Overview
Brief Summary
Biology
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Comprehensive Description
Description
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Distribution
Range Description
From his surveys carried out between 1962 and 1969, Coimbra-Filho concluded that L. rosalia was extinct in all but seven (Silva Jardim, Cabo Frio, Saquarema, Aruarama, Casimiro de Abreu, Rio Bonito, and São Pedro da Aldeia) of the 24 municipalities of its original range. The exhaustive survey by Kierulff (1993a,b; Kierulff and Procópio de Oliveira 1996; Kierulff and Rylands,2003) which covered the entire range of the species during 18 months between 1990 and 1992, showed that they remain in only 104.5 km² of forests in three regions: 1) near the coast (the Centro Hípico de Cabo Frio, with an estimated 29 individuals, and Campos Novos, with an estimated 36 individuals); 2) the Poço das Antas Biological Reserve and adjacent forests (with an estimated 360 individuals); and 3) on the hillsides of the Serra do Mar (with an estimated 74 individuals), there largely restricted to lowland forest patches. A further nine localities contained 12 isolated groups, totaling 60 individuals. These subpopulations were registered in just four of the municipalities reported by Coimbra-Filho (1969): Silva Jardim, Cabo Frio, Saquarema, and Aruarama, the latter two, however, maintaining only a single group each (Kierulff 1993a).
Burity et al. (2007) reported the occurrence of L. rosalia in the municipality of Duque de Caxias, near the Rio Taquara, in the Taquara Municipal Natural Park (19,000 ha), Rio de Janeiro, a westward extension of its current known range.
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Geographic Range
Lowland, coastal rain forest region in Southeast Brazil.
Biogeographic Regions: neotropical (Native )
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Range
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Physical Description
Morphology
Physical Description
The golden lion tamarin is between 200-366mm long (8-13in) with a tail length of between 315-400mm (12-15in). There is no sexual dimorphism. They have small, rounded heads adorned with a thick golden mane on the crown, cheeks, throat, ears and shoulders. Their bare faces are flat and have widely spaced nostrils. Their bodies are covered in long, soft silky hair with coloration ranging from pale golden to a rich reddish-gold. One interesting characteristic is that these tamarins have claws, not flattened fingernails. (Kleiman, 1981; Pearl, 1991; Sherr, 1996)
Average mass: 654.5 g.
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Ecology
Habitat
Habitat and Ecology
Marmosets and tamarins are distinguished from the other monkeys of the New World by their small size, modified claws rather than nails on all digits except the big toe, the presence of two as opposed to three molar teeth in either side of each jaw, and by the occurrence of twin births. They eat fruits, flowers, nectar, plant exudates (gums) and animal prey (including frogs, snails, lizards, spiders and insects).
Kierulff et al. (2002a) provide a comprehensive review of the behavioural ecology of the lion tamarins. They differ from other callitrichids in having long fingers and hands, which allow them to forage for prey efficiently in nooks and crannies and in epiphytic tank bromeliads. Lion tamarins live in extended family groups of usually 4 to 8 individuals. For L. rosalia, Dietz and Kleiman (1986) recorded a mean group size of 5.8 (range 3-11, n=21) at the Poço das Antas Biological Reserve. Generally, only one female per group breeds during a particular breeding season. They breed once a year. The groups defend home ranges of 40 to more than 100 ha (the size depending on availability and distribution of foods and second-growth patches). At the Poço das Antas Biological Reserve, L. rosalia groups use home ranges that average 45 ±16 ha (range 21-73 ha) (Dietz et al. 1997). At the União Biological Reserve, home ranges average 150 ±72 ha (range 65-229 ha) (Kierulff 2000).
French et al. (2002) review the reproductive biology of lion tamarins, Baker et al. (2002) review their mating system and group dynamics (focussing particularly on L. rosalia) and Tardif et al. (2002) aspects of infant care and development.
