Journal of Threatened Taxa | www.threatenedtaxa.org | 26 October 2025 | 17(10): 27594–27610

 

ISSN 0974-7907 (Online) | ISSN 0974-7893 (Print) 

https://doi.org/10.11609/jott.9902.17.10.27594-27610

#9902 | Received 05 May 2025 | Final received 26 August 2025 | Finally accepted 08 September 2025

 

 

Amphibians and reptiles of Chitwan National Park, Nepal: an updated checklist and conservation issues

 

Santosh Bhattarai 1, Bivek Gautam 2, Chiranjibi Prasad Pokheral 3  & Ram Chandra Kandel 4       

 

1,3 National Trust for Nature Conservation, Khumaltar Lalitpur, P.O. Box 3712, Kathmandu, Nepal.

1 Nepal Conservation and Research Center, Ratnanagar 06, Sauraha, Chitwan 44204, Nepal.

2 Biodiversity Research and Conservation Society, Tarakeshwar-11, Kathmandu, Nepal.

4 Department of National Parks and Wildlife Conservation, Babarmahal, P.O Box 860, Kathmandu, Nepal.

1 santosh.bhattarai@hotmail.com (corresponding author), 2 bivek.gautam2@gmail.com, 3 chiranpokharel@yahoo.com, 4 rckandel006@gmail.com

 

 

Editor: S.R. Ganesh, Kalinga Foundation, Agumbe, India.             Date of publication: 26 October 2025 (online & print)

 

Citation: Bhattarai, S., B. Gautam, C.P. Pokheral & R.C. Kandel (2025). Amphibians and reptiles of Chitwan National Park, Nepal: an updated checklist and conservation issues. Journal of Threatened Taxa 17(10): 27594–27610. https://doi.org/10.11609/jott.9902.17.10.27594-27610

  

Copyright: © Bhattarai et al. 2025. Creative Commons Attribution 4.0 International License. JoTT allows unrestricted use, reproduction, and distribution of this article in any medium by providing adequate credit to the author(s) and the source of publication.

 

Funding: Katie Adamson Conservation Fund, USA.

 

Competing interests: The authors declare no competing interests.

 

Author details: Santosh Bhattarai—conservation biologist at Nepal Conservation and Research Center, specializing in systematics, ecology, and conservation of reptiles and amphibians. Bivek Gautam—amphibian biologist and member of the IUCN SSC Amphibian Specialist Group. Dr. Chiranjibi Prasad Pokheral—conservation director at the National Trust for Nature Conservation, responsible for designing and implementing conservation projects in Nepal. Dr. Ram Chandra Kandel—director general of the Department of National Parks and Wildlife Conservation, overseeing protected area management and the implementation of conservation initiatives nationwide.

 

Author contributions: SB and BG conducted field surveys. SB generated funds, prepared manuscript, and submitted. BG, CPP and RCK reviewed the draft. CPP and RCK acquired necessary permissions for field surveys.

 

Acknowledgments: We acknowledge the support received from Chitwan National Park and National Trust for Nature Conservation. We thank wildlife technicians Dip Prasad Chaudhary, Tika Ram Tharu, Om Prakash Chaudhary, Binod Darai, Ramesh Darai, Tirtha Lama, Kapil Pokharel, Harkaman Lama, Suresh Shahi and Lal Bahadur Mahatara from Biodiversity Conservation Center, Sauraha for their support during the field work. We also thank NTNC-BCC team for logistics support. We would like to thank Katie Adamson Conservation Fund, USA to support herpetofauna research and conservation in Nepal. 

 

 

Abstract: An updated checklist of amphibians and reptiles of Chitwan National Park and its buffer zone is presented, which is essential for conservation management decision-making as the area is experiencing frequent stochastic events in recent years. A total of 89 species is listed from Chitwan National Park including—20 frogs & toads, 42 snakes, 14 lizards, 11 turtles, and two crocodile species. The confirmed record of Dudhwa Reed Frog Chirixalus dudhwaensis in Nepal is provided, and the occurrence of Eastern Bronze-back Tree Snake Dendrelaphis proarchos from Chitwan National Park, representing its westernmost known distribution in Nepal. In addition the presence of Hylarana tytleri and Sitana sivalensis is confirmed from Chitwan National Park. These findings contribute to filling critical knowledge gaps in species richness and offer updated insights into the taxonomy, natural history, and conservation status of herpetofauna in the park. Recent IUCN Red List mentions the geographic range of the Torrent Paha Frog Nanorana ercepeae from Chitwan National Park; based on the absence of verified records, we exclude it from updated checklist. We also suggest integrative taxonomic and ecological studies to uncover hidden diversity, and to inform evidence-based conservation strategies for amphibians and reptiles in Nepal.

