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The typical cattle production system in Ghana is predominantly pasture-based. Cattle are grazed all year round on natural pastures with minimal feed supplementation. The animals kept in this production system often experience inadequate nutrition and fluctuating nutrient supply affecting their productivity. There is presently limited information on the growth and reproductive performance of the Friesian x Sanga crossbred cattle (Plate 1) and factors influencing these performance traits. The growth and reproductive performance records of 150 Friesian x Sanga crossbred cattle, kept at the Animal Research Institute station in the Accra Plains of Ghana from April 1993 to October 2009 were evaluated to determine the effect of parity of cow, season of calving and sex of calf on birth weight, weaning weight, growth rate, age at first calving and calving interval. The birth weight and weaning weights of the calves averaged 21.8 ± 0.5 kg and 94.2 ± 3.8 kg, respectively, and were not (P > 0.05) affected by sex of calf, parity of cow or season of calving. Parity of cow affected (P < 0.05) weight of calf at 12 months. Calf weight at 12 and 18 months averaged 128.0 ± 3.4 kg and 159.9 ± 4.5 kg, respectively. Pre-weaning and post-weaning average daily gains were 0.33 ± 0.02 kg/day and 0.23 ± 0.03 kg/day, respectively, and were not significantly (P > 0.05) affected by sex of calf, parity of cow or season of calving. The mean age at first calving was 41.2 ± 1.2 months. Calving interval was prolonged averaging 441.6 ± 10.3 days and was significantly (P < 0.05) affected by parity of cow. Calving interval decreased with increasing parity of cow. The age at first calving and calving interval were not (P > 0.05) affected by either sex of calf or season of calving. The growth and reproductive performance of the Friesian x Sanga crossbred cattle was less than optimum. Improving their nutrition could impact, positively, on their productivity through fast growth, increased milk yield and early resumption of ovarian cycles after calving. Thus, results from this study should guide the development of appropriate strategies for increased meat and milk production in Friesian x Sanga crossbred cattle. Key words: Cattle, grazing, growth, pasture, reproduction, INTRODUCTION Livestock production is a major feature of Ghana's agriculture and contributes largely towards meeting food needs, providing drought power, cash income and manure to maintain soil fertility and texture. [...]

Angus x Hereford heifers (15 mo and AI to a single sire) were used to evaluate the effect of prenatal nutritional restriction on postnatal growth and regulation of glucose in plasma. Dams (d 32 of gestation) were stratified by BW and BCS and allotted to low [LN, 55% of NRC (1996) requirements, n = 7] or moderate nutrition [MN, 100% of NRC (1996) requirements, n = 7]. After 83 d of feeding, dams were commingled and received a diet in excess of requirements. Dams were allowed to calve naturally, and bull calves were castrated at birth. Dams and calves were maintained as a group until weaning, and calves were maintained as a group after weaning. Calves (15 mo of age) were adapted to a similar diet during 2 wk; catheters were placed in both jugular veins; and calves were confined in stalls. Two days later, calves were subjected to an intravenous glucose challenge and the next day to an insulin challenge. Dams had similar (P = 0.31) BW at the beginning of the experiment. At the end of restriction, LN dams weighed less (P [less than or equal to] 0.01) and had less BCS (P < 0.001) compared with MN dams. Length of gestation was not affected by prenatal nutritional treatment. Nutrient restriction during gestation did not influence birth weight or postnatal growth. Concentrations of glucose (P = 0.49) and insulin (P = 0.29) were not different in plasma of LN and MN calves before glucose infusion. Plasma concentrations of glucose, after intravenous administration of glucose, decreased more rapidly (P = 0.05) in LN compared with MN calves. Concentrations of glucose (P = 0.68) and insulin (P = 0.55) in plasma of LN and MN calves were similar after infusion of insulin. Nutritional restriction of dams during early gestation did not influence postnatal growth, but altered clearance of glucose after a bolus infusion of glucose. Key words: cattle, glucose, insulin, prenatal nutrition doi: 10.2527/jas.2010-3214

The objective of this study was to estimate (co)variance functions using random regression models on Legendre polynomials for the analysis of repeated measures of BW from birth to adult age. A total of 82,064 records from 8,145 females were analyzed. Different models were compared. The models included additive direct and maternal effects, and animal and maternal permanent environmental effects as random terms. Contemporary group and dam age at calving (linear and quadratic effect) were included as fixed effects, and orthogonal Legendre polynomials of animal age (cubic regression) were considered as random covariables. Eight models with polynomials of third to sixth order were used to describe additive direct and maternal effects, and animal and maternal permanent environmental effects. Residual effects were modeled using 1 (i.e., assuming homogeneity of variances across all ages) or 5 age classes. The model with 5 classes was the best to describe the trajectory of residuals along the growth curve. The model including fourth- and sixth-order polynomials for additive direct and animal permanent environmental effects, respectively, and third-order polynomials for maternal genetic and maternal permanent environmental effects were the best. Estimates of (co)variance obtained with the multi-trait and random regression models were similar. Direct heritability estimates obtained with the random regression models followed a trend similar to that obtained with the multi-trait model. The largest estimates of maternal heritability were those of BW taken close to 240 d of age. In general, estimates of correlation between BW from birth to 8 yr of age decreased with increasing distance between ages. Key words: growth curve, longitudinal data, Nellore cattle, random regression doi:10.2527/jas.2008-1511

