This article is about the Squamata order of reptiles. For the Roman scale armour, see Lorica squamata.
Scaled reptiles
Temporal range:
Early JurassicPresent, 199–0 Ma[1]
Eastern blue-tongued lizard
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Superorder: Lepidosauria
Order: Squamata
Oppel, 1811

The order Squamata, or the scaled reptiles, are the largest recent order of reptiles, comprising all lizards and snakes. With over 10,000 species,[3] it is also the second-largest order of extant vertebrates, after the perciform fish, and roughly equal in number to the Saurischia. Members of the order are distinguished by their skins, which bear horny scales or shields. They also possess movable quadrate bones, making it possible to move the upper jaw relative to the neurocranium. This is particularly visible in snakes, which are able to open their mouths very wide to accommodate comparatively large prey. They are the most variably sized order of reptiles, ranging from the 16 mm (0.63 in) dwarf gecko (Sphaerodactylus ariasae) to the 5.21 m (17.1 ft) green anaconda (Eunectes murinus) and the now-extinct mosasaurs, which reached lengths of 14 m (46 ft).

Among the other reptiles, squamates are most closely related to the tuatara, which strongly resembles lizards.


Slavoia darevskii, a fossil squamate

Squamates are a monophyletic sister group to the tuatara. The squamates and tuatara together are a sister group to crocodiles and birds, the extant archosaurs. Fossils of the squamate sister group, the Rhynchocephalia, appear in the Early Triassic,[4] meaning that the lineage leading to squamates must have existed as well. Modern squamates probably originated in the mid Jurassic,[4] when fossil relatives of geckos and skinks and snakes[5] appear; other groups, including iguanians and varanoids, first appear in the Cretaceous period. Also appearing in the Cretaceous are the polyglyphanodonts, a lizard group of uncertain affinities, and the mosasaurs, a group of predatory, marine lizards that grew to enormous sizes.[6] At the end of the Cretaceous, squamates suffered a major extinction at the K-T boundary[7] which wiped out polyglyphanodonts, mosasaurs, and a number of other groups.

The relationships of squamates have been debated. Although many of the groups originally recognized on the basis of morphology are still accepted, our understanding of their relationships to each other has changed radically as a result of studying their DNA. From morphological data, the iguanians were long thought to be the most ancient branch of the tree;[6] however, studies of the DNA suggest that the geckos represent the most ancient branch.[8] Iguanians are now united with snakes and anguimorphs in a group called the Toxicofera. DNA also suggests that the various limbless groups- snakes, amphisbaenians, and dibamids- are unrelated, and instead arose independently from lizards.


Trachylepis maculilabris skinks mating

The male members of the group Squamata have hemipenes, which are usually held inverted within their bodies, and are everted for reproduction via erectile tissue like that in the human penis.[9] Only one is used at a time, and some evidence indicates that males alternate use between copulations. The hemipenis has a variety of shapes, depending on the species. Often it bears spines or hooks, to anchor the male within the female. Some species even have forked hemipenes (each hemipenis has two tips). Due to being everted and inverted, hemipenes do not have a completely enclosed channel for the conduction of sperm, but rather a seminal groove that seals as the erectile tissue expands. This is also the only reptile group in which both viviparous and ovoviviparous species are found, as well as the usual oviparous reptiles. Some species, such as the Komodo dragon, can actually reproduce asexually through parthenogenesis.[10]

The Japanese striped snake has been studied in sexual selection

There have been studies on how sexual selection manifests itself in snakes and lizards. Snakes use a variety of tactics in acquiring mates.[11] Ritual combat between males for the females they want to mate with includes topping, a behavior exhibited by most viperids, in which one male will twist around the vertically elevated fore body of its opponent and forcing it downward. It is common for neck biting to occur while the snakes are entwined.[12]

Facultative parthenogenesis

The effects of central fusion and terminal fusion on heterozygosity

Parthenogenesis is a natural form of reproduction in which growth and development of embryos occur without fertilization. Agkistrodon contortrix (copperhead snake) and Agkistrodon piscivorus (cotton mouth snake) can reproduce by facultative parthenogenesis. That is, they are capable of switching from a sexual mode of reproduction to an asexual mode.[13] The type of parthenogenesis that likely occurs is automixis with terminal fusion (see figure), a process in which two terminal products from the same meiosis fuse to form a diploid zygote. This process leads to genome wide homozygosity, expression of deleterious recessive alleles and often to developmental abnormalities. Both captive-born and wild-born A. contortrix and A. piscivorus appear to be capable of this form of parthenogenesis.[13]

Reproduction in squamate reptiles is ordinarily sexual, with males having a ZZ pair of sex determining chromosomes, and females a ZW pair. However, the Colombian Rainbow boa, Epicrates maurus can also reproduce by facultative parthenogenesis resulting in production of WW female progeny.[14] The WW females are likely produced by terminal automixis.

