Tuatara are members of the taxon Rhynchocephalia and are most closely related to squamates (i.e., amphisbaenians, lizards, and snakes). Like squamates, tuatara are elongate and shed skin in large fragments. Unlike squamates, tuatara lack paired hemipenes (male copulatory organs).
The common name "tuatara" comes from Maori words meaning "spines on back," in reference to the crest on the backs of males and females. Tuatara have a lizard-like appearance: both groups are elongate with four limbs (most lizards) and both lizards and tuatara are known to shed their tails (caudal autotomy). The groups diverge, however, on the presence or lack of a paired hemipenes, the morphology of the teeth and skull, and other important features. Tuatara are long-lived species, reaching sexual maturity at about 20 years. Two species of tuatara, Sphenodon guntheri and Sphenodon punctatus, are located in New Zealand, and are the only species known to exist.
Source: National Biological Information Infrastructure (NBII) at http://www.nbii.gov
Molecular Biology and Genetics
Statistics of barcoding coverage
Specimens with Sequences:5
Specimens with Barcodes:2
Species With Barcodes:1
The tuatara is a reptile endemic to New Zealand which, though it resembles most lizards, is actually part of a distinct lineage, order Sphenodontia. The two species of tuatara are the only surviving members of its order, which flourished around 200 million years ago. Their most recent common ancestor with any other extant group is with the squamates (lizards and snakes). For this reason, tuatara are of great interest in the study of the evolution of lizards and snakes, and for the reconstruction of the appearance and habits of the earliest diapsids (the group that also includes birds, dinosaurs, and crocodiles).
Tuatara are greenish brown, and measure up to 80 cm (31 in) from head to tail-tip and weigh up to 1.3 kilograms (2.9 lb) with a spiny crest along the back, especially pronounced in males. Their dentition, in which two rows of teeth in the upper jaw overlap one row on the lower jaw, is unique among living species. They are further unusual in having a pronounced photo-receptive eye dubbed the "third eye", whose current function is a subject of ongoing research but is thought to be involved in setting circadian and seasonal cycles. They are able to hear although no external ear is present, and have a number of unique features in their skeleton, some of them apparently evolutionarily retained from fish. Although tuatara are sometimes called "living fossils", recent taxonomic and molecular work has shown that they have changed significantly since the Mesozoic era.
The name "tuatara" derives from the Māori language, and means "peaks on the back". As with many other Māori loanwords, the plural form is now generally the same as the singular in formal New Zealand English usage. "Tuataras" remains common in less formal speech, particularly among older speakers. The tuatara has been protected by law since 1895 (the second species, S. guntheri, was not recognised until 1989). Tuatara, like many of New Zealand's native animals, are threatened by habitat loss and introduced predators like the Polynesian Rat (Rattus exulans). They were extinct on the mainland, with the remaining populations confined to 32 offshore islands, until the first mainland release into the heavily fenced and monitored Karori Sanctuary in 2005.
During routine maintenance work at Karori Sanctuary in late 2008, a tuatara nest was uncovered, with a hatchling found the following autumn. This is thought to be the first case of tuatara successfully breeding on the New Zealand mainland in over 200 years, outside of captive rearing facilities.
Taxonomy and evolution
Tuatara, and their sister group Squamata (which includes lizards, snakes and amphisbaenians), belong to the superorder Lepidosauria, the only surviving taxon within Lepidosauromorpha. Squamates and tuatara both show caudal autotomy (loss of the tail-tip when threatened), and have a transverse cloacal slit. The origin of the tuatara probably lies close to the split between the Lepidosauromorpha and the Archosauromorpha. Though tuatara resemble lizards, the similarity is superficial, because the family has several characteristics unique among reptiles. The typical lizard shape is very common for the early amniotes; the oldest known fossil of a reptile, the Hylonomus, resembles a modern lizard.
Tuatara were originally classified as lizards in 1831 when the British Museum received a skull. The genus remained misclassified until 1867, when Albert Günther of the British Museum noted features similar to birds, turtles, and crocodiles. He proposed the order Rhynchocephalia (meaning "beak head") for the tuatara and its fossil relatives. Now, most authors prefer to use the more exclusive order name of Sphenodontia for the tuatara and its closest living relatives.
