Genetic correlations between horse show jumping competition traits in five European countries

Genetic correlations were computed for show jumping competition traits from national estimated breeding values (EBV) of stallions of five countries: Belgium, Denmark, France, Ireland and Sweden. Data involved 24,390 horses, i.e. 8993 stallions with EBV and their ancestors. There were 617 stallions with several EBVs in more than one country. Method involved MACE (Multi-Trait Across Country Evaluation) methodology based on deregressed proofs adapted to the existence of own performance for stallions and to missing EBVs for some ancestors. ASREML was used to estimate covariance with an equivalent multiple trait model described as a random regression model. Within country sire variances were considered as known. The estimated genetic correlations were high (0.86 to 0.88) especially for reliable estimates between Belgium, France, Sweden and between Sweden and Denmark, and relatively high (0.70 to 0.91) for other pairs. These results open perspectives for the international evaluation of sporthorses.     

Genetic relations of movement and free-jumping traits with dressage and show-jumping performance in competition of Dutch Warmblood horses

Genetic parameters for traits evaluated at the studbook entry inspection and genetic correlations with dressage and show-jumping performance in competition were estimated. Data comprised 36,649 Warmblood horses that entered the studbook between 1992 and 2002. The genetic analyses were performed using univariate and bivariate animal models. Heritabilities of the studbook entry traits were estimated in the range 0.15–0.40. The movement traits showed moderate to strong mutual genetic correlations, whereas the genetic correlations of movement traits with free-jumping traits were weak to moderate. The free-jumping traits showed strong to very strong mutual genetic correlations.

Competition results of 33,459 horses with performance in dressage and 30,474 horse with performance in show-jumping were linked to the studbook entry data to estimate the genetic relationship with performance in competition. Heritability estimates for dressage and show jumping were 0.14. Genetic correlations of the movement traits with dressage were moderate to strong, and with show-jumping weak to moderate. Genetic correlations of the free-jumping traits with dressage were weak to moderate and unfavourable. The free-jumping traits were genetically strong to very strong correlated to show-jumping. It was concluded that a selection of the traits evaluated at the studbook entry inspection will favourably contribute to estimation of breeding values for sport performance.     

Genetic parameters for strongyle and Nematodirus faecal egg counts in lambs and their relationships with performance traits

Genetic resistance to the gastro-intestinal parasites of lambs can contribute to sustainable systems of parasite control with associated benefits for health and welfare. This study reports estimates of the genetic parameters of strongyle egg counts (FEC), Nematodirus egg counts (NEM), faecal consistency scores (FCS) and their associations with growth and ultrasonic measurements of muscle (UMD) and fat (UFD) depths in lambs. The lambs were the progeny of 45 Bluefaced Leicester sires from Scottish Blackface and Hardy Speckled Face dams. Faecal samples were taken from lambs at 10, 14, 18, 22 and 26 weeks of age, giving 1024 to 3055 records per trait. Live weight was recorded for all lambs at 16 weeks and live weight, UMD and UFD were recorded in female lambs at 28 weeks. Mean FEC and NEM were significantly higher for twin versus single reared lambs, for male castrate versus female lambs and for the offspring of Scottish Blackface versus Hardy Speckled Face ewes. Heritability estimates for FEC were low (0.04 ± 0.02 to 0.20 ± 0.08) and showed a non-significant trend to increase with age. The phenotypic correlations between measures of FEC at different ages were low (0.06 to 0.34) but genetic correlations were not significantly different from one in most cases. Heritability estimates of NEM ranged from 0.05 ± 0.03 to 0.09 ± 0.05 and genetic correlations among counts at different ages were not significantly different from zero. FEC and NEM were strongly correlated genetically (0.62 to 0.93) and estimates of the genetic correlations between FEC and NEM with live weights (− 0.36 to 0.23), UMD (− 0.35 to 0.25) and UFD (0.08 to 0.55) were variable in sign, though not significantly different from zero. Heritability estimates for faecal consistency scores (FCS) were 0.06 ±0.03 to 0.11 ± 0.04, with strong genetic correlations between successive measures. FCS was not significantly correlated with FEC or lamb performance traits. It is concluded that selection for reduced strongyle egg counts in lambs at around 5–6 months of age will give favourable correlated responses in NEM in lambs, with limited correlated response in lamb performance or faecal consistency scores.     

