Short-beaked echidna

Description

Short-beaked echidnas are typically 30 to 45 cm (12 to 18 in) in length, with 75 mm (3 in) of snout, and weigh between 2 and 7 kg (4.4 and 15.4 lb). However, the Tasmanian subspecies, T. a. setosus, is smaller than its Australian mainland counterparts. Because the neck is not externally visible, the head and body appear to merge. The earholes are on either side of the head, with no external pinnae. The eyes are small, about 9 mm (0.4 in) in diameter and at the base of the wedge-shaped snout. The nostrils and the mouth are at the distal end of the snout; the mouth cannot open wider than 5 mm (0.2 in). The body of the short-beaked echidna is, with the exception of the underside, face and legs, covered with cream-coloured spines. The spines, which may be up to 50 mm (2 in) long, are modified hairs, mostly made of keratin. Insulation is provided by fur between the spines, which ranges in colour from honey to a dark reddish-brown and even black; the underside and short tail are also covered in fur.

The echidna's fur may be infested with the flea, Bradiopsylla echidnae, which is about 4 mm (0.16 in) long.

The limbs of the short-beaked echidna are adapted for rapid digging; they are short and have strong claws. Their strong and stout limbs allow it to tear apart large logs and move paving stones, and one has been recorded moving a 13.5 kg (30 lb) stone; a scientist also reported that a captive echidna moved a refrigerator around the room in his home. The power of the limbs is based on strong musculature, particularly around the shoulder and torso areas. The mechanical advantage of its arm is greater than that of humans, as its biceps connects the shoulder to the forearm at a point further down than for humans, and the chunky humerus allows more muscle to form.

The claws on the hind feet are elongated and curved backward to enable cleaning and grooming between the spines. Like the platypus, the echidna has a low body temperature—between 30–32 °C (86–90 °F)—but, unlike the platypus, which shows no evidence of torpor or hibernation, the body temperature of the echidna may fall as low as 5 °C (41 °F). The echidna does not pant or sweat and normally seeks shelter in hot conditions. Despite their inability to sweat, echidnas still lose water as they exhale. The snout is believed to be crucial in restricting this loss to sustainable levels, through a bony labyrinth that has a refrigerator effect and helps to condense water vapour in the breath. The echidna does not have highly concentrated urine, and around half of the estimated daily water loss of 120 g (4.2 oz) occurs in this manner, while most of the rest is through the skin and respiratory system. Most of this is replenished by its substantial eating of termites—one laboratory study reported ingestion of around 147 g (5.2 oz) a day, most of which was water. This can be supplemented by drinking water, if available, or licking morning dew from flora.

In the Australian autumn and winter, the echidna enters periods of torpor or deep hibernation. Because of its low body temperature, it becomes sluggish in very hot and very cold weather.

Like all monotremes, it has one orifice, the cloaca, for the passage of faeces, urine and reproductive products. The male has internal testes, no external scrotum and a highly unusual penis with four knobs on the tip, which is nearly a quarter of his body length when erect. The gestating female develops a pouch on her underside, where she raises her young.

The musculature of the short-beaked echidna has a number of unusual aspects. The panniculus carnosus, an enormous muscle just beneath the skin, covers the entire body. By contraction of various parts of the panniculus carnosus, the short-beaked echidna can change shape, the most characteristic shape change being achieved by rolling itself into a ball when threatened, so protecting its belly and presenting a defensive array of sharp spines. It has one of the shortest spinal cords of any mammal, extending only as far as the thorax. Whereas the human spinal cord ends at the first or second lumbar vertebra, for the echidna it occurs at the seventh thoracic vertebra. The shorter spinal cord is thought to allow flexibility to enable wrapping into a ball.