Inbreeding avoidance

When female sand lizards mate with two or more males, sperm competition within the females reproductive tract may occur. Active selection of sperm by females appears to occur in a manner that enhances female fitness.[15] On the basis of this selective process, the sperm of males that are more distantly related to the female are preferentially used for fertilization, rather than the sperm of close relatives.[15] This preference may enhance the fitness of progeny by reducing inbreeding depression.

Evolution of venom

See also: Venom

Recent research suggests that the evolutionary origin of venom may exist deep in the squamate phylogeny, with 60% of squamates placed in this hypothetical group called Toxicofera. Venom has been known in the clades Caenophidia, Anguimorpha, and Iguania, and has been shown to have evolved a single time along these lineages before the three groups diverged, because all lineages share nine common toxins.[16] The fossil record shows the divergence between anguimorphs, iguanians, and advanced snakes dates back roughly 200 Mya to the Late Triassic/Early Jurassic.[16] But the only good fossil evidence is from the Jurassic.[1]

Snake venom has been shown to have evolved via a process by which a gene encoding for a normal body protein, typically one involved in key regulatory processes or bioactivity, is duplicated, and the copy is selectively expressed in the venom gland.[17] Previous literature hypothesized that venoms were modifications of salivary or pancreatic proteins,[18] but different toxins have been found to have been recruited from numerous different protein bodies and are as diverse as their functions.[19]

Natural selection has driven the origination and diversification of the toxins to counter the defenses of their prey. Once toxins have been recruited into the venom proteome, they form large, multigene families and evolve via the birth-and-death model of protein evolution,[20] which leads to a diversification of toxins that allows the ambush predators the ability to attack a wide range of prey.[21] The rapid evolution and diversification is thought to be the result of a predator–prey evolutionary arms race, where both are adapting to counter the other.[22]

Humans and squamates

Bites and fatalities

See also: Snakebite
Map showing the global distribution of venomous snakebites

An estimated 125,000 people a year die from venomous snake bites.[23] In the US alone, more than 8,000 venomous snake bites are reported each year.[24]

Lizard bites, unlike venomous snake bites, are not fatal. The Komodo dragon has been known to kill people due to its size, and recent studies show it may have a passive envenomation system. Recent studies also show that the close relatives of the Komodo, the monitor lizards, all have a similar envenomation system, but the toxicity of the bites is relatively low to humans.[25] The Gila monster and beaded lizards of North and Central America are venomous, but not deadly to humans.


Though they survived the Cretaceous–Paleogene extinction event, many squamate species are endangered now due to habitat loss, hunting and poaching, illegal wildlife trading, alien species being introduced to their habitats (which puts native creatures at risk through competition, disease, and predation), and other anthropogenic causes. Because of this, some squamates species have recently become extinct, with Africa having the most extinct species of squamates. However, breeding programs and wildlife parks are trying to save many endangered reptiles from extinction. Zoos, private hobbyists and breeders help educate people about the importance of snakes and lizards.


Desert iguana from Amboy Crater, Mojave Desert, California

Historically, the order Squamata has been divided into three suborders:

Of these, the lizards form a paraphyletic group,[26] since "lizards" excludes the subclades of snakes and amphisbaenians. Studies of squamate relationships using molecular biology have found several distinct lineages, though the specific details of their interrelationships vary from one study to the next. One example of a modern classification of the squamates[2][27] found the following relationships:




