Genetic effects on ewe productivity of crossing D'man and Sardi breeds of sheep

Data from 364 ewes of Sardi (S), D'man (D), S x DS, DS x S, S x D, D x S (F1), F2, D x DS and DS x D breed groups mated to F1 rams were analyzed for fertility, number of lambs born alive, litter size at weaning, litter weight at weaning per ewe joined and mean lamb weight at 60 d. Each ewe was exposed in two seasons and had one or two lambings. Effects of breed group were significant for all traits. The highest number of lambs born alive and litter size at weaning were recorded in D'man (1.84 and 1.45, respectively) and D x DS (1.81 and 1.43, respectively). F1 ewes (S x D and D x S) had the highest fertility (.94) and litter weight at weaning per ewe exposed (13.8 kg). Mean lamb weight at 60 d was highest for S x DS and Sardi ewes (13.4 kg and 13.2 kg). D'man additive effects were positive and significant for number of lambs born alive, litter size at weaning and litter weight at weaning per ewe joined; were significant but negative for mean lamb weight at 60 d; and were not significant, although positive, for fertility. Significant individual heterosis was found for fertility, litter weight weaned and mean lamb weight at 60 d. Maternal heterosis and direct epistatic recombination effects were small for all traits.     

Genetic and environmental effects on growth to 1 year and viability of lambs from a crossbreeding study of D'man and Sardi breeds.

Genetic effects were estimated for growth to 1 yr and viability to 90 d of 882 lambs from a diallel cross of Sardi (S), D'man (D), and D'man x Sardi (DS) male and female parents. Sardi direct genetic effects were significantly higher than those of D'man for weights at birth and up to 2 mo, but the difference decreased thereafter and was in favor of D'Man at 6 mo. Sardi maternal ability was better than that of D'man for weights at all ages. Estimates of individual heterosis were small and negative for weight at birth, weight at 1 mo, and lamb viability and positive for other body weights; the estimate was significant for 12-mo weight. Estimates of maternal heterosis were small and did not approach significance for any trait. Epistatic recombination effects were generally small, but negative for all traits and significantly so for viability to 30 d. In general, the results, combined with those on reproduction and total lamb production of ewes of these groups, reported elsewhere, indicate that a population produced by inter se mating of animals 50% D, 50% S breeding is expected to have higher total lamb production than either purebred.     

Estimation of additive and non-additive genetic parameters for reproduction, growth and survival traits in crosses between the Moroccan D'man and Timahdite sheep breeds

Genetic breed differences, heterosis, recombination loss, and heritability for reproduction traits, lamb survival and growth traits to 90 days of age were estimated from crossing D'man and Timahdite Moroccan breeds. The crossbreeding parameters were fitted as covariates in the model of analysis. The REML method was used to estimate (co)variance components using an animal model. The first estimation of crossbreeding effects for Timahdite and D'man breeds shows that breed differences in litter traits are mainly of maternal genetic origin: +1.04 lambs, +1.88 kg, +0.60 lambs, and +2.23 kg in favour of D'man breed for litter size at lambing, litter weight at lambing, litter size at weaning, and litter weight at 90 days, respectively. The breed differences in lamb growth and survival are also of maternal genetic origin for the majority of traits studied, but in favour of the Timahdite breed: +3.48 kg, +45 g day⁻¹ and +0.19 lambs for weight at 90 days, for average daily gain between 30 and 90 days of age, and for lamb survival to 90 days, respectively. The D'man direct genetic effect was low and negative for survival and birth weight of lambs during the first month of life. All traits studied showed positive heterosis effects. Recombination loss effects were not significant. Therefore, crossbreeding of Timahdite with D'man breeds of sheep can result in an improved efficiency of production of saleable lambs. Heritability estimates were medium for litter size but low for the other reproduction traits. Direct heritabilities were low for body weights and lamb survival at 90 days and the corresponding maternal heritabilities showed, however, low to moderate estimates. For litter traits, the estimates of genetic and phenotypic correlations were positive and particularly high for genetic correlations.     