Genetic analyses for linear conformation traits in Pura Raza Español horses

A linear assessment methodology was developed for the conformational data in the Pura Raza Español horse (Andalusian horse). The final design included 31 linear traits (20 primary and 11 secondary). A total of 4158 records from 2512 horses collected during 2008 and 2011 were included in the genetic evaluation. The genetic analyses were executed twice, the first one only with the first conformation assessment record of each animal (dataset 1: 2512 horses and records), and the second one, only for animals with more than one conformation records available (dataset 2: 876 horses and 2522 records). Genetic parameters were estimated using REML methodology (in a linear animal model), and age, sex, geographic region and combination of appraiser×event were included as fixed effects in the model. For the analysis with dataset 2, permanent environment was also included as random effect. The pedigree file traced back the relationships to include a total of 12,385 (dataset 1) and 3025 (dataset 2) horses. After the repeatability and reproducibility of the system were evaluated, according to our results, the appraisers used the whole scale and showed an adequate level of repeatability (≥0.95), and the reproducibility of analyzed traits was over 0.90 for all traits. Despite the fact that the quality of the morphological assessment can be considered adequate, further training is recommendable for appraisers in order to improve uniformity. Heritabilities with dataset 1 were low-moderate, ranging from 0.06±0.026 (angle of shoulder) to 0.35±0.044 (head length) for the primary traits, and from 0.08±0.032 (frontal angle of knee) to 0.23±0.035 (head-neck junction) for the secondary ones. Heritabilities found with dataset 2 were slightly lower than those obtained with dataset 1. Genetic correlations between traits were also obtained, which ranged from 0.92 to 0.00 in both datasets. These results must be taken into account in order to reduce the number of traits routinely collected in this population.     

Genetic analysis of six production traits in Peruvian alpacas

In this study a total of 6499 records were obtained for fibre diameter (FD) and coefficient of variation of FD (CV), 3283 records for greasy fleece weight (GFW), staple length (SL) and shearing interval (SI) and 1802 records of textile value index (TV) obtained from an experimental herd of alpacas exploited in the Peruvian Altiplano.The estimated heritabilities were: 0.412 ± 0.015 (FD), 0.321 ± 0.013 (CV), 0.098 ± 0.016 (GFW), 0.070 ± 0.011 (SL), 0.061 ± 0.012 (SI) and 0.163 ± 0.017 (TV). No significant genetic correlation was found for the pairs FD-CV and CV-GFW whilst the pairs FD-GFW, FD-SI and FD-TV had significant genetic correlations of, respectively, 0.405 ± 0.081, − 0.395 ± 0.078 and − 0.746 ± 0.049. No significant correlations were found for SL except for the pair SL-SI (0.397 ± 0.099). The TV index also showed significant genetic correlations with CV of 0.125 ± 0.061 and with GFW of 0.490 ± 0.070. All estimates of permanent environmental effects (c²) associated with the six analysed traits were statistically significant ranging from 0.008 for SI to 0.259 for CV. Total repeatability for the analysed traits was low for SI (0.069) and SL (0.090), moderate for TV (0.299) and GFW (0.316) and high for FD (0.578) and CV (0.579). The permanent environmental effect associated with CV is significantly correlated with those of the other traits except for FD. The permanent environmental effects associated with GFW and SL seemed to be basically the same (estimated correlation of 0.916 ± 0.062). The permanent environmental effect for TV is highly correlated with those associated with GFW (0.498 ± 0.058) and SL (0.750 ± 0.137). Expected selection response for TV was higher when FD was considered as selection goal instead of TV itself.It would, therefore, be more efficient to use FD rather than empirical indices as selection criterion to increase textile value in Peruvian alpacas. The reported genetic parameters and correlation matrices can be useful to implement multitrait breeding value estimations for alpaca selection.     

