top of page

Sulawesi babirusa

Babyrousa celebensis

 

Status: Vulnerable

Did you know? Compared to the other two babirusa species, Sulawesi babirusa can be easily recognised thanks to their naked-looking body and impressive upper tusks.

Sulawesi babirusa - Josh More.jpg

Taxonomy

Phylogenetic studies suggest that babirusas diverged from other pigs in the Miocene, approximate between 10 and 19 million years ago, which could well be the time when they became first isolated on Sulawesi. Considering that the land connection between southern Sulawesi and Borneo was severed some 50 Mya, this suggests that a later land connection existed between Sundaland and Sulawesi, unless babirusas dispersed through rafting or swimming. The presence of two more genera of suids in Sulawesi (Celebochoerus and Sus), which must have split off from the main stock of Suidae at different times, is indicative of several invasions of ancestral suid types to Sulawesi over a great length of time.

The genus is monotypic within the subfamily Babyrousinae, or alternatively considered to form a tribe, Babyrousini, of the subfamily Suinae. All members of this genus were considered part of a single species, Babyrousa babyrussa, until recently, but following the split into several species, the nominate scientific name is now restricted to the Moluccan Babirusa from Buru and the Sula Islands. B. celebensis, the Sulawesi Babirusa, is the best-known babirusa, and the only species for which substantive ecological and behavioral information is available.

Distribution

B. celebensis occurs on the island of Sulawesi. The name specifically refers to animals from the north of the island, and the taxonomic identity of the individuals from central, eastern and southeastern Sulawesi remains undecided. We here follow the IUCN Red List and treat all individuals occurring on Sulawesi, as well as those previously known from the Muna, Buton and Lembeh Islands as belonging to B. celebensis, pending resolution of the taxonomy.

B. celebensis has been much reduced on the northern peninsula of Sulawesi, primarily due to over-hunting, and their distribution may now be largely limited to the western end of the Bogani Nani-Wartabone National Park, the Nantu Wildlife Reserve and the Panua Nature Reserve; all in the western half of the northern peninsula. The species still occurs in central Sulawesi and the eastern and southeastern peninsula, although precise information regarding the current extent of occurrence and area of occupancy is lacking. The species is unlikely to still occur on the severely deforested southern island of Muna, where the species used to occur. On Buton the species was not found during recent mammal surveys, and its continued presence on the island of Lembeh is also uncertain.

Descriptive notes

Head-body 85–110 cm; shoulder height 65–60 cm; weight up to 100 kg. B. celebensis is characterized by its sparse or absent body hair, a nearly hairless tail tuft, and long, relatively thick upper canines that emerge vertically, converge slightly and curl dorsally in a circle. The upper canines of males are generally long and thick, with the upper canines merging vertically and not crossing the lower canines in lateral view. The skulls of B. celebensis are longer than the two other species. They are relatively narrowed than one specimen from central Sulawesi, for which the taxonomic status remains unresolved as pointed out above. The lower (M1 and M3) and upper (M2 and M3) molars in B. celebensis are longer than in the other two species.

Unlike most other pig species, babirusas do not have the typical adaptations for rooting. The nose of babirusas lacks the rostral bone that in other pigs provides support for the tough connective tissue plate of the rhinarium.

Re-analyses of the soft tissue anatomy of the limbs and digestive tract of B. celebensis have revealed mistakes of identification in earlier work and the results have reversed the earlier suggestion that the babirusa was constructed in a significantly different way from the pig (Sus spp.); in general the muscular anatomies of the two species are very similar and the stomach of the babirusa does not resemble that of the ruminant.

Habitat

B. celebensis inhabits tropical rain forest. Whereas previously the animal had been reported to occur in low lying areas near coasts, recent anecdotal and survey reports indicate that the species is now confined mostly to the interior, on higher and less accessible ground. Although often associated with swamp and riverine areas, there is still insufficient data to be conclusive on the aquatic affinities of the species. The species frequently uses mineral salt-licks.