Many disparately related species were subsequently added to the Rhynchocephalia, resulting in what taxonomists call a "wastebasket taxon". Williston proposed the Sphenodontia to include only tuatara and their closest fossil relatives in 1925. Sphenodon is derived from the Greek for "wedge" (σφηνος/sphenos) and "tooth" (δόντι/odon(t)).
Tuatara have been referred to as living fossils, which means their group retains many basal characteristics from around the time of the squamate – rhynchocephalian split (220 MYA). However, taxonomic work on Sphenodontia has shown that this group has undergone a variety of changes throughout the Mesozoic, and a recent molecular study showed that their rate of molecular evolution is faster than of any other animal so far examined. Many of the niches occupied by lizards today were then held by sphenodontians. There was even a successful group of aquatic sphenodontians known as pleurosaurs, which differed markedly from living tuatara. Tuatara show cold weather adaptations that allow them to thrive on the islands of New Zealand; these adaptations may be unique to tuatara since their sphenodontian ancestors lived in the much warmer climates of the Mesozoic.
There are two extant species: Sphenodon punctatus and the much rarer Sphenodon guntheri, or Brothers Island tuatara, which is confined to North Brother Island in Cook Strait. The species name punctatus is Latin for "spotted", and guntheri refers to Albert Günther. S. punctatus was named when only one species was known, and its name is misleading, since both species can have spots. The Brother's Island tuatara (S. guntheri) has olive brown skin with yellowish patches, while the colour of the other species, (S. punctatus), ranges from olive green through grey to dark pink or brick red, often mottled, and always with white spots. In addition, S. guntheri is considerably smaller. A third, extinct species of Sphenodon was identified in November 1885 by William Colenso, who was sent an incomplete sub-fossil specimen from a local coal mine. Colenso named the new species S. diversum. Sphenodon punctatus is further divided into two subspecies: the Cook Strait tuatara (unnamed subspecies), which lives on other islands in and near Cook Strait, and the northern tuatara (Sphenodon punctatus punctatus), which lives on the Bay of Plenty, and some islands further north. A 2009 paper reexamined the genetic bases used to distinguish the two species of tuatara, and concluded that they only represent geographic variants, and only one species should be recognized.
The tuatara is considered the most unspecialised living amniote; the brain and mode of locomotion resemble that of amphibians and the heart is more primitive than that of any other reptile. Their lungs have a single chamber and lack bronchi. Both species are sexually dimorphic, males being larger. Adult S. punctatus males measure 61 cm (24 in) in length and females 45 cm (18 in). The San Diego Zoo even cites a length of up to 80 cm (31 in). Males weigh up to 1 kg (2.2 lb), and females up to 0.5 kg (1.1 lb). Brother's Island tuatara are slightly smaller, weighing up to 660 g (1.3 lb).
The tuatara's greenish brown colour matches its environment, and can change over its lifetime. Tuatara shed their skin at least once per year as adults, and three or four times a year as juveniles. Tuatara sexes differ in more than size. The spiny crest on a tuatara's back, made of triangular soft folds of skin, is larger in males, and can be stiffened for display. The male abdomen is narrower than the female's.
In the course of evolution, the skull has been modified in most diapsids from the original version evident in the fossil record. However, all the original features are preserved in that of the tuatara; it has two openings (temporal fenestra) on each side of the skull, with complete arches. In addition, the upper jaw is firmly attached to the skull. This makes for a very rigid, inflexible construction. Testudines (turtle and tortoise) skulls, which lack any temporal fenestra (anapsid condition), are sometimes considered to be the most primitive among amniotes, though there is strong evidence they may have lost the temporal holes rather than never having had them.
