Biomedical subjects

K E Gregory

Publications and source records attributed to K E Gregory.

At least 37 records · Page 2Linked to original sources

PubMed1999

Effects of twinning on postpartum reproductive performance in cattle selected for twin births.

The effects of twinning, dystocia, retained placenta, and body weight on postpartum reproduction were evaluated for 3,370 single and 1,014 twin births. Females were bred by AI for 40 d followed by 20 or 30 d of natural service with equal numbers bred and calved in spring and fall. Percentage of dams cyclic by the end of the AI period was lower (P<.05) for dams birthing and nursing a single calf (92.4%) than for dams birthing twins and nursing zero (98.7%) or two (94.7%) calves. Whereas the interval from parturition to first estrus was shorter (P<.01) for dams birthing and nursing a single (56.9 d) than for dams birthing twins and nursing one (68.5 d) or two (69.6 d) calves, length of the interval was further reduced by dystocia in nonlactating dams of either twins or singles (type of birth x dystocia, P<.05). Ensuing pregnancy rates were also affected by type of birth and dystocia. Without dystocia, dams birthing and nursing a single calf had a higher pregnancy rate (79.2%) than dams birthing twins and nursing one (61.7%) or two (66.3%) calves, whereas the lower ensuing pregnancy rates associated with dystocia in dams of singles (71.9%) resulted in similar rates among dams of singles and twins with dystocia (type of birth x dystocia; P<.01). Having a retained placenta resulted in a lower incidence of (93.5 vs. 96.4%, with vs. without; P<.05) and a longer interval to (64.7 vs. 59.2 d; P<.01) estrus while reducing subsequent pregnancy rates (X = 9.6%) in 3 of the 7 yr evaluated (retained placenta x year, P<.01). Because all parous females were bred during the same calendrical period, the shorter gestation length for twin calves (275.6 vs. 281.3 d) resulted in a longer interval from parturition to conception for twin births, whereas means for conception date differed by only 2 d between dams of twins and singles. Furthermore, a reduction (P<.01) in the interval to conception occurred with dystocia in dams of singles (89.3 vs. 85.0 d, without vs. with dystocia) and of twins nursed by zero (116.9 vs. 83.5 d), one (100.2 vs. 92.8 d), or two (96.1 vs. 97.2 d) calves. Another detriment to fertility was the higher incidence of fetal mortality or abortions associated with twin vs. single pregnancies (12.4 vs. 3.5%; P<.01). However, despite the lower conception rates for dams of twins, the increased prolificacy provides an opportunity to increase total beef production with a twinning technology.

Animals↗

PubMed1999

Estimation of direct, maternal, and grandmaternal genetic effects for weaning weight in several breeds of beef cattle.

Weaning weights from nine parental breeds and three composites were analyzed to estimate variance due to grandmaternal genetic effects and to compare estimates for variance due to maternal genetic effects from two different models. Number of observations ranged from 794 to 3,465 per population. Number of animals in the pedigree file ranged from 1,244 to 4,326 per population. Two single-trait animal models were used to obtain estimates of covariance components by REML using an average information method. Model 1 included random direct and maternal genetic, permanent maternal environmental, and residual environmental effects as well as fixed sex x year and age of dam effects. Model 2 in addition included random grandmaternal genetic and permanent grandmaternal environmental effects to account for maternal effects of a cow on her daughter's maternal ability. Non-zero estimates of proportion of variance due to grandmaternal effects were obtained for 7 of the 12 populations and ranged from .03 to .06. Direct heritability estimates in these populations were similar with both models. Existence of variance due to grandmaternal effects did not affect the estimates of maternal heritability (m2) or the correlation between direct and maternal genetic effects (r(am)) for Angus and Gelbvieh. For the other five populations, magnitude of estimates increased for both m2 and r(am) when estimates of variance due to grandmaternal effects were not zero. Estimates of the correlation between maternal and grandmaternal genetic effects were large and negative. These results suggest that grand-maternal effects exist in some populations, that when such effects are ignored in analyses maternal heritability may be underestimated, and that the correlation between direct and maternal genetic effects may be biased downward if grandmaternal effects are not included in the model for weaning weight of beef cattle.

Animals↗

PubMed1998

Germplasm evaluation in beef cattle-cycle IV: birth and weaning traits.

