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1.
Estimates of heritabilities and genetic correlations for calving ease over parities were obtained for the Italian Piedmontese population using animal models. Field data were calving records of 50,721 first- and 44,148 second-parity females and 142,869 records of 38,213 cows of second or later parity. Calving ability was scored in five categories and analyzed using either a univariate or a bivariate linear model, treating performance over parities as different traits. The bivariate model was used to investigate the genetic relationship between first- and second- or between first- and third-parity calving ability. All models included direct and maternal genetic effects, which were assumed to be mutually correlated. (Co)variance components were estimated using restricted maximum likelihood procedures. In the univariate analyses, the heritability for direct effects was .19 +/- .01, .10 +/- .01, and .08 +/- .004 for first, second, and second and later parities, respectively. The heritability for maternal effects was .09 +/- .01, .11 +/- .01, and .05 +/- .01, respectively. All genetic correlations between direct and maternal effects were negative, ranging from -.55 to -.43. Approximated standard errors of genetic correlations between direct and maternal effects ranged from .041 to .062. For multiparous cows, the fraction of total variance due to the permanent environment was greater than the maternal heritability. With bivariate models, direct heritability for first parity was smaller than the corresponding univariate estimate, ranging from .18 to .14. Maternal heritabilities were slightly higher than the corresponding univariate estimates. Genetic correlation between first and second parity was .998 +/- .00 for direct effects and .913 +/- .01 for maternal effects. When the bivariate model analyzed first- and third-parity calving ability, genetic correlation was .907 +/- .02 for direct effects and .979 +/- .01 for maternal effects. Residual correlations were low in all bivariate analyses, ranging from .13 for analysis of first and second parity to .07 for analysis of first and third parity. In conclusion, estimates of genetic correlations for calving ease in different parities obtained in this study were very high, but variance components and heritabilities were clearly heterogeneous over parities.  相似文献   

2.
First parity calving difficulty scores from Italian Piemontese cattle were analysed using a threshold mixed effects model. The model included the fixed effects of age of dam and sex of calf and their interaction and the random effects of sire, maternal grandsire, and herd‐year‐season. Covariances between sire and maternal grandsire effects were modelled using a numerator relationship matrix based on male ancestors. Field data consisted of 23 953 records collected between 1989 and 1998 from 4741 herd‐year‐seasons. Variance and covariance components were estimated using two alternative approximate marginal maximum likelihood (MML) methods, one based on expectation‐maximization (EM) and the other based on Laplacian integration. Inferences were compared to those based on three separate runs or sequences of Markov Chain Monte Carlo (MCMC) sampling in order to assess the validity of approximate MML estimates derived from data with similar size and design structure. Point estimates of direct heritability were 0.24, 0.25 and 0.26 for EM, Laplacian and MCMC (posterior mean), respectively, whereas corresponding maternal heritability estimates were 0.10, 0.11 and 0.12, respectively. The covariance between additive direct and maternal effects was found to be not different from zero based on MCMC‐derived confidence sets. The conventional joint modal estimates of sire effects and associated standard errors based on MML estimates of variance and covariance components differed little from the respective posterior means and standard deviations derived from MCMC. Therefore, there may be little need to pursue computation‐intensive MCMC methods for inference on genetic parameters and genetic merits using conventional threshold sire and maternal grandsire models for large datasets on calving ease.  相似文献   

3.
Calving ease scores from Holstein dairy cattle in the Walloon Region of Belgium were analysed using univariate linear and threshold animal models. Variance components and derived genetic parameters were estimated from a data set including 33 155 calving records. Included in the models were season, herd and sex of calf × age of dam classes × group of calvings interaction as fixed effects, herd × year of calving, maternal permanent environment and animal direct and maternal additive genetic as random effects. Models were fitted with the genetic correlation between direct and maternal additive genetic effects either estimated or constrained to zero. Direct heritability for calving ease was approximately 8% with linear models and approximately 12% with threshold models. Maternal heritabilities were approximately 2 and 4%, respectively. Genetic correlation between direct and maternal additive effects was found to be not significantly different from zero. Models were compared in terms of goodness of fit and predictive ability. Criteria of comparison such as mean squared error, correlation between observed and predicted calving ease scores as well as between estimated breeding values were estimated from 85 118 calving records. The results provided few differences between linear and threshold models even though correlations between estimated breeding values from subsets of data for sires with progeny from linear model were 17 and 23% greater for direct and maternal genetic effects, respectively, than from threshold model. For the purpose of genetic evaluation for calving ease in Walloon Holstein dairy cattle, the linear animal model without covariance between direct and maternal additive effects was found to be the best choice.  相似文献   

