Cephalophus silvicultoryellow-backed duiker

Ge­o­graphic Range

Cephalo­phus sil­vicul­tor is found through­out west­ern cen­tral Africa. Yel­low-backed duik­ers range from Guinea-Bis­sau east­ward to Uganda and Sudan, and as far south as An­gola and Zam­bia. Yel­low-backed duik­ers have the widest range in com­par­i­son to other for­est duiker species. They are typ­i­cally found in forested areas with dense un­der­story growth. ("The En­cy­clo­pe­dia of Mam­mals", 2001; Her­man and Sayama, 1951; Huff­man, 2004)

Habi­tat

Yel­low-backed duik­ers pre­fer forested habi­tats with dense un­der­growth, al­though they can be found in a va­ri­ety of forested habi­tats, in­clud­ing sa­van­nah and farm­land. There is ev­i­dence of in­ter­spe­cific com­pe­ti­tion be­tween yel­low-backed duik­ers and their larger rel­a­tives, Jentink's duik­ers (Cephalo­phus jentinki). In some sit­u­a­tions, Jentink's duik­ers may force yel­low-backed duik­ers out of pre­ferred habi­tat. (New­ing, 2001)

In cap­tiv­ity, yel­low-backed duik­ers are not tol­er­ant of cold tem­per­a­tures. They can­not be ex­posed to cli­mates of 7 de­grees Cel­sius (55 de­grees Fahren­heit) for a pro­longed time, but can tol­er­ate tem­per­a­tures of 43 de­grees Cel­sius (110 de­grees Fahren­heit). (Barnes, et al., 2002)

Phys­i­cal De­scrip­tion

The coat of yel­low-backed duik­ers is black or brown in color with a yel­low tri­an­gu­lar patch near the tail. This yel­low patch typ­i­cally will not ap­pear until about 1 month of age and will not be com­pletely de­vel­oped until about 10 months. Males and fe­males re­sem­ble each other in ap­pear­ance, al­though fe­males are slightly larger. The muz­zle area is a light gray color which sur­rounds their white lips. Both sexes have short, con­i­cal horns that grow be­tween 8.5 and 21 cen­time­ters long. ("The En­cy­clo­pe­dia of Mam­mals", 2001; Huff­man, 2004)

Young yel­low-backed duik­ers are born a dark brown color with spot­ted flanks and red un­der­sides. These cryp­tic col­ors help them re­main hid­den from preda­tors in the for­est. ("The En­cy­clo­pe­dia of Mam­mals", 2001; Huff­man, 2004)

Yel­low-backed duik­ers have unique scent glands lo­cated pos­te­rior to each eye. Un­like other an­te­lope species, these glands se­crete from a group­ing of pores, not from a soli­tary large open­ing. These scent glands are used to mark ter­ri­to­r­ial bound­aries. Yel­low-backed duik­ers are built for life in dense veg­e­ta­tion. The body is arched, with short forelegs and longer hindlegs for manu­ver­abil­ity. ("The En­cy­clo­pe­dia of Mam­mals", 2001; Huff­man, 2004)

Yel­low-backed duik­ers are one of the largest species of for­est duik­ers, rang­ing from 45 to 80 kilo­grams in the wild. The body is 115 to 145 cen­time­ters in length, with a short tail mea­sur­ing 11 to 18 cen­time­ters. Yel­low-backed duik­ers have the largest brain size rel­a­tive to body size than any other an­te­lope species. ("The En­cy­clo­pe­dia of Mam­mals", 2001)

  • Range mass
    45 to 80 kg
    99.12 to 176.21 lb
  • Range length
    115 to 145 cm
    45.28 to 57.09 in

Re­pro­duc­tion

Yel­low-backed duiker mat­ing pairs have been ob­served lick­ing and nib­bling each other so­cially. This be­hav­ior is also viewed be­tween moth­ers and calves. Adult duik­ers so­cially rub their pre­or­bital scent glands on other adults bod­ies and legs. Duiker mates also press these scent glands to­gether as a pos­si­ble sign of pair bond­ing. It is thought that fe­males de­fend ter­ri­to­ries that they share with males. How­ever, the pair bond may be fairly tran­si­tory. (Estes, 1991)

