Biomedical subjects

K A Leymaster

Publications and source records attributed to K A Leymaster.

At least 37 records · Page 2Linked to original sources

PubMed2000

Evaluation of Dorset, Finnsheep, Romanov, Texel, and Montadale breeds of sheep: I. Effects of ram breed on productivity of ewes of two crossbred populations.

Effects of Dorset, Finnsheep, Romanov, Texel, and Montadale breeds for performance as sires were estimated in the initial phase of a comprehensive evaluation of these breeds as contributors to sheep crossbreeding systems. Objectives were to evaluate the effects of ram breed, ewe breed, season of mating, and two-way interactions. Rams from the five breeds were single-sire-mated with ewes from two breed types to produce lambs over a 3-yr period. Ewes were assigned to one of three distinct 35-d mating seasons initiated each year in August, October, and December. A different sample of six rams per breed was used each year across all three seasons, and each ram was penned with ewes of both breeds. Traits evaluated and number of ewe records were conception rate and litter weaning weight per ewe exposed (n = 3,261) and number born, litter birth weight, average birth weight, number weaned, and litter weaning weight per ewe lambing (n = 2,751). Ram breed and ewe breed interacted (P < .01) for conception rate and litter weaning weight per ewe exposed, implicating mating preferences, particularly of Romanov rams. In mixed groups of ewes exposed to Romanov rams, conception rate was 12.7% lower and litter weight weaned was 8.4 kg lower in the ewe breed presumably less preferred for mating by the rams. On a per ewe exposed basis, Romanov-sired litters produced either the largest or the smallest values for litter weaning weight, depending on the breed of ewe. Effects of ram breed on number born and litter birth weight interacted (P < .05) with season of mating. The largest litters within each ram breed were associated with the October mating season. Montadale and Romanov rams sired larger and heavier litters from August matings than from December matings, whereas the opposite was true for Dorset-sired litters. Texel- and Finnsheep-sired litters were similar in size and weight from August and December matings. Breed of ram differences affected per ewe lambing productivity measurements (P < .01). Differences between ram breeds for ewe productivity were noted, with increased number born and improved survival of crossbred progeny to weaning for Romanov-sired litters. These results may have implications for using these ram breeds as sires in different crossbreeding systems. Structured mating systems or the creation of new composite populations involving these breeds could be used to match the resources, environment, and market of specific production situations.

Animals↗

PubMed1999

Genetic parameters for growth traits for a composite terminal sire breed of sheep.

Records of 9,055 lambs from a composite population originating from crossing Columbia rams to Hampshire x Suffolk ewes at the U.S. Meat Animal Research Center were used to estimate genetic parameters among growth traits. Traits analyzed were weights at birth (BWT), weaning (7 wk, WWT), 19 mo (W19), and 31 mo (W31) and postweaning ADG from 9 to 18 or 19 wk of age. The ADG was also divided into daily gain of males (DGM) and daily gain of females (DGF). These two traits were analyzed with W19 and with W31 in three-trait analyses. (Co)variance components were estimated with REML for an animal model that included fixed effects of sex, age of dam, type of birth or rearing, and contemporary group. Random effects were direct and maternal genetic of animal and dam with genetic covariance, maternal permanent environmental, and random residual. Estimates of direct heritability were .09, .09, .35, .44, .19, .16, and .23 for BWT, WWT, W19, W31, ADG, DGM, and DGF, respectively. Estimates of maternal permanent environmental variance as a proportion of phenotypic variance were .09, .12, .03, .03, .03, .06, and .02, respectively. Estimates of maternal heritability were .17 and .09 for BWT and WWT and .01 to .03 for other traits. Estimates of genetic correlations were large among W19, W31, and ADG (.69 to .97), small between BWT and W31 or ADG, and moderate for other pairs of traits (.32 to .45). The estimate of genetic correlation between DGM and DGF was .94, and the correlation between maternal permanent environmental effects for these traits was .56. For the three-trait analyses, the genetic correlations of DGM and DGF with W19 were .69 and .82 and with W31 were .67 and .67, respectively. Results show that models for genetic evaluation for BWT and WWT should include maternal genetic effects. Estimates of genetic correlations show that selection for ADG in either sex can be from records of either sex (DGM or DGF) and that selection for daily gain will result in increases in mature weight but that BWT is not correlated with weight at 31 mo.

