|Chamaeleo zeylanicus in Mangaon, Maharashtra, India|
Chameleons or chamaeleons (family Chamaeleonidae) are a distinctive and highly specialized clade of old world lizards. The approximately 180 species of chameleon come in a range of colours, and many species have the ability to change colours. Chameleons are distinguished by their zygodactylous feet; their very long, highly modified, rapidly extrudable tongues; their swaying gait; and crests or horns on their distinctively shaped heads. Most species, the larger ones in particular, also have a prehensile tail. Chameleons' eyes are independently mobile, but in aiming at a prey item, they focus forward in coordination, affording the animal stereoscopic vision. Chameleons are adapted for climbing and visual hunting. They are found in warm habitats that range from rain forest to desert conditions, various species occurring in Africa, Madagascar, southern Europe, and across southern Asia as far as Sri Lanka. They also have been introduced to Hawaii, California, and Florida, and often are kept as household pets.
The American English word chameleon is a simplified spelling of Latin chamaeleōn, a borrowing of the Greek χαμαιλέων (khamailéōn), a compound of χαμαί (khamaí) "on the ground" and λέων (léōn) "lion". The Greek word is a calque translating the Akkadian nēš qaqqari, literally "lion of the ground".
The Chamaeleonidae family was divided into two subfamilies, Brookesiinae and Chamaeleoninae, by Klaver and Böhme in 1986. Since that time, the validity of this subfamily designation has been the subject of much debate, although most phylogenetic studies support the notion that the pygmy chameleons of the subfamily Brookesiinae are not a monophyletic group. While some authorities have previously preferred to use the subfamilial classification on the basis of the absence of evidence principle, more recently these authorities have abandoned this subfamilial division and no longer recognize any subfamilies with the family Chamaeleonidae.
Change of color
Some chameleon species are able to change their skin coloration. Different chameleon species are able to vary their colouration and pattern through combinations of pink, blue, red, orange, green, black, brown, light blue, yellow, turquoise, and purple.
Color change in chameleons has functions in social signaling and in reactions to temperature and other conditions, as well as in camouflage. The relative importance of these functions varies with the circumstances, as well as the species. Color change signals a chameleon's physiological condition and intentions to other chameleons. Chameleons tend to show darker colors when angered, or attempting to scare or intimidate others, while males show lighter, multicolored patterns when courting females.
Some species, such as Smith's dwarf chameleon, adjust their colors for camouflage in accordance with the vision of the specific predator species (bird or snake) by which they are being threatened.
The desert-dwelling Namaqua chameleon also uses color change as an aid to thermoregulation, becoming black in the cooler morning to absorb heat more efficiently, then a lighter grey color to reflect light during the heat of the day. It may show both colors at the same time, neatly separated left from right by the spine.
Mechanism of color change
For a long time it was thought that chameleons change color by dispersion of pigment containing organelles within their skin. However, recent research on panther chameleons has shown that this is not the case. 
Chameleons have two superimposed layers within their skin that control their color and thermoregulation. The top layer contains a lattice of guanine nanocrystals, and by exciting this lattice the spacing between the nanocrystals can be manipulated, which in turn affects which wavelengths of light are reflected and which are absorbed. Exciting the lattice increases the distance between the nanocrystals, and the skin reflects longer wavelengths of light. Thus, in a relaxed state the crystals reflect blue and green, but in an excited state the longer wavelengths such as yellow, orange, and red are reflected.
The skin of a chameleon also contains some yellow pigments, which combined with the blue reflected by a relaxed crystal lattice results in the characteristic green color which is common of many chameleons in their relaxed state. The deeper layer of skins works in a similar fashion but primarily controls the amount of near-infrared light that is absorbed or reflected, and thus has a large effect on thermoregulation.
Other chameleon fossils include Chamaeleo caroliquarti from the Lower Miocene (about 13–23 mya) of the Czech Republic and Germany, and Chamaeleo intermedius from the Upper Miocene (about 5–13 mya) of Kenya.
The chameleons are probably far older than that, perhaps sharing a common ancestor with iguanids and agamids more than 100 mya (agamids being more closely related). Since fossils have been found in Africa, Europe and Asia, chameleons were certainly once more widespread than they are today. Although nearly half of all chameleon species today are found in Madagascar, this offers no basis for speculation that chameleons might originate from there. Monophyly of the family is supported by several studies.
