首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.
Variance components for greasy fleece weight in Rambouillet sheep were estimated. Greasy fleece weight was modeled either as repeated measurements on the same trait or as different traits at different ages. The original data were separated according to the age of the ewe at shearing into three classes; 1 yr, 2 and 3 yr, and older than 3 yr. An animal model was used to obtain estimates of genetic parameters with a REML algorithm. Total numbers of animals in pedigrees for the different age classes were 696, 729, and 573, respectively, and 822 for the repeated measures model across ages. The animal model included direct genetic, permanent environmental, and residual environmental random effects and fixed effects for age of ewe, shearing date as contemporary group, and number of lambs born. Days between shearings was used as a covariate. Single-trait analyses were initially done to obtain starting values for multiple-trait analyses. A repeated measures model across ages was also used. Estimates of heritability by age group were .42, .50, and .58 from three-trait (age class) analyses and for the repeated measures model the estimate was .57. Estimates of genetic correlations between fleece yields for 1 yr and 2 and 3 yr, 1 yr and >3 yr, and 2 and 3 yr and >3 yr classes were .88, .89, and .97, respectively. These estimates of genetic correlations suggest that a repeated measures model for greasy fleece weight is adequate for making selection decisions.  相似文献   

2.
Variance and covariance components for birth weight (BWT), as a lamb trait, and litter size measured on ewes in the first, second, and third parities (LS1 through LS3) were estimated using a Bayesian application of the Gibbs sampler. Data came from Baluchi sheep born between 1966 and 1989 at the Abbasabad sheep breeding station, located northeast of Mashhad, Iran. There were 10,406 records of BWT recorded for all ewe lambs and for ram lambs that later became sires or maternal grandsires. All lambs that later became dams had records of LS1 through LS3. Separate bivariate analyses were done for each combination of BWT and one of the three variables LS1 through LS3. The Gibbs sampler with data augmentation was used to draw samples from the marginal posterior distribution for sire, maternal grandsire, and residual variances and the covariance between the sire and maternal grandsire for BWT, variances for the sire and residual variances for the litter size traits, and the covariances between sire effects for different trait combinations, sire and maternal grandsire effects for different combinations of BWT and LS1 through LS3, and the residual covariations between traits. Although most of the densities of estimates were slightly skewed, they seemed to fit the normal distribution well, because the mean, mode, and median were similar. Direct and maternal heritabilities for BWT were relatively high with marginal posterior modes of .14 and .13, respectively. The average of the three direct-maternal genetic correlation estimates for BWT was low, .10, but had a high standard deviation. Heritability increased from LS1 to LS3 and was relatively high, .29 to .37. Direct genetic correlations between BWT and LS1 and between BWT and LS3 were negative, -.32 and -.43, respectively. Otherwise, the same correlation between BWT and LS2 was positive and low, .06. Genetic correlations between maternal effects for BWT and direct effects for LS1 through LS3 were all highly negative and consistent for all parities, circa -.75. Environmental correlations between BWT and LS1 through LS3 were relatively low and ranged from .18 to .29 and had high standard errors.  相似文献   

3.
The aim of this study was to estimate direct and maternal genetic parameters for calving difficulty score, stillbirth, and birth weight at first and later parities for Charolais and Hereford cattle in Sweden. Calving traits have long been recorded for pure-bred beef cattle in Sweden, but only birth weight has been used in the selection in order to avoid calving difficulties. Linear animal model analyses included records on birth weight for 60,309 Charolais and 30,789 Hereford calves born from 1980 to 1999, and calving traits for 74,538 Charolais and 37,077 Hereford calves born from 1980 to 2001. The frequencies of difficult calvings and stillbirths were approximately 6% at first and 1 to 2% at later parities for both breeds. Fewer than half the stillborn calves were born from difficult calvings. Heritabilities estimated for birth weight in different univariate and bivariate analyses for Charolais and Hereford calves born at first and later parities ranged from 0.44 to 0.51 for direct effects and 0.06 to 0.15 for maternal effects. Heritabilities on the observable scale for calving difficulty score of Charolais and Hereford, scored in three classes, ranged from 0.11 to 0.16 for direct and 0.07 to 0.12 for maternal effects at first parity, and lower at later parities. All estimated heritabilities for stillbirth were very low (0.002 to 0.016 on the observable scale). Direct-maternal genetic correlations were negative, with few exceptions. Genetic correlations between the traits and between parities within traits were generally moderate to high and positive. Calving difficulty score should be included in the genetic evaluation of beef breeds in Sweden, whereas progeny groups in Swedish beef populations are too small for stillbirth to be considered directly.  相似文献   

