Simias concolorsimakobou(Also: pig-tailed langur)

Ge­o­graphic Range

Simias con­color (the pig-tailed lan­gur) is presently found only on the Mentawai Is­lands off the west coast of Suma­tra in In­done­sia. This species has been elim­i­nated en­tirely from some is­lands due to log­ging and hunt­ing by hu­mans. (Bur­ton, 1995; Eudey and Mem­bers of the Pri­mate Spe­cial­ist Group 2000, 2004)

Habi­tat

The habi­tat of S. con­color in­cludes hill­sides in pri­mary forests. It is un­cer­tain whether S. con­color also re­sides in swamps and man­grove forests with dif­fer­ent sources stat­ing dif­fer­ent in­for­ma­tion re­gard­ing its pres­ence in these en­vi­ron­ments. This species is en­tirely ar­bo­real and only comes down from the trees when it is dis­turbed. (Bur­ton, 1995; Nowak, 1999)

Phys­i­cal De­scrip­tion

The body length of S. con­color ranges from 490 to 550 mm in males and from 460 to 550 mm in fe­males. The av­er­age weight is around 8.7 kg for males and 7.1 kg for fe­males. The tail length of S. con­color varies be­tween 14 and 15 cm. Two color va­ri­eties exist for S. con­color, a dark grey phase and a creamy buff phase, with the dark grey phase being more com­mon. The creamy buff phase is found in roughly one in four in­di­vid­u­als. The limbs are of equal length and the tail is rather short com­pared to other pri­mate species in the sub­fam­ily Colobi­nae. Adult pig-tailed lan­gurs have black faces and small snub-noses. The coat of the dark phase of S. con­color is black­ish-brown with light speck­led hair on the nape, shoul­der, and upper back. The tail of this species is not only short, but also hair­less, ex­cept for a small amount of hair at the tail tip. (Ankel-Si­mons, 2000; Bur­ton, 1995; Noë and Bshary, 2001)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    7.1 to 8.7 kg
    15.64 to 19.16 lb
  • Range length
    460 to 550 mm
    18.11 to 21.65 in

Re­pro­duc­tion

Males have been ob­served par­tic­i­pat­ing in dis­plays of strength that con­sist of leap­ing through the trees to at­tract mates. The so­cial group of S. con­color in­cludes one male and up to four fe­males with which the male mates. (Vogel and Win­kler, 1990; Woltan­ski, 2004)

Few data exist re­gard­ing the re­pro­duc­tive cycle of S. con­color, but it is be­lieved that a sin­gle birth oc­curs some­time dur­ing June and July. This species also ex­hibits sex­ual swelling, a trait that is rare in other Asian colobines. (Bur­ton, 1995)

  • Average number of offspring
    1

Lit­tle is known about the parental in­vest­ment of S. con­color, but there is in­for­ma­tion about their close rel­a­tives, pro­boscis mon­keys, Nasalis lar­va­tus. Fe­male N. lar­va­tus carry, nurse, and stay close to their young for about a year. While the males do not pro­vide as much care as the fe­males, they do pro­tect their young from males from other groups. (Woltan­ski, 2004)

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

Lifes­pan/Longevity

No in­for­ma­tion is avail­able re­gard­ing the lifes­pan and longevity of S. con­color, but its rel­a­tive N. lar­va­tus lives at least 23 years in cap­tiv­ity. (Woltan­ski, 2004)

Be­hav­ior

Lit­tle is known about the be­hav­ior of S. con­color be­cause there are so few in such a lim­ited ge­o­graph­i­cal range as well as the dif­fi­culty in spot­ting them in their dense for­est habi­tat. There are two dis­tinct group types ex­hib­ited in S. con­color, fam­ily groups and groups of all males; each ex­hibit unique be­hav­iors. The most com­mon type of group­ing is the fam­ily group of one male and up to 4 fe­males. These groups can be formed with a sin­gle adult cou­ple and their young or with more than one adult fe­male with a sin­gle male. Fam­ily group mem­bers main­tain very close prox­im­ity, rarely trav­el­ing more than 5 m (16 ft.) away from one an­other. They also re­strict vocal com­mu­ni­ca­tion, only using it at des­ig­nat­ing group bound­aries and as a warn­ing to preda­tors. The all male groups ex­hibit be­hav­iors that pro­duce ex­ces­sive noise as they travel through the for­est, com­mu­ni­cate with oth­ers, and leap in dis­plays of strength. (Ankel-Si­mons, 2000; Nowak, 1999; Tilson, 1977; Vogel and Win­kler, 1990)

  • Range territory size
    6600 to 202000 m^2

Home Range

The size of the av­er­age S. con­color ter­ri­tory is be­tween 16.3 and 50 acres (6.5 to 20 ha). In­di­vid­u­als are not ob­served deep in­side other ter­ri­to­ries, but are seen on the mar­gin of ad­ja­cent ter­ri­to­ries. Dur­ing en­coun­ters with other groups, the males ap­proach, make loud vo­cal­iza­tions and re­turn to their home ter­ri­tory with the other group mem­bers fol­low­ing be­hind. Chas­ing and fight­ing are gen­er­ally not ob­served dur­ing these en­coun­ters. (Tilson, 1977; Vogel and Win­kler, 1990)

Com­mu­ni­ca­tion and Per­cep­tion

Com­mu­ni­ca­tion be­tween in­di­vid­u­als and groups of S. con­color is achieved by pro­duc­ing loud calls in a se­ries of vo­cal­iza­tions rang­ing from 2 to 25 nasal barks. These barks can travel at least 500 m through the rain­for­est. The pur­pose of these calls is be­lieved to be to main­tain group struc­ture and bound­aries. Males call out with loud nasal barks and fe­males reply with sharp squeals. It is also likely that chem­i­cal cues are used widely in com­mu­ni­cat­ing re­pro­duc­tive state and that vi­sion and touch are im­por­tant. (Bur­ton, 1995; Tilson, 1977)

