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VARANUS BENGALENSIS (Bengal monitor):
UNUSUAL BEHAVIOUR AND FEEDING.
During July 2005, as part of the Knuckles
Expedition (De Silva, 2005), we conducted field
studies on thermoregulation in Calotes versicolor
at Hettipola (Meek et al., in press), an area that lies
on a flat plain at the edge of the Knuckles Massif
in Central Province, Sri Lanka. At the time of our
study, it was the dry season and operative
temperatures exceeded 40°C daily. We frequently
observed foraging V. bengalensis in the study area
and all the observations reported here relate to this
study site. Most sightings were after midday when
they appeared to be searching for prey species.
One lizard with an s.v. length of approximately 25
cm had a home site across from our hotel which
we often saw it return to either mid-afternoon or
evening. This individual was easily recognised
because of a damaged tail. One evening, an hour
or so after dark, one of us (E.J.) saw this individual
sitting partly outside its burrow in what appeared
to be a type of sentinel behaviour (see cover
illustration). It remained in this posture for some
time and never ventured from its home-site. The
lizard was approached (by E.J.) to a distance of
about 0.5 metre, but it made no effort to escape
and remained in its position. Air temperatures
were around 30°C and within normal body
temperature ranges recorded for this species
(Meek, 1978; Wikramanayake & Green, 1993;
review in Bennett, 1998).
The Bengal monitor is a typical varanid in that
it forages diurnally for a wide variety of animal
prey often over large distances (Auffenberg,
1994). Our observations at Hettipola indicated that
they foraged in both terrestrial and arboreal
microhabitats (Fig. 1). Dave (1960) observed
movement at night but in an extensive study and
review Auffenberg (1994) was unable to confirm
this although he refers to an observation by a Mr
Sanjeevaraj in Madras, India of a V. bengalensis
foraging at 02:00 hrs for toads under a street light.
We cannot confirm any feeding behaviour after
dark, but it is difficult to imagine the lizard
ignoring a prey animal if it wandered within
striking distance.
On the afternoon of July 22nd we were alerted
by hotel staff to a sub adult V. bengalensis (s.v.
length approximately 15 cm) that had captured an
adult Cricket frog or Paddie-field frog
(Limnonecton limnocharis) at the front of the hotel
and was in the process of swallowing it (Fig. 2).
The frog was swallowed initially by continually
being pushed against the ground then finally by
inertia movements. This is the usual method
employed by Varanids when the prey is large
relative to body size. Apparently, vertebrate prey is
comparatively rare in V. bengalensis (Bennett,
1998) and although is known to include frogs,
there are no records of L. limnocharis as a prey
species (Auffenberg, 1994). We observed another
individual (s.v. length approximately 20 cm)
eating six snails of an unknown species. Before
swallowing the lizard crushed the shells by
mastication then forced them into the stomach by
the usual inertia movements. Hard-shelled prey is
taken by adult Nile monitors (V. niloticus) and are
crushed before swallowing. There are ontogenetic
changes in the dentition for this dietary shift,
where the teeth become broader and molar-like
(e.g. Rieppel & Labhardt, 1979). We are not aware
of this condition in V. bengalensis.
Finally, on two occasions we fed dead bats to
foraging V. bengalensis (Fig. 3), one of which had
just previously been foraging on the branches of a
tree (Fig. 1). These were readily accepted
suggesting the lizards consume just about any prey
animal they come across. After consuming the bat
(at around 14:00 hrs), the first animal immediately
Number 95 - Herpetological Bulletin [2006] 31
NATURAL HISTORY NOTES
Figure 1. Arboreal foraging in Varanus bengalensis.
proofs temp.qxd 02/05/2006 11:19 Page 1
retreated to what appeared to be its home site
where it remained for the rest of the day. This may
have concerned digestion as the general
environmental temperatures at the time were high
– even at midnight air temperatures were in the
region of 28°C and by early morning still around
25°C, so basking to raise body temperatures may
have been unnecessary.
ACKNOWLEDGEMENTS
We thank Anslem De Silva for identifying the
frog, organising the field studies and obtaining
permission from the Forest Department and
Department of Wildlife Conservation, Sri Lanka to
carry out the research. Project Knuckles was partly
operated and partly funded by the University of
Edinburgh, Scotland.
REFERENCES
Auffenberg, W. (1994). The Bengal Monitor.
University Press of Florida, Gainesville FL.
