Genetic correlations between ewe reproduction and carcass and meat quality traits in Merino sheep

Genetic correlations between reproduction traits in ewes and carcass and meat quality traits in Merino rams were obtained using restricted maximum likelihood procedures. The carcass data were from 5870 Merino rams slaughtered at approximately 18 months of age that were the progeny of 543 sires from three research resource flocks over 7 years. The carcass traits included ultrasound scan fat and eye muscle depth (EMDUS) measured on live animals, dressing percentage and carcass tissue depth (at the GR site FATGR and C site FATC), eye muscle depth, width and area and the meat quality indicator traits of muscle final pH and colour (L*, a*, b*). The reproduction data consisted of 13 464 ewe joining records for number of lambs born and weaned and 9015 records for LS. The genetic correlations between reproduction and fat measurements were negative (range ?0.06 ± 0.12 to ?0.37 ± 0.12), with smaller correlations for live measurement than carcass traits. There were small favourable genetic correlations between reproduction traits and muscle depth in live rams (EMDUS, 0.10 ± 0.12 to 0.20 ± 0.12), although those with carcass muscle traits were close to zero. The reproduction traits were independent of meat colour L* (relative brightness), but tended to be favourably correlated with meat colour a* (relative redness, 0.12 ± 0.17 to 0.19 ± 0.16). There was a tendency for meat final pH to have small negative favourable genetic correlations with reproduction traits (0.05 ± 0.11 to ?0.17 ± 0.12). This study indicates that there is no antagonism between reproduction traits and carcass and meat quality indicator traits, with scope for joint improvement of reproduction, carcass and meat quality traits in Merino sheep.     

Genetic selection for increased mean and reduced variance of twinning rate in Belclare ewes

It is sometimes possible to breed for more uniform individuals by selecting animals with a greater tendency to be less variable, that is, those with a smaller environmental variance. This approach has been applied to reproduction traits in various animal species. We have evaluated fecundity in the Irish Belclare sheep breed by analyses of flocks with differing average litter size (number of lambs per ewe per year, NLB) and have estimated the genetic variance in environmental variance of lambing traits using double hierarchical generalized linear models (DHGLM). The data set comprised of 9470 litter size records from 4407 ewes collected in 56 flocks. The percentage of pedigreed lambing ewes with singles, twins and triplets was 30, 54 and 14%, respectively, in 2013 and has been relatively constant for the last 15 years. The variance of NLB increases with the mean in this data; the correlation of mean and standard deviation across sires is 0.50. The breeding goal is to increase the mean NLB without unduly increasing the incidence of triplets and higher litter sizes. The heritability estimates for lambing traits were NLB, 0.09; triplet occurrence (TRI) 0.07; and twin occurrence (TWN), 0.02. The highest and lowest twinning flocks differed by 23% (75% versus 52%) in the proportion of ewes lambing twins. Fitting bivariate sire models to NLB and the residual from the NLB model using a double hierarchical generalized linear model (DHGLM) model found a strong genetic correlation (0.88 ± 0.07) between the sire effect for the magnitude of the residual (V_E) and sire effects for NLB, confirming the general observation that increased average litter size is associated with increased variability in litter size. We propose a threshold model that may help breeders with low litter size increase the percentage of twin bearers without unduly increasing the percentage of ewes bearing triplets in Belclare sheep.     

Genetic parameters for production traits in New Zealand dual-purpose sheep, with an emphasis on dagginess