Lamb production and its components in pure breeds and composite lines. II. Breed effects and heterosis

Ewe performance was compared for five pure breeds of sheep (Finnsheep, F; Rambouillet, R; Dorset, D; Targhee, T; Suffolk, S) and the crosses in development of two maternal composite lines (C1 = 1/2F1/4R1/4D and C2 = 1/2F1/4T1/4S). The data involved 10,959 breeding season records of 4,219 ewes by 412 sires. Ewe production and the components (fertility, litter size, neonatal and preweaning lamb survival and mean lamb weaning weight) were adjusted for age and standardized across season of lambing and years. The D and F ewes produced more weight of lamb/ewe exposed than R, S and T ewes because of higher D and F fertility, higher D lamb survival and larger F litters. First cross and inter se generations of C1 and C2 ewes averaged 17 to 27% higher fertility than the parental mean. Litter size averaged about one lamb higher for F than for other pure breeds, but only slightly higher for C1 and C2 than for the mean of F and other breeds. Lower neonatal survival for F than for other breeds and crosses was associated with the larger F litters and with 2 to 8% positive heterosis in the crosses. Preweaning survival of suckled and nursery lambs was low for F and S and positive heterosis ranged from 9 to 19% in crosses. Mean lamb weaning weights were highest for S, lowest for F, with little heterosis in crosses. Crossbred ewes reared .3 to .4 more lambs than mean for parental pure breeds. Heterosis in C1 and C2 ranged from 11 to 28% for lambs born, 27 to 43% for lambs weaned and 29 to 44% for weight of lamb weaned/ewe exposed. Decline in heterosis with inter se mating of crosses was no greater than expected from the reduction in predicted heterozygosity.     

Lambing date and lamb production of spring-mated Rambouillet, Dorset and Finnsheep ewes and their F1 crosses

The reproductive performance of 255 Rambouillet (R), Dorset (D), Finnsheep (F) and F1 ewes born in 1978-1979 (group I) and 1979-1980 (group II) and managed in a semiconfinement fall/winter lambing system was evaluated through 4 yr of age of all ewes and through 5 yr for a portion of group I ewes. Ewes were with rams from approximately May 1 to late September each year, with a 2-wk break late in July/early August. Traits considered were fertility (ewes lambed/ewes exposed), lambing date, litter size, lamb survivial and 70-d lamb weights. Breeds and crossbred groups differed significantly in lambing date, with DR crossbred ewes earliest and F ewes latest. Repeatabilities for groups I and II were .31 and .22, .24 and .24 and .11 and .07 for lambing date, fertility and litter size, respectively. There was no significant heterosis in lambing date, although DR ewes in both groups I and II were superior to (D + R)/2, by about 1 wk on average. There was significant positive heterosis for fertility and traits of which fertility is a component in FR ewes in group I, but none in group II. The FD ewes showed negative heterosis for litter size, -.23 (P less than .05) for group I and -.09 for group II. The results indicate: F and FD ewes are not well adapted to the Mediterranean climate where this experiment was conducted; there is little, if any, useful heterosis in crosses among these three breeds for lambing date or other reproduction traits and RD and R ewes are most suitable of the groups tested, while late onset of the breeding season limits the usefulness of even 50% Finnsheep ewes for an autumn lambing system in this environment.     

Genetic implications of a simulation model of litter size in swine based on ovulation rate, potential embryonic viability and uterine capacity: I. Genetic theory

A simulation model of litter size in swine based on ovulation rate, uterine capacity and potential embryo viability was compared to three genetic models to clarify its genetic characteristics. The simulation model is equivalent to independent culling based on fixed levels of potentially viable embryos and uterine capacity. Litter size also can be described by a combination of additive, additive x additive, mean environment x additive, random environment and additive x random environment effects. A third genetic model that can describe the simulation model is the associative effects model, in which litter size is the result of grouping two genotypes. The fixed independent culling levels model predicts that genetic parameters will change as the component means change. This genetic model also predicts that selection on an index of ovulation rate and uterine capacity would improve selection response for litter size. This genetic model predicts asymmetry of correlated responses in ovulation rate and uterine capacity when selecting for high and low litter size. The nonadditive genetic model predicts covariances among relatives that are different from their additive relationships; however, simulated results did not detect any differences. The nonadditive genetic model also predicts that heterosis for litter size will differ among crosses based on the mean environment and on additive x additive genetic interaction. The associative effects model predicts that selection for litter size will always lead to a positive response in litter size.     