Chameleons vary greatly in size and body structure, with maximum total lengths varying from 15 mm (0.59 in) in male Brookesia micra (one of the world's smallest reptiles) to 68.5 cm (27.0 in) in the male Furcifer oustaleti. Many have head or facial ornamentation, such as nasal protrusions, or horn-like projections in the case of Trioceros jacksonii, or large crests on top of their heads, like Chamaeleo calyptratus. Many species are sexually dimorphic, and males are typically much more ornamented than the female chameleons.
Typical sizes of species of chameleon commonly kept as pets are:
|Scientific name||Common name||Length (male)||Length (female)||Color||Lifespan (years)|
|Chamaeleo calyptratus||Veiled chameleon||35–60 cm||25–33 cm||Green and light colors||about 5|
|Trioceros jacksonii||Jackson's chameleon||23–33 cm||25–33 cm||Green and light colors||5–10|
|Furcifer pardalis||Panther chameleon||38–53 cm||23–33 cm||Darker colors||about 5 (2–3 for birthing females)|
|Rieppeleon brevicaudatus||Bearded pygmy chameleon||5–8 cm||5–8 cm||Brown, beige, green||about 3–5|
|Rhampholeon spectrum||Spectral pygmy chameleon||8–10 cm||5–10 cm||Tan and gray||3–5|
|Rhampholeon temporalis||Usumbara pitted pygmy chameleon||6–10 cm||5–9 cm||Gray and brown||5–11|
The feet of chameleons are highly adapted to arboreal locomotion, though species such as Chamaeleo namaquensis, that have secondarily adopted a terrestrial habit, have retained the same foot morphology with little modification. On each foot, the five clearly distinguished toes are grouped into two fascicles. The toes in each fascicle are bound into a flattened group of either two or three, giving each foot a tongs-like appearance. On the front feet, the outer, lateral, group contains two toes, whereas the inner, medial, group contains three. On the rear feet, this arrangement is reversed, the medial group containing two toes, and the lateral group three. These specialized feet allow chameleons to grip tightly onto narrow or rough branches. Furthermore, each toe is equipped with a sharp claw to afford a grip on surfaces such as bark when climbing. It is common to refer to the feet of chameleons as didactyl or zygodactyl, though neither term is fully satisfactory, both being used in describing totally different feet, such as the zygodactyl feet of parrots or didactyl feet of sloths or ostriches, none of which is significantly like chameleon feet. Although "zygodactyl" is reasonably descriptive of chameleon foot anatomy, their foot structure does not resemble that of parrots, to which the term was first applied. As for didactyly, chameleons visibly have five toes on each foot, not two.
Some chameleons have a crest of small spikes extending along the spine from the proximal part of the tail to the neck; both the extent and size of the spikes varies between species and individuals. These spikes help break up the definitive outline of the chameleon, which aids it when trying to blend into a background.
Chameleons have the most distinctive eyes of any reptile. The upper and lower eyelids are joined, with only a pinhole large enough for the pupil to see through. Each eye can pivot and focus independently, allowing the chameleon to observe two different objects simultaneously. This gives them a full 360-degree arc of vision around their bodies. Prey is located using monocular depth perception, not stereopsis. Chameleons have very good eyesight for reptiles, letting them see small insects from a 5–10 meter distance.
Like snakes, chameleons do not have an outer or a middle ear, so there is neither an ear opening nor an eardrum. However, chameleons are not deaf: they can detect sound frequencies in the range of 200–600 Hz.
Chameleons can see in both visible and ultraviolet light. Chameleons exposed to ultraviolet light show increased social behavior and activity levels, are more inclined to bask and feed, and are also more likely to reproduce, as it has a positive effect on the pineal gland.
All chameleons are primarily insectivores that feed by ballistically projecting their long tongues from their mouths to capture prey located some distance away. While the chameleons' tongues are typically thought to be one and a half to two times the length of their bodies (their length excluding the tail), smaller chameleons (both smaller species and smaller individuals of the same species) have recently been found to have proportionately larger tongue apparatuses than their larger counterparts. Thus, smaller chameleons are able to project their tongues greater distances than the larger chameleons that are the subject of most studies and tongue length estimates, and can project their tongues more than twice their body length.
The chameleon tongue apparatus consists of highly modified hyoid bones, tongue muscles, and collagenous elements. The hyoid bone has an elongated, parallel-sided projection, called the entoglossal process, over which a tubular muscle, the accelerator muscle, sits. The accelerator muscle contracts around the entoglossal process and is responsible for creating the work to power tongue projection, both directly and through the loading of collagenous elements located between the entoglossal process and the accelerator muscle. The tongue retractor muscle, the hyoglossus, connects the hyoid and accelerator muscle, and is responsible for drawing the tongue back into the mouth following tongue projection.
