The objective of this study was to determine the proportion of forage in the diet which would maximize duodenal flow of unsaturated fatty acids in beef steers supplemented with linseed oil. A second objective was to determine how diets differing in forage content, but equal in nitrogen (N), energy and lipid supply, would affect the duodenal flow of C18:1 and conjugated linoleic acid (CLA) isomers. Eight Hereford×Friesian steers (533±13·6 kg), prepared with rumen and duodenal cannulae were offered one of four forage:concentrate (F:C) ratios: F80C20; F60C40; F40C60 and F20C80 on a dry-matter (DM) basis. All diets were offered at 0·013 body weight and designed to be isonitrogenous and isoenergetic with total lipid made up to 0·06 DM intake with linseed oil. The experimental design was a replicated incomplete 4×4 Latin square with three periods. Increasing the concentrate component in the diet from 0·20 to 0·60 reduced rumen pH from 6·58 to 6·37 and caused a small but significant shift in volatile fatty acid molar proportions, decreasing the non-glucogenic ratio. Rumen ammonia-nitrogen concentration was also significantly reduced with increasing concentrate, from 156·8 to 101·0 mg N per l on F80C20 and F20C80, respectively. Microbial nitrogen (MN) and the efficiency of microbial protein synthesis was significantly elevated as forage level decreased from 51·6 to 72·4 g/day and 17·2 to 27·3 g MN per kg organic matter apparently digested in the rumen, respectively for F80C20 and F20C80. Intake and duodenal flow of C18:1n-9 and C18:2n-6 were significantly higher with increasing concentrate level in the diet whereas C18:3n-3 intake and flow was not different, averaging 143·6 and 6·37 g/day, respectively. There were no differences in the flows of total C18:1 trans or CLA (47·7 and 1·79 g/day, respectively) across the diets. However, although not significantly different in duodenal flow there were trends (P<0·1) for an increasing proportion of trans-10 and a decreasing proportion of trans-11 when increasing the concentrate in the diet. Biohydrogenation of C18:2n-6 decreased from 0·91 to 0·85 when increasing concentrate in the diet from 0·20 to 0·40 but further increases had no effect. F:C ratio had little effect on the flow of unsaturated fatty acids, C18:1 trans and CLA to the duodenum of beef steers, and this may relate to the ability of the rumen to buffer the large changes in concentrate intake.

Duodenally and ruminally fistulated steers were offered grass silage and one of three concentrates at a ratio of 60: 40 (forage: concentrate on a dry-matter basis) : F0, F1 or F4 at 14 g/kg live weight. The concentrates were designed to be iso-lipid and to provide the same amount of sunflower oil but increasing amounts of fish oil : 0, 1 and 4 g per 100 g, respectively. Ruminal characteristics were measured along with fatty acid intakes and duodenal flows to determine the effect of fish oil on : ruminal pH, ammonia-N concentration, volatile fatty acid (VFA) concentration and polyunsaturated fatty acid (PUFA) metabolism. Fish oil had no significant effect on ruminal pH, ammonia-N concentration or the molar proportions of the major VFA, although total VFA concentration was significantly reduced at the highest level of fish oil inclusion. Fish oil significantly increased the flow of long chain PUFA, total conjugated linoleic acid and vaccenic acid to the duodenum and decreased the flow of stearic acid. Biohydrogenation, as determined by the net loss of fatty acid between the mouth and duodenum, of oleic and linolenic acid was not affected by fish oil inclusion and averaged 0·64 and 0·92, respectively. There was a small increase in the biohydrogenation of linoleic acid with increasing fish oil from 0·89 to 0·92 (P < 0·01) on F0 and F4, respectively. Biohydrogenation of the long chain PUFA C20 : 5(n-3) and C22 : 6(n-3) increased from 0·49 and 0·74 to 0·79 and 0·86 (P < 0·01), respectively when fish oil in the concentrate increased from 1 to 4 g per 100 g. The net effect of fish oil on lipid metabolism appears to inhibit the transition of vaccenic acid to stearic acid in the rumen resulting in a build up of this intermediate in the biohydrogenation pathway of C18 PUFA.

Six mature sheep, each fitted with a rumen cannula, were assigned to six diets in a 6 × 6 Latin-square design experiment to examine the effects of a yeast culture on ruminal metabolism, rumen liquid outflow rate, fibre digestion in the rumen and overall nutrient digestibility. The yeast culture (YC) was a commercial product composed of a yeast (Saccharomyces cerevisae) and the media on which it grew and dried so as to maintain its fermentative capacity. The six dietary treatments were three diets differing in hay dry matter (DM): concentrate DM ratio (90: 10, 65: 35 and 40: 60 designated low, medium and high concentrate respectively) each given either without or with a supplement of 4 g/day of YC. Treatment periods were of 3 weeks duration. There were significant effects of dietary forage: concentrate ratio on rumen function (P < 0·05). Rumen pH, rumen liquid outflow rate, rumen ammonia concentration, total volatile fatty acids concentration, and molar proportions of acetate, propionate and butyrate were not significantly affected by the inclusion of YC (P < 0·05). Supplemental YC did not affect the overall nutrient digestibility of organic matter, neutral-detergent fibre or gross energy measured in vivo. However, at every forage:concentrate ratio, YC increased the disappearance of hay organic matter from nylon bags incubated in the rumen for 24 h (P < 0·05). The values with and without YC were 0·482 and 0·432 for the low, 0·423 and 0·366 for the medium, and 0·360 and 0·321 for the high concentrate diets respectively. However, YC had no effect on hay disappearance when bags were incubated for 48 h. YC appeared to increase the initial rate of forage digestion in the rumen without altering overall food digestibility or the patern of production of fermentation end products.