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Journal ArticleDOI

Unrepeatable repeatabilities: a common mistake

C. M. Lessells, +1 more
- 01 Jan 1987 - 
- Vol. 104, Iss: 1, pp 116-121
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TLDR
The correct calculation of repeatability is outlined, a common mistake is pointed out, how the incorrectly calculated value relates to repeatable values is shown, and a method for checking published values and calculating approximate repeatability values from the F ratio is provided.
Abstract
-Repeatability is a useful tool for the population geneticist or genetical ecologist, but several papers have carried errors in its calculation We outline the correct calculation of repeatability, point out the common mistake, show how the incorrectly calculated value relates to repeatability, and provide a method for checking published values and calculating approximate repeatability values from the F ratio (mean squares among groups/ mean squares within groups) Received 6 February 1986, accepted 25 August 1986 REPEATABILITY is a measure used in quantitative genetics to describe the proportion of variance in a character that occurs among rather than within individuals Repeatability, r, is given by: r = (VG + VEg)/ VP, (1) where VG is the genotypic variance, VEg the general environmental variance, and Vp the phenotypic variance (Falconer 1960, 1981) In addition to its use in assessing the reliability of multiple measurements on the same individual, repeatability may be used to set an upper limit to the value of heritability (Falconer 1960, 1981) and to separate, for instance, the effects of "self" and "mate" on a character such as clutch size (van Noordwijk et al 1980) Repeatability is therefore a useful statistic for population geneticists and genetical ecologists Recently, we have noticed an increasing number of published papers and unpublished manuscripts in which repeatability was miscalculated Our purpose is fivefold: (1) to outline the correct method of calculating repeatability; (2) to point out a common mistake in calculating repeatability; (3) to show how much this mistake affects values of repeatability; (4) to provide a quick way of checking published estimates, and to calculate an approximate value of repeatability from published F ratios and degrees of freedom; and (5) to make recommendations for authors, referees, editors, and readers to prevent the promulgation and propagation of incorrect repeatability values in the literature CALCULATION OF REPEATABILITY Repeatability is the intraclass correlation coefficient (Sokal and Rohlf 1981), which is based on variance components derived from a one-way analysis of variance (ANOVA) The intraclass correlation coefficient is given by some statistical packages; otherwise it can be calculated from an ANOVA ANOVA is described in most statistics textbooks (eg Sokal and Rohlf 1981; Kirk 1968 gives a detailed treatment of more complex designs of ANOVA), so we will not repeat it here, but give the general form of the results from such an analysis in Table 1 Repeatability, r, is given by r = sA / (S + SA)' (2) where S2A is the among-groups variance component and s2 is the within-group variance component These variance components are calculated from the mean squares in the analysis of variance as:

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Citations
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Sexual Dimorphism in Melanin Pigmentation, Feather Coloration and Its Heritability in the Barn Swallow (Hirundo rustica)

TL;DR: Results show that pigmentation strategies vary in a complex manner according to sex and plumage region, and also among geographical populations, potentially reflecting adaptation to different natural and sexual selection regimes, and that some coloration components seem to be highly heritable.

Notes and Comments Birdsong Performance and the Evolution of Simple (Rather than Elaborate) Sexual Signals

TL;DR: In this paper, a comparative study across wood warbler (family Parulidae) showed that the elaboration of signals such as birdsong is not related to the strength of sexual selection across species.
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Male size determines reproductive output in a paternal mouthbrooding fish

TL;DR: The study reveals the benefits of mutual mate choice on size in this species: larger females provide larger eggs and larger males can brood heavier clutches, and suggests that females differentially allocate resources into the eggs according to the size of the mate.
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Song, sexual selection, and a song control nucleus (HVc) in the brains of European sedge warblers.

TL;DR: This study finds significant positive correlations between three song attributes (repertoire size, song complexity, and song length) and the size of HVc, a telencephalic nucleus that is essential for song learning and production, but finds no direct evidence that males who paired successfully had a larger HVC than unpaired males.
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Fecal glucocorticoid metabolites in wild yellow-bellied marmots: experimental validation, individual differences and ecological correlates.

TL;DR: This study performs biological and physiological validations of a minimally-invasive technique for assessing fecal corticosterone metabolites in captive and wild groups of yellow-bellied marmots and finds repeatable inter-individual differences in FCMs, suggesting this hormonal trait might be a meaningful target of selection.
References
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Book

Introduction to quantitative genetics

TL;DR: The genetic constitution of a population: Hardy-Weinberg equilibrium and changes in gene frequency: migration mutation, changes of variance, and heritability are studied.
Book

Experimental Design: Procedures for the Behavioral Sciences

Roger E. Kirk
TL;DR: This chapter discusses research strategies and the Control of Nuisance Variables, as well as randomly Randomized Factorial Design with Three or More Treatments and Randomized Block Factorial design, and Confounded Factorial Designs: Designs with Group-Interaction Confounding.
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