|Turtles from different families; clockwise from top-left: Red-bellied short-necked turtle, Indian flapshell turtle, Hawksbill sea turtle, and Galápagos tortoise|
|14 living families|
|Blue: sea turtles, black: land turtles|
Turtles are an order of reptiles known as Testudines, characterized by a special shell developed mainly from their ribs. Modern turtles are divided into two major groups, the Pleurodira (side necked turtles) and Cryptodira (hidden necked turtles), which differ in the way the head retracts. There are 360 living and recently extinct species of turtles, including land-dwelling tortoises and freshwater terrapins. They are found on most continents, some islands and, in the case of sea turtles, much of the ocean. Like other amniotes (reptiles, birds, and mammals) they breathe air and do not lay eggs underwater, although many species live in or around water.
Turtle shells are made mostly of bone; the upper part is the domed carapace, while the underside is the flatter plastron or belly-plate. Its outer surface is covered in scales made of keratin, the material of hair, horns, and claws. The carapace bones develop from ribs that grow sideways and develop into broad flat plates that join up to cover the body. Turtles are ectotherms or "cold-blooded", meaning that their internal temperature varies with their direct environment. They are generally opportunistic omnivores and mainly feed on plants and animals with limited movements. Many turtles migrate short distances seasonally. Sea turtles are the only reptiles that migrate long distances to lay their eggs on a favored beach.
Turtles have appeared in myths and folktales around the world. Some terrestrial and freshwater species are widely kept as pets. Turtles have been hunted for their meat, for use in traditional medicine, and for their shells. Sea turtles are often killed accidentally as bycatch in fishing nets. Turtle habitats around the world are being destroyed. As a result of these pressures, many species are extinct or threatened with extinction.
Naming and etymology
The word turtle is derived from the French tortue or tortre ('turtle, tortoise'). It is a common name and may be used without knowledge of taxonomic distinctions. In North America, it may denote the order as a whole. In Britain, the name is used for sea turtles as opposed to freshwater terrapins and land-dwelling tortoises. In Australia, which lacks true tortoises (family Testudinidae), non-marine turtles were traditionally called tortoises, but more recently turtle has been used for the entire group.
The name of the order, Testudines (// teh-STEW-din-eez), is based on the Latin word for tortoise, testudo; and was coined by German naturalist August Batsch in 1788. The order has also been historically known as Chelonii (Latreille 1800) and Chelonia (Ross and Macartney 1802), which are based on the Ancient Greek word for tortoise: χελώνη (chelone). Testudines is the official order name due to the principle of priority. The term chelonian is used as a formal name for members of the group.
Anatomy and physiology
The largest living species of turtle (and fourth-largest reptile) is the leatherback turtle, which can reach over 2.7 m (8 ft 10 in) in length and weigh over 500 kg (1,100 lb). The largest known turtle was Archelon ischyros, a Late Cretaceous sea turtle up to 4.5 m (15 ft) long, 5.25 m (17 ft) wide between the tips of the front flippers, and estimated to have weighed over 2,200 kg (4,900 lb). The smallest living turtle is Chersobius signatus of South Africa, measuring no more than 10 cm (3.9 in) in length and weighing 172 g (6.1 oz).
The shell of a turtle is unique among vertebrates and serves to protect the animal and provide shelter from the elements. It is primarily made of 50–60 bones and consists of two parts: the domed, dorsal (back) carapace and the flatter, ventral (belly) plastron. They are connected by lateral (side) extensions of the plastron.
The carapace is fused with the vertebrae and ribs while the plastron is formed from bones of the shoulder girdle, sternum, and gastralia (abdominal ribs). During development, the ribs grow sideways into a carapacial ridge, unique to turtles, entering the dermis (inner skin) of the back to support the carapace. The development is signaled locally by proteins known as fibroblast growth factors that include FGF10. The shoulder girdle in turtles is made up of two bones, the scapula and the coracoid. Both the shoulder and pelvic girdles of turtles are located within the shell and hence are effectively within the rib cage. The trunk ribs grow over the shoulder girdle during development.
The shell is covered in epidermal (outer skin) scales known as scutes that are made of keratin, the same substance that makes up hair and fingernails. Typically, a turtle has 38 scutes on the carapace and 16 on the plastron, giving them 54 in total. Carapace scutes are divided into "marginals" around the margin and "vertebrals" over the vertebral column, though the scute that overlays the neck is called the "cervical". "Pleurals" are present between the marginals and vertebrals. Plastron scutes include gulars (throat), humerals, pectorals, abdominals, and anals. Side-necked turtles additionally have "intergular" scutes between the gulars. Turtle scutes are usually structured like mosaic tiles, but some species, like the hawksbill sea turtle, have overlapping scutes on the carapace.
The shapes of turtle shells vary with the adaptations of the individual species, and sometimes with sex. Land-dwelling turtles are more dome-shaped, which appears to make them more resistant to being crushed by large animals. Aquatic turtles have flatter, smoother shells that allow them to cut through the water. Sea turtles in particular have streamlined shells that reduce drag and increase stability in the open ocean. Some turtle species have pointy or spiked shells that provide extra protection from predators and camouflage against the leafy ground. The lumps of a tortoise shell can tilt its body when it gets flipped over, allowing it to flip back. In male tortoises, the tip of the plastron is thickened and used for butting and ramming during combat.
Shells vary in flexibility. Some species, such as box turtles, lack the lateral extensions and instead have the carapace bones fully fused or ankylosed together. Several species have hinges on their shells, usually on the plastron, which allow them to expand and contract. Softshell turtles have rubbery edges, due to the loss of bones. The leatherback turtle has hardly any bones in its shell, but has thick connective tissue and an outer layer of leathery skin.
Head and neck
The turtle's skull is unique among living amniotes (which includes reptiles, birds and mammals), it is solid and rigid with no openings for muscle attachment (temporal fenestrae). Muscles instead attach to recesses in the back of the skull. Turtle skulls vary in shape, from the long and narrow skulls of softshells to the broad and flattened skull of the mata mata. Some turtle species have developed large and thick heads, allowing for greater muscle mass and stronger bites.
Turtles that are carnivorous or durophagous (eating hard-shelled animals) have the most powerful bites. For example, the durophagous Mesoclemmys nasuta has a bite force of 432 lbf (1,920 N). Species that are insectivorous, piscivorous (fish-eating), or omnivorous have lower bite forces. Living turtles lack teeth but have beaks made of keratin sheaths along the edges of the jaws. These sheaths may have sharp edges for cutting meat, serrations for clipping plants, or broad plates for breaking mollusks.
The necks of turtles are highly flexible, possibly to compensate for their rigid shells. Some species, like sea turtles, have short necks while others, such as snake-necked turtles, have long ones. Despite this, all turtle species have eight neck vertebrae, a consistency not found in other reptiles but similar to mammals. Some snake-necked turtles have both long necks and large heads, limiting their ability to lift them when not in water. Some turtles have folded structures in the larynx or glottis that vibrate to produce sound. Other species have elastin-rich vocal cords.
Limbs and locomotion
Due to their heavy shells, turtles are slow-moving on land. A desert tortoise moves at only 0.22–0.48 km/h (0.14–0.30 mph). By contrast, sea turtles can swim at 30 km/h (19 mph). The limbs of turtles are adapted for various means of locomotion and habits and most have five toes. Tortoises are specialized for terrestrial environments and have column-like legs with elephant-like feet and short toes. The gopher tortoise has flattened front limbs for digging in the substrate. Freshwater turtles have more flexible legs and longer toes with webbing, giving them thrust in the water. Some of these species, such as snapping turtles and mud turtles, mainly walk along the water bottom, as they would on land. Others, such as terrapins, swim by paddling with all four limbs, switching between the opposing front and hind limbs, which keeps their direction stable.
Sea turtles and the pig-nosed turtle are the most specialized for swimming. Their front limbs have evolved into flippers while the shorter hind limbs are shaped more like rudders. The front limbs provide most of the thrust for swimming, while the hind limbs serve as stabilizers. Sea turtles such as the green sea turtle rotate the front limb flippers like a bird's wings to generate a propulsive force on both the upstroke and on the downstroke. This is in contrast to similar-sized freshwater turtles (measurements having been made on young animals in each case) such as the Caspian turtle, which uses the front limbs like the oars of a rowing boat, creating substantial negative thrust on the recovery stroke in each cycle. In addition, the streamlining of the marine turtles reduces drag. As a result, marine turtles produce a propulsive force twice as large, and swim six times as fast, as freshwater turtles. The swimming efficiency of young marine turtles is similar to that of fast-swimming fish of open water, like mackerel.
Compared to other reptiles, turtles tend to have reduced tails, but these vary in both length and thickness among species and between sexes. Snapping turtles and the big-headed turtle have longer tails; the latter uses it for balance while climbing. The cloaca is found underneath and at the base, and the tail itself houses the reproductive organs. Hence, males have longer tails to contain the penis. In sea turtles, the tail is longer and more prehensile in males, who use it to grasp mates. Several turtle species have spines on their tails.
Turtles make use of vision to find food and mates, avoid predators, and orient themselves. The retina's light-sensitive cells include both rods for vision in low light, and cones with three different photopigments for bright light, where they have full-color vision. There is possibly a fourth type of cone that detects ultraviolet, as hatchling sea turtles respond experimentally to ultraviolet light, but it is unknown if they can distinguish this from longer wavelengths. A freshwater turtle, the red-eared slider, has an exceptional seven types of cone cell.
Sea turtles orient themselves on land by night, using visual features detected in dim light. They can use their eyes in clear surface water, muddy coasts, the darkness of the deep ocean, and also above water. Unlike in terrestrial turtles, the cornea, the curved surface that lets light into the eye, does not help to focus light on the retina, so focusing underwater is handled entirely by the lens, behind the cornea. The cone cells contain oil droplets placed to shift perception toward the red part of the spectrum, improving color discrimination. Visual acuity, studied in hatchlings, is highest in a horizontal band with retinal cells packed about twice as densely as elsewhere. This gives the best vision along the visual horizon. Sea turtles do not appear to use polarized light for orientation as many other animals do. The deep-diving leatherback turtle lacks specific adaptations to low light, such as large eyes, large lenses, or a reflective tapetum. It may rely on seeing the bioluminescence of prey when hunting in deep water.
