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Aipysurus laevis LACÉPÈDE, 1804

IUCN Red List - Aipysurus laevis - Least Concern, LC

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Higher TaxaElapidae (Hydrophiinae), Colubroidea, Caenophidia, Alethinophidia, Serpentes, Squamata (snakes)
Subspecies 
Common NamesE: Olive-brown seasnake 
SynonymAipysurus laevis LACÉPÈDE 1804: 210
Hypotropis jukesii GRAY 1846: 284
Aipysurus laevis — DUMÉRIL, BIBRON & DUMÉRIL 1854: 1326
Aipysurus fuliginosus DUMÉRIL, BIBRON & DUMÉRIL 1854: 1327
Aipysurus laevis — FISCHER 1856: 32
Aipysurus fuliginosus — FISCHER 1856: 32
Aipysurus laevis laevis — SMITH 1974: 95
Aipysurus laevis — COGGER 1983: 244
Aipysurus laevis — COGGER 2000: 703
Smithsohydrophis laevis
Aipysurus laevis — WALLACH et al. 2014: 22 
Distributionwaters around Indonesia (Timor), Papua New Guinea, east to New Caledonia, Australia (New South Wales?, Northern Territory, Queensland, Western Australia)

Type locality: Locker Is., off Onslow, Western Australia, in 21° 44'S, 114° 46'E., designated by Smith (1974). Neotype locality: near Locker Is., off Onslow, Western Australia, in 21° 44'S, 114° 46'E.  
Reproductionovovivparous 
TypesNeotype: WAM R22384, designated by Smith (1974). Original holotype in MNHN, now lost, from Australia, collected by F. Péron & C. Lesueur (M. Smith, 1926; L. Smith, 1974).
Holotype: BMNH 1946.1.9.53, from near Darnley Is., Torres Strait (as near Darnley Islands, Port Essington), Qld. [Hypotropis jukesii].
Holotype: MNHP 639, from New Caledonia [Aipysurus fuliginosus]. 
DiagnosisDIAGNOSIS (genus). Maxillary bone extends forward beyond palatine, as long as or longer than ectoptergyoid; 5–11 maxillary teeth behind front fangs; nostrils superior, nasal scales in contact with one another; head scales variable, either whole or broken into smaller scales; body scales imbricate, in 17–15 rows around body; ventrals large, 1 3 to 1 2 width of body, scales usually with medial keel, best developed posteriorly. (Modified after Smith 1926:13, Leviton et al. 2014)

Diagnosis: The species laevis is distinguished by 21 or 23 (rarely 19) scale rows and the presence of a loreal. For diagnosis of subspecies see under next taxon. (Smith 1974)

Description: The most massive member of the genus, maximum length: males 777 mm (subad.); females 1703 mm. Maximum girth: males 102 mm (subad.); females 225 mm. Head shields irregularly divided but generally retaining their colubroid outline.
Rostral wider than high. Nasals entire separated from 1 or 2 (rarely 3) preoculars by a loreal. Postoculars 2 or 3. Prefrontals 2 (in 86% of specimens), 3 or 4 (see comments under variation). Frontal rarely entire, usually divided asymqletrically into 3 or 4 pieces. Supraoculars transversely divided into two. Parietals always divided, their boundary indistinct. Anterior temporals usually 3. Upper labials 8-10 (9 in 74% of specimens); usually the first 3 (but up to the first 5) small owing to horizontal division; fourth to sixth entering orbit. Lower labials 7-9 (usually 8). One or two pairs of chin shields prominent; anterior pair sometimes, posterior pair always separated by one or two small scales.
Midbody scale rows 21 or 23 (once 19), the scales weakly imbricate. Ventrals: 142-159. Subcaudals: males 31-34, females 22-32. (Smith 1974)

Coloration: Uniform creamy-yellow or golden brown (one specimen brown). Head usually darker brown. Juveniles dark bluish-brown on back, broken by irregular pale golden bands one scale wide and 2-4 scales apart. Predominance of blue-brown decreases with age, it being super- seded by golden brown. Blue-brown recedes to tips of scales and persists longest on the back where it sometimes remains in subadults as several longitudinal rows of spots. (Smith 1974)

Variation: All specimens display some division of head shields. Most variable are the prefrontals; their number and orientation are related to variation in frontal length. When the frontal is not unduly prolonged forwards, the two prefrontals are roughly rectangular and in broad contact. With in~ creasing frontal length the prefrontals become long and narrow, obliquely orientated and only in short contact. A high prefrontal obliquity can be attained before the elongate anterior corner of the frontal is split off to form a median shield. In extreme cases of frontal elongation not only a median shield is formed but the elongate pre- frontals each divide transversely to form 4 prefrontals (or occasionally 3 . when only one side divides). (See M.A. Smith 1926: 20 fig. 10.)
Upper labials, especially the anterior ones, are prone to horizontal division, usually the first 3, sometimes 2 or 4 (once 5) divided. Ten upper labials occur occasionally, mainly because of vertical division of the basal portion of the horizontally divided sixth labial. Eight labials occur when the first and second labials fuse. With one exception (count of 22) subcaudal range is 25-34. (Smith 1974) 
CommentVenomous!

