Finishing performance and diet digestibility for feedlot steers fed corn distillers grains plus solubles and distillers solubles with and without oil extraction.

Three experiments evaluated the effects of corn oil removal using centrifugation in ethanol plants, on animal performance and digestion characteristics by finishing cattle fed by-products. In Exp. 1, 225 crossbred steers (300 ± 9.1 kg) were utilized in a randomized block design with a 2 × 2 + 1 factorial arrangement of treatments. Factors consisted of oil concentration [de-oiled (DO) or full fat (FF)] and by-product type [condensed distillers solubles (CDS) or modified distillers grains plus solubles (MDGS)] compared to a corn-based control. Fat concentration was 6.0% for DO CDS, 21.1% for FF CDS, 9.2% for DO MDGS, and 11.8% for FF MDGS. No oil concentration by by-product type interactions (P ≥ 0.17) were observed. There were no differences in DMI, ADG, or G:F between DO and FF CDS (P ≥ 0.29) or DO and FF MDGS (P ≥ 0.58). No differences (P ≥ 0.25) due to oil concentration were observed for carcass characteristics. Experiment 2 was a 5 × 5 Latin Square digestion trial with treatments similar to Exp. 1. Fat concentration was 8.7% or 15.4% for DO or FF CDS and 9.2% or 12.3% for DO or FF MDGS. Intake and total tract digestibility of fat were greater (P ≤ 0.02) for FF CDS compared with DO CDS. Digestible energy (megacalorie per kilogram), adjusted for intake, was greater (P = 0.02) for steers fed FF CDS compared to DO CDS. Average ruminal pH for cattle fed FF MDGS was greater than DO MDGS (P = 0.06). In Exp. 3, 336 yearling, crossbred steers (352 ± 19 kg) were utilized in a randomized block design with a 2 × 3 + 1 factorial arrangement of treatments. Factors included oil concentration (DO or FF) and inclusion [35%, 50%, and 65% wet distillers grains plus solubles (WDGS)] along with a corn-based control. The fat concentrations of DO and FF WDGS were 7.9% and 12.4%, respectively. A linear interaction (P < 0.01) was observed for DMI, which produced different slopes for DO and FF WDGS. No linear or quadratic interactions were observed for BW, ADG, or G:F (P ≥ 0.31). For the main effect of oil concentration, there were no statistical differences (P > 0.19) for final BW, ADG, or G:F. No statistical differences were observed for all carcass traits (P ≥ 0.34). Corn oil removal via centrifugation had minimal impact on finishing performance suggesting that cattle fed DO by-products will have similar performance to cattle fed FF by-products in dry-rolled and high-moisture corn diets.

A randomized controlled trial to evaluate the effects of dietary fibre from distillers grains on enterohemorrhagic Escherichia coli detection from the rectoanal mucosa and hides of feedlot steers.

Feeding high levels (≥40% dry matter) of distillers grains may increase the risk for cattle to carry enterohemorrhagic Escherichia coli (EHEC) O157. The mechanism for the increased risk is not known nor whether non-O157 EHEC are similarly affected. Our objective was to test whether the fibre content or other components of modified distillers grains plus solubles (MDGS) affects the probability for cattle to carry EHEC serogroups of public health importance. A 2 × 2 plus 1 factorial treatment arrangement within a randomized block design was utilized. Within each of four blocks, 25 feedlot pens (n = 8 steers/pen) were assigned randomly to (i) corn-based control diet; (ii) 20% dry matter (DM) MDGS; (iii) 40% DM MDGS; (iv) corn bran added to corn-based diet to match fibre of 20% MDGS or (v) 40% MDGS. Rectoanal mucosa swabs (RAMS) were collected on day (d)0, d35, d70 and d105; hide swabs were collected on the last feeding day. Samples were tested for EHEC by a molecular screening assay. The effects of fibre source and fibre level on EHEC carriage were tested using multilevel logistic regression (generalized linear mixed models; α = 0.05). EHEC O45 RAMS detection was associated with fibre level, source and sampling day. EHEC O103 RAMS detection increased by feeding 40% MDGS but not the corresponding corn bran diet. Hide contamination by EHEC O45 or O103 was less likely in cattle fed MDGS compared to corn bran diets. EHEC O111 RAMS detection decreased by feeding 40% MDGS but not by feeding the corresponding corn bran diet. Detection of EHEC O157 or O145 was not associated with dietary factors. Feeding 40% MDGS increased the probability for carriage of some EHEC serogroups but decreased probability of others, which indicated that EHEC serogroups have different risk factors associated with feeding MDGS and little association with dietary fibre.

Use of a complete starter feed in grain adaptation programs for feedlot cattle.

