Search

Objectives were to determine the effects of chromium propionate supplementation on growth performance, insulin and glucose metabolism, and carcass characteristics of beef cattle. Steers ( = 34) were stratified by BW and assigned to 1 of 2 treatments: 1) no supplemental Cr (Cont) or 2) 3 mg supplemental Cr·steer·d (CrP). Both supplements, Cont and CrP, were delivered via 0.454 kg ground corn top-dressed on the basal diet. There was no effect ( ≥ 0.45) of CrP on ADG, DMI, G:F, or final BW. However, steers fed CrP needed more ( = 0.10) days on feed (DOF) to achieve the same carcass back fat (BF) as steers fed Cont. There were no effects ( ≥ 0.41) of CrP on HCW, BF, or KPH. Steers fed CrP had increased ( = 0.01) dressing percentage (DP) and tended to have a 4.21 cm greater LM area ( = 0.15), decreased marbling scores ( = 0.11), and decreased intramuscular fat ( = 0.11) compared to steers fed Cont. There were no differences ( ≥ 0.25) in quality or yield grade distributions. A glucose tolerance test was conducted early (21 DOF) and late (98 DOF) in the finishing phase. There was a feedlot treatment (FT) × time × DOF interaction ( = 0.08) for glucose concentrations, but no other interactions ( ≥ 0.21) for glucose or insulin concentrations. There were no FT × DOF interactions ( ≥ 0.21) for insulin area under the curve (iAUC), insulin:glucose ratio, insulin or glucose baseline, or peak insulin or glucose concentrations. At 21 DOF, steers fed CrP had decreased glucose area under the curve (gAUC; = 0.01), decreased glucose clearance rate (; = 0.02), and increased glucose half-life (T; = 0.07) compared to steers fed Cont; however, by 98 DOF, no differences were observed between treatments. At 98 DOF, all steers, regardless of treatment, had increased ( < 0.01) peak glucose and insulin, , iAUC, insulin:glucose ratio, and baseline insulin when compared to values at 21 DOF, but gAUC and T decreased ( < 0.01). Although steers fed CrP tended ( = 0.11) to have increased baseline glucose concentrations compared to steers fed Cont, CrP supplementation did not affect ( ≥ 0.17) other measures of glucose or insulin. Results of this study indicate that CrP increased DP and tended to increase LM area but tended to decrease intramuscular fat, with no effect on growth performance. With increased DOF, all steers became more insulin resistant, using more insulin to clear less glucose, and these effects were not mitigated by CrP supplementation.

Objective: To investigate effects of low dietary vitamin A content on antibody responses in feedlot calves inoculated with an inactivated bovine coronavirus (BCoV) vaccine., Animals: 40 feedlot calves., Procedures: Calves were fed diets containing high (3,300 U/kg) or low (1,100 U/kg) amounts of vitamin A beginning on the day of arrival at a feedlot (day 0) and continuing daily until the end of the study (day 140). Serum retinol concentrations were evaluated in blood samples obtained throughout the study. Calves were inoculated IM with an inactivated BCoV vaccine on days 112 and 126. Blood samples obtained on days 112 and 140 were used for assessment of BCoV-specific serum IgG1, IgG2, IgM, and IgA titers via an ELISA., Results: The low vitamin A diet reduced serum retinol concentrations between days 112 and 140. After the BCoV inoculation and booster injections, predominantly serum IgG1 antibodies were induced in calves fed the high vitamin A diet; however, IgG1 titers were compromised at day 140 in calves fed the low vitamin A diet. Other isotype antibodies specific for BCoV were not affected by the low vitamin A diet., Conclusions and Clinical Relevance: Dietary vitamin A restriction increases marbling in feedlot cattle; however, its effect on antibody responses to vaccines is unknown. A low vitamin A diet compromised the serum IgG1 responses against inactivated BCoV vaccine, which suggested suppressed T-helper 2-associated antibody (IgG1) responses. Thus, low vitamin A diets may compromise the effectiveness of viral vaccines and render calves more susceptible to infectious disease.

Mature Angus-cross beef cows (n = 228) were used to evaluate effects of prepartum dietary energy source on postnatal growth and carcass composition of progeny in a 2-yr study. Starting at approximately 160 d of gestation, cows were fed diets consisting of 1 of 3 primary energy sources: grass hay (HY), corn (CN), or dried corn distillers grains with solubles (DG). The CN and DG diets were limit-fed to achieve similar energy intakes as cows fed HY. Following parturition, cows were fed a common diet and managed as a single group. Calves were weaned at an average of 185 ± 6 d of age and backgrounded for 28 d. A subset of progeny (n = 134) was individually fed a common finishing diet until slaughter, when each calf reached 1.2 ± 0.05 cm of backfat. A glucose tolerance test (GTT) was conducted in year 2 on 4 calves/treatment after 41 and 111 d on the finishing diet (DOF). Calf birth weights were greater (P = 0.002) in calves from cows fed CN and DG than calves from cows fed HY, and weaning BW (P = 0.08) was less for calves from cows fed HY vs. CN. Receiving BW, final BW, and HCW did not differ (P ≥ 0.16) among treatments. No difference (P ≥ 0.28) in ADG, morbidity, and mortality from birth to slaughter was observed among treatments. In response to a GTT, increased DOF resulted in greater (P ≤ 0.005) fasting insulin, faster glucose disappearance rate, and greater insulin:glucose area under the curve ratio. Glucose disappearance rate was greater (P = 0.01) in calves from cows fed CN than in calves from cows fed HY or DG. A greater initial insulin response (P = 0.005) was observed in calves from cows fed CN or DG than in calves from cows fed HY. Carcass traits used to measure yield grade did not differ (P ≥ 0.19) among treatments. Calves from dams fed CN had the lowest marbling score (P = 0.03) and intramuscular fat content (P = 0.07). These results indicate that prepartum maternal dietary energy source can alter fetal adipose tissue development and insulin sensitivity resulting in long-term effects on progeny's intramuscular fat deposition. Moreover, present findings suggest that increasing the number of days on a corn-based finishing diet increases insulin resistance in beef cattle.

Two experiments were conducted to evaluate the effects of monensin and dried distillers grains with solubles (DDGS) on ruminal metabolism in 8 fistulated steers. In Exp. 1, treatments were (DM basis): 1) 0 mg monensin/kg diet DM, 2) 22 mg monensin/kg diet DM, 3) 33 mg monensin/kg diet DM, and 4) 44 mg monensin/kg diet DM. The remainder of the diet was 10% corn silage, 60% DDGS, 10% corn, and 20% mineral supplement that used ground corn as the carrier. There was no effect (P > 0.80) of dietary monensin inclusion on DMI. Increasing dietary monensin did not affect (P > 0.05) ruminal VFA concentrations or lactic acid concentrations. There was no effect (P > 0.15) of increasing dietary monensin concentration on ruminal hydrogen sulfide gas (H(2)S) and liquid sulfide (S(2-)) concentrations, or ruminal pH. In Exp. 2, treatments were arranged in a 2 × 2 factorial and contained (DM basis): 1) 0 mg monensin/kg diet DM + 25% DDGS inclusion, 2) 0 mg monensin/kg diet DM + 60% DDGS inclusion, 3) 44 mg monensin/kg diet DM + 25% DDGS inclusion, and 4) 44 mg monensin/kg diet DM + 60% DDGS inclusion. The remainder of the diet was 15% corn silage, corn, and 20% mineral supplement that used ground corn as a carrier. With 60% dietary DDGS inclusion, DMI decreased (P < 0.01) when compared with 25% DDGS inclusion. With 25% DDGS in the diet, 0 h postfeeding acetate concentration was decreased compared with when 60% DDGS was fed (P < 0.01). A similar response (P < 0.01) occurred for total VFA concentrations at 0 h postfeeding. However, at 3 and 6 h postfeeding, propionate concentrations increased (P ≤ 0.05) in cattle fed the 60% DDGS diets, regardless of monensin inclusion. This increase in propionate concentrations contributed to the increase (P = 0.03) in total VFA concentrations at 3 h postfeeding when 60% DDGS diets were fed. There was no interaction detected (P > 0.05) for H(2)S or S(2-) concentrations in Exp. 2. Feeding 60% DDGS diets increased mean H(2)S by 71% when compared with feeding 25% DDGS diets. Similar to the response observed for H(2)S, feeding 60% DDGS diets increased mean S(2-) by 64% when compared with feeding 25% DDGS diets. Although these studies did not show beneficial effects of monensin supplementation on ruminal pH, VFA, or H(2)S concentrations, adverse rumen conditions, notably low ruminal pH, when high DDGS diets were fed may have precluded the effects of monensin from being realized.

Two feedlot studies were conducted to investigate the timing and duration of supplemental vitamin A withdrawal from feedlot cattle (Bos taurus) diets to reduce intramuscular adipose tissue vitamin A concentration and improve carcass quality. In Exp. 1, Angus crossbred steers (n = 84, BW = 211 ± 4 kg) were allotted to 4 treatments: no supplemental vitamin A for 227 d, no supplemental vitamin A for 112 d followed by 115 d of supplemental vitamin A, supplemental vitamin A for 112 d followed by no supplemental vitamin A for 115 d, or supplemental vitamin A for 227 d. In Exp. 2, Angus crossbred steers (n = 80, BW = 210 ± 5 kg) were allotted to 4 treatments: early weaning with or without supplemental vitamin A, and traditional weaning with or without supplemental vitamin A. In both experiments, serum vitamin A concentrations were greatest (P < 0.05) 56 d after cattle were weaned and placed in the feedlot, regardless of feedlot dietary vitamin A concentration. Hepatic vitamin A stores were dramatically decreased (P < 0.05) in the first 56 d and remained depressed as long as steers were not supplemented with vitamin A. At the end of the finishing period, vitamin A concentrations were less in intramuscular than subcutaneous adipose tissue. Growth was not affected by finishing cattle without supplemental dietary vitamin A (P > 0.10). Dietary vitamin A supplementation did not affect USDA yield grades. However, in Exp. 2, cattle without supplemental vitamin A had greater (P < 0.001) ether extractable lipid in the LM. Ether extractable lipid in the LM or marbling scores were enhanced when intramuscular adipose tissue vitamin A concentration was reduced in response to feeding diets without supplemental vitamin A.

The effects of 3 supplemental Cu concentrations on feedlot performance, mineral absorption, carcass characteristics, and ruminal S metabolism of cattle fed diets containing 60% dried distillers grains with solubles (DDGS) were evaluated in 2 experiments. Experiment 1 was conducted with 84 Angus-cross yearling steers and heifers (initial BW = 238 ± 36 kg), which were blocked by gender and allocated to 12 pens. Supplemental dietary Cu (tribasic copper chloride) treatments were: 1) 0 mg Cu/kg diet DM, 2) 100 mg Cu/kg diet DM, 3) 200 mg Cu/kg diet DM. The remainder of the diet was DDGS (60%), grass hay (10%), pelleted soy hulls (15%), and a vitamin-mineral supplement (15%). Diets were offered ad libitum throughout the finishing phase (168 d). Three cattle from each pen (n = 36) were harvested on d 168 and carcass data and liver samples were collected. Copper supplementation did not affect ADG (P = 0.22). However, the nonsignificant trend for increased ADG and decreased DMI led to a linear increase (P = 0.02) feed efficiency (G:F = 0.167, 0.177, and 0.177 for 0, 100, and 200 mg Cu/kg diet DM, respectively). The apparent absorption of Cu decreased quadratically (P = 0.07) and the apparent absorption of Mn and Zn were decreased linearly (P = 0.03 and P = 0.05, respectively) with increased Cu supplementation. Cattle supplemented with 100 or 200 mg Cu/kg diet DM had greater liver Cu concentrations (P < 0.01) than cattle that were not supplemented with Cu. There were no treatment effects (P > 0.10) on HCW, LM area, USDA yield grade, backfat, or marbling score. Experiment 2 was conducted with 6 ruminally fistulated steers that were fed the same diets as in Exp 1 in a replicated 3 × 3 Latin Square design. Copper supplementation did not affect (P > 0.10) ruminal pH or liquid S(2-) concentrations in steers consuming 60% DDGS diets (total dietary S = 0.55%). From 3 to 9 h after feeding, H(2)S gas concentration was decreased in those cattle supplemented with 100 mg Cu/kg diet. Concentration of H(2)S gas did not differ among cattle supplemented with 0 or 200 mg Cu/kg diet DM on 60% DDGS diets. Supplemental Cu improved feed efficiency in cattle consuming diets containing 60% DDGS; however, effects of Cu on rumen S metabolism were minimal even when supplemented at twice the maximum tolerable limit for beef cattle (NRC, 2000).

