The aim of this experiment was to study the effect of total replacement of oat hay by rosemary distillation residues (RR) on growth, carcass characteristics and meat quality of Barbarine lambs. A total of 21 lambs were divided into three groups. The control group (C) was offered 600 g of oat hay; the RR87 and RR60 groups received 600 g of pellets containing 87% and 60% of RR, respectively. The CP content was 9% and 14% for RR87 and RR60, respectively. All animals were supplemented by 600 g of concentrate. After 77 days of fattening, lambs were slaughtered. The DM and CP intakes were significantly increased with RR diets. The average daily gain was higher (P<0.001), while the feed conversion rate was lower for RR60 and RR87 than C group. The dressing percentage was similar for all groups. The tissular (muscle, fat and bone) and the regional (leg, shoulder, etc.) carcass composition did not differ among groups. The bony organs and gut weights were similar among groups, while functional ones (skin, liver, kidney and testicles) were significantly heavier for both RR groups than control. The ultimate pH, water cooking loss and color variables were similar among groups and the chemical composition (protein, fat, myoglobin, collagen and iron) did not differ also among groups. These results revealed the opportunity of RR use in fattening lambs without adverse effects on carcass and meat characteristics. Moreover, 9% CP in RR pellets are enough given the same growth performance recorded as that of RR with 14% CP.

The effects of feeding Cistus ladanifer (Cistus) and a blend of soybean and linseed oil (1 : 2 vol/vol) on fatty acid (FA) composition of lamb meat lipids and messenger RNA (mRNA) expression of desaturase enzymes was assessed. In total, 54 male lambs were randomly assigned to 18 pens and to nine diets, resulting from the combination of three inclusion levels of Cistus (50 v. 100 v. 200 g/kg of dry matter (DM)) and three inclusion levels of oil (0 v. 40 v. 80 g/kg of DM). The forage-to-concentrate ratio of the diets was 1 : 1. Longissimus muscle lipids were extracted, fractionated into neutral (NL) and polar lipid (PL) and FA methyl esters obtained and analyzed by GLC. The expression of genes encoding Δ5, Δ6 and Δ9 desaturases (fatty acid desaturase 1 (FADS1), fatty acid desaturase 2 (FADS2) and stearoyl CoA desaturase (SCD)) was determined. Intramuscular fat, NL and PL contents were not affected by oil or Cistus. Oil supplementation reduced (P<0.05) 16:0, c9-16:1, 17:0, c9-17:1 and c9-18:1 FA and increased (P<0.05) 18:2n-6, 18:3n-3 and the majority of biohydrogenation intermediates in NL. Cistus alone had few effects on FA of NL but interacted with oil (P<0.05) by increasing t10-18:1,t10,t12-18:2,t10,c12-18:2 and t7,c9-18:2. The t10-/t11-18:1 ratio increased with both Cistus and oil levels. The c9, t11-18:2 did not increase (P<0.05) with both oil and Cistus dietary inclusion. Oil reduced c9-16:1, 17:0, c9-17:1,c9-18:1, 20:4n-6, 22:4n-6 and 20:3n-9 proportions in PL, and increased 18:2n-6, 18:3n-3, 20:3n-3 and of most of the biohydrogenation intermediates. The Cistus had only minor effects on FA composition of PL. Cistus resulted in a reduction (P<0.05) of 20:5n-3 and 22:6n-3 in the meat PL. The expression level of SCD mRNA increased (P=0.015) with Cistus level, although a linear relationship with condensed tannins intake (P=0.11) could not be established. FADS1 mRNA expressed levels increased linearly (P=0.019) with condensed tannins intake. In summary, the inclusion of Cistus and oil in 1 : 1 forage-to-concentrate ratio diets resulted in a large increase in t10-18:1 and no increase in c9,t11-18:2 or n-3 long chain poor in polyunsaturated fatty acids in lamb meat.

