Evidence map›Paper›PMID 40478798›Full record

ArticlePloS one2025

Lateralized cerebellar connectivity differentiates auditory pathways in echolocating and non-echolocating whales.

Sophie Flem, Gregory Berns, Ben Inglis, Dillon Niederhut, Eric Montie, Terrence Deacon, Karla L Miller, Peter Tyack, Peter F Cook

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

4 citing papers in PubMed.

  1. Cortico-striatal network architecture shapes rhythmic biases in music.Cerebral cortex (New York, N.Y. : 1991) · 2026
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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

9 authors.

Sophie FlemPsychology Department, Division of Social Sciences, New College of Florida, Sarasota, Florida, United States of America.ORCID https://orcid.org/0009-0001-9605-1202
Gregory BernsDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Ben InglisHenry H. Wheeler Jr. Brain Imaging Center, University of California, Berkeley, Berkeley, California, United States of America.
Dillon NiederhutHenry H. Wheeler Jr. Brain Imaging Center, University of California, Berkeley, Berkeley, California, United States of America.ORCID https://orcid.org/0000-0002-9995-4378
Eric MontieDepartment of Natural Sciences, University of South Carolina Beaufort, Bluffton, South Carolina, United States of America.
Terrence DeaconAnthropology Department, University of California, Berkeley, Berkeley, California, United States of America.
Karla L MillerWellcome Centre for Integrative Neuroimaging, FMRIB, Nuffield Department of Clinical Neurosciences, University of Oxford, Headington, Oxford, United Kingdom.
Peter TyackBiology Department, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts, United States of America.
Peter F CookPsychology Department, Division of Social Sciences, New College of Florida, Sarasota, Florida, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the first application of diffusion tractography to a mysticete, which was analyzed alongside three odontocete brains, allowing the first direct comparison of strength and laterality of auditory pathways in echolocating and non-echolocating whales. Brains were imaged post-mortem at high resolution with a specialized steady state free precession diffusion sequence optimized for dead tissue. We conducted probabilistic tractography to compare the qualitative features, tract strength, and lateralization of potential ascending and descending auditory paths in the mysticete versus odontocetes. Tracts were seeded in the inferior colliculi (IC), a nexus for ascending auditory information, and the cerebellum, a center for sensorimotor integration. Direct IC to temporal lobe pathways were found in all animals, replicating previous cetacean tractography and suggesting conservation of the primary auditory projection path in the cetacean clade. Additionally, odontocete IC-cerebellum pathways exhibited higher overall tract strength than in the mysticete, suggesting they may play a role in supporting the rapid sensorimotor integration demands of echolocation. Further, in the mysticete, contralateral right IC to left cerebellum pathways were 17x stronger than those between left IC and right cerebellum, while in odontocetes, the laterality was reversed, and left IC to right cerebellum pathways were 2-4x stronger than those between right IC and left cerebellum. This lateralization may also relate to echolocation. Right cerebellum is responsible for integrating sensory and motor signals from the left cortical hemisphere, and in odontocetes, this hemisphere likely controls the contralateral right-side phonic lips, which have been empirically implicated in the production of echolocation clicks. We also found differences in the specific subregions of cerebellum targeted by the IC between the mysticete and odontocetes, some of which may also bear on hearing and vocal production. This study establishes foundational knowledge on mysticete brain connectivity and extends knowledge on pathways supporting hearing and auditory-motor integration across the order Cetacea.

Indexed as

Auditory PathwaysCerebellumEcholocationFunctional LateralityWhalesAnimalsDiffusion Tensor ImagingInferior Colliculi

Identifiers

PMID40478798
PMCPMC12143552

What OpenQuestion holds

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Registered trials

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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.