Genetic and phenotypic parameters were estimated for production and disease traits (including dagginess) from about 2 million pedigree-recorded animals born between 1990 and 2008 in New Zealand dual-purpose ram breeding flocks. This is the most comprehensive study of genetic parameter estimates for the New Zealand sheep industry to date and includes estimates that have not previously been reported. Estimates of heritability were moderate for BW at 8 mo (LW8), fleece weight at 12 mo (FW12), dagginess score at 3 and 8 mo (DAG3, DAG8; 0.31 to 0.37), typical for weaning weight (WWT), fecal egg count in summer (FEC1) and autumn (FEC2), and analogous Nematodirus counts (NEM1, NEM2; 0.17 to 0.21), and low for number of lambs born to ewes (NLB; 0.09). The genetic correlations among production traits, WWT, LW8, and FW12, were positive and moderate to high. Correlations of DAG3 and DAG8 with production and disease traits were low and mostly negative. The NLB had low, but typically positive, correlations with other traits. Disease traits also had low, but positive, correlations with production traits (WWT, LW8, and FW12), and were highly correlated among themselves. In general, the heritability estimate for BW and dagginess were greater than what is currently used in the New Zealand genetic evaluation service (Sheep Improvement Limited), and the availability of accurate estimates for dagginess plus parasite resistance and their genetic correlations with production traits will enable more accurate breeding values to be estimated for New Zealand sheep.     

Phenotypic and genetic parameter estimates for reproductive traits in Zandi sheep

This study reports on the phenotypic and genetic (co)variance components for reproductive traits in Zandi sheep, using between 1,859 and 2,588 records obtained from 577 ewes. The data were collected from the Khojir Breeding Station of Zandi sheep in Tehran, Iran from 1994 to 2008. The basic traits were litter size at birth (LSB), litter size at weaning (LSW), litter mean weight per lamb born (LMWLB), and litter mean weight per lamb weaned (LMWLW), and the composite traits were total litter weight at birth (TLWB) and total litter weight at weaning (TLWW). Genetic analyses were carried out using the restricted maximum likelihood method that was explored by fitting the additive direct genetic effects and permanent environmental effects of the ewes as random effects and the ewe age at lambing and lambing year as fixed effects for all of the investigated traits. Akaike’s information criterion was used to choose the most appropriate model. LSB, LSW, LMWLB, LMWLW, TLWB, and TLWW direct heritability estimates were 0.07, 0.05, 0.12, 0.10, 0.08, and 0.14, respectively. The estimated fractions of variance due to the permanent environmental effects of the ewe ranged from 0.03 for LMWLB to 0.08 for LMWLW and TLWW. Corresponding repeatability estimates ranged from 0.10 for LSW to 0.22 for TLWW. Direct genetic correlations varied from ?0.61 for LSB–LMWLB to 0.88 for LSB–LSW and LSB–TLWB. Results indicate that genetic change depends not only on the heritability of traits, but also on the observed phenotypic variation; therefore, improvement of non-genetic factors should be included in the breeding programs.     

Influence of maternal and additive genetic effects on offspring growth traits in Beetal goat

The purpose of the present study was to obtain estimates of variance components and genetic parameters for direct and maternal effects on various growth traits in Beetal goat by fitting four animal models, attempting to separate direct genetic, maternal genetic and maternal permanent environmental effects under restricted maximum likelihood procedure. The data of 3,308 growth trait records of Beetal kids born during the period from 2004 to 2019 were used in the present study. Based on best fitted models, the direct additive h² estimates were 0.06, 0.27, 0.37, 0.17 and 0.10 for birth weight (BWT), weight at 3 (WT3), 6 (WT6), 9 (WT9) and 12 (WT12) months of age, respectively. Maternal permanent environmental effects significantly contributed for 10% and 7% of total variance for BWT and WWT, respectively, which reduced direct heritability by 40 and 10% for respective traits from the models without these effects. For average daily gain (ADG1) and Kleiber ratios (KR1) up to weaning period (3 months) traits, maternal permanent environmental effects accounted for 7% and 8% of phenotypic variance, respectively, and resulted in a reduction of 6.6% and 5.4% in direct h² of respective traits. For post-weaning traits, the maternal effects were non-significant (p > .05) which indicates diminishing influence of mothering ability for these traits. High and positive genetic correlations were obtained among WT3-WT6, WT6-WT9 and WT9-WT12 with correlations of 0.96 ± 0.25, 0.84 ± 0.23 and 0.90 ± 0.13, respectively. Thus, early selection at weaning age can be practised taking into consideration maternal variation for effective response to selection in Beetal goat.     

