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1.
The aim of the study was to evaluate heterotic and combining ability effects for growth in nine chicken genotypes. A 3?×?3 complete diallel mating system involving two indigenous breeds named Venda (V) and Naked Neck (N) and one commercial broiler breed named Ross 308 (R) were used. The nine genetic groups of crosses were reared up from hatch to 13 weeks of age in deep litter open house. Body weights of 180 chicks (20 chicks per genetic group), recorded at 0, 3, 5, 7, 9, 11, and 13 weeks of age, were used to estimate heterosis, general combining ability (GCA), and specific combining ability (SCA). Results showed that the Ross 308 had the heaviest body weight at all weeks of measurement except for hatch. With respect to crosses, the V × R and its reciprocal cross, R × V had the heaviest body weights at 13 weeks. Heterosis estimates for body weight were higher in the Venda male × Ross 308 female and Venda male and Naked Neck female crosses. GCA was significant (P?≤?0.01) for body weight from hatch to 13 weeks of age while SCA and reciprocal effects were both significant (P?≤?0.05) for body weight at all ages of measurement except for hatch. The Ross 308 gave the highest positive effect of GCA for body weight except for hatch. V × N gave the highest and positive effects of SCA for body weight.  相似文献   

2.
  • 1.?A study was conducted to study direct dominance genetic and maternal effects on genetic evaluation of production traits in dual-purpose chickens. The data set consisted of records of body weight and egg production of 49 749 Mazandaran fowls from 19 consecutive generations. Based on combinations of different random effects, including direct additive and dominance genetic and maternal additive genetic and environmental effects, 8 different models were compared.

  • 2.?Inclusion of a maternal genetic effect in the models noticeably improved goodness of fit for all traits. Direct dominance genetic effect did not have noticeable effects on goodness of fit but simultaneous inclusion of both direct dominance and maternal additive genetic effects improved fitting criteria and accuracies of genetic parameter estimates for hatching body weight and egg production traits.

  • 3.?Estimates of heritability (h2) for body weights at hatch, 8 weeks and 12 weeks of age (BW0, BW8 and BW12, respectively), age at sexual maturity (ASM), average egg weights at 28–32 weeks of laying period (AEW), egg number (EN) and egg production intensity (EI) were 0.08, 0.21, 0.22, 0.22, 0.21, 0.09 and 0.10, respectively. For BW0, BW8, BW12, ASM, AEW, EN and EI, proportion of dominance genetic to total phenotypic variance (d2) were 0.06, 0.08, 0.01, 0.06, 0.06, 0.08 and 0.07 and maternal heritability estimates (m2) were 0.05, 0.04, 0.03, 0.13, 0.21, 0.07 and 0.03, respectively. Negligible coefficients of maternal environmental effect (c2) from 0.01 to 0.08 were estimated for all traits, other than BW0, which had an estimate of 0.30.

  • 4.?Breeding values (BVs) estimated for body weights at early ages (BW0 and BW8) were considerably affected by components of the models, but almost similar BVs were estimated by different models for higher age body weight (BW12) and egg production traits (ASM, AEW, EN and EI). Generally, it could be concluded that inclusion of maternal effects (both genetic and environmental) and, to a lesser extent, direct dominance genetic effect would improve the accuracy of genetic evaluation for early age body weights in dual-purpose chickens.

