Influence of protein nutrition and virginiamycin supplementation on feedlot growth performance and digestive function of calf-fed Holstein steers.

Two experiments were conducted to examine the influence of protein and virginiamycin (VM) supplementation on feedlot growth performance, digestion, and metabolizable AA (MAA) supply of calf-fed Holstein steers. Growth performance and dietary energetics were evaluated in 120 Holstein steers (127 ± 9 kg). During the initial 112-d feeding period, a steam-flaked corn-based diet was balanced to meet either 100% (MAB) or 87% (UREA) of MAA requirements. Diets were supplemented with or without 22.5 mg/kg VM in a 2 × 2 factorial arrangement. Subsequently (d 112 to 308), all steers received the UREA diet with or without VM. During the initial 112-d, MAB increased ADG, G:F, and dietary NE ( < 0.01). Thereafter, when all steers received the UREA diet, ADG, G:F, and dietary NE were not different ( > 0.10) across initial supplementation treatments. Overall (d 1 to 308), MAB did not affect ADG ( > 0.10) but enhanced G:F efficiency ( = 0.03) and dietary NE ( = 0.05). During the initial 112-d period and through the remainder of the experiment, VM increased G:F ( < 0.01) and dietary NE ( < 0.01). Four Holstein steers (146 ± 4 kg) with cannulas in the rumen and proximal duodenum were used in a 4 × 4 Latin square design to evaluate initial 112-d treatment effects on digestive function. There were no treatment effects ( > 0.10) on ruminal digestion of OM, NDF, starch, microbial efficiency, or total tract digestion of OM and NDF. The MAB increased indispensable AA flow to the small intestine ( < 0.01) and total tract digestion of N ( < 0.01) and starch ( = 0.04). Observed AA supply to small intestine was in agreement with expected supply ( = 0.96). Virginiamycin decreased ( = 0.04) nonammonia N flow to the small intestine and did not affect ( > 0.10) total tract N digestion. Extrapolating from AA supplies in the metabolism study, MAB satisfied indispensable AA requirements during the initial 112-d period, whereas the UREA diet met 73.5% and 79.2% of methionine and lysine requirements, respectively. During the subsequent periods (d 112 to 308) indispensable AA supplies exceeded theoretical requirements. We conclude that enhancements in energy utilization when diets are balanced to meet MAA requirements of calf-fed Holstein steers during the initial 112-d feedlot period remain appreciable throughout time on feed. Virginiamycin enhanced efficiency of energy utilization throughout the feedlot growing-finishing period.

Feeding value of supplemental curcas crude oil in finishing diets for feedlot lambs.

The objective of this experiment was to determine the feeding value of a mechanically extracted nontoxic variety of oil (JCO) as source of energy for feedlot lambs. Twenty Pelibuey × Katahdin lambs were individually fed a dry-rolled-corn-based finishing diet supplemented with 0%, 2%, 4%, or 6% JCO (diet dry matter basis). Supplemental JCO replaced dry rolled corn in the basal diet. Fatty acid composition of JCO was C16:0, 14.0%; C18:0, 8.2%; C18:1, 26.0%; C18:2, 50.3%, and C18:3, 0.4%. Daily intakes of JCO averaged 24.7, 51.1, and 77.3 g/day or 0.57, 1.08, and 1.62 g/kg LW for the 2%, 4%, and 6% levels of supplementation, respectively. Supplemental JCO did not affect ( = 0.33) dry matter intake (DMI), but tended to increase (linear effect, = 0.06) average daily gain, efficiency of gain (linear effect, < 0.01), and dietary net energy (linear effect, < 0.01) and decreased (linear effect, < 0.01) the ratio of observed/expected DMI. At low levels (20 g/kg diet dry matter) of supplementation, the net energy (NE) value of JCO corresponds closely (0.99) to the NE value assigned by current standards (), and this NE value decreased linearly as the inclusion level of JCO increased. There were not treatment effects on plasma metabolites. Across treatments, the concentrations of hemoglobin (11.64 ± 1.08 g/dL), hematocrit (39.15 ± 3.67%), glucose (85.2 ± 17.64 mg/dL), creatinine (1.43 ± 0.28 mg/dL), and urea (20.70 ± 4.35 mg/dL) were within normal (9-15 g/dL, 27%-40%, 50-90 mg/dL, 1.0-1.8 mg/dL, and 15-50 mg/dL, for hemoglobin, hematocrit, glucose, creatinine, and urea, respectively) ranges for healthy lambs. Based on DMI, performance and plasma metabolites observed in this study, nontoxic JCO is a suitable source of energy in finishing diets for lambs.

Evaluation of isoquinoline alkaloid supplementation levels on ruminal fermentation, characteristics of digestion, and microbial protein synthesis in steers fed a high-energy diet.

