Pygmy marmoset
TAXONOMY
Suborder: Haplorrhini Infraorder: Simiiformes Family: Cebidae Subfamily: Callitrichinae Genus: Callithrix Subgenus: Cebuella Species: C. pygmaea Subspecies: C. p. niveiventris, C. p. pygmaea Other names: Cebuella pygmaea; dwergzijdeaapje (Dutch); ouistiti mignon (French); chambira, chichico, leoncillo, micoleãozinho, or titi (Spanish); dvärgmarmosett or dvärgsilkesapa (Swedish)MORPHOLOGY

Callithrix pygmaea
RANGE
CURRENT RANGE MAPS (IUCN REDLIST): Callithrix pygmaea Found in Peru, Ecuador, Colombia, Bolivia, and Brazil, pygmy marmosets range over a large area and the subspecies are isolated by geographic barriers which include several large rivers. The northern subspecies, C. p. pygmaea, is found in the state of Amazonas, Brazil, southern Colombia, northern Bolivia, northeastern Ecuador, and eastern Peru (van Roosmalen 1997; Yépez et al. 2005). Its range is bound by the Rio Solimões and Rio Caquetá. C. p. niveiventris is found in eastern Peru and Amazonas, Brazil south of the Rio Solimões and north of the Rio Purus. It extends as far east as the Rio Madeira and is bound in the west by the Andes (van Roosmalen 1997; Groves 2001). Given their tiny body size and the type of forests in which they are found, wild pygmy marmosets have been poorly studied and there is a lack of detailed behavioral and ecological data (Soini 1982; Heymann &Soini 1999). Many short-term field studies were carried out in the late 1960s and early 1970s, but the first long-term field study of pygmy marmosets occurred in the mid-1970s to 1980s by Pekka Soini. His findings dramatically increased knowledge about pygmy marmoset social behavior and ecology (Kinzey 1997). Additionally, pygmy marmosets have been studied in captivity at the Anthropological Institutes of Zurich University in Switzerland and at the Wisconsin National Primate Research Center, adding to the knowledge of reproductive parameters, development, behavior patterns, and communication (Soini 1988).HABITAT
Pygmy marmosets occupy mature evergreen forests in and at the edges of periodically inundated river floodplains. They are habitat specialists that prefer areas with no more than two or three meters of standing water for more than three months out of the year and are found in highest densities in river-edge forests (Soini 1988). If they are found in highland areas, it is usually along small, seasonal forest streams that are subjected to frequent, minor flooding (Soini 1988). They utilize vertical strata of the forest from ground level up to 20 m (65.6 ft) and rarely venture into the highest level of the canopy. The understory is composed of reeds, tall grasses, and a few herbaceous plants, vines, shrubs, and saplings. There are also dense thickets formed by bamboo reeds, shrubs, and vines. The tallest trees in this area often have crown heights between 30 and 40 m (98.4 and 131 ft) which support hanging vines and epiphytes (Soini 1982). Data on rainfall and temperature have been reported for a study site in Peru in the Rio Maniti basin where the rainy season lasts from October to May and the dry season lasts from June to September (Soini 1982; Soini 1986). The highest amount of rain falls in March, with levels reaching more than 340 mm (1.12 ft). During the driest part of the year, only about 150 mm (5.9 in) of rain falls per month. Temperatures remain fairly constant throughout the year, hovering around 27° C (80° F) and 80% humidity (Soini 1982). In Ecuador at the Cuyabeno Faunal Production Reserve, average monthly rainfall from March to August exceeds 250 mm (9.84 in) with considerably drier periods during September through February. Average temperatures fluctuate between 22 and 29° C (71 to 84° F) with the rainy season seeing warmer temperatures (de la Torre &Snowdon 2002). Rivers begin to rise in the beginning of the dry season such that between February and June, the floodplain becomes inundated. During this time, there is an abundance of fruits, but as the floodplain dries out during the dry season, fruits also become noticeably scarce (Soini 1986).ECOLOGY
Characteristics such as elongated, sharp incisors and claw-like nails are adaptations to the very specific diet of the pygmy marmoset — gums and other exudates. They are exudativore –insectivores and spend the majority of their time gouging holes into trees or vines with their sharp lower teeth and then eating the gum, sap, resin, or latex that is exuded (Soini 1988). Holes are generally ten to 20 mm (.787 in) wide, four to 18 mm (.157 to .709 in) deep, and nearly perfectly circular. The “oldest” holes on a tree are closer to the ground and they get “newer” farther up the tree, indicating a pattern of usage (Ramirez et al. 1977). Insects make up the other important part of the diet, and grasshoppers are especially coveted. Pygmy marmosets forage in the crown foliage of trees at about five to 15 m off the ground, looking in vine-tangles and shrubby vegetation for spiders, orthopterans, butterflies, moths, beetles, and ants (Soini 1988). While 60 to 80% of their total feeding time is spent on exudates, they spend between 12 and 16% on insects, and supplement their diet with fruits, buds, flowers, nectars, and very occasionally small lizards (Soini 1988; Yépez et al. 2005).
