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Small Mammal Mail: Newsletter Celebrating The Most Useful Yet Most Neglected Mammals
Small Mammal Mail: Newsletter Celebrating The Most Useful Yet Most Neglected Mammals
Contents
Abstract
Lesser False Vampire Bat
(Megaderma spasma) has been
reported from various locations in
Indian subcontinent. In India,
there are reports on its
distribution from eastern, central
and southern states. This report
comprises of observations made
on M. spasma roost located on
the edge of Ratanmahal Wildlife
Sanctuary, Gujarat. This roost
comprised of 12 bats residing on
the underside of a tall community
water tank. Presence of wings of
grasshoppers and partially eaten
remains of unidentified insects
strewed on the floor provided
some evidence on diet Fig 1. M. spasma roost at Kanjeta village, near Ratanmahal Wildlife
preferences. This roost is Sanctuary, Central Gujarat, India
currently being monitored on a
seasonal basis.
Introduction
Chiropterans form one of the
largest congregations and
comprise of 25% of the total
existing mammalian species
(Mickleburgh et al., 2002), yet
they remain elusive due to their
nocturnal behaviour and secretive
lifestyle (Devkar et al 2013). The
forested areas of Central Gujarat
(western India) comprises of dry
deciduous habitats interspersed
with agricultural fields and
semiarid landscapes (Mistry 1997;
Devkar et al 2011). Lesser false
vampire bats (Megaderma
spasma, Linnaeus, 1758) are
widely distributed in south Asian
region from Philippines to Brunei
Darussalam stretching across
Indonesia, Malaysia, Myanmar,
Cambodia, Singapore, Sri Lanka,
Fig 2. Facial details of M. spasma
Bangladesh and India (Csorba et
al. 2011). In India, its
distribution has been reported Apart from an isolated report of
from Andaman & Nicobar Islands, Alam (2010) on sighting of M.
Andhra Pradesh, Assam, Goa, spasma from Gir National Park 1
Department of Zoology, Faculty of
Karnataka, Kerala, Maharashtra, and Sanctuary, there are no Science, The M.S.University of Baroda,
Vadodara.
Meghalaya, Mizoram, Tamil Nadu, reports on its distribution in 2
B 104, Premsagar Apartment, Nr.
West Bengal (Molur et al. 2002) Gujarat. Rameshwar Temple, Ellora Park,
Vadodara, Gujarat. Email:
and Odisha (Debata et al 2013). rvdevkar@rediffmail.com
Abstract
The Indian Crested Porcupine Hystrix indica is a
large rodent ranging across most of India and West
Asia (Menon 2003, Alkon and Saltz 1988). No
studies have been done on its presence and
distribution in the Eastern Ghats. The present note
is to report the first camera trap records of the
occurrence of the Hystrix indica from the Papikonda
National Park, in the northern Eastern Ghats of
Andhra Pradesh.
Introduction
The genus Hystrix includes eight species of noctural,
medium sized rodents equipped with quills,
belonging to the Mammalian order Rodentia, ranging
across Asia and Africa (Alkon and Saltz 1985, Alkon Indian Crested Porcupine Hystrix indica in location 1
and Saltz 1988, Corbet 1978). The Indian Crested
Porcupine Hystrix indica Kerr, 1792 is the only
member of its genus found in India, and occurs
widely throughout most of the country (Menon
2004, Johnsingh 2013). H. indica is classified as
Least Concern by the IUCN with a stable population
trend, although habitat loss could be potentially
affecting their population. There have been few
studies on their presence, distribution or ecology in
the Eastern Ghats, and none in the northern Eastern
Ghats (Srinivasulu and Nagulu 2002). The current
note records the occurrence of H. indica through the
first camera trap images in Papikonda National Park
(NP), located in the northern Eastern Ghats in
Andhra Pradesh.
References:
Alkon, P.U. and D. Saltz (1985). Potatoes and the
nutritional ecology of crested porcupines in a desert biome.
Journal of Applied Ecology 22, 727-737.
Abstract
This report is based on
investigation undertaken to study
the rodent diversity of Navegaon
National Park, district Gondia,
Maharashtra state; conducted
from January 2010 to December
2011. The study reports 14
rodent species under 10 genera of
3 families from the study area.
The standard size live traps were
used for trapping of the rodents,
whereas arboreal rodents were
observed with the help of
binoculars.