Gestation length, unassisted calving percentage, perinatal mortality, calf crop weaned (survival from birth to weaning), birth weight, and 200-d weaning weight of 2,597 calves born and 2,433 calves weaned are reported for F1 crosses resulting from matings of Angus, Hereford, Charolais, Gelbvieh, Pinzgauer, Shorthorn, Galloway, Longhorn, Nellore, Piedmontese, and Salers sires to Angus and Hereford dams (> or = 3 yr of age) in Cycle IV of the Germplasm Evaluation (GPE) Program at the U.S. Meat Animal Research Center. Hereford and Angus sires included 1) reference sires born from 1963 to 1971 used in previous cycles of the GPE Program, 2) sires born from 1982 to 1985 (1980s), and 3) sires born from 1983 to 1985 used in natural service clean-up matings. Effects of sire breed of calf were significant for gestation length, unassisted calving percentage, birth weight, and 200-d weaning weight. Gestation length was significantly longer for Nellore than for Charolais, Galloway, Longhorn, Piedmontese, and Salers, which were in turn longer than for Hereford-Angus and Shorthorn. Rankings for birth weight tended to be inversely related to those for calving ease, except for Shorthorn and Salers sires, which required low assistance relative to their heavy birth weights. Rankings for 200-d weight among AI-sired progeny were as follows: Charolais (231.3), Nellore (229.7), Salers (225.5), Shorthorn (223.8), 1980s Hereford-Angus (223.1), Piedmontese (220.0), Galloway (209.5), reference Hereford-Angus (210.1), and Longhorn (199.0); differences > or = 6.5 kg were significant.

Animals↗

PubMed1998

Relative contributions of subcutaneous and intermuscular fat to yields and predictability of retail product, fat trim, and bone in beef carcasses.

Carcass data from one side of 610 steers born from 1988 to 1990 in Cycle IV of the Germ Plasm Evaluation research program were analyzed to develop means for carcass traits and retail product percentages at two fat trim levels (.76 and .00 cm) by yield grade categories. Weights of subcutaneous (s.c.) fat and intermuscular (i.e.m.) fat were recorded separately at each trim level. Quadratic regression curves were plotted for percentages of roast and steak meat (R&S), retail product (RP), and fat trim components relative to incremental changes in USDA yield grade. Prediction equations were developed on a randomly chosen half of the 610 carcasses to predict weights and percentages of R&S, RP, and fat trim using carcass traits obtained at the time of USDA grading and then tested on the remaining half of the carcasses. In addition, prediction equations were developed using s.c. and i.e.m. fat plus carcass traits to evaluate the contribution of each to carcass fabrication yields. Percentage of RP, trimmed to either .76 cm or .00 cm of fat, decreased by an average of 3.5% for each full yield grade increase. Trimming to .00 cm of fat resulted in about 5.3% less RP compared to trimming to .76 cm. A prediction equation for percentage of RP trimmed to .00 cm using adjusted fat thickness, carcass weight, longissimus muscle area, and percentage of kidney knob had an R2 value of .54. The variations in percentage of R&S and percentage of RP at both trim levels were reduced by removing s.c. fat trimmed to .76 cm; however, considerable variation still existed. Subcutaneous fat expressed as a percentage of the sum of i.e.m. and s.c. fat increased as yield grade increased, but the percentage of i.e.m. fat was higher than the percentage of s.c. fat for all yield grades. On the basis of partial correlation coefficients, i.e.m. fat was approximately twice as important as s.c. fat in accounting for variations in fabrication yields.

Adipose Tissue↗

PubMed1998

A model of litter size distribution in cattle.

