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Table of Contents

1. Ecology
1A. Behaviour
1B. Flight
1C. Diet
1D. Reproduction
2. Description
3. Distribution & Habitat
4. Importance of bats around the world
5. Conservation
6. Taxonomy
6A. Type Specimen
6B. Phylogenetics
6C. Gene Sequence
7. References
The Cynopterus brachyotis, or more commonly known as the lesser dog-faced fruit bat, was first discovered near the serene Dewei river in lush Borneo by Muller on 12 September 1836. It belongs to the Megachiroptera (Megabats!) suborder within the Pteropodidae family of the order Chiroptera (bats). Although it is a species of megabat, this majestic creature is small, cuddly and cute but cannot and should not be brought home and domesticated. Still, you can adopt a bat today!

Watch this video on the conservation of baby fruit bats!




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1. Ecology

1A. Behaviour

Have you seen their large eyes?
The lesser dog-faced fruit bat usually cluster in small groups and forage with their keen sense of smell and sight. Unlike Microchiroptera bats, Megachiroptera bats are not capable of laryngeal echolocation as such a mechanism is too energetically expensive to retain. So, the lesser dog-faced fruit bat has its distinctive large eyes for smooth navigation at night.

In addition, the combination of sound and sight is required for the navigation of the lesser dog-face fruit bat. In a study (Heffner et al. 2008), it was shown that hearing is used to direct eyes to source of sound for sound localization.
Cynopterus brachyotis14.jpg
Taken by Doug Wechsler, under Some Rights Reserved



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Sleeping on beds is too boring.
All animals need to rest after a long day of feeding - bats are no different! As you may have seen on television or in movies, bats have very peculiar resting (roosting) behaviour. In the day, the lesser dog-faced fruit bat finds shelter in shaded trees, tree-ferns and near entrances of caves.
Cynopterus brachyotis24.jpg
Image from Wikimedia Commons

Roosting behaviour
  • Roosts in groups
  • Wings are wrapped around its body, leaving only its head in view
  • Hip joint rotated to allow its legs to turn outwards for perching on branches
  • Upside-down hanging posture is adopted so that it can quickly take-off when threatened


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The Perfect Life: Make a home and find a mate
Cynopterus brachyotis3.png
[A] to [F] are variants of Palmate type tents. (Tan et al. 1997)


Other than hanging upside-down in a tree, the lesser dog-faced fruit bat may make their own homes, known as roost tents, by chewing and collapsing leaves, stems and flower clusters. In Singapore and Malaysia, folded leaves of palms are used. To date, there are 4 known types of tents constructed by the furry lesser dog-faced fruit bat.

Types of tents

These tents serve to keep the furry little bats from vicious predators and also shelters them from wind and rain. An interesting fact about roost tents: Males make tents and recruit females (Tan et al, 1997). Males are also observed to have high roost fidelity as a resource defence strategy (Chaverri and Kunz 2006). Females will then choose males based on roost quality. Thus, males have high productivity pay-off if they successfully recruit females and exclude other males from roosts.
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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

1B. Flight



Bats are mammals with powered flight!
The body structure of bats enable them to fly great distances. Bats have modified skeletons and use various muscles for flight. They do not have reinforced sternums, unlike birds which power their flights with their breast muscles. Also unlike feathers on bird, bats have highly articulated and flexible wings which enable them to fly with greater manoeuvrability, increased lift and lesser drag.
Cynopterus branchyotis2.jpg
(Iriarte-Diaz and Swartz, 2008)


Much research has been conducted to detail the mechanisms of flight in bats, especially for the lesser dog-faced fruit bats. In this species, change in flight direction due to changes in body orientation during up-stroke has been observed. On the other hand, changes in flight direction is restricted during the down-stroke portion of the wing-beat cycle.
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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

1C. Diet



Lesser dog-faced fruit bat are fruigivores!
Do you know what is a fruigivore?

Cynopterus brachyotis23.jpg
Image by Fletcher & Baylis. Under Creative Commons

As a frugivore, the lesser dog-faced fruit bat usually eats fruits, figs, nectar and pollen from flowers. Leaves are high in protein while fruits are high in energy content to allow it to fly through the air.