The objective of this study was to evaluate the effects of the energy restriction of gestation of adult ewes from day 45 to day 115 on lamb live performance parameters, carcass and meat traits. In experiment I, dietary energy was restricted at 70% of the metabolizable energy (ME) requirements, after which ewes were re-fed ad libitum until lambing. In experiment II, dietary energy was restricted at 60% of the ME requirements, and ewes were re-fed to ME requirements until lambing. All ewes grazed together from the end of the restriction periods to weaning. Lambs were weaned and lot fed until slaughter. Feed intake, weight gain and feed efficiency were recorded, and body fat thickness and ribeye area (REA) were measured in the longissimus thoracis muscle. After slaughter, carcass weight and yield, fat depth, carcass and leg length, and frenched rack and leg weights and yields were determined. Muscle fiber type composition, Warner-Bratzler shear force, pH and color were determined in the longissimus lumborum muscle. In experiment I, energy restriction followed by ad libitum feeding affected lamb birth weight (P<0.05); however, no effects (P>0.05) were observed on later BW, REA, BF or carcass traits. Lambs born to non-restricted-fed ewes had higher (P<0.05) weight and yield of the frenched rack cut and their meat tended (P=0.11) to be tender compared with that of lambs from restricted ewes. The percentage of oxidative muscle fibers was lower for lambs born to non-restricted ewes (P<0.05); however, no effects of ewe treatment were observed on other muscle fiber types. For experiment II, energy restriction followed by ME requirements feeding, affected (P<0.01) pre-weaning live weight gain, weaning and final weights. Lambs from restricted ewes had higher (P<0.05) feed intake as % of leg weight and a trend to be less efficient (P=0.16) than lambs from unrestricted dams. Ribeye area and BF were not influenced by treatment. Treatment significantly affected slaughter weight, but had no effects on carcass yield and traits or on meat traits. The results obtained in both experiments indicate submitting ewes to energy restriction during gestation affects the performance of their progeny but the final outcome would depend on the ewe’s re-feeding level during late gestation and the capacity of the offspring to compensate the in utero restriction after birth.

For their glucose supply, ruminants are highly dependent on the endogenous synthesis in the liver, but despite the numerous studies that evaluated hepatic glucose production, very few simultaneously measured hepatic glucose production and uptake of all precursors. As a result, the variability of precursor conversion into glucose in the liver is not known. The present study aimed at investigating by meta-analysis the relationships between hepatic glucose net release and uptake of precursors. We used the FLuxes of nutrients across Organs and tissues in Ruminant Animals database, which gathers international results on net nutrient fluxes at splanchnic level measured in catheterized animals. Response equations were developed for intakes up to 41 g DM intake/kg BW per day of diets varying from 0 to 100 g of concentrate/100 g DM in the absence of additives. The net hepatic uptake of propionate, α-amino-N and l-lactate was linearly and better related to their net portal appearance (NPA) than to their afferent hepatic flux. Blood flow data were corrected for lack of deacetylation of the para-aminohippuric acid, and this correction was shown to impact the response equations. To develop response equations between the availability of precursors (portal appearance and hepatic uptake) and net glucose hepatic release, missing data on precursor fluxes were predicted from dietary characteristics using previously developed response equations. Net hepatic release of glucose was curvilinearly related to hepatic supply and uptake of the sum of precursors, suggesting a lower conversion rate of precursors at high precursor supply. Factors of variation were explored for the linear portion of this relationship, which applied to NPA of precursors ranging from 0.99 to 9.60 mmol C/kg BW per h. Hepatic release of glucose was shown to be reduced by the portal absorption of glucose from diets containing bypass starch and to be increased by an increased uptake of β-hydroxybutyrate indicative of higher body tissue mobilization. These relationships were affected by the physiological status of the animals. In conclusion, we established equations that quantify the net release of glucose by the liver from the net availability of precursors. They provide a quantitative overview of factors regulating hepatic glucose synthesis in ruminants. These equations can be linked with the predictions of portal absorption of nutrients from intake and dietary characteristics, and provide indications of glucose synthesis from dietary characteristics.