Estimation of genetic parameters for reproductive traits in shall sheep

The objective of this study was to estimate genetic parameters for reproductive traits in Shall sheep. Data included 1,316 records on reproductive performances of 395 Shall ewes from 41 sires and 136 dams which were collected from 2001 to 2007 in Shall breeding station in Qazvin province at the Northwest of Iran. Studied traits were litter size at birth (LSB), litter size at weaning (LSW), litter mean weight per lamb born (LMWLB), litter mean weight per lamb weaned (LMWLW), total litter weight at birth (TLWB), and total litter weight at weaning (TLWW). Test of significance to include fixed effects in the statistical model was performed using the general linear model procedure of SAS. The effects of lambing year and ewe age at lambing were significant (P?<?0.05). Genetic parameters were estimated using restricted maximum likelihood procedure, under repeatability animal models. Direct heritability estimates were 0.02, 0.01, 0.47, 0.40, 0.15, and 0.03 for LSB, LSW, LMWLB, LMWLW, TLWB, and TLWW, respectively, and corresponding repeatabilities were 0.02, 0.01, 0.73, 0.41, 0.27, and 0.03. Genetic correlation estimates between traits ranged from ?0.99 for LSW–LMWLW to 0.99 for LSB–TLWB, LSW–TLWB, and LSW–TLWW. Phenotypic correlations ranged from ?0.71 for LSB–LMWLW to 0.98 for LSB–TLWW and environmental correlations ranged from ?0.89 for LSB–LMWLW to 0.99 for LSB–TLWW. Results showed that the highest heritability estimates were for LMWLB and LMWLW suggesting that direct selection based on these traits could be effective. Also, strong positive genetic correlations of LMWLB and LMWLW with other traits may improve meat production efficiency in Shall sheep.     

Genetic parameters for ewe productivity traits in the Columbia, Suffolk and Targhee breeds

Estimates of repeatability and heritability were obtained for the following productivity traits of ewes: litter weight at birth (LWB) and weaning (LWW), litter size at birth (LSB), litter size alive at birth (NBA), litter size at weaning (LSW), neonatal survival rate (SRB) and preweaning survival rate (SRW). Phenotypic and genetic correlations were estimated for litter traits. The data set contained 6,394 ewe breeding records from three state stations over 10 yr on 1,731 ewes that were the progeny of 488 sires among three breeds (Columbia, Suffolk and Targhee). Pooled intra-station estimates of repeatability ranged from .11 to .22 for LWB and LWW among the three breeds. For litter size at birth, number born alive and litter size at weaning these estimates varied from .09 to .17 and for the survival traits (SRB and SRW) the variation was from .11 to .20. Intra-station estimates of heritability for the three breeds varied from .12 to .28 for LWB and LWW, and for LSB, NBA and LSW estimates varied from .05 to .35. Heritability estimates for survival traits (SRB and SRW) were low, ranging from .00 to .14. Phenotypic correlations among LWB, LWW, NBA and LSW ranged from .35 to .92 among the breed-station subclasses, with higher correlations occurring where a part-whole relationship existed. The study suggests that selection of ewes with high litter size at birth or at weaning and(or) litter weight at birth or at weaning will genetically improve total litter weight at weaning per ewe lambing.     