4.
Heritability of 2-yr-old heifer calving difficulty score was estimated in nine purebred and three composite populations with a total of 5,986 calving difficulty scores from 520 sires and 388 maternal grandsires. Estimates were 0.43 for direct (calf) genetic effects and 0.23 for maternal (heifer) genetic effects. The correlation between direct and maternal effects was -0.26. Direct effects were strongly positively correlated with birth weight and moderately correlated with 200-d weight and postweaning gain. Smaller negative correlations of maternal calving difficulty with direct effects of birth weight, weaning weight, and postweaning gain were estimated. Calving difficulty was scored from 1 to 7. Predicted heritabilities using seven optimal scores were similar to those using four scores. The predicted heritability using only two categories was reduced 23%. Phenotypic and direct genetic variance increased with increasing average population calving difficulty score. The estimated direct and maternal heritabilities for 2-yr-old calving difficulty score were larger than many literature estimates. These estimates suggested substantial variance for direct and maternal genetic effects. The direct effects of 2-yr-old calving difficulty score seemed to be much more closely tied to birth weight than were maternal effects.  相似文献   

5.
Direct and maternal (co)variance components and genetic parameters were estimated for growth and reproductive traits in the Kenya Boran cattle fitting univariate animal models. Data consisted of records on 4502 animals from 81 sires and 1010 dams collected between 1989 and 2004. The average number of progeny per sire was 56. Direct heritability estimates for growth traits were 0.34, 0.12, 0.19, 0.08 and 0.14 for birth weight (BW), weaning weight (WW), 12-month weight (12W), 18-month weight (18W) and 24-month weight (24W), respectively. Maternal heritability increased from 0.14 at weaning to 0.34 at 12 months of age but reduced to 0.11 at 24 months of age. The maternal permanent environmental effect contributed 16%, 4% and 10% of the total phenotypic variance for WW, 12W and 18W, respectively. Direct-maternal genetic correlations were negative ranging from −0.14 to −0.58. The heritability estimates for reproductive traits were 0.04, 0.00, 0.15, 0.00 and 0.00 for age at first calving (AFC), calving interval in the first, second, and third parity, and pooled calving interval. Selection for growth traits should be practiced with caution since this may lead to a reduction in reproduction efficiency, and direct selection for reproductive traits may be hampered by their low heritability.  相似文献   

6.
Non‐genetic factors influencing functional longevity and the heritability of the trait were estimated in South African Holsteins using a piecewise Weibull proportional hazards model. Data consisted of records of 161,222 of daughters of 2,051 sires calving between 1995 and 2013. The reference model included fixed time‐independent age at first calving and time‐dependent interactions involving lactation number, region, season and age of calving, within‐herd class of milk production, fat and protein content, class of annual variation in herd size and the random herd–year effect. Random sire and maternal grandsire effects were added to the model to estimate genetic parameters. The within‐lactation Weibull baseline hazards were assumed to change at 0, 270, 380 days and at drying date. Within‐herd milk production class had the largest contribution to the relative risk of culling. Relative culling risk increased with lower protein and fat per cent production classes and late age at first calving. Cows in large shrinking herds also had high relative risk of culling. The estimate of the sire genetic variance was 0.0472 ± 0.0017 giving a theoretical heritability estimate of 0.11 in the complete absence of censoring. Genetic trends indicated an overall decrease in functional longevity of 0.014 standard deviation from 1995 to 2007. There are opportunities for including the trait in the breeding objective for South African Holstein cattle.  相似文献   