Four Holstein steers with ruminal and duodenal cannulas were used in a 4 × 4 Latin square design to examine the effect of daily intake of 0, 2, 4 or 6 g/steer of standardized plant extract containing a mixture of quaternary benzophenanthridine alkaloids and protopine alkaloids (QBA+PA) on the characteristics of ruminal fermentation and characteristics of digestion. The basal diet consisted of a steam-flaked corn-based finishing diet that contained 62% corn and 12% sudangrass hay and the rest of diet was composed of mainly dried distillers grains, molasses, fat, and minerals. The source of QBA+PA used was Sangrovit-RS (Phytobiotics Futterzusatzstoffe GmbH, Eltville, Germany) and supplementation levels of 2, 4, and 6 g Sangrovit-RS∙steer∙d, which represented a net daily ingestion of approximately 6, 12, and 18 mg of QBA+PA compounds, respectively. Inclusion of QBA+PA linearly increased ( = 0.04) flow to the duodenum of nonammonia N and linearly decreased ( < 0.01) duodenal flows of ammonia N. Ruminal microbial efficiency (duodenal microbial N; g/kg OM fermented in the rumen) and protein efficiency (duodenal nonammonia N; g/g N intake) were increased ( < 0.05) as the level of QBA+PA increased. There were no effects of QBA+PA supplementation on ruminal, postruminal, and total tract digestion of OM, starch, and NDF, but postruminal and total tract digestion of N increased ( < 0.01) as the level of QBA+PA increased. Digestible energy of the diet tended to increase (linear affect, = 0.09) with QBA+PA supplementation. Ruminal pH and total VFA molar concentrations were not different between treatments. Ruminal NH-N concentration linearly decreased ( = 0.02) with QBA+PA supplementation. Ruminal molar proportion of acetate increased ( = 0.04) as the supplementation level of QBA+PA increased. It is concluded that QBA+PA supplementation enhances efficiency of N utilization in feedlot steers fed a steam-flaked corn-based finishing diet. This effect was due, in part, to enhanced ruminal microbial efficiency, decreased ruminal degradation of dietary nonammonia N, and enhanced postruminal N digestion.

Comparative feeding value of distillers dried grains plus solubles as a partial replacement for steam-flaked corn in diets for calf-fed Holstein steers: characteristics of digestion, growth performance, and dietary energetics.

Two experiments were conducted to examine the effect of level of dried distillers grains plus solubles (DDGS) supplementation (0, 10, 20, and 30%; DM basis), replacing steam-flaked (SF) corn in finishing diets, on characteristics of digestion (Exp. 1) and growth performance (Exp. 2) in calf-fed Holstein steers. In Exp.1, 4 cannulated Holstein steers (349 ± 12 kg) were used to evaluate treatment effects on characteristics of digestion. Ruminal NDF digestion tended to increase (quadratic effect, P = 0.09) and ruminal OM digestion decreased (linear effect, P = 0.01) with DDGS substitution. There were no treatment effects on duodenal flow of microbial N (MN). Substitution with DDGS increased (linear effect, P < 0.01) N flow to the small intestine. The undegradable intake protein (UIP) value of DDGS was 35%. Postruminal digestion of OM (linear effect, P = 0.04) and fatty acids (linear effect, P = 0.03) and total tract digestion of OM and GE decreased (linear effect, P < 0.03) with increasing level of DDGS substitution. Substitution with DDGS did not affect (P = 0.80) ruminal pH but increased (linear effect, P = 0.01) acetate:propionate molar ratio. In Exp.2, 144 Holsteins steer (112 ± 6 kg) were used in a 305-d trial to evaluate treatment effects on growth performance and carcass characteristics. During the initial 126 d, DDGS substitution increased ADG (linear effect, P = 0.03), G:F (quadratic effect, P = 0.03), and dietary NE (quadratic effect, P = 0.02), maximal for both at 20% DDGS inclusion rate. Based on estimated indispensable AA supply to the small intestine as a percentage of requirements during the initial 126-d period, histidine was first limiting followed by methionine. During the final 179-d period and overall (305-d feeding period), treatment effects on ADG and G:F were small (P ≥ 0.22). Compared with the other treatments, HCW was greater (3.4; P = 0.03) at the 20% level of DDGS substitution. The NE value for DDGS in SF corn-based diets for the calf-fed Holstein are consistent with current tabular standards. Extra-caloric value of DDGS as a metabolizable AA source is apparent during the initial growing phase. The UIP value of DDGS used in this study (35%) was considerably less than current tabular estimates (52%; NRC, 2000).

Feeding value of dried shredded sugarbeets as a partial replacement for steam-flaked corn in finishing diets for feedlot cattle.

Two experiments were conducted to evaluate the comparative feeding value of dried shredded sugarbeets (DSSB; 0, 20, and 40% of diet DM) as a replacement for steam-flaked corn (SFC) in finishing diets for feedlot cattle. In Exp. 1, 60 calf-fed Holstein steers (476 ± 6.3 kg) were used in a 97-d finishing trial. Substitution of SFC with DSSB did not affect ADG or DMI (P > 0.20). Increasing DSSB decreased gain efficiency (ADG:DMI; linear effect, P = 0.04) and dietary NE (linear effect, P = 0.03). Given that SFC has a NE(m) value of 2.38 Mcal/kg, the replacement NE(m) and NE(g) values for DSSB were 1.94 and 1.29 Mcal/kg, respectively. There were no treatment effects (P > 0.20) on carcass characteristics. In Exp. 2, 6 cannulated Holstein steers (205 kg) were used in a replicated 3 × 3 Latin square design to evaluate treatment effects on digestion. Ruminal digestion of starch, NDF, and feed N were not affected (P > 0.10) by DSSB, although ruminal OM digestion tended to increase (linear effect, P < 0.08). Replacing SFC with DSSB decreased flow of starch to the small intestine, but it increased flow of microbial N (linear effect, P = 0.05). There were no treatment effects (P > 0.14) on postruminal digestion of OM, NDF, starch, or feed N or total tract digestion of OM, starch, and N. Substitution of DSSB increased (linear effect, P = 0.05) total tract NDF digestion and decreased (linear effect, P = 0.05) dietary DE (Mcal/kg). Given that SFC has a DE value of 4.19 Mcal/kg, the replacement DE value of DSSB was 3.68 Mcal/kg. There were no treatment effects (P > 0.12) on ruminal pH or total VFA; however, DSSB decreased propionate (linear effect, P = 0.05) and increased acetate (linear effect, P = 0.07), butyrate (linear effect, P = 0.05), valerate (linear effect, P = 0.04), and estimated methane production (linear effect, P = 0.05). We concluded that DSSB may replace SFC in finishing diets at levels of up to 40% without detrimental effects on ADG and carcass characteristics. The NE value of DSSB is 82% that of SFC (DM basis). Partial replacement of SFC with DSSB alters ruminal VFA patterns, increasing estimated methane energy loss and slightly decreasing the efficiency of DE utilization.

