Boards of artificial pasture were prepared by threading the top two leaves of tillers from either ryegrass or kikuyu grass, in their vegetative stage of growth, through 5-mm-diameter holes in pressed hardwood sheets. The holes were spaced in rows from 10 to 50 mm apart, and, with one, two or three tillers per hole, tiller density ranged from 346 to 25 980/m2. Sward height was varied by pulling tillers different distances through the holes before they were fastened to the underside of the boards, and the mass of herbage dry matter ranged from 0.04 to 7.61 t/ha. In series I experiments, the effects of sward characteristics on ingestive behaviour of two sheep were examined, whereas, in series I1 experiments, pastures that were consumed at different rates were offered in pairs and the preference of one sheep observed.The rate of pasture intake was related to sward height only when tiller density was constant and to herbage mass per unit volume (bulk density) only at similar sward heights. Intake rate was better described by herbage mass per unit area but, at herbage availabilities of less than 1 t/ha, intake rate was several-fold greater when sheep grazed tall, sparse pastures than short, dense pastures. The best predictor of pasture intake rate was herbage mass per area effectively covered by one bite.Intake per prehending bite declined with a reduction in both sward height and density, and was also best described by herbage mass per area effectively covered by one bite. Prehending bite rate doubled as intake per bite declined from 200 to 10 mg dry matter. The rate of jaw movements during grazing was virtually unaffected by sward characteristics; prehending bites accounted for 20% of jaw movements when intake per bite was 200 mg dry matter and 80% of jaw movements with short, widely spaced swards.When two pastures with different sward characteristics were offered together, sheep generally preferred the one they could eat faster.*Part I, Aust.

No abstract

The present study revealed that CD affects a wide range of daily activities and that gluten consumption may be more common than anticipated with possible consequences on health.

I. Results of 298 nitrogen balance studies from experiments with male cross-bred lambs, ranging in weight from 3 to 38 kg, which had been either fasted, or fed entirely on liquid diets of varying protein content at various energy intakes up to ad lib. intake, were used to quantitatively describe the effects of the amount and quality of absorbed protein, energy intake and live weight on N balance and total N requirement of lambs.2. When N intake was less than the amount required, N balance was independent of energy intake, but linearly related to absorbed N and metabolic body-weight (live eight""^). In the fitted relationship, the coefficient of absorbed N was shown to be an estimate of the biological value of absorbed protein and the coefficient of metabolic body-weight was an estimate of the loss of endogenous N in both urine and faeces. For the milk-based diets used in the experiment biological value was 0'72 and the total endogenous N loss in urine and faeces was 148 mg N/kg075 per d. 3.When N intake was in excess of the amount required, N balance in lambs of a constant live weight increased linearly with metabolizable energy (ME) intake, at a rate that decreased with increasing live weight. Similarly at constant ME intake, N balance was a curvilinear decreasing function of metabolic body-weight. When N balance was expressed per unit metabolic body-weight, it was constant for lambs of all weights when ME intake was about 0.23 M J/kg0'76 per d, but it decreased linearly with increasing metabolic body-weight for ME intakes above this level.4. N balance of fasted lambs was several times less than predicted by either of the relationships established for fed animals, and was found to be linearly related to metabolic bodyweight.G . The effects of enerm intake and live weight on the total N requirement of lambs were -_ -determined. When total N requirement was expressed per unit of energy intake, it was found to be constant at 0-9 g N/MJ ME for all lambs irrespective of live weight when ME intake was 0.23 MJ/kg@75 per d. However, as ME intake/unit metabolic body-weight was raised above this level, N requirement/unit ME intake increased for lambs weighing less than c. 23 kg, but decreased for heavier animals.

In experiment 1, potential intake rates of several dried forages, varying widely in nutritive value, were measured by offering each alone to six hungry sheep for eight, separate 1-min periods. Intake rates ranged from 5.5 to 26.1 g/min, but, within each forage, it varied little between sheep (c.v. 13%) or between measurements with the same sheep (c.v. 8%). The forages were then offered in pairs in separate containers and preference for one forage was defined as the percentage of total intake derived from that forage. With the exception of a dried clover pasture, preference for a forage was strongly related to the rate at which it could be eaten. Reducing the length of wheaten straw particles from 30 to 10 mm increased intake rate from 5.5 to 12.4 g/min and resulted in an absolute preference for the short material. The mean preference for a forage over all comparisons was more strongly correlated with intake rate of the forage (r2 = 0.87) than with in vitro digestibility of organic matter (r2 = 0.30). In experiment 2, two wheaten straws and two wheaten hays were each chopped to two lengths and, within each forage, mixed (w/w) in the short : long ratios of 0 : 1, 1 : 2, 2 : 1 and 1 : 0. Mean intake rates were 7.3 and 12.5 g/min for the two straws and 15.7 and 23.2 g/min for the two hays. Within each forage, all mixtures were offered in pairs to establish preference. The slopes of regression equations relating preference (%) to intake rate (g/min) were 21.4, 17.0, 5.9 and 2.7 (%.min/g) for the four forages as mean intake rate increased from 7.3 to 23 2 g/min, which indicates that discrimination between forages with the same difference in intake rate was greater when mean intake rate was low. In experiment 3, finely ground clover pasture, lucerne hay, wheaten hay or wheaten straw were added to a base diet of either chopped lucerne or wheaten straw in the ratio 1 : 10. Although the additive had little effect on intake rate, sheep preferred lucerne to clover pasture and wheaten hay to wheaten straw. Equations developed from the results of experiment 2 to predict the preference for one forage over another on the basis of their relative intake rates, showed fair agreement with observations from experiment 1, particularly when the effects of acceptability factors such as taste, odour or feel were translated into differences in potential intake rate.