The objective of this research was to assess the genetic control of BW, hip height, and the ratio of BW to hip height (n = 5,055) in Brahman cattle through 170 d on feed using covariance function-random regression models. A progeny test of Brahman sires (n = 27) generated records of Brahman steers and heifers (n = 724) over 7 yr. Each year after weaning, calves were assigned to feedlot pens, where they were fed a high-concentrate grain diet. Body weights and hip heights were recorded every 28 d until cattle reached a targeted fatness level. M1 calves had records through 170 d on feed; subsequent records were excluded. Models included contemporary group (sex-pen-year combinations, n = 63) and age at the beginning of the feeding period as a covariate. The residual error structure was modeled as a random effect, with 2 levels corresponding to two 85-d periods on feed. Information criterion values indicated that linear, random regression coefficients on Legendre polynomials of days on feed were most appropriate to model additive genetic effects for all 3 traits. Cubic (hip height and BW:hip height ratio) or quartic (BW) polynomials best modeled permanent environmental effects. Estimates of heritability across the 170-d feeding period ranged from 0.31 to 0.53 for BW, from 0.37 to 0.53 for hip height, and from 0.23 to 0.6 for BW:hip height ratio. Estimates of the permanent environmental proportion of phenotypic variance ranged from 0.44 to 0.58 for BW, 0.07 to 0.26 for hip height, and 0.30 to 0.48 for BW:hip height ratio. Within-trait estimates of genetic correlation on pairs of days on feed (at 28-d intervals) indicated lower associations of BW:hip height ratio EBV early and late in the feeding period but large positive associations for BW or hip height EBV throughout. Estimates of genetic correlations among the 3 traits indicated almost no association of BW:hip height ratio and hip height EBV. The ratio of BW to hip height in cattle has previously been used as an objective measure of BCS in cows or calves; it may offer a unique assessment of body dimension. Results indicated that there is substantial additive genetic variation for this trait, and it may be possible to use EBV to increase BW without increasing frame score in Brahman cattle. Key words: Brahman, feedlot, height, random regression, body weight

Seventy Angus x Simmental calves (BW = 166.3 [+ or -] 4.2 kg) were used in a 3 x 2 factorial arrangement to determine the effect of age at feedlot entry and castration on growth, performance, and carcass characteristics. At 82 d of age, steers were castrated. Calves were placed in the feedlot at 111 (early-weaned), 202, or 371 (yearling) d of age. Steers were implanted with Synovex-S followed 93 d later with Revalor-S. Calves were harvested on an individual basis when fat thickness was estimated to be 1.27 cm. During the feedlot phase, yearlings gained faster (P < 0.01) than calves placed in the feedlot at 202 or 111 d of age (1.88, 1.68, and 1.62 kg/d, respectively); however, from 111 d of age until harvest, ADG was greatest for early-weaned calves, intermediate for cattle placed in the feedlot at 202 d of age, and lowest for yearlings (1.62, 1.47, and 1.21 kg/d, respectively; P < 0.01). Early-weaned calves spent the most days in the feedlot, followed by calves placed in the feedlot at 202 d of age; yearlings spent the fewest days in the feedlot (221, 190, and 163 d, respectively; P < 0.01). Total DMI when in the feedlot was similar (P = 0.22) among age groups; however, daily DMI was lowest for early-weaned calves, intermediate for calves placed in the feedlot at 202 d of age, and the highest for yearlings (7.1, 8.1, 10.5 kg/ d, respectively; P < 0.01). Early-weaned calves were the most efficient, followed by calves placed in the feedlot at 202 d of age; yearlings were the least efficient (227, 207, 180 g gain/kg feed, respectively; P < 0.01). Weight at harvest (682, 582, 517 kg, respectively; P < 0.01) and hot carcass weight (413, 358, 314 kg, respectively; P < 0.01) were greatest for yearlings, intermediate for cattle placed in the feedlot at 202 d of age, and lowest for early-weaned calves. Early-weaned calves had the smallest longissimus area, followed by calves placed in the feedlot at 202 d of age; yearlings had the largest longissimus area (77, 86, 88 [cm. sup.2], respectively; P < 0.01). Calves placed in the feedlot at 111 and 202 d of age had lower yield grades (3.2, 3.1, 3.5, respectively; P < 0.04), and produced fewer select carcasses than yearlings (25, 13, 48%, respectively; P < 0.01). Bulls and implanted steers both had an ADG of 1.7 kg/d when in the feedlot; however, bulls had a greater (P < 0.09) hot carcass weight (370 vs 354 kg) and a larger (P < 0.01) longissimus area (85.8 vs 81.3 cm2) than steers. Earlier feedlot placement resulted in greater quality grades but lower carcass weights. Key Words: Age Groups, Beef Cattle, Carcass Quality, Feedlots

