Herpetofauna of Katerniaghat Wildlife Sanctuary, Uttar
Pradesh, India
Abhijit Das1, Dhruvajyoti Basu 2, Laurel Converse 3 &
Su-resh C. Choudhury 4
1 Division of Herpetology, Aaranyak, Samanwoy Path, Beltola, Guwahati,
Assam 781028, India
2, 4 Katerniaghat
Foundation, India C-421, Sector-B, Mahanagar, Lucknow, Uttar Pradesh
226006, India
3 Laurel
Converse, 14 Eton Overlook, Rockville, MD 20850, USA
Email: 1 abhijit@aaranyak.org(corresponding author), 3 ghariallaurel@gmail.com, 4 wildcraft20@gmail.com
Date
of publication (online): 26 May 2012
Date
of publication (print): 26 May 2012
ISSN
0974-7907 (online) | 0974-7893 (print)
Editor: Indraneil Das
Manuscript
details:
Ms
# o2587
Received
27 September 2010
Final
received 07 March 2012
Finally
accepted 18 March 2012
Citation: Das, A., D. Basu, L. Converse & S.C. Choudhury (2012). Herpetofauna of
Katerniaghat Wildlife Sanctuary, Uttar Pradesh, India. Journal of Threatened Taxa4(5): 2553Ð2568.
Copyright: © Abhijit Das, Dhruvajyoti
Basu, Laurel Converse & Suresh C. Choudhury 2012. Creative Commons
Attribution 3.0 Unported License. JoTT allows unrestricted use of this article
in any medium for non-profit purposes, reproduction and distribution by
providing adequate credit to the authors and the source of publication.
Author Details
and Contribution: Abhijit Dasis currently working with the division of Herpetology, Aaranyak, a research
organization based in Guwahati. He is an avid herpetologist primary interested
is the taxonomy, biogeography and conservation initiatives of the herpetofauna
of northeastern India. He conducted the field surveys, identified the
specimens and wrote the mss.
Dhruvajyoti Basuwas associated with Katerniaghat Foundation and was one of the pioneers in
crocodile conservation and research in India. He extensively worked on the
distribution and status of Gharial throughout India and also closely associated
with the U.P. Forest Department Crocodile Breeding Programme, MCBT, WWF etc. He
passed away while conducting a Gharial survey in Assam in April, 2011. This paper is dedicated to the memory
of his indomitable spirit!! He shared past herpetological
observation from the area and guided the team during the survey
Laurel Conversewas with the Gharial Conservation Alliance, Madras Crocodile Bank Trust, Tamil
Nadu, India. Her primary research interest is captive breeding and ex-situ
conservation of crocodiles. She carried out the field surveys for along
with AD.
Suresh SChaudhuryis associated with the Katerniaghat Foundation, Lucknow, Uttar Pradesh, an
organization involved in conservation activities in the Terai landscape of
India. He is also a wildlife photographer. He was a member of the survey
team and also provided past information on the herpetofauna of the region.
Acknowledgements: We are thankful to the Uttar Pradesh
Forest Department for granting permission to conduct the study. Thanks to
Katerniaghat Wildlife Division for logistic support. Special thanks to Mr.
Ramesh K. Pandey, IFS, and Mr. Shukla for providing logistic support. The work is financially supported by
Conservation Leadership Programme. AD was supported by Rufford Small Grant, UK
and Aaranyak, Guwahati. Special thanks to Raja Chandramani Kant Singh, Babbu of
Katerniaghat foundation, Puja Chourasia, Subir Choufin for providing logistic
supports and being Field Company. Thanks to Indraneil Das, Romulus Whitaker,
S.U. Shravanakumar, Udayan Borthakur, Uttam Saikia, Sailendra Singh, Ashutosh
for sharing knowledge. We thank Ramrup, Shubai, Vinod, Santosh for assistance
in the field.
Abstract: A herpetofaunal inventory based on field
surveys, literature records and photographic records is presented for Katerniaghat
Wildlife Sanctuary and its environs, situated in the Terai region of Uttar
Pradesh, India. We list a total of
10 species of amphibians and 42 species of reptiles from the area. Compiled observations presented here
include biological notes on the Critically Endangered Gavialis
gangeticus and new locality records and natural history information of
poorly known species including Polypedates taeniatus and Sibynophis sagittarius. Besides recording members of currently
recognized species complexes, the study also documents species that were either
conferred to closely related species (e.g., Fejervarya cf. teraiensis) or their identity remains to
be ascertained (e.g., Kaloula sp.). The present study
indicates that species count at Katerniaghat Wildlife Sanctuary is likely to
increase with additional surveys and systematic work.
Keywords: Herpetofauna, India, inventory,
Katerniaghat Wildlife Sanctuary, Terai.
For figures, images -- click
here
INTRODUCTION
Katerniaghat Wildlife Sanctuary (27055ÕÐ28025ÕN & 810Ð81025ÕE),
is located in Bahraich District of Uttar Pradesh. This typical Terai ecosystem is spread over an area of 400km2and is characterized by extensive alluvial plains, wetlands, grasslands,
woodlands and moist forests. The
vegetation of the study area can be categorized into riverine forests, mixed
Sal forest, teak Tectona
grandis plantation, woodlands and alluvial grasslands. Except riverine forests which are
characterised by the dominance of moist evergreen species, all other categories
are deciduous in nature (Tripathi & Singh 2009). The riverine habitat (Girwa River) of the Sanctuary (18km
length) is bounded upstream by the Nepalese border and downstream by the
Girijapuri Barrage. The sanctuary
is home to large animals such as tiger, elephant, leopard and Gangetic dolphin,
and is regarded as an important habitat of the Critically Endangered Gavialis
gangeticus. The Sanctuary also
holds a key population of Crocodilus palustris and several freshwater turtle species. Past studies on herpetofauna include
those of Hallermann et al. (2001), Basu (1989) and Talukdar & Dasgupta
(1977). However, general
information on diversity and distribution of herpetofaunal species is scanty.
Study Area
The field investigations were conducted in
the following localities: Base Camp (28020.243ÕN
& 81007.855ÕE): Human habitation surrounded by degraded
grasslands, secondary growth and abandoned constructions; Boat point (28020.310ÕN
& 81007.858ÕE): Open grassland area and river; Girjapuri Barrage
road (28016.557ÕN & 81006.140ÕE): Forest road
surrounded by thick woodland and waterbodies; Vaisalot, Nishangada (28014.155ÕN
& 81012.919ÕE): Deciduous forest, teak plantation and swampy
areas; Mayla Nullah (28020.396ÕN
& 81006.876ÕE):
small channel of Girwa River having thick forest and cane brakes along two
sides; Kauriala (28018.401ÕN & 81005.586ÕE): large
riverine habitat with dense riverside grasslands; Bhabanipur Village (28019.968ÕN
& 81008.738ÕE): Human habitation and grazing lands, scrub and
open forest; Amba (28019.142ÕN, 81009.851ÕE): riverside
habitat with grazing lands and deciduous forest; Amba Ghat (28018.924ÕN & 81010.869ÕE):
riverside open area with human habitation and plantation areas; Watch Tower
Point (28019.968ÕN
& 81008.738ÕE): Riverside extensive riverside moist grassland;
Madhab Nullah (28020.277ÕN & 81006.135ÕE): channel of Girwa
River with extensive grassland and woodland on both side; Gharial Nesting
Island (28020.146ÕN & 81008.824ÕE): Sandy river
island with grassy patches, the mass gharial nesting spot; Mahadeva Taal: 28018.401ÕN
& 81005.586ÕE: Large wetland with extensive macrophytic growth
(Image 1).