Around 70% of total seed phosphorus is represented by phytate which must be hydrolysed to be bioavailable in non-ruminant diets. The limited endogenous phytase activity in non-ruminant animals make it common practice to add an exogenous phytase source to most poultry and pig feeds. The mature grain phytase activity (MGPA) of cereal seeds provides a route for the seeds themselves to contribute to phytate digestion, but MGPA varies considerably between species and most varieties in current use make negligible contributions. Currently, all phytases used for feed supplementation and transgenic improvement of MGPA are derived from microbial enzymes belonging to the group of histidine acid phosphatases (HAP). Cereals contain HAP phytases, but the bulk of MGPA can be attributed to phytases belonging to a completely different group of phosphatases, the purple acid phosphatases (PAPhy). In recent years, increased MGPAs were achieved in cisgenic barley holding extra copies of barley PAPhy and in the wheat HIGHPHY mutant, where MGPA was increased to ~6200 FTU/kg. In the present study, the effect of replacing 33%, 66% and 100% of a standard wheat with HIGHPHY wheat was compared with a control diet with and without 500 FTU of supplemental phytase. Diets were compared by evaluating broiler performance, ileal Ca and P digestibility and tibia development, using nine replicate pens of four birds per diet over 3 weeks from hatch. There were no differences between treatments in any tibia or bird performance parameters, indicating the control diet did not contain sufficiently low levels of phosphorus to distinguish effect of phytase addition. However, in a comparison of the two wheats, the ileal Ca and P digestibility coefficients for the 100% HIGHPHY wheat diets are 22.9% and 35.6% higher, respectively, than for the control diet, indicating the wheat PAPhy is functional in the broiler digestive tract. Furthermore, 33% HIGHPHY replacement of conventional wheat, significantly improved Ca and P digestibility over the diet-supplemented exogenous phytase, probably due to the higher phytase activity in the HIGHPHY diet (1804 v. 1150 FTU). Full replacement by HIGHPHY gave 14.6% and 22.8% higher ileal digestibility coefficients for Ca and P, respectively, than for feed supplemented with exogenous HAP phytase at 500 FTU. This indicates that in planta wheat PAPhys has promising potential for improving P and mineral digestibility in animal feed.

We investigated the effects of rumen-protected choline (RPC) and vitamin E (VITE) administration on milk production and status of folate, vitamin B12 and vitamin E during the periparturient period of dairy goats. Forty-eight Saanen multiparous goats were selected for the 72-day experiment, being moved to a maternity pen 30 days before expected parturition and assigned to one of the four experimental groups: control (CTR), no choline or vitamin E supplementation; choline (RPC), supplemented with 4 g/day choline chloride in rumen-protected form; vitamin E (VITE), supplemented with 200 IU/day vitamin E in rumen-protected form; and choline and vitamin E (RPCE), supplemented with 4 g/day RPC chloride and 200 IU/day vitamin E. Supplements were administered individually before the morning feed to ensure complete consumption, starting 30 days before kidding and continuing for 35 days after. During the experiment, milk yield and 4% fat-corrected milk (FCM) yield were, respectively, 210 and 350 g/day higher in RPC-supplemented goats than in non-supplemented goats. Milk fat concentration and fat yield were also increased by RPC treatment. Milk yield and composition were unaffected by vitamin E supplementation. There were no significant interactions between RPC and VITE for any of the variables measured. Plasma metabolites did not differ between treatments before and after kidding except that plasma folate at parturition was higher in RPC-supplemented goats. Neither choline nor vitamin E affected vitamin B12 plasma concentrations, while a time effect was evident after the second week of lactation, when B12 levels in each treatment group started to increase. Vitamin E administration resulted in plasma α-tocopherol levels that were 2 to 2.5 times higher than in non-supplemented goats. Overall, these results suggest that greater choline availability can improve milk production and methyl group metabolism in transition dairy goats.

