Biology:Agamidae

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Short description: Family of lizards

Agamidae
Temporal range: Cenomanian–recent
MC Siedleragame.jpg
Male Mwanza flat-headed rock agama (Agama mwanzae), in the Serengeti, Tanzania
Scientific classification e
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Squamata
Suborder: Iguania
Clade: Acrodonta
Family: Agamidae
Gray, 1827[1]
Subfamilies

6, see text

Agamidae is a family of over 550 species of iguanian lizards indigenous to Africa, Asia, Australia, and a few in Southern Europe. Many species are commonly called dragons or dragon lizards.

Overview

Phylogenetically, they may be sister to the Iguanidae, and have a similar appearance. Agamids usually have well-developed, strong legs. Their tails cannot be shed and regenerated like those of geckos (and several other families such as skinks), though a certain amount of regeneration is observed in some.[2][3] Many agamid species are capable of limited change of their colours to regulate their body temperature.[4] In some species, males are more brightly coloured than females,[5] and colours play a part in signaling and reproductive behaviours.[6] Although agamids generally inhabit warm environments, ranging from hot deserts to tropical rainforests, at least one species, the mountain dragon, is found in cooler regions. They are particularly diverse in Australia.[7][8][9]

This group of lizards includes some more popularly known, such as the domesticated bearded dragon, Chinese water dragon, and Uromastyx species.

One of the key distinguishing features of the agamids is their teeth, which are borne on the outer rim of their mouths (acrodonts), rather than on the inner side of their jaws (pleurodonts). This feature is shared with the chameleons and the tuatara, but is otherwise unusual among lizards. Agamid lizards are generally diurnal, with good vision, and include a number of arboreal species, in addition to ground- and rock-dwellers. Most need to bask in the sun to maintain elevated body temperatures, meaning they are heliothermic. They generally feed on insects and other arthropods (such as spiders), although for some larger species, their diet may include small reptiles or mammals, nestling birds, and flowers or other vegetable matter.[10]

Reproduction

The great majority of agamid species are oviparous.[11] The eggs are mostly found in damp soil or rotting logs to retain enough moisture during the incubation period. The clutch size varies from four to 10 eggs for most species, and incubation period lasts around 6–8 weeks. Specifically in the Leiolepidinae subfamily of agamids, all species use a burrowing system that reaches moist soil, where eggs are deposited in late spring/early summer or at the beginning of the dry season. The Leiolepidinae burrow system is also used for daily or seasonal retreats, as it allows them to regulate their body temperature or act as a refuge from predators.

Systematics and distribution

Ground agama (Agama aculeata) in Tanzania
Pondichéry fan-throated lizard Sitana ponticeriana from the Agaminae
Agamidae in Namibia

Very few studies of the Agamidae have been conducted. The first comprehensive assessment was by Moody (1980)[12] followed by a more inclusive assessment by Frost and Etheridge (1989).[13] Subsequent studies were based on mitochondrial DNA loci by Macey et al. (2000)[14] and Honda et al. (2000)[15] and also by sampling across the Agamidae by Joger (1991).[16] Few other studies focused on clades within the family, and the Agamidae have not been as well investigated as the Iguanidae.

The agamids show a curious distribution. They are found over much of the Old World, including continental Africa, Australia, southern Asia, and sparsely in warmer regions of Europe. They are, however, absent from Madagascar and the New World. The distribution is the opposite of that of the iguanids, which are found in just these areas, but absent in areas where agamids are found. A similar faunal divide is found in between the boas and pythons.[17]

Subfamilies

Among the Agamidae, six subfamilies are generally recognized:[18][19]

  • Agaminae (Africa, Europe and south Asia)
  • Amphibolurinae (Australia and New Guinea, one species in Southeast Asia)
  • Draconinae (South and Southeast Asia)
  • Hydrosaurinae (Hydrosaurus, Papua New Guinea, the Philippines, and Indonesia)
  • Leiolepidinae (Leiolepis, Southeast Asia)
  • Uromasticinae (Saara and Uromastyx, Africa and South Asia)

