirely new one.
In certain cases, some species have developed the additional ability to eavesdrop on the alarm calls of other species, gaining access to an additional source of information relevant to the presence of danger in the environment. This ability could be the consequence of a learned association between the alarm calls of another species and the presence of the predator, or it could be due to certain auditory properties common to the alarm calls of both species. More research is required to tease apart these possibilities. However, until recently, it was thought that the ability to identify and react to the alarm calls of other species was only possible in species that already had vocal communication. Several years ago, however, researchers from Princeton University observed this behavior in an unlikely species – a non-vocal reptile called the Galapagos marine iguana (Amblyrhynchus cristatus).
Prior to this observation, it was thought that non-vocal species, who did not have alarm calls themselves, would not be able to associate complex auditory stimuli with the presence of a predator. The Galapagos marine iguana does not have any vocalizations. Instead, they communicate by using visual and olfactory signals. However, they live among the Galapagos mockingbirds (Mimus parvulus), a species that does have auditory vocalizations and specific alarm calls. Further, since iguanas primarily live on the rocky shoreline, they are often unable to view hawks (their main predator) until it is too late. If they had the ability to eavesdrop on the alarm calls of the mockingbirds, they would possibly be able to engage their anti-predator behaviors significantly earlier and increase their chances of survival.
The researchers recorded two types of vocalizations from the Galapagos mockingbirds: their song calls and their alarm calls, and edited them into soundtracks each containing two or three examples of either type of call. The researchers would find a cluster of juvenile and female iguanas (the hawks mostly ignore the mature males) in three different sites on the coast of Santa Fe Island, and would play back the various mockingbird calls through a portable speaker system.
Galapagos Mockingbird
Previous research indicated that upon detecting a hawk, iguanas who were aggregated in a cluster would scatter in different directions, like many prey animals do, perhaps in an attempt to confuse the predator. Upon playback, the researchers noted the behavior of the iguanas. Their behaviors were coded as “non-response,” “alert,” (head raise, orienting towards the sound), or “escape” (walking or running away).
Forty-five percent of iguanas showed vigilance behavior during the playback of the alarm call, compared with only 28.1% of iguanas during the playback of the mockingbird songs, a statistically significant difference. This suggests that the Galapagos iguanas are able to eavesdrop on the alarm calls of the mockingbirds and respond accordingly. However, in addition to the type of playback, the time of day and the data collection site were also significant factors in predicting the proportion of iguanas responding to the playbacks.
Proportion of iguanas responding, according to type of call and site.
At each site, the iguanas successfully differentiated between the alarm calls and the songs, responding with escape behaviors more often subsequent to the alarm call. This is the first experimental evidence that a non-vocal species associated the alarm call of a different species with the presence of a nearby predator.
Recording sites on the island, with the general hunting flight trajectory of the hawks indicated with an arrow.
What might account for the different responses among recording sites? The authors speculate that differences in ambient noise could have contributed, resulting in changes in volume or sound quality. As each recording site was on the rocky coast of the island, the sound quality would be subject to wind and the sounds of the ocean. An alternative explanation, however, is that there are true differences between the sites, perhaps owing to slight variations in predator behavior or mockingbird vocalizations. The fact that the hawks on Santa Fe island begin their hunts each day on the northern side of the island and proceed south throughout the day might indeed result in higher predation rates at site three. If the hawks are successful at site three on a given day, they might not have any reason to continue on to sites one or two.
It was also noted that the iguanas were more responsive to the playbacks earlier in the day. One possibility is that these cold-blooded reptiles are more responsive earlier in the day, when their body temperature is lower, and they therefore require more time to escape due to their reduced agility. As the day continues, the sun passes overhead, and their body heat increases, their ability to escape more quickly might improve.
It is particularly impressive that these iguanas appear able to capitalize on the alarm calls of another species, the Galapagos mockingbird. By considering the environmental constraints placed on these iguanas by their specific location on the coast of Santa Fe Island, the elegance of evolution and natural selection becomes apparent.