Estimates of non-genetic effects and genetic parameters for body measures and subjectively scored traits in Finnhorse trotters

This study examined non-genetic effects and genetic parameters of body measures and subjectively scored traits in the Finnhorse trotter population. The data was based on studbook inspections from 1971 to 2004 covering observations on 6381 horses. There were five body measures – height at withers, height at croup, circumference of girth, length of body and circumference of cannon bone – and six subjectively scored traits – character, body conformation, leg stances, quality of legs, hooves and movements – included in the analyses. Multivariate mixed models were applied with year–sex and age as fixed effects and animal as a random effect. The year–sex effect had a significant influence on body measures and scored traits. Age at judging had a significant influence on all traits but height at withers and body conformation. Heritability estimates were from 0.53 to 0.78 for body measures and 0.10 to 0.19 for scored traits. Genetic correlations between body measures were highly positive, from 0.75 to 0.98, whilst genetic correlations between scored traits varied between − 0.20 and 0.51. Genetic correlations between body measures and scored traits were mainly negative, from − 0.38 to 0.09. Our results indicate that additive genetic effects are relevant determinants for body measures of Finnhorse trotters. The scored traits were of low to moderate heritability and were relevantly influenced by environmental effects.     

Genetic parameters of racing performance traits of Quarter horses in Brazil

The data used in the present study were recorded at the Jockey Club of Sorocaba for 5094 racing performance of 1350 Quarter Horses at the Paulista Race Track of Sorocaba, state of São Paulo, Brazil, from 1991 to 1997. The considered traits were time and final rank. The model used in analysis included random animal and permanent environmental effects, and race, sex, age and origin as fixed effects. The variance and covariance components were estimated by the restricted maximum likelihood for an animal model, using the derivative-free process method and the MTDFREML software. For the time, heritability was 0.17 (0.05), while estimate of repeatability 0.55 (0.05). The lower heritability for the final rank, 0.13 (0.04), indicate that this trait is not the most appropriate one for inclusion in programs of Quarter horse selection in Sorocaba racetrack. The repeatability estimate for rank was 0.44 (0.04) and the genetic correlation between this trait and time was 0.99.     

A review of genetic parameter estimates for wool, growth, meat and reproduction traits in sheep

Genetic parameters for a range of sheep production traits have been reviewed from estimates published over the last decade. Weighted means and standard errors of estimates of direct and maternal heritability, common environmental effects and the correlation between direct and maternal effects are presented for various growth, carcass and meat, wool, reproduction, disease resistance and feed intake traits. Weighted means and confidence intervals for the genetic and phenotypic correlations between these traits are also presented. A random effects model that incorporated between and within study variance components was used to obtain the weighted means and variances. The weighted mean heritability estimates for the major wool traits (clean fleece weight, fibre diameter and staple length) and all the growth traits were based on more than 20 independent estimates, with the other wool traits based on more than 10 independent estimates. The mean heritability estimates for the carcass and meat traits were based on very few estimates except for fat (27) and muscle depth (11) in live animals. There were more than 10 independent estimates of heritability for most reproduction traits and for worm resistance, but few estimates for other sheep disease traits or feed intake. The mean genetic and phenotypic correlations were based on considerably smaller numbers of independent estimates. There were a reasonable number of estimates of genetic correlations among most of the wool and growth traits, although there were few estimates for the wool quality traits and among the reproduction traits. Estimates of genetic correlations between the groups of different production traits were very sparse. The mean genetic correlations generally had wide confidence intervals reflecting the large variation between estimates and relatively small data sets (number of sires) used. More accurate estimates of genetic parameters and in particular correlations between economically important traits are required for accurate genetic evaluation and development of breeding objectives.     