The cosegregation between a genetic marker and the QTL in a well-designed mapping population is the basis for successful QTL mapping. Linkage disequilibria are, however, also expected among individuals that descended from the same breeding line, and some common haplotypes should carry on and segregate among individuals of the line. These identical by descent haplotypes make it possible to identify and locate the QTL segregating in the line. We report the identification of common haplotypes within commercial lines of Bos taurus and their associations with growth traits. One hundred and seventy six male calves and their 12 sires (9 to 30 male calves of each sire) of the Beefbooster, Inc., M1 line selected for maternal traits over 30 yr were genotyped using 16 microsatellite markers chosen from bovine chromosome 5 for the initial haplotype and growth association analysis. In order to verify the results from the M1 line, another 170 male calves and their 14 sires from the Beefbooster M3 line were genotyped using nine microsatellite markers chosen from bovine chromosome 5. The alleles of each male calf contributed by the sire and by the dam were identified, and haplotypes in the M1 line were established along 93% of bovine chromosome 5. The haplotypes in the M3 line were established along the chosen regions of bovine chromosome 5. Regression analysis detected 10 haplotypes in three chromosomal regions (0 to 30 cM, 55 to 70 cM, and 70 to 80 cM) that showed significant associations with birth weight, preweaning average daily gain, and average daily gain on feed in M1 line and 9 haplotypes associated with the growth traits in the same chromosomal regions in the M3 line at the comparisonwise threshold level. On average, the 19 haplotypes have an effect of 0.68 SD on the growth traits, ranging from 0.41 SD to 1.02 SD The results provide a useful reference for further positional candidate gene research and marker-assisted selection. Key Words: Cattle, Haplotypes, Quantitative Traits

Genetic parameters of mature weight are needed for effective selection and genetic evaluation. Data for estimating these parameters were collected from 1963 to 1985 and consisted of 32,018 mature weight records of 4,175 Hereford cows that were in one control and three selection lines that had been selected for weaning weight, for yearling weight, or for an index combining yearling weight and muscle score for 22 yr. Several models and subsets of the data were considered. The mature weight records consisted of a maximum of three seasonal weights taken each year, at brand clipping (February and March), before breeding (May and June), and at palpation (August and September). Heritability estimates were high (0.49 to 0.86) for all models considered, which suggests that selection to change mature weight could be effective. The model that best fit the data included maternal genetic and maternal permanent environmental effects in addition to direct genetic and direct permanent environmental effects. Estimates of direct heritability with this model ranged from 0.53 to 0.79, estimates of maternal heritability ranged from 0.09 to 0.21, and estimates of the genetic correlation between direct and maternal effects ranged from -0.16 to -0.67 for subsets of the data based on time of year that mature weight was measured. For the same subsets, estimates of the proportions of variance due to direct permanent environment and maternal permanent environment ranged from 0.00 to 0.09 and 0.00 to 0.06, respectively. Using a similar model that combined all records and included an added fixed effect of season of measurement of mature weight, direct heritability, maternal heritability, genetic correlation between direct and maternal effects, proportion of variance due to direct permanent environmental effects, and proportion of variance due to maternal permanent environmental effects were estimated to be 0.69, 0.13, -0.65, 0.00, and 0.04, respectively. Mature weight is a highly heritable trait that could be included in selection programs and maternal effects should not be ignored when analyzing mature weight data. Key Words: Beef Cattle, Growth, Heritability, Maternal Effects

Our objective was to determine the influence of bovine growth hormone (bGH) and bovine growth hormone-releasing factor (bGRF) administration on the mRNA abundance of lipoprotein lipase (LpL) and stearoyl-CoA desaturase (SCD). Primiparous Holstein cows received bGH, bGRF, or no treatment from 118 to 181 +/- 1 d postpartum. We hypothesized that bGH and bGRF treatment would increase the mRNA abundance of both SCD and LpL in the mammary gland with a corresponding reduction in adipose tissue. Milk yield significantly increased but milk fat percentage did not change as a result of bGH or bGRF treatment. Short-, medium-, and long-chain fatty acid concentrations in milk were not affected by either bGH or bGRF treatments, with the exception of a modest, but significant, increase in C16:1 and C18:1 following bGH treatment. Analysis was conducted on the genes encoding LpL (E.C. 3.3.1.34), a key enzyme involved in the uptake of fatty acids into tissues, and SCD (E.C. 1.14.99.5), which is the enzyme responsible for introducing A9 double bonds in fatty acids of 16 and 18 carbons in length. In adipose tissue, treatment with bGH and bGRF reduced the mRNA abundance of LpL to 14.6 and 25.7% respectively, of that observed for control animals. Similarly, these treatments reduced the SCD mRNA abundance to undetectable levels in adipose tissue. In mammary gland, bGH and bGRF had no significant impact on LpL mRNA abundance. Bovine GH did not significantly affect SCD mRNA abundance in the mammary gland, and bGRF reduced SCD mRNA abundance. From this study to examine the role of bGH and bGRF on the expression of the genes encoding these key lipogenic enzymes in cattle, we conclude that the increased substrate required for enhanced milk fatty acid yield may have been provided through redirection of nutrients to the mammary gland away from adipose tissue and through overall increased metabolism in the mammary gland. Key Words: Lipoprotein Lipase, Stearoyl-CoA Desaturase, Somatotropin, Cattle

