Genetic selection for increased sow prolificacy has resulted in decreased mean piglet birth weight. This study aimed to investigate the effect of l-carnitine (CAR) supplementation to sows during gestation and/or lactation on sow productivity, semitendinosus muscle (STM) maturity and lifetime growth in progeny. Sixty-four sows were randomly assigned to one of the four dietary treatments at breeding until weaning: CONTROL (0 mg CAR/d), GEST (125 mg CAR/d during gestation), LACT (250 mg CAR/d during lactation) and BOTH (125 mg CAR/d during gestation and 250 mg CAR/d during lactation). The total number of piglets born per litter was greater for sows supplemented with CAR during gestation (17·3 v. 15·8 (sem 0·52); P < 0·05). Piglet birth weight (total and live) was unaffected by sow treatment (P > 0·05). Total myofibre number (P = 0·08) and the expression level of selected myosin heavy chain genes in the STM (P < 0·05) were greater in piglets of sows supplemented with CAR during gestation. Pigs from sows supplemented with CAR during gestation had lighter carcasses at slaughter than pigs from non-supplemented sows during gestation (83·8 v. 86·7 (sem 0·86) kg; P < 0·05). In conclusion, CAR supplementation during gestation increased litter size at birth without compromising piglet birth weight. Results also showed that the STM of piglets born to sows supplemented with CAR during gestation was more developed at birth. However, carcass weight at slaughter was reduced in progeny of sows supplemented with CAR during gestation. The CAR supplementation strategy applied during gestation in this study could be utilised by commercial pork producers to increase sow litter size and improve offspring muscle development.

Currently, energy evaluation of fish feeds is performed on a digestible energy basis. In contrast to net energy (NE) evaluation systems, digestible energy evaluation systems do not differentiate between the different types of digested nutrients regarding their potential for growth. The aim was to develop an NE evaluation for fish by estimating the energy efficiency of digestible nutrients (protein, fat and carbohydrates) and to assess whether these efficiencies differed between Nile tilapia and rainbow trout. Two data sets were constructed. The tilapia and rainbow data set contained, respectively, eight and nine experiments in which the digestibility of protein, fat and energy and the complete energy balances for twenty-three and forty-five diets was measured. The digestible protein (dCP), digestible fat (dFat) and digestible carbohydrate intakes (dCarb) were calculated. By multiple regression analysis, retained energy (RE) was related to dCP, dFat and dCarb. In tilapia, all digestible nutrients were linearly related to RE (P<0·001). In trout, RE was quadratically related to dCarb (P<0·01) and linearly to dCP and dFat (P<0·001). The NE formula was NE=11·5×dCP+35·8×dFAT+11·3×dCarb for tilapia and NE=13·5×dCP+33·0×dFAT+34·0×dCarb–3·64×(dCarb)2 for trout (NE in kJ/(kg0·8×d); dCP, dFat and dCarb in g/(kg0·8×d)). In tilapia, the energetic efficiency of dCP, dFat and dCarb was 49, 91 and 66 %, respectively, showing large similarity with pigs. Tilapia and trout had similar energy efficiencies of dCP (49 v. 57 %) and dFat (91 v. 84 %), but differed regarding dCarb.

