Thryonomys gregorianuslesser cane rat

Ge­o­graphic Range

The genus Thry­on­o­mys is re­stricted to sub-Sa­ha­ran Africa. Thry­on­o­mys gre­go­ri­anus oc­curs through­out east­ern Africa and into west­ern Africa in the coun­tries of Cameroon, the Cen­tral African Re­pub­lic, Chad, the De­mo­c­ra­tic Re­pub­lic of Congo, Kenya, Malawi, Sudan, Tan­za­nia, Uganda, and Zam­bia. An iso­lated pop­u­la­tion also ex­ists in Zim­babwe and Mozam­bique. It is likely that pop­u­la­tions exist in An­gola, how­ever no records have been col­lected west of the Zam­bian bor­der. (An­to­nan­zas, et al., 2004; Skin­ner and Chim­imba, 2005)

Habi­tat

Lesser cane rats, oc­ca­sion­ally re­ferred to as sa­vanna cane rats, in­habit moist grass­lands dom­i­nated by ele­phant grass (Pen­nis­tum pur­pureum). They are also oc­ca­sion­ally found along the fringes of swamps and in wooded areas. In­di­vid­u­als usu­ally use tall grass for shel­ter, but have also been found dig­ging shal­low bur­rows or using rock crevices, ter­mite mounds, and aban­doned aard­vark or por­cu­pine holes. This species is con­sid­ered non-aquatic, dif­fer­ing in habi­tat pref­er­ence from the semi-aquatic Thry­on­o­mys swide­ri­anus. In­di­vid­u­als have been recorded up to al­ti­tudes of 2,600 m. (Ansell, 1966; King­don, 1984; Nowak, 1991; Sheppe and Os­borne, 1971)

  • Range elevation
    2,600 (high) m
    ft

Phys­i­cal De­scrip­tion

Thry­on­o­mys gre­go­ri­anus is the smaller of the two ex­tant species in the genus Thry­on­o­mys. Thry­on­o­mys swinde­ri­anus is the larger of the two species. Lesser cane rat body mea­sure­ments are: av­er­age head to tail length 380 mm; av­er­age tail length 90 mm; and av­er­age hind foot length 59 mm. Body mass can range from 2.65 to 7.5 kg. Thry­on­o­mys species are cov­ered with bris­tle-like hairs that grow in groups of five or six, and lay lon­gi­tu­di­nally along their bod­ies. They lack un­der­fur. Typ­i­cal body col­oration is speck­led gray­ish brown or yel­low­ish brown on the back and flanks, with grey or whitish under parts. The tail is sparsely cov­ered with short bris­tle-like hairs, with scales pre­sent be­tween hairs. The tail is brown­ish above and whitish un­der­neath. Ears are short, rounded, and hardly ex­tend be­yond the body pelage. The fore­foot has three well-de­vel­oped cen­tral dig­its, while the first and fifth dig­its are smaller and al­most non-func­tional. On the hind foot the dig­its are larger, but the first digit is ab­sent. Each foot pos­sesses a naked palm and thick, heavy claws. Lesser cane rats have short tails that barely ex­tend past their out­stretched hind foot. This is a dis­tin­guish­ing char­ac­ter­is­tic from their close rel­a­tive, T. swinde­ri­anus, which has a tail twice the length of the foot. Lesser cane rats have two paired mam­mae com­pared with three in T. swinde­ri­anus. The den­tal for­mula is: i 1/1, c 0/0, pm 1/1, m 3/3. Adult skulls can be iden­ti­fied by the place­ment of three groves on the an­te­rior sur­face of each upper in­cisor. The third, out­er­most groove is lo­cated near the out­side edge of the tooth, rather than along the mid­line of the tooth as in T. swinde­ri­anus. Most adult and ju­ve­nile skulls can also be dif­fer­en­ti­ated from T. swinde­ri­anus skulls by the pres­ence of a bar across each fora­men ovale, a square ap­pear­ance of the pair frontal bones when viewed dor­sally, and a right angle ori­en­ta­tion of the zy­go­matic arch and the dor­sal and ven­tral at­tach­ments of the outer rim of the in­fra­or­bital fora­men on the lat­eral side of the skull. (King­don, 1984; Nowak, 1991; Thomas, 1922; Van der Merwe, 2007)