As it has a tiny mouth, smaller fruits are swallowed while larger fruits are chewed. Sometimes it will just drink the juice after chewing and spit out the dehydrated pulp.


Piper Aduncum.jpg
Piper aduncum. Taken from Wikimedia Commons.

Adinandra dumosa.jpg
Adinandra dumosa. Taken by Ria Tan

Matico (Piper aduncum)
  • Present in Malaysia
  • Key species of plant that lesser dog-faced fruit bat feeds on
Tiup tiup (Adinandra dumosa)
  • Present in Singapore, mainly in secondary forest
  • Mutualistic relationship with lesser dog-faced fruit bat

In Malaysia, the keystone resources to sustain the population of bats are Ficus spp, Piper aduncum and Pternandra echinata. Seasonal feeding is also present for the lesser dog-faced fruit bats in Malaysia. It feeds mainly on fruits in months of March to June, which coincides with local fruiting seasons. On the remaining parts of the year, it feeds on floral parts.

In Singapore, it usually feeds on tiup tiup (Adinandra dumosa) in the secondary forest.
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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

1D. Reproduction

The lesser dog-faced fruit bat is polygynous, meaning that one male mates with more than one female partner. Similar to humans, both the male and female take care of their young. Females will reach sexual maturation at about 6 to 8 months, while males mature sexually later at about one-year old. The gestation period lasts approximately 14 to 16 weeks, after which nursing of young takes a surprisingly short 6 to 8 weeks. Mammals such as humans have gestation period of about 38 to 42 weeks, after which nursing of young takes years typically ranging from 16 to 21 years depending on culture.

Usually there is only one offspring per litter, with average of two litters per year. However, the mating season is dependent on location.

Different species of bats have different baculum structures!
The bone of the reproductive organ of male bats, namely baculum, can be used to determine different species of bats. In this instance, the lesser dog-faced fruit bat has a triangular shaped baculum located in glans dorsal to urethra (Krutzsch 1959).
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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

2. Description

Lesser_Dog-faced_Fruit_Bat.png

The Cynopterus brachyotis is the most common fruit bat to be found in Singapore. It belongs to the Megachiroptera suborder which are frugivores with long heads, long jaws, and large eyes for excellent vision. As a result, they do not require to use echolocation for navigation in the twilight and in caves.

Cynopterus brachyotis22.jpg
Taken from Wikimedia Commons, under Creative Commons

Although Megachiroptera refers to megabats, they are not necessarily huge in size and can range from as small as 6 cm to as large as having a wingspan of 1.7m and weighing up to 1.6kg. Of the Megachiroptera, the lesser dog-faced fruit bat is considered relatively small.

Interestingly, it has a lifespan of 20 to 30 years albeit possessing high basal metabolism rates, similar to other frugivorous species (McNab, 1989).


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Can you guess which one is the lesser dog-faced fruit bat?
Cynopterus branchyotis4.jpeg
Image from Wikimedia Commons

Black Flying Fox.jpg
Image from Wikimedia Commons

Pteropus_conspicillatus_with_baby.jpg
Image from Wikimedia Commons

BAT [A]
BAT [B]
BAT [C]
  • Small size
  • White wing bones
  • White edges of ears
  • Distinct collar
  • Short black hair
  • Large size with wingspan of more than 1m
  • Large size
  • Pale yellow fur around eyes

That's right! Bat [A] is the lesser dog-faced fruit bat.

Bat [A] : Lesser Dog-faced Fruit Bat, Cynopterus brachyotis
Bat [B] : Black Flying Fox, Pteropus alecto
Bat [C] : Spectacled Flying Fox, Pteropis conspicillatus


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How to know which one is the lesser dog-faced fruit bat?
Lesser dog-faced fruit bats typically mature between 70 to 127 millimetres for head and body, with an average wingspan of about 370 millimetres and average wing area of 21 cm2 (Hodgkison et al, 2004). At such a small size, it weighs only about 21 to 45 grams. The greyish young will develop into brown adults with collars, where the males have darker orange collars and the females have yellow collars. You can see that it gets its name from the characteristic long dog face and jaw which is obvious in the pictures below! Other features include dark spotted wings, white edges of ears and wing bones, long forearms of 55 to 92 millimetres, a small tail of about 6 to 15 millimetres and of course, large eyes.
Cynopterus branchyotis9.jpg
Image of Juvenile. Taken by The Darwin Initative Centre For Bat Research, under CC BY-NC-SA