The effect of dietary digestible protein (DP) and/or digestible energy (DE) levels on lysine (Lys) requirements, Lys utilisation efficiency and voluntary feed intake (VFI) were studied in rainbow trout fry when Lys was the first limiting indispensable amino acid or in excess in the diet. Two trials were conducted at 11·6°C with eighty-one experimental diets, containing 280 g DP/kg DM (low protein (LP), trial 1), 600 g DP/kg DM (high protein (HP), trial 1) or 440 g DP/kg DM (medium protein (MP), trial 2), 17 MJ DE/kg (low energy (LE)), 19·5 MJ DE/kg (medium energy (ME)) or 22 MJ DE/kg (high energy (HE)), and nine Lys levels from deeply deficient to large excess (2·3–36 g/kg DM). Each diet was given to apparent satiety to one group of fifty fry (initial body weight 0·85 g) for 24 (MP diets, trial 2) or 30 (LP and HP diets, trial 1) feeding days. Based on N gain data fitted with the broken-line model, the relative Lys requirement was significantly different with the dietary DP level, from 13·3–15·7 to 22·9–26·5 g/kg DM for LP and HP diets, respectively, but did not significantly change with the DE level for a same protein level. The Lys utilisation efficiency for protein growth above maintenance was constant across diets, suggesting no effect of either dietary DE or DP levels. In Lys excess, the VFI was markedly decreased by the DP level but not by the extra DE supply. Our results suggest that the relative Lys need is best expressed in terms of percentage of protein content for optimum fish feed formulation, at least in rainbow trout fry.

The dog chew studied here is a starch-based, twin-screw cooker extruded dog care and treat (C&T) product with oral health benefits. The manufacturing process and nutrient profile of such products are markedly different from those of main meal pet foods. Predicted metabolisable energy (PME) in pet food is calculated using equations derived from main meal feeding studies so it is unclear whether these equations can be applied to C&T products. The present study aimed to directly measure metabolisable energy (ME) content of the dog chew in dogs and compare with calculated PME. A batch of dog chews was manufactured and the product rendered micronutrient complete to allow solus feeding. Following a 3 d standard diet pre-feed phase, the test product was fed solus to a panel of seven adult dogs for a period of 8 d. Dietary intake was recorded daily and faecal matter collected for the last 5 d. Test product and pooled faecal samples were analysed for proximate nutrients, and digestibility coefficients were calculated as the difference in intake and faecal excretion (7–11 d). Digestible energy was converted to ME by correcting for energy losses in urine. PME was calculated using proximate analysis and modified Atwater factors according to National Research Council 2006. The results showed close agreement between actual ME (1272 (sd 12·1) kJ/100 g) and calculated PME (1268 (sd 12·6) kJ/100 g), indicating transferability of the NRC 2006 PME equations to the dog chew tested here.

Morphological and chemical characteristics of 11 warm season pasture weed species were defined. Goldenrod (Solidago altissima L.) was significantly taller and common ragweed (Ambrosia artemisiifolia L.) had the largest canopy diameter of the 11 species studied. Species ranged from 14 to 134 cm in height with canopy diameters of 25 to 70 cm. No direct correlation was found between individual leaf size and total leaf area. Macro- and micromineral content varied widely among species but all values obtained were considered high enough to meet the requirements of ruminant animals. Redroot pigweed (Amaranthus retroflexus L.) and horsenettle (Solanum carolinense L.) contained potentially toxic levels of nitrate. Five of the 11 species contained sufficient crude protein for ruminants and six of the 11 species were more than 50% digestible. Digestible energy values averaged 1.9 Mcal/kg for the 11 weeds evaluated.

This study examined the effect of including different dietary proportions of starch, protein and lipid, in diets balanced for digestible energy, on the utilisation efficiencies of dietary energy by barramundi (Lates calcarifer). Each diet was fed at one of three ration levels (satiety, 80 % of initial satiety and 60 % of initial satiety) for a 42-d period. Fish performance measures (weight gain, feed intake and feed conversion ratio) were all affected by dietary energy source. The efficiency of energy utilisation was significantly reduced in fish fed the starch diet relative to the other diets, but there were no significant effects between the other macronutrients. This reduction in efficiency of utilisation was derived from a multifactorial change in both protein and lipid utilisation. The rate of protein utilisation deteriorated as the amount of starch included in the diet increased. Lipid utilisation was most dramatically affected by inclusion levels of lipid in the diet, with diets low in lipid producing component lipid utilisation rates well above 1·3, which indicates substantial lipid synthesis from other energy sources. However, the energetic cost of lipid gain was as low as 0·65 kJ per kJ of lipid deposited, indicating that barramundi very efficiently store energy in the form of lipid, particularly from dietary starch energy. This study defines how the utilisation efficiency of dietary digestible energy by barramundi is influenced by the macronutrient source providing that energy, and that the inclusion of starch causes problems with protein utilisation in this species.