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3.
A total of 11,815 weight records from 23,94 Japanese Black calves was used to estimate direct, maternal, direct permanent environmental, and maternal permanent environmental effects on growth from birth to 356 d of age. The data were collected from a herd of Japanese Black cattle in Shiroshi city, Miyagi prefecture, Japan. A random regression model, including parity of dam and year-season of calving-sex of calf as fixed effects and animal, dam, animal permanent environmental, and maternal permanent environmental as random effects, was fitted to the data using Legendre polynomials for age of calf. Direct heritability estimates increased from 0.38 at birth to 0.65 at 120 d of age, decreased to 0.38 at 300 d, and then increased again up to 0.47 at 356 d. The ratio of animal permanent environmental variance to phenotypic variance decreased from 0.41 at birth to 0.12 at 90 d, and then increased gradually up to 0.40 at 270 d and oscillated around this value up to the end of the test period. Maternal genetic heritabilities increased from 0.04 at birth to 0.09 at 120 d and then decreased to 0.06 thereafter, whereas the variance ratios due to maternal permanent environment were fairly constant across the age trajectory, fluctuating around the value of 0.03. Direct genetic, phenotypic, maternal genetic, animal permanent environmental, and maternal permanent environmental correlations between different ages were all positive, and they generally decreased as the interval between ages increased. These correlations were lower between weights from nonadjacent ages than those between weights from adjacent ages. Results suggest that selection on preweaning weights would have a positive effect on weights at later ages.  相似文献   

4.
1. A total of 11 826 records from 2489 quails, hatched between 2012 and 2013, were used to estimate genetic parameters for BW (body weight) of Japanese quail using random regression models. Weekly BW was measured from hatch until 49 d of age. WOMBAT software (University of New England, Australia) was used for estimating genetic and phenotypic parameters.

2. Nineteen models were evaluated to identify the best orders of Legendre polynomials. A model with Legendre polynomial of order 3 for additive genetic effect, order 3 for permanent environmental effects and order 1 for maternal permanent environmental effects was chosen as the best model.

3. According to the best model, phenotypic and genetic variances were higher at the end of the rearing period. Although direct heritability for BW reduced from 0.18 at hatch to 0.12 at 7 d of age, it gradually increased to 0.42 at 49 d of age. It indicates that BW at older ages is more controlled by genetic components in Japanese quail.

4. Phenotypic and genetic correlations between adjacent periods except hatching weight were more closely correlated than remote periods. The present results suggested that BW at earlier ages, especially at hatch, are different traits compared to BW at older ages. Therefore, BW at earlier ages could not be used as a selection criterion for improving BW at slaughter age.  相似文献   


5.
The objective of this work was to estimate covariance functions for direct and maternal genetic effects, animal and maternal permanent environmental effects, and subsequently, to derive relevant genetic parameters for growth traits in Canchim cattle. Data comprised 49 011 weight records on 2435 females from birth to adult age. The model of analysis included fixed effects of contemporary groups (year and month of birth and at weighing) and age of dam as quadratic covariable. Mean trends were taken into account by a cubic regression on orthogonal polynomials of animal age. Residual variances were allowed to vary and were modelled by a step function with 1, 4 or 11 classes based on animal’s age. The model fitting four classes of residual variances was the best. A total of 12 random regression models from second to seventh order were used to model direct and maternal genetic effects, animal and maternal permanent environmental effects. The model with direct and maternal genetic effects, animal and maternal permanent environmental effects fitted by quadric, cubic, quintic and linear Legendre polynomials, respectively, was the most adequate to describe the covariance structure of the data. Estimates of direct and maternal heritability obtained by multi‐trait (seven traits) and random regression models were very similar. Selection for higher weight at any age, especially after weaning, will produce an increase in mature cow weight. The possibility to modify the growth curve in Canchim cattle to obtain animals with rapid growth at early ages and moderate to low mature cow weight is limited.  相似文献   

