The present study was carried out on 1243 kids (379 Black Bengal; 568 Jamunapari × Black Bengal and 296 Beetal × Black Bengal) born between 1981 and 1986. Data were analysed to study the influence of genetic group, sex, season of birth, type of birth, birth weight, dam's weight at kidding, filial generation and parity of dam (as covariate) on survivability of kids during the pre-weaning period (0 to 90 days of age). The overall survival rates during 0 to 15, 16 to 30, 31 to 60, 61 to 90 and 0 to 90 days of age were 81·68 (s.e. 2·89), 95·55 (s.e. 2·00), 90·77 (s.e. 2·33), 93·31 (s.e. 2·59) and 69·94 (s.e. 3·65) % respectively. Variation in survival rates from 0 to 15 days of age was significant due to genetic group (P < 0·01), birth weight (P < 0·01), dam's weight at kidding and parity of dams as a covariate (P < 0·05). Season of birth (P < 0·05), weight of kids (P < 0·01) and dam's weight at kidding (P < 0·01) had significant effects on survival rate during 0 to 90 days of age. Sex and type of birth had no significant effect on survival rates. The interaction effects of genetic groups with season of birth and sex on pre-weaning survival rates were not significant in all ages except the effect between genetic group and sex during 31 to 60 days of age. An improvement in survival rates during the period of study was noticed with the increase in filial generation number from Fj to F3, although the difference was not significant except from 61 to 90 days of age (P < 0·05). Birth weight of kids had a positive linear relationship with survivability during the pre-weaning period. Summer-born kids had a significantly lower survival rate than those born in the winter and monsoon periods from 16 to 30, 61 to 90 and from 0 to 90 days of age. A negative linear relationship was observed between dam's weight at kidding and survival rates of kids from 0 to 90 days of age except the 25 to 30 kg dams deviate. Heritability estimates of survival rates during pre-weaning periods were not significantly different from zero, indicating that improvement by simple selection is probably limited.

Four groups of eight lambs (four male + four female) of about 25 kg live weight were given a concentrate diet which was supplemented with either calcium (Ca) or Ca and phosphorus (P). The levels of Ca and P in the diets were set in relation to estimated requirements (R) as determined by the Technical Committee on Response to Nutrients (TCORN, 1990) and the four treatments were as follows: treatment A Ca and P = 1R; treatment B Ca = 2R P = 1R; treatment C Ca = 4R P = 1R; treatment D Ca = 4R P = 2R.

At about 50 kg live weight the lambs were slaughtered and their body composition was determined.

The composition of their gains was also determined using information obtained from a fifth group of lambs killed at the start of the trial. There were significant treatment effects in relation to body mineral composition with Ca and P levels being higher in lambs on treatments C and D compared with those on treatments A and B. Magnesium levels were also higher in lambs on treatment D. Lambs on treatments A and B grew at the same rate (0·t25 kg/day) and retained Ca and P in relation to live-weight gain at rates close to those on which TCORN (1990) based their estimates of requirements. Lambs on treatments C and D, however, retained these minerals at somewhat higher rates though this improvement in mineralization was accompanied by a slight reduction in growth rate and in some lambs on these treatments there were health problems due to the formation of kidney stones.

The levels of Ca and P recommended by TCORN (1990) for lambs are adequate for normal growth and mineralization. Some improvement in mineralization may be achieved by feeding these minerals at above recommended levels but this improvement would appear to be at the expense of a reduction in growth rate and an increased risk of urolith formation.

Central test data of two pig breeding companies were analysed to estimate sire × testing regime (S × T) interaction for ultrasonic backfat thickness (BT), life-time growth rate (GL) and growth rate during test (GT). Testing regime consisted of a combination of sex, test period and housing system (individual v. group housing). Data were analysed within five lines, with 5417, 8331, 3427, 2413 and 1263 records of progeny of 97, 162, 64, 69 and 33 sires, respectively. The data were collected from May 1983 until May 1987 (lines 1, 2 and 3) and from June 1985 until May 1987 (lines 4 and 5). Testing regime had a significant effect on BT (in three lines) and on GL and GT (in five lines). S × T interaction was significant only for BT in three lines and for GT in one line. Genetic correlations between identical traits, measured under the two testing regimes, varied from 0·64 to 1·00 for BT, from 0·65 to 1·00 for GL and from 0·62 to 1·00 for GT. Conclusively, within central test S × T interactions were relatively unimportant for BT, GT and GL.

The effect of grain processing and form of the concentrate mixture were studied on early-weaned Chios lambs (42 days of age) and Damascus kids (56 days of age). Forty-five, 36, 33 and 33 animals were used in trials 1 (lambs), 2 (lambs), 3 (kids) and 4 (kids), respectively. Within trials animals were divided on the basis of live weight and age into three groups. Treatments (three forms of concentrate mixture) were randomly allocated to one of the three groups. The treatments were: whole cereal (WGP) grains mixed with pellets made from the other ingredients of the concentrate mixture; pelleted (P), where all ingredients were ground and pelleted in 5-mm cubes; rolled cereal grains (RGP), where cereal grains were rolled and then mixed with pellets (5-mm cubes) made from the other ingredients of the concentrate mixture. Cereal grains comprised 774 g/kg concentrate mixture. Fattening diets were based on ad libitum feeding of concentrates and a daily allowance of 01 kg per animal of long lucerne hay. Digestion coefficients, outflow rate of small particles from the rumen and rumen metabolites were measured using five animals per species per treatment.