The tip of the upper jaw is beak-like and separated from the remainder of the jaw by a notch. There is a single row of teeth in the lower jaw and a double row in the upper, with the bottom row fitting perfectly between the two upper rows when the mouth is closed. This specific tooth arrangement is not seen in any other reptile; although most snakes have a double row of teeth in their upper jaw, their arrangement and function is different from the tuatara's. The jaws, joined by ligament, chew with backwards and forwards movements combined with a shearing up and down action. The force of the bite is suitable for shearing chitin and bone. The tuatara's teeth are not replaced, since they are not separate structures like real teeth, but sharp projections of the jaw bone. As their teeth wear down, older tuatara have to switch to softer prey such as earthworms, larvae, and slugs, and eventually have to chew their food between smooth jaw bones. The brain of Sphenodon fills only half of the volume of its endocranium. This proportion has been used by paleontologists trying to estimate the volume of dinosaur brains based on fossils. The use of tuataras as a model animal for dinosaur brain volume has been criticized because since bird brains occupy a greater portion of their skulls, and dinosaurs are the ancestors of birds, at least some dinosaurs must have had volumes intermediate between the two.
The eyes can focus independently, and are specialized with a duplex retina that contains two types of visual cells for both day and night vision, and a tapetum lucidum which reflects on to the retina to enhance vision in the dark. There is also a third eyelid on each eye, the nictitating membrane.
The tuatara has a third eye on the top of its head called the parietal eye. It has its own lens, cornea, retina with rod-like structures, and degenerated nerve connection to the brain, suggesting it evolved from a real eye. The parietal eye is only visible in hatchlings, which have a translucent patch at the top centre of the skull. After four to six months it becomes covered with opaque scales and pigment. Its purpose is unknown, but it may be useful in absorbing ultraviolet rays to manufacture vitamin D, as well as to determine light/dark cycles, and help with thermoregulation. Of all extant tetrapods, the parietal eye is most pronounced in the tuatara. The parietal eye is part of the pineal complex, another part of which is the pineal gland, which in tuatara secretes melatonin at night. It has been shown that some salamanders use their pineal body to perceive polarised light, and thus determine the position of the sun, even under cloud cover, aiding navigation.
Together with turtles, the tuatara has the most primitive hearing organs among the amniotes. There is no eardrum and no earhole, and the middle ear cavity is filled with loose tissue, mostly adipose (fatty) tissue. The stapes comes into contact with the quadrate (which is immovable) as well as the hyoid and squamosal. The hair cells are unspecialized, innervated by both afferent and efferent nerve fibres, and respond only to low frequencies. Even though the hearing organs are poorly developed and primitive with no visible external ears, they can still show a frequency response from 100–800 Hz, with peak sensitivity of 40 dB at 200 Hz.
Spine and ribs
The tuatara spine is made up of hourglass-shaped amphicoelous vertebrae, concave both before and behind. This is the usual condition of fish vertebrae and some amphibians, but is unique to tuatara within the amniotes.
The tuatara has gastralia, rib-like bones also called gastric or abdominal ribs, the presumed ancestral trait of diapsids. They are found in some lizards, where they are mostly made of cartilage, as well as crocodiles and the tuatara, and are not attached to the spine or thoracic ribs. The true ribs are small projections, with small, hooked bones, called uncinate processes, found on the rear of each rib. This feature is also present in birds. The tuatara is the only living tetrapod with well-developed gastralia and uncinate processes.
In the early tetrapods, the gastralia and ribs with uncinate processes, together with bony elements such as bony plates in the skin (osteoderms) and clavicles (collar bone), would have formed a sort of exo-skeleton around the body, protecting the belly and helped to hold in the guts and inner organs. These anatomical details most likely evolved from structures involved in locomotion even before the vertebrates ventured onto land. The gastralia may have been involved in the breathing process in early amphibians and reptiles. The pelvis and shoulder girdles are arranged differently to those of lizards, as is the case with other parts of the internal anatomy and its scales.
Tail and back
The spiny plates on the back and tail of the tuatara resemble those of a crocodile more than a lizard, but has the latter reptile's ability to break off its tail when caught by a predator, and then regenerate it. The tail and back are covered with spiny plates that, too, resemble modern crocodiles more than they do those of a lizard.