Callihrix pygmaea
Content last modified: June 30, 2005
Written by Kristina Cawthon Lang. Reviewed by Stella de la Torre.
Cite this page as: Cawthon Lang KA. 2005 June 30. Primate Factsheets: Pygmy marmoset (Callithrix pygmaea) Taxonomy, Morphology, & Ecology . <http://pin.primate.wisc.edu/factsheets/entry/pygmy_marmoset>. Accessed 2020 July 14.
SOCIAL ORGANIZATION AND BEHAVIOR
Groups of pygmy marmosets range in size from two to nine individuals, but average group size is five. Solitarily ranging individuals of both sexes are also seen. Most troops are composed of one dominant, reproductive female, a reproductive male, and the offspring from one to four litters (Soini 1993). Groups may also contain additional adult males or females that are unrelated to the reproductive female, but neither reproduce. The reproductive female is dominant over all group members, the breeding male is dominant over all males in the group, and, among the offspring, the older siblings are dominant over the younger siblings except for dependent infants, that are not part of the dominance hierarchy (Soini 1988). Dominance can be assessed by which animals displace others at gum feeding sites; dominant animals supplant subordinate individuals.
Callithrix pygmaea
REPRODUCTION
As is seen in other cooperatively breeding species, pygmy marmoset groups generally have only one dominant breeding female while other adult and subadult females remain in the group without breeding and help raise the offspring of the dominant female (Soini 1982; 1988; Schröpel 1998). Rather than beginning to mate when they reach puberty, young pygmy marmoset females are reproductively suppressed when they remain in their natal groups (Carlson et al. 1997). In Ecuador, de la Torre et al. reported on one group that appeared to have two breeding females, but this is not generally seen (2000). There is very limited data on age of reproductive maturity, but female captive pygmy marmosets reach sexual maturity between 15 and 17 months of age and if the young female remains in her natal group, fertility is suppressed through interactions with the dominant breeding female, her mother. There is some evidence that young females exhibit ovarian cycles while living in their natal groups, but they do not reproduce as long as there is a resident dominant female (Carlson et al. 1997). If the breeding female ceases to reproduce or disappears from the group, her oldest daughter will become the next dominant female, often breeding with her father. In captivity, when more than one female gives birth, the offspring of the younger female are often victims of neglect or infanticide by other group members (Schröpel 1998). Males are thought to reach sexual maturity around 16 months (Soini 1988).
