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Randomized complete block design experiments ( n = 6 experiments) evaluating steroidal implants (all from Merck Animal Health, Madison, NJ) were conducted in large-pen feedlot research facilities between 2015 and 2018 comparing an 80 mg trenbolone acetate (TBA) and 8 mg estradiol-17β (E 2 ) initial implant (Revalor-IH) and reimplanted with 200 mg TBA and 20 mg E 2 (Revalor-200; REPEATED) to a single 80 mg TBA and 8 mg E 2 uncoated; 120 mg TBA and 12 mg E 2 coated implant (Revalor-XH) at arrival (SINGLE) on growth and carcass responses in finishing heifers. Experiments occurred in Nebraska, Oklahoma, Washington, and Texas. Similar arrival processing was used across experiments where 17,675 heifers [initial body weight = 333 kg SEM (4.1)] were enrolled into 180 pens (90 pens per treatment with 65-240 heifers per pen) and fed for 145-222 d. Only REPEATED heifers were removed from their pen at reimplant. Diets contained monensin and tylosin, consisted of ingredients common to each region, and contained greater than 90% concentrate. Ractopamine hydrochloride was fed for a minimum of 28 d prior to harvest. Linear mixed models were used for all analyses; model-adjusted means for each implant group and the corresponding SEM were generated. Distributions of U.S. Department of Agriculture (USDA) quality grade (QG) and yield grade (YG) were analyzed as ordinal outcomes. No differences ( P ≥ 0.11) were detected for any performance parameters except dry matter intake (DMI), where SINGLE had greater ( P = 0.02) DMI (9.48 vs. 9.38 ± 0.127 kg) compared with REPEATED. Heifers implanted with REPEATED had greater ( P ≤ 0.02) hot carcass weight (HCW; 384 vs. 382 ± 2.8 kg), dressing percentage (64.54 vs. 64.22 ± 0.120%), and ribeye area (91.87 vs. 89.55 ± 0.839 cm 2 ) but less ( P ≤ 0.01) rib fat (1.78 vs. 1.83 ± 0.025 cm) and calculated YG (2.82 vs. 2.97 ± 0.040) and similar ( P = 0.74) marbling scores (503 vs. 505 ± 5.2) compared with SINGLE heifers. Distributions of USDA YG and QG were impacted ( P ≤ 0.03) by treatment such that REPEATED had fewer USDA Prime and YG 4 and 5 carcasses. Heifer growth performance did not differ between implant regimens, but HCW and muscling did, perhaps indicating that REPEATED may be suited for grid-based marketing, and SINGLE might be suited for heifers sold on a live basis depending upon market conditions and value-based grid premiums and discounts. However, these decisions are operational dependent and also may be influenced by factors including animal and employee safety, stress on animals, processing facilities, time of year, labor availability, and marketing strategies., (© The Author(s) 2020. Published by Oxford University Press on behalf of the American Society of Animal Science.)

The purpose of this experiment was to evaluate the effects of energy intake, implantation, and fat end point on feedlot performance and carcass composition of steers. Three hundred eighty-four yearling crossbred steers (368 +/- 23.1 kg) were allotted in a completely randomized design. Treatments were arranged in a 2 x 3 x 2 factorial experiment. Main effect factors were two levels of intake, three implant strategies, and two compositional fat end points at slaughter. The levels of intake were ad libitum (AL) and restricted (RS) intake (90% ad libitum). The three implant strategies were Revalor-S (REV) (120 mg trenbolone acetate, 24 mg estradiol), Synovex-Plus (SYN) (200 mg trenbolone acetate, 28 mg estradiol benzoate), and no implant (control). The compositional target end points were 1.0 and 1.4 cm s.c. fat cover over the 12th and 13th rib. Restricted-intake steers consumed 9.2% less (P < .01) DM than AL steers. Ad libitum-intake steers gained weight 15.5% more rapidly (P < .01) than RS-intake steers. Steers implanted with REV tended (P < .07) to gain faster than SYN steers, who in turn gained 15.2% more (P < .01) than control steers. Ad libitum-intake steers were 4.8% more (P < .01) efficient than RS steers. Steers fed to a targeted 1.4 cm s.c. backfat cover were 2.9% less (P < .05) efficient than steers fed to 1.0 cm, and steers implanted with either REV or SYN had similar (P = .47) feed efficiencies, whereas control steers had lower (P < .01) feed efficiencies. Steers fed to a targeted compositional fat end point of 1.4 cm had 1.3% higher (P < .01) dressing percentage (DP) than steers fed to 1.0 cm. Control and SYN steers had similar (P = .13) DP; however, REV steers had 6.1% greater (P < .01) DP than SYN steers. Steers fed to 1.4 cm s.c. fat end point had higher (P < .01) numerical yield grades than steers fed to 1.0 cm (3.34 vs 2.71). There was an interaction (P < .01) for intake level and implant for marbling score. Marbling scores were lower (P < .05) for RS x SYN and AL x REV than in other treatments. Steers on the RS x REV treatment were intermediate in marbling to all treatments except AL control, which was higher (P < .01) than RS x SYN, AL x REV, and RS x REV. No interaction for dry matter intake level and anabolic implants was observed for growth performance. The depression in carcass quality resulting from implanting is reduced as backfat increases from 1.0 to 1.4 cm at slaughter.

We conducted two trials to examine the effects of restricted vs full feeding and of grain processing method on feedlot performance, digestion, and mastication efficiency by Holstein steers in different growing-finishing systems. In Trial 1, 272 Holstein steers (177 +/- 9.98 kg) were blocked by weight and assigned to growing phase diets based on corn silage (SIL), steam-flaked corn that was either limit-fed (SFLF) or full-fed (SFFF), or whole corn that was limit-fed (WCLF) or full-fed (WCFF). Limit-fed steers were fed at levels predicted to allow daily gain of 1 kg/d. On d 112, all steers were switched to WCFF or SFFF diets until the mean BW of each treatment group was 545 kg. Overall, steers fed WCLF and SFLF during the growing phase and finished on SF were 8.1 and 6.6% more efficient at converting dietary ME to gain (P = .02 and .04, respectively) than steers in the SFFF group. In Trial 2, three ruminally and duodenally cannulated Holstein steers were fed whole (WC) and rolled corn (RC) diets at FF and LF intake in an incomplete replicated 2 x 2 switchback design. Ad libitum access to feed resulted in higher (P = .02) ruminal starch digestibility than did limit-feeding, and calves had higher total tract DM (P = .05) and starch (P = .03) digestion at the heavier BW. Limit-feeding whole corn resulted in increased particle size of masticate (P = .06) compared with full-feeding whole corn. Because of apparent differences in mastication efficiency between limit-fed and full-fed calves, grain processing method during periods of restriction and compensatory growth may be important considerations for managing growth in systems that incorporate limit-feeding.

