The sugar glider (Petaurus breviceps) is a small, omnivorous, arboreal, and nocturnal gliding possum. The common name refers to its predilection for sugary foods such as sap and nectar and its ability to glide through the air, much like a flying squirrel. They have very similar habits and appearance to the flying squirrel, despite not being closely related—an example of convergent evolution. The scientific name, Petaurus breviceps, translates from Latin as "short-headed rope-dancer", a reference to their canopy acrobatics.
The sugar glider is characterised by its pair of gliding membranes, known as patagia, which extend from its forelegs to its hindlegs. Gliding serves as an efficient means of reaching food and evading predators. The animal is covered in soft, pale grey to light brown fur which is countershaded, being lighter in colour on its underside.
The sugar glider, as strictly defined in a recent analysis, is only native to a small portion of southeastern Australia, corresponding to southern Queensland and most of New South Wales east of the Great Dividing Range; the extended species group, including populations which may or may not belong to P. breviceps, occupies a larger range covering much of coastal eastern and northern Australia, New Guinea, and nearby islands. Members of Petaurus are popular exotic pets.
Taxonomy and evolution The genus Petaurus is believed to have originated in New Guinea during the mid Miocene epoch, approximately 18 to 24 million years ago. The modern Australian Petaurus, along with New Guinean members of what were formerly considered P. breviceps, diverged from their closest living New Guinean relatives ~9-12 mya. They probably dispersed from New Guinea to Australia between 4.8 and ~8.4 mya, with the oldest Petaurus fossils in Australia being dated to 4.46 million years. This may have been possible due to sea level lowering from about 7 to 10 mya, resulting in land bridges between New Guinea and Australia.
The taxonomy of the species is complex, and is still not fully resolved. It was formerly understood to have a wide range across Australia and New Guinea, being the only glider to have this distribution, and to be divided into seven subspecies, with three occurring in Australia and four in New Guinea. This traditional subspecific division was based on small morphological differences, such as colour and body size. However, a 2010 genetic analysis using mitochondrial DNA indicates that these morphologically defined subspecies may not represent genetically unique populations.
Further studies have found significant genetic variation within populations traditionally classified in P. breviceps, sufficient to warrant splitting the species into multiple. The subspecies P. b. biacensis, from Biak Island off of New Guinea, was reclassified as a separate species, the Biak glider (Petaurus biacensis). In 2020, a landmark study suggested that P. breviceps actually comprised three cryptic species: the Krefft's glider (Petaurus notatus), found throughout most of eastern Australia and introduced to Tasmania, the savanna glider (Petaurus ariel), native to northern Australia, and a more narrowly defined P. breviceps, restricted to a small section of coastal forest in southern Queensland and most of New South Wales. In addition, other sugar glider populations throughout this range (such as those on New Guinea and the Cape York Peninsula) may represent undescribed species or be conspecific with previously described species. This indicates that contrary to previous findings of a large range (which in fact applied to P. notatus and, to a lesser extent, to P. ariel), P. breviceps is a range-restricted species that is sensitive to ecological disasters, such as the 2019-20 Australian bushfires, which significantly affected large portions of its habitat.
P. breviceps and P. notatus are estimated to have diverged ~1 million years ago, and may have originated from long term geographic isolation. The early-mid Pleistocene saw an uplifting of the Great Dividing Range, contributing to and coinciding with aridification of the interior of Australia, including on the western side of the range. This, as well as other climactic and geographic factors, may have isolated the ancestors of P. breviceps to refugia on the eastern, coastal side of the Great Dividing Range. This would be an example of allopatric speciation.
Distribution and habitat Sugar gliders are distributed in the coastal forests of southeastern Queensland and most of New South Wales. Their distribution extends to altitudes of 2000m in the eastern ranges. In parts of its range, it may overlap with Krefft's glider (P. notatus).
The sugar glider occurs in sympatry with the squirrel glider and yellow-bellied glider; and their coexistence is permitted through niche partitioning where each species has different patterns of resource use.
Like all arboreal, nocturnal marsupials, sugar gliders are active at night, and they shelter during the day in tree hollows lined with leafy twigs.
The average home range of sugar gliders is , and is largely related to the abundance of food sources; density ranges from two to six individuals per hectare (0.8–2.4 per acre).
Native owls (Ninox sp.) are their primary predators; others in their range include kookaburras, goannas, snakes, and quolls. Feral cats (Felis catus) also represent a significant threat.
Appearance and anatomy
The sugar glider has a squirrel-like body with a long, partially (weakly) prehensile tail. The length from the nose to the tip of the tail is about , and males and females weigh respectively. Heart rate range is 200–300 beats per minute, and respiratory rate is 16–40 breaths per minute. The sugar glider is a sexually dimorphic species, with males typically larger than females. Sexual dimorphism has likely evolved due to increased mate competition arising through social group structure; and is more pronounced in regions of higher latitude, where mate competition is greater due to increased food availability.