Effects of preslaughter withdrawal period on response of feedlot heifers to zilpaterol hydrochloride supplementation: growth performance and carcass characteristics.

Sixty-four crossbred heifers (451 +/- 23 kg) were used in a 42-d feeding trial (4 pens per treatment in a randomized complete block design) to evaluate the influence of preslaughter zilpaterol hydrochloride withdrawal period on growth performance and carcass characteristics. Heifers were fed a diet based on steam-flaked corn (2.13 Mcal of NE(m)/kg). Treatments were 1) control, no zilpaterol supplementation; 2) zilpaterol supplementation for 30 d, drug withdrawn from the diet 3 d preslaughter (ZIL-3); 3) zilpaterol supplementation for 30 d, drug withdrawn 6 d preslaughter (ZIL-6), and 4) zilpaterol supplementation for 30 d, drug withdrawn 12 d preslaughter (ZIL-12). Zilpaterol was supplemented at the rate of 0.15 mg/kg of BW daily. Intake of DM averaged 9.2 +/- 0.26 kg/d and was not affected (P > or = 0.36) by treatment. Compared with control heifers, ZIL-3 increased (P < 0.01) carcass-adjusted ADG (59%), G:F (57%), apparent dietary NE(m) (31%), and decreased observed/expected DMI (25%). Treatment with ZIL-3 did not affect marbling score (P = 0.49) or backfat thickness (P = 0.17), but compared with the control group, increased HCW (3.6%, P = 0.03), carcass dressing percentage (3.2%, P = 0.02), LM area (6.3%, P = 0.05), and reduced trimmed fat (31%, P = 0.03). Prolonging the period of zilpaterol withdrawal preslaughter tended to decrease carcass-adjusted ADG (linear, P = 0.11), G:F (linear, P = 0.08), apparent dietary NE(m) (linear, P = 0.11), and carcass dressing percentage (linear, P = 0.11). We conclude that growth performance and carcass yield responses to zilpaterol supplementation are negatively affected by prolonging the period of zilpaterol withdrawal beyond 3 d (the required minimum withdrawal period according to label). Drug withdrawal period may be a relevant factor in explaining variation in performance response to zilpaterol supplementation in commercial feedlots.

Influence of surfactant supplementation and maceration on the feeding value of rice straw in growing-finishing diets for Holstein steers.

Two trials were conducted to evaluate the interaction of the maceration process and surfactant (Tween 80) supplementation on feeding value of rice straw. Treatments were steam-flaked, corn-based diets containing 14% forage (DM basis), which was 1) Sudangrass hay; 2) ground rice straw; 3) ground rice straw plus 0.22% Tween 80; 4) macerated rice straw; and 5) macerated rice straw plus 0.22% Tween 80. In the maceration process, rice straw was passed through 2 sequentially placed pairs of corrugated rolls set at zero tolerance under a ram pressure of 62,050 millibars, similar to a conventional grain roller mill, except that the opposing rolls operated at different speeds (12 and 14 rpm, respectively). Sudangrass hay and rice straw (native and macerated) were ground through a 2.6-cm screen before incorporation into complete mixed diets. In trial 1, 125 Holstein steers (292 +/- 1.7 kg of BW) were used in a 188-d evaluation of the treatment effects on growth performance and carcass characteristics. In trial 2, 5 Holstein steers (224 +/- 3.5 kg of BW) with cannulas in the rumen and proximal duodenum were used in a 5 x 5 Latin square design to evaluate the treatment effects on digestion. There were no interactions between maceration and surfactant on growth or carcass characteristics. Tween 80 did not influence the feeding value of rice straw. Compared with grinding alone, maceration of rice straw increased the carcass-adjusted ADG (6%, P < 0.10), G:F (6%, P < 0.05), and dietary NE (5%, P < 0.05); DMI was similar across treatments. Assuming NE(m) and NE(g) of Sudangrass hay are 1.18 and 0.62 Mcal/kg, the NE(m) and NE(g) were 0.61 and 0.13 Mcal/kg for ground rice straw and 1.21 and 0.65 Mcal/kg for macerated rice straw. There were no treatment interactions on characteristics of digestion. Tween 80 did not influence ruminal or total tract digestion of OM, starch, NDF, or N. Compared with grinding alone, maceration of rice straw increased ruminal digestion of OM (7.7%, P < 0.10) and NDF (30.8%, P < 0.05), and total tract digestion of OM (2.3%, P < 0.10), NDF (21.1%, P < 0.01), and N (3.7%, P < 0.05). Total tract digestion of OM, NDF, starch, and N for the Sudangrass diet corresponded closely with that of the macerated rice straw diets. Maceration increases the feeding value of rice straw to a level similar to that of good-quality (flag stage of maturity) Sudangrass hay, which is attributable to increased OM and NDF digestion. Effects of surfactant supplementation on growth performance and digestion are not appreciable.