The objective of this study was to determine the effect of a subtherapeutic level of chlortetracycline (CTC) fed to growing beef steers under conditions of limited and adequate dietary protein on plasma concentrations of GH, thyroid-stimulating hormone (TSH), and thyroid hormones before and after an injection of thyrotropin-releasing hormone (TRH) + GHRH. Young beef steers (n = 32; average BW = 285 kg) were assigned to a 2 x 2 factorial arrangement of treatments of either a 10 or 13% crude protein diet (70% concentrate, 15% wheat straw, and 15% cottonseed hulls) and either a corn meal carrier or carrier + 350 mg of CTC daily top dressed on the diet. Steers were fed ad libitum amounts of diet for 56 d, and a jugular catheter was then placed in each steer in four groups (two steers from each treatment combination per group) during four consecutive days (one group per day). Each steer was injected via the jugular catheter with 1.0 [[micro]gram]/kg BW TRH + .1 [[micro]gram]/kg BW GHRH in 10 mL of saline at 0800. Blood samples were collected at -30, -15, 0, 5, 10, 15, 20, 30, 45, 60, 120, 240, and 360 min after releasing hormone injection. Plasma samples were analyzed for GH, TSH, thyroxine ([T.sub.4]), and triiodothyronine ([T.sub.3]). After 84 d on trial, the steers were slaughtered and the pituitary and samples of liver were collected and analyzed for 5[prime]-deiodinase activity. Feeding CTC attenuated the GH response to releasing hormone challenge by 26% for both area under the response curve (P < .03) and peak response (P < .10). Likewise, CTC attenuated the TSH response to releasing hormone challenge for area under the response curve by 16% (P < .10) and peak response by 33% (P < .02), and attenuated the [T.sub.4] response for area under the curve by 12% (P < .08) and peak response by 14% (P < .04). Type II deiodinase activity in the pituitary was 36% less (P < .02) in CTC-fed steers than in steers not fed CTC. The results of this study are interpreted to suggest that feeding subtherapeutic levels of CTC to young growing beef cattle attenuates the release of GH and TSH in response to pituitary releasing hormones, suggesting a mechanism by which CTC may influence tissue deposition in cattle. Key Words: Antibiotics, Chlortetracycline, Cattle, Somatotropin, Thyroxine, Triiodothyronine

Our objective was to determine to what extent rate and efficiency of protein gain in finishing cattle can be enhanced by feeding an amino acid-balanced mixture of undegraded intake proteins. The Cornell Net Carbohydrate and Protein System (CNCPS) model was used to formulate a corn-based diet that would meet the rumen requirements for 410-kg large-framed steers with an estrogen implant and fed an ionophore. The CNCPS model was also used to formulate a highly undegradable intake protein (UIP) mixture from meat and bone meal, blood meal, fish meal, and hydrolyzed feather meal to provide the amino acids needed to supplement those derived from microbial protein to better meet amino acid requirements for growth. Four Holstein steers weighing 407 kg were offered a 90:10 concentrate-forage diet at hourly intervals at 95% of ad libitum intake. The steers were injected with 500 [[micro]gram] of estradiol-17[Beta] at 12-h intervals to mimic the effects of an estrogenic implant. Treatments planned consisted of inclusion of the UIP mixture at 0, 2.5, 5, and 7.5% of the diet DM. Dry matter intake was fixed at 6.4 kg/d, and DM digestibility was not significantly affected by varying the amount of UIP addition. Apparent digestibility of N increased (P = .011) from 63.8 to 65.8, 70.7, and 71.5%, the amount of N absorbed increased (P = .001) from 73 to 84, 100, and 106 g/d, and N balance increased (P = .003) from 20 to 30, 33, and 39 g/d when UIP was fed at 0, 2.6, 5.2, and 7.8% of diet DM, respectively. The efficiency of N use increased 39.7%, and biological value increased 31.6% when the UIP mixture was added to the diet. Circulating concentrations of plasma urea N (PUN) were increased (P = .017) from 4.5 for the control diet to 5.7, 6.2, and 6.1 mg/dL when the UIP mixture was added at 2.6, 5.2, and 7.8%, respectively. Corresponding IGF-I concentrations were also increased from 491 to 558 and 624 ng/mL with 2.6 and 5.2% levels of UIP addition. Plasma glucose, NEFA, and insulin concentrations were not affected by feeding the UIP mix. The rate and efficiency of N use for growth improved with addition of an amino acid-balanced UIP mixture to the diet. Key Words: Cattle, Amino Acids, Nitrogen Metabolism

