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Tachyglossus aculeatus
short-beaked echidna


By Michelle Cason

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Monotremata
Family: Tachyglossidae
Genus: Tachyglossus
Species: Tachyglossus aculeatus

Geographic Range

Tachyglossus aculeatus is the most widely distributed extant monotreme. Subspecies of T. aculeatus are distributed throughout southern and eastern New Guinea, mainland Australia, Kangaroo Island, and Tasmania. This range includes large portions of the three countries of Australia, Indonesia, and Papua New Guinea. ("Tachyglossus aculeatus", 1991; Aplin, et al., 2008; Groves, 2005)

Biogeographic Regions
australian (Native )

Habitat

Range elevation
0 to 1,675 m
(0.00 to ft)

Short-beaked echidnas thrive in a variety of habitats including open woodlands, savanna, agricultural areas, semi-arid, and arid regions. Both coastal and highland areas in New Guinea are home to Tachyglossus aculeatus, along with a range of ecosystems in Australia from mild coastal regions to above snowline. Short-beaked echidnas have a broad altitudinal range from sea level to at least 1,675 meters. (Aplin, et al., 2008; Nicol and Anderson, 2007a)

Habitat Regions
temperate ; tropical ; terrestrial

Terrestrial Biomes
desert or dune ; savanna or grassland ; forest ; rainforest ; scrub forest ; mountains

Other Habitat Features
agricultural

Physical Description

Range mass
2 to 7 kg
(4.41 to 15.42 lb)

Range length
30 to 45 cm
(11.81 to 17.72 in)

Average basal metabolic rate
2.327 W
[External Source: AnAge]

Short-beaked echidnas are medium-sized mammals ranging in length from about 30 to 40 cm and in weight from about 2 to 7 kg. Depending on the subspecies and location, males or females may be larger. Short-beaked echidna spines are one of their most distinguishing characteristics. These spines cover the entire dorsal surface, including a small tail. Fur is also present and may be even longer than the spines in some subspecies. Tachyglossus aculeatus lacks external pinnae and teeth but does have hard pads in the back of the mouth. Short-beaked echidnas possess several adaptations to their foraging habits including tubular snouts, long sticky tongues, and front paws for digging. Males have non-venomous spurs on the ankles of their hind legs and females have pouches on their undersides. Both males and females have a cloaca through which feces, urine, and, in females, eggs pass. Males have penises they extend through the cloaca during mating. Short-beaked echidnas, and other monotremes, have low metabolic rates and low body temperatures, which may be related to such factors as diet and environmental variation. Short-beaked echidnas have larger brains than would be expected for their body mass. The cerebral cortex, in particular, is large and highly convoluted. (Nicol and Anderson, 2007a; Riek, 2008)

Other Physical Features
endothermic ; heterothermic ; bilateral symmetry

Sexual Dimorphism
sexes alike

Reproduction

Tachyglossus aculeatus has a courtship period between June and August that can last between a few days and several weeks depending on geographic region and subspecies. Females may be pursued by one or several males during this period. Observations of multiple males following individual females have led to the term “echidna train.” Females will mate with only one male per season. (Nicol and Anderson, 2007a)

Mating System
polygynous

Breeding interval
Short-beaked echidnas breed once a year.

Breeding season
Mating usually occurs June through August.

Range number of offspring
1 to 1

Average number of offspring
1
[External Source: AnAge]

Average gestation period
23 days

Average gestation period
22 days
[External Source: AnAge]

Average birth mass
0.3 kg
(0.66 lb)

Average birth mass
0.379 g
(0.01 oz)
[External Source: AnAge]

Range weaning age
150 to 200 days

Average age at sexual or reproductive maturity (female)
Sex: female

548 days
[External Source: AnAge]

Average age at sexual or reproductive maturity (male)
Sex: male

548 days
[External Source: AnAge]

Gestation in Tachyglossus aculeatus lasts about 23 days, after which the female will lay a single soft-shelled egg in her pouch for incubation. Eggs hatch 10 or 11 days later. Short-beaked echidnas exhibit a long lactation stage lasting between 150 and 200 days depending on geography and subspecies. When the young leave the pouch three months later, they are covered with spines. Maturation time is lengthy. Young reach full adult size after three to five years. Hatchlings have a mass of about 0.3 kg but will grow to weigh 0.7 to 2.1 kg by weaning. Weaning mass is 28 to 48% of adult mass. ("Tachyglossus aculeatus", 1991; Aplin, et al., 2008; Nicol and Anderson, 2007a)