7.
Data for gestation length, birth weight, calving difficulty (percent assisted) and survival from birth to weaning were analyzed from 4,639 calves by 290 sires of 14 Bos taurus breeds (Hereford, Angus, Jersey, South Devon, Limousin, Simmental, Charolais, Red Poll, Brown Swiss, Gelbvieh, Maine Anjou, Chianina, Pinzgauer and Tarentaise) mated to Hereford and Angus cows. The calves were produced over a 7-yr period in a germ plasm evaluation program. Variance components were estimated for breed of sire (sigma 2b), sire within breed of sire (sigma 2s) and progeny within sire (sigma 2w) random effects. Estimates of sigma 2b and sigma 2s direct genetic variance were similar for gestation length and calf survival. Estimates of sigma 2b genetic variance were greater than for sigma 2s for birth weight and calving difficulty. Estimates of total heritability [h2t = 4(sigma 2b + sigma 2s)/(4 sigma 2b + sigma 2s + sigma 2w)] and within-breed heritability (h2w = 4 sigma 2s/sigma 2s + sigma 2w) indicated that gestation length (h2t = .77, h2w = 64) and birth weight (h2t = .79, h2w = .46) are under a high degree of direct genetic control, calving difficulty (h2t = .42, h2w = .21) is under a moderate degree of direct genetic control and calf survival (h2t = .11, h2w = .07) is under a low degree of direct genetic control. Estimates of genetic correlation for between (rb) - and within-breed (rg) sources of genetic variation were comparable in direction, but tended to be stronger between than within breeds.(ABSTRACT TRUNCATED AT 250 WORDS)  相似文献   

8.
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   

9.
Published information on relative performance of beef breed crosses was used to derive combined estimates of purebred breed values for predominant temperate beef breeds. The sources of information were largely from the United States, Canada, and New Zealand, although some European estimates were also included. Emphasis was on maternal traits of potential economic importance to the suckler beef production system, but some postweaning traits were also considered. The estimates were taken from comparison studies undertaken in the 1970s, 1980s and 1990s, each with representative samples of beef breeds used in temperate agriculture. Weighting factors for breed-cross estimates were derived using the number of sires and offspring that contributed to that estimate. These weights were then used in a weighted multiple regression analysis to obtain single purebred breed effects. Both direct additive and maternal additive genetic effects were estimated for preweaning traits. Important genetic differences between the breeds were shown for many of the traits. Significant regression coefficients were estimated for the effect of mature weight on calving ease, both maternal and direct additive genetic, survival to weaning direct, and birth weight direct. The breeds with greater mature weight were found to have greater maternal genetic effects for calving ease but negative direct genetic effects on calving ease. A negative effect of mature weight on the direct genetic effect of survival to weaning was observed. A cluster analysis was done using 17 breeds for which information existed on nine maternal traits. Regression was used to predict breed-cross-specific heterosis using genetic distance. Only five traits, birth weight, survival to weaning, cow fertility, and preweaning and postweaning growth rate had enough breed-cross-specific heterosis estimates to develop a prediction model. The breed biological values estimated provide a basis to predict the biological value of crossbred suckler cows and their offspring.  相似文献   

10.
Calving difficulty was analyzed under threshold and linear models considering either a fixed or random herd-year effect. The aim of the study was to compare models for predicting breeding values according to the size of herd-year groups. When simulating data sets with small herds, in order to obtain an unbiased evaluation under a nonrandom and negative association of sire and herd effects, the best model for a practical evaluation was the fixed linear model. Field data included 246,576 records of the largest Charolais herds in France. Models were compared using the correlations of estimated breeding values between the different models. Although the best model from a theoretical point of view was a threshold model with a fixed herd-year effect, a linear model with a fixed herd-year effect was the best choice from a practical point of view for predicting direct effects for calving difficulty in beef cattle and was a sufficient choice for predicting the associated maternal effects for data set with large herds. Correlations between direct estimated breeding values under the reference model and the fixed linear model and the random threshold model were 0.94 and 0.91, respectively. Correlations between the corresponding maternal estimated breeding values were 0.94 and 0.98. Heritabilities of direct effects were 0.27 and 0.14 under fixed threshold and fixed linear models, respectively. The corresponding heritabilities of maternal effects were 0.18 and 0.13, and the genetic correlation between direct and maternal effects were -0.36 and -0.34, respectively.  相似文献   