4.
Comparison of the multi‐trait animal model and the traditional repeatability model was carried out using data obtained from 6,424 Landrace and 20,835 Yorkshire sows farrowed from January 2000 to April 2018 in order to estimate genetic parameters for litter traits at different parities. Specifically, records of the total number born (TNB), number born alive (NBA), total number of mortality (MORT), number of stillborn (NSB) and number of mummified pigs (MUM) were used. Although results showed the heterogeneity of heritability for litter traits at different parities, the mean heritability estimates from the multi‐trait model were found to be higher than those of the repeatability model for all traits in both pig breeds. In terms of genetic correlation between parities, a slight difference in genetic control in the first parity was noted for TNB and NBA in Landrace and Yorkshire pigs. The correlation between the first parity and later parities ranged from 0.48 to 0.74 for TNB and NBA in both breeds. Moreover, genetic correlation between parities for MORT and NSB was observed to be high for parities higher than 2 in Yorkshire pigs. For MUM, genetic correlation between the first and other parities was generally low in both breeds, indicating that culling pigs on the basis of MUM at the first parity could probably be unreasonable. Overall, the results of this study suggest that the multi‐trait approach for litter size traits is useful for the accurate estimation of genetic parameters.  相似文献   

5.
Fifteen models were compared for the birth weight of 33,994 lambs recorded at the U.S. Sheep Experimental Station (1950 to 1998). The initial intent was to estimate fractions of variance due to cytoplasmic line (c2; n = 892) and sire by cytoplasmic line interaction (sc2; n = 17,557). The basic model included direct genetic (fractional variance, a2; n = 35,684), maternal genetic (m2, with correlation r-am), and maternal permanent environmental (p2; n = 8,418) effects. The model with sc2 was significantly better than the basic model with and without c2. When other random effects were added, sc2 became zero. Significant effects were associated with random dam x year (dy2; n = 24,801), sire x dam (sd2; n = 23,924), and dam x number born (dn2; n = 12,944) interaction effects. Estimates with all effects in the model were a2, 0.24; m2, 0.19; r-am, 0.11; p2, 0.05; c2, 0.00; dn2, 0.04; dy2, 0.06; sd2, 0.05; sc2, 0.00. Estimates for a2, m2, and r-am were the same for all models. Estimate of p2 changed when other effects were added to the model. Largest estimates for nongenetic effects were: p2, 0.08; c2, 0.00; dy2, 0.13; sd2, 0.11; and sc2, 0.04. Regardless of whether Westell groups (n = 91) were in the model, estimates were similar. For weaning weight (120-d, n = 32,715), estimates of variances of effects added to the basic model were all near zero (a2, 0.18; m2, 0.12; r-am, -0.01; p2, 0.06). For number born (NB, n = 37,020) and fleece weight (FW, n = 36,197), animal permanent environmental effects were added to the model (ap2; n = 9,871 and 9,760) and r-am was dropped. For these traits, effects not in the basic model had small variances. Nonzero estimates with full model were a2, 0.10; ap2, 0.01; dy2, 0.02; and sc2, 0.01 for NB, and a2, 0.54; m2, 0.02; ap2, 0.02; dy2, 0.04; and sc2, 0.02 for FW. Cytoplasmic effects were not important. The addition of unusual random effects to the model did not change estimates for the basic parameters. Although some of these effects were significant, especially for BW, the effects on genetic evaluations are likely to be small.  相似文献   