 

Keywords: Chirixalus dudhwaensis, Chitwan-Annapurna Landscape, conservation, Dendrelaphis proarchos, diversity, herpetofauna, Hylarana tytleri, Nanorana ercepeae, new records, Sitana sivalensis, Terai-Arc Landscape.

 

 

 

Introduction

 

Nepal’s protected area network was designed and established to safeguard the country’s rich biodiversity, encompassing species, ecosystems, habitats, and genetic resources (MPFS 1988). At present, Nepal comprises 20 protected areas, including 12 national parks, six conservation areas, one wildlife reserve, and one hunting reserve (DNPWC 2025). The Department of National Parks and Wildlife Conservation (DNPWC) is the central authority responsible for the management and conservation of wildlife and their habitats within these areas. An essential prerequisite for effective wildlife conservation and management is that park managers possess a comprehensive understanding of the existing faunal diversity within their jurisdictional areas. Such knowledge is critical to identify species and populations that are in urgent need of targeted conservation interventions. Biodiversity documentation and periodic inventories, supported by validated scientific information, are foundational to evidence-based conservation planning (Boone et al. 2005). Conversely, gaps in biodiversity knowledge can hinder progress toward national and international biodiversity targets (Girardello et al. 2018).

In Nepal, wildlife conservation efforts have predominantly focused on large charismatic megafauna such as the Royal Bengal Tiger Panthera tigris, Greater One-horned Rhinoceros Rhinoceros unicornis, Asian Elephant Elephas maximus in the lowlands, and Snow Leopard Panthera uncia in the high Himalaya (Bhattarai et al. 2017a; Gautam et al. 2022). The increase in the population sizes of these species is often cited as indicators of conservation success (Rawat et al. 2020). Non-charismatic taxa, particularly herpetofauna (amphibians and reptiles), remain comparatively understudied, and largely neglected in conservation priorities (Bhattarai et al. 2017a, 2020; Gautam et al. 2020). Despite this general oversight, some targeted conservation actions have been implemented for select herpetofauna species. For instance, the conservation of the Gharial Gavialis gangeticus involves both in situ, and ex situ strategies, and its population status is relatively well documented (Acharya et al. 2017; Bhattarai et al. 2018; Poudyal et al. 2018; Yadav et al. 2022).

The present study aims to update the checklist of amphibians and reptiles of Chitwan National Park (CNP) and its buffer zone, thereby contributing to the broader understanding of the herpetofauna diversity in the park. The foundational work on the herpetofauna of CNP was conducted by Zug & Mitchell (1995), who reported 55 species. Earlier records, such as those by Fleming & Fleming (1973), and Kramer (1977), also documented snake species in Chitwan. Subsequent field guides and inventories (Schleich & Kästle 2002; Shah & Tiwari 2004; Kästle et al. 2013) enriched the knowledge base by including species with known distributions in the park.

More recently, efforts have been made to compile species-specific and locality-based lists, particularly of snakes (Pandey 2012), including the first record of the Siamese Cat Snake Boiga siamensis in Nepal (Pandey et al. 2018). Additionally, Psammodynastes pulverulentus was recently recorded for the first time in CNP (Bhattarai et al. 2017b). Many herpetological surveys have been locality or taxonomically restricted. For example, Lamsal (2014) conducted surveys exclusively in the Madi Valley of Chitwan, while Bhattarai et al. (2017a) focused on the Beeshazar and associated lakes complex – a Ramsar site of international importance. Other notable contributions include the descriptions of Rana chitwanensis (now treated as Hylarana chitwanensis) and Sphaerotheca maskeyi from the CNP (Das 1998; Schleich & Anders 1998), life history observations of turtles (Mitchell & Rhodin 1996), studies on turtle distribution (Khadka & Lamichhane 2020), studies on population and determinants of crocodile distribution and their socioeconomics (Nishan et al. 2023; Pathak et al. 2023) and post release growth of gharial (Khadka et al. 2022).

Importantly, herpetofauna taxonomy and nomenclature have undergone significant revisions in recent years. These changes, have yet to be incorporated into key conservation and management documents, including the official management plan of the Chitwan National Park (see CNP 2018). To address this gap, the present study provides an updated, taxonomically revised checklist of amphibians & reptiles of the CNP, and its buffer zone. The aim is to deliver up-to-date species list to support evidence-based management decisions and to highlight emerging conservation priorities.

