Performance by feedlot steers and heifers: daily gain, mature body weight, dry matter intake, and dietary energetics

Performance, DMI, diet composition, and slaughter data from 9,683 pens of steers and 5,009 pens of heifers that were fed high-concentrate diets for 90 d or more were obtained from 15 feedlots from the western United States and Canada. The data set included pen means for more than 3.1 million cattle fed between 1998 and 2004. Performance measurements assessed included ADG, DMI, dietary NE, shrunk initial weight (SIW), and shrunk final weight. Mature final weight (MFW) for cattle in each pen was estimated based on regression of slaughter weight against SIW and ADG across all pens. Equations were developed to standardize performance projections (ADG, MFW, and break-even values) and analyze feedlot cattle close-outs. Generally, as diet NE concentration increased, DMI was decreased but G:F, dressing percentage, and yield grade all increased. Pens of cattle with greater SIW had greater ADG, DMI, and shrunk final weight but a lower G:F and dressing percentage. Dressing percentage and yield grade were correlated positively. Equations of the NRC relating gain to NE intake explained 85 and 80% of the variation in DMI of steers and heifers, respectively, with mean ratios of predicted to observed DMI (DMIratio) at 1.000 +/- 0.0506 and 0.974 +/- 0.0490. However, a significant (P < 0.001) bias in the NRC estimate of DMI was detected (r(2) = 0.10 and 0.05, for steers and heifers) between the DMIratio and ADG in which DMIratio increased as ADG increased. This was due to inherent confounding of ADG and MFW in the original NE equation of Lofgreen and Garrett. Based on iterative optimization to minimize the difference between expected and observed DMI, revised equations for retained energy (RE, Mcal/kg) were developed for steers and for heifers: RE(steer) = 0.0606 x (LW x 478/MFW(steer))(0.75)ADG(0.905); RE(heifer) = 0.0618 x (LW x 478/MFW(heifer))(0.75)ADG(0.905), where LW = mean shrunk live weight. The revised equations decreased the SD of the DMIratio by 5.4% (from 0.0496 to 0.0469) and eliminated the bias in DMIratio that was related to ADG (r(2) = 0.0006). The similarity between the 2 equations derived for steers and for heifers for estimation of RE from ADG supports the concept that scaling by MFW accounts for energy utilization differences between sexes.     

Evaluation of the National Research Council (1996) dry matter intake prediction equations and relationships between intake and performance by feedlot cattle

Intake prediction equations of NRC based on initial BW and dietary NE(m) concentration were evaluated with a commercial feedlot database consisting of 3,363 pen means collected from 3 feedlots over a 4-yr period. The DMI predicted by NRC equations had significant (P < 0.01) mean and linear biases across the range of observed DMI in the database. In general, DMI was overpredicted by the NRC equations. Adjustment of the NE(m)-based prediction by use of a 12% increase in NE(m) concentration and a 4% decrease in predicted DMI associated with the feeding of monensin decreased bias. Dry matter intake predicted by the NE(m)-based monensin-adjusted, NE(m)- based, and initial BW equations explained 67, 66, and 64% of the variation in observed DMI, respectively. Relationships between ADG and G:F with DMI as a percentage of BW and NE(g) intake also were examined in the same data set. Across the wide range of average shrunk BW in the database (334.4 to 548.0 kg), ADG was positively related to DMI as a percentage of BW (P < 0.01); however, this relationship was not strong (r(2) = 0.17). Likewise, G:F showed little relationship with DMI as a percentage of BW (P < 0.01; r(2) = 0.05). By accounting for differences in maintenance energy requirements of pens with varying average BW, NE(g) intake was strongly and positively related to ADG (linear and quadratic, P < 0.01; R(2) = 0.70); however, G:F showed little relationship with NE(g) intake (P = 0.02; r(2) = 0.01). Our evaluations with measurements of DMI by cattle in commercial feedlots indicated the shortcomings of current published equations for predicting DMI and suggest the need for development of new equations with improved accuracy and precision. Furthermore, our data indicate that increasing NE(g) in- take increased ADG in a quadratic manner but did not affect G:F by pens of cattle in feedlots. These findings suggest a diminishing returns effect of energy intake on energy retention.     