The purpose of the present study was to compare digestibility of grass hay, faecal and plasma volatile fatty acid (VFA) concentrations, and faecal bacterial abundance in overweight and moderate-condition mares. Five overweight adult mixed-breed mares and five adult mixed-breed mares in moderate condition were housed individually and limit-fed orchard grass (Dactylis glomerata) hay at 20 g/kg body weight (as fed) daily for 14 d. Forage DM and fibre digestibility were determined using AOAC methods; digestible energy was measured using bomb calorimetry; plasma and faecal VFA concentrations were determined by use of GC and MS; faecal Firmicutes, Bacteroidetes, Fibrobacter succinogenes, Ruminococcus flavefaciens and total bacteria abundance was determined by quantitative real-time PCR using previously designed phylum-specific 16S ribosomal RNA gene primers. No differences in hay digestibility, faecal VFA concentrations or faecal bacterial abundance were detected between overweight and moderate-condition mares. Mean plasma acetate concentrations were higher (P = 0·03) in overweight (1·55 (range 1·43–1·65) mmol/l) v. moderate-condition (1·39 (range 1·22–1·47) mmol/l) mares. We conclude that the higher plasma acetate in overweight mares should be further investigated as a potential link between gut microbes and obesity in horses.

The effect of the type of non-protein energy (NPE) on energy utilisation in Nile tilapia was studied, focusing on digestible energy utilisation for growth (kgDE). Furthermore, literature data on kgDE across fish species were analysed in order to evaluate the effect of dietary macronutrient composition. A total of twelve groups of fish were assigned in a 2 × 2 factorial design: two diets (‘fat’ v. ‘starch’) and two feeding levels (‘low’ v. ‘high’). In the ‘fat’-diet, 125 g fish oil and in the ‘starch’-diet 300 g maize starch were added to 875 g of an identical basal mixture. Fish were fed restrictively one of two ration levels (‘low’ or ‘high’) for estimating kgDE. Nutrient digestibility, N and energy balances were measured. For estimating kgDE, data of the present study were combined with previous data of Nile tilapia fed similar diets to satiation. The type of NPE affected kgDE (0·561 and 0·663 with the ‘starch’ and ‘fat’-diets, respectively; P < 0·001). Across fish species, literature values of kgDE range from 0·31 to 0·82. Variability in kgDE was related to dietary macronutrient composition, the trophic level of the fish species and the composition of growth (fat:protein gain ratio). The across-species comparison suggested that the relationships of kgDE with trophic level and with growth composition were predominantly induced by dietary macronutrient composition. Reported kgDE values increased linearly with increasing dietary fat content and decreasing dietary carbohydrate content. In contrast, kgDE related curvilinearly to dietary crude protein content. In conclusion, energy utilisation for growth is influenced by dietary macronutrient composition.

