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Genetic parameters for stayability to six ages (ST1, . . ., ST6), for five measures of stayability to calving (SC2, . . ., SC6), and for five measures of stayability to weaning (SW2, . . ., SW6), were estimated using records of 2,019 Hereford cows collected from 1964 to 1979 from a selection experiment with a control line and three lines selected for weaning weight, yearling weight, and an index of yearling weight and muscle score. The model included birth year of the cow as a fixed effect and the cow's sire as a random effect. Analyses were performed with 1) a generalized linear mixed model for binary data using a probit link with a penalized quasi-likelihood function, and 2) with a linear mixed model using REML. Genetic trends were estimated by regressing weighted means of estimated transmitting abilities (ETA) of sires by birth year of their daughters on birth year. Environmental trends were estimated by regressing solutions for year of birth on birth year. Estimates of heritability (SE) for ST were between 0.09 (0.08) and 0.30 (0.14) for threshold model and between 0.05 (0.04) and 0.19 (0.09) for linear model. Estimates of heritability from linear model analyses transformed to an underlying normal scale were between 0.09 and 0.35. Estimates of heritability (SE) for SC were between 0.29 (0.10) and 0.39 (0.11) and between 0.18 (0.09) and 0.25 (0.08) with threshold and linear models. Estimates of heritability transformed to an underlying normal scale were between 0.30 and 0.40. Estimates of heritability (SE) for SW were between 0.21 (0.14) and 0.47 (0.19) and between 0.12 (0.08) and 0.26 (0.12) with threshold and linear models, respectively. Estimates of heritability transformed to an underlying normal scale were between 0.21 and 0.50. Estimates of genetic and environmental trends for all lines were nearly zero for all traits. Correlations between ETA of sires for stayability to specific ages, for stayability to calving, and for stayability to weaning with threshold and linear models ranged from 0.09 to 0.82, from 0.68 to 0.90, and from 0.67 to 0.87, respectively. Selection for stayability would be possible in a breeding program and could be relatively effective as a result of the moderate estimates of heritability, which would allow selection of sires whose daughters are more likely to remain longer in the herd. Selection for weaning and yearling weights resulted in little correlated response for any of the measures of stayability.

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

Retained heterosis for meat traits was estimated in F3 generation castrate males in three composite populations of beef cattle finished on two levels of dietary energy density (2.82 Mcal of ME and 3.07 Mcal of ME and 11.50% CP) and serially slaughtered at four end points at intervals of 20 to 22 d. Breed effects were evaluated in nine parental breeds (Red Poll [R], Hereford [H], Angus [A], Limousin [L], Braunvieh [B], Pinzgauer [P], Gelbvieh [G], Simmental [S], and Charolais [C]) that contributed to the three composite populations (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, and 1/4 A). Breed effects were important (P < .01) for all carcass and meat traits evaluated. Dietary energy density and slaughter group affected (P < .05) most traits evaluated. The effects of retained heterosis were not consistent among composites. For the mean of the three composites, retained heterosis was significant only for percentage of 9-10-11th rib fat and for percentage of retail product. Phenotypic correlations indicated that marbling score was a poor predictor of palatability attributes of individual carcasses. Estimates of heritability were intermediate to high for measures of fatness but were generally low for palatability attributes. The high negative genetic correlation (-.56) between percentage of retail product and marbling score and the relatively low genetic correlations between percentage of retail product and palatability attributes suggests the need for simultaneous attention to percentage of retail product and palatability attributes rather than to marbling score. Correlations among breed group means were generally high for measures of fatness with palatability attributes and were high and negative for percentage of retail product with marbling score and with other measures of fatness. Limited opportunity exists for selecting among breeds to achieve high levels of marbling in the longissimus muscle simultaneously with a high percentage of retail product. These results suggest that the most logical approach to resolution of the genetic antagonism between favorable carcass composition and less favorable palatability attributes is to form composite breeds with breed contributions organized to achieve an optimum balance between favorable carcass composition and desirable palatability attributes at optimum slaughter weights.

Selection in three lines of Hereford cattle for 1) weaning weight (WWL), 2) yearling weight (YWL), and 3) an index of yearling weight and muscle score (IXL) was studied. Remnant foundation cows and semen from seven foundation sires were used to establish an unselected control line for the last 11 yr of the experiment. Performance data collected over a 23-yr period on birth weight (BWT), weaning weight (WWT), postweaning gain (PWG), yearling weight (YWT), muscle score (MSC), and an index (IDX) giving equal weight to standard deviations of yearling weight and muscle score were analyzed. Generation interval of midparents was about 4.16 yr in each selected line. Sire and dam selection differentials, in standard deviation units per generation, for primary criteria were, respectively, 1.59 and .33 for WWT in WWL, 1.75 and .25 for YWT in YWL, and 1.42 and .25 for IDX in IXL. Components of direct and maternal genetic variances, direct-maternal covariance, and dam permanent environmental variance were estimated by REML. The average annual response of males and females in actual units for each trait in WWL, YWL, and IXL was, respectively, BWT, .22, .24, and .27 kg; WWT, .98, .63, and 1.26 kg; YWT, 2.43, 2.64, and 3.44 kg; and MSC, .053, .009, and .104 scores. Average selection responses in BWT, WWT, YWT, MSC, and IDX per unit of primary criteria in each selection line (all in standard deviation units) were .22, .20, .31, .10, and .24 for WWT in WWL; .23, .12, .32, .04, and .21 for YWT in YWL; and .27, .22, .40, .20, and .36 for IDX in IXL. Responses in bold type are realized heritability and others are correlated responses. Realized genetic correlations were .78 for WWT and YWT, .87 for WWT and IDX, and .86 for YWT and IDX. Responses for all traits in IXL were greater than in other selected lines.