Evaluation of the 1996 NRC beef model under western Canadian environmental conditions

Two feedlot trials were conducted to evaluate the 1996 NRC beef model under western Canadian conditions. In the first trial, 144 Charolais- (304.6 +/- 16.3 kg) and 144 Hereford- (295.1 +/- 20.8 kg) cross steers were used, whereas the second trial used 88 Angus- (289.7 +/- 15.0 kg), 88 Charolais- (299.8 +/- 17.9 kg), and 88 Hereford- (291.1 +/- 20.9 kg) cross steers. Diets were based on barley silage, rolled barley grain, canola meal, and cereal straw and were analyzed according to the 1996 NRC methodologies. Animal performance and environmental data were collected for 24 pens of steers per trial for the backgrounding and finishing periods. Levels 1 and 2 of the 1996 NRC model were used to generate predictions of DMI and ADG for each pen. Results showed that actual finishing DMI was accurately predicted for Trial 1 and for the combined trials but not for Trial 2. Predicted ADG was lower (P < 0.05) than actual ADG for all feeding periods except Level 1 of the Trial 1 finishing period. All ADG residuals were significant (P < 0.05), indicating inaccurate prediction of ADG in all feeding periods. The 1996 NRC model consistently predicted that protein was not limiting gain. Further investigations and model refinement regarding animal energy requirements under cold weather conditions and effects of limit feeding are required to increase the accuracy of the 1996 NRC model in predicting animal performance.     

Effects of supplementation on voluntary forage intake, diet digestibility, and animal performance

A data base was constructed to describe and estimate supplementation effects in nonlactating cattle consuming forage ad libitum. The data base included 66 publications on 126 forages (73 harvested and 53 grazed) and a total of 444 comparisons between a control, unsupplemented treatment and a supplemented treatment. Daily gains were reported for 301 comparisons and voluntary intake for 258. Direct measures of forage digestibility were reported for 202 comparisons, and total diet digestibility for 150. Supplements did not increase gain in all cases. Change in ADG due to supplement was not related closely to intake of supplemental TDN. Lowest increases in ADG were with native forages supplemented with molasses alone or with low intakes of molasses containing high levels of NPN. Greatest increases in gain were with improved forages, supplements with > 60% TDN, and supplemental CP intake > .05% of BW. Supplements decreased voluntary forage intake (VFI) when supplemental TDN intake was > .7% of BW, forage TDN:CP ratio was < 7 (adequate N), or VFI when fed alone was > 1.75% of BW. When supplements increased VFI, forage TDN: CP ratio was > 7 (N deficit), and VFI when fed alone was often low. There was little relationship between change in VFI and sources of supplemental CP and TDN. Supplements caused total diet TDN concentration to deviate from expected values by -10 to +5% of OM. When supplemental TDN intake was > .7% of BW, diet TDN concentration was always less than expected. There was little relationship between deviation from expected total diet TDN and type or composition of forages or supplements. Empirical multiple regression equations were developed to estimate effects of supplements on VFI and total diet TDN concentration. The most acceptable intake equation estimated VFI when fed with supplement (r2 = .84) That equation included VFI when fed alone, supplement intake, CP and TDN concentrations in forage and supplement, and classification codes describing forages and supplemental energy. The most acceptable equation for estimating total diet TDN concentration included only the expected total diet TDN concentration (r2 = .87). These equations may be used in nutritional models to account for associative effects.     

A net carbohydrate and protein system for evaluating cattle diets: III. Cattle requirements and diet adequacy.

The Cornell Net Carbohydrate and Protein System (CNCPS) has equations for predicting nutrient requirements, feed intake, and feed utilization over wide variations in cattle (frame size, body condition, and stage of growth), feed carbohydrate and protein fractions and their digestion and passage rates, and environmental conditions. Independent data were used to validate the ability of the CNCPS to predict responses compared to National Research Council (NRC) systems. With DMI in steers, the CNCPS had a 12% lower standard error of the Y estimate (Sy.x) and three percentage units less bias than the NRC system. For DMI in heifers, both systems had a similar Sy.x but the NRC had four percentage units less bias. With lactating dairy cows' DMI, the CNCPS had a 12% lower Sy.x. Observed NEm requirement averaged 5% under NRC and 6% under CNCPS predicted values at temperatures above 9 degrees C but were 18% over NRC and 9% under CNCPS at temperatures under 9 degrees C. Energy retained was predicted with an R2 of .80 and .95 and a bias of 8 and 4% for the NRC and CNCPS, respectively. Protein retained was predicted with an R2 of .75 and .85 with a bias of 0 and -1% for NRC and CNCPS, respectively. Biases due to frame size, implant, or NEg were small. Body condition scores predicted body fat percentage in dairy cows with an R2 of .93 and a Sy.x of 2.35% body fat. The CNCPS predicted metabolizable protein allowable ADG with a bias of 1.6% with a Sy.x of .07 kg compared to values of -30% and .10 kg, respectively for the NRC system.     