Increased intestinal permeability (IP) can lead to compromised health. Limited in vivo IP research has been conducted in chickens. The objectives of the current study were to develop a model of increased IP utilizing lipopolysaccharide (LPS Escherichia coli O55:B5) and to evaluate IP changes using the lactulose, mannitol and rhamnose (LMR) sugar permeability test. In addition, fluorescein isothiocyanate dextran (FITC-d), d-lactate, zonula occludens (ZO-1) and diamine oxidase (DAO) permeability tests were employed. Male Ross chickens were reared until day 14 on the floor in an animal care facility and then transferred to individual cages in three separate experiments. In each of experiments 1 and 2, 36 chicks were randomly allocated to receive either saline (control) or LPS (n=18/group). Lactulose, mannitol and rhamnose sugar concentration in blood was measured at 0, 30, 60, 90, 120 and 180 min in experiment 1, at 60, 90 and 120 min in experiment 2 and at 90 min in experiment 3 (n=16/group). Lipopolysaccharide was injected intraperitoneally at doses of 0.5, 1 and 1 mg/kg BW in experiments 1, 2 and 3, respectively, on days 16, 18 and 20, whereas control received sterile saline. On day 21, only birds in experiments 1 and 2 were fasted for 19.5 h. Chicks were orally gavaged with the LMR sugars (0.25 gL, 0.05 gM, 0.05 gR/bird) followed by blood collection (from the brachial vein) as per time point for each experiment. Only in experiment 3, were birds given an additional oral gavage of FITC-d (2.2 mg/ml per bird) 60 min after the first gavage. Plasma d-lactate, ZO-1 and DAO concentrations were also determined by ELISA in experiment 3 (n=10). Administration of LPS did not affect IP as measured by the LMR sugar test compared with control. This was also confirmed by FITC-d and DAO levels in experiment 3 (P>0.05). The plasma levels of d-lactate were decreased (P<0.05). Plasma levels of ZO-1 were increased in the third experiment only and did not change in the first two experiments. Lipopolysaccharide at doses of 0.5 and 1 mg/kg did not increase IP in this model system. In conclusion, the LMR sugar can be detected in blood 90 min after the oral gavage. Further studies are needed for the applicability of LMR sugars tests.

Scans of the m. longissimus and overlying fat at the 12th rib were taken, just prior to slaughter, on 254 lambs using the Scanogram and Danscanner ultrasonic machines. The lambs were from a ram breed trial and comprised six sire breed × five dam breed groups. Mean live weight at slaughter was 44·5 kg.

The precision with which scan measurements predicted comparable carcass measurements and carcass lean content (g/kg lean) was examined within groups with variation in live weight eliminated.

Residual s.d. for the prediction of carcass m. longissimus area from the corresponding scan measurement was 141 and 158 mm2 for the Scanogram and Danscanner respectively (s.d. of carcass m. longissimus area was 162mm2). Residual s.d. for the prediction of lean from the best combination of fat measurements was 32·0 for the Scanogram and 35·8 for the Danscanner (s.d. of lean was 38·5). M. longissimus did not increase the precision of lean prediction.

In a comparable evaluation of the Scanogram, involving 147 lambs, the residual s.d. for the prediction of lean was 24·0 (s.d. = 28·9).

The levels of precision obtained were low and it is debatable whether the ultrasonic techniques examined would be of value for carcass lean prediction in practical applications. They might be of use in selection programmes within nucleus flocks of the more important meat sire breeds or as an aid in experiments for differentiating between animals of widely differing composition.

Five randomized-block experiments were carried out over 2 years using British Friesian cows managed as three separate herds. The effects of offering cows different levels of concentrates, ranging from 0·8 to 7·2 kg/day, in addition to grass silage ad libitum during the winter period on reproductive performance was investigated. The effects of substituting 4 kg/day maize gluten, or 0·8 kg/day fish meal, for part or all of the standard concentrate were also examined.

Neither level of concentrates nor the inclusion of maize-gluten meal significantly affected reproductive performance even where milk production and quality was considerably influenced. The inclusion of fish meal improved conception rates to all services (0·64 v. 0·44; P < 0·05) and reduced the number of services required per conception (1·62 v. 2·31; P < 0·01).

