Notomys fuscusdusky hopping mouse

Ge­o­graphic Range

Dusky hop­ping-mice are dis­trib­uted from Ooldea in S Aus­tralia to past Lake Eyre to SW Queens­land. They also cur­rently in­habit the re­gions of SE West­ern Aus­tralia, S North­ern Ter­ri­tory, South­ern Aus­tralia, N New South Wales, and NE South Aus­tralia (south­ern Strzeleki Desert and the Cob­blers Desert). Since 1985, N. fus­cus spec­i­mens have been col­lected from Car­raweena, Mon­tecol­lina Bore and Quinyam­bie Sta­tion, and from Pel­i­can Wa­ter­hole. (Grizmick 1990, Honaki 1982, Nowak 1991, Ro­dent Ac­tion Plan http://​www.​anca.​gov.​au/​plants/​threaten/​sched123.​htm)

Habi­tat

Dusky hop­ping-mice in­habit sand dunes, grass­lands, tree and shrub heaths, and lightly wooded areas. The tem­per­a­ture of their habi­tat is usu­ally very high with desert-like con­di­tions. N. fus­cus also live in sand ridge habi­tats, which al­ter­nate with gib­ber flats and clay pans, in the Pel­i­can Wa­ter­hole area. (Grizmick 1990, Honaki 1982, Nowak 1991, Ro­dent Ac­tion Plan

http://​www.​anca.​gov.​au/​plants/​threaten/​sched123.​htm)

Phys­i­cal De­scrip­tion

N. fus­cus is char­ac­ter­ized by its strong in­cisor teeth, long tail, large ears, dark eyes, and ex­tremely length­ened and nar­row hind feet, which have only four sole pads. Head and body length is 91-177 mm, tail length is 125-225 mm, and weight is about 20-50 grams. Col­oration of the upper parts varies from pale sandy brown to yel­low­ish brown to ashy brown or gray­ish. The un­der­parts of dusky hop­ping-mice are white. The body cov­er­ing is fine, close and soft; and long hairs near the tip of the tail give the ef­fect of a brush. No­to­mys fus­cus has a well-de­vel­oped se­ba­ceous glan­du­lar area on the un­der­side of its neck or chest. Fe­males have four mam­mae. (Grizmick 1990, Honaki 1982, Nowak 1991)

Re­pro­duc­tion

Lit­tle is known of the breed­ing bi­ol­ogy of this species in the wild other than that it is an op­por­tunis­tic breeder. In cap­tiv­ity, its breed­ing pat­tern is polye­strous, with no ev­i­dence of sea­son­al­ity, thus it breeds through­out the year. The ges­ta­tion pe­riod is 38-41 days; a post­par­tum es­trus is not com­mon in N. fus­cus, but some fe­males enter es­trus 14-22 days after giv­ing birth. The es­trous cycle lasts about 7-8 days. Dusky hop­ping-mice rear lit­ters of 1-5 young. Their young weigh about 2-4 grams at birth and open their eyes at 18-28 days. The young cling to the nip­ples of the mother and are dragged about wher­ever she goes, and wean­ing oc­curs at about 30 days. Both sexes of N. fus­cus reach re­pro­duc­tive ma­tu­rity at 70 days. It was seen that one fe­male N. fus­cus pro­duced 9 lit­ters in her life­time of 26 months. Males are ca­pa­ble of breed­ing up to the age of 38 months. (Grizmick 1990, Honaki 1982, Nowak 1991)

  • Key Reproductive Features
  • gonochoric/gonochoristic/dioecious (sexes separate)
  • sexual