Retained heterosis for growth, carcass, and meat traits was estimated in F3 generation castrate male progeny in three composite populations finished on two levels of dietary energy density (2.82 Mcal of ME and 3.07 Mcal of ME and 11.50% CP) and serially slaughtered at four end points at intervals of 20 to 22 d. Breed effects were evaluated in nine parental breeds (Red Poll [R], Hereford [H], Angus [A], Limousin [L], Braunvieh [B], Pinzgauer [P], Gelbvieh [G], Simmental [S], and Charolais [C] that contributed to the three composite populations (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, and 1/4 A). Breed effects were important (P.01) for carcass weight, dressing percentage, fat thickness, and marbling score; for retail product, fat trim and bone percentages and weights at two levels of fat trim (8 and 0 mm); and for carcass lean, fat, and bone percentages and weights. Mean slaughter weight was 54.7 kg greater for the Simmental, Gelbvieh, and Charolais breeds than for the Limousin but did not differ (P.05) from Limousin in retail product weight or carcass lean weight because of higher dressing percentage, lower fat trim percentage, and lower bone percentage of Limousin. The effects of dietary energy density were important (P.01) for most traits. The interaction of breed group x dietary energy density generally was not important. Retained heterosis generally was significant for each composite population for weight of retail product, fat trim, bone, and carcass lean, fat, and bone. For percentage of retail product, fat trim, carcass lean, carcass fat, and chemical fat in the 9-10-11th rib cut, generally, heterosis was significant for composites MARC II and MARC III but not for composite MARC I (i.e., composites MARC II and MARC III had a lower percentage of retail product and carcass lean and a higher percentage of fat trim, carcass fat, and chemical fat in the 9-10-11th rib cut than the mean of contributing purebreds).

Summary Data from nine parental breeds and three composite populations described in the preceding article were used to calculate heritabilities and phenotypic and genotypic correlations among carcass and meat traits. Phenotypic correlations indicated that marbling was a poor predictor of longissimus muscle palatability a ttributes of the individual carcasses. Heritability estimates were intermediate to high for fatness measures but generally low for palatability attributes. The high negative genetic correlation (-.56) between percentage of retail product and marbling score and the relatively low genetic correlations between percentage of retail product and palatability attributes suggest simultaneous selection for percentage of retail product and palatability, rather than for marbling score. Correlations among breed group means were generally high between measures of fatness and palatability attributes and were high and negative between percentage of retail product and marbling score or other fatness measures. Thus, opportunity is limited to select among breeds for high levels of marbling and a high percentage of retail product at the same time. The most logical approach to resolving that genetic antagonism is to form composites from breeds that contribute an optimum balance between favorable carcass composition and desirable meat palatability.

Retained heterosis in F2 cows nursing F3 progeny was evaluated in 3-, 4-, and greater than or equal to 5-yr-old cows. Traits evaluated included milk yield at three stages of lactation and 200-d weight of progeny. Breed effects were evaluated in the nine parental breeds (Red Poll [R], Hereford [H], Angus [A], Limousin [L], Braunvieh [B], Pinzgauer [P], Gelbvieh [G], Simmental [S], and Charolais [C]) that contributed to the three composite populations (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). Breed effects were significant for 12-h milk yield, estimated 200-d milk yield, and 200-d weight of progeny. Herefords were lowest (P less than .05) for 12-h milk yield and estimated 200-d milk yield, and Braunvieh produced significantly more milk than all breed groups except Pinzgauer and Simmental, for which the difference approached significance. The correlation among breed group means (nine parental breeds and three composites) for 12-h milk yield with 200-d weight of progeny was .91. When 200-d weight was adjusted to a common estimated 200-d milk yield, Hereford, Angus, Red Poll, and Limousin did not differ (P greater than .05); all were significantly lighter than Braunvieh, Pinzgauer, Gelbvieh, Simmental, and Charolais, which did not differ (P greater than .05) from each other.(ABSTRACT TRUNCATED AT 250 WORDS)

The prevalence of bovine respiratory disease (BRD) was assessed in a population of 10,142 beef calves representing nine pure breeds and three composite populations born in 1983 through 1988. Twenty-four percent of the calves experienced at least one episode of respiratory disease during the 1st yr of life; frequencies over the six birth years ranged from 14 to 38%. The timing of respiratory disease outbreaks differed among birth years; in 4 of the 6 yr, more illness occurred in the pasture before weaning than in the feedlot after weaning. Frequencies of BRD during preweaning and postweaning periods were analyzed separately. Pure breeds and composite populations within a single preweaning location differed in frequency of illness during the preweaning period. However, not all possible breed comparisons could be made because preweaning location differed for the breed groups, and preweaning location had a significant effect on the frequency of respiratory disease in the preweaning period. The preweaning location effect did not carry through to the postweaning period. Pinzgauers had the highest BRD frequency within the feedlot (24.6%). The heritability estimates of BRD during the preweaning and postweaning periods did not differ significantly from 0 (.10 +/- .02 and .06 +/- .07, respectively). Although it is likely that response to selection for resistance to BRD would be slight using the animal's history of BRD as the selection criterion, including information on relatives or additional immune traits may improve the accuracy of an estimated breeding value for BRD resistance.