Diet

Diet and feeding behavior in B. celebensis remain poorly studied in the wild, but observations on captive animals provide a useful picture of their potential diet. The anatomical structure of the stomach and digestive tract suggest that B. celebensis is omnivorous. In zoos, adults of this species have been observed to chase, catch and eat small mammals and birds implying that they may show similar behavior in the wild. Observations of both wild and captive individuals suggest that species consumes a wide variety of leaf, root, and fruit material, with fruit supposedly being specifically important. Their jaws and teeth are strong enough to crack very hard nuts with ease. Not unlike the Bornean Bearded Pig, Sus b. barbatus, B. celebensis' apparent requirement for fruit-bearing trees as a component part of their environment has been implied, because as soon as mature trees were cleared by forestry operations or conversion to food crop production, the babirusas were no longer to be found in the area. Whether this is a result of changes in food resources or increased hunting pressure and disturbance from logging crews has not yet been clarified.

S. celebensis forages for food items on the ground, under logs and stones, in wet areas and on bushes and trees. Animals will stand with their forelimbs against tree trunks to reach hanging leaves and fruit, and will even stand on their hind limbs to pluck leaves from the trees.

Activity patterns

Based on observations on captive animals, B. celebensis appears to be mostly diurnal. These animals slept at night, which is consistent with the general lack of activity at night recorded in North Sulawesi. About an hour before sunrise at 6.00 individuals began to wake up and move about. Voiding of faecal material and urine occurs at this time, and animals appeared to prefer to defecate under branches and fallen tree trunks. Foraging extended throughout the day, but occupied a larger proportion of the time in the morning. From about mid-morning onwards an increasing proportion of the time was taken up with non-foraging activities. The animals were either wallowing or lying down. Both in the wild and in captivity, males have been observed to wallow more often than females.

Movements, home range and social organisation

The information available from field and captive studies indicates B. celebensis is a social species. Groups of up to 13 have been observed in the rainforest, especially around water, communal wallowing areas and salt licks. Rarely aggregations as large as 46 individuals comprising several distinct groups have congregated at salt licks. Most (i.e. 84%) of all sightings of solitary animals were of adult males. Single adult males were seen with single adult females, but never with two or more females unless young animals were present. Adult females were rarely seen without company; they were sometimes found together with other adult animals, but most often they were with young babirusa. Groups containing adult females and young numbered 84 (of the 226 groups studied), of which two thirds (56 groups) had no adult males present.

Very little is known about the ranging behavior of B. celebensis. Field observations suggest that the adult males have home ranges that overlap with those of a number of other adult males. Density estimates in two protected areas where the species still occurred in 2003 varied from 4.3–11.8 and 0.7–4.1 animals/km2.

 

Like other pigs, babirusas evidently swim well. A single adult male was reported approximately 500 m from the shore of a large lake in central Sulawesi, and even though it is not certain whether this is the same species as B. celebensis, it is likely that all babirusa species can swim and cover relatively large distances.

Reproduction

In zoological collections, B. celebensis may become sexually mature as early as five to ten months of age. However, it is likely that the age of sexual maturity in the wild is influenced by a number of factors including the level of nutrition. Precise data do not yet exist, but animals are unlikely to breed in the wild before they are one year old. Estrus cycle lengths of 28–42 days have been recorded but recent endocrine studies suggest it may lie between 35 and 37 days. Captive females generally re-cycle within 3 months after the birth of their young. Estrus lasts 2–3 days, and the female is not receptive to males at other times.

Gestation length is usually 155–158 days, though up to 171 days has been reported. The body weight of the sow increases during gestation. The normal litter size in B. celebensis is one or two uniformly brown colored piglets, but a low incidence of triplet births has been recorded both in zoos and in the wild, and a litter of four fetuses has been reported in utero in a wild female. Neonatal B. celebensis are small in size and weigh less than 800g at birth. There are usually four mammary glands, but an additional pair has sometimes been reported. Although the female can have a life span of as long as 24 years in captivity, it is unlikely that the animals in the wild live as long, perhaps no more than 7–12 years.

