Journal of Threatened Taxa | | 26 March 2017 | 9(3): 10014–10017






New distribution record of Nagarjunasagar Racer Platyceps bholanathi (Reptilia: Squamata: Colubridae) in Sigur, Nilgiris landscape, India


Arockianathan Samson 1, Palanisamy Santhoshkumar2, Balasundaram Ramakrishnan 3, Sivaraj Karthick 4 & Chandrashekaruni Gnaneswar 5


1,3,4 Mammalogy and Forest Ecology, Department of Zoology and Wildlife Biology, Government Arts College, Udhgamandalam, Nilgiris, Tamil Nadu 643002, India

2 Herpetology, Department of Zoology and Wildlife Biology, Government Arts Collage, Udhagamandalam, The Nilgiris, Tamil Nadu 643002, India

5 Zoology and Wildlife Biology, Government Arts College, Udhgamandalam, Nilgiris, Tamil Nadu 643002, India

1 (corresponding author), 2, 3, 4, 5



doi: | ZooBank:


Editor: Raju Vyas, Vadodara, Gujarat, India. Date of publication: 26 March 2017 (online & print)


Manuscript details: Ms # 3175 | Received 29 November 2016 | Final received 17 January 2017 | Finally accepted 22 February 2017


Citation: Samson, A., P. Santhoshkumar, B. Ramakrishnan, S. Karthick & C. Gnaneswar (2017). New distribution record of Nagarjunasagar Racer Platyceps bholanathi (Reptilia: Squamata: Colubridae) in Sigur, Nilgiris landscape, India. Journal of Threatened Taxa 9(3): 10014–10017;


Copyright: © Samson et al. 2017. Creative Commons Attribution 4.0 International License. JoTT allows unrestricted use of this article in any medium, reproduction and distribution by providing adequate credit to the authors and the source of publication.


Funding: Raptor Research & Conservation Foundation (RRCF).


Competing interests: The authors declare no competing interests.


Acknowledgments: Our whole-hearted thanks to the Principal Chief Conservator of Forests and Chief Wildlife Warden of Tamil Nadu state for giving us necessary permission to carry out the fieldwork. Our special thanks are due to the District Forest Officer, Nilgiri North Forest Division for providing permission and all logistic support to carry out the fieldwork. This observation record is part of a long term study on the project entitled “Conservation strategies for securing critically endangered White-rumped Vulture Gyps bengalensis and Long-billed Vulture Gyps indicus species in the Tamil Nadu part of the Nilgiri Biosphere Reserve” funded by the Raptor Research & Conservation Foundation (RRCF). We thank our field assistant Mr. R. Bomman, B. Vishnu, K. Manikandan and P. Prabhu for taking pains in collecting field data in the forests amidst elephants. Special thanks to P. Ravi Naturalist for the support and encouragement in the fieldwork.




The Nagarjunasagar Racer or Sharma’s Racer Platyceps bholanathi (Sharma, 1976) is a poorly-known snake endemic to southern India (Sharma 2003). Platyceps bholanathi was first described from Nagarjuna Hills (16031’N & 79014’E; 105m) in Guntur District, Andhra Pradesh, Eastern Ghats, southern India (Sharma 1976). Subsequently, this species was reported from other parts of southern India (Smart et al. 2014). It is classified under genus Platyceps Blyth, 1860 currently (Wallach et al. 2014). According to Sharma (1976 & 2003) this species is diurnal and found in rocky habitats covered with deciduous vegetation and its diet consists of Hemidactylus brookii geckos. In this note, we report for the first time, the occurrence of P. bholanathi from Nilgiris Landscape, Tamil Nadu, India. On 3 September 2016 at 15.30hr, we came across a dead snake on a rock in the Sigur (11.5312700N & 76.7697310E, elevation 945m) a rain-shadow area in the Nilgiris landscape, Tamil Nadu, India (Images 1 & 2). We measured the total body length (TBL), snout-vent length (SVL) and tail length (TaL) using an inch tape to the nearest mm.

