in

In situ swimming behavior of the Mariana snailfish Pseudoliparis swirei


Abstract

The hadal zone, defined as ocean depths below 6000 m, is one of Earth’s most extreme environments. The Mariana snailfish Pseudoliparis swirei is among the deepest known fishes, yet its natural behavior remains largely unknown. Here we quantify, for the first time, the three-dimensional swimming behavior of this species in its native habitat by analyzing video collected by a baited deep-sea lander at nearly 7000 m depth. Using an automated computer vision workflow that detects, tracks and infers visual depth from single camera footage, we reconstructed full trajectories for individual fish using 868 manually annotated instances. The results show that P. swirei exhibits a slow routine swimming speed of 0.16-0.18 m s⁻1 (0.62-0.80 body lengths s⁻1, mean ≈ 0.71 BL s⁻1), with low variability across individuals and only short acceleration events reaching up to ~ 0.50 m s⁻1. By combining reconstructed movement paths with a simple representation of near bottom flow, we estimate that the fish operates within a modest spatial range around the bait. A mechanistic advection-diffusion framework further indicates that P. swirei first detects bait odor at a distance of approximately 350 m. These findings provide the first quantitative view of locomotion in a hadal vertebrate, revealing gentle, steady gaits shaped by environmental constraints.

Data availability

The computer-vision analysis pipeline used for fish detection, monocular depth estimation, trajectory reconstruction, and swimming-speed calculation is openly available on GitHub at: https://github.com/chenyizi65/FishSpeed. The repository contains the scripts and configuration files required to reproduce the analyses. Data generated during this study are derived from deep-sea lander video recordings and processed outputs produced using this pipeline. Representative data are included in the manuscript and Supplementary Information.

References

  1. Xiao, X. et al. Microbial ecosystems and ecological driving forces in the deepest ocean sediments. Cell 188(5), 1363–1377 (2025).

    Google Scholar 

  2. Casey S: The Underworld: Journeys to the Depths of the Ocean: Random House; 2024, ISBN:9781804950906.

  3. Haddock, S. H. & Choy, C. A. Life in the midwater: The ecology of deep pelagic animals. Annu. Rev. Mar. Sci. 16(1), 383–416 (2024).

    Google Scholar 

  4. Gerringer, M. On the success of the hadal snailfishes. Integr. Organism. Biol. 1(1), obz004 (2019).

    Google Scholar 

  5. Gerringer, M. E., Linley, T. D., Jamieson, A. J., Goetze, E. & Drazen, J. C. Pseudoliparis swirei sp. nov.: A newly-discovered hadal snailfish (Scorpaeniformes: Liparidae) from the Mariana Trench. Zootaxa 4358(1), 161–177-161-177 (2017).

    Google Scholar 

  6. Jamieson, A. J. et al. New maximum depth record for bony fish: Teleostei, Scorpaeniformes, Liparidae (8336 m, Izu-Ogasawara Trench). Deep Sea Res. Part I Oceanogr. Res. Pap. 199, 104132 (2023).

    Google Scholar 

  7. Priede, I. G., Smith, K. L. Jr. & Armstrong, J. D. Foraging behavior of abyssal grenadier fish: Inferences from acoustic tagging and tracking in the North Pacific Ocean. Deep Sea Research Part A. Oceanographic Research Papers 37(1), 81–101 (1990).

    Google Scholar 

  8. Wang, K. et al. Morphology and genome of a snailfish from the Mariana Trench provide insights into deep-sea adaptation. Nat. Ecol. Evol. 3(5), 823–833 (2019).

    Google Scholar 

  9. Gerringer, M. et al. Habitat influences skeletal morphology and density in the snailfishes (family Liparidae). Front. Zool. 18, 1–22 (2021).

    Google Scholar 

  10. Schwarzhans, W. W. & Gerringer, M. E. Otoliths of the deepest-living fishes. Deep Sea Res. Part I Oceanogr. Res. Pap. 198, 104079 (2023).

    Google Scholar 

  11. Jiang, H., Du, K., Gan, X., Yang, L. & He, S. Massive loss of olfactory receptors but not trace amine-associated receptors in the world’s deepest-living fish (Pseudoliparis swirei). Genes 10(11), 910 (2019).

    Google Scholar 

  12. Gerringer, M. E., Linley, T. D. & Nielsen, J. G. Revision of the depth record of bony fishes with notes on hadal snailfishes (Liparidae, Scorpaeniformes) and cusk eels (Ophidiidae, Ophidiiformes). Mar. Biol. 168(11), 167 (2021).