On Santa Fe Island, hawks routinely approach begin their day hunting in the north, and proceed south throughout the day. It might make sense, therefore, that the iguanas generally orient towards the north so that they would be able to see the hawks coming. However, marine iguanas such as these must orient their bodies directly towards the sun, or at 180 degree angles to it, in order to survive. Without this thermoregulation, they would quickly overheat and die. The realities of their environmental requirements are directly at odds: face north to anticipate predation and risk overheating, or face the sun to avoid overheating and risk being eaten by an unseen hawk. The ability to capitalize on the auditory alarm vocalizations of another species – especially a species less constrained by body temperature needs – could therefore provide significant benefit. The evolution of this ability would allow the iguanas to simultaneously maintain their body temperature while maintaining awareness of potential threats of predation.
In order to confirm this evolutionary explanation, more research would be required to identify whether naive Galapagos iguanas, never exposed to the threat of predation or the calls of the mockingbirds, would recognize and respond to the alarm calls. The other possibility is that this is simply the result of associative learning of complex auditory information. In either case, the eavesdropping ability of this non-vocal reptile species is remarkable. For these iguanas, it truly is a sin to kill a mockingbird.
Vitousek MN, Adelman JS, Gregory NC, & Clair JJ (2007). Heterospecific alarm call recognition in a non-vocal reptile. Biology letters, 3 (6), 632-634. PMID: 17911047
Images: Galapagos marine iguana via Flickr/Max xx, mockingbird via Smugmug/Jerry Fiddler.
About the Author: Jason G. Goldman is a graduate student in developmental psychology at the University of Southern California, where he studies the evolutionary and developmental origins of the mind in humans and non-human animals. Jason is also Psychology and Neuroscience Editor for ResearchBlogging.org and Editor of Open Lab 2010. He lives in Los Angeles, CA. Follow on Google+. Follow on Twitter @jgold85.
The views expressed are those of the author and are not necessarily those of Scientific American.
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Sunday, February 19, 2012
Things to Consider Before Getting an Exotic Pet Exotic pets are very popular right now, but they have special needs and require a greater commitment, both of money and time, than do traditional pets like dogs and cats. Are you really ready for an exotic pet?
Exotic Reptile Pets: Shocking Truth to Keeping a Savannah Monitor
Jun 26, 2007 "Share your voice on Yahoo! websites. Start Here."
Savannah Monitors are excellent escape artists. Many years ago when living in the Jacksonville, Florida area one of the road reports was about one crossing a major road in Jacksonville. Most likely, this Savannah Monitor had used its talents to escape from its owner. They have sharp claws and will tear through screen like its paper. Savannah's have been known to tear up plywood up to ¼".
If you are going to keep one as a pet lizard, make sure you have plans it place for the Savannah Monitor's cage when they are adults. For juveniles, a 55 gallon aquarium is the right size. For full grown adults, the cage should be 1.5 to 2 times the length. This means you may need a cage 6-8 feet long and probably about 3-4 feet wide.
They like to be secluded and will constantly be hiding in their cage. The best way to tame them is to get a juvenile and handle it regularly. Wrapping the aquarium with backing on the two sides and the back will put the Savannah Monitor more at ease. This decorative background can be found in almost any pet store. Having a background of a desert or grassland would be the best choice for these shy lizards.
Since they are from Africa, the habitat needs to be hot and dry. The temperature should be 85-90 in the day and 70-80 at night. They need the full spectrum light and should have an additional heat source under the tank. Using hot rocks could cause severe burns on their belly.
Dirt would be the best substrate for them. Putting plants in the Savannah Monitor's cage would be a waste of time. They will trample them in their journeys. Use a large cat litter pan to give them all the water they need.
As juveniles, they will eat lots of crickets. These crickets should be dusted with calcium. Generally, as they get older, they will stop eating crickets and need to be fed mice. Adults should eat mice twice a week. For an occasional treat, Savannah Monitors can be fed low fat dog food, well cooked lean meats or even hard boiled eggs.