 

 

Material and Methods

 

Study area

Chitwan National Park is the oldest national park of Nepal (Established in 1973, area 952.63 km2, buffer zone 730 km2) and designated as UNESCO’s World Heritage Site in 1984 (under the criteria vii, ix, & x) for its exceptional natural beauty, supporting outstanding natural & biological systems, and processes, and for providing natural habitats for endangered fauna & flora (Image 1). The park comprises a mosaic of physiographic regions, including the Himalayan foothills, floodplains, Dun valleys, and the Siwalik (Chure) hills, with elevations ranging 100–900 m. The vegetation is primarily dominated by Sal Shorea robusta forests (DNPWC 2020), interspersed with 425 grassland patches that cover about 6.24% of the park’s area (CNP 2016). Additionally, 58 small and large natural wetlands within the park serve as critical habitats for numerous aquatic and semi-aquatic species, including a wide range of herpetofauna (CNP 2018). The landscape of the CNP has been shaped by three river systems: the Narayani, Rapti, and Reu rivers. Among these, the Narayani River—also known as the Gandaki and Trishuli Rivers upstream and as Gandak downstream in India—is of Himalayan origin, carrying a significant volume of meltwater from the Himalayas and serving as a perennial watercourse with substantial influence on the park’s hydrology, and sediment dynamics (Dahal et al. 2015). In contrast, the Rapti and Reu rivers originate from the Siwalik, and mid-hill regions to the east, and south of the park, respectively. These rivers are primarily rain-fed and exhibit strong seasonal fluctuations in discharge, particularly during the monsoon period (Gurung & Thapa 2016). Collectively, these river systems support a mosaic of aquatic and riparian habitats that are critical for the park’s biodiversity, including the ‘Critically Endangered’ Gharial Gavialis gangeticus (Bhuju et al. 2007; Poudyal et al. 2018; Yadav et al. 2022).

In 2003, the Beeshazar and associated lakes, located within the buffer zone of the CNP, were designated as a Ramsar Site—a wetland of international importance—further emphasizing the conservation value of the CNP’s aquatic habitats.

 

Methods

The data presented in this study are derived from a combination of field observations, rescue call records, and existing literature. Diurnal and nocturnal visual encounter surveys (VES) were conducted following Heyer et al. (1994) during multiple field visits across various habitats within both the core and buffer zones of CNP (Image 2). Surveys were conducted during the following periods: 02–08 August 2018, 17–30 July 2019, 8–15 August 2019, 3–14 September 2019, 2–5 February 2020, 16–24 June 2020, 14–29 July 2020, 10–21 August 2020, 5–15 June 2021, 19–25 July 2021, 11–19 August 2021, and 15–25 July 2023.

Survey teams consisted of three to four observers, who systematically searched all potential microhabitats that likely support amphibians and reptiles. This included active searches involving the turning of logs & stones, inspecting under leaf litter, peeling bark from fallen dead trees, and examining vegetation near water bodies, and forest edges. Diurnal surveys were conducted at 0900–1700 h, while nocturnal surveys were conducted at 1900–2300 h. In addition to systematic surveys, opportunistic data were also collected from rescue calls, mainly involving snakes, and crocodiles, received from local communities in the buffer zone. These opportunistic records contributed to the overall species richness data.

All individuals observed during surveys and rescue calls were identified to species level based on morphological characteristics, and photographic documentation, using standard field guides, and taxonomic literature (Smith 1935; Schleich & Kästle 2002; Shah & Tiwari 2004; Whitaker & Captain 2004; Lajmi et al. 2016; Das & Das 2017; David & Vogel 2021; Garg & Biju 2021; Gowande et al. 2021; Khatiwada et al. 2021; Vogel et al. 2022; Köhler et al. 2023). For taxonomic nomenclature, Frost (2025) for amphibians, and Uetz et al. (2025) for reptiles was followed.

 

 

Results

 

Species richness

The herpetofauna of CNP comprises 89 species, including 20 species of amphibians representing 14 genera, and five families; two species of crocodilians from two genera and two families; 11 species of turtles in seven genera and three families; 14 species of lizards across eight genera and four families; and 42 species of snakes representing 30 genera and 10 families (Table 1; Images 7–11). The Dhudhwa Reed Frog Chirixalus dudhwaensis Ray, 1992, is reported as a new species record for Nepal. Additionally, confirmed locality records of the Eastern Bronze-back Tree Snake Dendrelaphis proarchos (Wall, 1909), representing CNP as the westernmost known distribution of the species in Nepal is provided.  