  • Sexual Dimorphism
  • male larger
  • Range mass
    2.65 to 7.50 kg
    5.84 to 16.52 lb
  • Average length
    380 mm
    14.96 in

Re­pro­duc­tion

In Thry­on­o­mys species, males ini­ti­ate courtship by wag­ging their tails and tread­ing the hind legs. If the fe­male is at­tracted to these ac­tions, the pair will rear up and touch noses, fol­lowed by cop­u­la­tion. Male cane rats also use nose to nose push­ing duels to es­tab­lish a dom­i­nance hi­er­ar­chy within in their so­cial group, which pre­sum­ably in­flu­ences mate se­lec­tion by fe­males. (Ewer, 1968; King­don, 1984)

Al­though lit­tle is known about re­pro­duc­tion in T. gre­go­ri­anus, in most re­gions they seem to be sea­sonal breed­ers, re­pro­duc­ing dur­ing the wet­ter months. Two lit­ters a year are pos­si­ble under fa­vor­able con­di­tions. It is thought that Thry­on­o­mys species reach sex­ual ma­tu­rity after one year. Scarce records show preg­nant fe­males car­ry­ing 2 to 3 fe­tuses. Ges­ta­tion in Thry­on­o­mys lasts ap­prox­i­mately three months. Due to this low re­pro­duc­tive po­ten­tial, ex­ploited pop­u­la­tions may take long pe­ri­ods of time to re­cover. (Fiedler, 1994; King­don, 1984; Skin­ner and Chim­imba, 2005)

  • Breeding interval
    Two litters a year are possible under favorable conditions.
  • Breeding season
    Breeding usually occurs during the wetter months.
  • Average number of offspring
    2-3
  • Average gestation period
    3 months
  • Average age at sexual or reproductive maturity (female)
    1 years
  • Average age at sexual or reproductive maturity (male)
    1 years

Thry­on­o­mys gre­go­ri­anus young are born pre­co­cial, are ac­tive shortly after birth, de­velop rapidly, and are suck­led by the fe­male in grass nests (forms). (King­don, 1984)

  • Parental Investment
  • precocial
  • female parental care
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

It is thought that Thry­on­o­mys gre­go­ri­anus in­di­vid­u­als rarely live past three years. (King­don, 1984)

  • Range lifespan
    Status: wild
    3 (high) years

Be­hav­ior

Lesser cane rats are soli­tary in their habits, but can oc­cupy a re­stricted area with a small fam­ily of up to a dozen in­di­vid­u­als. They are pri­mar­ily noc­tur­nal, but are oc­ca­sion­ally ac­tive dur­ing the day. Dom­i­nance fight­ing be­tween males in­volves a nose to nose push­ing duel. Both in­di­vid­u­als push until one re­lieves pres­sure, caus­ing the dom­i­nant in­di­vid­ual to whip its rump around and hit its op­po­nent, knock­ing the weaker in­di­vid­ual off bal­ance. (Ewer, 1968; Nowak, 1991; Skin­ner and Chim­imba, 2005)

  • Range territory size
    3,000 to 4,000 m^2

Home Range

Thry­on­o­mys gre­go­ri­anus fam­ily groups have ter­ri­tory sizes of 3,000 to 4,000 square me­ters. (Nowak, 1991)

Com­mu­ni­ca­tion and Per­cep­tion

Thry­on­o­mys gre­go­ri­anus in­di­vid­u­als have poor eye­sight, but good senses of smell and hear­ing. Vo­cal­iza­tions in­clude whistling and low hoot­ing grunts. They will also thump their hind feet when alarmed. (King­don, 1984; Nowak, 1991)

