The critically endangered leaf-scaled (Aipysurus foliosquamaI) and short-nosed (A. apraefrontalis) sea snakes are currently recognised only from Ashmore and Hibernia reefs ~600km off the northwest Australian coast. Steep population declines in both species were documented over 15 years and neither has been sighted on dedicated surveys of Ashmore and Hibernia since 2001. We examine specimens of these species that were collected from coastal northwest Australian habitats up until 2010 (A.foliosquama) and 2012 (A. apraefrontalis) and were either overlooked or treated as vagrants in conservation assessments. Morphological variation and mitochondrial sequence data confirm the assignment of these coastal specimens to A. foliosquama (Barrow Island, and offshore from Port Hedland) and A.apraefrontalis (Exmouth Gulf, and offshore from Roebourne and Broome). Collection dates, and molecular and morphological variation between coastal and offshore specimens, suggest that the coastal specimens are not vagrants as previously suspected, but instead represent separate breeding populations. The newly recognised populations present another chance for leaf-scaled and short-nosed sea snakes, but coastal habitats in northwest Australia are widely threatened by infrastructure developments and sea snakes are presently omitted from environmental impact assessments for industry. Further studies are urgently needed to assess these species’ remaining distributions, population structure, and extent of occurrence in protected areas.
Citation: Sanders KL, Schroeder T, Guinea ML, Rasmussen AR (2015) Molecules and Morphology Reveal Overlooked Populations of Two Presumed Extinct Australian Sea Snakes (Aipysurus: Hydrophiinae). PLoS ONE 10(2): e0115679. doi:10.1371/journal.pone.0115679
Academic Editor: Michael Hart, Simon Fraser University, CANADA
Received: September 2, 2014; Accepted: November 14, 2014; Published: February 11, 2015
Copyright: © 2015 Sanders et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: Morphological data are within the paper. DNA sequences are available from Genbank under accession numbers KP205504-KP205513.
Funding: This work was funded by an Australian Research Council Future Fellowship (FT130101965 Sanders) to KLS, an Australian Biological Resources Study grant (ID: RF214-34) to KLS, Timor Sea survey grants from PTTEP (Exploration and Production Public Company Limited) Australasia to MLG, and a School of Conservation, Copenhagen, Research Fund 2012-13 grant to ARR. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: PTTEP Australasia generously funded survey trips to the Timor Sea reefs in 2012 and 2013. The authors’ statement of competing interests does not alter their adherence to PLOS ONE policies on sharing data and materials.
One in five reptile species might be at risk of extinction and many are thought to have become extinct within the last 50 years . Threats to reptiles include habitat loss and degradation , climate warming , and overharvest for food, traditional medicines and leather . Rediscoveries of presumed extinct species (e.g. ) inspire optimism, but many such rediscovered species remain at immediate risk of extinction and require urgent assessment of population status and threats in their remaining range to guide management actions[5, 6].
Viviparous sea snakes (Hydrophiinae) are the only extant group of fully marine reptiles, but remain very poorly understood with a recent IUCN Red List assessment listing 38% of species as data deficient [7,8]. Two species have been listed as critically endangered on the IUCN Red List and Australia’s EPBC Act (Environmental Protection and Biodiversity Act, 1999) due to their restricted distributions and documented population declines [7, 9, 10]. Aipysurus foliosquama (the leaf-scaled sea snake) and A. apraefrontalis (short-nosed sea snake) are currently recognised only from Ashmore and Hibernia reefs ~600km off the northwest Australian coast [11, 12, 13, 14] (Figs. 1 and 2). Surveys of these reefs undertaken in 1974 , between 1994 and 2007, and in 2012 and 2013 [15, 16, 17] indicated population declines of at least 90% in A. foliosquama and A. apraefrontalis over 15 years (three generation lengths). Neither species has been sighted on surveys of Ashmore and Hibernia (or any other Timor Sea reefs ) since 2001 despite dedicated search efforts in 2005, 2007, 2012 and 2013 . However, in 1982 a single specimen identified as A. foliosquama was collected offshore from Port Hedland, and in 2010 a beach-washed specimen also identified as A. foliosquama was collected on Barrow Island. These localities are close to the northwest Australian coast, approximately 800km from Ashmore and Hibernia (Fig. 1). Aipysurus apraefrontalis has also been recorded from the northwest Australian coast: in the Exmouth Gulf and offshore from Roebourne and Broome up until 2012 (this study and ) (Fig. 1) and from the Arafura Sea . These scattered specimens are searchable on museum collection databases (e.g. Atlas of Living Australia website at http://www.ala.org.au) but were treated as vagrants in the IUCN Red List and EPBC Act assessments on the assumption that breeding populations of both species are restricted to Ashmore and Hibernia [7, 9, 10]. Sea snakes are vulnerable to dispersal in strong currents during storms and locality records for many species include remote outliers.