Systems
- Terrestrial
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Habitat
They reside in dense forest that is entangled with many vines and has a high density of fruit. The climate is extremely humid. They occupy the closed canopy, often remaining 10-30 meters off the ground. They sleep in tree holes for protection from predators and warmth at night. (Sherr, 1996)
Terrestrial Biomes: rainforest
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Habitat
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Trophic Strategy
Food Habits
The golden lion tamarin is omnivorous (insectivorous and frugivorous). It eats spiders, snails, small lizards, eggs, small birds, fruits and vegetables. They eat insects using their long, slender fingers to probe into crevices in the tree bark. This technique is called "micromanipulation." It is uncommon that these tamarins will share food with others outside of their family members, but among the family members, some food sharing does take place. Juveniles, for example, playfully steal food from parents or siblings. (Sherr, 1996)
Animal Foods: birds; reptiles; eggs; insects; terrestrial non-insect arthropods; mollusks
Plant Foods: leaves; fruit
Primary Diet: omnivore
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Life History and Behavior
Life Expectancy
Lifespan/Longevity
Golden lion tamarins live at least 15 years.
Average lifespan
Status: wild: 15 years.
Average lifespan
Sex: male
Status: captivity: 24.8 years.
Average lifespan
Sex: female
Status: captivity: 22.0 years.
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Lifespan, longevity, and ageing
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Reproduction
Reproduction
There is one breeding pair per group. The rearing of young is a cooperative effort by all in the group, although the majority is done by the father.
Mating System: monogamous ; cooperative breeder
Golden lion tamarins normally breed twice per year, between September and March. Females give birth to twins after a gestation of 130 to 135 days. The age of sexual maturity is 18 months for females and 24 months for males.
Breeding interval: Golden lion tamarins breed twice a year.
Breeding season: Golden lion tamarins breed between September and March, the warmest and wettest time of year.
Average number of offspring: 2.
Range gestation period: 130 to 135 days.
Average weaning age: 90 days.
Average age at sexual or reproductive maturity (female): 18 months.
Average age at sexual or reproductive maturity (male): 24 months.
Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); viviparous
Average birth mass: 55.3 g.
Average number of offspring: 2.
Average age at sexual or reproductive maturity (male)
Sex: male: 730 days.
Average age at sexual or reproductive maturity (female)
Sex: female: 547 days.
At birth, the golden lion tamarin is fully furred with eyes open. It clings to its mother for the first few weeks and nurses for a period of 90 days. At about week 5, it begins to expand its curiousity and experience things on its own. In some cases, it has been observed that a parent prefers to tend to an offspring of its own sex, but with experienced parents, it did not make a difference. (Nowack, 1997; Pearl, 1991; Sherr, 1996)
Parental Investment: precocial ; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Male, Female); pre-independence (Protecting: Male, Female); post-independence association with parents; extended period of juvenile learning
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Conservation
Conservation Status
IUCN Red List Assessment
Red List Category
Red List Criteria
Version
Year Assessed
Assessor/s
Reviewer/s
Contributor/s
Justification
History
- 2003Endangered(IUCN 2003)
- 2000Critically Endangered
- 1996Critically Endangered(Baillie and Groombridge 1996)
- 1994Endangered(Groombridge 1994)
- 1990Endangered(IUCN 1990)
- 1988Endangered(IUCN Conservation Monitoring Centre 1988)
- 1986Endangered(IUCN Conservation Monitoring Centre 1986)
- 1982Endangered(Thornback and Jenkins 1982)
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Conservation Status
The golden lion tamarin is one of the rarest of all mammals in the wild, if not the rarest. It is certainly one of the most severely endangered of all primates in the world. There are only 400 left in the world, most on or near the Reserva Biologica de Poco des Antas in Rio de Janiero. The destruction of their habitat has accounted for their loss in numbers. The trees they live in are cut down for lumber, agriculture and housing. Large treeless areas prevent their spread.
There is hope because they have been bred successfully in captivity and this is continually raising their numbers. Reintroduction into the wild has been successful.