Diplodactylidae Underwood 1954

Pygopodidae Boulenger 1884





Sphaerodactylidae Underwood 1954










Gymnophthalmidae Merrem 1820

Teiidae Gray 1827




Rhineuridae Vanzolini 1951

Bipedidae Taylor 1951

Blanidae Kearney & Stuart 2004

Cadeidae Vidal & Hedges 2008

Trogonophiidae Gray 1865

Amphisbaenidae Gray 1865



Shinisauridae Ahl 1930 sensu Conrad 2006





Helodermatidae Gray 1837






Anguidae Gray 1825



Agamidae Gray 1827




Hoplocercidae Frost & Etheridge 1989











Leptotyphlopidae Stejneger 1892

Gerrhopilidae Vidal et al. 2010

Xenotyphlopidae Vidal et al. 2010

Typhlopidae Merrem 1820




Tropidophiidae Brongersma 1951





Xenopeltidae Bonaparte 1845


Pythonidae Fitzinger 1826



Bolyeriidae Hoffstetter 1946


Acrochordidae Bonaparte 1831










All recent molecular studies[28] suggest that several groups form a venom clade, which encompasses a majority (nearly 60%) of squamate species. Named Toxicofera, it combines the groups Serpentes (snakes), Iguania (agamids, chameleons, iguanids, etc.), and Anguimorpha (monitor lizards, Gila monster, glass lizards, etc.).[28]

List of extant families

FamilyCommon namesExample speciesExample photo
Gray, 1865
Tropical worm lizardsDarwin's worm lizard (Amphisbaena darwinii)
Taylor, 1951
Bipes worm lizardsMexican mole lizard (Bipes biporus)
BlanidaeMediterranean worm lizardsMediterranean worm lizard (Blanus cinereus)
Vidal & Hedges, 2008[29]
Cuban worm lizardsCadea blanoides
Vanzolini, 1951
North American worm lizardsNorth American worm lizard (Rhineura floridana)
Gray, 1865
Palearctic worm lizardsCheckerboard worm lizard (Trogonophis wiegmanni)
Gekkota (incl. Dibamia)
FamilyCommon namesExample speciesExample photo
Boulenger, 1884
Blind lizardsDibamus nicobaricum
Gray, 1825 (paraphyletic)
GeckosThick-tailed gecko (Underwoodisaurus milii)
Boulenger, 1884
Legless lizardsBurton's snake lizard (Lialis burtonis)
FamilyCommon namesExample speciesExample photo
Spix, 1825
Agamas Eastern bearded dragon (Pogona barbata)
Gray, 1825
ChameleonsVeiled chameleon (Chamaeleo calyptratus)
Frost & Etheridge, 1989
Casquehead lizardsPlumed basilisk (Basiliscus plumifrons)
Frost & Etheridge, 1989
Collared and leopard lizardsCommon collared lizard (Crotaphytus collaris)
Frost & Etheridge, 1989
Wood lizards or clubtailsClub-tail iguana (Hoplocercus spinosus)
IguanidaeIguanasMarine iguana (Amblyrhynchus cristatus)
Frost et al., 2001
Darwin's iguana (Diplolaemus darwinii)
Frost & Etheridge, 1989
Swifts Shining tree iguana (Liolaemus nitidus)
Frost & Etheridge, 1989
Madagascan iguanas Chalarodon (Chalarodon madagascariensis)
Frost & Etheridge, 1989
Earless, spiny, tree, side-blotched and horned lizardsGreater earless lizard (Cophosaurus texanus)
Frost & Etheridge, 1989 (+ Dactyloidae)
AnolesCarolina anole (Anolis carolinensis)
Frost & Etheridge, 1989
Neotropical ground lizards(Microlophus peruvianus)
Lacertoidea (excl. Amphisbaenia)
FamilyCommon NamesExample SpeciesExample Photo
GymnophthalmidaeSpectacled lizards Bachia bicolor
Oppel, 1811
Wall or true lizardsOcellated lizard (Lacerta lepida)
TeiidaeTegus or whiptailsGold tegu (Tupinambis teguixin)
FamilyCommon namesExample speciesExample photo
Oppel, 1811
Glass lizards, alligator lizards and slow wormsSlow worm (Anguis fragilis)
Gray, 1852
American legless lizardsCalifornia legless lizard (Anniella pulchra)
HelodermatidaeGila monstersGila monster (Heloderma suspectum)
Cope, 1866
Knob-scaled lizardsMexican knob-scaled lizard (Xenosaurus grandis)
Paleoanguimorpha or Varanoidea
FamilyCommon namesExample speciesExample photo
LanthanotidaeEarless monitorEarless monitor (Lanthanotus borneensis)
ShinisauridaeChinese crocodile lizardChinese crocodile lizard (Shinisaurus crocodilurus)
VaranidaeMonitor lizardsPerentie (Varanus giganteus)
FamilyCommon NamesExample SpeciesExample Photo
CordylidaeSpinytail lizards Girdle-tailed lizard (Cordylus warreni)
GerrhosauridaePlated lizardsSudan plated lizard (Gerrhosaurus major)
Oppel, 1811
SkinksWestern blue-tongued skink (Tiliqua occipitalis)
XantusiidaeNight lizardsGranite night lizard (Xantusia henshawi)
FamilyCommon namesExample speciesExample photo
Bonaparte, 1831[30]
File snakesMarine file snake (Acrochordus granulatus)
Stejneger, 1907[31]
Coral pipe snakesBurrowing false coral (Anilius scytale)
Cundall, Wallach and Rossman, 1993.[32]
Dwarf pipe snakesLeonard's pipe snake, (Anomochilus leonardi)
Gray, 1825[30] (incl. Calabariidae)
BoasAmazon tree boa (Corallus hortulanus)
Hoffstetter, 1946
Round Island boasRound Island burrowing boa (Bolyeria multocarinata)
Oppel, 1811[30] sensu lato (incl. Dipsadidae, Natricidae, Pseudoxenodontidae)
ColubridsGrass snake (Natrix natrix)
Fitzinger, 1843
Asian pipe snakesRed-tailed pipe snake (Cylindrophis ruffus)
Boie, 1827[30]
Cobras, coral snakes, mambas, kraits, sea snakes, sea kraits, Australian elapidsKing cobra (Ophiophagus hannah)
Bonaparte, 1845
Fitzinger, 1843[33]
Bibron's burrowing asp (Atractaspis bibroni)
Cope, 1861
Mexican burrowing snakesMexican burrowing snake (Loxocemus bicolor)
Romer, 1956
Fitzinger, 1826
PythonsBall python (Python regius)
Brongersma, 1951
Dwarf boasNorthern eyelash boa (Trachyboa boulengeri)
Müller, 1832
Shield-tailed snakes, short-tailed snakesCuvier's shieldtail (Uropeltis ceylanica)
Oppel, 1811[30]
Vipers, pitvipers, rattlesnakesEuropean asp (Vipera aspis)
Fitzinger, 1826
Gray, 1849
Sunbeam snakesSunbeam snake (Xenopeltis unicolor)
Scolecophidia (incl. Anomalepidae)
FamilyCommon namesExample speciesExample photo
Taylor, 1939[30]
Dawn blind snakesDawn blind snake (Liotyphlops beui)
Vidal et al., 2010[29]
Stejneger, 1892[30]
Slender blind snakesTexas blind snake (Leptotyphlops dulcis)
Merrem, 1820[34]
Blind snakesEuropean blind snake (Typhlops vermicularis)
Vidal et al., 2010[29]
Xenotyphlops grandidieri


