The common marmoset (Callithrix jacchus) is a New World monkey. It originally lived on the northeastern coast of Brazil, in the states of Piaui, Paraiba, Ceará, Rio Grande do Norte, Pernambuco, Alagoas and Bahia. Through release (both intentional and unintentional) of captive individuals, it has expanded its range since the 1920s to Southeast Brazil (its first sighting in the wild for Rio de Janeiro was in 1929), where it became an invasive species, raising concerns about genetic pollution of similar species, such as the buffy-tufted marmoset (Callithrix aurita), and predation upon bird nestlings and eggs.
|Common Marmoset at Aquazoo-Löbbecke-Museum, Düsseldorf|
|Scientific classification |
The whole-genome sequence of a female common marmoset was published on 20 July 2014. It became the first New World Monkey to have its genome sequenced.
Physical description and morphology
Common marmosets are very small monkeys with relatively long tails. Males and females are of similar size with males being slightly larger. Males have an average height of 188 mm (7.40 in) and females have an average height of 185 mm (7.28 in). Males weigh 256 g (9.03 oz) on average and females weigh 236 g (8.32 oz) on average. The pelage of the marmoset is multicolored, being sprinkled with brown, grey, and yellow. It also has white ear tufts and the tail is banded. Their faces have black across their nose area skin and have a white blaze on the forehead. The coats of infants are brown and yellow with the ear tuft developing later.
As with other members of the genus Callithrix, the common marmosets have claw-like nails known as tegulaes on most of their fingers. Only their halluxes (big toes) have the flat nails or ungulaes that most other primates have. Marmosets have an arboreal locomotion similar to squirrels. They can hang on to trees vertically and leap between them, as well as run across branches quadrupedally. Tegulaes are an adaptation of this type of locomotion. Other Callithrix traits shared include enlarged, chisel-shaped incisors and specialized cecums for their diet.
Range and ecology
Common marmosets are native only to east-central Brazil. They have been introduced into other areas and live within the cities of Rio de Janeiro and Buenos Aires, Argentina. Marmosets can be found in a number of forest habitats. They live in Atlantic coastal forests as well as semi-deciduous forests farther inland. They can also inhabit savanna forests and riverine forests. Marmosets are successful in dry secondary forests and edge habitats.
The common marmoset’s claw-like nails, incisor shape, and gut specialization reflect their unique diet which is primarily made of plant exudates and insects. Common marmosets feed on gum, sap, latex, and resin. They use their nails to cling to the side of a tree and, with their long lower incisors, chew a hole in the tree. The marmoset will then lick up the exudates or swoop them with the teeth. 20-70% of the marmoset’s feeding behavior is made of eating exudates.
Exudates provide marmosets with a reliable food source in the marmoset’s seasonal habitat. They rely on these foods particularly between January and April, when fruit is not abundant. A marmoset may visit a tree hole multiple times; including those made by other animals. In addition to exudates, insects also prove an important food source for marmosets, making 24-30% of their feeding time. The small size of the marmoset allows them to subsist on insects, as well as stalking and ambush them. Marmosets will also eat fruits, seeds, flowers, fungi, nectar, snails, lizards, tree frogs, bird eggs, nestlings, and infant mammals. It is possible that marmosets compete for fruit with birds, such as parrots and toucans, and with woolly opossums.
Common marmosets live in stable extended families with only a few members allowed to breed. A marmoset group can contain as many as 15 members, but a more typical number is nine. A marmoset family usually contains 1-2 breeding females, a breeding male, their offspring and their adult relatives, be it their parents or siblings. The females in a group tend to be closely related and males less so. Males do not mate with breeding females that they are related to. Marmosets may leave their natal groups when they become adults, in contrast to other primate species who leave at adolescence. Not much is known of the reasons marmosets leave their natal groups. Family groups will fission into new groups when a breeding male dies. Within the family groups, the breeding individuals tend to be more dominant. The breeding male and female tend to share dominance. However, between two breeding females, one is more dominant. In addition, the subordinate female is usually the daughter of the dominant one. For the other members, social rank is based on age. Dominance is maintained though various behaviors, postures and vocalizations and subordinates will groom their superiors.