Plasma urea levels were raised consistently by the feeding of fish meal and, with the exception of weeks 2 and 6 of lactation, by the feeding of higher levels of concentrates. From the 6th week of lactation levels of beta-hydroxybutyrate (BHB) in the blood were significantly higher in the group of cows receiving the highest level of concentrates. The BHB level at week 6 was correlated with the number of services required per conception.

A number of relationships between production factors and fertility are also presented.

A review of work reported in the literature was used to present quantitative descriptions of energy dispositioning in the growing pig. These are detailed in the text, which points to preferred values, as well as to anomalies and lacunae. The review was prepared with the objective of allowing from its content the inclusive and quantitative modelling of energy requirement. Requirement is approached as the sum of the component factors; maintenance, protein retention and lipid retention. Conventional expressions of maintenance requirement, as some function of pig mass, were found unconvincing in their variety of expression of coefficients and exponents. The review concluded that maintenance is properly related to protein turn-over, and thereby requires at least to include elements of concomitant protein metabolic activity. It was also judged that maintenance costs might be farm-specific. The energy requirements for activity, gaseous losses and disease were identified as important, but unsatisfactory in their quantification. Exploration of the energy costs of uncomfortable ambient temperatures suggested that whilst the responses of the pig are open to sophisticated and relatively exact calculation, the description of comfort remained inexact. The efficiency of retention of lipid by direct incorporation was high and may comprise a substantial proportion of the dietary lipid supply. There was little evidence of variation in the efficiency of utilization of metabolizable energy from carbohydrate for lipid retention. The linear-plateau paradigm for protein retention was adopted. The efficiency of utilization of energy for protein retention measured by a variety of approaches was found to be highly variable, prone to error and the literature confused. It was concluded that the efficiency of use of metabolizable energy for protein retention would be a function of at least: (a) the absorbed substrate being metabolized for the synthesis of body protein, (b) the rate of total protein tissue turn-over associated with the retention of newly accreted protein and not already accounted in the estimate of maintenance, (c) the mass of protein tissue involved in turn-over, and (d) the degree of maturity attained, and any influence maturity may have upon the rate of turn-over of total body protein. Algorithms for energy requirement are presented based upon protein turn-over and these appear to have some consistency with empirical findings.

Three groups of eight yearling Friesian steers were fed on pelleted diets containing ground barley straw, maize and soya bean meal, the percentages of straw in the diets being 10, 30 and 50 (treatments 1, 2 and 3). The crude protein level was adjusted to 12% in all diets on an air-dried basis.

Daily live-weight gain for treatment 2 was 7% greater than for treatment 1, and 12% greater than for treatment 3. Voluntary feed intake was also greater in treatment 2, by 16% when compared with treatment 1 and 4% when compared with treatment 3. The efficiency of feed conversion decreased by 10% for each 20% increase in dietary straw level.

Weight loss during lairage was greater on treatment 3, as were total gut fill and omasum weight. The bone content of carcasses was similar for all treatments; carcass lean was increased in treatment 2. Carcass and channel fat was severely depressed in treatment 3.

The results are discussed in relation to dietary effects on carcass composition.

To reduce nitrogen excretion (NEx) the effect of nitrogen supply on nitrogen retention (NR) and NEx was studied in pregnant sows during three parities. A nitrogen supply of 40 g/day (treatment L) was compared with 62 g/day (treatment C) during day 0 to 85 of pregnancy. In the last month of pregnancy nitrogen supply on treatment L was 50 g/day and on treatment C 74 g/day. Faecal digestible lysine supply followed the same pattern as nitrogen. Nitrogen and energy balances were measured during mid pregnancy (day 50 to 60; no. = 22) and late pregnancy (day 105 to 112; no. = 60). During mid pregnancy treatments had a minor affect on NR and energy metabolism. NEx on treatment L was proportionately about 0·40 lower than on treatment C. During late pregnancy NR was lower on treatment L than on treatment C. NEx on treatment L was proportionately reduced by 0·35 compared with treatment C. In parity 1 the lower NR on treatment L was compensated by a higher fat gain. Results indicate that nitrogen and faecal digestible lysine supply on treatment L were close to minimal requirement in late pregnancy. Assumed values for maintenance requirement of nitrogen (0·45 g N per kg M0·75) and efficiency of ingested nitrogen to NR (0·6) were in line with the results of the balance trials. The observed nitrogen retention of sows, especially during mid pregnancy, permits a reduced nitrogen supply to reduce NEx.