Skeletal muscle IGF-I and [Alpha]-actin mRNA responses to increased amino acid availability were investigated in young, rapidly growing steers. Four Holstein steers (208 kg BW) were surgically implanted with an abomasal cannula and jugular catheters and allowed 2 wk to recover. Steers were offered hourly a 43:57 forage:concentrate diet at 95% of ad libitum intake supplemented with continuous abomasal infusion of glucose (to replace 12.5% of metabolizable ad libitum energy intake) for 13 d before the start of abomasal infusion of 67 g of casein N/d. Biopsies of the liver and both semimembranosus muscles were removed and frozen in liquid N, and casein infusion was begun. Muscle biopsies were collected at 8, 16, 24, and 48 h, and on d 7 and 14. Nitrogen balance increased from 23.6 to 71.5 g/d (P < .001) within 24 h and remained elevated (mean = 58.4 g/d) during the 14 d of casein infusion. Plasma urea N increased from 4 to 9.5 mg/dL at 24 h and remained unchanged to d 14. Muscle IGF-I mRNA abundance increased to 215% of basal values at 16 h (P < .01), 244% of basal values at 24 h, and 222% of basal values at 48 h after initiation of casein infusion. Values reached a maximum of 274% of basal values on d 7 and then declined to near preinfusion levels on d 14. The IGF-I mRNA abundance was approximately 100 times higher in liver than in skeletal muscle and was not different on d 0 and 14. Although plasma IGF-I concentrations were numerically higher during the first 24 h of abomasal casein infusion, they were not significantly higher during the chronic phase of treatment. Plasma IGF binding protein (BP)-2 concentrations were higher at 16, 24, and 48 h after casein infusion was begun, but IGFBP-3 concentrations were not altered at these sampling times. Neither acute (first 24 h) nor chronic (daily) plasma insulin concentrations were altered by abomasal casein infusion. Plasma somatotropin concentrations were lower (P = .008) at 24 h of casein infusion and beyond. Results suggest that enhanced amino acid availability may modulate skeletal muscle protein synthesis and accretion through an autocrine or paracrine IGF-I influence. Key Words: Cattle, Skeletal Muscle, Growth, Nitrogen Metabolism, Casein

We studied the effect of protein and protein-free energy intake on the degradation rate of myofibrillar protein in preruminant calves in two experiments. Both experiments were similar in design but were performed with two live weight ranges: 80 to 160 kg (Exp. 1) and 160 to 240 kg (Exp. 2). In each experiment, calves were allocated to either an initial slaughter group or to one of 12 treatments (three calves per treatment), which consisted of six protein intake levels at each of two protein-free energy intake levels. Calves were slaughtered and analyzed for body composition when they had reached the target weight. A balance trial was performed when calves had reached 120 and 200 kg BW in Exp. 1 and 2, respectively. Myofibrillar protein degradation rate was measured by the urinary excretion of 3-methylhistidine. Correction of 3-methylhistidine excretion for myofibrillar protein mass was performed based either on the urinary creatinine excretion rate or on estimated body composition during the balance trial. In both experiments, fractional rates of myofibrillar protein degradation increased with increasing protein intake (P < .01). Fractional degradation rates increased with increasing protein-free energy intake in Exp. 1 (P < .10) and in Exp. 2 (P < .05). We conclude that the increased protein deposition rates, reported earlier, induced by nutrient intake are accompanied by increased myofibrillar protein degradation rates. Furthermore, we consider urinary creatinine excretion to be unreliable as an estimator of myofibrillar protein mass in experiments in which a large range of nutrient intakes is applied. Key Words: Veal Calves, Nutrient Intake, Methylhistidine, Protein Turnover, Creatinine

We conducted two experiments with preruminant calves weighing 80 to 240 kg to study the long-term nutritional regulation of circulating IGF-I, thyroxine ([T.sub.4]), and triiodothyronine ([T.sub.3]). The two experiments were similar in design but were performed with calves of two live weight ranges: 80 to 160 kg (Exp. 1) and 160 to 240 kg (Exp. 2). In each experiment, 36 calves were allocated to one of 12 dietary treatments, which consisted of six protein intake levels at each of two energy intake levels. Digestible protein intakes ranged between .90 and 2.72 g N[center dot][BW.sup.-.75][center dot][d.sup.-1] in Exp. 1 and between .54 and 2.22 g N[center dot][BW.sup.-.75][center dot][d.sup.-1] in Exp. 2. The energy intake levels were kept constant on a protein-free basis; increased energy intakes were realized by increasing energy intake from fat and carbohydrates in a fixed ratio. The digestible protein-free energy intakes were 663 and 851 kJ[center dot][BW.sup.-.75][center dot][d.sup.-1] in Exp. 1 and 564 and 752 kJ[center dot][BW.sup.-.75][center dot][d.sup.-1] in Exp. 2. Blood samples were taken 5 to 6 h after feeding once every 14 d until the calves reached their target weight. In both experiments, plasma IGF-I and [T.sub.4] concentrations increased with increasing protein intake (P < .01), but they were unaffected by protein-free energy intake (P > .10). In both experiments, plasma [T.sub.3] levels were markedly higher at the high protein-free energy intake level (P < .01) and increased slightly with increasing protein intake in Exp. 1 (P = .19) and Exp. 2 (P < .01). Results of these experiments suggest the involvement of IGF-I in the response of protein deposition to increased protein intakes and the involvement of the active thyroid hormone [T.sub.3] in the response of protein deposition to increased protein-free energy intakes. Key Words: Veal Calves, Protein Intake, Energy Intake, Insulin-Like Growth Factor, Triiodothyronine, Thyroxine

