Overview

Brief Summary

Biology

Dibblers are most active at dawn and dusk. They feed on ground-dwelling insects and other invertebrates but will also eat small lizards, small birds and small mammals. They are well adapted carnivores, with strong jaws and tiny sharp teeth, and are also incredibly agile and able to run through seemingly impenetrable undergrowth with ease. Not only are they well equipped for foraging in the undergrowth, but they can also run up trees and rocks. Their broad feet have claws on the toes, and grooves running along the feet pads which act as suckers (4).  Females have one oestrous cycle per year, and mating occurs in March or April (2). Following a gestation period of 44 days, the female gives birth to 8 young. The infants live and nurse in their mother's pouch for several weeks before growing too large (2).
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Comprehensive Description

Description

The dibbler is one of the rarest mammals in the world (2). It is a small marsupial carnivore found in Australia. Like other members of the dasyurid family, it has a distinctive pointed snout, well developed canines, 6-7 sharp cheek teeth and broad feet bearing sharp claws (3). Its small mouse-like body is covered in coarse fur which is brownish-grey in colour, with distinctive white speckles. The tail is hairy and tapering, and there are distinctive white markings around the eyes (3). Females, like most marsupials, have pouches in which they carry the newborns until they are fully developed (3).
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Distribution

Range Description

The Dibbler is endemic to south-western Australia. It occurs naturally in Fitzgerald River National Park and on the islands of Boullanger and Whitlock (Friend 2004). The species also occurs as translocated populations on Escape Island, Peniup, and Stirling Range National Park (Woolley 2008).
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Geographic Range

Although once widespread throughout southwest Australia, today Parantechinus apicalis is only found in small populations on the mainland. Two larger populations have recently been found inhabiting Boullanger and Whitlock Islands in Jurien Bay in Western Australia.

Biogeographic Regions: australian (Native )

  • Miller, S., R. Bencini, H. Mills, D. Moro. 2003. Food availability for the dibbler (Parantechinus apicalis) on Boullanger and Whitlock Islands, Western Australia. Wildlife Research, 30: 649-654. Accessed March 18, 2006 at www.publish.csiro.au/journals/wr.
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Historic Range:
Australia

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Range

This species is restricted to two small islands (Boullanger and Whitlock) off the southwest Western Australian coast. It also occurs on the Australian mainland in three widely separated areas (4).
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Physical Description

Morphology

Physical Description

Southern dibblers are small, with males averaging 145 mm in length and 60 to 100 g. Male southern dibblers found on the mainland are generally heavier than island individuals. Females are smaller at 140 mm average and 40 to 75 g. They have pointed snouts, long whiskers, and strong jaws with sharp teeth. There are also grooves on the pads of their feet which function in providing good traction. These, along with sharp claws, allow them a good grip on trees and rocks. Parantechinus apicalis has rather coarse fur with a freckled appearance. The fur is brownish grey above and grayish white with yellow underneath. They have hairy tapering tails and distinctive white rings around large eyes.

Range mass: 40 to 100 g.

Range length: 140 to 145 mm.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry ; polymorphic

Sexual Dimorphism: male larger

  • Moro, D. 2003. Translocation of captive-bred dibblers Parantechinus apicalis (Marsupialia: Dasyuridae) to Escape Island, Western Australia. Biological Conservation, 111: 305-315. Accessed March 18, 2006 at http://www.elsevier.com/locate/biocon.
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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
Dibblers are associated with scrub and heath communities. The time since fire appears to be important with older aged areas being preferred. It is possible that the species will occupy younger vegetation when foxes are excluded (Friend 2004). Dibblers eat a variety of arthropods, and some small vertebrates. Females may produce two litters annually (at least in captivity and on the islands) of up to eight young (Woolley 2008).

Systems
  • Terrestrial
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Habitat

Southern dibblers on Whitlock Island prefer dense vegetation such as dunal scrubland and succulent heath. This may be due to the protection it provides from predators or an increased abundance of insect prey. Interestingly, when released from captivity into the wild they take refuge in seabird burrows. On Boullanger Island there seemed to be no preference of habitat as the entire island is fairly regular and has no trees.