6.
Variance components for production traits were estimated using different models to evaluate maternal effects. Data analysed were records from the South African pig performance testing scheme on 22 224 pigs from 18 herds, tested between 1990 and 2008. The traits analysed were backfat thickness (BFAT), test period weight gain (TPG), lifetime weight gain (LTG), test period feed conversion ratio (FCR) and age at slaughter (AGES). Data analyses were performed by REML procedures in ASREML, where random effects were successively fitted into animal and sire models to produce different models. The first animal model had one random effect, the direct genetic effects, while the additional random effects were maternal genetic and maternal permanent environmental effects. In the sire model, the random effects fitted were sire and maternal grand sire effects. The best model considered the covariance between direct and maternal genetic effects or between sire and maternal grand sire effects. Fitting maternal genetic effects into the animal model reduced total additive variance, while the total additive variance increased when maternal grand sire effects were fitted into the sire model. The correlations between direct and maternal genetic effects were all negative, indicating antagonism between these effects, hence the need to consider both effects in selection programmes. Direct genetic correlations were higher than other correlations, except for maternal genetic correlations of FCR with TPG, LTG and AGES. There has been direct genetic improvement and almost constant maternal ability in production traits as shown by trends for estimated (EBVs) and maternal breeding values (MBVs), while phenotypic trends were similar to those for EBVs. These results suggest that maternal genetic effects should be included in selection programmes for these production traits. Therefore, the animal–maternal model may be the most appropriate model to use when estimating genetic parameters for production traits in this population.  相似文献   

7.
1. The objective of the study was to explore the genetic architecture of blood oxygen saturation (SaO) (an indicator trait, negatively correlated with ascites susceptibility), body weight (Weight) and fleshing score (Flesh, a measure of breast conformation) for 4 meat-type chicken lines reared in commercial conditions. 2. Genetic components, including heritabilities and genetic correlations, were estimated by Restricted Maximum likelihood for these traits measured at 6 weeks of age. 3. Data were collected over eight generations of selection and pedigrees comprised in excess of 130,000 birds. 4. Univariate analyses were performed to allow model definition and to obtain starting values for trivariate analyses. The basic model included a random animal effect and, in further models explored, a maternal environmental effect or a genetic maternal effect or both were fitted. Models were compared using likelihood ratio tests. 5. Estimated heritabilities for SaO ranged from 0.1 to 0.2, and there was no evidence of genetic maternal effects for SaO. The environmental maternal component was significant for one of the populations only. Estimated heritabilities for both Weight and Flesh were between 0.2 and 0.4, and there was evidence of environmental and genetic maternal effects for these traits in all populations. 6. Genetic correlations between SaO and Weight and between SaO and Flesh were low and negative. This suggests that, in principle, genetic selection to simultaneously increase SaO, and therefore decrease ascites susceptibility, and WEight and Flesh could be performed using traditional (marker-free) selection methods. We discuss how a putative interaction between ascites and production traits could jeopardise the success of such methods.  相似文献   

8.
Weight records of Brazilian Nelore cattle, from birth to 630 d of age, recorded every 3 mo, were analyzed using random regression models. Independent variables were Legendre polynomials of age at recording. The model of analysis included contemporary groups as fixed effects and age of dam as a linear and quadratic covariable. Mean trends were modeled through a cubic regression on orthogonal polynomials of age. Up to four sets of random regression coefficients were fitted for animals' direct and maternal, additive genetic, and permanent environmental effects. Changes in measurement error variances with age were modeled through a variance function. Orders of polynomial fit from three to six were considered, resulting in up to 77 parameters to be estimated. Models fitting random regressions modeled the pattern of variances in the data adequately, with estimates similar to those from corresponding univariate analysis. Direct heritability estimates decreased after birth and tended to be lowest at ages at which maternal effect estimates tended to be highest. Maternal heritability estimates increased after birth to a peak around 110 to 120 d of age and decreased thereafter. Additive genetic direct correlation estimates between weights at standard ages (birth, weaning, yearling, and final weight) were moderate to high and maternal genetic and environmental correlations were consistently high.  相似文献   