MATERIALS AND METHODS
Field records for the study comes from observations of AD and LC from 11 to 30 June 2008; 4 to 22 December 2008 and 28 February to 08 March 2009. However, the study also incorporates other literature records and reliable photographic records. Field observations were made opportunistically. Data have been supplemented with the earlier observations of DB and SC from in and around the Sanctuary. Active searches involving turning rocks and logs, peeling bark and digging through leaf litter. During the day, besides active search, basking reptiles were also searched along forest trails, forest edges and along river banks. Crocodiles were observed from motor boats, river shore transects and from watch tower. For frogs, observations were sometimes made on the basis of calls heard along forest trail, forest edges and along streams between 1800Ð2200 h, aided by flashlights. Records of road kills and dead specimens in fishing nets were studied and incorporated in this paper. Individuals of the species were captured by hand and released at the point of capture after examination or were observed using a binocular. A Canon Digital S3IS was used for photography. Data on locality, habitat and microhabitat, sex, reproductive data, syntopic species (if any) were recorded. Behavioural observations were recorded in a field data sheet. Morphometric data on specimens were used for identification. Frogs, lizards and snakes were released at their respective capture site once their specific identity and photography was over.
Geographic coordinates for survey sites
were recorded with a Garmin 12 receiver GPS. Interactions with local residents were held to make them
aware of the local herpetofauna and to supplement field observations. Species
were identified using the keys of Smith (1935, 1943); Schleich & KŠstle
(2002); Das (1995); and Dutta (1997). Nomenclature and taxonomic arrangement in the text follows Frost (2009)
for amphibian, Das (2003) and Uetz (2007) for reptiles.
Species account
Amphibians
Bufonidae Gray, 1825
Duttaphrynus melanostictus (Schneider, 1799): Recorded from Base camp, Girjapuri
Barrage, Bhabanipur and near staff quarters. Frequently encountered in and
around human habitations, plantations, river banks, under rocks, wood piles and
roadside areas.
Duttaphrynus stomaticus (LŸtken, 1862): Recorded from near Base camp during June
2008. The individual was feeding
on insects on a forest trail surrounded by human habitation and degraded
grassland at around 2000h.
Dicroglossidae Anderson, 1871
Hoplobatrachus tigerinus (Daudin, 1803): Calling aggregation was observed during
June. Individuals found to inhabit
temporary water pool, mud bank and open grassy space. Calling males are yellowish in colour dorsally. This colouration is reported to be an
indicator of good general physiological condition and sexual activity in males
(Abdulali 1985). Juveniles
observed in the month of June along the river bank. The species frequently
observed as road-kill on the segment between Katerniaghat to Bicchia.
Fejervarya cf. teraiensis (Dubois, 1984): Recorded from Boat point. Individuals had a broad cream coloured
mid dorsal line; dorsum with longitudinal skin folds, light in colour, whitish
patches along side of body, forelimb and hind limb not very distinctly
barred. Observed in moist grass
near river. Fejervarya
teraiensis was reported from Uttar Pradesh by Hegde et al. (2009) and
eastward up to Nagaland (Ao et al. 2003). However, the species is reported to be present in the entire Terai zone
of Nepal inhibiting 71Ð400 m elevation (Schleich & KŠstle 2002).
Fejervarya sp.: Recorded from Boat point and base camp. Individuals of the species are characterised by absence of a mid-dorsal line; dorsum with dark brown blotches, longitudinal skin fold absent, limbs barred throughout. It inhabits areas with moist grass near seasonal and perennial water bodies.
The species differs from Fejervarya
nepalensis in not having a mid dorsal line, from Fejervarya pierrei in absence of
middorsal line and long longitudinal skin folds, from F. teraiensis in having a small size (F. teraiensis,
SVL 43Ð51). However, the
species showed close resemblance with Fejervarya syhadrensis (absence of mid-dorsal
line, absence of dorsal longitudinal skin folds and small SVL 33mm) but only
differs in absence of reddish or orange patches which considered to be an
important character for F. syhadrensis (sensu Schleich & Kastle 2002). Further investigation with good sample
size might help in specific identity of this species.
Euphylectis cyanophlyctis (Schneider, 1799): Frequently
encountered in lentic and lotic habitats in and around the sanctuary. The species is used as fishing bait in
the fringe areas.
Microhylidae GŸnther, 1858
Kaloula sp. (Image 2): The first individual of this interesting microhylid was observed on 12 June 2008. It fell from a Cassia tree from a height of 6Ð7 m as it was dislodged from tree hole by a Varanus bengalensis. The second individual was recorded on 21 June at 1900h. Its head was protruding from a hole in a standing dead tree ca. 1.2m above ground. Both frogs were found near base camp close to grassland forest edge.
The two individuals showed colouration
similar to K. assamensis and morphometrical similarity to K. taprobanica however with different web
formula
(I 1Ú2 Ð1II 1Ú2 Ð2III2Ð2IV2 1Ú2 Ð 1Ú2 V). A similar animal is depicted in the
Schleich & KŠstle (2002) where it is treated under the nomen Kaloula
taprobanica. Due to paucity of
sample, we could not ascertain its specific status and suggest further study of
the Katerniaghat population.
Microhyla ornata (DumŽril & Bibron, 1841): Large calling aggregation was recorded
around base camp and boat point during June. Individuals call from moist grass and leaf litter of open
grassland especially after rains.
Rhacophoridae Hoffman, 1932
Polypedates taeniatus (Boulenger, 1906) (Image 3): Calling aggregation was observed during
16Ð21 June 2008 near boat point. Calling males were observed on moist grass blades, bushes and on ferns
and were located ca. 70cmÐ1.5m above the ground.
Ray (1991) reported the species as Rhacophorus tanieatus from Dudhwa National Park and recorded the habitat of the species as tall grassy patches near dense Sal Shorea robusta forest with considerable undergrowth of herbaceous plants. However, during this study individuals were only recorded from open grassland.
Type locality of the species is Purnia
(Bihar). We observed a colour photograph of the species from Behala area of
West Bengal. Eastward, the species
is recorded from north bank alluvial grasslands of Assam (Ahmed & Dutta
2000). Elsewhere, it was recorded
from Nepal and Bangladesh (Anders et al. 1998).