Introduction: Rodentia is a
largest order of mammals Fig 1. Indian Giant Squirrel
comprising 2277 species in 481
genera under 33 families (Wilson can be used as indicator consolidated account published on
and Reeder 2005). Rodents monitoring the distribution as well rodents is known from this study
include squirrels, rats, mice, as the density to indicate the area. The present investigation
voles, gerbils, hamsters, health of biotic system (William reports 14 species under 10
dormices, porcupines etc. They and Lidickes, 1989). The earliest genera of 03 families (Table 1).
are all mainly herbivores and their consolidated accounts on Indian
modes of feeding habits include rodents are available from the Material and Methods
gnawing, scraping or nibbling. works of Blyth (1863), Jerdon Study Area
Rodents are economically (1867), Sterndale (1884) and Navegaon National park is one of
important as some of them are Blanford (1888, 1891); which the well known nature reserve in
serious pests destroying crops, were further enhanced by the Vidarbha, situated in Gondia
fruit gardens, orchards, stored mammalian survey of India, district of eastern Maharashtra. It
food grains. Moreover they cause Myanmar and Ceylon through the lies between 20 45’ to 20 2’ N and
damage to the properties of collections during first quarter of 80 5’ to 80 15’ E. The study area
various kinds resulting in huge 20thcentury, organized by Bombay is located in Gondia wildlife
economic losses. Some of them Natural History Society (BNHS). division and surrounded by small
are carriers of serious diseases Later some of these reports were villages. Villagers graze their
like plague, leptospirosis, murine summarized in the form of key for cattle on the available grassland
typhus, etc. They have high identification & distribution by and forest area.
breeding rate and many show Wroughton (1918-1920). Out of
periodic increase in the population 33 families of rodents found in the Methodology
commencing with the availability world, seven families namely Field surveys were carried out in
of food. Sciuridae, Dipodidae, the fringe areas of Navegaon
Platacanthormyidae, Spalacidae, national park to trap rodents. The
Rodents are important link in food Cricetidae, Muridae and presences of squirrels were
chain between plants and the Hystricidae occur in India. Family ascertained by direct sightings, by
carnivorous predators hence it Muridae is the largest family hearing calls. To trap rodent
plays an important role in represented in India by 21 genera other than arboreal, live traps
ecosystems. One of the and 56 species followed by family were being used in different
important things is that rodent Suiuridae having 13 genera and
species always prefer a specific 27 species (Pradhan & Talmale,
1
habitat throughout its life than Assistant Professor Department of
2011). Navegaon National Park Zoology S.S.J. College, Arjuni/ Mor,
using the complex environmental because of its habitat richness Dist- Gondia
2
measures that define a particular Assistant Professor Department of
supports diversified fauna. Zoology M.B. Patel College, Deori, Dist-
habitat. Hence, certain rodents Perusal of literature shows no Gondia. Email: gpaliwal197@gmail.com
(Corresponding author)
Table 1. Systematic list of rodent species reported from Navegaon National Park.
Family: Muridae
5 Mus musculus castaneus House Mouse Undir C Sch: V
(Waterhouse)
6 Mus b. booduga (Gray) Little Field Mouse Shetatil Undir C Sch: V
7 Mus phillipsi (Wroughton) Small Spiny Mouse Undir U Sch: V
8 Rattus r. rufescens (Gray) House Rat Undir C Sch: V
9 Cremnomys blanfordi (Thomas) Branford’s White Tailed Undir U Sch: V
Mouse
10 Golunda e. ellioti (Gray) Indian Bush Rat Undir U Sch: V
13 Tetra indica indica (Hardiwicke) Indian Antelope Rat Gondedar Shepticha Undir C Sch: V
Family: Hystricidae
14 Hystrix indica (Kerr) Indian Porcupine Salinder U Sch:IV
Datta, A. and S.P. Goyal (2008). Responses of diurnal Wroughton, R.C. (1920). Summary of the results from
tree squirrels to selective logging in western Arunachal the Indian Mammal Survey of the Bombay Natural History
Pradesh. Current Science, 95 (7): 895-902. Society, Part III-VI. J. Bombay nay Hist. Soc., Part III,
26(2): 338-379; pt V, 26 (4): 955-967; pt VI, 27 (I):
57-85.
Bhati, U.S. (1988). Occurrence of an albino Rat-tailed Kahrau, W. (1972). Australian caves and caving.
Bat, Rhinopoma microphyllum kinneari Wroughton in the Perwinkle Books.
Indian Desert. J. Bombay Nat. Hist. Soc.,85(3): 608
Karim, K.B. (1983). A note on albino Rousettus
Devkar, R.V., S. Jayaraman, K. Upadhyay and P. Patel leschenaulti.Bat Res, News, 24(4):39-40.
(2011). Albino microchiropteran
Rhinopoma microphyllum Kinneri sighted in a bat colony Khajuria, H. (1973). Albinism in the lesser Rat-tailed Bat
inhabiting abandoned mines.Current Science, 100 (2): Rhinopoma h.harwickei Gray (Chiroptera:
165-166. Rhinopomatidae.) J. Bombay Nat. Hist. Soc., 70 (2): 197.
Herried, C.F. and R.B. Davis (1960). Frequency and Khajuria, H. (1984). Notes on some Central Indian Bats.
placement of white fur on free-tailed bats. J. Mammal., J. Zoological Society of India, 36 (1&2): 125-126.
41:117-119.