Effects of dried distillers grains and equivalent undegradable intake protein or ether extract on performance and forage intake of heifers grazing smooth bromegrass pastures

Crossbred heifers (n = 120; BW = 368 kg, SD = 39 kg) were used to determine effects of dried distillers grains (DDG) and relative contributions of undegradable intake protein (UIP) and fat (ether extract, EE) in DDG on ADG and forage intake (FI). Heifers rotationally grazed six 3.5-ha, smooth bromegrass paddocks (IVDMD = 65.7%, CP = 20.8%, UIP = 2.17%, DM basis). Heifers were blocked by previous ADG and allotted to treatments in a 3 x 3 + 1 factorial design. Factors were source and level of supplementation. Supplements were as follows: 1) DDG (UIP = 15.8%, EE = 9.67%), 2) corn gluten meal (CGM; UIP = 31.6%, EE = 0.83%), or 3) corn oil (OIL; UIP = 0.74%, EE = 19.3%). Amounts of DDG were 750, 1,500, or 2,250 g/d, whereas amounts of CGM and OIL were 375, 750, or 1,125 g/ d. Supplements containing CGM and OIL were fed in amounts that provided UIP and EE, respectively, equivalent to those of the DDG. Contrasts of interest were DDG vs. CGM and DDG vs. OIL. Control heifers were fed 250 g/d of a supplement containing corn bran and molasses (UIP = 0.92%, EE = 1.13%). Heifers were supplemented individually. Treatments were separated by regressing the response variables on grams of nutrient (DM, UIP, or EE) intake per kilogram of BW, because not all heifers consumed their allotment of supplement. Supplemental DDG resulted in a linear increase in ADG (P < 0.01), whereas CGM tended to increase ADG (P = 0.14) but at a rate that was 39% of that for DDG, representing a response to MP. Supplementation of OIL did not affect ADG (P = 0.25) and tended to result in ADG less than that of DDG (P = 0.09). Supplementation with DDG had no effect (P = 0.63) on FI when predicted by the use of chromic oxide but tended (P = 0.07) to decrease FI when it was predicted from ADG using NE equations. Despite the differences between methods in the significance of the effect of DDG, the rates of substitution agreed (-0.50 and -0.45 for chromic oxide and NE equations, respectively), suggesting that the chromic oxide method was less sensitive in assessing FI. Supplementation with CGM decreased FI (P < 0.01), but FI for CGM did not differ from that of DDG when the chromic oxide method was used (P = 0.19). Corn oil had no effect on FI (P = 0.42). Increased ADG and decreased FI observed from DDG supplementation is not independently explained by UIP or EE contained in DDG.     

A simulation model of forage yield, quality and intake and growth of growing cattle grazing cornstalks

A simulation model was developed to predict corn crop residue yield and quality and intake and performance of growing cattle grazing cornstalks. The model is wholly deterministic and integrates the effects of weather, residue supply and animal components. Low temperatures increase animal energy requirements, whereas snow cover decreases residue available. Residual grain and leaf are calculated from grain yield. Residue quantity and quality are reduced daily by environmental losses and animal consumption. Daily performance is predicted based on the nutrients obtained from residue and supplemental feed. Under unlimited roughage supply, leaf, husk and grain are primary diet components. Grain consumption decreases as the supply diminishes and forage quality decreases with time. Intake is calculated based on digestibility and fecal output = .0365 W.75. Forage availability affects intake in a curvilinear fashion. Energy gain is predicted by NRC equations and protein gain from metabolizable protein supply. The model underestimated intake of calves measured with chromic oxide and in vitro DM disappearance. Simulated daily gain (y, kg) of calves grazing at several stocking rates was related to observed daily gain (x, kg) by the equation y = .012 + .853 x (R2 = .71, Sy.x = .077). The model overestimated response to protein supplementation. Severe cold weather was predicted to reduce gains or cause weight loss due to increased energy requirements for maintenance. The model can be used as an aid in both research planning and cattle management.     

Energy requirement for maintenance and growth of Nellore bulls and steers fed high-forage diets

Data from three comparative slaughter experiments with individually fed Nellore bulls (n = 31) and steers (n = 66) were utilized to determine their NEm and NEg requirements when fed high-forage diets. The experimental design provided ranges in ME intake, BW, and ADG for the development of regression equations to predict NEm and NEg requirements. The Nellore bulls (Trial 1) were divided into two intake levels (ad libitum and 65% of the ad libitum). The steers (Trials 2 and 3) were allocated to three intake levels (ad libitum and 55 and 70% of the ad libitum). In both trials, there were three slaughter groups within each intake level. The three end points for the bulls were different days on treatment (100, 150, and 190 d and 130, 180, and 200 d, respectively, for older and younger animal subgroups). The steers were slaughtered when animals of the ad libitum treatment reached 400, 440, and 480 kg shrunk BW (SBW) on average for the first, second, and third group, respectively. For all body composition determinations, whole empty body components were weighed, ground, and subsampled for chemical analysis. In each of the trials, initial body composition was determined with equations developed from a baseline slaughter group, using SBW and empty BW (EBW), fat (EBF), and protein (EBP) as variables. The NEm was similar for bulls and steers; NEm averaged 77.2 kcal/ kg0.75 EBW. However, the efficiency of conversion of ME to net energy for maintenance was greater for steers than for bulls (68.8 and 65.6%, respectively), indicating that bulls had a greater ME requirement for maintenance than steers (5.4%; P < 0.05). Our analyses do not support the NRC (2000) conclusion that Nellore, a Bos indicus breed, has a lower net energy requirement for maintenance than Bos taurus breeds. An equation developed with the pooled data to predict retained energy (RE) was similar to the NRC (2000) equation. A second equation was developed to predict RE adjusted for degree of maturity (u): RE = (6.45 - 2.58/u) x EWG x e(0.469) x u), where u = current EBW/final EBW in which final EBW was 365 kg for steers and younger bulls and 456 kg for older bulls at 22% EBF, respectively.     

