Sugar supplementation can stimulate rumen microbial growth and possibly fiber digestibility; however, excess ruminal carbohydrate availability relative to rumen-degradable protein (RDP) can promote energy spilling by microbes, decrease rumen pH, or depress fiber digestibility. Both RDP supply and rumen pH might be altered by forage source and monensin. Therefore, the objective of this study was to evaluate interactions of a sugar source (molasses) with monensin and 2 forage sources on rumen fermentation, total tract digestibility, and production and fatty acid composition of milk. Seven ruminally cannulated lactating Holstein cows were used in a 5 x 7 incomplete Latin square design with five 28-d periods. Four corn silage diets consisted of 1) control (C), 2) 2.6% molasses (M), 3) 2.6% molasses plus 0.45% urea (MU), or 4) 2.6% molasses plus 0.45% urea plus monensin sodium (Rumensin, at the intermediate dosage from the label, 16 g/909 kg of dry matter; MUR). Three chopped alfalfa hay diets consisted of 1) control (C), 2) 2.6% molasses (M), or 3) 2.6% molasses plus Rumensin (MR). Urea was added to corn silage diets to provide RDP comparable to alfalfa hay diets with no urea. Corn silage C and M diets were balanced to have 16.2% crude protein; and the remaining diets, 17.2% crude protein. Dry matter intake was not affected by treatment, but there was a trend for lower milk production in alfalfa hay diets compared with corn silage diets. Despite increased total volatile fatty acid and acetate concentrations in the rumen, total tract organic matter digestibility was lower for alfalfa hay-fed cows. Rumensin did not affect volatile fatty acid concentrations but decreased milk fat from 3.22 to 2.72% in corn silage diets but less in alfalfa hay diets. Medium-chain milk fatty acids (% of total fat) were lower for alfalfa hay compared with corn silage diets, and short-chain milk fatty acids tended to decrease when Rumensin was added. In whole rumen contents, concentrations of trans-10, cis-12 C(18:2) were increased when cows were fed corn silage diets. Rumensin had no effect on conjugated linoleic acid isomers in either milk or rumen contents but tended to increase the concentration of trans-10 C(18:1) in rumen samples. Molasses with urea increased ruminal NH(3)-N and milk urea N when cows were fed corn silage diets (6.8 vs. 11.3 and 7.6 vs. 12.0 mg/dL for M vs. MU, respectively). Based on ruminal fermentation characteristics and fatty acid isomers in milk, molasses did not appear to promote ruminal acidosis or milk fat depression. However, combinations of Rumensin with corn silage-based diets already containing molasses and with a relatively high nonfiber carbohydrate:forage neutral detergent fiber ratio influenced biohydrogenation characteristics that are indicators of increased risk for milk fat depression.

Monensin (tradename: Rumensin) should reduce the extent of amino acid deamination in the rumen, and supplemental fat should decrease protozoal abundance and intraruminal N recycling. Because animal-vegetable (AV) fat can be biohydrogenated in the rumen and decrease its effectiveness as an anti-protozoal agent, we included diets supplemented with coconut oil (CNO) to inhibit protozoa. In a 6 × 6 Latin square design with a 2 × 3 factorial arrangement of treatments, 6 rumen-cannulated cows were fed diets without or with Rumensin (12 g/909 kg) and either no fat (control), 5% AV fat, or 5% CNO. The log10 concentrations (cells/mL) of total protozoa were not different between control (5.97) and AV fat (5.95) but were decreased by CNO (4.79; main effect of fat source). Entodinium and Dasytricha decreased as a proportion of total cells from feeding CNO, whereas Epidinium was unchanged in total abundance and thus increased proportionately. Total volatile fatty acid concentration was not affected by diet, but the acetate:propionate ratio decreased for CNO (1.85) versus control (2.95) or AV fat (2.58). Feeding CNO (23.8%) decreased ruminal neutral detergent fiber digestibility compared with control (31.1%) and AV fat (30.5%). The total-tract digestibility of NDF was lower for CNO (45.8%) versus control (57.0%) and AV fat (54.6%), with no difference in apparent organic matter digestibility (averaging 69.8%). The omasal flows of microbial N and non-ammonia N were lower for CNO versus control and AV fat, but efficiency of microbial protein synthesis was not affected. The dry matter intake was 4.5 kg/d lower with CNO, which decreased milk production by 3.1 kg/d. Main effect means of dry matter intake and milk yield tended to decrease by 0.7 and 1.2 kg/d, respectively, when Rumensin was added. Both percentage and production of milk fat decreased for CNO (main effect of fat source). An interaction was observed such that AV decreased milk fat yield more when combined with Rumensin. Using large amounts of supplemental fat, especially CNO, to decrease abundance of protozoa requires further research to characterize benefits versus risks, especiallywhen combined with Rumensin.