Chiromantis dudhwaensis (Ray, 1992) (Image 4): Calling aggregation of the species was
recorded near Base Camp and Ferry Ghat during June 2008. Calling individuals were photographed
from waterlogged and marshy areas inhabiting shrubs, grass blades and Ipomea sp. at
50cmÐ1.5m above substrate. A
detail note on the breeding habit of the species appears in Biswas (2000).
Reptiles
Gekkonidae Gray, 1825
Hemidactylus flaviviridis RŸpell, 1835 (Image 5): Base Camp, Watch Tower; Individuals also observed on Ficus tree
bark at 170cm height and under woodpiles near houses. This is the common house
gecko of the study area. Earlier records of the species is from Nishangada
(15km from the base camp) by Hallermann et al. (2001).
Hemidactylus brookii Gray, 1845: Individuals were found inhibiting house
walls up to 3m from the ground. However, majority of the encounters are from
low walls, culverts and on the ground. Gravid females observed in the month of June.
Employing a molecular systematic approach
Bauer et al. (2010) recovered two distinct clad what has long been considered a
single, but polytypic, Hemidactylus brookii. One consisting of specimens from Borneo (Sarawak), Myanmar, Peninsular
Malaysia and Karnataka, southwestern India, and another specimen from Sri Lanka,
Mauritius and Kerala, southwestern India. The name H.
brookii is restricted to the species occurring in East Asia and in parts of
India (including Karnataka, but probably most of the subcontinent). The
available name H.
parvimaculatus was applied to population of southern India and Sri Lanka and is found to be
restricted to that zone. Bauer et
al. (2010) also indicated towards further hidden species within Indian H. brookiipopulation. Keeping the taxonomic
uncertainty in mind and lacking detail in morphological and molecular data, we
keep our Katerniaghat taxa confer to Hemidactylus brookii pending further studies.
Hemidactylus frenatus Schlegel, 1836: One individual of the species was
photographed from Vaisalot of Nishangada. It was located under an information board of a teak plantation area by
day.
Agamidae Gray, 1827
Calotes versicolor (Daudin, 1802): Recorded from Base Camp, Nishangada,
Bhabanipur Village. Inhabit
grassland, scrub, plantation and human habitation. Majority of the individuals
were sighted in arboreal situations 30cmÐ4m above ground. Males in breeding colouration were
observed during June. In northern
India, they are known to lay eggs during summer (Das 2002). We observed juveniles during the month
of December.
Scincidae Gray, 1825
Eutropis carinata (Schneider, 1801): Observed from Bhawanipur Village during
June. A single individual was
foraging among leaf-litter of a teak plantation area close to human
habitations. Earlier, the species
had been recorded from Nishangada (Hallermann et al. 2001).
Lygosoma punctata (Gmelin, 1799) (Image 6): Recorded from near the base camp during
March 2009. The individual was
found among accumulated leaf-litter near degraded grassland and plantation area
at around 1100h.
Varanidae Merrem, 1820
Varanus bengalensis (Daudin, 1802): Individuals were sighted in
the backyard of human habitation, along the river bank, grassland, teak
plantation, agriculture fields and even seen crossing paved roads. Individuals were observed in arboreal situations ca. at 2Ð5 m
above ground. A juvenile was
observed during the month of June.
Varanus flavescens (Hardwicke & Gray, 1827): Photographed by SC on metalled forest road
in the buffer area of Katerniaghat Wildlife Sanctuary on 06 June 2010. The area was surrounded by teak
plantation area.
Typhlopidae Merrem, 1820
Ramphotyphlops brahminus (Daudin, 1803): Found inside a cracked floor of the base
camp at around 2130h.
Boidae Gray, 1825
Eryx conicus (Schneider, 1801): The record of the species is based on
Hallermann et al. (2001) from Nishangada.
Pythonidae Fitzinger, 1826
Python bivittatus Kuhl, 1820 (Image 7): Recorded
from near the base camp. During
June, one
individual was observed while it was crossing paved road at around 1840h.
surrounded by grassland and plantation area. Two basking individuals were
observed under thick Ipomea growth during February 2009 near abandoned Katerniaghat
railway station. This area is a
known nesting site for pythons in the area (Romulus Whitaker, pers. comm. June
2008). We observed remains of
eggshells, suggesting earlier nesting activity.
Python bivittatus is recently been re-assessed as a
distinct species by Jacobs et al. (2009). The westernmost distributional limit of this species is represented by
three disjunct wild populations known from Royal Chitwan National Park, Royal
Bardia National Park of Nepal and Corbett Tiger Reserve of India (Barker &
Barker 2008).
SC also photographed the same subspecies from
the nearby (90km to the west of Katerniaghat WLS) Dudhwa National Park in Uttar
Pradesh. Thus, report of Python bivittatusfrom Katerniaghat and Dudhwa further fill in the distributional gap in India.
Colubridae Oppel, 1811
Amphiesma stolatum (Linnaeus 1758): First sighting is from the Katerniaghat Forest Range Office while it was moving among leaflitter of a
teak plantation area during June 2008. Subsequently, on 14 June 2008, one dead
female was observed on a forest trail surrounded by Terai grasslands.
Boiga forsteni (DumŽril, Bibron & DumŽril, 1854):Hallermann et al. (2001) recorded the species from Nishangada area of the
sanctuary. The photograph of an
individual female (SVL 1680mm, TL 376mm) provided in that paper corresponds to
the variety 1 as described in Mohapatra et al. (2009).
Chrysopelia ornata (Shaw, 1802): Record of the species is based on Basu
(1989) who reported a specimen with pholidosis: ventral 214, subcaudals: 115,
scale row 18: 16.
Dendrelaphis tristis (Daudin, 1803) (Image 8): One male (SVL 670mm, TL: 315mm) from
human habitation and plantation forest edge near the base camp during March
2009. It was occupying a hole
within the entrance gate to a house. The individual was reported to be regularly using the hole from more than
20 days. The nearby areas include extensive lemon plantation and grassland.
Pholidosis: supralabials 9/9, 5 and 6
touches eye, infralabials 10/10, first five touches anterior genial, sixth
touches posterior genial, preocular: 1, postocular: 2, temporals: 2+2; ventral:
195, anal: 2; subcaudals: 110, dorsal scale rows: 15:15:11.
Enhydris sieboldii (Schlegel, 1837): A female individual
(SVL 645mm, TL 93mm) reported from Nishangada by Hallermann et al. (2001).
Lycodon aulicus (Linnaeus, 1758) (Image 9): First individual was found in a crevice of a wooden window frame ca. 2.5m above ground at around 1900h during June 2008. Another individual was obtained from a wall crack of the same building during June. One individual was killed by a Rattussp.
All the individuals had small yellowish
bars that broaden laterally and dissolve into yellowish edged lateral
scales. Thus, corresponds to the
variety forma typica.