  1. 1 2 Hutchinson, M. N.; Skinner, A.; Lee, M. S. Y. (2012). "Tikiguania and the antiquity of squamate reptiles (lizards and snakes)". Biology Letters. 8 (4): 665–669. doi:10.1098/rsbl.2011.1216. PMC 3391445Freely accessible. PMID 22279152.
  2. 1 2 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.
  3. http://www.reptile-database.org/db-info/SpeciesStat.html
  4. 1 2 Jones, M.E.; Anderson, C.L.; Hipsley, C.A.; Müller, J.; Evans, S.E.; Schoch, R.R. (2013). "Integration of molecules and new fossils supports a Triassic origin for Lepidosauria (lizards, snakes, and tuatara)". BMC Evolutionary Biology. 13: 208. doi:10.1186/1471-2148-13-208. PMC 4016551Freely accessible. PMID 24063680.
  5. Michael Caldwell et al. "The oldest known snakes from the Middle Jurassic-Lower Cretaceous provide insights on snake evolution", Nature Commynications, 27 January 2015, summarized in Christian Science Monitor, Joseph Dussault "How did snakes evolve? Fossil discovery holds clues.": accessed 28 January 2015
  6. 1 2 Gauthier, J.; Kearney, M.; Maisano, J.A.; Rieppel, O.; Behlke, A. (2012). "Assembling the squamate tree of life: perspectives from the phenotype and the fossil record". Bulletin Yale Peabody Museum. 53: 3–308. doi:10.3374/014.053.0101.
  7. Longrich, N.R.; Bhullar, A.-B.S.; Gauthier, J. (2012). "Mass extinction of lizards and snakes at the Cretaceous-Paleogene boundary". Proceedings of the National Academy of Sciences. 109: 21396–21401. doi:10.1073/pnas.1211526110. PMC 3535637Freely accessible. PMID 23236177.
  8. Pyron, R.A.; Burbrink, F.T.; Wiens, J.J. (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. PMC 3682911Freely accessible. PMID 23627680.
  9. "Iguana Anatomy".
  10. Morales, Alex (20 December 2006). "Komodo Dragons, World's Largest Lizards, Have Virgin Births". Bloomberg Television. Retrieved 2008-03-28.
  11. Shine, Richard; Langkilde, Tracy; Mason, Robert T (2004). "Courtship tactics in garter snakes: How do a male's morphology and behaviour influence his mating success?". Animal Behaviour. 67 (3): 477–83. doi:10.1016/j.anbehav.2003.05.007.
  12. Blouin-Demers, Gabriel; Gibbs, H. Lisle; Weatherhead, Patrick J. (2005). "Genetic evidence for sexual selection in black ratsnakes, Elaphe obsoleta". Animal Behaviour. 69 (1): 225–34. doi:10.1016/j.anbehav.2004.03.012.
  13. 1 2 Booth W, Smith CF, Eskridge PH, Hoss SK, Mendelson JR, Schuett GW (2012). "Facultative parthenogenesis discovered in wild vertebrates". Biol. Lett. 8 (6): 983–5. doi:10.1098/rsbl.2012.0666. PMC 3497136Freely accessible. PMID 22977071.
  14. Booth W, Million L, Reynolds RG, Burghardt GM, Vargo EL, Schal C, Tzika AC, Schuett GW (2011). "Consecutive virgin births in the new world boid snake, the Colombian rainbow Boa, Epicrates maurus". J. Hered. 102 (6): 759–63. doi:10.1093/jhered/esr080. PMID 21868391.
  15. 1 2 Olsson M, Shine R, Madsen T, Gullberg A, Tegelström H (1997). "Sperm choice by females". Trends Ecol. Evol. (Amst.). 12 (11): 445–6. PMID 21238151.
