The systematic use of the same genotype in several different environments provides information that can be used to estimate genotype by environment interaction (G ✕ E) variances and parameters. Data from the UK Suffolk Sire Referencing Scheme Ltd were used to investigate a range of sire and dam by environment interactions in lamb weight (at 8 weeks and scanning) and body composition traits (muscle and fat depth). These interactions were calculated in a DFREML mixed model containing direct additive, maternal additive, maternal environmental random variance components and the covariance between direct and maternal additive effects. Sire interactions with year, flock and flock-year and dam effects within and between litters were investigated. The addition of all G ✕ E (co)variance components resulted in an improved fit of the model for all traits. Sire interactions accounted for between 2 and 3% of the phenotypic variance in all traits, usually at the expense of both additive effects. Maternal litter environmental variance components ranged from 10% (fat depth and muscle depth) to 20% (8-week weight) of phenotypic variance. Most of this variation was found in the residual component of variance when the term was omitted from the model. When fitting sire G✕ E components in a model the covariance between direct and maternal additive genetic effects, as a proportion of phenotypic variance, was reduced to a low level (from –0·36 to –0·08 for 8-week weight). Genotype by environment interactions form a significant source of variation in lamb growth and composition traits and reduce the high negative correlation between additive effects found previously in these traits.

Survival data were simulated under the Weibull model in a half-sib family design, and about 50% of the records were censored. The data were analysed using the proportional hazard model (PHM) and, after transformation to survival scores, using a linear and a binary (logit) model (LIN and BIN, respectively), where the survival scores are indicators of survival during time period t given survival up to period t – 1. Correlations between estimated and true breeding values of sires (accuracies of selection) were very similar for all three models (differences were smaller than 0·3%). Daughter effects were however less accurately predicted by the LIN model, i.e.taking proper account of the distribution of the survival data yields more accurate predictions of daughter effects. The estimated variance components and regressions of true on estimated breeding values were difficult to compare for the LIN models, because estimated breeding values were expressed as additive effects on survival scores while the simulated true breeding values were expressed on the underlying scale. Also the differences in accuracy of selection between sire and animal model breeding value estimates were small, probably due to the half-sib family design of the data. To estimate breeding values for functional survival, i.e. the component of survival that is genetically independent of production (here milk yield), two methods were compared: (i) breeding values were predicted by a single-trait linear model with a phenotypic regression on milk yield; and (ii) breeding values were predicted by a two-trait linear model for survival and milk yield, and breeding values for survival corrected for milk yield were obtained by a genetic regression on the milk yield breeding value estimates. Both methods yielded very similar accuracies of selection for functional survival, and are expected to be equivalent.

Real-time ultrasound data of backfat thickness, longissimus muscle depth and longissimus area were carried out on 335 pigs (164 gilts and 171 barrows) using the Pie Medical Scanner 200 equipped with an ASP-18 probe and 3·5 MHz to predict carcass lean content in positive stress Pietrain (TT) and negative stress Pietrain (CC or CT). They were given food ad libitum and slaughtered at an average age of 213 days and an average weight of 101 kg. The day before slaughter, longitudinal and transverse images were taken at the last rib. After slaughter, the lean meat content was estimated by a CGM (capteur gras-maigre) equipped with an 8-mm diameter Sydel probe. The carcass lean proportion was higher in homozygote TT than homozygote CC and heterozygote CT individuals (P < 0·05). Gilts had more lean meat than barrows (P < 0·05). The correlation between the lean meat proportion and ultrasound backfat thickness (UBFT) or ultrasound longissimus muscle depth (ULMD) respectively was moderate. The prediction of lean meat proportion using UBFT, ULMD and ULMA gave an R2 which varied from 0·35 to 0·79. Real-time ultrasound is a tool that could potentially be used to predict the composition of pig carcasses before slaughter particularly if measurements can be taken with a higher degree of accuracy than at present.

