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Link to original content: http://pubmed.ncbi.nlm.nih.gov/37403037/
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Meta-Analysis
. 2023 Jul 5;23(1):30.
doi: 10.1186/s12862-023-02131-z.

Phylogenetic congruence, conflict and consilience between molecular and morphological data

Affiliations
Meta-Analysis

Phylogenetic congruence, conflict and consilience between molecular and morphological data

Joseph N Keating et al. BMC Ecol Evol. .

Abstract

Morphology and molecules are important data sources for estimating evolutionary relationships. Modern studies often utilise morphological and molecular partitions alongside each other in combined analyses. However, the effect of combining phenomic and genomic partitions is unclear. This is exacerbated by their size imbalance, and conflict over the efficacy of different inference methods when using morphological characters. To systematically address the effect of topological incongruence, size imbalance, and tree inference methods, we conduct a meta-analysis of 32 combined (molecular + morphology) datasets across metazoa. Our results reveal that morphological-molecular topological incongruence is pervasive: these data partitions yield very different trees, irrespective of which method is used for morphology inference. Analysis of the combined data often yields unique trees that are not sampled by either partition individually, even with the inclusion of relatively small quantities of morphological characters. Differences between morphology inference methods in terms of resolution and congruence largely relate to consensus methods. Furthermore, stepping stone Bayes factor analyses reveal that morphological and molecular partitions are not consistently combinable, i.e. data partitions are not always best explained under a single evolutionary process. In light of these results, we advise that the congruence between morphological and molecular data partitions needs to be considered in combined analyses. Nonetheless, our results reveal that, for most datasets, morphology and molecules can, and should, be combined in order to best estimate evolutionary history and reveal hidden support for novel relationships. Studies that analyse only phenomic or genomic data in isolation are unlikely to provide the full evolutionary picture.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Optimal morphological trees (i.e. most parsimonious trees and Bayesian maximum clade credibility trees) have similar congruence with the corresponding molecular trees (p = 0.167, ANOVA with repeated measures). Congruence is measured using the mean proportion of quartet statements that morphological trees share with molecular-only maximum clade credibility tree. The 32 points represent mean proportional congruence between the morphological and molecular trees for each inference method, per dataset
Fig. 2
Fig. 2
Treespace visualization of 32 empirical datasets using the quartet distance metric. Visualizations show Bayesian molecular-only posterior trees (blue crosses); Bayesian combined morphology and molecular posterior trees (open orange squares); Bayesian morphology only posterior trees (pink crosses); equal weighting most parsimonious trees (red triangles) and implied weighting most parsimonious trees (dark red circles). Trees sampled using various morphological methods tend to cluster together; molecular and combined trees tend to be more similar than molecular and morphology trees, but combined trees seldom completely overlap with molecular-only trees; combined analyses thus sample unique areas of treespace. (A1) Tetraodontiformes; (A2) Ostariophysi; (A3) Mollusca; (A4) Mammalia; (A5) Lemuriformes; (A6) Sphenisciformes; (B1) Hemiptera; (B2) Hymenoptera; (B3) Osteoglossiformes; (B4) Mysticeti; (B5) Arthropoda; (B6) Squamata; (C1) Serpentes; (C2) Palpimanoidea; (C3) Formicidae; (C4) Opiliones; (C5) Cetacea; (C6) Malacostraca; (D1) Rhynchonellida; (D2) Fabriciidae; (D3) Stygnopsidae; (D4) Chiroptera; (D5) Hydrophilidae; (D6) Tribelocephalinae; (E1) Apinae; (E2) Biblidinae; (E3) Caviidae; (E4) Abrotrichini; (E5) Hexactinellida; (E6) Hydroptilidae; (F1) Nephilidae; (F2) Actinopterygii. Silhouettes for C4, D3 and E6 were created by Gareth Monger, Jennifer Trimble and JCGiron respectively and are reproduced here under the CC BY 3.0 licence
Fig. 3
Fig. 3
Relationship between the proportion of morphological characters in the combined dataset and the distance between combined- and molecular-only trees. (A) Robinson-Foulds distance between the combined 50% majority rule consensus tree and the corresponding molecular-only 50% majority rule consensus tree against proportion of morphological characters; (B) quartet distance between the combined 50% majority rule consensus tree and the corresponding molecular-only 50% majority rule consensus tree against proportion of morphological characters

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