Phalanger gymnotisground cuscus

Ge­o­graphic Range

Ground cus­cuses (Pha­langer gym­no­tis) are found on the is­lands of New Guinea, Yapen, Mis­ool, Salawati and the Aru Is­lands. Al­though rare, they have also been sighted in south­ern­most re­gions of New Guinea. ("Ground Cus­cus", 2004; Flan­nery, 2004; Wil­son and Reeder, 2005)

Habi­tat

Pha­langer gym­no­tis oc­cu­pies a va­ri­ety of habi­tats in­clud­ing rain­forests, caves and gar­dens. It is found from sea level up to 2,700 m but is most com­mon at the lower end of its al­ti­tu­di­nal range. Pri­mar­ily ter­res­trial, P. gym­no­tis seeks refuge in dens, which are con­structed in caves, under trees, and along stream beds. It may also be found in cul­ti­vated gar­dens, de­spite close prox­im­ity to hu­mans. ("Ground Cus­cus", 2004; George, 1987; Leary, et al., 2010; Ma­jnep and Bul­mer, 2007; Ra­mono and Nash, 1992)

  • Range elevation
    0 to 2,700 m
    0.00 to ft

Phys­i­cal De­scrip­tion

Pha­langer gym­no­tis has a short, coarse, grey-brown or sil­ver-grey coat that con­tains a dark mid-dor­sal stripe. Fur con­tin­ues down the rump, cov­er­ing the top of the tail. The re­main­der of the tail is cov­ered in small bumpy growths that in­crease fric­tion for grip­ping. Pha­langer gy­mo­tis has lit­tle to no fur on the ears. The lack of fur on the ears and the dark dor­sal stripe dis­tin­guish P. gym­no­tis from other mem­bers of its par­ent genus, Pha­langer. At higher al­ti­tudes, tail fur is more dense and may have a white tip. Sim­i­lar to other mem­bers of Pha­langer, P. gym­no­tis has five dig­its on each foot, in­clud­ing a sin­gle op­pos­able digit on the hind feet. The op­pos­able digit is the only digit lack­ing a claw. Ground cus­cuses vary in mass from 1,500 g to 4,850 g and in length from 310 mm to 539 mm. Tail length makes up a sig­nif­i­cant por­tion of its body length and ranges from 290 mm to 335 mm. In­di­vid­u­als in the north­ern­most part of its range tend to be larger, while in­di­vid­u­als at higher al­ti­tudes are smaller than those a lower al­ti­tude. (Feiler, 1978; Flan­nery, 1995; Flan­nery, 2004; George, 1987; McNab, 2008)

The skulls of Pha­langer gym­no­tis fea­ture a pow­er­ful zy­go­matic arch and promi­nent sagit­tal crest, a nar­row ros­trum, and short paroc­cip­i­tal processes. Pha­langer gym­no­tis is fur­ther di­vided into two sub­species, P. gym­no­tis gym­no­tis and P. gym­no­tis leu­cip­pus, which are dif­fer­en­ti­ated by the wider palate and broader nasals of P. gym­no­tis gym­no­tis. The basal meta­bolic rate of P. gym­no­tis is 518.2 cm^3 oxy­gen/hour. Sex­ual di­mor­phism has not been re­ported in this species. (Feiler, 1978)

  • Range mass
    1,500.0 to 4,850.0 g
    to oz
  • Range length
    310.0 to 539.0 mm
    12.20 to 21.22 in
  • Average basal metabolic rate
    518.2 cm3.O2/g/hr

Re­pro­duc­tion

Lit­tle is known about breed­ing in Pha­langer gym­no­tis in the wild. In cap­tive pop­u­la­tions, males court fe­males by chas­ing and bit­ing prospec­tive mates when they are in es­trus. Chas­ing may occur dur­ing day­light hours, but is most com­mon at night, as Pha­langer gym­no­tis is noc­tur­nal. Al­though the mat­ing sys­tem is un­known, it is ei­ther polyg­y­nous or polyg­y­nan­drous, as males have been noted mat­ing with at least two dif­fer­ent fe­males. (Shoe­maker and Crox­ton, 1982)

Pha­langer gym­no­tis mates year round and gives birth to a sin­gle new­born. Al­though ges­ta­tion lasts 13 days, de­layed im­plan­ta­tion may occur, length­en­ing the time be­tween cop­u­la­tion and birth. Fe­males are al­most al­ways found to have a sin­gle young in their pouch, so the breed­ing in­ter­val is as­sumed to cor­re­spond with the length of time to in­de­pen­dence for young. Young re­main in the moth­ers pouch for ap­prox­i­mately three months, at which point they exit the pouch at night. They con­tinue to sleep in the pouch until the age of 5-7 months, when they leave per­ma­nently. Time to wean­ing is un­clear as the con­tin­ued use of the pouch makes wean­ing ob­ser­va­tions dif­fi­cult. ("Ground Cus­cus", 2004; Shoe­maker and Crox­ton, 1982)