In zoos, B. celebensis sows produce young at all times of the year, and may produce two litters within a 12 month period. However, since it seems likely that diet or seasonal factors would normally influence inter-birth intervals, litters may be produced less frequently in the wild. Observation in North Sulawesi revealed adult females accompanied by subadult animals as well as juveniles. However, there was no observable criterion with which to establish whether or not these youngsters of two different ages represented the progeny of consecutive litters from the same adult female.

Studies of the agonistic behavior of B. celebensis have so far revealed no evidence that the adult males normally use their teeth during male-male interactions. The ultimate form of agonistic behavior is described as “boxing”, and involves two males raising themselves off the ground until both are standing on their hind legs facing one another, leaning and paddling against the chest and shoulders of their opponent. Their snouts are held as high as possible. Females did not employ the same strategy.

Status and conservation

The species is listed as Vulnerable on The IUCN Red List. Adult B. celebensis appear to have few, if any, natural predators. There are no large native mammalian carnivores on Sulawesi, and the most likely predator are probably large snakes and crocodiles. The small numbers of young born suggest that the species is not adapted to a high rate of natural predation. Hunting by humans, however, with snares, nets, spears and dogs has undoubtedly been an important factor since prehistoric times, and widespread snare trapping constitutes the main threat to the remaining populations of B. celebensis in North Sulawesi and, more recently, elsewhere in Sulawesi. B. celebensis is apparently not hunted specifically for its own meat, but represents a by-catch to the hunting of the Sulawesi Warty Pig, Sus celebensis. Therefore, the population of B. celebensis in the wild is being placed under severe and increasing pressure by the market demand for wild pig meat.

 

The species is also increasingly threatened by commercial logging, and by the spread of other land-uses resulting in forest conversion and degradation. Total lowland forest loss on the island is estimated to be likely more than 75%.

The genus Babyrousa was accorded full protection under Indonesian law in 1931. Under its original taxonomic designation, B. babirussa, the species has been included on Appendix I of CITES since 1982, although international trade in this species is not thought to be have been an important issue.

B. celebensis occurs in several protected areas of various levels on Sulawesi (e.g. Bogani Nani Wartabone National Park, Lore Lindu National Park, Rawa Aopa Watumohai National Park, the Nantu Wildlife Reserve, the Panua Nature Reserve, Morowali Nature Reserve and others. As pointed out above, the taxonomic status of the central and southern Sulawesi animals remains unclear, and B. celebensis may therefore be much more restricted and highly endangered in northern Sulawesi.

Bibliography

Text adapted from: Meijaard, E., J. P. d'Huart, and W. L. R. Oliver. 2011. Family Suidae (Pigs). Pages 248-291 in D. E. Wilson, and R. A. Mittermeier, editors. Handbook of the Mammals of the World. Vol 2. Hoofed Mammals. Lynx Edicions, Barcelona, Spain.

 

Andreescu, I. & D. Murariu.  (1993).  L'anatomie du crane de Babyrousa babyrussa (L., 1758) (Mammalia, Suidae).  Travaux du Museum d'Histoire Naturelle "Grigore Antipa" 33: 397-409.

Bosma, A.A. & N.A. de Haan.  (1981).  The karyotype of Babyrousa babyrussa (Suidae, Mammalia).  Acta Zoologica et Pathologica Antverpiensia: 76.

Bowles, D.  (1986).  Social behaviour and breeding of babirusa Babyrousa babyrussa at the Jersey Wildlife Preservation Trust.  Dodo: 23.

Bowles, D., J. Bell & K. Leus.  (1993).  Agonistic behaviour in captive Babirusa (Babyrousa babyrussa).  Mammalian Biology 58: 18-30.