9.
Genetic parameters of mature weight are needed for effective selection and genetic evaluation. Data for estimating these parameters were collected from 1963 to 1985 and consisted of 32,018 mature weight records of 4,175 Hereford cows that were in one control and three selection lines that had been selected for weaning weight, for yearling weight, or for an index combining yearling weight and muscle score for 22 yr. Several models and subsets of the data were considered. The mature weight records consisted of a maximum of three seasonal weights taken each year, at brand clipping (February and March), before breeding (May and June), and at palpation (August and September). Heritability estimates were high (0.49 to 0.86) for all models considered, which suggests that selection to change mature weight could be effective. The model that best fit the data included maternal genetic and maternal permanent environmental effects in addition to direct genetic and direct permanent environmental effects. Estimates of direct heritability with this model ranged from 0.53 to 0.79, estimates of maternal heritability ranged from 0.09 to 0.21, and estimates of the genetic correlation between direct and maternal effects ranged from -0.16 to -0.67 for subsets of the data based on time of year that mature weight was measured. For the same subsets, estimates of the proportions of variance due to direct permanent environment and maternal permanent environment ranged from 0.00 to 0.09 and 0.00 to 0.06, respectively. Using a similar model that combined all records and included an added fixed effect of season of measurement of mature weight, direct heritability, maternal heritability, genetic correlation between direct and maternal effects, proportion of variance due to direct permanent environmental effects, and proportion of variance due to maternal permanent environmental effects were estimated to be 0.69, 0.13, -0.65, 0.00, and 0.04, respectively. Mature weight is a highly heritable trait that could be included in selection programs and maternal effects should not be ignored when analyzing mature weight data.  相似文献   

10.
A multivariate model was developed and used to estimate genetic parameters of body weight (BW) at 1–6 weeks of age of broilers raised in a commercial environment. The development of model was based on the predictive ability of breeding values evaluated from a cross-validation procedure that relied on half-sib correlation. The multivariate model accounted for heterogeneous variances between sexes through standardization applied to male and female BWs differently. It was found that the direct additive genetic, permanent environmental maternal and residual variances for BW increased drastically as broilers aged. The drastic increase in variances over weeks of age was mainly due to scaling effects. The ratio of the permanent environmental maternal variance to phenotypic variance decreased gradually with increasing age. Heritability of BW traits ranged from 0.28 to 0.33 at different weeks of age. The direct genetic effects on consecutive weekly BWs had high genetic correlations (0.85–0.99), but the genetic correlations between early and late BWs were low (0.32–0.57). The difference in variance components between sexes increased with increasing age. In conclusion, the permanent environmental maternal effect on broiler chicken BW decreased with increasing age from weeks 1 to 6. Potential bias of the model that considered identical variances for sexes could be reduced when heterogeneous variances between sexes are accounted for in the model.  相似文献   

11.
The objective of this work was to estimate covariance functions using random regression models on B-splines functions of animal age, for weights from birth to adult age in Canchim cattle. Data comprised 49,011 records on 2435 females. The model of analysis included fixed effects of contemporary groups, age of dam as quadratic covariable and the population mean trend taken into account by a cubic regression on orthogonal polynomials of animal age. Residual variances were modelled through a step function with four classes. The direct and maternal additive genetic effects, and animal and maternal permanent environmental effects were included as random effects in the model. A total of seventeen analyses, considering linear, quadratic and cubic B-splines functions and up to seven knots, were carried out. B-spline functions of the same order were considered for all random effects. Random regression models on B-splines functions were compared to a random regression model on Legendre polynomials and with a multitrait model. Results from different models of analyses were compared using the REML form of the Akaike Information criterion and Schwarz' Bayesian Information criterion. In addition, the variance components and genetic parameters estimated for each random regression model were also used as criteria to choose the most adequate model to describe the covariance structure of the data. A model fitting quadratic B-splines, with four knots or three segments for direct additive genetic effect and animal permanent environmental effect and two knots for maternal additive genetic effect and maternal permanent environmental effect, was the most adequate to describe the covariance structure of the data. Random regression models using B-spline functions as base functions fitted the data better than Legendre polynomials, especially at mature ages, but higher number of parameters need to be estimated with B-splines functions.  相似文献   