Relationship between body weight and level of fat supplementation on fatty acid digestion in feedlot cattle.

Eight Holstein steers with cannulas in the rumen and proximal duodenum were used in a split-plot design experiment to evaluate the interaction of body weight (175 vs. 370 kg) and level of fat supplementation (0, 3, 6, and 9% yellow grease) on characteristics of digestion and feeding value of fat in finishing diets. Dry matter intake was restricted to 2% of BW. There were no interactions between BW and level of fat supplementation (P > 0.10) on ruminal or total-tract digestion. Level of supplemental fat decreased (linear, P < 0.01) ruminal digestion of OM and NDF, and increased (linear, P < 0.05) ruminal N efficiency. There were no treatment effects (P > 0.10) on postruminal digestion of OM, NDF, and N. There tended to be an interaction (P < 0.10) between BW and level of fat supplementation on postruminal starch digestion. Increasing level of fat supplementation increased postruminal digestion of starch in heavier steers but did not affect starch digestion in lighter steers. There were no interactions (P > 0.10) between BW and level of fat supplementation on postruminal fatty acid digestion. Increasing level of fat supplementation decreased (linear, P < 0.01) postruminal fatty acid digestion, which was due to a decreased (linear, P < 0.01) postruminal digestion of C16:0 and C18:0. Supplemental fat decreased (linear, P < 0.01) total-tract digestion of OM and NDF. The estimated NEm (Mcal/kg) of yellow grease averaged (linear, P < 0.01) 6.02, 5.70, and 5.06 for the 3, 6, and 9% of level supplementation, respectively. We conclude that intestinal fatty acid digestion (FAD, %) is a predictable function (r2 = 0.89; P < 0.01) of total fatty acid intake per unit body weight (FAI, g/kg BW): FAD = 87.560 - 8.591FAI. Depressions in fatty acid digestion with increasing level of intake were due primarily to decreased intestinal absorption of palmitic and stearic acid. Level of fatty acids intake did not appreciably affect intestinal absorption of unsaturated fatty acid. Changes in intestinal fatty acid digestion accounted for most of the variation in the NE value of supplemental fat.

Interaction of dietary magnesium level on the feeding value of supplemental fat in finishing diets for feedlot steers.

A feeding trial involving 160 crossbred steers (357 kg) and a metabolism trial involving eight Holstein steers (189 kg) cannulated in the rumen and proximal duodenum were conducted to evaluate the interaction of dietary Mg level (.18 vs .32%, DM basis) and supplemental fat (0% supplemental fat vs 4% tallow [T], yellow grease [YG], or griddle grease [GG]) on growth performance and NE value of the diet. Dietary Mg level did not influence (P > .10) growth performance. Daily weight gain was lower (11%, P < .05) for steers fed GG than for those fed YG. Supplemental fat decreased (5%, P < .10) DMI and increased (P < .05) gain efficiency (7%). There was a fat x Mg level interaction (P < .01) for dietary NE. The increase in dietary NEg with T and YG supplementation was similar (8.6 vs 8.0%) for diets containing .18 and .32% Mg. In contrast, the increase in dietary NEg with GG supplementation was 8.9% with .18% dietary Mg, but the NEg value of the diet did not increase when GG was added to diets with .32% dietary Mg. Dressing percentage was lower (1.5%, P < .1) and retail yield was greater (2.2%, P < .05) for steers fed GG- than for steers fed YG-supplemented diets. Increasing dietary Mg level increased kidney, pelvic, and heart fat (5.5%, P < .05). There was a fat x Mg level interaction (P < .1) for marbling score. With diets containing no supplemental fat, increasing dietary Mg decreased (15.2%) the marbling score, and with diets containing supplemental fat, increasing dietary Mg increased (7.2%) the marbling score. Fat supplementation decreased (P < .01) ruminal and total tract digestion of OM (10 and 3.5%, respectively) and NDF (37 and 17%, respectively). Supplemental fat did not affect (P > .10) Ca digestion but decreased (41.7%, P < .01) apparent Mg digestion. Increasing dietary Mg level increased (77.7%, P < .05) apparent Mg digestion. There were no treatment effects (P > .10) on postruminal fatty acid digestion. Fat supplementation decreased (17.3%, P < .01) the acetate:propionate molar ratio. Total ruminal protozoal counts were increased (12.7%, P < .05) by increasing dietary Mg level and decreased (12.9%, P < .05) by fat supplementation. We conclude that supplemental fats may depress Mg absorption. Increasing dietary magnesium levels beyond current recommendations may increase marbling scores in cattle fed fat-supplemented diets but may not affect growth performance or dietary NE. The NE value of fat is a predictable function of level of fat intake.

Influence of ruminal biohydrogenation on the feeding value of fat in finishing diets for feedlot cattle.

