Geogale auritalarge-eared tenrec

Ge­o­graphic Range

Large-eared ten­recs are en­demic to the is­land of Mada­gas­car and are found in the south and south­west re­gions of the is­land. (Stephen­son, 2003)

Habi­tat

Ge­ogale au­rita is found widely dis­trib­uted in dry, de­cid­u­ous for­est, gallery forests, and spiny bush in south­ern and south­west­ern Mada­gas­car. The species has also been ob­served in the rain­for­est of the south­east. These are en­vi­ron­ments with large an­nual vari­a­tions in rain­fall. (Stephen­son, 2003)

Phys­i­cal De­scrip­tion

Large-eared ten­recs are small, shrew-like ten­recs with very short, soft pelage, hair-cov­ered tails, and large pin­nae. Dor­sal col­oration is vari­able, rang­ing from light gray to light red­dish-brown. Ven­trally, these an­i­mals are buffy white. Large-eared ten­recs are among the small­est liv­ing ten­recs, with wild-caught an­i­mals rang­ing in body mass from 5.0 to 8.5 g. The length of the head and body is 60 to 75 mm, and the total body length in­clud­ing the tail can be be­tween 90 and 105 mm.

Cer­tain char­ac­ters dis­tin­guish G. au­rita from other ten­recs. The den­tal for­mula is 2/2 1/1 3/2 3/3 = 34, whereas most ten­recs have 36 teeth. Fur­ther­more, large-eared ten­recs are the only mem­ber of the fam­ily Ten­re­ci­dae that ex­ibit post­par­tum oestrus, which al­lows fe­males to suckle a first lit­ter while a sec­ond lit­ter is de­vel­op­ing in utero.

Ge­ogale au­rita is het­erother­mic, and body tem­per­a­tures par­al­lel the sur­round­ing tem­per­a­ture at all times of year, al­though body tem­per­a­tures higher than am­bi­ent tem­per­a­ture are ob­served in preg­nant and lac­tat­ing fe­males. Low meta­bolic rate is cor­re­lated with this rel­a­tively low body tem­per­a­ture.

Testes are ab­dom­i­nal in G. au­rita, as they are in all other ten­recs. Mem­bers of the fam­ily Ten­re­ci­dae have a cloaca into which both the in­testi­nal and gen­i­touri­nary tracts empty. (Stephen­son, 2003)

  • Range mass
    5.0 to 8.5 g
    0.18 to 0.30 oz
  • Average mass
    6.0 g
    0.21 oz
  • Range length
    90 to 105 mm
    3.54 to 4.13 in
  • Average basal metabolic rate
    0.043 W
    AnAge

Re­pro­duc­tion

In­for­ma­tion on the mat­ing sys­tems of these ten­recs was not avail­able in the lit­er­a­ture re­viewed. Mat­ing sys­tems of ten­recs in gen­eral are poorly known. Most ten­recs are soli­tary, al­though some species ap­pear to form sta­ble long-term bonds be­tween males and fe­males, in­di­cat­ing that they may mate monog­a­mously. It is not known at this time what mat­ing sys­tem is em­ployed by G. au­rita. (Nowak, 1999)

Mat­ing takes place from late Sep­tem­ber to March. Be­cause these an­i­mals have a post-par­tum es­trus, they can pro­duce mul­ti­ple lit­ters dur­ing that time. Coital lock oc­curs dur­ing cop­u­la­tion and can last for more than 20 min­utes. Large-eared ten­recs are ca­pa­ble of ar­rest­ing the de­vel­op­ment of lit­ters, thus the ges­ta­tion pe­riod varies be­tween 54 and 69 days. Lit­ter size varies from 1 to 5 in­di­vid­u­als, and the weights of the neonates range from 0.5 to 0.8 g. The off­spring are al­tri­cial, and are born with closed eyes and ears. Young are weaned soon after the open­ing of eyes, which takes place after 21 to 33 days of age. (Stephen­son, 2003)

  • Breeding interval
    It is not known how often these animals breed in the wild.
  • Breeding season
    Breeding occurs in late September to March.
  • Range number of offspring
    1 to 5
  • Average number of offspring
    3.9
    AnAge
  • Range gestation period
    54 to 69 days
  • Range weaning age
    21 to 33 days

Parental care in this species has not been de­scribed. How­ever, be­cause G. au­rita is a mam­mal, we know that fe­males pro­vide ex­ten­sive ma­ter­nal care. Young are al­tri­cial, so it is likely that moth­ers pro­vide not just food to their young, but also pro­tec­tion, groom­ing, and shel­ter, until the time that the young are weaned and can care for them­selves. Male parental care is var­ied in mam­mals, and lack­ing spe­cific in­for­ma­tion for these ten­recs, it is im­pos­si­ble to spec­u­late upon. (Nowak, 1999; Stephen­son, 2003)

