Monodelphis kunsipygmy short-tailed opossum

Ge­o­graphic Range

Pygmy short-tailed opos­sums are a very poorly known species. Not many spec­i­mens of this mys­te­ri­ous mam­mal have been col­lected (about 15 in­di­vid­u­als total); the are from Bo­livia (seven) and the rest from Brazil and Ar­gentina. How­ever, the range of Mon­odel­phis kunsi prob­a­bly ex­tends to Peru since the re­ported col­lec­tion sites were in close prox­im­ity to the na­tional bor­ders of this coun­try. The first type spec­i­men of this opos­sum was col­lected in Bo­livia at "La Granja" near the west mar­gin of Itona­mas River, 4 km north of Mag­dalena (13° 18' S, 64° 09'W) at ap­prox­i­mately 200 m of el­e­va­tion. In Ar­gentina, the first spec­i­men of Mon­odel­phis kunsi was col­lected quite re­cently (2005) at 22° 18' 41.4'' S, 63° 58' 7.1''W, 700 m above sea level. (An­der­son, 1982; Jayat and Miotti, 2005; Salazar, et al., 1994; Var­gas, et al., 2003)

Habi­tat

Not much is known about the pre­ferred habi­tat of Mon­odel­phis kunsi. Based on the topog­ra­phy of the sites from which the spec­i­mens were col­lected, it ap­pears that M. kunsi oc­cupy a wide range of ter­res­trial habi­tats. Lo­ca­tions from which the spec­i­mens were col­lected are char­ac­ter­ized by a wide range of el­e­va­tions, from 200 m to 1500 m. One spec­i­men of the pygmy short-tailed opos­sum was col­lected in an area with thick brush, many rocks and fallen wood, and ground cov­ered by oc­ca­sional small forbs and ferns. The ground was steeply sloped (30°) and there was about 10 to 12 cm layer of mulch and lit­ter. In con­trast, an­other spec­i­men was col­lected in a ba­nana field about 30 m from a river. On this flat ter­race with very moist soil and about 2 cm of leaf lit­ter; the trees (7 to 8 m tall) and shrubs com­bined, pro­vided 30 to 60 % cover. While these two areas rep­re­sent some­what mod­er­ately dis­turbed ecosys­tems, pygmy short-tailed opos­sums have also been col­lected in quite pris­tine habi­tats. (An­der­son, 1982; Salazar, et al., 1994)

  • Range elevation
    200 to 1500 m
    656.17 to 4921.26 ft

Phys­i­cal De­scrip­tion

Mon­odel­phis kunsi is prob­a­bly the small­est species in the genus Mon­odel­phis. The mass of spec­i­mens lies be­tween 7.5 and 30 grams and length be­tween 103 and 147 mil­lim­iters. Mon­odel­phis kunsi lacks a sagit­tal crest on the skull and en­larged ca­nines. Un­like M. amer­i­cana and M. bre­vi­cau­data, pygmy short-tailed opos­sums have no dor­sal stripes or lat­eral red­den­ing. M. kunsi have throat glands cov­ered by thin fur. Over the body, the fur of these opos­sums is short, gen­er­ally warm brown on the dor­sal side and with whitish areas on the ven­tral side. The tail is bi­col­ored, darker dor­sally and buffy ven­trally; cov­ered by fine hair, ex­cept for the tip which may serve a tac­tile func­tion. The skull is small (about 22 mm in length) with no pos­tor­bital processes and a rel­a­tively blunt ros­trum. The head is cov­ered with nu­mer­ous mysta­cial, genal, supra­or­bital, and in­ter­ra­mal vib­ris­sae. The hind feet have no­tice­able webs be­tween dig­its 3 and 4 and a less con­spic­u­ous web be­tween dig­its 2 and 3. All mem­bers of the genus Mon­odel­phis lack ab­dom­i­nal pouches. (An­der­son, 1982)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    7.5 to 30 g
    0.26 to 1.06 oz
  • Range length
    103 to 147 mm
    4.06 to 5.79 in

Re­pro­duc­tion

Noth­ing is known about the re­pro­duc­tion of M. kunsi. It is pos­si­ble that these tiny opos­sums are promis­cu­ous, sim­i­larly to many other mem­bers of the fam­ily Didel­phi­dae. Gen­er­ally, species in this group are soli­tary and in­ter­act with each other only for the pur­pose of mat­ing. (Man­davia and Myers, 2004; Var­gas, et al., 2003)

Noth­ing is known about the re­pro­duc­tive be­hav­ior of Mon­odel­phis kunsi. Since M. kunsi are in the in­fr­a­class Metathe­ria (mar­su­pial mam­mals), they al­most cer­tainly have a short ges­ta­tion pe­riod and young fairly un­de­vel­oped at birth, as these traits gen­er­ally char­ac­ter­ize this group of an­i­mals. (An­der­son, 1982; Salazar, et al., 1994)

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

Noth­ing is known about the type of parental in­vest­ment in Mon­odel­phis kunsi. As in all mam­mals, lac­tat­ing fe­males nour­ish and pro­tect the de­vel­op­ing young. (An­der­son, 1982; Salazar, et al., 1994)

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

Lifes­pan/Longevity

The lifes­pan of Mon­odel­phis kunsi is un­known.