Animals↗

PubMed1999

Evaluation of the ovine callipyge locus: III. genotypic effects on meat quality traits.

A resource flock of 362 F2 lambs provided phenotypic and genotypic data to estimate effects of callipyge (CLPG) genotypes (NN, NC, CN, and CC) on meat quality traits. The mutant allele is represented as C, the normal allele(s) as N, and the paternal allele of a genotype is given first. Lambs of each genotype born in 1994 and 1995 were serially slaughtered in six groups at 3-wk intervals starting at 23 wk of age. Warner-Bratzler shear force and subjective evaluation of marbling were collected during both years from longissimus. Calpastatin activity was measured on longissimus from the 1994 group, and ELISA quantification of calpastatin protein was obtained from the 1995 group. Significant additive and paternal polar overdominance effects on meat quality traits were detected. This is in contrast to previous research that detected only polar overdominance effects on slaughter and carcass traits in this population. The magnitude of genotypic effects on shear force differed significantly between years; however, additive (P < .01), paternal polar overdominance (P < .001), and maternal dominance (P < .01) effects adjusted for variation in carcass weight were detected within each year. Shear force data adjusted to the mean slaughter age or carcass weight indicated that the means and variances of CN and CC genotypes were greater than values of NC and NN. Shear force values were greatest for CN and were intermediate for CC. The difference in shear force (adjusted for variation in slaughter age) between homozygous genotypes (additive effect) was supported by calpastatin activity data with 2-df F-tests of 3.66 (P < .05) and 11.84 (P < .001) at d 0 and 7 postmortem, respectively. Corresponding values for the paternal polar overdominance effects on calpastatin activity were 53.80 (P < .001) and 87.43 (P < .001). Calpastatin ELISA data (d 0, adjusted for slaughter age) exhibited a paternal polar overdominance effect exclusively with a 2-df F-test of 57.63 (P < .001). Additive and paternal polar overdominance effects on marbling adjusted for slaughter age had F-tests of 6.41 (P < .01) and 93.29 (P < .001), respectively. Consequences of increased longissimus shear force must be addressed if the advantages of CN lambs for dressing percentage and carcass composition are to be realized. Further research is needed to establish whether selection targeted at changing the background genome can mitigate the negative effects of the C allele on meat tenderness.

Animals↗

PubMed1998

A second-generation linkage map of the sheep genome.

A genetic map of Ovis aries (haploid n = 27) was developed with 519 markers (504 microsatellites) spanning approximately 3063 cM in 26 autosomal linkage groups and 127 cM (female specific) of the X Chromosome (Chr). Genotypic data were merged from the IMF flock (Crawford et al., Genetics 140, 703, 1995) and the USDA mapping flock. Seventy-three percent (370/504) of the microsatellite markers on the map are common to the USDA-ARS MARC cattle linkage map, with 27 of the common markers derived from sheep. The number of common markers per homologous linkage group ranges from 5 to 22 and spans a total of 2866 cM (sex average) in sheep and 2817 cM in cattle. Marker order within a linkage group was consistent between the two species with limited exceptions. The reported translocation between the telomeric end of bovine Chr 9 (BTA 9) and BTA 14 to form ovine Chr 9 is represented by a 15-cM region containing 5 common markers. The significant genomic conservation of marker order will allow use of linkage maps in both species to facilitate the search for quantitative trait loci (QTLs) in cattle and sheep.

Animals↗

PubMed1998

Evaluation of the ovine callipyge locus: II. Genotypic effects on growth, slaughter, and carcass traits.

