Overview

Distribution

Range Description

This species generally ranges through much of continental and insular Southeast Asia. On the mainland, it has been reported from southern Myanmar, southern Viet Nam (possibly southern Cambodia), through much of Peninsular Malaysia to Singapore. The species is found over much of Indonesia, being recorded from the islands of Sumatra, Bangka, the Mentawi Islands (Sipura, North Pagai and South Pagai), the Krakatau Islands, Java, Bali, Lombok, Sumbawa, Sumba, Savu, the Anamba Islands, the Natuna Islands (Bunguran Besar) and Siantan. It is present on the island of Timor (East Timor and Indonesia), and on Borneo (Brunei, Indonesia and Malaysia). The species is present throughout the Philippines, except for the Batanes/Babuyan region. There are records from the Philippines islands of Bohol, Bongao, Boracay, Cabo, Catanduanes, Culion, Leyte, Guimaras, Luzon (Abra, Cagayan, Ilocos Norte, Isabela, La Union, Quezon [Paguntalan pers. comm. 2006], Tarlac provinces), Marinduque, Mindanao (Agusan del Norte, Bukidnon, Cotabato, Davao del Norte, Davao del Sur, Davao Oriental, Lanao del Norte, Lanao del Sur, Maguindanao, Misamis Occidental, Misamis Oriental, North Cotabato, South Cotabato, Zamboanga del Norte, and Zamboanga del Sur provinces and Bongo Island), Mindoro, Negros, Palawan, Panay, Polillo (Alviola 2000), Tantangan, Dinagat (Gunther 1879) and Romblon (Timm and Birney 1980). In the Philippines it has been recorded from sea level to around 1,250 m asl. Outside of Southeast Asia, there is a report from Shaanxi in China (Smith and Xie 2008), and the species has been reported to be present in the Andaman and Nicobar Islands. However, as there are no voucher based records of this species from the Andaman and Nicobar Islands, and its presence within India is doubtful and it is not mapped here (C. Srinivasulu and Sanjay Molur pers. comm. 9 September 2007).
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Geographic Range

Pteropus vampyrus is found from Madagascar to Australia and in mainland Asia and Indonesia. It occurs in most of continental and insular Southeast Asia; from southern Myanmar and southern Vietnam through Malaysia to Singapore. It is present throughout most of Indonesia. This species is also found in southern Burma and southern Thailand and extends to the east Philippines, Sumatra, and Timor. Pteropus vampyrus is native to China, Indonesia, Malaysia, Myanmar, the Philippines, Singapore, Thailand, Timor-Leste, and Vietnam.

Biogeographic Regions: oriental (Native )

  • Wildscreen 2003-2011. 2011. "ARKive Images of Life on Earth" (On-line). Large flying fox (Pteropus vampyrus). Accessed March 30, 2011 at http://www.arkive.org/large-flying-fox/pteropus-vampyrus/#text=Facts.
  • Bates, P., C. Francis, M. Gumal. 2011. "The IUNC Red List of Threatened Species" (On-line). Pteropus vampyrus. Accessed March 30, 2011 at http://www.iucnredlist.org/apps/redlist/details/18766/0.
  • Kunz, T., D. Jones. 2000. Pteropus vampryrus. Mammalian Species, No. 642: 1-6. Accessed March 30, 2011 at http://www.science.smith.edu/departments/Biology/VHAYSSEN/msi/.
  • Tampa's Lowry Park Zoo, 2010. "Wallaroo Station Animal Fact Sheet" (On-line). Flying Fox Bat. Accessed April 15, 2011 at http://www.lowryparkzoo.com/bio_wallaroo_flying_fox.php.
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Physical Description

Morphology

Physical Description

Pteropus vampyrus is one of the largest bats in the world. Forearm length ranges from 180 to 220 mm, mean wingspan is 1.5 m, and body mas ranges from 0.6 to 1.1 kg. It has long pointed ears and a dog-like or fox-like face and head. Pelage varies in color and texture with age and sex . Upper dorsal fur is short and stiff, with longer, woolier fur on the venter. Head and upper body are covered with a dark mantle ranging in color from mahogany-red to black, and the venter is often darker than the rest of the body. Its wings have short rounded tips. Except for parts close to the body and the edge of the wing membrane, wing membranes lack fur. Young are born with dark skin and fur but become paler as they develop. Males have thicker and stiffer pelage than females and glandular neck tufts with dark bases. Pteropus vampyrus is different from most Pteropus in that it has darker underparts and a dark mantle. For example, P. giganteus and P. lylei have pale underparts that contrast with the darker dorsal pelage. Pelage color occasionally varies as a few P. vampyrus specimens have lighter mantles, and some have a gray or silver venter.