Four experiments evaluated the use of a complete starter feed (RAMP; Cargill Corn Milling, Blair, NE) for grain adaptation. In Exp. 1, 229 yearling steers (397 ± 28.4 kg BW) were used to compare a traditional adaptation program (CON) with adapting cattle with RAMP in either a 1- (RAMP-1RS) or 2- (RAMP-2RS) ration system. From d 23 to slaughter, cattle were fed a common finishing diet. In Exp. 2, 390 yearling steers (341 ± 14 kg BW) were used to compare accelerated grain adaptation programs with RAMP with 2 control treatments where RAMP was blended with a finishing diet containing either 25 (CON25) or 47.5% (CON47) Sweet Bran (Cargill Corn Milling) in 4 steps fed over 24 d to adapt cattle. Rapid adaptation treatments involved feeding RAMP for 10 d followed by a blend of RAMP and a 47% Sweet Bran finishing diet to transition cattle with 3 blends fed for 1 d each (3-1d), 2 blends fed for 2 d each (2-2d), or 1 blend fed for 4 d (1-4d). From d 29 to slaughter, all cattle were fed a common finishing diet. In Exp. 3, 300 steer calves (292 ± 21 kg BW) were used to compare the CON47 and 1-4d adaptation programs with directly transitioning cattle from RAMP, which involved feeding RAMP for 10 d and then switching directly to F1 on d 11 (1-STEP). From d 29 until slaughter, F2 was fed to all cattle. In Exp. 4, 7 ruminally fistulated steers (482 ± 49 kg BW) were used in a 35-d trial to compare the CON47 and 1-STEP adaptation programs. Ruminal pH and intake data from the first 6 d of F1and first 6 d of F2 were used to compare adaptation systems. Adaptation with RAMP-1RS and RAMP-2RS increased ( < 0.01) G:F compared with cattle adapted using CON in Exp. 1. Feeding RAMP-1RS increased ADG ( = 0.03) compared with CON. Intakes were similar ( = 0.39) among treatments. Daily gain, DMI, G:F, and carcass traits were similar ( > 0.11) among treatments in Exp. 2. Daily gain, DMI, and G:F were not different ( > 0.20) among treatments on d 39 or over the entire feeding period in Exp. 3. When F1 or F2 was being fed, DMI was similar ( ≥ 0.40) for CON47 and 1-STEP in Exp. 4. When F1 or F2 was being fed, 1-STEP cattle had lower average ruminal pH ( ≤ 0.03) and greater time below a pH of 5.3 ( ≤ 0.03). Using RAMP for grain adaptation improved performance compared with traditional adaptation. Rapid adaptation with RAMP decreased pH, but no performance differences were observed between long and rapid RAMP adaptation programs. Therefore, cattle started on RAMP do not require extensive adaptation before feeding a finishing diet with Sweet Bran.

Impact of microbial efficiency to predict MP supply when estimating protein requirements of growing beef cattle from performance.

Data from 16 trials were compiled to calculate microbial CP (MCP) production and MP requirements of growing cattle on high-forage diets. All cattle were individually fed diets with 28% to 72% corn cobs in addition to either alfalfa, corn silage, or sorghum silage at 18% to 60% of the diet (DM basis). The remainder of the diet consisted of protein supplement. Source of protein within the supplement varied and included urea, blood meal, corn gluten meal, dry distillers grains, feather meal, meat and bone meal, poultry by-product meal, soybean meal, and wet distillers grains. All trials included a urea-only treatment. Intake of all cattle within an experiment was held constant, as a percentage of BW, established by the urea-supplemented group. In each trial the base diet (forage and urea supplement) was MP deficient. Treatments consisted of increasing amounts of test protein replacing the urea supplement. As protein in the diet increased, ADG plateaued. Among experiments, ADG ranged from 0.11 to 0.73 kg. Three methods of calculating microbial efficiency were used to determine MP supply. Gain was then regressed against calculated MP supply to determine MP requirement for maintenance and gain. Method 1 (based on a constant 13% microbial efficiency as used by the beef NRC model) predicted an MP maintenance requirement of 3.8 g/kg BW and 385 g MP/kg gain. Method 2 calculated microbial efficiency using low-quality forage diets and predicted MP requirements of 3.2 g/kg BW for maintenance and 448 g/kg for gain. Method 3 (based on an equation predicting MCP yield from TDN intake, proposed by the Beef Cattle Nutrient Requirements Model [BCNRM]) predicted MP requirements of 3.1 g/kg BW for maintenance and 342 g/kg for gain. The factorial method of calculating MP maintenance requirements accounts for scurf, endogenous urinary, and metabolic fecal protein losses and averaged 4.2 g/kg BW. Cattle performance data demonstrate formulating diets to meet the beef NRC model recommended MP maintenance requirement (3.8 g/kg S) works well when using 13% microbial efficiency. Therefore, a change in how microbial efficiency is calculated necessitates a change in the proposed MP maintenance requirement to not oversupply or undersupply RUP. Using the 2016 BCNRM to predict MCP production and formulate diets to meet MP requirements also requires changing the MP maintenance requirement to 3.1 g/kg BW.

Technical note: Evaluation of urinary purine derivatives in comparison with duodenal purines for estimating rumen microbial protein supply in sheep.

A data set of individual observations was compiled from digestibility trials to examine the relationship between the duodenal purine bases (PB) flow and urinary purine derivatives (PD) excretion and the validity of different equations for estimating rumen microbial N (Nm) supply based on urinary PD in comparison with estimates based on duodenal PB. Trials (8 trials, = 185) were conducted with male sheep fitted with a duodenal T-type cannula, housed in metabolic cages, and fed forage alone or with supplements. The amount of PD excreted in urine was linearly related to the amount of PB flowing to the duodenum ( < 0.05). The intercept of the linear regression was 0.180 mmol/(d·kg), representing the endogenous excretion of PD, and the slope was lower than 1 ( < 0.05), indicating that only 0.43% of the PB in the duodenum was excreted as PD in urine. The Nm supply estimated by either approach was linearly related ( < 0.05) to the digestible OM intake. However, the Nm supply estimated through either of 3 published PD-based equations probably underestimated the Nm supply in sheep.

Evaluation of ractopamine hydrochloride (Optaflexx) on growth performance and carcass characteristics of finishing steers across different feeding durations.