Polyamines (putrescine, spermidine and spermine) are required for optimal growth in all cells, and are essential for cell proliferation and growth of cultured wool follicles, with an optimal concentration of spermidine required for the fibre elongation. The effects of a local supply of exogenous spermidine on the rate of cell division in the wool follicles, the length growth rate and diameter of fibres were therefore examined in Merino lambs. Three groups of eight lambs (40 kg) were given food at 1·2 ✕ maintenance. Spermidine was injected intradermally into a small patch (3 ✕ 3 cm) on the left flank three times per day for 7 days at one of three concentrations: 1·38, 2·75 or 4·58 џmol in 0·8 ml volume. The same volume of saline was injected into the contralateral side as a control. The concentration of spermidine in the skin patch 3 h after injection on day 7 increased by proportionately 018, 0·33 or 0·41 (P < 0001) respectively. The rates of cell division in the follicle bulb 3 h after the spermidine injection were proportionately 0104, 0184 and 0·283 higher compared with the contralateral side (P = 0078 overall) for the low, medium and high doses of spermidine respectively and differed between the three doses (P < 005). The fibre length growth rate, as measured using autoradiography, was proportionately 0099, 0117 and 0156 higher than that of the contralateral side (P < 0001 overall) for the low, medium and high doses of spermidine respectively, but differences between doses were not significant (P > 005). Spermidine injection did not result in a significant change in fibre diameter during the treatment period. The ratio of fibre length growth rate to fibre diameter was increased by the injection of spermidine (P < 0001). The results suggest that injecting extra spermidine into the skin altered spermidine homeostasis in the skin, stimulated cell proliferation and resulted in increased fibre growth.

Male beef calves in northern Australia are generally castrated under 6 months of age as an aid to management of animal behaviour and for the purpose of producing sufficiently fat carcasses at slaughter. It is also common for beef producers to administer hormone growth promotants, such as oestradiol, to increase the growth rates of steers at pasture. This experiment tested the hypothesis that delaying castration by 9 months would produce an increase in growth rate for the period while the cattle are retained as bulls without compromising management of animal behaviour. Bulls of three genotypes were castrated at 7 months or 16 months of age and half were treated with oestradiol after castration. Body weight (BW) and serum insulin-like growth factor-1 concentrations (IGF-1) were measured and behaviour was observed before and after the 16 month castration. At both 7 and 16 months of age, surgical castration of bulls caused no animal welfare problems. BW gain was affected by genotype with Bos taurus types having a lower BW gain than Bos indicus and F1-cross cattle. IGF-1 was similarly affected by genotype. Oestradiol treatment increased growth of the steers (early castrates) during the 9 months between castration times compared with non-implanted steers and bulls. Oestradiol implanted steers had similar BW gain from the late castration to slaughter, regardless of age at castration, which was greater than non-implanted early castrates which, in turn, was greater than the late castrates. Similar differences were observed for IGF-1 concentrations. Behaviour was not affected by genotype, oestradiol treatment or age of castration but this may have been an artefact of the design where all treatment groups were grazed together. Although delayed castration resulted in no behavioural or management problems, it did not produce a commercially useful increase in growth rate.

The effect of melatonin treatment on fur maturation period and hair follicle cycle in 4-month-old male and female chinchillas, kept under conditions of natural photoperiod, was studied. The animals were treated with continuous-release implants of melatonin (18 mg, group M, no. = 56), while no treatment was given to the control (group C, no. = 69). The effect on hair follicle activity cycle under conditions of normal hair growth (no. = 8) and after defleecing (no. = 8) and on number of hair fibres per follicle bundle (no. = 27) were measured by taking skin samples for histological examination once a month. The age at fur priming was reduced by 31 days (P < 0001) in the melatonin-treated chinchillas. When moulting began during the short-day period, the fur reached maturity 13 days (P < 005) sooner than when the moult began during the long-day period. Melatonin administration proved to be effective in these two periods. Melatonin treatment led to hair follicle activity decreasing at a faster rate, and the differences between treated and control groups from day 60 were significant (P < 005). The primary and secondary hair follicles reached the telogen phase 30 days earlier. Due to melatonin administration more fibres per follicle bundle were observed on the matured pelt (P < 005). At 4 months of age, following the removal of hair by defleecing, the growth of the first adult hair was studied without the presence of young-age hairs. No influence of defleecing as opposed to normal hair development on age at fur maturation or on the number of fibres per hair follicle bundle was observed. Within groups M and C the number of fibres per hair follicle bundle proved to be independent of age at first fur priming. No substantial differences between the groups were observed with respect to either body weight or pelt length at the time of pelting. According to these results, melatonin administration is effective in shortening the coat maturation period in growing chinchillas and causing corresponding changes in the hair follicle cycle.