Genetic increases in twinning of cattle could result in increased frequency of triplet or higher-order births. There are no estimates of the incidence of triplets in populations with genetic levels of twinning over 40% because these populations either have not existed or have not been documented. A model of the distribution of litter size in cattle is proposed. Empirical estimates of ovulation rate distribution in sheep were combined with biological hypotheses about the fate of embryos in cattle. Two phases of embryo loss were hypothesized. The first phase is considered to be preimplantation. Losses in this phase occur independently (i.e., the loss of one embryo does not affect the loss of the remaining embryos). The second phase occurs after implantation. The loss of one embryo in this stage results in the loss of all embryos. Fewer than 5% triplet births are predicted when 50% of births are twins and triplets. Above 60% multiple births, increased triplets accounted for most of the increase in litter size. Predictions were compared with data from 5,142 calvings by 14 groups of heifers and cows with average litter sizes ranging from 1.14 to 1.36 calves. The predicted number of triplets was not significantly different (chi2 = 16.85, df = 14) from the observed number. The model also predicted differences in conception rates. A cow ovulating two ova was predicted to have the highest conception rate in a single breeding cycle. As mean ovulation rate increased, predicted conception to one breeding cycle increased. Conception to two or three breeding cycles decreased as mean ovulation increased because late-pregnancy failures increased. An alternative model of the fate of ova in cattle based on embryo and uterine competency predicts very similar proportions of singles, twins, and triplets but different conception rates. The proposed model of litter size distribution in cattle accurately predicts the proportion of triplets found in cattle with genetically high twinning rates. This model can be used in projecting efficiency changes resulting from genetically increasing the twinning rate in cattle.

Animals↗

PubMed1998

Bayesian analysis of twinning and ovulation rates using a multiple-trait threshold model and Gibbs sampling.

The Multiple-Trait Gibbs Sampler for Animal Models programs were extended to allow analysis of ordered categorical data using a Bayesian threshold model. The algorithm is based on data augmentation, where a value on the unobserved underlying normally distributed variable (liability) is generated in each round of iteration for each categorical observation. The programs allow analysis of several continuous and ordered categorical traits. Categorical traits can have any number of response levels. Models can be different for each trait. The programs were used to analyze twinning and ovulation rates from a herd of cattle selected for twinning rate at the U.S. Meat Animal Research Center. Data included number of calves born at each parturition for the lifetime of a cow and number of eggs ovulated for several estrous cycles before first breeding as heifers. A total of 6,411 calvings was recorded for 2,087 cows with 83.2% single and 16.8% multiple births. A total of 19,849 ovulations was recorded for 2,332 heifers with 85.2% single and 14.8% multiple ovulations. Mean posterior estimates of heritability and fraction of variance accounted for by permanent environmental effects (PE) were .128 and .103 for twinning rate and .168 and .079 for ovulation rate. Mean posterior estimate of genetic correlation was .808, and correlation of PE effects was .517. Use of a threshold model could allow for more rapid genetic improvement of the twinning herd through improved identification and selection of genetically superior animals because of higher heritability on the underlying scale.

Algorithms↗

PubMed1997

Estimation of direct and maternal breed effects for prediction of expected progeny differences for birth and weaning weights in three multibreed populations.

Direct and maternal breed effects on birth and 200-d weights were estimated for nine parental breeds (Hereford [H], Angus [A], Braunvieh [B], Limousin [L], Charolais [C], Simmental [S], Gelbvieh [G], Red Poll [R], and Pinzgauer [P]) that contributed to three composite populations (MARC I = 1/4B, 1/4C, 1/4L, 1/8H, 1/8A; MARC II = 1/4G, 1/4S, 1/4H, 1/4A; and MARC III = 1/4R, 1/4P, 1/4H, 1/4A). Records from each population, the composite plus pure breeds and crosses used to create each composite, were analyzed separately. The animal model included fixed effects of contemporary group (birth year-sex-dam age), proportions of individual and maternal heterosis and breed inheritance as covariates, and random effects of additive direct genetic (a) and additive maternal genetic (m) with covariance (a,m), permanent environment, and residual. Sampling correlations among estimates of genetic fixed effects were large, especially between direct and maternal heterosis and between direct and maternal breed genetic effects for the same breed, which were close to -1. This resulted in some large estimates with opposite sign and large standard errors for direct and maternal breed genetic effects. Data from a diallel experiment with H, A, B, and R breeds, from grading up and from a top cross experiment were required to separate breed effects satisfactorily into direct and maternal genetic effects. Results indicate that estimation of direct and maternal breed effects needed to predict hybrid EPD for multibreed populations from field data may not be possible. Information from designed crossbreeding experiments will need to be incorporated in some way.

Aging↗

PubMed1997

Genetic and environmental parameters for ovulation rate, twinning rate, and weight traits in a cattle population selected for twinning.