Predicting growth and performance of Holstein steers

Refinements and additions were made to the growing cattle portion of the model of Fox et al. (1988) for predicting growth of Holstein steers. Based on observations of animal weight, DM intake (DMI), ADG, feed per gain (FPG) and diet ME, the modified model was tested on a database that included 299 feeding periods with Holstein steers fed in research trials over a period of 15 yr at Cornell University, the University of Minnesota and the University of Wisconsin. The modified model accounted for 93, 56 and 68% of the variation in DM intake, daily gain and feed required per unit gain, respectively. Averaged over all 299 periods in the database, the error in predicting DM intake, daily gain and feed required per unit gain was 1%, 4% and 2%, respectively. Analysis of residuals indicated that ME level did not influence the difference between predicted and observed values for DMI, ADG and FPG. Residuals analysis indicated that BW did not influence the difference between predicted and observed values for ADG and FPG but DMI of heavier cattle was overpredicted (P less than .01). These results indicated that the 8% increase in DMI for cattle over 318 kg was not warranted for the Holstein steers in this database, which were predominantly less than 15 mo at slaughter. The results of the validation indicate that this model accurately predicted performance of Holstein steers.     

Effects of ractopamine and protein source on growth performance and carcass characteristics of feedlot heifers

An experiment was conducted to determine the relationship between feeding ractopamine and different amounts of MP on growth and carcass characteristics of feedlot heifers. Seventy-two crossbred heifers (475 kg of initial BW) were fed individually a diet based on steam-flaked corn for ad libitum intake for 29 d. Heifers were implanted with 140 mg of trenbolone acetate and 14 mg of estradiol-17beta 60 d before the experiment. Treatments were arranged as a 2 x 3 factorial and included 0 or 200 mg of ractopamine-HCl (23 ppm)/ d, and urea, solvent soybean meal, or expeller soybean meal (ESBM) as the predominant protein supplement. The amounts of MP supplied by the urea, solvent soybean meal, and ESBM diets were 688, 761, and 808 g/ d, respectively, calculated according to level 1 of the NRC model. Body weights were obtained 1 d before ractopamine feeding and at slaughter. Blood samples were obtained 1 d before starting the experiment and 13 d later. Ractopamine improved ADG, efficiency of gain, carcass-adjusted ADG, and carcass-adjusted efficiency of gain (P < 0.01). For ADG, heifers demonstrated a ractopamine x protein source interaction (P < 0.05); heifers not fed ractopamine had greater ADG when fed ESBM than when fed urea, whereas for heifers fed ractopamine there were no differences (P > or = 0.10) among protein supplements. This interaction was not observed for carcass-adjusted ADG (P = 0.60). Final live weights (P = 0.02) and carcass weights (P = 0.01) were greater with ractopamine feeding. Carcass marbling scores and yield grades were not affected by ractopamine or protein source (P > or = 0.39). Plasma total alpha-amino N and glucose concentrations decreased more from pretreatment concentrations when heifers were fed ractopamine (P < 0.05). Feeding ractopamine to heifers for 28 d before slaughter improved ADG and efficiency of gain without any large effects on carcass characteristics. The MP supply does not need to be increased from that provided by finishing diets based on steam-flaked corn with urea as the primary N supplement to allow the maximal response to ractopamine by finishing heifers.     

Effects of supplement type on animal performance, forage intake, digestion, and ruminal measurements of growing beef cattle