Two experiments were conducted to evaluate the effects of ractopamine hydrochloride (RAC) dose and duration on growth performance and carcass characteristics of finishing steers. In Exp. 1, 336 crossbred steers (initial BW of RAC feeding = 539 kg [SD 22]) were used in a 2 × 2 factorial arrangement of treatments with one factor being RAC dose (0 or 200 mg/steer daily) and the other factor being RAC duration (28 or 42 d prior to harvest). There were no RAC dose × duration interactions ( ≥ 0.08) for growth performance or carcass characteristics. Feeding 200 mg RAC/steer daily increased ( < 0.01) live final BW by 9.0 kg compared with steers not fed RAC. Carcass-adjusted final BW, ADG, and G:F were greater ( < 0.01) for steers fed 200 mg RAC/d compared with steers not fed RAC. Hot carcass weight was 4.7 kg heavier ( < 0.01) for steers fed 200 mg RAC/d compared with steers not fed RAC. In Exp. 2, crossbred steers ( = 576; experiment initial BW = 408 kg [SD 29]) were used in a randomized block design with a 3 × 3 factorial arrangement of treatments. Factors included RAC dose (0, 300, and 400 mg/steer daily) and RAC duration (14, 28, or 42 d prior to harvest). There was a tendency ( ≤ 0.08) for an interaction of RAC dose × duration for final live BW, DMI, and live G:F; therefore, simple effects are presented. At 28 d, live final BW for steers fed 400 mg RAC/d were heavier ( < 0.01) than for steers fed 0 mg RAC/d. There was a tendency at 28 d for increased live final BW for steers fed RAC at 300 mg/d ( = 0.08) compared with steers fed RAC at 0 mg and for steers fed 400 mg RAC/d compared with steers fed 300 mg RAC/d ( = 0.06). Live final BW was greater ( < 0.01) for steers fed RAC for 42 d at 300 and 400 mg/d compared with steers fed 0 mg; however, live final BW was similar ( = 0.48) between steers fed 300 and 400 mg RAC/d. Despite no RAC dose × duration interaction ( = 0.30) for HCW, simple effects will be presented for consistency. Hot carcass weight was greater for steers fed 300 and 400 mg RAC/d for 28 and 42 d compared with steers fed 0 mg at 28 ( ≤ 0.02) and 42 d ( < 0.01). Feeding 300 mg RAC/d for 28 or 42 d increased HCW by 5.1 and 7.6 kg, respectively, compared with steers fed 0 mg RAC. Additionally, feeding 400 mg RAC/d for 28 or 42 d resulted in increases of 8.9 and 9.4 kg, respectively, in HCW compared with steers fed 0 mg RAC. In conclusion, our results confirm that feeding RAC improves growth performance and carcass weight, with an optimal duration of feeding RAC being 28 d.

Effects of agronomic factors on yield and quality of whole corn plants and the impact of feeding high concentrations of corn silage in diets containing distillers grains to finishing cattle.

Corn plants were sampled over 2 consecutive years to assess the effects of corn hybrid maturity class, plant population, and harvest time on whole corn plant quality and yield in Nebraska. A finishing experiment evaluated the substitution of corn with corn silage in diets with corn modified distillers grains with solubles (MDGS). The first 2 harvest dates were at the mid- and late-silage harvest times whereas the final harvest was at the grain harvest stage of plant maturity. Whole plant yields increased as harvest time progressed (yr 1 quadratic P < 0.01; yr 2 linear P < 0.01). However, differences in TDN concentration in both years were quite minimal across harvest time, because grain percentage increased but residue NDF in-situ disappearance decreased as harvest time was delayed. In the finishing experiment, as corn silage inclusion increased from 15 to 55% (DM basis) by replacing dry rolled and high moisture corn grain with corn silage in diets containing 40% MDGS, DMI, ADG, and G:F linearly decreased (P ≤ 0.01), with the steers on the 15% corn silage treatment being 1.5%, 5.0%, and 7.7% more efficient than steers on treatments containing 30, 45, and 55% corn silage, respectively. Calculated dietary NEm and NEg decreased linearly as corn silage inclusion increased indicating that net energy values were greater for corn grain than for corn silage. In addition, dressing percentage decreased linearly (P < 0.01) as silage inclusion increased suggesting more fill as silage inclusion increases in diets. Cattle fed greater than 15% corn silage in finishing diets based on corn grain will gain slower and be slightly less efficient and likely require increased days to market at similar carcass fatness and size. When 30% silage was fed with 65% MDGS, DMI, and ADG were decreased (P < 0.01) compared to feeding 30% silage with 40% MDGS suggesting some benefit to including a proportion of corn in the diet. Conversely, when 45% silage was fed with 40% MDGS, ADG, and G:F were greater (P < 0.04) than when 45% silage was fed with just grain implying a greater energy value for MDGS than for corn grain. Substituting corn silage for corn grain in finishing diets decreased ADG and G:F which would increase days to finish to an equal carcass weight; however, in this experiment, increasing corn silage levels with MDGS present reduced carcass fat thickness without significantly decreasing marbling score.

Digestibility and performance of steers fed varying inclusions of corn silage and modified distillers grains with solubles to partially replace corn in finishing diets.

