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Fish Eggs as the Apparent Sole Food Item for a Genus of Sea Snake, Emydocephalus (Krefft)
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inferred← citeshttps://doi.org/10.11646/zootaxa.4758.1.6zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1002/ece3.256openalex-snapshot
Sea snakes rarely venture far from home
inferred← citeshttps://doi.org/10.1002/jmor.1052050109openalex-snapshot
Venom glands and some associated muscles in sea snakes
inferred← citeshttps://doi.org/10.1007/s00227-021-03956-2openalex-snapshot
Resource use and the impacts of fisheries on two sympatric sea snake species on the west coast of India
inferred← citeshttps://doi.org/10.1007/s00265-004-0897-zopenalex-snapshot
All at sea: aquatic life modifies mate-recognition modalities in sea snakes (Emydocephalus annulatus, Hydrophiidae)
inferred← citeshttps://doi.org/10.1007/s00338-006-0192-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00338-012-0977-xopenalex-snapshot
Decline in sea snake abundance on a protected coral reef system in the New Caledonian Lagoon
inferred← citeshttps://doi.org/10.1007/s00338-012-1008-7openalex-snapshot
Effects of season, sex and body size on the feeding ecology of turtle-headed sea snakes (Emydocephalus annulatus) on IndoPacific inshore coral reefs
inferred← citeshttps://doi.org/10.1007/s00338-025-02615-yopenalex-snapshot
Dietary variation and seasonal changes in the fish egg eating specialist, Emydocephalus ijimae (Squamata: Reptilia) in mid-latitude coral reefs
inferred← citeshttps://doi.org/10.1007/s00442-005-0074-8openalex-snapshot
Do lizards and snakes really differ in their ability to take large prey? A study of relative prey mass and feeding tactics in lizards
inferred← citeshttps://doi.org/10.1007/s12526-022-01259-3openalex-snapshot
Diversity, distribution, and natural history of the marine snakes of Sri Lanka
inferred← citeshttps://doi.org/10.1016/j.parint.2023.102776openalex-snapshot
Polyphyly of the Dinurinae Looss, 1907 (Digenea: Hemiuridae) and resurrection of the Mecoderinae Skrjabin & Guschanskaja, 1954 based on novel collection of Tubulovesicula laticaudi Parukhin, 1969 from marine elapid snakes in Sri Lanka
inferred← citeshttps://doi.org/10.1046/j.0269-8463.2004.00803.xopenalex-snapshot
A novel foraging mode in snakes: browsing by the sea snake Emydocephalus annulatus (Serpentes, Hydrophiidae)
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2003.00213.xopenalex-snapshot
Intraspecific habitat partitioning by the sea snake Emydocephalus annulatus (Serpentes, Hydrophiidae): the effects of sex, body size, and colour pattern
inferred← citeshttps://doi.org/10.1080/00222938700770701openalex-snapshot
Adaptations of sea snakes that eat fish eggs; with a note on the throat musculature ofAipysurus eydouxi(Gray, 1849)
inferred← citeshttps://doi.org/10.1093/icb/ics069openalex-snapshot
Long-term Field Study of Sea Kraits in New Caledonia: Fundamental Issues and Conservation
inferred← citeshttps://doi.org/10.1093/icb/ics081openalex-snapshot
Effects of Oceanic Salinity on Body Condition in Sea Snakes
inferred← citeshttps://doi.org/10.1098/rsob.160054openalex-snapshot
The evolution of scale sensilla in the transition from land to sea in elapid snakes
inferred← citeshttps://doi.org/10.1098/rsos.182022openalex-snapshot
Ultrastructural evidence of a mechanosensory function of scale organs (sensilla) in sea snakes (Hydrophiinae)
inferred← citeshttps://doi.org/10.1098/rsos.231429openalex-snapshot
The adaptive significance of large size at birth in marine snakes
inferred← citeshttps://doi.org/10.1111/1365-2435.13446openalex-snapshot
A trait‐based framework for understanding predator–prey relationships: Trait matching between a specialist snake and its insect prey
inferred← citeshttps://doi.org/10.1111/bij.12422openalex-snapshot
Parental defence on the reef: antipredator tactics of coral-reef fishes against egg-eating seasnakes
inferred← citeshttps://doi.org/10.1111/brv.12201openalex-snapshot
Group living in squamate reptiles: a review of evidence for stable aggregations
inferred← citeshttps://doi.org/10.1111/evo.14379openalex-snapshot
Re‐evaluating the morphological evidence for the re‐evolution of lost mandibular teeth in frogs
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2006.00691.xopenalex-snapshot
Molecular phylogeny of sea snakes reveals a rapidly diverged adaptive radiation
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2012.01971.xopenalex-snapshot
Phenotypic divergence between seasnake (Emydocephalus annulatus) populations from adjacent bays of the New Caledonian Lagoon