(Sherr, 1996)
IUCN Red List of Threatened Species: endangered
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Status
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Trends
Population
Early estimates of population size ranged from 200-600 (Coimbra-Filho 1969; Coimbra-Filho and Mittermeier 1973, 1977), but it was only in 1991-1992 that a full and thorough census was carried out by Kierulff (1993a,b; Kierulff and Procópio de Oliveira 1996). Not including the population in the Poço das Antas Biological Reserve, the total number of individuals estimated was 272 in 55 groups. They were divided amongst 14 forests - four main subpopulations with six or more groups each and 12 groups isolated in 10 forest fragments each of 200 ha or less in area. The total area of forest containing Golden Lion Tamarins was 104.5 km². The majority of groups (29) were located in the municipality of Silva Jardim (53%), 24 groups were located in Cabo Frio (43%), and one group each were found in the municipalities of Saquarema and one in Araruama. At the time, the Poço das Antas Biological Reserve was known to harbor about 290 lion tamarins (Kierulff 1993a), giving a total population of 562 (range 470-631), close to the estimate of Coimbra-Filho in 1969.
During Kierulff?s (1993) census, the population of re-introduced lion tamarins was 118 individuals, but by December 2000, the number had risen to 359 (Kierulff et al. 2002a,b). A translocation programme, begun in 1994, established a new and thriving population in the União Biological Reserve, with six introduced groups resulting in a population of over 120 lion tamarins in the Reserve by mid-2001 (Kierulff et al. 2002a). The forests targeted for re-introduction are now believed to be at carrying capacity, and Kierulff and Procópio de Oliveira (1996) estimated that the União Biological Reserve (at 2,400 ha the second largest single block of lowland forest in the state, after the marginally larger Poço das Antas Biological Reserve with 2,760 ha of forest) can hold no more than about 158 lion tamarins (33 groups).
Since 1997, the numbers in the Poço das Antas Biological Reserve have been declining due to predation, and only 220 lion tamarins were recorded in December 2000 (see Franklin and Dietz 2001).
The current estimate of L. rosalia in the wild is now over 1,000. There are only very few forests available for further expansion of the population: Kierulff and Procópio de Oliveira (1996) identified a further four areas (two forest blocks, Rio Vermelho with 9 km², and the Morro de São João with 16 km², and two areas of fragmented forests, one of 16 km² along the BR101 at Gaviões and the other of 12 km² bordering the municipalities of Casimiro de Abreu and Silva Jardim) totalling 7,500 ha which could hold a further 500 lion tamarins (about 100 groups). Occupying all the habitat available, the Golden Lion Tamarin population as a whole would still remain below the minimum viable of 2,000 argued by Seal et al. (1991) and Ballou et al. (1998). Metapopulation management and reforestation are key strategies for the continued survival of this species in the wild (Kierulff 1993a; Kierulff and Procópio de Oliveira 1996).
Recorded population densities include:
Poço das Antas Biological Reserve - 12 individuals/km² or 1.96 groups/km² (Dietz et al. 1994)
Adjacent to Poço das Antas Biological Reserve - 5.1 individuals/km² or 1.17 groups/km² (Kierulff 1993a,b)
União Biological Reserve - 3.5 individuals/km² or 0.46 groups/km² (Kierulff 2000)
Campos Novos - 8.5 individuals/km² or 2.35 groups/km² (Kierulff 1993a,b).
Population Trend
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Threats
Threats
Deforestation in the state of Rio de Janeiro began in the 16th Century, with successive cycles of development supporting sugar cane plantations, coffee plantations, and in the last century particularly cattle breeding, besides persistent logging, charcoal production, and clearing for urbanization. The state is one of the most populous regions of Brazil, and today L. rosalia is limited to some few and isolated forest patches. Approximately 20% of the original range of L. rosalia is still forested, but 60% of this total is comprised of patches of 1,000 ha or less, 96% of which are less than 100 ha. The average size of the forest patches is 35 ha: smaller than the home range of a single lion tamarin group (Kierulff and Procópio de Oliveira 1996). Fires, set by cattle farmers adjacent to the remaining forest patches in the region, are a constant threat.
A study by Dietz et al. (2000) examined inbreeding depression in small (50 or less) isolated populations of L. rosalia. They concluded that it reduced probability of long-term survival by about one-third.