Turtles have no ear openings; the eardrum is covered with scales and encircled by a bony otic capsule, which is absent in other reptiles. Their hearing thresholds are high in comparison to other reptiles, reaching up to 500 Hz in air, but underwater they are more attuned to lower frequencies. The loggerhead sea turtle has been shown experimentally to respond to low sounds, with maximal sensitivity between 100 and 400 Hz.
Turtles have olfactory (smell) and vomeronasal receptors along the nasal cavity, the latter of which are used to detect chemical signals. Experiments on green sea turtles showed they could learn to respond to a selection of different odorant chemicals such as triethylamine and cinnamaldehyde, which were detected by olfaction in the nose. Such signals could be used in navigation.
The rigid shell of turtles is not capable of expanding and making room for the lungs, as in other amniotes, so they have had to evolve special adaptations for respiration. The lungs of turtles are attached directly to the carapace above while below, connective tissue attaches them to the organs. They have multiple lateral (side) and medial (middle) chambers (the numbers of which vary between species) and one terminal (end) chamber.
The lungs are ventilated using specific groups of abdominal muscles attached to the organs that pull and push on them. Specifically, it is the turtle's large liver that compresses the lungs. Underneath the lungs, in the coelomic cavity, the liver is connected to the right lung by the root, and the stomach is directly attached to the left lung, and to the liver by a mesentery. When the liver is pulled down, inhalation begins. Supporting the lungs is a wall or septum, which is thought to prevent them from collapsing. During exhalation, the contraction of the transversus abdominis muscle propels the organs into the lungs and expels air. Conversely, during inhalation, the relaxing and flattening of the oblique abdominis muscle pulls the transversus back down, allowing air back into the lungs.
Although many turtles spend large amounts of their lives underwater, all turtles breathe air and must surface at regular intervals to refill their lungs. Depending on the species, immersion periods vary between a minute and an hour. Some species can respire through the cloaca, which contains large sacs that are lined with many finger-like projections that take up dissolved oxygen from the water.
Turtles share the linked circulatory and pulmonary (lung) systems of vertebrates, where the three-chambered heart pumps deoxygenated blood through the lungs and then pumps the returned oxygenated blood through the body's tissues. The cardiopulmonary system has both structural and physiological adaptations that distinguish it from other vertebrates. Turtles have a large lung volume and can move blood through non-pulmonary blood vessels, including some within the heart, to avoid the lungs while they are not breathing. They can hold their breath for much longer periods than other reptiles and they can tolerate the resulting low oxygen levels. They can moderate the increase in acidity during anaerobic (non-oxygen-based) respiration by chemical buffering and they can lie dormant for months, in aestivation or brumation.
The heart has two atria but only one ventricle. The ventricle is subdivided into three chambers. A muscular ridge enables a complex pattern of blood flow so that the blood can be directed either to the lungs via the pulmonary artery, or to the body via the aorta. The ability to separate the two outflows varies between species. The leatherback has a powerful muscular ridge enabling almost complete separation of the outflows, supporting its actively swimming lifestyle. The ridge is less well developed in freshwater turtles like the sliders (Trachemys).
Turtles are capable of enduring periods of anaerobic respiration longer than many other vertebrates. This process breaks down sugars incompletely to lactic acid, rather than all the way to carbon dioxide and water as in aerobic (oxygen-based) respiration. They make use of the shell as a source of additional buffering agents for combating increased acidity, and as a sink for lactic acid.
In sea turtles, the bladder is one unit and in most freshwater turtles, it is double-lobed. Sea turtle bladders are connected to two small accessory bladders, located at the sides to the neck of the urinary bladder and above the pubis. Arid-living tortoises have bladders that serve as reserves of water, storing up to 20% of their body weight in fluids. The fluids are normally low in solutes, but higher during droughts when the reptile gains potassium salts from its plant diet. The bladder stores these salts until the tortoise finds fresh drinking water. To regulate the amount of salt in their bodies, sea turtles and the brackish-living diamondback terrapin secrete excess salt in a thick sticky substance from their tear glands. Because of this, sea turtles may appear to be "crying" when on land.
Turtles, like other reptiles, have a limited ability to regulate their body temperature. This ability varies between species, and with body size. Small pond turtles regulate their temperature by crawling out of the water and basking in the sun, while small terrestrial turtles move between sunny and shady places to adjust their temperature. Large species, both terrestrial and marine, have sufficient mass to give them substantial thermal inertia, meaning that they heat up or cool down over many hours. The Aldabra giant tortoise weighs up to some 60 kilograms (130 lb) and is able to allow its temperature to rise to some 33 °C (91 °F) on a hot day, and to fall naturally to around 29 °C (84 °F) by night. Some giant tortoises seek out shade to avoid overheating on sunny days. On Grand Terre Island, food is scarce inland, shade is scarce near the coast, and the tortoises compete for space under the few trees on hot days. Large males may push smaller females out of the shade, and some then overheat and die.
Adult sea turtles, too, have large enough bodies that they can to some extent control their temperature. The largest turtle, the leatherback, can swim in the waters off Nova Scotia, which may be as cold as 8 °C (46 °F), while their body temperature has been measured at up to 12 °C (54 °F) warmer than the surrounding water. To help keep their temperature up, they have a system of countercurrent heat exchange in the blood vessels between their body core and the skin of their flippers. The vessels supplying the head are insulated by fat around the neck.
Diet and feeding
Most turtle species are opportunistic omnivores; land-dwelling species are more herbivorous and aquatic ones more carnivorous. Generally lacking speed and agility, most turtles feed either on plant material or on animals with limited movements like mollusks, worms, and insect larvae. Some species, such as the African helmeted turtle and snapping turtles, eat fish, amphibians, reptiles (including other turtles), birds, and mammals. They may take them by ambush but also scavenge. The alligator snapping turtle has a worm-like appendage on its tongue that it uses to lure fish into its mouth. Tortoises are the most herbivorous group, consuming grasses, leaves, and fruits. Many turtle species, including tortoises, supplement their diet with eggshells, animal bones, hair, and droppings for extra nutrients.
Turtles generally eat their food in a straightforward way, though some species have special feeding techniques. The yellow-spotted river turtle and the painted turtle may filter feed by skimming the water surface with their mouth and throat open to collect particles of food. When the mouth closes, the throat constricts and water is pushed out through the nostrils and the gap in between the jaws. Some species employ a "gape-and-suck method" where the turtle opens its jaws and expands its throat widely, sucking the prey in.
The diet of an individual within a species may change with age, sex, and season, and may also differ between populations. In many species, juveniles are generally carnivorous but become more herbivorous as adults. With Barbour's map turtle, the larger female mainly eats mollusks while the male usually eats arthropods. Blanding's turtle may feed mainly on snails or crayfish depending on the population. The European pond turtle has been recorded as being mostly carnivorous much of the year but switching to water lilies during the summer. Some species have developed specialized diets such as the hawksbill, which eats sponges, the leatherback, which feeds on jellyfish, and the Mekong snail-eating turtle.
Communication and intelligence
While popularly thought of as mute, turtles make various sounds to communicate. Tortoises may bellow when courting and mating. Various species of both freshwater and sea turtles emit short, low-frequency calls from the time they are in the egg to when they are adults. These vocalizations may serve to create group cohesion when migrating. The oblong turtle has a particularly large vocal range; producing sounds described as clacks, clicks, squawks, hoots, various kinds of chirps, wails, hooos, grunts, growls, blow bursts, howls, and drum rolls.
Play behavior has been documented in some turtle species. In the laboratory, Florida red-bellied cooters can learn novel tasks and have demonstrated a long-term memory of at least 7.5 months. Similarly, giant tortoises can learn and remember tasks, and master lessons much faster when trained in groups. Tortoises appear to be able to retain operant conditioning nine years after their initial training. Studies have shown that turtles can navigate the environment using landmarks and a map-like system resulting in accurate direct routes towards a goal. Navigation in turtles have been correlated to high cognition function in the medial cortex region of the brain.
When sensing danger, a turtle may flee, freeze or withdraw into its shell. Freshwater turtles flee into the water, though the Sonora mud turtle may take refuge on land as the shallow temporary ponds they inhabit make them vulnerable. When startled, a softshell turtle may dive underwater and bury itself under the sea floor. If a predator persists, the turtle may bite or discharge from its cloaca. Several species produce foul-smelling chemicals from musk glands. Other tactics include threat displays and Bell's hinge-back tortoise can play dead. When attacked, big-headed turtle hatchlings squeal, possibly startling the predator.
Turtles are the only reptiles that migrate long distances, more specifically the marine species that can travel up to thousands of kilometers. Some non-marine turtles, such as the species of Geochelone (terrestrial), Chelydra (freshwater), and Malaclemys (estuarine), migrate seasonally over much shorter distances, up to around 27 km (17 mi), to lay eggs. Such short migrations are comparable to those of some lizards, snakes, and crocodilians. Sea turtles nest in a specific area, such as a beach, leaving the eggs to hatch unattended. The young turtles leave that area, migrating long distances in the years or decades in which they grow to maturity, and then return seemingly to the same area every few years to mate and lay eggs, though the precision varies between species and populations. This "natal homing" has appeared remarkable to biologists, though there is now plentiful evidence for it, including from genetics.
How sea turtles navigate to their breeding beaches remains unknown. One possibility is imprinting as in salmon, where the young learn the chemical signature, effectively the scent, of their home waters before leaving, and remember that when the time comes for them to return as adults. Another possible cue is the orientation of the earth's magnetic field at the natal beach. There is experimental evidence that turtles have an effective magnetic sense, and that they use this in navigation. Proof that homing occurs is derived from genetic analysis of populations of loggerheads, hawksbills, leatherbacks, and olive ridleys by nesting place. For each of these species, the populations in different places have their own mitochondrial DNA genetic signatures that persist over the years. This shows that the populations are distinct and that homing must be occurring reliably.
