Cream-coloured giant squirrels are arboreal. They spend their lives in the treetops of tropical forests and only go to ground level to reach trees that are not accessible from the canopy, or to escape predators. These animals are often observed residing within the middle of the tree canopy in lowland and hill forests with tall trees, they are not often found in agricultural areas. Southeast Asia, the habitat region of cream-coloured giant squirrels, is covered in tropical rainforests with a variety of plant life including shrubs, flowering plants, a wide variety of dipterocarps and other fruiting plants, like strangler figs. These regions have typical wet and dry seasons. (Aparajita and Goyal, 1996; Francis, 2008; MacKinnon, 1996; Meijaard and Sheil, 2008; Saiful and Nordin, 2004)
The world’s largest tree squirrels are included in genus Ratufa. Cream-coloured giant squirrels share a similar appearance and shape to other squirrel species, but differ in their size and coloration. Their weight ranges from 929 to 1,575 g and their head and body length is 322 to 350 mm, not including their tail. Their tails, which hang vertically when they are seated and extends horizontally while they are running, are longer than their bodies, ranging from 373 to 438 mm, giving them an overall length of more than 610 mm. Their coloration varies by location. Historically, 37 subspecies of cream-coloured giant squirrels have been described; however, 9 geographically and physically distinct subspecies are currently recognized. In general, these animals have orange to brown dorsal pelage and buffy to white ventral pelage, with a black tail, white cheeks and a thin black moustache. However, in Borneo and northern regions, these animals tend to be darker as compared to their paler counterparts found in the southern portions of their range. (Francis, 2008; Hayssen, 2008; Ng, et al., 2011; "Giant Squirrel (Ratufa Affinis)", 2013)
At present, very little is known about the mating systems of cream-coloured giant squirrels. The only studies presently available are in reference to captive individuals from closely related black giant squirrels (Ratufa bicolor). Newly introduced captive mates often begin building twig nests shortly after being housed together. Wild born captive pairs displayed distinct mating behaviors such as scent marking, chasing and grooming. Males inspect the female’s genitals before engaging in pre-copulatory chases after which, the males attempt to mount, if permitted, mating lasts about 1 to 3 seconds. The specific mating systems of this species are not known, however, most squirrel species engage in a polygynous mating system, although some species engage in a polygynandrous system as well. (Paulraj, 1988; Sherman and Wauters, 2001; Willis, 1980)
The gestation length of cream-coloured giant squirrels has not been reported, however, there appears to be a large variation in the gestation period of genus Ratufa. Grizzled giant squirrels (Ratufa macroura) have a reported 28-day gestation period, Black giant squirrels (Ratufa bicolor) have a 32-day gestation period and Indian giant squirrels (Ratufa indica) have a staggering 84-day gestation period. The lactation period for black giant squirrels has been reported at 35 days versus the 63-day period reported for grizzled giant squirrels. Cream-coloured giant squirrels have been noted to have litters that include 3 offspring. Captive black giant squirrels weigh between 75 and 77 grams at birth and first emerge from their nest 33 days after birth. In general, this genus has short gestation and lactation rates, relative to their size. Members of this genus typically only produce 2 litters per year, although they may be reproductively active throughout the year. (Hayssen, 2008; Tacutu, et al., 2013; Willis, 1980)
At this time, little information is known regarding the parental investment of cream-coloured giant squirrels. Both sexes participate in the construction of a large, round twig nest in the canopy, where young are born and raised. These nests are very large, similar in size to eagle aeries. In captivity, female black giant squirrels (Ratufa bicolor) wash, defend, move their young and repair and improve their nest. Due to their short gestation and lactation lengths, as well as their potentially year-round breeding, these animals have been described as using minimal but constant effort for breeding. (Francis, 2008; Hayssen, 2008; Paulraj, 1988; "Giant Squirrel (Ratufa Affinis)", 2013)
At this time, there is no data regarding the lifespan of cream-coloured giant squirrels. However, the maximum captive lifespan has been estimated for other members of their genus. Indian giant squirrels (Ratufa indica) may live up to 20 years in captivity and black giant squirrels (Ratufa bicolor) may live up to 19 years. (Tacutu, et al., 2013)