The effects of different energy sources in the lactation diet on sow and piglet performance were assessed in association with effects on the metabolic state of the sow around peak lactation. Either maize starch (S) or soya-bean oil (F) was added to a basal diet to provide 0·34 of total digestible energy (DE) intake, such that the experimental diets provided the same daily intakes of DE and crude protein. Twenty-four multiparous sows were allocated between two groups at farrowing, each given one of the two dietary treatments for a lactation period of 28 days. Sow weight and backfat (P2) as well as individual piglet weights were measured on a weekly basis. Litter sizes were standardized to 10 piglets. Milk samples were collected from sows on days 8, 12, 17, 21 and 25 of lactation to measure milk composition and prolactin concentrations. Blood samples were taken via an ear vein catheter from a subsample (7 S, 6 F) of sows on day 14 of lactation; two pre- and seven post-feeding samples were taken at 60-min intervals to measure plasma prolactin, insulin, glycerol, triglyceride, non-esterified fatty acid, urea, b-hydroxybutyrate and glucose concentrations. There was no effect of energy source on sow weight or P2 loss or on subsequent weaning-to-oestrus interval. Sows offered starch weaned more piglets than sows offered soya-bean oil (9·4 v. 8·4, P < 0·05). Litter weight gains were higher for S than F sows in week 3 of lactation (2·2 v. 1·7 kg/day, P < 0·05), irrespective of litter size. Significantly increased plasma urea and b-hydroxybutyrate concentrations and lower post-prandial increases in plasma glucose and insulin concentrations were observed in F sows around peak lactation. Neither milk nor plasma prolactin concentrations were significantly affected by dietary treatments. The metabolic indices indicated that the F diet was more limiting in dietary glucose availability, which was associated with impaired milk yield as indicated by poorer litter performance. In conclusion, this study suggests that starch is superior to fat as an energy source in sow lactation diets, particularly in the later stages of lactation.

The welfare of sows kept in two different group housing systems, namely voluntary cubicle pens housing small static groups and a split-yard housing system housing a large dynamic group, were examined. Each week, four newly weaned sows were introduced into either a voluntary cubicle pen or the split-yard system, with a total of eight groups of four sows introduced into each system. Behavioural and skin lesion data were recorded during the sows’ first 5 weeks in either system. Agonistic behaviours were performed more frequently during week 1 than in subsequent weeks in both housing systems (P < 0001). Sows in the voluntary cubicle pens spent more time standing inactive (P < 0001) and spent less time in exploratory (P < 005) and locomotory (P < 001) behaviours. However, sows in the split-yard system had higher skin lesion scores (P < 001) and engaged in more social (P < 005) and agonistic interactions (P < 005). These agonistic interactions included attacks (P < 005) and fleeing (P < 0001) throughout the 5-week observation period and fighting (P < 0001) during week 1 only. The split-yard system, therefore, appeared to offer sows a more stimulating social and physical environment than the voluntary cubicle pens, but also led to higher levels of aggression and skin damage. Both housing systems, therefore, appear to compromise sow welfare in different ways.

Feeder space allowance should be sufficient to ensure adequate access to food for all group members, irrespective of competitive ability. However, the influence of social group size on minimum feeder space requirement of pigs given food ad libitum is poorly understood. Performance, aggression and feeding behaviour were assessed over a 6-week period from 29·3 (s.e. 0·19) kg live weight, using four replicates of a 2 ✕ 2 factorial design with two group sizes (20 v. 80) (small and large) and two feeder space allowances (32·5 v. 42·5 mm per pig) (low and high). Food intake was significantly lower in the low feeder space allowance treatments (1·44 v. 1·56 (s.e.d. 0·050) kg per pig per day, P < 0·05) and group mean growth rate was reduced in the later phase between 41 and 56 kg live weight. There was no main effect of group size or interactive effect between group size and feeder space allowance on performance. Mean skin lesion score and the frequency of aggression given or received at the feeders was unaffected by treatment. Heavy weight pigs showed similar feeding behaviour in each treatment, but light pigs visited the feeder more frequently in groups of 20 (23·1 v. 16·0 (s.e.d. 2·04) visits per pig per day, P < 0·05) and spent the greatest time feeding when at a low feeder space allowance (5461 v. 4397 (s.e.d. 288·8) s per pig per day, P < 0·05). To avoid a depression in growth rate, pigs >40 kg should be allocated a minimum feeder space allowance of 42·5 mm per pig. There was little indication of a need to specify differential feeder space allowances according to group size.

