Acoustic superheroes: how seals mastered hearing on land and at sea

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The earliest eared seals, the 10 million-year-old Pithanotaria starii, improved their amphibious hearing abilities. Their in-air hearing was especially acute. Credit: Jamie Bran
The earliest eared seals, the 10 million-year-old Pithanotaria starii, improved their amphibious hearing abilities. Their in-air hearing was especially acute. Credit: Jamie Bran

New research from an international team of scientists has identified how a specialised tissue in the ears of seals enables them to hear both underwater and on land.

News release

From: Monash University

New research from an international team of scientists has identified how a specialised tissue in the ears of seals enables them to hear both underwater and on land.

The study, published today in Proceedings of the Royal Society B: Biological Sciences, reveals that the earliest marine seals evolved amphibious hearing over 26 million years ago. Amphibious hearing is the ability to hear effectively in both air and water. The findings suggest that amphibious hearing is fundamental to the lives of seals.

Lead author, Dr James Rule from the School of Biological Sciences at Monash University, conducted the research during his time as a postdoctoral researcher at London’s Natural History Museum and said pinnipeds (true seals, eared seals and walruses) have a unique superpower.

“Seals have a superpower, the ability to hear and communicate on land and in the ocean. How they hear sounds underwater, and when this remarkable ability evolved, has until now remained a mystery,” Dr Rule said.

“Our research found that amphibious hearing in seals originated roughly 26 million years ago. Most mammals are unable to hear properly underwater, but seals evolved ears specialised for hearing underwater without compromising their ability to hear on land. This evolutionary innovation facilitated the remarkable vocal diversity of pinnipeds, which allows them to communicate both on land and in the ocean.

“This ancient origin means that amphibious hearing is as fundamental to being a seal as their flippers,” Dr Rule said.

Together with evolutionary analysis of 3D scans of seal ears acquired by CT-imaging, data from both modern and fossil museum specimens and recent advances in pinniped evolution, researchers were able to understand the origins of their amphibious hearing and thus their complex underwater communication.

Dr Natalie Cooper, a Merit Researcher at the Natural History Museum, said pinnipeds have a remarkable variety of auditory and vocal abilities, which are rare in mammals.

“Sound behaves completely differently in air than it does under water, meaning an ear optimised for land usually fails in the ocean, and vice versa. Yet seals have evolved a highly specialised, dual-purpose auditory system that handles both mediums flawlessly. They are actively processing high-frequency acoustic sounds underwater and have sharp, directional hearing in both environments, making them true amphibious masters of sound,” Dr Cooper said.

The study is the largest dataset yet assembled of the ears of living and extinct pinnipeds, and their terrestrial relatives. The international team of researchers investigated whether proposed adaptations for amphibious hearing within pinnipeds differ from their nearest terrestrial relatives, when and how amphibious hearing evolved, and how pinnipeds balance the physical constraints of two markedly different auditory environments.

Professor Alistair Evans, Head of the EvoMorph Research Group, which specialises in the biology that influences the evolution, development and function of animals, said the research highlights just how rich and complex a seal's sensory experience truly is.

“Seals are the only creatures in their class to have evolved this sensory flexibility. It allows them to transition seamlessly between two entirely different acoustic worlds without a single drop in performance, giving them an evolutionary edge whether they are resting, hunting or communicating,” Professor Evans said.

Read the research paper: https://doi.org/10.1098/rspb.2026.0178

FURTHER INFORMATION

This research was conducted in collaboration with the Natural History Museum, Monash University, Museums Victoria, Imperial College London, Université de Poitiers, University of Liverpool, Tasmanian Museum and Art Gallery, University of Johannesburg, Australian National University, University of Bristol, Instituto Federal de Educação Ciência e Tecnologia do Rio Grande do Sul, Museum of New Zealand Te Papa Tongarewa, University of Otago, National Museum of Nature and Science, University of Tsukuba, Comenius University in Bratislava, Friedrich Schiller University Jena, Max Planck Institute for Evolutionary Anthropology and the American Museum of Natural History.

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conference:
Proceedings of the Royal Society B: Biological Sciences
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Organisation/s: Monash University, Museums Victoria, The Australian National University
Funder: J.P.R. was supported by a UKRI fellowship (SEAL: grant number EP/X021238/1) from the Engineering and Physical Sciences Research Council. Scans were funded from the following sources: NHMUK and LACM scans from UKRI EP/X021238/1, MSCA 748167/ECHO, and the Department of Anatomy and Developmental Biology (Monash University); USNM scans funded by Siobhán Cooke and the Center for Functional Anatomy and Evolution at Johns Hopkins School of Medicine; Peruvian fossil pinniped scans funded by CAPES 4240/08-1 (MEC/ Brazil), Centre of Ecology and Evolution/UCL Small Grant 2009/10 and DE-TAF-273 for access to DE-TAF under the SYNTHESYS Project; scan of Devinophoca† funded by the Slovak Research and Development Agency (grant number APVV-20-0079 to M.S.); scan of Puijila† funded by the Canadian Museum of Nature; scans of extant musteloids and pinnipeds were funded by a young researcher award from the Fondation des Treilles, a French-U.S. Fulbright Researcher program grant (both to C.G.) and a US NSF-DEB 1257572 grant and AMNH Frick Fund support (to J.J.F. and C.G.); travel expense to Poitiers were covered by a University grant to C.G. T.I.P was supported by a John Templeton Foundation Grant (JTF 62574; awarded to Emily J. Rayfield and Philip C. J. Donoghue; the opinions expressed in this article are those of the authors and do not necessarily reflect the views of the John Templeton Foundation) and a Leverhulme Trust Early Career Research Fellowship Grant (grant number: ECF-2025-468). T.P. was funded by an Australian Research Council DECRA Fellowship (DE220101296). A.R.E. was supported by the Australian Research Council (DP230100613).
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