Be­hav­ior

The se­ba­ceous glan­du­lar area is ac­tive in all adult males but is ac­tive in fe­males only dur­ing preg­nancy and lac­ta­tion. Nowak (1991) sug­gests that the glands are used for ter­ri­to­r­ial mark­ing and mark­ing of group mem­bers, in­clud­ing new­born young. Dusky hop­ping-mice are salta­to­r­ial and nor­mally move awk­wardly on all fours or make short hops. If star­tled, they bound rapidly using only their large hind feet. The mice dig their own bur­rows, some being of a sim­ple con­struc­tion but oth­ers being com­plex. The dusky hop­ping-mouse digs a bur­row on the flat top of a dune with a sin­gle tun­nel about 10 cm in di­am­e­ter, more than a meter below the sur­face and up to 5 m long. It is con­nected to the sur­face by up to 6 ver­ti­cal en­trance shafts that are dug from below and may end up any­where on the sur­face. A nest, con­sist­ing of a pad of finely chewed veg­e­ta­tion, is placed in the cen­ter of a small al­cove off the main shaft, and well-marked pads con­nect dif­fer­ent bur­rows along the top of the dune. The width of the en­trance shafts is crit­i­cal be­cause the an­i­mals move in them by hop­ping; they brace their backs against the sides with their forefeet be­tween hops. Progress when com­ing down a shaft is a head­long dive, with the back braced against the wall of the shaft and the forelegs used as a brake. If the en­ter­ing an­i­mal finds that the bur­row is blocked with loose sand, it often squeaks sev­eral times. This usu­ally at­tracts other oc­cu­pants and to­gether, from op­po­site sides, they rapidly clear the block­age. N. fus­cus is com­monly found in as­so­ci­a­tion with mar­su­pial coun­ter­parts and some­times shares the same tun­nel sys­tems. Liv­ing in groups of about five in­di­vid­u­als in one or two ad­ja­cent bur­rows sys­tems, the Dusky Hop­ping-mouse spends all its life on the dunes. Being a noc­tur­nal an­i­mal, it rests in its bur­row dur­ing the day, in­su­lated from the hot sur­face. At night, it for­ages on the top and sides of a dune, and rarely ven­tures more than a few me­ters away. Even in ap­par­ently fa­vor­able lo­cal­i­ties, pop­u­la­tion den­sity is low, with in­di­vid­u­als in­con­spic­u­ously con­gre­gated in a loose colony in a small area of a sand­hill. Dusky Hop­ping-mice calls in­clude twit­ter­ing dur­ing an­i­mated chases. How­ever, none of the sounds was as­so­ci­ated with threats or fight­ing. (Grizmick 1990, Honaki 1982, Nowak 1991)

Com­mu­ni­ca­tion and Per­cep­tion

Food Habits

No­to­mys fus­cus is like other hop­ping-mice in that it does not drink, but ob­tains all its water and food re­quire­ments from a diet of seeds, berries, leaves, green plants and oc­ca­sion­ally in­sects. (Grizmick 1990, Honaki 1982, Nowak 1991)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

No­to­mys fus­cus is used in stud­ies of re­pro­duc­tion be­cause of its rapid breed­ing cycle. Some stud­ies have in­cluded fe­male and male N. fus­cus re­pro­duc­tive anatomy and phys­i­ol­ogy, while other stud­ies have fo­cused on ge­netic analy­ses. (Baver­stock 1977, Breed 1982, Breed 1985)

Con­ser­va­tion Sta­tus

The N. fus­cus pop­u­la­tion is very small, and the species is rarely seen in its known habi­tats. Re­cent cap­ture rates sug­gests the num­bers of dusky hop­ping-mice to be 10 000. The rea­son for de­cline in `N. fus­cus <<No­to­mys fus­cus>` pop­u­la­tion size is not known. No­to­mys fus­cus is noted in the lists of ANZECC, and in Ap­pen­dix II of the Con­ven­tion in In­ter­na­tional Trade of En­dan­gered Species (CITES). IUCN con­sid­ers N. fus­cus to be a vul­ner­a­ble taxon with pop­u­la­tions that have been se­ri­ously de­pleted and whose ul­ti­mate se­cu­rity is not yet as­sured. There have been some ef­forts to as­sist the re­cov­ery of pop­u­la­tions of N. fus­cus by or­ga­ni­za­tions in­clud­ing the De­part­ment of En­vi­ron­ment and Nat­ural Re­sources, SA, and Qld De­part­ment of En­vi­ron­ment and Her­itage and Con­ser­va­tion Com­mis­sion of the North­ern Ter­ri­tory. Their re­cov­ery ob­jec­tives are to un­der­take a sur­vey to de­ter­mine the species' cur­rent dis­tri­b­u­tion, pop­u­la­tion size, and habi­tat re­quire­ments. (Refu­gia for Bi­o­log­i­cal Di­ver­sity in Arid and Semi-arid Aus­tralia http://​kaos.​erin.​gov.​au/​life/​general_​info/​biodivser_​4/​bio119.​html