  16. 1 2 Fry, B. G.; Vidal, N.; Norman, J. A.; Vonk, F. J.; Scheib, H.; Ramjan, S. F. R.; Kuruppu, S. (2006). "Early evolution of the venom system in lizards and snakes". Nature. 439: 584–588. doi:10.1038/nature04328. PMID 16292255.
  17. Fry, B. G.; Vidal, N.; Kochva, E.; Renjifo, C. (2009). "Evolution and diversification of the toxicofera reptile venom system". Journal of Proteomics. 72: 127–136. doi:10.1016/j.jprot.2009.01.009. PMID 19457354.
  18. Kochva, E (1987). "The origin of snakes and evolution of the venom apparatus". Toxicon. 25: 65–106. doi:10.1016/0041-0101(87)90150-4.
  19. Fry, B.G. (2005). "From genome to "Venome": Molecular origin and evolution of the snake venom proteome inferred from phylogenetic analysis of toxin sequences and related body proteins". Genome Research. 15: 403–420. doi:10.1101/gr.3228405.
  20. Fry, B. G.; Scheib, H.; Young, B.; McNaughtan, J.; Ramjan, S. F. R.; Vidal, N. (2008). "Evolution of an arsenal". Molecular & Cellular Proteomics. 7: 215–246. doi:10.1074/mcp.m700094-mcp200.
  21. Calvete, J. J.; Sanz, L.; Angulo, Y.; Lomonte, B.; Gutierrez, J. M. (2009). "Venoms, venomics, antivenomics". FEBS Letters. 583: 1736–1743. doi:10.1016/j.febslet.2009.03.029.
  22. Barlow, A.; Pook, C. E.; Harrison, R. A.; Wuster, W. (2009). "Coevolution of diet and prey-specific venom activity supports the role of selection in snake venom evolution". Proceedings of the Royal Society B: Biological Sciences. 276: 2443–2449. doi:10.1098/rspb.2009.0048. PMC 2690460Freely accessible. PMID 19364745.
  23. "Snake-bites: appraisal of the global situation" (PDF). Who.com. Retrieved 2007-12-30.
  24. "First Aid Snake Bites". University of Maryland Medical Center. Retrieved 2007-12-30.
  25. "Komodo dragon kills boy, 8, in Indonesia". msnbc. Retrieved 2007-12-30.
  26. Reeder, Tod W.; Townsend, Ted M.; Mulcahy, Daniel G.; Noonan, Brice P.; Wood, Perry L.; Sites, Jack W.; Wiens, John J. (2015). "Integrated Analyses Resolve Conflicts over Squamate Reptile Phylogeny and Reveal Unexpected Placements for Fossil Taxa". PLOS ONE. 10 (3): e0118199. doi:10.1371/journal.pone.0118199. PMC 4372529Freely accessible. PMID 25803280.
  27. Zheng, Yuchi; Wiens, John J. (2016). "Combining phylogenomic and supermatrix approaches, and a time-calibrated phylogeny for squamate reptiles (lizards and snakes) based on 52 genes and 4162 species". Molecular Phylogenetics and Evolution. 94 part B: 537–547. doi:10.1016/j.ympev.2015.10.009.
  28. 1 2 Fry, Brian G.; et al. (February 2006). "Early evolution of the venom system in lizards and snakes" (PDF). Nature. 439 (7076): 584–588. doi:10.1038/nature04328. PMID 16292255.
  29. 1 2 3
  30. 1 2 3 4 5 6 7 Cogger(1991), p.23
  31. "Aniliidae". Integrated Taxonomic Information System. Retrieved 12 December 2007.
  32. "Anomochilidae". Integrated Taxonomic Information System. Retrieved 13 December 2007.
  33. "Atractaspididae". Integrated Taxonomic Information System. Retrieved 13 December 2007.
  34. "Typhlopidae". Integrated Taxonomic Information System. Retrieved 13 December 2007.
Wikimedia Commons has media related to Squamata.
Wikispecies has information related to: Squamata