Among the 20 amphibian species recorded, three are classified as Vulnerable, 15 as Least Concern, one as Data Deficient, and one remains Not Evaluated, based on the IUCN Red List of Threatened Species. Similarly, among the 69 recorded reptile species, three species are classified as Critically Endangered, five species as Endangered, six species as Vulnerable, and four species as Near Threatened according to the IUCN Red List. Additionally, six species have not yet been evaluated, while the remaining 45 species are currently listed as Least Concern. These assessments reflect the varying conservation needs of amphibians and reptiles in the park, and underscore the importance of targeted conservation actions, especially for species at risk.

 

New records from Chitwan National Park, Nepal

Dhudhwa Reed Frog Chirixalus dudhwaensis Ray, 1992 is reported as a confirmed new country record for Nepal based on observation from CNP (Image 3). This record is located approximately 365 km east (air distance) from its type locality in Dudhwa National Park in India. The individual was observed calling in sympatry with Uperodon globulosus, Uperodon taprobanicus, and Microhyla nilphamarensis after a heavy rainfall.  Later, we also recorded this frog from Dhangadhi, Kailali in Sudoorpaschim Province.

The occurrence of Eastern Bronze-back Tree Snake Dendrelaphis proarchos (Wall, 1909) from Chitwan National Park is documented, representing the westernmost known distribution of the species in Nepal (Image 4). The D. proarchos were frequently observed in the Sauraha and Amaltari of the park. The record from CNP is approximately 900 km west of its type locality in Assam, India. D. proarchos was also observed from eastern Nepal, from Dharan forest, Miklajung, and Pathari, Morang in Koshi Province. Furthermore, Hylarana tytleri in Bandevi buffer zone community forest was also observed, which is a part of Barandabhar corridor forest (Image 5), and the Siwalik Fan-throated Lizard Sitana sivalensis from Triveni area of the park connected with Valmiki Tiger Reserve in India (Image 6).           

 

   

Discussion

 

The present study provides an update in the understanding of amphibian and reptile diversity in the CNP and its buffer zone. The documentation of 89 species underscores the park and buffer zone as a critical stronghold for amphibians and reptiles. This update represents a significant increase from earlier works, notably the 55 species of herpetofauna reported by Zug & Mitchell (1995), and 32 species of snakes reported by Pandey et al. (2018), and highlights the need for continuous, and systematic biodiversity assessments. The documentation of the Dudhwa Reed Frog Chirixalus dudhwaensis from the CNP as a new country record for Nepal indicates that suitable habitats for this species may be more continuous across the lowland Terai. Similarly, the observations of Eastern Bronze-back Tree Snake Dendrelaphis proarchos in the park’s Sauraha and Amaltari extends the known distribution of this species by nearly 900 km westward from its type locality in Assam, India. Although the occurrence of D. proarchos in Nepal was previously mentioned by Das & Das (2017), it lacked specific locality data; therefore, the observations from Chitwan National Park and from eastern Nepal provide the confirmed locality records for the species within the country. Likewise, the observation of Hylarana tytleri and Sitana sivalensis in CNP underpins the need for fine-scale herpetofauna surveys in the region. Hylarana tytleri, previously reported primarily from eastern Nepal (Schleich & Kästle 2002; Shah & Tiwari 2004) and with a single record from the Ghodaghodi Lake Complex in far-western Nepal (Shah & Tiwari 2004), warrants further confirmation to validate its occurrence in the far-western region.

The record of Sitana sivalensis from the Triveni area of the CNP is ca. 105 km east (air distance) from its type locality, Shivapur, Kapilbastu, Nepal, emphasizing the need for further targeted surveys along the Siwalik foothills. Given that the Triveni area is contiguous with the Valmiki Tiger Reserve in Bihar, India, species likely to be S. sivalensis from Valmiki Tiger Reserve was also observed during the transboundary rhino rescue. 

