Genotypic expression with different ages of dams: III. Weight traits of sheep.

Correlations between genetic expression in lambs when dams were young (1 yr), middle-aged (2 and 3 yr), or older (older than 3 yr) were estimated with three-trait analyses for weight traits. Weights at birth (BWT) and weaning (WWT) and ADG from birth to weaning were used. Numbers of observations were 7,731, 9,518, 9,512, and 9,201 for Columbia (COLU), Polypay (POLY), Rambouillet (RAMB), and Targhee (TARG) breeds of sheep, respectively. When averaged, relative estimates for WWT and ADG were similar across breeds. Estimates were variable across breeds. On average, direct heritability was greater when environment was young dams (.44 for BWT and .34 for WWT) than when environment was dams of middle age or older (.24 and .28 for BWT and .20 and .16 for WWT, respectively). Maternal heritability was greater when dams were middle-aged or older (.28 and .22 vs .18) for BWT but was greater when dams were younger (.10 vs .05 and .04) for WWT. The estimates of genetic correlations for direct effects across age of dam environments averaged .32 for birth weight and averaged .70 for weaning weight. Average estimates of maternal genetic correlations across age of dam classes were .36 or less for both BWT and WWT. Average estimates of correlations among maternal permanent environmental effects were .49 or less across age of dam classes. Total maternal effects accounted for .33 to .42 of phenotypic variance for BWT and for .09 to .26 of phenotypic variance for WWT. The average estimates of genetic correlations between expressions of the same genotypes with different ages of dams suggest that measurements of BWT of lambs with dams in young, middle, and older age classes should be considered to be separate traits for genetic evaluation and that for WWT measurements with young age of dam class and combined middle and older age of dam classes should be considered to be separate traits for genetic evaluation.     

Genetic parameter estimates for growth traits in Horro sheep

Variance components and genetic parameters were estimated for growth traits: birth weight (BWT), weaning weight (WWT), 6‐month weight (6MWT) and yearling weight (YWT) in indigenous Ethiopian Horro sheep using the average information REML (AIREML). Four different models: sire model (model 1), direct animal model (model 2), direct and maternal animal model (model 3) and direct–maternal animal model including the covariance between direct and maternal effects (model 4) were used. Bivariate analysis by model 2 was also used to estimate genetic correlation between traits. Estimates of direct heritability obtained from models 1–4, respectively, were for BWT 0.25, 0.27, 0.18 and 0.32; for WWT, 0.16, 0.26, 0.1 and 0.14; for 6MWT 0.18, 0.26, 0.16 and 0.16; and for YWT 0.30, 0.28, 0.23, and 0.31. Maternal heritability estimates of 0.12 and 0.23 for BWT; 0.19 and 0.24 for WWT; 0.09 and 0.09 for 6MWT and 0.08 and 0.14 for YWT were obtained from models 3 and 4, respectively. The correlations between direct and maternal additive genetic effects for BWT, WWT, 6MWT and YWT were –0.64, –0.42, 0.002 and –0.46, respectively. On the other hand, the genetic correlations between BWT and the rest of growth traits (WWT, 6MWT and YWT, respectively) were 0.45, 0.33 and 0.31, whereas correlations between WWT and 6MWT, WWT and YWT and 6MWT and YWT were 0.98, 0.84 and 0.87, respectively. The medium to high direct and maternal heritability estimates obtained for BWT and YWT indicate that in Horro sheep faster genetic improvement through selection is possible for these traits and it should consider both (direct and maternal) h² estimates. However, since the direct‐maternal genetic covariances were found to be negative, caution should be made in making selection decisions. The high genetic correlation among early growth traits imply that genetic improvement in any one of the traits could be made through indirect selection for correlated traits.     