Clason, A.T.  (1976).  A preliminary note about the animal remains from the Leang I Cave, South Sulawesi.  Modern Quaternary Research, SE Asia 2: 53-67.

Clayton, L. & D.W. MacDonald.  (1999).  Social Organization of the Babirusa (Babyrousa babyrussa) and Their Use of Salt Licks in Sulawesi, Indonesia.  Journal of Mammalogy 80: 1147-1157.

Clayton, L. & E.J. Milner-Gulland.  (2000).  The trade in wildlife in North Sulawesi, Indonesia. Pp. 473-496 in Hunting for sustainability in tropical forests, edited by J.G. Robinson and E.L. Bennett. New York: Columbia University Press.

Clayton, L.M., E.J. Milner-Gulland, D.W. Sinaga & A.H. Mustari.  (2000).  Effects of a proposed ex situ conservation program on in situ conservation of the babirusa, an endangered suid.  Cons. Biol. 14: 382-385.

Groves, C.  (1985).  The Sulawesi 'specials'. Archaic, strange, endemic.  Australian Natural History 21: 442-444.

Groves, C.P.  (1980).  Notes on the systematics of Babyrousa (Artiodactyla, Suidae).  Zoologische Mededelingen 55: 29-46.

Hooijer, D.A.  (1975).  Quaternary mammals west and east of Wallace's line.  Neth. J . Zool. 25: 46-56.

Houston, E.W., P.K. Hagberg, M.T. Fischer, M.E. Miller & C.S. Asa.  (2001).  Monitoring pregnancy in babirusa (Babyrousa babyrussa) with transabdominal ultrasonography.  Journal of Zoo and Wildlife Medicine 32: 366-372.

Lee, R.J., A.J. Gorog, A. Dwiyahreni, S. Siwu, J. Riley, H. Alexander, G.D. Paoli & W. Ramono.  (2005).  Wildlife trade and implications for law enforcement in Indonesia: a case study from North Sulawesi.  Biological Conservation 123: 477-488.

Lee, R.J., S.J. O'Brien, M.F. Kinnaird & A.A. Dwiyahreni.  (1999).  Impact of wildlife hunting in Sulawesi, Indonesia; with conservation recommendations. Bogor, Indonesia: WCS and PKA.

Leus, K.  (1996).  The habitat and diet of the Sulawesi babirusa (Babyrousa babyrussa). in Population and habitat viability assessment for the babirusa (Babyrousa babyrussa), edited by J. Manansang, A.A. Macdonald, D. Siswomartono, P. Miller, and U. Seal. Apple Valley, MN: Conservation Breeding Specialist Group (SSC/IUCN).

Leus, K., K.P. Bland, A.A. Dhondt & A.A. Macdonald.  (1996).  Ploughing behaviour of Babyrousa babyrussa (Suidae, Mammalia) suggests a scent-marking function.  Journal of Zoology 238: 209-219.

Leus, K., D. Bowles, J. Bell & A.A. Macdonald.  (1992).  Behaviour of the babirusa (Babyrousa babyrussa) with suggestions for husbandry.  Acta Zoologica et Pathologica Antverpiensia: 82.

Leus, K. & P. Vercammen.  (1996).  Behaviour of a male and female babirusa (Babyrousa babyrussa, Suidae, Mammalia) during the first five days after their move to a semi-natural enclosure.  Der Zoologische Garten, N.F. 66: 133-155.

Macdonald, A.A.  (1991).  Monographie des Hirschebers (Babyrousa babyrussa).  Bongo Sonderband 18: 69-84.

—.  (2006).  The Conservation of the Babirusa (Babyrousa babyrussa). Pp. 90-111 in Kumpulan makalah seminar sehari peduli anoa dan babirusa Indonesia, Bogor, 20 September 2005, edited by A.H.M. N. Sugiri, I. S. Suwelo & I. Djuwita. Bogor, Indonesia: Institut Pertanian Bogor.

