Evidence map›Paper›PMID 40360456›Full record

ArticleJournal of morphology2025

Intraspecific Sensory Diversity and the Decapod Claw: Patterns of Sensillation Are Heterochelic and Sexually Dimorphic In Pagurus bernhardus.

Ari Drummond, Tianna Holloway, Summer Nash, Alexander D M Wilson, Lucy M Turner, Mark Briffa, David T Bilton

Abstract read
In one paragraph

Article in Journal of morphology, 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

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

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.

Ari DrummondSchool of Marine and Biological Sciences, University of Plymouth, Plymouth, Devon, UK.ORCID 0009-0004-8403-6840
Tianna HollowaySchool of Marine and Biological Sciences, University of Plymouth, Plymouth, Devon, UK.
Summer NashSchool of Marine and Biological Sciences, University of Plymouth, Plymouth, Devon, UK.ORCID 0009-0004-0362-1686
Alexander D M WilsonSchool of Marine and Biological Sciences, University of Plymouth, Plymouth, Devon, UK.ORCID 0000-0002-7696-1671
Lucy M TurnerSchool of Marine and Biological Sciences, University of Plymouth, Plymouth, Devon, UK.ORCID 0000-0002-9052-9498
Mark BriffaSchool of Marine and Biological Sciences, University of Plymouth, Plymouth, Devon, UK.ORCID 0000-0003-2520-0538
David T BiltonSchool of Marine and Biological Sciences, University of Plymouth, Plymouth, Devon, UK.ORCID 0000-0003-1136-0848

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Information detection affects physiological performance and behaviour and is vital to survival and fitness. Despite the recognised importance of sensory adaptations in information acquisition and manipulation, many forms of sensory variation-from within individuals to between species-remain underexplored. To better understand the role of information in evolution, it is important to examine sensory variation as part of a cohesive framework of sensory diversity. Using the decapod claw, a structure well-recognised for its morphological variation, we investigated sensory diversity at the intraspecific level by assessing heterochely and sexual dimorphism in the chelar morphologies of Pagurus bernhardus hermit crabs. We employed a novel methodology using scanning electron microscopy (SEM) to assess moulted chelar tissue from both the major and minor claws. The shape, size, and sensillation (i.e., the distribution and abundance of sensilla) of both chelipeds were examined by geometric morphometric landmark analysis (GMLA), generalised Procrustes analysis (GPA), and linear mixed effects models. Hermit crabs exhibited heterochely and sexual dimorphism in both gross and sensory chelar morphologies. Sexual dimorphism was greater in the sensory morphology of the major claw, suggesting sex-based sensory specialisations, likely due to differences in mating roles and behaviours. In contrast, the minor claw's sensory morphology lacked sexual dimorphism, suggesting the sensory role of this appendage is equally important for both sexes. Our results highlight sensory variation as a fundamental aspect of functional morphology and emphasise the need to consider sexual dimorphism and body asymmetry in information acquisition. These findings contribute to a broader framework for studying sensory diversity, underscoring the importance of integrating sensory morphology, function, and ecology to fully understand the evolutionary implications of sensory specialisations.

Indexed as

AnomuraSensillaSex CharacteristicsAnimalsFemaleMaleMicroscopy, Electron, Scanningchelacrustaceahermit crabscanning electron microscopy (SEM)sensillasensory morphologysexual dimorphism

Identifiers

PMID40360456
PMCPMC12075039

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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.