  • Breeding season
    Phalanger gymnotis breed year round
  • Range number of offspring
    1 (low)
  • Average gestation period
    13 days
  • Range time to independence
    5 to 7 months

Young are al­tri­cial and re­main in the mother's pouch, not leav­ing per­ma­nently until the age of 5-7 months. The mother pro­vides milk, but time to wean­ing is un­known. Young exit the pouch first at night, at ap­prox­i­mately 3 months old. The young do not exit dur­ing the day to sleep alone until the age of 4 to 5 months. (Flan­nery, 1995; Shoe­maker and Crox­ton, 1982)

  • Parental Investment
  • altricial
  • female parental care
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
    • protecting
      • female
  • pre-independence
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

The lifes­pan of wild Pha­langer gym­no­tis is un­known, but in­di­vid­u­als at least 15 years of age have been recorded in cap­tiv­ity. (Flan­nery, 1995; Good­night, et al., 2007)

  • Range lifespan
    Status: captivity
    15 (high) years

Be­hav­ior

Out­side of mat­ing sea­son, Pha­langer gym­no­tis is soli­tary and aso­cial, and in­di­vid­u­als are often ag­gres­sive to­ward con­specifics. Fight­ing is com­mon and in­cludes hiss­ing, honk­ing, foot thump­ing and strik­ing op­po­nents with the fore­limbs. Pha­langer gym­no­tis con­structs ter­res­trial dens and for­ages in the mid to lower canopy at night. It gen­er­ally re­mains on low, sta­ble branches while for­ag­ing. Using a flex­i­ble, grip­ping tail and op­pos­able hind thumbs, P. gy­mo­tis is an ac­com­plished climber and can eas­ily tra­verse for­est habi­tats. Pha­langer gym­no­tis is al­most en­tirely noc­tur­nal, how­ever, some in­di­vid­u­als have been seen out­side their dens dur­ing the early morn­ing. ("Ground Cus­cus", 2004; Flan­nery, 1995; Shoe­maker and Crox­ton, 1982; Wil­son and Reeder, 2005)

Home Range

There is no in­for­ma­tion avail­able re­gard­ing the home range of Pha­langer gym­no­tis.

Com­mu­ni­ca­tion and Per­cep­tion

Pha­langer gym­no­tis uses urine and cloa­cal gland se­cre­tions as scent mark­ers. The scent, pro­duced by both males and fe­males, is said to smell like cof­fee. It likely uses pheromones to de­mar­cate ter­ri­to­r­ial bound­aries and to at­tract po­ten­tial mates. Ground cus­cuses com­mu­ni­cate vo­cally be­fore and dur­ing mat­ing and while fight­ing. While fight­ing, P. gym­no­tis hisses, honks, and foot thumps to com­mu­ni­cate ag­gres­sion. (Flan­nery, 1995; Shoe­maker and Crox­ton, 1982)

Food Habits

Pha­langer gym­no­tis is pri­mar­ily fru­giv­o­rous, but also con­sumes eggs, seeds, and leaves. It for­ages on the fruit and leaves of plants from nu­mer­ous gen­era, in­clud­ing Elaeo­car­pus, Ficus, Pip­turus, Pan­danus, Oe­nathe, Run­gia, and Ficus odoardii. Fruit is col­lected from trees and from the ground. Fe­male ground cus­cuses have been ob­served fill­ing their pouches with fruit and then re­turn­ing to their home dens where it is stored. (Flan­nery, 1995; Ganslosser and Et­ter-Ganslosser, 1990; Hume, et al., 1997; Mack and Wright, 2005; Wil­son and Reeder, 2005)

  • Animal Foods
  • eggs
  • Plant Foods
  • leaves
  • seeds, grains, and nuts
  • fruit

Pre­da­tion

Other than hu­mans, Pha­langer gym­no­tis has no doc­u­mented preda­tors. Hu­mans prey upon P. gym­no­tis using traps, dogs, and tra­di­tional hunt­ing meth­ods. The noc­tur­nal, soli­tary, and ar­bo­real habits of P. gym­no­tis likely re­duces risk of pre­da­tion. (Leary, et al., 2010; White­head, 2000)

Ecosys­tem Roles

Fruit dis­per­sion may be in­creased by Pha­langer gym­no­tis. As large fru­gi­vores, ground cus­cuses are one of the only species large enough to dis­perse vir­tu­ally all fruits in the New Guinean rain­for­est. By translo­cat­ing fruit and in­gest­ing seeds, P. gym­no­tis is likely an im­por­tant seed dis­perser through­out its ge­o­graphic range. Par­a­sites spe­cific to this species have not been doc­u­mented. (Mack and Wright, 2005; Shoe­maker and Crox­ton, 1982)

