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Home -> Kingdom Animalia -> Phylum Chordata -> Subphylum Vertebrata -> Class Mammalia -> Order Dasyuromorphia -> Family Dasyuridae -> Subfamily Dasyurinae -> Species Parantechinus apicalis

Parantechinus apicalis
southern dibbler



2008/06/15 07:13:18.507 GMT-4

By Megan Coughlin

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Dasyuromorphia
Family: Dasyuridae
Subfamily: Dasyurinae
Genus: Parantechinus
Species: Parantechinus apicalis

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 ).

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. ()

These animals are found in the following types of habitat:
temperate ; terrestrial .

Terrestrial Biomes:
desert or dune .

Physical Description

Mass
40 to 100 g
(1.41 to 3.52 oz)


Length
140 to 145 mm
(5.51 to 5.71 in)


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. ()

Some key physical features:
endothermic ; homoiothermic; bilateral symmetry ; polymorphic .

Reproduction

Breeding interval
Southern dibblers breed once yearly.

Breeding season
Breeding occurs from March to April.

Number of offspring
8 (average)

Gestation period
44 to 53 days

Time to independence
3 to 4 months

Age at sexual or reproductive maturity (female)
10 to 11 months

Age at sexual or reproductive maturity (male)
10 to 11 months

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. ()

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. ()

Key reproductive features:
semelparous ; iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous .

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).

Lifespan/Longevity

Extreme lifespan (wild)
1 to 3 years

Extreme lifespan (captivity)
2 to 3 years

Typical lifespan (wild)


Typical lifespan (captivity)


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. ()

Behavior

Southern dibblers are active at both dawn and dusk hunting for large insects. If necessary, they can jump or climb trees in order to catch their prey. During the day they take shelter and rest in logs or between rocks. In reintroduced populations they form groups which vary around 100 individuals. ()

Home Range

No information on home range sizes in southern dibblers is was found.

Key behaviors:
terricolous; crepuscular ; motile ; sedentary ; social .

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. ()

Communicates with:
visual ; acoustic ; chemical .

Perception channels:
visual ; tactile ; acoustic ; chemical .

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. ()

Primary Diet:
carnivore (insectivore ).

Animal Foods:
insects.

Plant Foods:
fruit; nectar.

Predation

Known predators

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. ()

Anti-predator adaptations::
cryptic .

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. ()

Economic Importance for Humans: Negative

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

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.

Ways that people benefit from these animals:
ecotourism .

Conservation Status

IUCN Red List: [link]:
Endangered.

US Federal List: [link]:
Endangered.

CITES: [link]:
No special 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. ()

Contributors

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

Megan Coughlin (author), University of Michigan. Phil Myers (editor, instructor), Museum of Zoology, University of Michigan.

References

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.

Collins, L. 1973. Monotremes and Marsupials. Washington: Smithsonian Institution Press.

Cooper, C., P. Withers. 2004. Influence of season and weather on activity patterns of the numbat (Myrmecobius fasciatus) in captivity. Australian Journal of Zoology, 52: 475-485. Accessed March 18, 2006 at http://www.publish.csiro.au/journals/ajz.

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.

Fisher, D., C. Dickman. 1993. Body size-prey relationships in insectivorous marsupials: tests of three hypotheses. Ecology, 74(6): 1871-1883. Accessed March 18, 2006 at http://www.jstor.org.

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.

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.

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.

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

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.

Strahan, R. 1983. The Australian Museum Complete Book of Australian Mammals. London-Sydney-Melbourne: Angus and Robertson Publishers.

Twigg, L., G. Martin, A. Eastman, D. King, W. Kirkpatrick. 2003. Sensitivity of some Australian animals to sodium fluoroacetate (1080): additional species and populations, and some ecological considerations. Australian Journal of Zoology, 51: 515-531. Accessed March 18, 2006 at http://www.publish.csiro.au/journals/ajz.

Wolfe, K., H. Mills, M. Garkaklis, R. Bencini. 2004. Post-mating survival in a small marsupial is associated with nutrient inputs from seabirds. Ecology, 85(6): 1740-1746.

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.

Woolley, P. 1988. Reproduction in the ningbing antechinus (Marsupialia: Dasyuridae): field and laboratory observations. Australian Wildlife Research, 15: 149-56.

Woolley, P. 1991. Reproductive pattern of captive Boullanger Island dibblers, Parantechinus apicalis (Marsupialia: Dasyuridae). Wildlife Research, 18: 157-63.

2008/06/15 07:13:22.389 GMT-4

To cite this page: Coughlin, M. and P. Myers. 2006. "Parantechinus apicalis" (On-line), Animal Diversity Web. Accessed July 04, 2008 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Parantechinus_apicalis.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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