Four Holstein steers (212 kg) with cannulas in the rumen and proximal duodenum were used in a 4 x 4 Latin square experiment to study the influence of degree of ruminal biohydrogenation (BH) on the feeding value of supplemental fat. Treatments consisted of an 88% concentrate finishing diet supplemented with 1) 2% yellow grease (control); 2) 4% formaldehyde-protected fat (Rumentek), 2% yellow grease (LBH); 3) 2% Rumentek, 4% yellow grease (MBH); or 4) 6% yellow grease (HBH). Ruminal BH of HBH, MBH, and LBH diets was 74, 68, and 54%, respectively. High-fat supplementation decreased (7%, P < .05) intestinal digestibility of 18:0 but increased intestinal digestibility of 18:1 (3%, P < .10), 18:2 (14%, P < .01), and 18:3 (23%, P < .05). Increases in intestinal digestibility of 18:0 (quadratic effect, P < .05), 18:1 (linear effect, P < .01), 18:2 (linear effect, P < .01), 18:3 (linear effect, P < .05), and total fatty acids (linear effect, P < .05) were inversely related to BH. For every 1% increase in the proportion of 18:1 fat entering the small intestine, the digestibility of 18:0 increased 1%. High-fat supplementation depressed ruminal digestion of OM (11%, P < .05), NDF (16%, P < .05), starch (6%, P < .05), and feed N (12%, P < .01). Formaldehyde-protein protection of fat diminished its depressing effects on ruminal digestion of NDF (quadratic effect, P < .10) and enhanced ruminal escape of feed N (linear effect, P < .10). Postruminal digestion of OM was greater (4.6%, P < .10) for high-fat diets. High-fat diets decreased (P < .05) total tract digestion of OM (1.9%), NDF (7.4%), and starch (.5%). Postruminal and total tract digestibility of OM, NDF, N, and starch was not affected (P > .10) by BH. In a 125-d finishing trial, 100 yearling steers (362 kg) were used to evaluate treatment effects on growth performance. High-fat diets did not affect (P > .10) ADG but increased (P < .10) feed efficiency (9%, P < .10), dietary NEm (7.6%, P < .05), and dressing percentage (9%, P < .05). The magnitude of the increase in dressing percentage was inversely related (linear effect, P < .10) to BH. We conclude that decreasing ruminal BH will increase postruminal digestibility of fat, and hence the NE value of dietary fat. The synergistic effect of increasing the proportion of 18:1 on intestinal digestion of fat enables higher levels of fat supplementation. Protecting fat from BH minimizes the detrimental effects of supplemental fat on fiber digestion.

Interaction of protein nutrition and laidlomycin on feedlot growth performance and digestive function in Holstein steers.

Two isonitrogenous diets (12.5% CP) containing 20 (20% NPN) or 40% (40% NPN) of the N as nonprotein N were evaluated with 0 or 10 mg laidlomycin propionate (LP)/kg in a 2 x 2 factorial arrangement. Changes in dietary NPN:N ratio were developed by partial substitution of urea N for fish meal N. In Trial 1, four Holstein steers (349 kg) with cannulas in the rumen and proximal duodenum were used to evaluate treatment effects on digestive function. Total tract OM digestion was slightly greater (1.2%, P < .10) for diets containing 20% of N as NPN, due to greater (3.4%, P < .05) postruminal OM digestion. Supplemental LP decreased passage of microbial N to the small intestine (7.4%, P < .10) and ruminal degradation of dietary CP (DIP, 8.1%, P < .10). Decreasing the NPN:N ratio decreased microbial N flow to the small intestine (7.5%, P < .10) and DIP (15%, P < .01) and increased (6%; P < .05) the flow of indispensable amino acids to the small intestine. Supplemental LP increased (P < .10) ruminal pH. There were no treatment effects (P > .10) on ruminal molar proportions of acetate or propionate. In Trial 2, 120 Holstein steers (122 kg) were used to evaluate treatment effects on growth performance. Decreasing the NPN:N ratio increased ADG (P < .01) by 36, 40, and 16%, respectively, for the initial three 56-d periods of the trial. Overall, ADG was 17% greater (P < .01) for cattle consuming diets containing 20 vs 40% NPN. Decreasing the NPN:N ratio increased (P < .01) gain efficiency by 17 and 14%, respectively, for the initial two 56-d periods. Overall, gain efficiency was 6% greater (P < .01) for diets containing 20% NPN. Dietary NPN:N ratio did not influence (P > .10) the NE value of diets. Supplemental LP did not affect DMI (P > .10) but increased ADG (6%, P < .01) and gain efficiency (5%, P < .05) and decreased (11%, P < .05) the maintenance energy requirements. Protein nutrition limited growth performance of calves receiving the 20% NPN diets during the initial 112 d of the trial. With the 40% NPN diets, protein nutrition limited growth performance throughout most of the trial (d 1 to d 224). We conclude that LP will enhance daily weight gain and gain efficiency of calf-fed Holstein steers. Conventional urea-based diets will not diminish response to LP, although they may not meet the metabolizable amino acid requirements of calf-fed Holsteins during the first three-quarters of the feeding period.

Influences of saturation ratio of supplemental dietary fat on digestion and milk yield in dairy cows.

Four multiparous, ruminally and duodenally cannulated Holstein cows in midlactation were utilized in a 4 x 4 Latin square to evaluate the effects of supplemental fat from sources varying in proportions of unsaturated and saturated fatty acids on nutrient digestion and lactation performance. All diets (45% alfalfa hay) contained 12% whole cottonseed (as-fed); treatments were no supplemental fat (control, 3% total fatty acids, dry matter basis) or additional 2% tallow, 2% yellow grease, or 2% blend (60% tallow: 40% yellow grease). The unsaturated to saturated fatty acid ratios were 1:1 for tallow and 2.5:1 for yellow grease. Dry matter intake, apparent ruminal and total tract digestibilities of organic matter, neutral detergent fiber, acid detergent fiber, N, and fatty acids, and microbial efficiency were similar across treatments. Microbial N flow to the duodenum was increased by yellow grease. Supplemental fat reduced the postruminal digestibility of fatty acids, primarily the saturated fatty acids; increasing saturation of the fat source magnified the reduction. Total volatile fatty acid concentrations and ruminal fluid pH were unaffected by fat supplementation or saturation level. Blend decreased ruminal pH and acetate to propionate ratio. Yields of milk and milk fat increased with fat supplementation. Concentrations and yields of trans vaccenic acid in milk increased linearly with the unsaturated fatty acid content of the fat supplement. Modest supplementation using highly unsaturated fats to diets containing whole cottonseed can increase milk production without disturbing rumen function, evident by the similar VFA concentrations, nutrient digestibilities, and milk composition.