Heterosis effects in F1 dams producing F2 progeny and retained heterosis in combined F2 and F3 dams producing F3 and F4 progeny were evaluated in dams 2 yr old, in dams greater than or equal to 5 yr old, and in dams of all ages. Traits included pregnant percentage, calf crop born percentage, calf crop weaned percentage, 200-d calf weight per heifer or cow exposed, and 200-d calf weight. Breed effects were evaluated in the nine parental breeds (Red Poll [R], Hereford [H], Angus [A], Limousin [L], Braunvieh [B], Pinzgauer [P], Gelbvieh [G], Simmental [S], and Charolais [C]) that contributed to the three composite populations (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). Breed effects were significant for all traits evaluated in the three age groupings and generally were greatest in 2-yr-old dams and smallest in dams greater than or equal to 5 yr old. Heterosis effects for 200-d calf weight were relatively uniform among age groupings and among the three composite populations and heterosis retained was equal to, or greater than, expectation based on retained heterozygosity. Heterosis effects in animals of all ages for reproductive traits in F1 dams producing F2 progeny differed among the three composite populations, as did heterosis retained in combined F2 and F3 dams producing F3 and F4 progeny. In dams of all ages, heterosis retained for reproductive traits in F2 and F3 dams producing F3 and F4 progeny did not differ (P greater than .05) from expectation based on retained heterozygosity in two of the three composite populations, but loss of heterosis was greater (P less than .05) than expectation based on retained heterozygosity in one of the three composite populations for calf crop born percentage, calf crop weaned percentage, and 200-d calf weight per heifer or cow exposed. This reduction was the result of increased fetal loss between pregnancy diagnosis and parturition.(ABSTRACT TRUNCATED AT 400 WORDS)

Records of Angus, Hereford, Shorthorn, and first-cross cows born from 1960 to 1963 were used to study the effect of age at first calving and culling policy on cumulative survival (SU), number of breeding seasons (BS), pregnancies (PG), calves born (CB) and alive at 72 h (C72) and at weaning (CW), calf weaning weights (WW), and input/output efficiency, up to 12 yr of age. The 155 cows born in 1960 and 1961 calved first at 3 yr of age (M3) and the 173 born in 1962 and 1963 calved at 2 yr of age (M2). Analyses included both actual culling of cows open in two consecutive years (AC) and imposed culling of any open cow (IC). Also, economic efficiency for no culling (NC) of cows for infertility after first calving and up to 10 yr of age was calculated. The model included cow birth year-sire breed of cow (Y-S), sires within Y-S, breed of cow's dam (D), and D x Y-S. Linear functions of Y-S were used to estimate means for M2 and M3 cows. Under AC, by 12 yr of age M2 exceeded M3 cows by 6.8% SU, 1.1 BS, 1.2 PG, 1.1 CB, 1.0 C72, .9 CW, and 138 kg WW (P less than .10). Under IC, M2 exceeded M3 cows by only .7% SU, .3 BS, .3 PG, .3 CB, .2 C72, and .1 CW; and M3 produced 24 kg more WW than M2 cows (P greater than .10). Economic efficiency was higher for M2 than for M3 cows (greater than 10% at 6 yr to greater than 5% at 12 yr culling age), regardless of culling policy. Economic efficiency was maximum when terminal age of cows was 6 to 9 yr for M2 and 8 to 9 yr for M3 cows. Repeatability of pregnancy was higher (P less than .05) for M3 (19%) than for M2 (2%) cows. Economic efficiency for M2 or M3 cows under NC was slightly poorer (2 to 3%) than under either AC or IC policies. Economic efficiency can be improved by managing heifers to calve first as 2-yr-olds under either mild or intense culling of open cows.

Heterosis effects were evaluated in F1, F2, and F3 generations of females and in the F1, F2, and combined F3 and F4 generations of males in three composite populations of beef cattle. Traits included weight, height, and condition scores at different ages, percentage of females reaching puberty at 368, 410, and 452 d, adjusted age, and adjusted weight of females at puberty and scrotal circumference and paired testicular volume of males. Breed effects were evaluated for the nine parental breeds (Red Poll [R], Hereford [H], Angus [A], Limousin [L], Braunvieh [B], Pinzgauer [P], Gelbvieh [G], Simmental [S], and Charolais [C]) that contributed to the three composite populations (MARC I = 1/4 C, 1/4 B, 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). Breed effects were significant for all traits evaluated. Heterosis was significant for weight, height, and condition score at all ages and for most measures of puberty in each generation of each composite and for the mean of the three composite populations. Heterosis for age at puberty was largely independent of heterosis effects on 368-d weight. Heterosis was significant for scrotal circumference and paired testicular volume in each generation of each composite and for the mean of the three composite populations. Heterosis effects on scrotal measurements are mediated both through heterosis effects on growth rate and through factors that are independent of growth rate. Correlation coefficients among breed group means and correlations of breed rank for scrotal measurements with puberty traits of females were greater than or equal to .88 (P less than .01) for all puberty traits except weight at puberty, which was not associated with scrotal measurements. There was close agreement in heterosis observed for most traits and expectation based on retained heterozygosity. These results support the hypothesis that heterosis in cattle for size, puberty, and scrotal measurement traits is due to dominance effects of genes.