We developed methods to integrate two published models that partitioned gains in empty body weight (EBW) to fat and fat-free matter. These models were based on separate mathematical formulations for growing and mature cattle. We assumed that as cattle grow from birth to maturity a transition would occur at some point in the life cycle from the growing to the mature mathematical formulation. This transition point and the rate at which the transition occurs between the two mechanisms were estimated from published data. Evaluation results with data on steers that were full-fed to grow from birth to 815 kg EBW showed that the methods used to integrate the two models provided an accurate prediction of empty body composition at final slaughter. Evaluation results with full-fed growing cattle that were slaughtered at market weights suggest that partitioning of EBW gains can be fully described by the mathematical formulation used for growing cattle. However, for cattle that were restricted in growth, then realimented, the results showed that a model with a transition to the mathematical formulation for mature cattle, during the realimentation phase, accurately predicted the observed final composition. These results suggest that the integrated model would accurately predict the changes in body composition of cattle of all ages, under different systems of nutritional management. Key Words: Beef Cattle, Growth Models, Body Composition

Partial stage and complete life-cycle growth curves of Brahman cattle were obtained for small, medium, and large frame sizes for a herd under grazing conditions in a subtropical environment. Data were grouped into three stages: birth to weaning (stage 1), weaning to 20 mo (males) or 32 mo (females) of age (stage 2), and 32 mo of age to maturity (females only; stage 3). Within each stage, multiplicative growth models were developed for each frame size and sex. Body weight growth on age t was represented as exp(a + bt + [ct.sup.2]) for stages 1 and 2, and as exp(A + B exp(kt)) for stage 3. The effects of sire and progeny within sire were considered in all models. For stages 2 and 3, the effect of season was also included. To obtain complete life-cycle curves, a growth stage-multiplicative model with stages 1 and 2 was defined; stage 3 was also included for females. Due to a 1-mo adaptation period after weaning, a transition stage between stages 1 and 2 was defined and represented by the model exp(a + bt). In stage 1, the shape of the growth curve differed (P < .05) among frame size groups; sex did not affect the shape of the growth curves, but bull calves had heavier (P < .05) weights than heifer calves. In stage 2, the shape of the growth curves did not differ among frame sizes, but BW differed among frame sizes (P < .05) and sex affected (P < .05) the shape of the growth curves. In stage 3, the shape of the growth curves differed (P < .05) among frame sizes. There were sire effects (P < .05) for stages 1 and 2, but sire effects were not significant for stage 3. Season effects were important (P < .05) for stages 1 and 2. These results suggest that variability in growth patterns provides an opportunity to use management and nutrition to improve production efficiency in cattle of different frame sizes. Key Words: Beef Cattle, Body Weight, Brahman, Growth Curve, Growth Models, Growth Stages

Birth (n = 308), weaning (n = 291), feedlot and carcass (n = 142), and yearling heifer traits (n = 139) were evaluated in [F.sub.1] calves sired by Brahman (BR), Borah (BO), and Tuli (TU) bulls and born to multiparous Hereford and Angus cows. Calves sired by BR were heaviest (P < .05) at birth and largest (P < .05) for cannon bone length. Tuli crosses were smaller (P < .05) for birth weight and cannon bone length than BR and BO crosses. No significant differences were observed for gestation length among sire breeds. Brahman crosses had larger (P < .05) weaning weight, hip height, and preweaning ADG than calves sired by BO and TU. Similar trends were observed for feedlot traits. Carcasses of BR crosses were heavier (P < .05) and had less (P < .05) internal fat than those of BO and TU crosses. Tulicrosses averaged greater (P < .05) skeletal maturity than BO crosses. Tuli crosses averaged greater marbling (P < .05) than BR crosses and less (P < .05) Warner-Bratzler shear force than BO crosses. No differences were observed in longissimus muscle area, fat thickness, or yield grade among sire breeds. Heifers sired by BR were heaviest (P < .05) and tallest (P < .05) at yearling measurement. Brahman [F.sub.1] heifers had larger (P < .05) pelvic height and pelvic area, due to larger skeletal frame size, than BO and TU [F.sub.1] heifers. These results indicate large differences in growth and skeletal size exist among calves sired by these three breeds. Several important differences also exist for carcass quality traits, but not for carcass yield traits, among these three breeds. Key Words: Tropical Cattle, Size, Growth, Carcass, Pelvic Area

