|Florida box turtle (Terrapene carolina)|
Batsch 1788 
|14 living families with 356 species|
|Blue: sea turtles, black: land turtles|
The order Testudines includes both living and extinct species. The earliest fossil turtles date from about 220 million years ago. So turtles are one of the oldest surviving reptile groups and a more ancient group than lizards, snakes and crocodiles.
Turtle, tortoise, or terrapin[change | change source]
Although the word turtle is widely used to describe all members of the order Testudines, it is also common to see certain members described as terrapins, tortoises or sea turtles, as well. How these names are used, if at all, depends on the type of English.
- British English describes these reptiles as turtles if they live in the sea; terrapins if they live in fresh or brackish water; or tortoises if they live on land.
- American English tends to use the word turtle as a general term for all species. "Tortoise" is used for most land-dwelling species, and oceanic species are usually referred to as sea turtles. The name "terrapin" is typically reserved only for the brackish water diamondback terrapin, Malaclemys terrapin.
- Australian English uses turtle for both the marine and freshwater species, but tortoise for the terrestrial species.
To avoid confusion, the word "chelonian" is popular among some who work with these animals, as a catch-all name. Unfortunately, Chelonia is also the name of a particular genus of turtles, so this conflicts with its use for the entire order Testudines.
Ecology and life history[change | change source]
Although many turtles spend much of their lives underwater, all turtles and tortoises breathe air, and must surface at regular intervals to refill their lungs. Some spend their whole lives on dry land.
Aquatic respiration in Australian freshwater turtles is being studied. Some species have large cloacal cavities that are lined with many finger-like projections. These projections, called papillae, have a rich blood supply, and increase the surface area. The turtles can take up dissolved oxygen from the water using these papillae, in much the same way that fish use gills to respire.
Like other reptiles, turtles lay eggs which are slightly soft and leathery. The eggs of the largest species are spherical, while the eggs of the rest are elongated. Sea turtles lay their eggs on dry, sandy beaches. Turtles can take many years to reach breeding age, and in many cases breed every few years rather than annually.
In some species, there is temperature-dependent sex determination. Temperature determines whether an egg develops into a male or a female: a higher temperature causes a female, a lower temperature causes a male. Large numbers of eggs are deposited in holes dug into mud or sand. They are then covered and left to incubate by themselves. When the turtles hatch, they squirm their way to the surface and head toward the water. No turtle mother cares for its young.
Long-lived[change | change source]
Researchers have recently discovered a turtle’s organs do not gradually break down or become less efficient over time, unlike most other animals. It was found that the liver, lungs, and kidneys of a centenarian turtle are almost identical with that of its young counterpart. This has inspired genetic researchers to begin examining the turtle genome for longevity genes.
Anatomy[change | change source]
Neck folding[change | change source]
Turtles are divided into two groups, according to how they evolved a solution to the problem of withdrawing their necks into their shells. The Cryptodira (hidden neck) can draw their necks in while contracting it under their spine. The Pleurodira (side neck), now found only in fresh water environments in the Southern hemisphere, contract their necks to the side. So, the important adaptation of head withdrawing evolved twice from ancestral turtles which did not have this ability.
Feeding[change | change source]
Turtles have a hard beak. Turtles use their jaws to cut and chew food. Instead of teeth, the upper and lower jaws of the turtle are covered by horny ridges. Carnivorous turtles usually have knife-sharp ridges for slicing through their prey. Herbivorous turtles have serrated-edged ridges that help them cut through tough plants. Turtles use their tongues to swallow food, but they cannot, unlike most reptiles, stick out their tongues to catch food.
Shell[change | change source]
The upper shell of the turtle is called the carapace. The lower shell that encases the belly is called the plastron. The carapace and plastron are joined together on the turtle's sides by bony structures called bridges.
The inner layer of a turtle's shell is made up of about 60 bones. It includes parts of the backbone and the ribs, meaning the turtle cannot crawl out of its shell. In most turtles, the outer layer of the shell is covered by horny scales called scutes that are part of its outer skin, or epidermis. Scutes are made up of a fibrous protein called keratin that also makes up the scales of other reptiles. These scutes overlap the seams between the shell bones and add strength to the shell. Some turtles do not have horny scutes. For example, the leatherback sea turtle and the soft-shelled turtles have shells covered with leathery skin instead.
Largest living[change | change source]
The largest chelonian is a marine turtle, the great leatherback sea turtle, which reaches a shell length of 200 cm (80 inches) and can reach a weight of over 900 kg (2,000 lb, or 1 short ton). Freshwater turtles are generally smaller, but with the largest species, the Asian softshell turtle Pelochelys cantorii, a few individuals have been reported to measure up to 200 cm or 80 in (Das, 1991). This dwarfs even the better-known alligator snapping turtle, the largest chelonian in North America, which attains a shell length of up to 80 cm (31½ in) and a weight of about 60 kg (170 lb).
The lagest fossil turtle, Archelon, was more than twice the length of the leatherback, at up to 4.5 metres.
Evolution[change | change source]
The first fossil proto-turtles come from Upper Triassic of the Mesozoic era, about 220 million years ago. Their shell evolved from bony extensions of their backbones and broad ribs that expanded and grew together to form a complete shell. It offered protection at every stage of its evolution, even when the bony component of the shell was not complete. This proved a long-lasting adaptation, and the group as a whole has survived many changes in the seas, and several extinction events.