Ovulation rate and litter size of Barbados, Targhee and crossbred ewes

Ovulation rate was measured in Barbados Blackbelly (United States strain; B), Targhee (T), Barbados X Targhee (B X T) and Barbados X Dorset-Targhee (B X DT) ewes at first and second estrus following synchronization of cycles early in the breeding season. Body weight at sponge removal differed (P less than .001) between B (30.9 kg) and T ewes (54.9 kg) and was intermediate for B X T (44.9 kg) and B X DT (43.5 kg) ewes. Ovulation rate was higher (P less than .01) at first and second estrus for B (1.86, 2.04), B X T (1.93, 2.04) and B X DT (1.72, 1.80) than for T (1.29, 1.40) ewes. Regressions of ovulation rate on body weight within the breed groups did not differ significantly from each other and the average was significant (b = .049 +/- .014 CL/kg at first estrus and b = .046 +/- .011 CL/kg at second estrus, where CL = number of corpora lutea), but differences between the groups in body weight did not explain the differences in ovulation rate. Litter size for B, B X T, B X DT and T groups was 1.71, 1.84, 1.84 and 1.28, respectively. The B X T ewes were superior to the average of the B and T ewes for ovulation rate (P less than .05) and litter size (P less than .01); there was no direct estimate of embryo survival, but the results indirectly indicate superiority of the crossbreds for this component also.(ABSTRACT TRUNCATED AT 250 WORDS)     

Performance of Polypay, Coopworth, and crossbred ewes: I. Reproduction and lamb production.

Six ewe genotypes, generated by mating Coopworth (C), Polypay (P), and Suffolk (S) rams to Polypay and Coopworth-type (Ct) ewes, were exposed to Hampshire rams for spring lambing from 1986 through 1990. Data from 1,092 exposures and 1,044 resultant lambings were used to analyze reproductive traits and lamb growth rates. Overall conception rate averaged 95% and ranged from 93% for S x Ct ewes to 97% for P x Ct ewes. Mean litter size at birth averaged 1.63 and ranged from 1.45 for C x C ewes to 1.75 for S x P ewes. Ewes from P dams had higher mean litter size (P less than .01) than those from Ct dams (1.73 vs 1.54), but differences between sire breeds were not significant. Incidence of lambing assistance was similar for ewes producing single or multiple lambs. Lamb birth weight influenced the level of assistance rendered to single-bearing but not to multiple-bearing ewes. Lambing assistance was not related to lamb survival, probably because the high surveillance level minimized trauma before assistance was rendered. Incidence of required assistance declined over subsequent parities. Lamb birth weights were affected by ewe genotype and increased with increasing ewe age. Survival of single-born lambs averaged 94% and was not affected by dam genotype. Survival of twins averaged 85%, ranging from 79% for lambs from S x Ct ewes to 89% for lambs from P x P ewes. Suffolk-sired ewes produced the heaviest mean birth and weaning weights for both singles and twins. Coopworth-sired ewes weaned heavier single lambs but lighter twins than P-sired ewes.     

Genetic variation in reproductive responses to a high-energy diet in mice

Effects of a high-energy diet on reproduction were studied in 300 mice from lines selected for litter size and(or) 6-wk BW (L+, increased litter size; W+, increased body weight; L+W-, increased litter size and decreased body weight; L-W+, decreased litter size and increased body weight; and K, randomly selected control). Mice received a high-energy diet (HED; 3.8 kcal/g of ME) or a standard diet (STD; 3.3 kcal/g of ME) from 8 to 11 wk of age and were then mated and evaluated for ovulation rate and embryo survival through 17 d of gestation. The HED increased ovulation rate in all lines (P less than .05). The line x diet interaction was significant, with increased ovulation rate due to HED ranging from 9.9% in W+ to 24.2% in L-W+. Within-line regression coefficients of ovulation rate on ME intake (kilocalories from 10 to 11 wk) varied from .08 +/- .04 (P less than .05) in L+W- to .177 +/- .05 (P less than .01) in L+. In contrast, nonsignificant increases were observed in litter size (live fetuses at 17 d of gestation) due to HED. Effects of HED on embryo survival rate were significantly negative in L+ and L+W-; the decrease in L+ was a result of preimplantation losses, and the decrease in L+W- was due to postimplantation losses. The line x diet interaction was significant for postimplantation embryo survival. The results indicate significant genetic variation in reproductive responses to a high-energy diet in mice.     