In trial 1, we evaluated the efficacy of a liquid feed (LF) containing cane molasses and corn steep liquor as carriers of suspended white grease (WG) without or with urea (U) or with soybean lipid (SL; a byproduct of soybean processing) compared with roasted soybeans plus tallow blended into respective concentrates in a 16-wk lactation study. The dry matter intake (DMI) and milk production for LF diets were either similar to or greater than respective controls, although SL decreased milk fat percentage. In trial 2, we compared LF without fat to LF plus WG or SL and also evaluated the dose response to increasing amount of LF + WG in a 16-wk lactation trial in which the LF products were added to respective total mixed rations. The DMI was increased and then decreased (quadratic response) with increasing LF + WG without a linear response. However, production of milk, protein, and fat increased linearly with corresponding quadratic responses, which we interpret to be a result of a limiting returns response from DMI and density of net energy for lactation. When LF plus SL was fed, milk fat percentage and yield decreased compared with the comparable amount of LF + WG. In a 12-wk lactation study (trial 3), we added 3.25 or 6.5% of the dry matter as LF (a different but generally similar product than the previous trials and without fat) to diets formulated to maintain comparable ruminal nonstructural carbohydrate digestibility by adding soybean hulls to decrease nonfiber carbohydrates (NFC) concentration; the 6.5% LF diet was without or with Rumensin (11.5 g/909 kg of dry matter). When 3.25% LF was added but NFC was decreased from 40 to 37%, cows increased DMI and production of milk fat. Adding Rumensin decreased DMI but maintained milk fat yield compared with its 6.25% LF control without Rumensin. In trials 1 and 3, apparent total tract nutrient digestibility was not affected by treatment. In conclusion, feeding LF at about 5% (trial 2, which contained WG, 1.6% added sugar) or 3.25% (trial 3, 1.7% added sugar) generally increased DMI and maintained or increased production of milk, protein, and fat.

Pelleting cottonseed (CS) improves handling characteristics. Our objectives were to determine whether increasing the particle size of the CS pellet or dilution of a smaller pellet with delinted CS would limit the rate of CS oil release to optimize digestibility of fatty acids (FA) and fiber while maintaining milk fat production. In a 5 x 5 Latin square design with 3-wk periods, 5 rumen-cannulated cows were fed 1) control with CS hulls (CSH) and CS meal plus tallow and Ca soaps of FA, 2) whole CS (WCS), 3) small CS pellets (SP; 0.44-cm die diameter), 4) larger CS pellets (LP; 0.52-cm die diameter), or 5) a blend of 1/2 SP plus 1/2 partially delinted CS (SPD). Diets contained 39.6% concentrate, 14.4% CS, and 46% forage (40:60, alfalfa hay:corn silage) on a DM basis and were balanced to have similar concentrations of CS protein, CS fiber, and total fat. In a production trial, dietary treatments were 1) WCS control, 2) LP, 3) SPD, and 4) SPD fed at 90%. Sixty cows averaging 105 d in milk were fed the WCS diet for 2 wk and then assigned to one of the 4 diets for 12 wk. Total tract digestibility of NDF was unaffected, but N digestibility was lower for SPD than for other treatments. Fatty acid digestibility was higher for SP and LP (82.6 and 82.3%) than for CSH or SPD treatments (78.8 and 75.3%), and WCS was intermediate (81.1%). The trans-11 C18:1 from cows fed SP and LP (6.58 and 6.24% of total milk FA) was greater than that from cows fed CSH, WCS, and SPD (3.23, 3.79, and 3.97%). The trans-10 C18:1 in milk fat from SP and LP (0.508 and 0.511%) was higher than that in WCS and SPD diets (0.316 and 0.295%); CSH was intermediate (0.429%). Using