Cynopterus brachyotis11.png
Image of Adult. Taken from Wikimedia Commons

Juvenile
Fur colour: Grey
Collar: No distinct collar
Adult
Fur colour: Brown
Collar: Females have yellow collars while males have dark orange collars


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Cynopterus branchyotis6.jpg
Taken by Phil Myers, under Creative Commons Attribution-Noncommercial-Share Alike

Cynopterus branchyotis8.jpg
Taken by Phil Myers, under Creative Commons Attribution-Noncommercial-Share Alike

Cynopterus branchyotis7.jpg
Taken by Phil Myers, under Creative Commons Attribution-Noncommercial-Share Alike

In the picture on the left, you can see the huge eye sockets in comparison to the skull for positioning the large eyes that allow the lesser dog-faced fruit bat to see well in the dark.
In the picture at the middle showing the underside of the skull, the long dog face is because of the elongated bony palate which forms the top of the mouth.
In the picture on the right, you can see the flat quadrate teeth adapted for biting through hard fruit skins and crushing fruits to bits.
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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

3. Distribution & Habitat

Mangroves-singapore.jpg
Mangroves. Taken by Mar Davies, under Creative Commons
Bukit-timah-singapore.jpg
Bukit Timah Primary Forest. Taken from Wikimedia Commons
Cynopterus branchyotis Distribution Map.png
Lesser dog-faced fruit bats can be found mainly in Southeast Asia and India. Areas include:


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Cynopterus brachyotis15.jpg
Lesser dog-faced fruit bat on palm tree. Image by Morten Strange, under Creative Commons

Cynopterus branchyotis5.jpeg

In Singapore, they can be found in a diverse array of landscapes ranging from rural to urban areas.
This includes:


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3 Tips to Help You Spot Your First Lesser Dog-faced Fruit Bat
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Crescent moon. Image from Creative Commons.

When is the best time?

How to know a lesser dog-faced fruit bat is nearby?

Where to search for better chances of finding one?




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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

4. Importance of bats around the world


Fruit bats are important seed dispersers!
The lesser dog-faced fruit bat is an important seed disperser and also a plant pollinator. It is able to retain viable seeds in gut for more than 12 hours, allowing long-distance seed disperser (Shilton et al. 1999). The mode of seed dispersal includes defecating or dropping seeds in flight, dispersing seeds over large areas (Tan et al, 1998). One study showed that this species of bats were able to disperse half of tree's original seed within a range of approximately 20 to 30m (Reiter et al. 2006) .

In Malaysia, the Ficus fistulosa is a key component in the diet of the lesser dog-faced fruit bat. So, the seeds of the Ficus fistulosa are mainly dispersed by the lesser dog-faced fruit bat with high percentage of germination (96 to 100% depending on the condition of seed after feeding) (Hodgkison et al, 2003). Hence there is a mutualistic relationship between the lesser dog-faced fruit bat and the Ficus fistulosa. In Singapore, a similar mutualistic relationship is seen between the lesser dog-faced fruit bat and the tiup tiup (Adinandra dumosa) (Phua et al. 1989).

In general, bats can also serve as indicator species to monitor biodiversity. More information can be obtained here.
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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

5. Conservation

LeastConcern.png

The lesser dog-faced fruit bat is categorised as of "least concern" because of its extensive presence in Southeast Asia and India, its ability to thrive in a diverse range of habitats (even in people's houses!) and its presumed large population. Also, its population numbers are not declining rapidly enough to qualify as being threatened. The slow decline in population numbers is primarily due to habitat loss from deforestation for timber and oil palm plantations. Even worse, conservation efforts for the lesser dog-faced fruit bat is poor as it is often seen as crop pests due to damage to fruit crops.

However, there are conservation programmes present for fruit bats around the world. They include scientific and charitable groups which help for bat monitoring, and local educational programmes. One example is bat cloud.
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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

6. Taxonomy

6A. Type Specimen

Definition of Type specimen: A type specimen is a physical specimen in which the scientific name of every taxon is based on.