Genetic correlations between similar traits in the Danish and Swedish Warmblood sport horse populations

Genetic correlations between phenotypically similar or related traits tested at young horse performance tests for Danish Warmblood (DWB) and Swedish Warmblood (SWB) horses were calculated using Multi-trait Across Country Evaluation (MACE). Data comprised stallions with an estimated breeding value (EBV) from the national genetic evaluations (NGE) based on at least 10 progeny tested in performance tests, and the ancestors of those stallions in two generations. The DWB data included 349 stallions and the SWB data 426 stallions. Of these, 28 had EBVs in both DWB and SWB. Additionally 151 pedigree animals were common between DWB and SWB. The dependent variables used were NGE results of stallions born 1980 and later, which reduced the number of common stallions with EBVs to 23. The genetic correlations were very high for jumping traits (0.99) and dressage related traits (0.89–0.97). For conformation traits correlations varied between 0.10 and 0.98. Because of the high genetic correlations and frequent use of same or closely related foreign stallions, breeders of both DWB and SWB would benefit from using the NGEs for performance traits across countries, although the genetic correlations do not consider differences in genetic merit levels between the populations. It would be feasible to perform a joint genetic evaluation using MACE, which would improve the reliability of estimated breeding values, and enable ranking of all stallions according to the national scale of each country.     

Genetic parameters for feed efficiency traits and their relationships with growth and carcass traits in Duroc pigs

Genetic parameters for feed efficiency traits of 380 boars and growth and carcass traits of 1642 pigs (380 boars, 868 gilts and 394 barrows) in seven generations of Duroc population were estimated. Feed efficiency traits included the feed conversion ratio (FCR), and nutritional (RFI(nut)), phenotypic (RFI(phe)) and genetic (RFI(gen)) residual feed intake. Growth and carcass traits were the age to reach 105-kg body weight (A105), loin eye muscle area (EMA), backfat (BF), intra-muscular fat (IMF) and meat tenderness. The mean values for RFI(phe) and RFI(gen) were close to zero and for RFI(nut) was negative. All the measures of feed efficiency were moderately heritable (h(2) = 0.31, 0.38, 0.40 and 0.27 for RFI(nut), RFI(phe), RFI(gen) and FCR respectively). The heritabilities for all growth and carcass traits were moderate (ranged from 0.37 to 0.45), except for BF, which was high (0.72). The genetic correlations of RFI(phe) and RFI(gen) with A105 were positive and high. Measures of RFI were correlated negatively with EMA. BF was more strongly correlated with measures of RFI (r(g) > or = 0.73) than with FCR (r(g) = 0.52). Selection for daily gain, EMA, BF and IMF caused favourable genetic changes in feed efficiency traits. Results of this study indicate that selection against either RFI(phe) or RFI(gen) would give a similar correlated response in carcass traits.     

Genetic parameters and trends for production and reproduction traits in Thai Landrace sows

Data from Thai Landrace sows were used to estimate the genetic parameters and trends for production and reproduction traits, over the first four parities. The reproduction traits investigated were age at first conception (AFC), total number of piglets born per litter (TB) and weaning to first service interval (WSI). The reproduction data was gathered from 9194 litters born between 1993 and 2005. The production measures were average daily gain (ADG) and backfat thickness (BF). These were recorded from 4163 boars and 15 171 gilts. Analyses were carried out using a multivariate animal model inputting average information restricted maximum likelihood procedures. Heritability estimates on the reproduction traits for AFC was 0.21, for TB in the first four parities it ranged from 0.02 to 0.11 and for WSI over the first three parities it ranged from 0.16 to 0.18. Heritability estimates for production traits were: 0.31 (ADG) and 0.45 (BF). AFC was genetically correlated favorably with TB (− 0.48) and WSI (0.35) in the first parity. Genetic trends were 4.71 g, − 0.23 mm and 0.23 days per year for ADG, BF and AFC respectively. There was no genetic progress for the other traits. It was concluded that selection for low AFC will increase TB and decrease WSI. The results further revealed that the ongoing selection being used improved growth rate and reduced backfat thickness. However, there was no genetic improvement in TB.     