Be­hav­ior

Noth­ing is known about the be­hav­ior of Mon­odel­phis kunsi. Like most other Didel­phids these opos­sums are prob­a­bly soli­tary ex­cept for the mat­ing sea­son. (Man­davia and Myers, 2004; Salazar, et al., 1994)

Home Range

Based on the meth­ods of Ra­bi­nowitz et al.(1986) and Arita et al.(1990) for de­ter­min­ing rar­ity, it was es­tab­lished that Mon­odel­phis kunsi has a wide dis­tri­b­u­tion but low den­si­ties lo­cally. (Salazar, et al., 1994)

Com­mu­ni­ca­tion and Per­cep­tion

Noth­ing is known about the com­mu­ni­ca­tion and per­cep­tion of Mon­odel­phis kunsi. It is pos­si­ble that this species de­pends on its sense of touch (nu­mer­ous vib­ris­sae on the head and feet) and smell as it moves about its en­vi­ron­ment. Other didel­phids rely pri­mar­ily on their senses of touch, smell, hear­ing, and, to a lesser ex­tent, sight. (An­der­son, 1982; Man­davia and Myers, 2004; Var­gas, et al., 2003)

Food Habits

Based on mor­pho­log­i­cal char­ac­ter­is­tics such as build, size and den­ti­tion; which are sim­i­lar to the mem­bers of the fam­ily So­ri­ci­dae, Mon­odel­phis kunsi is prob­a­bly in­vertiv­o­rous, or pos­si­bly om­niv­o­rous. The diet of M. kunsi is prob­a­bly de­ter­mined by the avail­abil­ity of food re­sources in a par­tic­u­lar area. (An­der­son, 1982; Var­gas, et al., 2003)

  • Animal Foods
  • insects

Pre­da­tion

Noth­ing is known about the preda­tors or anti-preda­tory be­hav­ior of Mon­odel­phis kunsi. These opos­sums are prob­a­bly preyed on by mam­mal car­ni­vores, rep­tiles, or preda­tory birds. Their small size and cryp­tic col­oration may help them to evade some pre­da­tion. (An­der­son, 1982; Man­davia and Myers, 2004)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Noth­ing is known about the role that M. kunsi plays in the ecosys­tem. These opos­sums could have an ef­fect on the pop­u­la­tion sizes of the in­sects on which they feed. If there is a preda­tor for which M. kunsi is the major food source, it is pos­si­ble that these opos­sums could have an im­pact on pop­u­la­tion size of this par­tic­u­lar preda­tor. (An­der­son, 1982; Man­davia and Myers, 2004; Var­gas, et al., 2003)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

There are no known pos­i­tive ef­fects of Mon­odel­phis kunsi on hu­mans. (An­der­son, 1982; Var­gas, et al., 2003; An­der­son, 1982; Var­gas, et al., 2003)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known neg­a­tive ef­fects of Mon­odel­phis kunsi on hu­mans.

Con­ser­va­tion Sta­tus

Ac­cord­ing to the IUCN Red List of Threat­ened Species Mon­odel­phis kunsi is an en­dan­gered species due to a de­cline in area of oc­cu­pancy, ex­tent of oc­cur­rence and/or qual­ity of habi­tat. Var­gas, Tar­ifa and Cortez (2003) re­ported that num­bers of M. kunsi are de­clin­ing due to human in­duced habi­tat degra­da­tion. They es­ti­mated that pop­u­la­tions de­clined as much as 50% in the last decade. (Var­gas, et al., 2003)

Other Com­ments

The name Mon­odel­phis is from the Greek word for "sin­gle womb" and the spe­cific ep­i­thet kunsi hon­ors Dr. Merle L. Kuns who ob­tained the type spec­i­men. (An­der­son, 1982)

Con­trib­u­tors

Tanya Dewey (ed­i­tor), An­i­mal Di­ver­sity Web.

Marcin Re­j­niak (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor, Phil Myers (ed­i­tor, in­struc­tor), Mu­seum of Zo­ol­ogy, Uni­ver­sity of Michi­gan-Ann Arbor.

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

agricultural

living in landscapes dominated by human agriculture.

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.

insectivore

An animal that eats mainly insects or spiders.

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.

omnivore

an animal that mainly eats all kinds of things, including plants and animals

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.

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.

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.

Ref­er­ences

An­der­son, S. 1982. Mon­odel­phis kunsi. Mam­malian Species, 190: 1-3.

Jayat, P., D. Miotti. 2005. Primer reg­istro de Mon­odel­phis kunsi (Didel­phi­mor­phia, Didel­phi­dae) para Ar­gentina. Mas­to­zo­olo­gia Neotrop­i­cal/ Jour­nal of Neotrop­i­cal Mam­mal­ogy, 12/2: 253-256. Ac­cessed Feb­ru­ary 20, 2006 at http://​redalyc.​uaemex.​mx/​redalyc/​pdf/​457/​45712214.​pdf.

Man­davia, A., P. Myers. 2004. "Mon­odel­phis bre­vi­cau­data (red-legged short-tailed op­po­sum)." (On-line). Ac­cessed March 15, 2006 at http://​animaldiversity.​ummz.​umich.​edu/​site/​accounts/​information/​Monodelphis_​brevicaudata.​html.

Salazar, J., M. Camp­bell, S. An­der­son, S. Gard­ner, J. Dun­num. 1994. New records of Bo­li­vian mam­mals. Mam­malia, 58/1: 125-130.

Var­gas, J., T. Tar­ifa, C. Cortez. 2003. Nuevos reg­istros de Mon­odel­phis adusta y Mon­odel­phis kunsi (Didel­phi­mor­phia: Didel­phi­dae) para Bo­livia. Mas­to­zo­olo­gia Neotrop­i­cal/Jour­nal of Neotrop­i­cal Mam­mal­ogy, 10/1: 123-131. Ac­cessed Feb­ru­ary 20, 2006 at http://​www.​cricyt.​edu.​ar/​mn/​indice/​pdf/​10_​1/​vargas.​pdf.