Ro­dent Ac­tion Plan http://​www.​anca.​gov.​au/​plants/​threaten/​sched123.​htm)

Other Com­ments

No­to­mys fus­cus means dusky south­ern mouse. Their large ears are not only for pick­ing up sounds of preda­tors but are also an adap­ta­tion for liv­ing in ex­treme heat. The large sur­face area of the ears al­lows the blood to flow and cool in the air, thus low­er­ing the body tem­per­a­ture by low­er­ing the tem­per­a­ture of the blood. Key threats are graz­ing by stock and rab­bits. Like other arid zone ro­dents, N. fus­cus is sub­ject to pe­ri­odic pop­u­la­tion fluc­tu­a­tions. The num­bers in the pop­u­la­tion fol­low the sea­sons of good rain­fall and plant growth. In times of sparse rain­fall, N. fus­cus is well adapted for sur­vival on ac­count of its abil­ity to ex­crete waste ni­tro­gen in the form of one of the most highly con­cen­trated urines known in a ro­dent. (Grizmick 1990, Honaki 1982, Nowak 1991, Refu­gia for Bi­o­log­i­cal Di­ver­sity in Arid and Semi-arid Aus­tralia http://​kaos.​erin.​gov.​au/​life/​general_​info/​biodivser_​4/​bio119.​html, Ro­dent Ac­tion Plan http://​www.​anca.​gov.​au/​plants/​threaten/​sched123.​htm)

Con­trib­u­tors

Ken­neth Kim (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

desert or dunes

in deserts low (less than 30 cm per year) and unpredictable rainfall results in landscapes dominated by plants and animals adapted to aridity. Vegetation is typically sparse, though spectacular blooms may occur following rain. Deserts can be cold or warm and daily temperates typically fluctuate. In dune areas vegetation is also sparse and conditions are dry. This is because sand does not hold water well so little is available to plants. In dunes near seas and oceans this is compounded by the influence of salt in the air and soil. Salt limits the ability of plants to take up water through their roots.

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.

sexual

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

tactile

uses touch to communicate

tropical savanna and grassland

A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.

savanna

A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.

temperate grassland

A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.

Ref­er­ences

Baver­stock, PR. Poly­mor­phism of the X-Chro­mo­some, Y-Chro­mo­some and Au­to­somes in the Aus­tralian Hop­ping Mice N. fus­cus. Chro­mo­soma.. 1977. 61(3): 243-56.

Breed, WG. Mor­pho­log­i­cal vari­a­tion in testes and ac­ces­sory or­gans of Aus­tralian ro­dents in gen­era No­to­mys. Jour­nal of Re­pro­duc­tive Fer­til­ity. 1982. 66(2): 607-13

Breed, WG. Mor­pho­log­i­cal vari­a­tion in fe­male re­pro­duc­tive tract of Aus­tralian ro­dents in gen­era No­to­mys. Jour­nal of Re­pro­duc­tive Fer­til­ity. 1985. 73(2): 379-84.

En­dan­gered Species in the Arid Zone http://​rubens.​anu.​edu.​au/​student.​projects/​rabbits/​endangered.​html

Grizmick, B. Grizmick's En­cy­clo­pe­dia of Mam­mals. Mc­Graw-Hill, Inc. New York, NY. 1990. 3: 202-203.

Honaki, J. Mam­mal Species of the World. Allen Press Inc. Lawrence, KA. 1982. 538.

Nowak, R. Walker's Mam­mals of the World. John's Hop­kins Uni­ver­sity Press. Bal­ti­more, MD. 1991. 824.

Refu­gia for Bi­o­log­i­cal Di­ver­sity in Arid and Semi-arid Aus­tralia http://​kaos.​erin.​gov.​au/​life/​general_​info/​biodivser_​4/​bio119.​html

Ro­dent Ac­tion Plan http://​www.​anca.​gov.​au/​plants/​threaten/​sched123.​htm

Wil­son, D. E., and D. M. Reeder. Mam­mal Species of the World, A Tax­o­nomic and Ge­o­graphic Ref­er­ence. 2nd edi­tion. Smith­son­ian In­sti­tu­tion Press, Wash­ing­ton. 1993. 2: 753.