Bennett, D. (1998). Monitor Lizards; Natural
History, Biology and Husbandry. Edition
Chimaira, Frankfurt am Main.
Dave, K.C. (1960). Contribution to the systematics,
distribution and ecology of the reptiles of the
deserts of Rajasthan with special reference to the
ecology of certain lizards. Proc. Indian Sci Congr.
47, 482–483.
De Silva, A. (2005). The Diversity of Dumbara
Mountains (Knuckles Massif, Sri Lanka): With
special reference to its herpetofauna.
Lyriocephalus special issue 6, vols 1& 2.
Rieppel, O & Labhardt, L. (1979). Mandibular
mechanics in Varanus niloticus. Herpetologica
35, 158–163.
Meek, R. (1978). On the thermal relations of two
oriental varanids, Varanus bengalensis nebulosis
and Varanus salvator. Cotswold Herpetological
Symposium 1978, 32–47.
Meek, R., Jolley E, De Silva, A., Goodawardene,
S.J. Drake, J., Chalalochani, H.M.N., Liyanage,
P.L.C.L.,Abeysekera, T.S., Mayadunna,
M.D.I.P.K., Somathilaka, S.A.U.S &
Chandrarathna. W.P.R (in press, 2005).
Altitudinal differences in thermoregulatory
behaviour in Calotes versicolor in the Knuckles
region, Sri Lanka. In DeSilva A, (Ed.) The
Diversity of the Dumbara Mountains (The
Knuckles Massif, Sri Lanka): With special
reference to its herpetofauna. Lyriocephalus
Special issue, 2005, 6 (Vols 1&2).
Wikramanayake, E.D. & Green, B. (1993).
Thermal ecology of microhabitat use by
sympatric Varanus bengalensis and Varanus
salvator in Sri Lanka. Copiea 1993, 709–714.
EDIE JOLLEY1 and ROGER MEEK2
1 16 Mountfields, Halifax, West Yorkshire, UK.
Email: ediejolley@yahoo.co.uk
2 7 Rue Georges Clemenceau, Chasnais, France.
Email: Rogermeek85@aol.com
32 Herpetological Bulletin [2006] - Number 95
Natural History Notes
Figure 2. Subadult V. bengalensis consuming an adult
Limnonecton limnocharis.
Figure 3. One of two specimens of V. bengalensis
consuming a dead bat offered by the authors.
proofs temp.qxd 02/05/2006 11:19 Page 2

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55; varanus bengalensis feeding behaviour (natural history note)

  • 1. VARANUS BENGALENSIS (Bengal monitor): UNUSUAL BEHAVIOUR AND FEEDING. During July 2005, as part of the Knuckles Expedition (De Silva, 2005), we conducted field studies on thermoregulation in Calotes versicolor at Hettipola (Meek et al., in press), an area that lies on a flat plain at the edge of the Knuckles Massif in Central Province, Sri Lanka. At the time of our study, it was the dry season and operative temperatures exceeded 40°C daily. We frequently observed foraging V. bengalensis in the study area and all the observations reported here relate to this study site. Most sightings were after midday when they appeared to be searching for prey species. One lizard with an s.v. length of approximately 25 cm had a home site across from our hotel which we often saw it return to either mid-afternoon or evening. This individual was easily recognised because of a damaged tail. One evening, an hour or so after dark, one of us (E.J.) saw this individual sitting partly outside its burrow in what appeared to be a type of sentinel behaviour (see cover illustration). It remained in this posture for some time and never ventured from its home-site. The lizard was approached (by E.J.) to a distance of about 0.5 metre, but it made no effort to escape and remained in its position. Air temperatures were around 30°C and within normal body temperature ranges recorded for this species (Meek, 1978; Wikramanayake & Green, 1993; review in Bennett, 1998). The Bengal monitor is a typical varanid in that it forages diurnally for a wide variety of animal prey often over large distances (Auffenberg, 1994). Our observations at Hettipola indicated that they foraged in both terrestrial and arboreal microhabitats (Fig. 1). Dave (1960) observed movement at night but in an extensive study and review Auffenberg (1994) was unable to confirm this although he refers to an observation by a Mr Sanjeevaraj in Madras, India of a V. bengalensis foraging at 02:00 hrs for toads under a street light. We cannot confirm any feeding behaviour after dark, but it is difficult to imagine the lizard ignoring a prey animal if it wandered within striking distance. On the afternoon of July 22nd we were alerted by hotel staff to a sub adult V. bengalensis (s.v. length approximately 15 