Reproduction and lifecycle
Turtles have a wide variety of mating behaviors but do not form pair-bonds or social groups. In green sea turtles, females generally outnumber males. In terrestrial species, males are often larger than females and fighting between males establishes a dominance hierarchy for access to mates. For most semi-aquatic and bottom-walking aquatic species, combat occurs less often. Males of these species instead may use their size advantage to mate forcibly. In fully aquatic species, males are often smaller than females and rely on courtship displays to gain mating access to females.
Courtship and mounting
Courtship varies between species, and with habitat. It is often complex in aquatic species, both marine and freshwater, but simpler in the semi-aquatic mud turtles and snapping turtles. A male tortoise bobs his head, then subdues the female by biting and butting her before mounting. The male scorpion mud turtle approaches the female from the rear, and often resorts to aggressive methods such as biting the female's tail or hind limbs, followed by a mounting.
Female choice is important in some species, and female green sea turtles are not always receptive. As such, they have evolved behaviors to avoid the male's attempts at copulation, such as swimming away, confronting the male followed by biting or taking up a refusal position with her body vertical, her limbs widely outspread, and her plastron facing the male. If the water is too shallow for the refusal position, the females resort to beaching themselves, as the males do not follow them ashore.
All turtles fertilize internally; mounting and copulation can be difficult. In many species, males have a concave plastron that interlocks with the female's carapace. In species like the Russian tortoise, the male has a lighter shell and longer legs. The high, rounded shape of box turtles are particular obstacles for mounting. The male eastern box turtle leans backward and hooks onto the back of the female's plastron. Aquatic turtles mount in water, and female sea turtles support the mounting male while swimming and diving. During copulation, the male turtle aligns his tail with the female's so he can insert his penis into her cloaca. Some female turtles can store sperm from multiple males and their egg clutches can have multiple sires.
Eggs and hatchlings
Turtles, including sea turtles, lay their eggs on land, although some lay eggs close near water that rises and falls in level, submerging the eggs. While most species build nests and lay eggs where they forage, some travel miles. The common snapping turtle walks 5 km (3 mi) on land, while sea turtles travel even further; the leatherback swims some 12,000 km (7,500 mi) to its nesting beaches. Most turtles create a nest for their eggs. Females usually dig a flask-like chamber in the substrate. Other species lay their eggs in vegetation or crevices. Females choose nesting locations based on environmental factors such as temperature and humidity, which are important for developing embryos. Depending on the species, the number of eggs laid varies from one to over 100. Larger females can lay eggs that are greater in number or bigger in size. Compared to freshwater turtles, tortoises deposit fewer but larger eggs. Females can lay multiple clutches throughout a season, particularly in species that experience unpredictable monsoons.
Most mother turtles do no more in the way of parental care than covering their eggs and immediately leaving, though some species guard their nests for days or weeks. Eggs vary between rounded, oval, elongated, and between hard- and soft-shelled. Most species have their sex determined by temperature. In some species, higher temperatures produce females and lower ones produce males, while in others, milder temperatures produce males and both hot and cold extremes produce females. There is experimental evidence that the embryos of Mauremys reevesii can move around inside their eggs to select the best temperature for development, thus influencing their sexual destiny. In other species, sex is determined genetically. The length of incubation for turtle eggs varies from two to three months for temperate species, and four months to over a year for tropical species. Species that live in warm temperate climates can delay their development.
Hatching young turtles break out of the shell using an egg tooth, a sharp projection that exists temporarily on their upper beak. Hatchlings dig themselves out of the nest and find safety in vegetation or water. Some species stay in the nest for longer, be it for overwintering or to wait for the rain to loosen the soil for them to dig out. Young turtles are highly vulnerable to predators, both in the egg and as hatchlings. Mortality is high during this period but significantly decreases when they reach adulthood. Most species grow quickly during their early years and slow down when they are mature.
Turtles can live long lives. The oldest living turtle and land animal is said to be a Seychelles giant tortoise named Jonathan, who turned 187 in 2019. A Galápagos tortoise named Harriet was collected by Charles Darwin in 1835; it died in 2006, having lived for at least 176 years. Most wild turtles do not reach that age. Turtles keep growing new scutes under the previous scutes every year, allowing researchers to estimate how long they have lived. They also age slowly. The survival rate for adult turtles can reach 99% per year.
Systematics and evolution
Zoologists have sought to explain the evolutionary origin of the turtles, and in particular of their unique shells. In 1914, Jan Versluys proposed that bony plates in the dermis, called osteoderms, fused to the ribs beneath them, later called the "Polka Dot Ancestor" by Olivier Rieppel. The theory accounted for the evolution of fossil pareiasaurs from Bradysaurus to Anthodon, but not for how the ribs could have become attached to the bony dermal plates.
More recent discoveries have painted a different scenario for the evolution of the turtle's shell. The stem-turtles Eunotosaurus of the Middle Permian, Pappochelys of the Middle Triassic, and Eorhynchochelys of the Late Triassic lacked carapaces and plastrons but had shortened torsos, expanded ribs, and lengthened dorsal vertebrae. Also in the Late Triassic, Odontochelys had a partial shell consisting of a complete bony plastron and an incomplete carapace. The development of a shell reached completion with the Late Triassic Proganochelys, with its fully developed carapace and plastron. Adaptations that lead to the evolution of the shell may have originally been for digging and a fossorial lifestyle.
The oldest known members of the Pleurodira lineage are the Platychelyidae, from the Late Jurassic. The oldest known unambiguous cryptodire is Sinaspideretes, a close relative of softshell turtles, from the Late Jurassic of China. During the Late Cretaceous and Cenozoic, members of the pleurodire families Bothremydidae and Podocnemididae became widely distributed in the Northern Hemisphere due to their coastal habits. The oldest known soft-shelled turtles and sea turtles appeared during the Early Cretaceous. Tortoises originated in Asia during the Eocene. A late surviving group of stem-turtles, the Meiolaniidae, survived in Australasia into the Pleistocene and Holocene.
The turtles' exact ancestry has been disputed. It was believed they were the only surviving branch of the ancient evolutionary grade Anapsida, which includes groups such as procolophonids and pareiasaurs. All anapsid skulls lack a temporal opening while all other living amniotes have temporal openings. It was later suggested that the anapsid-like turtle skulls may be due to backward evolution rather than to anapsid descent. Fossil evidence has shown that early stem-turtles possessed small temporal openings.
Some early morphological phylogenetic studies have placed turtles closer to Lepidosauria (tuataras, lizards, and snakes) than to Archosauria (crocodilians and birds). By contrast, several molecular studies place turtles either within Archosauria, or, more commonly, as a sister group to extant archosaurs, though an analysis conducted by Tyler Lyson and colleagues (2012) recovered turtles as the sister group of lepidosaurs instead. Ylenia Chiari and colleagues (2012) analyzed 248 nuclear genes from 16 vertebrates and suggested that turtles share a more recent common ancestor with birds and crocodilians. The date of separation of turtles and birds and crocodilians was estimated to be during the Permian. Through genomic-scale phylogenetic study of ultra-conserved elements (UCEs) to clarify the placement of turtles within reptiles, Nicholas Crawford and colleagues (2012) similarly found that turtles are closer to birds and crocodilians.
Using the draft (unfinished) genome sequences of the green sea turtle and the Chinese softshell turtle, Zhuo Wang and colleagues (2013) concluded that turtles are likely a sister group of crocodilians and birds. The external phylogeny of the turtles is shown in the cladogram below.
Modern turtles and their extinct relatives with a complete shell are classified within the clade Testudinata. The most recent common ancestor of living turtles, corresponding to the split between Pleurodira (side-necked species) and Cryptodira (hidden necked species), is estimated to have occurred around during the Late Triassic. Robert Thompson and colleagues (2021) comment that living turtles have low diversity, relative to how long they existed. Diversity has been stable, according to their analysis, except for a single rapid increase around the Eocene-Oligocene boundary some 30 million years ago, and a large regional extinction at roughly the same time. They suggest that global climate change caused both events, as the cooling and drying caused the land to become arid and turtles to become extinct there, while new continental margins opened up by the climate change provided habitats for other species to evolve.
The cladogram, from Nicholas Crawford and colleagues 2015, shows the internal phylogeny of the Testudines down to the level of families. The analysis by Thompson and colleagues in 2021 supports the same structure down to the family level.
Differences between the two suborders
Turtles are divided into two living suborders: Cryptodira and Pleurodira. The two groups differ in the way the neck is retracted for protection. Pleurodirans retract their neck to the side and in front of the shoulder girdles, whereas cryptodirans retract their neck backward into their shell. These motions are enabled by the morphology and arrangement of neck vertebrae. Sea turtles (which belong to Cryptodira) have mostly lost the ability to retract their heads.
The adductor muscles in the lower jaw create a pulley-like system in both subgroups. However, the bones that the muscles articulate with differ. In Pleurodira, the pulley is formed with the pterygoid bones of the palate, but in Cryptodira the pulley is formed with the otic capsule. Both systems help to vertically redirect the adductor muscles and maintain a powerful bite.
A further difference between the suborders is the attachment of the pelvis. In Cryptodira, the pelvis is free, linked to the shell only by ligaments. In Pleurodira, the pelvis is sutured, joined with bony connections, to the carapace and to the plastron, creating a pair of large columns of bone at the back end of the turtle, linking the two parts of the shell.
Distribution and habitat
Turtles are widely distributed across the world's continents, oceans, and islands with terrestrial, fully aquatic, and semi-aquatic species. Sea turtles are mainly tropical and subtropical, but leatherbacks can be found in colder areas of the Atlantic and Pacific. Living Pleurodira all live in freshwater and are found only in the Southern Hemisphere. The Cryptodira include terrestrial, freshwater, and marine species, and these range more widely. The world regions richest in non-marine turtle species are the Amazon basin, the Gulf of Mexico drainages of the United States, and parts of South and Southeast Asia.
For turtles in colder climates, their distribution is limited by constraints on reproduction, which is reduced by long hibernations. North American species barely range above the southern Canadian border. Some turtles are found at high altitudes, for example, the species Terrapene ornata occurs up to 2,000 m (6,600 ft) in New Mexico. Conversely, the leatherback sea turtle can dive over 1,200 m (3,900 ft). Species of the genus Gopherus can tolerate both below freezing and over 40 °C (104 °F) in body temperature, though they are most active at 26–34 °C (79–93 °F).