Feedlot producers often exceed NRC recommendations for vitamin A and D supplementation; however, increased concentrations of these vitamins have been shown to limit adipocyte differentiation in vitro. A feedlot trial was conducted using 168 Angus crossbred steers (BW = 284 ± 0.4 kg) allotted to 24 pens. The experiment had a 2 × 2 factorial arrangement of treatments: no supplemental vitamin A or D (NAND), 3,750 IU vitamin A/kg dietary DM with no supplemental vitamin D (SAND), no supplemental vitamin A and 1,860 IU vitamin D/kg dietary DM (NASD), and 3,750 IU and 1,860 IU vitamin A and D/ kg dietary DM (SASD), respectively. Serum, liver, and intramuscular and subcutaneous adipose tissue retinol concentrations were decreased in (P < 0.001) in cattle fed the no supplemental vitamin A diets (NAND and NASD combined) compared with those consuming supplemental vitamin A (SAND and SASD combined) diets. In addition, intramuscular retinol concentration was 38% less than in the subcutaneous depot. Serum 25(OH)D(3) concentrations were reduced (P < 0.001) during the first 70 d when cattle were fed no supplemental vitamin D diets (NAND and SAND combined); however, liver 25(OH)D(3) concentrations remained unchanged (P > 0.10) through d 184. Serum and liver 25(OH)D(3) concentrations increased (P < 0.001) with vitamin D supplementation (NASD and SASD combined). The DMI, ADG, G:F, and morbidity were not affected (P > 0.10) by dietary concentration of vitamin A or D. There were vitamin A and D interactions (P < 0.03) for backfat thickness and USDA Yield grade. Cattle fed the NAND diet had greater (P < 0.03) Yield grades than other treatments because of greater (P < 0.005) 12th rib backfat thickness in NAND steers than the NASD and SAND steers. Vitamin D concentrations were attenuated and minimal carcass adiposity responses to vitamin D supplementation were observed. Feeding a diet without supplemental vitamin A increased (P < 0.05) Quality grades and marbling scores and tended (P = 0.06) to increase ether extractable lipid of the LM. As retinol and 25(OH)D(3) concentrations in feedlot cattle declined as a result of a lack of dietary supplementation, adipose accretion increased, resulting in elevated Quality and Yield grades. Withdrawal of supplemental vitamin A, D, or both from the finishing diet of feedlot beef cattle had minimal impact carcass composition.

Quantification of the pro-vitamin A carotenoids in feedstuffs commonly fed to livestock has been ignored for many years. A greater dietary concentration of vitamin A has the potential to limit adipogenesis in cattle, thereby reducing carcass quality and value. A survey of 18 feedstuffs commonly fed to beef cattle was conducted for determination of vitamin A equivalents based on analysis of carotenoids. The pro-vitamin A carotenoids of interest were β-carotene, α-carotene, and β-cryptoxanthin. Collaborators in 5 states collected the feedstuffs and then shipped them to The Ohio State University for compilation and analysis. Carotenoids were extracted from the feedstuffs and then quantified using HPLC with photodiode array analysis. Fresh fescue pasture contained approximately 10 times more vitamin A equivalents than hay and 5 times more than corn silage (39,865, 2,750, and 6,900 IU of vitamin A/kg of DM for fresh pasture, hay, and corn silage, respectively). Beta-cryptoxanthin and α-carotene could not be detected in any forage samples. Hay and corn silage vitamin A equivalents decreased over extended periods of time from harvest to sample collection. Corn was the only feedstuff to have appreciable concentrations of all 3 pro-vitamin A carotenoids quantified. Corn processing had a minimal impact on the vitamin A equivalents. High-moisture corn contained 54% more vitamin A equivalents than whole shelled corn (378 and 174 IU of vitamin A/kg of DM, respectively). Pro-vitamin A carotenoids were more concentrated in corn coproducts than in whole shelled corn. The drying of distillers grains with solubles may significantly degrade β-carotene (800 and 480 IU/kg of DM for wet and dry distillers grains, respectively). Soybean-based feedstuffs contain a small concentration of pro-vitamin A carotenoids, at 55 and 45 IU of vitamin A/kg of DM for soybean meal and soybean hulls, respectively. Overall, there was considerable variation in the pro-vitamin A content of feedstuffs based on location and storage conditions. An extensive analysis of feedstuffs would need to be conducted for an accurate estimation of the vitamin A content of feedlot cattle diets.

Pasture management practices can affect forage quality and production, animal health and production, and surface and groundwater quality. In a 5-yr study conducted at the North Appalachian Experimental Watershed near Coshocton, Ohio, we compared the effects of two contrasting grazing methods on surface and subsurface water quantity and quality. Four pastures, each including a small, instrumented watershed (0.51-1.09 ha) for surface runoff measurements and a developed spring for subsurface flow collection, received 112 kg N ha(-1) yr(-1) and were grazed at similar stocking rates (1.8-1.9 cows ha(-1)). Two pastures were continuously stocked; two were subdivided so that they were grazed with frequent rotational stocking (5-6 times weekly). In the preceding 5 yr, these pastures received 112 kg N ha(-1) yr(-1) after several years of 0 N fertilizer and were grazed with weekly rotational stocking. Surface runoff losses of N were minimal. During these two periods, some years had precipitation up to 50% greater than the long-term average, which increased subsurface flow and NO(3)-N transport. Average annual NO(3)-N transported in subsurface flow from the four watersheds during the two 5-yr periods ranged from 11.3 to 22.7 kg N ha(-1), which was similar to or less than the mineral-N received in precipitation. Flow and transport variations were greater among seasons than among watersheds. Flow-weighted seasonal NO(3)-N concentrations in subsurface flow did not exceed 7 mg L(-1). Variations in NO(3)-N leached from pastures were primarily due to variable precipitation rather than the effects of continuous, weekly rotational, or frequent rotational stocking practices. This suggests that there was no difference among these grazing practices in terms of NO(3)-N leaching., (Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.)

The objectives of this research were to determine the interaction of monensin and haylage supplementation for steers fed 60% dried distillers grains (DDGS) on 1) mineral status, performance, and carcass characteristics, and on 2) ruminal pH, H(2)S, and short-chain fatty acid concentrations. In Exp. 1, Angus-cross steers (n=168; BW=277 ± 67 kg) were blocked by BW and allotted in a 2 × 2 factorial arrangement of treatments to 24 pens. Dietary treatments were 1) 0 mg of monensin/kg of diet + 0% haylage, 2) 33 mg of monensin/kg of diet + 0% haylage, 3) 0 mg of monensin/kg of diet + 10% haylage, and 4) 33 mg of monensin/kg of diet + 10% haylage. The remainder of the diet was 60% DDGS, 10% corn silage, 15% supplement, and corn (either 5 or 15%) on a DM basis. When supplemented with 0 mg of monensin/kg of diet, added haylage increased ADG by 5.7%, whereas when supplemented with 33 mg of monensin/kg of diet, added haylage increased ADG by 13% (P < 0.01). No interactions of monensin and haylage were observed for DMI or G:F (P ≥ 0.36). Haylage inclusion increased (P < 0.01) DMI and decreased (P < 0.01) G:F. No interactions (P > 0.05) on plasma mineral concentrations were observed; however, over time, plasma Cu concentrations decreased (P < 0.01), whereas plasma ceruloplasmin and S concentrations increased (P < 0.01). There were no treatment effects (P ≥ 0.08) on carcass characteristics. Cattle fed the 60% DDGS diets benefitted from increased dietary forage, and the effects of monensin and forage were additive for ADG and final BW. In Exp. 2, ruminally fistulated steers (n=8; BW = 346 ± 34 kg) were used in a replicated 4 × 4 Latin square design and were randomly assigned to the diets used in Exp. 1. Haylage inclusion increased ruminal pH from 1.5 through 12 h postfeeding, and the effects of monensin supplementation were additive (P < 0.05). From 1.5 through 9 h postfeeding, steers fed 33 mg of monensin/kg of diet tended to have reduced (P ≤ 0.10) concentrations of H(2)S when compared with steers fed 0 mg of monensin/kg of diet. Acetate:propionate ratios at 6 h postfeeding were 0.94, 0.93, 1.29, and 1.35 for diets 1 to 4, respectively (P < 0.01); total lactate was decreased regardless of treatment (range: 0.94 to 1.42 µmol/mL). Sulfuric acid in DDGS, not ruminal short-chain fatty acids, may be responsible for the low rumen pH observed and may influence the maximum inclusion of DDGS in cattle diets. Monensin supplementation decreased H(2)S concentration and may decrease the risk of polioencephalomalacia for cattle fed high-DDGS diets., (© 2011 American Society of Animal Science. All rights reserved.)

Energy density in growing diets may affect carcass quality of cattle; however, few reports have described the impact of energy source. The objectives of this research were to determine effects of source [dried distillers grains with solubles (DDGS) vs. corn] and amount (limit-fed to gain 0.9 vs. 1.4 kg of BW/d) of energy during the growing phase on feedlot performance and marbling. Angus-cross steers (144 head) were blocked by BW (average initial BW = 252 ± 36 kg), allotted within each block to 8 pens (6 steers/pen, 24 pens total), and randomly assigned to 1 of 4 feeding systems in a 2 × 2 factorial arrangement of treatments: 1) 65% DDGS fed to gain 0.9 kg of BW/d, 2) 65% DDGS fed to gain 1.4 kg of BW/d, 3) 65% corn fed to gain 0.9 kg of BW/d, and 4) 65% corn fed to gain 1.4 kg of BW/d. Fecal grab samples were collected on d 52 of the growing phase to determine digestibility of DM, ADF, NDF, ether extract (EE), and CP. After the 98-d growing phase, all steers were fed the same finishing diet. Steers were slaughtered by pen when average BW within the pen was 544, 522, and 499 kg for the large, medium, and small BW blocks, respectively. Average daily gain and DMI differed (P<0.01) by design during the growing phase. Compared with the corn-based diets, digestibilities of DM, NDF, and EE were decreased (P<0.02) when DDGS-based diets were fed during the growing phase, whereas the digestibility of N was increased (P<0.01). The ADG was greatest (P=0.02) during the finishing phase for steers fed to gain 0.9 kg of BW/d initially, but source of energy during the growing phase did not affect (P=0.24) finishing phase ADG. Steers fed to gain 0.9 kg of BW/d during the growing phase also had less backfat (P=0.08), decreased USDA yield grades (P=0.03), and greater LM area (P<0.01) than steers fed to gain 1.4 kg of BW/d. There was an interaction between energy source and amount for marbling scores (P=0.02). Steers fed corn-based diets to gain 0.9 kg of BW/d during the growing phase had the most marbling, whereas those fed to gain 0.9 kg of BW/d on DDGS had the least marbling; the remaining feeding systems were intermediate. Overall ADG and DMI were affected (P < 0.06) by both source and amount of energy fed during the growing phase. Feeding the DDGS-based diet to achieve greater ADG during the growing phase increased marbling, whereas feeding the corn-based diet to increase ADG during the growing phase decreased marbling., (© 2011 American Society of Animal Science. All rights reserved.)