A project was implemented in 1981 with the objective of increasing twinning rate in cattle. Daughters of foundation sires had twin calves at a frequency of from 8 to 13%, and foundation females had twin calves at an average frequency of 50%. Data were analyzed on twinning rate, ovulation rate, and weight traits. The h2 of ovulation rate increased from .11 to .38 for a single estrous cycle to the mean of eight estrous cycles. From all data, h2 for single observation of ovulation rate and twinning rate were .10 and .09, respectively. The r(g) between them was .75. The h2 of weight traits ranged from .42 to .54 when weight traits were analyzed pair-wise with ovulation rate and with twinning rate. The r(g) between weight traits with ovulation rate ranged from .15 to .30 and with twinning rate ranged from .24 to .39. Phenotypic mean twinning rate increased from 1.07 to 1.29 calves per parturition for females born 1981 through 1993, and adjusted mean predicted breeding value (PBV) increased from 1.07 to 1.33 calves per parturition. Phenotypic mean ovulation rate for fall of 1984 through fall 1994 birth groups increased from 1.11 to 1.26 per estrous cycle, and adjusted mean PBV for ovulation rate increased from 1.11 to 1.29 per estrous cycle. Because of the high r(g) (i.e., .75) between ovulation rate and twinning rate, and because of a h2 of .35 for ovulation rate for the mean of six estrous cycles, repeated records of ovulation rate in puberal heifers is an effective indirect selection criterion for twinning rate. The positive r(g) between growth traits and ovulation and twinning rate suggest the need for some compromise when the selection goal is increased twinning rate with no increase in growth and size.

Animals↗

PubMed1996

A search for quantitative trait loci for ovulation rate in cattle.

Seventy-seven polymorphic microsatellites were analysed in offspring of three elite sires that were part of the foundation of an experimental population selected for twinning rate at the US Meat Animal Research Center, Clay Center, Nebraska. All females were assessed for ovulation rate by rectal palpation of corpora lutea over 8-10 consecutive oestrous cycles from approximately 12 to 18 months of age, and associations between ovulation rate and sire allele were examined in each of the three sire groups. A preliminary analysis was performed using selectively genotyped daughters of each sire. Markers found significant or approaching significance were also genotyped in all daughters, sons and granddaughters of these sires. A test of marker associations limited to the granddaughter data provided an independent confirmation of marker effect and significance relative to the initial test with daughter data. Putative ovulation rate quantitative trait loci were detected on chromosomes 7 and 23. Marker UWCA20 on chromosome 7 was associated with an effect in excess of one phenotypic standard deviation and accounted for approximately 10% of phenotypic variation ovulation rate. Marker CYP21 (steroid 21-hydroxylase) on chromosome 23 was associated with an effect of slightly less than half a phenotypic standard deviation and accounted for approximately 4% of phenotypic variation.

Alleles↗

PubMed1996

Genetic (co)variances among birth weight, 200-day weight, and postweaning gain in composites and parental breeds of beef cattle.

Genetic and environmental (co)variances for birth weight, adjusted 200-d weight, and postweaning gain were estimated in nine parental and three composite populations of beef cattle. The parental breeds were Angus (A), Braunvieh (B), Charolais (C), Gelbvieh (G), Hereford (H), Limousin (L), Pinzgauer (P), Red Poll (R), and Simmental (S). The composites were MARC I (1/4 B, 1/4 C, 1/4 L, 1/8 H, 1/8 A), MARC II (1/4 G, 1/4 S, 1/4 H, 1/4 A), and MARC III (1/4 R, 1/4 P, 1/4 H, 1/4 A). Heritabilities of additive direct genetic effects for birth weight (.50) and postweaning gain (.49) were greater than for 200-d weight (.32). Heritabilities of additive maternal effects of .09 for birth weight and .10 for 200-d weight were much smaller than direct effect heritabilities. Heritabilities were larger in composites than in parental breeds for additive direct effects of all three traits but smaller for maternal 200-d weight. Correlations were high and positive for direct genetic effects of the three weight traits and higher in composites than in the parental breeds. Correlations between direct and maternal genetic effects for both birth weight and 200-d weight were near zero. Some differences in variances among populations were correlated with differences in weight and milk yield. Heavier populations had larger variances, supporting the use of logarithmic transformation of weights to stabilize variances among genetic groups. Increased average milk yield was correlated with decreased phenotypic variance of 200-d weight. Average milk yield was also implicated in the expression of direct and maternal genetic effects for 200-d weight and their covariance. Comparison of univariate and multivariate estimates of genetic variances suggested that it is important to include birth weight in multivariate analyses of all weight traits to account for increased preweaning mortality of calves with extremely heavy or light birth weights. Based on heritability estimates, within-herd selection in composites should be at least as effective as in purebreds. Some differences among populations in genetic parameters were indicated, especially maternal 200-d weight and its correlations with other traits.