Genetic parameters estimated with multitrait and linear spline-random regression models using Gelbvieh early growth data

Estimates of direct and maternal genetic parameters in beef cattle were obtained with a random regression model with a linear spline function (SFM) and were compared with those obtained by a multitrait model (MTM). Weight data of 18,900 Gelbvieh calves were used, of which 100, 75, and 17% had birth (BWT), weaning (WWT), and yearling (YWT) weights, respectively. The MTM analysis was conducted with a three-trait maternal animal model. The MTM included an overall linear partial fixed regression on age at recording for WWT and YWT, and direct-maternal genetic and maternal permanent environmental effects. The SFM included the same effects as MTM, plus a direct permanent environmental effect and heterogeneous residual variance. Three knots, or breakpoints, were set to 1, 205, and 365 d. (Co)variance components in both models were estimated with a Bayesian implementation via Gibbs sampling using flat priors. Because BWT had no variability of age at recording, there was good agreement between corresponding components of variance estimated from both models. For WWT and YWT, with the exception of the sum of direct permanent environmental and residual variances, there was a general tendency for SFM estimates of variances to be lower than MTM estimates. Direct and maternal heritability estimates with SFM tended to be lower than those estimated with MTM. For example, the direct heritability for YWT was 0.59 with MTM, and 0.48 with SFM. Estimated genetic correlations for direct and maternal effects with SFM were less negative than those with MTM. For example, the direct-maternal correlation for WWT was -0.43 with MTM and -0.33 with SFM. Estimates with SFM may be superior to MTM due to better modeling of age in both fixed and random effects.     

Genetic parameter estimates for growth traits and prolificacy in Raeini Cashmere goats

The main objectives of this study were to estimate genetic and phenotypic parameters for growth traits and prolificacy in the Raeini Cashmere goat. Traits included, birth weight (BWT), weaning weight (WWT), 6-month weight (6WT), 9-month weight (9WT), 12-month weight (12WT), average daily gain from birth to weaning (ADG1), average daily gain from weaning to 6WT (ADG2), average daily gain from 6WT to 12WT (ADG3), survival rate (SR), litter size at birth (LSB) and litter size at weaning (LSW) and total litter weight at birth (LWB). Data were collected over a period of 28 years (1982-2009) at the experimental breeding station of Raeini goat, southeast of Iran. Genetic parameters were estimated with univariate models using restricted maximum likelihood (REML) procedures. In addition to an animal model, sire and threshold models, using a logit link function, were used for analyses of SR. Age of dam, birth of type, sex and of kidding had significant influence (p < 0.05 or 0.01) all the traits. Direct heritability estimates were low for prolificacy traits (0.04 ± 0.01 for LSB, 0.09 ± 0.02 for LSW, 0.16 ± 0.02 for LWB and 0.05 ± 0.02 for SR) and average daily gain (0.12 ± 0.03 for ADG1, 0.08 ± 0.02 for ADG2, and 0.07 ± 0.03 for ADG3) to moderate for production traits (0.22 ± 0.02 for BWT, 0.25 ± 0.02 for WWT, 0.29 ± 0.04 for 6WT, 0.30 ± 0.02 for 9WT, 0.32 ± 0.05 for 12WT). The estimates for the maternal additive genetic variance ratios were lower than direct heritability for BWT (0.17 ± 0.03) and WWT (0.07 ± 0.02).     

Influence of maternal and additive genetic effects on offspring growth traits in Beetal goat

The purpose of the present study was to obtain estimates of variance components and genetic parameters for direct and maternal effects on various growth traits in Beetal goat by fitting four animal models, attempting to separate direct genetic, maternal genetic and maternal permanent environmental effects under restricted maximum likelihood procedure. The data of 3,308 growth trait records of Beetal kids born during the period from 2004 to 2019 were used in the present study. Based on best fitted models, the direct additive h² estimates were 0.06, 0.27, 0.37, 0.17 and 0.10 for birth weight (BWT), weight at 3 (WT3), 6 (WT6), 9 (WT9) and 12 (WT12) months of age, respectively. Maternal permanent environmental effects significantly contributed for 10% and 7% of total variance for BWT and WWT, respectively, which reduced direct heritability by 40 and 10% for respective traits from the models without these effects. For average daily gain (ADG1) and Kleiber ratios (KR1) up to weaning period (3 months) traits, maternal permanent environmental effects accounted for 7% and 8% of phenotypic variance, respectively, and resulted in a reduction of 6.6% and 5.4% in direct h² of respective traits. For post-weaning traits, the maternal effects were non-significant (p > .05) which indicates diminishing influence of mothering ability for these traits. High and positive genetic correlations were obtained among WT3-WT6, WT6-WT9 and WT9-WT12 with correlations of 0.96 ± 0.25, 0.84 ± 0.23 and 0.90 ± 0.13, respectively. Thus, early selection at weaning age can be practised taking into consideration maternal variation for effective response to selection in Beetal goat.     