Genetic regulation of the site of fat deposition is not well defined. The objective of this study was to investigate adipogenic differentiation state-specific gene expression in feedlot cattle (>75% Angus; <25% Simmental parentage) of varying adipose accretion patterns. Four groups of 4 steers were selected via ultrasound for the following adipose tissue characteristics: low subcutaneous-low intramuscular (LSQ-LIM), low subcutaneous-high intramuscular (LSQ-HIM), high subcutaneous-low intramuscular (HSQ-LIM), and high subcutaneous-high intramuscular (HSQ-HIM). Adipose tissue from the subcutaneous (SQ) and intramuscular (IM) depots was collected at slaughter. The relative expression of adipogenic genes was evaluated using quantitative PCR. Data were analyzed using the mixed model of SAS, and gene expression data were analyzed using covariate analysis with ribosomal protein L19 as the covariate. No interactions (P > 0.10) were observed between IM and SQ adipose tissue depots for any of the variables measured. Therefore, only the main effects of high and low accretion within a depot and the effects of depot are reported. Steers with LIM had smaller mean diameter IM adipocytes (P < 0.001) than HIM steers. Steers with HSQ had larger mean diameter SQ adipocytes (P < 0.001) than LSQ. However, there were no differences (P > 0.10) in any of the genes measured due to high or low adipose accretion. Preadipogenic delta-like kinase1 mRNA was greater in the IM than the SQ adipose tissue; conversely, differentiating and adipogenic genes, lipoprotein lipase, PPARγ, fatty acid synthetase, and fatty acid binding protein 4 were greater (P < 0.001) in the SQ than the IM depot. Intramuscular adipocytes were smaller than SQ adipocytes and had greater expression of the preadipogenic gene, indicating that more hyperplasia was occurring. Meanwhile, SQ adipose tissue contained much larger (P < 0.001) adipocytes that had a greater expression (P < 0.001) of differentiating and adipogenic genes than did the IM adipose tissue, indicating more cells were undergoing differentiation and hypertrophy. Adipogenic differentiation state-specific gene expression was not different in cattle with various phenotypes, but adipogenesis in the SQ and IM adipose tissues seems to occur independently.

Mature Angus-cross beef cows (n = 144) were used to determine effects of late gestation dietary energy source on pre- and postpartum cow performance in a complete randomized block design experiment. Cows were adapted to diets starting at 167 +/- 9 d of gestation and fed until 1 wk before expected calving date. Cows were fed 1 of 3 dietary energy sources: grass hay (HY), corn (CN), or dried distillers grains (DDGS). Cows allotted to HY were allowed ad libitum access to round-bale grass hay, and average hay disappearance was 12.4 kg/d. Limit-fed corn and DDGS diets contained 5.3 kg of whole-shelled corn or 4.1 kg of DDGS, respectively, plus 2.1 kg of hay, and 1.0 kg of supplement to meet cow nutritional needs during late gestation and to allow for an energy intake similar to HY. Every 21 d, BW, BCS, and ultrasound measurement of backfat between the 12th and 13th ribs were collected. At 210 d in gestation, jugular blood samples were collected from cows at 0, 3, 6, and 9 h postfeeding and were analyzed for glucose, insulin, NEFA, and blood urea N (BUN) concentrations. After parturition, cows were fed a common diet and managed similarly. Milk production was determined by weigh-suckle-weigh procedure on d 31, 100, and 176 postpartum. Cows fed DDGS during late gestation gained more (P = 0.04) BW than cows fed HY or CN; however, no difference in BCS change was detected (P = 0.28) among treatments. Plasma glucose concentrations were similar among treatments (P = 0.64), whereas insulin concentrations at 3 h postfeeding were greater (P = 0.002) for cows fed DDGS than those fed HY or CN. Plasma BUN concentrations were greater (P < or = 0.02) for cows fed DDGS vs. CN or HY up to 6 h postfeeding. Birth weight was greater (P < 0.001) for calves from cows fed CN and DDGS than for those fed HY, but this did not result in any differences in frequency of dystocia (P = 0.21). Prepartum energy source did not affect conception rates (P = 0.79), milk production (P > or = 0.51), or milk composition (P > or = 0.39). Maternal dietary energy source in late gestation did not affect pre- or postpartum cow performance, but did change plasma hormones and metabolites during gestation. Heavier birth weights in calves from cows fed CN or DDGS indicate the changes in maternal metabolism affected energy partitioning of nutrients to the fetus and subsequent fetal growth.

The effects of increased postruminal supply of casein, corn starch, and soybean oil on plasma concentrations of the gastrointestinal hormones ghrelin and oxyntomodulin (OXM) were investigated. Four mid-lactation Holstein cows were used in a 4 x 4 Latin square. Treatments were continuous abomasal infusions (23 h/d) for 7 d of water, soybean oil (500 g/d), corn starch (1100 g/d), or casein (800 g/d). Jugular vein plasma was obtained every 30 min for 7h on days 1 and 7. Soybean oil and casein infusion decreased preprandial plasma ghrelin concentration by approximately 20% on both d (time-by-treatment P<0.10); however, dry matter intake (DMI) was depressed only after 7 d of oil infusion. Infusion of soybean oil, corn starch, or casein did not change the plasma OXM concentration (P>0.20). The present data indicate that plasma ghrelin concentration is depressed immediately before feeding by the postruminal infusion of soybean oil and casein, but it is not affected during the postprandial period. Plasma ghrelin concentration was not altered (P>0.20), pre- or postfeeding, by increased postruminal supply of corn starch. In addition, plasma OXM concentration did not respond (P>0.20) to postruminal nutrient infusion. In conclusion, a decrease in DMI when fat is infused could be partially explained by the decrease in prefeeding plasma ghrelin concentration, but a decrease in prefeeding plasma ghrelin concentration is not always associated with a decrease in DMI, as observed for the infusion of casein. Plasma OXM concentration was not affected by postruminal infusion of macronutrients., (Copyright (c) 2010 Elsevier Inc. All rights reserved.)

Wagyu-sired (n = 20) and Angus-sired (n = 19) steers and heifers were used to compare the effects of sire breed on feedlot performance, carcass characteristics, and meat tenderness. Calves were weaned at 138 +/- 5 d of age and individually fed a finishing diet consisting of 65% whole corn, 20% protein/vitamin/mineral supplement, and 15% corn silage on a DM basis. Heifers and steers were slaughtered at 535 and 560 kg of BW, respectively. Carcasses were ribbed between the 12th and 13th (USDA grading system) and the 6th and 7th ribs (Japanese grading system) to measure fat thickness, LM area (LMA), and intramuscular fat (IMF). Two steaks were removed from the 12th rib location and aged for 72 h and 14 d to determine Warner-Bratzler shear force and cooking loss. Sire breed x sex interactions were not significant (P > 0.05). Angus-sired calves had greater (P < 0.05) ADG and DMI than Wagyu. Wagyu-sired calves had improved (P < 0.05) feed efficiency than Angus. Sire breed did not affect (P > 0.20) HCW, 12th-rib fat, or USDA yield grade. Carcasses of Wagyu had greater (P = 0.0001) marbling scores at the 12th rib than those of Angus (770.9 vs. 597.3 +/- 41.01, respectively). Carcasses of Wagyu also had greater (P < 0.02) 12th-rib IMF and 6th-rib IMF than Angus, resulting in a greater proportion of carcasses grading Prime (65.0 vs. 21.1%; P = 0.006). Carcasses from Wagyu tended (P = 0.08) to have greater LMA at the 12th rib, whereas Angus carcasses had greater (P < 0.05) LMA at the 6th rib. Steaks from Angus and Wagyu had similar (P > 0.50) tenderness at aging times of 72 h and 14 d. Cooking loss was greater (P < 0.01) for Angus than Wagyu steaks at 72 h and 14 d. Using Wagyu sires vs. Angus sires on British-based commercial cows combined with early weaning management strategies has the potential to produce a product with greater marbling, but is unlikely to significantly enhance tenderness.

Sixty-eight Angus-based steers (224 +/- 7.6 kg of BW) were used to evaluate the effects of a prolonged dietary vitamin A restriction on marbling and immunocompetency. Steers were allotted randomly to 1 of 2 treatments: LOW (no supplemental vitamin A) and HIGH (diet supplemented with 2,200 IU of vitamin A/kg of DM). Diets contained 60% high-moisture corn, 20% roasted soybeans, 10% corn silage, and 10% of a protein supplement. Steers were penned and fed individually. For the first 141 d, steers were program-fed to achieve a gain of 1.1 kg/d. The last 75 d of the experiment, steers were offered feed for ad libitum intake. At slaughter, serum and liver samples were taken to determine their retinol content. To evaluate immunocompetency, 10 steers per treatment were selected randomly on d 141 and received an ovalbumen vaccine, and 21 d later, the steers were revaccinated. On d 182, blood samples were taken from the vaccinated steers to determine serum antibody titers by ELISA. Steers were slaughtered after 216 d on feed. Carcass characteristics were determined, and LM samples were taken for composition analysis. Subcutaneous fat samples were taken for fatty acid composition analysis. Performance (ADG, DMI, and G:F) was not affected by vitamin A restriction (all P > 0.10). Hot carcass weight, 12th-rib fat, and yield grade did not differ between LOW and HIGH steers (all P > 0.10). Marbling score (LOW = 574 vs. HIGH = 568, P = 0.79) and i.m. fat (LOW = 5.0 vs. HIGH = 4.7% ether-extractable fat, P = 0.57) were not increased by vitamin A restriction. Serum (LOW = 18.7 vs. HIGH = 35.7 mug/dL, P < 0.01) and liver (LOW = 6.3 vs. HIGH = 38.1 mug/g, P < 0.01) retinol levels were lower in LOW steers compared with HIGH steers at slaughter. Response to ovalbumin vaccination was not affected by vitamin A restriction (LOW = 13.1 vs. HIGH = 12.8 log(2) titers, P = 0.60). Slight changes in the fatty acid profile of s.c. fat of the steers were detected. A greater proportion of MUFA (LOW = 41.7 vs. HIGH = 39.9%, P = 0.03) and fewer SFA (LOW = 47.1 vs. 48.7, P = 0.03) were observed in vitamin A-restricted steers. This suggests that vitamin A restriction may affect the activity of desaturase enzyme (desaturase activity index, LOW = 46.9 vs. HIGH = 44.9, P = 0.01). Feeding a low vitamin A diet for 216 d to Angus-based steers did not affect performance, marbling score, or animal health and immunocompetency. Slight changes in the fatty acid profile of s.c. fat were observed, suggesting that vitamin A restriction may have affected desaturase enzyme activity.

Angus-cross steers (n = 165; 295 +/- 16 kg of BW) were used evaluate the effect of low vitamin A diets with high-moisture corn (HMC) or dry corn (DC) on marbling and fatty acid composition. Steers were allotted to 24 pens (7 steers/pen), such that each pen had the same average initial BW. Treatments were randomly allotted to the pens. The experiment had a completely randomized design, with a 2 x 2 factorial arrangement of treatments: low vitamin A (Lo, no supplemental vitamin A) and HMC (LoHMC); LoDC; high vitamin A (Hi, supplemented with 2,200 IU of vitamin A/kg of DM) and HMC (HiHMC); and HiDC. Diets contained 76% corn, 10% corn silage, 11% protein supplement, and 3% soybean oil (DM basis). Samples of feed ingredients were collected for carotenoid analysis. Blood samples were collected for serum retinol determination. Steers were slaughtered after 145 d on feed. Carcass characteristics and LM composition were determined. Samples from the s.c. fat depot were analyzed for fatty acid composition. High-moisture corn had a greater vitamin A content, based on its carotenoid content, than DC (614 vs. 366 IU/kg of DM, P < 0.01). No vitamin A x corn type interactions were detected for feedlot performance, carcass characteristics, or serum, s.c. fat, or liver retinol concentration. Average daily gain, DMI, and G:F were not affected by vitamin A (P > 0.05). Marbling score and USDA quality grade were greater (P < 0.05) in Lo vs. Hi steers. Hot carcass weight, backfat, and yield grade were not affected by the treatments (P > 0.05). Vitamin A and corn type did not affect LM composition (DM, ash, CP, or ether-extractable fat, P > 0.05). Vitamin A supplementation increased (P < 0.06) serum retinol on d 112 and 145 and increased (P < 0.01) liver retinol at slaughter (Lo = 38.7 vs. Hi = 102.9 mug/g). The s.c. fat retinol concentrations were less (P < 0.01) for Lo (0.8 mug/g) than for Hi (1.4 mug/g) at slaughter. Cell diameter of adipocytes in the i.m. depot was not affected by dietary vitamin A (P > 0.05). A vitamin A x corn type interaction was observed (P < 0.05) for the s.c. fat cellularity. Feeding HMC increased the number of cells per square millimeter when Lo diets were fed (LoHMC = 128 vs. LoDC = 100 cells/mm(2), P < 0.05), but not when Hi diets were fed (HiHMC = 109 vs. HiDC = 111 cells/mm(2), P > 0.05). The CLA content of adipose tissue was not affected by the treatments. Regardless of the corn type used, feeding low vitamin A diets for 145 d to Angus-cross steers increased marbling and quality grade without affecting yield grade, animal health, or performance.