Recent studies have implicated insulin-like growth factor I (IGF-I) as an intraovarian regulator of follicular growth and differentiation. Therefore, we investigated the possibility that cattle selected for twin births may have increased concentrations of IGF-I within the ovarian follicle and(or) in peripheral blood. The estrous cycles of 14 cows with histories of producing twins and 12 control monotocous cows were synchronized with 35 mg of prostaglandin F2 alpha (PGF2 alpha). Blood and follicular fluid were collected 48-50 h post-administration of PGF2 alpha (follicular phase of the estrous cycle). Concentrations of IGF-I were measured by RIA after acid-ethanol treatment of serum or follicular fluid. Twin-producing cows had a greater (p less than 0.05) number of large (greater than or equal to 4 mm) follicles and 47% greater (p less than 0.05) concentrations of IGF-I in peripheral blood than control cows. Cattle selected for high twinning frequency also had greater (p less than 0.05) concentrations of IGF-I (+/- SE) in the two largest follicles than control (unselected) cows (327 +/- 28 vs. 243 +/- 29 ng/ml). IGF-I concentrations in pooled small (1-3.9 mm) follicles were less (p less than 0.05) than in large follicles but did not differ between control and twin-producing cattle. In addition, the percentage of IGF-I concentrations measured in follicular fluid to that of serum was lower (p less than 0.05) in small follicles than in large follicles, and was greater (p less than 0.05) in large follicles of control (93.2 +/- 5.3%) than twin-producing (76.2 +/- 4.4%) cattle.(ABSTRACT TRUNCATED AT 250 WORDS)

An elite, three-generation family from the USDA Meat Animal Research Center twinning population was examined for evidence of ovulation rate quantitative trait loci (QTL). This work was both a continuation of previously reported results suggesting evidence for ovulation rate QTL on bovine Chromosome (Chr) 7 and an extension of a genome-wide search for QTL. Additional markers were typed on Chr 7 to facilitate interval mapping and testing of the hypothesis of one versus two QTL on that chromosome. In addition, 14 other informative markers were added to a selective genotyping genome screening of this family, and markers exhibiting nominal significance were used to identify chromosomal regions that were then subjected to more exhaustive analysis. For Chr 7, a total of 12 markers were typed over a region spanning the proximal two-thirds of the chromosome. Results from interval mapping analyses indicated evidence suggestive of the presence of QTL (nominal P0.00077) within this region. Subsequent analysis with a model postulating two QTL provided evidence (P0.05) for two rather than one QTL on this chromosome. Preliminary analysis with additional markers indicated nominal significance (P0.05) for regions of Chrs 5, 10, and 19. Each of these regions was then typed with additional markers for the entire three-generation pedigree. Significant evidence (P0.000026) of ovulation rate QTL was found for Chrs 5 and 19, while support on Chr 10 failed to exceed a suggestive linkage threshold (P0.00077).

Postweaning growth, puberty, and pregnancy traits were evaluated for 783 F1 heifers sired by Angus, Hereford, Charolais, Shorthorn, Galloway, Longhorn, Nellore, Piedmontese, and Salers bulls and out of Angus and Hereford dams in Cycle IV of the Germplasm Evaluation (GPE) Program at the U.S. Meat Animal Research Center. The Hereford and Angus sires included a sample of bulls born from 1982 to 1985 (1980s HA) as well as reference sires born from 1963 to 1970 (REF HA) used in previous cycles of the GPE program. Breed group of sire had a significant (P.01) effect on age and weight at puberty, on 200-, 400-, and 550-d weights, on ADG from 200 to 400 and from 400 to 550 d, and 550-d hip height, but it did not influence (P.05) pregnancy rate. Mean age and weight at puberty were predicted from the cumulative distribution because of censoring of data in each tail of the distribution. Sire breed group rankings (and predicted means in days) for age at puberty were as follows: Piedmontese (332), Shorthorn (338), Charolais (348), REF HA (348), Galloway (351), 1980s HA (352), Salers (355), Longhorn (357), and Nellore (405). Sire breed group rankings (and predicted means in kilograms) for weight at puberty were Longhorn (283), Piedmontese (298), Galloway (305), REF HA (309), Shorthorn (329), 1980s HA (330), Salers (338), Nellore (341), and Charolais (345). Sire breed group rankings (and least squares means in kilograms) for 200-d weight were Charolais (229), Salers (225), Nellore (221), Shorthorn (220), Piedmontese (215), 1980s HA (215), Galloway (209), REF HA (206), and Longhorn (197), with differences8.3 kg significant. Rankings for 400-d weight (kilograms) were Charolais (390), Shorthorn (384), Salers (380), 1980s HA (374), Nellore (364), REF HA (356), Piedmontese (353), Galloway (348), and Longhorn (321), with differences11.5 kg significant. Rankings for 550-d weight (kilograms) were Charolais (445), Salers (430), Shorthorn (429), 80's HA (422), Nellore (420), Piedmontese (401), REF HA (398), Galloway (389), and Longhorn (371), with differences11.7 kg significant. Rankings for 550-d hip height (centimeters) were Nellore (132.2), Charolais (131.9), Salers (129.9), Shorthorn (129.5), Piedmontese (126.7), 1980s HA (126.1), Longhorn (125.3), Galloway (121.7), and REF HA (121.5), with differences1.35 cm significant. Breed of sire had significant effects on growth and puberty traits of heifers.

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.

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.

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.

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.

Least squares means, genetic ( ug) and phenotypic ( ap) standard deviations, and pheno- typic 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, Fa, F3, and F4 generations of three composite populations to which the nine purebreds contributed. Heritabilities (h2) and genetic (rg) and phenotypic (Ip) correlations were estimated for growth traits, calving difficulty of calves with dams of different ages, and gestation length. Coefficients of variation and ug 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 2 3 yr old and were sufficiently high (.27 and .3 1) 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 circumfer- ence ( .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 2 3 yr old. The rg of gestation length with birth weight was low (. 2 1) and was .57 and 54, respectively, with calving difficulty score and with percentage calving difficulty for calves with dams 2 3 yr old. Phenotypic correlations were relatively high among growth and size traits and were intermediate between birth weight and both expressions of calving difficulty in calves with 2-yr-old dams (.53 and .42) but were lower for calves with dams in other age classes.