In cap­tiv­ity, yel­low-backed duik­ers go into es­trus once per month through­out the year, last­ing 2 to 3 days. Ges­ta­tion is ap­prox­i­mately 7 months, after which fe­males give birth to one calf. Oc­ca­sion­aly, 2 calves are born. Fe­males may breed twice each year. Young yel­low-backed duik­ers stay hid­den for 1 to 2 weeks in the for­est. One male calf in cap­tiv­ity at the Los An­ge­les Zoo was weaned after 95 days, al­though oth­ers have been recorded at about 5 months. Fe­males are sex­u­ally ma­ture at 9 to 12 months of age, while males reach ma­tu­rity at 12 to 18 months. (Barnes, et al., 2002; Huff­man, 2004)

  • Breeding interval
    Yellow-backed duikers may breed twice each year.
  • Breeding season
    Yellow-backed duikers can breed throughout the year.
  • Range number of offspring
    1 to 2
  • Average number of offspring
    1
  • Average number of offspring
    1
    AnAge
  • Range gestation period
    4 (low) months
  • Average gestation period
    7 months
  • Range weaning age
    3.17 to 5 months
  • Range age at sexual or reproductive maturity (female)
    9 to 12 months
  • Range age at sexual or reproductive maturity (male)
    12 to 18 months

Young are weaned after ap­prox­i­mately 5 months. It is un­known how long young stay with the mother. The young re­main hid­den for their first week of life, after which they begin to emerge from hid­ing to browse on veg­e­ta­tion. (Huff­man, 2004)

  • Parental Investment
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-weaning/fledging
    • provisioning
      • female
  • extended period of juvenile learning

Lifes­pan/Longevity

In cap­tiv­ity, other species of Cephalo­phus can live 10 to 15 years. In the wild duik­ers can live 10 to 12 years. ("The En­cy­clo­pe­dia of Mam­mals", 2001; Huff­man, 2004)

  • Range lifespan
    Status: wild
    10 to 12 years
  • Average lifespan
    Status: captivity
    22.5 years
    AnAge

Be­hav­ior

Yel­low-backed duik­ers are a non-gre­gar­i­ous species. They rest alone dur­ing the day in "forms" - reg­u­larly used rest­ing places under fallen trees, in dense un­der­growth, or in root forms - and for­age at night. Males and fe­males share ter­ri­to­ries and loosely as­so­ci­ate for mat­ing. Duik­ers are ex­cep­tion­ally sus­cep­ti­ble to stress in cap­tiv­ity (cap­ture my­opa­thy). ("The En­cy­clo­pe­dia of Mam­mals", 2001; Barnes, et al., 2002; Kranz and Lump­kin, 1982)

Yel­low-backed duik­ers have also been seen rest­ing on the peaks of ter­mite mounds in order to gain a van­tage point. This and the fact that some fe­males have been ob­served with bro­ken horns, sug­gests that duik­ers ac­tively de­fend ter­ri­to­ries. Ter­ri­to­r­ial bound­aries are also marked with the max­il­lary glands. (Huff­man, 2004)

Home Range

Home range sizes are not known.

Com­mu­ni­ca­tion and Per­cep­tion

Yel­low-backed duik­ers com­mu­ni­cate with unique scent glands an­te­rior to the eyes. These max­il­lary glands are made of con­nec­tive tis­sues that sur­rounds 2 to 3 se­cre­tory lay­ers form­ing hair­less slits. The pres­ence of these glands cause the cheeks to swell. Duik­ers also have scent glands be­hind each hoof. Gland scents are used to com­mu­ni­cate ter­ri­to­r­ial bound­aries, re­pro­duc­tive sta­tus, and as a way of ce­ment­ing so­cial bonds. Yel­low-backed duik­ers also com­mu­ni­cate through grunts and shrill bleats. When alarmed, these duik­ers emit a shrill whis­tle, erect their dor­sal crest, and flee. ("The En­cy­clo­pe­dia of Mam­mals", 2001; Estes, 1991; Huff­man, 2004)