Tongue projection occurs at extremely high performance, reaching the prey in as little as 0.07 seconds, having been launched at accelerations exceeding 41 g. The power with which the tongue is launched, known to exceed 3000 W kg−1, exceeds that for which muscle is able to produce, indicating the presence of an elastic power amplifier to power tongue projection. The recoil of elastic elements in the tongue apparatus are thus responsible for large percentages of the overall tongue projection performance.
One consequence of the incorporation of an elastic recoil mechanism to the tongue projection mechanism is relative thermal insensitivity of tongue projection relative to tongue retraction, which is powered by muscle contraction alone, and is heavily thermally sensitive. While other ectothermic animals become sluggish as their body temperatures decline, due to a reduction in the contractile velocity of their muscles, chameleons are able to project their tongues at high performance even at low body temperatures. The thermal sensitivity of tongue retraction in chameleons, however, is not a problem, as chameleons have a very effective mechanism of holding onto their prey once the tongue has come into contact with it, including surface phenomena, such as wet adhesion and interlocking, and suction. The thermal insensitivity of tongue projection thus enables chameleons to feed effectively on cold mornings prior to being able to behaviorally elevate their body temperatures through thermoregulation, when other sympatric lizards species are still inactive, likely temporarily expanding their thermal niche as a result.
Distribution and habitat
Chameleons are primarily found in the mainland of sub-Saharan Africa and on the island of Madagascar, although a few species are also found in northern Africa, southern Europe, the Middle East, southern India, Sri Lanka, and several smaller islands in the western Indian Ocean. There are introduced, feral populations of veiled and Jackson's chameleons in Hawaii, and isolated pockets of feral Jackson's chameleons have been reported in California and Florida.
Chameleons inhabit all kinds of tropical and mountain rain forests, savannas, and sometimes deserts and steppes. The typical chameleons from the subfamily Chamaeleoninae are arboreal and usually found in trees or bushes, although a few (notably the Namaqua chameleon) are partially or largely terrestrial. Most species from the subfamily Brookesiinae, which includes the genera Brookesia, Rieppeleon, and Rhampholeon, live low in vegetation or on the ground among leaf litter. Many species of chameleons are threatened by extinction. Declining chameleon numbers are due to pollution and deforestation.
The oviparous species lay eggs three to six weeks after copulation. The female will dig a hole — from 10–30 cm (4–12 in), deep depending on the species — and deposit her eggs. Clutch sizes vary greatly with species. Small Brookesia species may only lay two to four eggs, while large veiled chameleons (Chamaeleo calyptratus) have been known to lay clutches of 20–200 (veiled chameleons) and 10–40 (panther chameleons) eggs. Clutch sizes can also vary greatly among the same species. Eggs generally hatch after four to 12 months, again depending on species. The eggs of Parson's chameleon (Calumma parsonii), a species which is rare in captivity, are believed to take more than 24 months to hatch.
The ovoviviparous species, such as the Jackson's chameleon (Trioceros jacksonii) have a five- to seven-month gestation period. Each young chameleon is born within the sticky transparent membrane of its yolk sac. The mother presses each egg onto a branch, where it sticks. The membrane bursts and the newly hatched chameleon frees itself and climbs away to hunt for itself and hide from predators. The female can have up to 30 live young from one gestation.
- The veiled chameleon, Chamaeleo calyptratus from Arabia, is insectivorous, but eats leaves when other sources of water are not available. It can be maintained on a diet of crickets. They can eat as many as 15–50 large crickets a day.
- Jackson's chameleon (Trioceros jacksonii) from Kenya and northern Tanzania eats a wide variety of small animals including ants, butterflies, caterpillars, snails, worms, lizards, geckos, amphibians, and other chameleons, as well as plant material, such as leaves, tender shoots, and berries. It can be maintained on a mixed diet including kale, dandelion leaves, lettuce, bananas, tomatoes, apples, crickets, and waxworms.
- The common chameleon of Europe, North Africa, and the Near East, Chamaeleo chamaeleon, mainly eats wasps and mantises; such arthropods form over three quarters of its diet.:5 Some experts advise that the common chameleon should not be fed exclusively on crickets; these should make up no more than half the diet, with the rest a mixture of waxworms, earthworms, grasshoppers, flies, and plant materials such as green leaves, oats, and fruit.:5–6
- Temperature influences the amount of food eaten.