Animals↗

PubMed1996

Effects of twinning on dystocia, calf survival, calf growth, carcass traits, and cow productivity.

This paper reports results from a long-term experiment with a primary objective to increase twinning rate in cattle at the Roman L. Hruska U.S. Meat Animal Research Center. Survival of singles was 13% higher (P < .01) than that of twins at birth, and the difference in survival in favor of singles was of similar magnitude at 72 h (12.9%, P < .01), 150 d (14.8%, P < .01), and 200 d (15.2%, P < .01). Survival of calves with no dystocia was higher than survival of calves with dystocia: 8.6% (P < .01) at birth, 10.8% (P < .01) at 72 h, 12% (P < .01) at 150 d, and 12.2% (P < .01) at 200 d. The effect of dystocia on survival was greater (P < .01) in twins than in singles at birth and at 72 h. Least squares means for dystocia were 20.4% in singles compared with 42.2% in twins. Most of the dystocia in singles resulted from a traction requirement (84.7%) of normal presentations, whereas most of the dystocia in twins (77.8%) resulted from malpresentations, with 59.2% of the malpresentations accompanied with a requirement for traction. Survival in singles ranged from 10.7% to 15.3% greater than in twins at different ages when there was no requirement for assistance in either singles or twins. Calves born as singles were 8.8 kg heavier (P < .01) at birth and 28 kg heavier (P < .01) at 200 d than calves born and reared as twins. Calf weight produced per cow calving was 53.1%, 54.7%, and 58.4% greater (P < .01) at birth, 150 d, and 200 d, respectively, in cows producing twins than in cows producing singles. Cows producing twins had 65.2% more (P < .01) live calves at 200 d than cows producing singles. Single male calves gained 74 g more per day than twin males from birth to 200 d, 45 g more (P < .01) per day from 200 d to slaughter and 57 g more (P < .01) per day from birth to slaughter. Differences between twin and single males in carcass traits were small. A sample of steers from the Twinning Project gained significantly faster and produced significantly more desirable carcasses than a sample of steers from a high performance reference population. Freemartins did not differ (P < .05) from normal females in growth traits, but freemartins had higher (P < .05) scores for marbling with a higher percentage (P < .05) of USDA Choice or better quality grade carcasses and lower estimated percentage retail product.

Analysis of Variance↗

PubMed1996

Genetic trend and environmental effects in a population of cattle selected for twinning.

A selection experiment was established in 1981 to increase twinning rate in cattle. Results reported are through 1993 calf crops. Estimates of genetic parameters for a two-trait twinning and ovulation rate model with genetic groups were as follows: heritabilities of .03 for twinning and .07 for ovulation rates with a genetic correlation of nearly 1.00 and fractional permanent environmental variances of .06 for twinning and .05 for ovulation rate. Corresponding estimates when group effects were ignored were as follows: heritabilities of .08 and .08 and fractional permanent environmental variances of .02 and .04 for twinning and ovulation rates, respectively. Twinning rate (percentage) in the project at the U.S. Meat Animal Research Center has increased in all cows born in the project by year of calving from 3.4% in 1982 to 28.5% in 1993, a phenotypic increase of 25.1%. The estimated genetic change in twinning of cows by year of calving using the groups model has been 15.2%. The increase in average genetic value by year of birth has been 18.2% in twinning and 15.0% in ovulation rate from 1980 through 1991. Solutions for seven selected groups of foundation animals ranged from -6.0 to 33.1% and influenced genetic trend.

Aging↗

PubMed1996

Variances of additive and dominance genetic effects for ovulation and twinning rates in a population selected for twinning.