Setzer, H.W. (1950). Albinism in bats. J. Mammal.,
Howell, K.M. (1980). Abnormal white colouration in three 31:350.
species of insectivorous African bats J. Zool. Lond., 191:
424-427 Smith, H.C. (1982). An albino little Brown Bat, Myotis
lucifugus from Aberto. Canada. Field Natur’., 96:217
Hsu, M.J. (2003). Albinism in Japanese House Bat
Pipistrellus abramus and the Formosan Uieda, W. (2000). A review of complete albinism in bats
leafnosed bat Hipposideros terasensis in Taiwan. with five new cases from Brazil.
Mammalia, 67(3); 451-453. Acta. Chiropt. 2: 97-106.
Melselvanur-Keelselvanur is a
famous location for the migratory
birds situated in the Kadaladi
Taluk (9° 13´N and 78° 32´E) of
the Ramnathapuram District,
Tamil Nadu. This place is being
used for nesting for more than
100 years largely Pelicans
(Pelecanus philippensis) and
Painted Stork (Mycteria
leucocephala). However many
ground nesting birds like Yellow-
wattled Lapwing (Vanellus
malabaricus) are also found in
this Bird Sanctuary. It is the
centre point of this district and is
one of the most important
tourism destinations in the district
[1]
.
Table: 1. Roost tree details of Indian cattle grazing and fire wood acuminata) is partially cultivated
Flying Fox recorded in Melselvanur- collection is strictly prohibited by local people which may attract
Keelselvanur Bird Sanctuary on 7th within the sanctuary. Many the foxes to roost in the
December 2013.
villages found nearby Bird sanctuary. Indigenous tribes are
Sanctuary within the radius of not found in this area and the
Tree No. of No. of
height in trees roosting bats 5km and banana (Musa local people are not harming to
Meters
8-10 1 130 Care Earth Trust, No. 3, 6th Street, Thillai Ganga Nagar, Nanganallur, Chennai.
Department of Zoology, Madras Christian College, Chennai. Email:
10-12 1 140 wildlife9protect@gmail.com
References
Molur, S., C. Srinivasulu, P. Bates
& C. Francis (2008). Pteropus
giganteus. The IUCN Red List of
Threatened Species. Version 2014.3.
<www.iucnredlist.org>. Downloaded
on 2 Feb 2014.
New Members
References
Feeroz, M.M. (eds). (2013).
Biodiversity of Chunati Wildlife
Sanctuary: Fauna. Arannayk
Foundation and Bangladesh Forest
Department, Dhaka, Bangladesh,
200pp.
The rapid assessment on flora Map 1. Bhutan's Protected Area map showing map of Thrumshingla National
and fauna in the park was first Park (Red line circle)
initiated in 1999-2001. The
record shows that there are 622
plant species, 68 species of
mammals and 337 species of
birds in the park (Doji, et al.
(2007). Thereafter, no specific
survey has been conducted on the
mammals in the park. Due to the
presence of prey species in the
two major rivers passing through
the park, the park is therefore
potentially known to occur Otters
but only one species of Otter
(Common Otter Lutra lutra) was
recorded during the survey in
1999-2001. The recent sighting
of Oriental Small-Clawed Otter or
Asian Small-Clawed Otter (Aonyx
cinerea) is a new record in the
area and for the park. The park
now has two species of Otters;
Common Otter (Lutra lutra) and
Oriental Small-Clawed Otter Map 2. Google earth map showing the location where Asian Small-Clawed
Otter was spotted
(Aonyx cinerea).
! A!
References
Dorji, T., N. Norbu, P. Dendup, T.B. Thapa, K.
Gyeltshen (2007). Mammals in Thrumshingla
National Park, A Rapid Assessment Report.
! B!
Reference
Fig 3. One
Ali, A. (2013). Indian Flying Fox of
Cesalpiniaceae
Assam. Scholars’ Press, Germany. plant near the
136pp roosting site
with fruits
*
Faculty Member, Institute of Forestry, Pokhara, Campus, Nepal.
Email: armalepushpa@gmail.com
Department of Biology, Prince of Songkla University, Hat Yai Thailand Centre for Ecology and Conservation,
University of Exeter in Cornwall, UK. Email: armalepushpa@gmail.com
Abstract
Eonycteris spelaea is recognized as the principal pollinator of most chiropterophilous plants in
SE Asia. The present study describes its feeding behaviour and clarifies its role in cross
pollinating these highly self-incompatible plants. Ten individuals of E. spelaea were radio-tracked
during the flowering period of durian (Durio zibethmus) and petai (Parkia speaosa) in an
agricultural mosaic in southern Thailand. Eonycteris spelaea makes a mean of seven visits per
hour to these trees and 80-86% of each feeding bout involves visits to multiple conspecific
trees. During each visit, 93% of D. zibethmus stigmas and 50% of-P. speaosa stigmas were
loaded with conspecific pollen. Eonycteris spelaea was the most common bat visitor to the
trees. High visitation frequency and conspecific pollen deposition by E. spelaea to D. zibethmus
and P. speaosa indicates that this nectarivorous bat is an effective pollinator. Mixed planting of
chiropterophilous trees in fruit orchards is recommended to ensure regular visits of E. spelaea.