Two experiments were conducted to determine the effects of supplement type on the rate of gain by heifers grazing bermudagrass and on the intake, apparent total-tract OM digestibility, ruminal fermentation, digesta kinetics, in situ DM digestibility, and forage protein degradation by steers fed prairie hay. In Exp. 1, 45 heifers (284+/-24 kg) grazed a bermudagrass pasture for 91 d in the late summer to determine the effects of no supplement (CON), or one of four individually fed monensin-containing (150 mg/[heifer x d]) supplements (MINCS; 0.1 kg of mineral mix with 0.2 kg [DM] of cottonseed hulls as a carrier/[heifer x d]), a pelleted protein supplement (PROT; 1 kg of DM, 242 g of degradable intake protein [DIP]/[heifer x d]), or high-fiber (HF) and high-grain (HG) (2 kg of DM, 243 and 257 g of DIP, respectively/[heifer x d]) pelleted energy supplements. In Exp. 2, four ruminally cannulated steers (311+/-22 kg) with ad libitum access to low-quality (4% DIP, 73% NDF, 40% ADF) prairie hay were individually fed monensin-containing (200 mg/[steer x d]) treatments consisting of 1) mineral mix + corn (MINCR; 0.1 kg of mineral and 0.4 kg of cracked corn [DM] as a carrier, 19 g of DIP/[steer x d]), 2) PROT (1.4 kg of DM, 335 g of DIP/[steer x d]), 3) HF, or 4) HG (2.9 kg of DM, 340 and 360 g of DIP, respectively/[steer x d]) in a 4 x 4 Latin square with 14-d adaptation and 6-d sampling periods. In Exp. 1, the HF-, HG-, and PROT-supplemented heifers had greater (P < 0.01) rates of gain than CON heifers, and the HF- and HG-supplemented heifers tended (P < 0.11) to gain more weight than those fed PROT. In Exp. 2, steers fed PROT consumed more (P < 0.05) hay OM than HF and HG, or MINCR. Total OM intake was greater (P < 0.01) by supplemented steers than MINCR-fed cattle. Hay OM digestibility was not affected (P = 0.19) by treatment, but total diet OM digestibility was greater (P < 0.01) for HF- and HG- than for MINCR- or PROT-fed steers. The rate of in situ DM digestibility was greater (P < 0.01) for HF, HG, and PROT than for MINCR. Results from these studies indicate that feeding milo- vs fiber-based energy supplements formulated to provide adequate DIP did not result in different forage intake, OM digestibility, or in situ DM digestibility, whereas both increased ADG in heifers consuming low-quality forages compared with unsupplemented or mineral- or protein-supplemented cattle. An adequate DIP:TDN balance decreased the negative associative effects often observed when large quantities of high-starch supplements are fed with low-quality hay.     

The influence of level of feeding on growth and serum insulin-like growth factor I and insulin-like growth factor-binding proteins in growing beef cattle supplemented with somatotropin

The objective of this study was to determine the effects of level of feeding on growth, feed efficiency (gain:feed; G:F), body composition (BC), and serum concentrations of somatotropin (ST), IGF-I, and IGF-binding proteins (BP) in growing beef cattle supplemented with bovine (b) ST. In each of two consecutive years, 40 growing beef cattle were blocked by weight (average BW: yr 1 = 316 kg, yr 2 = 305 kg) and used in a 2 x 2 factorial arrangement with main effects of bST (0 or 33 microg x kg BW(-1) x d(-1)) and level of feed intake (ad libitum [AL] or 0.75 AL). Relative to uninjected cattle, treatment with bST increased ADG 9.6% (1.14 vs 1.25 kg/d; P < 0.05) and increased G:F 8.1% (12.3 vs 13.3 gain [g]:feed [kg]; P < 0.05), whereas ADG in AL animals was 39% greater than that in 0.75 AL animals (1.39 vs 1.00 kg/d; P < 0.05). There was a tendency (P = 0.10) for a bST x level of feeding interaction, such that the increase in ADG with bST was greater in AL cattle than in 0.75 AL cattle (10.6 vs 7.8%; P = 0.10). Serum concentrations of ST were greater in 0.75 AL cattle than in AL cattle (13.0 vs 8.6 ng/mL; P < 0.05) and in bST-treated cattle than in uninjected cattle (16.3 vs 5.2 ng/mL; P < 0.05). Due to a bST x level of feeding interaction (P < 0.01), the magnitude of the increase in serum ST to exogenous bST was greater (P < 0.01) in 0.75 AL cattle than in AL cattle. Relative to uninjected cattle, treatment with bST increased (P < 0.05) serum concentrations of IGF-I and IGFBP-3 and reduced (P < 0.05) concentrations of IGFBP-2. Similarly, AL cattle had greater (P < 0.05) serum concentrations of IGF-I and IGFBP-3 and reduced (P < 0.05) IGFBP-2 compared with 0.75 AL cattle. In summary, treatment with bST increased growth rate and G:F and stimulated serum IGF-I and IGFBP-3 while reducing IGFBP-2. Feeding at 0.75 ad libitum intake reduced the magnitude of response for each of these variables. Thus, limit-feeding may reduce the effect of exogenous bST on growth rate by blunting bST-induced increases in IGF-I and IGFBP-3 and bST-induced decreases in IGFBP-2.     