Two finishing and 1 digestibility experiment evaluated the partial substitution of corn with corn silage and corn modified distillers grains with solubles (MDGS). Steers were used in Exp. 1 (n = 295; 467 ± 52 kg) and Exp. 2 (n = 225; BW = 348 ± 27 kg) in a 2 × 2 + 1 factorial arrangement of treatments with factors including corn silage (15 or 45%) and MDGS (20 or 40%) plus a control diet consisting of 5% cornstalks and 40% MDGS. In Exp. 1, there were tendencies for a corn silage × MDGS interaction for ADG, final BW, and G:F (P ≤ 0.08). In the overall F-test for G:F, there were no differences between the control treatment and 15:20, 15:40, or 45:40 (P ≥ 0.15), however, steers fed the control treatment had increased G:F compared to steers fed 45:20 treatment diets (P = 0.03). In Exp. 2, there were no corn silage × MDGS interactions (P ≥ 0.12). As corn silage increased in the diet, ADG, final BW, and G:F decreased (P ≤ 0.01). As MDGS increased from 20 to 40%, ADG and G:F tended to improve (P ≤ 0.07). In the overall F-test, the control was not different for G:F from 15:20, 45:20, or 45:40 (P ≥ 0.15), but had a 4.8% poorer G:F compared to 15:40 (P < 0.01). In Exp. 3, ruminally fistulated steers (n = 6) were used in a 5 × 6 Latin rectangle design and fed 15 or 45% corn silage with 20 or 40% MDGS as a 2 × 2 factorial. An additional diet consisting of 95% corn silage and 5% supplement was fed. There were no corn silage × MDGS interactions for nutrient intake, total tract digestibility, ruminal pH measurements, acetate: propionate ratio (A:P), or in-situ disappearance data (P ≥ 0.31) for the 2 × 2 factorial. As corn silage increased in the diet, DMI, NDF intake, ruminal pH, A:P, in-situ NDF disappearance of corn bran, and DM disappearance of corn increased (P ≤ 0.09) with decreases in DM and OM digestibility (P ≤ 0.03). As MDGS increased in the diet, there was an increase in NDF intake, total volatile fatty acid concentration, and NDF disappearance of corn bran (P ≤ 0.03) with no differences for any other tested variables (P ≥ 0.13). In general, increasing corn silage in place of corn in finishing diets containing MDGS results in a modest reduction in ADG and G:F with increases in ruminal pH.

Effect of corn residue harvest method with ruminally undegradable protein supplementation on performance of growing calves and fiber digestibility.

Two experiments evaluated the effects of corn residue harvest method on animal performance and diet digestibility. Experiment 1 was designed as a 2 × 2 + 1 factorial arrangement of treatments using 60 individually fed crossbred steers (280 kg [SD 32] initial BW; = 12). Factors were the corn residue harvest method (high-stem and conventional) and supplemental RUP at 2 concentrations (0 and 3.3% diet DM). A third harvest method (low-stem) was also evaluated, but only in diets containing supplemental RUP at 3.3% diet DM because of limitations in the amount of available low-stem residue. Therefore, the 3 harvest methods were compared only in diets containing supplemental RUP. In Exp. 2, 9 crossbred wethers were blocked by BW (42.4 kg [SD 7] initial BW) and randomly assigned to diets containing corn residue harvested 1 of 3 ways (low-stem, high-stem, and conventional). In Exp. 1, steers fed the low-stem residue diet had greater ADG compared with the steers fed conventionally harvested corn residue ( = 0.03; 0.78 vs. 0.63 kg), whereas steers fed high-stem residue were intermediate ( > 0.17; 0.69 kg), not differing from either conventional or low-stem residues. Results from in vitro OM digestibility suggest that low-stem residue had the greatest ( < 0.01) amount of digestible OM compared with the other 2 residue harvest methods, which did not differ ( = 0.32; 55.0, 47.8, and 47.1% for low-stem, high-stem, and conventional residues, respectively). There were no differences in RUP content (40% of CP) and RUP digestibility (60%) among the 3 residues ( ≥ 0.35). No interactions were observed between harvest method and the addition of RUP ( ≥ 0.12). The addition of RUP tended to result in improved ADG (0.66 ± 0.07 vs. 0.58 ± 0.07 for supplemental RUP and no RUP, respectively; = 0.08) and G:F (0.116 ± 0.006 vs. 0.095 ± 0.020 for supplemental RUP and no RUP, respectively; = 0.02) compared with similar diets without the additional RUP. In Exp. 2, low-stem residue had greater DM and OM digestibility and DE ( < 0.01) than high-stem and conventional residues, which did not differ ( ≥ 0.63). Low-stem residue also had the greatest NDF digestibility (NDFD; < 0.01), whereas high-stem residue had greater NDFD than conventional residue ( < 0.01). Digestible energy was greatest for low-stem residue ( < 0.05) and did not differ between high-stem and conventional residues ( = 0.50). Reducing the proportion of stem in the bale through changes in the harvest method increased the nutritive quality of corn residue.

Case Study: Supplementation of cow-calf pairs grazing smooth bromegrass pastures with ethanol by-products and low-quality forages.

Multiparous, lactating, crossbred (Simmental × Angus) beef cows with spring-born calves at side (n = 16 per year; 4 per pasture) were used each of 3 yr to evaluate supplementing modified distillers grains plus solubles mixed with low-quality forage on cow and calf performance while grazing. Cow-calf pairs were assigned randomly to treatment with 2 replications (pasture) per year for 3 yr. Treatments were (1) recommended stocking rate of 9.46 animal-unit month/ha with no supplementation (CON) or (2) double the recommended stocking rate (18.9 animal-unit month/ha) and supplemented with a 30:70 modified distillers grains plus solubles:cornstalks (DM) mixture (SUPP). To replace 50% of grazed forage DMI, SUPP pairs were fed an average of 1.13% of BW (DM) over the grazing season. Pairs grazed adjacent smooth bromegrass pastures for 130 d during the summer. Gain was not different (P = 0.19) between SUPP and CON cows (0.28 vs. 0.19 kg/d, respectively). Ending cow BW was not affected (P = 0.46) by treatment. Similarly, calf gain was not affected (P = 0.31) by supplementation. In studies where confined cow-calf pairs were fed average-quality (IVDMD = 52.9%) forage, DMI was 2.58% of pair BW. Based on these data, CON and SUPP pairs consumed 18.6 and 19.1 kg of DM, respectively, of total feed per pair daily. The SUPP pairs consumed 7.1 kg of DM/pair daily of the supplement, replacing approximately 35% of grazed forage intake. These data suggest mixtures of ethanol co-products and low-quality forages can be supplemented to replace grazed forage intake of cattle, allowing for increased stocking rate without affecting animal performance.

Suitable strategy to improve nitrogen utilization and reduce the environmental impact of Nellore bulls supplemented on tropical pasture.

