In Swedish Holstein dairy cattle, genetic effects on stillbirth and calving difficulty were studied in 411,409 first- and 281,193 second-calvers. A linear single-trait sire-maternal grandsire model and a threshold model using a Gibbs sampling technique were used to analyse calving data from 1985 to 1996. In first calving when using the linear model, the heritability of stillbirth on the visible scale was 4% for the direct effect and 3% for the maternal effect. For calving difficulty it was 6% and 5% for direct and maternal effects, respectively. In second calving the corresponding heritabilities for the two traits were considerably lower, less than 1%. Adjusting for calving difficulty in linear analysis of stillbirth halved the heritabilities for the direct and maternal effects in first calving. When using a threshold model, heritabilities for stillbirth in first-calvers were 12% and 8% for direct and maternal effects, respectively, and for calving difficulty they were 17% and 12%. At second calving corresponding heritabilities were 2 to 4% for stillbirth and 4 to 7% for calving difficulty. The correlation between direct and maternal effects was around -0.1, irrespective of whether the linear or the threshold model was used for first-calvers. The genetic correlations between bulls' EBV from first and second calving were 0.4 to 0.5 for direct and maternal effects in stillbirth, whereas they were 0.6 to 0.7 for calving difficulty. In first-calvers there was a substantial genetic variation in both traits, expressed by differences between breeding values of bulls, despite fairly low heritability. The results obtained in this study suggest that first-parity records should preferably be used for genetic evaluation of bulls for calving performance. In such routine evaluations both stillbirth and calving difficulty, and both direct and maternal effects, should be included.
The Baluchi breed is the most common native breed of Iran adapted to harsh environments in the eastern parts of the country. The data used in the present study, collected from two research flocks at the Abbasabad sheep breeding station in north-east Iran, included 20 534 animals descended from 363 sires, 5992 dams, 282 maternal grandsires, and 2865 maternal granddams during the period 1966 to 1989. The traits recorded were: birth weight (BW), weaning weight (WW), weight at 6 months (W6), weight at 12 months (YW), pre-weaning gain (WG), postweaning gain (PWG), lamb fleece weight (LFW), ewe fleece weight sheared before first joining (FW1) and adult ewe fleece weight (FW). Genetic parameters, estimated with restricted maximum likelihood and a two-trait animal model, were similar in the two flocks. Direct heritabilities for the various body weight traits were moderate and varied between 0-13 and 0-32, while the maternal heritabilities were low and varied between 0-01 and 0-12. Direct and maternal genetic correlations between WW and weights at later ages were moderate to high (0-59 to 0-96). Direct heritabilities of weight gain measures varied between 0-12 and 0-19, while no significant maternal influence on either of these weight gain measures could be detected. The estimates of direct genetic correlation between WG and PWG were positive and varied between 0-54 and 0-74, while negative maternal genetic correlation (-0-17 on average) between WG and PWG was detected. For LFW, direct heritability was low and no maternal heritability could be shown. For FW1, both direct and maternal genetic influences were demonstrated (0-07 to 0-26). Direct genetic correlation between LFW and FW1 was very low and close to zero, while maternal genetic correlation was positive and relatively high (0-72 on average). The relative contributions to phenotypic variance from variance components due to common environmental effects ranged from 0-01 to 0-15 for all traits. The repeatability of FW was low (0-03 to 0-12).
Genetic parameters were estimated for weights of lambs from birth to 1 d before slaughter and mature ewe weight (EMW) using REML procedures and single- and two-trait animal models. The data consisted of weight registrations from 5,001 animals descended from 131 sires, 788 dams, 48 maternal grandsires, and 530 maternal granddams in an experimental flock with Swedish finewool sheep. Direct heritabilities increased with lamb age from .07 for birth weight to .21 for weight before slaughter. Maternal heritabilities declined with age from .30 to .07. Direct-maternal genetic correlations were positive and increased with age from .11 for birth weight to .73 for weight before slaughter. For daily gain during shorter periods, direct heritability increased from .07 for the period from birth until 3 wk of age to .14 for the period from weaning until 1 d before slaughter. The values for maternal heritabilities were .16 and .03, respectively. The direct-maternal genetic correlations ranged from -.11 to .59. The direct heritability for EMW varied between analyses from .29 to .63. A nonsignificant maternal heritability of .22 was noted for EMW. Direct genetic correlations between EMW and various lamb weights varied between .36 to .85. Genetic correlations between direct effects on EMW and maternal effects on lamb weights varied between .39 and .53. Direct and maternal genetic correlations between the lamb weights were positive. The results showed that the maternal influence on lamb weights decreased with age. It was indicated that positive genetic relationships exist between ewe weight and maternal effects on lamb weight. Therefore, selection for larger lamb weights alone will not only increase ewe weights but also improve the maternal ability to the ewe.
