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Tarsipes rostratus
honey possum


By Yengin Loay

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Diprotodontia
Family: Tarsipedidae
Genus: Tarsipes
Species: Tarsipes rostratus

Geographic Range

Tarsipes rostratus is native to the south western tip of Western Australia, throughout the coastal-sand plain heathlands, which contains a diverse array plant communities. (Cooper and Cruz-Neto, 2009; Nagy, et al., 1995; Richardson, et al., 1986)

Biogeographic Regions
australian (Native )

Habitat

Preferred habitat of Tarsipes rostratus is banksia woodlands, which are rich in floral diversity. The overstory of banksia woodland habitat along the south western coast of Western Australia is dominated by Banksia attenuata (slender Banksia) and B. menziesii (firewood Banksia). Eucalyptus todtiana (coastal blackbutt), E. gomphocephala (Tuart), E. marginata (Jarrah), Allocasuarina fraseriana (Fraser’s sheoak), Nuytsia floribunda (christmas tree) and other Banksia species also occur, but far less frequently. Interspersed throughout the understory are various species in the families Proteaceae, Myrtaceae, Papilionaceae, and Epacridaceae (Maher et al., 2008). ("Restoration of banksia woodlands after the removal of pines Gnangara: evaluation of seeding trials.", 2008; Bradshaw and Bradshaw, 2002)

Habitat Regions
temperate ; terrestrial

Terrestrial Biomes
forest ; scrub forest

Physical Description

Range mass
6 to 18 g
(0.21 to 0.63 oz)

Range length
65 to 90 mm
(2.56 to 3.54 in)

Average basal metabolic rate
2.9 cm^3 oxygen/hour

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

Tarsipes rostratus has grey fur that is brown on the dorsal side with a dark stripe starting from the nape of the neck extending down towards the base of the tail. It has white and yellow ventral pelage on its underbelly that becomes orange on its sides. The head is dorsoventrally flattened with an elongated snout that is approximately two and a half times longer than its maximum width. Tarsipes rostratus has a brush-tipped protrusible tongue that is equal in length to the head. With the exception of the incisors, which are enlarged, the dentition of T. rostratus is greatly reduced. Its hands and feet have rough pads, opposable and elongated digits, with nails that do not project beyond the toe-pads. It has a prehensile tail that is hairless on the ventral surface near the tip. Tarsipes rostratus is sexually dimorphic, with females being approximately a third heavier than males. Females range in mass from 10 to 18 g, have a body length ranging from 70 to 90 mm, and a tail that measures from 75 to 105 mm in length. Males range in mass from 6 to 12 g, have a body length ranging from 65 to 85 mm, and a tail that measures from 70 to 100 mm in length. Despite females being slightly larger, there is no difference in head length between the sexes. (Bradshaw and Bradshaw, 2007; Cooper and Cruz-Neto, 2009; Nagy, et al., 1995; Richardson, et al., 1986; Withers, et al., 1990)

Tarsipes rostratus has a higher basal metabolic rate (BMR) and field metabolic rate (FMR) than most other marsupials. It has an average body temperature of 36.6 C, which is much higher than the typical marsupial, and a BMR of 2.9 cm^3 oxygen/hour. When in torpor, if its body temperature falls below 5 degrees C it is incapable of exiting torpor. Daily energy expenditures range from 25 to 30 kJ/day, which classifies them as hypermetabolic. In order to meet their high energy demands, its diet consists primarily of pollen and nectar. (Bradshaw and Bradshaw, 2007; Cooper and Cruz-Neto, 2009; Nagy, et al., 1995; Richardson, et al., 1986; Withers, et al., 1990)

Other Physical Features
endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism
female larger

Reproduction

Tarsipes rostratus mates several times a year in a non-seasonal pattern. Females are polyandrous and have small litters, usually between 2 and 3 offspring but potentially up to 4, with multiple paternities. Female polyandry results in sperm competition between males. The testes of male T. rostratus are very large relative to their body size, weighing more than 4% of their total body mass. Their testes contain sperm that is larger than any other mammal. Males compete for estrous females and courtship is limited with no ongoing association after copulation. (Bradshaw and Bradshaw, 2002; Oates, et al., 2007; Rose, et al., 1997; Wooller, et al., 2000; Wooller, et al., 1999)

Mating System
polyandrous

Breeding interval
Honey possums breed whenever conditions are favourable.

Breeding season
Honey possums breed year round.