Lycodon jara (Shaw, 1802): Talukdar & Dasgupta (1977) reported a
specimen of Lycodon jara from Katerniaghat and was the first record of the
species from Uttar Pradesh. Further western record of the species is from Dehradun and Rajaji
National Park (Hussain & Roy 1992). Although the species was repeatedly collected from Orissa, West Bengal,
Arunachal Pradesh (Boulenger 1913; Whitaker & Captain 2004; Abhijit Das
pers. obs. 2007) Assam (Sclater 1891; Das et al. 2009) Meghalaya (Sclater
1891), Manipur (Singh 1995) and Mizoram (Abhijit Das pers. obs. 2009). It is also known from Nepal and
Bangladesh.
Ptyas mucosa (Linnaeus, 1758) (Image 10): Single
individual was rescued from human habitation close to extensive Terai grassland
during June. Locally known as
ÒDhaminÓ.
Psammodynastes pulverulentus (Boie, 1827): The record of the species is from
Nishangada (ZMH R 04825), 5km south of the Nepal border by Hallermann et al.
(2001). In India, the southernmost
distributional limit of the species is Mahendragiri (18.560N &
84.210E; elev.1093m) Srikakulam District of Andhra Pradesh
(Mohapatra et al. 2010), northern West Bengal (Ahmed & Dasgupta 1992),
northeastern India (Ahmed et al. 2009). The Katerniaghat record appears to be the westernmost distributional
limit of the species. Also found
in Nepal, Bhutan, Bangladesh, Myanmar China, Laos, Cambodia, Vietnam, Thailand,
Taiwan and the Philippines (Schleich & KŠstle 2002; Das 2002).
Sibynophis sagittarius (Cantor, 1839) (Image 11): A specimen was observed and photographed
by DB in the area lying between Bhabanipur Village and Amba in March. It was
found below leaf-litter beneath riverine forest undergrowth adjoining a cattle
trail.
Sibynophis sagittarius is often considered as junior synonym of Sibynophis
subpunctatus (Wall 1907 & Morgan 1973). Captain et al. (2004) showed that S. sagittarius and S. subpunctatus are morphologically
distinct and geographically disjunct in their distribution. S. sagittariusis currently known from Himachal Pradesh, Uttarakhand, Uttar Pradesh, Madhya
Pradesh, Bihar, Orissa, West Bengal (Wall 1923; BMNH 1930.5.8. 161 dried skull;
Sclater 1891; Ahmed & Dasgupta 1992; Das 2002; Saikia et al. 2007; Dutta et
al. 2009). Record of the species
from northeastern India, Assam, Nicobars, Myanmar and Malaysia (Sclater 1891;
Boulenger 1893; Das 2002; Schleich & KŠstle 2002; Captain et al. 2004) are
doubtful or erroneous (Wall 1923; Ahmed & Dasgupta 1992; Ahmed et al. 2009;
www.calacademy.org/research/herpetology/myanmar). Elsewhere it is known from Nepal (Schleich & KŠstle
2002) and Bangladesh (Kabir et al. 2009).
Xenochrophis piscator (Schneider, 1799): One juvenile was
caught from the boat point while it was moving through moist grass near the
river during June. One individual (SVL 40cm, TL 10cm) was found in shallow
water near a sand bar of the Girwa River during December. Largest individual (SVL 80cm and TL:
30cm) was found dead on a fishing hook near Koriala-Girwa confluence. The individual had pholidosis: 145
ventrals, 83 subcaudals, anal: 2, 19:19:17 rows of scales, 9 supralabial of
which 4 and 5 touch eye, 9 infralabial, first 5 touch anterior genial,
postocular 2, preocular 1, temporal 2+2. The postocular streak not distinct and neck is without distinct
crossband. Only the outer edges of
the ventral scales were black.
Xenochrophis schnurrenbergeri Kramer, 1977: Specimen number ZMH R04814 collected from Nishangada, Uttar
Pradesh was reported by Hallermann et al. (2001) as Xenochrophis piscator piscator. This specimen was later identified
as Xenochrophis
schnurrenbergeri by Vogel & David (2006), and reported as a first
record of the species for northern India. Of late, X.
schnurrenbergeri is reported from Orissa, Bihar, West Bengal and Assam
(Ahmed et al. 2009, Purkayastha et al. 2010, Mohapatra et al. 2010). Also found in Nepal (Kramer 1977).
Elapidae Boie, 1827
Bungarus caeruleus (Schneider, 1801): One individual was observed near
Katerniaghat bus stop at night. The area is surrounded by human habitation.
Bungarus fasciatus (Schneider, 1801) (Image 12): One individual was photographed during
December 2007 near Katerniaghat forest range office. It was active on a forest trail at night (Ramesh Pandey,
pers. comm. June 2008).
Naja naja (Linnaeus, 1758) (Image 13): Recorded from Nishangada while it was crossing
a paved road surrounded by teak plantation area at 1030hr during June. The second individual was killed when
it entered human habitation near Base Camp. This venomous species is locally known as ÒPhitaraÓ.
Viperidae Boie, 1827
Daboia russelii (Shaw & Nodder, 1797): Observed in the Amba-Bhawanipur Village
watch tower point area in riverside habitat close to grassland-forest edge.
Juvenile observed basking in riverside grass patch close to forest trail. During summer, one adult was seen in a
tree hole at the base of the trunk.
Trionychidae Fitzinger, 1826
Chitra indica (Gray, 1831): Single individual was recorded basking on a flat, sandy riverbank of Amba ghat at around 1030h during December 2008. Two individuals of Nilssonia gangeticus were also observed at the same spot in December 2008. Local people narrated that the species start nesting from July and continue up to October. Das (1995) reported that in the Chambal region, the species nests from end August up to mid- September.
It is not conclusively known if double
clutching occurs in the species in which case the first clutch could be laid at
the beginning of the rainy season in July or even earlier in June when the
monsoon start, while the second clutch could follow about a month and half
later in AugustÐSeptember. Ashutosh Tripathi, studying the reproductive biology of the species
confirms its earliest nesting on 17 July in the Ganga River in Farrukhabad
District in Uttar Pradesh.
Nilssonia gangeticus (Cuvier, 1825): Recorded at various points along the 4km
Girwa River stretch from boat point to Amba Ghat. Frequently observed on newly emerged sandbars where they
bask with gharials. Individuals
often spotted while surfacing for breathing. One individual was seen feeding on submerged vegetation
during February 2009. In northern
India (Chambal River), Vasudevan (1998) recorded the nesting season from late
July to end of October with peak activity during late August. We presume that
similar nesting season prevail in Katerniaghat also.
Nilssonia hurum (Gray, 1831): Reported as Aspideretes hurumby Hallerman et al. (2001) from Nishangada area of the sanctuary. N. hurum has been reported from other parts of
the Terai by Das et al. (2010).
Lissemys punctata andersoni Webb, 1980 (Image 14): During August
2006, one individual was photographed in a grazing ground next to the Girwa
River (Ramesh Pandey, pers. comm. June 2008). Earlier, specimens (ZMH R00856-59) were reported from Monem
River, Nishangada by Hallermann et al. (2001).
