Journal of
Threatened Taxa | www.threatenedtaxa.org | 26 January 2019 | 11(1): 13132–13150
Marine snakes of Indian coasts: historical resume, systematic checklist,
toxinology, status, and identification key
S.R. Ganesh 1, T. Nandhini 2, V.
Deepak Samuel 3, C.R. Sreeraj 4, K.R. Abhilash 5,
R. Purvaja 6 & R. Ramesh 7
1 Chennai Snake Park, Raj Bhavan post,
Chennai, Tamil Nadu 600022, India.
2–7 National Centre for Sustainable Coastal
Management, Koodal Building, Anna University Campus, Chennai, Tamil Nadu
600025, India.
1 snakeranglerr@gmail.com (corresponding
author) 2 nandhu.vanan2389@gmail.com, 3 deepakocean@gmail.com,
4 crsreeraj@gmail.com, 5 abhilash@ncscm.res.in, 6
purvaja.ramachandran@gmail.com, 7 rramesh_au@yahoo.com
Abstract: We compile an up-to-date checklist of
26 species of marine snakes known from the Indian coastlines. We furnish
information on the original orthography, authorship, date of publication,
current binominal representation, synonymy and chresonymy lists for each
recognized taxon. In addition, we
provide details of name-bearing types, repository and type locality (both
original and subsequent restrictions where applicable) of the prevailing nomen
for all recognized species. We summarise
the history of research on Indian marine snakes from Linnaeus to the present
day, including taxonomic and regional treatises, and highlight the taxonomic
flux. We also provide a revised key for
this group to facilitate easier identification and support effective
conservation.
Keywords: Achrochrodide, annotated checklist,
Homalopsidae, Hydophiinae, India, literature review, synonymy.
doi: https://doi.org/10.11609/jott.3981.11.1.13132-13150 | ZooBank: urn:lsid:zoobank.org:pub:D6375F7A-DBC0-487B-8123-D78E402A30B5
Editor:
Chandrashekher U. Rivonker, Goa University, Taleigao Plateau, Goa. Date of
publication: 26 January 2019 (online & print)
Manuscript details: #3981
| Received 30 December 2017 | Final received 21 January 2019 | Finally accepted
23 January 2019
Citation: Ganesh, S.R., T. Nandhini, V.D. Samuel, C.R. Sreeraj, K.R. Abhilash, R.
Purvaja & R. Ramesh (2019). Marine snakes of Indian coasts: historical
resume, systematic checklist, toxinology, status, and identification key. Journal
of Threatened Taxa 11(1): 13132–13150; https://doi.org/10.11609/jott.3981.11.1.13132-13150
Copyright: Ganesh et al. 2019. Creative Commons
Attribution 4.0 International License. JoTT allows unrestricted use,
reproduction, and distribution of this article in any medium by adequate credit
to the author(s) and the source of publication.
Funding: None.
Competing interests: The authors declare no competing interests.
Author
Details: Dr.
S.R. Ganesh is a Scientist at the
Chennai Snake Park, conducting research on reptiles and amphibians of Southern
India. His research themes include documenting diversity of under-explored
eco-regions, updating and refining species characterizations and finding out
modern day distribution patterns with respect to south India’s
herpetofauna. Ms. T. Nandhini is working as a Junior Research Fellow in
the National Centre for Sustainable Coastal Management (NCSCM), Tamil Nadu, India. Her areas of interests are coastal biodiversity and
taxonomy. Dr. Deepak Samuel Vijay Kumar is working as a scientist in
the National Centre for Sustainable Coastal Management (NCSCM), Tamil Nadu, India. He is a taxonomist specializing on marine molluscs,
crustaceans and minor phyla. He is the Principal Investigator for the CoMBINe
Database Project. Dr. C.R. Sreeraj
is a marine biologist with specialisation on the taxonomy of coral reef fauna.
He is a scuba diver with more than ten years of experience on the coral reefs
of India. He holds a PhD in Marine Biology for working on the taxonomy and
ecology of opisthobranchiate mollusca. Earlier with NCSCM, he is currently
working as Scientist at the Sunderban Regional Centre of Zoological Survey of
India. Dr. K.R. Abhilash is
working as Scientist C in the National Centre for Sustainable Coastal
Management (NCSCM), Tamil Nadu, India. His
specialization is on marine biology and conservation. Dr.
Purvaja Ramachandran is working as Scientist G at the National Centre
for Sustainable Coastal Management (NCSCM), Tamil Nadu, India.
Her areas of specialization are coastal biodiversity, ecosystem management,
global climate change and nutrient biogeochemistry. Prof. Dr.
R. Ramesh is the Director of the National Centre for Sustainable Coastal
Management (NCSCM), Tamil Nadu, India. His areas of
specialization are Biodiversity conservation, Coastal Zone Management,
Biogeochemical Cycles and Global Climate Change.
The authors
are part of the Coastal and Marine Biodiversity Conservation Network (CoMBINe)
Database team involved in updating Species checklists and documenting recorded
Species information in Indian waters. This updated checklist is part of the
ongoing initiative to list out and update marine biodiversity of India.
Author
Contribution: SRG and VDS
conceived the study, with inputs from RP and RR. TN, CRS, KRA were involved in
literature survey. SRG led the writing with inputs from TN and VDS. All authors
eqaually participated in refining the manuscript, addressing editorial comments
and approving the final text.
Acknowledgements: We thank our
respective institutions for supporting our research activities. SRG thanks the
Board of Trustees of the Chennai Snake Park Trust for their encouragements. At
the NSCSM, the authors thank the authorities for supporting our research
activities. We thank Madras Crocodile Bank for extending library facilities.
SRG thanks Drs. Harold Voris (Field Museum of Natural History, Chicago, USA),
Ivan Ineich (Museum Nationale dHistoire Naturelle, France), Arne Redsted
Rasmussen (The Royal Danish Academy of Fine Arts, Copenhangen, Denmark) and
Kanishka Ukuwela (University of A’delaide, Australia / Rajarata University, Sri
Lanka) for their email exchanges, supply of important literature and general
discussions on the topic. Thanks are due to Mr. Vivek Sharma for giving his
photo of file snake, used in this article. We are grateful to the reviewers for
their lucid comments that improved this manuscript.
INTRODUCTION
Snakes which live completely or occasionally in marine and estuarine
environments comprise about 90% of living marine reptile species (Wallach et
al. 2014; Uetz & Hosek 2017). Marine
snakes are mainly found in warm tropical and subtropical coastal waters (Dunson
1975; Tu 1988; Heatwole 1999; Rasmussen et al. 2011; Wallach et al. 2014), and
are broadly classified as brackish water snakes, sea kraits and true sea
snakes. Occasionally sea snakes venture
into tidal river creeks far from the tide line, and similarly brackish water
snakes can swim into the sea (Rasmussen et al. 2011; Murphy 2012). Brackish water snakes comprise of wart snakes
(Acrochordidae) and mangrove water snakes (some species belonging to family
Homalopsidae), which are either non-venomous (Acrochordidae) or mildly venomous
(Homalopsidae) and have a cylindrical tapering tail (Whitaker & Captain
2004; Murphy 2007; Alfaro et al. 2008).
The true sea snakes (Elapidae: Hydrophiinae) are all
venomous with front fangs, and are distinguished by their laterally
compressed paddle-like or oar-shaped tail (Heatwole 1999). Two tribes, Hydrophiini (true sea snakes) and
Laticaudini (sea kraits) which are also highly venomous and have paddle-shaped
tail (Heatwole et al. 2012, 2016; Sanders et al. 2012), are present. Marine snakes live in a variety of habitats
like mangrove swamps, coral reefs and lagoons, mud flats and estuaries (Voris
& Murphy 2012). Water salinity has
been reported to greatly influence the distribution of marine snakes globally
(Gasperetti 1988; Brischoux et al. 2012).
As a
group of thoroughly aquatic and stenohaline taxa, true sea snakes
(Hydrophiinae) have several special adaptations (Brischoux & Shine
2011). Like all reptiles these snakes
undergo pulmonary respiration and have an elongated cylindrical lung on the
left side of their body for adequate gas exchange. They have nostril valves that regulate air
entering the lung so that they can remain under water for 0.5 to 2 hours during
a dive. True sea snakes have specialized
head-heart distance and lung morphology (Lillywhite et al. 2012b), and like
most marine snakes they have a salt-excretion gland under their tongue sheath
(Dunson & Dunson 1973). Sea snakes
have a paddle-shaped tail for efficient swimming (Aubert & Shine 2008) and
specialized visual systems to facilitate underwater habitat selection, foraging
and mating (Hart et al. 2012). Sea
kraits are known to possess a unique skin that is partially permeable to water
exchange (Dunson & Robinson 1976; Lillywhite et al. 2009). A recent study on true sea snakes has
revealed the existence of unique sense organs on the scales called sensilla
which are sensitive to light variations in the environment (Zimmermann &
Heatwole 1990; Crowe-Riddell et al. 2016).