This is not a flashy lizard, but enough lizard owners keep buying them for pets. They are not difficult to maintain, but should never be the first lizard as a pet.
Published by Jerry Robertson
I am a retail / small business consultant and author of three business books. View profile
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Reptiles as Pets and How to Buy Them Many retailers will tell you whatever they think you want to hear about any reptile just to make a sale. I am here to help you with the facts and what to look for so that you ca...
- Things to Consider Before Getting an Exotic Pet Exotic pets are very popular right now, but they have special needs and require a greater commitment, both of money and time, than do traditional pets like dogs and cats. Are you really ready for an exotic pet?
- Hedgehog as an Exotic Pet: Skin Disorder Complications Owning an exotic pet has become a fashion statement in the United States. When considering a hedgehog, be mindful of these potential health
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Iguana iguana: CLASSIFICATION
http://animaldiversity.ummz.umich.edu/site/accounts/classification/Iguana_iguana.html
To cite this page: Myers, P., R. Espinosa, C. S. Parr, T. Jones, G. S. Hammond, and T. A. Dewey. 2012. The Animal Diversity Web (online). Accessed at http://animaldiversity.org.
Reptilia
Information
Pictures
Specimens
Sounds
Classification
By Phil Myers
Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Sarcopterygii
Class: Reptilia
Reptilia, presented as a Class in our classification, includes turtles (Testudines), snakes and lizards (Lepidosauria), crocodiles and their relatives (Crocodilia), and birds (Aves), as well as a number of extinct groups. Reptiles (including birds!) are amniotes; that is, their eggs are protected from dessication and other environmental problems by an extra membrane, the amnion, not found in the first terrestrial vertebrates (amphibians). Mammals (Mammalia) are also amniotes, but they differ from reptiles in the structure of their skulls (especially the regions associated with chewing and hearing). Mammals also have hair and feed their young with milk produced by modified skin glands (mammary glands).
In addition to being amniotes, all reptiles have (or did have, in their evolutionary history) horny epidermal scales made of a particular kind of protein, paired limbs with 5 toes, skulls with a single occipital condyle, lungs instead of gills for respiration, and a 3 or 4 chambered heart. Their eggs are covered with a leathery or calcium-based shell (partially or completely lost in some species that give birth to live young), and fertilization occurs inside the female, rather than outside, as it does in most amphibians. Members of Reptilia generally share many additional traits, for example in their nervous and excretory systems, locomotion, and reproduction.
Why are birds included within Reptilia, and how are they and other members of this group related to each other? Both the fossil record and comparative analyses of living species (especially those based on molecular evidence) convincingly establish that, among living reptiles, birds and crocodiles are more closely related to each other than they are to lepidosaurs (snakes and lizards). The position of turtles is more controversial; in the past they were thought to represent an early branch of Reptilia. Recent evidence suggests they may have a special relationship with crocodiles and birds. Because birds clearly arise from within the groups we traditionally consider to be reptiles, not separately from them, most systematists now formally consider birds (Aves) to be a subgroup within Reptilia.
References:
Hickman, C. P. Jr., L. S. Roberts, and A. Larson. 2003. Animal Diversity, 3rd edition. McGraw Hill, Boston.
Laurin, M. and J. A. Gauthier. 2001. Amniota. http://tolweb.org/tree?group=Amniota&contgroup=Terrestrial_Vertebrates
Related Sites:
Savannah River Ecology Lab's Herpetology Homepage
Last updated 24 February 2004.
For More Information
Find Reptilia information at
Encyclopedia of Life
Contributors
Phil Myers (author), Museum of Zoology, University of Michigan.
To cite this page: Myers, P. 2001. "Reptilia" (On-line), Animal Diversity Web. Accessed February 19, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Reptilia.html
Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.
Sponsored in part by the Interagency Education Research Initiative,
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This material is based upon work supported by the National Science Foundation under Grants DUE-0633095 and DRL-0628151.