Genetic (co)variance components for ewe productivity traits in Katahdin sheep

The objective of this study was to estimate genetic parameters, in Katahdin sheep, for total weight of litter weaned per ewe lambing (TW) and its components, number of lambs born (NB), number of lambs weaned (NW), and average weight of lambs weaned (AW) measured as traits of the ewe. Weaning weights of lambs (WW) were adjusted to 60 d of age and for effects of ewe age, lamb sex, and type of birth and rearing and averaged over all lambs in the litter to obtain AW. The 60-d age-adjusted WW were adjusted for ewe age and lamb sex and summed over all lambs in the litter to obtain TW. A total of 2,995 NB and NW records, 2,622 AW, and 2,714 TW records were available from 1,549 ewes (progeny of 235 sires) over 4 yr. Heritabilities were initially estimated for each trait from univariate REML analyses. Estimates of genetic correlations were obtained from bi- and trivariate analyses. Models for NB, NW, AW, and TW included random ewe additive and permanent environmental effects. A random service sire effect was also fit for AW and TW. Heritabilities of TW, NB, NW, and AW from univariate analyses were 0.12, 0.12, 0.09, and 0.13 (all P < 0.01), respectively. Permanent environmental effects were significant (P < 0.01) for TW and AW. Genetic correlations of TW with NB, NW, and AW ranged from 0.27 to 0.33, 0.88 to 0.91, and 0.72 to 0.76, respectively; those of NB with NW and AW ranged from 0.70 to 0.75 and -0.01 to 0.02, respectively; and that between NW and AW ranged from 0.40 to 0.55. Genetic parameters were also obtained for lamb survival to weaning (LS) and WW measured as traits of the lamb, and the relationships between WW of the ewe as a lamb and her subsequent records for NB and NW were also estimated. A total of 5,107 LS and 5,444 WW records were available. Models for WW and LS included random animal and maternal genetic, maternal permanent environmental, and litter effects. Heritability of WW ranged from 0.15 to 0.20. There was no evidence of genetic effects on LS. Direct genetic correlations of WW with NB and NW were not significantly different from zero. The correlation between maternal genetic effects on WW, and animal genetic effects on NW, averaged 0.35. Results of this study indicate that there are no major antagonisms among TW and its components, so that selection for TW would not have adverse effects on any component traits and vice versa. Maternally superior ewes for WW appear to also be somewhat superior for NW.     

Performance of Djallonké Sheep under an Extensive System of Production in Faranah,Guinea

A total of 147 ewes, 4 rams and 188 lambs of their progeny of the Djallonké breed of sheep were used to study the factors affecting reproductive and growth traits and the causes of lamb mortality. Data on ewes were collected during a 12-month period, while those on the lambs born to 123 of the ewes were collected until they were 12 months of age. The average fertility and abortion rates were 0.84 and 0.09. The fertility rate increased and the abortion rate decreased with increasing age of the ewes (p<0.05). The number of lambs born per ewe joined, litter weight at birth per ewe joined and litter weight at weaning per ewe joined were 1.28, 3.5 kg and 17 kg, respectively. The average numbers of lambs born per ewe, lambs born alive per ewe, lambs born dead per ewe and lambs per ewe that died between birth and weaning were 1.53, 1.43, 0.03 and 0.3, respectively. The age of the ewes significantly (p<0.05) affected all these traits except the number of dead lambs and the index of fertility (94%). The age of the ewes significantly (p<0.05) affected the birth weight and the weight at 6 and 12 months of age, whereas the lambing season significantly (p<0.05) affected all the growth traits studied. The type of birth was the most important source of variation in body weights of lambs. Sex had no significant (p>0.05) effect on the growth traits studied. The complex `starvation–bad management–light body weight at birth' caused 48% of the lamb mortality between birth and weaning, while diarrhoea, pneumonia and internal and external parasites caused approximately 52% of the lamb mortality over the same period. The seasonal raw mortality rate of the lambs before weaning was highest in the humid season.     

Genetic variation of plasma insulin-like growth factor-1 in young crossbred ewes and its relationship with their maintenance feed intake at maturity and production traits