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.

Retained heterosis for different measures of gain efficiency was estimated in F3 generation castrate male progeny in three composite populations finished on two levels of dietary energy density (2.82 and 3.07 Mcal of ME and 11.50% CP) and serially slaughtered at four end points at intervals of 20 to 22 d. Breed effects were evaluated in nine parental breeds (Red Poll [R], Hereford [H], Angus [A], Limousin [L], Braunvieh [B], Pinzgauer [P], Gelbvieh [G], Simmental [S], and Charolais [C]) that contributed to the three composite populations (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, and 1/4 A). Gain efficiency was evaluated in time constant (0 to 207 d), gain constant (310 to 540 kg), carcass weight constant (333 kg), and retail product weight constant (225 and 210 kg) end points and to different marbling score and longissimus muscle fat end points. Expressions of gain efficiency included live weight gain/megacalories of ME and retail product weight/megacalories of ME. Significant differences were observed among breeds in all measures of gain efficiency. Breeds that had the smallest weight to maintain tended to be more efficient in live weight gain in the time constant period, whereas breeds with the highest rate of gain tended to be more efficient in the gain constant period. To marbling score or longissimus muscle fat end points, breeds with the lowest marbling scores and smallest percentage fat in the longissimus muscle on an age constant basis (e.g., Limousin and Gelbvieh) tended to be less efficient, whereas breeds with the highest marbling score and highest percentage of fat in the longissimus muscle on an age constant basis (e.g., Hereford and Angus) tended to be more efficient. Breeds with the highest percentage of retail product (Limousin and Gelbvieh) were more efficient to retail product weight end points, or when retail product weight was the measure of output. Steers fed the higher energy density diet were more efficient in live weight gain to time constant, live weight gain constant, marbling score constant, and longissimus fat constant end points and were more efficient in the production of retail product weight to retail product weight end points because of the shorter period of maintenance. Retained heterosis was not consistent among composites in different measures of gain efficiency. Higher initial weights resulting in greater requirements for maintenance had a negative effect in composites for most measures of gain efficiency.

Heterosis effects were evaluated in three composite populations in F1, F2, and F3 generations separately and combined in 1-yr-old and from 2- through greater than or equal to 7-yr-old beef cows. Traits included actual weight, weight adjusted to a common condition score, hip height, and condition score. Breed effects were evaluated in the nine parental breeds (Red Poll [R], Hereford [H], Angus [A], Limousin [L], Braunvieh [B], Pinzgauer [P], Gelbvieh [G], Simmental [S], and Charolais [C]) that contributed to the three composite populations (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). Breed group (parental breed and composite) effects were significant for all traits analyzed. The effects of heterosis were generally important (P less than .05) for all traits in F1, F2, and F3 generations separately and combined in the three composite populations. Generally, the magnitude of heterosis observed at 1 yr of age did not differ from that observed in cows from 2 through greater than or equal to 7 yr old. Adjusting weight to a common condition score resulted in an average reduction of heterosis effects on actual weight by approximately one-fourth. Thus, approximately one-fourth of the effects of heterosis on weight result from heterosis effects on condition score. Generally, retained heterosis in the F3 generation of either 1-yr-old or from 2-through greater than or equal to 7-yr-old cows of the three composite populations did not differ (P greater than .05) from expectation based on retained heterozygosity for the traits analyzed. These results support the hypothesis that heterosis for weight, hip height, and condition score of cows of these age classes is the result of dominance effects of genes.

A data set that was used to estimate covariance components with REML for an animal model with eight measures of ovulation rate treated as separate traits was used as a template to simulate data sets of eight multivari- ate normal traits that were then truncated to binomial traits. The model for simulation included eight measures on 610 animals with 1,071 animals in the numerator relationship matrix. Heritabili- ties were equal for the eight measures, and both genetic and phenotypic correlations among the measures were equal. Ten replications for each combination of heritability C15, .25, and .35) and genetic correlation (.50, .6& and .901 were simu- lated on the normal scale. For each replicate, estimates of the eight heritabilities and 28 genetic correlations were obtained by multiple-trait REML. The usual transformation of heritability estimated on the binomial scale overestimated heritability on the normal scale. Genetic correla- tions on the binomial scale seriously underesti- mated the correlations on the normal scale. Standard errors of the estimates obtained by replication were somewhat larger than the ap- proximate SE from REMLPK (the multitrait REML program of K. Meyer). A final set of 10 simulated replications with heritability of .25 and genetic correlation of 1.00 resulted in average estimates of .18 for heritability and of .66 for genetic correlation that agree closely with those from the analysis of measures of ovulation at eight estrous cycles used as a template; averages for heritabil- ity of .l6 and for genetic correlation of .66 were obtained .