Also shown are the distribution of coral reefs and the Northwest Commonwealth Marine Reserves Network.
Here, we examine morphology and mitochondrial sequences for the previously overlooked coastal specimens and A. foliosquama and A. apraefrontalis from Ashmore and Hibernia. These data verify the assignment of the coastal specimens to A. foliosquama (Barrow Island, and offshore from Port Hedland) and A.apraefrontalis (Exmouth Gulf, and offshore from Roebourne and Broome). Molecular and morphological variation between coastal and offshore specimens, in addition to their collection dates, indicate that the coastal specimens are not vagrants but instead represent overlooked breeding populations. We discuss conservation implications and provide revised accounts of the two species’ internal and external morphology, geographic distributions and ecology.
Material and Methods
We sampled six specimens of Aipysurus foliosquama: five from Ashmore Reef collected between 1996 and 1998 (SAMA R68139, SAMA R68145, SAMA R68144, SAMA R68146, SAMA R68143), and the specimen collected on Barrow Island in 2010 (WAM R150365). DNA tissues are not available for the other coastal A. foliosquama (from offshore Port Hedland). Four A. apraefrontalis were sampled: one collected on Ashmore in 1996 (SAMA R68142), two collected in the Exmouth Gulf in 2000 and 2012 (voucher specimens held in the Western Australian Museum: WAM R157818, WAM R154750) and one collected in 2012 on Cable Beach near Broome (WAM R174539). To our knowledge, no additional DNA tissues are available for coastal A. apraefrontalis. Because our study provides the first molecular data published for A. foliosquama we tested a sister species relationship between A. foliosquama and A. apraefrontalis by additionally sampling A. duboisii (recovered as the sister lineage to A. apraefrontalis in a phylogenetic analysis of five nuclear loci that included those two species but not A. foliosquama: ). Of the four A. duboisii sampled, one was from the Exmouth Gulf (WAM R154751), two were from Hibernia (NTMR17781, NTMR17785) and one was from Seringapatam Reef (no voucher specimen). Samples collected by the authors were obtained by snorkelling with nets (Ashmore, Seringapatam) or from beach-washed specimens (Broome) under Western Australia Department of Parks and Wildlife (DPaW) scientific permits, and animal ethics approval from the University of Adelaide Animal Ethics Committee (approval number 000018247) and Charles Darwin University Animal Ethics Committee. No endangered species were sacrificed during our study. Sampling localities are shown in Fig. 1.
Standard Proteinase K protocols were used to extract whole genomic DNA from tissues (liver biopsies and tail clippings) and fragments were amplified using HotMaster Taq polymerase reagents (Perkin Elmer). The double-stranded amplification products were visualised on 1.5% agarose gel. We sequenced 1100 bp of the mitochondrial cytb (cytochrome b) gene. Primers were Forward L14910 (5’- GAC CTG TGA TMT GAA AAACCA YCG TTG T -3′) and Reverse H16064 (5’- CTT TGG TTT ACA AGA ACA ATG CTT TA -3’) . Annealing temperatures ranged between 55 and 59°C. Double-stranded sequencing was outsourced to the Australian Genome Research Facility Ltd (AGRF) in Adelaide, Australia.
Sequences were checked for ambiguities, and alignments were assembled from consensus sequences of forward and reverse reads using Geneious Pro v5.1.7 software . Polymorphism and divergence statistics were calculated using DnaSP v5  and the Species Delimitation plugin for Geneious Pro . Phylogenetic analysis used Bayesian inference implemented in BEAST 1.8.0 . Various partitioning strategies and clock and substitution models were trialled during preliminary runs. Optimum convergence was achieved using the final analysis settings of: unlinked partitions of 1st + 2nd codon positions (GTRig) and 3rd positions (GTRig), a Yule tree model prior with a uniform distribution, and a strict clock model implying no branch rate variation. This analysis was run for 100,000,000 MCMC generations and sampled every 10,000 generations. Convergence was assessed in Tracer 1.4  by examining likelihood plots and histograms and effective sample sizes (ESS values) of the estimated parameters. The first 3000 sampled trees were excluded as burn-in and the remaining 7,000 were used to generate a maximum credibility tree with Tree Annotator 1.7.1 .
We examined 26 Aipysurus foliosquama from Ashmore and the two specimens from Barrow Island and Port Hedland; and 17 specimens of A. apraefrontalis: seven from Ashmore, six from the Exmouth Gulf, two from Roebourne and two from Broome. Two other coastal specimens provisionally identified as A. apraefrontalis are accessioned in the Western Australian Museum but were not available for study at the time of writing. Measurements and scale counts follow Smith  with the modification that scale rows were counted directly around the body (see ). The absolute position of the posterior tip of the heart and liver were determined in relation to the count of the adjacent ventral scales (VS), and their relative position is expressed as the percentage of the number (counted from head to rear) of the underlying ventral scale (%VS-heart, %VS-liver) (e.g. [29, 30]). Body length was measured from snout to vent and tail length from vent to tip of the tail.