  • Ecosystem Impact
  • disperses seeds

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Pha­langer gym­no­tis is hunted for its meat year round and is an im­por­tant pro­tein source for rural pop­u­la­tions through­out Papua New Guinea. In some com­mu­ni­ties, P. gym­no­tis is con­sumed only by se­nior el­ders of the com­mu­nity and is con­sid­ered to have med­i­c­i­nal qual­i­ties. (Dwyer, 1982; Leary, et al., 2010; White­head, 2000)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Ground cus­cuses may dwell in and around cul­ti­vated gar­dens and eat crops such as sweet pota­toes. (Ma­jnep and Bul­mer, 2007; Ra­mono and Nash, 1992)

  • Negative Impacts
  • crop pest

Con­ser­va­tion Sta­tus

Al­though hunt­ing has sig­nif­i­cantly re­duced local pop­u­la­tions of Pha­langer gym­no­tis, the species re­mains widely dis­trib­uted and is abun­dant through­out its ge­o­graphic range. It is clas­si­fied as a species of "least con­cern" on the IUCN's Red List of Threat­ened Species. In In­done­sia, P. gym­no­tis is pro­tected by law and can­not be cap­tured, kept or traded. Until re­cently, it was ac­cept­able for only the most se­nior mem­bers of many re­gional tribes in New Guinea to con­sume Pha­langer gym­no­tis, and as a re­sult, was in­fre­quently hunted. As food taboos in rural vil­lages changed dur­ing the 1970s and 1980s, P. gym­no­tis be­came an ac­cept­able food source for mem­bers of al­most all so­cial lev­els re­sult­ing in in­creased pres­sure from hunt­ing. ("Ground Cus­cus", 2004; Flan­nery, 2004; Ma­jnep and Bul­mer, 2007; Ra­mono and Nash, 1992; White­head, 2000)

Other Com­ments

Pha­langer gym­no­tis was for­merly a mem­ber of the genus Spi­lo­cus­cus, but mol­e­c­u­lar data led to its re­clas­si­fi­ca­tion. It in­cludes two sub­species, P. gym­no­tis gym­no­tis and P. gym­no­tis leu­cip­pus. (Feiler, 1978; Os­borne and Chris­tidis, 2002)

Con­trib­u­tors

Colleen Macke (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor, Phil Myers (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor, John Berini (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

Glossary

Australian

Living in Australia, New Zealand, Tasmania, New Guinea and associated islands.

World Map

acoustic

uses sound to communicate

altricial

young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.

arboreal

Referring to an animal that lives in trees; tree-climbing.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

chemical

uses smells or other chemicals to communicate

delayed implantation

in mammals, a condition in which a fertilized egg reaches the uterus but delays its implantation in the uterine lining, sometimes for several months.

drug

a substance used for the diagnosis, cure, mitigation, treatment, or prevention of disease

endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

female parental care

parental care is carried out by females

food

A substance that provides both nutrients and energy to a living thing.

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

frugivore

an animal that mainly eats fruit

herbivore

An animal that eats mainly plants or parts of plants.

island endemic

animals that live only on an island or set of islands.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

nocturnal

active during the night

pet trade

the business of buying and selling animals for people to keep in their homes as pets.

pheromones

chemicals released into air or water that are detected by and responded to by other animals of the same species

rainforest

rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.

scent marks

communicates by producing scents from special gland(s) and placing them on a surface whether others can smell or taste them

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

solitary

lives alone

stores or caches food

places a food item in a special place to be eaten later. Also called "hoarding"

suburban

living in residential areas on the outskirts of large cities or towns.

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

terrestrial

Living on the ground.

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

visual

uses sight to communicate

viviparous

reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.

year-round breeding

breeding takes place throughout the year

Ref­er­ences

2004. Ground Cus­cus. Pp. 64-65 in M Hutchins, D Kleiman, V Geist, eds. Grz­imek's An­i­mal Life En­cy­clo­pe­dia, Vol. 13, 2 Edi­tion. Farm­ing­ton Hills, MI: Thom­son Gale.

Dwyer, P. 1982. pp. 529-542. Jour­nal of An­i­mal Ecol­ogy, Vol. 51, No. 2: pp. 529-542.

Feiler, A. 1978. Be­merkun­gen über Pha­langer der "ori­en­talis-Gruppe". Pp. 385-395 in Zo­ol­o­gis­che Ab­hand­lun­gen, Vol. 34 Iss. 25. Leipzig, Ger­many: Akademis­che Ver­lags­ge­sellschaft Geest & Por­tig K.-G..

Flan­nery, T. 1995. Mam­mals of the South-West Pa­cific and Moluc­can Is­lands. Ith­ica, NY: Cor­nell Uni­ver­sity Presss.

