Estimates of genetic parameters for growth and skeletal measurements in Thai swamp buffalo

2000 ◽  
Vol 70 (3) ◽  
pp. 399-406
Author(s):  
K. Meyer ◽  
H. -U. Graser ◽  
A. Na-Chiangmai

AbstractEstimates of genetic parameters were obtained for weight, hip height, heart girth and shoulder to pin length measurements on Thai swamp buffalo, recorded at birth and weaning. Direct heritability estimates were 0·26 for weights at both ages and were low for skeletal measurements, ranging from 0·11 to 0·19. Low values could, in part at least, be caused by inaccuracies in recording. All traits were subject to maternal effects, permanent environmental maternal effects on traits recorded at weaning explaining proportionately up to 0·14 of the total variation. Estimates of genetic (direct and maternal) and permanent environmental correlations between traits recorded at the same time were high throughout, ranging from 0·83 to 0·97 for additive genetic effects and being close to unity otherwise. Except for heart girth measured at weaning, there appeared to be comparatively little genetic association between traits recorded at different times, direct additive correlation estimates ranging from 0·18 to 0·55 in contrast to estimates of 0·38 to 0·65 for correlations with heart girth at weaning.

1998 ◽  
Vol 66 (2) ◽  
pp. 349-355 ◽  
Author(s):  
M. Diop ◽  
L. D. Van Vleck

AbstractEstimates of (co)variance components and genetic parameters were obtained for birth (no. = 3909), weaning (no. = 3425), yearling (no. = 2763), and final weight (no. = 2142) for Gobra cattle at the Centre de Recherches Zootechniques de Dahra (Senegal), using single trait animal models. Data were analysed by restricted maximum likelihood. Four different animal models were fitted for each trait. Model 1 considered the animal as the only random effect. Model 2 included in addition to the additive direct effect of the animal, the environmental effect due to the dam. Model 3 added the maternal additive genetic effects and allowed a covariance between the direct and maternal genetic effects. Model 4 fitted both maternal genetic and permanent environmental effects. Inclusion of both types of maternal effects (genetic and environmental) provided a better fit for birth and weaning weights than models with one maternal effect only. For yearling and final weights, the improvement was not significant. Important maternal effects werefound for all traits. Estimates of direct heritabilities were substantially higher when maternal effects were ignored. Estimates of direct and maternal heritabilities with model 4 were 0·07 (s.e. 0·03) and 0·04 (s.e. 0·02), 0·20 (s.e. 0·05) and 0·21 (s.e. 0.05), 0·24 (s.e. 0·07) and 0·21 (s.e. 0·06), and 0·14 (s.e. 0·06) and 0.16 (s.e. 0·06) for birth, weaning, yearling and final weights, respectively. Correlations between direct and maternal genetic effects were negative for all traits, and large for weaning and yearling weights with estimates of -0·61 (s.e. 0·33) and -0·50 (s.e. 0·31), respectively. There was a significant positive linear phenotypic trend for weaning and yearling weights. Linear trends for additive direct and maternal breeding values were not significant for any trait except maternal breeding value for yearling weight.


2014 ◽  
Vol 59 (No. 7) ◽  
pp. 302-309 ◽  
Author(s):  
L. Vostrý ◽  
Z. Veselá ◽  
A. Svitáková ◽  
H. Vostrá Vydrová