Food Habits

Yel­low-backed duik­ers are se­lec­tive-for­ag­ing fru­gi­vores. Typ­i­cal diets are low in fiber. Starches are fer­mented quickly, with rapid pas­sage through the di­ges­tive tract. Along with fruit, yel­low-backed duik­ers eat leaves, seeds, buds, bark, and shoots. Four yel­low-backed duik­ers in the wild ate 71.3% fruit mat­ter and 28.6% dry weight. Oc­ca­sion­ally, these for­est an­telopes will kill and eat small an­i­mals, such as birds. Of the 28.6% dry weight, 0.1% was an­i­mal mat­ter. (Barnes, et al., 2002; Kranz and Lump­kin, 1982)

Yel­low-backed duik­ers spe­cial­ize on eat­ing fallen fruits and can con­sume fruits or seeds that are too large or hard for pri­mates and other fru­gi­vores to eat. Duiker cheek teeth are spe­cial­ized for chew­ing tough bark and roots. A long pointed tongue and mo­bile lips allow fo­liage to be eas­ily ob­tained and ma­nip­u­lated. Duik­ers search the ground for food using their hooves and snouts to dig. The large size of yel­low-backed duik­ers forces them to for­age al­most con­stantly. (Estes, 1991)

  • Animal Foods
  • birds
  • mammals
  • Plant Foods
  • leaves
  • roots and tubers
  • wood, bark, or stems
  • seeds, grains, and nuts
  • fruit

Pre­da­tion

Preda­tors of yel­low-back duik­ers in­clude African hunt­ing dogs, lions, and leop­ards. When they are alarmed, the typ­i­cal re­sop­nse is for the yel­low rump hairs to stand erect. A shrill call may be emit­ted be­fore dash­ing into the cover of un­der­brush habi­tat. Young duik­ers stay hid­den in the for­est for more than 7 days to evade preda­tors be­fore be­gin­ning to ven­ture out. When threat­ened, the re­sponse is to flee into dense for­est. Their habit of seem­ing to dive into the un­der­growth gives them their com­mon name, duiker, which is de­rived from Afrikaans for "div­ing buck." Yel­low-backed duik­ers also hold their yel­low rump hairs erect when ag­i­tated. (Huff­man, 2004; Kranz and Lump­kin, 1982; Huff­man, 2004; Kranz and Lump­kin, 1982)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

It is un­known how im­por­tant for­est duik­ers are in seed dis­per­sal in African forests. Duik­ers have been ob­served spit­ting out di­gested seeds after ru­mi­na­tion. Some seeds re­main in­tact and are dis­persed in this way. Duik­ers act as preda­tors on other seeds by dam­ag­ing them dur­ing di­ges­tion. Larger mam­mals also prey on adult and young duik­ers. (Feer, 1995)

Three new species of Coc­cidia have been found in for­est duik­ers. These par­a­sites were not found in any other wild or do­mes­tic African ru­mi­nant. Coc­cidia was doc­u­mented in Philan­tomba mon­ti­cola, Cephalo­phus dor­salis, and Cephalo­phus ni­grifrons. Cephalo­phus maxwelli was dis­cov­ered with the par­a­site Se­leno­mas ru­mi­nan­ticum. It is pos­si­ble that Coc­cidia species will be dis­cov­ered in C. sil­vicul­tor. (Her­man and Sayama, 1951; Pampiglione, et al., 1973)

  • Ecosystem Impact
  • disperses seeds

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Cephalo­phus sil­vicul­tor is an im­por­tant form of meat and money for peo­ple liv­ing in cen­tral and west­ern Africa. In many in­stances, yel­low-backed duiker meat is nec­es­sary bush­meat for local sur­vival. They are hunted with a va­ri­ety of meth­ods, in­clud­ing snares, shot­guns, or net­ting. At night, duik­ers are eas­ily shot be­cause they stand still when light is shone on them. (New­ing, 2001)

  • Positive Impacts
  • food
  • body parts are source of valuable material

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of Cephalo­phus sil­vicul­tor on hu­mans.