Influence of malic acid supplementation on ruminal pH, lactic acid utilization, and digestive function in steers fed high-concentrate finishing diets.

Two trials were conducted to evaluate the influence of malic acid supplementation on ruminal fermentation. In Trial 1, six Holstein steers (300 kg) with ruminal cannulas were used in a crossover design experiment to study the influence of malic acid (MA) on ruminal metabolism during glucose-induced lactic acidosis. Treatments consisted of a 77% steam-flaked barley-based finishing diet supplemented to provide 0 or 80 g/d of MA. After a 13-d dietary adjustment period, 1 kg of glucose was infused into the rumen 1 h after the morning feeding. Ruminal pH was closely associated (R2 = .70) with ruminal DL-lactate concentration. Malic acid supplementation increased (P < .01) ruminal pH 3 h after the glucose infusion. However, there were no treatment effects (P > .10) on ruminal VFA molar proportions or ruminal and plasma DL-lactate concentrations. In Trial 2, four Holstein steers (150 kg) with cannulas in the rumen and proximal duodenum were used in a crossover design experiment to evaluate the influence of MA supplementation on characteristics of digestion. Treatments consisted of an 81% steam-flaked barley-based finishing diet supplemented to provide 0 or 80 g/d of MA. There were no treatment effects (P > .10) on ruminal and total tract digestion of OM, ADF, starch, and feed N or on ruminal microbial efficiency. Malic acid supplementation increased (P < .05) ruminal pH 2 h after feeding. As with Trial 1, there were no treatment effects (P > .10) on ruminal VFA and DL-lactate concentrations. We conclude that supplementation of high-grain finishing diets with MA may be beneficial in promoting a higher ruminal pH during periods of peak acid production without detrimental effects on ruminal microbial efficiency or starch, fiber, and protein digestion. There were no detectable beneficial effects of MA supplementation on ruminal and plasma lactic acid concentrations in cattle fed high-grain diets.

The feeding value of dry-rolled and steam-flaked corn in finishing diets for feedlot cattle: influence of protein supplementation.

We used 80 medium-framed yearling crossbred heifers (357 kg) in a 110-d trial to evaluate the influence of dietary protein level (11 vs 14%) on the feeding value of dry-rolled (DRC) and steam-flaked corn (SFC). All diets contained 1% urea; cottonseed meal (CSM) was the source of supplemental undegradable intake protein (UIP). Steam flaking corn reduced DMI (9%, P < .10) and increased (P < .01) feed efficiency (14%), dietary NEm (13%), and NEg (15%). Steam flaking increased the NEm by 17% and NEg by 19%. Supplemental CSM decreased (P < .10) feed efficiency (7%) and dietary NEm (4%) and NEg (6%). There were no treatment effects (P > .10) on carcass characteristics. Steam flaking corn increased (P < .05) fecal pH and reduced (P < .01) fecal starch. Supplemental CSM increased (P < .01) fecal pH and reduced (P < .01) fecal starch. Four Holstein steers (413 kg) were used in a 4 x 4 Latin square experiment to evaluate treatment effects on digestive function. Steam flaking corn increased (P < .05) flow of nonammonia N (11%, P < .05) and microbial N (15%, P < .01) to the duodenum. Supplemental CSM increased the flow of microbial N (6%, P < .01), feed N (21%, P < .10), and nonammonia N (12%, P < .05) to the duodenum. The UIP value of CSM was 28% for the DRC diet and 52% for the SFC diet. Steam flaking corn increased (P < .01) ruminal starch digestion (26%) and total tract digestibility of OM (17%), N (15%), starch (19%), and GE (17%). Steam flaking increased the DE value of corn by 21%. Supplemental CSM did not influence (P > .10) postruminal or total tract starch digestion. Supplemental CSM decreased (7%, P < .10) the DE value of the diet. We conclude that increasing the postruminal protein supply of a corn-based finishing diet beyond that provided by urea supplementation, alone, will not enhance starch digestion or the energy value of the diet.

Influence of dietary magnesium level on growth-performance and metabolic responses of Holstein steers to laidlomycin propionate.

