Overview
Brief Summary
Biology
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Comprehensive Description
Description
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Distribution
Range Description
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Geographic Range
Golden-rumped lion tamarins (Leontopithecus chrysopygus) at one time inhabited the vast tropical forest in the Central and Western portions of the state of Sao Paulo, Brazil. Now L. chrysopygus is limited to only two areas. One is the 375 square kilometer Morro do Diabo State Forest Reserve in southwesten Sao Paulo. The other is the Caiteus Reserve, a 23 square kilometer reserve in central Sao Paulo. (Beacham 1998)
Biogeographic Regions: neotropical (Native )
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Range
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Physical Description
Morphology
Physical Description
L. chrysopygus is covered almost completely in silky, dense black hair. The only place this differs is in the hind quarters. The thighs, buttocks, and base of the tail are colored a reddish-brown. This is what gives the animal its common name, golden-rumped lion tamarin. The face of L. chrysopygus is not haired, as well as the hands and feet, these are colored dark gray to black. The hind limbs are generally longer than the forelimbs and the tail is not prehensile. All digits have a pointed sickle shaped nail, which is used for gripping trees, except the big toe which has a flat nail. The dental formula is as follows, 2/2 incisors, 1/1 canines, 3/3 premolars, 2/2 molars. Body length in L. chrysopygus is between 20 cm and 33.5 cm, tail length is usually 31.5 to 40 cm, and mass ranges from 300 to 700 g. (Beacham 1998; Nowak 1999; Wolters 1990)
Range mass: 300 to 700 g.
Average mass: 572.5 g.
Range length: 20 to 33.5 cm.
Other Physical Features: endothermic ; bilateral symmetry
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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 (see Rylands 1993; Kierulff et al. 2002a).
Coimbra-Filho (1970a,b, 1976a; Coimbra-Filho and Mittermeier 1977) studied their bevaviour in the wild, and Rylands (1993) and Kierulff et al. (2002a) provide a comprehensive review of the ecology, diet and behaviour of the lion tamarins. They differ from other callithrichids 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. chyrsopygus, Carvalho and Carvalho (1989) obtained a mean group size of 3.6 (range 2-7, n=9) in the Morro do Diabo State Park. 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). In the Morro do Diabo State Park, they have been found to have ranges exceeding 100 ha (113-199 ha: Valladares-Padua 1993; Valladares-Padua and Cullen Jr. 1994). Passos (1997) recorded a home range for his study group in the Ceatetus State Ecological Station of 277 ha.
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.
Size:
Adult male 575 g (n=4) (Rosenberger and Coimbra-Filho 1984).
Systems
- Terrestrial
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Habitat
Leontopithecus chrysopygus lives primarily in semideciduous forest of Sao Paulo. But it has also been know to occupy swamp forest and macega, a forest made up of mainly small bush-like trees. In these forests, L. chrysopygus lives approximately 3 to 12 meters above the ground, rarely going to the forest floor, giving it the classification of arboreal.
Range elevation: 0 to 700 m.
Habitat Regions: tropical ; terrestrial
Terrestrial Biomes: forest ; rainforest
- Nowak, R. 1999. Walker's Mammals Of The World. Baltimore: Johns Hopkins University Press.
- Flannery, S. 2000. "Golden-rumped Lion Tamarin (Leontopithecus chrysopygus)" (On-line). Accessed November 14, 2001 at http://www.primate.wisc.edu/pin/factsheets/leontopithecus_chrysopygus.html.
- Massicot, P. 2001. "Animal Info - Golden-rumped Lion Tamarin" (On-line). Accessed November 14, 2001 at http://www.animalinfo.org/species/primate/leonchrp.htm.
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Habitat
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Trophic Strategy
Food Habits
Leontopithecus chrysopygus eats mainly insects and fruits. When they are able to catch them, L. chrysopygus will eat small lizards, small birds, bird eggs, and small vertebrates. (Massicot 2001)
Animal Foods: birds; reptiles; eggs; insects
Plant Foods: fruit
Primary Diet: omnivore
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Associations
Ecosystem Roles
Golden-rumped lion tamarins may be important as seed dispersers in the ecosystems in which they live.
