Overview

Distribution

Range Description

This species is widely distributed from much of South Asia, through southern China, most of mainland and insular Southeast Asia. In South Asia this species is presently known from Bangladesh (Dhaka, Khulna and Rajsahi divisions), Bhutan (Phuntsholing), India (Andhra Pradesh, Arunachal Pradesh, Assam, Bihar, Chhattisgarh, Goa, Gujarat, Jammu and Kashmir, Jharkhand, Karnataka, Kerala, Madhya Pradesh, Maharashtra, Meghalaya, Nagaland, Nicobar Islands, Orissa, Rajasthan, Tamil Nadu, Tripura, Uttaranchal, Uttar Pradesh and West Bengal), Nepal (Central, Eastern, Far Western and Western Nepal), Pakistan (Sind) and Sri Lanka (Central, Eastern, North Central, Sabaragamuwa, Southern, Uva and Western provinces) (Molur et al. 2002). It has been recorded from sea level to an elevation of 400 m asl distributed widely in the region. In southern China, it is found from Tibet to Fujian (Smith and Xie 2008). In Southeast Asia, it ranges from Myanmar in the west, through Thailand, Lao PDR, Viet Nam and Cambodia to Peninsular Malaysia, and from here it occurs in Indonesia (the Mentawai Islands, Sumatra, western Java, Bali, Sumbawa and Sulawesi) and southern Borneo (Kalimantan [Indonesia]).
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Geographic Range

The short-nosed fruit bat is found in Sri Lanka, India, South China, S.E. Asia, Western Malaysia, and Sumatra and neighboring small islands.

Biogeographic Regions: oriental (Native )

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Physical Description

Morphology

Physical Description

These bats have a relatively long snout. Their upper parts are typically bright orange with paler underparts, but there is much variation. The fur is very fine and silky. The wing span of the adult is about 48 cm.

Average mass: 75 g.

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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
This species is found in a wide variety of habitats from rural areas, primary and secondary forested habitats to urban landscapes. It is found as small colonies consisting of 3-7 individuals, sometimes more; it roosts underside leaves, in flower and fruit clusters of Kitul Palm, on Saraka asoka trees and is known to build tents in the roosting trees. It feeds on a variety of fruits both wild and cultivated. It has a low but fast flight. It breeds twice a year, and in some areas is known to breed throughout the year and bears a single young (Bates and Harrison 1997).

Systems
  • Terrestrial
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Habitat

Cynopterus sphinx is common in tropical forests and areas where fruit crops are cultivated. They can also be found in grassland and mangrove forests. They typically nest high in palm trees. The bats chew the fronds of the palms to constuct fairly simple tents. These bats are also known to construct tents by closely interweaving the leaves and twigs of creeping vines which cover buildings, but such nests are constructed only when palms are not available.

Terrestrial Biomes: savanna or grassland ; forest ; rainforest ; scrub forest

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Trophic Strategy

Food Habits

These bats are frugivorous, they and locate their preferred food items by scent. They have been described as voracious feeders, eating more than their body weight in food in one sitting. Some preferred fruits include ripe guava, banana, chikus (a popular Indian fruit crop), dates and liches.

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Life History and Behavior

Life Expectancy

Lifespan/Longevity

Average lifespan

Status: captivity:
10 years.

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Lifespan, longevity, and ageing

Maximum longevity: 10 years (captivity) Observations: One specimen was still alive after 10 years in captivity (Richard Weigl 2005).
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Reproduction

Reproduction

In Central India, C. sphinx breeds twice per year. Females produce a single young at a time. The function of the female reproductive system is interesting in that each half of the bicornate uterus functions during alternate breeding cycles. The first pregancy cycle occurs from October through February/March. Mating occurs immediately postpartum, and a second offspring is born in July. Gestation 3-5 months. In 72% of bats, the first pregnancy occurs in the right horn of the uterus. The corpus luteum in the right ovary persists for some time after the pregancny and prevents ovulation from occuring in the right ovary during the second breeding cycle. This creats the pattern of alternate functioning of the two horns of the uterus. However, the corpus luteum in the left ovary does not persist until the beginning of the next breeding cycle. As yet, no reason has been found for the dominance of the right horn during the first breeding cycle.

Newborn bats weigh about 13.5 g and have a wingspan of 24 cm. By the time of weaning at 4 weeks of age, young bats weigh 25 g and have wings spanning 36 cm. Female short-nosed fruit bats reach sexual maturity at 5-6 months of age, but males are not capable of breeding until they are a year old.

Average birth mass: 11 g.

Average gestation period: 120 days.

Average number of offspring: 1.2.

Average age at sexual or reproductive maturity (male)

Sex: male:
525 days.

Average age at sexual or reproductive maturity (female)

Sex: female:
150 days.

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Molecular Biology and Genetics

Molecular Biology

Barcode data: Cynopterus sphinx

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

 
There are 32 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.
 