Range number of offspring
2 to 4

Average number of offspring
3
[External Source: AnAge]

Average gestation period
24 days
[External Source: AnAge]

Average birth mass
0.004 g
(0.00 oz)
[External Source: AnAge]

Range weaning age
60 (high) days

Range time to independence
60 (high) days

Range age at sexual or reproductive maturity (female)
90 (high) days

Range age at sexual or reproductive maturity (male)
90 (high) days

There is a strong association between reproductive success and diet in Tarsipes rostratus. Reproduction occurs during peak flowering periods when resources are abundant. In addition, breeding periods are affected by photoperiod and evidence suggests that the southern summer solstice triggers the first reproduction of the year. In general, breeding occurs from May to June, when day length begins to decrease and from September to October, when day length begins to increase. (Bradshaw and Bradshaw, 2002; Oates, et al., 2007; Wooller, et al., 2000; Wooller, et al., 1999)

Key Reproductive Features
iteroparous ; year-round breeding ; gonochoric/gonochoristic/dioecious (sexes separate); viviparous ; embryonic diapause

Tarsipes rostratus has the smallest young of any mammal, which are reared in the pouch for about 60 days. By 60 days old young are highly mobile, fully-furred, and have eyes that are completely open. Young become sexually mature around 90 days and females often breed before their young disperse. Due to a period of embryonic diapause, gestation in T. rostratus lasts from 60 to 80 days longer than in other marsupials. Unlike other mammals, embyonic diapause in T. rostratus is not controlled by lactation. (Bradshaw and Bradshaw, 2002; Oates, et al., 2007; Wooller, et al., 2000; Wooller, et al., 1999)

Parental Investment
female parental care ; pre-weaning/fledging (Provisioning: Female, Protecting: Female); pre-independence (Provisioning: Female, Protecting: Female)

Lifespan/Longevity

Range lifespan
Status: wild

1 to 2 years

Honey possums are relatively short lived, with a lifespan of 1 to 2 years. Lifespan of captive individuals has not been documented. (Wooller, et al., 1999)

Behavior

Honey possums are nocturnal or crepuscular and are relatively nonsocial. In captivity, however, they huddle in large groups when they sleep but no such behavior has been observed in natural populations. There is little evidence of territoriality, however, females are dominant to males. (Bradshaw and Bradshaw, 2002; Rose, et al., 1997; Wooller, et al., 1999)

Key Behaviors
nocturnal ; crepuscular ; daily torpor

Home Range

Females and males have individual home ranges but there is overlap between the home ranges of the different sexes. Male home ranges are much greater than those of females, primarily because they take refuge in a various locations throughout the day to avoid dominant females. Male honey possums can travel up to 114 m during the night to reach their feeding grounds. (Bradshaw and Bradshaw, 2002; Rose, et al., 1997)

Communication and Perception

Little is known of communication and perception in Tarsipes rostratus. In other possum species, it has been suggested that secretions from the holocrine gland are used to mark habitats and signal alarm. There is no evidence indicating that possums use scent marking to attract potential mates. (Woolhouse, et al., 1994)

Communication Channels
chemical

Other Communication Modes
scent marks

Perception Channels
visual ; acoustic

Food Habits

Tarsipes rostratus consumes pollen and nectar from a variety of flowering plants. It is the only flightless animal that feeds exclusively on pollen and nectar. Large amounts of pollen and nectar are consumed from plants belonging to the families Proteaceae, Epacridaceae, and Myrtacae. Tarsipes rostratus prefers to forage on Banksia spp., which are large plants with widely separated and exposed inflorescences from the family Proteaceae. The Mediterranean climate of south-west Western Australia is prone to recurrent fires, which has a significant effect on the population density of T. rostratus. Areas that remain unburnt for longer periods of time have larger plants, which bear more inflorescences. Plants with more inflorescences are correlated with increased abundance of T. rostratus. Its feet and prehensile tail are used for climbing, while their forepaws with elongated digits are used to manipulate flowers during feeding. In order to acquire the necessary nutrients from nectar, a substantial quantity of fluid must be consumed. As a result of the high water content in their diet in conjunction with their inability to concentrate urine, T. rostratus frequently excretes high volumes of dilute urine. (Bradshaw and Bradshaw, 2002; Everaardt, 2008; Richardson, et al., 1986; Slaven and Richardson, 1988; Sumner, et al., 2005; Wooller, et al., 1999)

Primary Diet
herbivore (Nectarivore )

Plant Foods
nectar; pollen

Predation

Known Predators


Aerial predators of honey possums, include barn owls (Tyto alba) and black-shouldered kites (Elanus caesuleus), and common terrestrial predators include red foxes (Vulpes vulpes) and feral cats (Felis domesticus). In certain parts of their range, Fitzgerald River National Park, other potential predators include tiger snakes (Notechis scutatus), southern monitors (Varanus rosenbergi), square-tailed kites (Lophoictinia isura), Australian kestrels (Falco cenchroides), brown falcons (Falco berigora), and boobook owls (Ninox novaeseelandiae). Honey possums are arboreal and are most commonly found in the lower canopy. As a result, the upper canopy likely provides shelter from aerial predators and being elevated off the forest floor likely decreases predation pressure from terrestrial predators. (Bradshaw and Bradshaw, 2002; Everaardt, 2003; Everaardt, 2008)

Ecosystem Roles

Honey possums are important pollinators for a number of different plants and are the principle pollinators of nodding banksia (Banksia nutans), which is common on the southern coast of Western Australia. (Wooller and Wooller, 2003)

Ecosystem Impact
pollinates

Economic Importance for Humans: Positive

There are no known positive effects of Tarsipes rostratus on humans.

Economic Importance for Humans: Negative

There are no known adverse effects of Tarsipes rostratus on humans.