12.
Weaning weights from Gelbvieh (GV; n = 82,138) and Limousin (LM; n = 88,639) calves were used to estimate genetic and environmental variance components with models that included different values for the correlation (lambda) between permanent environmental effects of dams and their daughters. Each analysis included fixed discrete effects of contemporary group, sex of calf, age of dam at calving, and month of calving, a fixed continuous effect of age of calf, random direct and maternal additive genetic effects, permanent environmental effects due to dams, and residual effects. The REML procedure was employed with a "grid search," in which the likelihood was computed for a series of values for lambda. For both breeds, models that included a nonzero value for lambda fitted the data significantly better than the model that did not include lambda. The maximum restricted likelihood was obtained for lambda of approximately -0.2 for both breeds. Estimates of residual and direct genetic variances were similar for all values of lambda, including zero; however, estimates of maternal genetic variance and maternal heritability increased slightly, and maternal permanent environmental variance and the proportion of the maternal variance to the total (phenotypic) variance decreased slightly, when the correlated structure for permanent environmental effects was assumed. As the value of lambda became more negative, absolute values of the direct-maternal genetic covariance and direct-maternal correlation estimates were decreased. Pearson and rank correlations for direct genetic, maternal genetic, and maternal environmental effects estimated with and without lambda were very high (>0.99). These results indicated that the linear relationship between maternal permanent environmental effects of dams and their daughters for weaning weight is negative but low in both breeds. Considering this relationship in the operational model did not significantly affect estimated breeding values, and thus, it may not be important in genetic evaluations.  相似文献   

13.
1. This study was to determine the effects of strain, age of the maternal flock and sex on morphological characteristics and composition of tibial bone of broilers from hatch to 48 d of age. 2. A total of 600 chicks was obtained from 2 strains of broiler breeder flocks (150/chicks/strain/maternal age). Maternal flock age was classified as young (32 to 35 weeks of age) or old (56 to 58 weeks of age). Birds were reared under standard feeding and lighting regimes. 3. On day 1, 16, 32 and 48, twelve birds were selected at random from each maternal group, strain and sex and killed. The wet bone weight and volume were measured. Morphological characteristics of tibia were determined using radiography. Bone breaking strength was tested. Tibia dry matter, ash content, mineral density and collagen level were determined. 4. A quadratic increase occurred with increase in age of broilers for all variables, except proximal width, medial cortex thickness and distal condyle width which increased in a linear manner. 5. Maternal age had a significant effect only on the variably measured at the time of hatch. On day of hatch bone weight, ash content and bone volume were affected by maternal age, but the extent of this also depended on the strain. 6. The differences observed between strains for bone anatomy and bone mineralisation during the rapid growth period of 16 d were not significant at later ages, with the exception of bone volume. Differences between sexes were evident from 16 to 49 d of age with females having lower values.  相似文献   

14.
1. The objectives of the present study were to estimate heritability and genetic correlations for feed efficiency and body weight (BW) in Japanese quail.

2. Recorded traits during different weeks of the growing period were BW from hatch to 35 d, feed intake (FI), feed conversion ratio (FCR) and residual feed intake (RFI) from hatch to 28 d of age.

3. Genetic parameters were estimated by restricted maximum likelihood method using ASREML software. The results showed that heritability estimates for BW ranged from 0.11 to 0.22, and maternal permanent environmental effect was the highest at hatch (0.45). FCR, RFI and FI showed moderate heritabilities ranging from 0.13 to 0.40.

4.Genetic correlations of BW28 with FI0–28 (0.88) and RFI0–28 (0.1) and genetic correlation of FI0–28 with FCR0–28 (0.13) and RFI0–28 (0.52) were positive. A negative genetic correlation was found between BW28 and FCR0–28 (?0.49). There was a high positive genetic correlation (0.67) between RFI0–28 and FCR0–28.