An experiment was conducted to examine the digestible energy (DE) content for weanling pigs in a cohort of wheats grown in Western Australia, and to establish relationships between DE content and their chemical composition. The 3 ✕ 3 ✕ 2 factorial experiment examined the wheat variety (Arrino, Stiletto and Westonia), growing location (high, medium and low rainfall zone) and harvest year (1999 and 2000). Pigs (no. = 5 per diet) aged about 28 days were given a diet at a level of 0·05 ✕ live weight containing 900 g/kg of the wheat and an acid-insoluble ash marker for 10 days, with samples of faeces collected from each pig for the final 5 days. The average live weight of pigs was 6·6 (s.d. 0·77) kg. The DE content of wheats harvested in 1999 varied by up to 1·3 MJ/kg, while wheats harvested in 2000 varied by up to 1·8 MJ/kg. When the 2 years’ data were combined, the DE content ranged from 12·5 to 14·4 MJ/kg. Both the variety and growing region significantly influenced (P < 0·05, P < 0·001, respectively in year 1999; P < 0·001, P < 0·01, respectively in year 2000) the DE content of wheat. Also, DE content of wheat differed significantly due to growing season (P < 0·001). Correlation studies between chemical composition and DE content of the wheats found significant inverse relationships between DE content and total xylose (r = –0·719, P < 0·05), insoluble xylose (r = –0·742, P < 0·05), neutral-detergent fibre (r = –0·839, P < 0·01), total-P (r = –0·833, P < 0·01), and phytate-P (r = –0·753, P < 0·05) contents with the wheats harvested in 1999. However, such relationships were not significant (P > 0·05) with the wheats harvested in 2000. In addition, the precipitation level (mm) during the growing season of wheats was strongly correlated (r = –0·821, P < 0·01) to the DE content of wheat in year 1999, but was not correlated in 2000. The results indicate that the genetic and environmental conditions during the growth of wheat have a significant impact on the utilization of plant energy in weaner pigs, and that greater attention needs to be paid to these influences in the assignment of energy values for wheats given to weaner pigs.

The intakes and in vivo apparent digestibilities (AD) of four forages: hay (H), haylage (HY), big-bale silage (BB) and clamp silage (CS), were investigated in Welsh cross pony geldings (live weight (LW) ca. 330 kg). The trial was a 4 ✕ 4 Latin-square design with diets offered at 1•65 g/kg dry matter (DM) per100 kg LW per day, in two equal meals. Food and faecal samples were analysed for DM, organic matter, crude protein (CP), gross energy, calcium (Ca), phosphorus (P), magnesium (Mg) and non-starch polysaccharide (NSP) composition and content. Significant differences (P < 0·05) in DM intakes (DMI) g/kg M0·75 were recorded between foods, where HY = BB = H > CS. For all measurements AD was significantly (P < 0·05) higher for BB and CS than for H, with HY being intermediate in all but digestibilities of Ca and Mg. Digestibility of NSP of BB and CS were significantly (P < 0·05) greater than for H and HY. The digestible energy (DE) of H, HY, BB and CS were 5·75, 9·09, 9·83 and 11·98 MJ/kg DM respectively, which coupled with the corresponding DMI resulted in all foods but H meeting the theoretical daily DE requirements of the ponies. Similarly, theoretical digestible CP requirements were met on all diets except H. NSP fractions accounted for 0·5 of daily DE in both H and BB, which were significantly (P < 0·05) higher than for CS and HY at 0·4 and 0·2 respectively. These results indicate that CS, BB and HY are readily digested by ponies and thus offer suitable high-energy alternatives to hay in horse rations.

An experiment was conducted to examine the effects of dietary lysine/digestible energy (DE) ratio (g/MJ) and dietary energy concentration on growth performance and body composition of young hybrid gilts from 9·1 to 25·4 kg live weight. Seven pigs were assigned to each of 10 dietary treatments consisting of lysine/DE ratios from 0·6 to 1·4 in 0·2 g/MJ increments and two DE concentrations (14·25 and 16·40 MJ/kg). Food was provided ad libitum and at 25·4 kg all pigs were slaughtered and body composition was determined. Responses to lysine/DE ratios were different for each DE concentration. The pigs given the 16·40 MJ/kg DE diets had a higher daily live-weight gain (DLWG) and nitrogen deposition rate (NDR) than those given the 14·25 MJ/kg diets up to the 1·2 g/MJ lysine/DE ratio. Beyond this point no DE effects were evident. Lipid deposition rate (LDR) was higher for all 16·40 MJ/kg diets as compared with the 14·25 MJ/kg diets and decreased with increasing lysine/DE ratio. The 14·25 MJ/kg diets resulted in increasing efficiency of nitrogen and gross energy utilization with increasing lysinel DE ratio up to the 1·0 g/MJ ratio after which it declined. Efficiency of lipid utilization decreased with increasing lysine/DE ratio for all 14·25 MJ/kg diets. The 16·40 MJ/kg diets resulted in a decrease in nitrogen and gross energy utilization efficiency with increasing lysine/DE ratio while lipid efficiency decreased up to the 1·0 g/MJ lysine/DE ratio after which it increased. Young hybrid pigs given high energy diets appear to be less sensitive to dietary lysine/DE ratio than those given lower energy diets. The optimum lysine/DE ratio for the genotype tested from 9 to 25 kg live weight was of the order of 1·2 g/MJ for both DE concentrations. The maximum DLWG and NDR of the genotype tested over the live-weight range of 9 to 25 kg appears to be of the order of 620 and 17 g/day (106 g/day protein deposition rate) respectively.