Institutional abbreviations follow : AMS = Australian Museum Sydney; BMNH = Natural History Museum London; NMNL = National Museum of Natural History Naturalis, Leiden; QM = Queensland Museum, Australia; SAMA = South Australian Museum; WAM = Western Australian Museum.
Aipysurus foliosquama: AMS R37143, AMS R40488, AMS R40489, AMS R40496, AMS R41516, AMS R41526, AMS R41537, AMS R44456, AMS R44576, AMS R44592, AMS R44597, AMS R44619, AMS R44872, AMS R44890, AMS R44896, AMS R44899, AMS R44902, AMS R44906, BMNH 19126.96.36.199 (holotype), NMNL 6430, SAMA R68139, SAMA R68145, SAMA R68144, SAMA R68146, SAMA R68143, WAM R129806 (all Ashmore Reef). AMS R104810 (offshore from Port Hedland).WAM R150365 (Bandicoot Bay, Barrow Island).
Aipysurus apraefrontalis: AMS R44616, AMS R44878, BMNH 19188.8.131.52 (holotype), BMNH 19184.108.40.206, BMNH 19220.127.116.11-22, SAMA R68142 (all Ashmore Reef). WAM R26415, WAM R31443, WAM R41261, WAM R43897, WAM R47748, WAM R157818 (all Exmouth Gulf). WAM R22961, QM J80569 (offshore from Roebourne).WAM R26716 (offshore from Broome), WAM R174539 (Cable Beach, Broome).
The final data matrix comprised 14 individuals of the three Aipysurus species and 1011 base pairs. Sequence data are deposited at GenBank (accession numbers KP205504-KP205513). Translation of the protein-coding cytb gene did not reveal frameshifts, unexpected stop codons or indels. Bayesian analyses yielded effective sample sizes (ESS values) well above 1000 for all parameters. The maximum clade credibility tree recovered Aipysurus foliosquama and A. apraefrontalis as reciprocally monophyletic sister species with a posterior probability (pp) of 0.98 (Fig. 3), and these formed a clade with A. duboisii that was supported by a pp of 1.0. The mean pairwise distance (HKY) between A. foliosquama and A. apraefrontalis was 4.3%, and these species showed 5.4–5.9% pairwise divergence from A. duboisii. Coastal samples of A. foliosquama and A. apraefrontalis represented unique haplotypes that formed strongly supported sister lineages to conspecifics from Ashmore (pp 1.0). Intraspecific pairwise distances were 0.7% between A. apraefrontalis from Ashmore and Exmouth/Broome, 1.0% between A. foliosquama from Ashmore and Barrow Island, and 1.2% between A. duboisii from Exmouth and Hibernia/Seringapatam.
Node support values (posterior probabilities) above 0.95 are shown. Scale bar indicates the number of substitutions per site.
Consistent with the molecular results, our morphological analyses clearly verified the identification of the Barrow Island and Port Hedland specimens to A. foliosquama (Table 1) and the remaining coastal specimens (Exmouth, Roebourne, Broome) to A. apraefrontalis (Table 2). We also found several differences between coastal and offshore specimens of both species: the two coastal specimens of A. foliosquama had higher ventral counts and more posterior relative heart positions than the other females examined from Ashmore (Table 1); coastal male A. apraefrontalis had higher ventral counts that did not overlap with conspecifics from Ashmore (Table 2) and reduced head relative to body size (not shown).
Aipysurus foliosquama Smith, 1926.
Smithohydrophis foliosquama 
External Morphological Characters: Teeth: 5–8 very small maxillary teeth behind poison fang, 5–7 palatine teeth, 22–23 pterygoid teeth, 15–16 dentary teeth. Scales: “Loreal” scale present;1–2 pre- and 2–3 postoculars; 7–8 supralabials; supralabials 1 and 2 invariably in contact with nasal, 3 and 4 or only 4 in contact with preocular, 4 and 5 or only 4 invariably in contact with eye; 2–3 anterior temporals; 7–9 infralabials; infralabials 1, 2 (sometimes divided), 3 and 4 in contact with anterior pair of sublinguals; infralabials 4 or none touching posterior pair of sublinguals. 19 scale rows on neck in males, 19 in females; 19 scale rows on body in males, 19 in females. 146–154 ventrals in males, 139–154 in females. Ventrals with a well-marked median keel and a deep notch on the posterior border. 23–27 subcaudals in males, usually 19–24 in females (but 29 in one paratype counted by Smith , however, we counted 27 subcaudals in the same specimen). Snout-vent length 80 cm in largest males, 95 cm in largest females. Tail length 10 cm in largest male, 11.5 cm in largest female.