The musculature of the face, jaw and tongue is specialised for feeding. The tongue is the animal's sole means of catching prey, and can protrude up to 180 mm (7 in) outside the snout. The snout's shape, resembling a double wedge, gives it a significant mechanical advantage in generating a large moment, so makes it efficient for digging to reach prey or to build a shelter. The tongue is sticky because of the presence of glycoprotein-rich mucus, which both lubricates movement in and out of the snout and helps to catch ants and termites, which adhere to it. The tongue is protruded by contracting circular muscles that change the shape of the tongue and force it forwards and contracting two genioglossal muscles attached to the caudal end of the tongue and to the mandible. The protruded tongue is stiffened by a rapid flow of blood, which allows it to penetrate wood and soil. Retraction requires the contraction of two internal longitudinal muscles, known as the sternoglossi. When the tongue is retracted, the prey is caught on backward-facing keratinous "teeth", located along the roof of the buccal cavity, allowing the animal both to capture and grind food. The tongue moves with great speed, and has been measured to move in and out of the snout 100 times a minute. This is partly achieved through the elasticity of the tongue and the conversion of elastic potential energy into kinetic energy. The tongue is very flexible, particularly at the end, allowing it to bend in U-turns and catch insects attempting to flee in their labyrinthine nests or mounds. The tongue also has an ability to avoid picking up splinters while foraging in logs; the factors behind this ability are unknown. It can eat quickly; a specimen of around 3 kg (6.6 lb) can ingest 200 g (7.1 oz) of termites in 10 minutes.

The echidna's stomach is quite different from other mammals. It is devoid of secretory glands and has a cornified stratified epithelium, which resembles horny skin. Unlike other mammals, which typically have highly acidic stomachs, the echidna has low levels of acidity, almost neutral, with pH in the 6.2–7.4 range. The stomach is elastic, and gastric peristalsis grinds soil particulates and shredded insects together. Digestion occurs in the small intestine, which is around 3.4 m (11 ft) in length. Insect exoskeletons and soil are not digested, being ejected in the waste.

Numerous physiological adaptations aid the lifestyle of the short-beaked echidna. Because the animal burrows, it must tolerate very high levels of carbon dioxide in inspired air, and will voluntarily remain in situations where carbon dioxide concentrations are high. It can dig up to a metre into the ground to retrieve ants or evade predators, and can survive with low oxygen when the area is engulfed by bushfires. The echidna can also dive underwater, which can help it to survive sudden floods. During these situations, the heart rate drops to around 12 beats per minute, around one-fifth of the rate at rest. This process is believed to save oxygen for the heart and brain, which are the most sensitive organs to such a shortage; laboratory testing has revealed the echidna's cardiovascular system is similar to that of the seal. Following the devastation of a bushfire, echidnas can compensate for the lack of food by reducing their daytime body temperature and activity through use of torpor, for a period of up to three weeks.

The echidna's optical system is an uncommon hybrid of both mammalian and reptilian characteristics. The cartilaginous layer beneath the sclera of the eyeball is similar to that of reptiles and avians. The small corneal surface is keratinised and hardened, possibly to protect it from chemicals secreted by prey insects or self-impalement when it rolls itself up, which has been observed. The echidna has the flattest lens of any animal, giving it the longest focal length. This similarity to primates and humans allows it to see distant objects clearly. Unlike placental mammals, including humans, the echidna does not have a ciliary muscle to distort the geometry of the lens and thereby change the focal length and allow objects at different distances to be viewed clearly; the whole eye is believed to distort, so the distance between the lens and retina instead changes to allow focusing. The visual ability of an echidna is not great, and it is not known whether it can perceive colour; however, it can distinguish between black and white, and horizontal and vertical stripes. Eyesight is not a crucial factor in the animal's ability to survive, as blind echidnas are able to live healthily.

Its ears are sensitive to low-frequency sound, which may be ideal for detecting sounds emitted by termites and ants underground. The pinnae are obscured and covered by hair, predators therefore cannot grab them in an attack, and prey or foreign material cannot enter, although ticks are known to reside there. The macula of the ear is very large compared to other animals, and is used as a gravity sensor to orient the echidna. The large size may be important for burrowing downwards.