6.
Abstract

In this study, genetic parameters were estimated for the Danish populations of Danish Marsk, Finnish Landrace, Gotland Pelt and Spel for birth weight (BW), average daily gain until two months (DG2) and litter size (LS). A multivariate animal model was used for estimation of genetic parameters, including fixed effects, both direct and maternal additive genetic effects, common litter effects and permanent environmental effects. Mean birth weight and DG2 ranged from, respectively, 3.39 kg and 262 g to 4.61kg and 286 g. Litter size ranged from 1.60 to 2.07. Direct heritability for BW ranged from 0.12 to 0.24, and maternal heritability for BW was about 0.23 for all breeds. Direct heritability of DG2 ranged from 0.19 to 0.33. The heritability for LS was between 0.08 and 0.13. The significant genetic correlations between the direct and maternal effect on both BW and DG2 were negative. The genetic correlations between the growth traits and LS were not uniform.  相似文献   

7.
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.  相似文献   

8.
Variance components, heritability (direct additive and maternal) and correlations (additive genetic, phenotypic, maternal genetic and environmental) of body weight (BW) and body size including length (BL), height (BH) and chest girth (BCG) at birth in Boer goats were estimated on the basis of 5096 records obtained from a Boer Goat Breeding Station in Yidu, China, during 2001–2005. The parameters were estimated using a DFREML procedure by excluding or including maternal genetic or permanent maternal environmental effects, four different analysis models were fitted in order to determine the optimum model for each trait. The environmental factors such as year, season, sex and litter size (LS, number of kids) were investigated as the fixed effects. The results showed that the maternal effects were important determinants of estimated the genetic parameters for birth traits. Year and season had significant effect on birth traits. Single births and male kids had the heaviest live weight and the largest body size at birth. The mean values and standard deviation (SD) of BW, BL, BH and BCG were 3.87 ± 0.85 kg, 31.67 ± 2.87 cm, 32.92 ± 2.80 cm, 33.46 ± 3.21 cm. The mean values and standard error (SE) of direct additive heritability estimates for BW, BL, BH and BCG calculated with the optimum model were 0.19 ± 0.08, 0.14 ± 0.07, 0.24 ± 0.09 and 0.25 ± 0.10, respectively. For all the birth traits, estimates of the correlations between direct additive and maternal genetic (ram) were negative. The estimates of additive genetic and phenotypic correlations among the birth traits were high and positive, and implied no genetic antagonisms among these traits analyzed. The estimates of maternal genetic correlations also were high and positive. Medium and positive environmental correlations indicated the important effects of environmental factors on early growth traits.  相似文献   

9.
Heritabilities and genetic correlations between birth weight (n = 13,741), adjusted 240-day weaning weight (WW, n = 8,806) and age at first calving (AFC, n = 3,955) of Brown Swiss cattle in Mexico were estimated. Data from 91 herds located in 19 of 32 states of Mexico from 1982 to 2006 were provided by the Mexican Brown cattle Breeder Association. Components of (co)variance, direct and maternal heritabilities were estimated for birth weight, WW and AFC using bivariate animal models. Direct and maternal heritabilities were 0.21 and 0.05 for birth weight, 0.40 and 0.05 for WW, whereas direct heritability for AFC was 0.08. The correlations between direct and maternal effects for birth weight and WW were −0.49 and −0.64, respectively. The genetic correlations between birth weight–WW and WW–AFC were 0.36 and −0.02, respectively. Under the conditions of this study, selection for increasing birth weight would increase WW, but increasing WW will not change AFC.  相似文献   

10.
The juvenile live weights, yearling fleece weight and wool characteristics of 2987 Romney progeny of 114 sires born over 9 breeding seasons in a fleece-weight-selected and a random control line were analysed. The high fleece weight-selected flock performance was higher (P < 0.001) for weaning weight and spring weight (6.9 and 8.4%), higher (P < 0.001) for greasy and clean fleece weight (23.8 and 24.3%), and also higher (P < 0.001) for FD by 1 μm, staple length by 6 mm, and wool yellowness by 0.3 unit than random control yearling sheep. Heritability estimates for weaning and spring live weight, greasy fleece weight, clean fleece weight, yield, fibre diameter, staple length, staple strength, loose wool bulk, brightness and yellowness were 0.15, 0.51, 0.35, 0.36, 0.40, 0.57, 0.41, 0.24, 0.46, 0.12 and 0.14 respectively. The heritability estimates are within the range of the long wool sheep breeds studied previously. The high selection differential achieved in the initial screening commercial flocks however facilitated to approach a selection response peak in a shorter selection duration and thus resulted in a non-significant genetic gain in greasy fleece weight when averaged over the 9 years of selection.  相似文献   