11.
Mortality records of 8,642 lambs from a composite population at the U.S. Meat Animal Research Center during the first year of life were studied using discrete survival analyses. Lamb mortality was studied across periods from birth to weaning, birth to 365 d of age, and weaning to 365 d of age. Animal-time data sets were created for each period using different time intervals: daily, weekly, fortnightly, and monthly. Each data set was analyzed using logistic and complementary log-log sire, animal, and maternal effects models. Explanatory variables included in the models were duration of time interval, sex, type of birth, contemporary group, age of dam, and type of upbringing (nursery or not). Similar estimates of explanatory variables were obtained within the same period across models and different time intervals. Heritability estimates from the complementary log-log models were greater than those from the comparable logistic models because of the difference in variance of the respective link functions. Heritability estimates from the complementary log-log sire model ranged from 0.13 to 0.21 for all periods. These estimates were greater than the complementary log-log animal model estimates that ranged from 0.04 to 0.12. Maternal effects were important early in life, with the maternal heritability slightly greater than the direct additive heritability. Negative correlations (-0.72 to -0.65) between direct additive and maternal effects was estimated. The similarity of results among survival analysis methods demonstrates that the discrete methodology is a viable alternative to estimate variance components in livestock survival data.  相似文献   

12.
Weaning weights from nine sets of Angus field data from three regions of the United States were analyzed. Six animal models were used to compare two approaches to account for an environmental dam-offspring covariance and to investigate the effects of sire x herd-year interaction on the genetic parameters. Model 1 included random direct and maternal genetic, maternal permanent environmental, and residual effects. Age at weaning was a covariate. Other fixed effects were age of dam and a herd-year-management-sex combination. Possible influence of a dam's phenotype on her daughter's maternal ability was modeled by including a regression on maternal phenotype (fm) (Model 3) or by fitting grandmaternal genetic and grandmaternal permanent environmental effects (Model 5). Models 2, 4, and 6 were based on Models 1, 3, and 5, respectively, and additionally included sire x herd-year (SH) interaction effects. With Model 3, estimates of fm ranged from -.003 to .014, and (co)variance estimates were similar to those from Model 1. With Model 5, grandmaternal heritability estimates ranged from .02 to .07. Estimates of maternal heritability and direct-maternal correlation (r(am)) increased compared with Model 1. With models including SH, estimates of the fraction of phenotypic variance due to SH interaction effects were from .02 to .10. Estimates of direct and maternal heritability were smaller and estimates of r(am) were greater than with models without SH interaction effects. Likelihood values showed that SH interaction effects were more important than fm and grandmaternal effects. The comparisons of models suggest that r(am) may be biased downward if SH interaction and(or) grandmaternal effects are not included in models for weaning weight.  相似文献   

13.
绵羊生长性状母本效应方差组分、遗传参数估计的研究   总被引:5,自引:0,他引:5  
本文利用公畜母畜模型和公畜外祖父模型估计了初生重、断奶重的直接加性遗传方差、母本遗传方差和遗传参数,得出初生重的直接加性遗传效应、母本遗传效应和总的加性遗传效应的遗传力分别为:0.164、0.101、0.103;断奶重相应的各遗传力为:0.076、0.108、0.081。初生重和断奶重二性状加性遗传效应和母本遗传效应间的遗传相关为:-0.57和-0.36。  相似文献   