Internal Morphological Characters: Tip of heart extending to ventral scale 36–42 in males, 40–44 in females. % VS heart 24.3–28.4 in males, 27.4–29.7 in females. Anterior end of liver situated at ventral scale 42–50 in males, 44–50 in females. %VS liver 28.3–33.6 in males, 28.7–33.7 in females. Heart and liver separated by 5–10 ventral scales in males, 3–6 in females. Body vertebrae: Aipysurus foliosquama shows a one to one correspondence between ventral body scales and vertebrae giving the same counts as heart and liver position in relation to the ventrals.
Colouration: Head brown above, same or lighter below. Body uniform tan-brown or purplish-brown, sometimes with whitish spots or bands on the sides and ventrally. Scales sometimes with dark margins. A pregnant female contained two large embryos, one with whitish bands around the body, the other with whitish bands only on the sides and ventrally.
Geographical Distribution: Aipysurus foliosquama is known from breeding populations at Ashmore and Hibernia Reefs in the Timor Sea [11,14, 16, 27, 32, 38, 45] that are now presumed extinct. The only other records are two specimens collected from Barrow Island and offshore from Port Hedland close to the northwest Australian coast (this study, Fig. 1).The type specimen was collected from Ashmore Reef .
Habitat and Biology: At Ashmore Aipysurus foliosquama has been found in shallow water not deeper than 10m, preferring areas heavily grown with corals [11, 16, 27, 32, 45]. Four prey species have been found in stomach contents of the Ashmore population. McCosker  reported jaws and a neurocranium identified to the family Labridae, presumably from a species of Halichoeres. Smith  reported that three specimens contained items identified as Platyglossus (= Halichoeres) trimaculatus. Voris  observed two specimens of the family Eleotridae and one specimen of the family Clinidae (Tripterygion). One pregnant female collected in January 1973 from Ashmore (AMS R44899) contained two full-term female embryos measuring 27 cm and 26.5 cm from head to vent.
Aipysurus apraefrontalis Smith, 1926.
Smithohydrophis apraefrontalis .
External Morphological Characters: Teeth: 5–6 maxillary teeth behind poison fang, 7–8 palatine teeth, 17–19 pterygoid teeth, 16dentary teeth. Scales: “Loreal” scale absent; 1 pre- and 2 postoculars; 6–8 supralabials; supralabials 1, 2 and 3 in contact with nasal, 3 and 4 in contact with preocular, 4 and 5 or 4, 5 and 6 in contact with eye, sometimes superlabial 5 divided horizontally; 1–3 anterior temporals. Prefrontal scales missing. 6–8 infralabials; infralabials 1, 2 and 3 in contact with anterior pair of sublinguals, sometimes only 1 and 2 or 1, 2 and 4; posterior sublinguals separated. Both pairs of sublinguals small. 17–19 scale rows on neck in males, 17–19 in females; 17 scale rows on body in males, 17 in females. Scales smooth or with a tubercle or short keel.141–158 ventrals in males, 148–152 in females. Ventrals large, at least three times as large as adjacent body scales. Each ventral scales with a deep notched and a median keel. 19–27 subcaudals in males, 19–25 in females. Snout-vent length 98 cm in largest males, 94 cm in largest females. Tail length 10.5 cm in largest male, 9 cm in largest female.
Internal Morphological Characters: Tip of heart extending to ventral scale 38–47 in males, 41–42 in females. % VS heart 26.0–29.7 in males, 27.6–27.7 in females. Anterior end of liver situated at ventral scale 45–47 in males, 47 in females. %VS liver 30.8–32.9 in males, 31.76 in females. Heart and liver separated by 5–7 ventral scales in males, 6 in females. Body vertebrae: Aipysurus apraefrontalis shows a one to one correspondence between ventral body scales and vertebrae giving the same counts as heart and liver position in relation to the ventrals.
Colouration: Head brown, body tan to dark brown or purplish-brown, paler ventrally, with cream or whitish scattered scales or/and with lighter brown cross-bands, which are mostly confined to the lower parts of the body. The posterior portion of the body scales often darker than the anterior.
Geographical Distribution: Aipysurus apraefrontalis has been collected from Ashmore and Hibernia Reefs but is absent from the other coral reefs of the Timor Sea (Cartier Island, Scott and Seringapatam Reefs). Specimens collected from the Exmouth Gulf, Roebourne and Broome (this study and ) were assigned to A. apraefrontalis (this study). Shuntov  collected A. apraefrontalis from the Arafura Sea but provided no further information. Golay et al.  mentioned this species as occurring in Javan waters (Indonesia), but we could not confirm this record with any specimens. Aipysurus apraefrontalis is then only known from Western Australia [11, 16, 27, 38, 45], but may be extinct or near-extinct on the Timor Sea reefs . The type specimen was collected from Ashmore Reef .