5. In conclusion, selection for increased BW and reduced FI in a selection index could be recommended to improve feed efficiency traits including FCR and RFI in Japanese quail.  相似文献   

15.
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.  相似文献   

16.
This study was conducted to evaluate the importance of maternal effect on body measurement traits at an early stage of growth, and to estimate the genetic relationships between direct and maternal effects and among body measurement traits at 0 month (0‐mo) and 4 months (4‐mo) of age in a population of Japanese Black calves. Body measurements and body weight of 889 Japanese Black calves were estimated with the use of an animal model by the Residual Maximum Likelihood procedure. Direct heritabilities were low to moderate, ranging between 0.17 ± 0.09 and 0.48 ± 0.13 at 0‐mo, and slightly lower, ranging between 0.15 ± 0.07 and 0.33 ± 0.13 at 4‐mo. Estimated maternal heritabilities were low to moderate, ranging between 0.08 ± 0.07 and 0.33 ± 0.07 at 0‐mo and 0.13 ± 0.06 to 0.33 ± 0.06 at 4‐mo. The direct genetic correlations between 0‐mo and 4‐mo were moderate to highly positive, ranging from 0.53 ± 0.23 to 0.96 ± 0.09. The estimated direct genetic correlation of chest width with other width traits was low and positive at both ages, whereas with hip width it was high and positive (0.80 ± 0.09) at 0‐mo, suggesting that simultaneous improvement of body width of the front and back parts is possible. Maternal genetic effects were relatively independent of direct genetic effects for body measurement traits and can be considered in genetic evaluation.  相似文献   

17.
There is limited genetic information relating calving difficulty and body weights to other productive and reproductive traits. Such information is useful for specifying selection criteria and for predicting economic consequences of selection. Genetic, maternal, and environmental covariances of six productive and reproductive measurements with calving difficulty, birth weight, 200-d weight, and 168-d postweaning gain were estimated in 12 experimental populations of cattle. Calf (direct) genetic effects resulting in longer gestation length were associated with increased calving difficulty and birth weight. Maternal genetic effects of increased gestation length and heavier birth weight were significantly associated. Lighter birth weight and reduced calving difficulty were associated with earlier heifer age at puberty. Increases in direct genetic effects of calving difficulty, 200-d weight, and postweaning gain were associated with a small increase in direct effect of scrotal circumference. Increased direct genetic effects of scrotal circumference were correlated with maternal effects decreasing calving difficulty and increasing 200-d weight. Direct effects of the skeletal measurements, yearling hip height, and heifer pelvic area were positively correlated with direct effects of calving difficulty, birth weight, 200-d weight, and postweaning gain, positively correlated with maternal effects for birth weight and 200-d weight, and negatively correlated with maternal calving difficulty. Percentage of retail product was positively associated with calving difficulty and negatively associated with 168-d gain. Predicted genetic change in calving difficulty resulting from one standard deviation of selection for either calving difficulty score or birth weight was much larger than for any other traits. Selection for 200-d weight, 168-d postweaning gain, hip height, pelvic area, or scrotal circumference was predicted to have opposite effects on direct and maternal calving difficulty. Estimated genetic correlations indicate some small to moderate relationships between calving difficulty and the measured productive and reproductive traits. However, selection for reduced calving difficulty should be based on calving difficulty score and(or) birth weight because of their superiority in predicted genetic change.  相似文献   

18.
The (co)variance components of BW at weaning (WW) were estimated for a Colombian multibreed beef cattle population. A single-trait animal model was used. The model included the fixed effect of contemporary group (sex, season, and year), and covariates including age of calf at weaning, age of cow, individual and maternal heterozygosity proportions, and breed percentage. Direct genetic, maternal genetic, permanent environmental, and residual effects were included as random effects. Direct, maternal, and total heritabilities were 0.23 +/- 0.047, 0.15 +/- 0.041, and 0.19, respectively. The genetic correlation between direct and maternal effects was -0.42 +/- 0.131, indicating that there may be antagonism among genes for growth and genes for maternal ability, which in turn suggests that improving WW by direct and maternal EPD may be difficult. A greater value for the direct heterosis effect compared with the maternal heterosis effect was found. Furthermore, the greater the proportion of Angus, Romosinuano, and Blanco Orejinegro breeds, the less the WW.  相似文献   