The genetic variation of plasma IGF-I in crossbred ewe lambs postweaning was evaluated together with its potential use as a physiological marker for selection in meat sheep. Genetic variation for IGF-I was analyzed among 1,246 young crossbred ewes that were the progeny of 30 sires from various maternal breeds and Merino dams. The estimate of heritability of IGF-I was 0.28 +/- 0.10, with sire breed not being significant. Genetic correlations were estimated between IGF-I and performance traits of the ewes, including feed intake, growth, body composition, wool, and reproduction over 3 matings. Although the genetic correlations had high standard errors because of the limited size of the data set, the correlation between IGF-I and grazing feed intake of the mature ewes at maintenance was positive (0.32 +/- 0.31). The genetic correlations of IGF-I with other traits ranged from positive and low to moderate for growth (0.05 to 0.36), positive for ultrasound eye muscle depth (0.15), and negative for ultrasound fat depth (-0.12) in the mature ewes, and close to zero for the wool traits. The genetic correlation between IGF-I and the average number of lambs born per ewe mated was negative (-0.18), whereas that for the average number of lambs weaned per ewe mated was positive (0.10). The parameters indicated that genetic variation exists for IGF-I in sheep, and selection for low IGF-I in young ewes may result in some reduction in feed intake and improvement in maintenance efficiency of mature ewes under grazing, with little impact on other production traits. However, the genetic correlations had high standard errors, and more precise estimates of these parameters are required for genetic evaluation and to predict with confidence the outcome of breeding programs.     

Genetic correlations among and between wool, growth and reproduction traits in Merino sheep

Summary Data from seven research resource flocks across Australia were combined to provide accurate estimates of genetic correlations among production traits in Merino sheep. The flocks represented contemporary Australian Merino fine, medium and broad wool strains over the past 30 years. Over 110 000 records were available for analysis for each of the major wool traits, and 50 000 records for reproduction and growth traits with over 2700 sires and 25 000 dams. Individual models developed from the single trait analyses were extended to the various combinations of two-trait models to obtain genetic correlations among six wool traits [clean fleece weight (CFW), greasy fleece weight, fibre diameter (FD), yield, coefficient of variation of fibre diameter and standard deviation of fibre diameter], four growth traits [birth weight, weaning weight, yearling weight (YWT), and hogget weight] and four reproduction traits [fertility, litter size, lambs born per ewe joined, lambs weaned per ewe joined (LW/EJ)]. This study has provided for the first time a comprehensive matrix of genetic correlations among these 14 wool, growth and reproduction traits. The large size of the data set has also provided estimates with very low standard errors. A moderate positive genetic correlation was observed between CFW and FD (0.29 ± 0.02). YWT was positively correlated with CFW (0.23 ± 0.04), FD (0.17 ± 0.04) and LWEJ (0.58 ± 0.06), while LW/EJ was negatively correlated with CFW (−0.26 ± 0.05) and positively correlated with FD (0.06 ± 0.04) and LS (0.68 ± 0.04). These genetic correlations, together with the estimates of heritability and other parameters provide the basis for more accurate prediction of outcomes in complex sheep-breeding programmes designed to improve several traits.     

Reproductive performance and genetic parameters in first cross ewes from different maternal genotypes

The reproduction of 2,846 crossbreed ewes with 7,899 records is reported. The ewes were progeny of mainly Merino dams and 91 sires from several maternal sire breeds including Border Leicester, East Friesian, Finnsheep, Coopworth, Corriedale, Booroola Leicester, and several others. There were 3 cohorts of ewes at each of 3 sites that were bred naturally to meat-type rams for each of 3 yr to evaluate reproduction and lamb production. At 2 sites, the ewes were mated in the autumn, first at 7 mo of age, and at 2 sites the ewes were mated in the spring, first at 14 or 17 mo of age. The cohorts of ewes and sites were genetically linked by 3 common sires. Mixed linear models were used to analyze ultrasound scanned pregnancy rate, fetal number, fertility (ewes lambing), litter size, lamb survival, number of lambs born (NLBj), number of lambs weaned (NLWj), and total weight of lamb weaned (TWWj) per ewe bred. Fixed effects included sire breed (1 to 10), environment (1 to 4, site and season of breeding: autumn, spring), breeding (1 to 3), cohort (1 to 3), and their interactions. The REML procedures were used to estimate (co)variance components. Ewe sire breed effects were significant (P < 0.01) for all the reproductive traits and breed means ranged from 0.75 to 0.96 for fertility, 1.22 to 2.08 for litter size, 0.70 to 0.90 for lamb survival, 0.99 to 1.66 for NLBj, 0.87 to 1.26 for NLWj, and 22.9 to 33.8 kg for TWWj, with the ranking of sire breeds varying for different traits. For all traits except lamb survival, the contrast between breeding 1 vs. 2 and 3 was considerably greater than the contrast between breeding 2 vs. 3, with significant environment x breeding interactions (P < 0.01). Estimates of heritability for the components of reproduction ranged from 0.03 +/- 0.02 for lamb survival to 0.19 +/- 0.05 for litter size, and those for the composite traits were 0.17 +/- 0.04 for NLBj, 0.13 +/- 0.04 for NLWj, and 0.17 +/- 0.04 for TWWj, with repeatability ranging from 0.10 to 0.19. Genetic and phenotypic correlations among the traits are reported. The significant variation among sire breeds of the crossbred ewes can be used to improve reproduction, although there was a change in the rank of the breeds for the various traits. There was considerable overlap between the breeds, and additional improvement could be achieved by exploiting the genetic variation between sires within breeds for all the ewe reproductive traits.     