An experiment was conducted to examine the effects of dietary lysine/digestible energy (DE) ratio (g/MJ) on growth performance and body composition of boars, gilts and castrated males from 25 to 90 kg live weight. Twelve pigs (four of each sex) were assigned to each dietary treatment consisting of lysine/DE ratios from 0·4 to 1·4, in 0·2 g/MJ increments. Food was provided at proportionately 0·90 ad libitum and at 90 kg all pigs were slaughtered and the body composition of two pigs per sex per treatment was determined. Responses to lysine/DE ratios were similar for all sexes up to the optimum level after which daily live-weight gain (DLWG) and nitrogen deposition rate (NDR) deteriorated in gilts and castrated males. This deterioration may have been due to energy used for deamination of excess protein not being availablefor growth processes. Lipid deposition rate (LDR) remained constant from the 0·4 to 0·8 g/MJ lysine/DE ratios and then decreased sharply to a lower plateau from the 1·0 to 1·4 g/MJ lysine/DE ratios suggesting that DE levels were adequate to meet NDR requirements up to the 1·0 g/MJ lysine/DE ratio when it became limiting. The optimum lysine/DE ratio for the genotype tested from 25 to 90 kg live weight was of the order of 0·95 to 1·0 g/MJ. The maximum NDR of the genotype tested appears to be of the order of 28 to 30 g/day (175 to 187 g/day protein deposition rate).

A total of 315 first parity sows were used in two experiments to establish the lactational and subsequent reproductive performance of first-litter sows in response to varying levels of dietary amino acids and digestible energy (DE) offered during lactation. In the first experiment, sows were offered five diets ranging in lysine content from 6·2 to 15·1 g/kg. In the second experiment sows were offered five diets with a similar lysine: DE ratio (0·88 to 0·85 g/MJ) but ranging in DE content from 12·6 to 15·1 MJ/kg. Voluntary food intake during lactation was unaffected by lysine or DE content of the diets. Piglet pre-weaning growth was similarly unaffected by dietary DE content but responded in a curvilinear manner with increasing dietary lysine. Sow body-weight loss during lactation was unaffected by dietary lysine but declined with increasing DE content up to 13·8 MJ/kg. Backfat loss was lowest for sows offered the lowest lysine diet and tended to reach a plateau at a dietary level of 10·6 g lysine per kg. In response to dietary DE content, backfat loss tended to be highest for sows offered the diet of lowest DE content and declined with increasing DE content up to 15·1 MJ DE per kg. The subsequent weaning to remating interval was unaffected by dietary DE content. Subsequent litter size was similarly unaffected by dietary DE content but was significantly higher for sows offered the two higher, compared with the two lower, lysine diets (10·7 v. 9·6 born alive, s.e.d. 0·5, P < 0·05). The results suggest that current amino acid recommendations for lactating first-litter sows are inappropriate and may be constraining both milk production and subsequent reproductive performance.