Among vertebrate orders, turtles are second only to primates in the percentage of threatened species. 360 modern species have existed since 1500 AD. Of these, 51–56% are considered threatened and 60% considered threatened or extinct. Turtles face many threats, including habitat destruction, harvesting for consumption, the pet trade, light pollution, and climate change. Asian species have a particularly high extinction risk, primarily due to their long-term unsustainable exploitation for food and medicine, and about 83% of Asia's non-marine turtle species are considered threatened. As of 2021, turtle extinction is progressing much faster than during the Cretaceous-Tertiary extinction. At this rate, all turtles could be extinct in a few centuries.
Turtle hatcheries can be set up when protection against flooding, erosion, predation, or heavy poaching is required. Chinese markets have sought to satisfy an increasing demand for turtle meat with farmed turtles. In 2007 it was estimated that over a thousand turtle farms operated in China. All the same, wild turtles continue to be caught and sent to market in large numbers, resulting in what conservationists have called "the Asian turtle crisis". In the words of the biologist George Amato, the hunting of turtles "vacuumed up entire species from areas in Southeast Asia", even as biologists still did not know how many species lived in the region. In 2000, all the Asian box turtles were placed on the CITES list of endangered species.
Harvesting wild turtles is legal in some American states, and there has been a growing demand for American turtles in China. The Florida Fish and Wildlife Conservation Commission estimated in 2008 that around 3,000 pounds of softshell turtles were exported weekly via Tampa International Airport. However, the great majority of turtles exported from the US between 2002 and 2005 were farmed.
Large numbers of sea turtles are accidentally killed in longlines, gillnets, and trawling nets as bycatch. A 2010 study suggested that over 8 million had been killed between 1990 and 2008; the Eastern Pacific and the Mediterranean were identified as among the areas worst affected. Since the 1980s, the United States has required all shrimp trawlers to fit their nets with turtle excluder devices that prevent turtles from being entangled in the net and drowning. More locally, other human activities are affecting marine turtles. In Australia, Queensland's shark culling program, which uses shark nets and drum lines, has killed over 5,000 turtles as bycatch between 1962 and 2015; including 719 loggerhead turtles and 33 hawksbill sea turtles, which are listed as critically endangered.
Native turtle populations can also be threatened by invasive ones. The central North American red-eared slider turtle has been listed among the "world's worst invasive species", pet turtle having been released globally. They appear to compete with native turtle species in eastern and western North America, Europe, and Japan.
World resting on four elephants on the back of the World Turtle. Western depiction of "The Hindu Earth", 1877
Terrapin shell leg rattles worn by lead Cherokee woman dancer, 20th century
Turtles have featured in human cultures across the world since ancient times. They are generally viewed positively despite not being "cuddly" or flashy; their association with the ancient times and old age have contributed to their endearing image.
In Hindu mythology, the World Turtle, named Kurma or Kacchapa, supports four elephants on his back; they, in turn, carry the weight of the whole world on their backs. The turtle is one of the ten avatars or incarnations of the god Vishnu. The yoga pose Kurmasana is named for the avatar. World Turtles are found in Native American cultures including the Algonquian, Iroquois, and Lenape. They tell many versions of the creation story of Turtle Island. One version has Muskrat pile up earth on Turtle's back, creating the continent of North America. An Iroquois version has the pregnant Sky Woman fall through a hole in the sky between a tree's roots, where she is caught by birds who land her safely on Turtle's back; the Earth grows around her. The turtle here is altruistic, but the world is a heavy burden, and the turtle sometimes shakes itself to relieve the load, causing earthquakes.
A turtle was the symbol of the Ancient Mesopotamian god Enki from the 3rd millennium BCE onward. An ancient Greek origin myth told that only the tortoise refused the invitation of the gods Zeus and Hera to their wedding, as it preferred to stay at home. Zeus then ordered it to carry its house with it, ever after. Another of their gods, Hermes, invented a seven-stringed lyre made with the shell of a tortoise. In the Shang dynasty Chinese practice of plastromancy, dating back to 1200 BCE, oracles were obtained by inscribing questions on turtle plastrons using the oldest known form of Chinese characters, burning the plastron, and interpreting the resulting cracks. Later, the turtle was one of the four sacred animals in Confucianism, while in the Han period, steles were mounted on top of stone turtles, later linked with Bixi, the turtle-shelled son of the Dragon King. Marine turtles feature significantly in Australian Aboriginal art. The army of Ancient Rome used the testudo ("tortoise") formation where soldiers would form a shield wall for protection.
In Aesop's Fables, "The Tortoise and the Hare" tells how an unequal race may be won by the slower partner. Lewis Carroll's 1865 Alice's Adventures in Wonderland features a Mock Turtle, named for a soup meant to imitate the expensive soup made from real turtle meat. In 1896, the French playwright Léon Gandillot wrote a comedy in three acts named La Tortue that was "a Parisian sensation" in its run in France, and came to the Manhattan Theatre, Broadway, New York, in 1898 as The Turtle. A "cosmic turtle" and the island motif reappear in Gary Snyder's 1974 novel Turtle Island, and again in Terry Pratchett's Discworld series as Great A'Tuin, starting with the 1983 novel The Colour of Magic. It is supposedly of the species Chelys galactica, the galactic turtle, complete with four elephants on its back to support Discworld. Turtles have been featured in comic books and animations such as the 1984 Teenage Mutant Ninja Turtles.
Some turtles, particularly small terrestrial and freshwater species, are kept as pets. The demand for pet turtles increased in the 1950s, with the US being the main supplier, particularly of farm-bred red-eared sliders. The popularity for exotic pets has led to an increase in illegal wildlife trafficking. Around 21% of the value of live animal trade is in reptiles, and turtles are among the more popularly traded species. Poor husbandry of tortoises can cause chronic rhinitis (nasal swelling), overgrown beaks, hyperparathyroidism (which softens their skeleton), constipation, various reproductive problems, and injuries from dogs. In the early 20th century, people in the United States have organized and gambled on turtle races.
As food and other uses
The flesh of captured wild turtles continues to be eaten in Asian cultures, while turtle soup was once a popular dish in English cuisine. Gopher tortoise stew has been popular with some groups in Florida. The supposed aphrodisiac or medicinal properties of turtle eggs created a large trade for them in Southeast Asia. Hard-shell turtle plastrons and soft-shell carapaces are widely used in traditional Chinese medicine; Taiwan imported nearly 200 metric tons of hard-shells from its neighbors yearly from 1999 to 2008. A popular medicinal preparation based on herbs and turtle shells is guilinggao jelly. The substance tortoiseshell, usually from the hawksbill turtle, has been used for centuries to make jewelry, tools, and ornaments around the Western Pacific. Hawksbills have accordingly been hunted for their shells. The trading of tortoiseshell was internationally banned in 1977 by CITES. Some cultures have used turtle shells to make music: Native American shamans made them into ceremonial rattles, while Aztecs, Mayas, and Mixtecs made ayotl drums.
A tortoiseshell comb; the material was expensive and decorative, and widely used for small items.
- Turtle Taxonomy Working Group (2017). Turtles of the World: Annotated Checklist and Atlas of Taxonomy, Synonymy, Distribution, and Conservation Status (PDF). Chelonian Research Monographs. Chelonian Research Monographs (no. 1). Vol. 7 (8th ed.). Chelonian Research Foundation: Turtle Conservancy. pp. 10, 24. doi:10.3854/crm.7.checklist.atlas.v8.2017. ISBN 978-1-5323-5026-9. OCLC 1124067380. Archived (PDF) from the original on February 25, 2021. Retrieved January 20, 2018.
- Dubois, Alan; Bour, Roger (2010). "The Distinction Between Family-Series and Class-Series Nominain Zoological Nomenclature, With Emphasis on the Nomina Created by Batsch (1788, 1789) and on the Higher Nomenclature of Turtles" (PDF). Bonn Zoological Bulletin. 57 (2): 149–171. Archived (PDF) from the original on October 9, 2022.
- Harper, Douglas. "turtle". Online Etymology Dictionary. Retrieved October 28, 2021.
- Orenstein 2012, p. 9.
- testudo. Charlton T. Lewis and Charles Short. A Latin Dictionary on Perseus Project.
- χελώνη. Liddell, Henry George; Scott, Robert; A Greek–English Lexicon at the Perseus Project
- "Chelonia". Merriam-Webster. Retrieved August 29, 2021.
- Franklin 2011, p. 14.
- Chen, Irene H.; Yang, Wen; Meyers, Marc A. (2015). "Leatherback Sea Turtle Shell: a Tough and Flexible Biological Design". Acta Biomaterialia. 28: 2–12. doi:10.1016/j.actbio.2015.09.023. PMID 26391496.
- "The Archelon". Black Hills Institute of Geological Research. Archived from the original on March 12, 2016. Retrieved December 23, 2018.
- Bonin, Franck; Devaux, Bernard; Dupré, Alain (2006). Turtles of the World. Johns Hopkins University Press. p. 230. ISBN 978-0-8018-8496-2.
- Frazier, Jack (2020). "Galapogos tortoises: Protagonists in the spectacle of life on Earth". In Gibbs, James; Cayot, Linda; Aguilera, Washington Tapia (eds.). Galapagos Giant Tortoises. Academic Press. p. 26. ISBN 978-0-12-817554-5.
- Iverson, John; Moll, Edward O (2002). "Turtles and tortoises". In Halliday, Tim; Adler, Kraig (eds.). The Firefly Encyclopedia of Reptiles and Amphibians. Firefly Books. pp. 118–129. ISBN 978-1-55297-613-5.
- Orenstein 2012, p. 22.
- Hutchinson, J. Howard (1996). "Introduction to Testudines: The Turtles". University of California Museum of Paleontology. Archived from the original on June 29, 2016. Retrieved June 4, 2003.
- Orenstein 2012, p. 16.
