Hapalemur griseusbamboo lemur

Ge­o­graphic Range

Ha­pale­mur griseus is the en­demic to Mada­gas­car. It is the most wide­spread of all bam­boo lemurs. Each of the 4 sub­species oc­cu­pies a slightly dif­fer­ent zone with Ha­pale­mur griseus griseus being the most widely dis­trib­uted sub­species. Ha­pale­mur griseus griseus is found through­out the east­ern rain­for­est zone ex­cept for the far south­ern por­tion. Ha­pale­mur griseus alaotren­sis is only found around Lac Alao­tra, liv­ing in reedbeds and float­ing reed is­lands. Ha­pale­mur griseus oc­ci­den­talis is found in small rain­for­est re­gion in north­west­ern Mada­gas­car. Ha­pale­mur griseus merid­ion­alis is only found near the Fort Dauphin area of ex­treme south­east Mada­gas­car. (Flan­nery, 2007; Grassi, 2001)

Habi­tat

Ha­pale­mur griseus is en­demic to Mada­gas­car. Av­er­age air tem­per­a­ture of this area is 21°C, but varies from 4°C to 30°C. The en­vi­ron­ment is typ­i­cally very humid. It is com­monly found in areas con­tain­ing bam­boo, marsh­lands, low­lands, and forests and pri­mar­ily in­hab­its pri­mary and sec­ondary forests. Four dif­fer­ent sub-species of Ha­pale­mur griseus have been doc­u­mented (H. g. griseus, H. g. alaotren­sis, H. g. oc­ci­den­talis, and H. g. meri­don­alis), all of which oc­cupy slightly unique habi­tats at dif­fer­ent el­e­va­tions through­out the species' ge­o­graphic range. The over­all range for the species occur from sea level to 2050 me­ters. (Flan­nery, 2007)

  • Range elevation
    0 to 2050 m
    0.00 to 6725.72 ft

Phys­i­cal De­scrip­tion

Ha­pale­mur griseus is a small to medium-sized lemur, with an av­er­age length of 66 cm and an av­er­age weight of 0.935 kg. Males tend to be slightly larger than fe­males. In gen­eral, H. griseus has grey fur; how­ever, four dif­fer­ent sub­species have been doc­u­mented, all of which ex­hibit sub­tle vari­a­tions in phys­i­cal ap­pear­ance. It has a non-pre­hen­sile tail, its fore­arms are shorter than its hindlimbs, it has sweat glands on its fore­arms and near its armpits, and it has a den­tal for­mula of 2:1:3:3. Ha­pale­mur griseus griseus is mostly gray with olive tones, a dark gray tail and lighter gray fur along the ven­ter. It has large ears, which are mostly hid­den in the fur, and its tail is longer than the head and body com­bined. Ha­pale­mur griseus alaotren­sis is darker than H. g. griseus, is slightly larger, and its large ears are also rel­a­tively hid­den by its fur. Its tail is gen­er­ally the same length as the head and body com­bined. Ha­pale­mur griseus oc­ci­den­talis is lighter than that of Ha­pale­mur griseus griseus and its large ears are rel­a­tively less hid­den. Its tail is longer than its head and body com­bined. Ha­pale­mur griseus merid­ion­alis is dark gray or beige. Its ears ex­tend out no­tice­ably from its fur, but to a lesser ex­tent than that of Ha­pale­mur griseus oc­ci­den­talis and its tail is equal to or slightly longer than the head and body com­bined. (Flan­nery, 2007; An­dri­a­holini­rina et alia, 2010)

  • Sexual Dimorphism
  • male larger
  • Average mass
    0.935 kg
    2.06 lb
  • Average mass
    1347.5 g
    47.49 oz
    AnAge
  • Average length
    66 cm
    25.98 in

Re­pro­duc­tion

Ha­pale­mur griseus pri­mar­ily lives in groups. Stud­ies have shown that 42% of groups have one adult male and one adult fe­male. Around 27% of groups have mul­ti­ple adults of each gen­der, 19% have two adult fe­males and 1 adult male, and 12% have two adult males and one adult fe­male. Most groups have more re­pro­duc­ing males than fe­males. Al­though most breed­ing re­la­tion­ships are monog­a­mous, they can also be polyg­y­nous. Polyg­y­nous groups tend to have more off­spring. Many groups also in­clude sub-adults. Mat­ing sea­son runs from June to July, with births oc­cur­ring in Oc­to­ber and No­vem­ber. Fe­males have on av­er­age one baby per year and they usu­ally once an­nu­ally. In­tra­group fe­males are often re­lated; how­ever, males tend to be un­re­lated. Mat­ing oc­curs al­most ex­clu­sively within group. One study found that only 8.5% of births had ex­tra-group pa­ter­nity. The sub-species H. g. alaotren­sis has a longer breed­ing sea­son than other sub-species of H. griseus. (Flan­nery, 2007)