Food Habits

Lesser cane rats are her­bi­vores that feed mainly on grasses and cane, but also feed on nuts, bark, fruits, and cul­ti­vated crops. They com­monly gnaw on rocks, bones, and ivory. Lesser cane rat habi­tat is typ­i­cally dom­i­nated by ele­phant grass and is there­fore con­sid­ered a prin­ci­pal food source. It is com­mon for ground­nut, sweet potato, cas­sava, maize, and pump­kin crops to be preyed on by these cane rats. Thry­on­o­mys gre­go­ri­anus in­di­vid­u­als also prac­tice co­prophagy. (King­don, 1984; Nowak, 1991; Opara, 2010)

  • Plant Foods
  • leaves
  • roots and tubers
  • wood, bark, or stems
  • seeds, grains, and nuts
  • fruit
  • Other Foods
  • dung

Pre­da­tion

Preda­tors in­clude hu­mans, ser­vals, leop­ards, viver­rids, pythons, and var­i­ous birds of prey. (Dro­nen, et al., 1999; King­don, 1984)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Lesser cane rats pro­vide nu­tri­tion as a prey species to their preda­tors. A species of anoplo­cephalid tape­worm, Thysan­o­tae­nia con­golen­sis, was dis­cov­ered in lesser cane rats in the Lake Kivv area of the De­mo­c­ra­tic Re­pub­lic of Congo. They are the only known host for this species of tape­worm. (Dro­nen, et al., 1999; King­don, 1984)

Com­men­sal/Par­a­sitic Species
  • anoplo­cephalid tape­worms (Thysan­o­tae­nia con­golen­sis)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Thry­on­o­mys species are in­ten­sively hunted as an im­por­tant source of pro­tein through­out their range. They are typ­i­cally hunted with dogs, spears, and fall-traps, or by burn­ing veg­e­ta­tion. It is es­ti­mated that, in West Africa, 80 mil­lion are har­vested an­nu­ally, equal­ing 300,000 met­ric tons of meat. To in­crease meat avail­abil­ity, Thry­on­o­mys species have been do­mes­ti­cated and cur­rently ef­forts are being made to ex­pand the in­dus­try. Greater cane rats are pre­ferred over lesser cane rats be­cause of their larger body size, how­ever it has been sug­gested that both species should be reared as part of the in­dus­try. Thry­on­o­mys species meat has more pro­tein than chicken, rab­bit, and guinea pig and lower fat than pork, beef, and lamb. The ex­pan­sion of this do­mes­ti­cated mar­ket may also re­lieve pres­sure on wild pop­u­la­tions of cane rats. (Fiedler, 1994; Hoff­mann, 2008a; How­ell, 1981; Jori, et al., 1995)

  • Positive Impacts
  • food

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Thry­on­o­mys species can do con­sid­er­able dam­age to sugar cane fields. Many plan­ta­tions pro­tect preda­tors, such as pythons so that they can prey on cane rats, less­en­ing crop dam­age. Cane rats also dam­age maize, mil­let, ground­nut, sweet potato, cas­sava, and pump­kin fields. (Nowak, 1991)

  • Negative Impacts
  • crop pest

Con­ser­va­tion Sta­tus

The ICUN Red List of Threat­ened Species lists lesser cane rats as a species of least con­cern due to their large pop­u­la­tion and wide dis­tri­b­u­tion. (Hoff­mann, 2008b)

Con­trib­u­tors

Brian Kiss (au­thor), Uni­ver­sity of Man­i­toba, Jane Wa­ter­man (ed­i­tor), Uni­ver­sity of Man­i­toba, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Ethiopian

living in sub-Saharan Africa (south of 30 degrees north) and Madagascar.

World Map

acoustic

uses sound to communicate

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

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

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

folivore

an animal that mainly eats leaves.

food

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

herbivore

An animal that eats mainly plants or parts of plants.

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

polygynous

having more than one female as a mate at one time

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

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

solitary

lives alone

tactile

uses touch to communicate

terrestrial

Living on the ground.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

tropical

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

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.