Expansion of the biodiesel industry has increased the crude glycerin (CG) supply. Crude glycerin has the potential of replacing corn in ruminant diets because the glycerol can be converted to glucose in the liver of ruminants, providing energy for cellular metabolism. The objective was to evaluate the effects of CG with urea, soybean meal, cottonseed meal, and corn gluten feed, respectively, on intake, digestibility, microbial protein yield, and efficiency of N utilization. Five Nellore bulls (initial BW of 448 kg [SD 14]) grazing tropical pasture were used in a 5 × 5 Latin square design. The supplements were control (no supplementation; only free-choice mineral mixture ad libitum), CG with urea (CG-Urea), CG with soybean meal, CG with cottonseed meal, and CG with corn gluten. Crude glycerin was used in all supplements to replace corn (15% of DM supplement). There were differences between CG-Urea and other supplements with regard to intake of DM (% of BW and total; < 0.01), OM ( < 0.01), CP ( < 0.01), and TDN ( < 0.01). The digestibility of CP was greater ( = 0.04) for animals supplemented with CG-Urea than for those fed other supplements. Animals supplemented with CG-Urea showed greater N intake ( < 0.01) and N ammonia ( = 0.04) than those supplemented with other treatments. Nitrogen retained (g/d) was not affected by protein source but was greater for cattle fed a protein supplement compared with cattle fed the control supplement ( < 0.01). Supplementing the animals with protein sources increased ( = 0.02) the daily production of rumen microbial nitrogen (g/d) compared with the control group. Microbial protein (g/d) was lesser for the control than for protein sources ( = 0.02). However, when expressed relative to TDN ( = 0.35) and CP ( = 0.82), there were no differences across treatments. Crude protein intake per digestible OM intake (g CP/kg digestible OM intake) was greater for animals fed protein sources compared with animals fed control supplements ( < 0.01). Based on nutrients intake and microbial protein yield, CG-Urea supplement has a greater feeding value compared with other protein sources. Crude glycerin, when used to replace corn in 15% of DM supplement, may be effective to improved N utilization and microbial protein yield in rumen of Nellore bulls grazing cv. Marandu.

Using Sweet Bran instead of forage during grain adaptation in finishing feedlot cattle.

Two trials evaluated adapting cattle to a finishing diet using wet corn gluten feed compared with traditional methods using forage. A 33-d grain adaptation metabolism trial (Exp. 1) compared decreasing wet corn gluten feed (Sweet Bran; Corn Milling unit, Cargill Corn Milling, Blair, NE) while increasing corn inclusion (SB) and a traditional grain adaptation system decreasing alfalfa hay while increasing corn with no Sweet Bran inclusion (CON). Ruminal pH, intake characteristics, and 24-h in situ digestibility were evaluated using 8 ruminally fistulated steers (291 kg BW [SD 19]). Steers (4/treatment) were adapted to finishing diets across 4 periods consisting of 5, 7, 7, and 7 d and then fed a finishing diet for 7 d. No period × adaptation diet interactions were observed ( ≥ 0.12). Average ruminal pH decreased ( < 0.01) whereas time and area below a pH of 5.6 increased ( ≤ 0.02) for the SB adaptation system compared with the CON adaptation system. Cattle adapted using SB had greater DMI than cattle adapted using CON ( < 0.01). As steers were adapted to finishing diets, DMI increased ( = 0.01), average ruminal pH decreased ( = 0.05), and time and area below a pH of 5.6 increased ( ≤ 0.04) for both treatments. Ruminal pH for CON steers decreased from 6.59 to 6.12 across periods as corn replaced alfalfa hay whereas ruminal pH decreased from 6.00 to 5.79 for SB steers. Steers adapted using SB had greater ( ≤ 0.05) in situ digestion of adaptation diets than steers adapted using CON for adaptation periods 3, 4, and 5. The SB diets were more digestible than the CON diets when incubated in either CON- or SB-fed steers for adaptation periods 1 and 2 ( < 0.01). Experiment 2 used 240 finishing steers (273 kg BW [SD 14]) to determine performance impacts of using Sweet Bran instead of forage to adapt cattle to finishing diets. Steers were fed either decreasing Sweet Bran inclusion while increasing corn (SB) or decreasing alfalfa hay inclusion while increasing corn (CON). Treatments were applied only during grain adaptation (26 d) and all steers were finished on a common diet containing 35% Sweet Bran for an additional 147 d. Steers adapted using SB had greater ( ≤ 0.01) final BW, ADG, G:F, and HCW compared with steers adapted using CON, even though treatments differed only the first 26 d. Grain adaptation treatment had no effect ( ≥ 0.13) on carcass quality. These results indicate that Sweet Bran can be used to adapt cattle to finishing diets instead of forage and improves ADG and G:F while decreasing the forage needs of feedlots.

Technical Note: Collection and preparation techniques change nutrient composition of masticate collected from esophageally fistulated cattle.