H. griseus comes into es­trus once a year. It typ­i­cally gives birth to only one off­spring, and rarely has twins. Breed­ing sea­son oc­curs dur­ing the dry sea­son (i.e., sum­mer or fall) and birthing typ­i­cally oc­curs dur­ing the rainy sea­son, dur­ing which time bam­boo, their pri­mary forge, is abun­dant. Ges­ta­tion lasts roughly 140 days and most young are com­pletely weaned by 20 weeks of age. Most fe­males are re­pro­duc­tively ma­ture by 2 years old, and most males are re­pro­duc­tively ma­ture by 3 years old. (Flan­nery, 2007; Williams, 2001; Grassi, 2001; An­dri­a­holini­rina et alia, 2010)

  • Breeding interval
    Hapalemur griseus breeds once yearly.
  • Breeding season
    Breeding season in Hapalemur griseus occurs during the dry season, from June-August.
  • Average number of offspring
    1
  • Average number of offspring
    1.2
    AnAge
  • Average gestation period
    140 days
  • Average gestation period
    140 days
    AnAge
  • Average weaning age
    20 weeks
  • Average age at sexual or reproductive maturity (female)
    2 years
  • Average age at sexual or reproductive maturity (female)
    Sex: female
    880 days
    AnAge
  • Average age at sexual or reproductive maturity (male)
    3 years

Av­er­age birth weight for Ha­pale­mur griseus is 45.2 g. The mother car­ries the in­fant in her mouth for about two weeks until young are strong enough to hold on. In­fants then cling to the mother until they are a lit­tle larger. Some­times the fa­ther or a sib­ling car­ries the in­fant, but most often it is the mother’s re­spon­si­bil­ity. Young are car­ried for ap­prox­i­mately 3 months; how­ever, once young be­come a lit­tle big­ger, they re­main in a tree while the mother searches for food. Once the in­fant is about three weeks old they are able to jump around, hop, and walk. Young can eat bam­boo by 6 weeks of age, but still de­pend on their mother to pro­vide them with food. Fe­males reach re­pro­duc­tive ma­tu­rity by 2 years of age, and males reach re­pro­duc­tive ma­tu­rity by 3 years of age. (Flan­nery, 2007)

Lifes­pan/Longevity

There is no in­for­ma­tion avail­able re­gard­ing the lifes­pan of Ha­pale­mur griseus in the wild. In cap­tiv­ity, records in­di­cate a max­i­mum age of 23 years. The pri­mary cause of death in the wild is pre­da­tion. (Flan­nery, 2007)

Be­hav­ior

Av­er­age group size for Ha­pale­mur griseus is around 4 in­di­vid­u­als. Groups are ter­ri­to­r­ial and males de­fend their group's ter­ri­tory from po­ten­tial ri­vals. Ter­ri­to­r­ial be­hav­ior in­cludes scent mark­ing, chas­ing, vo­cal­iza­tions, dis­plays, and star­ing. Con­fronta­tions are typ­i­cally not vi­o­lent and only 25% of these be­come ag­gres­sive. In­ter­group dis­putes usu­ally arise be­cause of an over­lap in ter­ri­to­ries. Al­though males are pri­mar­ily re­spon­si­ble for group pro­tec­tion, fe­males are dom­i­nant within the group. Once fe­males reach sub-adult­hood, they ei­ther dis­perse or re­main with their natal group. Males dis­perse upon reach­ing adult­hood, which oc­curs around three years of age. Ha­pale­mur griseus also ex­hibits la­trine be­hav­ior and takes turns defe­cat­ing in a sin­gle, cen­tral­ized lo­ca­tion. It fre­quently clings to trees and when mov­ing be­tween trees, it leaps from trunk to trunk. Move­ment is quadrupedal once in­di­vid­u­als de­scend to the ground. (Flan­nery, 2007)

  • Range territory size
    0.06 to 0.15 km^2
  • Average territory size
    0.1 km^2

Home Range

Home range size is highly vari­able in Ha­pale­mur griseus and de­pends on what re­gion of Mada­gas­car the in­di­vid­ual or group re­sides in. In some parks, home range has been found to be be­tween 0.06 km^2 and 0.1 km^2. In other parks, home range has been found to be around 0.15 km^2. In gen­eral, home range size is rel­a­tively small for H. griseus when com­pared to other bam­boo lemures. Ha­pale­mur griseus only ven­tures out of its home range dur­ing times of scarcity.