Evolutionary history

The oldest known unambiguous agamid is Protodraco from the mid-Cretaceous (early Cenomanian) aged Burmese amber of Myanmar, dating to around 99 million years ago. It is similar to primitive living Southeast Asian agamids.[20] Gueragama from the Late Cretaceous of Brazil may also be an agamid.[21] Jeddaherdan, a supposed agamid from the Late Cretaceous of Morocco, was later shown to be actually a young subfossil of the living genus Uromastyx.[22]

Predator responses

Body temperature helps determine the physiological state of these lizards and affects their predator responses. A positive correlation is seen between a flight response (running speed) and body temperature of various agamid species.[23] At higher body temperatures, these lizards tend to flee quickly from predators, whereas at lower temperatures, they tend to have a reduced running speed and show an increased fight response, where they are more likely to be aggressive and attack predators.

Certain physical features of some lizards of these species, such as frilled-neck lizards, play a role in their defensive responses, as well. During the mating season, males tend to display more of their frill, and give fight responses more often. Both males and females display their frills when they are threatened by predators, and during social interactions.[24]

References

  1. Dahms Tierleben. www.dahmstierlrben.de/systematik/Reptilien/Squamata/Iguania/agamidae.
  2. Thompson, M. B. (1993). "Estimate of the population structure of the e[a]stern water dragon, Physignathus lesueurii (Reptilia: Agamidae), along riverside habitat". Wildlife Research 20 (5): 613–9. doi:10.1071/WR9930613. 
  3. Ananjeva, Natalia B.; Bryan L. Stuart (2001). "The Agamid lizard Ptyctolaemus phuwtilmensis Manthey and Nabhitabhata, 1991 from Thailand and Laos represents a new genus". Russian Journal of Herpetology (Folium Publishing Company) 8 (3): 165–170. http://rjh.folium.ru/index.php/rjh/article/view/580. 
  4. de Velasco, Jesus Barraza; Glenn J. Tattersall (September 2008). "The influence of hypoxia on the thermal sensitivity of skin colouration in the bearded dragon, Pogona vitticeps". Journal of Comparative Physiology B 178 (7): 867–875. doi:10.1007/s00360-008-0274-8. PMID 18491114. 
  5. Cuervo, J.J.; R. Shine (10 July 2007). "Hues of a dragon's belly: morphological correlates of ventral coloration in water dragons". Journal of Zoology 273 (3): 298–304. doi:10.1111/j.1469-7998.2007.00328.x. 
  6. LeBas, Natasha R.; N. Justin Marshall (2000). "The role of colour in signaling and male choice in the agamid lizard Ctenophorus ornatus". Proceedings of the Royal Society of London B 267 (1442): 445–452. doi:10.1098/rspb.2000.1020. PMID 10737400. 
  7. Gray, JA; Sherratt, E; Hutchinson, MN; Jones, MEH (2019). "Changes in ontogenetic patterns facilitate diversification in skull shape of Australian agamid lizards". BMC Evolutionary Biology 19 (1): 7. doi:10.1186/s12862-018-1335-6. PMID 30621580. Bibcode2019BMCEE..19....7G. 
  8. "Exceptional disparity in Australian agamid lizards is a possible result of arrival into vacant niche". The Anatomical Record 302 (9): 1536–1543. 2019. doi:10.1002/ar.24096. PMID 30773845. 
  9. "Evolution of cranial shape in a continental-scale evolutionary radiation of Australian lizards". Evolution 73 (11): 2216–29. 2019. doi:10.1111/evo.13851. PMID 31580481. https://discovery.ucl.ac.uk/id/eprint/10088393/1/DRAGONS_submission1.pdf. 
  10. Cogger, H. G. (1994). Reptiles and Amphibians of Australia (6th ed.). Port Melbourne, Vic.: Reed. ISBN 978-0-7301-0088-1. OCLC 35576956. 