Protecting natural roost caves of E. spelaea is also essential in order to maintain the vital
ecosystem service provided by these bats.
Published in Journal of Pollination Ecology, Volume 15, Number 7, 2015, Pp. 44-50.
Website: http://www.pollinationecology.org/index.php
journal=jpe&page=article&op=view&path[0]=321&path[1]=111
Gulab Bagh in Udaipur city contains around 20,000-25000 macrochiropterans and is one of the
largest colony of Pteropus giganteus in Asiatic region. Investigations regarding bacterial
pathogens with potential for mutual transmission between bats and humans are sparse.
Gastrointestinal flora plays an important role in the health status of the host. In the present
study Enterococcus species (KF777815) was identified, isolated and characterized from fecal
contents of Pteropus giganteus inhabiting Gulab Bagh. Enterococcus species has been reported
to be responsible for a number of debilitating conditions in humans such as infections of the
urinary tract and also nosocomial infections, which could be life threatening in nature. The
presence of this microorganism in the gastrointestinal tract of Pteropus giganteus delineates a
novel mode of its transmission, not discussed till date.
Abstract
Fifty Sherman traps were used
for carrying out the study. A total
of six transects were laid in six
different habitat types along the
elevational gradients. Traps were
baited and kept for three
consecutive nights in each habitat
types. With 900 trap nights
spent in six habitat types, six
species of rodents were captured
and identified. The number of
individual capture was high for
Niviventer niviventer (50.4%, n=
64) and low for Dremomys
lokriah (0.79%, n= 1). From 6
habitat types, 127 individuals (25
Sikkim Mouse, Mus pahari; 64 Sikkim Rat (Rattus sikkimensis)
White-bellied Rat, Niviventer
niviventer; 4 Sikkim Rat, Rattus
sikkimensis; 1 Orange-bellied
Himalayan Squirrel, Dremomys
lokriah; and 11 Common House
Rat, Rattus rattus were captured.
All the species except Dremomys
lokriah were new record for the
Park. Among six species, Mus
pahari was the only species
captured in warm broadleaved
forest at the lowest elevation and
Niviventer eha in mixed conifer
and fir forest at the highest
elevations (M= 2234.09, SD=
563.259). Mus pahari was
recorded only from a single site in
the warm broadleaf forest.
Rattus rattus was found only in
Common House Rat (Rattus rattus)
dryland and likewise Dremomys
lokriah in bamboo forest. Species
Similarly, significant association of vegetation (Witmer, 2004).
richness (R= 1.23) was high in
was found between species They provide an essential prey
the higher elevations and low (R=
diversity and vegetation cover, r= base for many species of
0) in the lower elevations. Species
0.212, p< .001. predators. Many rodents, such as
diversity was very low (H'=
0.19-0.86) for all the habitat mice and voles, are important
Introduction food sources for predators like
types. However, Evenness Index
Rodents play very important role raptors, snakes and other small
was very high (E= 0.96) for dry
in the forest ecosystem in felids, making them a vital part of
land, medium for bamboo forest
dispersal of seed and spores, the ecosystem (DW, n.d).
(H'= 0.39) and low (E= 0.28) for
nutrient cycling and Rodents are important
wetland. Statistical analyses
decomposition through
showed that there were significant
consumption and shedding of *
Phrumsengla National Park,
association between species Department of Forest and Park
vegetation and also play an
diversity and habitat types, r= Services, Ministry of Agriculture and
important role in determining Forests, Royal Government of Bhutan.