11.
12.
Variance components and genetic parameters for greasy fleece weights of Muzaffarnagari sheep maintained at the Central Institute for Research on Goats, Makhdoom, Mathura, India, over a period of 29 years (1976 to 2004) were estimated by restricted maximum likelihood (REML), fitting six animal models including various combinations of maternal effects. Data on body weights at 6 (W6) and 12 months (W12) of age were also included in the study. Records of 2807 lambs descended from 160 rams and 1202 ewes were used for the study. Direct heritability estimates for fleece weight at 6 (FW6) and 12 months of age (FW12), and total fleece weights up to 1 year of age (TFW) were 0.14, 0.16 and 0.25, respectively. Maternal genetic and permanent environmental effects did not significantly influence any of the traits under study. Genetic correlations among fleece weights and body weights were obtained from multivariate analyses. Direct genetic correlations of FW6 with W6 and W12 were relatively large, ranging from 0.61 to 0.67, but only moderate genetic correlations existed between FW12 and W6 (0.39) and between FW12 and W12 (0.49). The genetic correlation between FW6 and FW12 was very high (0.95), but the corresponding phenotypic correlation was much lower (0.28). Heritability estimates for all traits were at least 0.15, indicating that there is potential for their improvement by selection. The moderate to high positive genetic correlations between fleece weights and body weights at 6 and 12 months of age suggest that some of the genetic factors that influence animal growth also influence wool growth. Thus selection to improve the body weights or fleece weights at 6 months of age will also result in genetic improvement of fleece weights at subsequent stages of growth.  相似文献   

13.
Genetic parameters for sow stayability were estimated from farrowing records of 10,295 Landrace sows and 8192 Large White sows. The record for sow stayability from parity k to parity k + 1 (k = 1, …, 6) was 0 when a sow had a farrowing record at parity k but not at parity k + 1, and 1 when a sow had both records. Heritability was estimated by using single-trait linear and threshold animal models. Genetic correlations among parities were estimated by using two-trait linear–linear and single-trait random regression linear animal models. Genetic correlations with litter traits at birth were estimated by using a two-trait linear–linear animal model. Heritability estimates by linear model analysis were low (0.065–0.119 in Landrace & 0.061–0.157 in Large White); those by threshold model analysis were higher (0.136–0.200 & 0.110–0.283). Genetic correlations among parities differed between breeds and models. Genetic correlation between sow stayability and number born alive was positive in many cases, implying that selection for number born alive does not reduce sow stayability. The results seem to be affected by decisions on culling made by farmers.  相似文献   

14.
In order to explore genetic variability of wool production and other quantitative traits, an 8-cohort divergent selection experiment for total fleece weight (TFW) was carried out in French Angora rabbits. Studies were made on the wool production of 669 female rabbits born between 1994 and 2001 and having produced wool from the third to 12th harvests. The aim of the selection experiment was to obtain two divergent lines (low and high) on total fleece weight. The studied traits included total fleece weight, weight of the two qualities of wool (WAJ1 and WAW1), homogeneity (HOM), live body weight at ages of 4 (LW4), 8 (LW8), 12 (LW12), 16 (LW16), and 20 (LW20) weeks and then 9 weeks before each harvest (9LW). A preliminary analysis of non-genetic factors was done with the GLM procedure. The genetic parameters and genetic trends were analysed using a BLUP animal model. Heritability estimates for TFW, WAJ1, WAW1, HOM, LW4, LW8, LW12, LW16, LW20 and 9LW were 0.38, 0.30, 0.10, 0.06, 0.30, 0.09, 0.14, 0.32, 0.39 and 0.45, respectively. Genetic and phenotypic correlations between TFW and WAJ1 were high (0.98 ± 0.01 and 0.89 ± 0.01, respectively). There was a low genetic correlation between TFW and 9LW (0.26 ± 0.12). After eight cohorts of selection, the divergence between the lines was approximately three genetic standard deviations. Selection for total fleece weight had a generally beneficial effect on fleece quality.  相似文献   