  • 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 long-eared ten­recs liv­ing in the wild is un­known but in cap­tiv­ity they have been ob­served to live for more than two and a half years. (Stephen­son, 2003)

  • Range lifespan
    Status: captivity
    more than two and a half (high) years
  • Typical lifespan
    Status: captivity
    2.5 (high) years

Be­hav­ior

Large-eared ten­recs are noc­tur­nal, poor-sighted an­i­mals that de­pend on au­di­tory and ol­fac­tory senses. They are mostly soli­tary an­i­mals, but male-fe­male pairs are oc­ca­sion­ally found liv­ing in prox­im­ity to each other. These an­i­mals are het­erother­mic and enter daily tor­por. They can often be found tor­pid in­side fallen logs and cav­i­ties of sand. (Stephen­son, 2003)

Home Range

The size of home range for these an­i­mals has not been re­ported, but given their small size, ter­ri­to­ries and home ranges are not likely to be very large.

Com­mu­ni­ca­tion and Per­cep­tion

Large-eared ten­recs use sound to lo­cate their ter­mite prey. Being a noc­tur­nal an­i­mal with poor eye­sight, G. au­rita de­pends on au­di­tory and ol­fac­tory senses. As in all mam­mals, tac­tile com­mu­ni­ca­tion is im­por­tant be­tween mates as well as be­tween moth­ers and their off­spring. Ac­coustic com­mu­ni­ca­tion be­tween mem­bers of this species has not been re­ported, but may occur. (Nowak, 1999; Pevel­ing, et al., 2003; Stephen­son, 2003)

Food Habits

Large-eared ten­recs are spe­cial­ized in­sec­ti­vores show­ing a clear pref­er­ence for ter­mites. Their diet con­sists ex­clu­sively of arthro­pods, which they lo­cate by using sound. They may also show a sig­nif­i­cant pref­er­ence for cer­tain species. (Pevel­ing, et al., 2003)

  • Animal Foods
  • insects

Pre­da­tion

Ge­ogale au­rita is preyed upon by var­i­ous groups of an­i­mals. Re­mains of large-eared ten­recs have been found in pel­lets from two species of owls: barn owls and Mada­gas­car long-eared owls. Other species ex­pected to be preda­tors of large-eared ten­recs are snakes, in­clud­ing Mala­gasy cat-eye snakes, which are as­so­ci­ated with the habi­tat where Ge­ogale is found, and car­ni­vores such as Mala­gasy nar­row-striped mon­gooses. (Good­man, et al., 1993a; Good­man, et al., 1993b)

Ecosys­tem Roles

Large-eared ten­recs are spe­cial­ized ter­mites feed­ers and thus act as sec­ondary con­sumers in an ecosys­tem. The species also pro­vides feed­ing op­por­tu­ni­ties for con­sumers at higher trophic lev­els. (Good­man, et al., 1993a; Pevel­ing, et al., 2003)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Habi­tats pop­u­lated by large-eared ten­recs are not densely pop­u­lated by hu­mans, thus no known spe­cific eco­nomic in­flu­ence on human so­ci­eties is known. (Stephen­son, 2003)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Large-eared ten­recs have no known spe­cific eco­nomic in­flu­ence on human so­ci­eties.

Con­ser­va­tion Sta­tus

Large-eared ten­recs do not ap­pear to be threat­ened, but as they are de­pen­dent on for­est habi­tats, their dis­tri­b­u­tion may de­crease with in­creas­ing loss of suit­able habi­tats. Other threats are in­di­rect ef­fects due to in­creased use of pes­ti­cides. Ge­ogale au­rita is a spe­cial­ized ter­mite feeder and ter­mites are af­fected by pes­ti­cides. Thus, the po­ten­tial ef­fect on G. au­rita ap­pears high. (Stephen­son, 2003; Tin­gle, et al., 2000)

Other Com­ments

Ge­ogale has tra­di­tion­ally been placed in the mono­typic sub­fam­ily Ge­o­gali­nae. An African ori­gin of ten­recs is widely ac­cepted. Some au­thor­i­ties sug­gest that Ge­ogale and the other ten­recs of Mada­gas­car share a com­mon an­ces­tor, and have di­verged from one an­other after a sin­gle col­o­niza­tion of the is­land. How­ever, there is some ev­i­dence that Ge­ogale may not have arizen from the same col­o­niza­tion event that links the other ten­recs of Mada­gas­car.

Cur­rently G. au­rita is con­sid­ered the sis­ter­group of the re­main­ing ten­recs, and it is the only liv­ing de­scen­dent along its branch; the re­main­ing Mala­gasy species are de­scen­dents of the other branch.