Adult tuatara are terrestrial and nocturnal reptiles, though they will often bask in the sun to warm their bodies. Hatchlings hide under logs and stones, and are diurnal, likely because adults are cannibalistic. Tuatara thrive in temperatures much lower than those tolerated by most reptiles, and hibernate during winter. They remain active at temperatures as low as 5 °C (41 °F), while temperatures over 28 °C (82 °F) are generally fatal. The optimal body temperature for the tuatara is from 16 to 21 °C (61 to 70 °F), the lowest of any reptile. The body temperature of tuatara is lower than that of other reptiles ranging from 5.2–11.2 °C (41–52 °F) over a day, whereas most reptiles have body temperatures around 20 °C (68 °F). The low body temperature results in a slower metabolism.
Burrowing seabirds such as petrels, prions, and shearwaters share the tuatara's island habitat during the bird's nesting season. The tuatara use the bird's burrows for shelter when available, or dig their own. The seabirds' guano helps to maintain invertebrate populations that tuatara predominantly prey on; including beetles, crickets, and spiders. Their diet also consists of frogs, lizards, and bird's eggs and chicks. The eggs and young of seabirds that are seasonally available as food for tuatara may provide beneficial fatty acids. Tuatara of both sexes defend territories, and will threaten and eventually bite intruders. The bite can cause serious injury. Tuatara will bite when approached, and will not let go easily.
Tuatara reproduce very slowly, taking ten to twenty years to reach sexual maturity. Mating occurs in midsummer; females mate and lay eggs once every four years. During courtship, a male makes his skin darker, raises his crests, and parades toward the female. He slowly walks in circles around the female with stiffened legs. The female will either submit, and allow the male to mount her, or retreat to her burrow. Males do not have a penis; they reproduce by the male lifting the tail of the female and placing his vent over hers. The sperm is then transferred into the female, much like the mating process in birds.
Tuatara eggs have a soft, parchment-like shell. It takes the females between one and three years to provide eggs with yolk, and up to seven months to form the shell. It then takes between 12 and 15 months from copulation to hatching. This means reproduction occurs at two- to five-year intervals, the slowest in any reptile. Wild tuatara are known to be still reproducing at about 60 years of age—"Henry", a 111-year-old tuatara at Southland Museum in Invercargill, New Zealand, became a father (possibly for the first time) on 23 January 2009.
The sex of a hatchling depends on the temperature of the egg, with warmer eggs tending to produce male tuatara, and cooler eggs producing females. Eggs incubated at 21 °C (70 °F) have an equal chance of being male or female. However, at 22 °C (72 °F), 80% are likely to be males, and at 20 °C (68 °F), 80% are likely to be females; at 18 °C (64 °F) all hatchlings will be females. There is some evidence that sex determination in tuatara is determined by both genetic and environmental factors.
Tuatara probably have the slowest growth rates of any reptile, continuing to grow larger for the first 35 years of their lives. The average lifespan is about 60 years, but they can live to be well over 100 years old. Some experts believe that captive tuatara could live as long as 200 years.
Distribution and threats
Tuatara were long confined to 32 offshore islands free of mammals. The islands are difficult to get to, and are colonised by few animal species, indicating that some animals absent from these islands may have caused tuatara to disappear from the mainland. However, kiore (Polynesian rats) had recently established on several of the islands, and tuatara were persisting, but not breeding, on these islands. Additionally, tuatara were much rarer on the rat-inhabited islands.
The recent discovery of a tuatara hatchling on the New Zealand mainland indicates that attempts to reestablish a breeding population on the mainland have had some success. The total population of tuatara of all species and subspecies is estimated to be greater than 60,000, but less than 100,000.
Eradication of rats
Tuatara were removed from Stanley, Red Mercury and Cuvier Islands in 1990 and 1991, and maintained in captivity to allow Polynesian rats to be eradicated on those islands. All three populations bred in captivity, and after successful eradication of the rats, all individuals including the new juveniles were returned to their islands of origin. In the 1991–92 season, Little Barrier Island was found to hold only eight tuatara, which were taken into in situ captivity, where females produced 42 eggs, which were incubated at Victoria University. The resulting offspring were subsequently held in an enclosure on the island, then released into the wild in 2006 after rats were eradicated there.