Con­ser­va­tion Sta­tus

Human ex­pan­sion has caused a change in some African habi­tats from ma­ture forests to clear­ings for agri­cul­ture, di­rectly im­pact­ing yel­low-duiler pop­u­la­tions, which rely on forested habi­tat. Yel­low-backed duik­ers re­quire dense for­est cover to hide, be­cause of their large size. Smaller duik­ers, such as blue duik­ers (Philan­tomba mon­ti­cola), can con­ceal them­selves in the more open habi­tats where they live. (Estes, 1991; Wilkie and Finn, 1990)

Other Com­ments

Cephalo­phus sil­vicul­tor is con­sid­ered one of the most evo­lu­tion­ar­ily an­ces­tral (prim­i­tive) African an­telopes that ex­ists today. ("The En­cy­clo­pe­dia of Mam­mals", 2001)

The name "duiker" comes from an African word mean­ing "diver". This refers to their ten­dency to run and hide in for­est cover when threat­ened. Cephalo­phus sil­vicul­tor can be bro­ken into its Greek roots. "Kephale" refers to the head, and "lo­phus" to a crest, both are as­so­ci­ated with a tuft of fur on the yel­low-backed duik­ers head. "Silva" means woods or for­est, and "cul­tor" im­plies a farmer or in­hab­i­tant, both these terms imply the an­i­mal lives in the for­est. (Huff­man, 2004)

Con­trib­u­tors

Tanya Dewey (ed­i­tor), An­i­mal Di­ver­sity Web.

Kristina De­Witt (au­thor), Uni­ver­sity of Wis­con­sin-Stevens Point, Chris Yahnke (ed­i­tor, in­struc­tor), Uni­ver­sity of Wis­con­sin-Stevens Point.

Glossary

Ethiopian

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

World Map

acoustic

uses sound to communicate

agricultural

living in landscapes dominated by human agriculture.

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.

food

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

forest

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

frugivore

an animal that mainly eats fruit

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).

monogamous

Having one mate at a time.

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.

scent marks

communicates by producing scents from special gland(s) and placing them on a surface whether others can smell or taste them

sedentary

remains in the same area

sexual

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

sexual ornamentation

one of the sexes (usually males) has special physical structures used in courting the other sex or fighting the same sex. For example: antlers, elongated tails, special spurs.

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.

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

"San Fran­cisco Zoo An­i­mals" (On-line). Yel­low-backed Duiker. Ac­cessed Oc­to­ber 13, 2006 at http://​www.​sfzoo.​org/​cgi-bin/​animals.​py?​ID=87.

2001. The En­cy­clo­pe­dia of Mam­mals. Pp. "542-545" in D Mac­Don­ald, ed. Barnes and Noble Inc.

Barnes, R., K. Greene, J. Hol­land, M. Lamm. 2002. Man­age­ment and Hus­bandry of Duik­ers at the Los An­ge­les Zoo. Zoo Bi­ol­ogy, 21/2: "107-121".

Estes, R. 1991. The Be­hav­ior Guide to African Mam­mals In­clud­ing Hoofed Mam­mals, Car­ni­vores, Pri­mates. Uni­ver­sity of Cal­i­for­nia Press. Ac­cessed No­vem­ber 29, 2006 at http://​books.​google.​com/​books?​hl=en&​lr=&​id=g977LsZHpcsC&​oi=fnd&​pg=PR11&​sig=73mHRqw7GQTw93UUcVXIIx7s6jM&​dq=duiker+mating+systems&​prev=http://​scholar.​google.​com/​scholar%3Fq%3Dduiker%2Bmating%2Bsystems%26hl%3Den%26lr%3D#​PRA1-PA90000,M1.