We evaluated protein sources for finishing steers in two randomized complete block design experiments. Experiment 1 used 144 steers (334 kg) with 2 x 3 factorially arranged treatments. Basal diets contained .9% urea or 5.6% soybean meal (SBM) and were either not supplemented or supplemented with additional protein (2%) from blood meal-corn gluten meal (BMCG) or SBM. Steers fed urea-containing diets consumed 4.6% (P < .10) more feed than those fed SBM-supplemented basal diets. On the basis of carcass weights, steers fed diets containing SBM as the basal protein source were 3.8% (P < .10) more efficient than those fed urea-containing diets; supplying additional SBM improved gain efficiency (G/F) 4.3% (P < .10) compared with BMCG. In Exp. 2, 384 steers (367 kg) were fed diets containing 1.0% urea (DM basis) and 10% roughage as either sorghum silage (four diets) or alfalfa hay (two diets). Additional protein was either not provided or provided (2%) as SBM, sunflower meal (SFM), or a 50:50 (N basis) SBM:SFM blend in silage-containing diets; for diets containing alfalfa, additional protein was either not provided or provided (2%) as SBM. Averaged across roughage source, added SBM tended (P = .16) to increase ADG. Dressing percent decreased (P = .09) with added SBM but was higher (P = .04) with alfalfa as roughage source. Feeding alfalfa vs sorghum silage as the roughage source increased carcass adjusted ADG 4.3% (P = .06) and G/F 4.8% (P = .02). Supplementing high-grain diets with SBM enhanced diet utilization, but BMCG was of little value.

Two trials were conducted to determine the effects of steam-flaked sorghum grain bulk density on animal performance, cost of production, and propensity to induce ruminal acidosis in feedlot steers. In Trial 1, 336 yearling steers (343 kg; SEM = .346) were fed diets for 125 d that contained sorghum grain (82.5%, DM basis) flaked to .283 (L), .322 (M), or .361 (H) kg/L (i.e., 22, 25, and 28 lb/bu). Steers fed L consumed 3.2% less DM than those fed H (linear, P < .05), resulting in 6.9% lower ADG (linear, P = .02) and 3.6% lower gain efficiency (linear, P < .15). Sorghum grain flaked to M and L had 16 and 46% greater starch gelatinization than H (measured using differential scanning calorimetry; linear, P = .002). Dressing percentage increased linearly (P < .05) with increasing flake density, but no other carcass measurements were affected by treatment. Increasing flake density increased mill production rate linearly (P < .01), resulting in the lowest energy usage per unit of flaked grain for the H treatment. Trial 2 was an acidosis challenge study that incorporated six ruminally cannulated steers (422 kg; SEM = .129) into a replicated 3 x 3 Latin square experiment. Reducing flake density resulted in linear reductions in ruminal pH following intake challenge at 3, 33, and 36 h after the d-12 challenge (P < .05). There was a linear increase in the area between the pH vs time curve and a line at pH 5.5 (P < .01) and 5.0 (P = .09) with decreasing flake density (28.0, 25.2, and 18.2 pH-hours below 5.5 and 9.6, 7.3, and 3.9 pH-hours below 5.0 for L, M, and H, respectively). Cattle consuming L also tended to have higher VFA concentrations (mM) at 36 h after challenge (P = .12). There was no significant treatment effect on ruminal lactate. Flaking sorghum grain to .283 and .322 kg/L resulted in reduced intake and poorer animal performance compared with .361 kg/L (58.7% starch gelatinization), higher susceptibility to subacute acidosis, and higher costs of production.

Two experiments were designed to evaluate dietary N source and concentration on finishing steer performance and nutrient digestion. In Exp. 1, 100 steers were used in a randomized complete block design experiment with 2 x 2 + 1 factorially arranged treatments. Diets contained 1.93 or 2.24% N supplemented by urea or soybean meal (SBM), or 2.24% N supplemented by cottonseed meal (CSM). Steers fed SBM-supplemented diets gained 13% faster (P < .01) and were 9% (P < .01) more efficient converting feed to gain than steers receiving urea. Steers fed diets containing 2.24% N were 4% (P < .05) more efficient than those fed diets containing 1.93% N. Steers fed CSM-supplemented diets gained 6% (P < .10) less efficiently than steers receiving SBM. Increasing dietary N with urea from 1.93 to 2.24% decreased carcass weights 3%, whereas increasing dietary N with SBM increased carcass weights 3%. Carcass-adjusted gains were reduced 8% by increasing urea from .9 to 1.5% but increased 7% by increasing SBM from 6.1 to 10.5% of DM. In Exp. 2, four ruminally and duodenally cannulated steers (390 kg) were used in a 4 x 4 Latin square design experiment to evaluate urea and SBM supplementation on digestion. Diets contained no supplemental N, 1.84% N with urea or SBM as the supplement, or 2.16% N with SBM as the supplement. Total tract starch digestion, duodenal microbial N flow, and efficiency of microbial protein synthesis in the rumen were higher (P < .10) in steers fed SBM- than in those fed urea-supplemented diets. Supplementation with SBM increased metabolizable protein supply and dietary energy utilization.