True sea snakes have also been reported to be
influenced by water loss and dehydration even at mid-sea (Lillywhite et
al. 2008, 2012a, 2014, 2015).
True
sea snakes shed their skins more frequently (every 2–6 weeks) than land snakes
(3–4 months), mainly to remove fouling marine organisms like algae, barnacles
and bryozoans (Mays & Nickerson 1968; Key et al. 1995). They are mainly ovoviviparous except for the
egg-laying sea kraits (Shetty & Shine 2002). They usually copulate for a long duration
lasting up to over 3 hours on the water surface (Heatwole 1999; Chanhome et al.
2011). The reproduction period ranges
from 4–11 months and most species reproduce annually (Rasmussen 1989, 1992,
1994; Shine 1988, 2005). Juvenile sea
snakes swim up to the water surface to breathe immediately after birth. In many
species, juveniles are brightly banded while the adults are unpatterned
(Heatwole 1999). Unlike snakes of the
tribe Hydrophinii, which are typically adapted to warm coastal waters (Heatwole
& Cogger 1993), the sea kraits (genus Laticauda Laurenti, 1768) are
semi-aquatic and can move well on land, as they often do for thermoregulation,
oviposition, skin shedding, prey digestion and assimilation (Heatwole &
Guinea 1993; Shine & Shetty 2001).
In
India, snakes have religious (Vogel 1926), medical (Whitaker & Andrews
1995) and socio-economic significance (Whitaker 1978). Scientific studies of Indian snakes by the
academic community started in the late 18th Century (Vijayaraghavan
2005), and currently a total of 26 marine snake species are recognized
(Whitaker & Captain 2004; Adimallaiah 2014): one species of file snake,
five species of brackish water snakes and 20 species of venomous sea snakes,
including two species of sea kraits (Aengals et al. 2018; Adimallaiah
2014). The file snake is restricted
mainly to mangrove areas and occasionally ventures into the sea along India’s
west coast, the Bengal coast and the Bay Islands’ coasts (Whitaker &
Captain 2004). The remaining snakes are
homalopsids, a family of rear-fanged aquatic snakes comprising of smooth water
snakes, mud snakes and mangrove snakes.
Of the five species of the homalopsid brackish water snakes, only one (Cerberus
rynchops) is widespread and common, whereas the other four (Cantoria
violacea, Dieurostus dussumierii, Fordonia leucobalia &
Gerarda prevostiana) are rather rare or range-restricted (Whitaker &
Captain 2004; Chandramouli et al. 2012; Kumar et al. 2012; Adimallaiah
2014). The following section presents an
in-depth description of Indian marine snakes.
HISTORY OF RESEARCH ON INDIAN MARINE
SNAKES
In the
18th Century Linnaeus described a few species of Indian marine
snakes, including Coluber laticaudatus (now Laticauda laticaudata
(Linnaeus, 1758)) and Anguis platura (now Hydrophis platurus
(Linnaeus, 1766)). Later the Scottish
naturalist Patrick Russell described a few more species using vernacular names
that were later given scientifical names by others, including Bokadam: Cerberus
rynchops (Schneider, 1799); Kerril patti: Hydrophis nigrocinctus
Daudin, 1803; Shootur sun and / or Kalla Shootur sun: Hydrophis
obscurus Daudin, 1803; Chittul: Hydrophis cyanocinctus
Daudin, 1803; Hoogli pattee and /or Valakadyen: Hydrophis schistosus Daudin,
1803; Shiddil: Hydrophis jerdoni (Gray, 1849) and Kadel
Nagam: Microcephalophis gracilis (Shaw, 1802) (Russell 1796, 1801). In the same century Schneider (1779)
described Hydrus granulatus (now Acrochordus granulatus (Schneider,
1799)), Hydrus rynchops (now Cerberus rynchops (Schneider, 1799),
Hydrus Colubrinus (now Laticauda colubrina (Schneider, 1799)) and
Hydrus fasciatus (now Hydrophis fasciatus (Schneider, 1799)).
In the
early 19th Century, Shaw (1802) described Hydrus spiralis
(now Hydrophis spiralis (Shaw, 1802)), Hydrus caerulescens (now Polyodontognathus
caerulescens Shaw, 1802), Hydrus curtus (now Hydrophis curtus)
and Hydrus gracilis (now Microcephalophis gracilis (Shaw, 1802).
Daudin (1803) described Hydrophis schistosus Daudin, 1803, H.
cyanocinctus Daudin, 1803, H. nigrocinctus Daudin, 1803, H.
obscurus Daudin, 1803 and Anguis mamillaris (now Hydrophis
mamillaris (Daudin, 1803) (also see Bour 2011). Schlegel (1837) described the brackish water
snakes Homalopsis leucobalia (now Fordonia leucobalia (Schlegel,
1837)). Eydoux & Gervais (1837)
described Coluber (Homalopsis) prevostianus (now Gerarda
prevostiana (Eydoux & Gervais, 1837)). Gray (1842, 1846, 1849)
described the sea snakes Aturia ornata (now Hydrophis ornatus
(Gray, 1842)), Hydrus stokesii (now Hydrophis stokesii (Gray,
1846)), Aturia lapemoides (now Hydrophis lapemoides (Gray, 1849))
and Kerilia jerdonii (now Hydrophis jerdonii (Gray, 1849)). André
Marie Constant Duméril (1774–1860), Gabriel Bibron (1805–1848) and Auguste
Henri André Duméril (1812–1870), zoologists associated with the Museum National
d’histoire Naturelle in Paris, France also studied sea snakes. Duméril et al. (1854) described Eurostus
dussumierii (now Dieurostus dussumierii Duméril, Bibron &
Duméril, 1854). Later, a German-born
zoologist working with the Natural History Museum, London, Albert Karl Ludwig
Gotthilf Günther described two species, Hydrophis stricticollis Günther,
1864 and Microcephalophis cantoris Günther, 1864 (see Günther
1864).
By the
late 19th Century no new species of Indian marine snakes were being
described (see Whitaker & Captain 2004).
The first regional treatise on Indian herpetology was
prepared by the British physician Thomas Caverhill Jerdon (1811–1872) (see
Jerdon 1854), followed by a treatise by Günther (1864). Museum-based stock-takings and catalogues
were also produced, including a description of the holdings of the Indian
Museum in Calcutta by William Theobald (Theobald 1868, 1876) and an expanded
herpetological catalogue from the same institution by museum director William
Lutley Sclater (Sclater 1891). George Albert Boulenger (1858-1937), a
Belgian-British zoologist, expanded and revised his early work on Indian
herpetology (Boulenger 1890) based on the collections of the London Museum
(Boulenger 1896).
In the
early 20th Century, Frank Wall, a British physician and
herpetologist who lived in South Asia wrote extensively about Indian snakes
(Campden-Main 1968, 1969). He published
a descriptive list of sea snake specimens preserved in the Indian Museum,
Calcutta (Wall 1906), and then what is perhaps the first monograph exclusively
dealing with sea snakes (Wall 1909).
Like Russell and Jerdon, Wall’s experience included studies of museum
specimens and a considerable amount of field observation. He worked with the
holdings of the Bombay Natural History Society Museum, the British Museum, the
Madras Museum and the Indian Museum in Calcutta (Wall 1906, 1909). In a more regional context, Prater (1924)
recorded snake species from the Islands of Bombay and Salsette and the
surrounding seas, and reported 11 species of sea snakes. Following Wall, Malcolm Arthur Smith
(1875-1958) expanded and refined the sea snake monograph (1926) and also the
work on Indian ophiology (1943), mainly based on collections in the London and
Indian museums.
In modern
times studies of Indian marine snakes have primarily consisted of regional
reviews (Table 1). Gyi (1970) revised
the Homalopsid snakes that also covered the Indian taxa. Ahmed (1975) studied
the sea snakes of the Indian Ocean based on the collection of Zoological survey
of India (ZSI), dealing with systematics, ecology and distribution of sea
snakes, recognizing 29 species. McCarthy (1986) elaborated on the relationships
of sea kraits, that also included Indian species. Das (2003) made an extensive overview of the
systematics, taxonomy and nomenclature of Indian reptiles, listing 23 species
of marine snakes including true sea snakes, sea kraits, file snakes and
brackish water snakes. Whitaker &
Captain (2004) published a field guide to the snakes of India that illustrated
and described 157 of over 270 species of Indian snakes, including 23 species of
marine snakes. They provided photographs
of several marine snakes providing a useful tool for species identification by
non-experts. Smith (1926) who considers H. hardwickii to not be part of
the Indian sea snake fauna, quotes Günther’s (1864)
remark that though its type specimen is believed to be from India, several
circumstances lead one to suppose that it is from Penang [in Malaysia]. Subsequently, H. hardwickii is treated
as a synonym of H. curtus (see Gritis & Voris 1990).
More
recently, several reviews on Indian taxa have appeared (Voris 1972, 2017;
Rasmussen 1989, 1992, 1994, 1997; Heatwole et al. 2005, 2012, 2017; Kharin
2005; Kharin & Czeblukov 2006; Somaweera et al. 2006; Somaweera &
Somaweera 2009; de Silva et al. 2011; Murphy et al. 2012; Sanders et al. 2013;
Wallach et al. 2014; Ukuwela et al. 2017).