    Google Scholar 

  13. Xu, H. et al. Evolution and genetic adaptation of fishes to the deep sea. Cell 188(5), 1393–1408 (2025).

    Google Scholar 

  14. Woodworth, B. et al. Swimming kinematics of deep-sea fishes. J. Fish Biol. 106(3), 805–822 (2025).

    Google Scholar 

  15. Drazen, J. C. & Seibel, B. A. Depth-related trends in metabolism of benthic and benthopelagic deep-sea fishes. Limnol. Oceanogr. 52(5), 2306–2316 (2007).

    Google Scholar 

  16. Priede, I. & Froese, R. Colonization of the deep sea by fishes. J. Fish Biol. 83(6), 1528–1550 (2013).

    Google Scholar 

  17. Gerringer M: On the Success of the Hadal Snailfishes: The Influence of Trophic Ecology, Life History, and Pressure Adaptation on Depth Zonation in the Planet’s Deepest-Living Fishes: University of Hawai’i at Manoa; 2017 http://hdl.handle.net/10125/62513.

  18. Bailey, D. M., Bagley, P. M., Jamieson, A. J., Collins, M. A. & Priede, I. G. In situ investigation of burst swimming and muscle performance in the deep-sea fish Antimora rostrata. J. Exp. Mar. Biol. Ecol. 285, 295–311 (2003).

    Google Scholar 

  19. Black J, Neuheimer A, Horn P, Tracey DM, Drazen J: Environmental, evolutionary, and ecological drivers of slow growth in deep-sea demersal teleosts. Marine Ecology Progress Series 2020, 658.

  20. Deng, X., Wagner, H.-J. & Popper, A. N. Comparison of the saccules and lagenae in six macrourid fishes from different deep-sea habitats. J. Acoust. Soc. Am. 141(5_Supplement), 3860–3861 (2017).

    Google Scholar 

  21. Stevens, D. W. et al. Rattail lebensspuren: Feeding impressions from deep-sea grenadiers. Deep Sea Res. Part I Oceanogr. Res. Pap. 200, 104152 (2023).

    Google Scholar 

  22. Linley, T. D. et al. Fishes of the hadal zone including new species, in situ observations and depth records of Liparidae. Deep Sea Res. Part I Oceanogr. Res. Pap. 114, 99–110 (2016).

    Google Scholar 

  23. Taira, K., Kitagawa, S., Yamashiro, T. & Yanagimoto, D. Deep and bottom currents in the Challenger Deep, Mariana Trench, measured with super-deep current meters. J. Oceanogr. 60, 919–926 (2004).

    Google Scholar 

  24. Jiang, H. et al. Three-layer circulation in the world deepest hadal trench. Nat. Commun. 15(1), 8949 (2024).

    Google Scholar 

  25. Collins, M. A., Priede, I. G. & Bagley, P. M. In situ comparison of activity in two deep-sea scavenging fishes occupying different depth zones. Proc. R. Soc. Lond. B Biol. Sci. 266(1432), 2011–2016 (1999).

    Google Scholar 

  26. Koslow, J. Energetic and life-history patterns of deep-sea benthic, benthopelagic and seamount-associated fish. J. Fish Biol. 49, 54–74 (1996).

    Google Scholar 

  27. Drazen, J. C. & Haedrich, R. L. A continuum of life histories in deep-sea demersal fishes. Deep Sea Res. Part I Oceanogr. Res. Pap. 61, 34–42 (2012).

    Google Scholar 

  28. Poulson, T. L. Adaptations of cave fishes with some comparisons to deep-sea fishes. Environ. Biol. Fish. 62(1), 345–364 (2001).

    Google Scholar 

  29. Warrant, E. J. & Locket, N. A. Vision in the deep sea. Biol. Rev. 79(3), 671–712 (2004).

    Google Scholar 

  30. Warrant, E. The eyes of deep–sea fishes and the changing nature of visual scenes with depth. Philos. Trans. R. Soc. Lond. B Biol. Sci. 355(1401), 1155–1159 (2000).

    Google Scholar 

  31. Shekhar G: Fisheries Acoustics: Understanding Aquatic Environments: Educohack Press; 2025, ISBN: 9789361526527.

  32. Bailey, D. M., Wagner, H.-J., Jamieson, A. J., Ross, M. F. & Priede, I. G. A taste of the deep-sea: The roles of gustatory and tactile searching behaviour in the grenadier fish Coryphaenoides armatus. Deep Sea Res. Part I Oceanogr. Res. Pap. 54(1), 99–108 (2007).

    Google Scholar 

  33. Horn, M. H. & Ferry-Graham, L. A. Feeding mechanisms and trophic interactions. In The ecology of marine fishes: California and adjacent waters 387–410 (2006).