Large flying foxes have robust skulls, with a nearly complete orbit and a thick, wide zygomatic arch. The postorbital processes reaches more than halfway to the zygomatic arch. The dental formula is 2/2, 1/1, 3/3, 2/3 for a total of 34 teeth. Upper canines have a prominent anterior groove and a smaller groove on the inner surface.

Range mass: 0.6 to 1.1 kg.

Average wingspan: 1.5 m.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: male larger; sexes colored or patterned differently

  • Hollister, N. 1913. A Review of the Philippine Land mammals in the United States National Museum. Washington: Washington Government Printing Office.
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Type Information

Type for Pteropus vampyrus
Collection: Smithsonian Institution, National Museum of Natural History, Department of Vertebrate Zoology, Division of Mammals
Sex/Stage: Male;
Preparation: Skin; Skull
Collector(s): E. Mearns
Year Collected: 1903
Locality: Pantar, Near Lake Lanao, Mindanao, Lanao Del Sur Province, Philippines, Asia
Elevation (m): 581
  • Type: Mearns, E. A. 1905 May 13. Proc. U.S. Nat. Mus. 28: 432.
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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
This tree roosting species is tolerant to some habitat disturbance; it occurs in primary, and secondary forest and uses adjacent agricultural areas for feeding (Rabor 1955; Rabor 1986; Rickart et al. 1993; Sanborn 1953). A study of the species habitat in the Subic Bay area, Luzon, indicated that the species preferred natural forest to disturbed or agricultural areas (T. Mildenstein pers. comm. 2006).

Systems
  • Terrestrial
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Habitat

Large flying foxes inhabit tropical forests and swamps. They occur primarily in secondary forests and use agricultural areas during forging bouts. Populations also occur on oceanic islands. During the day, groups often roost in large trees. Roost sites are often used for many years and trees become stripped of bark and foliage by the bats' sharp claws. Roosting trees are often found in mangrove forests, coconut groves, and mixed fruit orchards. Studies in Subic Bay, Philippines have shown that foraging locations range between 0.4 and 12 km from the roost. They prefer undisturbed forests in lowlands, beaches, and mangroves, for roosting and select against disturbed and agricultural areas. Large flying foxes are commonly found in riparian areas.

Habitat Regions: tropical ; terrestrial

Terrestrial Biomes: forest ; rainforest

Wetlands: swamp

Other Habitat Features: agricultural ; riparian

  • Mildenstein, T., S. Stier, C. Nuevo-Diego, S. Mills. 2005. Habitat selection of endangered and endemic large flying-foxes in Subic Bay, Phillipines. Biological Conservation, 126: 93-102.
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Trophic Strategy

Food Habits

Large flying foxes feed on flowers, nectar, and fruit such as bananas and mangos. Common foods also include the pollen and flowers of coconut, durian, and fig trees. When foraging, they slice the rind with their teeth and extract the fruit with their long tongue, which is also used for lapping up nectar. They can carry up to 200 g of food at a time. On a daily basis, large flying foxes can eat half of their body weight in fruit.

Plant Foods: leaves; fruit; nectar; pollen; flowers

Primary Diet: herbivore (Frugivore )

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Associations

Ecosystem Roles

Flying foxes are important frugivores in tropical forests. They serve as seed dispersers and pollinators of forest trees, including durian, which produce a high-priced fruit that is considered a delicacy in southeast Asia. Members of the genus Pteropus are often the only seed dispersers or pollinators large enough to carry the large fruit they feed upon. They also pollinate canopy trees when searching for nectar. Seed dispersal by large flying foxes is thought to play an important role in the regeneration of cleared forests. They are host to the parasitic nematode Litmosa maki, which inhabits the abdominal cavity. In malaysia, ectoparasites from the families Laelapidae, Nycteribiidae, and Spinturnicidae have also been reported.