Other aspects studied include marine snake ecology and conservation, and
the distribution and diversity of marine snakes along the coasts of India
(Murthy 1977 a,b; Lobo et al. 2005; Lobo 2006; Murthy
2007; Kannan & Rajagopalan 2008; Palot & Radhakrishnan 2010;
Adimallaiah 2014). Adimallaiah (2014)
reported the poorly-known mud snake Dieurostus
dussumierii from Kochi beach in the Malabar Coast (also see Chadramouli et
al. 2012; Kumar et al. 2012). In
Homalopsid snakes, some poorly-known Indian species
were researched (Alfaro et al.
2004; Somaweera et al. 2006; Chandramouli et al. 2012; Kumar et al. 2012; Das
et al. 2013; Vyas et al. 2013; Adimallaiah 2014; Murphy & Voris 2014;
Ukuwela et al. 2017). Lastly, Aengals et al. (2018) worked on an
updated checklist of Indian reptiles, featuring a total of 26 marine
snakes.
This
summary shows that there has been a considerable amount of work published
documenting Indian marine snakes since the 18th Century. Taxonomic inconsistency is evident, with
different authors having described the same species using different names or
synonyms. Major works from 1796 to 2004 are listed in Table 1, followed by a
synopsis for each species mainly sourced from Smith (1943), Golay et al.
(1993), Somawera & Somaweera (2009), Wallach et al. (2014) and Uetz &
Hosek (2017). An updated chreso-synonymy
(sensu Smith & Smith 1973; Dubois 2000), information of type specimen(s),
type locality and other pertinent data have also been updated to current
taxonomy.
SPECIES SYNOPSIS
Acrochordidae Bonaparte, 1831
File Snake Acrochordus granulatus
(Schneider, 1799)
Hydrus
granulatus Schneider,
1799 (sic)
Anguis
granulatus acrochordus Schneider, 1801
Acrochordus
fasciatus Shaw, 1802
Pelamis
granulatus — Daudin,
1803 (sic, for Pelamis granulata)
Chersydrus
[fasciatus] —
Cuvier, 1817
Chersydrus
granulatus — Merrem,
1820
Acrochordus
fasciatus — Raffles,
1822
Hydrus
granulatus — Raffles,
1822
Acrochordus
granulatus — Cantor,
1847
Chersydrus
annulatus Gray, 1849
Chersydrus
granulatus luzonensis Loverdige, 1938
Type
locality: “Madras, India” (fide Sang et al. 2009).
Type
specimen: unknown or lost (fide Sang et al. 2009; Wallach et al. 2014).
Homalopsidae Jan,
1863
Dussumier’s Mud Snake Dieurostus
dussumierii (Duméril, Bibron & Duméril, 1854)
Eurostus
dussumierii
Duméril, Bibron & Duméril, 1854
Hypsirhina
dussumieri — Jan, 1863 (nomen incorrectum)
Dieurostus
dussumieri —Berg, 1901
Hypsirhina
malabarica Werner,
1913
Enhydris
dussumieri — Smith,
1943
Enhydris
dussumieri — Murphy,
2007
Enhydris
dussumieri — Kumar
& Captain, 2011 (nomen incorrectum)
Enhydris
dussumierii —
Chandramouli et al., 2012
Dieurostus
dussumieri — Kumar et
al., 2012 (nomen incorrectum)
Dieurostus
dussumieri — Murphy
& Voris, 2014
Dieurostus
dussumierii —
Wallach et al., 2014
Type
locality: Malabar Coast, India / ‘Bengal’.
Type specimen:
Lectotype, Muséum National d’Histoire Naturelle, Paris, France, MNHN 3751
(after Wallach et al. 2014; contra Kumar et al. 2012).
Type
species: Eurostus dussumierii Duméril, Bibron & Duméril, 1854 is the
type species of the genus Dieurostus Berg, 1901.
Dog-faced Water Snake Cerberus rynchops
(Schneider, 1799)
Hydrus
rynchops Schneider,
1799
Boa
moluroides Schneider,
1801
Hydrus
cinereus Shaw, 1802
Coluber
cerberus Daudin, 1803
Hurria
bilineata Daudin,
1803
Python
rhynchops — Merrem,
1820
Homalopsis
cerberus — Fitzinger, 1826
Homalopsis
molurus H. Boie,
1826
Coluber
decipiens Oppel in
Boie, 1826
Homalopsis
rhynchops — Boie,
1827
Cerberus
cerberus — Cuvier, 1829
Homalopsis
rufotaeniatus
Wagler, 1833
Cerberus
grantii Cantor, 1836
Cerberus
cinereus — Cantor, 1839
Cerebrus
russellii — Fitzinger,
1843
Homalopsis
rhinchops (sic)
— Cantor, 1847; Mason, 1852
Cerberus
unicolor Gray, 1849
Cerberus
rhynchops — Günther,
1864
Cerberus
rhynchops — Anderson,
1871
Hurria
rynchops —
Stejneger, 1907
Type
locality: “Ganjam” (Orissa State, E India).
Type specimen:
Lectotype; specimen illustrated in Russell (1796), after Wallach et al. (2014).
Type
species: Hydrus rynchops Schneider, 1799 is the type species of the
genus Cerberus Cuvier, 1829.
Crab-eating Water Snake Fordonia
leucobalia (Schlegel, 1837)
Homalopsis
leucobalia Schlegel,
1837
Fordonia
leucobalia — Gray,
1842
Fordonia
unicolor Gray, 1849
Hemiodontus
leucobalia — Duméril,
Bibron & Duméril, 1854
Hemiodontus
chalybaeus Jan, 1863
Fordonia
bicolor Theobald,
1868
Fordonia
papuensis Macleay,
1877
Fordonia
variabilis Macleay,
1878
Fordonia
leucobalia — Smith,
1943
Type
locality: Timor (Indonesia) by lectotype designation
Type
specimen: Lectotype, Rijksmuseum van Natuurlijke Historie, Leiden, The
Netherlands RMNH 1161 (see Wallach et al. 2014).
Type
species: Homalopsis leucobalia Schlegel, 1837 is the type species of the
genus Fordonia Gray, 1842.
Glossy Marsh Snake Gerarda prevostiana
(Eydoux & Grevias, 1837)
Coluber
(Homalopsis) prevostianus Eydoux & Gervais, 1837
Gerarda
bicolor Gray, 1849
Campylodon
prevostianum —
Duméril, Bibron & Duméril, 1854
Gerarda
prevostiana —
Cope, 1862
Heleophis
flavescens Müller,
1884 (fide Smith, 1943)
Helipophis
flavescens Müller,
1884 (fide Murphy & Voris, 2014, in error)
Gerardia
prevostiana —
Wall, 1905
Type
locality: “Manille” (= Manila in Luzon, Philippines)
Type
specimens: Syntypes: Muséum national d’Histoire naturelle Paris, France, MNHN
3758 and MNHN 7593 (Wallach et al. 2014).
Remarks:
Type specimen details was stated to be unknown by Das et al. (2013).
Type species:
Coluber prevostianus Eydoux & Grevias, 1837
is the type species of the genus Gerarda Gray, 1849.
Mangrove Snake Cantoria violacea
Girard, 1858
Cantoria
violacea Girard,
1858
Hydrodipsas
elapiformis
Peters, 1859
Hemiodontus
elapiformis – Jan, 1863
Cantoria
elongata Günther,
1864 (nom. nov. pro Cantoria violacea Girard) – nomen nudum Wallach et
al., 2014
Cantoria
elapiformis –
Günther, 1869
Cantoria
dayana Stoliczka,
1870
Cantoria
dayana — Anderson,
1871
Cantoria
violacea —
Grandison, 1978
Type
locality: “Singapore”.
Type
specimen: Holotype; United States National Museum, Chicago, USA USNM 5523.
Type
species: Cantoria violacea Girard, 1858 is the type species of the genus
Cantoria Girard, 1858.
Remarks:
Precise Indian records of this species are from the Andaman Islands (Ghodke
& Andrews 2002).
Elapidae Boie, 1827
Common Sea Krait Laticauda
laticaudata (Linnaeus, 1758)
Coluber
laticaudatus Linnaeus, 1758
(part)
Laticauda
scutata Laurenti, 1768
Platurus
fasciatus Latreille,
1801
Platurus
laurenti Rafinesque,
1817 (non Platurus laurenti Daudin, 1803)
Aspisurus
laticaudatus — Gray
in Grey, 1841 (nomen incorrectum) – Wallach et al. 2014
Platurus
laticaudatus —
Girard, 1858
Platurus
fischeri Jan, 1859
Platurus
fasciatus Jan, 1859
Platurus
affnisi Anderson,
1871
Platurus
fischeri — Anderson,
1871
Platurus
muelleri Boulenger,
1896
Platurus
laticaudatus —
Wall, 1906
Laticauda
laticaudata —
Stejneger, 1907
Laticaudata
laticaudata —
Oshima, 1910
Laticauda
laticauda — Brehm,
1913
Laticauda
laticoudata — Khole,
1991
Type
locality: “Indiis”; by lectotype designation (see
Wallach et al. 2014).