Genetic implications of a simulation model of litter size in swine based on ovulation rate, potential embryonic viability and uterine capacity: II. Simulated selection

Direct selection for ovulation rate, uterine capacity, litter size and embryo survival and selection for indexes of ovulation rate with each of the remaining traits were simulated for a swine population. The relationships among these traits were determined from a simulation model that assumed that litter size was always less than or equal to both ovulation rate and uterine capacity. Heritabilities of ovulation rate and uterine capacity were assumed to be .25 and .20, respectively, and uncorrelated genetically and phenotypically. No additional genetic variation was assumed. Responses to weak selection pressure were simulated by recurrent updating of phenotypic variances and covariances combined with the heritabilities of ovulation rate and uterine capacity. Two indexes of ovulation rate and uterine capacity each resulted in 37% greater increase in litter size than direct selection for litter size. Indexes of ovulation rate and either litter size or embryo survival increased litter size by 21% more than direct selection for litter size. Selection for ovulation rate, uterine capacity or embryo survival was 6, 35 and 79%, respectively, less effective than direct selection for litter size. Responses to intense selection pressure were determined by direct simulation of genotypes and phenotypes of individuals. The two indexes of ovulation rate and uterine capacity exceeded direct selection for litter size by 39 and 27%. The indexes of ovulation rate and either litter size or embryo survival exceeded direct selection for litter size by 19 and 13%, respectively. Intense selection for ovulation rate or uterine capacity decreased selection response by 26 and 67%, respectively, relative to direct selection for litter size. Intense selection for embryo survival decreased litter size slightly.     

Lamb production and its components in pure breeds and composite lines. I. Seasonal and other environmental effects

Season of lambing and other environmental effects on ewe performance were analyzed for purebred Finnsheep (F), Rambouillet (R), Dorset (D), Targhee (T) and Suffolk (S) and the generations of crosses in development of two maternal composite lines (1/2F1/4R1/4D) and (1/2F1/4T1/4S) in accelerated (January, May and September) or annual April lambing. The data involved 10,959 ewe breeding season records for 4,219 ewes of 412 sire families over 4 yr. Various measures of ewe productivity and its components (fertility, litter size, neonatal and preweaning survival and weaning weight) were analyzed. Fertility was higher for annual April than for accelerated May or January lambing and was sharply lower for September lambing. Fertility of F and F-cross ewes was significantly higher for May and lower for January lambings relative to R and D ewes. Litter size also was higher in annual April (1.9) than in January (1.8) or May (1.7) and September (1.4). Neonatal and preweaning survival was higher in September when litter size was smaller. Mean weaning weights were depressed in the larger April and May litters. Thus, weight of lambs weaned/ewe exposed was higher for annual April than for May and January lambing and was very low for September lambing. Hormone treatment of ewes for September lambing increased fertility from 16 to 44% and litter size from 1.6 to 1.8. Short lambing interval (8 mo vs 12+ mo) reduced mean ewe fertility by five percentage points, and most for the January lambing of Finnsheep ewes.     

Comparison of Booroola Merino and Finnsheep: effects on productivity of mates and performance of crossbred lambs

Booroola Merino (BM) and Finnsheep (FS) rams were mated to FS and crossbred (CO) ewes to compare their effects on the productivity of their mates and the performance of their progeny. Effects of breed of ram and the interaction of breed of ram X breed of ewe were no significant for fertility, total number born, number born alive, litter birth weight, or number of lambs weaned by the ewe or in the nursery. Birth weights of FS- and BM-sired lambs were equal, but FS-sired lambs were heavier at weaning and 147 d of age. Compared with BM-sired lambs, survival from birth to weaning of dam-reared lambs was greater for FS-sired lambs produced by CO dams than for FS-sired lambs produced by FS dams. At a constant live weight, FS-sired lambs had a heavier carcass with less external fat thickness than BM-sired lambs. Percentage of ewe lambs reaching puberty was lowest and age at puberty was highest for the BM X CO cross; relatively small differences existed between the other three genotypes for these traits. Ewe lambs sired by BM had a greater ovulation rate than FS-sired ewe lambs. Embryo mortality was greater in BM X CO ewe lambs than in ewe lambs of the other three genotypes; the difference was larger for ewes with three ovulations than for ewes with two ovulations. The net result was that BM X CO ewe lambs averaged slightly fewer lambs born than FS X CO ewes. The BM X FS ewe lambs had larger litters than the FS ewes due to a substantially higher ovulation rate and only a slightly lower overall embryo survival rate. With the exception of ovulation rate and litter size, FS rams produced lambs with a more desirable level of performance than did BM rams.     