Callithrix pygmaea
PARENTAL CARE
All members of a pygmy marmoset group take some part in rearing the offspring of the dominant female. This greatly contributes to the survivability among wild pygmy marmosets which have a 67% rate of survival to the sixth month of life. Nearly 80% of total mortality in pygmy marmosets occurs within the first two months of life (Soini 1982). Infants are carried constantly for the first one to two weeks of life, but after this, a relatively unusual primate behavior is seen. Parents deposit two-week-old infants in specific, relatively protected places and leave them there for increasing longer time periods while the adults forage in the vicinity (Soini 1988; Heymann &Soini 1999). The most common places that infant pygmy marmosets are left include the crown of the group’s principal feeding tree or of another large tree in the group’s home range. This system of “baby-parking” is probably a way to decrease the cost of infant care which can include energetic costs of carrying the quickly growing infants, increased predator vigilance which distracts from feeding, and lost foraging opportunities because of decreased daily path length. Additionally, infants that are parked rather than traveling on the backs of other group members or moving around freely are less vulnerable to predation by birds of prey (Heymann & Soini 1999). When infants younger than two months are not parked in a tree, they are constantly being carried by one of the group members, with the oldest siblings (both male and female) doing a large majority of the carrying during this time (Soini 1982; 1988). From age two to five months, the infants start to move independently and are weaned by the end of the third month. Weaning begins as early as eight weeks, around the same time that infants begin to feed independently from already-gouged exudate holes. They do not begin to gouge their own feeding holes until much later in development (Soini 1988). From the age of six to 12 months, pygmy marmosets are considered juveniles and it is during this phase that the dominant female is likely to have another litter. Infant carrying in juveniles is seen starting at six months and they become completely independent feeders, gouging exudate holes and feeding from them. They enter the subadult stage from 12 to 18 months in which the only physical characteristics that differ from adults are their smaller body and genital sizes. Throughout this time of development, play behavior takes up a considerable part of the day. Pygmy marmoset infants, juveniles, and subadults either play solitarily by exploring, hanging, leaping, running, and imitating others or in groups by chasing and tumbling with others (Soini 1988). By 18 months, they are virtually indistinguishable from adults of any other age (Soini 1982).COMMUNICATION

Callithrix pygmaea
Content last modified: June 30, 2005
Written by Kristina Cawthon Lang. Reviewed by Stella de la Torre.
Cite this page as: Cawthon Lang KA. 2005 June 30. Primate Factsheets: Pygmy marmoset (Callithrix pygmaea) Behavior . <http://pin.primate.wisc.edu/factsheets/entry/pygmy_marmoset/behav>. Accessed 2020 July 14.
INTERNATIONAL STATUS
For individual primate species conservation status, please search the IUCN Red List. Also search the current scientific literature for primate conservation status (overall as well as for individual species), and visit CITES (Convention on International Trade in Endangered Species of Wild Fauna and Flora).
Callithrix pygmaea
LINKS TO MORE ABOUT CONSERVATION
CONSERVATION INFORMATION
- No current links for Callithrix pygmaea
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CONSERVATION NEWS
- Photos: researchers uncover top priority areas for Bolivian primates (Mongabay; June 28, 2010)
- Links for all species
ORGANIZATIONS INVOLVED IN Callithrix pygmaea CONSERVATION
Content last modified: June 30, 2005
Written by Kristina Cawthon Lang. Reviewed by Stella de la Torre.
Cite this page as: Cawthon Lang KA. 2005 June 30. Primate Factsheets: Pygmy marmoset (Callithrix pygmaea) Conservation . <http://pin.primate.wisc.edu/factsheets/entry/pygmy_marmoset/cons>. Accessed 2020 July 14.