The effects of high ambient temperature (T) on protein (PD) and lipid deposition (LD) and energy utilization were studied on 36 Piétrain ✕ (Landrace ✕ Large White) barrows according to a factorial design including two temperatures (23ºC for thermoneutrality and 30ºC for the high temperature) and four feeding levels. One feeding level corresponded to the voluntary food intake (VFI) at each temperature. Expressed as proportion of VFI at 23ºC, the actual feeding levels were 1·00, 0·90, 0·80, 0·70 at 23ºC and 0·80, 0·73, 0·68 and 0·62 at 30ºC. Animals were offered a wheat, maize and soya-bean meal based diet containing 187 g crude protein per kg and 0·95 g ileal standardized digestible lysine per MJ of net energy. Pigs were housed individually and had free access to water. The experiment started at 24 kg live weight and animals were slaughtered at 65 kg live weight and their body composition was measured. Slaughter of nine control pigs at the beginning of the experiment allowed calculation of the composition of gain (nutrients and energy) according to the comparative slaughter technique. Reduction of metabolizable energy (ME) intake resulted in a reduced live-weight gain at each T: the maximum gain was 1052 g/ day in pigs offered food ad libitum at 23ºC and the minimum (760 g/day) at the lowest intake at 30ºC. Visceral organ mass was lower at 30ºC than at 23ºC but was not affected by feeding level within T. Growth responses were described as polynomial or broken-line functions of ME intake (linear-plateau for PD). Both the slope and the plateau were influenced by T. At 30ºC, PDmax (143 g/day) was reached at 22·8 MJ ME per day, while at 23ºC PDmax (165 g/day) was reached at 28·4 MJ ME per day. In both cases, PDmax was reached at 0·88 of VFI at this temperature. Also the marginal response of PD to ME intake before the breakpoint was affected by T (5·9 and 4·5 g PD per MJ ME at 23ºC and 30ºC, respectively). At identical high ME intake (e.g. 0·80 of VFI at 23ºC), PD was greater at 23ºC than at 30ºC. In contrast, severe food restriction reduced PD at thermoneutrality more than an identical food restriction obtained at high ambient T. The results indicate that heat stress has a direct negative effect on PD and affects the partitioning of energy gain between protein and fat deposition.

A feeding trial was conducted to determine the adequate level of dietary choline for juvenile grass shrimp, Penaeus monodon, given diets containing different dietary lipid concentrations. Purified diets with six levels of choline chloride (0, 2000, 5000, 8000, 11000 and 14000 mg/kg diet) at either 50 or 110 g/kg lipid concentration were each given to three replicate groups of 15 shrimp (mean weight: 0·88 (s.d. 001) g) for 8 weeks. Results indicated that in the 50 g/kg lipid group, weight gain was highest in shrimp given the diets supplemented with 5000 mg choline per kg diet, intermediate in the group given 8000 mg choline per kg diet and lowest in the 14000 mg choline per kg diet and the unsupplemented control groups (P < 005); food efficiency (FE) was highest in shrimp given 5000 mg choline per kg diet, followed by the groups given > 8000 mg choline per kg diet and lowest for the unsupplemented control group. In the 110 g/kg lipid group, weight gain was highest in shrimp given the diets supplemented with 5000 and 8000 mg choline per kg diet, intermediate in the groups given 2000 and 14000 mg choline per kg diet and lowest in the control group; FE was higher in shrimp given 8000 mg choline per kg diet than in any of the other dietary groups; hepatic lipid concentration was higher in shrimp given < 2000 mg choline per kg diet than shrimp given > 5000 mg choline per kg diet. In both lipid groups, shrimp given < 2000 mg choline per kg diet had higher hepatosomatic index (HSI) than shrimp given > 5000 mg choline per kg diet. Of shrimp given <2000 mg choline per kg diet, those in the 110 g/kg lipid group had higher HSI and hepatic lipid concentration than those in the 50 g/kg lipid group. Analysis by polynomial regression of weight gain indicated that the optimum dietary choline requirements in juvenile grass shrimp were about 6400 mg/kg diet and 7800 mg/kg diet in 50 and 110 g/kg lipid diets, respectively.