The effects of the growth-promoting steroids estradiol-17 beta (E2), trenbolone acetate (TBA), and melengestrol acetate (MGA) in heifers on serum concentrations of E2 and trenbolone-17 beta (TBOH) were examined. Feed intake and growth performance were also measured. Serum concentrations of E2 and TBOH were measured on d 0, 1, 3, 5, 7, 13, 21, 28, 42, 56, 84, 112, and 140 in finishing heifers administered the following treatments: 1) control; 2) MGA, .5 mg per heifer daily; 3) Revalor-H (140 mg TBA + 14 mg E2); 4) Revalor-H + MGA; 5) Finaplix-H (200 mg TBA); and 6) Finaplix-H + MGA. Revalor-H implantation (Treatments 3 and 4) increased (P < .05) serum E2 concentrations; peak concentrations (67.5 pg/mL) occurred between d 21 and 56. Feeding MGA (Treatment 4) had no effect (P > .05) on this increase in serum E2 concentrations (63.3 pg/mL). From d 84 until d 140, serum E2 was greater (P < .05) for the Revalor-H treatment (average of 19 pg/mL) than for the control (7 pg/mL) or Finaplix-H treatments (6.5 pg/mL). Serum E2 concentrations increased numerically two- to threefold from d 56 to 140 in controls fed MGA, compared with controls not fed MGA. There was the expected increase in serum TBOH concentrations after TBA implantation in the Revalor-H and Finaplix-H treatments; concentrations were similar (P > .05) for Revalor-H (221 pg/mL) and Finaplix-H (280 pg/mL). After d 56, serum TBOH concentrations decreased in both treatments to 10 and 20% of these concentrations, respectively. Feeding MGA increased serum TBOH (P < .05). Dry matter intake by heifers did not differ among treatments. Feeding of MGA improved gains (P = .12) and efficiencies (P < .01) in nonimplanted heifers and had no effect (P > .4) on gains or efficiencies in Finaplix-implanted heifers.

Our objective was to determine whether beef heifers could be developed by delaying the majority of weight gain until the last third of the developmental period before the onset of the breeding season. Spring-born Angus x Hereford heifers were used in each of two consecutive years and were allotted at weaning to gain either .45 kg/d for the entire developmental period (yr 1 = 159 d, n = 40; yr 2 = 168 d, n = 40; EVENGAIN) or to gain .11 kg/d from d 0 to 112, followed by .91 kg/d from d 112 to 159 (yr 1, n = 40) or d 168 (yr 2, n = 40; LATEGAIN). Body weights and condition scores were determined at d 0, 112, and 159 (yr 1) or d 0, 112, and 168 (yr 2). Heifers were subjected to a 60-d breeding season. Frame scores and pelvic areas were determined at the conclusion of the breeding season. Actual daily gains for EVENGAIN heifers for yr 1 and yr 2 were .60 and .51 kg/d, respectively. LATEGAIN heifers gained .25 and .05 kg/d during the restricted phases from d 0 to 112, followed by 1.14 and 1.32 kg/d during the accelerated growth phases for yr 1 and 2, respectively. Body weight at the onset of the breeding season and weight at puberty were not different between treatments in either year. Age at puberty did not differ in yr 1, but, age at puberty in yr 2 was delayed (P < .01) in LATEGAIN (406.9 d) compared to EVENGAIN (386.3 d) heifers. The LATEGAIN and EVENGAIN heifers had similar pelvic areas, frame scores, and body condition scores in each year. First-service conception rates of both groups were similar in yr 1 (55.5 vs 55.3%). In yr 2, LATEGAIN heifers tended (P = .18) to have an increase in first-service conception rate compared to EVENGAIN heifers (71.1 vs 56.4%). No treatment differences occurred in either average age of conception or overall pregnancy rates at the conclusion of the breeding season for either year. The LATEGAIN heifers were developed to a similar BW on 12 (P < .01) and 2.5% (not statistically significant) less feed for yr 1 and 2, respectively, compared to EVENGAIN heifers. We interpret these data to indicate that delaying the majority of weight gain until late in heifer development may decrease costs without detrimental effects on reproductive performance.

In Exp. 1, 88 yearling steers (332 kg) were fed dry-rolled corn finishing diets to evaluate effects of dietary urea level on performance and carcass characteristics. Diets contained 0, .5, 1.0, or 1.5% urea (DM basis), which supplied all supplemental N, and 10% chopped prairie hay. Gains (P = .10) and gain efficiency (G/F; P < .05) were increased by .5% urea, with little improvement by additional urea. Regression analysis estimated optimal dietary urea at .9% of DM for ADG and G/F. Fat thickness (P < .05) and yield grade (P < .10) increased linearly with dietary urea level. In Exp. 2, four ruminally and duodenally cannulated steers (557 kg) were fed the diets used in Exp. 1 to evaluate effects of dietary urea on site and extent of digestion. True ruminal OM and starch digestion were increased 25 and 37%, respectively, by .5% urea, but higher urea levels did not differ from .5%. Flows of total N and microbial N to the duodenum were not affected by urea level. In Exp. 3, 100 yearling steers (347 kg) were fed dry-rolled corn finishing diets that contained 10% alfalfa hay as the dietary roughage to evaluate effects of dietary urea level on performance and carcass characteristics. Urea levels were 0, .35, .70, 1.05, or 1.40% urea (DM basis), with no other supplemental N provided. Dry matter intake (P = .10), ADG (P < .05), and G/F (P < .05) increased with intermediate concentrations of urea but decreased with the highest concentration. Regression analysis indicated that the optimal dietary urea level was .5% of DM for ADG and G/F. Urea increased dietary energy utilization but not metabolizable protein supply.

Three studies were conducted to evaluate amino acid utilization by cattle. In Exp. 1, five steers (580 kg) were fed 86% rolled corn diets with mixtures of amino acids containing up to 6 g/d DL-Met, 24 g/d L-Lys, 6 g/d L-Thr, and 3 g/d L-Trp. Treatments had little effect on ruminal fermentation, diet digestibility, N flow to the duodenum, or microbial efficiency. Ruminal concentrations of Met and Lys increased linearly (P < .05) with amino acid supplementation, whereas Thr responded quadratically, and Trp was not altered. In Exp. 2, four steers (414 kg) were used to measure effects of dietary monensin or laidlomycin propionate in high-grain diets supplemented with amino acids. Ionophores had no significant effect on ruminal fermentation or outflows of amino acids from the rumen. In Exp. 3, 100 steers (287 kg initial BW) were fed diets containing 1% of a nonprotein N source. Treatments were 1) no supplemental N (UREA), 2) UREA plus soybean meal (SBM), 3) UREA plus 2 g/d DL-Met, 8 g/d L-Lys, 2 g/d L-Thr, and 1 g/d L-Trp, or 4) UREA plus 4 g/d DL-Met, 16 g/d L-Lys, 4 g/d L-Thr, and 2 g/d L-Trp. During the growing period (diets based on whole-plant milo silage), gains were higher for SBM-supplemented steers than for UREA steers and intermediate for steers supplemented with amino acids. Few significant differences in performance were observed among treatments during the finishing phase (diets based on dry-rolled corn) or for the entire experiment, but cattle fed SBM or amino acids tended to be fatter and have better marbling scores and quality grades. Amino acids did not greatly alter ruminal fermentation or cattle performance.