To determine the effect of duration of dietary vitamin A restriction on site of fat deposition in growing cattle, 60 Holstein steers (BW = 218.4 +/- 6.55 kg) were fed a diet based on high-moisture corn, with 2,200 IU of supplemental vitamin A/kg of DM (control) or no supplemental vitamin A for a long (243 d; LR) or short (131 d; SR) restriction before slaughter at 243 d. The SR steers were fed the control diet for the first 112 d. Steers were penned individually and fed for ad libitum intake. Jugular vein blood samples for serum retinol analysis were collected on d 1, 112, and 243. Carcass samples were collected for composition analysis. Subcutaneous fat samples were collected for fatty acid composition. Fat samples from the i.m. and s.c. depots were collected to measure adipocyte size and density. Feedlot performance (ADG, DMI, and G:F) was not affected (P > 0.05) by vitamin A restriction. On d 243, the i.m. fat content of the LM was 33% greater (P < 0.05) for LR than for SR and control steers (5.6 vs. 3.9 and 4.2% ether extract, respectively). Depth of back-fat and KPH percentage were not affected (P = 0.44 and 0.80, respectively) by vitamin A restriction. Carcass weight, composition of edible carcass, and yield grade were similar among treatments (P > 0.10). Liver retinol (LR = 6.1, SR = 6.5, and control = 44.7 microg/g; P < 0.01) was reduced in LR and SR vs. control steers. On d 243, LR and SR steers had similar serum retinol concentrations, and these were lower (P < 0.01) than those of control steers (LR = 21.2, SR = 25.2, and control = 36.9 microg/dL). Intramuscular adipose cellularity (adipocytes/mm2 and mean adipocyte diameter) on d 112 and 243 was not affected (P > 0.10) by vitamin A restriction. Restricting vitamin A intake for 243 d increased i.m. fat percentage without affecting s.c. or visceral fat deposition, feedlot performance, or carcass weight. Restricting vitamin A intake for 131 d at the end of the finishing period appears to be insufficient to affect the site of fat deposition in Holstein steers.

A feedlot trial was conducted to determine the effect of dietary vitamin A concentration and roasted soybean (SB) inclusion on carcass characteristics, adipose tissue cellularity, and muscle fatty acid composition. Angus-crossbred steers (n = 168; 295 +/- 1.8 kg) were allotted to 24 pens (7 steers each). Four treatments, in a 2 x 2 factorial arrangement, were investigated: no supplemental vitamin A, no roasted soybeans (NANS); no vitamin A, roasted SB (20% of the diet on a DM basis; NASB); with supplemental (2,700 IU/kg) vitamin A, no roasted SB (WANS); and with supplemental vitamin A, roasted SB (WASB). Diets included high moisture corn, 5% corn silage, 10 to 20% supplement, and 20% roasted SB in the SB treatments on a DM basis. The calculated vitamin A concentration in the basal diet was < 1,300 IU/kg of DM. Blood samples (2 steers/pen) were collected for serum vitamin A determination. Steers were slaughtered after 168 d on feed. Carcass characteristics and LM composition were determined. Fatty acid composition of LM was analyzed, and adipose cellularity in the i.m. and s.c. depots was determined. No vitamin A x SB interactions were detected (P > 0.10) for cattle performance, carcass composition, or muscle fatty acid composition. Low vitamin A diets (NA) did not affect (P > 0.05) ADG, DMI, or G:F. Quality grade tended (P = 0.07) to be greater in NA steers. Marbling scores and the percentage of carcasses grading > or = Choice(-) were 10% greater for NA steers, although these trends were not significant (P = 0.11 and 0.13, respectively). Backfat thickness and yield grade were not affected (P > 0.26) by vitamin A supplementation. Composition of the LM was not affected (P > 0.15) by vitamin A or SB supplementation. Serum retinol at slaughter was 44% lower (P < 0.01) for steers fed NA than for steers supplemented with vitamin A (23.0 vs. 41.1 microg/dL). A vitamin A x SB interaction occurred (P < 0.05) for adipose cellularity in the i.m. depot; when no SB was fed, vitamin A supplementation decreased cell density and increased cell size. However, when SB was fed, vitamin A supplementation did not affect adipose cellularity. Adipose cellularity at the s.c. depot was not affected (P > 0.18) by vitamin A or SB treatments. Fatty acid profile of the LM was not affected by vitamin A (P > 0.05), but SB increased (P < 0.05) PUFA (7.88 vs. 4.30 g/100 g). It was concluded that feeding NA tended to increase marbling without affecting back-fat and yield grade. It appeared that NA induced hyperplasia in the i.m. but not in the s.c. fat depot.

Three experiments were conducted to determine the effects of cattle age and dietary forage level on the utilization of corn fed whole or ground to feedlot cattle. In Exp. 1, 16 steers were used to investigate the effects of cattle age and corn processing on diet digestibility. Two cattle age categories were evaluated (weanling [254 +/- 20 kg BW] and yearling [477 +/- 29 kg BW]; eight steers per group), and corn was fed either ground or whole to each cattle age category. Cattle age and corn processing did not affect (P > 0.10) diet digestibility of DM, OM, starch, CP, NDF or ADF, and no interactions (P > 0.10) between these two factors were detected. In Exp. 2, the effects of forage level and corn processing on feedlot performance and carcass characteristics were evaluated. One hundred eighty steers (310 +/- 40 kg BW) were allotted to 24 pens, and were fed one of the following diets: high-forage (18.2% corn silage) cracked corn (HFCC); high-forage shifting corn (whole corn for the first half of the trial, then cracked corn until harvest; HFSC); high-forage whole corn (HFWC); low-forage (5.2% corn silage) cracked corn (LFCC); low-forage shifting corn (LFSC); and low-forage whole corn (LFWC). For the high-forage diets, steers fed cracked corn had 7% greater DMI than those fed whole corn, whereas for the low-forage diets, grain processing did not affect DMI (interaction; P = 0.02). No interactions (P > 0.10) between forage level and corn processing were found for ADG and G:F. Total trial ADG and G:F, and percentage of carcasses grading USDA Choice, and carcass yield grade were not affected (P > 0.10) by corn processing. Cattle with fewer days on feed grew faster and more efficiently when cracked corn was fed, whereas cattle with longer days on feed had greater ADG and G:F when corn was fed whole (interaction; P < 0.10). In Exp. 3, the effects of forage level and corn processing on diet digestibility were evaluated. The high-forage cracked corn, high-forage whole corn, low-forage cracked corn, and low-forage whole corn diets used in Exp. 2 were fed to 16 steers (350 +/- 27 kg BW) in a digestion trial. No interactions (P > 0.10) between forage level and corn processing were detected for starch digestibility. Forage level and corn processing (grinding) did not affect (P > 0.10) diet DM, OM, starch, CP, and NDF digestibility. Processing corn did not provide additional benefits to feedlot cattle performance under these experimental conditions.

Seventy-three Holstein steers (initial BW 138.5 +/- 4.3 kg; approximately 3 mo of age) were allotted by BW to one of three growing-phase treatments to determine the effect of source and amount of energy on feedlot performance, and characteristics of subcutaneous (s.c.) and intramuscular (i.m.) adipose tissue. Treatment diets were 1) high concentrate fed ad libitum (ALC); 2) high forage fed ad libitum for 55 d, then a mid-level forage diet fed ad libitum for 98 d (ALF); or 3) limit-fed high concentrate to achieve a gain of 0.8 kg/d for 55 d, then to achieve a gain of 1.2 kg/d for 98 d (LFC). All steers were fed the ALC diet from d 154 to slaughter. Eight steers per treatment were selected after an average of 145 and 334 d on feed for determination of adipocyte cellularity and lipogenic enzyme activity at the end of the growing and finishing phases, respectively. Remaining steers were slaughtered after an average of 334 d on feed. At initial slaughter, ALC steers had a two- to threefold greater (P < 0.05) s.c. fat depth, and 1.9-fold greater (P < 0.01) longissimus muscle ether extract than steers in other groups. At final slaughter, LFC steers had a greater fat depth than ALF steers (P < 0.10) and had the greatest (P < 0.10) longissimus muscle ether extract. Increased fat depth for ALC steers at initial slaughter was a result of a greater (P < 0.05) mean adipocyte diameter in the s.c. depot. Mean i.m. adipocyte diameter followed the same trend (P < 0.16). The number of adipocytes per gram of s.c. fat was least for ALC and greatest for ALF (P < 0.10) at initial slaughter. Mean diameter and number of adipocytes per gram of i.m. and s.c. fat did not differ among treatments at final slaughter (after 180 d on a common finishing diet). High energy (ALC) increased activities of ATP-citrate lyase, fatty acid synthase, 6-phosphogluconate dehydrogenase, glucose-6-phosphate dehydrogenase, and malate dehydrogenase (P < 0.05), in the s.c. depot, and increased activities of ATP-citrate lyase and glucose-6-phosphate dehydrogenase (P < 0.10) in the i.m. depot at initial slaughter. Lipogenic enzyme activity in the s.c. depot at final slaughter did not differ among treatments. Glucose-6-phosphate dehydrogenase activity in the i.m. depot at final slaughter was lowest (P < 0.10) in ALF. Hypertrophy made a greater contribution to fat tissue growth than hyperplasia. Hypertrophy was affected by amount of energy, whereas hyperplasia was affected by source of energy. Differences diminished when cattle were fed the common finishing diet.

One hundred eighty-four Angus x Simmental steers (initial BW 161.7 +/- 3.4 kg) were used to determine whether different sources and amounts of energy in the growing phase could extend the growth curve and maintain high amounts of intramuscular fat deposition in early-weaned steers. Steers were allotted by source, age, and BW to one of four growing-phase (119 to 259 d of age) regimens. For three regimens, steers were weaned at 119 d of age and either 1) fed (DM basis) a 50% grain diet ad libitum (ALC); 2) limit-fed a 70% grain diet to achieve a gain of 0.8 kg/d from 119 to 192 d of age, and 1.2 kg/d from 193 to 259 d of age (LFC); or 3) fed a 60% haylage diet ad libitum from 119 to 192 d of age, and a 25% haylage diet ad libitum from 193 to 259 d of age (ALF). For the fourth regimen, steers were normal-weaned at 204 d of age and fed a silage diet from 205 to 259 d of age (NW). From 260 d of age to slaughter, all steers consumed a 70% grain (DM basis) diet. Limit-fed and ALF steers spent the most, and NW the least amount of time (P < 0.01) in the feedlot to achieve a target fat depth of 1.27 cm. Ad libitum-fed steers were the youngest (331 d), and NW the oldest (383 d) at slaughter (P < 0.01). Overall ADG was greatest for ALC and least for NW steers (P < 0.01). Overall, ALF steers consumed the most DM (P < 0.01). While in the feedlot, LFC and ALC steers were more efficient in converting feed to BW gain (P < 0.01) than ALF and NW steers. Normal-weaned had the least and ALC the greatest (P < 0.01) fat depth at 260 d of age. Consequently, NW steers produced the heaviest, and ALC the lightest (P < 0.01) carcasses at slaughter. Normal-weaned steers had the largest, and ALC and LFC steers had the smallest longissimus muscle area (P < 0.06). Growing phase dietary treatments did not affect (P > 0.20) yield grade. Marbling score did not differ (P > 0.35), but laboratory analysis revealed that ALC steers had the lowest percentage of fat (P < 0.02) in the longissimus muscle. Shear force was greatest (P < 0.08) for steaks from ALC and LFC steers, and least for steaks from ALF and NW steers. Feeding steers the ALC diet from 119 to 260 d of age hastened physiological maturity, decreased marbling scores, and decreased muscle tenderness compared with forage feeding (ALF, NW). Limit-feeding a high-grain diet also hastened physiological maturity and decreased muscle tenderness but did not decrease marbling scores. Source and amount of energy affected partitioning of fat deposition.