Feer, F. 1995. Seed Dis­per­sal in African For­est Ru­mi­nants. Jour­nal of Trop­i­cal Ecol­ogy, 11: 687-689. Ac­cessed De­cem­ber 01, 2006 at http://​www.​jstor.​org/​view/​02664674/​di008869/​00p0125a/​0?​frame=frame&​userID=8fec23ca@​uwsp.​edu/​01cce4405f00501b3ca63&​dpi=3&​config=jstor.

Geser, S., P. Dollinger. 2006. "World As­so­ci­a­tion of Zoos and Aquar­i­ums (WAZA)" (On-line). WAZA - World As­so­ci­a­tion of Zoos and Aquar­i­ums - Vir­tual Zoo. Ac­cessed Oc­to­ber 13, 2006 at http://​www.​waza.​org/​virtualzoo/​factsheet.​php?​id=119-009-009-014&​view=Antelopes.

Her­man, C., K. Sayama. 1951. Fur­ther Notes on Se­lenomonas from Cal­i­forn­ian Mam­mals. Trans­ac­tions of the Amer­i­can Mi­cro­scop­i­cal So­ci­ety: 185-187. Ac­cessed No­vem­ber 29, 2006 at http://​www.​jstor.​org/​view/​00030023/​sp050176/​05x0019s/​0?​frame=noframe&​userID=8fec23ca@​uwsp.​edu/​01cc99331300501b33b1a&​dpi=3&​config=jstor.

Huff­man, B. 2004. "An Ul­ti­mate Un­gu­late Fact Sheet" (On-line). Cephalo­phus sil­vicul­tor. Ac­cessed Oc­to­ber 13, 2006 at http://​www.​ultimateungulate.​com/​Artiodactyla/​Cephalophus_​silvicultor.​htm.

Kranz, K., S. Lump­kin. 1982. Notes on the Yel­low-backed duiker Cephalo­phus sylvicul­tor in cap­tiv­ity with com­ments on its nat­ural his­tory. In­ter­na­tional Zoo Year­book, 22: 232-240.

New­ing, H. 2001. Bush­meat Hunt­ing and Man­age­ment: im­pli­ca­tions of duiker ecol­ogy and in­ter­spe­cific com­pe­ti­tion. Bio­di­ver­sity and Con­ser­va­tion, 10: "99-118".

Pampiglione, S., G. Ricci-Bitti, M. Ka­bala. 1973. On Some Coc­cidia of Cephalo­phus in Zaire. Jour­nal of Wildlife Dis­ease, 9: 282-286. Ac­cessed No­vem­ber 29, 2006 at http://​www.​jwildlifedis.​org/​cgi/​reprint/​9/​4/​282.

Plow­man, A. 2002. Nu­tri­ent In­take and Ap­par­ent Di­gestibil­ity of Diets Con­sumed by Cap­tive Duik­ers at the Dambari Field Sta­tion, Zim­babwe. Zoo Bi­ol­ogy, 21: "135-147".

Wilkie, D., J. Finn. 1990. Slash-Burn Cul­ti­va­tion and Mam­mal Abun­dance in the Ituri For­est, Zaire. Biotrop­ica, Vol. 22, No. 1: pp. 90-99. Ac­cessed No­vem­ber 29, 2006 at http://​links.​jstor.​org/​sici?​sici=0006-3606%28199003%2922%3A1%3C90%3ASCAMAI%3E2.​0.​CO%3B2-V&​size=LARGE.

Woolf, N. 1986. New Hope for Ex­otic Species,. Bio­Science, Vol 36/No 9: 594-597. Ac­cessed No­vem­ber 29, 2006 at http://​www.​jstor.​org/​view/​00063568/​ap040293/​04a00040/​0?​frame=noframe&​userID=8fec23ca@​uwsp.​edu/​01cc99331300501b33b1a&​dpi=3&​config=jstor.