A total of 198, 27-day-old weanling gilts (7·7 kg) were used to study the associations between food intake characteristics measured in individual pigs but which were group-housed, and indicators of gut physiology at 5 days after weaning. All piglets were offered ad libitum access to food and water and were housed in pens (11 piglets per pen) equipped with feeding stations in order to determine the time between weaning and the start of the first food intake (latency time; h), and the increase in daily food intake (daily increase; g/kg0·75 per day) for each individual. Forty piglets were selected that either had an early (≤ 2 h) or a late (≥23 h) start of food intake and subsequently either had a relatively fast (≥18 g/kg0·75 per day) or slow (≤ 2 g/kg0·75 per day) increase in daily food intake so that there were four different groups. Five days after weaning, the 40 piglets were killed in order to determine histological (villous height, crypt depth, number of goblet cells) and functional (maltase and sucrase activities) measures in the proximal small intestine (SI), and microbial measures (ammonia and volatile fatty acid (VFA) concentrations) and dry-matter (DM) content in the distal SI, caecum and colon. Thirteen unweaned piglets were killed to serve as the reference group. Villous height/crypt depth ratio (P < 0·05), number (P < 0·01) of goblet cells on the villi and crypts, and sucrase activity (P < 0·001) in the proximal SI of the unweaned piglets were higher than in the weaned piglets. The proportion of branched-chain VFA (bcVFA; P < 0·01), ammonia-nitrogen (P < 0·001) and DM concentrations (P < 0·01) in the contents of the caecum as well as proportions of bcVFA in the contents of the colon of the unweaned piglets were higher than in the weaned piglets. Apart from a tendency towards an interaction (P < 0·1) between latency time and daily increase with regard to villous height/crypt depth ratio and number of goblet cells on the villi of the proximal SI, histology and function of the proximal SI and digesta characteristics of the distal SI, caecum and colon were not affected by latency time. Piglets with a fast increase in food intake tended to have longer villi on the proximal SI (P < 0·1), and had less acid-mucin containing goblet cells (P < 0·05) on these villi than had the piglets with a slow increase. The piglets with a fast increase had a higher DM content in the colon and tended to have a higher total VFA-concentration in the caecum than did their counterparts with a slow increase. The genotype of the piglets affected maltase (P < 0·01) and sucrase (P < 0·05) activities in the proximal SI and tended to affect the villous height/crypt depth ratio (P < 0·06). Genotype also affected total VFA concentrations (P < 0·05) and tended to affect the ammonia nitrogen (P < 0·1) in the colon and caecum, respectively. This study indicates that within the range of practical food intake levels recorded, the physiology and function of the gut is not markedly affected by the time between weaning and the onset of feeding or by the subsequent increase in daily food intake.

The effects of body condition score (BCS) of 2·0 or 3·0 units at calving (low v. moderate), post-partum energy intake at 0·6 or 1·0 MJ metabolizable energy (ME) per day per kg M0·75 (low v. high) and unrestricted or restricted (once daily) suckling on the ability of cows to ovulate were studied in a 2 ✕ 2 ✕ 2 factorial design with each treatment replicated eight times. Calf isolation and restricted suckling were imposed shortly after selection of the first dominant follicle (DF) to emerge after day 21 post partum. The episodic release of LH (sampled at 15-min intervals for 10 h) was determined 48 h before and 48 h after the day calf isolation and restricted suckling commenced. Additional blood samples were collected weekly for plasma insulin determination. The mean interval from calving to first ovulation was shorter for cows in moderate than low BCS at calving (47·8 v. 57·1 days, s.e.d. = 4·50, P < 0·05), and for cows suckling once daily than for those with unrestricted suckling (42·9 v. 62·0 days, s.e.d. = 4·50, P < 0·001). Post-partum nutrition did not affect this interval. Mean LH pulse frequency prior to the start of restricted suckling was higher for cows of moderate than low BCS at calving (3·2 v. 1·6 pulses per 10 h, s.e.d. = 0·60, P < 0·05). Subsequently, LH pulse frequency was higher for cows suckling once daily than for those with unrestricted suckling (4·0 v. 2·2 pulses per 10 h, s.e.d. = 0·82, P < 0·05). More cows in moderate than low BCS ovulated the first DF to emerge after day 21 post partum (within 4 to 6 days) in response to restricted suckling (69 v. 25%, P < 0·05). LH pulse frequency prior to restricted suckling increased (P < 0·05) with plasma insulin concentration (categorized as low, < 5; moderate, 5 to 8; and high, >8 mIU per l). There were indications of interactions between suckling treatment and BCS (P < 0·08), and suckling treatment and plasma insulin concentration (P < 0·06), on LH pulse frequency, which suggested that calf restriction could alleviate the suppressive effects of under nutrition on episodic LH release. Amongst cows suckling once daily, the non-ovulating animals had fewer LH pulses prior to restricted suckling and smaller, slower growing DF, indicating an inability of the DF to respond to increased LH pulse frequency following calf restriction. Cows of moderate BCS, particularly those with moderate to high levels of plasma insulin (³ 5 mIU per l), responded favourably to restricted suckling. In contrast, excessively thin cows with low plasma insulin concentrations (<5 mIU per l), that had most to gain from restricted suckling, responded poorly.

