1948
DOI: 10.3382/ps.0270375
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The Heritability of Resistance to Death in the Fowl

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Cited by 112 publications
(44 citation statements)
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“…Analysis of all-or-none traits has been examined by Wright (1933Wright ( , 1934, Lush et al (1948), Robertson and Lerner (1949), and Dempster and Lerner (1950), who assumed an underlying continuity with a threshold imposing discontinuity upon the phenotypic expression of the trait. Heritability is calculated from the percentage data (h) either by analysis of variance for binomial datathe procedure adopted here- (Lush et al, 1948), in which case h is r times the intraclass correlation coefficient, or from a 2 x .A chi-square analysis (Robertson and Lerner, 1949), in which case h is a function of the heterogeneity chi-squared in the 2 x X table.…”
Section: Methods (I) Ecological Comparison Of Collection Sitesmentioning
confidence: 99%
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“…Analysis of all-or-none traits has been examined by Wright (1933Wright ( , 1934, Lush et al (1948), Robertson and Lerner (1949), and Dempster and Lerner (1950), who assumed an underlying continuity with a threshold imposing discontinuity upon the phenotypic expression of the trait. Heritability is calculated from the percentage data (h) either by analysis of variance for binomial datathe procedure adopted here- (Lush et al, 1948), in which case h is r times the intraclass correlation coefficient, or from a 2 x .A chi-square analysis (Robertson and Lerner, 1949), in which case h is a function of the heterogeneity chi-squared in the 2 x X table.…”
Section: Methods (I) Ecological Comparison Of Collection Sitesmentioning
confidence: 99%
“…Analysis of all-or-none traits has been examined by Wright (1933Wright ( , 1934, Lush et al (1948), Robertson and Lerner (1949), and Dempster and Lerner (1950), who assumed an underlying continuity with a threshold imposing discontinuity upon the phenotypic expression of the trait. Heritability is calculated from the percentage data (h) either by analysis of variance for binomial datathe procedure adopted here- (Lush et al, 1948), in which case h is r times the intraclass correlation coefficient, or from a 2 x .A chi-square analysis (Robertson and Lerner, 1949), in which case h is a function of the heterogeneity chi-squared in the 2 x X table. However, because on a percentage scale variances differ according to the mean, probit transformation is advised as it makes the genetic variance independent of the threshold value in the population: The genetic variance on the underlying scale = where is the mean incidence in the population, and is the height of the ordinate of the standard normal curve corresponding to the abscissa value which cuts off a tail of area i. Heritability on the probit scale is = o/(1 + o), which may be compared to additive heritability on the percentage scale by the relationship ha = (2 .…”
Section: Methods (I) Ecological Comparison Of Collection Sitesmentioning
confidence: 99%
“…data. Lush et aL (1948) and Robertson and Lerner (1949) proposed an analysis of variance technique for the analysis of such data. Estimates of heritability obtained in this way can be converted onto a t Present address: Northern Pig Development Company, Manor House, Beeford,Driffield,North Humberside.…”
Section: Introductionmentioning
confidence: 99%
“…The hypothesis of a continuous, normal underlying genetic distribution (threshold character: Lush et al 1948;Robertson and Lerner 1949) does not apply directly to the genetic mechanisms underlying general viability where each cause of death can be considered a separate trait. The analysis here assumes that viability is under partial genetic control (genetic tolerance or susceptibility) and further that concepts such as genetic additivity and non-additivity do apply, but cannot be interpreted in the normal sense as for a trait such as body weight.…”
Section: Viabilitymentioning
confidence: 99%