Squamata

This article is about the Squamata order of reptiles. For the Roman scale armour, see Lorica squamata.
Scaled reptiles
Temporal range:
Early Jurassic - Present, 199–0 Ma[1]
Eastern blue-tongued lizard
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Superorder: Lepidosauria
Order: Squamata
Oppel, 1811
Subgroups[2]
black: Range of Squamata

The order Squamata, or the scaled reptiles, are the largest recent order of reptiles, comprising all lizards and snakes. With over 9,000 species, it is also the second-largest order of vertebrates, after the perciform fish. 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 tuataras, which strongly resemble lizards.

Evolution

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,[3] meaning that the lineage leading to squamates must have existed as well. Modern squamates probably originated in the mid Jurassic,[3] when fossil relatives of geckos and skinks and snakes[4] 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.[5] At the end of the Cretaceous, squamates suffered a major extinction at the K-T boundary [6] 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;[5] however, studies of the DNA suggest that the geckos represent the most ancient branch.[7] 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.

Reproduction

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.[8] 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.[9]

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.[10] 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.[11]

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.[12] The fossil record shows the divergence between anguimorphs, iguanians, and advanced snakes dates back roughly 200 Mya to the Late Triassic/Early Jurassic.[12] 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.[13] Previous literature hypothesized that venoms were modifications of salivary or pancreatic proteins,[14] but different toxins have been found to have been recruited from numerous different protein bodies and are as diverse as their functions.[15]

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,[16] which leads to a diversification of toxins that allows the ambush predators the ability to attack a wide range of prey.[17] 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.[18]

Humans and squamates

Bites and fatalities

See also: Snakebite
Map showing the global distribution of snakebite morbidity

An estimated 125,000 people a year die from venomous snake bites.[19] In the US alone, more than 8,000 venomous snake bites are reported each year.[20]

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.[21]

Conservation

Though they survived the most drastic changes in Earth's history, 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 many other unnecessary reasons. Because of this, some are in fact 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. Many zoos, private hobbyists and breeders educate people about the importance of snakes and lizards.

Classification

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,[22] 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] found the following relationships:

Squamata


Dibamidae



Gekkota



unnamed

Scincomorpha


unnamed

Lacertoidea (incl. Amphisbaenia)


Toxicofera

Ophidia (Serpentes)




Anguimorpha



Iguania







All recent molecular studies [23] 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.).[23]