Parameter estimates for number of lambs born at different ages and for 18-month body weight of Rambouillet sheep

Genetic parameters were estimated using REML with animal models for number of lambs born and 18-mo body weight in Rambouillet sheep. Number of lambs born was modeled either as repeated measurements on the same trait or as different traits at different ages. The original data for number of lambs born were separated according to age of the ewe into two classes: 2 and 3 yr, and older than 3 yr. Numbers of ewes with lambing records for the age classes were 653 and 466 with 1,106 and 1,118 records, respectively. For the data set that included all ages, the number of ewes was 684 with 2,224 records, and for 18-mo body weight the number of ewes measured was 557. For number of lambs born, the animal model included random genetic, permanent environmental, and residual environmental effects and fixed effects for age of ewe, year of lambing, and month of year of lambing. Lambing day within season was used as a covariate. For 18-mo body weight, year of birth of ewe was used as a fixed effect. Actual age in days when the ewe was weighed was used as a covariate. Estimates of heritability for number of lambs born by age group were .04, for 2- and 3-yr old ewes, and .06, for ewes greater than 3 yr old, from the two-trait (two age of ewe classes) analyses and .06 when all ages were included. Estimates of heritability for number of lambs born from the single-trait analyses were somewhat less than estimates from two-trait analyses. Estimate of genetic correlation between number of lambs born for the 2 and 3 yr and the >3 yr classes was near unity (1.00), which suggests that a repeated measures model for number of lambs born is adequate for making selection decisions. Estimate of genetic correlation between number of lambs born and 18-mo body weight was .35 with a heritability estimate of .48 for 18-mo body weight. The estimate of genetic correlation suggests that selection for increased number of lambs born would result in increased 18-mo body weight.     

Genetic correlations between growth and reproductive traits in Zandi sheep

For the first time, the current study reports the genetic and phenotypic correlations between growth and reproductive traits in Zandi sheep. The data were comprised of 4,309 records of lamb growth traits from 1,378 dams and 273 sires plus 2,588 records of reproductive traits from 577 ewes. These data were extracted from available performance records at Khojir Breeding Station of Zandi sheep in Tehran, Iran, from 1993 to 2008. Correlations were estimated from two animal models in a bivariate analysis using restricted maximum likelihood procedure between lamb growth traits [birth weight (BW), weaning weight at 3 months of age (WW), as well as six-month weight (6 MW)] and ewe reproductive traits [litter size at birth (LSB), litter size at weaning (LSW), total litter weight at birth (TLWB), and total litter weight at weaning (TLWW)]. The genetic correlations between BW and reproductive traits varied from low to high ranges from 0.10 for BW–LSB to 0.86 for BW–TLWB. WW was moderately (0.37) to highly (0.96) correlated with all the reproductive traits. Moreover, the genetic correlations were observed between 6 MW and reproductive traits, varied from 0.19 to 0.95. Relationships between growth and reproductive traits ranged from 0.01 for BW–LSW to 0.28 for BW–TLWB in phenotypic effects. Results indicated that selection to improve WW would have high effect on genetic response in TLWW, and also, these results could be effective for all of the reproductive traits in Zandi sheep.     