Heterosis effects were evaluated as traits of the dam in F2 progeny of F1 dams and F3 and 4 progeny of F2 and 3 dams in three composite populations of beef cattle. Traits included birth weight, birth date, calving difficulty percentage, and survival percentage at birth, 72 h, and weaning for calves with dams of different age classes. Breed effects were evaluated for the nine parental breeds (Red Poll [R], Hereford [H], Angus [A], Limousin [L], Braunvieh [B], Pinzgauer [P], Gelbvieh [G], Simmental [S], and Charolais [C]) that contributed to the three composite populations (MARC I = 1/4 C, 1/4 B, 1/4 L, 1/4 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). Among calves with 2-yr-old dams, breed effects were significant for birth weight, birth date, calving difficulty percentage, and survival percentage at birth but not at 72 h and weaning. Calf survival at weaning was lowest for smallest (less than mu - 1.5 sigma) and largest (greater than mu + 1.5 sigma) birth weight classes and did not differ among intermediate birth weight classes. Calves with difficult births with 2-yr-old dams were significantly heavier at birth (39.6 vs 35.4 kg) and had significantly lower survival at 72 h (87.1 vs 92.2%) and at weaning (77.4 vs 85.1%) than calves with 2-yr-old dams that did not experience difficult births. Among calves with dams greater than or equal to 3 yr old and from dams of all ages, breed group effects generally were significant for the traits analyzed. Important breed group effects on dystocia and survival traits were observed independent of breed group effects on birth weight. Effects of heterosis were significant for birth weight for each generation of each composite population and for the mean of the three composite populations. Generally, heterosis effects for calving difficulty percentage were not significant. Effects of heterosis generally were significant for date of birth (earlier) for each composite population and for the mean of the three composite populations. Heterosis effects on survival to weaning percentage generally were positive but generally were not significant. Heterosis retained for birth weight, birth date, and survival percentage in combined F3 and 4 generation progeny of combined F2 and 3 generation dams did not differ (P greater than .05) from expectation based on retained heterozygosity. These results support the hypothesis that heterosis in cattle for these traits is the result of dominance effects of genes.

Repeated measures of ovulation rate on puberal heifers should be an effective way to select for increased twinning rate. A reliable estimate of the genetic correlation between ovulation and twinning rates is needed to implement such selection and to predict its efficiency. Restricted maximum likelihood was used to estimate genetic correlations from subsets of data collected from the twinning project at the Roman L. Hruska U.S. Meat Animal Research Center. The animal model included numerator relationships among the animals and fixed effects of year-season of measurement, age at measurement, and birth group. Genetic correlations between averages of ovulation rates for three, four, five, six, seven, and eight estrous cycles and the occurrence of twins were, respectively, .62, .76, 1.00, 1.00, 1.00, and .98 based on observations on 200 to 325 puberal heifers. Corresponding phenotypic correlations ranged from .06 to .26. Genetic correlations between ovulation rate in a single estrous cycle and occurrence of twins were .38, .98, and .98, respectively, for 323, 430, and 283 cows with ovulation rate measured after measurement of twinning, in the same season as measurement of twinning, and more than 1 yr before measurement of twinning. Phenotypic correlations were .00, .07, and .00. Genetic and phenotypic correlations among ovulation rates at six consecutive estrous cycles averaged, respectively, .66 and .12 for 610 heifers. Heritabilities for ovulation rates in individual cycles averaged .16. No evidence of negative environmental covariance between ovulation rates in adjacent cycles was found. These results support the approach of indirectly selecting for twinning rate by measuring ovulation rates in estrous cycles of puberal heifers.

Heterosis effects for birth weight, ADG from birth to weaning, 200-d weight, ADG from weaning to 368 d, 368-d weight, 368-d height, 368-d condition score, and 368-d muscling score (males only) were evaluated separately for each sex in F1, F2, and combined F3 and F4 generations in three composite beef cattle populations. Breed effects were evaluated for the nine parental breeds (i.e., Red Poll [R], Hereford [H], Angus [A], Limousin [L], Braunvieh [B], Pinzgauer [P], Gelbvieh [G], Simmental [S], and Charolais [C]) that contributed to the three composite populations (MARC I = 1/4 C, 1/4 B, 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). Breed effects were significant for all traits evaluated. The large differences among breeds for growth and size traits in combined additive direct and additive maternal genetic effects (Gi + Gm) provide an opportunity to use genetic differences among breeds to achieve and maintain optimum additive genetic (breed) composition for growth and size traits to match cattle genetic resources to a wide range of production and marketing situations. Combined individual and maternal heterosis was significant in the F1, F2, and combined F3 and F4 generations for each composite population and for the mean of the three composite populations in both sexes for most of the traits evaluated. In both sexes, heterosis retained in combined F3 and F4 generations was greater (P less than .05) than expected based on retained heterozygosity for birth weight, ADG from weaning to 368 d, and for 368-d weight and did not differ (P greater than .05) from expectation for other traits. These results support the hypothesis that heterosis in cattle for traits related to growth and size is due to dominance effects of genes.

Records of 328 Angus, Hereford, Shorthorn, and first-cross cows produced from 1960 to 1963 were used to estimate heterosis (h) and individual (gI) and maternal (gM) average breed effects on cumulative survival (CS) by ages to 12 yr, longevity (L), and size (SI) and condition of incisors at 10 to 15 yr of age. Reasons for cow disposal were also studied. The 155 cows born in 1960 and 1961 first calved at 3 yr of age, and the 173 born in 1962 and 1963 first calved at 2 yr of age. Analyses for CS and L were done for both actual culling of cows open in two consecutive years (AC) and imposed culling of any open cow (IC). The model for CS and L included cow birth year-breed of cow's sire (Y-S), sires within Y-S, breed of dam (D), and D x Y-S. For SI, the model included breed of cow, year of recording, and quadratic effect of age. Linear contrasts were used to estimate h, gI, and gM for quantitative variables, and chi-square was used for discrete variables. Under both AC (P less than .05) and IC, crossbreds exceeded straightbreds in CS to 12 yr (16.7 and 8.5%) and L (1.36 and .99 yr). Estimates of gI and gM for CS and L were generally small, except for the low (P less than .05) gM of Shorthorn cows under IC. Mortality and culling for emaciation, cancer eye, or prolapse was less for crossbreds than for straightbreds and increased with age. Crossbreds had longer (P less than .01) and better (P less than .001) teeth than straightbreds. The longer productive life of crossbred cows reduces rearing costs for replacements and increases sales of calves and cull cows.

