Effects of rotating antibiotic and ionophore feed additives on volatile fatty acid production, potential for methane production, and microbial populations of steers consuming a moderate-forage diet.

Ionophores and antibiotics have been shown to decrease ruminal methanogenesis both in vitro and in vivo but have shown little evidence toward a sustainable means of mitigation. Feed additive rotation was proposed and investigated for methane, VFA, and microbial population response. In the present study, cannulated steers ( = 12) were fed a moderate-forage basal diet in a Calan gate facility for 13 wk. In addition to the basal diet, steers were randomly assigned to 1 of 6 treatments: 1) control, no additive; 2) bambermycin, 20 mg bambermycin/d; 3) monensin, 200 mg monensin/d; 4) the basal diet + weekly rotation of bambermycin and monensin treatments (B7M); 5) the basal diet + rotation of bambermycin and monensin treatments every 14 d (B14M); and 6) the basal diet + rotation of bambermycin and monensin treatments every 21 d (B21M). Steers were blocked by weight in a randomized complete block design where the week was the repeated measure. Rumen fluid was collected weekly for analysis ( = 13), and results were normalized according to individual OM intake (OMI; kg/d). Potential activity of methane production was not significantly different among treatments ( > 0.05). However, treatment tended to affect the CH-to-propionate ratio ( = 0.0565), which was highest in the control and lowest in the monensin, B21M, and B14M treatments (0.42 vs. 0.36, 0.36, and 0.33, respectively). The CH:propionate ratio was lowest in wk 2 and 3 ( < 0.05) but the ratio in wk 4 to 12 was not different from the ratio in wk 0. Week also affected total VFA, with total VFA peaking at wk 3 and plummeting at wk 4 (4.02 vs. 2.86 m/kg OMI; < 0.05). A significant treatment × week interaction was observed for the acetate-to-propionate (A:P) ratio, where bambermycin- and rotationally fed steers did not have a reduced A:P ratio compared with monensin-fed steers throughout the feeding period ( < 0.0001). Microbial analysis revealed significant shifts, but several predominant classes showed adaptation between 4 and 6 wk after additive initiation. There was no significant evidence to suggest that rotations of monensin and bambermycin provided additional benefits to steers consuming a moderate-forage diet at the microbial/animal and environmental level versus those continuously fed.

Search for exclusive multibody non- decays at the resonance.

Using data collected at the psi(3770) resonance with the CLEO-c detector at the Cornell e+e- storage ring, we present searches for 25 charmless decay modes of the psi(3770), mostly multibody final states. No evidence for charmless decays is found.

Absolute branching fraction measurements of exclusive D+ semileptonic decays.

Using data collected at the psi(3770) resonance with the CLEO-c detector at the Cornell e+e- storage ring, we present improved measurements of the absolute branching fractions of D+decays to K0e+ve, pi0e+ve, K*0e+ve, and p0e+ve, and the first observation and absolute branching fraction measurement of D+ --> omega e+ve. We also report the most precise tests to date of isospin invariance in semileptonic D0 and D+ decays.

Measurement of the muonic branching fractions of the narrow upsilon resonances.

The decay branching fractions of the three narrow Upsilon resonances to mu(+)mu(-) have been measured by analyzing about 4.3 fb(-1) e(+)e(-) data collected with the CLEO III detector. The branching fraction B(Upsilon(1S)-->mu(+)mu(-))=(2.49+/-0.02+/-0.07)% is consistent with the current world average, but B(Upsilon(2S)-->mu(+)mu(-))=(2.03+/-0.03+/-0.08)% and B(Upsilon(3S)-->mu(+)mu(-))=(2.39+/-0.07+/-0.10)% are significantly larger than prior results. These new muonic branching fractions imply a narrower total decay width for the Upsilon(2S) and Upsilon(3S) resonances and lower other branching fractions that rely on these decays in their determination.

Search for X(3872) in gammagamma fusion and radiative production at CLEO.

We report on a search for the recently reported X(3872) state using 15.1 fb(-1) of e(+)e(-) data taken in the sqrt[s] = 9.46-11.30 GeV region. Separate searches for the production of the X(3872) in untagged gammagamma fusion and e(+)e(-) annihilation following initial state radiation are made by taking advantage of the unique angular correlation between the leptons from the decay J/psi --> l(+)l(-) in X(3872) decay to pi(+)pi(-)J/psi. No signals are observed in either case, and 90% confidence upper limits are established as (2J+1)Gamma(gammagamma)(X(3872))B(X --> pi(+)pi(-)J/psi) < 12.9 eV and Gamma(ee)(X(3872))B(X- -> pi(+)pi(-)J/psi) < 8.3 eV.