Integration of ovulation rate, potential embryonic viability and uterine capacity into a model of litter size in swine

A mathematical model of litter size in swine was developed from ovulation rate, potential embryonic viability and uterine capacity. The model assumed that ovulation rate was reduced to potentially viable embryos by factors innate to the ovum and embryo. Potentially viable embryos then could be further reduced to uterine capacity, the maximum number of fetuses that a female can carry to term. Consequently, litter size can be no greater than either ovulation rate or uterine capacity. Means and variances of ovulation rate and potential embryonic viability used in the model were based on experimental results. The mean and variance of uterine capacity were varied until the simulated mean and variance of litter size were equal to experimental results. Simulated results of relationships among ovulation rate, embryo survival and litter size were similar to observed experimental relationships. Heritabilities of simulated litter size and embryo survival were similar to literature values when the heritability of ovulation rate was set at .25 and the heritability of uterine capacity was set at either .15 or .20. Litter size was simulated for 25 combinations of average ovulation rate and uterine capacity to develop equations relating mean ovulation rate and uterine capacity to litter size, embryo survival and correlations among them. Results suggest that changing either ovulation rate or uterine capacity independently will not result in large changes in litter size. Consequently, the model suggests that a single gene, hormonal manipulation or nutritional change will not result in large increases in litter size and that combinations of factors will be needed to increase litter size.     

Components of heterosis for growth traits and litter size in line crosses of mice after long-term selection

Strains selected for 54 generations for large 8-week weight (N8, S8), for small weight (N6, S6), for high 3–5-week gain and low 8-week weight (N1) as well as unselected randomly mated control strains (N9, S9) were crossed, and F ₁, F ₂ and both back crosses created. N strains are derived from a NMRI base, S strains from a synthetic four-way cross among inbred lines. Heterosis for 8-week weight (8-ww) was some 6%, but 30% for 3–5-week gain and it was on average negative (22%) for 5–8-week gain. When epistatic effects were taken into account, it appeared that heterosis for 8-ww was largely due to beneficial effects of non-parental gene combinations, i.e. additive × additive epistatic effects were negative. These non-parental combinations neutralized the mostly negative dominance effects. The latter were mostly positive for early gain but in all 9 line crosses negative for late gain. The digenic effects of the non-parental origin were not large enough to balance the negative dominance effects for late gain, so that heterosis was negative. It appears therefore that early and late gain are affected by different sets of genes. Maternal additive effects on 8-ww and early gain are smaller than direct additive effects but mostly of similar sign. For late gain there appears to be no connection with direct additive effects. Direct litter heterosis was almost 50% but much of this was due to positively acting recombinational gene combinations, while direct litter dominance was mostly negative. Maternal additive effects on litter size differed depending on whether they were estimated from dams with crossbred or with purebred litter. Heterosis was small in crosses between control strains. Heterosis caused by recombinant gene pairs should be amenable to improvement by selection.     

Ovulation rate, lambing rate, litter size and embryo survival of Rambouillet sheep selected for high and low reproductive rate

Ewes from lines selected for high and low reproductive rate and a control line bred and selected randomly were endoscopically examined 3 to 5 d after breeding to determine ovulation rates in the fall of 1985, 1986 and 1987. Fertility (ewes lambing per ewe exposed), lambing rate (lambs born per ewe exposed) and litter size (lambs born per ewe lambing) were evaluated at lambing in the spring of each year. Embryonic survival was estimated as the number of lambs born per corpora lutea. Ovulation rates were 1.28, 1.73 and 1.46 for low, high and control lines, respectively. More (P less than .01) single ovulations occurred in low-line ewes than in the other two lines; high-line ewes had more (P less than .01) twin ovulations than did low- or control-line ewes. Fertility did not differ among lines. Selection line affected (P less than .01) lambing rate at first and all services. Control-line ewes had mean lambing rates at first and all services that were intermediate between those of the low and high lines, which were different from each other. Line x age of ewe interactions existed (P less than .01) for lambing rate at all services and litter size at first and all services. High-line ewes had lower lambing rates and litter sizes as 2-yr-olds than other lines, but their performance increased steadily to 6-yr-olds, whereas the low and control lines remained relatively constant. Embryo survival differed (P less than .10) between lines, being 74%, 63% and 67% for low, high and control lines, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effect of selection for litter size and body weight on hormone-induced ovulation rate in mice.