Estimates of variances due to additive and dominance genetic effects and permanent and temporary environmental effects were obtained for ovulation and twinning rates from a composite population selected for twinning rate. Measures of ovulation rate after 11 mo of age on 2,317 heifers with a total of 19,209 measures were used. Twinning measures were on 1,522 first-parity cows, 1,311 later-parity cows with a total of 3,571 measures, and 1,704 all-parity cows with 5,100 measures. Models included fixed effects of year-season-age at calving for twinning, and year-season of birth, age in months, and calendar month of measurement for ovulation rate. Four analyses were performed for each sample: combinations of models with and without dominance effects and with and without covariates for fractions of inheritance from the seven foundation groups. Variance components as fractions of phenotypic variance for analysis of all ovulation rate measures were .076, .000, and .045 for additive, dominance, and permanent environmental effects with no foundation groups in the model and .069, .000, and .050 with foundation groups in the model. For sums of eight measures, the estimates were .287 and .000 for relative variances of additive and dominance effects with groups in the model and .316 and .000 with groups ignored. For twinning rate for first parity, estimates were .126 and .209 for relative variances of additive and dominance effects; for later parities, estimates were .045 and .035 for models including foundation group effects. The results suggest lack of dominance effects in expression of ovulation rate and the possibility of dominance effects for embryo and(or) fetal survival or conception rate because twinning rate is a function of ovulation, conception, and embryo and(or) fetal survival rates.

Aging↗

PubMed1996

Direct and maternal genetic covariances by age of dam for weaning weight.

Weaning weights of calves of dams at ages in years of 2, 3, and older were modeled to be three separate traits. Fixed effects were sex of calf-year of birth combinations for nine pure breeds and sex of calf-year of birth-generation for three composite populations. Random effects fitted for each trait were correlated direct and maternal genetic, maternal permanent environmental, and temporary environmental. Direct and maternal effects were correlated across traits. A multiple-trait, derivative-free REML algorithm was used to estimate the 30 (co)variance components. Number of animals per breed group ranged from 1,244 to 4,326. For the three traits for pure breeds, average proportions of phenotypic variance were .34, .31, and .27 for direct genetic; .16, .15, and .12 for maternal genetic; and .18, .20, and .17 for maternal environmental effects. Average correlations among the three traits were .84 for direct genetic, .78 for maternal genetic, and .71 for maternal environmental effects. Average of direct-maternal genetic correlations for pure breeds was .05. For the composite breeds, average proportions of phenotypic variances were .44, .46, and .36 for direct genetic; .06, .06, and .05 for maternal genetic; and .16, .14, and .14 for maternal environmental effects. Average correlations among the three traits were .93 for direct genetic, .76 for maternal genetic, and .85 for maternal environmental effects. Average direct-maternal genetic correlation was .09 for composites. No evidence was found for greater direct-maternal genetic correlation for earlier than for later ages of dam. Sign and magnitudes of direct-maternal genetic correlations seemed to differ among pure breeds and were reflected in composites from those parent breeds.

Aging↗

PubMed1995

Direct and maternal genetic responses to selection for weaning or yearling weight or for yearling weight and muscle score in Hereford cattle.

An experiment involving crosses among selection and control lines was conducted to partition direct and maternal additive genetic response to 20 yr of selection for 1) weaning weight (WWL), 2) yearling weight (YWL), and 3) an index of yearling weight and muscle score (IXL). Maternal response was estimated from reciprocal crosses among unselected sires and dams of control (CTL) and the selection lines. An Angus line was added to increase the number of reciprocal cross comparisons. Direct responses of WWL, YWL, and IXL linebreds compared with CTL were significant for all traits. Maternal genetic responses were much smaller than direct responses. Direct response in birth weight was largest for YWL, followed by WWL and IXL. Maternal effect of IXL on birth weight was larger and that of WWL and YWL was smaller than CTL. Direct responses in weaning weight did not differ greatly among selection lines; maternal response was greater for IXL than for WWL, which was selected for this trait, and response was negative for YWL. Responses in maternal effects on final weight were much reduced in Hereford crosses because of a negative relation between maternal responses in pre- and postweaning gains, especially in YWL and IXL. However, in Angus crosses, a positive association between pre- and postweaning gains increased maternal responses in final weight. Direct response for postweaning gain was greater in IXL than in YWL of WWL in Hereford crosses. In Angus crosses, YWL had larger direct responses for birth weight, preweaning gain, and postweaning gain than in other lines. The direct response for muscle score from selection in IXL, which was selected for muscle score and yearling weight, was greater than in other lines; maternal response was not important. The greatest gain in final weight was obtained when selection resulted in a favorable change in the total of direct and maternal effects pre- and postweaning, which in this experiment was provided by including a muscle score along with yearling weight as selection criteria.

Aging↗

PubMed1995

Predicting beef carcass cutability.