The effects of heterosis for gestation length, dystocia, calf survival, birth weight, 200-d weight, and ADG from birth to weaning were evaluated in F1, F2, and combined F3 and F4 generations in three composite populations. Breed effects were evaluated for the nine parental breeds (Red Poll, Hereford, Angus, Limousin, Braunvieh, Pinzgauer, Gelbvieh, Simmental, and Charolais) that contributed to the three composite populations. Breed effects were significant for all traits evaluated except survival at birth. The large differences among breeds in additive direct and additive maternal genetic effects offer a great opportunity to use the genetic differences among breeds to achieve and maintain optimum additive genetic (breed) composition to match genetic resources to a wide range of production-marketing ecosystems. There was no heterosis for gestation length. Mean heterosis for dystocia was significant estimated in F1 but not in F2 or in the combined F3 and F4 generations. Mean heterosis was not significant in any generation for survival at birth, to 72 h, and to weaning for the F1 generation; mean heterosis was significant for survival to weaning for the F2 generation and approached significance (P = .06) for the combined F3 and F4 generations. Mean heterosis over all composite populations and heterosis for each composite population were significant in all generations for weight at birth and at 200 d and for ADG from birth to weaning. Retained heterosis was not less than expected from retained heterozygosity in composite populations for the traits evaluated. These results suggest that heterosis for these traits likely is due to dominance effects and, thus, can be attributed to the recovery of accumulated inbreeding depression in the parental breeds.

An evaluation of natural twinning in beef cattle revealed that cows birthing twins had shorter (P less than .01) gestation lengths, more (P less than .01) retained placentas, more (P less than .01) dystocia, more (P less than .01) days to estrus, lower (P less than .01) conception rates and more (P less than .01) days to pregnancy than cows birthing singles. Days to estrus, conception rate and days to pregnancy were not affected by number of calves reared (1 vs 2) in cows birthing twins. Survival at birth was greater (P less than .01) for single- than for twin-born calves, but twins and singles did not differ (P greater than .05) in postnatal survival. When dystocia was experienced, calf survival at birth was 95% vs 73% for singles vs twins compared with 99% vs 92% when no dystocia was experienced. Calves born twins were lighter (P less than .01) at birth, 100 d and 200 d, but twins and singles did not differ in postweaning gains. Total calf weights at 100 d per cow calving were 12% greater (P less than .01) in cows birthing twins vs singles when twin calves reared by foster dams were excluded. The potential increase in cow productivity for total calf weight at 100 d is 40% if calf survival rates of twins with dystocia relative to survival rates of twins without dystocia were comparable to survival rates of singles with and without dystocia, and if cows birthing twins were fed and managed to obtain conception rates equal to those of cows birthing singles. Identification of cows gestating twins to provide for their higher prepartum nutritive requirements and calving assistance at parturition is necessary to make twinning in cattle an economically viable technology.

In the first part of the experiment, embryos of Brown Swiss-Hereford (BS-H) reciprocal crosses were transferred to BS and H recipient cows and embryos of Red Poll-Angus (RP-A) reciprocal crosses were transferred to RP and A recipient cows. Calves resulting from embryo transfers (ET) were weaned early (3 to 5 d). Males were castrated and their growth, feed efficiency and carcass composition were recorded. In the second part of the experiment, matings to produce reciprocal crosses were made by natural service (NS) between BS and H and between RP and A. Some of the offspring were weaned at 3 to 5 d; the remainder nursed their dams to an age of 150 to 180 d. Growth after 200 d, feed efficiency and carcass data were recorded on steers. Females produced in both parts of the experiment were reared for breeding, and post-200-d growth and age at puberty were recorded. Neither breed of recipient (uterine influence) nor breed of donor (cytoplasmic influence) had important effects on growth or carcass traits. Large differences were observed for most growth and carcass traits between offspring that were weaned early and those that nursed their dams. Effects of early weaning were greater in progeny of Brown Swiss and Red Poll dams than in progeny of Angus and Hereford dams. Prenatal maternal influences (e.g., ovum cytoplasm and uterine influence) are relatively small in comparison with postnatal maternal influences in contributing to maternal effects in beef cattle.

Foundation cows were selected using prior records from one of two sources, private herds or other projects at the Research Center. Comparing twinning rates before and after selection, the repeatability was lower for those from the first (.08) than for those from the second (.16) source with a combined value of .12. Realized heritability of single-parity twinning rate estimated from selection of parents and response in daughters of foundation females was .06. Paternal half-sib estimate of heritability of twinning rate was .02 +/- .07. Estimates of repeatability computed from calving records of females born in the project indicate that permanent environmental effects on twinning rate in cattle are small. Mean calving rate of females born in the project was 1.11 in the data set that included all data and 1.09 in the data set that excluded females from highly selected parents. Twinning rate was greater (P less than .05) in fall than in spring calving (1.13 vs 1.06). Data on twinning rate of a sample of the Swedish Friesian breed were summarized. Mean twinning rate of the Swedish Friesian breed is 2.57%. Age adjusted mean twinning rate of daughters of 32 half-sib sons of one particular Swedish Frieisan sire averaged 5.4% and ranged from .9% to 13.6%. There was no indication of a bimodal distribution, which would be expected if a single gene with a major effect on twinning rate were segregating. The estimated genetic standard deviation (sigma-xn) for mean twinning rates of the 32 sire progeny groups was 1.8%. Observed range among son progenies was .127 or 7.2 sigma-xn, in reasonable agreement with the hypothesis that twinning rate in this population is inherited as a quantitative trait.