Synonymy after COGGER 1983. Aipysurus laevis pooleorum SMITH 1974 has been elevated to species level. Kaiser et al. 2013 rejected the generic name Oceanius Wells 2007 and synonymized it with Aipysurus.

Type species: Aipysurus laevis LACÉPÈDE 1804 is the type species of the genus Aipysurus LACÉPÈDE 1804.

Habitat: marine. This species is known from 130-140 m depth in Australian waters (Greer 1997: 270).

Hybridization: A. laevis hybridizes with A. fuscus (Sanders et al. 2014) 
EtymologyNamed after Latin “laevis” = smooth. 
References
  • Aubret, Fabien. 2006. Aipysurus pooleorum Avian predation. Herpetological Review 37 (1): 93 - get paper here
  • Bauer, A. M. & SADLIER, R. A. 2000. The herpetofauna of New Caledonia. Contributions to Herpetology, 17; Society for Study Amphibians and Reptiles, Ithaca, New York.
  • Burns, G. & H. Heatwole 1998. Home Range and Habitat Use of the Olive Sea Snake, Aipysurus laevis, on the Great Barrier Reef, Australia Journal of Herpetology 32 (3): 350-358. - get paper here
  • Burns,Glen & Heatwole,Harold 2000. Growth, sexual dimorphism, and population biology of the olive sea snake, Aipysurus laevis, on the Great Barrier Reef of Australia. Amphibia-Reptilia 21 (3): 289-300 - get paper here
  • Cogger, H. G. 1975. The sea snakes of Australia and New Guinea. pp. 59-139 in Dunson, W. (ed. ) The Biology of Sea Snakes. Baltimore: University Park Press
  • Cogger, H. G. 2014. Reptiles and Amphibians of Australia, 7th ed. CSIRO Publishing, xxx + 1033 pp. - get paper here
  • Cogger, H.G. 2000. Reptiles and Amphibians of Australia, 6th ed. Ralph Curtis Publishing, Sanibel Island, 808 pp.
  • Duméril, A. M. C., Bibron, G. & DUMÉRIL, A. H. A., 1854. Erpétologie générale ou histoire naturelle complète des reptiles. Tome septième. Deuxième partie, comprenant l'histoire des serpents venimeux. Paris, Librairie Encyclopédique de Roret: i-xii + 781-1536 - get paper here
  • Ehmann, Harold 1992. Encyclopedia of Australian Animals: Reptiles. Angus & Robertson, Pymble, NSW, 495 pp.
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  • Kharin, V.E.; Cheblyukov, V.P. 2006. On a new record of a poorly known and rare sea snake Aipysurus tenuis Lönnberg et Andersson, 1913 (Serpentes: Hydrophiidae) in the waters of Australia. Russian Journal of Marine Biology 32 (3): 194-197. - get paper here
  • Kukoschek, V.; Heatwole, H.; Grech, A.; Burns, G.; Marsh, H. 2007. Distribution of two species of sea snakes, Aipysurus laevis and Emydocephalus annulatus, in the southern Great Barrier Reef: metapopulation dynamics, marine protected areas and conservation. Coral Reefs 26(2):291-307 - get paper here
  • LaCépède, B. G. E. L. 1804. Mémoire sur plusieurs animaux de la Nouvelle- Hollande dont la description n’a pas encore été publiée. Annales du Muséum National d’Histoire Naturelle, Paris, 4:184-211 - get paper here
  • LUKOSCHEK,VIMOKSALEHI; MICHELLE WAYCOTT and GLENN DUNSHEA 2005. Isolation and characterization of microsatellite loci from the Australasian sea snake, Aipysurus laevis. Molecular Ecology Notes 5: 879–881 - get paper here
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  • Redfield, J. A., Holmes, J. C. & Holmes, R. D. 1978. Sea snakes of the eastern Gulf of Carpentaria. Aust. J Mar. Freshwat. Res. 29: 325-334 - get paper here
  • Sanders, K.L., Rasmussen, A.R., Guinea, M.L. 2014. High rates of hybridisation reveal fragile reproductive barriers between endangered Australian sea snakes. Biological Conservation 171: 200 - 208 - get paper here
  • Shine, Richard; Claire Goiran, Catherine Shilton, Shai Meiri, Gregory P Brown 2019. The life aquatic: an association between habitat type and skin thickness in snakes. Biological Journal of the Linnean Society, blz136 - get paper here
  • Smith, L. A. 1974. The sea snakes of Western Australia (Serpentes: Elapidae: Hydrophiinae) with a description of a new subspecies. Rec. West. Aust. Mus. 3: 93-110 - get paper here
  • Smith, M. A. 1926. Monograph on the Sea Snakes. (Hydrophiidae). London: British Museum, xvii + 130 pp.
  • Swan, G.; Sadlier, R.; Shea, G. 2017. A field guide to reptiles of New South Wales. Reed New Holland, 328 pp.
  • Udyawer, V., Oxenham, K., Hourston, M., & Heupel, M. 2021. Distribution, fisheries interactions and assessment of threats to Australia’s sea snakes. Report to the National Environmental Science Program, Marine Biodiversity Hub. - get paper here
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  • Zimmerman, K. D.;Shohet, D. 1994. Observations on newborn olive sea snakes, Aipysurus laevis, and resulting divisions of its life cycle. The Snake 26 (1): 51-56
 
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