Every 3 mo for a 2-yr period, two weaned Holstein steer calves (94.5 kg) were randomly assigned to each of four slaughter age groups (3, 6, 9, and 12 mo). Urea dilution was performed before slaughter, and urea space (US) was calculated as total volume and as a percentage of body weight (BW) and empty body weight (EBW). The relationships between US (kg, % EBW and % BW), BW, and EBW and carcass soft tissue composition (protein, fat, moisture, and ash) were studied. One- and two-pool models were fitted using the urea dilution data and the coefficients of those equations (zero time, A + B), and the intercepts of compartments A and B were used to estimate body volume. Body weight and EBW effectively predicted the amount of water, fat, and protein in the carcass soft tissue. Equations expressed in kilograms were more accurate than those expressed as percentages. Urea space overestimated body water, probably because of the fast rate of urea disappearance in plasma. Correlation coefficients between US and carcass soft tissue water (kg) based on the pooled data ranged from .74 at 6 min to .48 at 42 min after infusion. The biexponential models coefficients explained more of the variation of carcass soft tissue composition than US; correlation coefficients using volume B and the soft tissue composition (in kg) with pooled data were .78 (water), .68 (fat), .69 (ash), and .76 (protein). The relationships between A and soft tissue composition were weaker (water .59, fat .51, ash .58 and protein .59). The highest correlation coefficients were obtained when A + B was used for water, fat, ash, and protein (.83, .70, .74 and .81, respectively). Equations combining BW, EBW, and two-model coefficients (A, B, A + B) explained much of the variation of soft tissue composition. No significant benefit was found in using the urea space at various times after infusion over BW or EBW alone to estimate carcass soft tissue composition in Holstein steers.

We studied the effects of supplement CP concentration on performance and forage use of cattle allowed ad libitum access to ammoniated wheat straw. During two consecutive winters, crossbred beef cows in late gestation (n = 87 in 1990-1991, n = 84 in 1991-1992) were used in a randomized complete block design with three pens per treatment. Cows were stratified by weight, body condition score (BCS), age, and breed and randomly assigned within strata to 1) control (C, no supplement), or 2 kg/d of 2) low-protein (LP) supplement (12% CP), 3) moderate-protein (MP) supplement (20.1% CP), or 4) high-protein (HP) supplement (31.7% CP) (DM basis). The feeding period was 84 d in 1990-1991 and 60 d in 1991-1992. Supplementation (C vs LP, MP, or HP) increased (P < .01) cow weight gains (32.7 vs 60.7, 62.8, and 72.4 kg, respectively) and improved (P < .01) BCS. Calf birth weights, weaning weights, and ADG were not affected by treatment (P > or = .20). Average calving date, percentage of cows cycling at the start of the breeding season and percentage pregnant after a 60-d breeding season were also similar (P > .20) among treatments. Sixteen ruminally fistulated steers (482 kg, four steers per treatment) were blocked by weight and assigned to the same four supplements in a 30-d digestion trial. Supplementation increased (P < .01) digestible DMI and forage DMI (P < or = .04) and tended (P = .09) to increase digestible NDF intake but did not alter (P > or = .15) apparent DM or NDF digestibility.(ABSTRACT TRUNCATED AT 250 WORDS)

Four ruminally and duodenally fistulated, 2-yr-old Angus x Hereford steers (average initial BW = 370 kg) were used to evaluate the effect of method of processing supplemental alfalfa on intake and digestion of dormant bluestem-range forage (2.8% CP, 78% NDF). Treatments (4 x 4 Latin square) were 1) control, no supplement; 2) ground and pelleted alfalfa hay (PELLET; 21% CP, 37% NDF); 3) ground and pelleted dehydrated alfalfa (DEHY; 21% CP, 44% NDF); and 4) longstem alfalfa hay (HAY; 20% CP, 37% NDF). All supplements were from a single cutting of alfalfa and fed at .5% BW (as-fed basis). Supplementing steers with alfalfa increased (P < or = .07) bluestem forage OM intake (FOMI); total OM intake (TOMI); true ruminal OM digestibility; total tract OM digestibility (TTOMD); total N, microbial N, and nonammonia-nonmicrobial N (NANM) flows to the duodenum; ruminal OM and fluid fill; fluid dilution rates; dietary DE concentration; and ruminal total VFA and NH3 N concentrations. Because of the enhanced FOMI and TOMI associated with alfalfa supplementation and the concomitant improvement in TTOMD, digestible OM intake (DOMI) also increased (P < .01) when supplemental alfalfa was fed. Method of processing alfalfa had little impact on forage utilization, except FOMI (P = .11), TOMI (P = .10), and ruminal OM fill (P = .09) tended to be greater when supplemental alfalfa pellets were dehydrated. Similarly, processing method tended to alter the molar proportions of some minor VFA. In conclusion, alfalfa supplementation exerted a dramatic impact on utilization of low-quality forage.(ABSTRACT TRUNCATED AT 250 WORDS)

Three experiments evaluated whether effects of altered frequency of supplementation on forage use and cow performance depended on supplement CP concentration and (or) grain type when fed to cattle eating low-quality forages. All experiments included supplementation frequency (daily = 7x; three times weekly = 3x) as one factor in a factorialized arrangement of treatments. In Exp. 1 and 2, the second factor was supplement CP concentration (10, 20, 30, and 40% CP), altered by changing the ratio of soybean meal to sorghum grain in supplements. Supplements were fed at 13.9 and 14.1 kg of DM/wk for Exp. 1 and 2, respectively. In Exp. 3, the second factor was supplement grain type (sorghum grain or corn) and supplements containing 21% CP were fed at 14.8 kg of DM/wk. In Exp. 1, eight ruminally fistulated steers (456 kg) consumed wheat straw ad libitum. Pregnant beef cows grazing dormant tallgrass prairie were used in Exp. 2 (475 kg; n = 128) and 3 (504 kg; n = 120). In Exp. 1, reducing supplementation frequency decreased (P < .01) straw intake but increased (P < or = .03) DM and NDF digestion. As CP concentration in supplements increased, straw DMI (P = .06) increased quadratically, whereas DM and NDF digestion increased linearly (P < .01). In Exp. 2, increasing CP concentration in supplements enhanced cows' ability to maintain BW and condition up to calving, with decreasing magnitude of difference between treatments at higher CP concentrations (P < .01). Increasing CP in supplements fed to the dams linearly (P = .05) increased calf weaning weight in Exp. 2. In Exp. 2 and 3, reducing supplementation frequency increased (P < or = .02) winter weight loss through calving. Grain type did not significantly affect most performance variables. In summary, response to supplementation frequency was not dependent on supplement CP concentration or grain type. Daily supplementation maximized forage intake and cow performance, although the magnitude of performance differences was not large.