0.396, p< .001, between species Email: jangyel_mangdip@yahoo.com
and elevation, r=0.536, p< .001. forest, structure, and succession (corresponding author)
Table 2: Diversity and species richness indices across six habitat types
Table 3. Length and weight data of six captured species in six habitat types
(TL= Tail length, EL= Ear length, HL= Head length, BL= Body length, Wt= Weight)
Species TL1 (Cm) EL2 (Cm) HL3 (Cm) BL4 (Cm) Wt5 (g)
Mean+SD (n) Mean+SD (n) Mean+SD (n) Mean+SD (n) Mean+SD (n)
M.pahari 6.78+0.52 (25) 0.96+0.25 (25) 2.04+0.39 (25) 7.24+0.76 (25) 13.82+2.47 (25)
N.niviventer 16.66+1.85 (65) 1.41+0.47 (65) 3.19+0.88 (65) 11.15+3.47 (65) 134.7+57.78 (25)
R.sikkimensis 16.13+1.31 (3) 1.48+0.34 (3) 3.43+0.79 (3) 14.0+3.39 (3) 157.50+40.31 (3)
N.eha 15.59+1.30 (22) 1.35+0.53 (22) 3.18+0.48 (22) 12.27+1.43 (22) 134.82+54.32 (22)
R.rattus 13.77+0.94 (11) 2.53+3.18 (11) 3.18+0.46 (11) 12.71+1.01 (11) 180.0+8.94 (11)
D.lokriah 18.00 (1) 2.80 (1) 4.50 (1) 18.00 (1) 200.00 (1)
1.Orange bellied Himalayan squirrel Rodentia Scuridae Callosciurinae Bangladesh, Bhutan, Least Concern
(Dremomys lokriah) India, Nepal
2.Himalayan White-bellied Rat Rodentia Muridae Murinae Bhutan, India, Nepal Least Concern
(Niviventer niviventer)
3.Little Himalayan Rat Rodentia Muridae Murinae India, Nepal Least Concern
(Niviventer eha )
4.Common House Rat Rodentia Muridae Murinae India, Bangladesh, Nepal, Least Concern
(Rattus rattus) Pakistan, Sri Lanka
5.Sikkim Rat Rodentia Muridae Murinae India, Nepal Least Concern
(Rattus sikkimensis)
6.Sikkim mouse Rodentia Muridae Murinae Bhutan, India Least Concern
(Mus pahari)
Further, the vegetation cover classes were areas in both the seasons (winter & summer) would
statistically analyzed to understand the strength of add more species list for the Park. Even, the current
relationship between species and vegetation cover study couldn’t cover alpine areas where some of the
class. The result shows that there was a significant species were reported to be present.
correlation between vegetation cover class of under-
story and the presence of species, r= 0.212 (p< In view of the above findings, the study
0.05) but has no correlation between species and recommends the following:
over-story vegetation cover class, r= 0.177 (p> • Similar study should be initiated during summer
0.05). This points out that for the rodents, under- season which would then supplement the present
storey vegetation cover is most important than the study conducted in winter season.
over-storey vegetation cover. Under-storey cover • Since this study couldn’t cover alpine areas,
can prevent rodents being exposed to predators and therefore, similar study is recommended for the
other dangers too. Corominas (2004) reported that alpine areas.
vegetation cover also provide food resources for • Mus pahari (Sikkim Mouse) is confirmed to be the
small mammals in the form of leaves, fruits, seeds restricted species captured only in warm
or insects. There was no strong significant broadleaved forest. Therefore, to protect and
correlation between average under-storey height of conserve this species, further study is needed on the
plants and average over-storey height of the plants, population status and habitat selection of Sikkim
r = 0.743 (p< 0.001). This illustrates that Mouse in the park. This would flag the current
irrespective of average height of overstorey and population status and conservation importance in its
understorey of a forest, rodents are found if there is habitats.
a good understorey cover. • Niviventer niviventer (White bellied rat) have wide
distribution range. Majority of individuals captured
Conclusions within study sites and outside study sites were
Ecological importance of rodents in the forest White bellied rat. Therefore, study on ecology and
ecosystem is understood very less by many distribution is felt necessary since this species may
foresters and public. In fact, rodent represents be important prey species for many of the iconic wild
major mammalian order on the earth. Conservation carnivores and raptors in the park.
of rodents would contribute to the conservation of • Strict monitoring and patrolling has to be carried
many wild carnivores and raptors. Due to the out by the park management in the Sikkim Mouse
diverse habitat present in Jigme Dorji National Park habitat at Tsorim Zampa to reduce disturbance and
(JDNP), the park seems to have more species of habitat destruction by the human activities.
rodents which are still undiscovered. The present • Since many species present were found out to be
study has been focused only in two Park Ranges long-tailed species, therefore use of Sherman trap
under JDNP. There are still three Park Range Offices size of 7.7 x 9.5 x 30.5 cm is recommended for
left where such study couldn’t cover. Covering those trapping rodents in Bhutan. Sherman trap size of 23
Introduction
The fulvous fruit bat, Rousettus leschenaultii Temperature, humidity and weather conditions were
(Megachiroptera: Pteropodidae) is a medium sized recorded every day morning inside the cage.
bat species (Body weight 92.50g; forearm length is Humidity in the day ranged from 95.32 to 98.64%
83mm) found in a variety of habitats ranging from and night from 95.29 to 99.15%. Day and night
tropical moist forest to urban environments. This temperature during study period ranged between
species roosts inside caves, old and ruined min 22.45oC and max 36oC and min 22.36oC and
buildings, temples, forts and disused tunnels. It is max 31.53oC respectively. Bats emerged from the
very widely distributed in South Asia, southern inner upper chamber to the open space of the cage
China and Southeast Asia. It lives in colonies every night for feeding the fruits. The timings of
consisting of a few to several thousands emergence of first bat and return of last bat were
(Sreenivasan and Bhat, 1974) and the colonies are observed and recorded for a period of three
often extremely noisy (Philips, 1980). R. consecutive years from 2000 to 2002 at weekly
leschenaulti uses tongue clicks as a crude form of interval and correlated with the timings of sunset
echolocation while navigating in the dark. They feed and sunrise respectively.
on fruits and flowers by using sense of olfaction as
seen in other megachiropteran bats. This bat plays Results
an important ecological role as a nocturnal pollinator This study reveals that in the captive colony of
and seed disperser. It exhibits two breeding cycles Rousettus leschenaultii, the timings of emergence of
in a year and bears a single young (Bates and first bat keep pace with the timings of sunset.