The most appropriate model for genetic parameters estimation for calving ease and birth weight in beef cattle was selected. A total of 27 402 field records were available from the Czech Charolais breed. For estimation of genetic parameters for calving ease and body weight, three bivariate models were tested: a linear-linear animal model (L-LM) with calving ease classified into four categories (1 – easy; 2–4 – most difficult), a linear-linear animal model (SC-LM) in which calving ease scores were transformed into Snell scores (Snell 1964) and expressed as percentage of assisted calving (ranging 0–100%), and a bivariate threshold-linear animal model (T-LM) with calving ease classified into four categories (1 – easy, 2–4 – most difficult). All tested models included fixed effects for contemporary group (herd × year × season), age of dam, sex and breed of a calf. Random effects included direct and maternal genetic effects, maternal permanent environmental effect, and residual error. Direct heritability estimates for calving ease and birth weight were, with the use of L-LM, SC-LM, and T-LM, from 0.096 ± 0.013 to 0.226 ± 0.024 and from 0.210 ± 0.024 to 0.225 ± 0.026, respectively. Maternal heritability estimates for calving ease and birth weight were, with the use of L-LM, SC-LM, and T-LM, from 0.060 ± 0.031 to 0.104 ± 0.125 and from 0.074 ± 0.041 to 0.075 ± 0.040, respectively. Genetic correlations of direct calving ease with direct birth weight ranged from 0.46 ± 0.06 to 0.50 ± 0.06 for all tested models; whereas maternal genetic correlations between these two traits ranged from 0.24 ± 0.17 to 0.25 ± 0.53. Correlations between direct and maternal genetic effects within-trait were negative and substantial for all tested models (ranging from –0.574 ± 0.125 to –0.680 ± 0.141 for calving ease and from –0.553 ± 0.122 to –0.558 ± 0.118 for birth weight, respectively), illustrating the importance of including this parameter in calving ease evaluations. Results indicate that any of the tested models could be used to reliably estimate genetic parameters for calving ease for beef cattle in the Czech Republic. However, because of advantages in computation time and practical considerations, genetic analysis using SC-LM (transformed data) is recommended.


1986 ◽  
Vol 28 (2) ◽  
pp. 306-312 ◽  
Author(s):  
L. R. McKay ◽  
P. E. Ihssen ◽  
G. W. Friars

The relative magnitude of additive genetic effects, nonadditive genetic effects, maternal effects, and common environmental effects was determined for size, growth, and condition factor in rainbow trout of various ages, from the egg to the yearling stage, using a factorial mating system. Heritability estimates for length and weight ranged from 0.09 to 0.32, except for dried egg weight, where no additive genetic variation was detected. Condition factors were more heritable than size, with heritability estimates ranging from 0.24 to 0.46. Maternal effects were only important for dried egg weight and early fry size, and decreased rapidly with age as heritability increased. Egg weight, fry size, and fry condition factors were influenced by common environmental effects and (or) nonadditive genetic effects, but confounding of these sources of variation prevented exact estimation of their relative magnitude. Nonadditive genetic effects were completely absent for yearling size but were present for yearling condition factors. Individual or between-family selection on size should produce some response unless selection is done on very young fry or families are housed separately. For very young fry or where families are not replicated across tanks, within-family selection will be necessary to identify genetically superior fish, because of strong maternal or common environmental effects. Genetic correlations between size or condition factors measured at different ages were all positive, so selection at one stage should improve size or condition factor at another.Key words: rainbow trout, growth, heritability, maternal effects, genetics.


1981 ◽  
Vol 30 (1) ◽  
pp. 51-57 ◽  
Author(s):  
C. C. Morton ◽  
R. M. Cantor ◽  
L. A. Corey ◽  
W. E. Nance

Taste threshold for phenylthiocarbamide (PTC) was measured in 393 offspring from the families of 85 monozygotic (MZ) twin pairs. PTC scores were bimodally distributed with modes at one and eight and the antimode at five. Because of the non-normality of the distribution, a jackknife procedure was used to obtain 95% confidence intervals for the estimates of genetic, maternal, and environmental parameters. Analyses which assumed no epistasis and which included additive genetic effects revealed that 37.9% of the observed variation in PTC threshold was due to additive genetic effects, 16.6% was due to dominance effects, 14.2% was due to maternal effects, 13.7% was due to a common sibship environment, and 17.6% was due to random environmental effects, yielding a broad sense heritability of 0.55 for the threshold ability to taste PTC. Analyses which did not include additive genetic effects revealed 26.6% of the observed variance was due to dominance effects, 23.6% to maternal effects, and 49.8% to environmental effects at the 0.67 confidence levels, but that environmental factors accounted for 72.4% and dominance effects for 23.6% of the observed variation at the 95% level.