REFERENCES
Carlson AA, Ziegler TE, Snowdon CT. 1997. Ovarian function of pygmy marmoset daughters (Cebuella pygmaea) in intact and motherless families. Am J Primatol 43(4): 347-55. Converse LJ, Carlson AA, Ziegler TE, Snowdon ST. 1995. Communication of ovulatory state to mates by female pygmy marmosets, Cebuella pygmaea. Anim Behav 49(3): 615-21. de la Torre S, Snowdon CT. 2002. Environmental correlates of vocal communication of wild pygmy marmosets, Cebuella pygmaea. Anim Behav 63(5): 847-56. de la Torre S, Snowdon CT, Bejarano M. 2000. Effects of human activities on wild pygmy marmosets in Ecuadorian Amazonia. Biol Cons 94(2): 153-63. de la Torre S, Yépez P. 2003. Environmental education: a teaching tool for the conservation of pygmy marmosets (Cebuella pygmaea) in the Ecuardorian Amazon. Neotrop Prim 11(2): 73-5. Groves C. 2001. Primate taxonomy. Washington DC: Smithsonian Inst Pr. 350 p. Heymann EW, Soini P. 1999. Offspring number in pygmy marmosets, Cebuella pygmaea, in relation to group size and the number of adult males. Behav Ecol Sociobiol 46(6): 400-4 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. Ramirez ML, Freese CH, Revilla C J. 1977. Feeding ecology of the pygmy marmoset, Cebuella pygmaea, in northeastern Peru. In: Kleiman DG, editor. The biology and conservation of the Callitrichidae; 1975 Aug 18-20; Washington DC. Washington DC: Smithsonian Inst Pr. p 91-104. Rowe N. 1996. The pictorial guide to the living primates. East Hampton (NY): Pogonias Pr. 263 p. Schröpel M. 1998. Multiple simultaneous breeding females in a pygmy marmoset group (Cebuella pygmaea). Neotrop Prim 6(1): 1-7. Snowdon CT, de la Torre S. 2002. Multiple environmental contexts and communication in pygmy marmosets (Cebuella pygmaea). J Comp Psych 116(2): 182-8. Soini P. 1982. Ecology and population dynamics of the pygmy marmoset, Cebuella pygmaea. Folia Primatol 39: 1-21. Soini P. 1986. A synecological study of a primate community in the Pcaya-Samiria National Reserve, Peru. Prim Cons 7: 63-71. Soini P. 1988. The pygmy marmoset, Genus Cebuella. In: Mittermeier RA, Coimbra-Filho AF, da Fonseca GAB, editors. Ecology and behavior of neotropical primates, Volume 2. Washington DC: World Wildly Fund. p 79-129. Soini P. 1993. The ecology of the pygmy marmoset, Cebuella pygmaea: some comparisons with two sympatric tamarins. In: Rylands AB, editor. Marmosets and tamarins: systematics, behaviour, and ecology. Oxford (UK): Oxford Univ Pr. p 257-61. Sussman RW. 2000. Primate ecology and social structure. Volume 2, New world monkeys. Needham Heights (MA): Pearson Custom. 207 p. van Roosmalen MGM. 1997. An eastern extension of the geographical range of the pygmy marmoset, Cebuella pygmaea. Neotrop Prim 5(1): 3-5. Yépez P, de la Torre S, Snowdon CT. 2005. Interpopulation differences in exudates feeding of pygmy marmosets in Ecuadorian Amazonia. Am J Primatol 66(2): 145-58. Ziegler TE, Snowdon CT, Bridson WE. 1990. Reproductive performance and excretion of urinary estrogens and gonadotropins in the female pygmy marmoset (Cebuella pygmaea). Am J Primatol 22(3): 191-203.Content last modified: June 30, 2005
IMAGES
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Callithrix pygmaea Photo: Alba Lucia Morales Jiménez |
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Callithrix pygmaea Photo: Alba Lucia Morales Jiménez |
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Callithrix pygmaea Photo: Allen M. Aisenstein |
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Callithrix pygmaea Photo: Anne Savage |
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Callithrix pygmaea Photo: Anne Savage |
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Callithrix pygmaea Photo: K. Fink |
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Callithrix pygmaea Photo: Luiz Claudio Marigo |
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Callithrix pygmaea Photo: Luiz Claudio Marigo |
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Callithrix pygmaea Photo: Luiz Claudio Marigo |
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Callithrix pygmaea Photo: P. Yépez |
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Callithrix pygmaea Photo: P. Yépez |
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Callithrix pygmaea Photo: P. Yépez |
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Callithrix pygmaea Photo: Verena Behringer |
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