Growth in animals is defined as accretion of protein, fat, and bone. Although growth typically is measured as the change in live weight, nutrient retention is estimated more precisely by measuring empty body weight and composition, whereas production economics are measured ideally through carcass weights and quality. As a percentage of live weight gain, carcass weight gain usually is a much higher percentage during the feedlot phase than during the growing phase of production because dressing percentage (ratio of carcass:live weight) increases with maturation and is greater with concentrate than with roughage diets. At a given fraction of mature body size (maximum body protein mass), body fat percentage seems to be a constant. Mature size may be altered genetically and nutritionally. Protein accretion declines to zero when cattle reach their mature body size (approximately 36% fat in empty body weight in modern cattle) even though mature animals can continue to accrete fat. Although fat accretion can be reduced by limiting the supply of net energy, rate of fat accretion by finishing steers given ad libitum access to high-concentrate diets seems to reach a plateau at approximately 550 g daily. Protein mass, in contrast, increases in proportion to empty body weight. The protein:fat ratio of the carcass can be increased through increasing mature size, by administering hormones or hormonal modifiers, by limiting energy intake during the growing period or finishing period, or by slaughtering cattle at an earlier stage of maturity. Energetically, efficiency of accretion of fat is approximately 1.7 times that of protein. But because more water is stored with deposited protein than with deposited fat, lean tissue gain is four times as efficient as accretion of fat tissue. Conversion of protein to fat is very inefficient, suggesting that excess protein is utilized inefficiently. Key Words: Growth, Fat, Protein, Deposition, Feedlot Cattle

Data from 2,101 Brangus calves born from 1986 to 1990 were analyzed with a REML procedure using a derivative-free algorithm in a mixed linear animal model to obtain variance component estimates of ultrasound-measured longissimus muscle area and fat thickness. Direct additive heritabilities (|Mathematical Expression Omitted~) of .39 and .40 were obtained for age-constant weaning and yearling longissimus muscle area (WLMA and YLMA, respectively), with a genetic correlation (|r.sub.g~) of .66 between them. The |r.sub.g~ of YLMA with birth weight (BWT), weaning weight (WWT), postweaning gain (PWG), yearling weight (YWT), frame score (FS), and scrotal circumference (SC) were .17, .29, .43, .38, .01, and .19, respectively. The |Mathematical Expression Omitted~ of age-constant yearling 12th rib fat thickness (FAT) was .14, and cattle averaged .44 cm (SD = .19). Positive |r.sub.g~ were obtained between FAT and WLMA (.19) and YLMA (.12). Negative |r.sub.g~ of FAT with WWT, YWT, and SC were -.17, -.53, and -.33, respectively. Positive |r.sub.g~ were obtained between FAT and BWT (.52), PWG (.44), and FS (.14). Maternal heritabilities |Mathematical Expression Omitted~ of WLMA, YLMA, and FAT were .01, .01, and .10, respectively. Weight-constant WLMA, YLMA, and FAT |Mathematical Expression Omitted~ were .36, .39, and .11, respectively. Selection based on either age-constant YLMA or FAT could potentially result in 1.06 |cm.sup.2~ or .005 cm change per year, respectively, which would be slightly greater than change from selection based on weight-constant YLMA or FAT. Selection based on WLMA or YLMA should be effective, and changes in these traits, growth, and SC should be possible in tandem. Genetic differences in ability to deposit fat probably were not expressed by these young cattle at the nutritional levels provided. Response to selection based on FAT should be minimal, and the effect of such selection on other traits is uncertain. There was no maternal influence on longissimus muscle areas; however, similar |Mathematical Expression Omitted~ and |Mathematical Expression Omitted~ for FAT indicate that variability in preweaning maternal environment has an effect on FAT equal to that of variability in an individual's own fattening ability.

: Double-muscled (DM) cattle possess more muscle fibers than do normal-muscled (NM) beef or dairy cattle. Serum-borne growth factors have been shown to modulate myogenesis. Media containing serum from 12 DM and 60 NM fetuses grouped by crown-rump lengths (CRL) of [is less than or equal to] 25, 26 to 50, 51 to 75, or > 75 cm were used to test the effect of fetal serum on L6 myoblast proliferation. Because DM and NM fetuses were similar in CRL at ages corresponding to 20- to 60-cm CRL, CRL was used to determine fetal age. Normal-muscled fetal serum-induced thymidine incorporation in L6 myoblasts was greater (P < .05) at CRL > 50- than at [is less than or equal to] 50-cm CRL. Mean incorporation tended to increase with CRL. Thymidine incorporation was 56, 41, and 41% greater (P < .05) with serum from DM fetuses than with that from NM fetuses at CRL of < 25, 26 to 50, and 51 to 75 cm, respectively. Morphological examination of cross-sections of the semitendinosus muscle showed that apparent muscle fiber number was greater (P < .05) for DM fetuses than for NM fetuses. These results confirm greater apparent muscle fiber number in DM cattle and show the existence of greater growth factor activity in serum of DM fetuses during early fetal development. This greater growth factor activity may play a role in bovine muscle fiber hyperplasia. Key Words: Bovine, Fetus, Double Muscling, Myoblast Proliferation, Muscle Fibers, Serum