A resource flock of 362 F2 lambs provided phenotypic and genotypic data to estimate effects of callipyge (CLPG) genotypes on growth, slaughter, and carcass traits. Lambs were serially slaughtered in six groups at 3-wk intervals starting at 23 wk of age to allow comparisons at different end points. Probabilities of CLPG genotypes were calculated at a position 86 cM from the most centromeric marker of chromosome 18. A contrast of CLPG genotypic effects, based on the paternal polar overdominance model, was used to evaluate callipyge and normal phenotypes. Relationships of traits with slaughter age, carcass weight, or 12th-rib fat depth for callipyge and normal phenotypic groups were estimated by regression. Callipyge and normal lambs did not differ for growth traits measured from birth to slaughter. Callipyge lambs produced 55.9% of live weight as chilled carcass weight compared with 51.7% for normal lambs at the same mean live weight of 48.32 kg. Lighter pelt, kidney-pelvic fat, and liver weights contributed to this advantage of callipyge lambs for dressing percentage (P < .001). Estimated accretion rates of carcass protein at the mean slaughter age were 12.5 and 10.2 g/d for callipyge and normal carcasses, respectively. Corresponding values for carcass fat were 35.2 and 42.1 g/d. Compositional differences in favor of callipyge carcasses were detected at constant values of slaughter age, carcass weight, and 12th-rib fat depth. Callipyge carcasses had 2.56 kg greater fat-free lean and 1.39 kg less fat than normal carcasses at the same mean age of 214.9 d (P < .001). The majority of these differences were established before the initial group was slaughtered and were maintained as age increased. Callipyge carcasses consisted of 24.3% fat and 71.3% fat-free lean, compared with 31.5 and 64.0% for normal carcasses at 25.6 kg of carcass weight. When evaluated at .49 cm of 12th-rib fat depth, callipyge lambs were 15.4 d older and produced 4.1 kg heavier carcasses with 4.3% less fat (P < .001). Effects of CLPG genotypic groups on carcass composition were greater than virtually all reported breed substitution effects. Use of the CLPG mutant allele in structured mating systems can dramatically increase production of lean lamb.

Age Factors↗

PubMed1998

Evaluation of the ovine callipyge locus: I. Relative chromosomal position and gene action.

Genotypic and phenotypic data were collected to estimate chromosomal position of the callipyge (CLPG) gene and to test gene action. Nine Dorset rams of extreme muscling phenotype and 114 Romanov ewes composed the grandparent generation of a resource flock of 362 F2 lambs segregating at the CLPG locus. The parent generation consisted of eight F1 sires and 138 F1 dams. The F2 lambs were serially slaughtered in six groups at 3-wk intervals starting at 23 wk of age to allow comparisons at different end points. A linkage group of 25 marker loci (mean of 708 informative meioses per marker) spanning 87.2 cM was developed and improved the previous known coverage and precision of marker order and interval distance from available maps of ovine chromosome 18. Probabilities of each CLPG genotype were calculated at 1-cM intervals (0 to 107 cM). Statistical models included effects of year, sex, sire, regressions on genotypic probabilities, and genotype-specific linear and quadratic regressions on appropriate covariates. Orthogonal contrasts of CLPG genotypic effects evaluated additive, maternal dominance, and paternally derived polar overdominance models of gene action. The most parsimonious model did not include the additive and maternal dominance genetic contrasts. From analyses of four key traits, a consensus for position of CLPG was obtained at 86 cM relative to the most centromeric marker. An F-test with 3 df representing polar overdominance was maximum at position 86 cM (F = 407.4; P < .00001) with leg score as the dependent variable. These results are consistent with assignment of the CLPG locus to the telomeric region of chromosome 18 and support the polar overdominance model of gene action proposed by Cockett et al. (1996). Furthermore, recombinant individuals with definitive phenotypes confined the position of CLPG to a 3.9-cM interval, facilitating positional cloning experiments.

Animals↗

PubMed1997

Extensive genomic conservation of cattle microsatellite heterozygosity in sheep.

We report the evaluation of 1036 bovine microsatellite primer pairs for their suitability as linkage markers in sheep. Approximately 58% (605/1036) of bovine primer pairs amplified a locus in sheep. Sixty-seven per cent (409/605) of amplified loci were detected as polymorphic. Marker heterozygosity, allele number and range of allele sizes were significantly lower in sheep than cattle sampled in this study. However, median fragment size was similar. These data suggest that high-resolution comparative linkage maps between closely related species can be constructed relatively efficiently.