Supplemental polyethylene glycol affects intake of and preference for sericea lespedeza by cattle

We tested the hypothesis that supplemental polyethylene glycol (PEG), a polymer that neutralizes the effects of tannins, would increase intake and preference of cattle for fresh-cut sericea lespedeza (SL; Lespedeza cuneata), a legume with high concentrations of condensed tannins. Sixteen crossbred steers (initial BW of 249 +/- 6.6 kg) were randomly assigned to 2 treatments: 1) grain supplement with PEG (PEG-S) and 2) grain supplement without PEG (control). To assess intake, we conducted a trial with 6 sample periods, each 6 d in duration, with steers fed SL and prairie hay (PH) in separate meals. Steers were fasted overnight and fed their respective supplements (with and without PEG) at 0800 h. Animals were then offered fresh-cut SL from 1050 to 1550 h, PH was fed from 1600 to 2000 h, and they were without food from 2000 to 0800 h the next day. To assess preference, we conducted 1-d tests in which steers had simultaneous access to SL and PH on the day following periods 2 to 6. As with the intake experiment, steers were fasted overnight and fed their respective supplements at 0800 h, but from 1050 to 1250 h all steers had access to SL and PH simultaneously. We weighed steers before and at the completion of the study and calculated ADG. Steers treated with PEG consumed more SL per unit of BW than control steers in periods 2 to 6 (period x treatment interaction, P < 0.001). In contrast, controls consumed more PH than steers given PEG (period x treatment x day interaction, P = 0.009). The PEG-S steers consumed more total DM (SL + PH) than controls in periods 3, 5, and 6 but not in periods 1, 2, and 4 (period x treatment interaction, P = 0.004). Sericea lespedeza intake as a percentage of total DMI was greater for the PEG-S steers every day except d 1 and 2 of period 1 (period x treatment x day interaction, P = 0.03). Averaged across the 5 preference tests, PEG-S steers selected a greater proportion of SL than did control steers (39 vs. 9%), and the magnitude of the difference was greater in the later tests (test x treatment interaction, P = 0.004). The PEG-S steers had greater ADG than controls (0.44 vs. 0.24 kg/d; P = 0.005). Our results indicate PEG increases intake of and preference for SL and suggest that PEG supplementation of cattle may increase intake of SL and improve ADG in pastures that contain SL.     

Net energy of ensiled wet corn gluten feed in corn silage diets for finishing steers.

Two trials were conducted to determine the NE value of ensiled wet corn gluten feed (WCGF) in corn silage finishing diets for beef cattle. In Trial 1, 96 Angus-crossbred yearling steers were fed corn silage-based diets containing 0, 20, 40, or 60% ensiled WCGF. Increased dietary WCGF resulted in improved DMI (linear, P less than .05), ADG (linear; P less than .05), and feed/gain (linear, P less than .05). Levels of WCGF had no (P greater than .05) effect on fat thickness, marbling, quality grade, carcass protein, and carcass fat. In Trial 2, four Angus-crossbred yearling steers were used in a 4 x 4 Latin square design to determine the effect of feeding 0, 20, 40, or 60% WCGF on DE and ME values. Level of WCGF had no (P greater than .05) effect on dietary DE and ME values. Regression equations were developed for predicting NEm (Y = 1.51 + .0009X; R2 = .22) and NEg (Y = 1.04 + .0028X; R2 = .35) in which Y = predicted diet NE values in megacalories/kilogram and X = percentage of dietary WCGF. The NEg value increased .06 Mcal/kg for each 20% increase in WCGF. Predicted NEm and NEg values for WCGF are 1.60 and 1.32 Mcal/kg, respectively.     

Nutritional management of horses competing in 160 km races

A survey was taken of dietary management and training schedules of 54 horses competing in two 160 km endurance races. A total of 52 owners, representing 54 horses, responded to a questionnaire distributed prior to the races. Diet and training schedules were compared between horses that successfully completed the races and those that were eliminated for metabolic reasons. Horses that completed the races were 11.5 +/- 4 years old, weighed 429 +/- 4.5 kg and were ridden 61 +/- 32 km a week when training. Feed intake was reported as "free choice hay or pasture" by 34 of the respondents. Dry matter (DM) hay intake in these horses was estimated to be 3% body weight (kg) minus the kg DM of grain fed, assuming a maximum intake. They were fed 12.3 +/- 2.3 kg feed per day consisting of 10 +/- 2.3 kg hay and 2.3 +/- 1.4 kg of grain. Most had free access to salt and were fed 1 +/- 1 vitamin/mineral supplement per day. Based on Nutritional Research Council (NRC) values for nutrient content of the reported feeds, diets contained 60 +/- 5% total digestible nutrients (TDN), 12 +/- 2% crude protein, 27 +/- 4% crude fiber, 0.72 +/- 0.4% calcium and 0.29 +/- 0.06% phosphorus. Maximum caloric intake was estimated to be 31.9 Mcal per day. Ratios of nutrients fed per kilometer trained were: kg TDN/km = .14 +/- .08, kg crude protein/km trained = .03 +/- .02, and kg crude fiber/km trained = .06 +/- .04.(ABSTRACT TRUNCATED AT 250 WORDS)     