Habitat Regions: temperate ; terrestrial

Terrestrial Biomes: desert or dune

  • Bencini, R., C. McCulloch, H. Mills, A. Start. 2001. Habitat and diet of the dibbler (Parantechinus apicalis) on two islands in Jurien Bay, Western Australia. Wildlife Research, 28: 465-468. Accessed March 18, 2006 at www.publish.csiro.au/journals/wr.
  • Mills, H., R. Bencini. 2000. New evidence for facultative male die-off in island populations of dibblers, Parantechinus apicalis. Australian Journal of Zoology, 48: 501-510. Accessed March 18, 2006 at http://www.publish.csiro.au/journals/ajz.
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Habitat

Inhabits dense heath habitat and appears to prefer sites with sandy soils (4).
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Trophic Strategy

Food Habits

Parantechinus apicalis is primarily insectivorous, eating whatever insects they can find. Being a generalist in this way may be advantageous due to fluctuating environmental conditions. Specifically P. apicalis has been found to eat grasshoppers (Orthoptera), cockroaches (Blattaria), beetles (Coleoptera), termites (Isoptera), and ants (Hymenoptera). Plant material, such as the berries of Rhagodia baccata, make up around 20% of its diet. Members of this species show no significant differences in their diet during different seasons.

Animal Foods: insects

Plant Foods: fruit; nectar

Primary Diet: carnivore (Insectivore )

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Associations

Ecosystem Roles

On the mainland southern dibblers prey on insects and are often prey to larger mammals. On the islands southern dibblers face little danger of predation but compete with introduced house mice for food.

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Predation

The color of the fur of southern dibblers is their best camouflage. They are also able to move easily and with speed through dense vegetation and, for these reasons, have few natural predators. Mainland populations are heavily preyed upon by introduced red foxes and feral cats.

Known Predators:

Anti-predator Adaptations: cryptic

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Life History and Behavior

Behavior

Communication and Perception

Southern dibblers do vocalize, but vocalization is usually only heard during mating and plays no role in the attraction of mates. There is no other information on how P. apicalis communicates, perceives its environment, or attracts mates, but related species rely heavily on sight and smell.

Communication Channels: visual ; acoustic ; chemical

Perception Channels: visual ; acoustic

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Life Expectancy

Lifespan/Longevity

In captivity and in the wild Parantechinus apicalis individuals live 2 to 3 years. Interestingly, on Boullanger Island males display semelparity where they die immediately after the breeding season. Extremely high energy demands during the breeding season, elevated levels of free corticosteroids in the blood, and related disease such as ulcers, anemia, and parasite infestation ultimately cause the death of males. Because mainland males survive for multiple breeding seasons, this male die-off could be environmentally determined. One possible explanation is the effect of nesting seabirds including bridled terns and white-faced storm petrels on resources. Seabirds affect nutrients in the soil; post-breeding survival is significantly higher on Whitlock Island which has many seabirds, 18 times more nutrients in the soil and a larger amount of insects.

Range lifespan

Status: wild:
1 to 3 years.

Range lifespan

Status: captivity:
2 to 3 years.

Typical lifespan

Status: wild:
2 to 3 years.

Typical lifespan

Status: captivity:
2 to 3 years.

  • Kraaijeveld, K., F. Kraaijeveld-Smit, G. Adcock. 2003. Does female mortality drive male semelparity in dasyurid marsupials?. Proc. R. Soc. Lond. B (Suppl.), 270: 251-253.
  • Dickman, C., R. Braithwaite. 1992. Postmating mortality of males in the dayurid marsupials, Dasyurus and Parantechinus. Journal of Mammalogy, 73(1): 143-147. Accessed March 18, 2006 at http://www.jstor.org.
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Lifespan, longevity, and ageing

Maximum longevity: 5.5 years (captivity) Observations: These animals are expected to live more than 3 years in the wild (Bernhard Grzimek 1990). One specimen lived 5.5 years in captivity (Richard Weigl 2005).
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Reproduction

Reproduction

Typical behaviors prior to and during mating include sniffing of the cloacal and facial regions and rump by both the male and female. This behavior is common and increases in intensity as the female approaches estrous. Chases and attempted mountings are frequent. The male may chase the female or vice versa. Often the animals vocalize when they are chasing or attempting mountings. Mountings are initiated by the male and there are many attempts that are unsuccessful. Chasing and unsuccessful mountings may occur up to 15 days prior to copulation. Successful mountings involve the male clasping the female in a neck-grip and a single copulation may continue for a few hours.

Mating System: polygynandrous (promiscuous)

Paranechinus apicalis will mate throughout March and April. Although females are only able to breed once annually, males may be able to breed in multiple seasons. The gestation period for southern dibblers is long compared to other small dasyurids, 44 to 53 days. Once females give birth they carry up to eight young in a shallow pouch. The young are dependent on the female for 3 to 4 months and usually disperse in September and October, reaching sexual maturity in 10 to 11 months.