Geoemydidae Theobald, 1868
Cyclemys gemeli Fritz,
Guicking, Auer, Sommer, Wink & Hundsdšrfer, 2008: Fritz et al. (2008) showed that sub adult
female ZMH R00288 collected from Nishangada, Bahraich, Uttar Pradesh, India,
approximately 5km S. Nepali border, leg. G.A. von Maydell during German India
Expedition 1955/1957 represents the newly described Cyclemys gemeli thus making the record as the
westernmost distributional limit of the species in India. Elsewhere, the species is reported from
localities in northeastern India and northern West Bengal (Das et al. 2009;
Praschag et al. 2009).
Geoclemys hamiltonii (Gray, 1831): One shell (SCL 31cm) was observed near a
seasonal water pool at the grassland-deciduous forest edge. Forest staff narrated that the turtle
was presumably killed and eaten by local ÔTharuÕ people.
Hardella thurjii (Gray,
1831):Observed by SC in streams and rivulets leading to Mahadeva Tal. Earlier, Das
(1995) reported the species from the Katerniaghat Wildlife Sanctuary. H. thurjii is apparently less frequently
encountered in large rivers and more frequently in smaller slow flowing streams
and wetlands such as beels in Assam. Similar suitable habitats also available in Katerniaghat Wildlife
Sanctuary. Thus we presume that,
further survey will record new distributional localities for the species from
the study area.
Melanochelys trijuga (Schweigger, 1914) (Image 15): An individual male (CCL 12cm, PL 8cm.)
encountered while it was crossing Barrage road at around 1730hr during June
2008. The area is surrounded by
thick forest and water bodies.
Based on subspecific characters provided
in Das (1995), we refer our individual to the subspecies Melanochelys
trijuga indopeninsularis.
Melanochelys tricarinata (Blyth, 1856) (Image 16): First male (CCL: 190mm, PL: 120mm.
carapace width: 97mm) was recorded from Watch tower road on 21 June 2008 at
1620hr. It was crossing the forest
trail surrounded by extensive terai grassland. The males carry a distinct plastral concavity. One female (PL 115mm, SCL 135mm) was
recorded during March 2009 while it was crossing grassland trail at 0850h.
Morenia petersi (Anderson, 1879) (Image 17): Recorded from near Mahadeva Tal in the
month of December 2008. Mahadeva Tal is a large wetland/Marsh area with
extensive macrophytic growth. In
Uttar Pradesh, the species was reported from Dudhwa National Park (Javed &
Hanfee 1995). In India, Morenia petersiis known from Uttarakhand (Bahuguna 2010), Bihar and West Bengal (Das 1995),
Assam (Ahmed et al. 2009). Also
found in Bangladesh and Nepal.
Pangshura tectum (Gray, 1831) (Image 18): Two basking individuals were observed
from Maila Nullah during June. The
individuals were observed on logs close to thick cane brake of Maila
Nullah. During February, one complete
shell (SCL 82mm, PL 74.25mm) was obtained from near a temporary water pool of
grassland-deciduous forest edge. During October 2009, SC photographed an individual on the left efflux
embankment of Girwa Barrage while it was crossing the road in the evening. This species appears to avoid open
large rivers unlike the closely related P. tentoria and P. smithii which were recorded from
Girwa river.
Pangshura tentoria (Gray, 1834) (Image 19): Most frequently observed turtle species
during the study period. Sighting records are from Boat point, watch tower,
Amba and Bhabanipur. Individuals
frequently observed while basking on river-side logs as well as in mid
river. Individuals also observed
on accumulated vegetation on a log sharing the basking space with juvenile
Gharial.
Egg lying was observed during December 2008. A total of nine nests were traced from flat sandbank of Amba Ghat. The nests are located at a distance of 15Ð 32m from water and are close to grassy patches. The clutch size observed as 7Ð9 elongated eggs measuring 44.40 x 25.15 mm. One female (CCL 230mm, SCL 215mm, PL 225mm) found while it was digging the sand at around 1300h. Urinates when captured.
Hallermann (2001) reported the subspecies P. tentoria
tentoria from Nishangada, however, our individuals correspond to the
subspecies Pangshura
tentoria flaviventer in having an unpatterned yellowish plastron, a
yellowish stripe on first three vertebrae, head brownish with a pink patch
behind the eyes. Schleich &
KŠstle (2002) regarded P. tentoria flaviventer as distinct species without detail
description. However, we maintain
the P.
tentoria flaviventer following Fritz & Havas (2007).
Pangshura smithii (Gray, 1863): Single individual was photographed while it was basking on a log close to watch tower river bank at around 0930hr during March 2009. Two individuals of P. tentoriawere also basking on the same log.
We are unable to comment on the subspecific status of the individual encountered. The nominate subspecies Pangshura smithii smithii characterised by a blotched plastron is known from Katerniaghat (Das 1995).
Crocodylidae Cuvier, 1807
Crocodylus palustris Lesson, 1831 (Image 20): Recorded from Boat point, Nesting Island,
Madhab Nullah, Mayla Nullah, Bhabanipur, Barrage, Amba and Occur syntopically
with Gharial. However, from the
observed comparative abundance of the two species it would seem that the
Gharial is more abundant in the open river which is avoided by Mugger, the
latter preferring stagnant and semi stagnant habitats of wetlands and smaller
streams. Basking individuals were
observed on sandbanks, sandbars, vegetated river bank as well as mudbank. Large individuals found inhabiting
small rivulets ca. 2Ð3 km away from the main channel. Capable of climbing
ca. >600 riverbank and utilise riverbanks with grassy ledges for
resting. Muggers were also found
inhabiting small to large wetlands with extensive macrophytic growth. An individual feeding on a bovine
carcass was observed during July. During August, one individual was recorded to
feed on a Gharial hatchling.
In Katerniaghat, nesting season coincides
with that of the Gharial and a nest was located in July on the same river
Island where communal nesting of Gharial occurred. The nest was 24cm deep, clutch size is 18 eggs and each egg
measured 77.20 x 49.74 mm.
Gavialidae Gmelin, 1789
Gavialis gangeticus (Gmelin, 1789) (Image 21): Basking individuals were observed on sand banks and sand bars. Newly created sand bars are frequently used and those in the mid river or which are remotely placed sand bars are preferred for basking. Besides using sand banks, juveniles also bask on mud banks and on emergent logs or vegetation lodged into the river bed. Basking places sometimes shared with Crocodilus palustris, Nilssonia gangeticus, Pangshura tentoria, Dendrocygna javanica and Tadorna ferruginea. The highest count for a single day was 105 individuals on 09 December 2008 of which 35 were recognized as adults. Largest number of adult males with ÒgharasÓ were eight on 20 December 2008. During high water in JuneÐJuly, large individuals were observed inside small sub channels, 1Ð2 km from main river channels. Communal nesting was observed on a 40m long and 6Ð7 m wide sandy island with grassy patches. Nesting began in March. Nests were observed as 32Ð40 cm deep. One nest had 46 eggs. Average size of the eggs measured 82.21 x 60.07. Hatchlings measuring SVL 132Ð150 mm, TL 180Ð190 mm (N = 5) observed on 16 June 2008. Five to six hatchlings were seen taking refuge near grassy roots or in depressions along the river bank.