The type specimen for this species is collected in Dewei river in Borneo, and described by Muller in 1938. However, the current location of the type specimen is unknown.


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6B. Phylogenetics


Species level phylogeny of bats
Cynopterus brachyotis-tree of life.jpg
Image from Tree of Life


Tree of life is constructed using Cytochome b sequences for 648 bats, including 550 named species. This data supports the division of bats into megachiroptera and micrchroptera during evolution. This tree serves to approximate the species level phylogeny of bat Chiroptera until other detailed species level phylogenies are available.



Cynopterus brachyotis phylogenetic tree.png
(Bastian et al. 2003)

Phylogenetic relationships between the species of Megachiroptera are investigated using complete cytochrome b genes sequences, with samples collected from islands of Luzon and Mindanao in Philippines. The phylogenetic tree, generated using both neighbor joining and maximum likelihood methods, shows close evolutionary relationship between Cynopterus brachyotis, Ptenochirus jagori and Pteropus vampyrus.


Status of Cynopterus brachyotis as a single species
The current state of Cynopterus brachyotis is uncertain due to variations of bats, namely in size and colour, that is present in the species.
phylogenetic tree 2.png
(Campbell et al. 2004)


Research by (Campbell et al. 2004) has shown that Cynopterus brachyotis comprises of a complex of distinct lineages. In the figure above, two alternative phylogenetic hypothesis has been constructed using cytochome b. Although the position on the tree and the evolutionary relationships within the clades differ significantly, 6 distinct lineages within this species has been shown clearly and they are named according to their place of origin as follows: Forest, Sunda, India, Myanmar,Sulawesi and Philippines. In addition, C. sphinx and C. horsfieldi also formed monophyletic groups within C. brachyotis species complex.

Four lineages from India, Myanmar, Sulawesi and Philippines are well defined geographically. However, two lineages in Malaysia, Sunda and Forest are sympatric and ecologically distinct. Hence, these two lineages are thus further investigated.

Cynopterus brachyotis-tree.jpg
(Abdullah et al. 2006)


Another research has also shown that there are different morphological forms in Cynopterus brachyotis in Kubah National Park in Malaysia. The morphological measurements used as character states include ear length, tail length, body length and wing span. Using UPGMA cluster analysis on these morphological features, the figure above shows that the small form and large form of Cynopterus brachyotis lies in two distinct clades. Cynopterus brachyotis belonging to the large form clade in the Sunda lineage is found in open areas, orchards and argicultural areas while the smaller form in the Forest lineage is confined in closed habitat or primary forest.

In addition, the type specimen of Cynopterus brachyotis is clustered together with the large form of Cynopterus brachyotis.

In support of this findings, micro-satellite data also showed the presence of two lineages in Southern Thailand, Malaysia and Borneo (Fong PH. 2011).

phylogenetic tree.png
(Jayaraj et al. 2012)


Cynopterus brachyotis-morphology.png
Morphological measurements(Jayaraj et al. 2012)


Another model was also done to differentiate the fruit bats of C. horsfieldii, Sunda and Forest lineages in Malaysia. As the forearm length is usually employed to distinguish these two lineages during field studies, it will not have high accuracy due to variations in forearm length measurements. Thus, this study (Jayaraj et al. 2012) tried to develop a list of features to attempt to classify the lineages for both field studies and museum specimens. These features include skull, dental and external measurements. UGPMA cluster analysis of 28 characters on morphological measurements showed separate clades of C. horsfieldii, C.cf.brachyotis Forest and Cynopterus brachyotis.

In conclusion, more research has to be done to further identify and correctly separate the lineages within Cynopterus brachyotis species. Conservation has to be planned to ensure that all six form do not go extinct. The two lineages Indian and Forest are restricted within the forest habitat, which is becoming increasingly fragmented due to forest loss, thus having higher risks of being endangered.

6C. Gene Sequence


There are 25 barcode sequences of Cynopterus brachyotis from BOLD and GenBank. Example of these sequences include COX1 and cytochrome B. More information can be obtained here.

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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

Thank for reading my page! Have a nice day!
Baby Fruit Bat.png

Are you still interested in learning more about bats?
Learn more about Bats and Biodiversity here!