inferred← citeshttps://doi.org/10.1111/j.1096-3642.1969.tb00716.xopenalex-snapshot
Notes on the Australian sea-snake Ephalophis greyi M. Smith (Serpentes : Elapidae, Hydrophiinae) and the origin and classification of sea-snakes
inferred← citeshttps://doi.org/10.1111/j.1096-3642.1972.tb00028.xopenalex-snapshot
The genera of sea‐snakes of the Hydrophis group(Serpentes: Elapidae)
inferred← citeshttps://doi.org/10.1111/j.1442-9993.2005.01524.xopenalex-snapshot
Synchrony in capture dates suggests cryptic social organization in sea snakes (Emydocephalus annulatus, Hydrophiidae)
inferred← citeshttps://doi.org/10.1111/j.1469-7998.1970.tb02054.xopenalex-snapshot
Character analysis: an empirical approach applied to advanced snakes
inferred← citeshttps://doi.org/10.11606/d.41.2007.tde-24082007-173431openalex-snapshot
Isolamento e caracterização de toxinas do veneno de Bothrops alcatraz Marques, Martins e Sazima, 2002 e aspectos coevolutivos com a dieta
inferred← citeshttps://doi.org/10.11646/zootaxa.3431.1.1openalex-snapshot
Aipysurus mosaicus, a new species of egg-eating sea snake (Elapidae: Hydrophiinae), with a redescription of Aipysurus eydouxii (Gray, 1849)
inferred← citeshttps://doi.org/10.1186/s12862-020-01725-1openalex-snapshot
Visual adaptation of opsin genes to the aquatic environment in sea snakes
inferred← citeshttps://doi.org/10.2108/zsj.20.461openalex-snapshot
Growth and Reproduction of the Sea Snake, Emydocephalus ijimae, in the Central Ryukyus, Japan: a Mark and Recapture Study
inferred← citeshttps://doi.org/10.2307/1444667openalex-snapshot
Marine Snake Diets: Prey Composition, Diversity and Overlap
inferred← citeshttps://doi.org/10.2330/joralbiosci1965.23.691openalex-snapshot
Devolutive dentitions of the sea snake, Emydocephalus ijimae
inferred← citeshttps://doi.org/10.3158/0015-0754(2006)108[1:tpdisr]2.0.co;2openalex-snapshot
The Palatal Dentition in Squamate Reptiles: Morphology, Development, Attachment, and Replacement
inferred← citeshttps://doi.org/10.3354/meps10177openalex-snapshot
Trophic consequences of pelagic life-style in yellow-bellied sea snakes
inferred← citeshttps://doi.org/10.3389/fmars.2018.00399openalex-snapshot
Future Directions in the Research and Management of Marine Snakes
inferred← citeshttps://doi.org/10.3390/toxins5112172openalex-snapshot
Three-Fingered RAVERs: Rapid Accumulation of Variations in Exposed Residues of Snake Venom Toxins
inferred← citeshttps://doi.org/10.3724/sp.j.1245.2014.00255openalex-snapshot
Food Habits and Distribution of the Lake Taal Sea Snake(Hydrophis semperi Garman 1881) and the Sympatric Little File Snake(Acrochordus granulatus Schneider 1799) in Lake Taal, Philippines
inferred← citeshttps://doi.org/10.3853/j.0067-1975.31.1978.219openalex-snapshot
Underwater observations on sea snake behaviour
inferred← citeshttps://doi.org/10.5281/zenodo.13271845openalex-snapshot
A review of gastrolith function with implications for fossil vertebrates and a revised classification
inferred← citeshttps://doi.org/10.6084/m9.figshare.13294466openalex-snapshot
Additional file 1 of Visual adaptation of opsin genes to the aquatic environment in sea snakes
inferred← citeshttps://doi.org/10.6084/m9.figshare.13294469openalex-snapshot
Additional file 2 of Visual adaptation of opsin genes to the aquatic environment in sea snakes
inferred← citeshttps://doi.org/10.6084/m9.figshare.13294472openalex-snapshot
Additional file 3 of Visual adaptation of opsin genes to the aquatic environment in sea snakes
inferred← citeshttps://doi.org/10.6084/m9.figshare.13294475openalex-snapshot
Additional file 4 of Visual adaptation of opsin genes to the aquatic environment in sea snakes
inferred← citeshttps://doi.org/10.6084/m9.figshare.13294478openalex-snapshot
Additional file 5 of Visual adaptation of opsin genes to the aquatic environment in sea snakes
inferred← citeshttps://doi.org/10.6084/m9.figshare.13294481openalex-snapshot
Additional file 6 of Visual adaptation of opsin genes to the aquatic environment in sea snakes
inferred← citeshttps://doi.org/10.6084/m9.figshare.13294484openalex-snapshot
Additional file 7 of Visual adaptation of opsin genes to the aquatic environment in sea snakes
inferred← citeshttps://doi.org/10.6084/m9.figshare.13294487openalex-snapshot
Additional file 8 of Visual adaptation of opsin genes to the aquatic environment in sea snakes
inferred← citeshttps://doi.org/10.7554/elife.66926openalex-snapshot
Rampant tooth loss across 200 million years of frog evolution
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