In 24 individually housed feedlot steers that weighed 275 kg, clostridial vaccines were compared for size of injection site reactions, systemic inflammatory response caused by vaccination, and impact on feed consumption. Vaccines were a bacterin/toxoid containing antigens from multiple clostridial species (7-way), and a Clostridium perfringens type C and D toxoid; sterile physiologic saline solution was used as the control. Injection site reactions were observed in all vaccinated cattle. Differences in size of lesions were found, with cattle given the 7-way vaccine (7-way group) having the largest lesions. The inflammatory-response to vaccination, measured by serum concentration of the acute-phase protein haptoglobin, was significantly (P < 0.05) increased in both vaccinated groups over that of controls. However, the 7-way group had higher postinjection values than did the group given type C and D toxoid. The 7-way group had a significant (P < 0.05) 20% decrease in feed consumption in response to the second injection of vaccine. These findings are indicative of potential negative effects of multiple clostridial vaccinations.

The relationship between serum-neutralizing antibody against Fusobacterium necrophorum leukotoxin and hepatic abscesses was investigated in cattle fed diets supplemented with or without tylosin. Sixteen cattle (eight each in tylosin and in control groups) were inoculated intraportally with F. necrophorum. Ultrasonographic scanning showed that all control animals developed hepatic abscesses after inoculation. In the tylosin group, two animals were free of abscess by d 7 and one was free by d 14. Leukotoxin-neutralizing antibody titers were low on d 0, but increased (P < .05) markedly after intraportal inoculation in both groups. In a second study, blood was collected at the time of slaughter from 141 feedlot cattle (36 fed diets with tylosin and 105 fed diets without tylosin), and livers were examined for presence or severity of hepatic abscesses at slaughter. The incidences of hepatic abscesses were 32% in the control group and 6% in the tylosin group. Antibody was detected in all animals; however, antibody titers were greater (P < .05) in cattle with abscessed liver than those without, and greater (P < .01) in the nontylosin than in the tylosin group. Abscess score and antibody titer were correlated (r = .34; P < .0001). We conclude that F. necrophorum leukotoxin is highly antigenic and that anti-leukotoxin antibody titer is related to the severity of hepatic abscesses.

One feedlot trial (116 d; 192 steers) with a factorial arrangement of treatments was conducted to determine effects of supplemental fat and ionophores in corn-based finishing diets. Factors were level of fat (0 or 4% tallow) and ionophore type (none [N], lasalocid [L], monensin plus tylosin [MT], or daily rotation of L and MT [LMT]); L, M, and T were fed at 31, 25, and 10 ppm (DM basis), respectively. Fat and ionophore interacted for DMI (P < .10), ADG (P < .01), and gain:feed G/F, P < .05). Compared with 0%-fat diets, 4% fat decreased (P < .005) DMI by steers fed MT by 8.9%. In 0%-fat diets, MT increased (P < .05) ADG and G/F compared with N or L; however, this increase was negated or reversed in 4%-fat diets. Fat and ionophore interacted (P < .16) on dietary NE concentration. In the 0%-tallow diet, MT increased NEm and NE(g) by 5.1 and 7.0%, respectively, but MT had not effect on NE concentration of the 4%-tallow diet. Alternate feeding of L and MT did not increase animal performance above that of separate, continuous feeding. Six ruminally fistulated steers were used in a metabolism study to evaluate potential mechanisms underlying the interactions observed in the feedlot trial. Treatments were the same as the feedlot trial, except that LMT was not included. Ruminal digesta kinetics were not altered (P > .30) by the addition of fat or ionophores to the diet. Fat and ionophore interacted (P < .05) for molar proportions of ruminal acetate and propionate.(ABSTRACT TRUNCATED AT 250 WORDS)

Forty Angus x Hereford 2-yr-old primiparous cows (358 kg) were used to determine the effects of source and amount of CP on performance, reproductive function, and metabolic status of suckled primiparous cows. A 2 x 2 factorial treatment arrangement was used; cows received either 100 or 150% of NRC recommendations for CP in diets that contained either soybean meal (low escape = L) or corn gluten meal/blood meal (high escape = H) as the principal supplemental protein source. Resulting treatments were 100-L, 100-H, 150-L, and 150-H. Cows were individually fed diets for 100 d or until they were observed to be in standing estrus. Diets were isoenergetic and limit-fed to meet NRC recommendations for NE, Ca, and P for 364-kg, 2-yr-old primiparous cows producing 4.5 kg of milk daily and gaining .23 kg/d. Increased CP tended (P = .09) to increase ADG in cows, but body condition score was unaffected. Increased CP and use of a CP source with higher potential for ruminal escape increased ADG in calves from d 0 to 97 (P = .002 and .04, respectively), which corresponded with numerical changes in milk production. Feeding high escape CP sources decreased plasma glucose and urea N (P = .04 and .0001, respectively). Increased CP tended (P = .12) to increase plasma glucose and increased (P = .0001) plasma urea N. Treatment had no effect on profiles of LH or progesterone. Although numerical differences in conception rate seemed large for 100-L compared with the remaining treatments, statistical significance was not detected.(ABSTRACT TRUNCATED AT 250 WORDS)

One hundred forty British x Exotic crossbred, yearling steers (370 kg) were used in a 2 x 2 factorial experiment to evaluate main effects and the interaction of grain type (steam-flaked sorghum grain [SFSG] or steam-flaked corn [SFC]) and level of supplemental far (0 or 4% yellow grease [YG]) on feedlot performance, diet NE concentration, carcass traits, and chemical composition and sensory properties of longissimus muscle. Steer performance and estimated dietary NEm and NEg values were not different between SFSG and SFC. Supplemental YG improved (P less than or equal to .05) gain/feed and estimated NEm and NEg of both SFSG and SFC diets. Compared with steers fed SFSG, steers fed SFC had a more yellow (P less than .05) subcutaneous fat color. Supplemental YG had an additive effect (P less than .025) on yellow color of subcutaneous fat but improved (P less than .08) the lean color of longissimus muscle. Grain type or supplemental YG had no effect on sensory properties or mechanical shear of longissimus muscle. Longissimus muscle cholesterol content was elevated (P less than .05) by supplemental YG (.49 vs .52 mg/g of wet tissue for 0 vs 4% YG, respectively); however, the biological significance of this result is questionable. Similarly, effects of YG on increased (P less than .05) stearic acid concentration and a higher concentration (P less than .05) of linoleic acid measured in longissimus muscle of steers fed SFSG vs SFC were small in magnitude. These data indicate that under the conditions of this experiment, NE contents of SFSG and SFC were similar.(ABSTRACT TRUNCATED AT 250 WORDS)

