Tuatara

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Tuatara
Temporal range: Early
Ma
[1]
Northern tuatara (Sphenodon punctatus punctatus)

Least Concern  (IUCN 3.1),[2][3]

Relict (NZ TCS)[4]
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Rhynchocephalia
Family: Sphenodontidae
Genus: Sphenodon
Gray, 1831 (conserved name)
Species:
S. punctatus
Binomial name
Sphenodon punctatus
(Gray, 1842) (conserved name)
Native range (New Zealand)
Current distribution of tuatara (in black):[5][6][7] Circles represent the North Island tuatara, and squares the Brothers Island tuatara. Symbols may represent up to seven islands.
Synonyms
  • Sphaenodon
    (Gray, 1831) (rejected name)
  • Hatteria
    (Gray, 1842) (rejected name)
  • Rhynchocephalus
    (Owen, 1845) (rejected name)

The tuatara (Sphenodon punctatus) is a species of reptile endemic to New Zealand. Despite its close resemblance to lizards, it is part of a distinct lineage, the order Rhynchocephalia.[8] The name tuatara is derived from the Māori language and means "peaks on the back".[9]

The single extant species of tuatara is the only surviving member of its order, which was highly diverse during the Mesozoic era.[10] Rhynchocephalians first appeared in the fossil record during the Triassic, around 240 million years ago,[11] and reached worldwide distribution and peak diversity during the Jurassic, when they represented the worlds dominant group of small reptiles. Rhynchocephalians underwent a great decline during the Cretaceous with their youngest records outside New Zealand dating to the Paleocene. Their closest living relatives are squamates (lizards and snakes). Tuatara are of interest for studying the evolution of reptiles.

Tuatara are greenish brown and grey, and measure up to 80 cm (31 in) from head to tail-tip and weigh up to 1.3 kg (2.9 lb)[12] with a spiny crest along the back, especially pronounced in males. They have two rows of teeth in the upper jaw overlapping one row on the lower jaw, which is unique among living species. They are able to hear, although no external ear is present, and have unique features in their skeleton.

Tuatara are sometimes referred to as "

DNA sequence, nearly twice that of humans.[14]

The tuatara (Sphenodon punctatus) has been protected by law since 1895.

Karori Wildlife Sanctuary (now named "Zealandia") in 2005.[20]

During routine maintenance work at Zealandia in late 2008, a tuatara nest was uncovered,[21] with a hatchling found the following autumn.[22] This is thought to be the first case of tuatara successfully breeding in the wild on New Zealand's North Island in over 200 years.[21]

Taxonomy and evolution

Relationships of the tuatara to other living reptiles and birds, after Simões et al. 2022[23]

Reptilia
Lepidosauria

Squamata (lizards and snakes)

Rhynchocephalia (tuatara)

Archelosauria

Testudines
(turtles, including tortoises)

Archosauria

Crocodilia (crocodilians)

Aves
(birds)


Tuatara, along with other now-extinct members of the order Rhynchocephalia, belong to the superorder Lepidosauria, the only surviving taxon within Lepidosauromorpha along with the order Squamata, which includes lizards and snakes. Squamates and tuatara both show caudal autotomy (loss of the tail-tip when threatened), and have transverse cloacal slits.[24]

Tuatara were originally classified as lizards in 1831 when the

A.C.L.G. 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.[26]

At one point many disparately related species were incorrectly referred to the Rhynchocephalia, resulting in what taxonomists call a "wastebasket taxon".[27] Williston proposed the Sphenodontia to include only tuatara and their closest fossil relatives in 1925.[27] However, Rhynchocephalia is the older name[26] and in widespread use today. Sphenodon is derived from the Greek for "wedge" (σφήν, σφηνός/sphenos) and "tooth" (ὀδούς, ὀδόντος/odontos).[28] Many scholars use Sphenodontia as a subset of Rhynchocephalia, including almost all members of Rhynchocephalia aside from the most primitive representatives of the group.[29]

The earliest rhynchocephalian,

Sphenodontinae, the clade which includes the tuatara, are known from the Early Jurassic of North America. The earliest representatives of this group are already very similar to the modern tuatara.[31] Rhynchocephalians underwent a great decline during the Cretaceous period,[32] possibly due to competition with mammals and lizards,[33] with their youngest record outside of New Zealand being of Kawasphenodon known from the Paleocene of Patagonia in South America.[34]