Two experiments determined effects of collection and preparation techniques on nutrient composition of masticate samples from esophageally fistulated cattle. In Exp. 1, 12 esophageally fistulated cattle were maintained on 2 precollection diets, high CP (24% CP; = 6) or low CP (7.7% CP; = 6), for 8 d. On d 9, the esophageal plug was removed, screen bottom bags were attached, and each cow was offered fresh grass. Immediately after fresh grass sample collection was complete, dry grass (hay) was offered and a sample was collected. Blood samples were collected and analyzed for serum urea nitrogen concentration. Masticate samples of both fresh and dry grass were divided and each was either squeezed by hand until no more saliva could be removed or remained unsqueezed. In Exp. 2, 10 esophageally fistulated cattle were fitted with either screen ( = 5) or solid ( = 5) bottom collection bags after removal of the esophageal plug and presented grass hay, fresh grass, alfalfa hay, or fresh alfalfa. In Exp. 1, the precollection diet did not affect ( = 0.49) CP content of masticate even though serum urea nitrogen tended to be greater ( = 0.08) for high- vs. low-CP precollection diets. Forage harvest type offered (fresh vs. hay) interacted ( = 0.01) with preparation technique (squeezed vs. unsqueezed) for CP, where CP decreased in squeezed fresh samples ( < 0.001) but not in squeezed grass hay samples ( = 0.98). In Exp. 2, ingestion greatly increased levels of ash ( < 0.001). Crude protein was greater ( < 0.004) before ingestion for all samples except grass hay ( = 0.43). Levels of NDF were similar before and after ingestion ( > 0.15) for all samples except fresh alfalfa, which was greater after ingestion ( = 0.002). Ingestion status did not affect in vitro OM disappearance (IVOMD; > 0.34) except for grass hay, which was greater after ingestion ( < 0.001). Bag type (screen vs. solid) did not affect ash and NDF ( > 0.31), except for fresh alfalfa, which were greater ( < 0.03) for solid bottom bags. Bag type did not affect alfalfa CP ( = 0.71) but did affect grass CP, which was lower ( = 0.02) for solid bottom bags. Bag type did not affect IVOMD ( > 0.33). More ( = 0.01) fresh forage than hay was recovered through the esophageal opening. Previous diet did not impact masticate samples but squeezing impacted CP levels of high-quality forage and therefore should not be performed. Nutrient values should be reported on an OM basis.

Effects of grind size when alkaline treating corn residue and impact of ratio of alkaline-treated residue and distillers grains on performance of finishing cattle.

Two studies were conducted to optimize use of alkaline-treated corn stover and wheat straw and distillers grains as partial corn replacements. In Exp. 1, a finishing experiment used 30 pens (12 steers/pen) of calf-fed steers (initial BW = 374 ± 23.9 kg) with a 2 × 2 + 1 factorial arrangement of treatments with 6 replications per treatment. Factors were grind size, where corn stover was processed through a 2.54- or 7.62-cm screen, and chemical treatment (corn stover either fed in native, non-treated form [NT; 93.4% DM] or alkaline treated [AT; 5% CaO hydrated to 50% DM]). No interactions (P ≥ 0.38) were noted between grind size and chemical treatment. Feeding AT compared with NT improved (P ≤ 0.02) final BW, ADG, and G:F. Reducing grind size improved (P ≤ 0.01) ADG and G:F, and no interaction with chemical treatment was observed. Steers fed AT had similar DMI, ADG, G:F, and carcass characteristics compared with a 5% roughage control that contained 15 percentage units (DM basis) more corn. In Exp. 2, 60 individually fed steers (initial BW = 402 ± 61.4 kg) were randomly assigned to 10 diets. Six treatments evaluated 10, 25, or 40% dry-rolled corn (DRC), which was replaced with either a 2:1 or 3:1 ratio (DM basis) of modified distillers grains plus solubles (MDGS) and treated corn stover analyzed as a 2 × 3 factorial. An additional 3 treatments were added where a 3:1 ratio of MDGS:straw were compared with a 3:1 ratio of MDGS:stover. As DRC increased, G:F (P = 0.06) quadratically increased for 3:1 MDGS:stover diets. Increasing DRC increased (P = 0.07) G:F in treated stover diets, regardless of ratio. Increasing DRC increased (P = 0.10) ADG for 3:1 ratios for both straw and stover. Reducing grind size, feeding a maximum of 20% treated crop residue, and maintaining at least 25% corn in the diet are strategies for optimizing cattle performance when replacing dry-rolled and high-moisture corn with treated crop residues and distillers grains.

Effects of stocking rate on forage nutrient composition of Nebraska Sandhills upland range when grazed in early summer.

Twelve 2-ha, Nebraska Sandhills upland range paddocks were used in a 2-yr study to determine effects of stocking rate on grazed forage nutrient value in early summer. Paddocks contain a mixture of native cool- and warm-season grasses with forbs as a minor component. Stocking rates were 0 (control), 0.57 (light), and 0.85 (heavy) animal unit months per ha, respectively. Three esophageally fistulated cows collected diet samples on May 14 (d 0), May 21 (d 7), May 28 (d 14), and June 4 (d 21) in 2013 and 2014. Ten quadrats per paddock were clipped and separated into current or previous year growth on each diet sampling date. All samples were analyzed for CP, NDF, and in vitro OM disappearance, which was adjusted to an in vivo OM basis (). For diet samples, treatment interacted ( < 0.001) with sampling date for CP, NDF, and IVOMD. However, treatment and date did not interact ( ≥ 0.32) for clipped samples. Diets collected in control paddocks had greater ( < 0.05) IVOMD and CP and lower NDF compared with light and heavy stocking rate paddocks on d 7, 14, and 21 but light stocking rate paddocks did not differ ( ≥ 0.26) from heavy stocking rate paddocks on any sampling day except d 21 NDF ( = 0.03). In general, previous year growth IVOMD, CP, and NDF were not affected ( ≥ 0.11) by treatment. Generally, current year growth IVOMD and CP were not affected ( ≥ 0.22) by treatment. Current year growth NDF did not differ ( = 0.23) among stocking rates on d 0, but control paddock had lower ( = 0.02) NDF than light and heavy on d 7, 14, and 21. In stocked paddocks, diet samples had greater ( < 0.01) IVOMD and CP and lower NDF than current and previous year growth except IVOMD on d 0 where diet and current year growth did not differ ( = 0.34). Generally, in control paddocks, current year growth and diet samples had greater ( < 0.01) IVOMD and CP than previous year growth. Control paddocks had greater ( < 0.01) forage accumulation than stocked paddocks on d 7, 14, and 21; however, light and heavy stocked paddocks did not differ ( ≥ 0.29). On d 0 it was estimated that 96% of the diet was current year growth and only 4% previous year growth, whereas on d 21, 70% of the diet was current year growth vs. 30% previous year growth. Stocking pastures decrease current year growth forage mass and therefore diet nutritive value by forcing cattle to consume diets containing previous year growth in early summer.