There were no significant differences between diets for live-weight gain in lambs. On the other hand, kids on the P diet gained more weight and had better food to gain ratio than the other two diets. Feeding the P diet resulted in a significant decrease of acetate and butyrate molar proportion ( P < 0·001) and an increase (P < 0·001) of propionate molar proportion. Similarly, feeding the P diet resulted in a significant reduction in ruminal pH (P < 0·01) and NH,-N (P < 0·05) concentration. Outflow rate (% per h) of small particles from the rumen was lower from lambs and kids on the P diet (P < 0·001). There were no significant differences between species and/or among diets for apparent digestion coefficients and nitrogen balance.

Finn Dorset ewes were offered forage ad libitum from week 16 of pregnancy until lambing and were either unsupplemented (U) or given 600 g/day of concentrates (S). Grass silage and white clover silage, ensiled separately and having similar dry matter concentrations, were offered in four mixtures with white clover proportions of 0, 0·20, 0·40 and 0·60 on a fresh basis. Forage intake was significantly higher for mixtures containing higher proportions of clover (9·1, 10·5, 12·3 and 13·6 g organic matter (OM) per kg live weight) and the ewes gained more weight (33, 65, 178 and 174 g/day) and had smaller losses in body condition score (–0·59, –0·49, –0·39 and –0·17). Higher proportions of clover in the diet in late pregnancy also resulted in significantly higher growth rates of lambs during lactation, when a common diet was offered.

The number of foetuses carried in pregnancy had significant effects on intake and some aspects of performance. For ewes carrying singles, twins and multiples respectively, mean daily forage intakes were 12·2, 11·9 and 10·4 g OM per kg live weight and losses in body condition score were –0·05, –0·40 and –0·62.

Offering the supplement reduced forage intake and for treatments U and S respectively, mean daily values were 12·6 and 10·2 g OM per kg live weight. Whilst the supplemented ewes had smaller losses in body condition score in late pregnancy (–0·54 v. –0·28), lamb birth weights and growth rates were significantly increased only for ewes which had carried three or more foetuses in pregnancy and reared their two heaviest lambs.

One hundred and thirty crossbred gilts (Yorkshire × Duroc × Hampshire) were exposed to either natural (40 lux) or supplemental lighting (700 lux) beginning at 8 weeks of age. Gilts received supplemental lighting from 40-W flourescent bulbs from 05·15 to 09·00 h and 16·30 to 20·15 h from 9 September to 22 April. At 4 months of age, all gilts were exposed daily for 15 min to mature boars five times weekly. Twelve gilts from each group were slaughtered at 4, 5, 6 and 7 months of age. All gilts were bled from indwelling cannulas at 20-min intervals for 4 h the day preceding slaughter. In addition, blood samples were drawn weekly from 17 gilts in each group from 7 to 9 months of age and analysed for progesterone to determine age of puberty. Twelve of 17 gilts that received supplemental lighting reached puberty at 228 (s.e. 11) days of age whereas 11 of 16 gilts that received natural lighting reached puberty at 252 (s.e. 7) days of age (P = 0·07). No significant differences occurred in anterior pituitary gland weight or pituitary concentration of LH, mean concentrations of serum LH or number of LH secretory spikes between natural and supplemental-lighted gilts at each month (all P > 005). Concentration of oestradiol-17β and progesterone in follicular fluid was similar between treatment groups within months and follicular size (P > 0·05). Content of GnRH in the stalk-median eminence, preoptic area and hypothalamus proper were also similar between treatment groups (P > 0·05). In summary, supplemental lighting reduced the age of puberty in gilts without a detectable change in pituitary, hypothalamic or ovarian parameters.

The consistency of differences between varieties in nutritive value of cereal straws was tested over 3 years consecutively for nine varieties of spring barley and 10 varieties of winter wheat straw and over 2 years consecutively for 12 varieties of winter barley and six varieties of oats. For all varieties there were large year-to-year differences in nutritive value measured by ruminal degradation characteristics using the nylon bag technique. For spring barley there were large differences between varieties and the correlations between varieties in different years were mostly in excess of r = 0·90 for 48-h degradability and maximum potential degradability. For winter wheat the correlations between varieties for different years were lower but mostly significant. For the winter barley differences between varieties were less, but even so differences between varieties in different years were significant. For oats differences between the varieties were small and there was no significant correlation within varieties between years. The results suggest that the nutritive value of cereal straws is generally consistent between years and is a characteristic that could be improved by selection.