Alleles↗

PubMed1997

A simulation model including ovulation rate, potential embryonic viability, and uterine capacity to explain litter size in mice: I. Model development and implementation.

Litter size in mice was studied using a model including ovulation rate, potential embryonic viability, and uterine capacity. Simulated results were compared with experimental results from a selection experiment with mice. The four criteria of selection were selection on number born (LS), selection on an index of ovulation rate and ova success (IX), selection on number born to unilaterally ovariectomized females (UT), and unselected control (LC). Comparisons were made to statistics of the base generation and to responses after 13 generations of selection. Phenotypic and genetic statistics for uterine capacity were generated so that simulations produced the experimental means, standard deviations, and correlations between left and right litter size, as well as responses in number born using the LS, IX, and UT criteria. Statistics for the simulated data generally agreed with observed values. Simulated heritability in the base generation for uterine capacity was .065. Experimental and simulated responses per generation in litter size through 13 generations of selection were .15 and .16, .17 and .18, and .10 and .11 for LS, IX, and UT, respectively. Simulated responses in uterine capacity after 13 generations were 2.19, 1.60, and 3.40 for LS, IX, and UT, respectively. Simulated means for the base generation were 13.22 and 16.30 for ovulation rate and uterine capacity, respectively. Uterine capacity was an important component of the variability in litter size; however, ovulation rate was the more limiting component.

Algorithms↗

PubMed1997

A simulation model including ovulation rate, potential embryonic viability, and uterine capacity to explain litter size in mice: II. Responses to alternative criteria of selection.

Direct selection for litter size was compared with selection for ovulation rate, ova success, or uterine capacity and for indexes of ovulation rate with ova success or uterine capacity. Selection was simulated for 10 generations in a mouse population based on a model integrating ovulation rate, potential embryonic viability, and uterine capacity. Two indexes including ovulation rate (OR) and ova success (OS) were I = .291 x OR + 2.19 x OS and I = .165 x OR + .736 x OS. Heritabilities for ovulation rate and ova success, assumed in the simulation and to derive the indexes, were .25 and .06, respectively. Both indexes resulted in the same response in litter size, 12.9% greater than response to direct selection for litter size. Two indexes including OR and uterine capacity (TUC = true total uterine capacity; UC = uterine capacity measured as number born for a female with right ovary excised) were I = .881 x OR + .223 x TUC and I = .876 x OR + .568 x UC. Heritabilities assumed for uterine capacity were .09 (TUC) and .065 (UC). The first index assumed true parameters for uterine capacity (TUC) and resulted in a response in litter size that was 23.9% greater than direct selection. The second index was calculated using parameters estimated under a unilateral-ovariectomy model and resulted in response that was 14.7% greater than direct selection. Selection for OR, TUC, UC, or OS resulted in responses that were 4.5, 48.5, 38.7, or 74.8%, respectively, less than that from direct selection for litter size.

Animals↗

PubMed1995

Development and evaluation of a regression equation of prediction for fat-free soft tissue in heterogenous populations of cattle.

Regression equations to predict kilograms of fat-free soft tissue (the sum of water and protein from chemical analyses) were developed from data collected on 526 steers and heifers. Straightbred animals representing Angus, Braunvieh, Charolais, Gelbvieh, Hereford, Limousin, Pinzgauer, Red Poll, and Simmental breeds of cattle contributed to the data set. Cattle ranged in slaughter weight and age from approximately 350 to 575 kg and from 13 to 23 mo, respectively. Diets (100% ground alfalfa, 67% ground alfalfa and 33% ground corn or 33% ground alfalfa and 67% ground corn) were cross-classified with breed and sex. Estimative traits included in the equation were warm carcass weight, fat depth at the 12th rib, and body impedance. Carcass soft-tissue samples were taken for determination of chemical constituents. The prediction equation accounted for 94% of the variation in fat-free soft tissue of the carcass. Adjusting for breed-sex-diet contemporary groups increased the R2 value by 2% units. The prediction model was evaluated using data collected on 65 steers sired by Charolais or by Hereford bulls at the Ft Keogh Livestock and Range Research Laboratory (Miles City, MT). Postweaning feeding strategies and slaughter ages varied among these animals. Carcass weight, back fat depth, and resistive impedance measures were recorded. Carcass soft-tissue samples were taken for determination of chemical constituents. Values of estimator variables recorded at Ft. Keogh were used in the regression equation to predict fat-free soft tissue for each animal. The values for kilogram of fat-free soft tissue determined from chemical analysis were regressed on predicted fat-free soft tissue. the results indicate that fat-free soft tissue of carcasses can be accurately predicted using estimative traits that do not diminish carcass value.