- Cebra-Thomas, Judith; Tan, Fraser; Sistla, Seeta; Estes, Eileen; Bender, Gunes; Kim, Christine; Riccio, Paul; Gilbert, Scott F. (2005). "How the Turtle Forms its Shell: a Paracrine Hypothesis of Carapace Formation" (PDF). Journal of Experimental Zoology Part B: Molecular and Developmental Evolution. 304B (6): 558–569. doi:10.1002/jez.b.21059. ISSN 1552-5007. PMID 15968684.
- Gaffney, Eugene S. (1990). "The Comparative Osteology of the Triassic Turtle Proganochelys". Bulletin of the American Museum of Natural History (194): 1–263. hdl:2246/884. OCLC 263164288. Archived from the original on May 16, 2021. Retrieved May 16, 2021.
- Schoch, Rainer R.; Sues, Hans‐Dieter; Benson, Roger (2019). "The Origin of the Turtle Body Plan: Evidence from Fossils and Embryos". Palaeontology. 63 (3): 375–393. doi:10.1111/pala.12460. ISSN 0031-0239.
- Orenstein 2012, pp. 16–17.
- Pritchard, Peter C. H. (2008). "Evolution and Structure of the Turtle Shell". In Wyneken, Jeanette; Bels, V. L.; Godfrey, Matthew H. (eds.). Biology of Turtles. CRC Press. p. 56. ISBN 978-0-8493-3339-2. OCLC 144570900.
- Orenstein 2012, pp. 22–26.
- Orenstein 2012, pp. 22–23, 26–27.
- Franklin 2011, p. 18.
- Orenstein 2012, p. 33.
- Franklin 2011, p. 28.
- Herrel, Anthony; O'Reilly, James C.; Richmond, Alan M. (2002). "Evolution of Bite Performance in Turtles". Journal of Evolutionary Biology. 15 (6): 1083–1094. CiteSeerX 10.1.1.484.5540. doi:10.1046/j.1420-9101.2002.00459.x. S2CID 54067445.
- Orenstein 2012, pp. 33–34.
- Orenstein 2012, p. 34.
- Orenstein 2012, p. 36.
- P. Russell, Anthony; M. Bauer, Aaron (2020). "Vocalization by extant nonavian reptiles: A synthetic overview of phonation and the vocal apparatus". The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology. 304 (7): 1478–1528. doi:10.1002/ar.24553. PMID 33099849. S2CID 225069598.
- Capshaw, Grace; Willis, Katie L.; Han, Dawei; Bierman, Hilary S. (2020). "Reptile sound production and perception". In Rosenfeld, Cheryl S.; Hoffmann, Frauke (eds.). Neuroendocrine Regulation of Animal Vocalization. Academic Press. pp. 101–118. ISBN 978-0-12-815160-0.
- Orenstein 2012, p. 38.
- Davenport, John; Munks, Sarah A.; Oxford, P. J. (February 22, 1984). "A Comparison of the Swimming of Marine and Freshwater Turtles". Proceedings of the Royal Society of London. Series B. Biological Sciences. 220 (1221): 447–475. Bibcode:1984RSPSB.220..447D. doi:10.1098/rspb.1984.0013. ISSN 0080-4649. JSTOR 35758. S2CID 84615412.
- Orenstein 2012, pp. 38–40.
- Orenstein 2012, p. 40.
- Fritsches, Kerstin A.; Warrant, Eric J. (2013). "Vision". In Wyneken, Jeanette (ed.). The Biology of Sea Turtles. CRC Press. pp. 31–58. ISBN 978-1-4398-7308-3. OCLC 828509848.
- Granda, Alan M.; Dvorak, Charles A. (1977). "Vision in Turtles". The Visual System in Vertebrates. Handbook of Sensory Physiology. Vol. 7 / 5. Berlin, Heidelberg: Springer Berlin Heidelberg. pp. 451–495. doi:10.1007/978-3-642-66468-7_8. ISBN 978-3-642-66470-0. ISSN 0072-9906.
- Jacobs, Gerald (1981). "Reptiles: The Turtle". Comparative Color Vision. New York: Academic Press. pp. 102–105. ISBN 978-0-12-378520-6.
- Willis, Katie L. (2016). "Underwater Hearing in Turtles". Advances in Experimental Medicine and Biology. 875: 1229–1235. doi:10.1007/978-1-4939-2981-8_154. ISBN 978-1-4939-2980-1. PMID 26611091.
- Martin, Kelly J.; Alessi, Sarah C.; Gaspard, Joseph C.; Tucker, Anton D.; Bauer, Gordon B.; Mann, David A. (2012). "Underwater Hearing in the Loggerhead Turtle (Caretta caretta): a Comparison of Behavioral and Auditory Evoked Potential Audiograms". Journal of Experimental Biology. 215 (17): 3001–3009. doi:10.1242/jeb.066324. ISSN 1477-9145. PMID 22875768. S2CID 459652.
- Orenstein 2012, pp. 35–36.
- Manton, Marion; Karr, Andrew; Ehrenfeld, David W. (1972). "Chemoreception in the Migratory Sea Turtle, Chelonia mydas". The Biological Bulletin. 143 (1): 184–195. doi:10.2307/1540338. ISSN 0006-3185. JSTOR 1540338. Archived from the original on June 6, 2021. Retrieved June 6, 2021.
- Cordeiro, Tábata E. F.; Abe, Augusto S.; Klein, Wilfried (April 2016). "Ventilation and Gas Exchange in Two Turtles: Podocnemis unifilis and Phrynops geoffroanus (Testudines: Pleurodira)" (PDF). Respiratory Physiology & Neurobiology. 224: 125–131. doi:10.1016/j.resp.2014.12.010. hdl:11449/158795. ISSN 1569-9048. PMID 25534144. S2CID 37446604. Archived from the original on July 24, 2021. Retrieved September 25, 2019.
- Lyson, Tyler R.; Schachner, Emma R.; Botha-Brink, Jennifer; Scheyer, Torsten M.; Lambertz, Markus; Bever, G. S.; Rubidge, Bruce S.; de Queiroz, Kevin (November 7, 2014). "Origin of the Unique Ventilatory Apparatus of Turtles". Nature Communications. 5: 5211. Bibcode:2014NatCo...5.5211L. doi:10.1038/ncomms6211. ISSN 2041-1723. PMID 25376734.
- Lee, Stella Y.; Milsom, William K. (2016). "The Metabolic Cost of Breathing in Red-eared Sliders: An Attempt to Resolve an Old Controversy". Respiratory Physiology & Neurobiology. 224: 114–124. doi:10.1016/j.resp.2015.10.011. ISSN 1569-9048. PMID 26524718. S2CID 5194890.
- Orenstein 2012, p. 41.
- Lambertz, Markus; Böhme, Wolfgang; Perry, Steven F. (July 2010). "The Anatomy of the Respiratory System in Platysternon megacephalum Gray, 1831 (Testudines: Cryptodira) and Related Species, and its Phylogenetic Implications". Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology. 156 (3): 330–336. doi:10.1016/j.cbpa.2009.12.016. ISSN 1095-6433. PMID 20044019.
- Klein, Wilfried; Codd, Jonathan R. (2010). "Breathing and Locomotion: Comparative Anatomy, Morphology and Function". Respiratory Physiology & Neurobiology. 173: S26–S32. doi:10.1016/j.resp.2010.04.019. ISSN 1569-9048. PMID 20417316. S2CID 28044326.
- Morera-Brenes, Bernal; Monge-Nájera, Julián (2011). "Immersion Periods in Four Neotropical Turtles". UNED Research Journal. 3 (1): 97. doi:10.22458/urj.v3i1.212. Archived from the original on August 9, 2020. Retrieved June 11, 2020.
- Priest, Toni E.; Franklin, Craig E. (December 2002). "Effect of Water Temperature and Oxygen Levels on the Diving Behavior of Two Freshwater Turtles: Rheodytes leukops and Emydura macquarii". Journal of Herpetology. 36 (4): 555–561. doi:10.1670/0022-1511(2002)036[0555:EOWTAO]2.0.CO;2. ISSN 0022-1511. JSTOR 1565924. S2CID 85279910.
- Wyneken, Jeanette (2008). "The Structure of Cardiopulmonary Systems of Turtles: Implications for Behavior and Function". In Wyneken, Jeanette; Bels, V. L.; Godfrey, Matthew H. (eds.). Biology of Turtles. CRC Press. pp. 213–224. ISBN 978-0-8493-3339-2. OCLC 144570900.
- Jackson, Donald C. (2002). "Hibernating Without Oxygen: Physiological Adaptations of the Painted turtle". Journal of Physiology. 543 (Pt 3): 731–737. doi:10.1113/jphysiol.2002.024729. PMC 2290531. PMID 12231634.
- Miller, Jeffrey D.; Dinkelacker, Stephen A. (2008). "Reproductive Structures and Strategies of Turtles". In Wyneken, Jeanette; Bels, V. L.; Godfrey, Matthew H. (eds.). Biology of Turtles. CRC Press. p. 234. ISBN 978-0-8493-3339-2. OCLC 144570900.
- Wyneken, Jeanette; Witherington, Dawn (February 2015). "Urogenital System" (PDF). Anatomy of Sea Turtles. 1: 153–165. Archived (PDF) from the original on June 8, 2019. Retrieved May 18, 2021.
- Bentley, Peter J. (2013). Endocrines and Osmoregulation: A Comparative Account in Vertebrates. Springer. p. 143. ISBN 978-3-662-05014-9. Archived from the original on May 31, 2021. Retrieved May 18, 2021.
- Franklin 2011, p. 31.
- Pough, F. Harvey; Janis, Christine M. (2019). "16. Turtles". Vertebrate Life (10th ed.). New York: Sinauer Associates. pp. 283–299. ISBN 978-1-60535-607-5. OCLC 1022979490.
- Orenstein 2012, p. 231.
- Franklin 2011, pp. 29–30.
- Orenstein 2012, p. 237.
- Orenstein 2012, p. 235.
- Van Damme, Johan; Aerts, Peter (1997). "Kinematics and Functional Morphology of Aquatic Feeding in Australian Snake-necked Turtles (Pleurodira;Chelodina)". Journal of Morphology. 233 (2): 113–125. doi:10.1002/(SICI)1097-4687(199708)233:2<113::AID-JMOR3>3.0.CO;2-7. PMID 9218349. S2CID 32906130.