Reproduction and parenting
Common marmosets have a complex mating system. It was thought that they were monogamous, however both polygamy and polyandry have also been observed. Nevertheless, most matings are monogamous. Even in groups with two breeding females, the subordinate female often mates with males from other groups. Subordinate females usually do not give birth to fit offspring. Nevertheless, mating with extra-group males may allow the female to find potential mates in the future. Females that mate successfully but lose their young move to other groups and may gain dominant breeding positions.
The breeding individuals in a group need the other members to help raise their young. Thus the pair will behaviorally and physiologically suppress the reproduction of the other members of the group. Since these suppressed individuals are likely related to the breeding pair, they have an incentive to care for the young as they share genes with them. In addition, the presence of a related male affects female ovulation. Laboratory studies have shown that female ovulation does not occur when their fathers are around, but does occur when an unrelated male is there instead. They will also display aggressive behavior towards their mothers, possibly to displace them.
When conditions are right for them to breed, adult females breed regularly for the rest of their lives. Females flick their tongues at males to solicit mating. The gestation period lasts for five months, and females are ready to breed again around ten days after giving birth. There are five months in between each parturition and they give birth twice a year. Marmosets commonly give birth to two non-identical twins. Because of this, females are under stress during pregnancy and lactation, and need help from the other members of the family. Infant marmosets instinctively cling to their mothers back and do not voluntarily let go for the first two weeks. After that, they become very active and explore their environment. The breeding male (likely the father) will begin handling the twins, and all members of the family will care for them. In the following weeks, the young spend less time on their mother’s back and more time moving around and playing. Infants are weaned at three months. At five months they enter their juvenile stage. At this time, they have more interactions with family members other than their parents, and there is rough play for to establish their future status. Another set of infants may be born and the previous young will carry and play with them. Marmosets become sub-adults between nine and 14 months, act like adult and go through puberty. At 15 months, they reach adult size and are sexually mature but can not breed until they are dominant.
Common marmosets employ a number of vocal and visual communications. To signal alarm, aggression, and submission, marmosets use the "partial open mouth stare," "frown," and "slit-stare", respectively. To display fear or submission, marmosets flatten their ear-tufts close to their heads. Marmosets have two alarm calls: a series of repeating calls that get higher with each call, known as "staccatos"; and short trickling calls given either intermittently or repeatedly. These are called "tsiks". Marmoset alarm calls tend to be short and high-pitched. Marmosets monitor and locate group members with vibrato-like low-pitched generic calls called "trills". Marmosets also employ "phees" which are whistle-like generic calls. These serve to attract mates, keep groups together, defend territories, and locate missing group members. Marmosets will use scent gland on their chests and anogenital regions to mark objects. These are meant to communicate social and reproductive status.
The common marmoset remains an abundant species and are not currently threatened. Nevertheless, its habitat had been degraded at a fast rate, with around 67% of the cerrado region cleared for human use in the 1990s and around 80% cleared for cultivation more recently. In addition, marmosets are captured and traded as pets. Though popular as pets, they become difficult to control as they get older and are thus abandoned or killed. Common marmosets have also been used for medical experiments. They are used as such in Europe more so than in the United States, and are the most common non-human primates to be experimented on. They are used as model organisms in areas of research such as teratology, periodontal disease, reproduction, immunology, endocrinology, obesity, and aging.
The genome of a female marmoset was published in 2014. It became the first non-human primate, among the New World Monkeys, to have its complete genome sequenced. The genome size is 2.26 Gb, and contains 21,168 genes. Segmental duplications added a total of 138 Mb of non-redundant sequences (4.7% of the whole genome), slightly less than observed in human or chimpanzee (~5%), but more than in orangutan (3.8%).
- Groves, C.P. (2005). Wilson, D.E.; Reeder, D.M. (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Baltimore: Johns Hopkins University Press. p. 131. ISBN 0-801-88221-4. OCLC 62265494.