The total body length (TBL) of the Sigur specimen was 246mm with a snout to vent length (SVL) of 176mm and tail length (TaL) of 70mm. It had 19:19:13 dorsal scale, 208 ventral scales and 110 pairs of subcaudal scales. This specimen is confirmed to be Platyceps bholanathi following major key characters with available literature (Sharma 1976; Guptha et al. 2012; Seetharamaraju & Srinivasulu 2013; Ganesh et al. 2013; Sharma et al. 2013; Smart et al. 2014), scalation like ventral scales 208; subcaudal scales 110; scale rows 19:19:13; preocular 1, presubocular 1, postoculars 2, loreal 1, supralabials 9 (5th and 6th touching the eye) and temporal 2+2. Morphology characters such as head broader than the neck, eye has round pupil, pointed snout. Top of head is light brown witha number of irregular shaped markings of dark brown, margined by black (Image 1b). One black streak starts from the lower part of the eyes and reaches till the posterior lip. One dark brown patch starts from the temporal and reaches the posterior lower temporal (Image 1a,c). A long slender body, with a longer tail with a pointed end. Dorsal side has light grayish-brown color bands, black edged, starting from the neck, the bands become faint mid body and are completely absent on tail parts (Image 1a).







Platyceps gracilis (Günther, 1862) is another Indian species of Coluber, reported only from a few localities from four Indian states, Rajasthan, Gujarat, Madhya Pradesh and Maharashtra (Smart et al. 2014). P. gracilis scalation, morphology characters and habitat type is similar to Platyceps bholanathi (Ganesh et al. 2013; Smart et al. 2014); however, based on the following three major comparison characters with available literature clearly indicates that the Sigur specimen (P. bholanathi) differs from P. gracilis in: (i) Sigur specimen has 19:19:13 dorsal scale rows vs. 21:21:15 in P. gracilis (Ganesh et al. 2013); (ii) Sigur specimen has a nuchal blotch that has a round posterior margin (Image 1a,b) vs. P. gracilis, the blotch usually appears to have an inverse V at its posterior margin (Smart et al. 2014); (iii) Sigur specimen has a dark brown parietal bar that is interrupted laterally by light coloration at the post-temporal area adjacent to the parietal scales (Image 1a,b) vs. In P. gracilis, dark parietal bar widens towards the last two supralabials, typically forming an inverted “Y” (Smart et al. 2014).

In the literature, observations of juveniles were reported in the month of July during the southwest monsoon (TL 295mm) (Guptha et al. 2012) and November in the northeast monsoon (TL 320mm) (Ganesh et al. 2013). But in the present case, we observed this juvenile specimen in the month of September (northeast monsoon). Our individual was smaller in size (TL 246mm) compared to earlier reports. This finding indicates that this season is possibly the breeding season of Platyceps bholanathi in this region and more observations are required for better understanding of the breeding season of this endemic snake species.

The habitat type was determined by referring to Champion & Seth (1968). The specimen was found in a rocky habitat with dry thorn forests (Image 3), which is similar to earlier reported habitat of deciduous vegetation (Sharma 1976, 2003), deciduous forest patch (Guptha et al. 2012), rocky boulders or hillocks intermixed with sparsely scattered scrublands (Ganesh et al. 2013), semi desert scrub forest containing evergreen thorny vegetation (Sharma et al. 2013), scattered scrub vegetation and rocky outcrops (Seetharamaraju & Srinivasulu 2013) and mixture of dry deciduous scrub forest and thorn scrub (Smart et al. 2014). This result clearly indicates the role of dry and rocky hills in supporting such species. Protection of this habitat in future conservation plans will be useful to conserve such a poorly known endemic species.

According to previous studies, the distribution of Platyceps bholanathi encompasses the discontinuous Eastern Ghats mountains in southern India, including the states of Andhra Pradesh and Telangana (Sharma 1976; Guptha et al. 2012; Ganesh et al. 2013; Seetharamaraju & Srinivasulu 2013), Karnataka (Sharma et al. 2013) and Tamil Nadu (Ganesh et al. 2013; Smart et al. 2014) (Image 2). Our new record significantly extends the range from all earlier records (nearest previous record 160km northeast) (Image 2). Moreover, past records of the distribution of this snake were only in the Eastern Ghats regions of southern India. The Sigur Plateau is the connective junction of the Western Ghats and the Eastern Ghats region (Samson et al. 2016); therefore this species extends its distribution to the Western Ghats landscape also. Our record is important because it not only significantly extends the range from earlier records (Image 2) but it is also the first report of this species from the Nilgiri Landscape. We however suggest further studies on more sightings / collections of this taxon from the dry forests of Nilgiris landscape to conclusively prove its occurrence in Mudumalai. Elsewhere in the Western Ghats, cases of uncertain snake identification-based range extensions have been reported with caution (Harikrishnan et al. 2007), a stance that we too follow here. We believe that our present note will encourage further studies on this group and throw open prospects to resolve such issues.









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