No abstract

Three steers with simple rumen and abomasal cannulas were given ground and pelleted diets containing predominantly dried grass meal (DG) or rolled barley (RB). Diets were given at frequencies of two or eight feeds/d in a simple changeover design. Chromic oxide and polyethylene glycol were given as flow markers and flows (g/24 h) of organic matter (OM), nitrogenous and carbohydrate compounds were calculated. Ribonucleic acid and 35S were used as microbial markers and diaminopimelic acid (DAP) as a bacterial marker. Frequency of feeding had no significant effect on mean rumen pH, ammonia levels or liquid outflow rates with either diet. Rumen volume was decreased and abomasal digesta flow increased on Diet DG with more feeds but these parameters were unaffected with Diet RB. Increased feeding frequency with both feeds resulted in increased numbers of protozoa. There were no significant effects of feeding frequency of Diet DG on the abomasal flows of any of the nitrogenous constituents measured. However, there was a significant increase in microbial-N flow from 33 to 43 g/d with more frequent feeding of diet RB which was not reflected in bacterial-N flow as measured by DAP. The apparent digestion of OM in the rumen, expressed as g/g intake with diet DG was 0.41 and 0.31 for two feeds and eight feeds/d respectively. Corresponding values for diet RB were 0.56 and 0.63 respectively. The reduction in OM digestion with frequent feeding of diet DG was reflected in similarly reduced rumen digestibilities of all dietary carbohydrate components whereas the increase in OM digestion with diet RB was reflected only by the component sugars of the dietary fibre. The efficiencies of microbial protein synthesis (expressed as gMN/kg ADOM) increased from 36 to 46 when the feeding frequency of diet DG was increased from two to eight times/d. No significant effect of frequency of feeding was found for diet RB. Mouth to abomasum degradation of feed-N (expressed as g/g intake) of 0.64 was unaffected by the number of feeds of diet DG but was significantly increased from 0.55 to 0.82 when eight rather than two feeds/d of diet RB were given.

SummaryNormal and brown midrib-3 (bm3) maize plants of three genotypes (Inra 188, Inra 240 and Inra 258) were sampled at three stages of maturity. Whole crop and plant components were analysed for in vitro digestible organic matter in the dry matter (DOMD) and the concentration of neutral detergent fibre, cellulose, hemicellulose, xylose, soluble sugars, starch and total nitrogen in the dry matter.The concentrations of total nitrogen, neutral detergent fibre, cellulose, hemicellulose and xylose were similar in both normal and bm3 plants. Xylose was the main constituent sugar of hemicellulose forming 70–75% of the total hemicellulose. The higher concentration of soluble sugars and lower concentration of starch in the bm3 plants was attributed to the later maturity of the bm3 plants.The bm3 gene significantly reduced lignin synthesis in the whole plant and plant components at all harvests. The mean concentration of lignin in the normal and bm3 plants were 2·2 and 1·4%, respectively. The ferulic and p-coumaric acid concentrations in the bm3 plants were 1·31 and 0·93 mg/g D.M. compared with 1·59 and 1·16 mg/g D.M. for the normal plants, respectively.The in vitro DOMD values for the bm3 plants were significantly higher (P < 0.05) than their normal counterparts.

Steers fitted with simple rumen and abomasal cannulas were given isoenergetic diets of approximately equal amounts of untreated (UT) barley straw and concentrates (flaked maize +tapioca) alone (BS) or with urea (BSU) or fishmeal (BSF). Similar diets were also given in which the barley straw had been treated (AT) with NaOH (BSA, BSAU and BSAF respectively). The diets were given in a 6 X 6 Latin square design. Feed components and abomasal digesta samples were analysed for neutral (NDF) and acid (ADF) detergent fibres and for monosaccharide constituents of structural polysaccharides. Hemicellulose contents were estimated as the sum of xylose + arabinose (X + A) and by the difference between ash-free NDF and ash-free ADF (NDF-ADF). Cellulose was estimated as @-linked glucose (C) and by the difference between ash-free ADF and lignin (ADF-L).lo3 Ruthenium and PEG were given as flow markers and flows (g24h-') at the abomasum of carbohydrate components estimated in these ways were calculated. Approximately 98% (by wt.) of the cellulose (C) found in original feed and digesta samples was recovered in both NDF and ADF. Recoveries of hemicellulose (X + A) in NDF from UT straw, AT straw and abomasal digesta were approximately 92, 48 and 50%, respectively. The ADF fraction of feeds and digesta contained 3-6 and 10-17% of the nitrogen and xylose, respectively, present in the original samples. Mouth to abomasum digestibilities of hemicellulose (NDF-ADF) for diets BS, BSU, BSF, BSA, BSAU and BSAF were 39, 62, 67, 29, 61 and 76%, respectively. Corresponding values for cellulose (ADF-L) were 37, 34, 50, 45, 48, and 63%, respectively. The use of NDF-ADF and ADF-L as measures of hemicellulose and cellulose contents, respectively, of feeds and digesta, and the digestibility of these carbohydrate fractions between mouth and abomasum of steers are discussed.

Friesian steers, virtually protozoa free, were equipped with simple rumen and abomasal cannulas. They were given diets consisting of approximately equal proportions of ground, pelleted alkali treated straw and a rolled barley, tapioca mixture supplemented with urea + casein (UC), soybean meal (SBM), 'normal' white fishmeal (NDF) or white fishmeal designated as being of 'low' rumen degradability (LDF). The diets were isoenergetic (the protein sources replacing part of the tapioca) and they were given in amounts to supply sufficient metabolizable energy (ME) to support an average growth rate of 0.5 kg/d. Rumen degradable nitrogen (RDN): ME values were estimated to be 2.08, 1.40, 1.90 and 1.66 for diets UC, SBM, NDF and LDF respectively. RNA, alpha-epsilon-diaminopimelic acid and 35S (added as sulphate) were used as bacterial markers. Chromic oxide and polyethylene glycol (PEG) were given as flow markers and flows (g/24 h) at the abomasum of organic matter (OM) and nitrogenous constituents were calculated. Rumen volumes and ruminal liquid fractional outflow rates were measured using PEG. Samples of mixed rumen bacteria separated from strained rumen digesta from animals receiving diet UC contained significantly less DAP-N (0.322 g/kg DM) than those from animals receiving diets SBM, NDF or LDF (0.530 g/kg DM). Mean rumen volume (approximately 15 l) and liquid fractional outflow rates (approximately 0.105/h) were similar on all diets but there was appreciable variation between animals. The proportion of OM intake digested in the rumen was similar on all diets. The proportional contribution of bacterial-N to the total non-ammonia-N passing the abomasum based on mean values derived from DAP and 35S as markers was 0.57, 0.47, 0.39 and 0.31 for diets UC, SBM, NDF and LDF respectively. Corresponding values based on RNA were 0.71, 0.50, 0.48 and 0.35 respectively. Bacterial-N (RNA) flows at the abomasum were 31, 25, 26 and 20 g/d for diets UC, SBM, NDF and LDF respectively. Corresponding values for 35S and DAP were 26, 24, 21 and 18 g/d respectively. Values derived from RNA flows were consistently and significantly higher (P less than 0.01) than those based on DAP or 35S. Mean estimated efficiencies of bacterial protein synthesis (g bacterial-N/kg OM truly digested) were 15, 15, 14 and 12 for diets UC, SBM, NDF and LDF respectively.(ABSTRACT TRUNCATED AT 400 WORDS)