Genetic parameters of growth and in vivo computerized tomography based carcass traits in Pannon White rabbits

Genetic parameters for average daily gain between the age of 5 and 10 weeks (ADG), the average cross-sectional area of the m. Longissimus dorsi (L) (between the 2nd–3rd and 4th–5th lumbar vertebrae-based on in vivo computerized tomography (CT)) and dressing out percentage (DoP) were estimated in a group of 28,686 Pannon White rabbits reared in 5044 litters and born between 2000 and 2003. Using multivariate animal models with Bayesian procedures, estimated heritabilities were moderate and moderately high for ADG, L and DoP (0.21 to 0.29, 0.25 to 0.42 and 0.19 to 0.71, respectively). Litter effects were moderate for ADG, L and DoP estimates (0.20 to 0.22, 0.10 to 0.18 and 0.09 to 0.30, respectively). Genetic correlation coefficient estimates between ADG and L and ADG and DoP were moderate and negative (− 0.41 to − 0.01, − 0.70 to + 0.10). A moderately high positive genetic correlation was found between L and DoP (0.13 to 0.83).     

Heritability of clinical tail-biting and its relation to performance traits

Clinical tail-biters were identified over a 12-month period at a commercial nucleus pig-breeding farm that had a history of tail-biting problems. The breed, gender, and relative size of the tail-biters were recorded. Using pedigree data for all the pigs on the farm at the time of observations, the heritability of the tail-biting behaviour was estimated for purebred Large White (LW) and Landrace (LR) pigs. The incidence of tail-biting was 2.8% for Large White and 3.5% for Landrace (breed effects, P<0.10). Tail-biting was found to be heritable in Landrace (h²=0.05±0.02, P<0.05 as a 0-1 trait, equivalent to h²=0.27 as a continuous trait), but not heritable in Large White pigs (h²=0.00±0.00, as a 0-1 trait). In the Landrace population, tail-biting was unfavourably genetically correlated with leanness [lean tissue growth rate (LTGR; r_g=0.27, P<0.05), and back fat (BF) thickness at 90 kg (r_g=−0.28, P<0.05)]. It is concluded that past selection for desirable production traits may have resulted in increased predisposition to exhibit tail-biting behaviour. From the correlations and covariance matrix reported, it would be possible to develop a selection index to reduce the predisposition to exhibit tail-biting behaviour through selective breeding.     

Estimation of genetic parameters of conformation traits in Iranian Thoroughbred horses

The aim of this study was to estimate the genetic parameters of conformation traits in Iranian Thoroughbred race horses. The data set included the conformation records of 607 Thoroughbred horses. In this study, 10 conformation traits were recorded. The effect of sex was significant for length of back line (P < 0.05), withers height (P < 0.05), circumference of front cannon (P < 0.001), and circumference of hind cannon (P < 0.001). The effect of age was significant for all traits (P < 0.01). The genetic parameters were estimated by the restricted maximum likelihood (REML) method using DFREML program. The heritability estimates were for head length 0.39, length of back line 0.41, length of shoulder 0.24, heart girth 0.49, chest width 0.22, withers height 0.38, front cannon height 0.27, circumference of front cannon 0.30, hind cannon height 0.29 and circumference of hind cannon 0.34. The estimates of genetic correlation ranged from 0.18 to 0.96 and those of phenotypic correlation varied from 0.16 to 0.83.     

Genetic and phenotypic parameter estimates for growth traits in Boer goat

An understanding of influencing factors and genetic principles affecting the growth traits is needed to implement optimal breeding and selection programs. In this study, heritabilities (direct additive and maternal) of body weights at birth (BW0), 90 days (BW90) and 300 days (BW300) of age and average daily gains from birth to 90 days (ADG0-90), birth to 300 days (ADG0-300) and 90 days to 300 days (ADG90–300) of age in Boer goats were estimated on the basis of 1520 Boer goats at Boer Goat Breeding Station in Yidu, China, during 2002–2007. The parameters were estimated using a DFREML procedure by excluding or including maternal genetic or permanent maternal environmental effects, four analysis models were fitted in order to optimize the model for each trait. Influencing factors such as parity, litter size, kidding year and season, as well as sex of kids and some significant interactions among these factors were investigated as the fixed effects for the models. The results showed that the birth year and maternal genetic effects such as parity and litter size of dam were important determinants of the genetic parameter estimates for pre-weaning growth traits, and environmental effects such as birth year, season and sex of kids had some significant effect on post-weaning growth traits. The mean values and standard errors (SE) of direct additive heritability estimates calculated with the optimum model were 0.17 ± 0.07, 0.22 ± 0.08, 0.07 ± 0.07, 0.10 ± 0.08, 0.30 ± 0.12 and 0.08 ± 0.10 for BW0, BW90, ADG0-90, BW300, ADG0-300 and ADG90–300, respectively. For pre-weaning weights, correlation estimates between direct additive and maternal genetic (r_a–m) effect were high and negative ranging from − 0.74 to − 0.86.     