Food Habits

This species eats leaves, fruits, and berries. Feed­ing oc­curs after sun­rise near the trees used for sleep­ing and again in the af­ter­noon. Adult males lead the for­ag­ing and the fe­males and young fol­low be­hind . (Bur­ton, 1995; Tilson, 1977)

  • Plant Foods
  • leaves
  • fruit
  • flowers

Pre­da­tion

The only known enemy or preda­tor of S. con­color is man. Other large preda­tors on the Mentawai Is­lands in­clude crested ser­pent ea­gles (Spi­lor­nis cheela) and pythons (Python retic­u­la­tus), both may also prey on S. con­color. (Vogel and Win­kler, 1990; Whit­ten and Whit­ten, 1982)

Ecosys­tem Roles

There is lit­tle avail­able in­for­ma­tion on the ecosys­tem role of the pig-tailed lan­gur. They may aid in seed dis­per­sal of trop­i­cal fruit­ing trees.

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Pig-tailed lan­gur meat is con­sid­ered a del­i­cacy. These are im­por­tant mem­bers of the ecosys­tems in which they live, they could con­tribute to the de­vel­op­ment of the eco­tourism in­dus­try in the Mentawai is­lands. (Bur­ton, 1995)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse af­fects of S. con­color on hu­mans.

Con­ser­va­tion Sta­tus

Pig-tailed lan­gurs are listed as an en­dan­gered species under the IUCN. The pop­u­la­tion con­sists of fewer than 10,000 in­di­vid­u­als. Habi­tat loss due to log­ging is the main cause of pop­u­la­tion de­cline. Hunt­ing is also a major prob­lem, es­pe­cially in the Pagai Is­lands be­cause S. con­color meat is con­sid­ered a del­i­cacy. This species re­ceives pro­tec­tion at the Teit­eibatti Wildlife Re­serve, lo­cated on the only is­land that pro­vides such se­cu­rity. It is be­lieved that the pop­u­la­tion size of S. con­color has de­creased by 50% dur­ing the last decade and will most likely con­tinue to drop an­other 50% dur­ing the next decade. (Bur­ton, 1995; Eudey and Mem­bers of the Pri­mate Spe­cial­ist Group 2000, 2004; Nowak, 1999)

Other Com­ments

This species was pre­vi­ously rec­og­nized under the name Nasalis con­color.

Con­trib­u­tors

Tanya Dewey (ed­i­tor), An­i­mal Di­ver­sity Web.

Lyn­d­say Rankin (au­thor), Michi­gan State Uni­ver­sity, Bar­bara Lun­dri­gan (ed­i­tor, in­struc­tor), Michi­gan State Uni­ver­sity.

Glossary

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.

arboreal

Referring to an animal that lives in trees; tree-climbing.

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

diurnal
  1. active during the day, 2. lasting for one day.
ecotourism

humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.

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.

folivore

an animal that mainly eats leaves.

food

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

frugivore

an animal that mainly eats fruit

herbivore

An animal that eats mainly plants or parts of plants.

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.

oriental

found in the oriental region of the world. In other words, India and southeast Asia.

World Map

polygynous

having more than one female as a mate at one time

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.

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

social

associates with others of its species; forms social groups.

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.

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

Ankel-Si­mons, F. 2000. Pri­mate Anatomy: An In­tr­duc­tion. San Diego, Cal­i­for­nia: Aca­d­e­mic Press.

Bur­ton, F. 1995. The Mul­ti­me­dia Guide to the Non-hu­man Pri­mates. Scar­bor­ough, On­tario: Pren­tice Hall Canada.

Eudey, A., Mem­bers of the Pri­mate Spe­cial­ist Group 2000. 2004. "IUCN Red List of Threat­ened Species: Simias con­color" (On-line). Ac­cessed March 16, 2006 at http://​www.​iucnredlist.​org/​search/​details.​php?​species=20229.

Nowak, R. 1999. Pig-tailed Lan­gur. Pp. 596-597 in Walker's Mam­mals of the World, Vol. 1, 6th Edi­tion. Bal­ti­more: The Johns Hop­kins Uni­ver­sity Press.

Noë, R., R. Bshary. 2001. Colobus and Leaf Mon­keys. Pp. 380-395 in D Mac­don­ald, ed. The En­cy­clo­pe­dia of Mam­mals, Vol. 2, Re­vised Edi­tion. New York: Facts on File.

Tilson, R. 1977. So­cial or­ga­ni­za­tion of simakobu mon­keys (Nasalis con­color) in Siberut Is­land, In­done­sia. Jour­nal of Mam­mal­ogy, 58(2): 202-212.

Vogel, C., P. Win­kler. 1990. Lan­gurs and Colobi. Pp. 296-324 in S Parker, ed. Grz­imek's En­cy­clo­pe­dia of Mam­mals, Vol. 2, 1 Edi­tion. New York: Mc­Graw-Hill Pub­lish­ing Com­pany.

Whit­ten, A., J. Whit­ten. 1982. Pre­lim­i­nary ob­ser­va­tions of the Mentawai macaque on Siberut Is­land, In­done­sia. In­ter­na­tional Jour­nal of Pri­ma­tol­ogy, 3(4): 445-459.

Woltan­ski, A. 2004. "Nasalis lar­va­tus" (On-line). An­i­mal Di­ver­sity Web. Ac­cessed April 18, 2006 at http://​animaldiversity.​ummz.​umich.​edu/​site/​accounts/​information/​Nasalis_​larvatus.​html.