Potorous tridactyluslong-nosed potoroo

Ge­o­graphic Range

Po­torous tri­dacty­lus is widely dis­trib­uted in south­east­ern Aus­tralia and Tas­ma­nia and can be found in coastal New South Wales, south­east­ern Queens­land, coastal, near-coastal, and north­east­ern areas of Vic­to­ria, and the south­west­ern cor­ner of West­ern Aus­tralia (Cen­sus of Aus­tralian Ver­te­brate Species 1995 http://​www.​erin.​gov.​au/​life/​species/​fauna/​cavs81_​mammals.​html, Menkhorst 1995, Mor­ris 1965, Stra­han 1995, and Walker 1975).

Habi­tat

Rel­a­tively thick ground cover is an es­sen­tial com­po­nent of a po­toroo habi­tat; there­fore, these an­i­mals in­habit forests and woods where above-ground nests of dry veg­e­ta­tion can be built among grass tus­socks, under bushes, and in low, thick shrubs (Kowal­ski 1976, Matthews 1971, Mor­ris 1965, Stra­han 1995, Walker 1975). In ad­di­tion, po­toroos uti­lize a wide va­ri­ety of wet for­est and wet scrub habi­tats de­vel­oped on sandy loam soils where an­nual rain­fall ex­ceeds 760 mm (Menkhorst 1995). Fi­nally, P. tri­dacty­lus are usu­ally found at al­ti­tudes be­tween sea level and 250 m, but they has been ob­served at al­ti­tudes up to 650 m (Menkhorst 1995).

Phys­i­cal De­scrip­tion

Po­torous tri­dacty­lus is a rab­bit-sized rat-kan­ga­roo with an elon­gated muz­zle (Matthews 1971 and Mor­ris 1965). The length of its head and body is ap­prox­i­mately 300-400 mm, while its tail is about 150-260 mm long (Stra­han 1995 and Walker 1975). Its pelage is straight, soft, and loose with a grey or a light chest­nut brown col­oration of its upper parts, a gray­ish or whitish un­der­side, and often a white tipped tail (Matthews 1971, Mor­ris 1965, and Walker 1975). The me­dian claws of its manus (fore foot) - well adapted for scratch­ing and dig­ging - are very long and sharp (Hume 1982, Matthews 1971, and Mor­ris 1965). Po­torous has a down­ward-curv­ing, semi­prehen­sile tail used for car­ry­ing bun­dles of nest­ing ma­te­ri­als (Matthews 1971 and Mor­ris 1965). Its den­tal for­mula is 3/1, 1/0, 2/2, 4/4; it also has well-de­vel­oped ca­nines and bun­odont mo­lars (Mor­ris 1965 and Myers 1997). Po­toroos have en­larged hind feet and pow­er­ful hind limbs which be­stow them with adept hop­ping abil­i­ties at high speeds and a rab­bit-like gait at slower speeds (Myers 1997). Fi­nally, P. tri­dacty­lus has a well-de­vel­oped mar­supium that opens an­te­ri­orly and con­tains 4 mam­mae (teats) (Myers 1997 and Stra­han 1995). It is in­ter­est­ing to note that P. tri­dacty­lus pop­u­la­tions show con­sid­er­able mor­pho­log­i­cal vari­a­tion (Stra­han 1995). Over a dis­tance of only 200 km from the west­ern to the east­ern coast of north­ern Tas­ma­nia, the av­er­age size of these crea­tures nearly dou­bles and their coat color changes from ru­fous brown to grey-brown (Stra­han 1995). In ad­di­tion, the snout is rel­a­tively short in an­i­mals from Queens­land and in­creases pro­por­tion­ally in size in more south­ern pop­u­la­tions, being most elon­gate and nar­row in Tas­ma­nia (Stra­han 1995). Fi­nally, the pro­por­tion of in­di­vid­u­als with a white tip on their tail in­creases from zero at the north­ern ex­trem­ity of the range to 80% in Tas­ma­nia (Stra­han 1995).

Po­torous tri­dacty­lus, or the "three-toed po­toroo," is one of the first mam­mals recorded from Aus­tralia (Stra­han 1995). Its name comes from an er­ro­neous de­scrip­tion in Sur­geon-Gen­eral White's Jour­nal of a Voy­age to New South Wales in which he re­ferred to the foot of this crea­ture as hav­ing only three toes (due to the con­join­ing of its sec­ond and third dig­its) (Stra­han 1995). There­fore, the syn­dacty­lous con­di­tion found in P. tri­dacty­lus is re­spon­si­ble for the mis­nomer that has stuck with this an­i­mal ever since (Stra­han 1995).