Cream-coloured giant squirrels are solitary. Social interaction usually only occurs during mating season, during which time, they are seen only in pairs. They are arboreal and spend the vast majority of their time in the forest canopy, using the dense foliage as protection from predators. When threatened they bristle their fur and make loud calls. These animals are diurnal; they are active after dawn and return to their nests before dusk. Their nests usually have a globular shape and are found in the crown of tall trees. (Becker, et al., 1985; Francis, 2008; McConkey and Chivers, 2004)
The home range size of cream-coloured giant squirrels has not been reported, however, there are typically 11 individuals found per km2. (MacKinnon, 1996)
In general, squirrels mark their territory by scratching and removing bark from tree branches and marking these areas with urine. Both male and female cream-coloured giant squirrels have been noted scent marking by dragging their anogenital region across territory areas. During territorial scent marking, the animals release a very small amount of urine, as opposed to the scent marking performed by females in estrus, which involves a larger release of urine. Cream-coloured giant squirrels produce a variety of vocalizations including a staccato mating call, harsh chatter, which can be heard for several meters and is likely used territorially and a much softer “hgip…hgip” call, whose function is unknown. (Francis, 2008; Gurnell, 1987; Paulraj, 1988)
Cream-coloured giant squirrels find the majority of their food in tree tops, where they spend most of their time. These animals primarily consume plant parts such as leaves, fruit, bark and seeds; however, they also consume insects. Dipterocarp seeds play a larger role in their diet during periods of mast fruiting, when large amounts of seeds are produced and deposited. While eating, cream-coloured giant squirrels allow their tail to hang down, using it as a counterbalance, this leaves their hands free for manipulating food. (Curran and Leighton, 2000; Nakagawa, et al., 2005; "Giant Squirrel (Ratufa Affinis)", 2013; Saiful and Nordin, 2004)
Cream-coloured giant squirrels face predation from a variety of predators including cats, snakes, raptors and humans. Because they are arboreal, their main threats are birds, such as crested serpent eagles (Spilornis cheela). Their defense behaviors include bristling their fur and darting for cover, while calling loudly. Indigenous people often use the squirrel as a food source, hunting with shotguns and blowpipes. (Becker, et al., 1985)
Cream-coloured giant squirrels are a food source for larger predators, such as birds of prey. Their role in the seed dispersal of mast-fruiting trees like dipterocarps has been studied, however, fruit is not their preferred food source and is only consumed when other food is lacking. (Curran and Leighton, 2000)
Although human use of this species appears to be limited, cream-colored giant squirrels are hunted and eaten by native people. (Becker, et al., 1985)
There are no known negative impacts of this species on human populations.
Currently, cream-coloured giant squirrels are classified as ‘near threatened’ by the IUCN, with a decreasing trend in the global population. The largest factor behind these population declines appears to be loss of habitat throughout their range due to human related activities. Studies of protected forest sites in Borneo show that areas under protection show a higher rate of forest loss than those outside of the boundary. Removal of large trees is especially detrimental, as they are used by this species for nesting and feeding. (Duckworth, et al., 2008; Meijaard and Sheil, 2008)
Jessica Branson (author), Northern Michigan University, Leila Siciliano Martina (author), Animal Diversity Web Staff, John Bruggink (editor), Northern Michigan University.
uses sound to communicate
Referring to an animal that lives in trees; tree-climbing.
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
uses smells or other chemicals to communicate
animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.
parental care is carried out by females
A substance that provides both nutrients and energy to a living thing.
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
having the capacity to move from one place to another.
the area in which the animal is naturally found, the region in which it is endemic.
an animal that mainly eats all kinds of things, including plants and animals
found in the oriental region of the world. In other words, India and southeast Asia.
rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.
communicates by producing scents from special gland(s) and placing them on a surface whether others can smell or taste them
offspring are all produced in a single group (litter, clutch, etc.), after which the parent usually dies. Semelparous organisms often only live through a single season/year (or other periodic change in conditions) but may live for many seasons. In both cases reproduction occurs as a single investment of energy in offspring, with no future chance for investment in reproduction.
reproduction that includes combining the genetic contribution of two individuals, a male and a female
uses touch to communicate
Living on the ground.