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1. Ecology | 2. Description | 3. Distribution & Habitat | 4. Importance of bats around the world | 5. Conservation | 6. Taxonomy | 7. References |

7. References


Abdullah MT, Jayarajand VK and Abdullah M.T. Preliminary investigation on the validation of Small and Large Forms of Cynopterus brachyotis in Malaysia. Sarawak Museum Journal 62: 223-236.

Bastian T. Severo, Jr., Kazuaki Tanaka, Rea Victoria P. Anunciado, Nelson G. Natural, Augusto C. Sumalde, and Takao Namikawa. 2003. Phylogenetic relationships among megachiropteran species from the two major islands of the Philippines, deduced from DNA sequences of the cytochrome b gene. Can. J. Zool. 79: 1671 - 1677.

Brian K. McNab. 1989. Temperature Regulation and Rate of Metabolism in Three Bornean Bats. Journal of Mammalogy. Vol. 70, No. 1. pp. 153-161

Campbell P, Schneider CJ, Adnan AM, Zubaid A, Kunz TH. 2004. Phylogeny and phylogeography of Old World fruit bats in Cynopterus brachyotis complex. Mol Phylogenetic Evolution 33 (3): 764 - 781.

Gloriana Chaverri and Thomas H. Kunz. 2006. Roosting Ecology of the Tent-Roosting Bat Artibeus watsoni (Chiroptera: Phyllostomidae) in Southwestern Costa Rica. Biotropica. Vol. 38, No. 1. pp. 77-84

Heffner R. S, Koay G., Heffner H. E. 2008. Sound localization Acuity and its Relation to Vision in large and Small Fruit-eating bats: Non-ecolocating species, Eidolon helvum and Cynopterus brachyotis. Hear Res. 241 (1-2): 80 - 86.

Hodgkison Robert, Balding Sharon T. , Akbar Zubaid and Thomas H. Kunz. 2004. Habitat Structure, Wing Morphology, and the Vertical Stratification of Malaysian Fruit Bats (Megachiroptera: Pteropodidae). Journal of Tropical Ecology , Vol. 20, No. 6. pp. 667-673

J. Reiter, E. Curio, B. Tacud, H. Urbina and F. Geronimo. 2006. Tracking Bat-Dispersed Seeds Using Fluorescent Pigment. Biotropica , Vol. 38, No. 1. pp. 64-68

Jayaraj V.K., Charlie J. Laman and Mohd T. Abdullah. 2012. A Predictive Model to Differentiate the Fruit Bats Cynopterus brachyotis and C. cf. brachyotis Forests from Malaysia using Multivariate Analysis. Zoological Studies 51 (2): 259 - 271.

Philip H. Krutzsch. 1959. Variation in the Os Penis of Tropical Fruit Bats. Journal of Mammalogy , Vol. 40, No. 3 (Aug., 1959), pp. 387-392

Phua, P.B. & Corlett, R.T., 1989. Seed Dispersal by the Lesser Short-nosed Fruit Bat (Cynopterus brachyotis, Pteropodidae, Megachiroptera). Malayan Nature Journal, 42: 251-256.

Robert Hodgkison, Sharon T. Balding, Akbar Zubaid and Thomas H. Kunz. 2003. Fruit Bats (Chiroptera: Pteropodidae) as Seed Dispersers and Pollinators in a Lowland Malaysian Rain Forest. Biotropica , Vol. 35, No. 4. pp. 491-502

Shilton L. A, Altringham J. D, Compton S. G, Whittaker R. J. 1999. Old World fruit bats can be long-distance seed disperser through extended retention of viable seeds in the gut. Proc Biol Sci. 266 (1416): 219.

Tan K. H , A. Zubaid & T.H. Kunz. 1997. Tent construction and socialorganization in Cynopterus brachyotis (Muller) (Chiroptera: Pteropodidae) in Peninsular Malaysia,Journal of Natural History, 31:11, 1605-1621

Tan, K.H., Zubaid, A. and Kunz, T.H. 1998. Food habits of Cynopterus brachyotis in Peninsular Malaysia. Journal of Tropical Ecology, 14: 299 - 307.

Tan K. H, A. Zubaid, T. H. Kunz. 2000. Fruit dispersal by Lesser Dog-faced Fruit Bat. Malayan Natural Journal, 54:1, 57-62.