Habitat and Biology: At Ashmore Aipysurus apraefrontalis seems to be confined to shallow water at depths no greater than 10m . It has been reported primarily from reef flat and reef edge habitats but compared to A. foliosquama seems to prefer sandy bottom habitats less heavily grown with coral [11, 32]. Some specimens were found in cavities under dead coral debris fully exposed at low tide  or resting beneath small coral overhangs or coral heads in 1–2 m of water . Specimens from the Exmouth Gulf were collected in prawn trawl nets, presumably from inter-reef habitats .
Stomach contents data are available only for the Ashmore population, with one specimen reported to contain a ‘small eel’  and two specimens containing gobies (Eleotridae) . Two male specimens collected in the Exmouth Gulf in late June 1973 and July 2004 had very rugous ventral scales indicating breeding condition; a single gravid female was collected in Exmouth Gulf in late November 1967.
Our molecular and morphological data confirm the assignment of coastal northwest Australian specimens to Aipysurus foliosquama (Barrow Island, and offshore from Port Hedland) and A. apraefrontalis (Exmouth Gulf, and offshore from Roebourne and Broome). For both species, coastal specimens represent moderately divergent mitochondrial haplotypes not present in sampled conspecifics from Ashmore. Morphological differences are also found between coastal and Ashmore/Hibernia specimens: The two coastal A. foliosquama females have more ventral scales and more posterior relative heart positions than conspecific females from Ashmore (Table 1); coastal A. apraefrontalis have more ventrals in males (Table 2) and consistently smaller heads relative to body size compared to Ashmore specimens (not shown). These molecular and morphological differences suggest that the coastal specimens are not vagrants as previously suspected, but instead represent separate breeding populations. Collection dates of the coastal specimens further support this interpretation: A. foliosquama was collected on Barrow Island in 2010, and A. apraefrontalis was most recently collected from the Exmouth Gulf in 2004 and Broome in 2012; these records postdate both species’ disappearance from Ashmore and Hibernia where they were last sighted in 2001. Rediscoveries of presumed extinct reptiles are rare but usually involve longer intervals between disappearance and rediscovery. The Pygmy Blue-Tongue lizard  was rediscovered after 40 years, and the La Palma Giant Lizard and Terror Skink remained undetected in their known ranges for hundreds of years [55, 56]. The ‘false extinction’ of these lizards and the two Aipysurus sea snakes can, at least partially, be explained by the chronic lack of basic distributional and ecological data for most reptiles .
Molecular analysis of additional samples might resolve whether one or both Aipysurus species originated on the isolated Timor Sea reefs or dispersed there following a coastal origin. However, pairwise cytb distances between coastal and offshore lineages of 1% (A. foliosquama) and 0.7% (A. apraefrontalis) suggest recent connections, probably within the last few hundred thousand years (based on substitution rates estimated for cytochrome b in hydrophiines: ). Given the close molecular and morphological affinities of the coastal and offshore specimens we recommend that the newly recognised coastal populations remain in A. foliosquama and A. apraefrontalis. However, rapid speciation and post-speciation mitochondrial introgression have both been reported in sea snakes (e.g. ) and with further study might also be found here.
If A. foliosquama and A. apraefrontalis are indeed extinct at Ashmore and Hibernia, then the newly recognised coastal populations present another chance for these species’ survival. An urgent priority for conservation will be to assess the two species’ remaining distributions and population connectivity. The three coastal localities for A. apraefrontalis (Exmouth Gulf, ~600km to the north-north-east off Roebourne, and a further ~800km north-north-east off Broome: Fig. 1) suggest this species has a fairly large geographic range (extent of occurrence: ). However, the area of habitat it occupies within this range (area of occupancy:) is likely to be small given that coral reefs are highly fragmented on the northwest Australian coast (Fig. 1). The two coastal A. foliosquama specimens were collected ~350km apart, but whether this species also has a wider distribution remains to be discovered. Aipysurus foliosquama is known only from heavily grown coral habitats (e.g. [11, 45]) so might have a smaller area of occupancy than A. apraefrontalis.
