This study was designed to investigate the effects of a humate supplement on rumen ammonia N (RAN), serum urea N (SUN) and live performance i n beef cattle finishing diets. Twenty-four English cross steers (BW 432+5 kg) were stratified by weight, randomly assigned to individual pens and fed one of the four diets, containing 0 (control), 0.5, 1.0 or 1.5% humiclfulvic acid, for 56 d. Control diets contained 33.3 mgl kg monensin. Steers were weighed at d 0, 28 and 56. Blood (jugular veni-puncture) samples and rumen (esophageal tube) samples were taken prior to feeding on d 0 and there after prior to and 4 h post feeding on d 28 and 56. Rumen fluid p H was determined immediately, acidified with HCl and stored (-2OC) for subsequent RAN analysis. Serum was also stored (-2OC) for analysis of SUN. During the 56 d period there was no difference in DMI (P>0.58), ADG (P>0.24) or G:F (P>0.28) between treatments. There were no two or three way interactions for SUN (P>0.95), RAN (P>0.87) or rumen p H (P>0.15). There was a tendency for a cubic response (P

Two experiments were conducted to examine the effect of growth rate to similar age or BW on fat deposition in stocker cattle grazing dormant native range (DNR) or winter wheat pasture (WP). In each experiment, fall-weaned Angus steers were randomly allotted to 1 of 4 stocker production programs: 1) control, 1.02 kg/d of a 40% CP cottonseed meal-based supplement during grazing of DNR (CON); 2) corn/soybean meal-based supplement fed at 1% of BW during grazing of DNR (CORN); 3) grazing WP at a high stocking rate to achieve a low rate of BW gain (LGWP); and 4) grazing WP at a low stocking rate to achieve a high rate of BW gain (HGWP). In Exp. 1, a subset of steers (3 steers per treatment) was harvested after winter grazing (138 d) at similar age. The remaining WP steers were transitioned into the finishing phase, whereas DNR steers were allowed to graze the same native range pastures for another 115 d without supplementation before entering the feedyard. In Exp. 2, steers grazed their respective pastures until each treatment reached an estimated HCW of 200 kg (262, 180, 142, and 74 d, respectively, for the CON, CORN, LGWP, and HGWP treatments), at which time a subset of steers (4 steers per treatment) were selected for intermediate harvest before finishing. In both experiments, the remaining steers were fed a finishing diet to a common 12th-rib fat thickness of 1.27 cm. In Exp. 1, winter grazing ADG was 0.19, 0.52, 0.68, and 1.37 ± 0.03 kg/d; and in Exp. 2, winter/summer grazing ADG was 0.46, 0.61, 0.83, and 1.29 ± 0.02 kg/d, respectively for CON, CORN, LGWP, and HGWP treatments. At intermediate harvest in Exp. 1, HGWP steers had greater (P < 0.01) 12th-rib fat thickness and marbling scores, compared with the other treatments. However, in Exp. 2, LGWP steers had greater (P < 0.01) marbling scores compared with HGWP steers, which were greater than DNR steers. At final harvest in Exp. 1, LGWP steers had greater (P < 0.01) 12th-rib fat thickness and smaller LM area, compared with the other treatments; however, there were no differences (P = 0.99) in final marbling scores. In Exp. 2, CON steers had lower (P < 0.05) 12th-rib fat thickness and tended (P = 0.10) to have greater marbling scores, compared with the other treatments. These data suggest that changes in the partitioning of fat among depots during the stocker phase may not be reflected after finishing when steers are fed to a common 12th-rib fat thickness.