Genetic differences in natural vs hormone-induced ovulation rates were compared in immature female mice from five lines that had undergone long-term single-trait and antagonistic index selection for litter size and(or) 6-wk BW. Lines used were control (K); high litter size (L+); high BW (W+); low litter size and high BW (L-W+); and high litter size and low BW (L+W-). Natural ovulation rate at a mean age of 34.3 d and hormone-induced (5 IU of pregnant mare's serum gonadotropin followed 2 d later by 5 IU of human chorionic gonadotropin) superovulation rate at a fixed age of 31 d were obtained. Total number of eggs ovulated was affected by line (P less than .001), treatment (P less than .001), and line x treatment interaction (P less than .001). Line differences were subsequently tested within treatment because of the significant line x treatment interaction. Line differences were important (P less than .001) for natural ovulation, hormone-induced ovulation, and response to hormones. Mean natural ovulation rates for K, L+, W+, L-W+, and L+W- were 14.1, 19.8, 15.1, 13.6, and 16.4, respectively. Selection changed ovulation rate by 40, 16, 7, and -4% in the L+, L+W-, W+ and L-W+ lines, respectively (P less than .01). Hormone-induced ovulation rates in K, L+, W+, L-W+, and L+W- were 32.3, 24.6, 19.6, 20.9, and 22.1, respectively. Exogenous hormones increased ovulation by 18.2, 4.8, 4.6, 7.3, and 5.7 ova for K, L+, W+, L-W+, and L+W-, respectively (P less than .001). Lines with lower natural ovulation rates had higher responses to superovulation. Increased ovulation rate due to treatment ranged from 24.3% in L+ to 129% in K. These results indicate significant differences among lines in ovarian response to exogenous hormones.     

Reproduction in Javanese sheep: evidence for a gene with large effect on ovulation rate and litter size

Three breeds of Javanese sheep are described briefly and data suggesting the segregation of a gene with large effect on ovulation rate and litter size are presented. The three breeds are Javanese Thin Tail (JTT), Javanese Fat Tail (JFT) and Semarang (SEM), the last possibly a substrain of JTT. All three breeds have mean mature ewe weights under 30 kg. Ovulation rate and litter size did not differ significantly among the three; all had litter sizes of up to 4 or 5 with a mean for mature ewes of approximately 2. Ovulation rate ranged from 1 to 5 and had an average within-breed repeatability of .8 within season and .65 between seasons. Within-breed repeatability of litter size was .35 +/- .06. Prenatal survival in pregnant ewes with two, three and four or more ovulations averaged 93, 88 and 86% over two seasons. Dams that had at least one ovulation rate or litter size record greater than or equal to 3 produced two groups of daughters in approximately equal numbers: one group with many records greater than or equal to 3 and mean ovulation rate and litter size of 2.73 and 2.31, respectively, and one group with ovulation rates and litter sizes of 1 or 2 and corresponding means of 1.39 and 1.38. Dams with ovulation rate or litter size records of only 1 or 2 produced daughters in which over 90% had records of only 1 or 2. Estimated heritabilities for the mean of approximately three ovulation rate or litter size records from these daughter-dam comparisons exceeded .7. These results suggest segregation of a Booroola-type gene, one copy of which increases ovulation rate by about 1.3 and litter size by .9 to 1.0. Relationships between duration of estrus and ovulation rate, and between timing of release of luteinizing hormone and number of eggs shed, resemble the pattern in Booroola Merino more closely than that in Finnish Landrace or Romanov, supporting the hypothesis of a major gene.     

