Rhyncholestes raphanurusChilean shrew opossum

Ge­o­graphic Range

Chilean shrew opos­sums (Rhyn­c­holestes rapha­nu­rus) have only been found in a small ge­o­graphic range that cov­ers south­ern Chile, Chiloe Is­land and a small part of south­ern Ar­gentina (ap­prox­i­mately 40 de­grees south lat­i­tude and 70 de­grees west lon­gi­tude). These an­i­mals have been cap­tured at el­e­va­tions from sea level to 1,135 m. Only two spec­i­mens have been cap­tured in Ar­gentina. This species was once thought to be rare; how­ever, it is pos­si­ble that they are abun­dant in lim­ited habi­tat types. (Meserve, et al., 1982; Pat­ter­son and Gal­lardo, 1987)

Habi­tat

Chilean shrew opos­sums re­side in tem­per­ate for­est habi­tats. Fa­vor­able mi­cro­cli­mates in­clude wet areas of south­ern beech (Nothofa­gus species) forests with plenty of coarse, woody de­bris and a thick un­der­story of shrub cover. These mar­su­pi­als are more fre­quently caught at el­e­va­tions lower than 600 me­ters. (Kelt and Mar­tinez, 1989)

  • Range elevation
    0 to 1135 m
    0.00 to 3723.75 ft

Phys­i­cal De­scrip­tion

Chilean shrew opos­sums are small mam­mals. Their body size can range from 10 to 13 cm. Their ven­tral and dor­sal por­tions are dark brown or gray. Their tail is shorter than their head to body length and is solid in color, with short, sparse hairs. Their body shape is shrew-like in ap­pear­ance and their ears are small and rounded. Den­tal pat­terns are used to de­ter­mine gen­der in this species, males have con­i­cal, sin­gle rooted upper ca­nines and fe­males have dou­ble-rooted ca­nines, re­sem­bling pre­mo­lars. (Pat­ter­son and Gal­lardo, 1987; Red­ford and Eisen­berg, 1992)

  • Sexual Dimorphism
  • sexes alike
  • Range length
    10 to 13 cm
    3.94 to 5.12 in

Re­pro­duc­tion

Lit­tle is known about caenolestid mat­ing sys­tems. The seem­ingly soli­tary be­hav­ior of Chilean shrew opos­sums, as well as the ran­dom dis­tri­b­u­tion of re­sources in their en­vi­ron­ment sug­gests a polyg­y­nan­drous (promis­cu­ous) mat­ing sys­tem. An­other hy­poth­e­sis sug­gests that these an­i­mals live in fam­ily groups and have a monog­a­mous mat­ing sys­tem. How­ever, nei­ther hy­poth­e­sis has been tested. (Kelt and Mar­tinez, 1989)

Few stud­ies have been con­ducted on the re­pro­duc­tive cycle of Chilean shrew opos­sums. Fe­males do not have a pouch and pos­sess five to seven teats. Pat­terns of teat de­vel­op­ment sug­gest lit­ters of 5 to 7 or greater. There is ev­i­dence that fe­males are ca­pa­ble of re­pro­duc­ing any time of the year, as lac­tat­ing fe­males have been cap­tured in Feb­ru­ary, March, May, Oc­to­ber, No­vem­ber and De­cem­ber. Males are thought to be re­pro­duc­tively ac­tive all year as well. They pos­sess a cleft penis and paired sperm. (Nowak, 1999; Pat­ter­son and Gal­lardo, 1987)

  • Breeding interval
    Breeding intervals are unknown in Chilean shrew opossums.
  • Breeding season
    Chilean shrew opossums may breed throughout the year.
  • Range number of offspring
    5 to 7

Lit­tle is known about parental care of Chilean shrew opos­sums. Re­searchers have never cap­tured a fe­male with young; this may sug­gest that these an­i­mals use a nest to raise their young. In close suc­ces­sion, an adult male, an adult fe­male and two ju­ve­niles were cap­tured in one trap, lead­ing to the hy­poth­e­sis that Chilean shrew opos­sums live in fam­ily groups. If this is ac­cu­rate, both male and fe­male par­ents may par­tic­i­pate in the care of their young. How­ever, this hy­poth­e­sis has not yet been tested. (Pat­ter­son and Gal­lardo, 1987)

  • Parental Investment
  • altricial
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female

Lifes­pan/Longevity

No data has been gath­ered on the life span of Chilean shrew opos­sums. Few trapped in­di­vid­u­als have been re­cap­tured, mak­ing it dif­fi­cult to judge their life span. Be­cause of their small body size, it is likely that they do not live more than a few years. (Meserve, et al., 1982)

Be­hav­ior

Chilean shrew opos­sums are usu­ally caught at night, in­di­cat­ing that they are noc­tur­nal. They are often caught near bur­rows and under logs and ap­pear to be semi-fos­so­r­ial, for­ag­ing under leaf lit­ter for in­sects. Lack of re­cap­ture may in­di­cate trap shy­ness, high post-cap­ture mor­tal­ity or a large home range. (Kelt and Mar­tinez, 1989)

Home Range

Due to lack of re­cap­ture data or radio track­ing, home range size is not known for Chilean shrew opos­sums.