2013 ◽  
Vol 56 (1) ◽  
pp. 276-284 ◽  
Author(s):  
M. Madad ◽  
N. Ghavi Hossein-Zadeh ◽  
A. A. Shadparvar ◽  
D. Kianzad

Abstract. The objective of this study was to estimate genetic parameters for milk yield and milk percentages of fat and protein in Iranian buffaloes. A total of 9,278 test-day production records obtained from 1,501 first lactation buffaloes on 414 herds in Iran between 1993 and 2009 were used for the analysis. Genetic parameters for productive traits were estimated using random regression test-day models. Regression curves were modeled using Legendre polynomials (LPs). Heritability estimates were low to moderate for milk production traits and ranged from 0.09 to 0.33 for milk yield, 0.01 to 0.27 for milk protein percentage and 0.03 to 0.24 for milk fat percentage, respectively. Genetic correlations ranged from −0.24 to 1 for milk yield between different days in milk over the lactation. Genetic correlations of milk yield at different days in milk were often higher than permanent environmental correlations. Genetic correlations for milk protein percentage ranged from −0.89 to 1 between different days in milk. Also, genetic correlations for milk percentage of fat ranged from −0.60 to 1 between different days in milk. The highest estimates of genetic and permanent environmental correlations for milk traits were observed at adjacent test-days. Ignoring heritability estimates for milk yield and milk protein percentage in the first and final days of lactation, these estimates were higher in the 120 days of lactation. Test-day milk yield heritability estimates were moderate in the course of the lactation, suggesting that this trait could be applied as selection criteria in Iranian milking buffaloes.


2013 ◽  
Vol 43 (12) ◽  
pp. 2215-2220 ◽  
Author(s):  
Priscilla Regina Tamioso ◽  
Jaime Luiz Alberti Filho ◽  
Laila Talarico Dias ◽  
Rodrigo de Almeida Teixeira

The study aimed to estimate the components of (co)variance and heritability for weights at birth (BW), weaning (WW) and 180 days of age (W180), as well as the average daily gains from birth to weaning (ADG1), birth to 180 days of age (ADG2) and weaning to 180 days of age (ADG3) in Suffolk sheep. Thus, three different single-trait animal models were fitted, considering the direct additive genetic effect (Model 1), the direct additive genetic and maternal permanent environmental effects (Model 2), and in Model 3, in addition to those in Model 2, the maternal additive genetic effect was included. After comparing models through the likelihood ratio test (LRT), model 3 was chosen as the most appropriate to estimate heritability for BW, WW and ADG1. Model 2 was considered as the best to estimate the coefficient of heritability for W180 and ADG2, and model 1 for ADG3. Direct heritability estimates were inflated when maternal effects were ignored. According to the most suitable models, the heritability estimates for BW, WW, W180, ADG1, ADG2 and ADG3 were 0.06, 0.08, 0.09, 0.07, 0.08 and 0.07, respectively, indicating low possibility of genetic gain through individual selection. The results show the importance of including maternal effects in the models to properly estimate genetic parameters even at post-weaning ages.


1999 ◽  
Vol 79 (4) ◽  
pp. 433-439 ◽  
Author(s):  
J. J. Tosh ◽  
R. A. Kemp ◽  
D. R. Ward

Variance components were estimated for weight at birth, weaning, and 365 d of age, and yearling ultrasonic backfat thickness in a multibreed population of beef cattle. Data (n = 5880) were available on F1 animals and various crosses leading up to, and including, a composite breed (7/16 British, 1/4 Charolais, 1/4 Simmental, and 1/16 Limousin). Single- and two-trait analyses were conducted using an animal model and derivative-free REML procedures. Covariates representing fractional contributions of each of the four purebred groups and average heterotic effects, both direct and maternal, accounted for breed composition. Direct and maternal genetic, maternal permanent environmental, and residual effects were the random variables. Only minor differences existed between parameter estimates obtained from the various analyses. Mean direct heritabilities were 0.51, 0.33, 0.48, and 0.37 for weight at birth, weaning, and 365-d, and backfat, respectively, which, though well within the range of published estimates, seemed higher than average, indicating diversity in the founding purebreds. Mean maternal heritabilites were 0.09, 0.13, and 0.08 for the three consecutive weights. A likelihood ratio test showed maternal heritability and(or) the direct-maternal correlation was important (P < 0.001) for 365-d weight. Averaged across weights, the direct-maternal correlation was 0.07, lacking evidence of genetic antagonism. No age of dam or random maternal effects on backfat were apparent. Phenotypic correlations between weight at birth and weaning and weight at weaning and 365-d were 0.46 and 0.76, respectively. Though moderate between birth and weaning weight, maternal genetic and permanent environmental correlations between weaning and 365-d weight approached unity, demonstrating maternal carryover effects. Phenotypic and genetic correlations of 0.19 and –0.13, respectively, implied a limited association between 365-d weight and backfat, which possibly would have been stronger had fat been measured later in life. Estimates of variance components suitable for general use can be obtained from data from multibreed animals by considering breed and heterotic effects. Key words: Beef cattle, crossbreds, genetic parameters, heritability, maternal effects


