Evidence map›Paper›PMID 40877967›Full record

ArticleMovement ecology2025

Wiggle and glide: fine-scale telemetry reveals unique diving strategies in benthic-foraging sea snakes.

Shannon Coppersmith, Claire Goiran, Kate Laura Sanders, Jenna Margaret Crowe-Riddell, Olivier Chateau, Richard Shine, Vinay Udyawer

Abstract read
In one paragraph

Article in Movement ecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Shannon CoppersmithSchool of Biological Sciences, The University of Adelaide, Adelaide, South Australia, Australia. shannon.coppersmith@adelaide.edu.au.ORCID http://orcid.org/0000-0002-7178-7731
Claire GoiranISEA & LabEx Corail, Université de La Nouvelle-Calédonie, Nouméa, New Caledonia, New Caledonia.ORCID http://orcid.org/0000-0002-1649-4418
Kate Laura SandersSchool of Biological Sciences, The University of Adelaide, Adelaide, South Australia, Australia.ORCID http://orcid.org/0000-0002-9581-268X
Jenna Margaret Crowe-RiddellSchool of Biological Sciences, The University of Adelaide, Adelaide, South Australia, Australia.ORCID http://orcid.org/0000-0003-2794-2914
Olivier ChateauLaboratory of Marine Biology and Ecology, Aquarium des Lagons, Nouméa, New Caledonia, New Caledonia.ORCID http://orcid.org/0000-0003-1153-6284
Richard ShineSchool of Natural Sciences, Macquarie University, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0001-7529-5657
Vinay UdyawerSharks Pacific, Rarotonga, Cook Islands.ORCID http://orcid.org/0000-0001-5812-0740

Funding

Australian Research Council DE240100501Australian Research Council FL120100074PADI Foundation 28454Parks Australia QT4C7PG
6 · The paper itself

Abstract

backgroundThe efficient acquisition of two critical but spatially separated resources -food and oxygen- governs the daily movements and diving patterns of air-breathing aquatic animals. Unlike pinnipeds, turtles and seabirds, fully marine ('true') sea snakes spend their entire lifecycle at sea and have evolved specialised movement behaviours. However, fine-scale data on the diving behaviour of free-ranging sea snakes remain scarce, limiting our understanding of their ecology and vulnerability to anthropogenic threats.

methodsWe used acoustic telemetry to track five individuals of two benthic-foraging sea snake species (Hydrophis stokesii, H. major) in Exmouth Gulf, Western Australia, and Baie des Citrons, New Caledonia. Each snake was continuously tracked using a directional hydrophone for up to 18 h, generating high-resolution, three-dimensional dive paths. After filtering, we analysed 106 dives from 46 h of tracking.

resultsSea snakes primarily conducted U- and S-shaped dives and spent on average 97.2% of their time submerged. Most U-shaped dives were characterised by limited vertical and horizontal movement. S-shaped dives were more complex, with variable time on the seafloor and occasionally interrupted gradual ascents. Dive duration was positively correlated with post-dive surface interval, while depth and duration of the gradual ascent phase were influenced by environmental depth. We also identified distinctive, repetitive undulations ('wiggles') in the depth profiles of several dives completed by all three tracked H. stokesii.

conclusionsThese high-resolution data provide the first insights into the fine-scale diving patterns of benthic-foraging sea snakes. Like surface-foraging species, they appear to regulate air intake based on environmental depth and may be neutrally buoyant in the gradual ascent phase of S-shaped dives. We hypothesise that this phase facilitates efficient horizontal travel, despite potential increases in predation risk. The 'wiggles' observed in H. stokesii may have a functional role in buoyancy control, energy conservation, or foraging. Our study contributes to a deeper understanding of sea snake diving strategies, with implications for their ecology, physiology, and conservation.

Indexed as

Acoustic telemetryBehaviourBiologgingEnergeticsSensory

Identifiers

PMID40877967
PMCPMC12395837

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.