Type
specimen: Lectotype; Naturhistoriska Riksmuseet, Stockholm, Sweden NRM (NHRM
Lin-87).
Type
species : Coluber laticaudatus Linnaeus, 1758 is the type species
of the genus Laticauda Laurenti, 1768.
Yellow-lipped Sea Krait Laticauda
colubrina (Schneider, 1799)
Hydrus
colubrinus Schneider,
1799
Coluber
laticaudatus
Linnaeus, 1758 (part)
Platurus
colubrinus — Wagler,
1830
Coluber
platycaudatus Oken,
1836 (nomen substitutum)
Hydrophis
colubrina — Schlegel,
1837
Hydrus
colubrinus — Begbie,
1846
Laticauda
scutata (non
Laurenti, 1768) Cantor, 1847
Platurus
fasciatus var.
colubrina — Fischer, 1856
Platurus
laticaudatus var.
B. — Günther, 1858 (part)
Platurus
colubrinus — Fischer,
1884
Platurus
colubrinus —
Boulenger, 1896 (part)
Laticauda
colubrina —
Stejneger, 1907
Laticauda
celubrina —
Deraniyagala, 1977 (nomen incorrectum)
Type
locality: “East Indian Ocean” (Bauer 1998)
Type
specimen: Holotype; Zoologische Museum, Berlin, Germany, ZMB 9078
Malacca Sea Snake Hydrophis
caerulescens (Shaw, 1802)
Hydrus
caerulescens Shaw,
1802 (sic)
Polyodontus
annulatus Lesson,
1834
Hydrophis
caerulescens —
Gray, 1842
Hydrophis
hybrida Schlegel,
1844
? Hydrophis
colubrinus Jerdon, 1854
Hydrophis
protervus Jan, 1859
Hydrophis
wertmani Jan, 1859
Hydrophis
frontalis Jan, 1863
Hydrophis
polydonta Jan, 1863
Hydrophis
polyodontus Jan, 1872
in Jan & Sordelli, 1870-1881
Hydrophis
caerulescens thai Smith, 1920
Polyodontognathus
caerulescens —
Wall, 1921
Hydrophis
coerulescens — Bouquet,
1964 (nomen incorrectum)
Hyhdrophis
caerulscens — Deraniyagala,
1977 (nomen incorrrectum)
Hydrophis
coerelescens — Lin, 1975
(nomen incorrectum)
Aturia
caerulescens — Welch, 1994
Hydrophis
caerulescens — Sanders et al., 2013
Polyodontognathus
caerulescens — Wallach et al., 2014
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946.1.3.90,
from “East-Indian” (= Indian Ocean).
Type
locality: Indian Ocean (as East-Indian); however, label on type cites type
locality as “Indian Ocean: Vizagapatam” (see Smith 1926).
Short Sea Snake Hydrophis curtus (Shaw,
1802)
Hydrus
curtus Shaw, 1802
Hydrophis
flaviventris Siebold,
1827
Hydrophis
pelamidoides
Schlegel, 1837
Lapemis
curtus — Gray,
1842
Lapemis
loreatus Gray, 1843
Hydrus
pelamoides Hallowel,
1845 (nomen emendatum)
Hydrophis
pelamiodes Duméril, 1853
(nomen incorrectum)
Hydrophis
pelamidoides — Duméril,
Bibron & Duméril, 1854
Hijdrophis
pelamidioides Bleeker, 1856
(nomen emendatum)
Hydrophis (Pelamis) pelamidoides var.
annulata Fischer, 1856
Hydrophis (Pelamis) pelamidoides —
Fischer, 1856
Hydrophis
problematicus Jan, 1859
Hydrophis
propinquus Jan, 1859
Hydrophis
abbreviatus Jan, 1863
Hydrophis
brevis Jan, 1863
Hydrophis
loreata — Günther,
1864
Hydrophis
fayreriana Anderson,
1871
Hydrophis
fayeri Fayer, 1871
(nomen emendatum)
Hydrophis
pelamidoides unimaculatus Peters in Martens, 1876
Hydrophis
pelamoides Hilgendorf,
1876 (in error)
Hydrophis
hardwickei — Boettger,
1888 (emendation)
Hydrophis
abreviatus — Casto
de Elera, 1895 (nomen incorrectum)
Enhydris
curtus — Werner,
1895
Hydrophis
pelmoides -— Khan,
1982 (nomen incorrectum)
Hydrophis
abbreviataus —
Culotta & Pickwell, 1993 (nomen incorrectum)
Hydrophis
curtus — Sanders et al., 2013
Lapemis
curtus — Wallach et al., 2014
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946.1.17.59.
Type
locality: “East-India”, none stated more precisely.
Annulated Sea Snake Hydrophis
cyanocinctus Daudin, 1803
Hydrophis
cyanocinctus
Daudin, 1803
Leioselasma
striata Lacépède, 1804
Hydrophis
chittul
Rafinesque-Schmaltz, 1817
Hydrophis
striata — Schlegel,
1837
Hydrophis
sublaevis Gray, 1842
(in part)
Hydrophis
subannulata Gray,
1849
Hydrophis
aspera Gray, 1849
?
Hydrophis striatus — Duméril, Bibron & Duméril, 1854
Hydrophis
striata — Fischer,
1856
Hydrophis
westermani Jan, 1859
Hydrophis
westermanni — Jan, 1863 (emendation)
Hydrophis
trachyceps Theobald,
1868
Hydrophis
crassicollis
Anderson, 1871
Hydrophis
tuberculatus
Anderson, 1871
Hydrophis
dayanus Stoliczka,
1872
Hydrophis
tenuicollis
Peters, 1872
Hydrophis
asperrimus Murray,
1886
Hydrophis
taprobanica Haly,
1887
Hydrophis
phipsoni Murray, 1887
Hydrophis
cyanocincta — Boulenger,
1887
Distira
cyanocincta — Werner, 1895
Distira
cyanocincta — Boulenger,
1896
Distira
saravacensis Boulenger,
1900
Distira
sarawacensis — Shelford,
1901 (nomen emendatum)
Hydrophis
cyanocyneta —
Anonymous, 1902 (nomen incorrectum)
Distira
longissima Rosén, 1905
Distina
cyanocincta — Aiyar, 1906
(nomen incorrectum)
Disteira cyanocincta — Stejneger, 1907
Distra
cyanocincta — Castellani
& Chalmers, 1913 (nomen incorrectum)
Leioselasma [sic] cyanocincta — Wall, 1921
Leioselasma
cyanocincta — Prater, 1924
Hydrophis
cyanocinctus — Smith, 1943
Hydrophis
asperriums — Meyers,
1947 (nomen incorrectum)
Hydrophys
cyanocinctus —
Anthony, 1955 (nomen incorrectum)
Disteira
saravaciensis —
Culotta & Pickwell, 1993 (nomen incorrectum)
Hydrophis
asperiums — Culotta
& Pickwell, 1993 (nomen incorrectum)
Hydrophis
cyanocinctus —
Sanders et al., 2013
Leioselasma
cyanocincta —
Wallach et al., 2014
Type
specimen: Holotype; The Natural History Museum, London, UK, BMNH 1946.1.9.23
(see Wallach et al. 2014).
Type
locality: “Coromandel” Coast of eastern peninsular India, precisely the
Sunderban in Bengal.
Remarks:
Type material was misreported to be lost by Sang et
al. (2009). The nomen Hydrophis dayanus Stoliczka, 1872 has varying
been considered as a synonym of H. cyanocinctus Daudin, 1803 and H.
lapemoides (Gray, 1849) (see Das et al. 1998).
Banded Sea Snake Hydrophis fasciatus (Schneider,
1799)
Hydrus
fasciatus Schneider,
1799 (sic)
Hydrophis
laticauda -Latreille in
Sonnini & Latreille, 1801
Anguis
xiphura Hermann,
1804
Hydrophis
lanceolatus Oken,
1817
Hydrus
chlorus Merrem, 1820
Disteira
fasciata — Fitzinger,
1826
Hydrus
chloris Gray in
Griffith & Pidgeon, 1831 (nomen emendatum)
Pelamis
Lindsayi Gray in
Griffith & Pidgeon, 1831
Hydrophis
gracilis (not of
Shaw 1802) Schlegel, 1837 (part)
Aturia
Lindsayi — Gray,
1842
Colubrinus
hydrus Duméril, Bibron & Duméril, 1854
Hydrophis
fasciatus — Duméril,
Bibron & Duméril, 1854
Hydrophis
chloris Günther
1864 (non H. cloris Daudin, 1803)
Hydrophis
Lindsayi — Anderson,
1871
Hydrophis
fasciatus — Peters,
1872
Hydrophis
leptodira Boulenger,
1896
Hydrophis
fasciatus — Boulenger,
1896
Hydrophis
rhombifer Boulenger,
1900
Hydrophis
lindsays — Mocquard, 1904 (nomen incorrectum)
Disteira
fasciata — Stejneger,
1907 (part)
Hydrophis
lindsaya — Wall, 1921
(nomen incorrectum)
Micromastophis
fasciatus — Prater,
1924
Aturia fasciata
— Wall, 1921
Hydrophis
fasciatus — Smith,
1943
Hydrophis
fasciatus faciatus — Lin, 1975 (nomen incorrectum)
Pelamis
fasciataus — Culotta
& Pickwel, 1993 (nomen incorrectum)
Type
specimens: Lectotype; Zoologisches Museum Berlin, Germany, ZMB 2836.