Chameleons are parasitized by nematode worms, including threadworms (Filarioidea). Threadworms can be transmitted by biting insects such as ticks and mosquitoes. Other roundworms are transmitted through food contaminated with roundworm eggs; the larvae burrow through the wall of the intestine into the bloodstream.
- χαμαιλέων, Henry George Liddell, Robert Scott, A Greek-English Lexicon, on Perseus
- χαμαί, Henry George Liddell, Robert Scott, A Greek-English Lexicon, on Perseus
- λέων, Henry George Liddell, Robert Scott, A Greek-English Lexicon, on Perseus
- Dictionary.com entry for "chameleon"
- Klaver, C. & Böhme, W. (1986). "Phylogeny and classification of the Chamaeleonidae (Sauria) with special reference to hemipenis morphology". Bonner Zoologische Monographien 22: 1–64.
- Tilbury, Colin (2010). Chameleons of Africa, An Atlas including the chameleons of Europe, the Middle East and Asia. Frankfurt: Edition Chimaira. ISBN 3899734513.
- Townsend, T.; Larson, A. (2002). "Molecular phylogenetics and mitochondrial genomic evolution in the Chamaeleonidae (Reptilia, Squamata)". Molecular Phylogenetics and Evolution 23 (1): 22–36. doi:10.1006/mpev.2001.1076. PMID 12182400.
- Raxworthy, C. J.; Forstner, M. R. J.; Nussbaum, R. A. (2002). "Chameleon radiation by oceanic dispersal". Nature 415 (6873): 784–787. doi:10.1038/415784a. PMID 11845207.
- Townsend, T. M., Tolley, K. A., Glaw, F., Böhme, W. & Vences, M. (2011). "Eastward from Africa: Palaeocurrent-mediated chameleon dispersal to the Seychelles islands". Biological Letters 7 (2): 225–228. doi:10.1098/rsbl.2010.0701.
- Tolley, K. A., Townsend, T. M. & Vences, M.; Townsend; Vences (2013). "Large-scale phylogeny of chameleons suggests African origins and Eocene diversification". Proceedings of the Royal Society Part B 280 (1759): 20130184. doi:10.1098/rspb.2013.0184.
- Tilbury, Colin (2014). "Overview of the Systematics of the Chamaeleonidae". In Tolley, Krystal A.; Herrel, Anthony. The Biology of Chameleons. Berkeley: University of California Press. pp. 151–174. ISBN 9780520276055.
- Chameleons. National Geographic Explorer (Student Magazine) – Featured Article
- Stuart-Fox, D.; Moussalli, A. (2008). "Selection for Social Signalling Drives the Evolution of Chameleon Colour Change". PLoS Biology 6 (1): e25. doi:10.1371/journal.pbio.0060025. PMC 2214820. PMID 18232740.
- Harris, Tom. "How Animal Camouflage Works". How Stuff Works. Retrieved 2006-11-13.
- Richard D. Bartlett (1995). Chameleons: Everything about Selection, Care, Nutrition, Diseases, Breeding, and Behavior. Barron's Educational Series. p. 7. ISBN 978-0-8120-9157-1. Retrieved 31 August 2013.
- Young, Emma (2008) Chameleons fine-tune camouflage to predator's vision. New Scientist
- Teyssier, Jeremie; Saenko, Suzanne V.; Milinkovitch Dirk can der Marel & Michel C. (2015). "Photonic crystals cause active colour change in chameleons." nature Communications (6). http://www.nature.com/ncomms/2015/150302/ncomms7368/full/ncomms7368.html
- Maisano, Jessie (27 August 2003). "Digimorph". Chamaeleo calyptratus, Veiled Chameleon. University of Texas at Austin. Retrieved January 10, 2012.
- Tolley, Krystal; Burger, Marius (2007). Chameleons of Southern Africa. Struik. pp. 26–28. ISBN 1-77007-375-2.
- Glaw, Frank; Vences, Miguel (1994). A Field Guide to Amphibians and Reptiles of Madagascar (2nd ed.). Köln: M. Vences & F. Glaw Verlags GbR. ISBN 3-929449-01-3.
- Longbottom, Wil (February 14, 2012). "Discovered: The mini-meleon that is one of the smallest reptiles on the planet". Daily Mail (London).
- Ott, M.; Schaeffel, F.; Kirmse, W. (1998). "Binocular vision and accommodation in prey-catching chamaeleons". Comparative Physiology A 182 (3): 319–330. doi:10.1007/s003590050182.