  34. Blankenship, L. E. & Levin, L. A. Extreme food webs: Foraging strategies and diets of scavenging amphipods from the ocean’s deepest 5 kilometers. Limnol. Oceanogr. 52(4), 1685–1697 (2007).

    Google Scholar 

  35. Xu, H., Fang, C. & He, S. Deciphering the life adaptation in extreme high pressure: Genomic breakthroughs and ecological insights in fish from hadal zone. Innovation https://doi.org/10.1016/j.xinn.2025.100915 (2025).

    Google Scholar 

  36. Xu, H., Fang, C., Wang, C., Gan, X. & He, S. Lipidome and proteome analyses provide insights into Mariana Trench snailfish (Pseudoliparis swirei) adaptation to the hadal zone. Water Biol. Secur. 3(4), 100295 (2024).

    Google Scholar 

  37. Srivastava A: A textbook of vertebrate zoology: Academic Guru Publishing House; 2024, ISBN: 978–81–970707–1–6.

  38. Howard J: Fish biology and fisheries: Scientific e-Resources; 2019.

  39. Gerringer, M. E. et al. Distribution, composition and functions of gelatinous tissues in deep-sea fishes. R. Soc. Open Sci. 4(12), 171063 (2017).

    Google Scholar 

  40. Gerringer, M. et al. Habitat influences skeletal morphology and density in the snailfishes (family Liparidae). Front. Zool. 18(1), 16 (2021).

    Google Scholar 

  41. Blanton, J. M. et al. Microbiomes of hadal fishes across trench habitats contain similar taxa and known piezophiles. mSphere 7(2), e00032-e122 (2022).

    Google Scholar 

  42. Gerringer, M. E. et al. Observations of deep-sea fishes at depths 250 to 6300 m off Puerto Rico. ICES J. Mar. Sci. 83(1), fsaf234 (2026).

    Google Scholar 

  43. Yagi, M., Anzai, S. & Tanaka, S. Dive deep: Bioenergetic adaptation of deep-sea animals. Zool. Sci. 42(1), 83–95 (2025).

    Google Scholar 

  44. Xu, W. et al. Chromosome-level genome assembly of hadal snailfish reveals mechanisms of deep-sea adaptation in vertebrates. Elife 12, RP87198 (2023).

    Google Scholar 

  45. Barcan, A. S. et al. Understanding the transfer and persistence of antimicrobial resistance in aquaculture using a model teleost gut system. Anim. Microbiome 7(1), 18 (2025).

    Google Scholar 

  46. Barcan, A. S. et al. Modulatory effects of Boletus edulis on the gut microbiota in Atlantic salmon (Salmo salar) utilizing an artificial teleost gut model. Anim. Microbiome 7(1), 111 (2025).

    Google Scholar 

  47. Zhang J, Wang Y: A video dataset for hadal snailfish along with the benchmark. Deep Sea Research Part I: Oceanographic Research Papers 2025:104517.

  48. Amin, S. U., Abbas, M. S., Kim, B., Jung, Y. & Seo, S. Enhanced anomaly detection in pandemic surveillance videos: An attention approach with EfficientNet-B0 and CBAM integration. IEEE Access https://doi.org/10.1109/access.2024.3488797 (2024).

    Google Scholar 

Download references

Acknowledgements

This work was supported by the project 2025YFE0218900. We are grateful to R/V Tansuo Yihao for their contributions in lander deployment.

Funding

This study was supported by National Natural Science Foundation of China (42376149) and Shenzhen Key Laboratory of Advanced Technology for Marine Ecology (ZDSYS20230626091459009).

Author information

Authors and Affiliations

Authors

Contributions

A.S.B. analyzed the data and wrote the first draft of the manuscript. Y.C. performed the video analysis, frame-based calculations, and prepared the figures. J.Z., J.L., L.H., and A.S.B. reviewed the manuscript. Y.W. conceived the study.

Corresponding author

Correspondence to
Yong Wang.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Supplementary Information 1. (download DOCX )

Supplementary Information 2. (download DOCX )

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Cite this article

Chen, Y., Barcan, A.S., Zhang, J. et al. In situ swimming behavior of the Mariana snailfish Pseudoliparis swirei.
Sci Rep (2026). https://doi.org/10.1038/s41598-026-48409-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1038/s41598-026-48409-2

Keywords

  • Snailfish
  • Hadal trench
  • Swimming speed
  • Deep-sea fish
  • Biomechanics


Source: Ecology - nature.com

Carbon removal project supports Maine’s blue economy, broader marine health

Soil organic carbon stabilization by organic amendments through iron gate and enzyme latch mechanisms

Back to Top