The leathery snout is keratinised and covered in mechano- and thermoreceptors, which provide information about the surrounding environment. These nerves protrude through microscopic holes at the end of the snout, which also has mucous glands on the end that act as electroreceptors. Echidnas can detect electric fields of 1.8 mV/cm—1000 times more sensitive than humans—and dig up buried batteries. A series of push rods protrude from the snout. These are columns of flattened, spinous cells, with roughly an average diameter of 50 micrometres (0.0020 in) and a length of 300 micrometres (0.012 in). The number of push rods per square millimetre of skin is estimated to be 30 to 40. Longitudinal waves are believed to be picked up and transmitted through the rods, acting as mechanical sensors, to allow prey detection.

A well-developed olfactory system may be used to detect mates and prey. A highly sensitive optic nerve has been shown to have visual discrimination and spatial memory comparable to those of a rat. The brain and central nervous system have been extensively studied for evolutionary comparison with placental mammals, particularly with its fellow monotreme, the platypus. The average brain volume is 25 ml (0.88 imp fl oz; 0.85 US fl oz), similar to a cat of approximately the same size; while the platypus has a largely smooth brain, the echidna has a heavily folded and fissured, gyrencephalic brain similar to humans, which is seen as a sign of a highly neurologically advanced animal. The cerebral cortex is thinner, and the brain cells are larger and more densely packed and organised in the echidna than the platypus, suggesting evolutionary divergence must have occurred long ago. Almost half of the sensory area in the brain is devoted to the snout and tongue, and the part devoted to smell is relatively large compared to other animals.

The short-beaked echidna has the largest prefrontal cortex relative to body size of any mammal, taking up 50% of the volume in comparison to 29% for humans. This part of the brain in humans is thought to be used for planning and analytical behaviour, leading to debate as to whether the echidna has reasoning and strategising ability. Experiments in a simple maze and with a test on opening a trap door to access food, and the echidna's ability to remember what it has learnt for over a month, has led scientists to conclude its learning ability is similar to that of a cat or a rat.

The echidna shows rapid eye movement during sleep, usually around its thermoneutral temperature of 25 °C (77 °F), and this effect is suppressed at other temperatures. Its brain has been shown to contain a claustrum similar to that of placental mammals, linking this structure to their common ancestor.

Ecology and behaviour

No systematic study of the ecology of the short-beaked echidna has been published, but studies of several aspects of their ecological behaviour have been conducted. They live alone, and, apart from the burrow created for rearing young, they have no fixed shelter or nest site. They do not have a home territory they defend against other echidnas, but range over a wide area. The range area has been observed to be between 21–93 ha (52–230 acres), although one study in Kangaroo Island found the animals there covered an area between 9–192 ha (22–474 acres). Overall, the mean range areas across the various regions of Australia were 40–60 ha (99–148 acres). There was no correlation between sex and range area, but a weak one with size. Echidnas can share home ranges without incident, and sometimes share shelter sites if not enough are available for each animal to have one individually.

Short-beaked echidnas are typically active in the daytime, though they are ill-equipped to deal with heat because they have no sweat glands and do not pant. Therefore, in warm weather, they change their patterns of activity, becoming crepuscular or nocturnal. Body temperatures above 34 °C (93 °F) are believed to be fatal, and in addition to avoiding heat, the animal adjusts its circulation to maintain a sustainable temperature by moving blood to and from the skin to increase or lower heat loss. In areas where water is present, they can also swim to keep their body temperatures low. The "thermoneutral zone" for the environment is around 25 °C (77 °F), at which point the metabolism needed to maintain body temperature is minimised. The echidna is endothermic, and can maintain body temperatures of around 32 °C (90 °F). It can also reduce its metabolism and heart rate and body temperature.