The ADW Team gratefully acknowledges their support.
Color Variatiions occur in different regions as iguanas are present throughout South and Central America and Mexico
By Fred Gingell
Home
Kingdom Animalia
Phylum Chordata
Subphylum Vertebrata
Superclass Gnathostomata
Class Sarcopterygii
Class Reptilia
Order Squamata
Family Iguanidae
Genus Iguana
Species Iguana iguana
Iguana iguana
Common Green Iguana
Geographic Range
Green iguanas, Iguana iguana, occur throughout Central and South America, from Sinaloa and Veracruz, Mexico, south to the Tropic of Capricorn in Paraguay and southeast Brazil. This large lizard also inhabits many islands throughout the Caribbean region and the coastal eastern Pacific, and has been introduced into southern Florida and in Hawaii. This is the largest known lizard to occur within the borders of the United States (Conant and Collins, 1998; Campbell, 1998). (Campbell, 1998; Conant and Collins, 1998)
Biogeographic Regions
nearctic
Habitat
Green Iguanas are arboreal lizards that live high in the tree canopy. Juveniles establish areas lower in the canopies while older mature iguanas reside higher up. This tree dwelling habit allows them to bask in the sun, rarely coming down except when females dig burrows to lay eggs. Although preferring an arboreal (forested) environment, they can adjust well to a more open area. No matter where they inhabit, they prefer to have water around as they are excellent swimmers and will dive beneath the water to avoid predators (Conant and Collins 1998). (Alberts, et al., 2004; Campbell, 1998; Conant and Collins, 1998)
Habitat Regions
tropical
Terrestrial Biomes
forest
Aquatic Biomes
lakes and ponds; rivers and streams; temporary pools; coastal
Wetlands
swamp
Other Habitat Features
suburban
Physical Description
Range mass
4 to 8 kg
(8.81 to 17.62 lb)
Average mass
7 kg
(15.42 lb)
Range length
2 (high) m
(6.56 (high) ft)
Average length
1.75 m
(5.74 ft)
Within three years, a young, 12 gram hatchling iguana can become a 1 kg adult (de Vosjoli, 1992). Upon hatching, the length of green iguanas ranges from 17 to 25 cm. Most mature iguanas weigh between 4 and 6 kg, but some in South America, with proper diet can reach up to 8 kg. These large lizards can reach head to tail lengths of around 2 m.
Although called green iguanas, these animals are actually variable in color. The adults become more uniform in color with age, whereas the young may appear more blotchy or banded between green and brown. Color of an individual may also vary based upon its mood, temperature, health, or social status. Such color alteration may aide these animals in thermoregulation. In the morning, while body temperature is low, skin color will be darker, helping the lizard to absorb heat from sunlight. However, as the hot mid-day sun radiates upon them, these animals become lighter or paler, helping to reflect the sun rays and minimizing the heat absorbed. Active dominant iguanas usually have a darker color than lower-ranked iguanas living the same environment (Frye, 1995). Most color variation seen in this species is exhibited by males, and may be attributed in part to sex steroids. Six to eight weeks prior to and during courtship, males may acquire a bright orange or gold hue, although coloration is still related to dominance status (Frye, 1995). Mature females, for the most part, retain their green coloring.
Other distinguishing features of this species include a pendulous dewlap under the throat, a dorsal crest made up of dermal spines that run from the mid neck to the tail base, and a long tapering tail. The dewlap is more developed in adult males than females. Extensions of the hyoid bones stiffen and support the leading edge of this structure, which is used in territorial defense or when the animal is frightened. This fleshy structure also serves in heat absorption and dissipation when it is extended.
The laterally situated eyes are protected mainly by a immovable eyelid and freely mobile lower eyelid (Oldham and Smith, 1975). On the dorsal midline of the skull behind the eyes is a parietal eye. This sense organ, although not a true "eye," serves as a meter for solar energy, and aids in the maturation of sex organs, thyroid gland, and endocrine glands (Frye, 1995). The visual effect of this "eye" is mostly limited to the detection of predatory shadows from above.