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Predation
The main predators of golden-rumped lion tamarins are small cats, birds of prey, and snakes. They avoid predation by being part of a social organization, so that more individuals are alert to potential dangers and will give warning signals to other members of their troupe. (Wolters 1990)
Known Predators:
- small cats (Felidae)
- birds of prey (Falconiformes and Strigiformes)
- snakes (Serpentes)
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Known predators
Strigiformes
Serpentes
Felidae
Falconiformes
This list may not be complete but is based on published studies.
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Known prey organisms
Reptilia
Aves
This list may not be complete but is based on published studies.
- Myers, P., R. Espinosa, C. S. Parr, T. Jones, G. S. Hammond, and T. A. Dewey. 2006. The Animal Diversity Web (online). Accessed February 16, 2011 at http://animaldiversity.org. http://www.animaldiversity.org
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Life History and Behavior
Life Expectancy
Lifespan/Longevity
Leontopithecus chrysopygus in the wild will live for approximately ten years. In captivity the longest lived golden-rumped lion tamarin lived for 28 years. (Nowak 1999)
Average lifespan
Status: wild: 10 years.
Range lifespan
Status: captivity: 28 (high) years.
Average lifespan
Status: captivity: 17.9 years.
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Lifespan, longevity, and ageing
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Reproduction
Reproduction
Most cases have found L. chrysopygus to be monogamous when mating but there has been some polyandy observed in certain populations. In populations where there is more than one adult male per social group the female may mate with several males to confuse the males as to paternity of her young. This causes males to provide assistance in the care of offspring that may be their own.
Mating System: monogamous ; polyandrous
Golden-rumped lion tamarins give birth most frequently to twins, though triplets and quadruplets have been reported. In other species of lion tamarin, gestation lasts from 125 to 132 days. Lion tamarins give birth during the rainy season, usually from September through March.
Breeding season: Breeding occurs from September through March, the wet season..
Range number of offspring: 1 to 4.
Average number of offspring: 2.
Range gestation period: 125 to 132 days.
Range weaning age: 2 to 3 months.
Range age at sexual or reproductive maturity (female): 16 to 24 months.
Range age at sexual or reproductive maturity (male): 16 to 24 months.
Both male and female golden-rumped lion tamarins aid in the rearing of offspring. The young are born well-furred and with their eyes open, but are entirely dependent on adults for their care. For the first 2 to 3 weeks newborns stay primarily with the mother. After three weeks the father will carry the young for much of the day, bringing them to their mother every 2 to 3 hours for feeding. The offspring are weaned after 2 to 3 months but usually don't leave the family group until they reach sexual maturity, at 16 to 24 months. (Nowak 1999)
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
- 2003Critically Endangered(IUCN 2003)
- 2000Critically Endangered
- 1996Critically Endangered
- 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
L. chrysopygus is listed as one of the world's rarest mammals. It is estimated that only about 700 are still living in both the wild and captivity. (Massicot 2001)
US Federal List: threatened
CITES: appendix i
IUCN Red List of Threatened Species: endangered
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Status
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Trends
Population
Population Trend
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Threats
Threats
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Threats
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Management
Conservation Actions
The species is recorded from Morro do Diabo State Park (34,441 ha, of which 23,800 ha is forest), and Caetetus State Ecological Station (2,178 ha). A new (federal) Ecological Station of 5,500 ha was decreed in July 2002 – Mico-Leão-Preto Ecological Station in São Paulo. It covers three forest fragments containing Black Lion Tamarins.
The isolation and small size of the existing populations is being addressed through metapopulation management, which includes the captive population founded on individuals taken from the Morro do Diabo State Park, in the 1970s and later, in 1983-1985 as part of the rescue operation in the inundation area of the Rosana hydroelectric dam (Rylands et al. 2002a). Current efforts are focussing on the genetic health of these populations (translocation, managed dispersal and re-introduction) (Valladares-Padua et al. 2000; Valladares-Padua, Ballou et al. 2002), environmental education (Pádua and Valladares-Padua 1997; Pádua et al. 2002), the preservation of remaining forest fragments, with and without lion tamarins, and the creation of corridors to link forest patches to establish larger areas of continuous forest (Pádua and Valladares-Padua 1997; Cullen Jr. et al. 2001; Valladares-Padua et al. 2000; Valladares-Padua, Ballou et al. 2002; Valladares-Padua, Padua et al. 2002).