Thirty young male sheep were given air-dried foliage of Acacia cyanophylla Lindl. ad libitum and 400 g oat hay. Animals were divided into five equal groups each of which was supplemented with either 300 g concentrate with (CPEG) or without (C) 20 g polyethylene glycol 4000 (PEG) or urea-containing feedblocks with (BUPEG) or without (BU) PEG. One other treatment was PEG-containing feedblock without urea (BPEG). PEG was used to preferentially bind A. cyanophylla condensed tannins (CT). Feedblocks (BU, BPEG and BUPEG respectively) were made from olive cake (395, 376 and 353), wheat bran (263, 250 and 235), wheatfeeds (132, 125 and 118), quicklime (88, 83 and 78), salt (44, 42 and 39), mineral and vitamin supplement (12, 10 and 10), urea (66, 0 and 59) and PEG (0, 114 and 107 g/kg). These diets were used in growth (60 days) and metabolism (7 days) studies. Urea-containing feedblocks, as compared with concentrate, were higher in crude protein (CP; 235 v. 116 g/kg DM) and lower in metabolizable energy (6 v. 10 MJ/kg DM). The type of supplement (i.e. concentrate v. feedblocks) had no effect (P > 0·05) on A. cyanophylla DM intake, CP and neutral-detergent fibre (NDF) digestibilities and nitrogen (N) retention. However, concentrate-containing diets exhibited higher DM and organic matter (OM) digestibilities (P < 0·05), urinary excretion of allantoin (P < 0·05), microbial N supply (P < 0·001) and average daily gain (P < 0·001). PEG supply increased DM intake of A. cyanophylla, CP digestibility, N retention, allantoin voided in urine, microbial N supply and lamb growth. PEG-containing feedblocks enriched (BUPEG) or not (BPEG) with urea had similar effect on A. cyanophylla intake, DM, OM and NDF digestibilities, allantoin in urine, microbial N supply and average daily gain. These findings suggested that urea inclusion in feedblocks are not necessary and thus the feeding cost may be reduced. The higher amount of microbial N and daily gain in lambs given concentrate as compared with those on feedblock-supplemented diets was ascribed to the level of energy which was low in the latter diets. Enrichment of feedblocks with energy-rich ingredients such as molasses or cactus fruits could be a solution. This work confirmed that tannins depressed the nutritive value of this shrub species and lamb growth. However, the reduction was not drastic in the absence of PEG in the diet. Feedblock diet (BU) matched maintenance requirements of lambs while lambs on concentrate-supplemented diet (C) grew at a rate of 78 g/day. The choice between these two supplements will depend upon farm conditions and objectives.

Twenty-five male Barbarine lambs aged approximately 150 days were divided into five groups. All the animals received 400 g/day of oat hay and Acacia cyanophylla Lindl. foliage ad libitum. Two groups also received 300 g/ day of a mixture (70: 30) of processed barley and wheat bran, with or without 20 g polyethylene glycol 4000 (PEG), groups CPEG and C respectively. The three other groups had free access to feedblocks based on olive cake, and containing urea, urea and PEG, or PEG, groups BU, BUPEG and BPEG respectively. Lambs were slaughtered at age 230 days and meat quality was determined in the longissimus thoracis et lumborum muscle. Lean colour was significantly affected by dietary condensed tannins. Lightness (L*) was higher in those animals that did not receive PEG (P < 0·001) indicating that condensed tannins can cause lighter meat colour. This difference was not due to the ultimate pH, which was not affected by the inclusion of PEG in the diet. Meat from groups that received supplementation of concentrate had lower values of resistance to the Warner-Bratzler shear device compared with those that received feedblocks. This result was confirmed by a taste panel, that found samples from groups C and CPEG more tender than samples from groups BU, BUPEG and BPEG. Inclusion of PEG in the diet increased intensity of flavour (P < 0·05) but had no effect on overall acceptability. Meat from animals that had received the concentrate had higher overall acceptability (P < 0·05) than meat from animals that received the feedblocks. No differences were found in meat chemical composition.

