Black crested gibbon

The black crested gibbon (Nomascus concolor) is a Critically Endangered species of gibbon found in China, Laos, and northern Vietnam, with four subspecies.

Black crested gibbon[1]
Temporal range: Pleistocene to Recent[2]
CITES Appendix I (CITES)[4]
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Primates
Suborder: Haplorhini
Infraorder: Simiiformes
Family: Hylobatidae
Genus: Nomascus
Species:
N. concolor
Binomial name
Nomascus concolor
(Harlan, 1826)
Subspecies
  • Nomascus concolor concolor
  • Nomascus concolor lu
  • Nomascus concolor jingdongensis
  • Nomascus concolor furvogaster
Black crested gibbon range
Synonyms

Hylobates concolor

Taxonomy

The taxonomy of the species is confused. Previously grouped in the genus Hylobates, currently four subspecies are recognised.[3]

  • Central Yunnan black crested gibbon (Nomascus concolor jingdongensis), Yunnan province, China
  • West Yunnan black crested gibbon (N. c. furvogaster), Yunnan province, China
  • Laotian black crested gibbon (N. c. lu), Laos
  • Tonkin black crested gibbon (N. c. concolor), northern Vietnam

Description

The length from the head to the end of body is 43–54 cm (17–21 in) and it weighs from 6.9 to 10 kg (15 to 22 lb).[5] The species exhibits sexual dichromatism, the male is completely black, while the female is a golden or buff colour with variable black patches, including a black streak on the head.[5]

Behavior

Gibbons are forest dwellers and are well known for their habit of swinging between the branches of the rainforest on their long arms, a method of locomotion known as brachiation. Gibbons are also adept, however, at walking upright, both on the ground and in the trees. Black crested gibbons live in small family groups consisting of a monogamous male and female and their offspring; occasionally groups reportedly may contain additional mature females. These apes are predominantly arboreal and the group forages and sleeps amongst the trees. Led by the female, the breeding pair partakes in vigorous bouts of singing in the morning, which hauntingly echo through the forest. These 'duets' are believed to be essential in pair bond formation and reinforcement, and also serve to advertise the presence of the group within the territory. A single young is born every two to three years and the infant is usually weaned once it reaches two years old;

Black crested gibbons feed preferentially on ripe, sugar-rich fruit, such as figs, but occasionally consume vitamin-rich leaf buds, and rarely eat animals.

Group living

Black-crested gibbons live arboreally in small groups, most of which consist of a pair of adults, one male and one female, and their offspring. It has been observed that some groups consist of one adult male living with two to four females and their offspring. The group could potentially include one infant, one juvenile, one adolescent, and one sub adult.[6] Groups have been found to be territorial, like other species of gibbons. Territories are limited by the availability of the male for territory defense. Thus, group and territory size would be limited. With a large group, territory defense would not be favored by kin selection due to the group consisting of less-closely related individuals.[7] Though the research is not explicit, there can be some assumptions made about altruism within groups. Since the majority of groups are living in monogamous relationships with both males and females displaying aggression when another individual enters,[7] it is likely that kin selection plays a major role in determining behavior of the group. Kin recognition is thought to be favored for maternal-offspring relationships. This is largely due to primates' uncertainty over paternity, even in pair-bonding species due to female promiscuity.[8] Social behaviors within groups will evolve according to Hamilton's rule.[9]

Mating

Gibbons were previously reported to practice monogamous sexual relationships.[7] They are known to form pair bonds, as well documented in the majority of gibbon species.[8] Upon the discovery of single male, multi-female living groups, the question arose to determine if all females were mating. The observation that offspring of similar ages lived within a multi-female group confirmed that polygyny did in fact occur. The current hypothesis remains that both monogamous and polygamous relationships exist.[6] There may be various selection pressures for polygyny within previously monogamous groups. Parents tend to be hostile towards maturing offspring, with males leaving the group more quickly than females do.[6] Yet, upon tolerance by the mother, adult female offspring may remain in the group, as the group continues to forage and feed as family members. The mutual tolerance of females is likely to be caused by "weak territoriality of females".[6] Further selection occurs due to the birth interval for a single female averaging 2–2.5 years. Male fitness would benefit from inseminating other females during a birth interval.[6] This hypothesis is supported by the large scrotal size allowing for increased sperm production.[6] Other observations have been made that males will share child carrying to place less of a burden on the female, delaying her interbirth time.[7] The conflicting observations support the hypothesis that black-crested gibbons demonstrate both monogamous and polygamous sexual relationships.

Singing

All gibbon species are known to produce loud and long song bouts, lasting for 10–30 minutes. The black-crested gibbon sings in the morning, sometimes in duets initiated by the male. The males choose the highest tree branches, often near ridges. The songs are thought to be used for resource defense, mate defense, pairbonding, group cohesion and mate attraction.[10]

Distribution and habitat

The black crested gibbon has a discontinuous distribution across southwestern China, northwestern Laos, and northern Vietnam. One thousand years ago, gibbons which may have been crested gibbons (Nomascus) were found over a large part of southern and central China up to the Yellow River.[3]

The four subspecies are geographically separated. The Tonkin black crested gibbon (Nomascus concolor concolor) occurs in southern China (southwestern Yunnan) and northern Vietnam (Lào Cai, Yên Bái, Sơn La, and Lai Châu provinces), between the Black and Red Rivers. The West Yunnan black crested gibbon (N. c. furvogaster) occurs in a small area near the Burma border, west of the Mekong, in southwestern Yunnan, southern China. The Central Yunnan black crested gibbon (N. c. jingdongensis) occurs in a small region around the Wuliang Mountains, between the Mekong and Chuanhe rivers in west-central Yunnan. The Laotian black crested gibbon (N. c. lu) occurs in northwestern Laos in an isolated population on the east bank of the Mekong in Laos.[3]