Conservation Status

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

US Federal List [Link]
No special status

CITES [Link]
No special status

State of Michigan List [Link]
No special status

According to the IUCN Red List of Threatened Species, honey possums are a species of “least concern”. Due to their relative abundance and broad distribution, there are no major threats to their existence. However, bushfires can result in significant habitat loss. In addition, water mold (Phytophthora cinnamomi), which is prevalent in many high humidity environments, can cause plant pathogens that could decrease resource abundance for honey possums. Finally, feral cats may have a negative effect on honey possum abundance. (Friend, et al., 2008)

For More Information

Find Tarsipes rostratus information at

Contributors

Yengin Loay (author), University of Manitoba, Jane Waterman (editor), University of Manitoba, John Berini (editor), Special Projects.

References

Gnangara Department of Environment and Conservation. Restoration of banksia woodlands after the removal of pines Gnangara: evaluation of seeding trials.. Perth, AU: Murdoch University. 2008. Accessed February 24, 2011 at http://www.water.wa.gov.au/sites/gss/Content/reports/Restoration%20Banksia%20woodlands%20-%20evaluation%20of%20seeing%20trials.pdf.

Bradshaw, S., F. Bradshaw. 2007. Isotopic measurements of field metabolic rate (FMR) in the marsupial honey possum (Tarsipes rostratus). Journal of mammalogy, 88: 401-407.

Bradshaw, S., F. Bradshaw. 2002. Short-term movements and habitat use of the marsupial honey possum (Tarsipes rostratus). Journal of Zoology, 258: 343-348.

Cooper, C., A. Cruz-Neto. 2009. Metabolic, hygric and ventilatory physiology of a hypermetabolic marsupial, the honey possum (Tarsipes rostratus). Journal of Comparative Physiology, 179: 773-781.

Everaardt, A. 2003. "The impact of fire on the honey possum Tarsipes rostratus in the Fitzgerald River National Park, Western Australia." (On-line pdf). Murdoch University Research Repository. Accessed March 04, 2011 at http://researchrepository.murdoch.edu.au/66/2/02Whole.pdf.

Everaardt, A. 2008. The impact of fire upon the size and flowering of three honey possum foodplants at the western end of the Fitzgerald River National Park, Western Australia. Western Australian Naturalist, 26: 85-98.

Friend, T., K. Morris, A. Burbidge, N. McKenzie. 2008. "Tarsipes rostratus" (On-line). IUCN Red List of Threatened Species. Accessed November 11, 2010 at http://www.iucnredlist.org/apps/redlist/details/40583/0.

Nagy, K., C. Meienberger, S. Bradshaw, R. Wooller. 1995. Field metabolic rate of a small marsupial mammal, the honey possum (Tarsipes rostratus). Journal of Mammalogy, 76: 862-866.

Oates, J., F. Bradshaw, S. Bradshaw, E. Stead-Richardson, D. Philippe. 2007. Reproduction and embryonic diapause in a marsupial: Insights from captive female honey possums, Tarspies rostratus (Tarsipedidae). General and Comparative Endocrinology, 150: 445-461.

Richardson, K., R. Wooller, B. Collins. 1986. Adaptations to a diet of nectar and pollen in the marsupial Tarsipes rostratus (Marsupialia: Tarsipedidae). Journal of Zoology, 208: 285-297.

Rose, R., C. Nevison, A. Dixson. 1997. Testes weight, body weight and mating systems in marsupials and monotremes. Journal of Zoology, 243: 523-531.

Slaven, M., K. Richardson. 1988. Aspects of the Form and Function of the Kidney of the Honey Possum, Tarsipes rostratus. Australian Journal of Zoology, 36: 465-471.

Sumner, P., C. Arrese, J. Partridge. 2005. The ecology of visual pigment tuning in an Australian marsupial: the honey possum Tarsipes rostratus. Journal of Experimental Biology, 208: 1803-1815.

Withers, P., K. Richardson, R. Wooller. 1990. Metabolic Physiology of Euthermic and Torpid Honey Possums, Tarsipes rostratus. Australian Journal of Zoology, 37: 685-93.

Woolhouse, A., R. Weston, B. Hamilton. 1994. Metabolic physiology of euthermic and torpid honey possums, Tarsipes rostratus. Australian Journal of Zoology, 37: 685-693.

Wooller, R., K. Richardson, G. Bradly. 1999. Dietary constraints upon reproduction in an obligate pollen and nectar-feeding marsupial, the honey possum (Tarsipes rostratus). Journal of Zoology, 248: 279-287.

Wooller, R., K. Richardson, C. Garavanta, V. Saffer, K. Bryant. 2000. Opportunistic breeding in the polyandrous honey possum, Tarsipes rostratus. Australian Journal of Zoology, 48: 669-680.

Wooller, R., S. Wooller. 2003. The role of non-flying animals in the pollination of Banksia nutans. Australian Journal of Botany, 51: 503-507.

To cite this page: Loay, Y. 2011. "Tarsipes rostratus" (On-line), Animal Diversity Web. Accessed May 23, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tarsipes_rostratus.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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