Evidence map›Paper›PMID 38944324›Full record

ArticleActa biomaterialia2024

Flexural rigidity of hawkmoth antennae depends on the bending direction.

Adam Puchalski, Zoë McCarthy, Alexandre Varaschin Palaoro, Arthur A Salamatin, Agnes Nagy-Mehesz, Guzeliya Korneva, Charles E Beard, Jeffery Owens, Peter H Adler, Konstantin G Kornev

Abstract read
In one paragraph

Article in Acta biomaterialia, 2024. 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

10 authors.

Adam PuchalskiDepartment of Materials Science and Engineering, Clemson University, Clemson, SC 29634, USA.
Zoë McCarthyDepartment of Materials Science and Engineering, Clemson University, Clemson, SC 29634, USA.
Alexandre Varaschin PalaoroDepartment of Materials Science and Engineering, Clemson University, Clemson, SC 29634, USA.
Arthur A SalamatinDepartment of Materials Science and Engineering, Clemson University, Clemson, SC 29634, USA.
Agnes Nagy-MeheszDepartment of Bioengineering, Clemson University, Clemson, SC 29634, USA.
Guzeliya KornevaDepartment of Bioengineering, Clemson University, Clemson, SC 29634, USA.
Charles E BeardDepartment of Plant and Environmental Sciences, Clemson University, Clemson, SC 29634, USA.
Jeffery OwensAir Force Civil Engineer Center, Tyndall Air Force Base, Florida, USA.
Peter H AdlerDepartment of Plant and Environmental Sciences, Clemson University, Clemson, SC 29634, USA.
Konstantin G KornevDepartment of Materials Science and Engineering, Clemson University, Clemson, SC 29634, USA. Electronic address: kkornev@clemson.edu.

Funding

Transnational Research Imaging Core (TRI)P30GM131959 · NIGMS · CLEMSON UNIVERSITY · PI VYAVAHARE, NAREN R · 2019 to 2023
$5.9M
NIGMS NIH HHS P30 GM131959
6 · The paper itself

Abstract

To probe its environment, the flying insect controllably flexes, twists, and maneuvers its antennae by coupling mechanical deformations with the sensory output. We question how the materials properties of insect antennae could influence their performance. A comparative study was conducted on four hawkmoth species: Manduca sexta, Ceratomia catalpae, Manduca quinquemaculata, and Xylophanes tersa. The morphology of the antennae of three hawkmoths that hover while feeding and one putatively non-nectar-feeding hawkmoth (Ceratomia catalpa) do not fundamentally differ, and all the antennae are comb-like (i.e., pectinate), markedly in males but weakly in females. Applying different weights to the free end of extracted cantilevered antennae, we discovered anisotropy in flexural rigidity when the antenna is forced to bend dorsally versus ventrally. The flexural rigidity of male antennae was less than that of females. Compared with the hawkmoths that hover while feeding, Ceratomia catalpae has almost two orders of magnitude lower flexural rigidity. Tensile tests showed that the stiffness of male and female antennae is almost the same. Therefore, the differences in flexural rigidity are explained by the distinct shapes of the antennal pectination. Like bristles in a comb, the pectinations provide extra rigidity to the antenna. We discuss the biological implications of these discoveries in relation to the flight habits of hawkmoths. Flexural anisotropy of antennae is expected in other groups of insects, but the targeted outcome may differ. Our work offers promising new applications of shaped fibers as mechanical sensors. STATEMENT OF SIGNIFICANCE: Insect antennae are blood-filled, segmented fibers with muscles in the two basal segments. The long terminal segment is muscle-free but can be flexed. Our comparative analysis of mechanical properties of hawkmoth antennae revealed a new feature: antenna resistance to bending depends on the bending direction. Our discovery replaces the conventional textbook scenario considering hawkmoth antennae as rigid rods. We showed that the pectinate antennae of hawkmoths behave as a comb in which the bristles resist bending when they come together. This anisotropy of flexural resistance offers a new mode of environmental sensing that has never been explored. The principles we found apply to other insects with non-axisymmetric antennae. Our work offers new applications for shaped fibers that could be designed to sense the flows.

Indexed as

Arthropod AntennaeAnimalsBiomechanical PhenomenaFemaleMaleManducaMothsTensile StrengthBendingFlexural rigidityHawkmothsInsect antennaeLepidoptera

Identifiers

PMID38944324
PMCPMC11369912

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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.