cm) that had captured an adult Cricket frog or Paddie-field frog (Limnonecton limnocharis) at the front of the hotel and was in the process of swallowing it (Fig. 2). The frog was swallowed initially by continually being pushed against the ground then finally by inertia movements. This is the usual method employed by Varanids when the prey is large relative to body size. Apparently, vertebrate prey is comparatively rare in V. bengalensis (Bennett, 1998) and although is known to include frogs, there are no records of L. limnocharis as a prey species (Auffenberg, 1994). We observed another individual (s.v. length approximately 20 cm) eating six snails of an unknown species. Before swallowing the lizard crushed the shells by mastication then forced them into the stomach by the usual inertia movements. Hard-shelled prey is taken by adult Nile monitors (V. niloticus) and are crushed before swallowing. There are ontogenetic changes in the dentition for this dietary shift, where the teeth become broader and molar-like (e.g. Rieppel & Labhardt, 1979). We are not aware of this condition in V. bengalensis. Finally, on two occasions we fed dead bats to foraging V. bengalensis (Fig. 3), one of which had just previously been foraging on the branches of a tree (Fig. 1). These were readily accepted suggesting the lizards consume just about any prey animal they come across. After consuming the bat (at around 14:00 hrs), the first animal immediately Number 95 - Herpetological Bulletin [2006] 31 NATURAL HISTORY NOTES Figure 1. Arboreal foraging in Varanus bengalensis. proofs temp.qxd 02/05/2006 11:19 Page 1
  • 2. retreated to what appeared to be its home site where it remained for the rest of the day. This may have concerned digestion as the general environmental temperatures at the time were high – even at midnight air temperatures were in the region of 28°C and by early morning still around 25°C, so basking to raise body temperatures may have been unnecessary. ACKNOWLEDGEMENTS We thank Anslem De Silva for identifying the frog, organising the field studies and obtaining permission from the Forest Department and Department of Wildlife Conservation, Sri Lanka to carry out the research. Project Knuckles was partly operated and partly funded by the University of Edinburgh, Scotland. REFERENCES Auffenberg, W. (1994). The Bengal Monitor. University Press of Florida, Gainesville FL. Bennett, D. (1998). Monitor Lizards; Natural History, Biology and Husbandry. Edition Chimaira, Frankfurt am Main. Dave, K.C. (1960). Contribution to the systematics, distribution and ecology of the reptiles of the deserts of Rajasthan with special reference to the ecology of certain lizards. Proc. Indian Sci Congr. 47, 482–483. De Silva, A. (2005). The Diversity of Dumbara Mountains (Knuckles Massif, Sri Lanka): With special reference to its herpetofauna. Lyriocephalus special issue 6, vols 1& 2. Rieppel, O & Labhardt, L. (1979). Mandibular mechanics in Varanus niloticus. Herpetologica 35, 158–163. Meek, R. (1978). On the thermal relations of two oriental varanids, Varanus bengalensis nebulosis and Varanus salvator. Cotswold Herpetological Symposium 1978, 32–47. Meek, R., Jolley E, De Silva, A., Goodawardene, S.J. Drake, J., Chalalochani, H.M.N., Liyanage, P.L.C.L.,Abeysekera, T.S., Mayadunna, M.D.I.P.K., Somathilaka, S.A.U.S & Chandrarathna. W.P.R (in press, 2005). Altitudinal differences in thermoregulatory behaviour in Calotes versicolor in the Knuckles region, Sri Lanka. In DeSilva A, (Ed.) The Diversity of the Dumbara Mountains (The Knuckles Massif, Sri Lanka): With special reference to its herpetofauna. Lyriocephalus Special issue, 2005, 6 (Vols 1&2). Wikramanayake, E.D. & Green, B. (1993). Thermal ecology of microhabitat use by sympatric Varanus bengalensis and Varanus salvator in Sri Lanka. Copiea 1993, 709–714. EDIE JOLLEY1 and ROGER MEEK2 1 16 Mountfields, Halifax, West Yorkshire, UK. Email: ediejolley@yahoo.co.uk 2 7 Rue Georges Clemenceau, Chasnais, France. Email: Rogermeek85@aol.com 32 Herpetological Bulletin [2006] - Number 95 Natural History Notes Figure 2. Subadult V. bengalensis consuming an adult Limnonecton limnocharis. Figure 3. One of two specimens of V. bengalensis consuming a dead bat offered by the authors. proofs temp.qxd 02/05/2006 11:19 Page 2