Genetic parameters for testes traits in swine

Data were collected from 1,245 Duroc boars and 527 Yorkshire boars. This represents 128 Duroc and 57 Yorkshire sires. Body weights, testis length and combined testes width at 140 and 168 d were obtained. Of these boars, 432 were castrated at a later age to evaluate relationships between in situ measures and excised testis traits. Heritabilities for testis length, width and volume at 140 d ranged from .16 to .25 in both Duroc and Yorkshire data. Heritabilities for testis measurements at 168 d ranged from .16 to .36 in both data sets. Favorable negative genetic relationships were found between in situ testis measures and age to 104 kg and backfat adjusted to 104 kg. Correlations among in situ measurements were high and positive. All excised testicular traits were highly heritable except for right epididymis weight and excised testis width. Correlation estimates among excised testis traits were generally positive. Phenotypic and genetic correlation estimates between live (in situ testis and growth performance traits) measurements and excised testis traits were generally favorable. This study suggests that in situ testis measurements should be good predictors of sperm production. It also suggests that selection for testis size should not be antagonistic to selection for growth performance traits.     

Genetic analysis of behavior traits in swine production

Estimates of genetic parameters related to pig behavior under stressful situations are required before selection programs can be designed to produce more docile pigs. Pig behavior was evaluated in a pedigreed Landrace–Duroc–Yorkshire composite population. Piglets were evaluated for their response to handling at 1 d of age (n=11069), being placed on their back for 60 s at ~24 d of age (n=975), and being confined in a scale while backfat measurements were being collected (n=9035). Feeding behavior was monitored in a growing–finishing facility (n=1162) including preferences for feeding positions. Feeders were placed along a fence with one end adjacent to a gate (gate-end) and the other end open. An animal model was fitted to the data using WOMBAT where litter was included for d 1 activity scores and backtest traits. Fixed effects of sex, pen/year-season/date of collection in all analyses along with scorer (d 1 activity score) and a covariate of age (d 154 weight and backfat). Multiple trait models were fit to estimate genetic covariances among traits. All estimates of heritability were significantly different than zero. Activity scores and backtest traits had the lowest estimates of heritability (0.15–0.19), measures of feeding behavior were more variable (0.16–0.60) while production data had high heritabilities (>0.5). Genomic heritability estimates were similar to standard heritability estimates for most traits, except traits measured at a young age. All traits measured during the backtest had strong genetic correlations and similar estimated heritability. Among feeding behavior traits, number of meals/d and average meal length were highly correlated with total daily meal time. In addition, animals that preferred to eat alone avoided the open-end position at the feeder. The only behavioral traits with genetic correlations significantly different from zero with production traits were associated with feeding behavior where animals that ate longer meals and spent more time at the feeder/d tended to be heavier and fatter at 154 d. In addition, animals that ate more meals/d were fatter and animals that preferred the gate-end position of the feeder were heavier. Pigs with more reactive personalities tended to eat fewer meals/d, each longer in duration, and they preferred the gate-end feeder position. The measures of pig behavior studied were heritable and selection for more docile pigs should not have large detrimental effects on performance.     