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Threats
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Management
Conservation Actions
The first conservation initiatives for Leontopithecus rosalia began with field surveys and initiation of a breeding programme for the species by Adelmar Coimbra-Fillho and Alceo Magnanani in the late 1960s (Coimbra-Filho and Magananini 1972; Magnanini and Coimbra-Filho 1972; Coimbra-Filho 1976a,b). Kleiman (1972) set up an international breeeding programme and studbook for the captive populations in 1972, and initiated the The Golden Lion Tamarin Conservation Program (GLTCP) of the National Zoological Park, Smithsonian Institution, in 1983. The GLTCP is still active and includes field research, reintroduction, environmental education, and habitat restoration programmes, centered on the Poço das Antas Biological Reserve, created in 1972 in Rio de Janeiro (Magnanini 1978).
Golden Lion Tamarins occur in the Poço das Antas Biological Reserve (5,500 ha, of which 2,760 ha is forested), União Biological Reserve (3,260 ha, of which 2,400 ha is forested), Bacia do Rio São João / Mico-leão-dourado Environmental Protection Area (150,700 ha), and Taquara Municipal Natural Park (19,000 ha) (Burity et al. 2007).
There is active management of the Poço das Antas and União Biological Reserves, and a stable, managed population in captivity maintained at about 490 animals. However, there is little room for expansion for the population, considering the extreme fragmentation and reduced forest cover within its range. Current and future conservation efforts are attacking this problem with reforestation and the establishment of corridors.
There is an International Committee for the Conservation and Management of lion Tamarins, set up in 1990 by the Brazilian Government (Instituto Chico Mendes de Conservação da Biodiversidade of the Ministry of the Environment) (see Rambaldi et al. 2002).
Reviews of the conservation measures and programmes in place and underway for the lion tamarins are provided by Rylands et al. (2002a), Rambaldi et al. (2002), Kierulff et al. (2002b), Beck et al. (2002), Valladares-Padua et al. (2002), Padua et al. (2002), and Kleiman and Rylands (2002b).
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Conservation
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Relevance to Humans and Ecosystems
Benefits
Economic Importance for Humans: Negative
Conservation efforts have made valuable land unavailable for human use. (Nowack, 1997; Sherr, 1996)
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Economic Importance for Humans: Positive
At one time, people captured and sold golden lion tamarins as pets. Their rapid decline in numbers has thwarted many people's desires for these exotic pets. They were also exploited in zoos and used in laboratories. (Nowack, 1997)
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Wikipedia
Golden lion tamarin
The golden lion tamarin (Leontopithecus rosalia, Brazilian Portuguese: [ˈmiku ʎiˈɐ̃w̃ dowˈɾadu], mico-leão-dourado) also known as the golden marmoset, is a small New World monkey of the family Callitrichidae. Native to the Atlantic coastal forests of Brazil, the golden lion tamarin is an endangered species with an estimated wild population of approximately 1,500 individuals spread between 3 different locations along southeastern Brazil, and a captive population maintained at approximately 490 individuals among 150 zoos.[4][3]
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Physical characteristics
The golden lion tamarin gets its name from its bright reddish orange pelage and the extra long hairs around the face ears which give it distinctive mane.[5] Its face is dark and hairless. It is believed that the tamarin gets hair color from sunlight and carotenoids in its food.[6] The golden lion tamarin is the largest of the callitrichines. It is typically around 261 mm (10.3 in) and weighs around 620 g (1.4 lb). There is almost no size difference between males and females. As with all callitrichines, the golden lion tamarin has tegulae, which are claw-like nails, instead of ungulae or flat nails found in all other primates, including humans. Tegulaes enable tamarins to cling to the sides of tree trunks. It may also move quadrupedally along the small branches, whether through walking, running, leaping or bounding.[7] This gives it a locomotion more similar to squirrels than primates.
Habitat and distribution
The golden lion tamarin has a very limited distribution range, as overtime they've lost all but 2–5% of their original habitat in Brazil.[8] Today, this tamarin is confined to three small areas of the tropical rain forest in southeastern Brazil: Poço das Antas Biological Reserve, Fazenda União Biological Reserve, private land through the Reintroduction Program.[4] The first population estimate made in 1972 approximated the count at between 400 and 500. By 1981 the population was reduced to less than 200. Surveys from as recent as 1995 suggest that there may only be at most 400 Golden Lion Tamarins left in the wild. Tamarins live along the far southeastern border of the country in the municipalities of Silva Jardim, Cabo Frio, Saquarema, and Araruama.[9] However, they have been successfully reintroduced to the municipalities of Rio das Ostras, Rio Bonito, and Casimiro de Abreu.[10] Tamarins live in coastal lowland forests less than 300 m (984 ft) above sea level.[11] They can be found in hilltop forests and swamp forests.