  • Range mass
    0.7 to 1.8 kg
    1.54 to 3.96 lb
  • Average basal metabolic rate
    2.556 W
    AnAge

Re­pro­duc­tion

In eu­ther­ian mam­mals the op­ti­mum tem­per­a­ture for sper­mato­ge­n­e­sis is sev­eral de­grees cooler than deep body tem­per­a­ture (Tyn­dale-Bis­coe 1973). There­fore, these mam­mals have de­vel­oped a scro­tum as an adap­ta­tion for re­mov­ing their testes from a re­gion of deep body tem­per­a­ture to one that is cooler and closer to the op­ti­mum tem­per­a­ture for sper­mato­ge­n­e­sis (Tyn­dale-Bis­coe 1973). Po­torous tri­dacty­lus is a non-eu­ther­ian mam­mal; yet, male po­toroos have adopted the above eu­ther­ian adap­ta­tion. Fe­male po­toroos are poly­oestrus such that pe­ri­ods of oestrus and prog­es­ta­tion al­ter­nate cycli­cally and pro­vide the op­por­tu­nity to con­ceive at a sec­ond or sub­se­quent oestrus if the first is in­fer­tile (Tyn­dale-Bis­coe 1973). The 42 day oestrus cycle of P. tri­dacty­lus is at the upper limit of that ob­served in mar­su­pi­als, while its ges­ta­tion pe­riod is about 38 days (Menkhorst 1995 and Tyn­dale-Bis­coe 1973).

Sex­ual ma­tu­rity among males and fe­males is reached at about 12 months, and re­pro­duc­tive po­ten­tial is about 2.5 young/year (Menkhorst 1995). Both sexes mate promis­cu­ously, and breed­ing is con­tin­u­ous through­out the year with peaks in early spring and early sum­mer (Menkhorst 1995).

Fe­males give birth to a sin­gle new­born weigh­ing nearly 300 mg . The young suck­les in the mother's mar­supium for up to 120-130 days (Menkhorst 1995 ; Tyn­dale-Bis­coe 1973). Birth is often fol­lowed by a post-par­tum oestrus; mat­ing at this time re­sults in an em­bryo which re­mains dor­mant until the ex­ist­ing young leaves the pouch nat­u­rally or dies (Menkhorst 1995). After the ex­ist­ing young va­cates the mar­supium or dies, the qui­es­cent em­bryo re­sumes de­vel­op­ment and is born ap­prox­i­mately 30 days later (Menkhorst 1995). In­ter­est­ingly, new­born off­spring of P. tri­dacty­lus and other mar­su­pi­als are much less de­vel­oped at birth than pla­cen­tal off­spring, and in fact, they re­sem­ble a human fetus after the first trimester of ges­ta­tion (Myers 1997). After the young po­toroo leaves the pouch, it will con­tinue to suckle and fi­nally be weaned after about 170 days (Menkhorst 1995).

  • Key Reproductive Features
  • gonochoric/gonochoristic/dioecious (sexes separate)
  • sexual
  • Average number of offspring
    1
    AnAge
  • Average gestation period
    30 days
    AnAge
  • Average age at sexual or reproductive maturity (female)
    Sex: female
    400 days
    AnAge

Lifes­pan/Longevity

  • Average lifespan
    Status: captivity
    14.5 years
    AnAge

Be­hav­ior

Po­torous tri­dacty­lus is noc­tur­nal and rarely ven­tures far from cover dur­ing pe­ri­ods of ac­tiv­ity (Stra­han 1995). The wide di­etary spec­trum and dig­ging habits of P. tri­dacty­lus are strong sur­vival tools (Hume 1982). These have proved in­valu­able in al­low­ing them to sur­vive after brush fires that de­stroy all avail­able food sources apart from those un­der­ground (a sit­u­a­tion that causes many other mam­mals to per­ish) (Hume 1982). Long-nosed po­toroos are seden­tary crea­tures who live rel­a­tively soli­tary ex­is­tences ex­cept dur­ing pe­ri­ods of mat­ing or when they have young at foot (Menkhorst 1995, Stra­han 1995). Male home ranges of ap­prox­i­mately 47 acres over­lap the 12.5 acre ranges of fe­males, and there is some in­di­ca­tion that the home ranges of males do not over­lap (Mac­don­ald 1984). Po­torous tri­dacty­lus may live in the wild or in cap­tiv­ity for a pe­riod of over seven years, but longevi­ties of four or five years are much more com­mon (Menkhorst 1995, Walker 1975).

Com­mu­ni­ca­tion and Per­cep­tion

Food Habits

Po­torous tri­dacty­lus is an om­ni­vore and ob­tains much of its food by dig­ging shal­low holes with the claws of its fore feet (Hume 1982). Plant ma­te­r­ial - cran­ber­ries, fungi, grasses, juicy stems, roots, and tu­bers - con­sti­tute its main nu­tri­tional source through­out the year (Hume 1982, Matthews 1971, Mor­ris 1965). Of these fungi are the most com­monly eaten, while grasses are eaten only dur­ing win­ter when total food avail­abil­ity is at its low­est lev­els (Hume 1982). In­sects and their lar­vae com­pose a mea­ger 1-2% of the win­ter diet of P. tri­dacty­lus, but this can in­crease to 21% dur­ing the sum­mer when in­sect abun­dance aug­ments (Hume 1982 and Stra­han 1995). Fi­nally, it is in­ter­est­ing to note that in order to ob­tain a suf­fi­cient amount of fungi, po­toroos are forced to use a va­ri­ety of widely scat­tered feed­ing areas (Hume 1982).