In Exp. 1, 31, 24, and 17 mature, pregnant Simmental x Angus cows (initial BW = 662.0 +/- 10.4 kg) in each of 3 yr were used to determine the efficacy of stockpiled orchardgrass, limit-fed corn, or ad libitum hay for maintaining cows in mid- to late gestation, respectively. In Exp. 2, 24 mature, pregnant crossbred cows (initial BW = 677.7 +/- 9.4 kg) per treatment in each of 3 yr were used to determine the efficacy of stockpiled orchardgrass, limit-fed corn, or ad libitum hay for maintaining cows in late gestation and early lactation, respectively. Each year, cows were assigned to treatment by BW. From November to February or from January to April, respectively, nutritional needs for mid- to late gestation (Exp. 1) or late gestation and early lactation (Exp. 2) were met either by 1) rotating cows on approximately 15.2 or 21.7 ha of predominantly orchardgrass pasture, set aside and fertilized in late August, 2) limit-feeding approximately 5.8 kg of whole shelled corn, 1.1 kg of a pelleted supplement, and 1.2 kg of hay daily, or 3) ad libitum feeding of round-baled hay. During extreme weather conditions, cows grazing stockpiled orchardgrass were limit-fed a grain-based diet. Postcalving weight (P < 0.10) was greatest for limit-fed cows in Exp. 1 and lowest for cows grazed on stockpiled orchardgrass; cows given ad libitum access to hay were intermediate in weight and did not differ from cows limit-fed or cows grazed on stockpiled orchardgrass (641.8, 657.4, and 634.0 kg, respectively). Calving date, calf birth and weaning weight, and conception rate did not differ among treatments (P > 0.15) in Exp. 1. In Exp. 2, weight at weaning did not differ among treatments (P > 0.17); however, postcalving weight (P < 0.01) was greatest for cows given ad libitum access to hay, intermediate for limit-fed cows, and lowest for cows grazed on stockpiled orchardgrass (674.8, 652.4, and 624.5 kg). Body condition score at any time point did not differ among treatments (P > 0.38), nor did calving date, calf birth and weaning weights, and conception rate (P > 0.12). Because of the few differences in cow performance, selection of energy sources for beef cows can be made based on economics. The cost to feed a cow hay in early to mid-gestation was nearly double that of limit-feeding the corn-based diet or grazing stockpiled orchardgrass. Because of lower quality pastures, the cost to graze cows on stockpiled orchardgrass during late gestation and early lactation was not as cost effective as limit feeding a corn-based diet.

Seventy-three crossbred steers (initial BW = 170.5 +/- 5.5 kg) from The Ohio State University (Exp. 1) and 216 crossbred steers (initial BW 135.4 +/- 4.4 kg) from the University of Illinois (Exp. 2) were used to determine the effect of source of energy and rate of growth on performance, carcass characteristics, and glucose and insulin profiles on early-weaned steers. Effects of the diets used in Exp. 1 and 2 on ruminal pH and VFA concentrations were quantified using ruminally fistulated steers (Exp. 3). Cattle were weaned at an average age of 119 d in all experiments and were allotted by age, BW, and breed to one of four diets: high-concentrate, fed ad libitum (ALCONC), high-concentrate fed to achieve a gain of either 1.2 kg/d (1.2CONC) or 0.8 kg/d (0.8CONC), or high-fiber, fed ad libitum (ALFIBER). At 218 d of age, all steers were placed on the ALCONC diet until slaughter. Steers were implanted with Compudose at the initiation of all experiments and with Revalor-S when they were estimated to be 100 d from slaughter. When steers in Exp. 1 averaged 181 and 279 d of age, serum samples were collected to determine glucose and insulin concentrations. Steers were slaughtered when a fat thickness of 1.27 cm was reached (Exp. 1) or after 273 d on feed (Exp. 2). In Exp. 1, days in the feedlot (P < 0.01) and age at slaughter (P < 0.01) were lowest for ALCONC and ALFIBER steers, and greatest for 0.8CONC steers. Overall, ADG was greatest for ALCONC and lowest for 0.8CONC steers; feed efficiency was lowest (P < 0.01) for ALFIBER steers. Final BW did not differ (P > 0.57) among treatments. At 181 and 218 d of age, serum insulin was increased (P < 0.10) and intramuscular fat percentage was greatest (P < 0.07), respectively, for ALCONC steers. In Exp. 2, overall ADG (P < 0.06) and final BW (P < 0.04) were greatest for ALCONC and lowest for 1.2CONC and 0.8CONC steers. Overall feed efficiency was greatest for 0.8CONC and lowest for ALFIBER (P < 0.01). Growing phase diet did not affect marbling score at 218 d of age or at slaughter (P > 0.81). In Exp. 3, differences in ruminal pH after feeding may have been a consequence of increasing acetate (ALFIBER), propionate (ALCONC), or a combination of VFA (0.8CONC and 1.2CONC), respectively (diet x time after feeding, P < 0.10). Controlling growth by limit-feeding a high-concentrate diet for only 100 d does not extend the growth curve of early-weaned steers or enhance intramuscular fat deposition at slaughter compared to ad libitum intake of a high-concentrate or high-fiber diet.

Seventy Angus x Simmental calves (BW = 166.3 +/- 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 feed-lot at 202 d of age; yearlings had the largest longissimus area (77, 86, 88 cm2, 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.

Sixty-three Angus x Simmental calves were allotted to a bull or a steer group based on sire, birth date, and birth weight to determine effects of castration status on performance, carcass characteristics, and circulating insulin-like growth factor I (IGF-I) concentrations in early-weaned cattle. At 75 d of age, calves in the steer group were castrated. Calves were not creep-fed prior to weaning. All calves were weaned and weighed at an average age of 115 d and transported by truck to the OARDC feedlot in Wooster, OH. Performance and carcass characteristics were measured in three phases. Phase 1 was from 115 to 200 d of age, phase 2 was from 201 to 277 d of age, and phase 3 was from 278 d of age to slaughter. Before implantation, four bulls and four steers were selected for serial slaughter and carcass evaluation. Steers were implanted with Synovex-C at 130 d of age and with Revalor-S at 200 and 277 d of age. Serum samples were collected from all calves on the day of implantation, 28 and 42 d after implantation, and at slaughter and analyzed for circulating IGF-I concentration. Bulls gained 9.7% faster (1.75 vs 1.60 kg/d; P < 0.01), consumed 25 kg more DM (521 vs 496 kg; P = 0.11), and were 3.3% more efficient (282 vs 273 g/kg, P < 0.10) than steers in phase 1. However, steers gained 10.5% faster (1.62 vs 1.46 kg/d; P < 0.02), consumed similar amounts of DM, and were 6.5% more efficient than bulls (214 vs 201 g/kg; P < 0.06) in phase 2. Overall gains and efficiency were similar between bulls and steers; however, bulls consumed 140 kg more DM (P < 0.05), were 27 kg heavier (P < 0.05), and had to stay in the feedlot 18 more days (P < 0.05) than steers to achieve a similar amount of fat thickness. Implanted steers had greater concentrations of circulating IGF-I than bulls (P < 0.01), and the pattern of IGF-I concentration over time was affected by castration status (castration status x time interaction; P < 0.01). Synovex-C had a lower impact on circulating IGF-I concentration (implant effect, P < 0.01) than either Revalor-S implant. Eighty-five percent of both bulls and steers had marbling scores sufficient to grade low Choice or better. Bulls achieved their target fat thickness later, increased muscle growth, and deposited fat more favorably than steers, possibly due to a gradual increase in IGF-I concentration as the testicles grew rather than the large fluctuations in IGF-I concentration observed in steers following implantation.

In Exp. 1, 36 individually penned steers (initial BW = 294 +/- 3.8 kg) were used to determine effects of dietary CP percentage and programming gain on performance and carcass characteristics. Steers were fed to achieve a predicted gain of 1.13 kg/d for the first 84 kg of gain and 1.36 kg/d for the next 124 kg of gain and were offered feed for ad libitum consumption for the final 58 kg of gain before slaughter. In these three phases of growth, steers were fed diets, sequentially, with the following CP percentages: HHH (16, 13.5, and 12.5%), LHH (9, 13.5, and 13%), or LLL (9, 9, and 9%). When predicted gain was 1.13 kg/d, ADG was greater (P < 0.01) for steers in the HHH (1.09 kg/d) vs LHH and LLL (0.83 kg/d) systems. When predicted gain was 1.36 kg/d, ADG and gain efficiency were greatest (P < 0.01) for steers in the LHH system. Overall ADG and gain efficiency were greater (P < 0.01) for steers in the HHH (1.46 kg/d, 0.194) and LHH systems (1.38 kg/d, 0.190), compared with steers in the LLL (1.21 kg/d and 0.166) system. Carcass fat thickness was lower for steers in the LHH (0.74 cm) system than for steers in the LLL system (1.09 cm). In Exp. 2, 18 individually penned steers (initial BW = 225 +/- 5.8 kg) were either offered a 13% CP diet for ad libitum intake (AL) throughout the 134-d experiment or fed a high- (16% CP; PI-HH) or low- (10% CP; PI-LH) CP diet and fed to achieve a predicted gain of 1.13 kg/d for the first 85 d of the experiment. Steers in the PI-HH and PI-LH feeding regimens were then offered a 13% CP diet for ad libitum consumption from d 86 to 134. Fractional protein accretion rate was greater (P < 0.01) for steers in the PI-HH and PI-LH feeding regimens than for steers in the AL regimen at d 92, 106, and 120. Fractional breakdown and synthesis rates were not affected (P = 0.63) by feeding regimen. Increased ADG and gain efficiency of steers during compensatory growth periods may in part be due to greater fractional accretion rates of skeletal muscle protein.

Two experiments were conducted to investigate the effects of proportion of dietary corn silage during periods of feed restriction on performance of steers. In Exp. 1, Simmental x Angus steer calves (n = 107; initial BW = 273 +/- 3.8 kg) were allotted to 12 pens with eight or nine steers/pen and four pens/treatment. Periods of growth were 273 to 366 kg BW (Period 1), 367 to 501 kg BW (Period 2), and 502 to 564 kg BW (Period 3). In two of the dietary regimens, steers were given ad libitum access to feed throughout the experiment and were fed either a 15% corn silage diet in each period or an 85, 50, and 15% corn silage diet in Periods 1, 2, and 3; respectively. In the third feeding regimen, a programmed intake feeding regimen was used. Steers were fed a 15% corn silage diet in each period. However, feed intake was restricted to achieve a predicted gain of 1.13 kg/d in Period 1 and 1.36 kg/d in Period 2, and feed was offered for ad libitum consumption in Period 3. For the entire experiment, ADG was similar (P = 0.41) among treatments and feed efficiency was lower (P < 0.10) for steers in the corn silage regimen than for steers in the programmed intake and ad libitum regimens. In Exp. 2, Simmental x Angus steer calves (n = 106; initial BW = 233 +/- 2 kg) were allotted by BW to 12 pens (three pens/treatment) and fed in three periods similar to those described in Exp. 1. Four feeding regimens were investigated: 1) AL; steers were offered a 15% corn silage diet for ad libitum consumption in all three periods; 2) PI; DMI was programmed to achieve gains as described in Exp. 1; 3) CS-HLL; programmed intake as described above except diets contained 85, 15, and 15% corn silage in Periods 1, 2, and 3, respectively; and 4) CS-HIL; same feeding regimens as CS-HLL, except diets contained 85, 50, and 15% corn silage in Periods 1, 2, and 3, respectively. Steers were given ad libitum access to feed in Period 3. Overall ADG was lower (P < 0.05) for steers in the CS-HLL and CS-HIL feeding regimens than for steers in the AL and PI regimens; feed efficiency was greatest for steers in the PI regimen. Few effects of feeding regimen on carcass characteristics were observed.