Energy and protein requirements for growth and maintenance of F1 Nellore x Red Angus bulls, steers, and heifers

A comparative slaughter trial was conducted with 36 F1 Nellore x Red Angus calves (12 steers, 12 bulls, and 12 heifers), averaging 274 kg of BW, to assess the net requirements of protein and energy for growth and maintenance. Three cattle from each group (i.e., steers, bulls, and heifers) were slaughtered at the beginning of the trial to determine the initial body composition. The remaining calves were randomly assigned to 1 of 3 treatments: maintenance (diet containing 70% of DM as corn silage fed at 1.2% of BW daily) or concentrate at 0.75 or 1.5% of BW daily with corn silage available for ad libitum consumption. The diets were isonitrogenous (2% N, DM basis). The experimental design provided ranges in ME intake, BW, and ADG for the development of regression equations to predict the maintenance requirements for NE and net protein (MRNE and MRNP, respectively) and the growth requirement for NE and net protein (GRNE and GRNP, respectively). After 84 d of growth, the cattle were slaughtered. The cleaned gastrointestinal tracts, organs, carcasses, heads, hides, tails, feet, blood, and tissues were weighed to measure empty BW (EBW). These parts were ground separately and subsampled for chemical analyses. For each animal within a period, DMI was measured daily and samples of feces were collected to determine diet digestibility. There were no differences in MRNE (P = 0.06) among groups. The combined data indicated a MRNE of 71.2 kcal x kg(-0.75) of EBW x d(-1), with a partial efficiency of use of ME to NE(m) of 0.71. The partial efficiency of use of ME to NE for growth was 0.54 for bulls, 0.47 for steers, and 0.54 for heifers. The GRNE for steers and heifers were similar (P = 0.15) but were 18.7% greater (P = 0.03) for steers and heifers than for bulls. The MRNP did not differ among groups and averaged 2.53 g of CP x kg(-0.75) of EBW x d(-1). Likewise, GRNP was not different among groups. The percentage of retained energy deposited as protein (RE(p)) increased as the content of retained energy in the gain (RE(c), Mcal/kg of empty body gain) decreased. The RE(p) equation of the pooled data was 46.5 x e(-0.2463 x RE(c)). We conclude that the energy requirement of crossbred Bos indicus x Bos taurus for maintenance might be less than that of purebred Bos taurus and that RE(p) is nonlinearly, negatively correlated with RE(c). The GRNE was less for bulls than for steers and heifers. However, we found no differences in MRNE, MRNP, and GRNP for bulls, steers, and heifers of Nellore x Red Angus crossbreds.     

Effects of placing cattle on feed at two-month intervals and housing on feedlot performance and carcass grades

A 5-yr study was conducted involving the placement of yearling steers on feed at 2-mo intervals under three different housing systems. A total of 3,571 steers (180 pens) initially averaging 318 kg was used. Evaluations were made for DM intake, ADG, feed efficiency (FE), carcass quality (QG), and yield grades (YG). Cattle were assigned to either an open lot with overhead shelter (S), an open lot without overhead shelter (NS), or an open-front confinement building (C). Each treatment consisted of two lots of 20 steers each per interval per trial. Corn grain provided 85% of the energy; the remainder was supplied by corn silage and protein supplement. Cattle were fed 140 to 180 d to achieve an average slaughter weight of 500 kg. The main effects of year (Y), month (M), and housing (H) affected DM intake, ADG, FE, and final live weight (P less than .01). The interactions for Y x M, M x H and Y x M x H affected ADG (P less than .05). Month and H affected hot carcass weight (P less than .01). Year affected YG, and year and month affected QG (P less than .01). Month effects on DM intake and ADG indicated that cattle started in May had the highest intake and ADG (P less than .05) and that cattle started in November had the lowest (P less than .05) DMI and ADG. Month effects on FE indicated that cattle were most efficient when placed on feed during March, May, and July (5.82, 5.72, and 5.66 kg DM/kg gain; P less than .05).(ABSTRACT TRUNCATED AT 250 WORDS)     