Predicting individual feed requirements of cattle fed in groups.

A published model designed to predict individual feed required for the observed shrunk BW and ADG of growing cattle when fed in groups was modified and evaluated to improve its accuracy. This model is needed to accurately bill feed and compute cost of gain in marketing programs based on individual animal management. Because of its importance in predicting energy required for growth, a database of 401 steers was used to develop an equation to predict percentage of empty-body fat (EBF) from carcass measurements (12th rib fat thickness, hot carcass weight, USDA quality grade, and longissimus muscle area), which accounted for 61% of the variation in EBF with no bias (P > 0.1). When tested with an independent data set of 951 steers, the equation accounted for 51% of the variation with 1% proportional bias. The large variation in the carcass measurements at a particular EBF observed in this study indicates further improvement is limited by the inability of carcass measurements to account for variation in fat distribution in the various carcass components. Because of its importance in setting the target end point, a database of 1,355 steers and heifers was used to determine the relationship between EBF and USDA quality grade. These data indicate growing and finishing cattle reach Select and low-Choice quality grades at an EBF of 26.15 +/- 0.19 and 28.61 +/- 0.20%, respectively (P < 0.05). A data set of 228 steers from different breeds from two serial slaughter studies indicated 14.26 +/- 1.52 kg of empty BW change are required to increase EBF one percentage unit for cattle fed high-energy diets; this adjustment is needed to adjust final shrunk BW to the target EBF end point. The model to predict DM required with modifications developed in this study was evaluated with data from 365 individually fed cattle and it accounted for 74% of the variation in observed DM consumed with no bias (P > 0.1). When the revised model was applied to a commercial feedlot data set containing 12,105 steers and heifers, the total observed DM consumed was predicted with a bias of less than 1%. The model presented in this study accounts for differences known to affect animal requirements (breed type, BW and ADG, and weight at the target EBF end point) and can be used to fairly allocate feed to individuals fed in a group under commercial feedlot conditions.

Influence of high-starch vs high-fiber energy supplements on performance of stocker cattle grazing wheat pasture and subsequent feedlot performance.

A 3-yr study was conducted to determine effects of high-starch (HS) or high-fiber (HF) energy supplements on performance of fall-weaned steer calves (n = 192, Exp. 1 and 2; n = 84, Exp. 3) grazing winter wheat pasture (Triticum aestivum variety 2157) and subsequent feedlot performance. The steers received 1) no supplement (CL) other than free-choice access to a commercial mineral mixture or 2) were hand-fed 6 d/wk either a corn-based HS supplement, or 3) a soybean hull/wheat middling-based HF supplement. In Exp. 1 (1989-1990), a fourth treatment provided ad libitum access to the HF supplement (SFHF). Supplements contained 88 mg of monensin/kg and the combination of ionophore, minerals and salt (8%) was used to limit intake of the SFHF supplement. Target level of daily consumption of all supplements was .75% of mean BW. Stocking density was increased by 33% (i.e., from 1.24 to 1.65 steers/ha) in Exp. 1 and 3, and by 22 to 44% in Exp. 2 when supplements were fed. Subsequent to grazing wheat pasture in Exp. 2 and 3, feedlot performance and carcass quality (Exp. 2 only) of the cattle were measured. Over the 3-yr period (pooled analysis), mean daily supplement consumption was .65% BW. Daily gains were increased (P < .001) .15 kg by supplementation and were .92, 1.06, and 1.08 kg for CL, HS, and HF, respectively. Daily gains were not influenced (P > .45) by type of energy supplement. Mean supplement conversions (kilograms asfed.kilogram of increased gain-1.hectare-1) were 5.4 for HS and 5.0 for HF and did not differ (P > .95). Subsequent feedlot daily gain was decreased .09 kg (P < .05) by supplementation in Exp. 2 but not in Exp. 3 (P > .80). This supplementation program for growing cattle on wheat pasture allowed stocking density to be increased by approximately one-third and increased daily gains by .15 kg.