ABCMA644-07|ROM MAM 116144|Cynopterus sphinx| ---------------------------------------ACTCTGTACCTTCTGTTTGGCGCTTGAGCTGGAATAGTTGGCACCGCCCTC---AGTCTACTAATTCGAGCAGAACTTGGCCAACCAGGTGCACTATTAGGAGAT---GACCAAATTTACAATGTCATCGTAACAGCCCACGCATTTGTAATAATTTTCTTCATGGTGATGCCCATTATAATCGGAGGCTTTGGAAACTGACTGATCCCTCTGATA---ATTGGTGCCCCAGACATAGCCTTTCCCCGAATAAACAATATGAGTTTCTGACTTCTCCCTCCCTCATTCCTACTCCTGTTAGCCTCCTCAACAGTAGAAGCCGGCGCCGGAACCGGATGGACAGTTTACCCTCCTCTAGCCGGTAACTTAGCCCACGCAGGAGCCTCAGTGGACCTG---GCGATTTTCTCTCTACACCTGGCCGGAGTCTCATCCATTCTAGGGGCCATTAATTTTATTACAACAATTATCAACATAAAACCGCCAGCTCTGTCCCAATATCAAACCCCCTTGTTTGTTTGATCAGTCCTAATTACCGCTGTATTGCTCCTTCTATCCCTACCAGTCCTAGCCGCT---GGTATTACGATACTACTTACAGATCGAAATTTGAATACTACTTTCTTTGACCCTGCTGGAGGAGGAGACCCGATTCTATATCAACACCTC------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- 
-- end --

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Statistics of barcoding coverage: Cynopterus sphinx

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 31
Species: 120
Species With Barcodes: 1

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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
LC
Least Concern

Red List Criteria

Version
3.1

Year Assessed
2008

Assessor/s
Bates, P., Bumrungsri, S., Molur, S. & Srinivasulu, C.

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

Contributor/s

Justification
Listed as Least Concern because, although it is seldom recorded, it has a relatively wide distribution, is tolerant of a broad range of habitats, has a presumed large population, and because it is unlikely to be declining fast enough to qualify for listing in a more threatened category.

History
  • 1996
    Lower Risk/least concern
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Conservation Status

IUCN Red List of Threatened Species: least concern

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Population

Population
This is a widespread and very common species. In South Asia, it is considered to be more adaptable than C. brachyotis, and the population of C. sphinx seems to be stable (Molur et al. 2002, C. Srinivasulu pers. comm. September, 2007).

Population Trend
Increasing
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Threats

Threats

Major Threats
There are no major threats to this species as a whole. In South Asia, it is locally threatened in parts of its range through deforestation, generally resulting from logging operations and the conversion of land to agriculture and for construction of dams and other developmental activities. It is also under threat due to hunting for medicinal purposes (Molur et al. 2002). In Southeast Asia, it is a pest species of orchards and is hunted for food in some parts of the range. In China, there is some habitat loss and the species is hunted for medicinal purposes.
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Management

Conservation Actions

Conservation Actions
As it is present in many protected areas and is very adaptable, no direct conservation measures are currently needed for this species as a whole. In South Asia, this species like most other fruit bats in India is considered a vermin under Schedule V of the Indian Wildlife (Protection) Act. It has been recorded from protected areas in India like Point Calimere Wildlife Sanctuary in Tamil Nadu, Coringa Wildlife Sanctuary, Kawal Wildlife Sanctuary, Nagarjunasagar Srisailam Tiger Reserve in Andhra Pradesh, Kanha National Park in Madhya Pradesh, Indravati National Park in Chattisgarh. Taxonomic studies, population monitoring and lobbying with the government to accord it a non-vermin status are recommendations (Molur et al. 2002). Molecular taxonomic studies to know the variations in the population are recommended (C. Srinivasulu pers. comm. 10 October, 2007).
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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Negative

Short-nosed fruit bats inflict serious damage on many fruit crops, and are viewed by local people as a pest species. In addition, these bats are possible vectors for Japanese encephalitis, a very serious disease in humans.

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Economic Importance for Humans: Positive

These bats are important dispersers of date palm seeds, and pollinate many night blooming flowers.

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Wikipedia

Greater short-nosed fruit bat

The greater short-nosed fruit bat or short-nosed Indian fruit bat (Cynopterus sphinx) is a species of megabat in the Pteropodidae family. It is found in South and Southeast Asia.[1]

Contents

Description

These bats have a relatively long snout. Their upper parts are brown to grey-brown with paler under parts. The fur is very fine and silky. The ears and wing bones of C. sphinx are edged in white. Lower cheek teeth rounded without accessory cusps. The wing span of the adult is about 48 cm. Juveniles are lighter than adults. Average forearm length 70.2mm (64-79mm).[2]

Habitat

It is found in Pakistan, Bangladesh, Bhutan, Cambodia, China, India, Indonesia, Laos, Malaysia, Myanmar, Philippines, Sri Lanka, Thailand, and Vietnam. C. sphinx is common in tropical forests and areas where fruit crops are cultivated. They can also be found in grassland and mangrove forests. They typically nest high in palm trees. The bats chew the fronds of the palms to construct fairly simple tents. These bats are also known to construct tents by closely interweaving the leaves and twigs of creeping vines which cover buildings, but such nests are constructed only when palms are not available.

