As the dairy industry continues to grow, more dairy calves are available for dairy, beef, and veal purposes. Rearing systems must be highly efficient to make this industry cost efficient, making the evaluation of rearing methods important to establish the most practical method. A study was designed and conducted to evaluate effects of housing and feeding systems on performance of neonatal Holstein bull calves. Treatments (2 × 2 factorial arrangement) consisted of: 1) individually housed, bottle-fed (n = 5 bull calves); 2) individually housed, bucket-fed (n = 5 bull calves); 3) group-housed, bottle-fed (n = 5 pens; 4 bull calves/pen); and 4) group-housed, bucket- (trough) fed (n = 5 pens; 3 or 4 bull calves/pen). Feeding treatments began on d 7 when calves had been acclimated to their new environment. Body weight measurements were collected every 7 d and blood samples were collected on d 0, 28, 55, and 66 for β-hydroxybutyrate (BHBA) concentration as a gross indicator of ruminal development. No housing × feeding interactions or feeding treatment effects were observed (P > 0.10). Average DMI (dry feed plus milk replacer) was increased (P < 0.05) for group-housed vs. individual animals after d 41, and final BW was greater (P < 0.05) for group-housed calves compared with individually housed calves. Feed efficiency and ADG, however, remained similar (P > 0.10) for all treatments. Fecal scores (P > 0.26), CV for BW (P > 0.26), and BHBA concentrations (P > 0.14) showed no differences among treatments. Housing system had greater effect on calf performance compared with milk feeding regimen.

Red Angus steers (n = 24; 260 ± 25 kg) were used to analyze the effects of supplementation of zilpaterol hydrochloride (ZH) under heat stress conditions on respiration rate (RR), rectal temperature (RT), growth performance (GP), and carcass traits (CT). Steers were randomly assigned to a 2 x 2 factorial treatment arrangement (n = 6/group) with factors including heat stress (HS; THI=71 to 83) or thermal neutral (TN; THI=27 to 39) conditions and with/without supplementation of ZH (0 or 8.38 mg/kg/d on 88% DM basis). Steers were provided 9 d to acclimate to tie stalls rooms under TN conditions before starting the study. TN steers were pair-fed to the average daily dry matter intake (DMI) of HS steers. Ad libitum water consumption (WC) was recorded daily. HS and TN steers were harvested on d 22 and 23, respectively. By design, DMI was not different between environments (P = 0.43). DMI also did not differ between supplement groups (P = 0.31). RT, RR, and WC were greater (P &lt; 0.01) in HS steers compared to TN steers. There was a supplement by environment interaction (P = 0.02) for RT, as HS steers fed ZH had lower RT than HS control steers (39.1 vs 39.5 ℃). ADG was 20% higher (P = 0.04) in HS steers compared to TN steers. CT did not differ (P = &gt;0.05) due to environment, treatment, or interactions between environment and ZH supplementation. Our results suggest that feedlot steers under our experimental conditions display some sensitivity to HS through GP, RR, and RT, however, this did not translate to an impact on CT. Furthermore, ZH supplementation under HS conditions appears to impact thermoregulatory responses positively, yet this did not impact GP or CT.

Supplementation with a β- adrenergic agonist (β-AA) for 21 days in Brahman steers under heat stress conditions (HS) was evaluated with respect to feedlot performance and carcass merit. Twenty-four Brahman steers (kg = 338 ± 39) were housed in two controlled environment chambers with one of two environmental (ENV) conditions 1) heat stress (HS; THI = 73 to 85) and 2) thermoneutral (TN; THI = 68) with either Zilpaterol hydrochloride (ZL) or soymeal supplementation (CN) using a randomly assigned in a 2 x 2 factorial design (n=6/group). Daily data were collected for dry matter intake, water intake, respiratory rate (RR), and rectal temperature (RT). At the end of 21 d period, total weight gain was used to calculate average daily gain (ADG) and gain to feed. Blood samples were collected from the jugular vein on days -7, 3, 10, and 21 for cortisol analysis, and biological impedance analysis (BIA) was determined on days 3, 10, and 21 on each animal. Steers were harvested at 544 kg on average post supplementation/environment conditions, and carcass merit was determined. There were no differences (P &gt; 0.05) in feedlot performance. Brahmans exposed to heat stress had greater RR during the heat stress periods of the experiment, regardless of supplementation. Environment and day interactions (P &lt; 0.04) were observed for RT, HS steers had a greater RT on d 8 but similar RT on d 15 and 19. Stressed steers with ZL had higher RT (P &lt; 0.05) than TN/CN steers on d 11. There was no interaction (P &gt; 0.05) between environmental conditions and CN and ZH supplementation for cortisol concentrations. Regardless of environmental treatment or supplementation, no difference (P &gt; 0.05) was associated with BIA characteristics. There were no differences (P &gt; 0.05) for hot carcass weight, cold carcass weight, USDA yield grade, 12th rib loin eye area, marbling score, KPH percentage, and 12th rib fat thickness between groups. Twelfth-rib loin eye area lean color from HS/CN had higher lightness (L*) (P &lt; 0.05) than TN/CN steers. HS/CN steers present a similar (L*) to ZL in TN and HS conditions. Redness-greenness (a*) was greater (P = 0.01) in carcasses from HS steers with or without ZL than TN/ZL but similar to TN/CN. Steers exposed to HS and CN had a higher (P = 0.02) change of 12th rib lean color from yellow to blue (b*) than TN steers with CN and ZL. Supplementation with β-AA did not negatively impact growth, carcass performance, or carcass merit in heat-stressed steers.