Recently, Mirza et al. (2024) described a new species of a vine snake, Ahaetulla longirostris, from adjoining Valmiki Tiger Reserve. Accordingly, Ahaetulla cf. nasuta can be recognized from Chitwan National Park as A. longirostris, since the true A. nasuta is now considered restricted to Sri Lanka (Mallik et al. 2020). Similarly, Gowande et al. (2021) reassessed the taxonomy of the Calotes versicolor complex in southern Asia and assigned the populations from the Gangetic plains to Calotes vultuosus (Harlan, 1825), based on a combination of morphological characters, including a smaller to medium body size, and a dorsal crest composed of relatively smaller scales that gradually decrease in size towards the tail compared to C. versicolor. The observations of Calotes from CNP agree with the diagnostic characters of C. vultuosus. Therefore, the Chitwan population is considered to represent C. vultuosus. Likewise, the Banded Kukri Snake Oligodon arnensis is treated as O. russelius, as suggested by Bandara et al. (2022), for Eutropis macularia as E. trivittata (Amarsinghe et al. 2022), Rabdophis subminiatus as R. helleri (David & Vogel 2021),Hemidactylus brookii as H. kushmorensis (Lajmi et al. 2016) and Boiga ochracea as B. stoliczkae (Köhler et al. 2023). A detailed specimen-based study is recommended, incorporating both morphological and molecular approaches, to confirm the taxonomic status of above-mentioned species in Nepal.  

Malhotra et al. (2025) recently downgraded Trimeresurus salazar to a subspecies of Trimeresurus septentrionalis, noting that whole genome analyses are currently underway. The field observations of Trimeresurus populations from CNP and other lowland regions of Nepal, differ from T. septentrionalis specimens collected from its type locality in Pokhara, situated in the mid-mountain region of Nepal, and are more consistent with the description provided by Vogel et al. (2022). Accordingly, the Chitwan population is treated as T. salazar (Mirza et al. 2020). Furthermore, earlier literature reports a GenBank accession number (AF171909) for a specimen collected from Mahottari District in Madhesh Province located in the lowland Terai region of Nepal (Malhotra & Thorpe 2004), mentioned as Trimerusurus albolabris. To resolve these uncertainties, a comprehensive sampling of Trimerusurus from lowland, mountains, and valleys are needed for a detailed comparative study to clarify taxonomic status, and evolutionary relationship within Trimeresurus sepentrionalis complex.

Two frog species, namely, Sphaerotheca maskeyi (Schleich & Anders, 1998) and Rana chitwanensis (now Hylarana chitwanensis) (Das, 1998), were described from CNP, while Narayanghat Whipping Frog Polypedates zed (Dubois, 1987) was described from Narayanghat, Chitwan; hardly 5 km away from the CNP, and Barandabhar (Bhattarai et al. 2017a). The known distributions of H. chitwanensis and Polypedates zed remain restricted to their respective type localities at Kasara, CNP, and Narayanghat, respectively. Hylarana chitwanensis was recorded from the Temple Tiger area and the Bagai area of the CNP, and observed calling males from Bagai during the monsoon season. These observations provide additional locality records for Hylarana chitwanensis, a species that has been poorly documented since its description. No Polypedates zed were detected during the survey, although P. maculatus was observed from the area. Given the significant urban expansion of Narayanghat into a metropolitan area, it is imperative to conduct targeted surveys combining fieldwork, and molecular methods, including comparison with the holotype, and related congeners, to ascertain the continued presence of P. zed in the wild. As for the dicroglossid frog Minervarya syhadrensis (Annandale, 1919), current scholarship suggests that it may be restricted to the hills of Peninsular India, especially the Western Ghats (Phuge et al. 2020). Some publications (Khatiwada et al. 2021) report M. syhadrensis also from Nepal, which may require additional re-confirmation. Hence, the sightings are conservatively represented from Nepal as M. cf. syhadrensis, requiring additional confirmation of their species identity.

 

Conservation concerns

This article highlights the erroneous inclusion of Torrent Paha Frog Nanorana ercepeae in the CNP and Shuklaphanta National Park in the recent IUCN Red List assessment. Nanorana ercepeae was originally described from Bajhang in far-western Nepal. The species is known to inhabit temperate forests associated with montane streams in the proximity of coniferous forests; occurring at elevations of 1700–2700 m (Schleich & Kästle 2002; Shah & Tiwari 2004; Alley et al. 2013). In contrast, CNP is characterized by sub-tropical forests with a known elevation of approximately 100–900 m (DNPWC 2020), which likely represent unsuitable habitats for Nanorana ercepeae. Furthermore, no verified records for the species exist within the park. This correction is crucial, as inaccurate species lists can mislead conservation priorities, and management interventions.