Breeding interval: Southern dibblers breed once yearly.

Breeding season: Breeding occurs from March to April.

Average number of offspring: 8.

Range gestation period: 44 to 53 days.

Range time to independence: 3 to 4 months.

Range age at sexual or reproductive maturity (female): 10 to 11 months.

Range age at sexual or reproductive maturity (male): 10 to 11 months.

Key Reproductive Features: semelparous ; iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); viviparous

Average number of offspring: 8.

The extent of parental investment in southern dibblers involves the female carrying and protecting her young in a shallow pouch. She provides food and protection until the young reach independence and disperse in 3 to 4 months.

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

  • Woolley, P. 1988. Reproduction in the ningbing antechinus (Marsupialia: Dasyuridae): field and laboratory observations. Australian Wildlife Research, 15: 149-56.
  • Collins, L. 1973. Monotremes and Marsupials. Washington: Smithsonian Institution Press.
  • Miller, S., R. Bencini, H. Mills, D. Moro. 2003. Food availability for the dibbler (Parantechinus apicalis) on Boullanger and Whitlock Islands, Western Australia. Wildlife Research, 30: 649-654. Accessed March 18, 2006 at www.publish.csiro.au/journals/wr.
  • Moro, D. 2003. Translocation of captive-bred dibblers Parantechinus apicalis (Marsupialia: Dasyuridae) to Escape Island, Western Australia. Biological Conservation, 111: 305-315. Accessed March 18, 2006 at http://www.elsevier.com/locate/biocon.
  • Wolfe, K., H. Robertson, R. Bencini. 2000. The mating behavior of the dibbler, Parantechinus apicalis, in captivity. Australian Journal of Zoology, 48: 541-550. Accessed March 18, 2006 at http://www.publish.csiro.au/journals/ajz.
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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
EN
Endangered

Red List Criteria
B1ab(iii)

Version
3.1

Year Assessed
2008

Assessor/s
Friend, T., Burbidge, A. & Morris, K.

Reviewer/s
Lamoreux, J. & Hilton-Taylor, C. (Global Mammal Assessment Team)

Justification
Listed as Endangered because its extent of occurrence is less than 5,000 km2, its distribution is severely fragmented, and there is continuing decline in the extent and quality of its habitat.

History
  • 1996
    Endangered
  • 1994
    Endangered
    (Groombridge 1994)
  • 1990
    Indeterminate
    (IUCN 1990)
  • 1988
    Indeterminate
    (IUCN Conservation Monitoring Centre 1988)
  • 1986
    Indeterminate
    (IUCN Conservation Monitoring Centre 1986)
  • 1982
    Indeterminate
    (Thornback and Jenkins 1982)
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Conservation Status

In 1902 southern dibblers were thought to be extinct but were rediscovered in 1967. They have been threatened by human development, habitat destruction and burning, and the introduction of foxes and cats. Southern dibblers are presently undergoing extensive conservation efforts including successful translocations of captive-bred individuals to Escape Island. Although this project is fairly new, initial success is high with three generations surviving after the initial relocation.

US Federal List: endangered

CITES: no special status

IUCN Red List of Threatened Species: endangered

  • Mills, H., B. Spencer. 2003. Polymorphic microsatellites identified in an endangered dasyurid marsupial, the dibbler (Parantechinus apicalis). Molecular Ecology Notes, 3: 218-220.
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Current Listing Status Summary

Status: Endangered
Date Listed: 12/02/1970
Lead Region: Foreign (Region 10) 
Where Listed:


Population detail:

Population location: entire
Listing status: E

For most current information and documents related to the conservation status and management of Parantechinus apicalis, see its USFWS Species Profile

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Status

Classified as Endangered (EN B1+2ce) on the IUCN Red List 2003 (1).
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Population

Population
The Dibbler is a rare species (Woolley 2008). The global population consists of about 500-1,000 mature individuals, but there have been some declines. The three island populations include a total of 200 individuals. The (reintroduced) adult population on Escape Island is about 30 individuals. The island populations have declined in the last few decades. Population size fluctuates significantly with rainfall. This species lives only for about one year.