A species of sphenodontine is known from the

Saint Bathans Fauna. Whether it is referable to Sphenodon proper is not entirely clear, but is likely to be closely related to tuatara. The ancestors of the tuatara were likely already present in New Zealand prior to its separation from Antarctica around 82-60 million years ago.[33]


Cladogram of the position of the tuatara within Sphenodontia, after Simoes et al., 2022:[35]

Species

While there is currently considered to be only one living species of tuatara, two species were previously identified: Sphenodon punctatus, or northern tuatara, and the much rarer Sphenodon guntheri, or Brothers Island tuatara, which is confined to

Latin for "spotted",[37] and guntheri refers to German-born British herpetologist Albert Günther.[38] A 2009 paper re-examined the genetic bases used to distinguish the two supposed species of tuatara, and concluded they only represent geographic variants, and only one species should be recognized.[18] Consequently, the northern tuatara was re-classified as Sphenodon punctatus punctatus and the Brothers Island tuatara as Sphenodon punctatus guntheri. Individuals from Brothers Island could also not be distinguished from other modern and fossil samples based on jaw morphology.[39]

The Brothers Island tuatara has olive brown skin with yellowish patches, while the colour of the northern tuatara ranges from olive green through grey to dark pink or brick red, often mottled, and always with white spots.

subfossil specimen from a local coal mine. Colenso named the new species S. diversum.[42] Fawcett and Smith (1970) consider it a synonymous to the subspecies level based on a lack of distinction.[43]

Description

Size comparison of male S. punctatus and human
Skeleton of the tuatara


Tuatara are the largest reptile in New Zealand.[44] Adult S. punctatus males measure 61 cm (24 in) in length and females 45 cm (18 in).[24] Tuatara are sexually dimorphic, males being larger.[24] The San Diego Zoo even cites a length of up to 80 cm (31 in).[45] Males weigh up to 1 kg (2.2 lb), and females up to 0.5 kg (1.1 lb).[24] Brother's Island tuatara are slightly smaller, weighing up to 660 g (1.3 lb).[41]

Their lungs have a single chamber with no

bronchi.[46]

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,[40] 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.[47]

Skull

Skull diagram in top down and side-on views

Unlike the vast majority of lizards, the tuatara has a complete lower temporal bar closing the lower

Sphenodontinae, rather than a primitive trait retained from early diapsids. The complete bar is thought to stabilise the skull during biting.[48]

The tip of the upper jaw is chisel-or beak-like and separated from the remainder of the jaw by a notch,[26] this structure is formed from fused premaxillary teeth, and is also found in many other advanced rhynchocephalians.[49] The teeth of the tuatara, and almost all other rhynchocephalians, are described as acrodont, as they are attached to the apex of the jaw bone. This contrast with the pleurodont condition found in the vast majority of lizards, where the teeth are attached to the inward-facing surface of the jaw. The teeth of the tuatara are extensively fused to the jawbone, making the boundary between the tooth and jaw difficult to discern, and the teeth lack roots and are not replaced during the lifetime of the animal, unlike those of pleurodont lizards.[50] It is a common misconception that tuatara lack teeth and instead have sharp projections on the jaw bone,[51] though histology shows that they have true teeth with enamel and dentine with pulp cavities.[52] 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.[53]

The tuatara possesses palatal dentition (teeth growing from the bones of the roof of the mouth), which is ancestrally present in reptiles (and tetrapods generally).[54] While many of the original palatal teeth present in reptiles have been lost,[54] like all other known rhynchocephalians, the row of teeth growing from the palatine bones have been enlarged, and like other members of Sphenodontinae the palatine teeth are orientated parallel to the teeth in the maxilla, and during biting the teeth of the lower jaw slot between the two upper tooth rows.[55] The structure of the jaw joint allows the lower jaw to slide forwards after it has closed between the two upper rows of teeth.[56] This mechanism allows the jaws to shear through chitin and bone.[24]

The brain of Sphenodon fills only half of the volume of its endocranium.[57] This proportion has actually been used by paleontologists trying to estimate the volume of dinosaur brains based on fossils.[57] However, the proportion of the tuatara endocranium occupied by its brain may not be a very good guide to the same proportion in Mesozoic dinosaurs since modern birds are surviving dinosaurs but have brains which occupy a much greater relative volume in the endocranium.[57]

Sensory organs

Close-up of a tuatara's head

Eyes

The eyes can

colour vision, possibly even at low light levels.[59]