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.

young precocial

young are relatively well-developed when born

Ref­er­ences

Ansell, W. 1966. Thry­on­o­mys gre­go­ri­anus and Thry­on­o­mys swinde­ri­anus in Zam­bia. The Puku, 4: 1-16.

An­to­nan­zas, R., S. Sen, P. Mein. 2004. Sys­tem­at­ics and phy­logeny of the cane rats (Ro­den­tia: Thry­on­o­myi­dae). Zo­o­log­i­cal Jour­nal of the Lin­nean So­ci­ety, 142: 423-444.

Dro­nen, N., S. Simeik, J. Scharn­ing­hausen, R. Pitts. 1999. Thysan­o­tae­nia con­golen­sis n. sp. (Ces­toda: Anoplo­cephal­i­dae) in Lesser Sa­vanna Cane Rat, Thry­on­o­mys gre­go­ri­anus from De­mo­c­ra­tic Re­pub­lic of Congo, Africa. The Jour­nal of Par­a­sitol­ogy, 85: 90-92.

Ewer, R. 1968. Form and func­tion on the grass cut­ter, Thry­on­o­mys swinde­ri­anus Temm. (Ro­den­tia: Thry­on­o­myi­dae)). Ghana Jour­nal of Sci­ence, 9: 131-141.

Fiedler, L. 1994. Ro­dent pest man­age­ment in east­ern Africa. Rome: Food and Agri­cul­ture Or­ga­ni­za­tion of the United Na­tions.

Hoff­mann, L. 2008. The yield and nu­tri­tional value of meat from African un­gu­lates, camel­i­dae, ro­dents, ratites, and rep­tiles. Meat Sci­ence, 80: 94-100.

Hoff­mann, M. 2008. "Thry­on­o­mys gre­go­ri­anus" (On-line). ICUN Red List of Threat­ened Species. Ver­sion 2011.2. Ac­cessed No­vem­ber 29, 2011 at www.​icunredlist.​org.

How­ell, K. 1981. A note on the iden­ti­fi­ca­tion of cane rats, with records from Dar es Salaam. Bul­letin - East Africa Nat­ural His­tory So­ci­ety, 1981: 41-43.

Jori, F., G. Men­sah, E. Ad­janohoun. 1995. Grass­cut­ter pro­duc­tion: and ex­am­ple of ra­tio­nal ex­ploita­tion of wildlife. Bio­di­ver­sity and Con­ser­va­tion, 4: 257-265.

King­don, J. 1984. Thry­on­o­myid Ro­dents. Pp. 696-704 in East African Mam­mals, Vol. 2, Part B (hares and ro­dents). Chicago, Illi­nois: Uni­ver­sity of Chicago Press.

Nowak, R. 1991. Cane Rats. Pp. 956-957 in Walker's mam­mals of the world, Vol. 2, 5th Edi­tion. Bal­ti­more: The John Hop­kins Uni­ver­sity Press.

Opara, M. 2010. Grass­cut­ter: the haema­tol­ogy and major par­a­sites. Re­search Jour­nal of Par­a­sitol­ogy, 5: 214-223.

Sheppe, W., T. Os­borne. 1971. Pat­terns of use of a flood plain by Zam­bian mam­mals. Eco­log­i­cal Mono­graphs, 41: 179-205.

Skin­ner, J., C. Chim­imba. 2005. Lesser canerat. Pp. 96-97 in The mam­mals of the South African sub­re­gion, 3rd Edi­tion. Cam­bridge: Cam­bridge Uni­ver­sity Press.

Thomas, O. 1922. On the an­i­mals known as ground-hogs or cane-rats in Africa. An­nals & Mag­a­zine of Nat­ural His­tory, 9: 388-392.

Van der Merwe, M. 2007. Dis­crim­i­nat­ing be­tween Thry­on­o­mys swinde­ri­anus and Thry­on­o­mys gre­go­ri­anus. African Zo­ol­ogy, 42: 165-171.