Ecosystem Impact: disperses seeds; pollinates

Commensal/Parasitic Species:

  • Brown, M. 1997. Durio - A Bibliographic View. New Delhi, India: International Plant Genetics Resources Institute.
  • Muscarella, R., T. Fleming. 2007. The role of frugivorous bats in tropical forest succession. Biological Reviews, Vol 82, Issue 4: 573-590. Accessed April 16, 2011 at http://apps.isiknowledge.com/full_record.do?product=BIOSIS&search_mode=GeneralSearch&qid=1&SID=2CcoAkk5ePb45E12@GO&page=4&doc=31.
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Predation

Pteropus vampyrus is commonly hunted for food and sport throughout its geographic range. In peninsular Malaysia, an estimated 22,000 flying foxes are legally hunted each year. No other information exits on potential predators of this species. Its nocturnal and roosting lifestyle likely decreases risk of predation.

Known Predators:

  • Ardea, A. 2009. "The Telegraph" (On-line). Large flying fox: world's biggest bat being hunted to extinction. Accessed March 30, 2011 at http://www.telegraph.co.uk/earth/wildlife/6087109/Large-flying-fox-worlds-biggest-bat-being-hunted-to-extinction.html.
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Life History and Behavior

Behavior

Communication and Perception

During flight, Pteropus vampyrus tends to remain silent. During feeding, however, it is often very noisy. Returning to the roost at dawn is also associated with loud vocalizations, which are used in territorial behavior and to help maintain inter-individual spacing at roost sites. Evidence suggests that P. vampyrus vocalizes to communicate emotion as well. It uses vision rather then echolocation for in-flight navigation, and they find food using their acute senses of sight and smell.

Communication Channels: visual ; tactile ; acoustic

Other Communication Modes: choruses ; pheromones ; scent marks

Perception Channels: visual ; acoustic

  • Mohd-Azlan, J., A. Zubaid, T. Kunz. 2011. Distribution, relative abundance, and conservation status of the large flying fox, Pteropus vampyrus, in peninsular Malaysia:a preliminary assessment. Acta Chiropterologica, 3(2): 149-162.
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Life Expectancy

Lifespan/Longevity

Pteropus vampyrus can live 15 to 30 years in captivity, and an average of 15 years in the wild.

Average lifespan

Status: wild:
15 years.

Range lifespan

Status: captivity:
15 to 30 years.

  • Oakland Zoo, 2011. "Conservation and Education; Oakland Zoo" (On-line). Malayan Flying Fox. Accessed April 03, 2011 at http://www.oaklandzoo.org/animals/mammals/bat-malayan-flying-fox.
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Lifespan, longevity, and ageing

Maximum longevity: 20.9 years (captivity) Observations: This is the largest species of the genus in wingspan (Ronald Nowak 1999).
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Reproduction

Reproduction

Pteropus vampyrus is most often polygynous, with males protecting a small harem and mating with up to ten females. Dominant males occupy the best roosting sites, and there is a social hierarchy among males.

Mating System: polygynous

Unlike other pteropods, which have fused horns on the baculum, Pteropus vampyrus has a saddle-shaped baculum. It ranges from 4.5 to 8.2 mm and is wider than it is long. Females typically give birth to only one offspring per year. Synchronous birthing occurs within each population, and timing depends on local geography and seasonality. In peninsular Malaysia, mating peaks from November to January. In Thailand, birthing peaks during March and April and in the Philippines it peaks during April and May. In captive populations, birthing peaks during May and June. Mean body mass newborns is 133g (20-30% of maternal body mass) and their forearm length is around 79.5 mm. Mothers carry their young during the first few days after parturition, then leave them at the roost during foraging bouts. Young are weaned by 2 to 3 months after birth.

Breeding interval: once yearly

Breeding season: Mating season varies according to local geography and climate

Range number of offspring: 1 to 2.

Average number of offspring: 1.

Range gestation period: 140 to 192 days.

Average birth mass: 133 g.

Range weaning age: 2 to 3 months.

Average age at sexual or reproductive maturity (female): 2 years.