15.
16.
Objective To compare haematological values and lymphocyte phenotypes in the peripheral blood of fleece rot-resistant and -susceptible sheep.
Procedure Experiments were conducted on 2- and 3-year-old Merino rams, flock 1 (17 rams) and flock 2 (32 rams), respectively. Within each flock, individual rams were classified as fleece rot-resistant or -susceptible, based on established criteria. Total and differential white cell counts, and indirect fluorescent antibody tests specific for B cells and T cells were performed on all sheep. The concentration of various subsets of circulating lymphocytes was then determined in each sheep.
Results There were no significant differences between fleece rot-resistant and -susceptible sheep from either flock in the mean total or differential white cell counts. However, fleece rot-resistant rams in flock 1 did have a significantly higher concentration of circulating SBU-T1+ cells than fleece rot-susceptible rams from the same flock. No such difference was noted in the rams from flock 2. While all rams in flock 1 were free of clinical fleece rot, 24 rams in flock 2 (comprising all 17 fleece rot-susceptible and 7 of 15 fleece rot-resistant animals) had clinical signs of the disease. Fleece rot-free rams in this flock (irrespective of their classification as fleece rot-resistant or -susceptible) had significantly higher concentrations of circulating SBU-T1+ cells compared with fleece rot-affected animals. They also had significantly higher concentrations of circulating B cells, and total lymphocytes.
Conclusions An examination of peripheral blood lymphocyte subsets in fleece rot-resistant and -susceptible sheep revealed a possible association between resistance to fleece rot and the concentration of circulating SBU-T1+ cells.  相似文献   

17.
We estimated genetic parameters for number born alive (NBA) from the first to the seventh parities in Landrace and Large White pigs using three models. Analyzing 55,160 farrowing records for 12,677 Landrace dams and 43,839 for 10,405 Large White dams, we used a single‐trait animal model to estimate the heritability of NBA at each parity and a two‐trait animal model and a single‐trait random regression model to estimate the genetic correlations between parities. Heritability estimates of NBA at each parity ranged from 0.08 to 0.13 for Landrace and from 0.05 to 0.16 for Large White. Estimated genetic correlations between parities in all cases were positive. Genetic correlations between the first and second parities were slightly lower than those between other neighboring parities. Genetic correlations between more distant parities tended to be lower, in some cases <0.8. The results indicate the necessity to investigate the applicability of evaluating NBA at different parities as different traits (e.g., the first and later parities), although a repeatability model might still be reasonable.  相似文献   

18.
本研究旨在分析影响多胎细毛羊出生重和断奶重的因素,为优质多产细毛羊的选育奠定基础.利用SPSS19.0软件对多胎细毛羊羔羊的初生重和断奶重进行了描述性统计分析,并利用SAS9.2软件的GLM(最小二乘方差分析)程序对新疆科创畜牧繁育中心2009-2019年多胎细毛羊1 567条产羔记录分析出生年份、出生月份、性别和母羊...  相似文献   

19.
Metabolizable energy requirements of the ewe increase during pregnancy due to increases in fetal and maternal metabolism. Fetal metabolism is related to total weight of the fetuses. Fetal number is a primary contributor to fetal weight. Litter birth weight represents the culminated fetal growth of the litter and can be used to estimate the effect of fetal metabolism on energy requirements of the ewe. We hypothesized that litter weight in sheep would increase at a decreasing rate with increasing litter size. Birth weights of lambs born to yearling (11 to 15 mo) and mature ewes (> 34 mo) were collected on litters born to Dorset, Rambouillet, Suffolk, Finnsheep, Romanov, and Composite III ewes mated to produce straightbred lambs. Litter birth weight expressed as a function of litter size increased at a decreasing rate and the quadratic term differed from zero for mature Rambouillet, Suffolk, Finnsheep, Romanov, and Composite III litters (P < 0.042). The quadratic coefficient differed among breeds. In yearlings, litter weight increased at a decreasing rate for Suffolk ewes (P = 0.002). The quadratic term for the relationship between litter weight and litter size did not differ from zero for Finnsheep (P = 0.39) or Romanov litters (P = 0.07). The hypothesis that litter weight increases at a decreasing rate with increased litter size is supported by experimental results.  相似文献   

20.
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   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号