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

The small num­ber and large size of P. tri­dacty­lus chro­mo­somes has led to the use of their cells - es­pe­cially those of the kid­ney and the testis - in tis­sue cul­ture stud­ies (Tyn­dale-Bis­coe 1973).

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Po­torous tri­dacty­lus and other rat-kan­ga­roos have been re­garded by farm­ers as pests be­cause of their affin­ity for crops (Mor­ris 1965).

Con­ser­va­tion Sta­tus

Po­torous tri­dacty­lus is still quite com­mon through­out Aus­tralia, al­though it and other rat-kan­ga­roos have ex­pe­ri­enced pop­u­la­tion de­creases at­trib­uted to the fol­low­ing: small size, com­pe­ti­tion with rab­bits for suc­cu­lent food, the spread­ing of poi­soned bait meant for the pop­u­la­tion con­trol of rab­bits, pre­da­tion by the in­tro­duced Eu­ro­pean fox and feral cats, and sport hunt­ing (Hume 1982, Matthews 1971, Mor­ris 1965). Most re­gional pop­u­la­tions are rel­a­tively se­cure, since the species oc­curs in con­ser­va­tion re­serves; how­ever, one iso­lated pop­u­la­tion in the Grampians re­gion of Vic­to­ria is at risk be­cause most of its very lo­cal­ized habi­tat is out­side the Na­tional Park bound­ary (Menkhorst 1995). The fre­quent oc­cur­rence of sub­fos­sil re­mains in cave de­posits in­di­cate that P. tri­dacty­lus was much more com­mon in the past (Stra­han 1995). It is not clear to what ex­tent its de­cline is the re­sult of human ac­tiv­i­ties, but it is ob­vi­ous that very large areas of suit­able habi­tat along the east­ern coast of Aus­tralia have been re­moved by land clear­ing (Stra­han 1995).

Other Com­ments

In De­cem­ber 1994 Gilbert's Po­toroo, Po­torous tri­dacty­lus gilberti, was re­dis­cov­ered at Two Peo­ples Bay Na­ture Re­serve east of Al­bany, West­ern Aus­tralia. This po­toroo was thought to be ex­tinct for 125 years prior to this dis­cov­ery, and after fur­ther in­spec­tion, three more an­i­mals were cap­tured. In total, two adult males, a sub-adult male, and two fe­males, each with a pouch young, have been cap­tured ( http://​www.​environment.​gov.​au/​life/​end_​vuln/​animals/​potoroo.​html 1997 and Stra­han 1995). Other com­mon names for P. tri­dacty­lus are the Long-nosed rat-kan­ga­roo and the Wal­laby Rat (Stra­han 1995).

Con­trib­u­tors

Nathan Lan­des­man (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Australian

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

World Map

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

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.

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.

scrub forest

scrub forests develop in areas that experience dry seasons.

sexual

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

tactile

uses touch to communicate

Ref­er­ences

Hume, I. D. 1982. Di­ges­tive phys­i­ol­ogy and nu­tri­tion of mar­su­pi­als. Cam­bridge Uni­ver­sity Press, Cam­bridge.

Mac­don­ald, D. 1984. En­cy­clo­pe­dia of Mam­mals. Facts on File Pub­li­ca­tions, New York City.

Matthews, L. H. 1971. The Life of Mam­mals. Vol­ume Two. Uni­verse Books, New York City.

Menkhorst, P. W. 1995. Mam­mals of Vic­to­ria: Dis­tri­b­u­tion, ecol­ogy, and con­ser­va­tion. Ox­ford Uni­ver­sity Press, Mel­bourne.

Mor­ris, D. 1965. The Mam­mals: A guide to the liv­ing species. Harper & Row Pub­lish­ers, New York City.

Myers, P. 1997. An­i­mal Di­ver­sity Web. http://​www.​oit.​itd.​umich.​edu/​projects/​ADW/​

1995. Cen­sus of Aus­tralian Ver­te­brate Species Web­page. http://​www.​erin.​gov.​au/​life/​species/​fauna/​cavs81_​mammals.​html

1997. http://​www.​environment.​gov.​au/​life/​end_​vuln/​animals/​potoroo.​html

Stra­han, R. 1995. Mam­mals of Aus­tralia. Smith­son­ian In­sti­tu­tion Press, Wash­ing­ton, D.C.

Tyn­dale-Bis­coe, H. 1973. Life of Mar­su­pi­als. Amer­i­can El­se­vier Pub­lish­ing Com­pany, Inc., New York City.

Walker, E. P. 1975. Mam­mals of the World. Third Edi­tion. Vol­ume One. The Johns Hop­kins Uni­ver­sity Press, Bal­ti­more.