Average age at sexual or reproductive maturity (male): 2 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); viviparous

Pteropus vampyrus offspring are born with eyes open and fully furred, but in many ways are altricial. They are carried with the mother initially, then left in the roost after a couple of days so that the mother can feed. Mothers nurse young for the first 2 to 3 months after parturition, or until weaning is complete, which can be anywhere from 3 to 5 months. All parental care is provided by the mother, though males often help protect and defend their harem.

Parental Investment: altricial ; female parental care ; pre-fertilization (Provisioning, Protecting: Male); pre-hatching/birth (Provisioning: Female, Protecting: Male, Female); pre-weaning/fledging (Provisioning: Female, Protecting: Male, Female); pre-independence (Provisioning: Female, Protecting: Female)

  • Kunz, T., D. Jones. 2000. Pteropus vampryrus. Mammalian Species, No. 642: 1-6. Accessed March 30, 2011 at http://www.science.smith.edu/departments/Biology/VHAYSSEN/msi/.
  • Organization for Bat Conservation, 2011. "Organization for Bat Conservation" (On-line). Malayian Flying Fox. Accessed April 16, 2011 at http://www.batconservation.org/drupal/malayan-flying-fox.
  • Tampa's Lowry Park Zoo, 2010. "Wallaroo Station Animal Fact Sheet" (On-line). Flying Fox Bat. Accessed April 15, 2011 at http://www.lowryparkzoo.com/bio_wallaroo_flying_fox.php.
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Molecular Biology and Genetics

Molecular Biology

Barcode data: Pteropus vampyrus

The following is a representative barcode sequence, the centroid of all available sequences for this species. 

 
There are 2 barcode sequences available from BOLD and GenBank.  Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species.  See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
 
ABRVN411-06|ROM MAM 110949|Pteropus vampyrus| ---------------------------------------ACTTTGTATTTACTATTCGGCGCCTGAGCTGGCATGGTCGGAACGGCCCTC---AGCCTACTAATCCGAGCAGAACTGGGCCAACCAGGAACTCTACTGGGCGAC---GACCAAATTTACAATGTAATCGTAACAGCCCACGCATTCGTAATAATCTTCTTTATGGTTATACCAATTATAATTGGAGGCTTCGGAAACTGGCTTGTGCCACTAATG---ATCGGAGCTCCGGACATGGCATTCCCCCGAATAAATAACATGAGCTTCTGACTTCTGCCTCCATCGTTCCTACTTCTGCTAGCCTCATCAACAGTAGAGGCCGGTGCTGGAACAGGGTGAACAGTATATCCACCTTTAGCCGGTAATCTAGCACATGCCGGAGCCTCAGTAGATCTG---GCAATTTTCTCACTTCACTTGGCTGGTATCTCATCAATCCTGGGTGCCATTAATTTTATTACAACTATTATCAATATAAAACCCCCGGCTCTATCCCAGTATCAAACCCCACTGTTCGTTTGATCTGTCTTAATCACGGCCGTCTTACTCCTCCTATCTCTACCAGTGCTAGCCGCC---GGAATTACGATACTGTTAACAGATCGTAACCTAAATACCACCTTTTTCGACCCTGCAGGAGGGGGAGACCCAATTCTATATCAACACCTA------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- 
-- end --

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Statistics of barcoding coverage: Pteropus vampyrus

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 2
Species: 2
Species With Barcodes: 1

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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
NT
Near Threatened

Red List Criteria

Version
3.1

Year Assessed
2008

Assessor/s
Bates, P., Francis, C., Gumal, M., Bumrungsri, S., Walston, J., Heaney, L. & Mildenstein, T.

Reviewer/s
Hutson, A.M., Racey, P.A. (Chiroptera Red List Authority) & Cox, N. (Global Mammal Assessment Team)

Contributor/s

Justification
Listed as Near Threatened because this species is in significant decline (but at a rate of probably less than 30% over ten years or three generations) because it is being over-harvested for food over much of its range, and because of ongoing degradation of its primary forest habitat, making the species close to qualifying for Vulnerable under criterion A.

History
  • 1996
    Lower Risk/least concern
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Conservation Status

The IUCN Red List of Threatened Species classifies Pteropus vampyrus. Its populations are in significant decline, and major threats include chronic over-harvesting and the destruction of its primary habitats. If harvesting continues at its current rate, P. vampyrus could disappear from western Malaysia in as little as 6 years. In the Philippines, major threats include hunting and targeting due to noise. Hunting of P. vampyrus has more than doubled since 1996. Likewise, in 2003, an estimated 4,500 large flying foxes were killed in a single location and sold into trade. Habitat destruction due to deforestation is also a major threat to their persistence in Malaysia.