Energy metabolism in lactating beef heifers

To obtain measurements of energy balance in lactating beef cows, respiration calorimetry and digestion trials were conducted using seven lactating (613 kg BW) and three nonlactating (598 kg BW) Hereford x Angus heifers fed a pelleted 75% alfalfa:25% concentrate diet. Five measurements of energy balance were obtained at 6- to 7-wk intervals beginning 6 to 10 wk postpartum in lactating heifers and at 6-wk intervals in nonlactating heifers. Milk yield was measured using a combination of weigh-suckle-weigh and machine milking to adapt heifers to milking by machine without the use of oxytocin. Heifers were milked only by machine during measurements of energy balance. Weekly milk yield averages ranged from 8.2 kg/d at wk 5 postpartum to 3.2 kg/d at wk 32 postpartum. When scaled to BW(.75), the regression of NE1 on ME intake and the regression of ME intake on NE1 were remarkably similar to previously published regressions for measurements obtained from lactating Holstein-Friesian cows. The average daily maintenance energy requirement from these regressions was 503 kJ ME/kg BW(.75), a value similar to the average value reported previously for lactating Holstein-Friesian cows (488 kJ/kg (BW.75)). This is in contrast to numerous published comparisons of the maintenance requirements of cattle breed types in the nonlactating state and current NRC standards for estimating maintenance energy requirements of beef and dairy cattle. The results of the present study suggest that when expressed on the basis of BW(.75) the efficiency of utilization of incremental ME above maintenance for milk and tissue energy (i.e., NE1) is similar among lactating Hereford x Angus heifers and lactating Holstein-Friesian cows. The breeds differ in terms of their propensity for milk yield and the resulting partition of ME between milk synthesis and tissue energy retention.     

Effects of supplemental energy and/or degradable intake protein on performance,grazing behavior,intake, digestibility,and fecal and blood indices by beef steers grazed on dormant native tallgrass prairie

To evaluate the effects of balancing total diet degradable intake protein with dietary total digestible nutrients (TDN), we conducted two studies during 2 yr with 100 (302 +/- 8 kg initial BW) mixed-breed yearling steers and 12 ruminally cannulated steers (526 +/- 28 kg). Steers individually received one of four supplements 5 d/wk while grazing dormant native tallgrass prairie. Supplements included: 1) corn and soybean meal, balanced for total diet degradable intake protein in relation to total diet TDN (CRSBM), 2) corn and soybean hulls, equal in supplemental TDN to CRSBM (CORN), 3) soybean meal, equal in supplemental degradable intake protein to CRSBM (SBM), or 4) a cottonseed hull-based control supplement (CONT). At each feeding (5 d/wk), steers consumed 13.6, 13.6, or 4.2 g of dry matter/kg of body weight, or 178 g of DM, respectively, of supplement. Steers fed CRSBM had greater (P < 0.01) average daily gain than cattle fed CORN or SBM. Feeding soybean meal (CRSBM, SBM) resulted in improved (P < 0.01) efficiency of supplement. Grazing time, intensity, and harvesting efficiency were reduced (P < 0.05) by corn supplementation (CRSBM and CORN), whereas the number of grazing bouts per day was increased (P < 0.08). Intake and digestibility of forage organic matter were reduced (P < 0.01) for steers supplemented with corn (CORN and CRSBM) vs cattle not fed corn (SBM and CONT). Total diet digestibility (P < 0.12) and digestible organic matter intake (P < 0.01) were greater for CRSBM-fed steers than for cattle fed either CORN or SBM. Steers fed CRSBM had greater (P < 0.01) fecal nitrogen and serum insulin than cattle fed CORN or SBM. Corn-fed cattle had lesser (P < 0.01) fecal pH and ADF concentrations than steers not consuming grain. Cattle fed supplements with soybean meal (CRSBM and SBM) had greater (P < 0.01) serum urea nitrogen than steers fed supplements without soybean meal (CORN, CONT). Supplemented steers grazing dormant tallgrass prairie had a greater rate of gain, with the greatest response in animal performance occurring when grain supplements were balanced for total diet degradable intake protein in relation to total diet TDN. These results lead us to suggest that grain-supplemented cattle grazing dormant tallgrass prairie require a balance of total diet degradable intake protein in relation to total diet TDN to optimize animal performance.     

Evaluation in Appalachian pasture systems of the 1996 (update 2000) National Research Council model for weaning cattle

This study was conducted to evaluate the accuracy of the National Research Council's (2000) Nutrient Requirements of Beef Cattle computer model when used to predict calf performance during on-farm pasture or dry-lot weaning and backgrounding. Calf performance was measured on 22 farms in 2002 and 8 farms in 2003 that participated in West Virginia Beef Quality Assurance Sale marketing pools. Calves were weaned on pasture (25 farms) or dry-lot (5 farms) and fed supplemental hay, haylage, ground shell corn, soybean hulls, or a commercial concentrate. Concentrates were fed at a rate of 0.0 to 1.5% of BW. The National Research Council (2000) model was used to predict ADG of each group of calves observed on each farm. The model error was measured by calculating residuals (the difference between predicted ADG minus observed ADG). Predicted animal performance was determined using level 1 of the model. Results show that, when using normal on-farm pasture sampling and forage analysis methods, the model error for ADG is high and did not accurately predict the performance of steers or heifers fed high-forage pasture-based diets; the predicted ADG was lower (P < 0.05) than the observed ADG. The estimated intake of low-producing animals was similar to the expected DMI, but for the greater-producing animals it was not. The NRC (2000) beef model may more accurately predict on-farm animal performance in pastured situations if feed analysis values reflect the energy value of the feed, account for selective grazing, and relate empty BW and shrunk BW to NDF.