In the Hen and Chicken Islands, Pacific rats were eradicated on Whatupuke in 1993, Lady Alice Island in 1994, and Coppermine Island in 1997. Following this program, juveniles have once again been seen on the latter three islands. In contrast, rats persist on Hen Island of the same group, and no juvenile tuatara had been seen there as of 2001. In the Alderman Islands, Middle Chain Island holds no tuatara, but it is considered possible for rats to swim between Middle Chain and other islands that do hold tuatara, and the rats were eradicated in 1992 to prevent this. Another rodent eradication was carried out on the Rangitoto Islands east of D’Urville Island, to prepare for the release of 432 Cook Strait tuatara juveniles in 2004, which were being raised at Victoria University as of 2001.
Brothers Island tuatara
Sphenodon guntheri is present naturally on one small island with a population of approximately 400. In 1995, 50 juvenile and 18 adult Brothers Island tuatara were moved to Titi Island in Cook Strait, and their establishment monitored. Two years later, more than half of the animals had been re-sighted and all but one had gained weight. In 1998, 34 juveniles from captive breeding and 20 wild caught adults were similarly transferred to Matiu/Somes Island, a more publicly accessible location within Wellington Harbour. The captive juveniles were from induced layings from wild females.
In late October 2007, it was announced that 50 tuatara collected as eggs from North Brother Island and hatched at Victoria University were being released onto Long Island in the outer Marlborough Sounds. The animals had been cared for at Wellington Zoo for the last five years and have been kept in secret in a specially built enclosure at the zoo, off display.
Sphenodon punctatus naturally occurs on 29 islands and its population is estimated to be over 60,000 individuals. In 1996, 32 adult northern tuatara were moved from Moutoki Island to Moutohora. The carrying capacity of Moutohora is estimated at 8500 individuals, and the island could allow public viewing of wild tuatara. In 2003, sixty northern tuatara were introduced to Tiritiri Matangi Island from Middle Island in the Mercury group. They are occasionally seen sunbathing by visitors to the island.
A mainland release of S. punctatus occurred in 2005 in the heavily fenced and monitored Karori Sanctuary. The second mainland release took place in October 2007, when a further 130 were transferred from Stephens Island to the Karori Sanctuary. In early 2009 the first recorded wild-born offspring were observed.
There are several tuatara breeding programmes within New Zealand. Southland Museum and Art Gallery in Invercargill, was the first to have a tuatara breeding programme; they breed Sphenodon punctatus. Hamilton Zoo, Auckland Zoo and Wellington Zoo also breed tuatara for release into the wild. The Victoria University of Wellington maintains a research programme into the captive breeding of tuatara, and the Pukaha Mount Bruce Wildlife Centre keeps a pair and a juvenile. The WildNZ Trust has a tuatara breeding enclosure at Ruawai. On 28 January 2009, the 11th of 11 eggs belonging to tuataras Henry and Mildred hatched. This rare occurrence came after Henry had surgery to remove a cancerous tumor that was inhibiting both his ability and desire to breed.
Tuatara feature in a number of indigenous legends, and are held as ariki (God forms). Tuatara are regarded as the messengers of Whiro, the god of death and disaster, and Māori women are forbidden to eat them. Tuatara also indicate tapu (the borders of what is sacred and restricted), beyond which there is mana, meaning there could be serious consequences if that boundary is crossed. Māori women would sometimes tattoo images of lizards, some of which may represent tuatara, near their genitals. Today, tuatara are regarded as a taonga (special treasure).
The tuatara was featured on one side of the New Zealand 5 cent coin, which was phased out in October 2006. Tuatara was also the name of the Journal of the Biological Society of Victoria University College and subsequently Victoria University of Wellington, published from 1947 until 1993. It has now been digitised by the New Zealand Electronic Text Centre, also at Victoria.
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