Type
locality: None given. Smith (1926, 96) stated that the type of Hydrophis
fasciatus was labelled “East Indies.”
Type
species: Hydrus fasciatus Schneider, 1799 is the type species of the
genus Hydrophis Latreille in Sonnini & Latreille, 1801.
Jerdon’s Sea Snake Hydrophis
jerdonii (Gray, 1849)
Eryx
shiddil Wagler, 1825
(nomen ineditum)
Hydrus
shiddil Boie, 1827
(nomen nudum)
Kerilia
jerdonii Gray, 1849
(sic)
Hydrus
cantori Jerdon,
1854
Hydrophis
jerdonii — Anderson,
1871
Distira
jerdonii Boulenger,
1896
Hydrophis
jerdonii —
Boulenger, 1912
Kerilia
jerdonii — Wall,
1921
Kerilia
jerdoni siamensis Smith, 1926
Hydrophis
jerdone — Culotta
& Pickwell, 1993 (nomen incorrectum)
Hydrophis
jerdonii — Sanders
et al., 2013
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946.1.10.11.
Type
locality: Madras, India.
Type
species: Kerilia jerdoni Gray, 1849 is the type species of the genus Kerilia
Gray, 1849. The validity of the subspecies has been questioned before (see
Rasmussen & Anderson 1990).
Persian Gulf Sea Snake Hydrophis
lapemoides (Gray, 1849)
Aturia
lapemoides Gray, 1849
Hydrophis
lapemoides — Günther,
1864
Hydrophis
holdsworthii
Günther, 1872
Hydrophis
stewartii Anderson,
1872
Distira
lapemioides — Boulenger,
1890 (nomen emendatum)
Distira
lapemoides — Werner, 1895
Distira
lapemoides — Wall, 1909
Lioselasma [sic] lapemidoides [sic] — Wall,
1921
Distira
lapimoides — Phisalix,
1922 (nomen incorrectum)
Disteira
lapemoides — Werner, 1924
Hydrophis
lapemoides — Smith, 1926
Lioselasma
lapemoides — Culotta and Pickwell, 1993
Chitulia
lapemoides — Kharin,
2005
Hydrophis
lapemoides — Sanders
et al., 2013
Type
specimen: Lectotype; The Natural History Museum London, UK, BMNH 1946.1.7.2
(after Wallach et al. 2014).
Type
locality: Ceylon, now Sri Lanka.
Bombay Gulf Sea Snake Hydrophis
mamillaris (Daudin, 1803)
Anguis
mamillaris Daudin,
1803
Hydrophis
tesselatus —
Murray, 1886
Hydrophis
mammillaris —
Wall, 1906 (nomen emendatum)
Lioselasma mamillaris — Wall, 1921 (sic)
Leioselasma
mamillaris — Smith,
1926
Hydrophis
mamillaris — Smith,
1943
Aturia
mamillaris — Welch,
1994
Hydrophis
mamillaris — Das, 1996
Hydrophis
mammillaris [sic]
— Khan, 2002 (incorrect spelling)
Chitulia
mamillaris — Kharin,
2005
Hydrophis
mamillaris — Sanders
et al., 2013 (by implication)
Chitulia
(Dolichodira) mamillaris — Kharin, 2012
Chitulia
mamillaris — Wallach
et al., 2014
Type
specimen: Neotype; The Natural History Museum London, UK, BMNH 1861.12.30.38
(Wallach et al. 2014).
Type
locality: “Vizagapatam” (=Vishakhapatnam), in northeastern Andhra Pradesh,
India.
Black-banded Sea Snake Hydrophis
nigrocinctus
Daudin, 1803
Hydrophis
nigrocinctus
Daudin, 1803
Hydrophis
nigro-cinctus —
Duméril, Bibron & Duméril, 1854
Hydrophis
nigrocincta —
Fischer, 1856
Hydrophis
nigro-cincta —
Viaud-Grant-Marias, 1880 (nomen illegitimum)
Hydrophis
nigrocyneta —
Anonymous, 1902 (nomen incorrectum)
Melanomystax
nigrocinctus —
Wall, 1921
Hydrophis
nigrocinctus —
Smith, 1943
Disteira
walli Kharin,
1989
Disteira
nigrocincta —
Welch, 1994
Disteira
nigrocinctus —
Rasmussen, 1997
Disteira
nigrocincta —
Wallach et al., 2014
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946.1.10.13,
depicted in Russell, 1801, p. 7, pl. 6.
Type
locality: salted waters of a river near Calcutta, Sundarban, West
Bengal, India.
Estuarine Sea Snake Hydrophis
obscurus Daudin, 1803
Hydrophis
obscura Daudin,
1803
Hydrophis
cloris Daudin,
1803
Hydrophis
shooter Rafinesque-Schmaltz,
1817
Pelamis
chloris — Merrem,
1820 (nomen emendatum)
Leioselasma
obscura — Fitzinger,
1827
Hydrophis
subcinctus Gray, 1842
Hydrophis
coronata Günther,
1864
Hydrophis
latifasciata
Günther, 1864
Hydrophis
subcincta — Günther,
1864
Hydrophis
coronata — Anderson,
1871
Porrecticollis
obscurus — Wall,
1921
Hydrophis
obscurus — Smith,
1943
Porreticollis
obscurus — Culotta
& Pickwell, 1993 (nomen incorrectum)
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946.1.9.27
(specimen depicted in Russell, 1801, pl. 8).
Type
locality: Sandbarbans, now Sunderban, West Bengal, India.
Cochin Banded Sea Snake Hydrophis
ornatus (Gray, 1842)
Aturia
ornata Gray, 1842
Hydrophis
laevis Lütken,
1863 (nomen praeoccupatum)
Hydrophis
ellioti Günther,
1864
Hydrophis
ornata — Günther,
1864
Hydrophis
godeffroyi Peters, 1879
Hydrophis
ellioti — Boulenger,
1887
Distira
andamanica Annandale,
1905
Distira
mjobergi Lönnberg &
Andersson, 1913
Distira
godeflovi -— Phisalix,
1922 (nomen incorrectum)
Disteira
ornata — Taylor, 1922
Hydrophis
inornatus — Smith,
1926
Distira
ornata godeffroi — Takahashi, 1935 (nomen incorrectum)
Hydrophis
ornatus — Smith,
1943
Hydrophis
ornatus maresinensis Mittleman, 1947
Hydrophis
ornata godeffrayi — Wang & Wang, 1956 (nomen incorrectum)
Hydrophis
maresianus Kelmmer,
1963 (nomen emendatum)
Hydrophis
ernata—
Deraniyagala, 1974 (nomen incorrectum)
Hydrophis
oranatus — Tamiya
& Puffer, 1974 (nomen incorrectum)-
Hydrophis
elliotti — Culotta
& Pickwell, 1993 (nomen incorrectum)
Chitulia
ornata — Wallach
et al., 2014
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946.1.23.72.
Type
locality: none given; later restricted to Indian Ocean by Günther (1864).
Black and Yellow Sea Snake Hydrophis
platurus
(Linnaeus, 1766)
Anguis
platura Linné, 1766
Anguis
platuros — Gmelin,
1789 (nomen incorrectum)
Hydrus
bicolor Schneider,
1799
Pelamis
bicolor —
Schneider, 1799
Pelamis
platuros [sic]
Daudin, 1803
Pelamis
bicolor — Daudin,
1803
Natrix
dorsalis Rafinesque-Schmaltz,
1817
Ophinectes
lutens
Rafinesque-Schmaltz, 1817
Pelamis
schneideri
Rafinesque-Schmaltz, 1817 (nomen substitutum)
Hydrophis
pelamis Schlegel,
1837 (nomen substitutum)
Pelamis
ornata Gray, 1842
(non Aturia ornata Gray, 1842)
Pelamis
bicolor var.
maculata Duméril, Bibron & Duméril, 1854 (nomen nudum)
Pelamis
bicolor var.
variegata Duméril, Bibron & Duméril, 1854
Pelamis
bicolor var.
sinuata Duméril, Bibron & Duméril, 1854
Hydrophis
(Pelamis) bicolor var. alternans Fischer, 1855
Hydrophis
(Pelamis) bicolor var. sinuata — Fischer, 1855
Pelamijs
bicolor — Bleeker,
1856 (nomen emendatum)
Hydrophis (Pelamis) bicolor var. alternans Fischer, 1856 (nomen
substitutum pro P. variegata).