Fossils of the freshwater Odontochelys semitestacea or "half-shelled turtle with teeth", from the later Triassic, have been found in southwest China. Odontochelys displays a complete bony plastron and an incomplete carapace, similar to an early stage of turtle embryonic development. By the Upper Jurassic, turtles had radiated widely, and their fossil history becomes easier to read.
Their exact ancestry has been a puzzle. Early amniotes had no openings in the skull behind the eyes. Openings developed in both Sauropsid and Synapsid skulls. They made the skull lighter, gave attachment points for muscles, and gave room for muscle bulges. But turtles do not have these skull openings. They were called 'anapsids', meaning 'no openings'.
Eventually it was suggested that turtles evolved from sauropsids which had skull openings, but turtles lost them as part of their evolution towards heavy defensive armour. All molecular studies have strongly upheld the placement of turtles within diapsids; some place turtles within Archosauria, or as a sister group to extant archosaurs.
The earliest known fully shelled turtles are the late Triassic Odontochelys, Chinlechelys and Proganochelys. The first-named genus was aquatic, but the second was probably terrestrial. They already had many advanced turtle traits, and thus probably had many millions of years of preceding turtle evolution and species in their ancestry. They did lack the ability to pull their heads into their shell (and they had a long neck), and (Odontochelys) had a long, spiked tail ending in a club, a body form similar to that of ankylosaurs, resulting from convergent evolution.
Turtles are divided into two living suborders, the Cryptodira and the Pleurodira. The Cryptodira is the larger of the two groups and includes all the marine turtles, the terrestrial tortoises, and many of the freshwater turtles. The Pleurodira are sometimes known as the side-necked turtles, a reference to the way they withdraw their heads into their shells. This smaller group mostly consists of freshwater turtles.
Related pages[change | change source]
References[change | change source]
- Li, Chun; Xiao-Chun Wu; Olivier Rieppel; Li-Ting Wang; Li-Jun Zhao (November 27, 2008). "An ancestral turtle from the Late Triassic of southwestern China". Nature 456 (7221): 497–501. doi:10.1038/nature07533. PMID 19037315.
- Turtle Taxonomy Working Group (2017). Turtles of the World: Annotated Checklist and Atlas of Taxonomy, Synonymy, Distribution, and Conservation Status (8th Ed.) (PDF). Chelonian Research Monographs. 7. pp. 1–292. doi:10.3854/crm.7.checklist.atlas.v8.2017. ISBN 9781532350269.
- Bonin F; Devaux B. & Dupré A. 2006. Turtles of the world, transl. P.C.H. Pritchard. Johns Hopkins University Press, Baltimore.
- "Archelon-Enchanted Learning Software". Enchantedlearning.com. Retrieved 2009-03-14.
- James E. Barzyk Turtles in crisis: the Asian food markets. The article itself is not dated, but mostly refers to data in the range 1995–2000.
- The word 'terrapin' is derived from the Algonquian word for this animal. "San Diego Zoo's animal bytes: turtle & tortoise". Retrieved September 12, 2011.
- 'Chelonia' is based on the Ancient Greek word χελώνη, chelōnē; Modern Greek χελώνα, chelōna; meaning turtle/tortoise
- All but ageless: turtles face their biggest threat: humans
- Li C. et al 2008. An ancestral turtle from the late Triassic of southwestern China. Nature 456 (7221): 497–501. doi:10.1038/nature07533. PMID 19037315.
- Rieppel O. & DeBraga M. 1996. Turtles as diapsid reptiles. Nature 384 (6608): 453–5. doi:10.1038/384453a0.
- Mannena, Hideyuki & Li, Steven S. 1999. Molecular evidence for a clade of turtles. Molecular Phylogenetics and Evolution 13 (1): 144–148. doi:10.1006/mpev.1999.0640. PMID 10508547.
- Zardoya R. & Meyer A. 1998. Complete mitochondrial genome suggests diapsid affinities of turtles. Proc Natl Acad Sci USA 95 (24): 14226–14231. doi:10.1073/pnas.95.24.14226. PMC 24355. PMID 9826682.
- Iwabe N. et al 2004. Sister group relationship of turtles to the bird-crocodilian clade revealed by nuclear DNA-coded proteins. Molecular Biology and Evolution 22 (4): 810–813. doi:10.1093/molbev/msi075. PMID 15625185. http://mbe.oxfordjournals.org/content/22/4/810.long. Retrieved 2010-12-31.
- Roos, Jonas; Aggarwal, Ramesh K. & Janke, Axel 2007 Extended mitogenomic phylogenetic analyses yield new insight into crocodylian evolution and their survival of the Cretaceous–Tertiary boundary. Molecular Phylogenetics and Evolution 45 (2): 663–673. doi:10.1016/j.ympev.2007.06.018. PMID 17719245.
- Katsu Y. et al 2010. From reptilian phylogenomics to reptilian genomes: analyses of c-Jun and DJ-1 proto-oncogenes. Cytogenetic and Genome Research 127 (2–4): 79–93. doi:10.1159/000297715. PMID 20234127.
- Benton M J., Michael J. (2000). Vertebrate Paleontology (2nd ed.). London: Blackwell Science. ISBN 978-0-632-05614-9., 3rd ed. 2004 ISBN 978-0-632-05637-8
- Joyce W.G. et al. 2009. A thin-shelled reptile from the Late Triassic of North America and the origin of the turtle shell. Proc Biol Sci. 276(1656):507-13. PubMed A thin-shelled reptile from the Late Triassic of North America and the origin of the turtle shell. - PubMed - NCBI
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