Anthropomorphic greenhouse gases are raising the temperature of the earth and threatening ecosystems. Since 1950 atmospheric carbon dioxide has increased 28%, while methane has increased 70%. Methane, over the first 20 years after release, has 80-times more warming potential as a greenhouse gas than carbon dioxide. Enteric methane from microbial fermentation of plant material by ruminants contributes 30% of methane released into the atmosphere, which is more than any other single source. Numerous strategies were reviewed to quantify their methane mitigation potential, their impact on animal productivity and their likelihood of adoption. The supplements, 3-nitrooxypropanol and the seaweed, Asparagopsis, reduced methane emissions by 40+% and 90%, respectively, with increases in animal productivity and small effects on animal health or product quality. Manipulation of the rumen microbial population can potentially provide intergenerational reduction in methane emissions, if treated animals remain isolated. Genetic selection, vaccination, grape marc, nitrate or biochar reduced methane emissions by 10% or less. Best management practices and cattle browsing legumes, Desmanthus or Leucaena species, result in small levels of methane mitigation and improved animal productivity. Feeding large amounts daily of ground wheat reduced methane emissions by around 35% in dairy cows but was not sustained over time.

1. A mathematical model is described, which simulates the metabolism of absorbed nutrients (amino acids, acetic acid, butyric acid, glucose, lipid and propionic acid) in growing sheep.2. The basic assumption of the model is that each nutrient is partitioned between synthetic, oxidative or intermediate reactions with rates of reaction which are described using enzyme kinetics. These rates depend on the relationship between maximum reaction rates, constants of affinity and inhibition and the concentrations of metabolites as determined by the model.3. Synthetic reactions calculate fat and protein deposition while intermediate reactions involve the production of ATP and NADPH. There is a total of twelve state variables and the model, programmed in CSMP and ACSL, is solved by integration of twelve differential equations. 4. The model calculates the efficiency of utilization of metabolizable energy for different nutrient inputs and the results may be interpreted in terns of fluxes through the metabolite pools. Simulations using inputs representing forage-and concentrate-based diets indicated decreased efficiency for the forage at high levels of intake and possible reasons for this were further studied in simulations where the inputs of protein and glucose were varied.

Grains rich in starch constitute the primary source of energy for both pigs and humans, but there is incomplete understanding of physiological mechanisms that determine the extent of digestion of grain starch in monogastric animals including pigs and humans. Slow digestion of starch to produce glucose in the small intestine (SI) leads to undigested starch escaping to the large intestine where it is fermented to produce short-chain fatty acids. Glucose generated from starch provides more energy than short-chain fatty acids for normal metabolism and growth in monogastrics. While incomplete digestion of starch leads to underutilised feed in pigs and economic losses, it is desirable in human nutrition to maintain consistent body weight in adults. Undigested nutrients reaching the ileum may trigger the ileal brake, and fermentation of undigested nutrients or fibre in the large intestine triggers the colonic brake. These intestinal brakes reduce the passage rate in an attempt to maximise nutrient utilisation, and lead to increased satiety that may reduce feed intake. The three physiological mechanisms that control grain digestion and feed intake are: (1) gastric emptying rate; (2) interplay of grain digestion and passage rate in the SI controlling the activation of the ileal brake; and (3) fermentation of undigested nutrients or fibre in the large intestine activating the colonic brake. Fibre plays an important role in influencing these mechanisms and the extent of their effects. In this review, an account of the physiological mechanisms controlling the passage rate, feed intake and enzymatic digestion of grains is presented: (1) to evaluate the merits of recently developed methods of grain/starch digestion for application purposes; and (2) to identify opportunities for future research to advance our understanding of how the combination of controlled grain digestion and fibre content can be manipulated to physiologically influence satiety and food intake.