Estimates of (co)variance components for productive and composite reproductive traits in Iranian Cashmere goats

The objective of this study was to estimate variance and covariance components, in Iranian Cashmere goats, for birth weight (BWT) and weaning weight (WWT) performances of kids and total weight of kids weaned (TWW) per doe joined at first (TWW1), second (TWW2) and third (TWW3) parities by REML procedures using univariate and multivariate animal models. The analysis was based on 2313 records of kids and 940 records of does. Through ignoring or including maternal additive genetic or maternal permanent environmental effects, four different models were fitted for BWT and WWT performances. For TWW performances only two models (without or with service sire effect) were used. Models were compared using likelihood ratio test. Direct additive genetic and maternal permanent environmental effects had significant influence on BWT and WWT performances. These effects accounted for 9.4% and 15.6%, and 13.9% and 6.7% of phenotypic variation, respectively. No significant effect of service sire was observed on TWW. The estimates of heritabilities were 0.072, 0.109 and 0.082 for TWW1, TWW2 and TWW3, respectively. Direct genetic correlations among all performances were positive and low (for BWT with TWW) to high (for BWT with WWT and WWT with TWW). The corresponding estimates for phenotypic and residual correlations were moderate and lower than genetic correlations. The high genetic correlation among WWT and TWW suggests that direct selection on TWW1 or indirect selection on WWT would increase total weight of kids weaned per doe joined.     

Estimates of (co)variance components and genetic parameters for body weights and first greasy fleece weight in Malpura sheep

Estimates of (co)variance components and genetic parameters were calculated for birth weight (BWT), weaning weight (WWT), 6 month weight (6WT), 9 month weight (9WT), 12 month weight (12WT) and greasy fleece weight at first clip (GFW) for Malpura sheep. Data were collected over a period of 23 years (1985–2007) for economic traits of Malpura sheep maintained at the Central Sheep & Wool Research Institute, Avikanagar, Rajasthan, India. Analyses were carried out by restricted maximum likelihood procedures (REML), fitting six animal models with various combinations of direct and maternal effects. Direct heritability estimates for BWT, WWT, 6WT, 9WT, 12WT and GFW from the best model (maternal permanent environmental effect in addition to direct additive effect) were 0.19 ± 0.04, 0.18 ± 0.04, 0.27, 0.15 ± 0.04, 0.11 ± 0.04 and 0.30 ± 0.00, respectively. Maternal effects declined as the age of the animal increased. Maternal permanent environmental effects contributed 20% of the total phenotypic variation for BWT, 5% for WWT and 4% for GFW. A moderate rate of genetic progress seems possible in Malpura sheep flock for body weight traits and fleece weight by mass selection. Direct genetic correlations between body weight traits were positive and ranged from 0.40 between BWT and 6WT to 0.96 between 9WT and 12WT. Genetic correlations of GFW with body weights were 0.06, 0.49, 0.41, 0.19 and 0.15 from birth to 12WT. The moderately positive genetic correlation between 6WT and GFW suggests that genetic gain in the first greasy fleece weight will occur if selection is carried out for higher 6WT.     

Genetic evaluation of Ethiopian Boran cattle and their crosses with Holstein Friesian for growth performance in central Ethiopia

Breed additive and non-additive effects, and heritabilities of birth weight (BWT), weaning weight (WWT), 6 months weight (SMWT), yearling weight (YWT), eighteen months weight (EWT), 2 years weight (TWT) and average daily weight gain from birth to 6 months (ADG1) and from 6 months to 2 years (ADG2) were estimated in Ethiopian Boran (B) cattle and their crosses with Holstein Friesian (F) in central Ethiopia. The data analysed were spread over 15 years. Ethiopian Boran were consistently lighter (p < 0.01) than the B-F crosses at all ages. Ethiopian Boran also gained lower weight than all the crosses. At birth, 50% F crosses were significantly (p < 0.01) lighter than all the other crosses. However, the differences in SMWT, YWT, EWT, TWT, ADG1 and ADG2 were all non-significant among the crosses. The individual additive breed differences between B and F breeds were positive and significant (p < 0.01) for all traits. The individual heterosis effects were significant (p < 0.05) for all traits except WWT for which the effect was non-significant. The maternal heterosis effects were significant (p < 0.01) for BWT (2.5 kg) and WWT (-3.0 kg). The heritability estimates for all traits in B and crosses were generally moderate to high indicating that there is scope for genetic improvement through selection. Selection within B and crossbreeding should be the strategy to enhance the growth performance under such production systems.     