The scales or plates on the head are larger and more irregular than the scales on the rest of the body. Below the tympanum there is a large rounded scale called the subtympanic plate. (De Vosjoli, 1992; Frye, 1995; Oldham and Smith, 1975)
Other Physical Features
ectothermic
Sexual Dimorphism
male larger; sexes colored or patterned differently; male more colorful; ornamentation
Development
Approximately 65 days after mating, a female is ready to lay her eggs. The size and number of eggs produced varies depending upon her size, her nutritional status, and her maturity. Eggs measure around 15.4 mm in diameter, and 35 to 40 mm in length (Frye, 1995). Over a three day period, an average of 10 to 30 leathery white or pale-cream colored eggs are deposited into a nest. Nests are located 45 cm to more than a meter deep, and may be shared with other females if nesting areas are limited. After laying the eggs, females may return to the nest several times but do not stay to guard it.
Incubation lasts from 90 to 120 days. Temperature should range from 85 to 91 degrees Fahrenheit. The hatchlings pip the egg open using a special egg tooth, called the caruncle, that falls off shortly after hatching. Absorbed yolk provides most of the nourishment for the first week or two of an iguana's life.
There are no major morphological changes in these animals as they age, except that they grow. However, diet is related to age. The young, with higher need for protein, are more likely to consume insects and eggs than are mature individuals. (Frye, 1995; Kaplan, 2002)
Reproduction
Most green iguanas reach sexual maturity between three and four years of age, although maturity can be reached earlier. Iguanas tend to breed in the dry season, ensuring that young hatch in the wet season when food is more readily available (de Vosjoli, 1992).
Mating appears to be polygynandrous. Courtship occurs within a defined territory where more than one female may be present. Conflicts between males are not uncommon. Courtship behavior of males includes head bobbing, extending and retraction of the dewlap, and nuzzling or biting a female’s neck (Frye, 1995). Dominant males may also mark rocks, branches, and females with a waxy pheromone-containing substance secreted from their femoral pores.
During mating, the male approachs the female and climbs on her back, straddling her. To restrain his mate, he grips the her shoulder skin with his teeth, sometimes causing wounds. The male then pairs his cloacal vent up with the female's and inserts one of his hemipenes into her cloaca. Copulation can last for several minutes. Female iguanas can can save sperm for several years (Frye, 1995), allowing them to fertilize eggs at a much later date. (De Vosjoli, 1992; Frye, 1995)
Mating System
polygynandrous (promiscuous)
Breeding interval
These animals breed annually.
Breeding season
Green iguanas breed in the dry season.
Range number of offspring
65 (high)
Average number of offspring
10-30
Range gestation period
59 to 84 days
Average gestation period
65 days
Range age at sexual or reproductive maturity (female)
2.5 to 5 years
Average age at sexual or reproductive maturity (female)
3-4 years
Range age at sexual or reproductive maturity (male)
3 to 5 years
Females lay their eggs about 65 days after mating (eggs take 59 to 84 days to develop before they are laid). Over the course of three days, females may up to 65 eggs, each measuring around 15.4 mm in diameter, and 35 to 40 mm in length (Frye, 1995). Eggs are deposited into nests which are located 45 cm to more than a meter deep, and may be shared with other females if nesting areas are limited.
Incubation lasts from 90 to 120 days. Temperature should range from 85 to 91 degrees Fahrenheit. The hatchlings pip the egg open using a special egg tooth, called the caruncle, that falls off shortly after hatching. Absorbed yolk provides most of the nourishment for the first week or two of an iguana's life. Young are independent from birth.