Genetic correlations between competition traits and traits scored at breeding field-tests in Icelandic horses

Relationships between breeding field-test traits and competition traits were studied to investigate whether the latter could be usefully included in the genetic evaluation of Icelandic horses. The current method of genetic evaluation is based on records from breeding field-tests only. The breeding field-test data included 16 401 individual records of Icelandic horses evaluated in 11 countries during 1990–2005. Competition results included 18 982 records of 3790 horses competing in sport and gæðinga competitions in Iceland and Sweden during 1998–2004. In the breeding field-tests, eight conformation traits and eight riding ability traits were scored; height of withers was also recorded. These traits were analysed together with the competition traits tölt(comp), 4-gait, 5-gait and pace test, in bivariate analyses. Animal models were used; the fixed effects for breeding field-test traits included sex by age interaction and country by year interaction. For the competition traits the model included fixed effects of sex, age and event, and a random permanent environmental effect. Estimated heritabilities and genetic correlations for breeding field-test traits were consistent with earlier results; heritabilities ranged from 0.20 to 0.67, and moderate to high genetic correlations were estimated between many of the riding ability traits, and between riding ability traits and some conformation traits. The estimated heritabilities for competition traits were about 0.20, and genetic correlations between competition traits varied from − 0.12 to 1.00. In general, high genetic correlations were estimated between breeding field-test riding ability traits and competition traits. Moderately positive genetic correlations were found between some breeding field-test conformation traits and competition traits. Competition traits add information relating to the breeding goal of the Icelandic horse; they should therefore be added to genetic evaluation in future.     

Genetic analysis of competition data on Icelandic horses

In a study of the possibility of using competition data in the genetic evaluation of Icelandic horses, data from competitions held in Iceland between 1999 and 2004 and in Sweden between 1998 and 2004 were analyzed to estimate the genetic parameters of competition performance traits. The data-sets from both countries included 18 982 records of 3790 horses in 379 different events. Two types of competition were included: sport competitions and gæðinga competitions performed on oval tracks and on a straight track. Each type of competition involves several disciplines in which the horses are ridden in the various gaits. The traits analyzed were two different measures of four-gait, five-gait and tölt, and one pace trait. In both the four-gait and five-gait tests the gaits walk, trot, tölt and gallop are exhibited. In the five-gait test, pace is also exhibited. The traits tölt and pace are performances of these single gaits. Highly correlated and similar traits were combined, and three new traits relating to tölt, four-gait and five-gait were formed. No large differences in means or standard deviations of traits were found between countries. All traits were approximately normally distributed. Genetic parameters were estimated using linear animal models including the fixed effects of sex, age and event for all traits, and the level of discipline was included for some traits. Random permanent environmental effects were also included. Estimated heritabilities were moderate to high, ranging from 0.18 to 0.21 for sport-competition traits, from 0.33 to 0.35 for gæðinga-competition traits and from 0.19 to 0.22 for combined traits. Estimated genetic correlations between different sport-competition traits varied from 0.63 to 0.96, and between the two gæðinga-competition traits it was estimated at 0.43. Genetic correlations between sport- and gæðinga-competition traits ranged from − 0.42 to 1.00. It was concluded that competition traits are suitable to include in genetic evaluations.     

A Note on the Heritability of Reactivity Assessed at Field Tests for Danish Warmblood Horses

Temperament traits in horses, especially reactivity, are an important trait in relation to human–horse accidents and the welfare of the horses. However, so far, temperament is often not included in many horse breeding programs. Most of the behavioral genetic studies in horses have been based on indirect indications of a sire effect and not on estimations of the heritability of temperament traits. Therefore, the aim of this study was to estimate the heritability of behavior reactions related to reactivity observed in a practical situation, that is, during the evaluation of the conformation of the horse at field tests. The study included 323 3-year-old Warmblood horses. Data were analyzed according to an animal model, and the estimation was based on restricted maximum likelihood. Results showed a low (0.17) heritability of reactivity. Probably because of the limited number of horses in the study, a high standard error was untainted. Nevertheless, results suggested a genetic variation of reactivity when assessed at field tests, but further research is needed before reactivity can be incorporated as a selection criteria into a breeding program.