In addition to brief and light bouts of torpor throughout the year, the echidna enters periods during the Australian winter when it hibernates, both in cold regions and in regions with more temperate climates. During hibernation, the body temperature drops to as low as 4 °C (39 °F). The heart rate falls to four to seven beats per minute—down from 50 to 68 at rest—and the echidna can breathe as infrequently as once every three minutes, 80 to 90% slower than when it is active. Metabolism can drop to one-eighth of the normal rate. Echidnas begin to prepare for hibernation between February and April, when they reduce their consumption and enter brief periods of torpor. Males begin hibernating first, while females that have reproduced start later. During periods of hibernation, the animals average 13 separate bouts of torpor, which are broken up by periods of arousal lasting 1.2 days on average. These interruptions tend to coincide with warmer periods. Males end their hibernation period in mid-June, while reproductive females return to full activity in July and August; nonreproductive females and immature echidnas may not end hibernation until two months later. During euthermia, the body temperature can vary by 4 °C per day. The metabolic rate is around 30% of that of placental mammals, making it the lowest energy-consuming mammal. This figure is similar to that of other animals that eat ants and termites; burrowing animals also tend to have low metabolism generally.

Echidnas hibernate even though it is seemingly unnecessary for survival; they begin their hibernation period while the weather is still warm, and food is generally always plentiful. One explanation is that echidnas maximize their foraging productivity by exercising caution with their energy reserves. Another hypothesis is that they are descended from ectothermic ancestors, but have taken to periodic endothermy for reproductive reasons, so that the young can develop more quickly. Supporters of this theory argue that males hibernate earlier than females because they finish their contribution to reproduction first, and they awake earlier to undergo spermatogenesis in preparation for mating, while females and young lag in their annual cycle. During the hibernation period, the animals stay in entirely covered shelter.

Short-beaked echidnas can live anywhere with a good supply of food, and regularly feast on ants and termites. They are believed to locate food by smell, using sensors in the tips of their snouts, by shuffling around seemingly arbitrarily, and using their snout in a probing manner. A study of echidnas in New England (New South Wales) has shown that they tend to dig up scarab beetle larvae in spring when the prey are active, but eschew this prey when it is inactive, leading to the conjecture that echidnas detect prey using hearing. Vision is not believed to be significant in hunting, as blind animals have been observed to survive in the wild.

Echidnas use their strong claws to pull apart nests and rotting logs to gain access to their prey. They avoid ants and termites that secrete repulsive liquids, and have a preference for the eggs, pupae and winged phases of the insects. Echidnas hunt most vigorously towards the end of the southern winter and early in spring, when their fat reserves have been depleted after hibernation and nursing. At this time, ants have high body fat, and the echidna targets their mounds. The animal also hunts beetles and earthworms, providing they are small enough to fit in a 5 mm (0.20 in) gap. The proportion of ants and termites in their diets depends on the availability of prey, and termites make up a larger part in drier areas where they are more plentiful. However, termites are preferred, if available, as their bodies contain a smaller proportion of indigestible exoskeleton. Termites from the Rhinotermitidae family are avoided due to their chemical defences. Scarab beetle larvae are also a large part of the diet when and where available. In the New England study, 37% of the food intake consisted of beetle larvae, although the echidna had to squash the prey in its snout as it ingested it, due to size.

Echidnas are powerful diggers, using their clawed front paws to dig out prey and create burrows for shelter. They may rapidly dig themselves into the ground if they cannot find cover when in danger. They bend their belly together to shield the soft, unprotected part, and can also urinate, giving off a pungent liquid, in an attempt to deter attackers. Males also have single small spurs on each rear leg, believed to be a defensive weapon that has since been lost through evolution. Echidnas typically try to avoid confrontation with predators. Instead, they use the colour of their spines, which is similar to the vegetation of the dry Australian environment, to avoid detection. They have good hearing and tend to become stationary if sound is detected.