Data from experimental programmes designed to investigate the effect of chemical structure of fats upon their apparent digestible energy (DE) value for pigs were subjected to regression analysis. For growing pigs, over the approximate live-weight range 30 to 90 kg, 25 data points were available, with fats evaluated having a range in the ratio of unsaturated to saturated fatty acids (U/S) from 0·66 to 15·67 and in free fatty acid (FFA) content from 8 to 818 g/kg. Sixteen data points were available for young pigs of approximately 12 kg live weight with a range in U/S from 0·62 to 5·71 and in FFA content from 54 to 756 g/kg. The wide range of values for U/S and FFA content had been obtained by blending different fats and, therefore, represented both the range and extremes likely to be found in the formulation of pig diets. Derivation of prediction equations for DE were based upon a series of non-linear regression analyses employing, in sequence, U/S, U/S + FFA content and U/S × FFA content. The DE offats could be predicted from U/S and FFA content with equations accounting for 0·802 and 0·768 of the variation in DE values for growing and young pigs respectively. The most appropriate equation for pigs of all live weights employed U/S and FFA content additively (U/S + FFA content). The equation for growing pigs was DE (MJ/kg) = 36·898 – (0·0046FFA (g/kg)) — 7·33e(–0·906U/S) and for young pigs was DE (MJ/kg) = 37·890 — (0·0051FFA (g/kg)) –8·20e(–0·515U/S). Comparisons revealed that differences between the two age groups, with lower values achieved with younger pigs, -were more pronounced the lower U/S and the higher FFA content of the fat.

The effect of degree of saturation (ratio of unsaturated to saturated fatty acids, U/S) and free fatty acid (FFA) content of fats upon their digestible energy (DE) values was investigated in post-weaning pigs. The two fats evaluated were soya-bean oil (SO) and tallow (T) (representing extremes of saturation) together with their acid oils (SAO and TAO respectively) providing high FFA levels). Blends of the four fats provided treatments with varying FFA content and U/S ratios. The experimental fats were evaluated by substitution, at 40, 80 and 120 g/kg into a basal diet, in a randomized-block design, with 98 gilts and 98 boars of approximately 12 kg live weight. Pigs had been weaned at 28 days of age and experimental diets were given 7 days after weaning. When pigs obtained a weight of 10 kg the inert marker titanium dioxide was added to the diets as a reference substance. A 5-day adjustment period was allowed followed by a 5-day collection period of faeces by grab sampling. Fat content of food and faeces, with methodology based on acid hydrolysis, allowed calculation of apparent digestible fat (AFD) of experimental diets. Analysis of variance demonstrated effects of fats, rates of inclusion, and fats × rates (P < 0·001 in all cases). There was no effect of sex. Extrapolation of the function obtained by regressing AFD of diets (y) on rate of inclusion of fat (x) to × = 1000 generated values for the fats. The product of the coefficient of fat apparent digestibility of fats and their respective gross energies gave DE values for fats which were: SO = 37·2 MJ/kg, SAO = 35·0 MJ/kg, T = 34·3 MJ/kg and TAO = 27·4 MJ/kg. Data for fat blends intermediary between these fats showed that DE improved as a function of U/S and that DE declined linearly with increasing FFA content.

Information on diet composition, daily energy expenditure, energy storage and the utilization of energy in the prey are important factors when evaluating the food consumption of minke whales (Balaenoptera acutorostrata) during their summer stay in northern waters. The purpose of the present study was in this context to obtain information on the digestible energy (DE) of different prey selected by minke whales. An in vitro three-stage digestion technique, simulating the different compartments of the digestive system, has been developed. The initial step simulated the anaerobic microbial fermentation of substrate in the fortestomach. The next stage included the addition of pepsin (EC 3.4.23.1)–HCI, simulating ventricle enzymic decomposition, and finally, in the third step, fresh extract from duodenal contents was used to simulate enzymic intestinal degradation of the remaining components of the food. The inoculum was normally obtained from animals which had recently eaten the prey to be tested. In such tests we obtained a dry matter disappearance (DMD) and a DE for herring (Clupea harengus) of 80·4 (SD 5·0)% (n 18) and 92·1 (SD 3·7) % (n 16) respectively, and a DMD of krill (Thysanoessa sp.) of 83·4 (SD 4·9)% (n 6). The DMD of krill was reduced to 73·8 (SD 7·3)% (n 8) while the DE was 70·6 (SD 10·4) % (n 7) when inoculum from whales which had recently eaten cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) was used. These results indicate a high digestibility of the most common species of prey in these animals, and also that the whales have little difficulty in changing from one prey species to another.