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.

Brown Swiss-Hereford (BS-H) reciprocal cross embryos were transferred to BS and H recipient cows and Red Poll-Angus (RP-A) reciprocal cross embryos were transferred to RP and A recipient cows to estimate the relative contributions of ovum cytoplasm and uterine influences to prenatal maternal effects. Calves resulting from embryo transfers (ET) were weaned early (3 to 5 d). Reciprocal cross mating also were made by natural service (NS) between BS and H and between RP and A breeds; part of the offspring were weaned at 3 to 5 d, and the remainder nursed their dams to an age of 150 to 180 d. This was done to estimate breed differences in prenatal and postnatal effects combined and to separate the effects of prenatal maternal influences from postnatal maternal influences of these breeds. Females produced in both ET and NS parts of the experiment were retained to produce three calf crops to an age of about 4.5 yr. The following traits were analyzed: percentage of conception rate; percentage of calf survival; percentage of calves produced per cow exposed; birth and weaning weights of calves produced; and periodic weights, heights, and condition scores of females to an age of 4.5 yr. Neither breed of donor (cytoplasmic influence) nor breed of recipient (uterine influence) had consistently important effects on the traits evaluated. In NS matings, differences between reciprocal crosses were small for most of the traits evaluated. Method of rearing (nursed vs weaned at 3 to 5 d) had no effect on reproductive and maternal traits for RP-A reciprocal cross females, but females that nursed generally were heavier, were taller, and had higher condition scores at most ages than early-weaned females. For the BS-H reciprocal cross, early-weaned females were favored over females reared by their dams in percentage of calves produced per cow exposed, but the method of rearing did not affect other reproductive or maternal traits. BS-H reciprocal cross females that nursed their dams were heavier at 550 d and were heavier and had higher condition scores at an age of 34 mo than early-weaned females.

The potential of ovulation rate before 18 to 21 mo of age in puberal heifers as an indirect selection criterion for twinning rate was considered. Heritability (h2) was .07 +/- .03 for single observations and .34 +/- .18 for the mean of 7.9 estrous cycles per heifer. Estimated repeatability (r) of ovulation rate was less than or equal to h2, indicating negligible permanent environmental effects. Expected h2 for mean ovulation rate (assuming h2 = r = .07 for single observations) for increasing numbers of estrous cycles would be as follows: 4, .23; 6., 31; 8, .38; and 10, .43. About 50% of the heifers produced no multiple ovulations, but 27% produced multiple ovulations in more than 15% of their estrous cycles. Ovulation rate varied seasonally and increased about .01 per month of age (P less than .05). Genetic correlation of mean ovulation rate with adjusted 368-d weight was low (.08 +/- .32). Ovulation rate in postpartum cows was higher (P less than .05) in fall than in spring (1.15 vs 1.08). In postpartum cows, estimated h2 = .24 +/- .13 and r = .17. Mean ovulation rate for postpartum cows was 1.12 vs 1.09 in puberal heifers, accounting in part for the higher h2. Pregnancy rate was higher (P less than .05) in multiple- than in single-ovulating cows. Effects of ovulation rate on embryonic survival were small (P greater than .05). Unilateral and bilateral multiple ovulations were not different in embryonic survival. Accuracy of ovulation rate determination by palpation per rectum was lower in multiple- than in single-ovulating postpartum cows, because some unilateral multiple corpora lutea, especially, were recorded as singles. Results suggest that use of ovulation rate in puberal heifers should permit effective indirect selection for twinning rate among yearling heifers based on individual performance and among young sires based on ovulation rate of sibs and daughters.

A total of 280 young bulls representing five breed groups with an average age of about 1 yr were assigned to five experimental treatments as follows: (1) emasculator castration at d 0, (2) surgical castration at d 0, (3) intact, (4) intact and implanted at d 0 and 70 with 36 mg of zeranol and (5) intact and implanted at d 0 with 72 mg zeranol. All animals were slaughtered and carcass data were collected after a feeding period of 141 d. Method of castration did not affect rate of gain. Intact males not implanted with zeranol gained 38.6% more (P less than .01) during the 141 d period than castrate males. Intact males from the two zeranol implant treatment groups did not differ from each other in gain, but averaged 11.1% more (P less than .01) during the 141 d period than males from the intact treatment group not implanted. Castrate males required 40.4% more (P less than .01) metabolizable energy (ME) and dry matter (DM)/kg gain than intact males not implanted, but intact males implanted with zeranol did not require less (P greater than .05) ME or DM/kg gain than intact males not implanted. Males castrated at about 1 yr showed a progressive decrease in secondary sex characteristics during the 141 d feeding period, while males from the three intact treatments showed a progressive increase. Zeranol did not have an effect on testicular weight or on aggressive male behavioral characteristics. Castrate males had greater (P less than .01) fat thickness at 12th rib, higher (P less than .01) marbling score and lower (P less than .01) cutability and retail product percentage than the males from the three intact treatments, which did not differ (P greater than .05) from each other in traits associated with carcass composition. The effect of treatment on lean color score, though significant, was not of major importance; all treatments produced meat of acceptable color. The longissimus muscle of castrate males had a finer texture (P less than .01) than longissimus muscle from males from intact treatments, which did not differ from each other (P greater than .05).