Harrison 1997). Similarly, the timings of return of the last bat keep
pace with the timings of sunrise. The circadian
In 1994, a huge colony of R. leschenaultii consisting periodicity of flight activity of the colony was ca. 24
of about 15,000 individuals was observed in a hours as seen in the natural habitats. A linear
temple premises at Cheranmahadevi in Tirunelveli pattern was demonstrated in the time of emergence
district, (Chandrasekaran and Marimuthu 1994). In of the first bat in relation to time of sunset
addition, 5 different colonies with a few thousands (y=1.1012x-0.0645; R=0.946), and the time of
of individuals roosting in temples and old buildings return of last bat to the time of sunrise (y=0.733x
were also observed in the study area. These +0.0608; R=0.878). During the breeding seasons,
colonies vanished in the vicinity within a short the bats emerge later and return earlier while
period due to renovation of these old structures and compared to the other months of the year. The
unavailability of preferred roosting sites. So we flight activity rhythm and the circadian periodicity
attempted to rear this bat species in semi-natural were also persisted throughout the study period of
conditions for the purpose of rehabilitation and three years from 2000 to 2002 (Figure 1).
conservation. During rearing of this bat population, Moreover, the fulvous fruit bats, R. leschenaultii,
we could observe persistence of circadian flight were healthy and well adapted to the captive
activity rhythm continuously for years. conditions, feeding on the local available fruits and
breeding during the seasons as found in the wild
Materials and Methods populations.
Field observations and survey of Rousettus
leschenaultii were performed in Tirunelveli district Discussion
since 1990 and captive rearing was carried out in The light-dark cycle is the most powerful entraining
Thrissur from 2000 to 2002, for the purpose of agent in synchronizing the activity-rest patterns of
convenience. In this study, 5 specimens (3 females animals especially the higher vertebrates (Aschoff et
and 2 males) were brought from Palayamkottai to al. 1982). The timings of sunset and sunrise and
Thrissur on October 1999. These bats were placed the onset and end of activity of the animals are used
in wire-mesh cage (dimension 3m x 2m x 1.3m). as reference points to compare and demonstrate
The cage was kept in an open courtyard of a house seasonal changes in their phase relationship
with a tile roof. Drinking water was kept on the (Aschoff et al. 1972; Chandrashekaran et al. 1983).
floor ad libitum and plantain slices were provided on In the wild, a similar pattern has been observed, in
the floor daily at about 6 p.m. All the females were
with pups on 05.02.2000 and again with pups on
29.06.2000 during second parturition. The captive 1&2
Kailath Tharavadu, Venginissery, Paralam, Thrissur,
Kerala.
population increased to 12 bats on 16.08.2001 and 3
Research Department of Zoology, St. John’s College,
subsequently to 19 individuals on 31.12.2002. Palayamkottai, Tamil Nadu. E.mail:
isaacsuthakar@yahoo.com
the timings of emergence and return of foraging for medicinal purposes and local consumption. It is
flight activity of R. leschenaultii as reported by King classified as a vermin under Schedule V of the
Immanuel (2002). In addition, the variation in Indian Wildlife (Protection) Act. In spite, it has been
emergence and return activity was influenced by the recorded from protected areas in India like
breeding season as reported for Pteropus giganteus Namdapha Biosphere in Arunachal Pradesh,
in the wild environment (Suthakar Isaac and Nagarhole Wildlife Sanctuary in Karnataka,
Sudhakaran, 2005). Sambalpur Wildlife Sanctuary in Orissa, Indravathi
National Park in Chattisgarh, Kanha National Park in
This species is more suitable for captive rearing and Madhya Pradesh. This species should be monitored
it is a good research specimen as this species can periodically to record changes in population
survive well in captive conditions and accept the dynamics and awareness activities are to be taken
local seasonal fruits. This bat also breeds twice a up to mitigate threats to this species.
year in captivity as seen in the wild populations. So
this bat species can be bred and rehabilitated where References:
these bat populations are dwindling and used as Aschoff, J., S. Daan, J. Figala, and K. Mueller (1972).
research specimen. Recently, this fulvous fruit bat Precision of entrained circadian activity rhythms under
has been used as non-primate laboratory models to natural photoperiodic conditions. Naturwissenschaften 6 :
276-277.
study menstruation and menstrual dysfunction
Aschoff, J., S. Daan, and K.I. Honma (1982).