Many reptile species such as Yellow Tortoise Indutestudo elongata, Three Striped-roofed Turtle Batagur dhongoka face critical endangerment similar to the gharial Gavialis gangeticus. These species, unlike the Gharial, receive no conservation attention in Nepal. This neglect is particularly concerning for Batagur dhongoka; for which further verification is needed to confirm its occurrence in Nepal. Likewise, earlier literature reports the occurrence of Red-crowned Roofed Turtle Batagur kachuga from Nepal (Schleich & Kästle 2002; Shah & Tiwari 2004; Aryal et al. 2010). The known population of Batagur dhongoka and B. kachuga is not known from Nepal (Das et al. 2019; Praschag et al. 2019) and the distribution of B. kachuga in Nepal is erroneous, and unlikely to occur as its known distribution is only from Chambal River system in India, and Ganga River is the northern-most distribution limit (S. Singh pers. comm.). Similarly, ‘Endangered’ species such as Chitra indica; Nilssonia gangetica, N. hurum, and Varanus flavscens also require urgent conservation attention due to continuing threats such as habitat loss, pollution, and illegal exploitation similar to those impacting Gharials (Poudyal et al. 2018; Yadav et al. 2022).

 

Conservation implications

The tigers and rhinos are the nucleus of conservation interventions in the CNP. All the conservation activities such as grassland management through cutting, slash & burn practices, and wetland restoration are primarily designed, and implemented to support these species. Additionally, community engagement activities such as outreach sessions, and involvement of community-based anti-poaching units, focus mainly on these priority taxa. These units receive frequent specialized training in species-specific conservation practices, particularly for tigers and rhinos.

The ‘Critically Endangered’ Gharial has attracted targeted conservation efforts such as population monitoring, nest monitoring, protection, and nest relocation have been implemented to safeguard the Gharial population in the rivers of the CNP and at Gharial Conservation and Breeding Center (GCBC), located at the headquarters of the CNP at Kasara (Poudyal et al 2018; Khadka et al. 2022a). The GCBC is well managed, with hundreds of Gharials reared annually, and released into the wild through a head-start program. In contrast, management efforts at the Turtle Breeding Center (TBC) remain limited, with only a few documented initiatives, such as the successful nest relocation of Chitra indica (Khadka et al. 2022b). Despite these initiatives, the aquatic habitats of the CNP remain under significant anthropogenic pressure. Both legal and illegal activities, including the distribution of fishing licenses to selected river-dependent communities, and the widespread illegal use of gill nets threaten the Gharial’s survival. Entanglement in fishing nets is among the greatest direct threats, often resulting in injury or mortality. Given these challenges, it is imperative that conservation efforts in the CNP adopt more inclusive activities that address the shared threats faced by amphibians and reptiles, beyond the priority taxa.

The updated checklist in this study offers a baseline for future herpetological research and conservation planning in the CNP. The findings highlight the herpetofauna richness of the CNP and its buffer zone. Given the increasing frequency of stochastic events such as floods, wildfires, and anthropogenic pressures, maintaining updated information, and implementing adaptive management strategies are essential to ensure the long-term persistence of herpetofauna communities in the park. Therefore, it is recommended to use integrative taxonomic approaches, combining molecular, morphological, and ecological data to resolve cryptic diversity for effective conservation actions.

 

 

Table 1. Checklist of amphibians and reptiles of Chitwan National Park, Nepal with their current IUCN Red List status.

 

Species name

Common name

Red List status

AMPHIBIANS

Family: Bufonidae Gray, 1825

1

Duttaphrynus melanostictus (Schneider, 1799)

Common Asian Toad

LC

2

Firouzophrynus stomaticus (Lütken, 1864)

Marbled Toad

LC

Family: Microhylidae Günther, 1858 (1843)

3

Microhyla nilphamariensis Howlader, Nair, Gopalan, & Merilä, 2015

Nilphamari Narrow-mouth Frog

LC

4

Uperodon globulosus (Günther, 1864)

Globular Balloon Frog

LC

5

Uperodon taprobanicus (Parker, 1934)

Painted Frog

LC

Family: Dicroglossidae Anderson, 1871

6

Euphlyctis adolfi (Gunther, 1860)

Skittering Frog

LC

7

Fejervarya orissaensis (Dutta, 1997)

Odisha Cricket Frog

LC

8

Hoplobatrachus tigerinus (Daudin, 1802)

Indian Bull Frog

LC

9

Minervarya chilapata Ohler, Deuti, Grosjean, Paul, Ayyaswamy, Ahmed, & Dutta, 2009