Macdonald, A.A., D. Bowles, J. Bell & K. Leus.  (1993).  Agonistic behaviour in captive babirusa (Babyrousa babyrussa).  Zeitschrift für Säugetierkunde 58: 18-30.

Macdonald, A.A. & K. Leus.  (1995).  Creating a public understanding of the biology of the babirusa (Babyrousa babyrussa) within a caring zoo environment.  Ibex J.M.E. 3: 37-40.

MacKinnon, J.  (1981).  The structure and function of the tusks of babirusa.  Mammal Review 11: 37-40.

Manansang, J., A. Macdonald, D. Siswomartono, P. Miller & U. Seal.  (1996).  Babirusa (Babyrousa babyrussa). Population and habitat viability assessment 22-26 July 1996, Taman Safari Indonesia, Cisarua, Java Barat, Indonesia. Pp. i-vi, 1-190: IUCN/SSC Conservation Breeding Specialist Group.

Meijaard, E. & C. Groves.  (2002a).  Proposal for taxonomic changes within the genus Babyrousa.  Asian Wild Pig News 2.

Meijaard, E. & C.P. Groves.  (2002b).  Upgrading three subspecies of babirusa (Babyrousa sp.) to full species level.  Asian Wild Pig News 2: 33-39.

Melisch, R.  (1994).  Observation of swimming babirusa Babyrousa babyrussa in Lake Poso, Central Sulawesi, Indonesia.  Malayan Nature Journal 47: 431-432.

—.  (1995).  Babirusa skulls on sale in south Sulawesi.  Traffic Bulletin 15: 99.

Milner-Gulland, E.J.  (2001).  The exploitation of spatially structured populations.  Conservation Biology Series 6: 87-109.

Milner-Gulland, E.J. & L. Clayton.  (2002).  The trade in babirusas and wild pigs in North Sulawesi, Indonesia.  Ecol. Econ 42: 165-183.

Mohr, E.  (1958).  Zur Kenntnis des Hirschebers, Babirussa babyrussa Linné 1758.  Zoologischer Garten 25: 50-69.

Patry, M., K. Leus & A.A. Macdonald.  (1995).  Group structure and behaviour of babirusa (Babyrousa babyrussa) in northern Sulawesi.  Australian Journal of Zoology 43: 643-655.

Peters, C.T.M.  (1985).  De babiroesa: het hertzwijn.  Dieren 5: 135-139.

Rajchl, O.  (2007).  Babirusa - Babyrousa babyrussa (Linnaeus, 1758).  Fauna Bohemiae Septentrionalis 32: 23-28.

Randi, E., V. Lucchini & C. Hoong Diong.  (1996).  Evolutionary genetics of the suiformes as reconstructed using mtDNA sequencing.  Journal of Mammalian Evolution 3: 163-194.

Rice, E.K.  (1988).  The babirusa: a most unusual southeast Asian pig.  Animal Kingdom 91: 46-47.

Riley, J.  (2002).  Current Wildlife Conservation Society research and conservation of Sulawesi’s suids.  Asian Wild Pig News 2: 4-8.

Sody, H.J.V.  (1949).  Notes on some Primates, Carnivora and the babirusa from the Indo-Malayan and Indo-Australian regions.  Treubia 20: 121-190.

Van Wees, S., J. Nujboer, H. Everts & A.C. Beynen.  (2000).  Apparent digestibility of macronutrients in captive babirusa (Babyrousa babyrussa).  Journal of Zoo and Wildlife Medicine 31: 508-511.

Wemmer, C. & D. Watling.  (1982).  Eye colour polymorphism in the Babirusa pig.  Malayan Nature Journal 36: 135-136.

Wiles, P.R., A.A. MacDonald, J. Burton & I.A.H. Mustari.  (2002).  Records of babirusa and warty pigs in SE Sulawesi.  Asian Wild Pig News 2.

bottom of page