Animals↗

PubMed1995

Relationships among heat production, body weight, and age in Suffolk and Texel ewes.

The objective of this study was to test the null hypothesis that heat production (HP) was equivalent between Suffolk and Texel ewes at common fasted BW and at common ages. Open-circuit respiration calorimetry was used to estimate HP in 48 Suffolk and 48 Texel ewes at eight ages (10, 15, 20, and 28 wk of age and 1.5, 2.5, 3.5, and 4.5 yr of age). Sheep were individually penned in an environmentally controlled building 6 to 10 d before sample collection. Feed was removed 55 h before sample collection. Heat production measurements were made from 55 and 71 h of the feed restriction. Suffolk ewes had greater mature weights (P < .01) and reached maturity more rapidly than Texel ewes (P < .05). At a common weight, Texel ewes had a lower HP than Suffolk ewes. The ratio of HP:BW declined as ewes aged, as indicated by the fact that the slope of the log-transformed data was negative and less than 1 (P < .01). The models predict that Suffolk ewes had a lower HP:BW than Texel ewes at a common age, but when ewes were compared at common proportions of mature weight HP:BW did not differ between breeds. Breed differences in HP seem to be the result of differences between breeds in maturing rate.

Aging↗

PubMed1993

Estimates of maturing rates and masses at maturity for body components of sheep.

Weight data for fleece-free empty body, carcass and offal components, and their chemical constituents (protein, water, lipid, and ash) were collected via serial slaughter techniques. Rams sired by a sheep breed of high genetic merit for growth were slaughtered from birth through 48 mo of age. Approximately six rams were killed at each of 13 slaughter ages. The data were fit with a nonlinear function Yt = A(1-Be-kt) to provide estimates of rates of maturing (k) and weight at maturity (A) for components of interest. Except for the testes, all tissues met the convergence criterion. The proportion of offal components relative to empty BW was greatest at birth and steadily declined after this time. Rates of maturing for visceral organs (except for the heart) and the protein constituent of the offal were of greater magnitude than the carcass and nonprotein constituents of both the offal and carcass. Estimated maturing rate and weight at maturity for lipid of the carcass exceeded corresponding estimates of the offal lipid. Evidence was provided suggesting that the developmental patterns of body components may be established by functional demand.

Animals↗

PubMed1993

Comparison of Texel- and Suffolk-sired crossbred lambs for survival, growth, and compositional traits.

Texel sheep were imported from Finland and Denmark for evaluation as a terminal sire population relative to the Suffolk breed. The objective was to estimate effects of sire breed on fitness, growth, and compositional traits of crossbred progeny that were serially slaughtered at 63, 105, 147, and 189 d of age. A total of 325 lambs, sired by 19 Texel and 20 Suffolk rams, were born to mature, half-Finnsheep ewes during a 2-yr period. Carcass traits were recorded on 183 lambs. Texel-sired lambs had greater survival to weaning (P = .06) and similar birth and weaning weights compared with Suffolk progeny. Lambs by Texel sires grew 11% less rapidly from 63 to 189 d of age. Estimated accretion rates of carcass fat at 189 d of age were 96.1 and 78.5 g/d for Suffolk and Texel progeny, respectively. Corresponding values for carcass protein were 17.4 and 16.0 g/d. At fixed ages, area of the longissimus muscle did not differ between sire breeds. Texel progeny weighed less at 189 d of age, producing lighter, leaner carcasses of shorter length (P < .05). Compositional differences were not detected when sire breeds were compared at 25 kg of carcass weight. However, Texel progeny had significantly greater depth of fat at the 12th rib and weight of kidney-pelvic fat. Data indicated that Texel-sired lambs deposited proportionally more subcutaneous and less intermuscular fat than did lambs by Suffolk sires. Due to the apparent advantage in lamb survival and the observation that Texel progeny produce lean carcasses relative to the intermediate growth rate and mature size characteristic of the breed, it is concluded that Texel sheep can be used effectively as a terminal sire breed.