  11. Bauer, Aaron M. (1998). Encyclopedia of Reptiles and Amphibians. San Diego: Academic Press. pp. 134–136. ISBN 978-0-12-178560-4. 
  12. Moody, S. M. (1980). Phylogenetic relationships and historical biogeographical relationships of the genera in the family Agamidae (Reptilia: Lacertilia) (PhD). Ann Arbor: University of Michigan. 8017324.
  13. Frost, Darrel R.; Richard Etheridge (28 September 1989). "A phylogenetic analysis and taxonomy of iguanian lizards (Reptilia: Squamata)". University of Kansas Museum of Natural History Miscellaneous Publications (University of Kansas Museum of Natural History) 81: 1–65. https://www.biodiversitylibrary.org/item/55046. Retrieved 5 January 2012. 
  14. Macey, J. Robert; James A. Schulte II; Allan Larson. (2000). "Evolution and phylogenetic information content of mitochondrial genomic structural features illustrated with acrodont lizards". Systematic Biology 49 (2): 257–277. doi:10.1093/sysbio/49.2.257. PMID 12118408. .
  15. Honda, Masanao; Hidetoshi Ota; Mari Kobayashi; Jarujin Nabhitabhata; Hoi-Sen Yong; Showichi Sengoku; Tsutomu Hikida (2000). "Phylogenetic Relationships of the Family Agamidae (Reptilia: Iguania) Inferred from Mitochondrial DNA Sequences". Zoological Science 1991 (3): 616–622. doi:10.2108/0289-0003(2000)17[527:PROTFA2.0.CO;2]. ISSN 0289-0003. http://repository.kulib.kyoto-u.ac.jp/dspace/bitstream/2433/57223/1/K093.pdf. 
  16. Joger, Ulrich (1 August 1991). "A Molecular Phylogeny of Agamid Lizards". University of Kansas Museum of Natural History Miscellaneous Publications (American Society of Ichthyologists and Herpetologists) 81 (3): 616–622. doi:10.2307/1446389. 
  17. Heads, Michael (2014). "3 Global affinities of Australasian Groups §Indian + Pacific Ocean Groups". Biogeography of Australasia: A Molecular Analysis. Cambridge University Press. pp. 119. ISBN 9781107041028. 
  18. Agamidae, UniProt Taxonomy
  19. B. Ananjeva, Natalia (October 2010). "Asian Agamid lizards (Agamidae, Acrodonta, Sauria, Reptilia): Phylogenetic and taxonomic diversity". Taprobanica: The Journal of Asian Biodiversity 2 (2): 65. doi:10.4038/tapro.v2i2.3144. 
  20. Wagner, Philipp; Stanley, Edward L.; Daza, Juan D.; Bauer, Aaron M. (August 2021). "A new agamid lizard in mid-Cretaceous amber from northern Myanmar". Cretaceous Research 124: 104813. doi:10.1016/j.cretres.2021.104813. Bibcode2021CrRes.12404813W. https://linkinghub.elsevier.com/retrieve/pii/S0195667121000604. 
  21. Apesteguía, Sebastián; Daza, Juan D.; Simões, Tiago R.; Rage, Jean Claude (September 2016). "The first iguanian lizard from the Mesozoic of Africa". Royal Society Open Science 3 (9): 160462. doi:10.1098/rsos.160462. ISSN 2054-5703. PMID 27703708. Bibcode2016RSOS....360462A. 
  22. Vullo, Romain; Bailon, Salvador; Dauphin, Yannicke; Monchot, Hervé; Allain, Ronan (November 2022). "A reappraisal of Jeddaherdan aleadonta (Squamata: Acrodonta), the purported oldest iguanian lizard from Africa" (in en). Cretaceous Research 143: 105412. doi:10.1016/j.cretres.2022.105412. 
  23. Hertz, Paul E.; Huey, Raymond B.; Nevo, Eviatar (1982-08-01). "Fight versus flight: Body temperature influences defensive responses of lizards" (in en). Animal Behaviour 30 (3): 676–679. doi:10.1016/S0003-3472(82)80137-1. ISSN 0003-3472. https://www.sciencedirect.com/science/article/pii/S0003347282801371. 
  24. Shine, Richard (May 1990). "Function and evolution of the frill of the Frillneck Lizard, Chlamydosaurus Kingii (sauria: Agamidae)". Biological Journal of the Linnean Society 40 (1): 11–20. doi:10.1111/j.1095-8312.1990.tb00531.x. 

External links

Wikidata ☰ Q191102 entry