- Franklin 2011, p. 30.
- Orenstein 2012, p. 239.
- Orenstein 2012, p. 229.
- Giles, Jacqueline C.; Davis, Jenny; McCauley, Robert D.; Kuchling, Gerald (2009). "Voice of the Turtle: The Underwater Acoustic Repertoire of the Long-necked Freshwater Turtle, Chelodina oblonga". The Journal of the Acoustical Society of America. 126 (1): 434–443. Bibcode:2009ASAJ..126..434G. doi:10.1121/1.3148209. PMID 19603900.
- Pryke 2021, p. 39.
- Ferrara, Camila R.; Vogt, Richard C.; Sousa-Lima, Renata Santoro (2012). "Turtle Vocalizations as the First Evidence of Posthatching Parental Care in Chelonians" (PDF). Journal of Comparative Psychology. 127 (1): 24–32. doi:10.1037/a0029656. PMID 23088649. Archived (PDF) from the original on September 2, 2017. Retrieved September 1, 2017.
- Burghardt, Gordon M.; Ward, B.; Rosscoe, Roger (1996). "Problem of Reptile Play: Environmental Enrichment and Play Behavior in a Captive Nile Softshelled Turtle, Trionyx triunguis". Zoo Biology. 15 (3): 223–238. doi:10.1002/(SICI)1098-2361(1996)15:3<223::AID-ZOO3>3.0.CO;2-D.
- Davis, K. M.; Burghardt, Gordon M. (2007). "Training and Long-term Memory of a Novel Food Acquisition Task in a Turtle (Pseudemys nelsoni)". Behavioural Processes. 75 (2): 225–230. doi:10.1016/j.beproc.2007.02.021. PMID 17433570. S2CID 34130920.
- "Reptiles Known as 'Living Rocks' Show Surprising Cognitive Powers". Nature. Animal Behaviour. 576 (7785): 10. 29 November 2019. Bibcode:2019Natur.576...10.. doi:10.1038/d41586-019-03655-5. S2CID 208613023.
- Gutnick, Tamar; Weissenbacher, Anton; Kuba, Michael J. (13 November 2019). "The Underestimated Giants: Operant Conditioning, Visual Discrimination and Long-term Memory in Giant Tortoises". Animal Cognition. 23 (1): 159–167. doi:10.1007/s10071-019-01326-6. ISSN 1435-9456. PMID 31720927. S2CID 207962281.
- Salas, Cosme; Broglio, Cristina; Rodríguez, Fernando (2003). "Evolution of Forebrain and Spatial Cognition in Vertebrates: Conservation across Diversity". Brain, Behavior and Evolution. 62 (2): 72–82. doi:10.1159/000072438. ISSN 0006-8977. PMID 12937346. S2CID 23055468.
- Reiter, Sam; Liaw, Hua-Peng; Yamawaki, Tracy M.; Naumann, Robert K.; Laurent, Gilles (2017). "On the Value of Reptilian Brains to Map the Evolution of the Hippocampal Formation". Brain, Behavior and Evolution. 90 (1): 41–52. doi:10.1159/000478693. ISSN 0006-8977. PMID 28866680. S2CID 13763864.
- Orenstein 2012, pp. 252–253.
- Franklin 2011, p. 40.
- Orenstein 2012, pp. 252–253, 301.
- Southwood, Amanda; Avens, Larisa (2009). "Physiological, Behavioral, and Ecological Aspects of Migration in Reptiles". Journal of Comparative Physiology B. 180 (1): 1–23. doi:10.1007/s00360-009-0415-8. ISSN 0174-1578. PMID 19847440. S2CID 20245401. Archived from the original on July 24, 2021. Retrieved June 6, 2021.
- Lohmann, Kenneth J.; Lohmann, Catherine M. F.; Brothers, J. Roger; Putman, Nathan F. (2013). "Natal Homing and Imprinting in Sea Turtles". In Wyneken, Jeanette (ed.). The Biology of Sea Turtles. CRC Press. pp. 59–78. ISBN 978-1-4398-7308-3. OCLC 828509848.
- Pearse, Devon E. (2001). "Turtle Mating Systems: Behavior, Sperm Storage, and Genetic Paternity". Journal of Heredity. 92 (2): 206–211. doi:10.1093/jhered/92.2.206. PMID 11396580.
- Booth, Julie; Peters, James A. (1972). "Behavioural Studies on the Green Turtle (Chelonia mydas) in the Sea". Animal Behaviour. 20 (4): 808–812. doi:10.1016/S0003-3472(72)80155-6.
- Berry, James F.; Shine, Richard (1980). "Sexual Size Dimorphism and Sexual Selection in Turtles (order Testudines)". Oecologia. 44 (2): 185–191. Bibcode:1980Oecol..44..185B. doi:10.1007/bf00572678. PMID 28310555. S2CID 2456783.
- Berry, James; Iverson, John (December 2011). "Kinosternon scorpioides (Linnaeus 1766) – Scorpion Mud Turtle" (PDF). Conservation Biology of Freshwater Turtles and Tortoises: 063.1–063.15. doi:10.3854/crm.5.063.scorpioides.v1.2011. ISBN 978-0-9653540-9-7. Archived (PDF) from the original on February 4, 2019. Retrieved August 20, 2019.
- Orenstein 2012, pp. 270–271.
- Orenstein 2012, p. 270.
- Franklin 2011, p. 33.
- Ripple, J. (1996). Sea Turtles. Voyageur Press. p. 26. ISBN 978-0-89658-315-3.
- Franklin 2011, pp. 20–22.
- Orenstein 2012, p. 260.
- Orenstein 2012, p. 277.
- Orenstein 2012, pp. 273, 276.
- Franklin 2011, p. 37.
- Orenstein 2012, p. 274.
- Ye, Yin-Zi; Ma, Liang; Sun, Bao-Jun; Li, Teng; Wang, Yang; Shine, Richard; Du, Wei-Guo (2019). "The Embryos of Turtles can Influence their own Sexual Destinies". Current Biology. 29 (16): 2597–2603.e4. doi:10.1016/j.cub.2019.06.038. ISSN 0960-9822. PMID 31378606.
- Orenstein 2012, p. 286.
- Orenstein 2012, p. 294.
- Orenstein 2012, pp. 301–302.
- Millward, Adam (February 27, 2019). "Introducing Jonathan, the World's Oldest Animal on Land at 187 Years Old". Guinness World Records. Archived from the original on August 9, 2020. Retrieved July 14, 2020.
- Franklin 2011, pp. 44–45.
- Warner, Daniel A.; Miller, David A. W.; Bronikowski, Anne M.; Janzen, Fredric J. (2016). "Decades of Field Data Reveal that Turtles Senesce in the Wild". PNAS. 113 (23): 6502–6507. Bibcode:2016PNAS..113.6502W. doi:10.1073/pnas.1600035113. PMC 4988574. PMID 27140634.
- Rieppel, Olivier (2017). Turtles as Hopeful Monsters: Origins and Evolution. Indiana University Press. p. 195. ISBN 978-0-253-02507-4. OCLC 962141060.
- Lyson, Tyler R.; Bever, Gabriel S. (2020). "Origin and Evolution of the Turtle Body Plan". Annual Review of Ecology, Evolution, and Systematics. 51 (1): 143–166. doi:10.1146/annurev-ecolsys-110218-024746. S2CID 225486775.
- Cadena, Edwin; Joyce, Walter G. (April 2015). "A Review of the Fossil Record of Turtles of the Clades Platychelyidae and Dortokidae". Bulletin of the Peabody Museum of Natural History. 56 (1): 3–20. doi:10.3374/014.056.0101. ISSN 0079-032X. S2CID 56195415.
- Evers, Serjoscha W.; Benson, Roger B. J. (January 2019). Smith, Andrew (ed.). "A new phylogenetic hypothesis of turtles with implications for the timing and number of evolutionary transitions to marine lifestyles in the group". Palaeontology. 62 (1): 93–134. doi:10.1111/pala.12384. S2CID 134736808.
- Pérez-García, Adán (September 2, 2017). "A new Turtle Taxon (Podocnemidoidea, Bothremydidae) Reveals the Oldest Known Dispersal Event of the Crown Pleurodira from Gondwana to Laurasia". Journal of Systematic Palaeontology. 15 (9): 709–731. doi:10.1080/14772019.2016.1228549. ISSN 1477-2019. S2CID 88840423.
- Ferreira, Gabriel S.; Bandyopadhyay, Saswati; Joyce, Walter G. (November 15, 2018). "A Taxonomic Reassessment of Piramys auffenbergi, a Neglected Turtle from the late Miocene of Piram Island, Gujarat, India". PeerJ. 6: e5938. doi:10.7717/peerj.5938. ISSN 2167-8359. PMC 6240434. PMID 30479901.
- Hirayama, Ren; Isaji, Shinji; Hibino, Tsuyoshi (2013). Brinkman, Donald B.; Holroyd, Patricia A.; Gardner, James D. (eds.). Kappachelys okurai gen. et sp. nov., a New Stem Soft-Shelled Turtle from the Early Cretaceous of Japan. Morphology and Evolution of Turtles. Dordrecht: Springer Netherlands. pp. 179–185. doi:10.1007/978-94-007-4309-0_12. ISBN 978-94-007-4308-3.
- Evers, Serjoscha W.; Barrett, Paul M.; Benson, Roger B. J. (May 2019). "Anatomy of Rhinochelys pulchriceps (Protostegidae) and Marine Adaptation During the Early Evolution of chelonioids". PeerJ. 7: e6811. doi:10.7717/peerj.6811. ISSN 2167-8359. PMC 6500378. PMID 31106054.
- Hofmeyr, Margaretha D.; Vamberger, Melita; Branch, William; Schleicher, Alfred; Daniels, Savel R. (July 2017). "Tortoise (Reptilia, Testudinidae) Radiations in Southern Africa from the Eocene to the Present". Zoologica Scripta. 46 (4): 389–400. doi:10.1111/zsc.12223. S2CID 88712318.