(Zhang et al 2007).
Zeitgebers, entrainment and masking: some unsettled
question. In : Aschoff, J., Daan, S., and Groos G.A. (eds)
In South Asia, while majority of populations are Vertebrate circadian systems. Springer, Berlin Heidelberg,
generally stable, this species is locally threatened by pp 13-24 430.
human interference to roosting sites due to tourism Bates, P.J.J. and D.L. Harrison (1997). Bats of the
related developmental activities, loss of preferred Indian Subcontinent. Harrison Zoological Museum, Kent,
roosting sites, persecution by humans by means of xiv+268pp.
poisoning, fumigation activities and stoning, hunting
Continued on Page 39 ...
Painted Bat Kerivoula picta (Pallas, 1767) of Painted Bats from Maharashtra as well as from
(Vespertilionidae: Chiroptera) is relatively smallest different parts of India. Recently, Korad & Yardi
bat, comparable with the size of a large moth. It (2004) and Korad et al (2010) have recorded many
flies with up and down flutter like a moth. Fur is bat species during their surveys in Pune city and
bright orange on dorsal surface and warm buff on Pune district respectively. However, there are no
ventral surface with bright orange and black wings, sightings of any Painted Bat from these surveys.
makes this bat unmistakable. It has hairy face with Bates & Harrison (1997) have indicated that the
large, funnel- shaped ears. Despite of their bright Painted Bats are widely distributed. It seems that
colours, they are camouflaged in dead down- these bats have very patchy distribution in all over
hanging leaves of banana plants or other similar India. Hence, there is a need to undertake
hiding places where they roost during the daytime systematic surveys to study their distributional
either singly or occasionally in pairs. They feed on status, population ecology, breeding habits (except
small insects (Prater 1971, Bates & Harrison 1997, a note by Ramachandran & Jayson, 1994)
Menon 2003, Johnsingh & Manjrekar (Eds) 2013). throughout the India and particularly in Jalgaon and
These bats are listed as Least Concern as per The Dhulia districts (where huge areas are under banana
IUCN Red List of Threatened Species (2014). plantations) as well as in coastal and Western Ghats
districts of Maharashtra state.
Painted Bats are distributed in Indian Subcontinent
mostly in south-east Asia, Sri Lanka, Bangladesh Acknowledgments
and India. State-wise distribution in India is in Authors are thankful to Dr. P.S. Bhatnagar and Dr.
Assam, Sikkim, West Bengal, Orissa, S.S. Talmale, Scientists, Zoological Survey of India,
Andhra Pradesh, Tamil Nadu, Kerala, Karnataka, Pune and Jabalpur for their valuable suggestions.
Goa, Maharashtra and Rajasthan (Bates & Harrison Authors are also thankful to Mr. Rajiv Mule Sub-
1997, Alfred et al 2006, Pradhan & Talmale, 2012). Editor of “Lokmat” Satara for the information;
Menon (2003) has indicated that they occurred in Abhijit Nale, Datta Chavan, Vinay Chavan, Rahul
forest of Western Ghats and Assam. In all the Thombare, Atul Rajmane and Jitendra Patole team
above mentioned states there are hardly one or two of Wildlife Protection and Research Society Satara,
records of their occurrence (Bates & Harrison 1997). Maharashtra, for their support in the field work.
However, in the state of Maharashtra ten previous
records are available, mostly from Mumbai region, References
two from Satara and one each from Pune and Thane Alfred, J.R.B., A.K Das & A.K Sanyal (2006). Animals
districts (Table 1a). of India : Mammals. ENVIS-Zoological Survey of India,
236pp
There was a news (with photograph) in “Lokmat”- a Bates, P.J.J. & D.L. Harrison (1997). Bats of Indian
Subcontinent. Harrison Zoological Museum Publication,
Marathi Newspaper, Satara on 29th April, 2015 that a
Seven Oaks, Kent TN13 3AQ, England, 252pp.
local person observed a Painted Bat on the banana
Blanford, W.T. (1888-91). The Fauna of British India:
plant. So, the second author (AS) visited the place Mammalia. Taylor & Francis, London, 617 pp.
called Hamdabad village next evening on 30th April, Brosset, A. (1962). The Bat of Central and Western
2015 and he confirmed the occurrence of the India. Part 3. Journal of Bombay Natural History Society,
Painted Bat. Hence, it was then decided to 59 (3): 707-746
undertake preliminary survey in and around Satara Gavand, M. & N. Chaturvedi (1999). Status of Painted
to locate the presence of these bats, if any. During Bat Kerivoula Picta (Pallas, 1767) in Maharashtra. Journal
5th to 18th May, 2015 surveys were carried out of Bombay Natural History Society, 96 (2): 309
particularly in localities like Ajinkyatara Fort, IUCN (2014). IUCN Red List of Threatened Species.