Finishing performance of feedlot cattle fed condensed distillers solubles.

Two experiments evaluated the effects of condensed distillers solubles (CDS) on performance and carcass characteristics of finishing beef cattle. In Exp. 1, 250 crossbred steers (initial BW = 355 ± 18 kg) were fed 0, 9, 18, 27, or 36% CDS (DM basis) which replaced a portion of urea and a 1:1 ratio of dry-rolled corn (DRC) and high-moisture corn (HMC). Steers were divided into 3 BW blocks and were assigned randomly to 25 pens. Dietary fat increased from 3.7 to 9.4% as CDS inclusion increased from 0 to 36%. Intake decreased linearly ( < 0.01) as CDS increased. A quadratic response was observed for ADG ( = 0.01) and G:F ( < 0.01) with maximum gain calculated at 20.8% CDS and maximum G:F at 32.5% CDS inclusion, which was 12% more efficient than those fed 0% CDS. Experiment 2 was designed as a 2 × 4 factorial using 400 crossbred steers (initial BW = 339 ± 15 kg) evaluating 0, 7, 14, or 21% CDS (DM basis) in 2 base byproduct diets containing either 20% modified distillers grains plus solubles (MDGS) or 20% Synergy (a blend of wet corn gluten feed and MDGS). Steers were divided into 2 BW blocks and were assigned randomly to 40 pens. A tendency for a base diet × CDS inclusion interaction was observed for ADG, HCW, and final BW ( < 0.10). Gain increased linearly ( = 0.01) and tended to increase quadratically ( = 0.09) in MDGS diets, with maximum calculated ADG at 16% CDS inclusion. Inclusion of CDS had no effect on ADG in Synergy-based diets. Increasing CDS resulted in a linear increase in G:F ( < 0.01) regardless of basal diet. Condensed distillers solubles may be included in the diet at greater than 30% (DM basis) without other byproducts and improve animal performance. Likewise, CDS can be fed in combination with other byproduct feeds but with less improvement in performance.

Effects of roughage source and inclusion in beef finishing diets containing corn wet distillers' grains plus solubles.

Two experiments were conducted to determine the effects of roughage source and inclusion in diets containing wet distillers' grains plus solubles (WDGS) on finishing cattle performance and ruminal metabolism. In Exp. 1, 385 crossbred steer calves (initial BW = 346 kg [SD 29]) were used in a finishing trial. A control diet with no roughage inclusion was compared with 6 diets containing either alfalfa hay (ALF), corn silage (CSIL), or corn stalks (CSTK) at 2 inclusions as a 3 × 2 factorial. Alfalfa hay was included at 4 (low) or 8% (standard) of diet DM. Diets containing CSIL or CSTK were formulated to provide total dietary NDF equal to the low and standard ALF inclusion diets. The final diets contained 6.13 and 12.26% CSIL or 3.04 and 6.08% CSTK (DM basis). All diets contained 30% WDGS and a 1:1 mixture of dry-rolled and high-moisture corn (DM basis). Cattle fed no roughage had reduced ( < 0.01) DMI and tended ( ≤ 0.10) to have the lowest final BW and ADG compared with cattle fed roughage. There were no differences ( ≥ 0.11) in DMI, ADG, or G:F due to roughage source. Cattle fed a standard inclusion of roughage had greater ( ≤ 0.04) DMI and ADG compared with cattle fed diets with low inclusion, regardless of roughage source. Feed efficiency tended to be different among treatments ( = 0.09), with cattle fed no roughage having greater G:F than all treatments ( ≤ 0.06) except cattle fed the low level of CSTK, which had a similar G:F ( = 0.48). Feed efficiency was not affected by source of roughage ( = 0.23) or inclusion of roughage ( = 0.49). In Exp. 2, 6 ruminally fistulated steers (347 kg BW [SD 25]) were used in a 6 × 6 Latin square design. Treatments were arranged as a 2 × 3 factorial with ALF or CSTK included at zero, low, or standard levels similar to Exp. 1. Apparent total tract digestibility (%) of DM, OM, and NDF decreased linearly ( ≤ 0.07) due to increasing roughage inclusion. Average, maximum, and minimum ruminal pH increased linearly ( ≤ 0.09) as roughage inclusion was increased. Based on the results of this study, low levels of CSTK improved cattle performance relative to low inclusions of ALF or CSIL. Diets with standard inclusions of ALF, CSIL, or CSTK had similar performance. Roughage sources can be exchanged to provide equal NDF in finishing diets containing 30% WDGS without negatively impacting finishing cattle. Based on ADG, eliminating roughages when 30% WDGS was included in finishing diets was not beneficial.

FORAGES AND PASTURES SYMPOSIUM: Optimizing the use of fibrous residues in beef and dairy diets.