The faecal egg count (FEC) and total egg output is reduced in parasite-resistant sheep and breeding sheep for resistance should reduce infective larval contamination of pastures. This research compares lambs and rams from the parasite-resistant flock, Rylington Merinos, with unselected controls at the same level of larval challenge and the same level of food supply in an animal-house environment. The sheep were penned individually. The parasite resistant sheep excreted 0·85-fold less eggs than the control animals after infection with Trichostrongylus colubriformis and Ostertagia circumcincta for 12 or 18 weeks. During the infection period the parasite resistant lambs had higher plasma immunoglobulin concentration and higher ratio of globulin to albumin than the control animals. In the mature rams these genotype differences diminished. They also had lighter mass of the small intestine with a higher proportion of mucosa, but heavier mass of the large intestine. Parasite infection caused a depletion of blood glutathione in the lambs given food at maintenance or 1·5 × maintenance, and the parasite-resistant sheep (both lambs and rams) also had lower glutathione concentration. Maintaining good body nutrient reserve before the infection reduced the egg output in the early stage of the infection. Food intake had little effect on worm egg production in young sheep given food at maintenance or above. It is suggested that an improvement of nutrition, sulphur-containing amino acids in particular, is required to recover the loss of productive performance caused by the infection.

Maturing patterns of carcass muscle, fat and bone and of body organs were established relative to live weight, using data from 20 Dorset Horn rams and 20 Dorset Horn wethers. The sheep were fed a pelleted ration from soon after weaning and individual sheep of both groups slaughtered at 6-kg increments in live weight from 18 kg to maturity at approx. 100 and 96 kg for the rams and wethers, respectively. This small difference in mature weight was mostly due to the weight of the testes and the increased weight of the head in mature rams.

As proportions of live weight, the mature rams had more carcass muscle and bone and less carcass fat than the mature wethers. In the mature animals the body organs in general comprised similar proportions of live weight in the two groups. However the head, hide and blood were proportionately heavier in the mature rams. The liver and alimentary tract were heavier in the mature wethers.

The maturing patterns for the three carcass tissues were not different for the two groups. However, many of the body organs matured on different patterns in the rams and wethers.

As the mature live weights and the maturing patterns for carcass tissues and some body organs were not different for the two groups, comparisons of the proportions of these tissues in rams and wethers would yield similar conclusions on an equal weight basis, as on the basis of the same proportion of maturity. However, comparisons of the proportions comprised by some body organs need to take account of different maturing patterns, as comparisons at different stages of maturity will each give different answers.

In each of two trials, three groups of eight cows, with condition scores of 1-5 to 2, 2-5 to 3 and 3-5 to 4 at calving, were given a complete diet for the first 16 weeks of lactation. Food intake, milk yield, live weight and condition score were measured, and related to levels of plasma glucose and free fatty acids, serum insulin, prolactin and progesterone in weekly blood samples, in an attempt to explain differences in food intake.

In both trials, levels of plasma free fatty acids were high after calving for all cows and declined rapidly until week 8, after which they were fairly constant. Glucose and insulin levels increased after calving, producing curves similar to that for dry-matter intake in the first 8 weeks of lactation. Prolactin levels fluctuated too markedly to provide useful information. Progesterone levels increased until week 7 and then fluctuated at 3-week intervals coincident with oestrus. Dry-matter intake was negatively correlated with free fatty acid levels and positively correlated with insulin in trial 1, and with glucose and progesterone in both trials.