Evaluation of the ovine callipyge locus: IV. Genotypic effects on reproductive traits

A resource population of ewes derived from Dorset and Romanov grandparents was generated over 5 yr to provide genotypic and phenotypic data to estimate effects of each callipyge genotype on component traits of reproduction. Effects on ovulation rate were estimated from data recorded by examination of ovaries from serially slaughtered ewe lambs (n = 174) born in 1994 and 1995. Productivity and longevity through 5 yr of age were recorded on a total of 265 F2 ewes produced in 1996 through 1998. Number of lambs born, birth weights, and weaning weights of lambs were calculated for each ewe. Weaning weight was recorded for each lamb and adjusted for age to 56 and 32 d for dam- and nursery-reared lambs, respectively. Longevity was determined as a binary trait based on the presence or absence of the ewe in the breeding flock at 5 yr of age. Ewes generated 937 records for breeding weight and 925 records for conception rate, which was determined on ewes exposed and still present at the start of each lambing season. Seven hundred seventeen records were analyzed for traits based on the number of ewes lambing. Genotypes for the causative callipyge mutation were determined using a matrix-assisted laser desorption/ionization time-of-flight mass spectrometry assay. Each ewe was classified into 1 of 4 genotypes; NMatNPat, NMatCPat, CMatNPat, or CMatCPat, where N represents wild type and C represents the mutant allele. The mean ovulation rate of the ewe lambs genotyped NMatNPat was greater (P < 0.02) than that exhibited by NMatCPat; however, the estimated difference of 0.25 ovum in the ewe lambs did not affect the number born. The live weight of NMatCPat ewes at breeding was 2.5 kg less than that of other genotypes (P < 0.01). The callipyge genotype class did not significantly affect conception rates, fecundity, maternal ability, or ewe longevity. Maintaining a ewe flock to produce homozygous mutant rams for use in terminal sire mating systems presents no unusual problems from a reproduction standpoint.     

Genetic parameter estimates for growth traits in Horro sheep

Variance components and genetic parameters were estimated for growth traits: birth weight (BWT), weaning weight (WWT), 6‐month weight (6MWT) and yearling weight (YWT) in indigenous Ethiopian Horro sheep using the average information REML (AIREML). Four different models: sire model (model 1), direct animal model (model 2), direct and maternal animal model (model 3) and direct–maternal animal model including the covariance between direct and maternal effects (model 4) were used. Bivariate analysis by model 2 was also used to estimate genetic correlation between traits. Estimates of direct heritability obtained from models 1–4, respectively, were for BWT 0.25, 0.27, 0.18 and 0.32; for WWT, 0.16, 0.26, 0.1 and 0.14; for 6MWT 0.18, 0.26, 0.16 and 0.16; and for YWT 0.30, 0.28, 0.23, and 0.31. Maternal heritability estimates of 0.12 and 0.23 for BWT; 0.19 and 0.24 for WWT; 0.09 and 0.09 for 6MWT and 0.08 and 0.14 for YWT were obtained from models 3 and 4, respectively. The correlations between direct and maternal additive genetic effects for BWT, WWT, 6MWT and YWT were –0.64, –0.42, 0.002 and –0.46, respectively. On the other hand, the genetic correlations between BWT and the rest of growth traits (WWT, 6MWT and YWT, respectively) were 0.45, 0.33 and 0.31, whereas correlations between WWT and 6MWT, WWT and YWT and 6MWT and YWT were 0.98, 0.84 and 0.87, respectively. The medium to high direct and maternal heritability estimates obtained for BWT and YWT indicate that in Horro sheep faster genetic improvement through selection is possible for these traits and it should consider both (direct and maternal) h² estimates. However, since the direct‐maternal genetic covariances were found to be negative, caution should be made in making selection decisions. The high genetic correlation among early growth traits imply that genetic improvement in any one of the traits could be made through indirect selection for correlated traits.     