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
uses sight to communicate
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
breeding takes place throughout the year
Royal Society SEARRP. 2013. "Giant Squirrel (Ratufa Affinis)" (On-line). Stability of Altered Forest Ecosystems. Accessed February 18, 2013 at http://www.safeproject.net/animal-sightings/giant-squirrel-ratufa-affinis/.
Aparajita, D., S. Goyal. 1996. Comparison of Forest Structure and Use by the Indian Giant Squirrel (Ratufa indica) in Two Riverine Forests of Central India. Biotropica, 28: 394-399.
Becker, P., M. Leighton, J. Payne. 1985. Why Tropical Squirrels Carry Seeds Out of Source Crowns. Journal of Tropical Ecology, 1: 183-186.
Curran, L., M. Leighton. 2000. Vertebrate Responses to Spatiotemporal Variation in Seed Production of Mast-Fruiting Dipterocarpaceae. Ecological Society of America, 70: 101-128.
Duckworth, J., E. Meijaard, B. Giman, K. Han. 2008. "Ratufa affinis" (On-line). IUCN Red List of Threatened Species. Accessed April 01, 2013 at http://www.iucnredlist.org/details/19376/0.
Francis, C. 2008. A Field Guide to the Mammals of South-East Asia. London: New Holland Publishers.
Gurnell, J. 1987. The Natural History of Squirrels. New York, New York: Facts on File, Inc.
Hayssen, V. 2008. Reproductive effort in squirrels: Ecological, phylogenetic, allometric, and latitudinal patterns. Journal of Mammology, 89:3: 582-606.
MacKinnon, K. 1996. The Ecology of Kalimantan: Indonesian Borneo. United Kingdom: Oxford University Press.
McConkey, K., D. Chivers. 2004. Low mammal and hornbill abundance in the forests of Barito Ulu, Central Kalimantan, Indonesia. Oryx, 38: 439-447.
Meijaard, E., D. Sheil. 2008. The persistence and conservation of Borneo's mammals in lowland rain forests managed for timber: observations, overviews and opportunities. Ecological Restoration, 23: 21-34.
Nakagawa, M., Y. Takeuchi, T. Kenta, T. Nakashizuka. 2005. Predispersal Seed Predation by Insects vs. Vertebrates In Six Dipterocarp Species in Sarawak, Malaysia. Biotropica, 37: 389-396.
Ng, P., R. Corlett, H. Tan. 2011. Singapore Biodiversity: An Encyclopedia of the Natural Environment and Sustainable Development. Singapore: Editions Didier Millet.
Paulraj, S. 1988. Breeding behaviour of the Malay giant squirrel Ratufa bicolor at Arignar Anna Zoological Park. International Zoo Yearbook, 27: 279-282.
Saiful, A., M. Nordin. 2004. Diversity and Density of Diurnal Squirrels in a Primary Hill Dipterocarp Forest, Malaysia. Journal of Tropical Ecology, 20: 45-49.
Sherman, P., L. Wauters. 2001. Squirrels. Pp. 598-608 in D MacDonald, S Norris, eds. The Encyclopedia of Mammals, Vol. 1. London: The Brown Reference Group.
Tacutu, R., T. Craig, A. Budovsky, D. Wuttke, G. Lehmann, D. Taranukha, J. Costa, V. Fraifeld, J. de Magalhaes. 2013. "An Age: The Animal Aging and Longevity Database" (On-line). Human Aging Genomics Resources: Integrated databases and Tools for the Biology and Genetics of Aging. Accessed September 22, 2013 at http://genomics.senescence.info/species/.
Willis, R. 1980. Breeding the Malayan giant squirrel Ratufa bicolor at London Zoo. International Zoo Yearbook, 20:1: 218-220.