- Le Berre and Bartlett, p. 31
- Chamaeleon News, August 2004
- Anderson, C.V.; Sheridan, T.; Deban, S.M. (2012). "Scaling of the ballistic tongue apparatus in chameleons". Journal of Morphology 273 (11): 1214–1226. doi:10.1002/jmor.20053. PMID 22730103.
- Anderson, Christopher V. (2009) Rhampholeon spinosus feeding video. chamaeleonidae.com
- Herrel, A., Meyers, J.J., Nishikawa, K.C. & De Vree, F. (2001). "Morphology and histochemistry of the hyolingual apparatus in chameleons". Journal of Morphology 249 (2): 154–170. doi:10.1002/jmor.1047. PMID 11466743.
- de Groot, J.H. & van Leeuwen, J.L. (2004). "Evidence for an elastic projection mechanism in the chameleon tongue". Proceedings of the Royal Society of London B 271 (1540): 761–770. doi:10.1098/rspb.2003.2637.
- Anderson, C.V. and Deban, S.M. (2010). "Ballistic tongue projection in chameleons maintains high performance at low temperature". Proceedings of the National Academy of Science of the United States of America 107 (12): 5495–5499. Bibcode:2010PNAS..107.5495A. doi:10.1073/pnas.0910778107.
- Anderson, C.V. and Deban, S.M. (2012). "Thermal effects on motor control and in vitro muscle dynamics of the ballistic tongue apparatus in chameleons". Journal of Experimental Biology 215 (24): 4345–4357. doi:10.1242/jeb.078881.
- Herrel, A., Meyers, J.J., Aerts, P. & Nishikawa, K.C. (2000). "The mechanics of prey prehension in chameleons" (PDF). Journal of Experimental Biology 203 (Pt 21): 3255–3263. PMID 11023845.
- Glaw, Frank; Vences, Miguel (1994). A Field Guide to Amphibians and Reptiles of Madagascar, 2nd edition. Köln: M. Vences & F. Glaw Verlags GbR. ISBN 3-929449-01-3.
- "African Rainforest". Jackson's Chameleon. Toronto Zoo. Retrieved January 9, 2012.
- Dever, Jennifer (December 5, 2007). "Common Chameleon" (PDF). Common Chameleon. usfca.edu. Retrieved January 9, 2012.
- "Reptiles and Amphibians". Veiled Chameleon. Smithsonian National Zoological Park. Retrieved January 9, 2012.
- Le Berre and Bartlett, p. 110
- Le Berre and Bartlett, p. 109
- Sloboda, Michal and David Modrý (2006). "New species of Choleoeimeria (Apicomplexa: Eimeriidae) from the veiled chameleon, Chamaeleo calyptratus (Sauria: Chamaeleonidae), with taxonomic revision of eimerian coccidia from chameleons". Folia Parasitologica 53 (2): 91–97. doi:10.14411/fp.2006.012. PMID 16898122.
- Le Berre, François and Bartlett, Richard D. (2009) The Chameleon Handbook. Barron's Educational Series. 3rd Edition. ISBN 0764141422.
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- Anderson, C.V. & Deban, S.M. (2010): Ballistic tongue projection in chameleons maintains high performance at low temperature. Proceedings of the National Academy of Science of the United States of America 107 (12): 5495–5499. doi:10.1073/pnas.0910778107
- Anderson, C.V. & Deban, S.M. (2012): Thermal effects on motor control and in vitro muscle dynamics of the ballistic tongue apparatus in chameleons. Journal of Experimental Biology 215 (24): 4345–4357. doi:10.1242/jeb.078881
- Anderson, C.V., Sheridan, T. & Deban, S.M. (2012): Scaling of the ballistic tongue apparatus in chameleons. Journal of Morphology 273: 1214–1226. doi:10.1002/jmor.20053
- de Groot, J.H. & van Leeuwen, J.L. (2004): Evidence for an elastic projection mechanism in the chameleon tongue. Proceedings of the Royal Society of London B 271: 761–770. doi:10.1098/rspb.2003.2637
- Herrel, A., Meyers, J.J., Nishikawa, K.C. & De Vree, F. (2001): Morphology and histochemistry of the hyolingual apparatus in chameleons. Journal of Morphology 249: 154–170.
- Linda J. Davison. Chameleons: Their Care and Breeding. Hancock House Publishers, 1997.
- Philippe de Vosjoli. Essential Care of Chameleons. Advanced Vivarium Systems, 2004.