Hydrophis
(Pelamis) bicolor — Fischer, 1856
Hydrophis
(Pelamis) bicolor var. sinuata — Fischer, 1856
Hydrophis
bicolor chinensis Jan, 1859
Pelamis
tricolor Bennett, 1862
Pelamides
platurus — Blyth,
1863 (nomen incorrectum)
Hydrophis
bicolor maculata Jan, 1863 (nomen nudum)
Hydrophis
bicolor maculata Jan, 1872 in Jan & Sordelli, 1870-1881
Pelamis
platurus — Stoliczka, 1872
Hydrus
platurus —
Boulenger, 1896
Hydrus
platyurus — Lydekker,
1901 (nomen incorrectum)
Hydrus
platurus linnaeus — Castellani & Chalmers, 1910 (nomen
incorrectum)
Pelamydrus
platurus —
Stejneger, 1910
Hydrus
platurus pallidus Wall, 1921
Hydrus
platurus subobscurus Wall, 1921
Pelamydrus
platalus — Nagai,
1928 (nomen incorrectum)
Pelamas
platurus — Deam, 1938
(nomen incorrectum)
Pelamiris
platurus — Daniel,
1949 (nomen incorrectum)
Pelamis
platura brunnea Deraniyagala,
1955
Pelamis
platura fasciata
Deraniyagala, 1955
Pelamis
platura leucostriata Deraniyagala, 1955
Pelamis
platura neuricatenata Deraniyagala, 1955
Pelamis
platura neurileucura Deraniyagala, 1955
Pelamis
platura tricolor
Deraniyagala, 1955
Pelamis
platyura —
Deraniyagala, 1977 (nomen incorrectum)
Palemis
platurus — Felger
& Moser, 1985 (nomen incorrectum)
Pelamydrus
platarus — Culotta
& Pickwell, 1993 (nomen incorrectum)
Hydrophis
platurus — Sanders
et al., 2013
Type
specimen(s): Cabinet of Natural Wonders of F. Ziervogel, pharmacist to the
Royal Court in Stockholm, fide E. Thorsell (in litt.) ;
but stated to be in Department of Vertebrate Zoology, Stockholm, Stockholm,
Sweden, NHR fide Wall (1921) (see Wallach et al. 2014).
Type
locality: Unknown, erroneously cited as Suriname (Wallach et al. 2014)
Remarks:
Holotype was stated to be unknown by Sang et al. (2009).
Type
species: Hydrus bicolor Schneider, 1799 is the
type species of the genus Pelamis Daudin, 1803.
Hook-nosed Sea Snake Hydrophis
schistosus Daudin, 1803
Hydrophis
schistosus Daudin,
1803
Enhydris
valakadin Rafinesque-Schmaltz,
1817
Hydrophis
cianura
Rafinesque-Schmaltz, 1817
Hydrophis
hoglin
Rafinesque-Schmaltz, 1817
Hydrus
valakadjen — Boie
in Schlegel, 1826 (nomen incorrectum)-
Hydrophis
flaviventris Siebold,
1827
Hydrus
valakadyn — Boie,
1827 (nomen incorrectum)
Disteira
russelii Fitzinger,
1827 (based on Russell 1801)
Polyodontes
annulatus Lesson,
1832 in Bélanger, 1831-1834
Hydrophis
schistosa (not of
Daudin, 1803) Schlegel, 1837
Hydrophis
bengalensis Gray,
1842
Hydrophis
subfasciata Gray,
1842
Enhydrina
valakadyen — Gray, 1849
(nomen emendatum)
Thalassophis
werneri Schmidt,
1852
Thalassophis
werneria Duméril,
Bibron & Duméril, 1854 (nomen emendatum)
Hydrophis
schistosus — Duméril
& Bibron & Duméril, 1854
Hydrophis
schistosa — Fischer,
1856
Enhydrina
schistosa —
Stoliczka, 1870
Enhydrina
valakadyen —
Stoliczka, 1870
Enhydrina
valacadyen -—
Anderson, 1872 (nomen incorrectum)
Hydrophis
fasciatus (not of
Schneider, 1799) — Jan, 1872
Hydrophis
schistosus — Jan, 1872
Entrydrina
bangaensis —
Phipson, 1887 (nomen incorrectum)
Enhydrina
valakadien —
Boulenger, 1890 (nomen emendatum)
Enhydrina
vikadien — Boettger,
1892 (nomen incorrectum)
Enhydrina
schistosa — Van
Denburgh, 1895
Enhydrina
velakadien —
Flower, 1899 (nomen incorrectum)
Enhydrina
valacadjen -—
Kathariner, 1900 (nomen incorrectum)
Enhydrina
schistoza — Codoceo,
1956 (nomen incorrectum)
Enhydrina
schitosa — Bouquet,
1964 (nomen incorrectum)
Enhydrena
schistose — Chippaux
& Goyffon, 1983 (nomen incorrectum)
Enhydria
schistose — Murthy,
1986 (nomen incorrectum)
Enhydrina
valacadien —
Culotta & Pickwell, 1993 (nomen incorrectum)
Disteira
schistosa — McDowell,
1972
Hydrophis
schistosus — Sanders
et al., 2013
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH
1946.1.10.7.
Type
locality: Tranquebar (now Tarangampadi), Tamil Nadu, India.
Type
species: Hydrophis schistosus Daudin, 1803 is the type species of the
genus Enhydrina Gray, 1849.
Yellow Sea Snake Hydrophis
spiralis (Shaw, 1802)
Hydrus
spiralis Shaw, 1802
Hydrus
brugmannii Boie in
Schlegel, 1826 (nomen nudum)
Hydrophis
brugmansii Boie, 1827
(nomen emendatum)
Hydrophis
melanurus Wagler,
1828
Hydrophis
sublaevis Gray, 1842
(in part)
Hydrophis
spiralis — Duméril,
Bibron & Duméril, 1854
Hydrophis
rappi Jan, 1863
(nomen nudum)
Hydrophis
robusta Günther, 1864
Hydrophis
robsustus -—
Theobald, 1868
Hydrophis
rappii Jan, 1872 in Jan & Sordelli, 1870-1881
Hydrophis
temporalis Blanford,
1881
Hydrophis
bishopii Murray,
1884
Hydrophis
aurifasciata
Murray, 1886
Hydrophis
melanocinctus Wall,
1906
Hydrophis
brugmansii —
Boulenger, 1912
Distira
brugmansi — Stone,
1913
Lioselasma [sic] spiralis — Wall, 1921
Distira
spiralis typica Raj,
1926
Hydrophis
spiralis — Smith,
1943
Leioselasma
spiralis — Prater,
1924
Hydrophis
rapii -— Culotta
& Pickwell, 1993 (nomen incorrectum)
Leiocephalus
spiralis — Das, 1996
Leioselasma
spiralis — Wallach
et al., 2014
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH
1946.1.6.94.
Type
locality: Indian Ocean.
Remarks:
Perhaps the largest of true sea snakes, at least among those found in Indian
waters (Wall 1909; Smith 1926, 1943; Whitaker & Captain 2004).
Stoke’s Sea Snake Hydrophis
stokesii (Gray, 1846)
Hydrus
stokesii Gray, 1846
Hydrus
major Shaw, 1802
(part)
Hydrophis
schizopholis
Schmidt, 1846
Hydrus
annulatus Gray, 1849
Hydrophis
schizopholis —
Duméril, Bibron & Duméril, 1854
Astrotia
schizopholis —
Fischer, 1856
Hydrophis
güntheri Theobald,
1868 (nomen praeoccupatum)
Hydrophis
granosa Anderson,
1871
Hydrophis
guttata Murray,
1887
Disteira
stokesii— Boulenger,
1896
Astrotia
stokesi — Wall,
1909
Astrossii
stokesii — Lowe,
1932 (nomen incorrectum)
Astrokia
stokesi — Ruiter,
1958 (nomen incorrectum)
Astoria
stokesi — Sawai,
1976 (nomen incorrectum)
Astroria
stokesi — deSilva,
1976 (nomen incorrectum)
Astrocia
stokessi — Khole,
1991 (nomen incorrectum)
Hydrophois
guentheri -— Cogger, 1983
(nomen corrigendum)
Hydrophis
stokesii — Sanders
et al., 2013
Astrotia
stokesii — Wallach
et al., 2014
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946. 1. 17. 12.
Type
locality: Australian Seas.
Type
species: Hydrus stokesii Gray in Stokes, 1846 is the type species
of the genus Astrotia Fischer, 1855.
Narrow-collared Sea Snake Hydrophis
stricticollis Günther, 1864
Hydrophis
stricticollis
Günther, 1864
Hydrophis
neglectus Wall, 1906
Distira
neglecta — Wall, 1909
Aturia
stricticollis —
Welch, 1994
Chitulia
stricticollis —
Kharin, 2005
Chitulia
(Dolichodira)
stricticollis — Kharin, 2012
Hydrophis
stricticollis —
Sanders et al., 2013
Chitulia
stricticollis —
Wallach et al., 2014
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946.1.6.90.