Parietal eye (third eye)

Like some other living vertebrates, including some lizards, the tuatara has a third eye on the top of its head called the parietal eye (also called a pineal or third eye) formed by the parapineal organ, with an accompanying opening in the skull roof called the pineal or parietal foramen, enclosed by the parietal bones.[60] It has its own lens, a parietal plug which resembles a cornea,[61] retina with rod-like structures, and degenerated nerve connection to the brain. The parietal eye is visible only 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.[24] It likely serves to regulate the circadian rhythm and possibly detect seasonal changes, and help with thermoregulation.[24][60]

Of all extant tetrapods, the parietal eye is most pronounced in the tuatara. It is part of the pineal complex, another part of which is the pineal gland, which in tuatara secretes melatonin at night.[24] Some salamanders have been shown to use their pineal bodies to perceive polarised light, and thus determine the position of the sun, even under cloud cover, aiding navigation.[62]

Hearing

Together with

efferent nerve fibres, and respond only to low frequencies. Though the hearing organs are poorly developed and primitive with no visible external ears, they can still show a frequency response from 100 to 800 Hz, with peak sensitivity of 40 dB at 200 Hz.[63]

Odorant receptors

Animals that depend on the sense of smell to capture prey, escape from predators or simply interact with the environment they inhabit, usually have many odorant receptors. These receptors are expressed in the dendritic membranes of the neurons for the detection of odours. The tuatara has several hundred receptors, around 472, a number more similar to what birds have than to the large number of receptors that turtles and crocodiles may have.[59]

Spine and ribs

The tuatara spine is made up of hourglass-shaped amphicoelous vertebrae, concave both before and behind.[51] This is the usual condition of fish vertebrae and some amphibians, but is unique to tuatara within the amniotes. The vertebral bodies have a tiny hole through which a constricted remnant of the notochord passes; this was typical in early fossil reptiles, but lost in most other amniotes.[64]

The tuatara has

gastralia, rib-like bones also called gastric or abdominal ribs,[65] 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.[51] 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 exoskeleton around the body, protecting the belly and helping 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 from those of lizards, as is the case with other parts of the internal anatomy and its scales.[66]

Tail and back

The spiny plates on the back and tail of the tuatara resemble those of a crocodile more than a lizard, but the tuatara shares with lizards the ability to break off its tail when caught by a predator, and then regenerate it. The regrowth takes a long time and differs from that of lizards. Well illustrated reports on tail regeneration in tuatara have been published by Alibardi and Meyer-Rochow.[67][68] The cloacal glands of tuatara have a unique organic compound named tuataric acid.

Age determination

Currently, there are two means of determining the age of tuatara. Using microscopic inspection, hematoxylinophilic rings can be identified and counted in both the phalanges and the femur. Phalangeal hematoxylinophilic rings can be used for tuatara up to ages 12–14 years, as they cease to form around this age. Femoral rings follow a similar trend, however they are useful for tuatara up to ages 25–35 years. Around that age, femoral rings cease to form.[69] Further research on age determination methods for tuatara is required, as tuatara have lifespans much longer than 35 years (ages up to 60[9] are common, and captive tuatara have lived to over 100 years).[70][71][72] One possibility could be via examination of tooth wear, as tuatara have fused sets of teeth.

Physiology

West Coast

Adult tuatara are

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. Juveniles are typically active at night, but can be found active during the day. The juveniles' movement pattern is attributed to genetic hardwire of conspecifics for predator avoidance and thermal restrictions.[73] Tuatara thrive in temperatures much lower than those tolerated by most reptiles, and hibernate during winter.[74] They remain active at temperatures as low as 5 °C (41 °F),[75] 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.[76] The body temperature of tuatara is lower than that of other reptiles, ranging from 5.2–11.2 °C (41.4–52.2 °F) over a day, whereas most reptiles have body temperatures around 20 °C (68 °F).[77] The low body temperature results in a slower metabolism
.