Key Reproductive Features
iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); fertilization ; oviparous

Subspecies vary in their strategies of caring for young. Short-beaked echidnas on Kangaroo Island forage with the young in the pouch immediately post-hatching. After 45 to 55 days, mothers will deposit their young in nursery burrows, where the young will remain until weaning. Mothers return every five to ten days to nurse the young. Short-beaked echidnas in Tasmania remain in nursery burrows with the young for 25 to 35 days post-birth. Mothers then return to the burrow every three to five days to nurse. Other subspecies exhibit variations of parental care ranging between these two extremes. Mothers do not have nipples or teats, but nurse young through pores connected to their paired mammary glands. (Nicol and Anderson, 2007a)

Parental Investment
altricial ; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female)

Lifespan/Longevity

Range lifespan
Status: wild

45 (high) years

Range lifespan
Status: captivity

50 (high) days

Average lifespan
Status: captivity

50.0 years
[External Source: Max Planck Institute for Demographic Research]

Average lifespan
Status: captivity

49.4 years
[External Source: Max Planck Institute for Demographic Research]

The longest recorded lifespan for Tachyglossus aculeatus is 50 years in captivity. There are anecdotal accounts of wild individuals living as long as 45 years. There is no doubt this species is particularly long-lived, especially for its size. A lifespan of 50 years is 3.7 times longer than would be expected based on echidna body size. Other long-lived mammals have been observed to have peroxidation-resistant membrane composition, which describes the ratio between polyunsaturates and monounsaturates in membrane lipids. Short-beaked echidna membranes were found to have lower polyunsaturate and higher monounsaturate levels than expected. This composition indicates peroxiclation-resistant cellular membranes in T. aculeatus. Lifespan is also associated with the production of free radicals, which is proportional to metabolic rate. Short-beaked echidnas have notably low metabolic rates, with the exception of times of arousal from torpor. During these arousal periods, metabolic rates increase by up to nine times that of basal metabolic rates and free radical production is high. Therefore, T. aculeatus is thought to have stress resistance that contributes to a long lifespan. A large and complexly-structured brain may be involved with longevity in T. aculeatus. Such brain characteristics are often correlated with life history traits like slow maturation and single births in other mammals. These traits, in turn, correlate with a long lifespan. (Hulbert, et al., 2008; Nicol and Anderson, 2007a)

Behavior

Short-beaked echidnas are semi-fossorial, digging in substrate for hibernation cover and to construct nursery burrows. They decrease energy usage by hibernating from early autumn to late spring. Short-beaked echidnas reduce their body temperature to 8 to 10 degrees C during torpor and use behavioral thermoregulation to maintain that preferred body temperature. During early hibernation, individuals prefer cooler soil temperatures compared with the coldest period of hibernation, at which time they will move to warmer hibernacula. During hibernation there are periodic arousals from torpor. The timing of hibernation seasons varies by subspecies, geographic location, sex, and reproductive state. Short-beaked echidnas are flexible in their exploitation of substrates for hibernacula, commonly using leaf litter and grass tussocks. (Nicol and Anderson, 2007b; Nicol and Anderson, 2007a)

Key Behaviors
terricolous; fossorial ; diurnal ; nocturnal ; crepuscular ; sedentary ; hibernation ; solitary

Home Range

Short-beaked echidnas nest at temporary sites, and have overlapping home ranges. Their movements depend on food availability and not territoriality. ("Tachyglossus aculeatus", 1991; Nicol and Anderson, 2007a)

Communication and Perception

Short-beaked echidnas sense other echidnas predominantly through smell. Recent findings suggest feces piles act as an important intra-specific form of communication. (Elridge and Mensing, 2007; Nicol and Anderson, 2007a)

Communication Channels
chemical

Other Communication Modes
scent marks

Food Habits

Adult short-beaked echidnas eat ants, termites, and other invertebrates. They make foraging pits by disturbing the soil when looking for food, and they prefer foraging under the canopies of large trees. Their long snouts and sticky tongues reflect their specialized diet. Short-beaked echidnas dig into ant and termite nests with their front paws and poke their long, sticky tongue into nest crevices and grinds insects with its tooth pads. Their foraging habits make separating soil from food difficult. Thus, much of their feces consists of soil. (Elridge and Mensing, 2007; Nicol and Anderson, 2007a)

Primary Diet
carnivore (Insectivore )