Adipose Tissue↗

PubMed1993

Uterine function in Meishan pigs.

The Meishan pig provides a biological model with the genetic capacity to express a high prolificacy. This prolificacy can be partially attributed to a higher ovulation rate and a higher rate of prenatal survival at a given ovulation rate throughout gestation than in European breeds. Both early embryonic survival (factors inherent to the ovum and uterus, which occur before day 25 of gestation) and uterine capacity (factors inherent to uterine limitation, which occur from 30 days of gestation to parturition) may contribute to prenatal survival. Crossbreeding studies show that the prolificacy of Meishan pigs is primarily of maternal origin, but not whether the effects occur via the ovum, uterus or systemic factors. Although there have been few comparative studies on uterine function for prolific pigs, experiments relating to three general areas have been reported. During neonatal uterine development, endometrial gland development occurs shortly after birth in Meishan and European breeds. Tissue culture for 24 h showed that secretion of at least three uterine proteins (one identified as retinol-binding protein) increased in clear temporal association with development of the endometrial gland. The secretion of two additional proteins appears to change in a breed-specific manner. Although regulatory roles for uterine proteins remain to be defined, biochemical events associated with neonatal endometrial gland development may affect subsequent adult uterine function. During the time of maternal recognition of pregnancy or early gestation, reports suggest that uterine secretions are enhanced in Meishan pigs, which may partially explain their increased prolificacy. However, other studies show smaller embryo and placental weights at day 30 of gestation, suggesting that prolificacy of Meishan females is related to a maternal ability to control embryo/fetal and placental growth. During the later fetal period (uterine capacity) in European pigs, endometrial response to a crowded uterine environment is minimal, but the conceptus responds to a crowded uterine environment by altering placental function; similar experiments using Meishan pigs are in progress. Once the regulatory determinants of uterine function are understood, improvements can possibly be made in the reproductive efficiency of all swine.

Animals↗

PubMed1991

Straightbred comparison of a composite population and the Suffolk breed for performance traits of sheep.

A terminal sire Composite population was formed by mating Columbia rams to Hampshire-Suffolk crossbred ewes. Subsequent generations were produced by inter se mating. The objective was to compare Composite sheep to purebred Suffolks for numerous performance traits. Young ewes lambing at 1 yr of age were evaluated separately from mature ewes (2, 3, 4, and 5 yr old) of each population. Composite and Suffolk populations did not differ significantly in components of litter weaning weight per young ewe joined. Mature Composite ewes produced more wool than Suffolk ewes. Fertility of mature ewes did not differ significantly between populations. The greater prolificacy (P less than .01) of mature Suffolk ewes was offset by a lower survival to weaning (P less than .01), particularly for twin-born lambs. Consequently, mature Composite and Suffolk ewes did not differ for number weaned and litter weaning weight per ewe joined. The average birth weight of lambs born to young and mature Composite ewes was greater (P less than .02) than the average birth weight of Suffolk lambs. The average weaning weight of lambs born to young Composite ewes was greater (P less than .05) than that of lambs born to young Suffolk ewes. Breed differences were not detected for preweaning daily gains, weaning weights, and postweaning daily gains of ewe lambs born to mature ewes. Likewise, weights of ewes at 125 d of age and weights of mature ewes at breeding did not differ significantly between breeds.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1991

Effects of breed, heterosis, age of dam, litter size, and birth weight on lamb mortality.