Ecology

Burrowing seabirds such as

lux.[81] The eggs and young of seabirds that are seasonally available as food for tuatara may provide beneficial fatty acids.[24] Tuatara of both sexes defend territories, and will threaten and eventually bite intruders. The bite can cause serious injury.[82] Tuatara will bite when approached, and will not let go easily.[83]

Tuataras are parasitised by the

tuatara tick (Archaeocroton sphenodonti), a tick that directly depends on tuataras.[84]

Reproduction

A male tuatara named Henry, living at the Southland Museum and Art Gallery, is still reproductively active at 111 years of age.[70]
Tuatara juvenile (Sphenodon punctatus)

Tuatara reproduce very slowly, taking 10 to 20 years to reach sexual maturity.

eggs once every four years.[87] 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 allow the male to mount her, or retreat to her burrow.[88] Males do not have a penis; they have rudimentary hemipenes; meaning that intromittent organs are used to deliver sperm to the female during copulation. They reproduce by the male lifting the tail of the female and placing his vent over hers. This process is sometimes referred to as a "cloacal kiss". The sperm is then transferred into the female, much like the mating process in birds.[89] Along with birds, the tuatara is one of the few members of amniota to have lost the ancestral penis.[90]

Tuatara eggs have a soft, parchment-like 0.2 mm thick shell that consists of calcite crystals embedded in a matrix of fibrous layers.[91] 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.[24] Survival of embryos has also been linked to having more success in moist conditions.[92] Wild tuatara are known to be still reproducing at about 60 years of age; "Henry", a male tuatara at Southland Museum in Invercargill, New Zealand, became a father (possibly for the first time) on 23 January 2009, at age 111, with an 80 year-old female.[71][72][70]

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.[9] Some evidence indicates sex determination in tuatara is determined by both genetic and environmental factors.[93]

Tuatara probably have the slowest growth rates of any reptile,

tRNA genes. In humans, selenoproteins have a function of antioxidation, redox regulation and synthesis of thyroid hormones. It is not fully demonstrated, but these genes may be related to the longevity of this animal or may have emerged as a result of the low levels of selenium and other trace elements in the New Zealand terrestrial systems.[59]

Genomic characteristics

The most abundant LINE element in the tuatara is L2 (10%). Most of them are interspersed and can remain active. The longest L2 element found is 4 kb long and 83% of the sequences had ORF2p completely intact. The CR1 element is the second most repeated (4%). Phylogenetic analysis shows that these sequences are very different from those found in other nearby species such as lizards. Finally, less than 1% are elements belonging to L1, a low percentage since these elements tend to predominate in placental mammals.[59] Usually, the predominant LINE elements are the CR1, contrary to what has been seen in the tuatara. This suggests that perhaps the genome repeats of sauropsids were very different compared to mammals, birds and lizards.[59]

The genes of the major histocompatibility complex (MHC) are known to play roles in disease resistance, mate choice, and kin recognition in various vertebrate species. Among known vertebrate genomes, MHCs are considered one of the most polymorphic.[95][96] In the tuatara, 56 MHC genes have been identified; some of which are similar to MHCs of amphibians and mammals. Most MHCs that were annotated in the tuatara genome are highly conserved, however there is large genomic rearrangement observed in distant lepidosauria lineages.[59]

Many of the elements that have been analyzed are present in all amniotes, most are mammalian interspersed repeats or MIR, specifically the diversity of MIR subfamilies is the highest that has been studied so far in an amniote. 16 families of SINEs that were recently active have also been identified.[59]

The tuatara has 24 unique families of DNA transposons, and at least 30 subfamilies were recently active. This diversity is greater than what has been found in other amniotes and in addition, thousands of identical copies of these transposons have been analyzed, suggesting to researchers that there is recent activity.[59]

Around 7,500 

Spumavirus.[59]

More than 8,000 non-coding RNA-related elements have been identified in the tuatara genome, of which the vast majority, about 6,900, are derived from recently active transposable elements. The rest are related to ribosomal, spliceosomal and signal recognition particle RNA.[59]

The mitochondrial genome of the genus Sphenodon is approximately 18,000 bp in size and consists of 13 protein-coding genes, 2 ribosomal RNA and 22 transfer RNA genes.[59]

DNA methylation is a very common modification in animals and the distribution of CpG sites within genomes affects this methylation. Specifically, 81% of these CpG sites have been found to be methylated in the tuatara genome. Recent publications propose that this high level of methylation may be due to the amount of repeating elements that exist in the genome of this animal. This pattern is closer to what occurs in organisms such as zebrafish, about 78%, while in humans it is only 70%.[59]

Conservation

Tuatara are absolutely protected under New Zealand's

Convention on International Trade in Endangered Species (CITES) meaning commercial international trade in wild sourced specimens is prohibited and all other international trade (including in parts and derivatives) is regulated by the CITES permit system.[98]