Type
locality: Bay of Bengal, India.
Viperine Sea Snake Hydrophis
viperinus (Schmidt, 1852)
Thalassophis
viperina Schmidt,
1852
Diseira
praescutata Duméril, 1853
(nomen nudum)
Diseira
praescutata Duméril,
Bibron & Duméril, 1854
Hydrophis
doliata (not of
Lacépède, 1804) Fischer, 1856
Hydrophis
obscurus (not of
Daudin, 1803) Jan, 1859 (nomen praeoccupatum)
Hydrophis
nigra Anderson,
1872
Hydrophis
jayakari Boulenger,
1887
Hydrophis
plumbea Murray,
1887
Hydrophis
viperinus — Boettger,
1888
Distira
viperina —
Boulenger, 1896
Disteira
viperina —
Stejneger, 1907
Praescutata
viperina — Wall,
1921
Thalassophina
viperina — Smith,
1926
Thallassophina
viperina — Corkil,
1932 (nomen incorrectum)
Thalassophinae
viperina —
Maegraith, 1958 (nomen incorrectum)
Praescutata
viperine — Sayed,
1972 (nomen incorrectum)
Paraescutata
viperina — Khan,
1982 (nomen incorrectum)
Enhydrus
plumbea — Culotta
& Pickwell, 1993 (lapsus calami)
Thalassophina
veperina — Culotta
& Pickwell, 1993 (nomen incorrectum)
Hydrophis
viperinus — Sanders et al., 2013
Thalassophina
viperina — Wallach
et al., 2014
Type
specimen: Holotype; Zoologisches Museum Hamburg, Germany, ZMH 404, destroyed in
World War II (see Wallach et al. 2014).
Type
locality: coast of Java.
Type
species: Thalassophis viperina Schmidt, 1852 is the type species of the
genera Praescutata Wall, 1921 and Thalassophina Smith, 1926.
Remarks:
Smith (1926) whilst erecting the genus Thalassophina, overlooked the
existing senior nomen Praescutata Wall, 1921, a stance that he corrected
later (Smith 1943). Praescutata
Wall, 1921 is also regarded by some authorities as a nomen ineditum (see
Wallach et al. 2014).
Cantor’s Small-headed Sea Snake Microcephalophis
cantoris (Günther, 1864)
Hydrophis
cantoris Günther, 1864
Distira
gillespiae Boulenger,
1899
Microcephalophis
cantoris — Wall, 1921
Microcephalophis
cantori Lin, 1975
(nomen incorrectum)
Hydrophis
(Microcephalophis) cantoris — Kharin, 2004
Microcephalophis
cantoris — Sanders et al., 2013; Wallach et al., 2014
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946.1.18.30.
Type
locality: Penang, Malaysia.
Common Small-headed Sea Snake Microcephalophis gracilis (Shaw, 1802)
Hydrus
gracilis Shaw, 1802
(sic)
Disteira
gracilis —
Fitzinger, 1826
Microcephalophis
gracilis — Lesson,
1834
Hydrus
kadell-nagam Boie,
1827 (based on Russell, 1801) (nomen incorrigendum)
Hydrus
garcilis — Mason, 1852
(nomen emendatum)
Thalassophis
microcephala Schmidt, 1852
Hydrophis
microcephalus — Duméril,
Bibron & Duméril, 1854
Hydrophis
gracilis — Duméril,
Bibron & Duméril, 1854
Hydrophis
microcephala — Fischer,
1856
Hydrophis
gracilis — Fischer,
1856
Hydrophis
leprogaster Duméril, 1853
(nomen nudum)
Hydrophis
leprogaster Duméril &
Bibron in Fischer, 1856
Hydrophis
guentheri Theobald, 1868
Hydrophis
guntherii — Murray,
1884 (nomen emendatum)
Distira
gracilis — Wall,
1909
Hydrophis
rostralis Smith, 1917
Microcephalophis
gracilis gracilis Smith, 1926
Microcephaloides
gracilis — Barret,
1950 (nomen incorrectum)
Distevia
gracilis — Okada,
1953 (nomen incorrectum)
Microcephalus
graculis —
Saint-Girons, 1967 (nomen incorrectum)
Microcephalophus
gracilis — Vitt, 1987
(nomen incorrectum)
Microcephalophus
gracilis microcephalophis — Culotta & Pickwell, 1993 (nomen incorrectum)
Microcephalophis
gracilis — Culotta
& Pickwell, 1993 (nomen incorrectum)
Hydrophis (Microcephalophis) gracilis
— Kharin, 2004
Microcephalophis
gracilis microcephalus — Kharin, 2005
Microcephalophis
gracilis — Sanders et
al., 2013
Microcephalophis
gracilis — Wallach
et al., 2014
Type
specimen: Holotype; The Natural History Museum London, UK, BMNH 1946.1.17.37.
Type
locality: none given.
Type
species: Hydrus gracilis Shaw, 1802 is the type species of genus Microcephalophis
Lesson, 1832.
Remarks:
One of the few sampled genera of true sea snakes found in Indian waters that
was not nested within Hydrophis group taxa (Sanders et al. 2013).
THREATS AND CONSERVATION STRATEGIES
The major
threat to the survival of marine snakes in India is not known precisely but
their primary or direct threat is considered to be death by entangling in
fishing nets when caught as bycatch by the trawlers, in fact those which
survive are killed by the fishermen. The
indirect threat is due to the degradation of their ecosystems like coral reef
and destruction of mangrove forest habitat.
Sea snakes are caught as the bycatch in trawls, and it is assessed that
roughly 50% of mortality is by suffocating or being smashed
by the heaviness of the catch in the trawls (Ward 2000; Wassenberg et al. 2001;
Milton et al. 2009). Mass bycatch
mortality of sea snake (Hydrophis schistosus) was reported in Goa
(Padate et al. 2009). In 2015 another
such instance was noted, resulting in a mass mortality in two consecutive days
where around 60–80 dead sea snakes lay scattered over
20–30 meter stretch on shore. This
occurred because of the operation of shore seines pulled down to the shore and
the catch landed by the fishermen. Sea snakes when encountered get killed intentionally as their presence is perceived as a threat by the
local community (Jamalabad 2015).
Prawn trawling and boat seine nets are also among the top threats for
sea snakes. In a study reported from Puducherry coast, nearly 234 Hydrophis
schistosus were found trapped in 316 trawling nets. In 63 boat seine nets around 103 sea snakes
were found entangled (Muthukumaran et al. 2015). Though some southeastern Asian countries exploit
sea snakes for their meat for food and animal food purpose, in India they are
not exploited for food industries, but yet many other threats doom the marine
snakes in India (Das 2012; Sarker 2013; Cao et al. 2014).
A legal
management plan for the conservation of marine snake species in India is the
Indian Wildlife (Protection) Act, 1972 wherein the species are protected under
Schedule IV. Status of
the world’s sea snakes according to IUCN category has been enumerated by
Livingstone (2009) and several threatened species find place in that
list. Lukoschek et al. (2013) reported
on inexplicable declines in sea snake populations in Great Barrier Reef of
Australia. Although marine snakes are
designated as scheduled species in India to prevent exploitation, there is a
need for better understanding on the impacts and vulnerability assessments of
marine snakes. There is no major study
on the environmental impacts and direct human threats to marine snakes are
practically unknown, therefore we require a multidisciplinary effort (Elfes et
al. 2013). Implementation
of long-term bycatch monitoring programme to obtain baseline evidence on the
abundance of the sea snake species.
The most fundamental aspect of conservation effort is to analyze the
areas of high biodiversity and the distribution of threatened species (Brooks
et al. 2006; Hoffman et al. 2008).
BITES AND TOXINOLOGY
Bites and toxinology of sea snakes, particularly with reference to
Indian scenario have been briefly reviewed by Vijayaraghavan & Ganesh
(2015) and Whitaker & Martin (2015).
This is sumamrised in the following: “Sea snake bites are consensually
accepted as being potentially lethal to human beings and produce symptoms such
as are postsynaptic neurotoxic activity, attenuated twitch blockade,
degenerative changes in the central nervous system, petechiae and ecchymoses
throughout the viscera, distal tubular necrosis in the kidney, lung emphysema
and patchy edema, slight endocardial fibrosis, coronary sclerosis,
centrilobular degeneration and necrosis in the liver, porter round-cell
infiltration in the liver, and myoglobinuria”.
Toxinology of sea snake envenomations have been
compiled by Reid (1979), Pickwell (1994) and Takasaki (1998). Ali et al. (2000) reported the bite
management of an India species Hydrophis cyanocinctus, based on Malyan
case studies. Lomonte et al. (2014)
reported the envenomation and treatment of the bites of Hydrophis platurus
based on a study from Central America.