Behaviour and ecology
The Golden lion tamarin is for a maximum of 12 hours daily. It uses different sleeping dens each day.[12][13] By frequently moving their sleeping nests around, groups minimize the scent left behind, reducing the likelihood of predators finding them.[14] The first activities of the day are traveling and feeding on fruits. As the afternoon nears, tamarins focus more on insects. By late afternoon, they move to their night dens.[12] Tamarin groups use hollow tree cavities, dense vines or epiphytes as sleeping sites. Sites that are between 11 and 15 m (36 and 49 ft) off the ground are preferred. The golden lion tamarin tends to be active earlier and retire later in the warmer, wetter times of the years as the days are longer.[12] During drier times, it forages for insects longer as they become more scarce.[12][13]
The golden lion tamarin has a diverse, omnivorous diet consisting of fruits, flowers, nectar, bird eggs, insects and small vertebrates. They rely on microhabitats for foraging and other daily activities and tamarins will use bromeliads, palm crowns, palm leaf sheaths, woody crevices, lianas, vine tangles, tree bark, rotten logs, and leaf litters.[12][13] The golden lion tamarin uses its fingers to extract prey from crevices, under leaves, and in dense growth; a behavior known as micromanipulation.[15] It is made possible by elongated hands and fingers. Insects make up to 10–15% of its diet. Much of the rest is made of small, sweet, pulpy fruits.[12] During the rainy season, golden lion tamarin mainly eat fruit, however during drier times, it must eat more of other foods like nectar and gums.[12] Small vertebrates are also consumed more at these times as insects become less abundant.
Social structure
Golden lion tamarins are social and groups typically consist of 2-8 members.[16] These groups usually consist of one breeding adult male and female but may also have 2–3 males and one female or the reverse.[16] Other members include subadults, juveniles and infants of either sexes. These individual are typically the offspring of the adults. When there is more than one breeding adult in a group, one is usually dominant over the other and this is maintained through aggressive behavior. The dominance relationship between males and females depend on longevity in the group. A newly immigrated male is subordinate to the resident adult female who inherited her rank from her mother.[17] Both males and females may leave their natal group at the age of four, however females may replace their mothers as the breeding adult, if they die, which will lead to the dispersal of the breeding male who is likely her father.[18] This does not happen with males and their fathers. Dispersing males join groups with other males and remain in them until they find an opportunity to immigrate to a new group. The vast majority of recruits to groups are males.[18] A male may find an opportunity to enter into a group when the resident male dies or disappears. Males may also aggressively displace resident males from their group; this is usually done by two immigrant males who are likely brothers. When this happens, only one of the new males will be able to breed and will suppress the reproduction of the other.[19] A resident male may also leave a vacancy when his daughter becomes the breeding female and he must disperse to avoid inbreeding.[19] Golden lion tamarins are highly territorial and groups will defend their home range boundaries and resources from other groups.[20]
Tamarins emit "whine" and "peep" calls, which are associated with alarm and alliances respectively.[21] "Clucks" are made during foraging trips or during aggressive encounters, whether directed at conspecifics or predators.[22] "Trills" are used to communicate over long distances to give away an individual’s position. "Rasps" or "screeches" are usually associated with playful behavior. Tamarins communicate though chemicals marked throughout their territories. Reproductive males and females scent mark the most and their non-reproductive counterparts rarely do so. Dominant males use scent marking to show their social status and may suppress the reproductive abilities of the other males.