Two experiments were conducted to investigate a feeding regimen in which a programmed amount of feed was offered daily to control growth rate of steers. In Exp. 1, steers (n = 107, 309 +/- 3 kg) were used to determine effects of offering ad libitum access to feed (AL) vs a programmed intake feeding regimen (PI) and the number of days steers were fed (168 vs 203) on performance and carcass characteristics. Steers in the programmed intake feeding regimen were fed to achieve a predicted gain of 1.13 kg/d for the first 78 kg of gain, 1.36 kg/d for the next 124 kg of gain, and were given ad libitum access to feed for the final 54 or 103 kg of gain before slaughter (for steers fed for 168 d or 203 d, respectively). Feed efficiency was greater (P < 0.02) for steers in the PI than for those in the AL feeding regimen (0.193 vs 0.183 kg gain/kg feed, respectively). From d 169 to 203, steers in the PI feeding regimen had greater (P < 0.06) ADG (1.60 vs 1.38 kg/d) and similar (P = 0.38) feed efficiency than steers in the AL regimen. In Exp. 2, steers (n = 96; 308 +/- 3 kg BW) were offered feed ad libitum throughout the experiment (AL) or were programmed to gain at a high (PI-H) or low (PI-L) growth rate. For the first 78 kg of gain, intake was restricted to achieve predicted gains of 1.13 kg/d (PI-L) or 1.25 kg/d (PI-H). For the next 124 kg of gain, intake was restricted to achieve predicted gains of 1.36 kg/d (PI-L) or 1.47 kg/d (PI-H). Feed was offered ad libitum for the final 58 kg of gain. Overall ADG was similar (P > 0.37) among feeding regimens despite lower DMI for the steers in the PI-L and PI-H feeding regimens than for those in the AL regimen. Feeding regimen did not affect (P < 0.22) carcass characteristics. Programmed intake feeding regimens sustained growth rate and feed efficiency for an extended period of time without detrimental effects on carcass characteristics.

One hundred forty-three Angus x Simmental crossbred steers (initial BW = 155.1 +/- 4.5 kg) were used in a 2-yr study (yr 1, n = 67; yr 2, n = 76) to determine the effects of weaning age, implant regimen, and the weaning age x implant regimen interaction on steer growth and performance, organ mass, carcass characteristics, and cooked beef palatability. Steers were early-weaned at an average age of 108 d (EW) or normally weaned at an average age of 202 d (NW) and allotted by weight to an aggressive or nonaggressive implant regimen. On their respective weaning dates, EW and NW steers were penned individually and fed a grain-based diet until they were slaughtered at a final BW of 546 kg. A subsample of steers (n = 2 per treatment) were slaughtered at 254 kg. At 254 kg, EW steers implanted with the aggressive implant regimen had 64% greater backfat depth than those implanted with the nonaggressive implant regimen; conversely, NW steers implanted with the aggressive implant regimen had 52% lower backfat depth than those implanted with the nonaggressive implant regimen (weaning status x implant regimen interaction; P < 0.01). A similar interaction was observed for empty visceral organ weights. Early-weaned steers were younger (354.7 vs 372.4 d; P < 0.01) at final slaughter but were in the feedlot longer (246.5 vs 169.6 d; P < 0.01) than NW steers, whereas the aggressive implant regimen decreased days fed (203.3 vs 212.7; P < 0.07) compared to the nonaggressive implant regimen. Overall ADG was greater for EW than for NW steers (1.61 vs 1.50 kg/d; P < 0.01) and for the aggressive compared with the nonaggressive implant regimen (1.59 vs 1.52 kg/d; P < 0.02). Early-weaned steers consumed less DM per day (7.4 vs 8.5 kg/d; P < 0.01) and were more efficient (0.217 vs 0.208 kg/kg; P < 0.02) but consumed more total DM (1,817 vs 1,429 kg; P < 0.01) than NW steers while in the feedlot. Implant regimen did not affect DMI (P > 0.37) or feed efficiency (P > 0.15). Weaning status did not affect carcass characteristics (P > 0.14), final empty body composition (P > 0.25), or final longissimus muscle composition (P > 0.18); however, steaks from EW steers had higher (P < 0.05) taste panel tenderness and juiciness ratings than steaks from NW steers. The aggressive implant regimen decreased yield grade (P < 0.02), but did not affect quality grade (P > 0.86) compared to the nonaggressive implant regimen. Placing early-weaned steers on an aggressive implant regimen is a viable management option.

Two experiments were conducted to determine supplemental CP requirements for feedlot steers prescription-fed to achieve stepwise increases in ADG during the feeding period. In Exp. 1, 106 steers (initial BW = 285.7 +/- 3.4 kg) were allotted to 12 pens. Treatments consisted of ad libitum consumption of a 12% CP diet throughout the experiment (AL12%), prescription intake of a 12% CP diet (PI12%), or prescription intake of high-CP diets (PIHCP). The PIHCP diets were formulated to provide the same grams of CP per day as the AL12% diet. Steers in the prescription intake feeding regimens were fed to gain 1.13 kg/d for the first 87 kg of gain and 1.36 kg/d for the next 134 kg of gain and were offered feed for ad libitum consumption for the final 52 kg of gain before slaughter at 559 kg. Overall ADG was lower (P < 0.05) for steers fed PI12% and PIHCP diets than for those fed the AL12% diet (1.48 and 1.50 vs 1.60 kg/d, respectively). Total DM intake was lower (P < 0.08) for steers fed the PI12% and PIHCP diets than for steers fed the AL12% diet (1,359, 1,370, and 1,421 kg, respectively). Dressing percentage, back-fat thickness, and quality grade were lower (P < 0.05) for steers fed the PI12% and PIHCP diets than for steers fed the AL12% diet. In Exp. 2, 142 steers (initial BW = 285.4 +/- 3.1 kg) were allotted to 16 pens. System 1 was ad libitum consumption of a 12% CP diet throughout the experiment. Steers in Systems 2, 3, 4, and 5 were subjected to the same prescription intake strategy as steers in Exp. 1. During the three phases of growth (1.13 kg/d, 1.36 kg/d, and ad libitum), steers were fed the following CP concentrations: System 2(12, 14, and 12%); System 3(12, 14, and 14%); System 4(12, 16, and 12%); and System 5(12, 16, and 14%). No differences (P > 0.06) in total steer performance, carcass characteristics, or carcass chemical composition were observed among systems. Increasing percentage of CP in diets of prescription-fed steers to provide the same daily intake of CP as steers consuming feed ad libitum was not beneficial.

Two experiments were conducted to determine the effects of diet on growth of steers weaned at approximately 100 vs 205 d of age. In Exp. 1, a 2 x 2 x 2 factorial experiment was conducted using 78 Angus crossbred cow-calf pairs. The factors examined were age at weaning (early, at 103+/-3 d [EW] vs normal, at 203+/-3 d [NW]), feeding strategy (ad libitum vs postweaning programmed intake), and dietary CP concentration (100 vs 120% of NRC [1984] recommended levels). Early-weaned calves had a greater (P < .001) ADG than NW calves from 103 to 203 d and reached market weight at 385 d vs 418 d for NW calves (P < .001). Likewise, steers offered feed for ad libitum consumption reached market weight at 394 d, compared with 409 d for programmed-intake steers (P < .05). In Exp. 2, 64 Angus crossbred steers were either weaned at 93+/-3 d and fed one of four diets, weaned at 210+/-3 d without access to creep feed, or weaned at 210+/-3 d with access to creep feed for 60 d prior to weaning. Early-weaned calves were heavier (P < .01) than NW calves at 210 d if fed either 100 or 90% concentrate diets, and they had greater (P < .001) backfat thickness at 210 d but no difference (P > .10) in longissimus muscle area compared to EW calves fed a 60% concentrate diet. At slaughter, 80 to 100% of steers on all treatments graded low Choice or higher. Feeding high-concentrate diets to EW beef calves accelerated growth rate and fat deposition early in the feeding period and may be a way to provide young cattle for a high-quality beef market.

Four trials were conducted to determine the efficacy of using trainer animals to improve the health and performance of newly arrived feedlot calves. For all trials, trainer animals were given 3 wk to adapt to the feedlot before arrival of the feeder calves and initiation of the trials. Trainer animals were present with newly received feedlot calves for 14 d after arrival and then were removed from the pens for the remaining 14 d of the experiments. In Trial 1, trainer animals were six crossbred beef steers and six mature cull beef cows. Newly received calves were allotted to 18 pens with 10 calves/pen. Six pens contained a trainer steer and six pens contained a trainer cow. Similar procedures were used for the subsequent three trials, except 12 trainer cows and 24 pens were used, and in Trial 4 half of the calves were allotted to pasture paddocks for 14 d before placement in their feedlot pens. During wk 1 of Trial 1, calves with trainer cows and steers gained weight more rapidly (P < .10) than those without a trainer animal (1.12 vs .67 kg/d, respectively). During wk 2, this trend was reversed and overall gains did not differ (P > .20) among treatment groups. Morbidity was 16.7 for control calves, 28.3% for calves with trainer steers, and 8.3% for calves with trainer cows. Four of six trainer steers required antibiotic treatment for respiratory disease. On d 1, a greater (P < .05) percentage of calves in the trainer cow group (81.7%) were observed eating during the first 30 min after feeding compared with either the steer trainer group (60%) or the control group containing no trainer animal (48.3%). This trend continued on d 2 but was not evident on d 3 or 7. In Trial 2, overall gains were 10% greater (P < .06) and final BW was higher (P < .01) for calves with trainer cows than for those without trainers. Trainer cows resulted in a substantial reduction (P < .01) in calf morbidity compared with calves housed alone. In Trial 3, trainer cows did not improve performance or health of newly received calves. More (P < .07) calves with trainers than without were eating 5 min after feeding on d 1, 2, 4, and 8. In Trial 4, the presence of trainer cows the first 2 wk did not affect (P > .27) gains. However, calves placed on pasture after arrival had lower (P < .03) gains during wk 1 than those housed in the feedlot. Calves placed in pasture paddocks upon arrival had more than twice (P < .01) the incidence of morbidity of those placed directly in the feedlot. In these trials, trainer cows had a significant effect on eating behavior of newly received calves, but health and performance benefits were variable.

Newly arrived feedlot calves undergo numerous stressors that result in 1) transient endocrine responses, 2) altered products of energy and protein metabolism, 3) changes in appetite and growth rate, 4) possible limited compromise of digestive and rumen function, and 5) a challenged immune system. The most consistent endocrine and metabolic responses to marketing, transport, and feedlot adaptation are seen with cortisol and epinephrine. In contrast to earlier work done with indirect in vitro gas production measurements, recent research has shown that the ruminal microbial population is able to effectively digest available substrate immediately following a calfs weaning, trucking, and 24 h of feed and water deprivation. Additionally, a period of feed and water deprivation up to 72 h coupled with 8 h of trucking does not reduce the concentration or total numbers of either the viable cellulolytic or total bacteria present in the rumen of newly weaned or feedlot-adapted calves. However, ruminal volume, DM, total weight of ruminal contents, and total protozoal numbers decrease as duration of feed deprivation increases. To compensate for the reduced DMI that occurs in the first 2 wk after arrival at the feedlot, increased nutrient density is needed to meet an animal's requirements for nutrients. Limited data suggest that newly arrived calves prefer a diet that is similar in moisture and texture to feeds with which they are familiar. Additionally, modification of the stress-associated behavior using trainer animals may improve the feed intake of newly received calves and may reduce calf morbidity.

Five ruminally fistulated 3-yr-old mature Holstein steers (average BW 691+/-23 kg) were used in a 5 x 5 Latin square experiment with a 2 x 2 + 1 fact orial arrangement of treatments. Effects of protein concentration and protein source on nutrient digestibility, excretion of DM and fecal N, ruminal fluid volume and dilution rate, ruminal characteristics, and in situ DM disappearance of whole shelled corn, ground corn, and orchardgrass hay were measured in steers limit-fed high-concentrate diets at 1.5% of BW. A negative control basal diet (NC; 9% CP) was supplemented to achieve either 11 or 14% CP; supplemental CP was either from soybean meal (11 and 14% SBM) or a 50:50 ratio of CP from urea and soybean meal (11 and 14% U). Dry matter and OM digestibilities were 5% greater (P < .07) for steers fed the SBM diets than for those fed the U diets. Starch digestibility did not differ (P > .10) among steers fed any of the diets. Nitrogen source did not affect (P > .10) apparent N digestibility or fecal N excretion; however, steers fed the NC diet had the lowest (P < .10) apparent N digestibility compared with those fed all other diets. Ruminal fluid volume was lower (P < .06) when steers were fed the NC diet compared with all other diets; there were no differences (P > .74) among diets for ruminal fluid dilution rate. In general, ruminal ammonia N and VFA molar proportions were not affected by protein source or concentration. Although CP concentration affected (P < .06) in situ DM disappearance of ground corn, CP concentration did not (P > .48) affect total tract digestion of DM or OM. This indicates that CP concentration may have affected site of digestion, but not extent of digestion. When mature ruminants were limit-fed a corn-based diet to meet primarily a maintenance function, protein source and concentration had little effect on measures of nutrient digestion.