Population Trend
Decreasing
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Threats

Threats

Major Threats
Introduced foxes and cats are known to prey on this species, and are found throughout its known mainland range, though they are not present on the islands. The plant disease Phytophthora cinnamomi is a threat to Dibblers, as it adversely alters their habitat. Introduced mice are also a potential threat on Boullanger and Whitlock Islands, due to competition (Friend 2004). Because this species is dependent on habitat that has not been recently burned, frequent and intense fire is a major threat.
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Threats

This species has been lost from 90% of its former range in Australia (4). It is not known why this marsupial is so rare, although surveys suggest various factors. Land clearing and habitat fragmentation are thought to be significant causes of its decline. In addition, the frequent burning of heathland and litter may reduce the availability of invertebrates in the area. Predation by introduced mammals such as foxes and cats are also considered a threat to this species (4).
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Management

Conservation Actions

Conservation Actions
The Dibbler is listed as a threatened species under Australian law. It occurs in a few protected areas. A recovery plan has been developed for the species for the 2003-2013 period (Friend 2004). Captive breeding has allowed for the translocation of Dibblers to three locations.

Recommendations in the recovery plan (Friend 2004), include: monitoring known populations; surveying for additional populations; protecting populations from threatening processes (including the prevention of exotic predators from the islands, controlling foxes and cats at mainland sites, implementing fire management, preventing the spread of Phytophthora cinnamomi); studying the feasibility of eradicating introduced mice from Boullanger and Whitlock Islands; maintaining and expanding captive breeding populations for further translocations; and promoting awareness of Dibbler conservation among the public and among land managers.
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Conservation

In 1992 a recovery plan for this species was developed by the International Union for the Conservation of Nature and Natural Resources (IUCN), addressing the threats facing this species (4). Predation by foxes and cats has now been brought under control by The Department of Conservation and Land Management (CALM) and, in the last decade, dibbler numbers have started to increase (5). Perth Zoo has been working with CALM to establish a captive breeding stock of over 100 individuals of this species (6). They have also translocated a group of dibblers to Escape Island; a predator free island which has suitable habitat for this marsupial. Here, radio tracking devices and trapping practices will be used to monitor the populations (5). Considering that the dibbler was on the brink of extinction, this recovery plan has been a great success. It is however essential to maintain these conservation efforts as the dibbler is still regarded as a severely endangered animal (1).
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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Negative

There are no known adverse affects of Parantechinus apicalis on humans.

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Economic Importance for Humans: Positive

There are no known positive affects of Parantechinus apicalis on humans. They are a member of a unique fauna and may be of ecotourist interest because of their rarity.

Positive Impacts: ecotourism

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Wikipedia

Dibbler

Dibbler is the common name for Parantechinus apicalis, an endangered species of marsupial. It is an inhabitant of the southwest mainland of Western Australia and some offshore islands. It is a member of the Dasyuromorphia order, and the only member of the genus, Parantechinus. The Dibbler is a small, carnivorous, nocturnal, with speckled fur that is white around the eyes.

Contents

Description

The Dibbler is 10–16 cm long with a 7.5-12.0 cm tail; it weighs 40-125g. The distinctive features of this dasyurid include a white eye-ring, gray-brown fur flecked with white hairs, and a short tapering tail. It has strong jaws and large canine teeth for killing prey, which include small vertebrates such as mice, birds and lizards, as well as insects and other invertebrates. The breeding season for the species is March–April.

The Dibbler is found in Southwestern Western Australia, It is also found on Boullanger Island and Whitlock Island and Escape Island off Jurien Bay.,[2] some national parks/reserves, including Fitzgerald River National Park, Peniup Creek Reserve (where it was re-introduced) and at the Stirling Range National Park (where it was re-introduced). Dibblers weigh about 40–100 grams (1.4–3.6 oz) and eat insects, small reptiles, and nectar. The Dibbler is a solitary, mostly nocturnal species.

The Dibblers habitat is an unburnt vegetation area with a thick litter layer and sandy soils. They can be found sleeping in hollow logs and caves during the day.

The two main locations where Dibblers live are Whitlock and Boullanger, which are two little islands just off Jurien Bay. They have also been recorded at Torndirrup Peninsula south of Albany. Specimens have been obtained by traps located on Banksia attenuata.[3]

Taxonomy

Classification

The Dibbler is the only member of its genus, Parantechinus, which indicates that it is an "antechinus-like (animal)".[4] The specific epithet, apicalis, means "pointed". This genus formerly included the Sandstone Dibbler, now placed in the genus Pseudantechinus.