Reproduction
The mating system of the golden lion tamarin is largely monogamous. When there are two adult males in a group only one of them will mate with the female. There are cases of a male mating with two females, usually a mother and daughter.[16] Reproduction is seasonal and depends on rainfall.[23] Mating is at its highest at the end of the rainy season between late March to mid-June and births peak during the September–February rains.[23] Females are sexually mature between of 15–20 months but it isn't until they are 30 months old when they can reproduce.[22] Only dominant females can reproduce and will suppress the reproduction of the other females in the group.[24] Males may reach puberty by 28 months.[23] Tamarins have a four month gestation period. Golden lion tamarin groups exhibit cooperative rearing of the infants. It is due to the fact that tamarins commonly give birth to twins and to a lesser extent, triplets and quadruplets. A mother is not able to provide for her litter and needs the help of the other members of the group.[25] The younger members of the groups may lose breeding opportunities but they gain parental experience in helping rear their younger siblings.[17] In their first 4 weeks, the infants are completely dependent on their mother for nursing and carrying. By week five, the infant spend less time on their mother’s back and begin to explore their surroundings. Young reach their juvenile stage at 17 weeks and will socialize other group members. The subadult phase is reached at 14 months and a tamarin first displays adult behaviors.
Conservation status
Threats to the golden lion tamarin population include illegal logging, poaching, mining, urbanization and infrastructure development and the introduction of alien species. This species was first listed as endangered in 1982, rising to critically endangered in 1996.[3] The Golden Lion Tamarins are also listed under Appendix I in CITES.[26] By 2003 the successful establishment of a new population at União Biological Reserve enabled downgrading the species to endangered,[27] but the IUCN warns that extreme habitat fragmentation from deforestation means the wild population has little potential for any further expansion.[3] In an attempt to curb the golden lion tamarin's precipitous decline, several conservation programs have been undertaken. The intent is to strengthen the wild population and maintain a secure captive population in zoos worldwide. The survival rate of re-introduced animals has been encouraging, but destruction of unprotected habitat continues.
References
- ^ Groves, C. (2005). Wilson, D. E.; Reeder, D. M. eds. Mammal Species of the World (3rd ed.). Baltimore: Johns Hopkins University Press. pp. 133. OCLC 62265494. ISBN 0-801-88221-4. http://www.bucknell.edu/msw3/browse.asp?id=12100214.
- ^ Rylands AB and Mittermeier RA (2009). "The Diversity of the New World Primates (Platyrrhini)". In Garber PA, Estrada A, Bicca-Marques JC, Heymann EW, Strier KB. South American Primates: Comparative Perspectives in the Study of Bahavior, Ecology, and Conservation. Springer. pp. 23–54. ISBN 978-0-387-78704-6.
- ^ a b c d Kierulff, M.C.M., Rylands, A.B. & de Oliveira, M.M. (2008). Leontopithecus rosalia. In: IUCN 2008. IUCN Red List of Threatened Species. Downloaded on 1 March 2009.
- ^ a b national zoological park, Smithsonian. "Current Status of Golden Lion tamarin". Smithsonian National Zoological Park. http://nationalzoo.si.edu/SCBI/EndangeredSpecies/GLTProgram/InWild/CurrentStatus.cfm. Retrieved 26 March 2012.
- ^ Rowe N. (1996) The pictorial guide to the living primates. East Hampton (NY): Pogonias Pr.
- ^ Kleiman DG, Hoage RJ, Green KM. (1988) "The lion tamarins, Genus Leontopithecus". In: Mittermeier RA, Coimbra-Filho AF, da Fonseca GAB, editors. Ecology and behavior of neotropical primates, Volume 2. Washington DC: World Wildl Fund. p 299-347.
- ^ Sussman RW. (2000) Primate ecology and social structure. Volume 2, New world monkeys. Needham Heights (MA): Pearson Custom.
- ^ Wildlife Trust, Durrel Concervation. "Golden Lion Tamarin | Durrell Wildlife Concervation Trust". Durrell Wildlife Conservation Trust. http://www.durrell.org/animals/mammals/golden-lion-tamarin/. Retrieved 26 March 2012.
- ^ Kierulff MCM, Rylands AB. (2003) Census and distribution of the golden lion tamarin (Leontopithecus rosalia). Am J Primatol 59(1): 29-44.
- ^ Kierulff MCM, Rambaldi DM, Kleiman DG. (2003) "Past, present, and future of the golden lion tamarin and its habitat". In: Galindo-Leal C, de Gusmão Câmara I, editors. The Atlantic Forest of South America: biodiversity status, threats, and outlook. Washington DC: Island Pr. p 95-102.
