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Interrogating Random and Systematic Measurement Error in Morphometric Data

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A Correction to this article was published on 06 March 2024

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Abstract

Measurement error is present in all quantitative studies, and ensuring proper biological inference requires that the effects of measurement error are fully scrutinized, understood, and to the extent possible, minimized. For morphometric data, measurement error is often evaluated from descriptive statistics that find ratios of subject or within-subject variance to total variance for a set of data comprising repeated measurements on the same research subjects. These descriptive statistics do not typically distinguish between random and systematic components of measurement error, even though the presence of the latter (even in small proportions) can have consequences for downstream biological inferences. Furthermore, merely sampling from subjects that are quite morphologically dissimilar can give the incorrect impression that measurement error (and its negative effects) are unimportant. We argue that a formal hypothesis-testing framework for measurement error in morphometric data is lacking. We propose a suite of new analytical methods and graphical tools that more fully interrogate measurement error, by disentangling its random and systematic components, and evaluating any group-specific systematic effects. Through the analysis of simulated and empirical data sets we demonstrate that our procedures properly parse components of measurement error, and characterize the extent to which they permeate variation in a sample of observations. We further confirm that traditional approaches with repeatability statistics are unable to discern these patterns, improperly assuaging potential concerns. We recommend that the approaches developed here become part of the current analytical paradigm in geometric morphometric studies. The new methods are made available in the RRPP and geomorph R-packages.

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Data Availability

All data from simulattion experiments can be generated with scripts in the Supplementary material. Data for the empirical example can be found at the Dryad Digital Repository: https://doi.org/10.5061/dryad.t9888.

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Notes

  1. If only one machine was the cause of inconsistency, it would be clear which machine it was, regardless of the exactness of any machine to produce the true configuration.

  2. Often the terms, “Procrustes residuals” and “Procrustes coordinates” are used almost interchangeably. Procrustes coordinates are the mean configuration after GPA, plus the Procrustes residuals, which are the deviations of configuration-specific coordinates from the mean. Either can be used in most analyses, producing the same results, as the mean shape would be constant for every research observation.

  3. Despite the imprecision of the automated digitizer compared to the researcher, the configurations it produces are accurate with respect to the researcher’s.

  4. There is not a strict need for replicate balance in the research design (see “Discussion”). However, issues like heterogeneity of variance among subjects might be more difficult to interpret with replicate imbalance.

  5. It is important to realize that the same strategy (within-subject RRPP) is used to obtain sampling distributions, whether Roy’s maximum root or \(SNR\) are used as test statistics. Alternative statistics could also be used. Generally, \(P\)-values and \(Z\)-scores will be similar in terms of interpretation but not perfectly rank-correlated unless they are linear transformations of each other, like \(SNR\) and \(F\). However, alternative sampling distribution strategies are not needed if different statistics are used.

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Acknowledgements

We thank P.D. Polly and an anonymous reviewer for helpful comments on an earlier version of this paper. We also thank the MorphMet listserv—and A. Cardini in particular—for a discussion of measurement error, which made clear to us that current recommendations regarding measurement error in morphometrics were inadequate, and required a rethink. The present paper takes the nascent ideas we expressed in that thread, and converts them into fully developed analytical methods. This work was sponsored in part by National Science Foundation Grants DBI-1902694 and DEB-2146220 (to MLC), and DBI-1902511 and DEB-2140720 (to DCA). All analyses in this paper were performed in R (R Core Team, 2023), using the packages, geomorph (Adams et al., 2023; Baken et al., 2021) and RRPP (Collyer & Adams, 2018, 2023). The functions measurement.error, plot.measurement.error, focusMEonSubjects, interSubVar and plot.interSubVar in RRPP, and gm.measurement.error in geomorph, contain all new analytical approaches described in this paper.

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Contributions

M.L.C and D.C.A wrote the main manuscript. M.L.C wrote computer scripts, and prepared figures and tables. Both authors reviewed the manuscript.

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Correspondence to Michael L. Collyer.

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The authors declare that they have no known conflicts of interest.

Additional information

The original online version of this article was revised: “In this article, a typo occurs in equation 9, \(\begin{aligned} SS_{replicate}= & {} trace({\textbf{S}}_{subject}) \nonumber \\= & {} trace\left( \left( \hat{{\textbf{Z}}}^T_{sr|s} - \hat{{\textbf{Z}}}_{s}\right) ^T \left( \hat{{\textbf{Z}}}^T_{sr|s} - \hat{{\textbf{Z}}}_{s}\right) \right) , \end{aligned}\), should have read as \(\begin{aligned} SS_{replicate}= & {} trace({\textbf{S}}_{replicate}) \nonumber \\= & {} trace\left( \left( \hat{{\textbf{Z}}}^T_{sr|s} - \hat{{\textbf{Z}}}_{s}\right) ^T \left( \hat{{\textbf{Z}}}^T_{sr|s} - \hat{{\textbf{Z}}}_{s}\right) \right) , \end{aligned}\)”.

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Supplementary file 1 (ZIP 6201 KB)

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Collyer, M.L., Adams, D.C. Interrogating Random and Systematic Measurement Error in Morphometric Data. Evol Biol 51, 179–207 (2024). https://doi.org/10.1007/s11692-024-09627-6

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  • DOI: https://doi.org/10.1007/s11692-024-09627-6

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