The genus Parantechinus contains only the single species, Parantechinus apicalis, the Dibbler. It was first described in 1842 by John Edward Gray, who placed it in the genus Phascogale. He identified the specimen as being Australasian in origin. The genus Parantechinus was created for the species in 1947 by George Henry Hamilton Tate. The species was also assigned to the genus Antechinus, before being split to own genus. There are various arrangements of the genera in this section of Dasyuridae family, many of which are supported by molecular systematics, and their relationship remains unresolved.[3]

Common name

The name 'Dibbler' is used by government and scientific authorities, and in popular usage, to refer to this species exclusively.[5][6][7][8] In the Dibbler Recovery Plan, Senior DEC scientist, Dr. Tony Friend notes

Strahan (2003) introduced the common name "southern dibbler" for P. apicalis [Parantechinus apicalis] and "northern dibbler" for the sandstone antechinus" [Pseudantechinus bilarni][3] ... the well-established use of "dibbler" to refer only to P. apicalis is recommended and is followed in this plan."[9]

A number of common names derive from previous systematic arrangements. John Gould gave several names from the Nyoongar/Noongar language; Marn-dern and Wy-a-lung are from northern areas, Dib-bler is from the dialect spoken in the King George Sound region.[10] The practice of restoring traditional names to marsupial species has conserved this common name. Gould referred to the species as the Freckled Antechinus,[3] and it has also been known as the Speckled Marsupial Mouse.

The online edition of Mammal Species of the World gave the name Southern dibbler in 2009.[11] A species known as the Northern (or Sandstone) Dibbler, Pseudantechinus bilarni, is found in the Northern Territory. This species has been distinguished by the name Southern Dibbler, however this name is given in The Mammals of Australia (2008),[12] the formative guide for Australian mammal nomenclature worldwide.

Conservation status

The Dibbler was believed to have become extinct until it was rediscovered in 1967 at Cheyne Beach on the south coast of Western Australia after a gap of 80 years. It remains an endangered species.

The Perth Zoo in Western Australia operates a conservation project for the Dibbler which is helpful in its survival and breeding, and along with the Department of Environment and Conservation have helped to breed and release more dibblers into the wild.

In the early 19th century, dibblers were widely distributed across Western Australia. By 1884, they were declared extinct, but some were found on the southern coast of Western Australia in 1967. They are threatened by habitat loss (land clearing, forest fires) and predators. Their predators are mainly feral foxes and feral cats.

References

  1. ^ Friend, T., Burbidge, A. & Morris, K. (2008). Parantechinus apicalis. In: IUCN 2008. IUCN Red List of Threatened Species. Downloaded on 28 December 2008. Database entry includes justification for why this species is listed as endangered
  2. ^ Menkhorst, Peter (2001). A Field Guide to the Mammals of Australia. Oxford University Press. p. 58. 
  3. ^ a b c d Friend, Tony (2003). "Dibbler (Parantechinus apicalis) Recovery Plan". Dibbler Recovery Team. Department of Conservation and Land Management (DEC). http://www.environment.gov.au/biodiversity/threatened/publications/recovery/p-apicalis/pubs/p-apicalis.pdf. Retrieved 2009-04-26. 
  4. ^ Woolley, P.A. (1995). "Southern Dibbler". In Strahan, Ronald. The Mammals of Australia. Reed Books. pp. 72–73. 
  5. ^ Bencini, R., McCulloch, C., Mills, H.R., Start, A.N., 2001. Habitat and diet of the dibbler (Parantechinus apicalis) on two small islands in Jurien Bay, Western Australia. Wildlife Research 28, 465–468.
  6. ^ Fuller, P.J., Burbidge, A.A., 1987. Discovery of the Dibbler, Parantechinus apicalis, on islands at Jurien Bay. The Western Australian Naturalist 16, 177–181.
  7. ^ Miller, S., Bencini, R., Mills, H., Moro, D. Food availability for the dibbler, Parantechinus apicalis, on Boullanger and Whitlock Islands, Western Australia. Australian Journal of Zoology (in press).
  8. ^ Mills, H.R., Bencini, R., 2000. New evidence for facultative male dieoff in island populations of dibblers, Parantechinus apicalis. Australian Journal of Zoology 48, 501–510.
  9. ^ Dibbler Recovery Plan (html)
  10. ^ Friend citing Gould, J. 1863. The Mammals of Australia. Taylor and Francis, London.
  11. ^ Groves, C. (2005). Wilson, D. E.; Reeder, D. M. eds. Mammal Species of the World (3rd ed.). Baltimore: Johns Hopkins University Press. pp. 26. OCLC 62265494. ISBN 0-801-88221-4. http://www.bucknell.edu/msw3/browse.asp?id=10800032. 
  12. ^ The Mammals of Australia 3rd Ed. 2008. Reed New Holland. Edited by Steve Van Dyck & Ronald Strahan. ISBN 978-1-877069-25-3
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