Four metabolism trials were conducted. Trials 1 and 2 (Tl, T2) investigated degree of saturation of fats (ratio of unsaturated to saturated fatty acids, U/S) on digestible energy (DE) content. Fats evaluated were rape oil (RO) and tallow (T) for Tl (U/S 15·67 and 0·97 respectively) and RO and palm oil (PO) for T2 (U/S 15·33 and 0·85 respectively). Three fats of intermediary U/S for each trial were produced by blending the two fats in proportions to give U/S of 3·18,2·08 and 1·49 in both trials. Trials 3 and 4 (T3, T4) investigated the effect of free fatty acid (FFA) content of fats on DE value. Fats were soya-bean oil (SO) and soya-bean acid oil (SAO) for T3 (FFA 6·2 and 626·0 g/kg respectively) and T and tallow acid oil (TAO) for T4 (FFA 44·3 and 818·2 g/kg fat respectively). Three fats of intermediary FFA for each trial were formed by blending the two fats in the ratios of 72:25, 50: 50 and 25: 75 in both trials. The FFA content of the blends were 161·2, 316·1 and 471·1 g/kg fat for T3 and 237·8, 431·3 and 624·7 g/kg fat for T4. All trials evaluated five fats by substitution, at 40, 80 and 120 g/kg into a basal diet, in a cross-over design, with 16 gilts of 25 kg initial live weight evaluating 16 diets over four time periods. Diets were offered for 10 days followed by a 5-day collection period using the marker to marker technique. Fat content of food and faeces, with methodology based on acid hydrolysis, allowed calculation of apparent digestible fat (AFD) of experimental diets. Analysis of variance gave effects of fats (P < 0·001 for Tl, T3 and T4 and P = 0·014 for T2), rates of inclusion (P < 0·001 for all trials), and fats × rates (P > 0·05, P > 0·05, P < 0·001, P < 0·01 for T1, T2, T3 and T4 respectively). Extrapolation of the function obtained by regressing AFD of diets (y) on rate of inclusion of fat (x) to × = 1000 generated values for the fats. The product of the coefficient of apparent fat digestibility of fats and their respective gross energies gave DE values for fats which were MJ/kg: T1 RO = 35·8 and T = 31·2; T2 RO = 36·7 and PO = 33·1; T3 SO = 374 and SAO = 32·8 and T4 T = 33·8 and TAO = 28·9. Data for fat blends intermediary between the two fats showed that DE improved exponentially as a function of U/S and that DE declined linearly with increasing FFA content.

A sugar-beet fibre preparation (SBF) was incorporated into a semi-synthetic rat diet at a level of 100 g/kg. The material caused no feed aversion, and gain of live weight was unimpaired. SBF appeared to be slightly more fermentable than wheat bran and only marginally less effective as a faecal bulking agent when compared with equalized intakes of non-starch polysaccharide. SBF did not stimulate mucosal cell turnover in the small intestine. Some enlargement of the caecum was observed in animals given SBF, but it was no greater than that of animals given wheat bran. Animals given SBF had a lower serum cholesterol concentration than both the fibre-free controls and those given wheat bran. This hypocholesterolaemic effect was less than that of guar gum however. The partial digestibility of energy for SBF was 0.64, and its partial digestible energy value was 11.3 kJ (2.7 keal)/g. The partial digestibility of energy for non-starch polysaccharide in SBF was estimated to be 0.53 and its partial digestible energy value was 9.1 kJ (2.2 kcal)/g. This value was not significantly different from that expected for unavailable carbohydrate in mixed human diets.