The first Gharial population survey in
Katerniaghat was in 1975Ð1976, and previous to our work, the last study
of Gharial was done in 2001Ð2002 (Singh 1978; Srivastava 1981; Singh
2003). From 2008Ð09, we
found 27 nests; a 7% increase since 2001 and 96% increase since 1975. Nests were found in seven sites. Additionally, one clutch was found in
shallow water and five eggs were deposited in the open on a sand bar (not in a
nest). Two nests were destroyed by flooding/erosion. The island on which most Gharial had nested since 1988 was
completely destroyed by floods during July 2008, and most nests were lost. The concentration of nests in such
small areas makes the population vulnerable. A detailed paper on gharial
population and habitat study in Katerniaghat WS is in preparation.
Discussion
Based on field and literature records, the
study documents 42 species of reptiles belonging to 14 families and 32 genera and
10 species of amphibians belonging to four families and eight genera. The family Colubridae is the most
speciose genus with 12 species; Geoemydidae with nine species; Trionychidae and
Dicroglossidae with four species; Gekkonidae three species; families Bufonidae,
Microhylidae, Rhacophoridae, Varanidae, Scincidae, Elapidae each with two
species; Agamidae, Typhlopidae, Boidae, Pythonidae, Viperidae, Crocodilidae,
and Gavialidae with a single species each.
The record of Calotes maria, a Khasi Hill endemic agamid by Hallermann et al. (2001) from Nishangada, Uttar Pradesh, needs to be verified. As the collection in that paper also includes specimens collected from northeastern India and northern West Bengal, so we presume that record s of C. maria, E. multifasciata and H. platyurus might have been collected from eastern India and the collection localities are mistakenly recorded as ÒNishangadaÓ.
During the present survey, few herpetofaunal species were recorded, the identity of which are either unknown or conferred to closely related species (e,g, Kaloula sp., Fejervarya sp. Fejervarya cf. teraiensis). These provisionally identified species may represent previously unknown species, or are members of cryptic species complexes.
According to Bain et al. (2003), most of the species complexes are widespread, although the member species can have only limited ranges within this broad range. Members of the species complexes encountered are Calotes versicolor (Zug et al. 2006), Lycodon aulicus, Xenochrophis piscator (Vogel & David 2006).
Sankaran (1989) reported Dendrelaphis pictus from Dudhwa National Park which appears to be the westernmost distributional limit for the species and also indicates its possible occurrence in Katerniaghat. However, D. pictus is regarded as a species complex and several populations from south-east Asia and Sundaland have been recently described as new with the taxonomy of the group in the subcontinent remaining unresolved (Rooijen & Vogel 2008; Vogel & Rooijen 2008). Boiga trigonata, reported as fairly common in the Terai and Duns of Nepal (Fleming & Fleming 1974), might also occur in Katerniaghat. Similarly, we predict the occurrence ofCoelognathus helena helena, Lycodon striatus, Psammophis condanarus, Oligodon arnensis and even rare species like Oligodon kheriensis and Elachistodon westermanni.
The Girwa River is recorded within the natural distribution of Batagur dhongoka and Batagur kachuga (Fritz & Havas 2007) and recorded from nearby areas of Terai (Mitchell & Rhodin 1996) in southern Nepal. DB collected secondary information on occurrence of both the species from Katerniaghat Sanctuary. However, subsequent field surveys failed to record the two species from the Sanctuary. Thus, it has been hypothesized that the two species are either locally extirpated from their habitats in the Girwa or have become extremely rare because of ecological changes as a result of storage of water after the construction of barrage at Kailashpuri. Thus, while considering the reptilian diversity of Katerniaghat Wildlife Sanctuary the possibility of local extirpations of several species as a result of deforesteation in Nepal and modification of river courses and discharge should also be given cognizance.
The Sanctuary is one of the last remaining habitats of the Critically Endangered Gharial (Choudhury et al. 2011). Among the threatened species, Gravialis gangeticus, Crocodilus palustris, Chitra indica, Nilssonia hurum, Nilssonia gangeticus, Melanochelys tricarinata, Pangshura tecta, Geoclemys hamiltoni, Python bivittatus, Varanus bengalensis and Varanus flavescens have been accorded the highest legal protection status, under Schedule I of Indian Wildlife (Protection) Act, 1972. Naja naja, Ptyas mucosa and Xenochrophis piscator are listed in Schedule II; all other snake species are listed under Schedule IV of the Act.
The reptilian fauna of Katerniaghat Sanctuary predominantly composed of Indo-Malayan genera (Amphiesma, Chrysopelea, Crocodylus, Cyclemys, Enhydris, Lygosoma, Naja, Psammodynastes, Python, Ramphotyphlops, Varanus and Xenochrophis), followed by genera of Indian radiations (Bungarus, Gavialis, Hemidactylus, Lissemys, Pangshura and Melanochelys) and transitional elements (Boiga, Chitra, Dendrelaphis, Lycodon, Morenia and Sibynophis) (sensu Das 1996). Originally, the Terai was almost entirely covered by dense tropical forest, with grasslands or scrub (Schleich & Kaestle 2002). This might have provided in colonization of wet zone species (Cyclemys gemeli, Chrysopelea ornata, Python bivittatus and Psammodynastes pulverulentus) in the Katerniaghat. Basu (1989) also opined that the humid and well-forested areas of Terai and bhabar provide an exclusive corridor of suitable habitat for the spread of reptiles from afforested areas in the east, deep into the Gangetic plain areas.
Katerniaghat Wildlife Sanctuary represents
one of the last remaining Terai ecosystems and hence it is of tremendous
conservation concern. Considering
the dearth of knowledge on diversity, distribution and natural history of the
herpetofauna of the region, the present study assumes significance. However, the field observation of the
study is limited to a single peak monsoon month (JuneÐJuly) and
subsequent two visits are during winter month where herpetofaunal activity is
limited due to low temperature. Thus it is almost certain that the present inventory only represents a
fraction of the actual herpetofaunal assemblage and additional survey will
reveal hitherto unrecorded species.
References
Abdulali, H. (1985). On the export of frog legs from India. Journal of the
Bombay Natural History Society 82(2): 347Ð375.
Ahmed, S. & G. Dasgupta (1992). Reptilia, pp. 1Ð65. In: Ghosh,
A.K. (ed.). State
Fauna Series 3: Fauna of West Bengal: Part - 2 (Reptilia, Amphibia, Fishes, Hemichordata
and Archaezoology). Zoological Survey
of India, Calcutta, 381pp.
Ahmed, M.F. & S.K. Dutta (2000). First record of Polypedates
taeniatus (Boulenger 1906) from Assam, north-eastern India. Hamadryad25(1): 49Ð50.