Timing of sexual maturity varies. Animals may be able to breed as early as their second year, but may not breed until as late as their fifth year. (Frye, 1995)
Key Reproductive Features
iteroparous
Parental investment includes the risk of mating and laying eggs. Eggs are provisioned with nutrients by the mother. Females choose nesting sites, presumably as a means of caring for their offspring. However, after eggs are laid, there is no direct investment in the young. (De Vosjoli, 1992)
Parental Investment
pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Male, Female)
Lifespan/Longevity
Range lifespan
Status: captivity
20 (high) years
Average lifespan
Status: wild
8 years
Average lifespan
Status: captivity
10 years
Average lifespan
Sex: female
Status: captivity
12.4 years
[External Source: Max Planck Institute for Demographic Research]
Iguanas can live for more than 20 years in captivity, although wild iguanas are thought to live only about 8 years. Proper nutrition for growth is a concern for captive management of these animals. Improper housing and nutrition can shorten a captive iguana's lifespan. (De Vosjoli, 1992; Frye, 1995)
Behavior
In the wild, most disputes between iguanas take place over basking sites. There is usually adequate food for these herbivorous lizards, but good perches are limited. Basking is important for increasing body temperature and aiding digestion.
During the breeding season, males become territorial and display head bobbing, dewlap extension, and color changes. They will bite at each other. Injuries in the wild are rare, as there is ample space for males to retreat when threatened. However, in captivity where space is limited, injuries are more common. Females may also display some of these behaviors when nesting sites are limited.
Green iguanas may travel considerable distances in several cases. Females migrate to the same nesting site for several years in a row, then travel back to their home territory once their eggs are laid. Hatchlings may disperse over large distances as well (Alberts et. al., 2004).
When frightened, an iguana will usually freeze or hide. If caught, twisting and rotating around or tail whipping may occur. Like many other lizards, iguanas can autotomatize, or drop of part of their tail. This gives them a chance to escape before their predator figures out what is going on. A new tail will sprout from the autotomatized spot and regrow with in a year, though not to the length it was before. (Alberts, et al., 2004)
Key Behaviors
arboreal
Communication and Perception
These animals are known to use visual signals, such as head bobbing and dewlap extension, as means of communicating with rivals. In extreme cases, physical contact is involved in altercations. In addition, males scent mark females as well as branches. Hissing, which is a form of auditory communication, sometimes occurs.
Communication Channels
visual
Other Communication Modes
mimicry
Perception Channels
visual
Food Habits
Green iguanas are primarily herbivorous. They occasionally eat a small amount of carrion or invertebrates. Green leafy plants or ripe fruits are their preferred foods.
Green iguanas use their tongues to help manipulate the food and bite small enough pieces to swallow, with little or no chewing. The food mixes with enzymes in the stomach before moving to the small intestine where pancreatic enzymes and bile are mixed with it. Most digestion occurs in the sacculated colon, where microflora break down the cellulose (Frye, 1995). Microflora are essential for hind-gut digestion of the hard to digest diet of this species. Hatchling iguanas are inclined to eat feces from adults, which may be an adaptation for acquiring this much need microflora (Alberts et.al., 2004). This microflora breaks the food down and makes it available for absorption.
Iguanas require a high amount of dietary protein in their first two to three years for adequately fast growth. During this time period, young iguanas may consume insects and spiders. Older iguanas that have reached close to maximum growth consume a low phosphorous, high calcium, leafy diet for their maintenance requirements.
Iguanas are ectothermic. Their body temperature is mainly dependent upon the environmental temperature. Low environmental temperatures inhibit an iguana's appetite and digestive enzymes. Active eating usually occurs when the environmental temperatures are between 77 and 95 degrees Fahrenheit (Frye, 1995). Basking is an important aid to digestion. Iguanas may cease eating prior to or during skin shedding. Females may refuse to eat during later stages of egg development. Individuals who are overly stressed or in a new environment may also refuse to eat. (Alberts, et al., 2004; Frye, 1995)
Animal Foods
eggs; insects; terrestrial worms
Plant Foods
leaves; fruit; flowers
Predation
Known Predators
Homo sapiens
hawks
large birds
One of the best methods for iguanas to avoid predation is their cryptic coloration. Because they look like so much of their green environment, they can remain immobile when a predator has been spotted, and go unnoticed themselves. Young iguanas may be found in small groups, and use the "selfish-herd" or "more eyes are better" strategy to avoid predators. Iguanas prefer to bask in tree limbs that over-hang water so when threatened by a predator they can dive into the water and swim swiftly away. In addition to these strategies for avoiding predation, green iguanas are able to shed a large portion of their tail, thus distracting predators and allowing the "rest" of the animal to escape.