Chilapata Rainpool Frog

VU

10

Minervarya nepalensis (Dubois, 1975)

Nepal Cricket Frog

LC

11

Minervarya pierrei (Dubois, 1975)

Pierre's Cricket Frog

LC

12

Minervarya cf. syhadrensis (Annandale, 1919)

Syhadra Cricket Frog

LC

13

Minervarya teraiensis (Dubois, 1984)

Terai Cricket Frog

LC

14

Sphaerotheca maskeyi (Schleich & Anders, 1998)

Maskey's Burrowing Frog

LC

Family: Ranidae Batsch, 1796

15

Amolops mahabharatensis Khatiwada, Shu, Wang, Zhao, Xie, & Jiang, 2020

Mahabharat Cascade Frog

VU

16

Hylarana chitwanensis (Das, 1998)

Chitwan Frog

DD

17

Hylarana tytleri Theobald, 1868

Yellow-striped Frog

LC

Family: Rhacophoridae Hoffman, 1932 (1858)

18

Chirixalus dudhwaensis Ray, 1992

Dudhwa Reed Frog

VU

19

Polypedates maculatus (Gray, 1830)

Common Tree Frog

LC

20

Polypedates taeniatus (Boulenger, 1906)

Six-lined Bush Frog

LC

REPTILES

Family: Crocodylidae Cuvier, 1807

21

Crocodylus palustris (Lesson, 1831)

Mugger Crocodile

VU

Family: Gavialidae Adams 1854

22

Gavialis gangeticus (Gmelin, 1789)

Gharial

CR

Family: Geoemydidae Theobald 1868

23

Batagur dhongoka (Gray, 1834)

Three-striped Roofed Turtle

CR

24

Melanochelys tricarinata (Blyth, 1856)

Tricarinate Hill Turtle

EN

25

Melanochelys trijuga (Schweigger, 1812)

Black Pond Turtle

LC

26

Pangshura smithii (Gray, 1863)

Brown Roofed Turtle

NT

27

Pangshura tecta (Gray, 1830)

Indian Roofed Turtle

VU

28

Pangshura tentoria (Gray, 1834)

Indian Tent Turtle

LC

Family: Testudinidae Batsch, 1788

29

Indotestudo elongata (Blyth, 1854)

Elongated tortoise

CR

Family: Trionychidae Gray, 1835

30

Chitra indica (Gray 1831)

Narrow-headed Softshell Turtle

EN

31

Lissemys punctata (Bonnaterre, 1789)

Indian Flapshell Turtle

VU

32

Nilssonia gangetica (Cuvier, 1825)

Gangetic Softshell Turtle

EN

33

Nilssonia hurum (Gray, 1830)

Peacock Softshell Turtle

EN

Family: Agamidae Gray, 1827

34

Calotes vultuosus (Harlan, 1825)

Changeable Lizard

LC

35

Sitana sivalensis Schleich, Kästle, & Shah, 1998

Sivalik Fan-throated Lizard

LC

Family: Gekkonidae Gray, 1825

36

Hemidactylus cf. kushmorensis Murray, 1884

 Kushmore House Gecko

 

37

Hemidactylus flaviviridis Rüppell, 1835

Yellow-bellied House Gecko

LC

38

Hemidactylus frenatus Duméril & Bibron, 1836

Common House Gecko

LC

39

Hemidactylus garnotii Duméril & Bibron, 1836

Fox Gecko

LC

Family: Scincidae Gray, 1825

40

Ablepharus sikimmensis (Blyth, 1854)

Sikkim Ground Skink

LC

41

Eutropis carinata (Schneider, 1801)

Common Ground Skink

LC

42

Eutropis macularia (Blyth, 1853)

Bronze Ground Skink

LC

43

Eutropis trivittata (Hardwicke & Gray, 1827)

Striped Ground skink

LC

44

Riopa albopunctata Gray, 1846

White-spotted Supple Skink

LC

45

Sphenomorphus maculatus (Blyth, 1853)

Spotted Forest Skink

LC

Family: Varanidae Merrem, 1820

46

Varanus bengalensis (Daudin, 1802)

Bengal Monitor

NT

47

Varanus flavescens (Hardwicke & Gray, 1827)

Golden Monitor

EN

Family: Erycidae Bonaparte, 1831

48

Eryx conicus (Schneider, 1801)

Common Sand Boa

NT

49

Eryx johnii (Russell, 1801)