It is likely that echidnas are keystone species in the ecosystem health in Australia, due to their contribution through bioturbation, the reworking of soils through their digging activity. This is based on the estimation that a single echidna will move up to 204 m³ (7,200 cu ft) of soil a year, that it is the most widespread of any terrestrial Australian species, is relatively common, and that other bioturbators have been heavily impacted by human settlement.

In Australia, they are most common in forested areas with abundant, termite-filled, fallen logs. In agricultural areas, they are most likely to be found in uncleared scrub; they may be found in grassland, arid areas, and in the outer suburbs of the capital cities. Little is known about their distribution in New Guinea. They have been found in southern New Guinea between Merauke in the west and the Kelp Welsh River, east of Port Moresby, in the east, where they may be found in open woodland.

Echidnas have the ability to swim, and have been seen cooling off near dams during high temperatures. They have also been seen crossing streams and swimming for brief periods in seas off Kangaroo Island. They swim with only the snout above water, using it as a snorkel.

Reproduction

The solitary short-beaked echidna looks for a mate between May and September; the precise timing of the mating season varies with geographic location. In the months before the mating season, the size of the male's testes increases by a factor of three or more before spermatogenesis occurs. Both males and females give off a strong, musky odour during the mating season, by turning their cloacas inside out and wiping them on the ground, secreting a glossy liquid believed to be an aphrodisiac. During courtship—observed for the first time in 1989—males locate and pursue females. Trains of up to 10 males, often with the youngest and smallest male at the end of the queue, may follow a single female in a courtship ritual that may last for up to four weeks; the duration of the courtship period varies with location. During this time, they forage for food together, and the train often changes composition, as some males leave and others join the pursuit. In cooler parts of their range, such as Tasmania, females may mate within a few hours of arousal from hibernation.

Before mating, the male smells the female, paying particular attention to the cloaca. This process can take a few hours, and the female can reject the suitor by rolling herself into a ball. After prodding and sniffing her back, the male is often observed to roll the female onto her side and then assume a similar position himself so the two animals are abdomen to abdomen, having dug a small crater in which to lie. They can lie with heads facing one another, or head to rear. If more than one male is in the vicinity, fighting over the female may occur. Each side of the bilaterally symmetrical, rosette-like, four-headed penis (similar to that of reptiles and 7 centimetres (2.8 in) in length) is used alternately, with the other half being shut down between ejaculations. Sperm bundles of around 100 each appear to confer increased sperm motility, which may provide the potential for sperm competition between males. This process takes between a half and three hours. Each mating results in the production of a single egg, and females are known to mate only once during the breeding season.

Fertilisation occurs in the oviduct. Gestation takes between 21 and 28 days after copulation, during which time the female constructs a nursery burrow. Following the gestation period, a single, rubbery-skinned egg between 13 and 17 mm (0.5 and 0.7 in) in diameter and 1.5 and 2.0 g (0.053 and 0.071 oz) in weight is laid from her cloaca directly into a small, backward-facing pouch that has developed on her abdomen. The egg is ovoid, leathery, soft, and cream-coloured. Between laying and hatching, some females continue to forage for food, while others dig burrows and rest there until hatching. Ten days after it is laid, the egg hatches within the pouch. The embryo develops an egg tooth during incubation, which it uses to tear open the egg; the tooth disappears soon after hatching.

Hatchlings are about 1.5 centimetres (0.6 in) long and weigh between 0.3 and 0.4 grams (0.011 and 0.014 oz). After hatching, young echidnas are known as "puggles". Although newborns are still semitranslucent and still surrounded by the remains of the egg yolk, and the eyes are still barely developed, they already have well-defined front limbs and digits that allow them to climb on their mothers' bodies. Hatchlings attach themselves to their mothers' milk areolae, specialised patches on the skin that secrete milk—monotremes lack nipples—through about 100–150 pores. The puggles were thought to have imbibed the milk by licking the mother's skin, but they are now thought to feed by sucking the areolae.