Three experiments were conducted to evaluate supplementation of dried distillers grains with solubles (DGS) to spring-calving beef cows (n = 120; 541 kg of initial BW; 5.1 initial BCS) consuming low-quality forage during late gestation and early lactation. Supplemental treatments included (DM basis) 1) 0.77 kg/d DGS (DGSL); 2) 1.54 kg/d DGS (DGSI); 3) 2.31 kg/d DGS (DGSH); 4) 1.54 kg/d of a blend of 49% wheat middlings and 51% cottonseed meal (POS); and 5) 0.23 kg/d of a cottonseed hull-based pellet (NEG). Feeding rate and CP intake were similar for DGSI and POS. In Exp. 1, cows were individually fed 3 d/wk until calving and 4 d/wk during lactation; total supplementation period was 119 d, encompassing 106 d of gestation and 13 d of lactation. Tall-grass prairie hay (5.6% CP, 50% TDN, 73% NDF; DM basis) was fed for ad libitum intake throughout the supplementation period. Change in cow BW and BCS during gestation was similar for DGSI and POS (-5.0 kg, P = 0.61 and -0.13, P = 0.25, respectively) and linearly increased with increasing DGS level (P < 0.01). Likewise, during the 119-d supplementation period, BW and BCS change were similar for DGSI and POS (-72 kg, P = 0.22 and -0.60, P = 0.10) and increased linearly with respect to increasing DGS (P < 0.01). The percentage of cows exhibiting luteal activity at the beginning of breeding season (56%, P = 0.31), AI conception rate (57%, P = 0.62), or pregnancy rate at weaning (88%, P = 0.74) were not influenced by supplementation. In Exp. 2, 30 cows from a separate herd were used to evaluate the effect of DGS on hay intake and digestion. Supplementation improved all digestibility measures compared with NEG. Hay intake was not influenced by DGS (P > 0.10); digestibility of NDF, ADF, CP, and fat linearly increased with increasing DGS. In Exp. 3, milk production and composition were determined for cows (n = 16/treatment) of similar days postpartum from Exp. 1. Daily milk production was not influenced by supplementation (6.3 kg/d, P = 0.25). Milk fat (2.1%) and lactose (5.0%) were not different (P > 0.10). Milk protein linearly increased as DGS increased (P < 0.05) and was greater for DGSI compared with POS. Similar cow performance was achieved when cows were fed DGS at the same rate and level of CP as a traditional cottonseed meal-based supplement. Increasing amounts of DGS did not negatively influence forage intake or diet digestibility.

Sixteen ruminally cannulated crossbred steers (529 ± 45 kg initial body weight, BW) were used to evaluate in situ dry matter (DM), neutral detergent fiber (aNDF), and N degradation characteristics of low-quality prairie hay, blood urea-N (BUN) and rumen fermentation parameters in steers provided a protein supplement with or without Micro-Aid ® (MA; plant derived saponin). Steers were allowed ad libitum access to chopped prairie hay (49 g crude protein (CP)/kg DM and 738 g aNDF/kg DM) and randomly assigned to one of four treatments: (1) no supplement (C), (2) cottonseed meal and wheat middlings: 920 g DM/d (PC; positive control), (3) MA added to PC to supply 1 g MA/d (MA1), and (4) MA added to PC to supply 2 g MA/d (MA2). Steers were individually supplemented 920 g DM once daily at 08:00 along with a vitamin and mineral mix to ensure requirements were met. Orthogonal contrasts were used to determine the effects of protein supplementation, addition of MA and level of MA inclusion. During in situ phase, forage samples were incubated for a 96 h period. Protein supplementation increased DM intake (DMI), particulate passage rate (Kp), and rumen digestibility of DM and NDF (P < 0.001), but there was no effect on rumen N degradability. The inclusion of MA did not impact DMI in either phase. Compared to PC, MA decreased K p (27.8 and 22.7 g DM/kg/h, respectively; P = 0.02), resulting in an increase in rumen aNDF and DM digestibility (P < 0.001). However, there was no influence of MA on apparent total tract digestibility in the metabolism phase. Rumen protozoa concentrations were suppressed (P = 0.01) with MA inclusion while lactate concentrations and microbial crude protein (MCP) flow to the small intestine were increased (P = 0.05). There was no impact on BUN, rumen ammonia, pH, volatile fatty acid (VFA) concentrations or N balance for MA compared to PC diets. Supplementation improved N balance, MCP synthesis and increased total concentrations of VFA and independent acetate and propionate concentrations. In conclusion, including MA in protein supplements increased rumen DM and a NDF digestibility of forage, reduced protozoa concentrations and increased daily outflow of MCP. This is indicative of increased rumen fermentation rate and may ultimately impact animal performance via increased energy and amino acid supply to the small intestine. However, more research is needed to validate this potential impact on animal performance.