passage rates estimated from the NRC, disappearance of total FA in situ was estimated to be 17.7, 44.2, 46.6, and 35.0% for WCS, SP, LP, and SPD, respectively. In the production trial, a diet x week interaction was explained by a trend for progressively greater milk production for SPD and SPD90 than for WCS or LP. Milk fat was lower for LP (2.74%) and SPD90 (2.85%) than for WCS or SPD (3.07 and 3.08%). The fat yield was lower for LP than for SPD (1.09 and 1.30 kg/d); WCS and SPD90 were intermediate (1.23 and 1.21 kg/d). Although having a lower FA digestibility, SPD appeared to minimize negative effects of free oil from SP in the rumen, explaining higher DMI and milk production compared with WCS or LP.

Since the addition of either ruminal fluid or a combination of phenylacetic and phenylpropionic acids (PAA/PPA) has previously been shown to dramatically improve cellulose degradation and growth of Ruminococcus albus, it was of interest to determine the effects of these additives on xylan-grown cultures. Although cell-bound xylanase activity increased when either PAA/PPA or ruminal fluid was added to the growth medium, total xylanase did not change, and neither of these supplements affected the growth or xylan-degrading capacity of R. albus 8. Similarly, neither PAA/PPA nor ruminal fluid affected xylan degradation by multiple strains of R. albus when xylan prepared from oat spelts was used as a carbohydrate source. These results show that the xylanolytic potential of R. albus is not conditional on the availability of PAA/PPA or other components of ruminal fluid.Ruminococcus albus is a gram-positive anaerobe widely recognized for its high cellulolytic activity. A distinguishing feature of R. albus isolates is their dependence on the provision of micromolar concentrations of phenylacetic and phenylpropionic acids (PAA/PPA) for optimal rates of growth and cellulose degradation (12,16,18,19,20). PAA/PPA appear to be necessary for the formation of cell-associated, high-molecularweight protein complexes believed to be cellulosomes (13). Many isolates of R. albus have also been shown to degrade xylan and the hemicellulose fraction of plant cell walls (3, 9). Greve et al. (11) demonstrated that R. albus strain 8 produces several enzymes involved in xylan degradation, including ␤-1,4-xylanase, ␤-xylosidase, and ␣-arabinofuranosidase. The strain was also shown to ferment glucose and xylose residues present in alfalfa cell wall preparations in preference to other sugars (11). However, there are no data on the possible effect(s) from either PAA/PPA or other components of ruminal fluid on xylan degradation and growth of R. albus. Considering that heteroxylans represent a major part of the plant cell wall, it was of interest to determine whether optimal rates of R. albus growth, as well as xylan degradation, would be conditional on the provision of PAA/PPA or ruminal fluid.Bacterial strains and growth experiments. R. albus strains 8, B199, and 7 were obtained from the culture collection at the National Center for Agricultural Utilization Research, U.S. Department of Agriculture, Peoria, Ill. In the experiments described here the strains were cultured at 39°C in a semidefined medium, described by Champion et al. (5), containing 5% (vol/vol) clarified ruminal fluid (RF) or the same medium with ruminal fluid omitted but supplemented with either 25 M each of PAA and PPA (PA) or sterile water (WO). Carbohydrate sources were included at a concentration of 0.4% (wt/vol). Pebble-milled Whatman No. 1 filter paper was used in cellulose-containing media, and the xylan preparations (birchwood and oat spelt) were purchased from Sigma Chemical Co., St. Louis, Mo. The bacterial strains were passed no less than three times in the respective...