Animal Foods
insects; terrestrial non-insect arthropods

Predation

Known Predators


Predation is not a major threat to short-beaked echidnas, even though feral cats, pigs, dingoes, and goannas are occasional predators. Animal predators are mostly a threat to young in burrows and to subadults. Adults escape predation by hiding beneath rocks or logs, or digging into the ground until only the spiny back is exposed. Short-beaked echidnas can also curl up to protect their undersides. Despite the minimal defense of many hibernaculum materials, predation on hibernating individuals does not seem to be a problem. After introduced predators, the biggest influence on T. aculeatus mortality is the threat of motor vehicles. Over-hunting by humans may become a problem in some areas of New Guinea. (Aplin, et al., 2008; Nicol and Anderson, 2007a)

Anti-predator Adaptations
cryptic

Ecosystem Roles

The foraging pits short-beaked echidnas create become resource traps and affect soil biogeochemistry. Tachyglossus aculeatus may be important in maintaining proper nutrient circulation through small-scale patchiness in semi-arid regions. (Elridge and Mensing, 2007)

Ecosystem Impact
creates habitat; soil aeration

Economic Importance for Humans: Positive

Short-beaked echidnas are hunted for food and for ceremonial purposes, especially in New Guinea. They maintain small-scale patchiness, which is an important ecosystem service that keeps semi-arid regions functioning properly. Their diet of ants, termites, and other invertebrates may contribute to the control of these species. (Aplin, et al., 2008; Elridge and Mensing, 2007; Nicol and Anderson, 2007a)

Positive Impacts
food ; body parts are source of valuable material; controls pest population

Economic Importance for Humans: Negative

Because short-beaked echidnas can live in agricultural areas, they may disrupt fields and gardens while foraging. (Nicol and Anderson, 2007a)

Negative Impacts
crop pest

Conservation Status

IUCN Red List of Threatened Species [Link]
Least Concern
More Information

US Federal List [Link]
No special status

CITES [Link]
Appendix I

As of 2008, the IUCN listed Tachyglossus aculeatus as a species of Least Concern. Short-beaked echidnas have a broad distribution, a large total population with a stable trend, and are tolerant of many habitat types. They occur in protected areas and appear to lack major threats. The IUCN did suggest monitoring the number of T. aculeatus killed on major tourist roads. (Aplin, et al., 2008)

For More Information

Find Tachyglossus aculeatus information at

Contributors

Tanya Dewey (editor), Animal Diversity Web, University of Michigan Museum of Zoology.

Michelle Cason (author), University of Alaska Fairbanks, Link Olson (editor, instructor), University of Alaska Fairbanks.

References

1991. Tachyglossus aculeatus. Pp. xviii-xix, 2-3 in R Strahan, ed. The Australian Museum Complete Book of Australian Mammals. New South Whales: Cornstalk Publishing.

Aplin, K., C. Dickman, L. Salas, K. Helgen. 2008. Tachyglossus aculeatus. 2008 IUCN Redlist of Threatened Species. Accessed November 15, 2008 at www.iucnredlist.org.

Elridge, D., A. Mensing. 2007. Foraging pits of the short-beaked echidna (Tachyglossus aculeatus) as small-scale patches in a semi-arid Australian woodland. Soil Biology & Biochemistry, 39: 1055-1065.

Groves, C. 2005. Tachyglossus aculeatus. Pp. 1-2 in D Wilson, D Reeder, eds. Mammal Species of the World: A Taxonomic Reference, Vol. 1. Washington: Smithsonian Institution Press.

Hulbert, A., L. Beard, G. Grigg. 2008. The exceptional longevity of an egg-laying mammal, the short-beaked echidna (Tachyglossus aculeatus) is associated with peroxidation-resistant membrane composition. Experimental Gerontology, 43: 729-733.

Nicol, S., N. Anderson. 2007. Cooling rate and body temperature regulation of hibernating echidnas (Tachyglossus aculeatus). Journal of Experimental Biology, 210: 586-592.

Nicol, S., N. Anderson. 2007. The history of an egg-laying mammal, the echidna (Tachyglossus aculeatus). Ecoscience, 14: 275-285.

Riek, A. 2008. Relationship between metabolic rate and body weight in mammals: effect of the study. Journal of Zoology, 276: 187-194.

To cite this page: Cason, M. 2009. "Tachyglossus aculeatus" (On-line), Animal Diversity Web. Accessed May 16, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tachyglossus_aculeatus.html

Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.

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