Behaviour and breeding

The species is gregarious, and typically roosts in same sex groups of 8-9 individuals. The sexes remain separate until the mating season, when group size increases. They are polygynous and it is usual for 6-10 males and 10-15 females to share palm frond tents during the breeding season.[3] C. sphinx is the only non-primate species to show fellatio, which enhances copulation time in the species. Copulation by males is dorsoventral and the females lick the shaft or the base of the male's penis, but not the glans which has already penetrated the vagina. While the females do this, the penis is not withdrawn and research has shown a positive relationship between length of the time that the penis is licked and the duration of copulation. Post copulation genital grooming has also been observed.[4] Males stay with females for some time after mating, but later return to same sex groups.

Cynopterus sphinx fellatio no music.ogg
Female bats perform fellatio to increase copulation time. This species is the only non-primate to exhibit this behaviour[4]

The adult sex ratio is very female biased. Researchers attribute this to the relatively rapid maturation of females compared to males. In Central India, C. sphinx breeds twice per year. Females produce a single young at a time. Each half of the bicornate uterus functions during alternate breeding cycles. The first pregnancy cycle occurs from October through February/March. Mating occurs immediately postpartum, and a second offspring is born in July. Gestation period is about 3–5 months. In 72% of bats, the first pregnancy occurs in the right horn of the uterus. The corpus luteum in the right ovary persists for some time after the pregnancy and prevents ovulation from occurring in the right ovary during the second breeding cycle. This creates the pattern of alternate functioning of the two horns of the uterus. However, the corpus luteum in the left ovary does not persist until the beginning of the next breeding cycle. As yet, no reason has been found for the dominance of the right horn during the first breeding cycle.[5][6] Newborn bats weigh about 13.5 g and have a wingspan of 24 cm. By the time of weaning at 4 weeks of age, young bats weigh 25 g and have wings spanning 36 cm. Female short-nosed fruit bats reach sexual maturity at 5–6 months of age, but males are not capable of breeding until they are a year old.[7]

These bats are frugivorous, locate their preferred food items by scent. They have been described as voracious feeders, eating more than their body weight in food in one sitting. Some preferred fruits include ripe guava, banana, chikoo, dates and lychees.

Short-nosed fruit bats inflict serious damage on many fruit crops, and are considered pests. In addition, these bats are possible vectors for Japanese encephalitis, which is serious disease in humans.[8] These bats are important dispersers of date palm seeds, and pollinate many night blooming flowers.

Notes

  1. ^ Bates, P; Bumrungsri, Molur S. & Srinivasulu, C. (2008). "IUCN entry for C. sphinx". IUCN Red List of Threatened Species.. http://www.iucnredlist.org/search/details.php/6106/all. Retrieved 2009-10-28. 
  2. ^ Bates, P.J.J; D.A. Harrison (1997). Bats of the Indian Subcontinent. Harrison Zoological Museum. pp. 258. ISBN 0951731319. 
  3. ^ Balasingh, J; J. Suthakar-Isaac, S., and R. Subbaraj (1993). "Tent roosting by the frugivorous bat Cynopterus sphinx in southern India". Current Science 65 (5): 418. http://www.ias.ac.in/j_archive/currsci/65/5/418/viewpage.html. 
  4. ^ a b Tan, Min; Gareth Jones, Guangjian Zhu, Jianping Ye, Tiyu Hong, Shanyi Zhou, Shuyi Zhang, Libiao Zhang (October 28, 2009). Hosken, David. ed. "Fellatio by Fruit Bats Prolongs Copulation Time". PLoS ONE 4 (10): e7595. Bibcode 2009PLoSO...4.7595T. doi:10.1371/journal.pone.0007595. PMC 2762080. PMID 19862320. http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0007595. Retrieved October 28, 2009. 
  5. ^ Advani, R (1982). "Feeding, foraging and roosting behavior of the fruit eating bats and damage to fruit crops in Rajasthan and Gujarat". Saeugeteirkundliche mitteilungen 30 (1): 46–48. 
  6. ^ Sandhu, S; A. Gopalakrishna. (1984). "Some observations on the breeding biology of Cynopterus sphinx in central India". Current Science 53 (22): 1189–1192. 
  7. ^ Krishna, A; C.J. Dominic (1983). "Growth of young and sexual maturity of 3 species of Indian Bats". Journal of Animal Morphology and Physiology 30 (1–2): 162–168. 
  8. ^ Banjeree, K; Ilkal, M.A., and P.K. Deshmikh. (1984). "Susceptibility of Cynopterus sphinx (frugivorus bat) and Suncus minimus (house shrew) to Japanese encephalitis virus". Indian Journal of Medical Research 79 (1): 8–12. 

References

  • Nowak, Ronald. 1991 Walker's Mammals of the World, Fifth edition. Johns Hopkins University Press, Baltimore and London.

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