Com­mu­ni­ca­tion and Per­cep­tion

Lit­tle is known about the com­mu­ni­ca­tion of Chilean shrew opos­sums or how they per­ceive their en­vi­ron­ment. They likely have poor eye­sight due to their noc­tur­nal ac­tiv­ity and small eyes. Vib­ris­sae are used to sense in­sects and ob­jects in the en­vi­ron­ment. Ex­am­i­na­tion of their brains shows large ol­fac­tory bulbs, in­di­cat­ing an acute sense of smell. (Pat­ter­son and Gal­lardo, 1987)

Food Habits

Chilean shrew opos­sums are semi-fos­so­r­ial, for­ag­ing in the lit­ter layer for soil in­ver­te­brates (54% of diet) and earth­worms (7%). An­other prin­ci­ple com­po­nent of their diet is plant ma­te­r­ial and fungi (39%). When cap­tur­ing these an­i­mals, suc­cess­ful traps are com­monly baited with rolled oats. (Meserve, et al., 1988)

  • Animal Foods
  • insects
  • terrestrial non-insect arthropods
  • mollusks
  • terrestrial worms
  • Plant Foods
  • seeds, grains, and nuts
  • Other Foods
  • fungus

Pre­da­tion

Lit­tle data has been gath­ered on pre­da­tion of Chilean shrew opos­sums. Like most small mam­mals, they are likely a food base for noc­tur­nal car­ni­vores. Pos­si­ble ver­te­brate preda­tors in­clude vari­able hawks, white-tailed kites, Amer­i­can kestrels, black-chested buz­zard ea­gles, Har­ris's hawks, bur­row­ing owls, great horned owls, barn owls, culpeos, long-tailed snakes and Peru slen­der snakes. Chilean shrew opos­sums are small, cryp­tic, noc­tur­nal an­i­mals and likely avoid most pre­da­tion by being dif­fi­cult to find. (Jak­sic, et al., 1980; Nowak, 1999)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Other than their con­sump­tion of in­sects, earth­worms, plant ma­te­r­ial and fungi, lit­tle is known about the ecosys­tem roles of Chilean shrew opos­sums. (Meserve, et al., 1988)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Due to few stud­ies, eco­nomic im­por­tance of Chilean shrew opos­sums is not known.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Due to few stud­ies, eco­nomic im­por­tance of Chilean shrew opos­sums is not known.

Con­ser­va­tion Sta­tus

As of 2012, Chilean shrew opos­sums were listed as a near threat­ened species by the IUCN (In­ter­na­tional Union for Con­ser­va­tion of Na­ture and Nat­ural Re­sources). These an­i­mals are vul­ner­a­ble due to habi­tat loss and degra­da­tion. (Diaz and Teta, 2008)

Con­trib­u­tors

Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor, Leila Si­cil­iano Mar­tina (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

An­drew Moore (au­thor), Uni­ver­sity of Wis­con­sin-Stevens Point, Chris Yahnke (ed­i­tor, in­struc­tor), Uni­ver­sity of Wis­con­sin-Stevens Point.

Glossary

Neotropical

living in the southern part of the New World. In other words, Central and South America.

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.

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.

carnivore

an animal that mainly eats meat

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.

forest

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

insectivore

An animal that eats mainly insects or spiders.

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.

mycophage

an animal that mainly eats fungus

native range

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

nocturnal

active during the night

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.

sedentary

remains in the same area

sexual

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

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.

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

Diaz, M., P. Teta. 2008. "Rhyn­c­holestes rapha­nu­rus" (On-line). IUCN Red List of Threat­ened Species. Ac­cessed June 04, 2013 at www.​iucnredlist.​org.

Jak­sic, F., H. Greene, J. Yanez. 1980. The guild struc­ture of a com­mu­nity of preda­tory ver­te­brates in cen­tral Chile. Oe­colo­gia, 49: 21-28.

Kelt, D., D. Mar­tinez. 1989. Notes on dis­tri­b­u­tion and ecol­ogy of two mar­su­pi­als en­demic to the Val­vid­ian forests of south­ern South Amer­ica. Jour­nal of Mam­mal­ogy, 70: 220-224.

Meserve, P., B. Lang, B. Pat­ter­son. 1988. Trophic re­la­tions of small mam­mals in a Chilean Tem­per­ate For­est. Jour­nal of Mam­mal­ogy, 69: 721-730.

Meserve, P., R. Murua, O. Lopetegui, J. Rau. 1982. Ob­ser­va­tions on the Small Mam­mal Fauna of a Pri­mary Tem­per­ate Rain For­est in South­ern Chile. Jour­nal of Mam­mal­ogy, 63: 315-317.

Nowak, R. 1999. Mam­mals of the World. Bal­ti­more, Mary­land: John Hop­kins Uni­ver­sity Press.

Pat­ter­son, B., M. Gal­lardo. 1987. Mam­malian Species- Rhyn­c­holestes rapha­nu­rus. Amer­i­can So­ci­ety of Mam­mal­o­gists, 286: 1-5.

Red­ford, K., J. Eisen­berg. 1992. Mam­mals of the Neotrop­ics- The South­ern Cone. Chicago, Illi­nois: Uni­ver­sity of Chicago Press.