An agro-economic simulation model was developed to facilitate comparison of the impact of management, market and biological factors on the cost of providing ruminant livestock with feed grown on the farm (home produced feed). Unpredictable year-to-year variation in crop yields and input prices were identified as quantifiable measures of risk affecting feed cost. Stochastic analysis was used to study the impact of yield and input price risk on the variability of feed cost for eight feeds grown in Ireland over a 10-year period. Intensively grazed perennial ryegrass was found to be the lowest cost feed in the current analysis (mean cost €74/1000 Unité Fourragère Viande (UFV)). Yield risk was identified as the greatest single factor affecting feed cost variability. At mean prices and yields, purchased rolled barley was found to be 3% less costly than home-produced spring-sown barley. However, home-produced spring barley was marginally less risky than purchased barley (coefficient of variation (CV) 0·063 v. 0·064). Feed crops incurring the greatest proportion of fixed costs and area-dependent variable costs, including bunker grass silage, were the most sensitive to yield fluctuations. The most energy input-intensive feed crops, such as grass silage, both baled and bunker ensiled, were deemed most susceptible to input price fluctuations. Maize silage was the most risky feed crop (CV 0·195), with potential to be both the cheapest and the most expensive conserved feed.

The effects of yeast Saccharomyces cerevisiae, either inactivated (by osmotic pressure, designated IY) or provided as a culture containing live yeast cells (YC), on ruminal fermentation of two different diets were investigated in vitro. Total mixed rations (TMR) having forage:concentrate ratios of 0·6:0·4 (medium–high forage diet) and 0·2:0·8 (low-forage diet) were incubated in batch cultures of mixed ruminal micro-organisms to which either IY (to reach concentrations of 500 and 250 mg product/l incubation medium) or YC (at a concentration of 150 mg product/l) were added directly as powder. To evaluate the effects of the additive on ruminal microbial population, sheep used as donors of rumen fluid were allocated to three experimental groups: Control (no additive), IY and YC, that received a diet with the corresponding additive for 10 days. With both diets, YC decreased ruminal pH compared to control, whereas IY had no effect. Adding yeast products to the high-fibre diet affected total volatile fatty acid (VFA) production and VFA composition, in general with a slight increase in IY and a significantly greater increase in response to the addition of YC. Ammonia nitrogen (P=0·006), total gas production (P<0·001) and in vitro dry matter disappearance (IVD) (P<0·001) showed the highest values with YC. Methane production was higher than the control when the IY inoculum was used, and increased even more with the YC inoculum (P<0·001). With the high-concentrate TMR, no effects on total VFA concentration were observed when yeast additives were used. Similar trends were shown for lactate and methane production and total gas production, where values tended to be higher when using the YC inoculum (P values of 0·055, <0·001, 0·006 and <0·001, respectively). After 144 h of incubation, differences were observed only with the high-fibre diet in the cumulative gas production at 24 h of incubation and in the average fermentation rate, which was greater with YC, although the asymptotic gas production was not affected. These results indicate that live yeasts affect ruminal fermentation slightly more than inactivated yeasts, although both products require a regular administration and some adaptation of the ruminal microbial population for the stimulatory effects to become apparent. The effects of yeasts on ruminal fermentation are diet-dependent, being more noticeable with a high-fibre substrate, and subtle with a high-concentrate diet.

A method is proposed for estimating the percentage of dietary protein that is degraded by microbial action in the rumen when protein supplement is added to a specified ration. The potential degradability, p, is measured by incubating the supplement in artificial-fibre bags in the rumen and is related to incubation time, t, by the equation p = a+b(1 – e-ct). The rate constant k, measuring the passage of the supplement from the rumen to the abomasum, is obtained in a separate experiment in which the supplement is combined with a chromium marker which renders it completely indigestible. The effective percentage degradation, p, of the supplement, allowing for rate of passage, is shown to be p = a+[bc/(c+k)] (1-e-(e+k)t) by time, t, after feeding. As t increases, this tends to the asymptotic value a+bc/(c+k), which therefore provides an estimate of the degradability of the protein supplement under the specified feeding conditions.

The method is illustrated by results obtained with soya-bean meal fed as a supplement to a dried-grass diet for sheep. The incubation measurements showed that 89% of the soya-bean protein disappeared within 24 h and indicated that it was all ultimately degradable with this diet.

When the dried grass was given at a restricted level of feeding the allowance for time of retention in the rumen reduced the estimate of final degradability to 71% (69% within 24 h). With ad libitum feeding there was a faster rate of passage and the final degradability was estimated to be 66% (65% within 24 h).

A rapid method for measuring gas production during incubation of feedingstuffs with rumen liquor in vitro is described. Gas production in 24 h from 200 mg feed dry matter was well correlated with digestibility of organic matter, determined in vivo with sheep. Multiple regression analysis, when it included data from proximate analysis, resulted in an equation (R = 0·98) for prediction of metabolizable energy content, based on 30 experiments with rations varying in protein and crude fibre content, and 59 other experiments with concentrates. Energy content was in the range of 7·7–13·2 MJ ME/kg D.M. (± S.D. = 11·17 ± 1·08). The residual standard deviation of the equation was 0·25 MJ. Gas production was measured in calibrated syringes. The only chemical determinations needed are dry matter, protein and fat. Differences in activity between batches of rumen liquor are corrected by reference to gas production with standard feedingstuffs (hay meal and maize starch).

The recovery in the faeces of the n-alkanes of herbage (odd-chain, C27–C35) and of dosed artificial alkanes (even-chain, C28 and C32) was studied in twelve 4-month-old castrated male lambs. The lambs received three levels of cut, fresh perennial ryegrass or a mixed diet of perennial ryegrass (0·70) and a barley-based concentrate (0·30) (500–900 g D.M./day). C28 and C32 n-alkanes (130 mg each), absorbed onto shredded paper, were given once daily for 17 days to test whether the recoveries of herbage and dosed alkanes were similar to enable their use as markers for determining the herbage intake of grazing sheep. Stearic and palmitic acids (130 mg each) were given with the dosed alkanes to half of the animals with the objective of facilitating emulsification of the dosed alkanes within the digestive tract.

With the exception of C27 n-alkane, the faecal recoveries of all alkanes were unaffected by diet, feeding level or emulsifying agent. Faecal recovery of odd- chain herbage n-alkanes increased with increasing C-chain length. The recovery of the dosed C28 n-alkane was slightly greater than the recoveries of both C27, and C29 n-alkanes of herbage. The recoveries of the dosed C32 n-alkane and the herbage C33-alkane were the same.

The mean herbage intake estimated using C33 and C32 n-alkanes was identical to the actual herbage intake. Other alkane pairs gave slight underestimates of herbage intake ranging from 3·5% for the C28–C29 pair to 7·6% for the C27–C28 pair. No cyclical pattern of n-alkane excretion throughout the day was observed. Examination of daily variations in faecal alkane concentrations indicated that the start of alkane dosing should precede the sampling of faeces by at least 6 days.

These results suggest that accurate estimation of herbage intake in grazing sheep is possible from the simultaneous use of dosed C32 and herbage C33 n-alkanes as markers.

The method may be particularly useful in enabling unbiased estimates of herbage intake to be made in animals receiving supplementary feed.