There is a well-managed captive breeding programme, although it has not been as successful as those for Leontopithecus rosalia and L. chrysomelas, probably because of a very reduced founder stock (Ballou et al. 2002). However, it is growing and, despite having few founders, is now also contributing significantly to the metapopulation management programme currently udnerway by Valladares-Padua and his team (Valladares-Padua and Ballou 1996; Valladares-Padua and Martins 1996; Valladares-Padua 1997; Valladares-Padua et al. 2000; Medici 2001; Valladares-Padua, Ballou et al. 2002). The first translocation of a wild L. chrysopygus group was carried out in 1995, and the first experimental re-introduction, was carried out in July 1999 by combining an adult male born in the Jersey Zoo, UK, with two wild females (Valladares-Padua et al. 2000).
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Conservation
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Relevance to Humans and Ecosystems
Benefits
Economic Importance for Humans: Negative
There are no negative effects of lion tamarins on humans.
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Economic Importance for Humans: Positive
L. chrysopygus is periodically captured and sold in Brazil as pets, though this has a negative impact on this imperiled species. The charismatic quality of lion tamarins makes them excellent candidates for ecotourism activities. (Beacham 1998)
Positive Impacts: pet trade ; ecotourism
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Wikipedia
Black lion tamarin
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The black lion tamarin (Leontopithecus chrysopygus) also known as the golden-rumped lion tamarin is a lion tamarin endemic to the Brazilian state of São Paulo, almost exclusively at the Morro do Diabo State Park. The lion tamarins are the most rare of the New World monkeys and for this reason, little is known about them.[4] This black lion tamarin was thought to be extinct 65 years until rediscovery in 1970.[5] This species is the most endangered of all the species within Leontopithecus.[5] The IUCN has the black lion tamarin listed as endangered on their red list [3] because the total number of individuals is estimated to be around 1000.[5] On the other hand there are experts who perceive this as a grave overestimate because recent studies have shown that the average range size for a black lion tamarin is closer to 106 ha rather than 66 ha that was previously estimated.[5]. The average range size for a black lion tamarin has been estimated to be 64 to 127 ha.[5] The black lion tamarin is usually found in groups ranging from 4-9 individuals. It lives in secondary and primary forests along the circumference of its home range. These forests are broken down into three distinct sections a scrub forest, a dry land forest, and a swamp.[5] The average weight of the black lion tamarin is 590 - 640 g (ARKive).
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Diet
The diet of the black lion tamarin is seasonal and varies with the different environments that the tamarin moves between.[5] For example, when the tamarin is in the dryland forest, it usually eats a variety of fruits .[5] while in a swampy environment they predominantly feed on the gum of different trees.[5] In addition to seasonal variation the black lion tamarin seems to have daily and monthly cycles of food preferences as well.[6] Independent of the environment they occupy, tamarins spend long periods each day in search for different types of insects and spiders to feed on. On average 80% of their time can be attributed to the search for insects, whether the black lion tamarin is physically digging or surveying for prey from above.[5] Therefore their diet probably contains relatively high levels of protein. The search for insects and spiders can be broken down into two parts. The first part is physically looking for insects in areas that are on the forest ground that include leaf-litter, tree roots and decomposing trees. The places that the tamarins look for these insects are very intentional. They are consistently looking under dry palm leaves, loose bark, and tree cavities for extended periods. They use their hands that have specialized fingers for this type of prying.[3] The second and main part of looking for insects is scanning from a tree. This is usually 4 meters above the forest floor. These black lion tamarins also eat the gum and fruit of trees. This has been recorded to be above the 10-meter mark. Because of the readily accessible fruits and gum, time spent looking for it was totaled to be 12.8% of their day compared to 41.2% of their day surveying high in the trees for insects and spiders.[5]
Infant survival rate and care
During the spring, summer and fall months (August to March in Brasil), the black lion tamarins are mating and having their offspring. [7] Usually they have one litter per year, yet in 20% of the population of females, there can be two litters per year.[7] While this is unusual, this has no baring on the mortality rate of the children of either litter. The mean litter size is roughly 2 infants for a female who has one litter that year. For a female that has two litters that year, she will usually have 3 or 4 offspring that year.[7]In most mammals there is a usually 50:50 ratio of males to females. However, in the black lion tamarin species there is almost always a 60:40 male to female distribution within all the litters of a given population.[7] Most of the deaths of infants within a population occur within the first two weeks after birth. The lowest survival rates of newborns were encountered in the care of a first time mother. Contrary to all conservation efforts, the number of animals that survive to adulthood in the wild is 10% higher than those that are in captivity.[7] This means that the tamarins have a better chance surviving in the wild.[7]