Flan­nery, T. 2004. Pos­sums of the world : a mono­graph of Pha­langeroidea. Chatswood, NSW, Aus­tralia: Geo Pro­duc­tions.

Ganslosser, U., R. Et­ter-Ganslosser. 1990. Pha­langers. Pp. 308-309 in S Parker, ed. Grizmek's En­cy­clo­pe­dia of Mam­mals, Vol. 1, 1990 Edi­tion. Hast­ings-on-Hud­son, NY: Mc­Graw-Hill, Inc..

George, G. 1987. Char­ac­ter­i­sa­tion of the Liv­ing Species of Cus­cus. Pp. 513-515 in M Archer, ed. Pos­sums and Opos­sums: Stud­ies in Evo­lu­tion, Vol. 2. Chip­ping Nor­ton, NSW: Sur­rey Beatty & Sons.

Good­night, A., G. Couto, E. Green, M. Bar­rie, G. Myers. 2007. Chemother­apy and Ra­dio­ther­apy for Treat­ment of Cu­ta­neous Lym­phoma in a Ground Cus­cus. Jour­nal of Zoo and Wildlife Med­i­cine, Vol. 39, Iss.3: 472-475.

Hamil­ton, A., M. Springer. 1999. DNA Se­quence Ev­i­dence for Place­ment of the Ground Cus­cus, Pha­langer gym­no­tis , in the Tribe Pha­lan­gerini (Mar­su­pi­alia: Pha­lan­geri­dae). Jour­nal of Mam­malian Evo­lu­tion, Vol. 6 Iss. 1: 1-17.

Hume, I., M. Run­cie, J. Caton. 1997. Di­ges­tive phys­i­ol­ogy of the ground cus­cus (Pha­langer gym­no­tis), a New Guinean pha­lan­gerid mar­su­pial. Aus­tralian Jour­nal of Zo­ol­ogy, Vol. 45 Iss. 6: 561-571.

Leary, T., R. Sin­gadan, J. Men­zies, K. Hel­gen, D. Wright, A. Al­li­son, L. Salas, C. Dick­man. 2010. "Pha­langer gym­no­tis" (On-line). The IUCN Red List of Threat­ened Species. Ac­cessed Feb­ru­ary 26, 2011 at http://​www.​iucnredlist.​org/​apps/​redlist/​details/​16856/​0.

Mack, A., D. Wright. 2005. The Fru­gi­vore Com­mu­nity and the Fruit­ing Plant Flora in a New Guinea Rain­for­est: Iden­ti­fy­ing Keyston Fru­gi­vores. Pp. 185-194 in A Mack, ed. Trop­i­cal Fruits and Fru­gi­vores: The Search for Strong In­ter­ac­tors. Hei­del­berg, Ger­many: Springer Nether­lands.

Ma­jnep, I., R. Bul­mer. 2007. An­i­mals the An­ces­tors Hunted. Be­lair SA, Aus­tralia: Craw­ford House.

McNab, B. 2008. The Com­par­a­tive En­er­get­ics of New Guinean Cus­cuses (Metathe­ria: Pha­lan­geri­dae). Jour­nal of Mam­mal­ogy, Vol. 85 Iss. 5: 1145-1151.

Os­borne, M., L. Chris­tidis. 2002. Mol­e­c­u­lar re­la­tion­ships of the cus­cuses, brush­tail and scaly-tailed pos­sums (Pha­lan­geri­nae). AUS­TRALIAN JOUR­NAL OF ZO­OL­OGY, vol:50 iss:2: 135-149.

Ra­mono, W., S. Nash. 1992. Con­ser­va­tion of Mar­su­pi­als and Monotremes in In­done­sia. Pp. 13-19 in M Kennedy, ed. Aus­tralian Mar­su­pi­als and Monotremes. Gland, Switzer­land: IUCN. Ac­cessed April 06, 2011 at http://​data.​iucn.​org/​dbtw-wpd/​edocs/​1992-026.​pdf.

Shoe­maker, A., J. Crox­ton. 1982. Hus­bandry and Re­pro­duc­tion of the Ground Cus­cus Pha­langer-gym­no­tis in Cap­tiv­ity. In­ter­na­tional Zoo Year­book, Vol. 22 Iss.1: 176-180.

White­head, H. 2000. Food Rules: Hunt­ing, Shar­ing and Taboo­ing Game in Papua New Guinea. Ann Arbor, MI: The Uni­ver­sity of Michi­gan Press.

Wil­son, D., D. Reeder. 2005. Pha­langer gym­no­tis. Pp. 46 in D Wil­son, D Reeder, eds. Mam­mal Species of the World, Vol. 1, 3 Edi­tion. Bal­ti­more, Mary­land: The Johns Hop­kins Uni­ver­sity Press.