Com­mu­ni­ca­tion and Per­cep­tion

Ha­pale­mur griseus has scent glands that as­sist in ol­fac­tory com­mu­ni­ca­tion with group mem­bers and ri­vals. Many forms of com­mu­ni­ca­tion occur on or with pa­pyrus plants, in­clud­ing sub­strate mark­ing. When sub­strate mark­ing, in­di­vid­u­als scratch pa­pyrus leaves with their teeth and ei­ther rub the piece of pa­pyrus on its scent glands or uri­nate on it. Ha­pale­mur griseus also per­forms scent mark­ing with its tail by rub­bing the fore­arm scent glands along the length of the tail while watch­ing star­ing at a rival. Other forms of com­mu­ni­ca­tion in­clude run­ning around a patch of veg­e­ta­tion in cir­cles to iden­tify ones lo­ca­tion, by con­fronting in­di­vid­u­als, by chas­ing away in­di­vid­u­als, and by star­ing. Tac­tile com­mu­ni­ca­tion is largely re­stricted to so­cial groom­ing. Vocal com­mu­ni­ca­tion of H. griseus is ac­com­plished through a va­ri­ety of grunts, clicks, screeches, trem­bles, teeth grind­ing, and purrs. In­fants often purr when licked by their mother and per­form a high-pitched dis­tress call when sep­a­rated from its mother. When re­united with their young, moth­ers cre­ate a grunt-like sound. Ha­pale­mur griseus also per­forms mat­ing calls, low-in­ten­sity alarm calls, high-in­ten­sity alarm calls, in­tim­i­da­tion calls, and calls that are used to iden­tify the lo­ca­tion of con­specifics. (Flan­nery, 2007)

Food Habits

The pri­mary for­age of Ha­pale­mur griseus is bam­boo. There are over 40 species of bam­boo, but the main species con­sumed by H. griseus is giant bam­boo. Al­though bam­boo is con­sid­ered toxic due to high con­cen­tra­tions of cyanide found through­out the plant, bam­boo lemurs do not ex­pe­ri­ence cyanide poinson­ing. The mech­a­nism of how this is ac­com­plished is still un­known. A typ­i­cal diet for this species is 72% bam­boo, 16% grasses, 5% fruits, 4% leaves (usu­ally from var­i­ous lianas), and 3% from other sources. Ha­pale­mur griseus eats the bases and the inner walls of young bam­boo shoots. It feeds through one side of its mouth and chews the bam­boo on the other side. Around 70% of its time is spent feed­ing on bam­boo. Food pref­er­ences are con­tin­gent on time of year and re­source avail­abil­ity. Fe­males tend to eat more than the males be­cause of the phys­i­o­log­i­cal stress in­duced by ges­ta­tion and lac­ta­tion. (Flan­nery, 2007)

  • Plant Foods
  • leaves
  • wood, bark, or stems
  • fruit

Pre­da­tion

Known preda­tors in­clude Mala­gasy tree boas as well as other boas, ring-tailed mon­gooses, hu­mans, fos­sas, owls, and Mada­gas­car ser­pent ea­gles. Other po­ten­tial preda­tors in­clude other rap­tors, lemurs, dogs, and cats. Vi­sual mon­i­tor­ing and vocal com­mu­ni­ca­tion are the pri­mary means of evad­ing pre­da­tion by H. griseus. In ad­di­tion, their ar­bo­real na­ture likely re­duces risk of pre­da­tion as well. (Flan­nery, 2007; Williams, 2001)

Ecosys­tem Roles

Other than their role as prey for a num­ber of Mala­gasy preda­tors, lit­tle is known of the po­ten­tial im­pact of Ha­pale­mur griseus on their local en­vi­ron­ment. Major preda­tors of H. griseus in­clude Mala­gasy tree boas as well as other boas, ring-tailed mon­gooses, hu­mans, fos­sas, owls, and Mada­gas­car ser­pent ea­gles. There is no in­for­ma­tion avail­able re­gard­ing par­a­sites of this species. (Flan­nery, 2007; Williams, 2001)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Ha­pale­mur griseus is hunted by hu­mans through­out their ge­o­graphic range and is also col­lected for the local pet trade. (An­dri­a­holini­rina et alia, 2010)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of Ha­pale­mur griseus on hu­mans. Ques­tions have been raised about the po­ten­tial trans­mis­sion of zoonotic dis­eases from lemurs to hu­mans and do­mes­tic an­i­mals.