Food sharing
During the first few months after birth, the infant is unable to obtain food on its own. For this reason, the infant will latch onto the back of the parent and will ride them and will receive food from the parents. The first 4 to 5 weeks after birth they drink milk. After that the parents and other members of the group share food with the infants. Usually, until the age of approximately 15 weeks, the newly born infant will receive more food from others through sharing than through self-feeding. Because they feed on a large number of insects and spiders, the inexperienced tamarins rely on the older members of the group to share with them. Sharing involves both offers from the parents and begging by the infant.[8] Offers from the members of the group is highest around week 7 yet ceases at around 20 weeks after the infants' birth. After 15 weeks, there is a slow decline in sharing till about 26 weeks were food sharing was practically non-existent.[8]
Calling structure and taxonomy
Within Leontopithecus, the black lion tamarin is the largest in size and has the lowest pitched calls.[4] In addition to their lower pitch, the black lion tamarin also uses longer notes than the other species of the genus. The taxonomy of the black lion tamarin was debated because one group of taxonomists classify the lion tamarins by their geography into different species, while other taxonomists place them all into one species and then divide them into subspecies. Most recently they have agreed to focus classification predominantly on their geography. Sometimes characteristics such as long calls are analyzed to be used to classify different species, similar to birds that sing.[4] These calls of the black lion tamarin can be used to defend a territory, maintain cohesion within the group, attracting a mate, and contacting individuals who might have lost physical proximity with the group. Most calls can be recorded in the morning, and can be attributed to the reuniting of mated pairs. These mated pairs are coupled up throughout the mating season. For the sake of differentiating within the genera, a black lion tamarin’s call is one whose syllables have the greatest range from start to finish yet start lowest.[4]
Status and threats
As mentioned previously, the black lion tamarin is the most endangered of all the species within Leontopithecus. For this reason, there have been several attempts to bring the tamarins into captivity and to salvage what little home they have left within the Morro do Diabo State Park. The natural habitat of this animal has been exploited and destroyed through deforestation. This is the primary threat to the black lion tamarin.[5] For this reason the IUCN have recorded that the number of individuals within the species is declining. Another threat is from people hunting them in some of the unprotected forests that the black lion tamarin inhabits. Some of these forests include the Fazenda Rio Claro and the Fazenda Tucano.[9] In these parks there are roughly 3.66 and 1.0 individuals per square kilometer respectively.[9] Hunting could cause the black lion tamarins to become entirely endemic to the Morro do Diabo State Park. Some black lion tamarins are being taken into captivity to breed to increase the number of individuals of black lion tamarins.
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=12100213.
- ^ 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 Behavior, Ecology, and Conservation. Springer. pp. 23–54. ISBN 978-0-387-78704-6.
- ^ a b c Kierulff, M. C. M., Rylands, A. B., Mendes, S. L. & de Oliveira, M. M. (2008). Leontopithecus chrysopygus. In: IUCN 2008. IUCN Red List of Threatened Species. Downloaded on 2 January 2009.
- ^ a b c d Snowdon, Charles T., and Alexandra Hodun. "Long-Call Structure and Its Relation to Taxonomy in Lion Tamarins." American Journal of Primatology 11.253-26 (1986). Web.
- ^ a b c d e f g h i j k l Albernaz, Ana L. "Home Range Size and Habitat Use in the Black Lion Tamarin." International Journal of Primatology 18.6 (1997). Web.
- ^ Camargo Passos, Fernando De, and Alexine Keuroghlian. "Foraging Behavior and Microhabitats Used by Black Lion Tamarins, Leontopithecus Chrysopygus." Revista Brasileira De Zoologia 16.219-222 (1999). Web.
- ^ a b c d e f French, Jeferey A. "Reproduction in Captive Lion Tamarins (Leontopithecus): Seasonality, Infant Survival, and Sex Ratios." American Journal of Primatology 39.17-33 (1996). Web.
- ^ a b Feistner, Anna T.C., and Eluned C. Price. "Food Sharing in Black Lion Tamarins (Leontopithecus Chrysopygus)." American Journal of Primatology 52.47-54 (2000). Web.
- ^ a b Cullen, L., E. R. Bodmer, and C. Valladares-Padua. "Ecological Consequences of Hunting in Atlantic Forest Patches, Sao Paulo, Brazil." Oryx 35.2 (2001). Web.
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