Hawks and other large birds are potential predators of juvenile iguanas. Humans are another one of major predators of green iguanas. Humans eat both iguanas and their eggs. Humans also use these reptiles for crocodile bait, and poach them for the pet trade.
Like many other animals, green iguanas also suffer from habitat destruction.
Anti-predator Adaptations
cryptic
Ecosystem Roles
In addition to helping disperse seeds, iguanas provide a source of food for larger predatory animals, including humans. Like other amphibians and reptiles, iguanas can be indicators of environmental changes (Kaplan, 2002). Reptiles are more sensitive to environmental changes than are humans, and by watching their responses, we can be alerted to possible problems before they are large enough for us to detect with our own senses. (Kaplan, 2002; Phillips, 1990)
Ecosystem Impact
disperses seeds
Economic Importance for Humans: Positive
Iguanas are farmed in some countries as a source of food and leather, as well as for the pet trade. Due to their large size, iguana hides provide a source of luxury leather that can be made into boots, belts or purses. The pet industry also prizes iguanas; most are sold in the United States, Europe, and Japan. Iguanas also make an interesting tourist attraction in resort areas.
Exploitation of iguanas has resulted in marked declines in their numbers in some parts of their range. (Campbell, 1998). (Campbell, 1998)
Positive Impacts
pet trade
Economic Importance for Humans: Negative
The most adverse effect green iguanas have on humans would be eating exotic tropical foliage in gardens. They do not pose any major problems for humans.
Conservation Status
IUCN Red List [Link]
No special status
US Federal List [Link]
No special status
CITES [Link]
Appendix II
Although some populations have suffered from poaching and collection for the pet trade, green iguanas are not considered a conservation risk at this time. All Iguana species are listed under CITES Appendix II.
For More Information
Find Iguana iguana information at
Encyclopedia of Life
Contributors
Nancy Shefferly (editor), Animal Diversity Web Staff.
Fred Gingell (author), Michigan State University, James Harding (editor, instructor), Michigan State University, , 205 Museum, Michigan State University, East Lansing, MI 48824.
References
Alberts, A., R. Carter, W. Hayes, E. Martins. 2004. Iguanas: Biology and Conservation. Berkeley and Los Angeles, Californa: University of California Press.
Campbell, J. 1998. Amphibians and Reptiles of Norther Guatemala,the Yucatan, and Belize. Oklahoma: University of Oklahoma Press.
Conant, R., J. Collins. 1998. Peterson Field Guides: Reptiles and Amphibians of Eastern & Central North America, 3rd Edition. New York: Houghton Mifflin Company.
De Vosjoli, P. 1992. The Green Iguana Mannual. Lakeside, California: Advanced Vivarium Systems.
Frye, F. 1995. Iguana Iguana, Guide for Successful Captive Care. Malabar, Florida: Krieger Publishing Company.
Kaplan, M. 2002. "Journal Abstracts: Iguana iguana Visual and Chemical Reception" (On-line). Accessed July 14, 2005 at http://www.anapsid.org/iguana/sight2.html.
Oldham, J., H. Smith. 1975. Laboratory Anatomy of the Iguana. Dubuque, Iowa: WM. C. Brown Company.
Phillips, J. 1990. Iguana iguana: a model species for studying the ontogeny of behavior/hormone interactions. Exp Zool Suppl, 4: 167-169. Accessed January 03, 2005 at http://www.anapsid.org/iguana/sight2.html.
To cite this page: Gingell, F. 2005. "Iguana iguana" (On-line), Animal Diversity Web. Accessed February 19, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Iguana_iguana.html
Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.
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