Ahmed, M.F., A. Das & S.K. Dutta
(2009). Reptiles and
Amphibians of Northeast India, A Photographic Guide. Aaranyak, Guwahati,
168pp.
Anders, C.C., A. Deiner & H.H.
Schleich (1998). First
record of Polypedates
taeniatus (Boulenger 1906) from Nepal (Amphibia, Anura:
Rhacophoridae). In: Schleich, H.H.
& W. Kastle, (eds.). Contribution to
the Herpetology of South Asia (Nepal, India). Veroff Fuhlrott Museum 4:
73Ð86; Wuppertal.
Ao,
J.M., S. Bordoloi & A. Ohler (2003). Amphibian fauna of Nagaland with nineteen
new records from the state including five new records for India. ZoosÕ Print
Journal 18(6): e1117Ð1125.
Bahuguna, A. (2010). Morenia petersi. Geographical distribution. Herpetological Review 41(2): 242.
Bain, R.H., A. Lathrop, R.W. Murphy, N.
Orlov & H.T. Cuc (2003). Cryptic species of a cascade frog from Southeast Asia:
taxonomic revisions and descriptions of six new species. American Museum Novitates(3417):1Ð60.
Barker, D.G. & T.M. Barker (2008). The distribution of the Burmese Python, Python molurus bivittatus. Bulletin of Chicago Herpetological Society43(3):33Ð38.
Basu, D. (1989). Range extension of Chrysopelia
ornata Shaw (Reptilia:Colubridae) with comments of the distribution of some
snakes in north India. Journal of the
Bombay Natural History Society 86(1): 110Ð111.
Bauer, A.B., T.R. Jackman, E. Greenbaum,
A. desilva, V.B. Giri & I. Das (2010). Molecular evidence for the taxonomic
status of Hemidactylus
brookii group taxa (squamata: Gekkonidae). Herpetological Journal 20:129Ð138.
Biswas, S. (2000). Notes on the breeding habits of Chirixalus
dudhwaensis Ray 1992, from Uttar Pradesh, north India. Hamadryad 25(2): 200Ð203.
Boulenger, G.A. (1893). Catalogue of The Snakes in the British
Museum (Natural History)ÑVolume I. Containing families Typhlopidae, Glauconiidae,
Boidae, Ilsiidae, Uropeltidae, Xenopeltidae and Colubridae Aglyphae. British Museum. (Natural History),
London, xii+448pp+28plates.
Boulenger, G.A. (1913). A list of reptiles obtained by N.H.
Stevens in the upper Assam and the eastern Himalayas. Record of the
Indian Museum 9: 337Ð338.
Captain, A., D.J. Gower, P. David &
A.M. Bauer (2004).Taxonomic status of the colubrid snake Sibynophis subpunctatus (Dumeril Bibron & Dumeril 1854). Hamadryad28(1&2): 90Ð94.
Choudhury, B.C., L.A.K. Singh, R.J. Rao, D. Basu, R.K. Sharma,
S.A. Hussain, H.V. Andrews, N. Whitaker, R. Whitaker, J. Lenin, T. Maskey, A.
Cadi, S.M.A. Rashid, A.A. Choudhury, B. Dahal, U.W.K. Ko, J. Thorbjarnarson
& J.P. Ross (2007). Gavialis gangeticus. In: IUCN 2011. IUCN Red List of Threatened Species. Version
2011.2. <www.iucnredlist.org>. Downloaded on 18 May 2012.
Das, I. (1995). Turtles and
Tortoises of India. World Wide
Fund for Nature-India and Oxford University Press, Bombay, xi+179pp.
Das, I. (1996). Biogeography of
the Reptiles of South Asia. Krieger Publishing Company, Malabar, Florida,
16pls.+vii+87pp.
Das, I. (2002). A Photographic Guide to Snakes and Other
Reptiles of India. New Holland Publishers (UK) Ltd., London, 144pp.
Das, I. (2003). Growth of knowledge on the reptiles of
India, with an introduction to systematics, taxonomy and nomenclature. Journal of the
Bombay Natural History Society 100(2&3): 446Ð501.
Das, I., D. Basu & S. Singh (2010). Nilssonia hurum (Gray 1831): Peacock soft-shell Turtle,
pp.048.1Ð048.6. In: Rhodin, A.G.H., P.C.H. Pritchard, P.P. Van Dijk, R.A.
Saumure, K.A. Buhlmann, J.B. Iverson & R.A. Mittermeier (eds.). Conservation
Biology of Freshwater Turtle and Tortoises: A Compilation Project of the
IUCN/SSC Tortoise and Freshwater Turtle specialist group. Chelonian
Research Monographs No. 5.
Das, A., U. Saikia, B.H.C.K. Murthy, S.
Dey & S.K. Dutta (2009). A herpetofaunal inventory of Barail Wildlife
Sanctuary and adjacent regions, Assam, northeastern India. Hamadryad34(1): 117Ð134.
Dutta, S.K. (1997). Amphibians of India and Sri Lanka (checklist and bibliography). Odyssey
Publishing House, Bhubaneswar, xiii+342pp+xxii.
Dutta, S.K., M.V. Nair, P.P. Mohapatra
& A.K. Mahapatra (2009). Amphibians
and Reptiles of Simlipal Biosphere Reserve. Regional Plant Resource Center,
Bhubaneswar, 174pp.
Fleming, R.L. (Jr.) & R.L. Fleming
(Sr.) (1974). Some
snakes from Nepal. Journal of the Bombay Natural History Society 70(3): 426Ð437.
Fritz, D.G., M. Auer, R.S. Sommer, M. Wink
& A.K. Undsdorfer (2008).Diversity of Southeast
Asian leaf turtle genus Cyclemys: how many leaves on its tree of life? Zoologica Scripta 37(4):367Ð390.
Fritz, U. & P. Havas (2007). Checklist of chelonians of the world. Vertebrate Zoology 57(2): 149Ð368.
Frost, D.R. (2009). Amphibian species of the world: an online reference. Electronic database accessible at
http://research.amnh.org/herpetology/amphibian/index.php. American Museum of
Natural History, New York. Online
version 5.3. dated 12 February 2009.
Hallermann, J., N.B. Ananjeva & N.L.
Orlov (2001). On
a remarkable collection of Reptiles and Amphibians collected by the German
India Expedition 1955Ð1958. Russian
Journal of Herpetology 8(1):
59Ð68.
Hegde, V.D., S. Roy & B. Lal (2009). First record of Terai Cricket Frog Fejervarya
teraiensis (Dubois 1984) from Uttar Pradesh. Record of Zoological Survey of India 109 (Part I): 109Ð110.
Hussain, A. & P. Roy (1992). Occurrence of Twin Spotted Wolf
Snake Lycodon
Jara (Shaw) (Dipsadidae: Lycodontinae) in Rajaji National Park and Doon
Valley, Uttar Pradesh. Journal of the Bombay Natural History Society 90: 112Ð113.