Effective recovery of the two species will further depend on threat distributions in their remaining range and the extent of their occurrence in protected areas. The northwest Commonwealth Marine Reserves Network includes 13 reserves  but large areas outside of these reserves are impacted by trawl-fishing, seismic surveys for oil and gas exploration, and destructive infrastructure developments. Of particular concern are mining and oil and gas projects that involve dredging and dumping marine sediment . These activities are predicted to have areas of influence that can exceed 1000 square kilometres  potentially impacting protected reefs. A recent study linked dredging-induced sedimentation from the Gorgon natural gas project with coral stress and disease at Barrow Island and the nearby Montebello reefs . Such threats to coral habitats will directly impact reef-specialists such A. foliosquama; one of the two coastal specimens of this species was beach-washed on the south coast of Barrow Island close to the Gorgon dredging and spoil disposal sites. Many other development projects are planned or underway in the Kimberley, Pilbara and mid-west coast (e.g. ). Hence, the inclusion of sea snakes in environmental impact studies for industry should be an immediate priority for marine conservation managers in northwest Australia.
PTTEP Australasia generously funded our survey trips to the Timor Sea reefs in 2012 and 2013. Additional travel and laboratory work was funded by Australian Research Council and Australian Biological Resources Study grants to Kate Sanders, and School of Conservation, Copenhagen Research Fund 2012–13 to Arne R. Rasmussen. The Australian Genomics Research Facility in Adelaide conducted the molecular laboratory work. Paul Doughty provided access to specimens and tissues at the Western Australian Museum. Brad Maryan first identified the Barrow Island specimen as Aipysurus foliosquama. The Department of Environment and Conservation, Western Australia, and DSEWPaC in Canberra granted us permission to conduct field research on sea snakes.
Conceived and designed the experiments: KLS. Contributed reagents/materials/analysis tools: KLS ARR MLG. Wrote the paper: KLS ARR TS MLG. Generated and analysed molecular data: KLS. Generated and analysed morphological data: KLS ARR. Created the map figure: TS.
- 1. Böhm M, Collen B, Baillie JE, Bowles P, Chanson J, et al. (2013) The conservation status of the world’s reptiles. Biol Conserv 157: 372.
- 2. Sinervo B, Méndez-de-la-Cruz F, Miles DB, Heulin B, Bastiaans E, et al. (2010) Erosion of lizard diversity by climate change and altered thermal niches. Science 328:894–899. doi: 10.1126/science.1184695. pmid:20466932
- 3. Nijman V, Shepherd CR, Mumpuni , Sanders KL (2012) Overexploitation and illegal trade of reptiles in Indonesia. Herpetological Journal 22: 83–89.
- 4. Armstrong G, Reid J (1992) The rediscovery of the Adelaide pygmy bluetongue Tiliqua adelaidensis (Peters, 1863). Herpetofauna (Sydney)22: 3
- 5. Scheffers BR, Joppa LN, Pimm SL, Laurance WF (2012) What we know and don’t know about earth's missing biodiversity. Trends Ecol. Evol.27: 501. doi: 10.1016/j.tree.2012.05.008. pmid:22784409
- 6. Scheffers BR, Yong DL, Harris JBC, Giam X, Sodhi NS (2011) The world's rediscovered species: Back from the brink? PloS one 6: e22531. doi: 10.1371/journal.pone.0022531. pmid:21818334
- 7. IUCN (2012) IUCN Red List Categories and Criteria: Version 3.1. Second edition. Gland, Switzerland and Cambridge, UK: IUCN. (Available online: www.iucnredlist.org/technical-documents/categories-and-criteria).
- 8. Elfes CT, Livingstone SR, Lane A, Lukoschek V, Sanders KL, et al. (2013) Fascinating and forgotten: The conservation status of marine elapid snakes. Herp. Cons. Bio.8: 37.
- 9. TSSC (Threatened Species Scientific Committee) (2010) Listing advice for Aipysurus apraefrontalis (short-nosed sea snake).
- 10. TSSC (Threatened Species Scientific Committee) (2010). Listing advice for Aipysurus foliosquama (Leaf-scaled Sea Snake).
- 11. Minton SA, Heatwole H (1975) Sea snakes from three reefs of Sahul Shelf. In The biology of sea snakes: 141–144. Dunson W. A. (Ed.). Baltimore: London & Tokyo.
- 12. Storr GM, Smith LA, Johnstone RE (2002) Snakes of Western Australia. Western Australian Museum, Perth.
- 13. Guinea ML (1995) The sea turtles and sea snakes of Ashmore Reef Nature Reserve. In Report to the Australian Nature Conservation Agency: 67). the Northern Territory University, Darwin.
- 14. Cogger HG (2014) Reptiles and amphibians of Australia. 7 edn. Collingwood, Victoria: CSIRO Publishing. doi: 10.1682/JRRD.2014.01.0007. pmid:25626113
- 15. Guinea ML (2007) Sea snakes of Ashmore Reef, Hibernia Reef and Cartier Island with comments on Scott Reef. In Consultant’s report to The Department of the Environment and Water Resources, Canberra.
