Evidence map›Paper›PMID 38970781›Full record

ArticleSystematic biology2025

Exploring Phylogenetic Signal in Multivariate Phenotypes by Maximizing Blomberg's K.

Philipp Mitteroecker, Michael L Collyer, Dean C Adams

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Article in Systematic biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Philipp MitteroeckerDepartment of Evolutionary Biology, University of Vienna, Djerassiplatz 1, 1030 Vienna, Austria.ORCID 0000-0002-5308-3837
Michael L CollyerDepartment of Science, Chatham University, 107 Woodland Road, Pittsburgh, PA 15232, USA.ORCID 0000-0003-0238-2201
Dean C AdamsDepartment of Ecology, Evolution, and Organismal Biology, Iowa State University, 2200 Osborne Dr, Ames, IA 50011, USA.ORCID 0000-0001-9172-7894

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to the hierarchical structure of the tree of life, closely related species often resemble each other more than distantly related species; a pattern termed phylogenetic signal. Numerous univariate statistics have been proposed as measures of phylogenetic signal for single phenotypic traits, but the study of phylogenetic signal for multivariate data, as is common in modern biology, remains challenging. Here, we introduce a new method to explore phylogenetic signal in multivariate phenotypes. Our approach decomposes the data into linear combinations with maximal (or minimal) phylogenetic signal, as measured by Blomberg's K. The loading vectors of these phylogenetic components or K-components can be biologically interpreted, and scatterplots of the scores can be used as a low-dimensional ordination of the data that maximally (or minimally) preserves phylogenetic signal. We present algebraic and statistical properties, along with 2 new summary statistics, KA and KG, of phylogenetic signal in multivariate data. Simulation studies showed that KA and KG have higher statistical power than the previously suggested statistic Km⁢u⁢l⁢t, especially if phylogenetic signal is low or concentrated in a few trait dimensions. In 2 empirical applications to vertebrate cranial shape (crocodyliforms and papionins), we found statistically significant phylogenetic signal concentrated in a few trait dimensions. The finding that phylogenetic signal can be highly variable across the dimensions of multivariate phenotypes has important implications for current maximum likelihood approaches to phylogenetic signal in multivariate data.

Indexed as

ClassificationModels, BiologicalPhenotypePhylogenyAnimalsComputer SimulationMultivariate AnalysisSkullCranial shapemultivariate evolutionphylogenetic generalized least squaresphylogenyrelative eigenanalysis

Identifiers

PMID38970781
PMCPMC11958371

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