Estimates of (co)variance components and genetic parameters for growth traits in Sirohi goat

Data were collected over a period of 21 years (1988–2008) to estimate (co)variance components for birth weight (BWT), weaning weight (WWT), 6-month weight (6WT), 9-month weight (9WT), 12-month weight (12WT), average daily gain from birth to weaning (ADG1), weaning to 6WT (ADG2), and from 6WT to 12WT (ADG3) in Sirohi goats maintained at the Central Sheep and Wool Research Institute, Avikanagar, Rajasthan, India. Analyses were carried out by restricted maximum likelihood, fitting six animal models with various combinations of direct and maternal effects. The best model was chosen after testing the improvement of the log-likelihood values. Heritability estimates for BWT, WWT, 6WT, 9WT, 12WT, ADG1, ADG2, and ADG3 were 0.39 ± 0.05, 0.09 ± 0.03, 0.06 ± 0.02, 0.09 ± 0.03, 0.11 ± 0.03, 0.10 ± 0.3, 0.04 ± 0.02, and 0.01 ± 0.01, respectively. For BWT and ADG1, only direct effects were significant. Estimate of maternal permanent environmental effect were important for body weights from weaning to 12WT and also for ADG2 and ADG3. However, direct maternal effects were not significant throughout. Estimate of c ² were 0.06 ± 0.02, 0.03 ± 0.02, 0.06 ± 0.02, 0.05 ± 0.02, 0.02 ± 0.02, and 0.02 ± 0.02 for 3WT, 6WT, 9WT, 12WT, ADG2, and ADG3, respectively. The estimated repeatabilities across years of ewe effects on kid body weights were 0.10, 0.08, 0.05, 0.08, and 0.08 at birth, weaning, 6, 9, and 12 months of age, respectively. Results suggest possibility of modest rate of genetic progress for body weight traits and ADG1 through selection, whereas only slow progress will be possible for post-weaning gain. Genetic and phenotypic correlations between body weight traits were high and positive. High genetic correlation between 6WT and 9WT suggests that selection of animals at 6 months can be carried out instead of present practice of selection at 9 months.     

Investigation of genotype by country interactions for growth traits for Charolais populations in Australia,Canada, New Zealand and USA

Evidence of heterogeneity of parameters and genotype by country interactions was investigated for birth weight (BWT), weaning weight (WWT) and postweaning gain (PWG) between Australian (AUS), Canadian (CAN), New Zealand (NZ) and USA populations of Charolais cattle. An animal model was fit to data sets for each individual country to compare the within-country parameter estimates for homogeneity. The direct heritability estimates of BWT in AUS (0.34) and NZ (0.31) were less than CAN (0.55) and USA (0.47). Maternal BWT heritabilities (0.13–0.18), direct WWT heritabilities (0.22–0.27), and maternal WWT heritabilities (0.12–0.18) were similar across all four countries. Direct PWG heritability for AUS (0.14) was smaller than the same estimate in the other three countries (0.24–0.31). The phenotypic variances for all three traits were similar across AUS, CAN and USA; however, NZ was higher for BWT and WWT and lower for PWG. A multiple trait animal model that considered each trait as a different trait in each country was also fit to the data for pairs of countries. Direct (maternal) estimated genetic correlations for BWT for AUS–CAN, AUS–USA, USA–CAN, NZ–CAN and NZ–USA were 0.88 (0.86), 0.85 (0.82), 0.88 (0.82), 0.85 (0.83), and 0.84 (0.80), respectively. Direct (maternal) estimated genetic correlations for WWT for AUS–CAN, AUS–USA, USA–CAN, NZ–CAN and NZ–USA were 0.96 (0.91), 0.95 (0.90), 0.95 (0.91), 0.95 (0.92), and 0.95 (0.92), respectively. Direct estimated genetic correlations for PWG for AUS–CAN, AUS–USA, USA–CAN, NZ–CAN and NZ–USA were 0.89, 0.91, 0.94, 0.90, and 0.91, respectively. The magnitude of the across-country genetic correlations indicates that genotype by country interactions were biologically unimportant. However, strong evidence exists for heterogeneity of parameters across the countries for some traits and effects. Therefore, combining these countries into one single analysis to produce a common set of genetic values will depend on the development of methods to adjust for heterogeneous parameters for models containing both direct and maternal effects, and for circumstances where constant variance ratios or heritabilities are not present across populations.     