We used 216 Holstein steers (151 kg) in a 262-d trial to evaluate the influence of dietary magnesium level (.19, .25, and .32%) and laidlomycin propionate (LP; 0 vs 11 ppm, air-dry basis) on growth performance and NE value of the diet. During the initial 112 d of the trial, LP increased (P < .01) ADG (6.3%) and feed efficiency (4.2%). From d 112 until slaughter, LP increased (P < .05) ADG (9.7%) and feed efficiency (4.5%). Across the 262-d feeding period, LP supplementation enhanced (P < .01) ADG (8.9%) and feed efficiency (6.3%). There was an interaction (P < .05) between dietary Mg and LP on NE value of the diet. The enhancement in NE value of the diets owing to LP with .19, .25, and .32% dietary Mg were .5, 3.0, and 5.9%, respectively. Six Holstein steers (302 kg) were used in a 6 x 6 Latin square experiment to evaluate treatment effects on characteristics of ruminal and total tract digestion. There were no treatment interactions (P > .10) on site and extent of digestion of OM, starch, and N. Supplemental Mg increased (quadratic effect, P < .10) ruminal OM digestion. Neither LP nor dietary Mg level affected (P > .10) ruminal digestion of starch and feed N. Supplemental LP decreased (15%, P < .05) ruminal microbial efficiency. Total tract digestion of OM and N increased (linear effect, P < .01) with increasing dietary Mg level. There were interactions between LP and dietary Mg level on ruminal soluble-Mg concentration (linear effect, P < .01) and Mg absorption (quadratic effect, P < .05). Apparent total tract Mg digestion increased owing to LP (P < .01) and dietary Mg level (linear effect, P < .01). There were no treatment effects (P > .10) on ruminal pH. Dietary Mg level did not influence (P > .10) ruminal VFA concentrations or molar proportions. Supplemental LP increased (14%; P < .10) total ruminal VFA concentration but did not affect (P > .10) VFA molar proportions. We conclude that LP will increase daily weight gain and feed efficiency of calf-fed Holstein steers and that this response may be enhanced by increasing dietary Mg level.

An evaluation of ruminally degradable intake protein and metabolizable amino acid requirements of feedlot calves.

Ruminally degradable intake protein (DIP) and metabolizable indispensable amino acid (MIAA) requirements of feedlot steers were evaluated. Dietary treatments consisted of isocaloric 80% concentrate steam-flaked corn-based diets containing either .8% urea, 1.5% fish meal (FM), 3.0% FM, 4.5% FM, or 4.5% soybean meal (SBM). Treatment effects on characteristics of ruminal and total tract digestion were evaluated using four Holstein steers (249 kg) with cannulas in the rumen and proximal duodenum. Ruminal digestibility of OM (RDOM; P < .05) and feed N (P < .01) and microbial N flow (MNF; P < .01) to the small intestine were greater with urea as the supplemental N source. The level of DIP was closely associated (R2 = .89) with MNF. Postruminal digestibility of OM was greater (P < .05) for FM than for urea-supplemented diets, compensating for lower RDOM. There were no treatment effects (P > .10) on DOM. As the level of FM was increased, MIAA increased linearly (P < .01). Intestinal MIAA were similar (P > .10) for urea- and SBM-supplemented diets. Treatment effects on 56-d growth performance were evaluated using 100 medium-framed crossbred steers (231 kg). Daily weight gain (linear effect; P < .01), DM intake (linear effect; P < .10), feed efficiency (linear effect; P < .05), and diet NE (linear effect; P < .05) increased with level of FM supplementation. Daily weight gain (P < .10) and DM intake (P < .05) were greater for urea- than for SBM-supplemented diets. Using bovine tissue as the reference protein, the biological value (based on chemical score) of the intestinal chyme protein averaged 73%; methionine was first-limiting. There was a close association (R2 = .99) between methionine supply to the small intestine and observed/expected dietary NE. The metabolizable methionine requirement (MMETR, g/d) of medium-framed feedlot steers can be reliably predicted from measures of BW and ADG (MMETR = 1.565 + .0234ADG[268 - (29.4 x .0557BW(.75)ADG(1.097))/ADG] + .0896BW(.75)). There was a very close association (R2 = .89) between DIP and MNF (MNF = 13.7DIP - .66DIP(2) + 25.9). At maximal observed synthesis, DIP accounted for 76% of the MNF. A minimum of 100 g DIP/kg of total tract digestible OM was required to maximize RDOM and MNF.

Feeding value of cottonseed meal for feedlot cattle.

One hundred twenty crossbred steers (294 kg, initially) were used in a 141-d finishing trial. Four concentrations (8, 16, 24, and 32% of diet DM) of cottonseed meal (CSM, prepressed solvent-extracted) replaced steam-flaked corn in a corn-based finishing diet. Increasing level of CSM decreased ADG (linear component, P < .10), feed efficiency (linear component, P < .01), and dietary NE (linear component, P < .01). Observed dietary NE was 99% of expected at 8 and 16% CSM but 95% of expected at higher levels of inclusion (linear component, P < .05). Level of CSM did not influence (P > .10) dressing percentage, longissimus area, fat thickness, or retail yield. Eight Holstein steers (285 kg) were used in a replicated 4 x 4 Latin square design to evaluate treatment effects on characteristics of digestion. Ruminal digestibility of OM decreased (linear component, P < .05) as CSM increased, although ruminal digestibility of starch and feed N were not affected (P > .10). Ruminal escape protein from CSM was 58%. Total tract starch digestion was not altered (P > .10), but total tract digestibility of OM and GE decreased (linear component, P < .05) and digestion of N increased (linear component, P < .01) as CSM replaced steam-flaked corn. The ratio of observed to expected DE value of the diets was similar across CSM levels, averaging .99. Thus, comparative DE value of CSM was not affected by level of inclusion, averaging 3.32 Mcal/kg. We conclude that the NEm and NEg values of CSM are 1.88 and 1.24 Mcal/kg, respectively, and in close agreement with tabular values. However, CSM should not exceed 16% of DMI, because higher levels may depress cattle performance and replacement value of CSM.

Influence of dietary sulfur level on growth performance and digestive function in feedlot cattle.