- Rylands AB & Mittermeier RA (2009). "The Diversity of the New World Primates (Platyrrhini)". In Garber PA, Estrada A, Bicca-Marques JC, Heymann EW & Strier KB (eds.). South American Primates: Comparative Perspectives in the Study of Behavior, Ecology, and Conservation. Springer. pp. 23–54. ISBN 978-0-387-78704-6.
- Rylands, A. B.; Mittermeier, R. A.; Oliveira, M. M. & Keirulff, M. C. M. (2008). "Callithrix jacchus". IUCN Red List of Threatened Species. Version 2008. International Union for Conservation of Nature. Retrieved 2 January 2009.
- Linnaeus, Carl (1758). Systema naturæ. Regnum animale (10th ed.). pp. 27, 28. Retrieved 19 November 2012.
- Macdonald, David, ed. (1985). Primates. All the World's Animals. Torstar Books. p. 50. ISBN 978-0-920269-74-9.
- Brandão, Tulio Afflalo (December 2006). "BRA-88: Micos-estrelas dominam selva urbana carioca" (in Portuguese). Rio de Janeiro. Archived from the original on 14 August 2009. Retrieved 10 April 2009.
- Worley, Kim C; Warren, Wesley C; Rogers, Jeffrey; Locke, Devin; Muzny, Donna M; et al. (2014). "The common marmoset genome provides insight into primate biology and evolution". Nat Genet. 46 (8): 850–857. doi:10.1038/ng.3042. PMC 4138798. PMID 25038751.
- Baylor College of Medicine. "Marmoset sequence sheds new light on primate biology and evolution". ScienceDaily. Retrieved 21 July 2014.
- Rowe, N. (1996). Pictorial Guide to the Living Primates. East Hampton: Pogonias Press. ISBN 978-0-9648825-0-8.
- Groves C. (2001) Primate taxonomy. Washington DC: Smithsonian Inst Pr.
- Garber PA, Rosenberger AL, Norconk MA. (1996) "Marmoset misconceptions". In: Norconk MA, Rosenberger AL, Garber PA, editors. Adaptive radiations of neotropical primates. New York: Plenum Pr. p 87-95.
- Kinzey WG. 1997. "Synopsis of New World primates (16 genera) ". In: Kinzey WG, editor. New world primates: ecology, evolution, and behavior. New York: Aldine de Gruyter. p 169-324.
- Rylands AB, Coimbra-Filho AF, Mittermeier RA. 1993. "Systematics, geographic distribution, and some notes on the conservation status of the Callitrichidae". In: Rylands AB, editor. Marmosets and tamarins: systematics, behaviour, and ecology. Oxford (England): Oxford Univ Pr. p 11-77.
- Rylands AB, de Faria DS. (1993) "Habitats, feeding ecology, and home range size in the genus Callithrix". In: 'Rylands AB, editor. Marmosets and tamarins: systematics, behaviour, and ecology. Oxford (England): Oxford Univ Pr. p 262-72.
- Ferrari, SF; Lopes Ferrari, MA (1989). "A re-evaluation of the social organization of the Callitrichidae, with reference to the ecological differences between genera". Folia Primatol. 52 (3–4): 132–47. doi:10.1159/000156392. PMID 2515129.
- Stevenson MF, Rylands AB. (1988) "The marmosets, genus Callithrix". In: Mittermeier RA, Rylands AB, Coimbra-Filho AF, da Fonseca GAB, editors. Ecology and behavior of neotropical primates, Volume 2. Washington DC: World Wildlife Fund. p 131-222.
- Digby, LJ (1995). "Social organization in a wild population of Callithrix jacchus: II, Intragroup social behavior". Primates. 36 (3): 361–75. doi:10.1007/bf02382859.
- Ferrari, SF; Digby, LJ (1996). "Wild Callithrix group: stable extended families?". Am J Primatol. 38: 19–27. doi:10.1002/(sici)1098-2345(1996)38:1<19::aid-ajp3>3.3.co;2-f.