Increased corn prices over the past decade have altered land use away from traditional forage in favor of corn. Accordingly, beef and dairy producers have had to adopt nontraditional forage resources into their production systems, many of which have become available as a result of increased corn production. Corn residues have become more available due to increases in corn hectares and yield. The individual plant components (i.e., husk, leaf, and stem) vary in fiber digestibility (NDF digestibility estimates = 40.5, 31.4, and 0.6% ± 0.8 for husk, leaf, and stalk, respectively). Stocking cattle to consume 3.6 kg forage/25.5 kg of grain allows cattle to graze selectively; selection of husks and leaves improves cattle performance. Byproducts of the wet and dry milling industries can be supplemented to calves grazing corn residues to provide protein and energy. Optimal gains were observed when these byproducts were supplemented at approximately 2.5 kg/d to 250-kg growing calves. Gestating beef cows do not require supplemental inputs when grazing corn residue, if stocked appropriately. Alkaline treatment of crop residues improves their feeding value. Concentrations of up to 20% harvested corn residue treated with calcium oxide can be included in finishing diets with an average of 1.3% reduction in G:F when diets contain 40% wet or modified distillers grains. Conversely, when untreated corn residues are included in similar finishing diets, G:F is reduced by 13.4%. Calcium oxide-treated residues included in beef growing diets increases DMI and ADG without significant improvements in G:F. Calcium oxide treatment of corn residues has been evaluated in dairy diets by replacing corn or corn silage with variable results. Efficient use of nontraditional fiber sources, such as corn milling byproducts and corn residue, are critical to the future viability of ruminant animal production.

Effects of twenty percent alkaline-treated corn stover without or with yucca extract on performance and nutrient mass balance of finishing steers fed modified distillers grains-based diets.

Two experiments were conducted with 192 steers each (during the winter [November to May] or summer [June to October]) to evaluate 3 diets with or without Yucca schidigera extract in a 3 × 2 factorial on steer growth performance and N mass balance. One factor was diet (DM basis): 1) 5% untreated corn stover, 51% corn, and 40% modified distillers grains plus solubles (MDGS; CON); 2) 20% calcium oxide-treated corn stover (CaO added at 5% of stover DM), 40% MDGS, and 36% corn (TRT); or 3) 20% untreated corn stover, 40% MDGS, and 36% corn (NONTRT). The other factor was dietary extract at 0 (NOYE) or 1.0 g/d per steer (YE). No interaction between diet and YE was detected (P > 0.51) for growth performance and carcass traits in winter and only for DMI in summer. Final BW, ADG, DMI, or G:F were not different (P ≥ 0.28) between cattle fed CON and TRT, whereas cattle fed NONTRT had lesser ADG, HCW, and G:F compared to CON and TRT in the winter experiment. During the summer, final BW and ADG tended to be greater (P ≥ 0.07) for CON compared to TRT. Cattle fed TRT had reduced (P < 0.01) G:F compared to CON. No difference was observed (P ≥ 0.36) between YE and NOYE in the winter experiment for performance or carcass traits. In the summer, cattle fed YE had greater (P < 0.02) HCW, ADG, and DMI compared to NOYE. In the summer experiment, cattle fed YE had greater (P < 0.01) N intake, N excretion, and amount of N lost (kg/steer) compared to NOYE, but no difference (P = 0.33) was observed for percentage of N volatilized (% of excretion). Diet had no effect (P > 0.18) on amount (kg/steer) or percentage of N volatized in the winter or summer. All diets had similar amounts (P > 0.13) of DM and OM removed from the pen surface in both summer and winter. Feeding CaO-treated corn stover as a partial grain replacement had no impact on performance in winter but decreased G:F in summer. Although high-fiber diets increased the amount of OM on pen surfaces, they did not impact N volatilized. Feeding a Y. schidigera extract did not affect N balance or manure characteristics.

Digestibility and performance of steers fed low-quality crop residues treated with calcium oxide to partially replace corn in distillers grains finishing diets.

Two studies were conducted to identify methods for treating crop residues to improve digestibility and value in finishing diets based on corn grain and corn wet distillers grain with solubles (WDGS). In Exp. 1, 336 yearling steers (initial BW 356 ± 11.5 kg) were used in a 2 × 3 + 1 factorial arrangement of treatments with 6 pens per treatment. Factors were 3 crop residues (corn cobs, wheat straw, and corn stover) and 2 treatments where crop residues were either fed (20% diet DM) in their native form (NT) or alkaline treated with 5% CaO (DM basis) and hydrated to 50% DM before anaerobic storage (AT). Intakes were not affected by diet (F test; P = 0.30). An interaction between chemical treatment and residue (P < 0.01) was noted for final BW, ADG, G:F, and HCW. Greater final BW was observed for treated stover (4.6%) and straw (5.6%) compared with NT residues; however, AT and NT cobs were similar. Treated straw (9.7%) and stover (12.5%) resulted in greater ADG (P < 0.01) and improved G:F (10.7% and 5.0%, respectively; P < 0.01) compared with NT forms. In Exp. 2, ruminally fistulated steers (n = 5) were used in an unbalanced 5 × 7 incomplete Latin square design with a 2 × 3 + 1 factorial arrangement of treatments. Factors were crop residue (corn cobs, wheat straw, and corn stover) and chemical treatment (NT or AT) fed at 25% of diet DM. Greater DM (73.7% vs. 66.1%; P < 0.01), OM (77.0% vs. 68.5%; P < 0.01), fat (89.2 vs. 85.2; P = 0.02), and NDF (66.8% vs. 51.5%; P < 0.01) digestibilities were noted for AT than for NT. However, no difference (P > 0.10) was observed between control (46% corn; DM basis) and AT (31% corn; DM basis) for DM digestibility (70.7% vs. 73.7%) or OM digestibility (72.1% vs. 77.0%). Dry matter intakes were not different between treated and untreated diets (P = 0.38), but lower (P < 0.01) NDF intake was observed for treated diets (3.1 vs. 3.5 kg/d), suggesting that CaO treatment was effective in solubilizing some carbohydrate. These data suggest that 15% replacement of corn and 10% untreated residue with treated forage result in a nutrient supply of OM similar to that of the control. The improvements in total tract fiber digestibility that occurred when treated forages were fed may have been related to increased digestibility of recoverable NDF and not to increased ruminal pH. Feeding chemically treated crop residues and WDGS is an effective strategy for replacing a portion of corn grain and roughage in feedlot diets.