Distribution and threats

Tuatara were once widespread on New Zealand's main North and South Islands, where

subfossil remains have been found in sand dunes, caves, and Māori middens.[99] Wiped out from the main islands before European settlement, they were long confined to 32 offshore islands free of mammals.[19] The islands are difficult to get to,[100] 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 become established on several of the islands, and tuatara were persisting, but not breeding, on these islands.[101][102] Additionally, tuatara were much rarer on the rat-inhabited islands.[102] Prior to conservation work, 25% of the distinct tuatara populations had become extinct in the past century.[5]

The recent discovery of a tuatara hatchling on the mainland indicates that attempts to re-establish a breeding population on the New Zealand mainland have had some success.[103] The total population of tuatara is estimated to be between 60,000[24] and 100,000.[104]

Climate change

Tuatara have temperature-dependent sex determination meaning that the temperature of the egg determines the sex of the animal. For tuatara, lower egg incubation temperatures lead to females while higher temperatures lead to males. Since global temperatures are increasing, climate change may be skewing the male to female ratio of tuatara. Current solutions to this potential future threat are the selective removal of adults and the incubation of eggs.[105][106]

Eradication of rats

Tuatara were removed from

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.[107]

In the

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.[6]

Brothers Island tuatara

Sphenodon punctatus 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

Matiu/Somes Island, a more publicly accessible location in Wellington Harbour. The captive juveniles were from induced layings from wild females.[6]

In late October 2007, 50 tuatara collected as eggs from North Brother Island and hatched at

Long Island in the outer Marlborough Sounds. The animals had been cared for at Wellington Zoo for the previous five years and had been kept in secret in a specially built enclosure at the zoo, off display.[108]

There is another out of country population of Brothers Island tuatara that was given to the

San Diego Zoological Society and is housed off-display at the San Diego Zoo facility in Balboa.[109]
No successful reproductive efforts have been reported yet.

Northern tuatara

S. punctatus punctatus naturally occurs on 29 islands, and its population is estimated to be over 60,000 individuals.

Moutoki Island to Moutohora. The carrying capacity of Moutohora is estimated at 8,500 individuals, and the island could allow public viewing of wild tuatara.[6] In 2003, 60 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.[110][111]

Karori Sanctuary
are given coloured markings on the head for identification.

A mainland release of S.p. punctatus occurred in 2005 in the heavily fenced and monitored

Stephens Island to the Karori Sanctuary.[112] In early 2009, the first recorded wild-born offspring were observed.[113]

Captive breeding

The first successful breeding of tuatara in captivity is believed to have achieved by Sir Algernon Thomas at either his University offices or residence in Symonds Street in the late 1880s or his new home, Trewithiel, in Mount Eden in the early 1890s.[citation needed]

Several tuatara breeding programmes are active in New Zealand.

Southland Museum and Art Gallery in Invercargill was the first institution to have a tuatara breeding programme; starting in 1986 they bred S. punctatus and have focused on S. guntheri more recently.[114]

Hamilton Zoo, Auckland Zoo and Wellington Zoo also breed tuatara for release into the wild. At Auckland Zoo in the 1990s it was discovered that tuatara have temperature-dependent sex determination. The Victoria University of Wellington maintains a research programme into the captive breeding of tuatara, and the Pūkaha / Mount Bruce National Wildlife Centre keeps a pair and a juvenile.[citation needed]

The WildNZ Trust has a tuatara breeding enclosure at Ruawai. One notable captive breeding success story took place in January 2009, when all 11 eggs belonging to 110 year-old tuatara Henry and 80 year-old tuatara Mildred hatched. This story is especially remarkable as Henry required surgery to remove a cancerous tumour in order to successfully breed.[94]

In January 2016, Chester Zoo, England, announced that they succeeded in breeding the tuatara in captivity for the first time outside its homeland.[115]

Cultural significance

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.[116] Tuatara also indicate tapu (the borders of what is sacred and restricted),[117] beyond which there is mana, meaning there could be serious consequences if that boundary is crossed.[117] Māori women would sometimes tattoo images of lizards, some of which may represent tuatara, near their genitals.[117] Today, tuatara are regarded as a taonga (special treasure) along with being viewed as the kaitiaki (guardian) of knowledge.[118][119]

The tuatara was featured on one side of the

New Zealand Electronic Text Centre, also at Victoria.[120]

In popular culture

See also

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Further reading

External links