- Lazaro-Perea, C (2001). "Intergroup interactions in wild common marmosets, Callithrix jacchus: territorial defense and assessment of neighbours". Anim Behav. 62: 11–21. doi:10.1006/anbe.2000.1726.
- Arruda, MF; Araujo, A; Sousa, MBC; Albuquerque, FS; Albuquerque, ACSR; Yamamoto, ME (2005). "Two breeding females within free-living groups may not always indicate polygyny: alternative subordinate female strategies in common marmosets (Callithrix jacchus)". Folia Primatol. 76 (1): 10–20. doi:10.1159/000082451. PMID 15711070.
- Baker, JV; Abbott, DH; Saltzman, W (1999). "Social determinants of reproductive failure in male common marmosets housed with their natal family". Anim Behav. 58 (3): 501–13. doi:10.1006/anbe.1999.1200.
- Saltzman, W; Severin, JM; Schultz-Darken, NJ; Abbott, DH (1997). "Behavioral and social correlates of escape from suppression of ovulation in female common marmosets with the natal family". Am J Primatol. 41: 1–21. doi:10.1002/(sici)1098-2345(1997)41:1<1::aid-ajp1>3.0.co;2-0.
- Yamamoto ME. (1993) From dependence to sexual maturity: the behavioural ontogeny of Callitrichidae". In: Rylands AB, editor. Marmosets and tamarins: systematics, behaviour, and ecology. Oxford (England): Oxford Univ Pr. p 235-54.
- Jones CB. (1997) "Quantitative analysis of marmoset vocal communication". In: Pryce C, Scott L, Schnell C, editors. Marmosets and tamarins in biological and biomedical research: proceedings of a workshop. Salisbury (UK): DSSD Imagery. p 145-51.
- Cavalcanti RB, Joly CA. (2002) "Biodiversity and conservation priorities in the cerrado region". In: Oliveira PS, Marquis RJ, editors. The cerrados of Brazil: ecology and natural history of a neotropical savanna. New York: Columbia Univ Pr. p 351-67.
- Duarte-Quiroga, A; Estrada, A (2003). "Primates as pets in Mexico City: an assessment of the species involved, source of origin, and general aspects of treatment". Am J Primatol. 61 (2): 53–60. doi:10.1002/ajp.10108.
- Abbott, DH; Barnett, DK; Colman, RJ; Yamamoto, ME; Schultz-Darken, NJ (2003). "Aspects of common marmoset basic biology and life history important for biomedical research". Comp Med. 53 (4): 339–50. PMID 14524409.
- Rylands AB. (1997) "The callitrichidae: a biological overview". In: Pryce C, Scott L, Schnell C, editors. Marmosets and tamarins in biological and biomedical research: proceedings of a workshop. Salisbury (UK): DSSD Imagery. p 1-22.
- Venter, J. C. (2001). "The Sequence of the Human Genome". Science. 291 (5507): 1304–1351. CiteSeerX 10.1.1.112.7735. doi:10.1126/science.1058040. PMID 11181995.
- McPherson, John D.; Marra, Marco; Hillier, LaDeana; Waterston, Robert H.; Chinwalla, Asif; et al. (2001). "A physical map of the human genome". Nature. 409 (6822): 934–941. doi:10.1038/35057157. PMID 11237014.
- The Chimpanzee Sequencing and Analysis Consortium (2005). "Initial sequence of the chimpanzee genome and comparison with the human genome". Nature. 437 (7055): 69–87. doi:10.1038/nature04072. PMID 16136131.
- Locke, Devin P.; Hillier, LaDeana W.; Warren, Wesley C.; Worley, Kim C.; Nazareth, Lynne V.; et al. (2011). "Comparative and demographic analysis of orang-utan genomes". Nature. 469 (7331): 529–533. doi:10.1038/nature09687. PMC 3060778. PMID 21270892.
|Wikispecies has information related to Common Marmoset|