Further reading

  • Bebler, John L.; King, F. Wayne (1979). The Audubon Society Field Guide to Reptiles and Amphibians of North America. New York: Alfred A. Knopf. p. 581. ISBN 0-394-50824-6. 
  • Capula, Massimo; Behler (1989). Simon & Schuster's Guide to Reptiles and Amphibians of the World. New York: Simon & Schuster. ISBN 0-671-69098-1. 
  • Cogger, Harold; Zweifel, Richard (1992). Reptiles & Amphibians. Sydney: Weldon Owen. ISBN 0-8317-2786-1. 
  • Conant, Roger; Collins, Joseph (1991). A Field Guide to Reptiles and Amphibians Eastern/Central North America. Boston, Massachusetts: Houghton Mifflin Company. ISBN 0-395-58389-6. 
  • Ditmars, Raymond L (1933). Reptiles of the World: The Crocodilians, Lizards, Snakes, Turtles and Tortoises of the Eastern and Western Hemispheres. New York: Macmillan. p. 321. 
  • Evans, SE (2003). "At the feet of the dinosaurs: the origin, evolution and early diversification of squamate reptiles (Lepidosauria: Diapsida)". Biological Reviews, Cambridge. 78: 513–551. doi:10.1017/S1464793103006134. PMID 14700390. 
  • Evans SE. 2008. The skull of lizards and tuatara. In Biology of the Reptilia, Vol.20, Morphology H: the skull of Lepidosauria, Gans C, Gaunt A S, Adler K. (eds). Ithica, New York, Society for the study of Amphibians and Reptiles. pp1–344. Weblink to purchase
  • Evans, SE; Jones, MEH (2010). "The origin, early history and diversification of lepidosauromorph reptiles. In Bandyopadhyay S. (ed.), New Aspects of Mesozoic Biodiversity". 27 Lecture Notes in Earth Sciences. 132: 27–44. doi:10.1007/978-3-642-10311-7_2. 
  • Freiberg, Dr. Marcos; Walls, Jerry (1984). The World of Venomous Animals. New Jersey: TFH Publications. ISBN 0-87666-567-9. 
  • Gibbons, J. Whitfield; Gibbons, Whit (1983). Their Blood Runs Cold: Adventures With Reptiles and Amphibians. Alabama: University of Alabama Press. p. 164. ISBN 978-0-8173-0135-4. 
  • McDiarmid, RW; Campbell, JA; Touré, T (1999). Snake Species of the World: A Taxonomic and Geographic Reference. 1. Herpetologists' League. p. 511. ISBN 1-893777-00-6. 
  • Mehrtens, John (1987). Living Snakes of the World in Color. New York: Sterling. ISBN 0-8069-6461-8. 
  • Rosenfeld, Arthur (1989). Exotic Pets. New York: Simon & Schuster. p. 293. ISBN 0-671-47654-8. 
This article is issued from Wikipedia - version of the 11/24/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.