Due to den­tal sim­i­lar­i­ties to Ge­ogale in a fos­sil found in Miocene de­posits of Kenya, this fos­sil was orig­i­nally placed in Ge­ogale. These den­tal sim­i­lar­i­ties were con­sid­ered too spe­cial­ized to give rise to the re­main­ing ten­recs, thus the an­ces­tor of Ge­ogale must have had col­o­nized Mada­gas­car in­de­pen­dently.

The iden­ti­fi­ca­tion of this fos­sil has since been dis­puted, and is now tax­o­nom­i­cally placed as Par­a­geogale. The phy­lo­ge­netic re­la­tion­ship to other mem­bers of the fam­ily Ten­re­ci­dae re­mains un­cer­tain, but mol­e­c­u­lar and mor­pho­log­i­cal ev­i­dence sug­gests a sis­ter re­la­tion­ship, thus sup­port­ing a two col­o­niza­tions hy­poth­e­sis. (Olson and Good­man, 2003; Po­duschka and Po­duschka, 1985)

Con­trib­u­tors

Thomas Nielsen (au­thor), Uni­ver­sity of Alaska Fair­banks, Link E. Olson (ed­i­tor, in­struc­tor), Uni­ver­sity of Alaska Fair­banks.

Nancy Shef­ferly (ed­i­tor), An­i­mal Di­ver­sity Web.

Glossary

Ethiopian

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

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

embryonic diapause

At about the time a female gives birth (e.g. in most kangaroo species), she also becomes receptive and mates. Embryos produced at this mating develop only as far as a hollow ball of cells (the blastocyst) and then become quiescent, entering a state of suspended animation or embryonic diapause. The hormonal signal (prolactin) which blocks further development of the blastocyst is produced in response to the sucking stimulus from the young in the pouch. When sucking decreases as the young begins to eat other food and to leave the pouch, or if the young is lost from the pouch, the quiescent blastocyst resumes development, the embryo is born, and the cycle begins again. (Macdonald 1984)

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.

fertilization

union of egg and spermatozoan

forest

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

heterothermic

having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.

insectivore

An animal that eats mainly insects or spiders.

island endemic

animals that live only on an island or set of islands.

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

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.

scrub forest

scrub forests develop in areas that experience dry seasons.

seasonal breeding

breeding is confined to a particular season

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

Good­man, S., O. Lan­grand, C. Rax­wor­thy. 1993. Food habits of the Mada­gas­car long-eared owl Asio mada­gas­carien­sis in two habi­tats in south­ern Mada­gas­car. Os­tritch, 64: 79-85.

Good­man, S., O. Lan­grand, C. Rax­wor­thy. 1993. The food habits of the barn owl Tyto alba at three sites on Mada­gas­car. Os­tritch, 64: 160-171.

Nowak, R. 1999. Walker's Mam­mals of the World, Sixth Edi­tion. Bal­ti­more and Lon­don: The Johns Hop­kins Uni­ver­sity Press.

Olson, L., S. Good­man. 2003. Phy­logeny and bio­geog­ra­phy of ten­recs. Pp. 1235-1242 in S Good­man, J Ben­stead, eds. The Nat­ural His­tory of Mada­gas­car. Chicago and Lon­don: The Uni­ver­sity of Chicago Press.

Pevel­ing, R., A. McWilliam, P. Nagel, H. Ra­solo­manana, Ra­holi­jaona, L. Rako­to­mi­an­ina, A. Ravon­in­ja­tovo, C. De­whurst, G. Gib­son, S. Rafanomezana, C. Tin­gle. 2003. Im­pact on lo­cust con­trol on har­vester ter­mites and en­demic ver­te­brate preda­tors in Mada­gas­car. Jour­nal of Ap­plied Ecol­ogy, 40: 729-741.

Po­duschka, W., C. Po­duschka. 1985. Zur frage des gat­tungsna­mens von "<<Ge­ogale" aletris>> But­ler und Hop­wood 1957 *<<Mam­malia>>: <<In­sec­tivora>>) aus dem Miozän Ostafrikas. Zeitschrift fur Säugertierkunde, 50: 129-140.

Stephen­son, P. 2003. Lipo­ty­phla (In­sec­tivora): Ge­ogale au­rita, Large-eared Ten­rec. Pp. 1265-1267 in S Good­man, J Ben­stead, eds. The Nat­ural His­tory of Mada­gas­car. Chicago and Lon­don: The Uni­ver­sity of Chicago Press.

Tin­gle, C., J. Rother, C. De­whurst, S. Lauer, W. King. 2000. "Pes­ti­cide Ac­tion Net­work" (On-line pdf). Ac­cessed De­cem­ber 02, 2004 at http://​www.​pan-uk.​org/​briefing/​fipronil.​pdf.