- 16. Guinea ML, Whiting SD (2005) Insights into the distribution and abundance of sea snakes at Ashmore Reef. The Beagle 1: 199.
- 17. Guinea ML (2012) Surveys of the Sea Snakes and Sea Turtles on Reefs of the Sahul Shelf, Monitoring Program for the Montara Well Release Timor Sea. DEWHA Final Report Survey 2012.
- 18. Moore GI, Richards ZT (2014) New records of sea snakes at mid-shelf shoals of Australia’s North West Shelf. Mar. Biodiv. DOI 10.1007/s12526-014-0267-7
- 19. Shuntov VP (1971) Sea snakes of the North Australian shelf. Ekologiia 4: 65.
- 20. Sanders KL, Lee MSY, Mumpuni , Bertozzi T, Rasmussen AR (2013) Multilocus phylogeny and recent rapid radiation of the viviparous sea snakes (Elapidae, Hydrophiinae). Mol. Phylogenet. Evol. 66: 575–591. doi: 10.1016/j.ympev.2012.09.021. pmid:23026811
- 21. Burbrink FT, Lawson R, Slowinski JB (2000) Mitochondrial DNA phylogeography of the polytypic North American rat snake (Elaphe obsoleta): A critique of the subspecies concept. Evolution 54: 2107. pmid:11209786 doi: 10.1111/j.0014-3820.2000.tb01253.x
- 22. Drummond AJ, Ashton B, Buxton S, Cheung M, Cooper A, et al. (2010) Geneious v5.0.4.
- 23. Librado P, Rozas J (2009) Dnasp v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics 25: 1451. doi: 10.1093/bioinformatics/btp187. pmid:19346325
- 24. Masters BC, Fan V, Ross HA (2011) Species Delimitation—a Geneious plugin for the exploration of species boundaries. Mol. Ecol. Resour.11: 154–157. doi: 10.1111/j.1755-0998.2010.02896.x. pmid:21429114
- 25. Drummond A.J, Suchard MA, Xie D, Rambaut A (2012) Bayesian phylogenetics with beauti and the beast 1.7. Mol. Biol. Evol. 29: 1969. doi: 10.1093/molbev/mss075. pmid:22367748
- 26. Rambaut A, Drummond AJ (2007) Tracer v1.4.
- 27. Smith MA (1926) Monograph of the sea-snakes (Hydrophiidae). Printed by order of the Trustees of the British Museum (Natural History) London.
- 28. Thomas RA (1976) Dorsal scale row formulae in snakes. Copeia 1976: 837. doi: 10.2307/1443484
- 29. Rasmussen AR (1989) An analysis of Hydrophis ornatus (Gray), H. lambertiSmith, and H. inornatus (Gray) (Hydrophiidae, Serpentes) based on samples from various localities, with remarks on feeding and breeding biology of H. ornatus. Amphibia-Reptilia 10: 397. doi: 10.1163/156853889x00043
- 30. Rasmussen AR (1993) The status of the Persian Gulf sea snake Hydrophis lapemoides (Gray, 1849)(Serpentes, Hydrophiidae). Bull. Nat. Hist. Mus. Zool. 59: 97.
- 31. Leviton AE, Gibbs RH, Heal E, Dawson CE (1985) Standards in herpetology and ichthyology Part I. Standard symbolic codes for institutional resource collections in herpetology and ichthyology. Copeia 1985: 802.
- 32. Cogger HG (1975) Sea snakes of Australia and New Guinea. In The biology of sea snakes: 59–139. Dunson W. A. (Ed.). Baltimore London & Tokyo: University Park Press.
- 33. Cogger HG (1992) Reptiles and amphibians of Australia. 5th edn. Chatswood New South Wales and Cornell University Press, New York.: Reed International Books. pmid:25144096
- 34. Cogger HG, Cameron EE, Cogger HM (1983) Hydrophiidae. In Zoological catalogue of Australia. Amphibia and reptilia: 241–256). Canberra: Australian: Government Publishing Service.
- 35. David P, Ineich I (1999) Les serpents venimeux du monde: Systématique et répartition. Dumerilia(Paris) 3: 3.
- 36. Golay P, Smith HM, Broadley DG, Dixon JR, McCarthy C, et al. (1993) Endoglyphs and other major venomous snakes of the world. A checklist. Geneva: Herpetological Data Centre, Azemiops.
- 37. Greer AE (1997) The biology and evolution of Australian snakes. Sydney New South Wales, Australia: Surrey Beatty and Sons. pmid:25165803
- 38. Heatwole H, Cogger HG (1994) Sea snakes of Australia. In Sea snake toxinology: 167–205. Gopalakrishnakone P. (Ed.). Singapore: Singapore University Press.