Efficiency of limit-feeding a whole shelled corn-based diet as an alternative to a conventional forage-based diet for nonlactating dairy cattle was determined. Twelve nonlactating, multiparous Holstein cows (initial BW 642+/-50 kg) were used in a randomized complete block design. Nutrient digestibility, excretion of DM, N, and P, performance of cows, and feed costs were measured. Both diets were formulated to provide equal daily intakes of NE1, protein, vitamins, and minerals, according to National Research Council recommendations. Dry matter intake was restricted by 30% for cows fed the high-corn diet compared with the high-forage diet (6.8 vs 9.6 kg/ d, respectively); therefore, concentrations of nutrients in the high-corn diet were increased to compensate for decreased DMI. Diets were fed once daily, and cows had unlimited access to fresh water. After a 28-d adaptation period, cows were placed in metabolism stalls for a 6-d total collection of feces and urine. The limit-fed, high-corn diet had a 15% greater DM digestibility than the high-forage diet. A 29% decrease in DMI for the high-corn diet vs the high-forage diet resulted in a 40% decrease in fecal DM excretion. Starch digestibility and digestibility of whole corn kernels were not affected (P > or = .62) by diet. Despite similar N intakes, total N excretion was 22% greater (P < .01) for cows fed the high-forage diet than for those limit-fed the high-grain diet. Cow weight and condition score change did not differ (P > .10) between diets. Feed costs were reduced by $.38/d with the high-corn diet vs the high-forage diet. Limit-feeding a corn-based diet is an economically and nutritionally viable alternative to forage-based diets for nonlactating Holstein cows.

In Trial 1, 108 crossbred steer calves (initial BW 295 kg) were allotted to 12 pens and used in a 186-d feedlot trial to determine the effects of increasing or decreasing roughage level on feedlot performance and carcass characteristics. Four dietary treatments were investigated: 1) 85% concentrate diet fed for 186 d, 2) 100% concentrate diet fed for 186 d, 3) 85% concentrate diet fed for 84 d followed by a 100% concentrate diet for the remaining 102 d, and 4) 100% concentrate diet for 84 d followed by an 85% concentrate diet for the remaining 102 d. Corn silage was added as roughage. During the first 84 d, level of dietary concentrate did not affect (P > .10) ADG. Steers switched to the 85% concentrate diet for the last 102 d had higher (P < .05) DMI than those fed the 100% concentrate diet; they did not exhibit an increase in ADG. Finishing phase feed efficiency was highest (P < .05) for steers continually fed 100% concentrate, lowest (P < .05) for steers continually fed 85% concentrate, and intermediate for steers whose concentrate level was switched during the trial. Carcass characteristics were not affected (P > .10) by concentrate level regimen. In Trial 2, 108 crossbred steer calves (initial BW 319 kg) were allotted to 12 pens and used in a 158-d trial to determine whether feedlot performance could be enhanced by manipulating roughage level and grain processing. Factors investigated were staged increases in concentrate level (70 to 85 to 100%) vs staged decreases in concentrate level (100 to 85 to 70%) and whole vs rolled high-moisture corn. Corn silage was added as roughage. Diet concentrate levels were changed on d 56 and 112. During the first 56 d, steers fed 70% concentrate diets grew 11% faster (P < .05) and consumed 19% more feed (P < .05) than those fed 100% concentrate diets. Steers fed rolled corn gained 8% faster (P < .06) and were 7% more efficient (P < .06) than those fed whole corn. During the last period (d 113 to 158), ADG was not affected (P > .10) by concentrate level or corn processing. Although increasing roughage during the feeding period increased feed intake in these trials, steer performance was not enhanced. Processing high-moisture corn did not affect feedlot performance.

In Trial 1, 161 Angus x Simmental crossbred steers (initial BW 305 +/- 1.0 kg) were used in a completely randomized design experiment to determine the effects of intake restriction and programmed gain on cattle performance and carcass composition and characteristics. Five feeding systems were tested using step-wise increases in programmed intake level. Initially steers were fed to gain 1.13 kg/d. Intake was then increased to achieve a gain of 1.36 kg/d. At the end of the feeding period, steers had ad libitum access to feed. Duration of intake restriction and the period of unrestricted intake was varied. Feeding steers at restricted intakes and then increasing daily gain by increasing feed intake using four different schedules all reduced (P < .05) daily feed intake and total feed intake compared with providing ad libitum access to feed throughout the trial. Furthermore, daily feed efficiency was increased (P < .05) by two of the feeding systems compared with offering ad libitum access to feed throughout the trial. The feeding system used did not affect (P > .10) quality grade of the carcasses. In Trial 2, 77 individually penned Angus x Simmental crossbred steers (initial BW 273 +/- 1.2 kg) were used to determine the effects of various feed intake restriction systems. For systems 1 through 4, multiple periods of restriction and realimentation were investigated; the duration and magnitude of restriction were varied. Feed intake was not restricted for steers in system 5. The feed restriction systems used in this experiment did not result in decreased total feed intake or changes in carcass composition as compared with offering ad libitum access to feed. Reducing total energy intake seems to be a prerequisite to altering feed efficiency of steers in limit-feeding systems.

Three experiments were conducted to determine the effects of supplemental fat and CP concentration in diets of newly received steers. In Exp. 1, 72 steers (initial BW 201 +/- 17 kg) were used in a 2 x 2 x 2 factorial experiment to determine effects of fat (Megalac, a calcium soap of palm fatty acids [CS]) concentration (0 vs 2%), CP concentration (12 vs 14%), and CP source (spray-dried blood meal [BM] vs soybean meal [SBM]) in receiving diets. Steers fed BM ate 22.8% more during wk 1 and 15.0% more during wk 2 if there was no CS in their diets compared with steers fed BM plus 2% CS (P < .05). In Exp. 2, 160 steers (initial BW 247 +/- 16 kg) were used in a randomized complete block design experiment to determine effects of adding CS (0, 2, or 4%) to 14% CP diets containing BM. No differences (P > .10) in ADG or feed efficiency (FE) occurred due to CS. In Exp. 3, 186 steers (initial BW 243 +/- 20 kg) were used in a randomized complete block design experiment to determine effects of supplemental fat source in receiving diets on steer performance. Diets contained either 0% added fat (control), 4% CS, or 4% animal-vegetable blend (AV). Feeding AV improved (P < .05) ADG and FE during wk 2 and FE for the total trial. Addition of AV to high-protein (15 to 22% CP) receiving diets improved FE, and CS resulted in no improvements in performance.

Three experiments were conducted to determine the efficacy of limit-feeding corn-based diets as an alternative to hay for beef cows in gestation and early lactation. Seventy or 71 mature, pregnant Simmental crossbred cows (average weight = 589 +/- 10 kg) were used in each trial. Each of 29 or 30 cows was fed approximately 5 kg of whole shelled corn, 1.2 kg of a pelletted supplement, and 1 kg of hay daily from November to April to meet nutritional needs for gestation. The remaining 41 cows were fed first-cutting round-baled hay free choice. Cows with ad libitum hay intake consumed approximately twice as much feed as cows limit-fed the corn-based diet. Body weight change during the winter was not affected (P > .10) by feeding system in Trials 1 and 2. Limit-feeding the corn-based diet had no detrimental effects on subsequent cow performance or conception rate or on calf weaning weight following summer grazing on pasture. The cost to feed a cow hay was nearly double that of limit-feeding corn-based diet. Two additional experiments were conducted to determine the effect of supplemental monensin (200 mg/d) on performance of gestating Simmental-Angus first-calf heifers fed corn-based diets. In Trial 4, monensin-supplemented heifers were fed 10% less corn than control heifers. In Trial 5, both groups were fed equal amounts of feed. No adverse effects of feeding the corn-based diets were observed. It was concluded from these trials that corn-based diets can meet the nutrient requirements of pregnant beef cattle without adverse effects on production and at a lower cost than feeding hay.

Three experiments were conducted with Simmental x Angus crossbred steers to determine the effects of energy source and level on performance of newly arrived feedlot calves. In trial 1, 68 steers (initial BW 215 +/- 9.4 kg) were used in a 2 x 3 factorial experiment to determine the effects of receiving diet and previous creep feed on performance. Diets were composed primarily of either corn silage, corn silage + alfalfa pellets + dry corn, or dry corn + alfalfa pellets. For the 41-d trial, calves fed the corn silage-based diet had greater (P < .05) ADG and feed efficiencies than calves fed the other two diets. In Trial 2, 60 steers (initial BW 212 +/- 4.6 kg) were used in a 28-d completely randomized design experiment to determine the effects of 16% CP receiving diets containing 70, 75, 80 or 85% concentrate on performance. There were no differences (P > .10) in ADG or feed efficiency due to dietary concentrate level. In Trial 3, 77 steers (initial BW 226.3 +/- 3.0 kg) were used in a 2 x 3 factorial experiment to determine the effects of dietary concentrate and protein levels on performance during a 28-d receiving period. The factors were concentrate level (70 vs 85% concentrate) and protein level (12.5%, 16%, or phase-fed at 23%, 17%, 14%, and 12.5% during wk 1, 2, 3, and 4, respectively). During wk 1, calves fed the 85% concentrate diet had greater (P < .01) DMI, ADG, and feed efficiency compared with 70% concentrate. Calves fed the 16% CP and phase-fed protein diets had greater (P < .01) DMI, ADG, and greater (P < .02) feed efficiency than calves fed the 12.5% CP diets. Receiving diets containing at least 16% CP and > 70% concentrates are beneficial to calves during the first week after feedlot arrival.

Two experiments were conducted to determine the effects of length of feed and water deprivation on ruminal microbes and ruminal characteristics. In Exp. 1, treatments were as follows: 1) weaned, but not trucked (0 h), 2) weaned, trucked, and fasted for 48 h (48 h), and 3) weaned, trucked, and fasted for 72 h (72 h). On d 0 (arrival back at the feedlot after treatment), DMI, ruminal contents (P < .05) decreased as length of feed and water deprivation increased. However, on d 4, there were no longer any differences (P > .10) in DMI or weight of ruminal contents. On d 0, percentage of ruminal DM in the 48- and 72-h treatment groups was lower (P < .01) than in the 0-h treatment group, but there were no differences (P > .10) by d 4. After the steers used in Exp. 1 had been in the feedlot for 28 h, they were reallotted, and the three treatments (except for weaning) were repeated; the 0-h group remained at the feedlot. On d 0, DMI of the 48-h group was lower (P < .05) than that of the 0-h group; DMI of the 72-h group was intermediate. On d 0, the 0-h treatment group had a greater ruminal DM percentage than the 48- and 72-h treatment groups (P < .05); however, due to large within-treatment variation the total weight of ruminal contents did not differ (P > .10) among treatments. There were no decreases (P > .10) in cellulolytic or total bacterial concentration or in the ruminal numbers of cellulolytic or total bacteria due to length of feed and water deprivation on d 0 in either Exp. 1 or 2. In both trials, 48 and 72 h of feed and water deprivation decreased (P < .05) protozoal numbers on d 0 and 4 compared with the 0-h treatment group.

In Trial 1, 240 crossbred steers (initial BW 243 +/- 8 kg) were used in a 2 x 4 factorial experiment to determine the effects of receiving diet CP concentration (12, 14, 16, or 18%) and source (spray-dried blood meal [SDBM] vs soybean meal [SBM]) on steer performance. There were linear (P < .01) increases in ADG and feed efficiency during wk 1. For the entire trial, there was an increase (P < .01) in feed efficiency with increasing CP concentration and diets containing SDBM compared with those containing SBM. In Trial 2, 240 crossbred steers (initial BW 246 +/- 14 kg) were used in a completely randomized design experiment to determine the effects of receiving diet CP concentration (11, 14, 17, 20, 23, or 26%) on steer performance. Average daily gain and feed efficiency increased (P < .01) with increasing CP concentration during wk 1. There were quadratic (P < .01) responses to CP concentration for final weight, ADG, and feed efficiency. In Trial 3, 216 steers (initial BW 238 +/- 1 kg) were used to determine the effects of receiving diet protein sources on steer performance. The control diet used SBM as the supplemental CP source and was formulated to contain 12.5% CP. The other five protein sources were corn gluten meal (CGM), ring-dried blood meal (RDBM), SDBM, fish meal (FM), and SBM. For these five CP sources, diets were formulated to contain 23% CP during wk 1, 17% CP during wk 2, and 12.5% CP during wk 3 and wk 4. During wk 1, control steers had the lowest ADG (P < .07) and feed efficiency (P < .01) whereas steers fed RDBM and SDBM had the highest (P < .01) feed efficiency. Increased CP concentrations are needed early in the receiving period, when DMI is low.