Version 2014.3 www.iucnredlist.org downloaded on 22
Sajjangarh, Thoseghar, Chalkewadi, Patan and areas
March 2014.
between these hill ranges. Out of all these localities, Johnsingh, A.J.T. & N. Manjrekar (Eds) (2013). Bats.
Painted Bats were observed only in the area of In: Mammals of South Asia. Vol.1, 614 pp, Universal Press
Thoseghar village, on 16th May, 2015. Besides this, (India) Pvt. Ltd., Hyderabad.
recently a specimen collected at Patan, Satara
district by the 4th author (BVJ) has been deposited
in the collection of Zoological Survey of India, Pune. 1
Scientist (Retd.)Zoological Survey of India, W.R.C, Pune.
Email: mahabal.anil@gmail.com
All these recent additional records from Satara 2
Wildlife Protection and Research Society, Satara
district have been compiled in the (Table 1b). Email: amitsayyedsatara@gmail.com (corresponding author)
3
Scientist, Zoological Survey of India, W.R.C, Pune
Email: shrikantj123@yahoo.com
A perusal of literature revealed that there is no 4
Asstt. Professor, Department of Zoology Balasaheb Desai
much information available on distributional records College, Patan, Satara district, Maharashtra
Korad, V.S. & K.D. Yardi (2004). Ecological study and Conservation Status and Taxanomy. Publ.by Nature Books
faunistic survey of bats from Pune Corporation limits, India, Kolkata, 488 pp.
Maharashtra State, India. Records of Zoological Survey of Prater, S.H. (1971). The Book of Indian Mammlas. Third
India, 102 (1&2) : 115-136. (Revised) Edition, Bombay Natural History Society,
Korad, V.S., M.C. Gaikwad & A.L. Koratkar (2010). Bombay. 324 pp.
Studies on diversity, distribution and habitat preference of Ramchandran, K.K. & E.A. Jayson (1994). Note on the
Bat species in Pune district, Maharashtra. Records of breeding period of Painted Bat (Kerivoula picta). Journal of
Zoological Survey of India, Occassional Paper No. 311: Bombay Natural History Society, 91 (3): 447.
1-52. Talmale, S.S. (2007). Studies on Small Mammal Diversity
Menon, V. (2003). A Field Guide to Indian Mammals. in Maharashtra State. Thesis Submitted to University of
Dorling Kindersley (India) Pvt. Limited and Penguin Book Pune. 431 pp. (Unpublished, Personal Communication).
India (P) Ltd., Delhi, 201 pp Wroughton, R.C. (1916). Report No. 22: Koyna Valley
Pradhan, M.S. & S.S. Talmale (2012). Indian Mammals. [311-316]. Bombay Natural History Society’s Mammal
Checklist with Comments on Type Locality, Distribution, Survey of India, Burma and Ceylon. Journal of Bombay
Natural History Society, 24: 219-316.
Chandrashekaran, M.K. and G. Marimuthu (1994). A Sreenivasan, M.A. and H.R. Bhat (1974). Records of a
huge colony of the dog bat, Rousettus leschenaulti, in piebald fulvous fruitbat, Rousettus leschenaultia
South India. Bat Res. News 35(4): 82. (Desmarest). J. Bombay Nat. Hist. Soc. 71(30:598-600.
Chandrashekaran, M.K., R. Subbaraj and K. Sripathi Suthakar Isaac, S. and M.R. Sudhakaran (2005).
(1983). Reference phases and circadian rhythm. J Influence of breeding on the seasonal flight activity rhythm
Interdiscipl Cycle Res 14:43 52. in the Indian flying fox, Pteropus giganteus under natural
King Immanuel, J. (2002). Ecological studies on the conditions. Abstracts of the XVII National Symposium on
behavior of the Indian fulvus fruit bat, Rousettus Chronobiology. 1-3 October 2005, Banarus Hindu
leschenaulti (Chiroptera: Pteropodidae). Ph.D. thesis, University, Varanasi, India.
Manonmaniam Sundaranar University, Tirunelveli. Zhang, X., Cheng Zhu, Haiyan Lin, Qing Yang, Qizhi
Philips, W.W.A. (1980). Manual of the Mammals of Sri Ou, Yuchun Li, Zhong Chen, Paul Racey, Shuyi Zhang,
Lanka. Part I. Wildlife and Nature protection Society of Sri and Hongmei Wang (2007). Wild fulvous fruit bats
Lanka. 1-116. (Rousettus leschenaulti) exhibit human-like menstrual
cycle. Biology of Reproduction 77, 358–364.
Editor: Sally Walker; Technical Advisors: Sanjay Molur, B.A. Daniel, R. Marimuthu;
and Publication Assistants: Latha Ravikumar and Radhika Suresh.
CCINSA and RISCINSA are an activity of Zoo Outreach Organization (ZOO) and
Wildlife Information Liaison Development (WILD) in association with CBSG, South
Asia and RSG, South Asia.