Tan et al. (2015a) reported on envenomation management in Malaysia, for
one of India’s widespread and fairly defensive species of sea snake – Hydrophis
schistosus. Tan et al. (2015b, 2016)
reported on cross-neutralisation by Malayan anti-cobra antivenom, of sea snake
envenomations in two species – H. schistosus and H. curtus, both
of which occur in India. Cases of
fatality from sea snake (Hydrophis schistosus) bites were documented in
Sri Lanka (Vithanage & Thirumavalavan 2013; Kularatne et al. 2014). The portion on snake envenomations by
McGoldrick & Marx (1991) and Fenner (1998) may also be referred.
CONCLUSION
Indian
marine snakes have been scientifically known and described as early as the late
18th Century, yet, there are many radical changes in their classification at
species-level, genus-level and even family-level up to this day. Conflicting consensus on the taxonomy and
nomenclature is far higher for this group than other snakes in India.
Many
are widespread along the coast of the country, but still newer observations and
records turn up. Some are so rare that
they have been sporadically sighted and not adequately documented by
researchers.
Many
are potentially venomous and known to cause life-threatening envenomations in
adult humans. As of date, specific
anti-venom is unavailable for the bites and their venoms are poorly researched
in India.
Some species are encountered by fishermen while entangled in the fishing
gears, especially the bottom trawling nets.
Often, a sharp hook-shaped pole is used to peg and throw them back into
the sea. Snakes brought ashore are
usually discarded on the shores or at the landing sites.
Despite
being so, the biology and natural history for many species still remain obscure
with no proper field observations and scientific studies.
Marine
species are well-protected statutorily in most areas,
both inside and outside marine protected areas (MPAs). Marine snakes often get prejudiced and killed
/ harmed directly by people when encountered.
India
with many zoos and serpentaria has a poor history of captive stock and studies
on marine snakes in such captive care facilities.
Fraught
with so many paradoxes and challenges, it is hoped that this overview will
stimulate further research interest and attract conservation attention towards
this group of snakes.
Table 1. Records of
sea snakes from Indian waters from 1796 to 2004. Number in entries denote
the numbers of nominal representations (i.e., synonyms) for each species as
currently recognized. Abbreviations:
Rus: Russell (1796-1809), Jerd: Jerdon (1854), Gthr: Günther (1864), Blgr:
Boulenger (1890), Scltr: Sclater (1891), Wall: Wall (1909), Smt: Smith (1943),
Ahm: Ahmed (1975), WC: Whitaker & Captain (2004), NA: not applicable. * indicates usage of vernacular names.
|
Species |
Rus* |
Jerd |
Gthr |
Blgr |
Scltr |
Wall |
Smt |
Ahm |
WC |
|
Acrochordus granulatus |
|
1 |
1 |
1 |
1 |
NA |
1 |
NA |
1 |
|
Dieurostus dussumierii |
|
|
|
|
|
NA |
1 |
NA |
1 |
|
Cerberus rynchops |
1 |
1 |
1 |
1 |
1 |
NA |
1 |
NA |
1 |
|
Fordonia leucobalia |
|
|
1 |
1 |
1 |
NA |
1 |
NA |
1 |
|
Gerarda prevostiana |
|
|
|
1 |
1 |
NA |
1 |
NA |
1 |
|
Cantoria violacea |
|
|
1 |
1 |
1 |
NA |
1 |
NA |
1 |
|
Laticauda colubrina |
|
1 |
|
1 |
1 |
1 |
1 |
1 |
1 |
|
L. laticaudata |
|
|
1 |
1 |
1 |
1 |
1 |
1 |
1 |
|
Hydrophis caerulescens |
|
|
1 |
1 |
1 |
1 |
1 |
1 |
1 |
|
H. curtus |
|
1 |
1 |
1 |
1 |
1 |
1 |
1 |
1 |
|
H. cyanocinctus |
1 |
1 |
1 |
3 |
2 |
1 |
1 |
1 |
1 |
|
H. fasciatus |
|
|
1 |
1 |
1 |
1 |
1 |
1 |
1 |
|
H. jerdoni |
1 |
|
1 |
1 |
1 |
1 |
1 |
1 |
1 |
|
H. lapemoides |
|
|
1 |
1 |
1 |
1 |
1 |
1 |
1 |
|
H. mamillaris |
|
|
|
1 |
|
1 |
1 |
1 |
1 |
|
H. nigrocinctus |
1 |
1 |
1 |
2 |
1 |
1 |
1 |
1 |
1 |
|
H. obscurus |
2 |
|
1 |
3 |
3 |
2 |
1 |
1 |
1 |
|
H. ornatus |
|
|
1 |
1 |
|
1 |
1 |
1 |
1 |
|
H. platurus |
|
1 |
1 |
1 |
1 |
1 |
1 |
1 |
1 |
|
H. schistosus |
2 |
1 |
|
2 |
1 |
1 |
1 |
1 |
1 |
|
H. spiralis |
|
|
1 |
2 |
1 |
1 |
1 |
1 |
1 |
|
H. stokesi |
|
|
1 |
1 |
|
1 |
1 |
|
1 |
|
H. stricticollis |
|
|
1 |
|
|
|
1 |
1 |
1 |
|
H. viperinus |
|
|
|
2 |
1 |
1 |
1 |
1 |
1 |
|
Microcephalophis cantoris |
|
|
1 |
1 |
1 |
1 |
1 |
1 |
1 |
|
M. gracilis |
1 |
1 |
1 |
1 |
1 |
1 |
1 |
1 |
1 |
For
images/figures – click here
Key to Indian marine
snakes
“The classification
of sea snakes has proved to all observers a most difficult task, in fact has given
more trouble than that of any other Ophidian family” - Wall, 1906
“This group [i.e.
sea snakes] is admittedly a difficult one, and has lead to considerable
diversity of opinion among herpetologists …” - Smith, 1926
The following key has
been, to certain extent, modified from Smith (1943); however, in certain cases
the arrangement has been newly devised for certain groups, based on customized
set of character-states largely due to the change in generic allocation and the
number of species in each group.
A. No enlarged teeth, skin very coarse
and loosely attached
..................................................................... Acrochordus
granulatus
B. Enlarged maxillary fangs at the rear of jaw; grooved
I. Nasal scales touch one another; parietals broken up; scales keeled
............................................................... Cerberus rynchops
II. Nasal scales separated by internasal; parietals entire;
scales usually smooth
a. Midbody scalerows 25–27, loreal present ................................................................................................
Dieurostus
dussumierii
b. Midbody scalerows 25–27, loreal absent
.......................................................................................................
Fordonia
leucobalia
c. Midbody scalerows 17, nasal scale
smaller than internasal
.......................................................................... Gerarda
prevostiana
d. Midbody scalerows 19, nasal scale larger than internasal
.............................................................................. Cantoria violacea
C. Enlarged maxillary fangs at the front of jaw; not grooved
but hollow
I. Ventral scales very wide, extending to the full belly width
.............................................................................................
Laticauda
a. Midbody scalerows 19; prefrontals
2; no azygous extra scale
................................................................................
L.
laticaudata
b. Midbody scalerows 21–25; prefrontals
3, often with an extra azygous scale
............................................................ L. colubrina
II. Ventrals scales much reduced in width, without any median
groove
i. Head scales not normal; parietals scales often broken–up
................................................................................
Hydrophis
curtus
ii. Head scales normal, neck slightly narrower than trunk; two
(or three) anterior temporals
a. Midbody scalerows 39–45; ventrals
296–330 ........................................................................................................
H. nigrocinctus
b. Midbody scalerows 37–47; ventrals
300–390
......................................................................................................
H. cyanocinctus
c. Midbody scalerows 45–55; ventrals
374–452
..........................................................................................................
H. stricticollis
d. Midbody scalerows 33–55; ventrals
209–312 ..............................................................................................................
H. ornatus
e. Midbody scalerows 43–51; ventrals
314–372
.........................................................................................................
H. lapemoides
f. Midbody scalerows 35–43; ventrals
302–390
..........................................................................................................
H. mamillaris
g. Midbody scalerows 38–54; ventrals
253–334 ......................................................................................................
H. caerulescens
h. Midbody scalerows 47–59; ventrals grooved, paired, 226–286
....................................................................................
H. stokesii
i. No distinct mental groove; black and yellow colouration
............................................................................................
H. platurus
iii. Head normal; neck as wide as other parts of trunk; usually
one anterior temporal
a. Midbody scalerows 19–21; snout
declivous
..................................................................................................................
H. jerdoni
b. Midbody scalerows 39–55; mental
elongate, hidden in a groove .............................................................................
H. schistosus
iv. Head and neck very thin and much narrower than rest of the
trunk
a. One anterior temporal; midbody
scalerows 47–58
....................................................................................................
H. fasciatus
b. two or three
anterior temporals; midbody scalerows 29–37; ventrals 300–338
....................................................... H. obscurus
v. Ventral scales posteriorly with median furrow, partly or
fully divided, spiny and tuberculate
a. Prefrontal not touching 3rd supralabial; ventrals
220–287.................................................................... Microcephalophis
gracilis
b. Prefrontal touching 3rd supralabial; ventrals
404–468 ................................................................................................
M. cantoris
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