14.
Mating and calving records for 47,533 first-calf heifers in Australian Angus herds were used to examine the relationship between days to calving (DC) and two measures of fertility in AI data: 1) calving to first insemination (CFI) and 2) calving success (CS). Calving to first insemination and calving success were defined as binary traits. A threshold-linear Bayesian model was employed for both analyses: 1) DC and CFI and 2) DC and CS. Posterior means (SD) of additive covariance and corresponding genetic correlation between the DC and CFI were -0.62 d (0.19 d) and -0.66 (0.12), respectively. The corresponding point estimates between the DC and CS were -0.70 d (0.14 d) and -0.73 (0.06), respectively. These genetic correlations indicate a strong, negative relationship between DC and both measures of fertility in AI data. Selecting for animals with shorter DC intervals genetically will lead to correlated increases in both CS and CFI. Posterior means (SD) for additive and residual variance and heritability for DC for the DC-CFI analysis were 23.5 d2 (4.1 d2), 363.2 d2 (4.8 d2), and 0.06 (0.01), respectively. The corresponding parameter estimates for the DC-CS analysis were very similar. Posterior means (SD) for additive, herd-year and service sire variance and heritability for CFI were 0.04 (0.01), 0.06 (0.06), 0.14 (0.16), and 0.03 (0.01), respectively. Posterior means (SD) for additive, herd-year, and service sire variance and heritability for CS were 0.04 (0.01), 0.07 (0.07), 0.14 (0.16), and 0.03 (0.01), respectively. The similarity of the parameter estimates for CFI and CS suggest that either trait could be used as a measure of fertility in AI data. However, the definition of CFI allows the identification of animals that not only record a calving event, but calve to their first insemination, and the value of this trait would be even greater in a more complete dataset than that used in this study. The magnitude of the correlations between DC and CS-CFI suggest that it may be possible to use a multitrait approach in the evaluation of AI and natural service data, and to report one genetic value that could be used for selection purposes.  相似文献   

15.
Weaning weight records of 44,357 Australian Angus calves produced by 1,020 sires in 90 herds were used to evaluate the importance of sire x herd interactions. Models fitted fixed effects of contemporary group (herd-year-date of weighing subclass), sex, calf age, and dam age and random effects of sire or of sire and sire x herd interaction using REML. Effects of standardizing the data, including sire relationships and including dam maternal breeding values (MBV) as a covariate were also investigated. Sire x herd interactions were found (P less than .05) in all cases and, in the most complete model, accounted for 3.3% of phenotypic variance. Across-herd heritabilities ranged from .19 to .28. Differential nonrandom mating among herds seemed to occur in the data. Significant sire x herd effects were observed for dam MBV, and adjustment for dam MBV yielded the smallest estimates of interaction variance and across-herd heritability. If sire x herd interactions were due only to genotype x environment interaction, within-herd heritabilities would range from .33 to .49. These estimates are larger than previously reported estimates. Thus, unreported environmental effects common to progeny of individual sires may also be involved in the observed interaction but could not be disentangled from true genotype x environment interaction effects using these data. Results of these analyses suggest that some accommodation of sire x herd interaction effects on weaning weight may be needed in beef cattle genetic evaluations, but a compelling case for development of herd-specific breeding value prediction cannot be made.  相似文献   

16.
Data from 2,089 laboratory rats utilized in selection experiments were used to estimate maternal influence on growth from weaning (21 d) to 16 wk of age. Adjustment factors were calculated for the effects of sex, generation, litter size, inbreeding of the dam and inbreeding of the offspring on the body weights. The effect of line of sire was included in the analysis of variance models. Covariances among paternal half-sibs, full-sibs, offspring-dam, and individuals with the same maternal grandsire were equated to theoretical causal components of variance in a series of simultaneous equations. From these, estimates of heritability, maternal influence and other environmental influences on the weights of the animals were calculated. Estimates of additive genetic effects were negative at weaning and increased to positive intermediate values during postweaning growth. Maternal influence due to additive genetic effects was of primary importance at weaning and tended to diminish at later stages of growth. An antagonism was indicated between maternal environment and genes affecting the offspring's growth. Maternal influence is an important factor at weaning and during the postweaning growth of a litter-bearing species such as the laboratory rat.  相似文献   