Analyses were conducted to develop and test the efficacy of beef carcass cutability prediction equations. Data from 1,602 calf-fed steer carcasses (Germplasm Utilization Project; GPU) were used to develop the equations and an additional 1,160 calf-fed steer carcasses (Germplasm Evaluation Project; GPE) were used to validate the equations. In both experimental groups, USDA yield grade ranged from < 1 to > 5 and the SD of yield grade was > .8 indicating a relatively large amount of variation in carcass cutability. Models were developed to predict boneless, totally trimmed retail product yield (RPYD), fat trim yield (FATYD), and bone yield (BONEYD) using 1) carcass traits, 2) carcass traits and wholesale rib dissection traits, 3) carcass traits and 9-10-11 rib dissection traits, and 4) carcass traits and 9-10-11 rib dissection and chemical traits. For each dependent variable, the best single predictor was a wholesale rib dissection trait, and the best higher order model contained at least one wholesale rib dissection trait. Equations developed explained 87, 88, and 77% of the variation in RPYD, FATYD, and BONEYD, respectively. When validated against GPE carcasses, models developed from GPU carcasses explained 74, 78, and 69% of the phenotypic variation and 96, 94, and 84% of the genetic variation in RPYD, FATYD, and BONEYD, respectively. Prediction of carcass cutability using carcass and wholesale rib dissection traits should allow for rapid, precise, and cost-effective assessment of variation in cutability.

Animals↗

PubMed1995

Genetic and phenotypic (co)variances for growth and carcass traits of purebred and composite populations of beef cattle.

Least squares means, genetic (sigma g), and phenotypic (sigma p) standard deviations, and phenotypic coefficients of variation (CV) were estimated on an age-constant basis for growth, carcass, and meat traits of castrate males from 12 breed groups combined, for 9 purebreds combined, and for the F3 generation of three composite populations combined to which the nine purebreds contributed. Also, heritabilities (h2) and genetic (rg) and phenotypic (rp) correlations were estimated among growth, carcass, and meat traits for all breed groups combined involving 1,594 individuals that were the progeny of 306 sires (214 purebred and 92 composites). Coefficients of variation and sigma g generally were similar for composites and contributing purebreds for growth and size-related traits. For traits relating to carcass composition and meat quality, means, sigma p, or CV for composites and contributing purebreds generally were similar. Generally, estimates of sigma g and h2 were similar among all breed groups combined, contributing purebreds combined, and composites combined. Generally, rg were high among all measures of carcass fat, indicating major difficulty in achieving a high percentage of retail product simultaneously with a high fat content of the longissimus muscle that is required for carcass quality grade. Generally, rp were of smaller magnitude than rg. All rp of marbling score or percentage of ether-extracted fat in the longissimus muscle with all end-use properties relating to palatability including shear force, and sensory evaluation of tenderness, juiciness, and flavor were below .30.

Animals↗

PubMed1995

Genetic and phenotypic (co)variances for production traits of intact male populations of purebred and composite beef cattle.

Least squares means, genetic (sigma g) and phenotypic (sigma p) standard deviations, and phenotypic coefficients of variation (CV) were estimated for growth traits of intact males from 12 breed groups combined, for nine purebreds combined, and for the F1, F2, F3, and F4 generations of three composite populations to which the nine purebreds contributed. Heritabilities (h2) and genetic (rg) and phenotypic (rp) correlations were estimated for growth traits, calving difficulty of calves with dams of different ages, and gestation length. Coefficients of variation and sigma g generally were similar for composites and contributing purebreds. Generally, estimates of h2 were similar for all breed groups combined, contributing purebreds combined, and composites combined. Estimates of h2 for calving difficulty were higher for calves with 2-yr-old dams than for calves with dams > or = 3 yr old and were sufficiently high (.27 and .31) to be a useful selection criterion for reducing calving difficulty. Mean h2 pooled within all breed groups ranged from .35 for 200-d weight and 368-d weight to .48 for 368-d height. Estimates of h2 for subjective scores of anatomical traits were only slightly lower than those for growth and size traits. The h2 of scrotal circumference (.43) was similar to those for growth and size traits. Genetic correlations between birth weight and calving difficulty were similar for 1) calves with dams of all ages, 2) calves with 2-yr-old dams, and 3) calves with dams > or = 3 yr old.(ABSTRACT TRUNCATED AT 250 WORDS)

Aging↗