Two experiments were conducted to evaluate performance and forage utilization characteristics of beef cattle fed ammoniated wheat straw (AWS) unsupplemented except for minerals or supplemented with energy and protein. In Exp. 1, 194 crossbred beef cows (BW = 472 kg) in late gestation were allotted by weight, breed type, and age during two consecutive winters to 12 drylot pens (three pens/treatment) for a 60-d feeding trial. The AWS (3% NH3 wt/wt) was tubground through a 7.6-cm screen, and cows were allowed ad libitum access to the AWS. In Exp. 2, 16 ruminally fistulated Angus x Hereford steers (BW = 300 kg) were blocked by weight and randomized to treatments in a 35-d intake-digestion trial. Daily supplementation treatments in both experiments were Control, no supplemental energy or protein; LSG, 1.36 kg of sorghum grain (SG); HSG, 2.72 kg of SG; and SG + SBM, 1.02 kg of SG + .34 kg of soybean meal (SBM). All animals received .23 kg of mineral mixture formulated to meet a pregnant cow's mineral requirements. Supplements LSG and SG + SBM were fed to provide the same daily ME, and HSG and SG + SBM were fed to provide the same daily CP. Cows were managed as one group during and after calving. In Exp. 1, all supplements increased gain (P less than .01) vs Control, and cows fed SG + SBM had higher (P = .05) gains than those fed LSG. The SG + SBM supplement increased (P less than .01) change in cow body condition score compared with LSG.(ABSTRACT TRUNCATED AT 250 WORDS)

Wheat and high-moisture corn (HMC) were fed singly and in three combinations using dry-rolled wheat (DRW) (ratios of 75:25, 50:50, and 25:75, respectively, Trial 1), or singly and in two combinations using steam-rolled wheat (SRW) (ratios of 67:33 and 33:67, respectively, Trial 2) to finishing beef cattle fed a high-concentrate diet. In situ rate of starch digestion (Trial 3) was measured on grains used in Trial 1 (excluding the 25 HMC: 75 DRW mixture) and ground dry corn. In Trial 1 (132 d), gain/feed did not differ (P greater than .10); however, final weight, hot carcass weight, and ADG decreased linearly (P less than .05) and DMI exhibited a cubic response (P less than .05) as the percentage of wheat in the diet increased. Carcass characteristics were not different. In Trial 2 (113 d), there were no differences attributable to treatment for ADG, DMI, gain/feed, or carcass characteristics. Positive associative responses for gain efficiency (gain/feed) were greatest for the first increment of wheat addition (25% DRW and 33% SRW in Trials 1 and 2, respectively) and for the early portion of the feeding period (57 and 28 d for Trials 1 and 2, respectively), indicating a more rapid diet adaptation and(or) less propensity for subacute acidosis. In Trial 3, the treatment grains or mixtures did not differ in rate of starch digestion. Although the differences were not statistically significant, starch in the 100% wheat diet was digested twice as fast as the 100 or 75% HMC mixtures.(ABSTRACT TRUNCATED AT 250 WORDS)

A 111-d finishing study evaluated animal growth and carcass characteristics using 138 steers (366 kg) in a randomized complete block design with a 2 x 3 factorial arrangement of treatments. The dietary treatments consisted of no supplemental fat or 3.5% tallow or soybean oil soapstock (SS) fed with .6% and .9% dietary Ca. Fat increased DMI (P less than .05) but interacted with Ca level (P less than .05) for gain/feed and ADG. All diets containing fat or .9% Ca were converted more efficiently to gain than the .6% Ca, no supplemental fat diet (P less than .05). The .9% Ca interacted with fat source to decrease gain (P less than .05) and tended to decrease efficiency in the tallow diet but improved efficiency (P less than .05) and tended to improve gain in the no-fat diet. In the SS diet, .9% Ca had no effect on ADG, DMI, or efficiency of gain. Fat addition increased backfat (P less than .10) and interacted with Ca on hot carcass weight, final weight, and dressing percentage (P less than .05). Feeding fat increased the proportion of 18:0 (P less than .02) and decreased the proportion of 16:1 fatty acids (P less than .06) in intermuscular fat. A replicated 3 x 3 Latin square design, using six Holstein steers (349 kg) fed three diets, with no supplemental fat or 3.5% SS or tallow with 1.0% Ca, was used to explore the effects of fat sources when fed with high Ca on digestion and metabolism. Ruminal fluid pH was higher (P less than .10) when steers were fed fat. Adding fat did not affect (P greater than .10) duodenal or ileal pH, VFA proportions or total concentration, or ruminal liquid volume or flow rate. Liquid retention time was shorter and liquid rate of passage was higher (P less than .05) with dietary fat addition. Adding fat did not affect site or extent of starch or DM digestion. There was net synthesis of 16:0, 18:0, and 18:1 fatty acids in the rumen. When steers were fed tallow, synthesis of 16:0 and 18:0 fatty acids in the rumen was lower (P less than .10) than when steers were fed SS. Feeding fat tended to decrease (P = .11) bacterial N flowing at the duodenum but did not affect nonbacterial N or total N. Fat addition seems to affect ruminal kinetics, and the effects may vary with fat source, particularly relative to fatty acid synthesis and digestion.

Ruminal samples were collected at slaughter from 98 steers consuming a high-grain diet and receiving either no fat, or 2, 4, 6, or 8% supplemental tallow. Tallow supplementation tended (P = 0.11) to increase average ciliated protozoan numbers, however, the occurrence of defaunated animals was higher in the 8% fat treatment than in the control group. Entodinium spp. were the only protozoans that survived in all treatments, and total numbers ranged up to 3.2 x 10(6)/g of ruminal contents. Although increasing tallow supplementation induced a defaunating effect in many animals, the response was unpredictable and protozoa occasionally proliferated irrespective of fat level.