17.
Records for yearling scrotal circumference (SC; n = 7,580), age at puberty in heifers (AP; n = 5,292), age at first calving (AFC; n = 4,835), and pregnancy, calving, or weaning status following the first breeding season (PR1, CR1, or WR1, respectively; n = 7,003) from 12 Bos taurus breeds collected at the Meat Animal Research Center (USDA) between 1978 and 1991 were used to estimate genetic parameters. Age at puberty (AP) was defined as age in days at first detected ovulatory estrus. Pregnancy (calving or weaning) status was scored as one for females conceiving (calving or weaning) given exposure during the breeding season and as zero otherwise. The final model for SC included fixed effects of age of dam at breeding (AD), year of breeding (Y), and breed (B) and age in days at measurement as a covariate. Fixed effects in models for AP and AFC were AD, Y, B, and month of birth. Fixed effects in models for PR1, CR1, and WR1 included AD, Y, and B. For all traits, random effects in the model were direct genetic, maternal genetic, maternal permanent environmental, and residual. Analyses for a three-trait animal model were carried out with SC, AP, and a third trait (the third trait was AFC, PR1, CR1, or WR1). A derivative-free restricted maximum likelihood algorithm was used to estimate the (co)variance components. Direct and maternal heritability estimates were 0.41 and 0.05 for SC; 0.16 and 0.03 for AP; 0.08 and 0.00 for AFC; 0.14 and 0.02 for PR1; 0.14 and 0.03 for CR1; and 0.12 and 0.01 for WR1. Genetic correlations between direct and maternal genetic effects within trait were -0.26, -0.63, -0.91, -0.79, -0.66, and -0.85 for SC, AP, AFC, PR1, CR1, and WR1, respectively. Direct genetic correlations between SC and AP and between those traits and AFC, PR1, CR1, and WR1 ranged from -0.15 (between SC and AP) to 0.23 (between AP and WR1). Estimates of heritability indicate that yearling SC should respond to direct selection better than AP, AFC, PR1, CR1, and WR1. Variation due to maternal genetic effects was small for all traits. No strong genetic correlations were detected between SC and female reproductive traits or between AP and the other female traits. These results suggest that genetic response in female reproductive traits through sire selection on yearling SC is not expected to be effective.  相似文献   

18.
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   

19.
This study is based on 12708 first-parity and 7062 second-parity Yorkshire litters from Swedish nucleus herds; and on 1037 first-parity Yorkshire litters from an experimental herd. Gestation length was analysed together with litter size, piglet mortality and average piglet growth rate. A sire–dam model was used to estimate direct (litter) and maternal (sow) genetic effects. Direct heritability for gestation length was 0.3. Maternal heritability was estimated at 0.2 in nucleus data and 0.3 in experimental data. The maternal genetic correlation between gestation length and litter size was negative. The genetic correlations between gestation length and number stillborn were not consistent between the two data sets. Genetic correlations between gestation length and number dead after birth were negative. Genetic correlations between gestation length and average birth weight and piglet growth rate were positive. We conclude that gestation length is influenced by the genotype of the piglets and the genotype of the sow. Selection for prolonged gestation would probably improve piglet survival after birth and piglet growth; it might, however, result in more stillbirths.  相似文献   

20.
Generalized mixed linear, threshold, and logistic sire models and Markov chain, Monte Carlo simulation procedures were used to estimate genetic parameters for calving rate and calf survival in a multibreed beef cattle population. Data were obtained from a 5-generation rotational crossbreeding study involving Angus, Brahman, Charolais, and Hereford (1969 to 1995). Gelbvieh and Simmental bulls sired terminal-cross calves from a sample of generation 5 cows. A total of 1,458 cows sired by 158 bulls had a mean calving rate of 78% based on 4,808 calving records. Ninety-one percent of 5,015 calves sired by 260 bulls survived to weaning. Mean heritability estimates and standard deviations for daughter calving rate from posterior distributions were 0.063 +/- 0.024, 0.150 +/- 0.049, and 0.130 +/- 0.047 for linear, threshold, and logistic models, respectively. For calf survival, mean heritability estimates and standard deviations from posterior distributions were 0.049 +/- 0.022, 0.160 +/- 0.058, and 0.190 +/- 0.078 from linear, threshold, and logistic models, respectively. When transformed to an underlying normal scale, linear sire, mixed model, heritability estimates were similar to threshold and logistic sire mixed model estimates. Posterior density distributions of estimated heritabilities from all models were normal. Spearman rank correlations between sire EPD across statistical models were greater than 0.97 for daughter calving rate and for calf survival. Sire EPD had similar ranges across statistical models for daughter calving rate and for calf survival.  相似文献   

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