Selection for ovulation rate in rabbits

An experiment of selection for ovulation rate was carried out. Animals were derived from a synthetic line first selected 12 generations for litter size, then 10 generations for uterine capacity. Selection was relaxed for 6 generations. Selection was based on the phenotypic value of ovulation rate with a selection pressure on does of 30%. Males were selected from litters of does with the highest ovulation rate. Males were selected within sire families in order to reduce inbreeding. Ovulation rate was measured in the second gestation by a laparoscopy, 12 days after mating. Each generation had about 80 females and 20 males. Results of three generations of selection were analyzed using Bayesian methods. Marginal posterior distributions of all unknowns were estimated by Gibbs sampling. Heritabilities of ovulation rate (OR), number of implanted embryos (IE), litter size (LS), embryo survival (ES), fetal survival (FS), and prenatal survival (PS) were 0.44, 0.32, 0.11, 0.26, 0.35, and 0.14, respectively. Genetic correlation between OR and LS was 0.56, indicating that selection for ovulation rate can augment litter size. Response to selection for OR was 1.80 ova. Correlated responses in IE and LS were 1.44 and 0.49, respectively. Selection for ovulation rate may be an alternative to improve litter size.     

Production of prolific microsheep by embryo transfer into large non-prolific sheep

The Garole is a prolific breed of microsheep that possesses the FecB gene, which increases ovulation rate. The purpose of this study was to compare embryo production by multiple ovulation in seven Garole ewes with that in seven normal size, non-prolific Malpura ewes, and assess the influence of the large body size of Awassi crossbred recipient ewes on the birth-weight of Garole lambs. Oestrus was synchronised with two intramuscular injections of 7.5 mg prostaglandin F(2alpha) administered 10 days apart. The donor ewes were superovulated by the use of pregnant mare serum gonadotrophin and follicle-stimulating hormone. The onset and duration of oestrus were similar in both breeds. The Garole donors had higher total mean (se) ovarian responses (15.6 [3.6] v 9.1 [2.3]), ovulation rate (13.6 [3.1] v 8.4 [2.2]) and produced more transferable embryos (6.0 [3.5] v 4.0 [0.9]) than the Malpura donors, but the differences were not statistically significant. The Garole lambs produced by embryo transfer were on average 57.8 per cent heavier at birth than contemporary Garole lambs produced by natural mating.     

Progestagen supplementation during early pregnancy does not improve embryo survival in pigs

Progesterone supplementation during early pregnancy may increase embryo survival in pigs. The current study evaluated whether oral supplementation with an analogue of progesterone, altrenogest (ALT), affects embryo survival. A first experiment evaluated the effect of a daily 20-mg dosage of ALT during days 1-4 or 2-4 after onset of oestrus on embryo survival at day 42 of pregnancy. A control group (CTR1) was not treated. The time of ovulation was estimated by transrectal ultrasound at 12-h intervals. Altrenogest treatment significantly reduced pregnancy rate when start of treatment was before or at ovulation: 25% (5/20) compared to later start of treatment [85% (28/33)] and non-treated CTR1 [100% (23/23)]. Altrenogest treatment also reduced (p < 0.05) number of foetuses, from 14.6 ± 2.6 in CTR1 to 12.5 ± 2.5 when ALT started 1-1.5 days from ovulation and 10.7 ± 2.9 when ALT started 0-0.5 days from ovulation. In a second experiment, sows with a weaning-to-oestrous interval (WOI) of 6, 7 or 8-14 days were given ALT [either 20 mg (ALT20; n = 49) or 10 mg (ALT10; n = 48)] at day 4 and day 6 after onset of oestrus or were not treated (CTR2; n = 49), and farrowing rate and litter size were evaluated. Weaning-to-oestrous interval did not affect farrowing rate or litter size. ALT did not affect farrowing rate (86% vs 90% in CTR2), but ALT20 tended to have a lower litter size compared with CTR2 (11.7 ± 4.1 vs 13.3 ± 3.1; p = 0.07) and ALT10 was intermediate (12.3 ± 2.9). In conclusion, altrenogest supplementation too soon after ovulation reduces fertilization rate and embryo survival rate and altrenogest supplementation at 4-6 days of pregnancy reduces litter size. As a consequence, altrenogest supplementation during early pregnancy may reduce both farrowing rate and litter size and cannot be applied at this stage in practice as a remedy against low litter size.