Variance components due to direct genetic, maternal genetic and permanent environmental effect for growth and feed-efficiency traits in young male Japanese Black cattle

Variance components and genetic parameters were estimated using data recorded on 740 young male Japanese Black cattle during the period from 1971 to 2003. Traits studied were feed intake (FI), feed‐conversion ratio (FCR), residual feed intake (RFI), average daily gain (ADG), metabolic body weight (MWT) at the mid‐point of the test period and body weight (BWT) at the finish of the test (345 days). Data were analysed using three alternative animal models (direct, direct + maternal environmental, and direct + maternal genetic effects). Comparison of the log likelihood values has shown that the direct genetic effect was significant (p < 0.05) for all traits and that the maternal environmental effects were significant (p < 0.05) for MWT and BWT. The heritability estimates were 0.20 ± 0.12 for FI, 0.14 ± 0.10 for FCR, 0.33 ± 0.14 for RFI, 0.19 ± 0.12 for ADG, 0.30 ± 0.14 for MWT and 0.30 ± 0.13 for BWT. The maternal effects (maternal genetic and maternal environmental) were not important in feed‐efficiency traits. The genetic correlation between RFI and ADG was stronger than the corresponding correlation between FCR and ADG. These results provide evidence that RFI should be included for genetic improvement in feed efficiency in Japanese Black breeding programmes.     

Effect of including relationships in the estimation of genetic parameters of beef calves.

Variances and covariances for birth weight, gain from birth to weaning (ADG), and 205-d weight were obtained from a sire-dam model and a sire-maternal grandsire model for a herd of Angus and a herd of Hereford cattle. Estimates of direct additive genetic variance (sigma 2A), maternal additive genetic variance (sigma 2M), covariance between direct and maternal additive genetic effects (sigma AM), permanent environmental variance (sigma 2PE), and residual variance (sigma 2e) were obtained both with and without the inverse of the numerator relationship matrix (A-1) included. Estimates of heritability for direct genetic effects (h2A), maternal genetic effects (h2M), and the correlation between direct and maternal effects (rAM) for birth weight were .37, .18, and -.01 in Angus and .53, .23, and -.19 in Herefords, respectively, for the analyses without A-1. For the analyses with A-1, estimates of h2A, h2M, and rAM were .42, .22, and -.12 for Angus and .58, .22, and -.13 for Herefords, respectively. Estimates of h2A, h2M, and rAM for ADG were .43, .15, and -.44 in Angus and .52, .38, and -.03 in Herefords, respectively, without A-1. With A-1, estimates of h2A, h2M, and rAM were .57, .15, and -.32 for Angus and .58, .39, and -.05 for Herefords, respectively. Estimates of h2A, h2M, and rAM for 205-d weight were .49, .15, and -.46 for Angus and .58, .43, and -.06 for Herefords, respectively, without A-1. With A-1, estimates of h2A, h2M, and rAM were .63, .16, and -.36 for Angus and .66, .43, and -.08 for Herefords, respectively. Estimates of h2A were higher with A-1 than without A-1, but estimates of h2M were similar. Using variances and covariances obtained from analyses including A-1 generally gave higher estimates of direct breeding values than using variances and covariances obtained from analyses not including A-1. Both Pearson product-moment and Spearman rank correlations were high (.99) between estimates of breeding values from the two analyses, although some changes in rank did occur.     

Genetic parameters for nuclear and nonnuclear inheritance in three synthetic lines of beef cattle differing in mature size.