Eight Holstein steers (four at 300 kg, four at 406 kg) fitted with an elevated carotid artery, hepatic portal and mesenteric venous catheters, and abomasal and ileal cannulas were used in several 4 x 4 Latin square experiments to evaluate small intestinal starch digestion. They were fed alfalfa hay at 1.5% of BW and abomasally infused with water or glucose, corn starch or corn dextrin (one carbohydrate per Latin square) at 20, 40 or 60 g/h, with subsequent determination of small intestinal disappearance and net portal glucose absorption. Increasing the amount of all three carbohydrates infused abomasally increased the amount of carbohydrate disappearing in the small intestine. Increased infusion of glucose caused a continual increase (linear, P less than .01) in net glucose absorption, whereas net glucose absorption for starch and dextrin was maximal at the 20 g/h infusion (quadratic, P less than .05). With the 60 g/h infusion, 94% of the glucose but only 38% of starch and 29% of small intestinal dextrin disappearance could be accounted for as net glucose absorption, leaving a large portion of starch and dextrin disappearance unaccounted for. Of the infused starch and dextrin passing the ileum, 5.8 and 7.3%, respectively, was unpolymerized glucose, indicating that, at least in the distal small intestine, complete starch hydrolysis exceeded the capacity for glucose disappearance. It is concluded that only about 35% of the raw corn starch disappearing in the steer's small intestine resulted in net portal glucose absorption.

Fluctuations in ciliated protozoan concentrations were monitored in 40 individually fed crossbred heifers that were stepped up to an 85% concentrate diet either slowly (12 days) or rapidly (3 days), with or without monensin (30 ppm). Ruminal fluid was withdrawn from all animals by stomach tube at the start of the study, after each group reached full feed, and at 14-day intervals thereafter throughout the finishing period until termination (day 119). Neither monensin nor speed of step-up affected (P greater than 0.10) total protozoan concentrations, ruminal pH, or lactic acid concentrations. Average protozoan concentrations peaked on day 5, progressively declined until day 56, and then increased (P less than 0.05), suggesting an adaptation to ruminal conditions. Concentrations of Isotricha spp. were higher (P less than 0.05) on the final two sampling dates than at any other time. After day 28, Entodinium, Isotricha, and Polyplastron were the only surviving genera. Protozoa were not detected in 11 heifers on day 42 and day 56, but only two animals were defaunated on day 119, indicating either exogenous or endogenous refaunation. Average protozoan concentrations were not different (P greater than 0.25) between ruminal samples collected by stomach tube the day before slaughter (2.8 x 10(5)/g) and digesta samples collected the next day (1.6 x 10(5)/g). In feedlot cattle, defaunation apparently is transitory and individual animals harbor a dynamic protozoan population that fluctuates in response to changing ruminal conditions.

Two trials that utilized 356 yearling steers were conducted to evaluate the effects of fat sources (3.5% of diet dry matter) in steam-flaked milo finishing diets. Fats differed in fatty acid composition and level of free fatty acids. In Trial 1, soybean oil, tallow and yellow grease were compared to a nonfat control. Feeding fat increased (P less than .05) daily gain, feed efficiency, estimated diet NE concentration, carcass weight and dressing percentage of steers. In Trial 2, fat treatments were control, acidulated soybean soapstock (SBSS), tallow, a blend of 70% SBSS:30% tallow, and yellow grease. Feeding tallow or the SBSS:tallow blend improved (P less than .05) feed efficiency and estimated dietary NE compared to control. Proportions of palmitic, stearic, oleic, linoleic and linolenic acid in longissimus muscle of steers were altered (P less than .05) by source of supplemental fat. Potential variability in animal response to fat blends was demonstrated by differences in animal response to yellow grease in the two trials. It was concluded that fats vary in feeding value and may alter carcass composition, contrary to putative thought. Further, potential associative effects of fat blends and interactions of fat with other dietary components in high-grain finishing diets require further investigation.

Ruminal samples were collected at slaughter from 364 unfasted steers fed different finishing diets to obtain information on numbers and species distribution of ciliated protozoa in feedlot cattle. Total numbers of protozoa averaged 1.59 X 10(5)/g of ruminal contents. A total of 47 steers (12.9%) were defaunated, but 4.1% of the steers possessed numbers of protozoa greater than 10(6)/g. Entodinium species did not always dominate the protozoan populations; 41 faunated steers (11.2%) were devoid of entodinia, and 79 additional steers (21.7%) possessed populations dominated (greater than 50%) by other genera. Isotricha was the most commonly occurring genus supplanting Entodinium, but Polyplastron and Epidinium were frequently present in high concentrations. Tallow and soybean soapstock supplementation reduced (P less than .05) numbers of protozoa in steers consuming wheat diets. However, yellow grease supplementation did not affect numbers of protozoa in steers fed either sorghum or corn diets. Average ruminal pH was 6.20 on the wheat diet, 6.05 on the corn diet, and 5.69 and 6.23 for the two sorghum diets, respectively. We found no correlation between ruminal pH and numbers of protozoa on any diet. The presence of relatively high protozoan concentrations and few defaunated animals in feedlot cattle necessitates reevaluation of the role that ciliated protozoa play in ruminal metabolism of animals fed processed, high-concentrate diets.

Two experiments were conducted to determine the influence of dietary roughage concentration and feed intake on finishing steer performance and ruminal metabolism. In Exp. 1, 126 steers (334 kg) were used in a completely randomized design and fed (120 d) diets of steam-rolled wheat without roughage or containing 5, 10 or 15% roughage (50% alfalfa hay:50% corn silage). Steers fed 5 or 10% roughage gained faster (quadratic, P less than .05) and were more efficient (quadratic, P less than .05) than steers fed 15% or no roughage. In Exp. 2, six ruminally cannulated steers (447 kg) were used in a 6 x 6 latin square design and fed (twice daily) diets of steam-rolled wheat without roughage or containing 5 or 15% alfalfa hay at twice or three times NE required for maintenance. Increasing dietary roughage increased (linear, P less than .01) ruminal liquid passage 38%, indigestible ADF passage 63%, Yb-labeled wheat passage 75% and fiber fill 31%. The rate of in situ starch digestion tended to increase (linear, P = .16), and ruminal VFA concentration was 40 mM higher (P less than .01) at 4 h after feeding with increased roughage. Increased feed intake increased (P less than .05) ruminal starch fill, fiber fill, liquid fill and liquid passage 23%, Yb-labeled wheat passage 50% and Dry-labeled hay passage 20%. It reduced protozoa five- to sixfold (P less than .01) but doubled total bacterial counts (P less than .01). Ruminal NH3N was lower (P less than .01) and total VFA concentration was 50 mM higher (P less than .01) at 4 h after feeding. The acetate:propionate ratio was reduced from 2.3 to 1.3 (P less than .01) with increased intake. Adding roughage to a steam-rolled wheat diet increased passage and tended to increase rate of starch digestion; increased feed intake with its associated effects on ruminal fill and passage dramatically shifted the microbial population and fermentation end products.