The Convention on International Trade in Endangered Species of Fauna and Flora (CITES) lists Pteropus vampyrus under Appendix II. Efforts to conserve P. vampyrus are underway, and hunting laws have been established to reduce harvest rates. Unfortunately, anti-poaching laws and harvest limits are difficult to enforce. Currently, colony management on small islands appears to be the most effective protection of P. vampyrus. Due to its migratory behavior and its tendency to travel long distances during nocturnal foraging bouts, a more regional management approach may be necessary to successfully conserve this species.

US Federal List: no special status

CITES: appendix ii

IUCN Red List of Threatened Species: near threatened

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Population

Population
In the Philippines, this species formerly occurred in many large colonies, but these are now greatly reduced in size and number (Heideman and Heaney 1989; Mickleburgh et al. 1992; Mudar and Allen 1986; Rickart et al. 1993). The largest colony identified as this species found in Subic Bay (Luzon) contained almost 20,000 individuals (Paguntalan pers. comm. 2006). It is a moderately common species on Palawan Island in spite of continuing hunting pressure (Esselstyn et al. 2004). On Mindoro, it has been found in Sablayan municipality (Occidental Mindoro province) in mixed colonies of up to 52,000 individuals (Garcia pers. comm. 2006). In Thailand, the species has not been recorded from some localities for over 100 years. The largest colonies in Thailand now consist of 3,000 individuals (S. Bumgrunsri pers. comm. 2006). In Sabah (Malaysia) populations have probably undergone a serious decline (C. Francis pers. comm. 2006).

Population Trend
Decreasing
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Threats

Threats

Major Threats
In the Philippines, while hunting for food has resulted in population declines in some areas, the species appears to be able to change roosting locations in order to avoid heavy hunting pressure (Garcia pers. comm. 2006). In Thailand, hunting is considered to be the major threat to this species (S. Bumgrunsri pers. comm. 2006), and it seems possible that hunting is also a major threat in other parts of the species range. In addition to overhunting, the species is generally threatened by the loss of lowland forest throughout much of its range, however, it somewhat adaptable to secondary or modified habitats, providing suitable roosting sites are available.
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Management

Conservation Actions

Conservation Actions

This species is listed on Appendix II of CITES. In view of the species wide range, it seems probable that it is present in many protected areas. There is a need to protect important roosting sites for this species, and to regulate any hunting pressure so that populations are sustainably harvested. Regular field surveys and monitoring of known populations should be undertaken. Further studies are needed to clarify the taxonomic status of populations currently allocated to this species, as Pteropus vampyrus might represent a species complex.

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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Negative

In some areas, large flying foxes are viewed as agricultural pests, as forage sites often include fruit farms. They are also exceptionally noisy while feeding, and many farmers use flapping or whirling devices and bright lights to deter them. Large flying foxes carry a number of zoonotic diseases such as the Hendra virus and the Nipah virus. Nipah virus first appeared in humans in Malaysia in 1998, followed by cases in Bangladesh and India. Evidence suggests that large flying foxes are reservoirs for a number of different henipaviruses, including Nipah. In particular, it is suspected that this species was the reservoir hosts of the 1998 Nipah outbreak in pigs and humans. The long distance movements of large flying foxes increases its potential to transfer these diseases to other countries in the Australian and Asian regions.

Negative Impacts: injures humans (carries human disease); crop pest; causes or carries domestic animal disease

  • Breed, A., H. Field, C. Smith, J. Meers. 2010. Bats Without Borders: Long-Distance Movements and Implications for Disease Risk Management. Ecohealth, Vol 7, Issue 2: 204-212.
  • Hassan, N., S. Saad, Z. Shohaimi. 2010. Characterization of Nipah virus from naturally infected pteropus vampyrus bats, Malaysia. Emerging Infecitous Diseases, 16/12: 1990.
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Economic Importance for Humans: Positive

As a pollinator and seed disperser, Pteropus vampyrus plays an important role in maintaining forest structure and composition throughout its geographic range. Humans hunt P. vampyrus for sport, and there is a significant international market, both legal and illegal, for its meat and the various by-products that are used in traditional medicines. For example, its fat is valued in Pakistan, where some believe it helps cure rheumatism, and others claim that its meat can help cure asthma. Shipments of P. vampyrus carcasses have been confiscated on numerous occasions in Guam, and trade continues to be monitored.

