We investigated the effects of dietary carbohydrates on the composition and pH of fecal material and on the ammonia emission from the slurry of growing pigs. Thirty-four barrows (BW approximately 40 kg) were randomly allotted to 1 of 10 diets. A basal diet was formulated to meet all requirements for protein, amino acids, minerals, and vitamins. The control diet was composed of the basal diet plus heat-treated cornstarch. In the other diets, the cornstarch in the control diet was replaced with three levels of either coconut expeller, soybean hulls, or dried sugar beet pulp. Feces were collected separately from urine in a balance experiment. Feces were mixed with a standardized urine (ratio of 1:2.5, wt/wt) to form a slurry. A sample of this slurry was placed in an in vitro system to determine the pH and the ammonia emission for 16 d at 20 degrees C. The fecal and slurry DM contents decreased (P < .001) and the total VFA concentrations increased (P < .001) when the level of dietary carbohydrates increased. The pH and the ammonia emission decreased as the level of carbohydrates increased (P < .001). The addition of soybean hulls to the diet had the greatest effect on reducing the pH and ammonia emission (P < .001), and the effects of sugar beet pulp and coconut expeller were approximately the same. A linear relationship was found between the intake of dietary nonstarch polysaccharides (NSP) and the ammonia emission (P < .001). For each 100-g increase in the intake of dietary NSP, the slurry pH decreased by approximately .12 unit and the ammonia emission from slurry decreased by 5.4%. We conclude that replacing cornstarch in the diet with components that have a high concentration of fermentable carbohydrates increases the VFA concentration of feces and slurry and reduces the pH and ammonia emission from the slurry of growing pigs.

Two experiments were conducted to quantify the effects of protein intake on protein and fat deposition rates at two protein-free, energy intake levels in 90 preruminant Holstein Friesian x Dutch Friesian calves. The two experiments were similar in design, but were performed in two different weight ranges: 80 to 160 kg BW and 160 to 240 kg BW in Exp. 1 and 2, respectively. In each experiment, calves were allocated to either an initial slaughter group or to one of 12 treatments (three calves per treatment), which consisted of six protein intake levels at each of two protein-free energy intake levels. Calves were slaughtered and analyzed for body composition when they had reached the target weight. A balance study was conducted when calves reached 120 and 200 kg BW in Exp. 1 and 2, respectively. Protein digestibility increased with increasing protein intake in both experiments (P < .001). Average daily gain of the empty body varied between 640 and 1,340 g/d and between 420 and 1,370 g/d in Exp. 1 and 2, respectively, and was affected by protein (P < .001) and protein-free energy intake (P < .001). The calves responded to increased protein intake by increasing their protein (P < .001) and fat (P < .01) deposition rates. Maximum protein deposition was reached in the second experiment at 244 g/d. Extra protein-free energy intake resulted mainly in extra fat deposition (P < .001), but also increased the protein deposition (P < .01), even at low protein intake levels. In both experiments, the response of protein deposition rate to increased protein intakes was low: about 30% of the extra ingested protein was deposited. These results clearly demonstrate a low priority for partitioning dietary protein into protein gain in these calves.

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Single-cell ingredients (SCI) are a relatively broad class of materials that encompasses bacterial, fungal (yeast), microalgal-derived products or the combination of all three microbial groups into microbial bioflocs and aggregates. In this review we focus on those dried and processed single-cell organisms used as potential ingredients for aqua-feeds where the microorganisms are considered non-viable and are used primarily to provide protein, lipids or specific nutritional components. Among the SCI, there is a generalised dichotomy in terms of their use as either single-cell protein (SCP) resources or single-cell oil (SCO) resources, with SCO products being those oleaginous products containing 200 g/kg or more of lipids, whereas those products considered as SCP resources tend to contain more than 300 g/kg of protein (on a dry basis). Both SCP and SCO are now widely being used as protein/amino acid sources, omega-3 sources and sources of bioactive molecules in the diets of several species, with the current range of both these ingredient groups being considerable and growing. However, the different array of products becoming available in the market, how they are produced and processed has also resulted in different nutritional qualities in those products. In assessing this variation among the products and the application of the various types of SCI, we have taken the approach of evaluating their use against a set of standardised evaluation criteria based around key nutritional response parameters and how these criteria have been applied against salmonids, shrimp, tilapia and marine fish species.

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