- ^ Rylands AB, Kierulff MCM, de Souza Pinto LP. (2002). "Distribution and status of lion tamarins". In: Kleiman DG, Rylands AB, editors. Lion tamarins: biology and conservation. Washington DC: Smithsonian Inst Pr. p 42- 70.
- ^ a b c d e f g Kierulff MCM, Raboy BE, de Oliveira PP, Miller K, Passos FC, Prado F. (2002) "Behavioral ecology of lion tamarins". In: Kleiman DG, Rylands AB, editors. Lion tamarins: biology and conservation. Washington DC: Smithsonian Inst Pr.
- ^ a b c Dietz JM, Peres CA, Pinder L. (1997) "Foraging ecology and use of space in wild golden lion tamarins (Leontopithecus rosalia)". Am J Primatol 41(4): 289-305.
- ^ Facts, Monkey. "Golden Lion Tamarin". Infoqis Publishing Co.. http://www.monkeyworlds.com/golden-lion-tamarin.html. Retrieved 26 March 2012.
- ^ National Zoological Park, Smithsonian. "About Gold Lion Tamarins - National Zoo". http://nationalzoo.si.edu/SCBI/EndangeredSpecies/GLTProgram/Learn/default.cfm. Retrieved 26 March 2012.
- ^ a b c Dietz JM, Baker AJ. (1993) "Polygyny and female reproductive success in golden lion tamarins, Leontopithecus rosalia". Anim Behav 46(6): 1067-78.
- ^ a b Bales KL. (2000) Mammalian monogamy: dominance, hormones, and maternal care in wild golden lion tamarins. Ph.D dissertation, University of Maryland.
- ^ a b Baker AJ, Dietz JM. (1996) "Immigration in wild groups of golden lion tamarins (Leontopithecus rosalia)". Am J Primatol 38(1): 47-56.
- ^ a b Baker AJ, Bales K, Dietz JM. (2002) "Mating system and group dynamics in lion tamarins". In: Kleiman DG, Rylands AB, editors. Lion tamarins: biology and conservation. Washington DC: Smithsonian Inst Pr. p 188-212.
- ^ Peres CA. (2000) "Territorial defense and the ecology of group movements in small-bodied neotropical primates". In: Boinski S, Garber PA, editors. On the move: how and why animals travel in groups. Chicago: Univ Chicago Pr. p 100-23.
- ^ Ruiz-Miranda CR, Kleiman DG. (2002) "Conspicuousness and complexity: themes in lion tamarin communication". In: Kleiman DG, Rylands AB, editors. Lion tamarins: biology and conservation. Washington DC: Smithsonian Inst Pr. p 233-54.
- ^ a b Kleiman DG, Hoage RJ, Green KM. (1988) "The lion tamarins, Genus Leontopithecus". In: Mittermeier RA, Coimbra-Filho AF, da Fonseca GAB, editors. Ecology and behavior of neotropical primates, Volume 2. Washington DC: World Wildl Fund. p 299-347.
- ^ a b c French JA, de Vleeschouwer K, Bales K, Hiestermann M. (2002) "Lion tamarin reproductive biology". In: Kleiman DG, Rylands AB, editors. Lion tamarins: biology and conservation. Washington DC: Smithsonian Inst Pr.
- ^ French JA, Bales KL, Baker AJ, Dietz JM. (2003) "Endocrine monitoring of wild dominant and subordinate female Leontopithecus rosalia". Int J Primatol 24(6): 1281-1300.
- ^ Tardif SD, Santos CV, Baker AJ, Van Elsacker L, Feistner ATC, Kleiman DG, Ruiz-Miranda CR, Moura AC de A, Passos FC, Price EC et al. (2002) "Infant care in lion tamarins". In: Kleiman DG, Rylands AB, editors. Lion tamarins: biology and conservation. Washington DC: Smithsonian Inst Pr. p 213-32.
- ^ Atlanta, Zoo. "Golden Lion Tamarin". Atlanta Fulton County Zoo, Inc.. http://www.zooatlanta.org/home/animals/mammals/golden_lion_tamarin. Retrieved 26 March 2012.
- ^ Translocations of Golden Lion Tamarins – history and status as of MAY 2006
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