Con­ser­va­tion Sta­tus

Ha­pale­mur griseus is clas­si­fied as vul­ner­a­ble on the IUCN's Red List of Threat­ened Species. Al­though it is cur­rently rec­og­nized as com­mon, pop­u­la­tions are de­creas­ing due to hunt­ing and the pet trade. In ad­di­tion, habi­tat loss due the clear­ing of bam­boo stands and slash-and-burn agri­cul­ture have had a neg­a­tive im­pact on the range and abun­dance of this species. CITES (the Con­ven­tion on In­ter­na­tional Trade in En­dan­gered Species of Wild Fauna and Flora) lists H. griseus under Ap­pen­dix I and it oc­curs in a num­ber of na­tional parks and habi­tat re­serves. (An­dri­a­holini­rina et alia, 2010)

Con­trib­u­tors

John Hibbs (au­thor), Augs­burg Col­lege, Kevin Potts (ed­i­tor), Augs­burg Col­lege, John Berini (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

Glossary

Ethiopian

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

World Map

acoustic

uses sound to communicate

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

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.

female parental care

parental care is carried out by females

folivore

an animal that mainly eats leaves.

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.

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).

marsh

marshes are wetland areas often dominated by grasses and reeds.

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.

pet trade

the business of buying and selling animals for people to keep in their homes as pets.

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.

scent marks

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

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

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

Ref­er­ences

An­dri­a­holini­rina et alia, 2010. "Ha­pale­mur griseus" (On-line). The IUCN Red List of Threat­ened Species. Ac­cessed April 18, 2011 at http://​www.​iucnredlist.​org/​apps/​redlist/​details/​9673/​0.

Flan­nery, S. 2007. "Gray Gen­tle Lemur (Ha­pale­mur griseus)" (On-line). The Pri­mata. Ac­cessed April 15, 2011 at http://​www.​theprimata.​com/​hapalemur_​griseus.​html.

Grassi, C. 2001. The Be­hav­ioral Ecol­ogy of Ha­pale­mur griseus griseus: The In­flu­ences of Mi­cro­hab­i­tat and Pop­u­la­tion Den­sity on this Small-bod­ied Prosimian Fo­li­vore. Uni­ver­sity of Texas. Ac­cessed April 21, 2011 at http://​icte.​bio.​sunysb.​edu/​pdf_​files/​GrassiDissertation.​pdf.

Gron, K. 2010. "Pri­mate Info Net" (On-line). Ha­pale­mur. Ac­cessed April 19, 2011 at http://​pin.​primate.​wisc.​edu/​factsheets/​entry/​bamboo_​lemur/​taxon.

Niev­ergelt, C., T. Mutschler, A. Feist­ner, D. Woodruff. 2002. So­cial Sys­tem of the Alao­tran Gen­tle Lemur (Ha­pale­mur griseus alaotren­sis): Ge­netic Char­ac­ter­i­za­tion of Group Com­po­si­tion and Mat­ing Sys­tem. Amer­i­can Jour­nal of Pri­ma­tol­ogy, 57: 157-176. Ac­cessed April 19, 2011 at http://​polymorphism.​scripps.​edu/​Reprints/​AJP-CN-2002.​pdf.

Ralaina­solo, F., P. Wae­ber, J. Rat­sim­bazafy, J. Durbin, R. Lewis. 2006. The Alao­tra gen­tle lemur: Pop­u­la­tion es­ti­ma­tion and sub­se­quent im­pli­ca­tions. MADA­GAS­CAR CON­SER­VA­TION & DE­VEL­OP­MENT, 1/1: 9-10. Ac­cessed April 19, 2011 at http://​www.​ajol.​info/​index.​php/​mcd/​article/​viewFile/​44044/​27559.

Williams, G. 2001. "Ha­pale­mur griseus griseus" (On-line). Wel­come to Ra­nomafana Na­tional Park. Ac­cessed April 18, 2011 at https://​web.​archive.​org/​web/​20110913140122/​http://​icte.​bio.​sunysb.​edu/​rano.​biodiv/​Mammals/​Hapalemur-griseus/​index.​html.