The black crested gibbon inhabits tropical evergreen, semievergreen, deciduous forests in subtropical and mountainous areas. It generally lives in high altitudes, from 2100 to 2400 m above sea level, where most of their food resources are concentrated. In Vietnam and Laos, the species is found at lower altitudes, while in China, it has been observed as high as 2689 meters.[5]

Conservation

The black crested gibbon is listed as critically endangered on the IUCN Red List. An estimated 1300 to 2000 individuals are left in the wild.[3] The western black crested gibbons were included on the State Forestry Bureau of China's list of 12 flagship and keystone species for biodiversity protection in 2021.[11] While under protection, there was still a noticeable decline in population size at Wuliangshan National Nature Reserve.[12] It was discovered that the gray langurs are suppressing the black crested gibbon's potential recovery.[12] The gray langurs and black crested gibbons have similar diets and ranges; however, gray langurs have an advantage by having a more comprehensive dietary list, a larger group, and faster life history.[13] The black crested gibbon inhabits the evergreen broad-leaved forests that take a long time to regenerate, making it challenging for the gibbons to connect with other groups.[14] Ecological corridors were put in place in the Hengduan Mountain in China to help restore connections between different groups, increase overall well-being, and decrease the risk of extinction.[15]

References
  1. Groves, C. P. (2005). "Order Primates". In Wilson, D. E.; Reeder, D. M (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. p. 180. ISBN 978-0-8018-8221-0. OCLC 62265494.
  2. "Fossilworks: Nomascus concolor". www.fossilworks.org.
  3. Pengfei, F.; Nguyen, M.H.; Phiaphalath, P.; Roos, C.; Coudrat, C.N.Z.; Rawson, B.M. (2020). "Nomascus concolor". IUCN Red List of Threatened Species. 2020: e.T39775A17968556. doi:10.2305/IUCN.UK.2020-2.RLTS.T39775A17968556.en. Retrieved 19 November 2021.
  4. "Appendices | CITES". cites.org. Retrieved 14 January 2022.
  5. Cheng, Clarence (2011). Sargis, Eric; McCormick, Gale (eds.). "Nomascus concolor". Animal Diversity Web. Retrieved 29 December 2011.
  6. Jiang, Xuelong, Yingxiang Wang, and Qiang Wang. "Coexistence of Monogamy and Polygyny in Black-crested Gibbon (Hylobates concolor).” Primates, 40(4): 607-611.
  7. Brockelman, Warren Y. "Ecology and the Social Systems of Gibbons. The Gibbons Developments in Primatology: Progress and Prospects. 211-239. 2009
  8. Silk, Joan B. "Kin Selection in Primate Groups". International Journal of Primatology. Vol. 23, No. 4, August 2002.
  9. Silk, Joan B. "Practicing Hamilton’s rule: kin selection in primate groups". Cooperation in Primates and Humans: Mechanisms and Evolution. 2006.
  10. Fan, Peng-Fei, Wen Xiao, Sheng Huo, and Xue-Long Jiang. "Singing Behavior and Singing Functions of Black-Crested Gibbons at Mt. Wuliang, Central Yunnan, China". American Journal of Primatology. Vol 71: 539-547. 2009.
  11. Fan, Peng-Fei; Zhang, Lu; Yang, Li; Huang, Xia; Shi, Kai-Chong; Liu, Guo-Qing; Wang, Chun-Hua (18 March 2022). "Population recovery of the critically endangered western black crested gibbon (Nomascus concolor) in Mt. Wuliang, Yunnan, China". Zoological Research. 43 (2): 180–183. doi:10.24272/j.issn.2095-8137.2021.390. ISSN 2095-8137. PMC 8920850. PMID 35008133.
  12. Chen, Yuan; Ma, Chi; Yang, Li; Guan, Zhenhua; Jiang, Xuelong; Fan, Pengfei (1 August 2020). "Asymmetric competition between sympatric endangered primates affects their population recovery". Biological Conservation. 248: 108558. doi:10.1016/j.biocon.2020.108558. ISSN 0006-3207. S2CID 225472295.
  13. Chen, Yuan; Ma, Chi; Yang, Li; Guan, Zhenhua; Jiang, Xuelong; Fan, Pengfei (1 August 2020). "Asymmetric competition between sympatric endangered primates affects their population recovery". Biological Conservation. 248: 108558. doi:10.1016/j.biocon.2020.108558. ISSN 0006-3207. S2CID 225472295.
  14. Wu, Jiacheng; Delang, Claudio O.; Li, Yijie; Ye, Quan; Zhou, Jie; Liu, Huan; He, Hongming; He, Wenming (1 September 2021). "Application of a combined model simulation to determine ecological corridors for western black-crested gibbons in the Hengduan Mountains, China". Ecological Indicators. 128: 107826. doi:10.1016/j.ecolind.2021.107826. ISSN 1470-160X.
  15. Wu, Jiacheng; Delang, Claudio O.; Li, Yijie; Ye, Quan; Zhou, Jie; Liu, Huan; He, Hongming; He, Wenming (1 September 2021). "Application of a combined model simulation to determine ecological corridors for western black-crested gibbons in the Hengduan Mountains, China". Ecological Indicators. 128: 107826. doi:10.1016/j.ecolind.2021.107826. ISSN 1470-160X.
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