Genetic parameters for nuclear and cytoplasmic genetic effects were estimated from preweaning growth data collected on three synthetic lines of beef cattle differing in mature size. Lines of small-, medium-, and large-framed calves were represented in each of two research herds (Rhodes and McNay). Variance components were estimated separately by herd and size line for birth weight and 205-d weight (WW) by REML with an animal mode using an average of 847 and 427 calf records from Rhodes and McNay, respectively. Model 1 included effects of fixed year, sex of calf, age of dam, and random additive direct (a), additive maternal genetic (m), covariance (a,m), permanent environment affecting the dam, and residual error. Model 2 differed from Model 1 by including random cytoplasmic lineage effects and by ignoring permanent environmental effects. Model 1--direct (maternal) heritability estimates for birth weight at Rhodes were .62(.03) for small, .67(.06) for medium, and .30(.11) for large lines. Genetic correlations between direct and maternal effects for birth weight were .67, -.16, and .48 for the respective size groups. For WW at Rhodes, direct (maternal) heritability estimates were .30(.29), .30(.14), and .10(.16) for small, medium, and large lines, respectively, with genetic correlations of -.34 (small), -.12 (medium), and .17 (large). Heritability estimates at McNay were similar to those at Rhodes, except that maternal genetic heritabilities for WW were smaller (.10, small; .01, medium; .00, large). Model 2--estimates for nuclear genetic effects were consistent with the estimates from Model 1. Cytoplasmic variance accounted for 0 to 5% of the total random variance in birth weight. For WW, cytoplasmic variance was negligible at Rhodes and accounted for 4% of the total random variance in the large line at McNay, averaging less than the permanent environment. Results failed to indicate that cytoplasmic variance was important for preweaning performance.     

Genetic parameters and relationships between hip height and weight in Brahman cattle

Genetic parameters for weaning hip height (WHH), weaning weight (WWT), postweaning hip height growth (PHG), and hip height at 18 mo of age (HH18) and their relationships were estimated for Brahman cattle born from 1984 to 1994 at the Subtropical Agricultural Research Station, Brooksville, FL. Records per trait were 889 WHH, 892 WWT, and 684 HH18. (Co)variances were estimated using REML with a derivative-free algorithm and fitting three two-trait animal models (i.e., WHH-WWT, WHH-PHG, and WWT-HH18). Heritability estimates of WHH direct effects were 0.73 and 0.65 for models WHH-WWT and WHH-PHG and were 0.29 and 0.33 for WWT direct for models WHH-WWT and WWT-HH18, respectively. Estimates of heritability for PHG and HH18 direct were 0.13 and 0.87, respectively. Heritability estimates for maternal effects were 0.10 and 0.09 for WHH for models WHH-WWT and WHH-PHG and 0.18 and 0.18 for WWT for models WHH-WWT and WWT-HH18, respectively. Heritability estimates for PHG and HH18 maternal were 0.00 and 0.03. Estimates of the genetic correlation between direct effects for the different traits were moderate and positive; they were also positive between WHH and WWT maternal and WWT and HH18 maternal but negative (-0.19) between WHH and PHG maternal, which may indicate the existence of compensatory growth. Negative genetic correlations existed between direct and maternal effects for WHH, WWT, PHG, and HH18. The correlation between direct and WWT maternal effects was low and negative, moderate and negative between WHH direct and PHG maternal, and high and negative (-0.80) between WWT direct and HH18 maternal. There is a strong genetic relationship between hip height and weight at weaning that also affects hip height at 18 mo of age. Both product-moment and rank correlations between estimated breeding values (EBV) for direct values indicate that almost all of the same animals would be selected for PHG EBV if the selection criterion used was WHH EBV, and that it is possible to accomplish a preliminary selection for HH18 EBV using WHH EBV. Correlations between breeding values for WHH, WWT, and HH18 indicate that it will be possible to identify animals that will reduce, maintain, or increase hip height while weaning weight is increased. Thus, if the breeding objective is to manipulate growth to 18 mo of age, implementation of multiple-trait breeding programs considering hip height and weight at weaning will help to predict hip height at 18 mo of age.     