Estimating non-genetic and genetic parameters of pre-weaning growth traits in Raini Cashmere goat

Data and pedigree information used in the present study were 3,022 records of kids obtained from the breeding station of Raini goat. The studied traits were birth weight (BW), weaning weight (WW), average daily gain from birth to weaning (ADG) and Kleiber ratio at weaning (KR). The model included the fixed effects of sex of kid, type of birth, age of dam, year of birth, month of birth, and age of kid (days) as covariate that had significant effects, and random effects direct additive genetic, maternal additive genetic, maternal permanent environmental effects and residual. (Co) variance components were estimated using univariate and multivariate analysis by WOMBAT software applying four animal models including and ignoring maternal effects. Likelihood ratio test used to determine the most appropriate models. Heritability ( \texth_\texta² ) \left( {{\text{h}}_{\text{a}}^2} \right) estimates for BW, WW, ADG, and KR according to suitable model were 0.12 ± 0.05, 0.08 ± 0.06, 0.10 ± 0.06, and 0.06 ± 0.05, respectively. Estimates of the proportion of maternal permanent environmental effect to phenotypic variance (c ²) were 0.17 ± 0.03, 0.07 ± 0.03, and 0.07 ± 0.03 for BW, WW, and ADG, respectively. Genetic correlations among traits were positive and ranged from 0.53 (BW-ADG) to 1.00 (WW-ADG, WW-KR, and ADG-KR). The maternal permanent environmental correlations between BW-WW, BW-ADG, and WW-ADG were 0.54, 0.48, and 0.99, respectively. Results indicated that maternal effects, especially maternal permanent environmental effects are an important source of variation in pre-weaning growth trait and ignoring those in the model redound incorrect genetic evaluation of kids.     

Dominance genetic and maternal effects for genetic evaluation of egg production traits in dual-purpose chickens

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

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

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

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

     

Aggressive behaviour of sows at mixing and maternal behaviour are heritable and genetically correlated traits

This study was designed to estimate genetic variation in aggressive behaviour of sows at mixing, and in maternal ability for the same sows. The study included 835 sows observed for number of mild or severe aggressions performed (F_A1, F_A2), or received (F_R1, F_R2) during 30 min after grouping. Maternal ability was recorded as sows' response to vocalisation from their piglets when these were handled. Maternal behaviour was studied in 1076 sows as a body reaction (MBR) to their piglets being handled after farrowing. Genetic covariances were estimated using a multi-trait animal model, assuming traits to be normally distributed. The heritabilities of performed aggression traits were intermediate (h² F_A1=0.17, h² F_A2=0.24), but lower for received aggression (h² F_R1=0.06, h² F_R2=0.04), and heritability of maternal behaviour was also low (h²=0.08). Although estimates of genetic correlations had large standard errors, they indicate that less aggressive sows were stronger responding mothers (r_g=−0.3). We conclude that performed aggression in sows is a heritable trait, and selection against aggression is possible without offsetting maternal behaviour.     

Flock dynamics of desert Barki sheep in relation to age structure

Reproduction data of 8689 ewe records spread over 40 years (from 1960 to 2000) representing 2952 breeding Barki ewes were used in this study. The flock belonged to the Desert Research Center in Egypt. Flock dynamics of nine age groups (2–10 yrs) were assessed. Two parameters were used to evaluate flock dynamics, net reproduction rate (R_o) (number of ewe- lambs reaching joining age and produced by each ewe during its lifetime in the flock) and intrinsic rate of increase (r_m) (flock growth when no resource is limiting). Age of ewe had a highly significant (P < 0.01) effect on number of ewes lambing per ewe joined (E_PJ), number of lambs born per ewe joined (L_BJ), number of lambs weaned per ewe joined (L_WJ) and number of ewe lambs reaching joining age per ewe joined (L_EJ.J). All estimates tended to increase with dams age up to four years and decreased thereafter. The results of R_o and r_m showed that the studied flock must consist of 5 age groups to maintain its size and replace itself. It may be recommended to cull the breeding ewe at the age of 6 years to accelerate genetic improvement.