19.
Correlated effects of selection for components of litter size on growth and backfat thickness were estimated using data from 3 pig lines derived from the same base population of Large White. Two lines were selected for 6 generations on either high ovulation rate at puberty (OR) or high prenatal survival corrected for ovulation rate in the first 2 parities (PS). The third line was an unselected control (C). Genetic parameters for individual piglet BW at birth (IWB); at 3 wk of age (IW3W); and at weaning (IWW); ADG from birth to weaning (ADGBW), from weaning to 10 wk of age (ADGPW), and from 25 to 90 kg of BW (ADGT); and age (AGET) and average backfat thickness (ABT) at 90 kg of BW were estimated using REML methodology applied to a multivariate animal model. In addition to fixed effects, the model included the common environment of birth litter, as well as direct and maternal additive genetic effects as random effects. Genetic trends were estimated by computing differences between OR or PS and C lines at each generation using both least squares (LS) and mixed model (MM) methodology. Average genetic trends for direct and maternal effects were computed by regressing line differences on generation number. Estimates of direct and maternal heritabilities were, respectively, 0.10, 0.12, 0.20, 0.24, and 0.41, and 0.17, 0.33, 0.32, 0.41, and 0.21 (SE = 0.03 to 0.04) for IWB, IW3W, IWW, ADGBW, and ADGPW. Genetic correlations between direct and maternal effects were moderately negative for IWB (-0.21 +/- 0.18), but larger for the 4 other traits (-0.59 to -0.74). Maternal effects were nonsignificant and were removed from the final analyses of ADGT, AGET, and ABT. Direct heritability estimates were 0.34, 0.46, and 0.21 (SE = 0.03 to 0.05) for ADGT, AGET, and ABT, respectively. Direct and maternal genetic correlations of OR with performance traits were nonsignificant, with the exception of maternal correlations with IWB (-0.28 +/- 0.13) and ADGPW (0.23 +/- 0.11) and direct correlation with AGET (-0.23 +/- 0.09). Prenatal survival also had low direct but moderate to strong maternal genetic correlations (-0.34 to -0.65) with performance traits. The only significant genetic trends were a negative maternal trend for IBW in the OR line and favorable direct trends for postweaning growth (ADGT and AGET) in both lines. Selection for components of litter size has limited effects on growth and backfat thickness, although it slightly reduces birth weight and improves postweaning growth.  相似文献   

20.
Estimates of (co)variance components were obtained for weights at birth, weaning and 6, 9 and 12 months of age in Chokla sheep maintained at the Central Sheep and Wool Research Institute, Avikanagar, Rajasthan, India, over a period of 21 years (1980–2000). Records of 2030 lambs descended from 150 rams and 616 ewes were used in the study. Analyses were carried out by restricted maximum likelihood (REML) fitting an animal model and ignoring or including maternal genetic or permanent environmental effects. Six different animal models were fitted for all traits. The best model was chosen after testing the improvement of the log-likelihood values. Direct heritability estimates were inflated substantially for all traits when maternal effects were ignored. Heritability estimates for weight at birth, weaning and 6, 9 and 12 months of age were 0.20, 0.18, 0.16, 0.22 and 0.23, respectively in the best models. Additive maternal and maternal permanent environmental effects were both significant at birth, accounting for 9% and 12% of phenotypic variance, respectively, but the source of maternal effects (additive versus permanent environmental) at later ages could not be clearly identified. The estimated repeatabilities across years of ewe effects on lamb body weights were 0.26, 0.14, 0.12, 0.13, and 0.15 at birth, weaning, 6, 9 and 12 months of age, respectively. These results indicate that modest rates of genetic progress are possible for all weights.  相似文献   

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