The fur coat on the sugar glider is thick, soft, and is usually blue-grey; although some have been known to be yellow, tan or (rarely) albino. A black stripe is seen from its nose to midway on its back. Its belly, throat, and chest are cream in colour. Males have four scent glands, located on the forehead, chest, and two paracloacal (associated with, but not part of the cloaca, which is the common opening for the intestinal, urinal and genital tracts) that are used for marking of group members and territory. Scent glands on the head and chest of males appear as bald spots. Females also have a paracloacal scent gland and a scent gland in the pouch, but do not have scent glands on the chest or forehead.
The sugar glider is nocturnal; its large eyes help it to see at night and its ears swivel to help locate prey in the dark. The eyes are set far apart, allowing more precise triangulation from launching to landing locations while gliding. Sugar gliders have demonstrated trichromacy in behavioral testing with sensitivity in the ultraviolet/blue, green, and red ranges. Ultraviolet sensitivity is corroborated by genetic evidence. The physiological source of their middle wavelength sensitivity is not yet confirmed.
Each foot on the sugar glider has five digits, with an opposable toe on each hind foot. These opposable toes are clawless, and bend such that they can touch all the other digits, like a human thumb, allowing it to firmly grasp branches. The second and third digits of the hind foot are partially syndactylous (fused together), forming a grooming comb. The fourth digit of the forefoot is sharp and elongated, aiding in extraction of insects under the bark of trees.
The gliding membrane extends from the outside of the fifth digit of each forefoot to the first digit of each hind foot. When the legs are stretched out, this membrane allows the sugar glider to glide a considerable distance. The membrane is supported by well developed tibiocarpalis, humerodorsalis and tibioabdominalis muscles, and its movement is controlled by these supporting muscles in conjunction with trunk, limb and tail movement.
Lifespan in the wild is up to 9 years; is typically up to 12 years in captivity, and the maximum reported lifespan is 17.8 years.
Biology and behaviour
Gliding The sugar glider is one of a number of volplane (gliding) possums in Australia. It glides with the fore- and hind-limbs extended at right angles to the body, with feet flexed upwards. The animal launches itself from a tree, spreading its limbs to expose the gliding membranes. This creates an aerofoil enabling it to glide or more. For every travelled horizontally when gliding, it falls . Steering is controlled by moving limbs and adjusting the tension of the gliding membrane; for example, to turn left, the left forearm is lowered below the right.
This form of arboreal locomotion is typically used to travel from tree to tree; the species rarely descends to the ground. Gliding provides three dimensional avoidance of arboreal predators, and minimal contact with ground dwelling predators; as well as possible benefits in decreasing time and energy consumption spent foraging for nutrient poor foods that are irregularly distributed. Young carried in the pouch of females are protected from landing forces by the septum that separates them within the pouch.
Torpor Sugar gliders can tolerate ambient air temperatures of up to through behavioural strategies such as licking their coat and exposing the wet area, as well as drinking small quantities of water. In cold weather, sugar gliders will huddle together to avoid heat loss, and will enter torpor to conserve energy. Huddling as an energy conserving mechanism is not as efficient as torpor. Before entering torpor, a sugar glider will reduce activity and body temperature normally in order to lower energy expenditure and avoid torpor. With energetic constraints, the sugar glider will enter into daily torpor for 2–23 hours while in rest phase. Torpor differs from hibernation in that torpor is usually a short-term daily cycle. Entering torpor saves energy for the animal by allowing its body temperature to fall to a minimum of to . When food is scarce, as in winter, heat production is lowered in order to reduce energy expenditure. With low energy and heat production, it is important for the sugar glider to peak its body mass by fat content in the autumn (May/June) in order to survive the following cold season. In the wild, sugar gliders enter into daily torpor more often than sugar gliders in captivity. The use of torpor is most frequent during winter, likely in response to low ambient temperature, rainfall, and seasonal fluctuation in food sources.
Diet and nutrition
Sugar gliders are seasonally adaptive omnivores with a wide variety of foods in their diet, and mainly forage in the lower layers of the forest canopy. Sugar gliders may obtain up to half their daily water intake through drinking rainwater, with the remainder obtained through water held in its food. In summer they are primarily insectivorous, and in the winter when insects (and other arthropods) are scarce, they are mostly exudativorous (feeding on acacia gum, eucalyptus sap, manna, honeydew or lerp). Sugar gliders have an enlarged caecum to assist in digestion of complex carbohydrates obtained from gum and sap.
To obtain sap or gum from plants, sugar gliders will strip the bark off trees or open bore holes with their teeth to access stored liquid. Little time is spent foraging for insects, as it is an energetically expensive process, and sugar gliders will wait until insects fly into their habitat, or stop to feed on flowers. Gliders consume approximately 11 g of dry food matter per day. This equates to roughly 8% and 9.5% of body weight for males and females, respectively.