- Poropat, Stephen F.; Kool, Lesley; Vickers-Rich, Patricia; Rich, Thomas H. (April 3, 2017). "Oldest Meiolaniid Turtle Remains from Australia: Evidence from the Eocene Kerosene Creek Member of the Rundle Formation, Queensland". Alcheringa: An Australasian Journal of Palaeontology. 41 (2): 231–239. doi:10.1080/03115518.2016.1224441. ISSN 0311-5518. S2CID 131795055.
- Rieppel, Olivier; DeBraga, M. (1996). "Turtles as Diapsid Reptiles" (PDF). Nature. 384 (6608): 453–455. Bibcode:1996Natur.384..453R. doi:10.1038/384453a0. S2CID 4264378.
- Zardoya, Rafael; Meyer, Axel (1998). "Complete Mitochondrial Genome Suggests Diapsid Affinities of Turtles" (PDF). PNAS. 95 (24): 14226–14231. Bibcode:1998PNAS...9514226Z. doi:10.1073/pnas.95.24.14226. ISSN 0027-8424. PMC 24355. PMID 9826682. Archived from the original on July 24, 2021. Retrieved October 31, 2018.
- Mannen, Hideyuki; Li, Steven S.-L. (October 1999). "Molecular Evidence for a Clade of Turtles". Molecular Phylogenetics and Evolution. 13 (1): 144–148. doi:10.1006/mpev.1999.0640. PMID 10508547.
- Iwabe, Naoyuki; Hara, Yuichiro; Kumazawa, Yoshinori; Shibamoto, Kaori; Saito, Yumi; Miyata, Takashi; Katoh, Kazutaka (December 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.
- Roos, Jonas; Aggarwal, Ramesh K.; Janke, Axel (November 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, Yoshinao; Braun, Edward L.; Guillette, Louis J. Jr.; Iguchi, Taisen (March 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. S2CID 12116018.
- Lyson, Tyler R.; Sperling, Erik A.; Heimberg, Alysha M.; Gauthier, Jacques A.; King, Benjamin L.; Peterson, Kevin J. (2012). "MicroRNAs Support a Turtle + Lizard Clade". Biology Letters. 8 (1): 104–107. doi:10.1098/rsbl.2011.0477. PMC 3259949. PMID 21775315.
- Chiari, Ylenia; Cahais, Vincent; Galtier, Nicolas; Delsuc, Frédéric (2012). "Phylogenomic Analyses Support the Position of Turtles as the Sister Group of Birds and Crocodiles (Archosauria)". BMC Biology. 10 (65): 65. doi:10.1186/1741-7007-10-65. PMC 3473239. PMID 22839781.
- Crawford, Nicholas G.; Faircloth, Brant C.; McCormack, John E.; Brumfield, Robb T.; Winker, Kevin; Glen, Travis C. (2012). "More than 1000 Ultraconserved Elements Provide Evidence that Turtles are the Sister Group to Archosaurs" (PDF). Biology Letters. 8 (5): 783–786. doi:10.1098/rsbl.2012.0331. PMC 3440978. PMID 22593086. Archived (PDF) from the original on August 10, 2012. Retrieved September 21, 2014.
- Wang, Zhuo; Pascual-Anaya, Juan; Zadissa, Amonida; et al. (2013). "The Draft Genomes of Soft-shell Turtle and Green Sea Turtle Yield Insights into the Development and Evolution of the Turtle-specific Body Plan". Nature Genetics. 45 (6): 701–706. doi:10.1038/ng.2615. PMC 4000948. PMID 23624526.
- Joyce, Walter G.; Anquetin, Jérémy; Cadena, Edwin-Alberto; Claude, Julien; Danilov, Igor G.; Evers, Serjoscha W.; Ferreira, Gabriel S.; Gentry, Andrew D.; Georgalis, Georgios L.; Lyson, Tyler R.; Pérez-García, Adán (December 2021). "A Nomenclature for Fossil and Living Turtles Using Phylogenetically Defined Clade Names". Swiss Journal of Palaeontology. 140 (1): 5. doi:10.1186/s13358-020-00211-x. ISSN 1664-2376. S2CID 229506832.
- Böhmer, Christine; Werneburg, Ingmar (2017). "Deep Time Perspective on Turtle Neck Evolution: Chasing the Hox Code by Vertebral Morphology". Scientific Reports. 7 (1): 8939. Bibcode:2017NatSR...7.8939B. doi:10.1038/s41598-017-09133-0. PMC 5566328. PMID 28827543.
- Thomson, Robert C.; Spinks, Phillip Q.; Shaffer, H. Bradley (February 8, 2021). "A Global Phylogeny of Turtles Reveals a Burst of Climate-associated Diversification on Continental Margins". Proceedings of the National Academy of Sciences. 118 (7): e2012215118. Bibcode:2021PNAS..11812215T. doi:10.1073/pnas.2012215118. ISSN 0027-8424. PMC 7896334. PMID 33558231.
- Crawford, Nicholas G.; Parham, James F.; Sellas, Anna B.; Faircloth, Brant C.; Glenn, Travis C.; Papenfuss, Theodore J.; Henderson, James B.; Hansen, Madison H.; Simison, W. Brian (2015). "A Phylogenomic Analysis of Turtles". Molecular Phylogenetics and Evolution. 83: 250–257. doi:10.1016/j.ympev.2014.10.021. ISSN 1055-7903. PMID 25450099.
- Knauss, Georgia E.; Joyce, Walter G.; Lyson, Tyler R.; Pearson, Dean (September 21, 2010). "A New Kinosternoid from the Late Cretaceous Hell Creek Formation of North Dakota and Montana and the Origin of the Dermatemys mawii Lineage". Paläontologische Zeitschrift. Springer Science and Business Media LLC. 85 (2): 125–142. doi:10.1007/s12542-010-0081-x. ISSN 0031-0220. S2CID 129123961.
- Joyce, Walter G.; Anquetin, Jérémy; Cadena, Edwin-Alberto; et al. (February 9, 2021). "A Nomenclature for Fossil and Living Turtles Using Phylogenetically Defined Clade Names". Swiss Journal of Palaeontology. 140 (1): 5. doi:10.1186/s13358-020-00211-x. ISSN 1664-2384.
- Werneburg, Ingmar; Wilson, Laura A. B.; Parr, William C. H.; Joyce, Walter G. (March 1, 2015). "Evolution of Neck Vertebral Shape and Neck Retraction at the Transition to Modern Turtles: an Integrated Geometric Morphometric Approach". Systematic Biology. 64 (2): 187–204. doi:10.1093/sysbio/syu072. ISSN 1063-5157. PMID 25305281.
- Herrel, Anthony; Van Damme, Johan; Aerts, Peter (2008). "Cervical Anatomy and Function in Turtles". In Wyneken, Jeanette; Bels, V. L.; Godfrey, Matthew H. (eds.). Biology of Turtles. CRC Press. pp. 163–186. ISBN 978-0-8493-3339-2. OCLC 144570900.
- Orenstein 2012, p. 110.
- Ferreira, Gabriel S.; Lautenschlager, Stephan; Evers, Serjoscha W.; et al. (March 26, 2020). "Feeding Biomechanics Suggests Progressive Correlation of Skull Architecture and Neck Evolution in Turtles". Scientific Reports. 10 (1). article 5505. Bibcode:2020NatSR..10.5505F. doi:10.1038/s41598-020-62179-5. ISSN 2045-2322. PMC 7099039. PMID 32218478.
- Wise, Taylor B.; Stayton, C. Tristan (2017). "Side-necked Versus Hidden-necked: Comparison of Shell Morphology Between Pleurodiran and Cryptodiran Turtles". Herpetologica. 73 (1): 18–29. doi:10.1655/HERPETOLOGICA-D-15-00038. JSTOR 26534349. S2CID 90226667.
- Pough, F. Harvey (2001). "Reptiles, Biodiversity of". Encyclopedia of Biodiversity. Elsevier. pp. 146–151. doi:10.1016/b0-12-226865-2/00233-9. ISBN 978-0-12-226865-6.
- Ferreira, Gabriel S.; Bronzati, Mario; Langer, Max C.; Sterli, Juliana (2018). "Phylogeny, Biogeography and Diversification Patterns of Side-necked Turtles (Testudines: Pleurodira)". Royal Society Open Science. 5 (3): 171773. Bibcode:2018RSOS....571773F. doi:10.1098/rsos.171773. ISSN 2054-5703. PMC 5882704. PMID 29657780.
- Buhlmann, Kurt A.; Akre, Thomas S. B.; Iverson, John B.; et al. (2009). "A Global Analysis of Tortoise and Freshwater Turtle Distributions with Identification of Priority Conservation Areas" (PDF). Chelonian Conservation and Biology. 8 (2): 116–149. doi:10.2744/CCB-0774.1. S2CID 85942804. Archived (PDF) from the original on May 9, 2021. Retrieved May 9, 2021.
- Ultsch, Gordon R. (May 15, 2006). "The Ecology of Overwintering Among Turtles: Where Turtles Overwinter and its Consequences". Biological Reviews. 81 (3): 339–367. doi:10.1017/s1464793106007032. ISSN 1464-7931. PMID 16700968. S2CID 32939695.
- Degenhardt, William G.; Christiansen, James L. (1975). "Distribution and Habitats of Turtles in New Mexico". The Southwestern Naturalist. 19 (1): 21–46. doi:10.2307/3669787. JSTOR 3669787.
- Dodge, Kara L.; Galuardi, Benjamin; Miller, Timothy J.; Lutcavage, Molly E. (2014). "Leatherback Turtle Movements, Dive Behavior, and Habitat Characteristics in Ecoregions of the Northwest Atlantic Ocean". PLOS ONE. 9 (3): e91726. Bibcode:2014PLoSO...991726D. doi:10.1371/journal.pone.0091726. PMC 3960146. PMID 24646920.
- Meyer, Rachelle (2008). "Gopherus spp". U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory. Archived from the original on September 16, 2020. Retrieved May 9, 2021.