Positive Impacts: food ; body parts are source of valuable material; source of medicine or drug

  • Feldhamer, G., L. Drickamer. 2007. Mammology: Adaptation, Diversity, Ecology. Johns Hopkins University: Johns Hopkins University Press.
  • Struebig, M., M. Harrison, S. Cheyne, S. Limin. 2007. Intensive hunting of large flying foxes Pteropus vampyrus natunae in Central Kalimantan, Indonesian Borneo. Oryx, Vol 41, No 3: 390-393.
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Wikipedia

Large Flying Fox

The Large Flying Fox (Pteropus vampyrus), also known as the Greater Flying Fox, Malaysian Flying Fox, Kalang or Kalong, is a species of megabat in the family Pteropodidae.[1] Like the other members of the genus Pteropus, or the Old World fruit bats, it feeds exclusively on fruits. It is noted for being the largest member of the bat family by wingspan. It, as with all other Old World fruit bats, lacks the ability to echolocate. It should not be confused with Acerodon jubatus which is also large.

Contents

Description

The large flying fox is among the largest species of bats. It weighs 0.6 (1.3 lbs) to 1.1 kg (2.4 lbs) and has a wingspan of 1.5 m (4.9 ft) on average. As with all megabats, it has a fox-like face, hence its name. It lacks a tail and has pointed ears. The hairs on much of its body is long and wooly but are shorter and more erect on the upper back.[2] The mantle hairs tend to be the longest.[3] The color and texture of the coat differ between sexes and age classes.[4] Males tend to have slightly stiffer and thicker coats than females.[2] Immature individuals are almost all dull gray-brown.[5] Young have a dark-colored mantle that becomes lighter in males when they mature.[2] The head has hairs that range in color mahogany-red and orange-ochreous to blackish. The ventral areas are brown or blackish, tingled with chocolate, gray or silver.[4] The mantle can vary from pale dirty-buff to orange yellow, while the chest is usually dark-golden brown or dark russet.[2] The large flying fox has a large and robust skull. The dental formula is Upper: 2.2.1.1, lower: 2.3.2.3. It has a total of 34 teeth.[3] The large flying fox's wing are short and somewhat rounded at the tips. This allows them to fly slowly but with great maneuverability.[2] Wing membranes are only haired near the body.

Ecology

The large flying fox ranges from Malay Peninsula, stretching to the Philippines in the east and Sumatra, Java, Borneo and Timor in the south.[6] In certain areas, the bat prefers coastal regions, but it can also be found at elevation up to 1,370 m.[7]

Flying foxes inhabit as primary, mangrove forest, coconut groves , mixed fruit orchards and a numer of other habitats.[8] During the day, trees in mangrove forests and coconut groves may be used as roosts.[4] In Malaysia, flying foxes prefer in lowland habitats below 365m.[9] In Borneo, flying foxes inhabit the coastal areas by move to nearby islands to feed on fruit.[5] Flying fox roost in the thousands (maximum). One colony was recorded numbering around 2,000 individuals in a mangrove forest in Timor.[4] In general, mangrove roosts have lower numbers of resting bats compared to lowland roost sites which could mean that mangroves forests are only used temporarily.[9]

This species primarily eats on flower, nectar and fruit. When all three food item are available, flower and nectar are preferred.[3][4][5] The pollen, nectar and flower of coconut and durian trees as well as the fruits of rambutan, fig and langsat trees are consumed. Flying foxes will also eat mangoes and bananas.[4][9][10] With fruit, the flying fox prefers the pulp, and slices open the rind to get it.[10] With durian tree flowers, the flying fox can lick up the nectar without do apparent damage to the flower.[2]

Behaviour and life history

Colonies of large flying foxes fly in a scattered stream.[3] They may fly to their feeding grounds for up to 50 km in one night. Vocalization are not made during flight.[3] Large flocks fission into family or feeding groups upon arrival at feeding grounds.[2] Flying foxes may circle a fruit tree before landing, and usually land on the tips of branches in an upright position, then falling into a head-down position from which they feed.[2] Feeding aggregations tend to be very noisy.[11]

Flowers on trees are the basis territories in this species. Territoral behavior includes growling and the spreading of wings.[11] During antagonistic behavior, individuals maintain specing with wrists/thumbs sparing, bites, and loud vocalizations.[4] When moving to a suitable resting place after landing, an individual may fight with conspeifics along the way.[4] A roosting flying fox is positioned upside down with its wings wrapped up.[12] When it gets too warm, a flying fox fans itself with its wings.[4] Roosting bats are restless until mid morning.