- 39. Hibbard E (1975) Eyes and other sense organs of sea snakes. In The biology of sea snakes: 355–382. Dunson W. A. (Ed.). Baltimore: London & Tokyo.
- 40. Lukoschek V, Beger M, Ceccarelli D, Richards Z, Pratchett M (2013) Enigmatic declines of Australia’s sea snakes from a biodiversity hotspot. Biol. Conserv. 166: 191. doi: 10.1016/j.biocon.2013.07.004
- 41. Minton SA (1975a) Geographic distribution of sea snakes. In The biology of sea snakes: 21–31. Dunson W. A. (Ed.). Baltimore: London & Tokyo.
- 42. Minton SA (1975b) Serological relationships of sea snakes and their evolutionary implication. In The biology of sea snakes: 33–55. Dunson W. A. (Ed.). Baltimore: London & Tokyo.
- 43. Rasmussen AR (2002) Phylogenetic analysis of the "true" aquatic elapid snakes Hydrophiinae (sensu Smith et al. 1977) indicating two independent radiations into water. Steenstrupia 27: 47.
- 44. Rasmussen AR, Murphy JC, Ompi M, Gibbons JW, Uetz P (2011) Marine reptiles. PLoS ONE 6: 1. doi: 10.1371/journal.pone.0027373
- 45. Smith LA (1974) The sea snakes of Western Australia (Serpentes: Elapidae, Hydrophiinae), with a description of a new subspecies. Rec. West. Aust. Mus. 3: 93.
- 46. Sutherland SK (1983) Australian animal toxins the creatures their toxins and care of the poisoned patient. New York: Oxford University Press. pmid:25121320
- 47. Voris HK (1977) A phylogeny of the sea snakes (Hydrophiidae). Fieldiana Zoology 70: 79. doi: 10.5962/bhl.title.7200
- 48. Wallach V, Williams KL, Boundy J (2014) Snakes of the world: A catalogue of living and extinct species. Boca Raton: CRC Press. doi: 10.1682/JRRD.2014.01.0007. pmid:25626113
- 49. Kharin VE (1981) A review of sea snakes of the genus Aipysurus (Serpentes: Hydrophiidae). Zool. Zh. 60: 257.
- 50. Kharin VE (2005) A check-list of sea snakes (Serpentes: Laticaudidae, Hydrophiidae) of the world ocean. Tinro140: 71.
- 51. Kharin VE, Czeblukov VP (2006) On a new record of a poorly known and rare sea snake Aipysurus tenuisLönnberg et Andersson, 1913 (Serpentes: Hydrophiidae) in the waters of Australia. Russ. J. Mar. Biol.32: 194. doi: 10.1134/s1063074006030072
- 52. Wells RW (2007) Some taxonomic and nomenclatural considerations on the Class Reptilia in Australia. The sea snakes of Australia. An introduction to the members of the families Hydrophiidae and Laticaudidae in Australia, with a new familial and generic arrangement. Aust. Biodiv. Rec. 8: 1.
- 53. McCosker JE (1975) Feeding behavior of Indo-Australian Hydrophiidae. In The biology of sea snakes: 217–232. Dunson W. A. (Ed.). Baltimore: London & Tokyo.
- 54. Voris HK (1972) The role of sea snakes (Hydrophiidae) in the trophic structure of coastal ocean communities. J. Mar. Biol. Assoc. India 14: 429.
- 55. Miras JAM, Martínez-Solano I (2009) Gallotia auaritae. The IUCN Red List of Threatened Species. Version 2014.2. www.iucnredlist.org. Downloaded on 06 November 2014.
- 56. Sadlier RA, Whitaker AH, Bauer AM (2010) Phoboscincus bocourti. The IUCN Red List of Threatened Species. Version 2014.2. www.iucnredlist.org. Downloaded on 06 November 2014.
- 57. Sanders KL, Lee MSY, Leys R, Foster R, Keogh JS (2008) Molecular phylogeny and divergence dates for Australasian elapids and sea snakes (Hydrophiinae): evidence from seven genes for rapid evolutionary radiations. J. Evol. Biol. 21: 682–695. doi: 10.1111/j.1420-9101.2008.01525.x. pmid:18384538
- 58. Director of National Parks (2013) Draft North-west Commonwealth Marine Reserves Network Management Plan 2014–24.Canberra: Director of National Parks.
- 59. Masini R, Jones R, Sim C(2011) Node 1—Dredging science: Science plan. Western Australia Marine Science Institute: 23.
- 60. Pollock JF, Lamb JB, Field SN, Heron SF, Schaffelke B, et al. (2014) Sediment and turbidity associated with offshore dredging increase coral disease prevalence on nearby reefs. PLOS one 9(7): e102498. doi: 10.1371/journal.pone.0102498. pmid:25029525