The effect of ruminal degradable protein source in roughage diets on nutrient digestibility and animal growth was evaluated in two trials using lambs. In trial 1, two qualities of alfalfa and smooth brome hays replaced 0, 15, 30 or 100% of an ammonia (NH3)-treated corn cob negative control diet in a digestion trial using 26 mixed breed wethers (31.8 kg). Fifteen or 30% inclusion of hay increased (P less than .01) dry matter (DM) intake, regardless of hay type or quality. Cell wall intake was highest for 100% high quality brome hay. Positive associative action on digestibility of DM and cell walls occurred with 30% of each hay tested when diets were fed ad libitum. Measured at equal intakes, DM and cell wall digestibilities were affected by forage type X level and forage quality X level interactions (P less than .01), which showed that the magnitude of associative action was greater for 30% of high vs low quality and alfalfa vs brome hay, respectively. Magnitude of associative response on cell wall digestibility was more highly correlated to degradable N (r = .88) than cell solubles (r = .64) content of hay. In trial 2, 72 young growing lambs were allotted to three sources of supplemental ruminal degradable N (NH3, casein, corn steep liquor) superimposed upon two levels of alfalfa hay (0 or 30% of diet DM). Diets containing 0% alfalfa were supplemented with ruminal escape protein equivalent to that supplied by 30% alfalfa hay.(ABSTRACT TRUNCATED AT 250 WORDS)

Three trials involving 513 exotic crossbred steers were conducted to determine the effect of zeranol implanting in the suckling and growing phases on subsequent feedlot performance and carcass characteristics. Treatments were 1) unimplanted control, 0000; 2) implanted twice in the finishing phase, 00II; 3) implanted in the growing phase and twice in the finishing phase, 0III; 4) implanted in the suckling phase and twice in the finishing phase, I0II; 5) implanted in the suckling and growing phases with a single implant in the finishing phase, III0; and 6) implanted in the suckling and growing phases and twice in the finishing phase, IIII. Implanting in the suckling period did not significantly affect preweaning gain. Implanting in the growing period produced a treatment x trial interaction (P less than .05), but zeranol increased gains by an average of 8.4% over the three trials. Growing period gain was not influenced by implanting during suckling. Implanting twice during the finishing period increased gain (P less than .05) over unimplanted and III0 steers. Finishing gain was not influenced by previous suckling and(or) growing implant treatment. Lifetime ADG of steers was increased (P less than .05) by all implant treatments compared with unimplanted controls. Zeranol tended (P = .14) to improve feed conversion in the finishing phase. All implant treatments increased hot carcass weight (P less than .05), and all but III0 reduced fat deposition, as indicated by lower quality grade (P less than .05). Other carcass characteristics were not significantly affected by treatment. These trials demonstrated that implanting in the suckling and(or) growing phases of production did not reduce performance in the finishing phase.

The influence of mechanically separated alfalfa fractions on intake, digestibility and rate of ruminal passage was investigated using 48 lambs (32 kg) in a digestion trial. Whole plant pre-bloom alfalfa (25% crude protein) or fractions (presscake, dehydrated presscake, protein coagulum, dehydrated protein coagulum, whole juice or deproteinized juice) were added to a 3% ammonia (NH3)-treated corn cob negative control diet at levels equal to 20% wholeplant alfalfa dry matter (DM); eight treatments, six lambs/treatment. Ad libitum intake was greater (P less than .05) for alfalfa fiber (presscake) or juice supplemented diets compared with 20% direct cut alfalfa. Dry matter intake, digestibility of DM and cell walls, and rate of passage were highly correlated when diets were fed ad libitum. At equal DM intakes, dehydrated vs wet presscake increased (P less than .05) DM and cell wall digestibility. Heating of the protein may have reduced degradation rate and consequently a slower release of nutrients for microorganisms in the rumen. Whole vs deproteinized juice increased digestibility of cob DM (P = .11) and cell walls (P = .13), suggesting a response to level of degradable alpha-amino N. Whole and deproteinized juice increased cell wall digestibility compared with the negative control by 23.0 and 18.5 percentage units, respectively, suggesting that degradable alpha amino-N and cell solubles or other nutrients interacted to maximize microbial fiber digestion. Total and branch-chain volatile fatty acids measured at 6, 12 and 18 h post-feeding were highly correlated with nutrient digestibility. Ruminal NH3-N measured at 18 h was negatively correlated with dry matter (r = -.74) and cell wall (r = -.72) digestibility, showing that alfalfa supplies nutrients required by ruminal microorganisms for NH3 assimilation and fiber digestion. The mode of alfalfa associative action in high fiber diets is in supplying ruminal microorganisms with degradable protein and (or) other nutrients, rather than altering ruminal retention time.

Three trials evaluated associative action of alfalfa in ammonia (NH3)-treated corn residue diets and(or) potential ruminal degradable protein X escape protein interactions. In trial 1, 128 crossbred steers (250 kg) were fed 0 or 3% NH3-treated residue diets replaced by 0, 15, 30 or 100% of alfalfa hay. Basal diets were formulated to contain adequate metabolizable and crude protein but were nearly devoid of ruminal degradable protein. Ammonia treatment increased (P less than .02) dry matter (DM) intake of residues. Pooled across residue treatment, intake increased linearly (P less than .01) with increased level of alfalfa. A residue treatment X level of alfalfa interaction (P less than .02) for daily gain resulted because the response to level of alfalfa was linear (P less than .01) for nontreated residues and quadratic (P less than .01) for NH3-treated residues. Similar responses (P less than or equal to .07) were found for efficiency of gain, indicating that addition of 15 or 30% alfalfa promoted greater associative action for combinations involving NH3-treated vs nontreated residues. In an in vitro trial (trial 2) with the same corn cob and alfalfa diets used in trial 1, NH3 treatment increased (P less than .01) in vitro DM disappearance and rate of cell wall digestion of corn cobs. Alfalfa had no effect on rate of nontreated cob cell wall digestion, but increased (P less than .01) the rate for NH3-treated cobs.(ABSTRACT TRUNCATED AT 250 WORDS)