- Wallace, Bryan P.; Lewison, Rebecca L.; McDonald, Sara L.; McDonald, Richard K.; Kot, Connie Y.; Kelez, Shaleyla; Bjorkland, Rhema K.; Finkbeiner, Elena M.; Helmbrecht, S'rai; Crowder, Larry B. (April 5, 2010). "Global Patterns of Marine Turtle Bycatch". Conservation Letters. Wiley. 3 (3): 131–142. doi:10.1111/j.1755-263x.2010.00105.x. ISSN 1755-263X.
- Montgomery, Madeline (April 15, 2021). "Environmentalists Fight Against New Law that Could Kill Thousands of Sea Turtles". WPEC. Archived from the original on April 17, 2021. Retrieved May 11, 2021.
- Rhodin, Anders G. J.; Stanford, Craig B.; van Dijk, Peter Paul; Eisemberg, Carla Camilo; et al. (2018). "Global Conservation Status of Turtles and Tortoises (order Testudines)" (PDF). Chelonian Conservation and Biology. 17 (2): 135–161. doi:10.2744/CCB-1348.1. S2CID 91937716.
- Rhodin, Anders G. J.; Walde, Andrew D.; Horne, Brian D.; van Dijk, Peter Paul; Blanck, Torsten; Hudson, Rick, eds. (2011). Turtles in Trouble: The World's 25+ Most Endangered Tortoises and Freshwater Turtles – 2011. Turtle Conservation Coalition. OCLC 711692023. Archived from the original on March 5, 2011. Retrieved March 5, 2011.
- Pryke 2021, pp. 160–166.
- Pryke 2021, p. 156.
- Pryke 2021, p. 157.
- van Dijk, Peter Paul (2002). "The Asian Turtle Crisis". In Halliday, Tim; Adler, Kraig (eds.). The Firefly Encyclopedia of Reptiles and Amphibians. Firefly Books. pp. 134–135. ISBN 978-1-55297-613-5.
- McCallum, Malcolm (2021). "Turtle Biodiversity Losses Suggest Coming Sixth Mass Extinction". Biodiversity and Conservation. 30 (5): 1257–1275. doi:10.1007/s10531-021-02140-8. ISSN 0960-3115. S2CID 233903598. Archived from the original on July 24, 2021. Retrieved March 12, 2021.
- Draven, James (May 30, 2018). "Are Turtle Hatcheries Unethical?". National Geographic. Archived from the original on June 13, 2019. Retrieved May 10, 2021.
- Sea Turtle Conservation Beach Management and Hatchery Programmes (PDF). Centre for Herpetology/ Madras Crocodile Bank Trust, Tamil Nadu. 2003. Archived (PDF) from the original on November 12, 2020. Retrieved April 7, 2021.
- Chacon, Didiher; Sanchez, Juan; Calvo, Jose Joaquin; Ash, Jenny (2007). Manual Para el Manejo y la Conservación de las Tortugas Marinas en Costa Rica; con énfasis en la operación de proyectos en playa y viveros [Manual for the management and conservation of sea turtles in Costa Rica; with emphasis on the operation of beach and nursery projects] (PDF) (in Spanish). Latin American Sea Turtles and WIDECAST (Wider Caribbean Sea Turtle Network). Archived (PDF) from the original on July 24, 2021. Retrieved April 7, 2021.
- "Turtle Farms Threaten Rare Species, Experts Say". Fish Farmer. March 30, 2007. Archived from the original on February 18, 2012. Retrieved November 1, 2012.
- Cheung, Sze Man; Dudgeon, David (November–December 2006). "Quantifying the Asian Turtle Crisis: Market Surveys in Southern China, 2000–2003". Aquatic Conservation: Marine and Freshwater Ecosystems. 16 (7): 751–770. doi:10.1002/aqc.803.
- Amato, George (2007). A Conversation at the Museum of Natural History (.flv). POV25. Archived from the original (video) on November 12, 2021. Retrieved November 1, 2012.
- Bennett, Elise (February 20, 2020). "Report: Refusal to Ban Trapping Threatens Turtles in Nine States, Enables Illegal Trade". Center for Biological Diversity. Retrieved August 5, 2021.
- Hylton, Hilary (May 8, 2007). "Keeping U.S. Turtles Out of China". Time. Archived from the original on May 12, 2007. Retrieved November 1, 2012.
- Pittman, Craig (October 9, 2008). "China Gobbling Up Florida Turtles". St. Petersburg Times. Archived from the original on September 20, 2016. Retrieved August 18, 2016.
- Thom, Mitchell (November 20, 2015). "Queensland's Shark Control Program Has Snagged 84,000 Animals". Action for Dolphins. Archived from the original on December 24, 2020. Retrieved December 25, 2018.
- Lambert, Max R.; et al. (2019). "Experimental Removal of Introduced Slider Turtles Offers New Insight into Competition with a Native, Threatened Turtle". PeerJ. 7: e7444. doi:10.7717/peerj.7444. PMC 6698372. PMID 31435491.
- Pryke 2021, p. 107.
- Pryke 2021, pp. 9–10.
- Pryke 2021, pp. 63–68.
- McLellan, Liz; Nickson, Amanda; Benn, Jo (June 2005). "Marine turtle conservation in the Asia Pacific region" (PDF). WWF. Archived (PDF) from the original on July 24, 2021. Retrieved July 22, 2021.
- Mallinson, James (December 9, 2011). "A Response to Mark Singleton's Yoga Body by James Mallinson". Academia. Archived from the original on July 24, 2021. Retrieved January 4, 2019. revised from American Academy of Religions conference, San Francisco, 19 November 2011.
- Iyengar, Bellur K. S. (1979) . Light on Yoga: Yoga Dipika. Thorsons. pp. 288–291. ISBN 978-1-85538-166-7.
- Converse, Harriet Maxwell; Parker, Arthur Caswell (1908). Myths and Legends of the New York State Iroquois. University of the State of New York. p. 33. Archived from the original on May 22, 2021. Retrieved May 22, 2021.
- Filice, Michelle (November 6, 2018). "Turtle Island". The Canadian Encyclopedia. Archived from the original on May 20, 2021. Retrieved May 22, 2021.
- Pryke 2021, pp. 44–48.
- Pryke 2021, p. 56.
- Anonymous; Evelyn-White, Hugh G. (1914). "Hymn 4 to Hermes". Cambridge, Massachusetts: Harvard University Press. Lines 26–65. Archived from the original on May 11, 2021. Retrieved May 11, 2021.
- Pryke 2021, pp. 49–52.
- "The Tortoise and the Hare". Aesopica: Aesop's Fables in English, Latin, and Greek. Archived from the original on August 16, 2019. Retrieved May 11, 2021.
- Pryke 2021, p. 139.
- Carroll, Lewis (1901) . "The Mock-Turtle's Story". Alice's Adventures in Wonderland. Harper & Brothers. p. 128. OCLC 1049742993.
- Pryke 2021, p. 135.
- "Mock Turtle Soup". Merriam-Webster. Archived from the original on October 20, 2012. Retrieved December 22, 2020.
- Anon (April 1, 1899). "Brooklyn Life [Theater]". Brooklyn Life. p. 31. Archived from the original on May 22, 2021. Retrieved May 22, 2021.
it is primarily a very amusing farce. The plot is slight, and concerns chiefly the proverbial fickle-mindedness of woman.
- Pryke 2021, p. 137.
- Pryke 2021, pp. 118–120.
- Greenberg, Harvey R. (April 15, 1990). "Just How Powerful Are Those Turtles?". The New York Times. Archived from the original on June 12, 2018. Retrieved May 11, 2021.
- Pryke 2021, pp. 148–151.
- Reid, Siuna A. (2017). "Current Trends in the Husbandry and Veterinary Care of Tortoises" (PDF). Testudo. 8 (4): 58–68. Archived (PDF) from the original on July 31, 2019. Retrieved July 31, 2019.
- Pryke 2021, p. 181.
- Pryke 2021, pp. 181–183.
- Pryke 2021, pp. 120–122.
- Barzyk, James E. (November 1999). "Turtles in Crisis: The Asian Food Markets". Tortoise Trust. Archived from the original on February 22, 2015. Retrieved November 1, 2012.
- Clarkson, Janet (2010). Soup : a global history. Reaktion. p. 115. ISBN 978-1-86189-774-9. OCLC 642290114.
- "Recipes from Another Time". Smithsonian. October 2001. Archived from the original on August 19, 2016. Retrieved August 19, 2016.
- Chen, Tien-Hsi; Chang, H.-C.; Lue, Kuang-Yang (2009). "Unregulated Trade in Turtle Shells for Chinese Traditional Medicine in East and Southeast Asia: the Case of Taiwan". Chelonian Conservation and Biology. 8 (1): 11–18. doi:10.2744/CCB-0747.1. S2CID 86821249.
- Zhang, Huan; Wu, Min-Yi; Guo, De-Jian; et al. (2013). "Gui-ling-gao (turtle jelly), a traditional Chinese functional food, exerts anti-inflammatory effects by inhibiting iNOS and pro-inflammatory cytokine expressions in splenocytes isolated from BALB/c mice". Journal of Functional Foods. 5 (2): 625–632. doi:10.1016/j.jff.2013.01.004. hdl:10397/16357.
- Cox, Lisa (November 12, 2018). "Hawksbill Turtle Poaching to be Fought with DNA Technology". The Guardian. Retrieved August 7, 2021.
Hawksbills are the only sea turtles hunted for their shells, despite international trade in hawksbill products being banned more than 20 years ago.
- "Global Status of the Hawksbill Sea Turtle: The Tortoiseshell Trade". Sea Turtle Conservancy. 2007.
- Pryke 2021, pp. 58–60.
- Strieker, Gary (April 10, 2001). "Tortoiseshell Ban Threatens Japanese Tradition". CNN. Archived from the original on December 15, 2006. Retrieved May 11, 2021.
- Franklin, Carl J. (2011). Turtle: A Extraordinary Natural History 245 Million Years in the Making. Crestline. ISBN 978-0-7858-2775-7.
- Orenstein, Ronald (2012). Turtles, Tortoises and Terrapins: a Natural History. Firefly Books. ISBN 978-1-77085-119-1. OCLC 791162481.
- Pryke, Louise (2021). Turtle. Reaktion Books. ISBN 978-1-78914-336-2. OCLC 1223025640.