List of extant families

Amphisbaenia
FamilyCommon namesExample speciesExample photo
Amphisbaenidae
Gray, 1865
Tropical worm lizardsDarwin's worm lizard (Amphisbaena darwinii) -
Bipedidae
Taylor, 1951
Bipes worm lizardsMexican mole lizard (Bipes biporus)
BlanidaeMediterranean worm lizardsMediterranean worm lizard (Blanus cinereus) -
Cadeidae
Vidal & Hedges, 2008[24]
Cuban worm lizardsCadea blanoides -
Rhineuridae
Vanzolini, 1951
North American worm lizardsNorth American worm lizard (Rhineura floridana)
Trogonophidae
Gray, 1865
Palearctic worm lizardsCheckerboard worm lizard (Trogonophis wiegmanni) -
Gekkota (incl. Dibamia)
FamilyCommon namesExample speciesExample photo
Dibamidae
Boulenger, 1884
Blind lizardsDibamus nicobaricum -
Gekkonidae
Gray, 1825 (paraphyletic)
GeckosThick-tailed gecko (Underwoodisaurus milii)
Pygopodidae
Boulenger, 1884
Legless lizardsBurton's snake lizard (Lialis burtonis)
Iguania
FamilyCommon namesExample speciesExample photo
Agamidae
Spix, 1825
Agamas Eastern bearded dragon (Pogona barbata)
Chamaeleonidae
Gray, 1825
ChameleonsVeiled chameleon (Chamaeleo calyptratus)
Corytophanidae
Frost & Etheridge, 1989
Casquehead lizardsPlumed basilisk (Basiliscus plumifrons)
Crotaphytidae
Frost & Etheridge, 1989
Collared and leopard lizardsCommon collared lizard (Crotaphytus collaris)
Hoplocercidae
Frost & Etheridge, 1989
Wood lizards or clubtailsClub-tail iguana (Hoplocercus spinosus) -
IguanidaeIguanasMarine iguana (Amblyrhynchus cristatus)
Leiosauridae
Frost et al., 2001
- Darwin's iguana (Diplolaemus darwinii) -
Liolaemidae
Frost & Etheridge, 1989
Swifts Shining tree iguana (Liolaemus nitidus)
Opluridae
Frost & Etheridge, 1989
Madagascan iguanas Chalarodon (Chalarodon madagascariensis) -
Phrynosomatidae
Frost & Etheridge, 1989
Earless, spiny, tree, side-blotched and horned lizardsGreater earless lizard (Cophosaurus texanus)
Polychrotidae
Frost & Etheridge, 1989 (+ Dactyloidae)
AnolesCarolina anole (Anolis carolinensis)
Tropiduridae
Frost & Etheridge, 1989
Neotropical ground lizards(Microlophus peruvianus)
Lacertoidea (excl. Amphisbaenia)
FamilyCommon NamesExample SpeciesExample Photo
GymnophthalmidaeSpectacled lizards Bachia bicolor
Lacertidae
Oppel, 1811
Wall or true lizardsOcellated lizard (Lacerta lepida)
TeiidaeTegus or whiptailsGold tegu (Tupinambis teguixin)
Neoanguimorpha
FamilyCommon namesExample speciesExample photo
Anguidae
Oppel, 1811
Glass lizards, alligator lizards and slow wormsSlow worm (Anguis fragilis)
Anniellidae
Gray, 1852
American legless lizardsCalifornia legless lizard (Anniella pulchra)
HelodermatidaeGila monstersGila monster (Heloderma suspectum)
Xenosauridae
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)
Scincoidea
FamilyCommon NamesExample SpeciesExample Photo
CordylidaeSpinytail lizards Girdle-tailed lizard (Cordylus warreni)
GerrhosauridaePlated lizardsSudan plated lizard (Gerrhosaurus major)
Scincidae
Oppel, 1811
SkinksWestern blue-tongued skink (Tiliqua occipitalis)
XantusiidaeNight lizardsGranite night lizard (Xantusia henshawi)
Alethinophidia
FamilyCommon namesExample speciesExample photo
Acrochordidae
Bonaparte, 1831[25]
File snakesMarine file snake (Acrochordus granulatus)
Aniliidae
Stejneger, 1907[26]
Coral pipe snakesBurrowing false coral (Anilius scytale)
Anomochilidae
Cundall, Wallach and Rossman, 1993.[27]
Dwarf pipe snakesLeonard's pipe snake, (Anomochilus leonardi)
Boidae
Gray, 1825[25] (incl. Calabariidae)
BoasAmazon tree boa (Corallus hortulanus)
Bolyeriidae
Hoffstetter, 1946
Round Island boasRound Island burrowing boa (Bolyeria multocarinata)
Colubridae
Oppel, 1811[25] sensu lato (incl. Dipsadidae, Natricidae, Pseudoxenodontidae)
ColubridsGrass snake (Natrix natrix)
Cylindrophiidae
Fitzinger, 1843
Asian pipe snakesRed-tailed pipe snake (Cylindrophis ruffus)
Elapidae
Boie, 1827[25]
Cobras, coral snakes, mambas, kraits, sea snakes, sea kraits, Australian elapidsKing cobra (Ophiophagus hannah)
Homalopsidae
Bonaparte, 1845
-
Lamprophiidae
Fitzinger, 1843[28]
Bibron's burrowing asp (Atractaspis bibroni)
Loxocemidae
Cope, 1861
Mexican burrowing snakesMexican burrowing snake (Loxocemus bicolor)
Pareatidae
Romer, 1956
-
Pythonidae
Fitzinger, 1826
PythonsBall python (Python regius)
Tropidophiidae
Brongersma, 1951
Dwarf boasNorthern eyelash boa (Trachyboa boulengeri)
Uropeltidae
Müller, 1832
Shield-tailed snakes, short-tailed snakesCuvier's shieldtail (Uropeltis ceylanica)
Viperidae
Oppel, 1811[25]
Vipers, pitvipers, rattlesnakesEuropean asp (Vipera aspis)
Xenodermatidae
Fitzinger, 1826
-
Xenopeltidae
Gray, 1849
Sunbeam snakesSunbeam snake (Xenopeltis unicolor)
Scolecophidia (incl. Anomalepidae)
FamilyCommon namesExample speciesExample photo
Anomalepidae
Taylor, 1939[25]
Dawn blind snakesDawn blind snake (Liotyphlops beui)
Gerrhopilidae
Vidal et al., 2010[24]
-
Leptotyphlopidae
Stejneger, 1892[25]
Slender blind snakesTexas blind snake (Leptotyphlops dulcis)
Typhlopidae
Merrem, 1820[29]
Blind snakesEuropean blind snake (Typhlops vermicularis)
Xenotyphlopidae
Vidal et al., 2010[24]
Xenotyphlops grandidieri -

References

  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 3391445. 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. 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 4016551. PMID 24063680.
  4. 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
  5. 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.
  6. 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 3535637. PMID 23236177.
  7. 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 3682911. PMID 23627680.
  8. "Iguana Anatomy".
  9. Morales, Alex (2006-12-20). "Komodo Dragons, World's Largest Lizards, Have Virgin Births". Bloomberg Television. Retrieved 2008-03-28.
  10. 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.
  11. 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.
  12. 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.
  13. 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.
  14. 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.
  15. 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.
  16. 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.
  17. 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.
  18. 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 2690460. PMID 19364745.
  19. "Snake-bites: appraisal of the global situation" (PDF). Who.com. Retrieved 2007-12-30.
  20. "First Aid Snake Bites". University of Maryland Medical Center. Retrieved 2007-12-30.
  21. "Komodo dragon kills boy, 8, in Indonesia". msnbc. Retrieved 2007-12-30.
  22. 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.
  23. 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.
  24. 1 2 3
  25. 1 2 3 4 5 6 7 Cogger(1991), p.23
  26. "Aniliidae". Integrated Taxonomic Information System. Retrieved 12 December 2007.
  27. "Anomochilidae". Integrated Taxonomic Information System. Retrieved 13 December 2007.
  28. "Atractaspididae". Integrated Taxonomic Information System. Retrieved 13 December 2007.
  29. "Typhlopidae". Integrated Taxonomic Information System. Retrieved 13 December 2007.
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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, Australia: 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. 

External links

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