Genetics and non-genetics parameters of body weight for post-weaning traits in Raini Cashmere goats

Genetic parameters were estimated for 6-month weight (W6), 9-month weight (W9), 12-month weight (W12), average daily gain from birth to 6 months old (ADG6), and Kleiber ratio at 6 months (KL6) traits using 6,442 records obtained from a Raini Cashmere goat flock. The parameters were estimated using the restricted maximum likelihood procedure and applying four animal models excluding or including maternal additive genetic and permanent environmental effects. Heritability estimates for W6, W9, W12, ADG6, and KL6, under the most appropriate model were 0.028, 0.26, 0.29, 0.02, and 0.25, respectively. The estimates of genetic and phenotypic correlations among W6, W9, W12, and ADG6 were high and ranged from 0.73 to 0.99. The estimates of genetic and phenotypic correlations among KL6 and others traits were negative and low. Thus, these estimates of genetic parameters may provide a basis for deriving selection indices for postweaning growth traits also low genetic correlation between growth traits with KL6, it is possible to increase efficiency in Raini kids by multitrait selection.     

Investigation of genotype x environment interactions for weaning weight for Herefords in three countries

The objective of this study was to investigate the possibility of genotype x environment interactions for weaning weight (WWT) between different regions of the United States (US) and between Canada (CA), Uruguay (UY), and US for populations of Hereford cattle. Original data were composed of 487,661, 102,986, and 2,322,722 edited weaning weight records from CA, UY, and US, respectively. A total of 359 sires were identified as having progeny across all three countries; 240 of them had at least one progeny with a record in each environment. The data sets within each country were reduced by retaining records from herds with more than 500 WWT records, with an average contemporary group size of greater than nine animals, and that contained WWT records from progeny or maternal grand-progeny of the across-country sires. Data sets within each country were further reduced by randomly selecting among remaining herds. Four regions within US were defined: Upper Plains (UP), Cornbelt (CB), South (S), and Gulf Coast (GC). Similar sampling criteria and common international sires were used to form the within-US regional data sets. A pairwise analysis was done between countries and regions within US (UP-CB vs S-GC, UP vs CB, and S vs GC) for the estimation of (co)variance components and genetic correlation between environments. An accelerated EM-REML algorithm and a multiple-trait animal model that considered WWT as a different trait in each environment were used to estimate parameters in each pairwise analysis. Direct and maternal (in parentheses) estimated genetic correlations for CA vs UY, CA vs US, US vs UY, UP-CB vs S-GC, UP vs CB, and S vs GC were .88 (.84), .86 (.82), .90 (.85), .88 (.87), .88 (.84), and .87 (.85), respectively. The general absence of genotype x country interactions observed in this study, together with a prior study that showed the similarity of genetic and environmental parameters across the three countries, strongly indicates that a joint WWT genetic evaluation for Hereford cattle could be conducted using a model that treated the information from CA, UY, and US as a single population using single population-wide genetic parameters.     

New genetic parameters to exploit genetic variability in low input production systems

Under low input production systems, low heritabilities for growth traits have been a major limiting factor for recommending selection to improve animal productivity. Heritabilities low values were usually due to a large error variance leading to a dilution of the genetic variability. A total of 11,802 Barbarine lambs, from 606 breeding rams and 2428 breeding ewes, born during the period 1972–2002 and raised in a low production system were used in this study. The objective was to derive new genetic parameters that reflect in a proper way the available genetic variabilities for growth traits even under a low production system. Three classical heritability estimators and two new proposed genetic parameters (ratios) were computed and compared: the additive (h²a), the maternal (h²m), the total (h²t) heritabilities, the additive genetic ratio (a²) and the genetic maternal ratio (m²). Main results of this study showed that the direct animal model has led to higher heritability estimates than the animal maternal model. Estimates were 0.30, 0.30 and 0.31 for weights at 10 days, 30 days and 90 days, respectively. For average daily gains, estimates were 0.22 and 0.26 between 10–30 days and 30–90 days, respectively. Under maternal model, h²a varied from 0.05 to 0.08, h²m varied from 0.08 to 0.12 and h²t varied from 0.11 to 0.17. Maternal heritabilities were higher than additive heritabilities, but both remained relatively small. Values of additive genetic ratios were 0.20, 0.19, 0.20, 0.32 and 0.39 for W10, W30, W90 ADG13 and ADG39, respectively. The maternal genetic ratios were 0.41, 0.45, 0.37, 0.41 and 0.40 for W10, W30, W90, ADG13 and ADG39, respectively. These results showed that a² and m² describe better the contribution of the additive and maternal effects to the available genetic variability compared to classical heritability estimates because they remain unaffected by the residual error variance even under low-input production systems. These new parameters (ratios) represent, consequently, appropriate indicators for the contribution of the additive and maternal genetic effects to the total genetic variability and encourage breeders to find ways to exploit them.     