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.
There are two types of 1-day field tests available for young Swedish Warmblood sport horses; one test for 3-year olds and one more advanced test for 4-year olds. Conformation, gaits and jumping ability are evaluated at both tests. Studies on various genetic parameters were based on about 20 000 tested horses. The data for 4-year olds consisted of 30 years of testing. The aims of the study were to estimate genetic parameters for results from different time periods, and to estimate heritabilities for, and genetic correlations between, traits scored in the two tests. The judgement of traits was shown to have been changed during the 30 years of testing, resulting in changes in higher heritabilities in, and stronger genetic correlations between, later time periods. In the first time period, records showed higher residual and lower genetic variances than in the subsequent time periods. Genetic correlations between traits recorded in the first and last time period deviated considerably from unity. Further studies are needed to investigate how to treat data from the early period in genetic evaluations. Heritabilities were moderate to high for conformation traits (0.24 to 0.58) at both types of tests, except for correctness of legs (0.08). The heritabilities for gait traits were also moderate to high (0.37 to 0.53). For jumping traits, the heritabilities ranged between 0.17 and 0.33. The highly positive genetic correlations (0.82 to 0.99) between corresponding traits tested at the simpler test for 3-year olds and at the ridden test of 4-year olds implied that it would be desirable to include the test results of 3-year olds into the genetic evaluation as breeding values for Swedish Warmbloods for many years has only been based on results from 4-year olds.
For many years, the breeding value estimation for Swedish riding horses has been based on results from Riding Horse Quality Tests (RHQTs) of 4-year-olds only. Traits tested are conformation, gaits and jumping ability. An integrated index including competition results is under development to both get as reliable proofs as possible and increases the credibility of the indexes among breeders, trainers and riders. The objectives of this study were to investigate the suitability of competition data for use in genetic evaluations of horses and to examine how well young horse performance agrees with performance later in life. Competition results in dressage and show jumping for almost 40 000 horses from the beginning of the 1960s until 2006 were available. For RHQT data of 14 000 horses judged between 1988 and 2007 were used. Genetic parameters were estimated for accumulated competition results defined for different age groups (4 to 6 years of age, 4 to 9 years of age and lifetime), and for different birth year groups. Genetic correlations were estimated between results at RHQT and competitions with a multi-trait animal model. Heritabilities were higher for show jumping than dressage and increased with increasing age of the horse and amount of information. For dressage, heritabilities increased from 0.11 for the youngest group to 0.16 for lifetime results. For show jumping corresponding values increased from 0.24 to 0.28. Genetic correlations between competition results for the different age groups were highly positive (0.84 to 1.00), as were those between jumping traits at RHQT and competition results in show jumping (0.87 to 0.89). For dressage-related traits as 4-year-old and dressage competition results the estimated genetic correlations were between 0.47 and 0.77. We suggest that lifetime results from competitions should be integrated into the genetic evaluation system. However, genetic parameters showed that traits had changed during the over 35-year period covered due to the development of the sport, which needs to be considered in future genetic evaluations.Keywords: riding horses, dressage, show jumping, performance test, genetic parameters ImplicationsTo estimate reliable breeding values of Swedish Warmblood horses and to reduce bias due to pre-selection of horses for competition, it is important to integrate all available information from both young horse tests and competitions. Lifetime competition results are recommended and high genetic correlations were estimated between results in competition and results from tests of 4-year-old. The equestrian sport has changed during the 20th century, and this study shows that competition results do not mean the same throughout the 35-year long period of recording. Future studies will investigate how to handle competition data from different time periods in genetic evaluations.
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