Eight ruminally fistulated steers, 7 to 8 mo old, were used in a completely randomized, 2 x 2 factorial experiment to determine the effects of energy density and protein source in receiving diets on in situ DM, NDF, and N disappearance, concentrations of ruminal bacteria, protozoa, ammonia, and pH. Two energy densities (1.80 and 1.48 Mcal/kg of NEm) and two protein sources (spray-dried blood meal [SDBM] and soybean meal [SBM]) were compared. Fistulated steers were weaned, transported by truck, and held in a sale barn before their arrival at the feedlot. On d 0 (day of arrival at the feedlot), DMI was 62% of DMI on d 7 after arrival. Overall, feeding a high-energy diet resulted in lower (P < .01) in situ DM disappearance (DMD) of orchardgrass than feeding a low-energy diet at both 24 and 48 h. In situ 24-h DMD averaged 46.6% on d-3 and 41.6% on d 0, whereas 48-h in situ DMD on d -3 and 0 averaged 58.2 and 58.6%, respectively, indicating the ruminal microbial population was not inhibited in its ability to digest available substrate. Additionally, there were no differences (P > .10) in 48-h in situ NDF disappearance between d -3 and 0 (58.8 vs 57.8%), respectively. No differences (P > .10) occurred in the concentration of total bacteria, or cellulolytic bacteria, due to feed and water deprivation. Concentration of total protozoa was lower (P < .05) on d 0 than at any other time. Entodinium averaged 72.5% of genera before weaning, and more than 90% of genera found on all treatments by d 21. Diplodinium and Epidinium percentages tended to decline after weaning. Isotricha concentrations were low and Dasytricha were eliminated after d 7. In conclusion, the concentration of ruminal bacteria and the ability to digest available substrate were not decreased immediately after weaning, trucking, and 24 h of feed and water deprivation.

Two experiments were conducted to determine the effects of restricted feeding on performance, carcass characteristics, and composition. In Trial 1, 36 individually penned steer calves (280 +/- 13 kg BW) were fed all-concentrate diets at intake levels of ad libitum and 90 and 80% of ad libitum. Trial 2 used 36 individually penned steer calves (298 +/- 14 kg BW) fed corn silage-based growing diets for 84 d followed by 91% concentrate finishing diets. Intakes were as described for Trial 1. Compared with steers with ad libitum intake, ADG was reduced (P < .005) .15 and .25 kg for steers fed 90 and 80% of ad libitum intake, respectively, in Trial 1. In Trial 2, growing phase ADG was reduced (P < .005) .15 and .24 kg for the 90 and 80% of ad libitum feed intake, respectively. Finishing phase ADG was reduced (P < .005) .12 and .21 kg for the 90 and 80% of ad libitum intake, respectively. Feed efficiency was not affected by intake when all-concentrate diets were fed in Trial 1, or when a corn silage-based diet was fed in the growing phase of Trial 2. During the finishing phase of Trial 2, feed efficiency was increased when intake was restricted. Carcass quality grade and 12th rib backfat were reduced (P < .04) with decreases in daily feed intake when all-concentrate diets were fed. However, no effect on carcass characteristics was observed in Trial 2. Liver and heart weights were not affected by daily feed intake. Serum triiodothyronine (T3) concentrations tended (P = .11) to decrease for cattle receiving restricted intakes of all-concentrate diets and were decreased (P < .04) with intake restriction in Trial 2. Carcass fat content was reduced (P < .02), whereas carcass protein and water were increased (P < .06) with reductions in daily feed intake in both trials. We concluded that restrictedly feeding growing-finishing steer calves does not decrease feed efficiency and actually may improve feed efficiency. Restrictedly fed steers had reduced maintenance requirements, and lean tissue accretion represented a greater percentage of their total gain.

The effects of restricted feeding on site and extent of digestion, flow of N-containing compounds to the duodenum, and ruminal metabolism were determined. In Trial 1, corn silage-based diets were fed at one of three intakes to three ruminally and duodenally fistulated steers (420 +/- 4.4 kg BW) in a repeated 3 x 3 Latin square experiment. Feeding levels were 100% of ad libitum intake, 90% of ad libitum intake, and 80% of ad libitum intake. Site of digestion was not affected by restricted feeding; however, extent of DM, NDF, and apparent N digestion were increased (P < .03) 2.8, 4.1, and 6.2 percentage units for each 1-kg restriction in DM intake. Restricted feeding increased (P < .06) ruminal pH and ammonia concentrations, decreased (P < .05) ruminal liquid dilution rate, and had no major effects on bacterial concentrations. In Trial 2, all-concentrate diets based on whole shelled corn were fed at 100, 90, or 80% of ad libitum intake to six ruminally and duodenally fistulated steers (440 +/- 4.1 kg BW) in a replicated 3 x 3 Latin square experiment. Restricted feeding increased (P < .06) apparent ruminal DM digestion; however, true ruminal OM digestibility was not affected. Extent of apparent N digestion increased 3.0 percentage units for each 1-kg restriction in DMI. Ruminal pH was not affected by restricted feeding; however, ruminal ammonia concentrations increased (P < .06) and ruminal liquid dilution rate decreased (P < .04) with restricted feeding. In both Trials, total N flow to the duodenum was approximately 100% of N intake for the 80% of ad libitum intake. Flow of N exceeded N intake in a linear (P < .01) manner as DMI increased. Decreases in duodenal N flow when intake was restricted resulted from decreases (P < .01) in bacterial N flowing to the duodenum, and also in decreases (P < .01) in non-ammonia, non-bacterial N flow when whole shelled corn-based diets were fed. We concluded that restrictions in digestible energy intake are less than the DM restriction when corn silage-based diets are fed but are equal to the DM restriction when whole shelled corn-based diets are fed. Also, restricted feeding strategies reduce the flow of N to the duodenum from both bacterial and feed origins.

The effects of intake (ad libitum and 70% of ad libitum) and corn processing (whole or rolled) on digestion, ruminal metabolism, and blood metabolites were determined in a 2 x 2 factorial experiment using eight ruminally fistulated steers. All-concentrate diets were fed with adjustments to dietary concentrations of N, vitamins, and minerals to ensure equal daily intake of these nutrients. Digestion of DM, OM, and starch were affected by an intake x processing interaction (P < .03). Starch digestion for the low-intake, whole-corn diet was much lower than that for the other three diets. This decrease in starch digestion was the major reason for the interaction. Nitrogen digestion was improved (P < .03) with limited intake but was not affected by processing. Ruminal volume and ruminal turnover (percentage/hour) were both reduced (P < .03) on the low-intake diet. Molar proportion of acetate was reduced and propionate was increased (P < .01) for steers receiving high intake of rolled corn compared with the other three diets. Butyrate concentrations were increased (P < .01) when corn was rolled before feeding. Ruminal pH was higher immediately before feeding for steers receiving whole corn than for those receiving rolled corn. Decreases in pH were observed for rolled corn 2 to 9 h after feeding, suggesting a faster rate of fermentation of rolled corn than of whole corn. Concentrations of blood glucose and insulin were not affected by intake or processing. It was concluded that processing corn can improve DM and OM digestibility if intake is restricted and that N digestion is improved with restricted feeding.(ABSTRACT TRUNCATED AT 250 WORDS)

Sixty Angus crossbred steers (initial BW, 237 kg) were used in a 2 x 2 factorial experiment to determine the effects of energy density and protein source in receiving diets on steers performance and total tract nutrient digestion. The factors compared were energy density (1.80 vs 1.48 Mcal/kg of NEm, referred to as high-energy and low-energy, respectively) and protein source (ring-dried blood meal [BM] vs soybean meal [SBM]). Diets containing BM resulted in a 10.6% greater (P < .09) ADG and a 7.6% improvement (P < .05) in efficiency of feed utilization compared with those containing SBM. High-energy diets resulted in an 8.7% improvement (P < .05) in feed efficiency vs low-energy diets. Dry matter digestibility (DMD), NDF digestibility (NDFD), and CP digestibility (CPD) were exceptionally high during wk 1, when DMI was approximately 1.5 kg/d. Nutrient digestibility declined during wk 2 and 3, as intake increased, before stabilizing between wk 4 and 6. Additionally, NDFD was not consistently lower (P > .10) during this study for high-energy diets than for low-energy diets. The results of the overall performance data indicate that, compared to SBM, feeding BM may improve ADG and feed efficiency during the receiving period when dietary CP is approximately 13%. Additionally, DMD, NDFD, and CPD were higher on d 7 than at any other time, indicating that by d 7 ruminal function was not adversely affected. Therefore, it seems that the reduced feed intake and growth rate normally seen during the first 2 wk in the feedlot is not caused by a reduction in diet digestibility.

The objective of this study was to determine the effects of soybean meal (SBM) or spray-dried blood meal (BM) supplementation of diets based on untreated (UNT-WS) or alkaline hydrogen peroxide-treated wheat straw (AHP-WS). A 4 x 4 Latin square design with a 2 x 2 factorial arrangement of treatments was used. Variables included nutrient digestion and flow to the duodenum. Four Simmental steers (average weight 477 kg) fitted with ruminal and duodenal cannulas were fed 65% UNT-WS or AHP-WS based diets in 12 equal portions daily. Diets were formulated to contain 10% CP. Chromic oxide was used as the digesta flow marker and purines were used as the microbial marker. There were no straw type x protein source interactions. Total tract and ruminal OM digestibility were approximately 25% greater (P < .04) when AHP-WS was fed than when UNT-WS was fed. Source of protein did not affect (P > .10) OM or fiber digestion in the rumen or total tract. Ruminal digestion of NDF and ADF was increased (P < .01) by 51 and 40%, respectively, when AHP-WS was fed than when UNT-WS was fed. Main effect means (P > .10) for N flow to the duodenum as a percentage of N intake were 128.2, 142.5, 133.4, and 137.6 for UNT-WS, AHP-WS, SBM, and BM treatments, respectively. Despite increased (P < .01) ruminal OM digestion for AHP-WS, microbial N flow to the duodenum was greater (P < .01) when UNT-WS was fed than when APH-WS was fed.(ABSTRACT TRUNCATED AT 250 WORDS)

A 4 x 4 Latin square metabolism trial with a 2 x 2 factorial arrangement of treatments was conducted to determine N kinetics in steers. Steers were fed either untreated (UNT-WS) or alkaline hydrogen peroxide-treated wheat straw (AHP-WS) based diets supplemented with soybean meal (SBM) or blood meal (BM). Single doses of (15NH4)2SO4 were infused into ruminal pools to determine N kinetics. Ruminal NH3N concentrations (main effects) were 3.81, 1.65, 3.18, and 2.28 mg/dL in steers when fed diets that contained UNT-WS, AHP-WS, SBM, and BM, respectively. Ruminal N pool size was greater (P < .05) for UNT-WS than for AHP-WS diets and also was greater (P < .10) for SBM than for BM diets. Nitrogen flux rate into the rumen was not affected (P > .10) by diet. However, production rate of N from the ruminal pool was greater (P < .05) for UNT-WS than for AHP-WS diets and greater (P < .10) for SBM than for BM diets. Nitrogen recycled into the rumen was 33% greater (P < .05) for AHP-WS than for UNT-WS diets and 26% greater (P < .05) for BM than for SBM diets. Nitrogen recycling (percentage of N intake) was 33, 56, 36, and 49% for UNT-WS, AHP-WS, SBM, and BM diets, respectively. The blood urea N (BUN) concentrations were 10.23, 4.58, 7.15, and 7.65 mg/dL for UNT-WS, AHP-WS, SBM, and BM diets, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)