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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population geneticists and genetical ecologists Recently, we have noticed an increasing number of published papers and unpublished manuscripts in which repeatability was miscalculated Our purpose is fivefold: (1) to outline the correct method of calculating repeatability; (2) to point out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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Post-hatching parental care masks the effects of egg size on offspring fitness: a removal experiment on burying beetles

TL;DR: A parental removal experiment on the burying beetle Nicrophorus vespilloides is reported in which it is found that the parent's presence or absence had a strong main effect on larval body mass, whereas there was no detectable effect of egg size.
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Age differences in blue tit Parus caeruleus plumage colour: within-individual changes or colour-biased survival?

TL;DR: The observed pattern of age dichromatism in blue tit Parus caeruleus UV/ blue structural crown coloration suggests that both male and female yearlings could benefit from being less ornamented and hence that sexual selection might be acting on both sexes simultaneously in this species.
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Survival costs of reproduction in the blue tit (Parus caeruleus): a role for blood parasites?

TL;DR: This work uses a path analytical approach to investigate whether a change in parasite resistance after manipulation of reproductive effort translates into altered survival in female blue tits, and shows a negative relationship between reproductive effort and parasite resistance, although evident only in first–year breeders.
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Skin carotenoid concentration correlates with male hunting skill and territory quality in the kestrel Falco tinnunculus

TL;DR: Investigation of the yellow-orange colouration of the tarsi of the kestrel Falcotinnunculus in relation to sex, diet and to different aspects of male reproductivebehaviour suggests that in the common kestREL carotenoid based colouration is important as an indicator of male quality.
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Effect of sexual dimorphism in bill length on foraging behavior: an experimental analysis of hummingbirds.

TL;DR: It is suggested that no single mechanism is responsible for the evolution of sexual dimorphism in bill lengths of hummingbirds, but rather that the dimorphisms probably reflects the combined effects of reproductive role division and intersexual food competition, and possibly, sexual 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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