Javed, S. & F. Hanfee (1995). Freshwater turtles of Dudhwa National
Park and their conservation. Hamadryad 20: 21Ð26.
Kabir, S.M.H., M. Ahmed, A.T.A Ahmed,
A.K.A. Rahman, Z.U. Ahmed, Z.N.T. Begum, M.A. Hassan, & M. Khondker (eds.)
(2009). Amphibians and
Reptiles. In: Encyclopaedia of the flora and fauna of Bangladesh. Asiatic Society of Bangladesh, Dhaka.
Kramer, E. (1977). Zur Schlangenfauna Nepals. Review Suisse
Zoology 84: 721Ð761.
Mitchell, J.C. & A.G.J. Rhodin (1996). Observation on the natural history and
exploitation of the turtles of Nepal with life history notes on Melanochelys
trijuga. Chelonian
Conservation and Biology 2(1): 66Ð72
Mohapatra, P.P., A. Das, F. Tillack &
S.K. Dutta (2009).Taxonomy, natural history and distribution of Boiga forsteni (Dumeril, Bibron et
Dumeril, 1854) (Serpentes: Colubridae) from Orissa, India. Russian Journal of Herpetology 16(4):
243Ð254.
Mohapatra, P.P., A. Das & S.K. Dutta
(2010). Psammodynastes
pulverulentus -
geographiocal distribution. Herpetological
Review 41(1): 111.
Mohapatra, P.P., S.K. Dutta, & S.P.
Parida (2010). Report
of Xenochrophis
schnurrenbergeri Kramer, 1977 (Serpentes: Natricidae) from Orissa, India. Russian Journal
of Herpetology 17(2): 94Ð96.
Morgan, E.C. (1973). Snakes of the subfamily Sibynophiinae.
PhD Thesis. University of Southwestern Louisiana, Lafayette, 260pp.
Praschag, P., A.K. Hundsdorfer & U.
Fritz (2009). Further specimens and phylogenetic
position of the recently described leaf turtle species Cyclemys gemeli (Testudines:
Geoemydidae). Zootaxa 2008: 29Ð37.
Purkayastha, J., M. Das, S. Sengupta, S.K. Dutta (2010). Notes on Xenochrophis schnurrenbergeri Kramer, 1977 (Serpentes: Colubridae)
from Assam, India with some comments on its morphology and distribution. Herpetology Notes 3: e175Ð180.
Ray, P. (1991). On
the natural distribution of the rare tree frog Rhacophorus taeniatus Boulenger, 1906
(Anura: Rhacophoridae), with notes on its biology and osteology.Journal of the
Bombay Natural History Society 88(3): 376Ð380.
Rooijen, J.V. & G. Vogel (2008). Contributions to a review of the Dendrelaphis
pictus complex (Serpentes: Colubridae) Ð 1. Description of a sympatric species. Amphibia-Reptilia 29: 101Ð115.
Saikia, U., D.K. Sharma & R.M. Sharma (2007). Checklist of the reptiles of
Himachal Pradesh, India. Reptile Rep8: e6Ð9.
Sankaran, R. (1989). Range extension of Painted
Bronzeback Tree Snake Dendrelaphis pictus (Gmelin). Journal of the Bombay Natural History Society255.
Schleich, H.H. & W. KŠstle (eds). (2002). Amphibians and Reptiles of Nepal. A.R.G. Gantner Verlag K.
G., Ruggell, Liechtenstein, x+1201pp.
Sclater, W.L. (1891). Notes on the snakes in the
Indian Museum with description of several new species. Journal of Asiatic Society of Bengal, Calcutta 60:
230Ð250.
Singh, S. (1995). On a collection of reptiles and
amphibians of Manipur. Geobios New
Report 14(2): 135Ð145.
Singh, V.B. (1978). Status of the gharial in Uttar Pradesh
and its rehabilitation. Journal of the Bombay Natural History Society 75(3): 668Ð683.
Singh, V.P. (2003). Evaluation of Gharial Rehabilitation U.P.
Forestry Project: Report Prepared for Biodiversity Research, Terai Nature
Conservation Society, 63pp.
Smith, M.A. (1935). The Fauna of British India, Ceylon and
Burma: Amphibia and Reptilia, Vol. IIÑSauria. Taylor and Francis Ltd.,
London, xii+445pp.
Smith, M.A. (1943). The Fauna of British India, Ceylon and
Burma, including the whole of the Indo-Chinese region. Reptilia and
Amphibia. Vol. IIIÑSerpentes.
Taylor and Francis, London, xii+583pp+1 folding map.
Srivastava, A.K. (1981). Biology of Indian Gharial Gavialis gangeticus,
with special reference to its behaviour. PhD Thesis. Department of Zoology,
University of Lucknow, 217pp.
Talukdar, S.K & G. Dasgupta (1977). Natural distribution of the
wolf Snake Lycodon
Jara (Shaw) (Serpentes: Colubridae) in Northern India. Newsletter of the Zoological Survey of India3(5): 276Ð277.
Tripathi, K.P. & B. Singh (2009). Species diversity and vegetation structure
across various strata in natural and plantation forests in Katerniaghat
Wildlife Sanctuary, north India. Tropical Ecology50(1): 191Ð200.
Uetz, P. (2007). The reptile
database. <http://www. reptile-database.org>. On-line version dated
18 January 2009.
Vasudevan, K. (1998). Reproductive ecology of the Indian
Softshell Turtle Aspideretes gangeticus, in northern India. Chelonian Conservation and Biology 3(1):
96Ð99.
Vogel, G. & P. David (2006). On the taxonomy of the Xenochrophis
piscator complex (Serpentes, Natricidae), pp. 241Ð246. In: Vences, M. & J. Kšhler, T.
Ziegler & W. Bšhme (eds.). Herpetologia
Bonnensis II. Proceedings of
the 13th Congress of the Societas Europaea Herpetologica. Societas Europaea
Herpetologica, Bonn.
Vogel, G. & J.V. Rooijen (2008). Contributions to a review of the Dendrelaphis
pictus (Gmelin 1789) complex-2. The eastern forms (Serpentes: Colubridae). Herpetozoa21(1/2): 3Ð29.
Wall, F. (1907). Reduction in the species of the
genus Polydontophis. Suppression of P. subpunctatus. Journal of the Bombay Natural History Society 17:
823Ð824.
Wall, F. (1923). A hand-list of the snakes of
the Indian Empire. Journal of the Bombay Natural History Society. 29: 598Ð632.
Whitaker, R. & A. Captain (2004). Snakes of India - The Field Guide. Draco
Books, Chennai, xiv+481pp.
Zug,
G.R., H.H.K. Brown, J.A. Schulte & J.V. Vindum (2006). Systematics of the garden lizards, Calotes
versicolor Group (Reptilia, Squamata, Agamidae), in Myanmar: central dry
zone populations. Proceedings of the California Academy of Science 57(2):
35Ð68.