A total of 317 dairy and beef cattle, offered grass silage-based diets, have been subjected to energy metabolism measurements in calorimetric chambers in 11 feeding experiments at this Institute. In addition the silages (no. = 33) were also given individually to sheep as a sole food at maintenance feeding level for measurement of energy intake and outputs (faeces and urine). The digestible (DE) and metabolizable (ME) energy concentrations of mixed diets for sheep at maintenance were estimated using these measured silage data, predicted silage methane energy output and tabulated energy values of concentrates. The objective of the present study was to use treatment mean data (no. = 59), derived from the cattle (production level) (MEprod or DEprod) and the sheep (maintenance level) (MEmaint or DEmaint), to evaluate the combined effects of animal species and level of feeding on dietary ME or DE concentration. The mean-square prediction error technique and the sensitivity test both indicated that there was little bias derived from the deviation of the slope (line bias) when relating MEprod (DEprod) with cattle to MEmaint (DEmaint) with sheep. Relating feeding level to the decline in ME or DE concentration (from maintenance to production level) revealed that the constant had no significant effect on the relationship, suggesting that there was little difference in dietary ME or DE concentration between sheep and cattle when given food at maintenance. ME d and DE d were significantly related to MEmaint and DEmaint (P < 0001) respectively. These two relationships were however influenced (P < 0001) by level of feeding above maintenance (FL-1). There was little effect of silage DM proportion in the total diets (S/T) on the depression of ME concentration from maintenance to production levels, while this effect on the depression of DE concentration was significant (P < 0001). Therefore, the following two equations are recommended to calculate MEprod and DEprod concentrations respectively for cattle using data obtained with sheep at maintenance. Alternatively, with each unit increase in feeding level above maintenance, dietary ME and DE concentrations respectively were reduced by proportionately 0016 and 0025 for grass silage-based diets, irrespective of the effect of forage proportion on the latter. MEprod = [1 068 - 0019 ✕ (FL-1)] ✕ MEmaint - 0·755 DE d = [0·891 + (-0027 + 0018 ✕ S/T) ✕ (FL-1)] ✕ DEmaint + 1·355

Two 4-week experiments were conducted to examine the effect of type of supplement, offered through automatic feeders at pasture, on supplement intake and grazing behaviour by multiparous spring-calving Holstein-Friesian cows grazing continuously stocked grass pastures. Four supplement formulations were used: a dairy concentrate containing 180 g crude protein per kg fresh weight (treatment DC), a high digestible undegraded protein supplement (treatment HP), a high starch, low protein supplement (treatment HS) and a high fibre supplement (treatment HF). In experiment 1, groups of eight cows were provided with access to one of diets DC, HP or HS, with a maximum of 4 kg being available during each of two periods, between 16:00 and 03:30 h and between 03:30 and 14:30 h. During experiment 2, groups of eight cows were provided access to diet DC, HP, HS or HF, up to a maximum of 8 kg between 16:00 and 14:30 h the following day. Detailed measurements of grazing, ruminating and supplement eating behaviour were made using jaw movement recorders and the transponder-controlled out-of-parlour feeder software. Treatment had no effect on intake rate per min or daily intake of supplement in either experiment, but did affect the temporal pattern of concentrate meals. Treatment did not affect grazing bite mass, bite rate or intake rate in either experiment. During experiment 1, compared with treatment DC, treatment HS reduced total eating time, total grazing jaw movements and daily herbage intake and increased ruminative mastications per bolus and ruminative mastications per kg grass OM intake. In experiment 2, compared with treatment DC, only treatment HS reduced total eating time, total grazing jaw movements and daily herbage intake. Treatments HS and HF both increased ruminative mastications per bolus. The results indicate that when supplements are available at pasture there is a conflict between the time required to consume supplements and herbage and that supplement type can affect both the temporal pattern of supplement intake and subsequent grazing activity.