Female large flying fox gestations are at their highest between November to January in Peninsular Malaysia, but some births occur in other months.[8] In Thailand, gestations may take place during the same period with young being born in March or early April.[3][8] Females apparently enter partus during April and May in the Philippines.[12] This species usually give birth to only one young.[3] For the first days, the mothers carrying their youngs but leave than at the roost when they go on their foraging trips.[2] The young are weaned by 2–3 months.[3]

Status

A recent update by the IUCN has listed the species as Near Threatened and mentioned its near-vulnerable status with the following reasons.[13]

"Listed as Near Threatened because this species is in significant decline (but at a rate of probably less than 30% over ten years or three generations) because it is being over-harvested for food over much of its range, and because of ongoing degradation of its primary forest habitat, making the species close to qualifying for Vulnerable under criterion A."

One threat to the large flying fox is habitat destruction.[8] Flying fox are sometimes hunted for food and the controls on hunting seem to be unenforceable.[2] In some areas, farmers consider flying foxes pests as they sometimes feed on their orchards.[9]

References

  1. ^ Simmons, Nancy B. (16 November 2005). "Order Chiroptera". In Wilson, Don E.; Reeder, DeeAnn. Mammal Species of the World (3rd ed.). Johns Hopkins University Press. pp. 345-346. ISBN 978-0-8018-8221-0. OCLC 62265494. http://www.bucknell.edu/msw3/browse.asp?id=13800382. 
  2. ^ a b c d e f g h i j Kunz, T., D. Jones. 2000. "Pteropus vampryrus". Mammalian Species, No. 642: 1-6.
  3. ^ a b c d e f g h Lekagul B., J. A. McNeely. 1977. Mammals of Thailand. Association for the Conservation of Wildlife, Bangkok, Thailand.
  4. ^ a b c d e f g h i Goodwin R. E. 1979. The bats of Timor. Bullentin of the American Museum of Natural History, 163:75-122.
  5. ^ a b c Payne J., C. M. Francis, K. Philps. 1985. A field guide to the mammals of Borneo. The Sabah Society, Kota Kinabulu, Malayisa.
  6. ^ Corbet G. B., J. E. Hill. 1992. Mammals of the Indomalayan region: a systematic review. Oxford University Press.
  7. ^ Medway L. 1965. Wild mammals of Malaya (Peninsular Malaysia) and Singapore. Oxford University Press.
  8. ^ a b c d Heideman P. D., L. D. Heaney. 1992. Pteropus vampyrus. Pp. 140-143 in Old World fruit bats: an action plan for the family Pteropodidae (S. P. Mickleburgh, A. M. Hutson, P. A. Racy, eds). ICUN Survival Commission, Gland, Switzerland.
  9. ^ a b c d Lim B. L. 1966. "Abundance and distribution of Malaysian bats in different ecological habitats", Federated Museums Journal 11:61-76.
  10. ^ a b Davis D. D. 1962. "Mammals of the lowland rainforest of North Borneo", Bulletin of National Museum, Singapore 31:1-129.
  11. ^ a b Gould E. 1978. "Foraging behavior of Malaysian nectar-feeding bats", Biotropica 10:184-193.
  12. ^ a b Rabor D. 1977. Philippine birds and mammals, University of Philippines Press.
  13. ^ P. Bates, C. Francis, M. Gumal, S. Bumrungsri, J. Walston, L. Heaney & T. Mildenstein (2008). "Pteropus vampyrus". IUCN Red List of Threatened Species. Version 3.1. International Union for Conservation of Nature. http://www.iucnredlist.org/apps/redlist/details/18766. Retrieved November 13, 2010. 
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