Postweaning growth and carcass characters of 110 steers from a complete two-breed diallel of the Devon and Hereford breeds were examined under two environments. Additive and nonadditive effects were estimated using linear contrasts for several growth and carcass traits. Steers from each of the four breed groups were grown postweaning to slaughter in high- and low-nutrition environments. Weights were recorded every 2 mo. At slaughter, hot carcass weight, longissimus muscle area, kidney and channel fat, and subcutaneous fat at nine sites were measured. Heterosis for postweaning growth rate was 3.9% (P < .01) and for slaughter weight 5.0% (P < .01). Within the low-nutrition environment during periods of slow and fast growth, the Devons and Herefords performed differently. The growth rate of the steers differed in the two environments; however, heterosis for slaughter weight was of the same magnitude in both environments. No differences existed between the straightbreds or between the reciprocal crosses for slaughter weight. Crossbred carcasses were 7.4% heavier (P < .01) than the straightbred carcasses; however, this effect was removed after adjustment for differences in slaughter weight. Heterosis for longissimus muscle area and carcass fatness were not significant after adjusting for carcass weight. Additive differences occurred for carcass traits. Devon carcasses had more kidney and channel fat (P < .05) at a constant hot carcass weight and differences occurred in the partitioning of fat within the subcutaneous depot. No significant maternal effects were observed for the carcass traits measured. Crossbreeding increased carcass weight without altering composition, and relative performance was not affected by the diverse environments. Key Words: Beef, Diallel Crossing, Carcass Composition, Growth Rate, Heterosis J. Anim. Sci. 1992. 70:2688-2694, Results of an experimental study indicated that carcass weight of steers can be increased by cross breeding without affecting other carcass traits. Post-weaning carcass traits and growth of pure bred Devon and Hereford steers and associated cross-breeds reared under conditions of high-nutrition and low-nutrition were assessed. Four groups of steers, Devon, Hereford, Hereford x Devon and Devon x Hereford were assessed for postweaning growth. Carcass characteristics such as carcass weight and subcutaneous fat were measured at the time of slaughter. Nutritional availability influenced growth rate but did not influence heterosis for slaughter weight.

The effect of nitrogen supplementation using fish meal or fish meal and urea on growth and composition of steers kept on a hay- or silage-based diet was examined. Silage-fed cattle showed improvement in weight gain which was further enhanced by protein supplementation during the growing phase. Growth during the finishing phase was dependent on choice of forage with silage-fed steers exhibiting higher growth rates. Carcass composition was not affected by any of the treatments.

The objectives of this study were to determine the efficacy of various doses of rbST on ADG and feed efficiency (FE) and to describe carcass composition changes in finishing beef steers. In Exp. 1, 96 crossbred beef steers (393 kg) received daily i.m. injections of buffer or 33, 100, or 300 [Mu]g/kg of BW of rbST (0ST, 33ST, 100ST, 300ST. In Exp. 2, 200 crossbred beef steers (417 kg) received daily i.m. injections of buffer or 8.25, 16.5, 33, or 66 [Mu]g/.kg of BW of rbST (0ST, 8.25ST, 16.5ST, 33ST, 66ST). Treatments were administered until steer BW per pen averaged 540 kg in Exp. 1 and 560 kg in Exp. 2. An 86% concentrate:14% roughage diet was fed once daily (CP: 16.5% in Exp. 1, 20.2% in Exp. 2). In Exp. 1, growth performance of steers receiving rbST was dose-dependent; ADG changed linearly (P = .01), DMI decreased linearly (P = .03), and FE changed quadratically (P < .03). The 33ST steers responded with improved ADG and FE, 100ST with improved FE, and 300ST with lower ADG and poorer FE, compared with 0ST. In Exp. 2, the ADG response was quadratic (P = .01), DMI decreased linearly (P = .003), and FE improved quadratically (P = .004) with increasing dose of rbST. Steers receiving 16.5ST and 33ST responded with improved ADG and FE, whereas steers receiving 8.25ST and 66ST responded with improved FE but not ADG relative to 0ST steers. In Exp. 1 and 2, rbST administration altered carcass composition by increasing carcass protein and decreasing carcass fat. Our results indicate that a daily dose between 16.5 and 33 [Mu]g/kg of BW was required to optimize both ADG and FE in finishing beef steers; however, the dose response for changes in carcass chemical composition had not attained a plateau even at 300 [Mu]g/kg of BW. Key Words: Somatotropin, Growth, Steers, Carcasses, Recombinant bovine somatotropin was administered at constant concentrations and different volumes to determine efficacy of variable doses on growth performance of beef steers. An optimal dose of 13 micrograms per kilogram body weight per day elicited an increased rate of body weight gain, improved carcass composition and efficiency of feed utilization on steers given high concentrate and high-protein diet during the finishing phase.