They have been observed ingesting large amounts during each feeding period, and mothers may leave them unattended in the burrow for between five and ten days to find food. Studies of captives have shown they can ingest milk once every two or three days and then increase their mass by 20% in one milk-drinking session lasting between one and two hours. Around 40% of the milk weight is converted into body mass, and as such, a high proportion of milk is converted into growth; a correlation with the growth of the puggle and its mother's size has been observed. By the time the puggle is around 200 g (7.1 oz), it is left in the burrow while the mother forages for food, and it reaches around 400 g (14 oz) after around two months. Juveniles are eventually ejected from the pouch at around two to three months of age, because of the continuing growth in the length of their spines. During this period, the young are left in covered burrows while the mothers forage, and the young are often preyed upon. Suckling gradually decreases until juveniles are weaned at about six months of age. The duration of lactation is about 200 days, and the young leave the burrow after 180 to 205 days, usually in January or February, at which time they weigh around 800 and 1,300 g (28 and 46 oz). There is no contact between the mother and young after this point.

The composition of the milk secreted by the mother changes over time. At the moment of birth, the solution is dilute and contains 1.25% fat, 7.85% protein, and 2.85% carbohydrates and minerals. Mature milk has much more concentrated nutrients, with 31.0, 12.4 and 2.8% of the aforementioned nutrients, respectively. Near weaning, the protein level continues to increase; this may be due to the need for keratin synthesis for hair and spines, to provide defences against the cold weather and predators.

The principal carbohydrate components of the milk are fucosyllactose and saialyllactose; it has a high iron content, which gives it a pink colour. The high iron content and low levels of free lactose differ from eutherian mammals. Lactose production is believed to proceed along the same lines as in the platypus.

The age of sexual maturity is uncertain, but may be four to five years. A 12-year field study found the short-beaked echidna reaches sexual maturity between five and 12 years of age, and the frequency of reproduction varies from once every two years to once every six years. In the wild, the short-beaked echidna has an average lifespan of 10 years, though they can live as long as 40. The longest-lived specimen reached 49 years of age in a zoo in Philadelphia. In contrast to other mammals, echidna rates of reproduction and metabolism are lower, and they live longer, as though in slow motion, something caused, at least in part, by their low body temperature, which rarely exceeds 33 °C (91 °F), even when they are not hibernating.

Like its fellow monotreme the platypus, the short-beaked echidna has a system of multiple sex chromosomes, in which males have four Y chromosomes and five X chromosomes. Males appear to be X₁Y₁X₂Y₂X₃Y₃X₄Y₄X₅, while females are X₁X₁X₂X₂X₃X₃X₄X₄X₅X₅. Weak identity between chromosomes results in meiotic pairing that yields only two possible genotypes of sperm, X₁X₂X₃X₄X₅ or Y₁Y₂Y₃Y₄, thus preserving this complex system.

Homosexual behaviours between males have been observed in captivity; this has sometimes led to cloacal injuries being observed following the interactions.

Conservation status

The short-beaked echidna is common throughout most of temperate Australia and lowland New Guinea, and is not listed as endangered. In Australia, it remains widespread across a wide range of habitats, including urban outskirts, coastal forests and dry inland areas, and is especially widespread in Tasmania and on Kangaroo Island.

The most common threats to the animal in Australia are motor vehicles and habitat destruction, which have led to localised extinctions. In Australia, the number of short-beaked echidnas has been less affected by land clearance than have some other species, since they do not require a specialised habitat beyond a good supply of ants and termites. As a result, they can survive in cleared land if the cut-down wood is left in the area, as the logs can be used as shelters and sources of insects. However, areas where the land has been completely cleared for single crops that can be mechanically harvested, such as wheat fields, have seen extinctions. Over a decade-long period, around one-third of echidna deaths reported to wildlife authorities in Victoria were due to motor vehicles, and the majority of wounded animals handed in were traffic accident victims. Studies have shown they often choose to traverse drainage culverts under roads, so this is seen as a viable means of reducing deaths on busy roads in rural areas or national parks where the animals are more common.