The objective of this study was to determine the effects on animal performance and rumen digestion characteristics of supplementing cattle grazing autumn grass offered at two levels of allowance, with concentrates formulated from different carbohydrate sources. Seventy-two steers (494 (s.e. 38·4) kg) were assigned to one of six treatments which were arranged in a two grass allowances (5·5 or 11 kg grass dry matter (DM) per head per day) by three concentrate types (starch, starch + fibre or fibre-based diets) factorial design. The experiment commenced on 22 August and had a mean duration of 84 days. Concentrates were formulated to have similar metabolizable energy and crude protein and animals were offered 5 kg per head daily. Grass allowances were offered daily and concentrates were offered individually. Six rumen fistulated steers were used concurrently in a Latin square design to determine the effect of the diets on rumen digestion characteristics. Grass and concentrates degradabilities were measured using the nylon bag technique. The concentrate DM was degraded at 0·189, 0·102 and 0·094 per h for the starch, starch + fibre and fibre-based diets, respectively. Concentrate carbohydrate source and grass allowance did not affect (P > 0·05) degradation rate of grass DM or nitrogen in the rumen, rumen fluid pH, rumen fluid concentration of volatile fatty acids, total lactic acid or ammonia concentration or plasma concentration of glucose, urea or beta-hydroxybutyrate. Animals offered the low grass allowance had larger (P < 0·05) diurnal variation in the rumen fluid acetate: propionate ratio than those offered the high grass allowance. Increasing grass allowance increased (P < 0·01) carcass gain whereas concentrate type had no effect. There was no interaction between concentrate carbohydrate source and grass allowance on any of the production variables measured. It is concluded that the rumen environment in cattle grazing autumn grass buffered the effects of concentrate carbohydrate degradability such that similar productivity was achieved with each concentrate.

The nutritional value of a pelleted fattening concentrate mixture, in which heat-sterilized poultry litter (PL) was included at rates of 0, 15, 25 and 35%, was studied. A digestion and nitrogen balance trial was carried out with rams, and a feeding trial was carried out with intact male cattle from the age of 8 mo to slaughter at 14 mo.

Digestibility of crude protein was related inversely to PL content of the diet. This decrease in digestibility was not accompanied by a decrease in the quality of the protein digested.

Gross and digestible energy contents of the diets were related inversely to their PL content. There were no significant differences in blood urea concentration. A concentrate mixture containing 1% urea but otherwise similar to the control, was included in the feeding trial.

There were no significant differences in rate of live-weight or carcass gain between treatments. The differences in degree of fatness of the carcasses tended to be related inversely to PL% in the diet, but they were small and reached significance only with the extreme treatments. Feed intake on PL-containing diets was higher than on the control diet, but feed conversion efficiency was impaired when the proportion of PL exceeded 25%. No significant correlations were found between total volatile fatty acids in rumen liquor and daily live-weight gain.

Data on 2120 lambs produced over 7 years in the Animal Breeding Research Organization synthetic Dam Line (49% Finn, 22% East Friesian, 16 % Border Leicester and 13 % Dorset Horn) were analysed by least squares. The effects of sex, age of dam, year of birth, birthrearing class, and age of lamb on weights at birth and at 4, 8, 12 and 16 weeks of age were all appreciable. However, pooled within-year correction factors should be adequate in adjusting records for selection. Heritability estimates for weights at the five ages ranged from 0·17 to 0·24 by the sire component method and from 0·18 to 0·28 by regression of offspring on dam. Previous reports of differences in heritability in singles and in twins were not confirmed. Estimates of the genetic correlations among the various lamb weights were high (0·62 to 1·04) indicating that selection for weight at one age should result in increased weights at all ages.