Using ammonium sulfate, three levels of dietary S (.15, .20, and .25%, DM basis) were evaluated in a finishing trial with 108 yearling crossbred heifers (384 kg). The basal diet contained (DM basis) 4% alfalfa hay, 6% sudangrass hay, 74% steam-flaked corn, 4% yellow grease, 6% cane molasses, and 6% protein-mineral supplement. Increasing dietary S decreased ADG (quadratic effect, P < .10), DMI (linear effect, P < .10), feed efficiency (quadratic effect, P < .10), diet NE (quadratic effect, P < .10), and longissimus muscle area (linear effect, P < .05). Six Holstein steers (218 kg) with cannulas in the rumen and proximal duodenum were used to evaluate treatment effects on characteristics of digestion. Treatment effects on ruminal and total tract digestion of OM and N were small (P > .10). However, ruminal digestion of ADF and starch was slightly lower (quadratic effect, P < .10), and postruminal digestion of ADF and starch was correspondingly greater (quadratic effect, P < .05) with supplemental S. Dietary S level did not influence (P > .10) ruminal synthesis of microbial N. Increasing dietary S did not influence (P > .10) ruminal pH or lactic acid. Increasing S decreased molar proportions of acetate (quadratic effect, P < .10) and increased molar proportions of propionate (linear effect, P < .10). We conclude that S in excess of .20% of dietary DM may have detrimental effects on growth performance and dietary NE. Excessive dietary S may also compromise carcass merit by decreasing longissimus muscle area.

Interaction of dietary calcium and supplemental fat on digestive function and growth performance in feedlot steers.

Four Holstein steers (261 +/- 2 kg) with cannulas in the rumen and proximal duodenum were used in a 4 x 4 Latin square experiment to evaluate the interaction of dietary Ca (.45 vs. 90%) and supplemental fat (0 vs 5% yellow grease) on characteristics of digestion. There were no treatment interactions (P > .10). Supplemental Ca did not influence (P > .10) digestibility of OM, NDF, starch, N, and fatty acids. Supplemental fat decreased ruminal (21%, P < .05) and total tract (3%, P < .01) digestibility of OM and ruminal (25%, P < .10) and total tract (20%, P < .01) digestibility of NDF. Supplemental fat increased (P < .10) ruminal microbial efficiency. Ruminal free Ca was not affected (P > .10) by Ca intake but was closely associated with ruminal pH and fatty acid intake (R2 = .84). Apparent ruminal Ca absorption was generally negative, being increased (P < .05) by Ca supplementation and decreased (P < .10) by fat supplementation. Postruminal (P < .05) and total tract (P < .01) apparent Ca absorption was increased by Ca supplementation. Supplemental fat did not influence (P > .10) postruminal or total tract Ca absorption. One hundred forty-four medium-frame crossbred steers were used to evaluate treatment effects on feedlot growth performance. There were no treatment interactions (P > .10). Increasing dietary Ca did not influence (P > .10) steer performance. Supplemental fat decreased (P < .01) DMI and increased NE value of the diet (P < .01). It is concluded that increasing dietary Ca from .45 to .9% in high-grain finishing diets will not affect the feeding value of supplemental fat and that high levels (5%) of supplemental fat will not have a detrimental effect on Ca absorption.

Influence of dietary magnesium level on metabolic and growth-performance responses of feedlot cattle to laidlomycin propionate.

A metabolism trial and a growth-performance trial were conducted to evaluate the interaction of dietary magnesium level (.18 vs .32%) and laidlomycin propionate (LP) (0 vs 11 ppm, airdry basis) on utilization of a high-energy finishing diet by feedlot steers. There were no treatment effects (P > .10) on ruminal and total tract digestion of OM and ADF. However, there was an interaction (P < .05) between magnesium level and LP on ruminal starch digestion. With LP, magnesium level had no effect on ruminal starch digestion. Without LP, increasing dietary magnesium decreased ruminal starch digestion. Laidlomycin propionate decreased (P < .10) ruminal degradation of feed N (13.9%) and microbial efficiency (8.9%) and increased (P < .10) total tract N digestibility. There were no treatment interactions (P > .10) on site and extent of magnesium digestion. Magnesium absorption decreased with increased dietary magnesium (11.6%, P < .05) and LP (16.9%, P < .01). There was an interaction (P < .10) of treatments on postabomasal calcium absorption. With the low magnesium level LP increased calcium absorption, whereas with the higher magnesium level LP decreased calcium absorption. There was an interaction between magnesium level and LP on ruminal pH at .5 h (P < .05) and 8 h (P < .10) after feeding. In general, ruminal pH increased with LP supplementation at the lower magnesium level and decreased with LP supplementation at the higher magnesium level. There were interactions (P < .05) between magnesium level and LP on ruminal VFA molar proportions and estimated methane production. At the lower magnesium level, the effects of LP on VFA molar proportions were small. At the higher magnesium level, however, LP decreased (13.2%) molar proportions of acetate and increased (26.5%) molar proportions of propionate. There was an interaction (P < .05) between magnesium level and LP on feed intake. At the lower magnesium level, LP increased (3.9%) feed intake; at the higher magnesium level LP decreased (4.4%) intake. Increasing dietary magnesium enhanced ADG (6%, P < .10). Both magnesium and LP enhanced (2.8%, P < .10) diet NE, and this effect was strictly additive. There were no effects (P > .10) of magnesium level or LP on plasma magnesium concentrations. Plasma calcium concentrations were decreased by supplemental magnesium (15.2%, P < .05) and increased by LP (16.0%, P < .01). We conclude that dietary magnesium levels modulate the metabolic and performance responses of feedlot steers to supplemental LP.