Despite their spines, they are preyed on by birds of prey, the Tasmanian devil, dingoes, snakes, lizards, goannas, cats, and red foxes, although almost all victims are young. Goannas are known for their digging abilities and strong sense of smell, and are believed to have been the main predators of the echidna before the introduction of eutherian mammals. Dingoes are known to kill echidnas by rolling them over onto their backs and attacking their underbellies. A tracking study of a small number of echidnas on Kangaroo Island concluded that goannas and cats were the main predators, although foxes—absent in Kangaroo Island—would be expected to be a major threat.

They were eaten by indigenous Australians and the early European settlers of Australia. Hunting and eating of the echidna in New Guinea has increased over time and caused a decline in the population and distribution areas; it is now believed to have disappeared from highland areas. The killing of echidnas was a taboo in traditional culture, but since the tribespeople have become increasingly Westernised, hunting has increased, and the animals have been more easily tracked down due to the use of dogs.

Infection with the introduced parasitic tapeworm Spirometra erinaceieuropaei is considered fatal for the echidna. This waterborne infection is contracted through sharing drinking areas with infected dogs, foxes, cats, and dingos, which do not die from the parasite. The infection is seen as being more dangerous in drier areas, where more animals are sharing fewer bodies of water, increasing the chance of transmission. The Wildlife Preservation Society of Queensland runs an Australia-wide survey, called Echidna Watch, to monitor the species. Echidnas are also known to be affected by other tapeworms, protozoans and herpes-like viral infections, but little is known of how the infections affect the health of the animals or the populations.

Although it is considered easy to keep echidnas healthy in captivity, breeding is difficult, partly due to the relatively infrequent cycle. In 2009, Perth Zoo managed to breed some captive short-beaked echidnas, and in 2015 the first zoo-born echidnas were successfully bred there. Until 2006, only five zoos have managed to breed short-beaked echidnas, but no captive-bred young have survived to maturity. Of these five institutions, only one in Australia—Sydney's Taronga Zoo—managed to breed echidnas, in 1977. The other four cases occurred in the Northern Hemisphere, two in the United States and the others in western Europe. In these cases, breeding occurred six months out of phase compared to Australia, after the animals had adapted to Northern Hemisphere seasons. The failure of captive breeding programs has conservation implications for the endangered species of echidna from the genus Zaglossus, and to a lesser extent for the short-beaked echidna.

Cultural references

Short-beaked echidnas feature in the animistic culture of indigenous Australians, including their visual arts and stories. The species was a totem for some groups, including the Noongar people from Western Australia. Many groups have myths about the animal; one myth explains it was created when a group of hungry young men went hunting at night and stumbled across a wombat. They threw spears at the wombat, but lost sight of it in the darkness. The wombat adapted the spears for its own defence and turned into an echidna. The fictional character Knuckles the Echidna from Sonic the Hedgehog is a red short-beaked echidna who possesses superhuman strength.

The short-beaked echidna is an iconic animal in contemporary Australia, notably appearing on the five-cent coin (the smallest denomination), and on a $200 commemorative coin released in 1992. The anthropomorphic echidna Millie was a mascot for the 2000 Summer Olympics.

General references

• Augee, M. L.; Gooden, B. A. (1993). Echidnas of Australia and New Guinea. Sydney: Australian National History Press. ISBN 978-0-86840-046-4.
• Augee, M. L. (1983). Strahan, R. (ed.). The Australian Museum Complete Book of Australian Mammals. Angus & Robertson. pp. 8–9. ISBN 0-207-14454-0.
• Griffiths, M. (1989). "Tachyglossidae". In Walton, D. W.; Richardson, B. J. (eds.). Fauna of Australia (PDF). Vol. 1B: Mammalia. Australian Government Publishing Service. pp. 407–435. ISBN 978-0-644-06056-1. Archived from the original on 16 July 2017.