It has become common practice in pig fattening production systems to castrate young boar piglets without the use of anaesthesia. In this study, we examined whether or not CO2 gas is capable of inducing an acceptable anaesthetic state during which castration can be performed. The first step was to identify the most promising CO2/O2 mixture. Based on the results from this first experiment, a mixture of 70% CO2 + 30% O2 was chosen for further investigation as a potential anaesthetic during the castration of young piglets. Thereby, it was established whether the duration and depth of anaesthesia were acceptable for castration where the animal has to be insensible and unconscious. Physiological effects were assessed based on electroencephalogram (EEG) and electrocardiogram (ECG) measurements, blood gas values and behavioural responses. During the induction phase, the only typical behaviour the piglets exhibited when exposed to the 70/30 gas mixture was heavy breathing. All piglets (n = 25) lost consciousness after approximately 30 s according to the EEG. Heart rate decreased slowly during the induction phase, a serious drop occurred when piglets lost their posture. Immediately after this drop, the heart rate neared zero or showed a very irregular pattern. Shortly after loss of posture, most animals showed a few convulsions. None of the animals showed any reaction to castration in behaviour and/or on the EEG and ECG. On average, the piglets recovered within 59 s, i.e. EEG returned to its pre-induction pattern and piglets were able to regain a standing position. After 120 s, heart rate returned to pre-induction levels. In order to explore the usage range of CO2 concentration, 24 piglets were exposed to 60% CO2 + 20% O2 + 20% N2 for up to 30 s after loss of consciousness (as registered on EEG), and castrated after removal from the chamber. Sixteen of the 24 animals showed a reaction to the castration on the EEG. To establish the maximum time piglets survive in 70% CO2 + 30% O2, five piglets were placed in this mixture for 3 min. Two of them died. After that, four piglets were placed in this mixture for 2 min after unconsciousness, one died after 2 min. It was concluded from this study that it is possible to anaesthetise piglets with a mixture of 70% CO2 + 30% O2, but that there are limits to its safety in terms of CO2 concentration and duration of exposure. Before implementation for practical use, further research is essential to assess the limits of gas concentration and exposure times.

An experiment was carried out on pigs to provide a test of two current conceptual frameworks available for the understanding and prediction of food intake. Framework 1 assumes that food intake will be that which allows potential (genetic) performance to be achieved. If this is not achieved then it is because intake is being constrained. Framework 2 sees food intake as being a consequence of a process of optimization such that biological efficiency (the ratio of net energy ingested to oxygen consumed) is maximized. Both frameworks predict that a reduction in temperature will increase the intake of a high quality food. For a food of low quality framework 2 predicts that intake will also be increased when temperature is decreased while framework 1 predicts that it will not. This difference between the predictions of the two frameworks allows them to be tested by means of an experiment in which foods of different quality were given to animals at different environmental temperatures.

Forty pigs were randomly allocated to a control (C) food based on micronized wheat with 13·1 MJ digestible energy (DE) and 232 g crude protein (CP) per kg fresh food, or one of two high bulk foods. The high bulk foods contained either 650 g/kg of unmolassed sugar-beet pulp (SBP) or 650 g/kg of wheat bran (WB). Half the pigs were maintained at a thermoneutral temperature of 22ºC for 14 days followed by a cold temperature of 12ºC for 14 days. The other half were maintained at 12ºC for a period of 14 days followed by a temperature of 22ºC for 14 days. Food intake was recorded daily and live weight twice weekly.

There was a highly significant food ✕ temperature interaction ( P < 0·001) for food intake. A reduction in temperature resulted in an increase in food intake on C and WB but had no effect on the intake of SBP. There was a highly significant effect of both temperature and food on intake ( P < 0·001). A reduction in temperature resulted in a significant increase in food intake, intake on WB was higher than that of either C or SBP. There was no overall effect of temperature on live-weight gain although a reduction in temperature resulted in a non-significant increase in the gain of C and reduction in the gain of WB and SBP. There was a highly significant effect of food ( P < 0·001) on live-weight gain, as gain on C was higher than that on either WB or SBP.

The results of the experiment were in agreement with the predictions set forward by the first framework that growing pigs are eating to achieve maximum performance subject to constraints.