Red Sand Boa

NT

Family: Pythonidae Fitzinger, 1826

50

Python bivittatus Kuhl, 1820

Burmese Python

VU

Family: Colubridae Oppell, 1811

51

Ahaetulla laudankia Deepak, Narayanan, Sarkar, Dutta & Mohapatra, 2019

Laudanka Vine Snake

LC

52

Ahaetulla longirostris Mirza, Pattekar, Verma, Stuart, Purkayastha, Mohapatra, & Patel, 2024

Long-snout Vine Snake

 

53

Boiga stoliczkae (Wall, 1909)

Tawny Cat Snake

LC

54

Boiga siamensis Nootphand, 1971

Siamese Cat Snake

LC

55

Boiga trigonata (Schneider, 1802)

Common Cat Snake

LC

56

Boiga westermanni (Reinhardt, 1863)

Indian Egg-eating Snake

LC

57

Chrysopelea ornata (Shaw, 1802)

Ornate Flying Snake

LC

58

Coelognathus helena (Daudin, 1803)

Common Trinket Snake

LC

59

Coelognathus radiatus (Boie, 1827)

Copper-headed Trinket Snake

LC

60

Dendrelaphis tristis (Daudin, 1803)

Common Bronze-back Tree Snake

LC

61

Dendrelaphis proarchos Wall, 1909

Eastern Bronze-back Tree Snake

 

62

Gongylosoma calamaria (Günther, 1858)

Calamaria Reed Snake

LC

63

Lycodon aulicus (Linnaeus, 1758)

Common Wolf Snake

LC

64

Lycodon jara (Shaw, 1802)

Twin-spotted Wolf Snake

LC

65

Lycodon striatus (Shaw, 1802)

Barred Wolf Snake

LC

66

Oligodon kheriensis Acharji & Ray, 1836

Coral Red Kukri Snake

LC

67

Oligodon russelius (Daudin, 1803)

Russell's Kukri Snake

 

68

Ptyas mucosa (Linnaeus, 1758)

Common Rat Snake

LC

69

Sibynophis sagittarius (Cantor, 1839)

 

LC

Family: Homalopsidae Bonaparte, 1845 

70

Enhydris enhydris (Schneider, 1799)

Rainbow Water Snake

LC

71

Ferania sieboldii (Schlegel, 1837)

Siebold's Water Snake

LC

Family: Psammophidae Bourgeois, 1968

72

Psammophis condanarus (Merrem, 1820)

Common Sand Snake

LC

Family: Psammodynastidae Das, Greenbaum, Brecko, Pauwels, Ruane, Pirro, & Merilä, 2024

73

Psammodynastes pulverulentus (Boie, 1827)

Common Mock Viper

LC

Family: Natricidae Bonaparte, 1838

74

Amphiesma stolatum (Linnaeus, 1758)

Striped Keelback Snake

LC

75

Fowlea piscator (Schneider, 1799)

Checkered Keelback Snake

LC

76

Herpetoreas platyceps (Blyth, 1854)

Mountain Keelback Snake

LC

77

Rhabdophis helleri Schmidt, 1925

Red-necked Keelback Snake

 

78

Xenochrophis cerasogaster (Cantor, 1839)

Painted Keelback Snake

VU

Family: Elapidae F. Boie, 1827

79

Bungarus caeruleus (Schneider, 1801)

Common Krait

LC

80

Bungarus fasciatus (Schneider, 1801)

Banded Krait

LC

81

Bungarus lividus Cantor, 1839

Lesser Black Krait

LC

82

Naja kaouthia Lesson, 1831

Monocled Cobra

LC

83

Naja naja (Linnaeus, 1758)

Common Cobra

LC

84

Ophiophagus hannah (Cantor, 1836)

King Cobra

VU

85

Sinomicrurus macclellandi (Reinhardt, 1844)

MacClelland's Coral Snake

LC

Family: Typhopidae Merrem, 1820

86

Argyrophis diardii (Schlegel, 1839)

Diard's Blind Snake

LC

87

Indotyphlops braminus (Daudin, 1803)

Common Blind Snake

LC

Family: Viperidae Oppel, 1811

88

Daboia russelii (Shaw & Nodder, 1797)

Russell's Viper

LC

89

Trimeresurus salazar Mirza, Bhosale,
Phansalkar, Sawant, Gowande, & Patel, 2020

Salazar Pit-viper

 

LC—Least Concern | DD—Data Deficient | VU—Vulnerable | NT—Near Threatened | EN—Endangered | CR—Critically Endangered.

 

 

For images - - click here for full PDF

 

 

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