Sources of individual plus maternal effects on lamb mortality were studied in data collected at the U.S. Meat Animal Research Center from 1980 to 1985 for paternal and maternal breeds lambing yearly and for maternal breeds lambing at 8-mo intervals. Records included 16,881 lambs born. Breeds included were Finnsheep (F), Dorset (D), Rambouillet (R), Suffolk (S), Targhee (T), Composite 1 (C1 = F/2, D/4, R/4), Composite 2 (C2 = F/2, S/4, T/4), and Composite 3 (C3 = Columbia/2, S/4, Hampshire/4), Traits analyzed were perinatal, postnatal, and total mortality to 60 d of age and postnatal respiratory, digestive, starvation, injury, and other or unknown causes of mortality. The least squares analyses included breed, year, sire within breed-year, sex, linear and quadratic season and age of dam covariates (Model 1), plus litter size (Model 2), plus birth weight (Model 3), and significant two-way interactions. Age of dam, litter size, and birth weight all had important, often quadratic, effects that differed among breeds. Models 1, 2, and 3, respectively, reduced variation by 8, 10, and 16% for perinatal, 7, 8, and 12% for postnatal, and 9, 11, and 20% for total mortality. In Model 1, breed means ranged from 3.5 to 16.2% for perinatal, 7.2 to 21.1% for postnatal, and 16.7 to 32.8% for total mortality. Respiratory and starvation problems were major causes of postnatal mortality. Heterosis for lamb survival retained in composites was 9% for C1 and 18% for C2. Mortality was 1 to 5% higher for males than for females.(ABSTRACT TRUNCATED AT 250 WORDS)

Age Factors↗

PubMed1991

Genetic and phenotypic variation in sources of preweaning lamb mortality.

Information on causes of mortality to 8 wk weaning for 16,881 lambs of 10 line-breed groups by 594 sires born over a 5-yr period was analyzed by least squares procedures to estimate sire variance and covariance components within line and year-season. Heritability estimates were approximately 5% for total mortality in the binomial scale and near 10% when converted to a normal scale. Average heritability estimates in the binomial and normal scale were, respectively, 4 and 12% for perinatal and 3 and 7% for postnatal mortality. The heritability estimates for respiratory problems were inconsistent; binomial-scale estimates ranged from 0 to 7% in different populations. Regression adjustment for effects of variation in litter size and birth weight caused only minor changes in the heritability estimates. Comparison of covariances among half-sibs vs full-sibs indicated very large maternal effects on perinatal mortality but smaller and less consistent effects on sources of postnatal mortality. Phenotypic correlations among sources of mortality indicated a 26% greater influence of postnatal than perinatal mortality on variation in total mortality, but both the genetic and phenotypic correlations between those two components were slightly negative. These results suggest that the use of family and progeny test selection for transmitted effects on both perinatal and postnatal lamb viability should be effective.

Animals↗

PubMed1991

Effect of limited feed intake on growth of subcutaneous adipose tissue layers and on carcass composition in swine.

Little is known about the function of individual backfat layers in swine. Our objective in this study was to evaluate differential growth of each backfat layer in pigs fed different amounts of the same diet. Relationships of growth of backfat layers to deposition of carcass protein and ether extract were also studied. Feed intake levels were ad libitum, 92.5% of ad libitum, and 85% of ad libitum for 36 barrows averaging 95 d of age and 37.8 kg of weight at the start of the study. Chemical composition of the carcass soft tissue was determined at the end of the 84-d study. Daily gain tended to decrease (P less than .10) and conversion of feed to gain improved (P less than .15) as feed intake decreased. The daily depositions (g/d) of protein and ether extract were 62.9 and 205 for the ad libitum group, 61.1 and 176 for the 92.5% intake group, and 59.3 and 153 for the 85% intake group, respectively. The compositional effect of limiting feed intake for 84 d was to produce less carcass soft tissue of greater lean content. Overall backfat depths were 31.5, 29.6, and 27.8 mm for the ad libitum, 92.5, and 85% intake groups, respectively. The outer backfat layer differed among groups; the 92.5 and 85% groups were thinner than the ad libitum group. Relative to the ad libitum group, the change in depth of the middle backfat layer was 86 and 75% for the 92.5 and 85% intake groups (P less than .01). The inner backfat layer was not affected significantly by level of feed intake.(ABSTRACT TRUNCATED AT 250 WORDS)

Adipose Tissue↗