2010 ◽  
Vol 53 (5) ◽  
pp. 600-608
Author(s):  
T. Szwaczkowski ◽  
M. Grzech ◽  
A. Borowska ◽  
E. Wencek ◽  
A. Wolc

Abstract. Direct and maternal additive genetic and mitochondrial variances of duck meat performance traits were estimated using AI-REML algorithm. Records of 3 099 (5 010 pedigreed birds) from six consecutive generations were included. The following four traits were investigated: body weight at 3rd week, body weight at 7th week, sternum crest length at 7th week (in cm), and breast muscles thickness at 7th week (in cm). The data were analysed via three single trait linear animal models: I – additive genetic model, II – model extended to additive maternal effects; III– as model II with mitochondrial effects as random. Adequacy of the models was examined by Akaike´s information criterion (AIC). Relatively high direct additive heritability estimates were obtained for body weight at 3rd week (0.4326–0.4546) and body weight at 7th week (0.5322–0.6088) whereas lower estimates were obtained for sternum crest length (0.1756–0.2744) and breast muscles thickness (0.1369–0.2932). The maternal heritabilities were moderate and also considerably depended on the model used. For all of the studied traits a negative covariance between direct and maternal genetic effects was found. Mitochondrial heritabilities were very low. Generally, on the basis of criteria employed, the model III can be suggested for analysis of body weight whereas for other traits model II seems to be suitable.


1999 ◽  
Vol 22 (3) ◽  
pp. 363-367 ◽  
Author(s):  
M. Diop ◽  
J. Dodenhoff ◽  
L.D. Van Vleck

Estimates of genetic parameters for birth (N = 3909), weaning (N = 3425), yearling (N = 2764) and final (N = 2144) weights were obtained from the records of Gobra cattle collected at the Centre de Recherches Zootechniques de Dahra, Senegal. Three animal models were fitted to obtain estimates by REML using an average information (AI) approach. Model 1 considered random direct, maternal genetic and maternal permanent environmental effects. In model 2, a general grandmaternal effect was added to the random effects considered in model 1, and in model 3, the general grandmaternal effect was divided into grandmaternal genetic and grandmaternal permanent environmental effects. All models allowed covariances among genetic effects. The inclusion of grandmaternal effects in models 2 and 3 did not change the estimates of the genetic parameters compared to model 1. Variances attributable to grandmaternal effects became negative and were set close to zero, except for yearling weight for which grandmaternal heritability was 0.03 ± 0.03. The estimates for direct and maternal heritabilities were, respectively, 0.08 ± 0.03 and 0.03 ± 0.02 for birth, 0.20 ± 0.05 and 0.21 ± 0.05 for weaning, 0.26 ± 0.07 and 0.16 ± 0.07 for yearling and 0.14 ± 0.06 and 0.16 ± 0.06 for final weights. The estimates of the genetic correlation between direct and maternal effects for birth, weaning, yearling and final weights were -0.17 ± 0.40, -0.58 ± 0.32, -0.52 ± 0.34 and -0.34 ± 0.37, respectively. For yearling weight with grandmaternal heritability estimated to be only 0.03, model 3 gave estimates of the genetic correlation between direct and grandmaternal effects and between maternal and grandmaternal effects of 0.28 ± 0.48 and -0.33 ± 0.67, respectively. Estimates of direct and maternal heritabilities were unchanged when grandmaternal effects were not included in the model.


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