Evidence map›Paper›PMID 30518326›Full record

ArticleBMC evolutionary biology2018

Alpha shapes: determining 3D shape complexity across morphologically diverse structures.

James D Gardiner, Julia Behnsen, Charlotte A Brassey

Abstract read
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Article in BMC evolutionary biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. New perspectives on head and neck allometry and ecomorphology in tetrapods.Biological reviews of the Cambridge Philosophical Society · 2026
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  9. Generative modeling of biological shapes and images using a probabilisticbioRxiv : the preprint server for biology · 2024
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

James D GardinerInstitute of Ageing and Chronic Disease, University of Liverpool, Liverpool, L7 8TX, UK.
Julia BehnsenManchester X-ray Imaging Facility, University of Manchester, Manchester, M13 9PL, UK.
Charlotte A BrasseySchool of Science and the Environment, Manchester Metropolitan University, Manchester, M1 5GD, UK. c.brassey@mmu.ac.uk.ORCID 0000-0002-6552-541X

Funding

Biotechnology and Biological Sciences Research Council BB/N010957/1
6 · The paper itself

Abstract

backgroundFollowing recent advances in bioimaging, high-resolution 3D models of biological structures are now generated rapidly and at low-cost. To use this data to address evolutionary and ecological questions, an array of tools has been developed to conduct shape analysis and quantify topographic complexity. Here we focus particularly on shape techniques applied to irregular-shaped objects lacking clear homologous landmarks, and propose a new 'alpha-shapes' method for quantifying 3D shape complexity.

methodsWe apply alpha-shapes to quantify shape complexity in the mammalian baculum as an example of a morphologically disparate structure. Micro- computed-tomography (μCT) scans of bacula were conducted. Bacula were binarised and converted into point clouds. Following application of a scaling factor to account for absolute size differences, a suite of alpha-shapes was fitted per specimen. An alpha shape is formed from a subcomplex of the Delaunay triangulation of a given set of points, and ranges in refinement from a very coarse mesh (approximating convex hulls) to a very fine fit. 'Optimal' alpha was defined as the refinement necessary in order for alpha-shape volume to equal CT voxel volume, and was taken as a metric of overall 'complexity'.

resultsOur results show that alpha-shapes can be used to quantify interspecific variation in shape 'complexity' within biological structures of disparate geometry. The 'stepped' nature of alpha curves is informative with regards to the contribution of specific morphological features to overall 'complexity'. Alpha-shapes agrees with other measures of complexity (dissection index, Dirichlet normal energy) in identifying ursid bacula as having low shape complexity. However, alpha-shapes estimates mustelid bacula as being most complex, contrasting with other shape metrics. 3D fractal dimension is identified as an inappropriate metric of complexity when applied to bacula.

conclusionsAlpha-shapes is used to calculate 'optimal' alpha refinement as a proxy for shape 'complexity' without identifying landmarks. The implementation of alpha-shapes is straightforward, and is automated to process large datasets quickly. We interpret alpha-shapes as being particularly sensitive to concavities in surface topology, potentially distinguishing it from other shape complexity metrics. Beyond genital shape, the alpha-shapes technique holds considerable promise for new applications across evolutionary, ecological and palaeoecological disciplines.

Indexed as

Imaging, Three-DimensionalAnimalsBiological EvolutionFractalsMalePenis

Identifiers

PMID30518326
PMCPMC6282314

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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.