Comparison of methods of estimating variance components in pigs

Components of variance due to average effects of genes (sigma 2g), environmental effects common to littermates (sigma 2c), and environmental effects peculiar to individual pigs (sigma 2e) were estimated (--) by the Pseudo Expectation Approach (PE). Data were litter size (LS), backfat (BF; centimeter) and ADG (kilograms/day) collected from the Nebraska Gene Pool swine population between 1967 and 1986. Mean square errors (MSE) for h--2 and c--2 (sigma--2g and sigma--2c divided by phenotypic variance) by PE and nested ANOVA and h2 estimated by offspring on parent regression (REGOP) were evaluated using simulation of 200 repetitions of the Nebraska Gene Pool population. Parameter values for sigma 2g, sigma 2c, and sigma 2e used in simulations were PE estimates from the Gene Pool population. Estimates of h2 from PE were .18 +/- .06 for LS, .56 +/- .06 for BF, and .16 +/- .05 for ADG. Estimates of c2 from PE were .01 +/- .03 for LS, .09 +/- .02 for BF, and .19 +/- .03 for ADG. Compared with REGOP, PE yielded h--2 with smaller MSE for BF and ADG and larger MSE for LS. The MSE of PE was smaller than the MSE of the nested ANOVA estimate for all estimates and traits. These results were interpreted to suggest that considerable gains in precision in estimation of genetic parameters could be achieved by accounting for all relationships in lieu of accounting for only half- and full-sib relationships or parent-offspring relationships.     

Genetic parameters for production traits in New Zealand dual-purpose sheep, with an emphasis on dagginess

Genetic and phenotypic parameters were estimated for production and disease traits (including dagginess) from about 2 million pedigree-recorded animals born between 1990 and 2008 in New Zealand dual-purpose ram breeding flocks. This is the most comprehensive study of genetic parameter estimates for the New Zealand sheep industry to date and includes estimates that have not previously been reported. Estimates of heritability were moderate for BW at 8 mo (LW8), fleece weight at 12 mo (FW12), dagginess score at 3 and 8 mo (DAG3, DAG8; 0.31 to 0.37), typical for weaning weight (WWT), fecal egg count in summer (FEC1) and autumn (FEC2), and analogous Nematodirus counts (NEM1, NEM2; 0.17 to 0.21), and low for number of lambs born to ewes (NLB; 0.09). The genetic correlations among production traits, WWT, LW8, and FW12, were positive and moderate to high. Correlations of DAG3 and DAG8 with production and disease traits were low and mostly negative. The NLB had low, but typically positive, correlations with other traits. Disease traits also had low, but positive, correlations with production traits (WWT, LW8, and FW12), and were highly correlated among themselves. In general, the heritability estimate for BW and dagginess were greater than what is currently used in the New Zealand genetic evaluation service (Sheep Improvement Limited), and the availability of accurate estimates for dagginess plus parasite resistance and their genetic correlations with production traits will enable more accurate breeding values to be estimated for New Zealand sheep.     

Estimation of Genetic Parameters and Variance Components for Growth Traits of Nguni Cattle in Limpopo Province,South Africa

Estimates of (co)variance and genetic parameters of birth, weaning (205 days) and yearling (365 days) weight were obtained using single-trait animal models. The data were analysed by restricted maximum likelihood, fitting an animal model that included direct and maternal genetic and permanent environmental effects. The data included records collected between 1976 and 2001. The pedigree information extended as far back as early 1960s. The heritabilities for direct effects of birth, weaning and yearling weights were 0.36, 0.29 and 0.25, respectively. Heritability estimates for maternal effects were 0.13, 0.16 and 0.15 for birth, weaning and yearling weights, respectively. The correlations between direct and maternal additive genetic effects were negative for all traits analysed. The results indicate that both direct and maternal effects should be included in a selection programme for all the traits analysed.