Evidence map›Paper›PMID 40877013›Full record

ArticleJournal of fish biology2025

Structural and developmental insights into the muscles involved in lionfish (Pterois spp.) vocalisations.

Roxanne B Holmes, Nadia M Hamilton, Katharine E Criswell, Keturah Z Smithson, James E Herbert-Read, Lucille Chapuis

Erratum issuedAbstract read
In one paragraph

Article in Journal of fish biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Roxanne B HolmesDepartment of Zoology, University of Cambridge, Cambridge, UK.ORCID https://orcid.org/0000-0001-5561-0621
Nadia M HamiltonDepartment of Zoology, University of Cambridge, Cambridge, UK.
Katharine E CriswellDepartment of Biology, Saint Francis University, Loretto, Pennsylvania, USA.
Keturah Z SmithsonDepartment of Zoology, University of Cambridge, Cambridge, UK.
James E Herbert-ReadDepartment of Zoology, University of Cambridge, Cambridge, UK.ORCID https://orcid.org/0000-0003-0243-4518
Lucille ChapuisDepartment of Biological Sciences, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0003-3001-983X

Funding

This work was supported by the Whitten Programme in Aquatic Biology, The Cambridge SBS Fieldwork Fund and the Darwin College Travel Fund awarded to R.B.H, J.H-R was supported by the Whitten Programme in Aquatic Biology and L.C was funded by the European Union Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie agreement 897218Whitten Programme in Aquatic Biology
6 · The paper itself

Abstract

Vocal signalling is an important mode of communication in fishes. The two species of lionfish in the Pterois complex, the Indo-Pacific lionfish (Pterois volitans) and the red lionfish (Pterois miles), are both known to produce different types of sounds with sonic muscles attached to the swimbladder. However, the specific mechanism and the functions of these vocalisations in these invasive species are still unknown. We used three-dimensional bioimaging to describe the anatomy of the sonic muscles of both species. We further quantified the muscles of P. volitans to specifically explore how muscles developed across ontogeny and to test the hypothesis that sonic muscles would show sexual dimorphism if they were a sexually selected trait. Both P. volitans and P. miles showed a physoclistous swimbladder with a bilaterally symmetric pair of extrinsic sonic swimbladder muscles (ESSMs), which have been suggested to control buoyancy and generate vocalisations. Both species also displayed an additional pair of anterior extrinsic muscles, which projected dorsoventrally from the spinal column and inserted onto the anterior wall of the swimbladder, potentially also having a role in sound production. Both types of sonic muscles were present across ontogeny. Quantification of the posterior belly of the ESSMs in P. volitans showed that both the length and mass of these muscles in both mature and immature individuals increased linearly with body size. There were no ontogenetic or sex differences in sonic muscle investment between individuals. Given the primary function of these muscles is to control the swimbladder for buoyancy, this may constrain the modification of these muscles relative to body size, or they may have no differences in their acoustic function between sexes or across ontogeny.

Indexed as

Air SacsMusclesPerciformesVocalization, AnimalAnimalsFemaleMaleSex Characteristicsdissectioninvasive speciesmicro‐CT scanningvocalisation

Identifiers

PMID40877013
PMCPMC12861829

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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.