The performance of housed ewes, shorn at various stages during pregnancy and offered silages ad libitum made from grass harvested at two contrasting stages of growth, was studied. The mean increase in silage dry matter (DM) intake due to shearing (0·11 kg/day; P > 0·05) was small in comparison with that resulting from offered earlier-cut silage (0·27 kg/day; P < 0·001). The mean increase in twin lamb birth weight from ewes shorn at least 6 weeks before lambing was almost 1 kg per lamb (P < 0·01) with no significant effect on ewe live-weight change. Greatest increase in lamb birth weight (1·11 kg; P < 0·01) was produced by shearing several times during pregnancy, with least response (0·23 kg; P < 0·05) from shearing once only, 4 weeks before lambing. The effect of silage quality on lamb birth weight was not significant, despite the large difference in DM intake of the two silages. This difference in intake was reflected by ewe live-weight change over pregnancy with those ewes offered early-cut silage gaining 5·57 kg while those offered late-cut silage lost 4·53 kg (P < 0·001). There was a marked fall in respiration rate and rectal temperature after each shearing and, compared with shorn ewes, unshorn ewes had a mean gestation length which was 2·04 days shorter (P < 0·01). In terms of lamb growth rates, ewe milk yields and milk composition, the performance on all treatments after turn-out to pasture was satisfactory and no significant carry-over effect of treatments applied during pregnancy were observed during the first 5 weeks of lactation.

The effects on reproductive performance of different strategies of pasture management designed to conserve herbage in situ during the late growing season for use during the pre-mating and mating period were studied in three experiments over 3 years with Greyface ewes. Two experiments with 341 ewes compared set-stocking of pasture at 12 ewes per ha on two initial levels of herbage mass with a conservation strategy which left half of the area ungrazed and grazed the other half of the area at 24 ewes per ha from late August until mid October (2 weeks before the start of mating) after which the total area was grazed at 12 ewes per ha. In a third experiment with 124 ewes, the conservation strategy left a quarter of the area ungrazed and varied stocking rate to a minimum of 12 ewes per ha to maintain two initial levels of herbage mass on the other three-quarters of the area and then compared set-stocking at six ewes per ha on this area with set-stocking at 18 ewes per ha on the previously ungrazed quarter of the area during the pre-mating and mating period.

Initial levels of herbage mass were within the range of 2000 to 2100 kg dry matter (DM) per ha (7 cm sward height; high) and 1500 to 1700 kg DM per ha (4 to 5 cm; low). Mean herbage accumulation rates between August and October were estimated to be 25 and 44 kg DM per ha per day in the first two experiments. Initial live weight and body condition score also varied considerably between years and subsequent response was influenced by herbage growth rate. Where mean ewe body condition was within the score 2·75 to 3·00, range over the mating period and herbage mass on set-stocked areas was not higher than 2200 kg DM per ha (8 cm sward height) in the pre-mating period or not lower than 1300 kg DM per ha (3·5 cm) at about 3 weeks after mating, the strategy of management did not influence reproductive performance in terms of the number of lambs born. Within these limits, however, reproductive performance was positively related to herbage mass in late August (low = 1·60, high = 1·94).

When herbage mass fell below the 1300 kg DM per ha level before or during mating, reproductive performance was improved by a herbage-conservation strategy which maintained ewe body-condition score within the 2·75 to 3·00 range. When herbage mass and growth rate were high, reproductive performance was also improved by a herbage-conservation strategy which restricted the development of excessive body condition before mating by avoiding the increase in barrenness shown to derive from very high levels of body condition.

It is common for sows in commercial practice to lose body weight during lactation and if the loss is excessive then performance may be impaired. However, there is little information on the composition of this loss of body weight. In a 2 × 2 factorial experiment gilts were given daily either 2·7 (H) or 1·5 (L) kg food during gestation and either a high (H) (mean intakes of 3·4 and 4·9 kg/day for the H-H and L-H groups, respectively) or low (L, 2·0 kg/day) food intakes during a 31-day lactation. Seventy-three animals were slaughtered at various stages over all treatments and body composition determined by chemical analysis. The content of lipid (Li, kg) and protein (Pr, kg) in the empty body were closely related to live weight (LW, kg) and depth of backfat measured by ultrasound (P2, mm); Li = 0·381 LW + 1·042 P2 - 31·099 (R = 0·95) and Pr = 0·11 LW - 013 P2 + 4·46 (R = 0·67). Prediction equations were used to predict the composition of animals from a previous experiment (Mullan and Williams, 1989). Increasing food intake prior to farrowing increased the amount of lipid (67 v. 38 kg), protein (20 v. 17 kg), water (73 v. 63 kg) and ash (5 v. 4 kg) in the empty body at farrowing. For sows given 2·0 kg/day food during lactation about half of the total loss of body weight was lipid (835 and 570 g/day for the H-L and L-L groups, respectively) and proportionately 0-10 was protein tissue (165 and 125 g/day, respectively). When sows were fed to appetite the heaviest animals lost both lipid (520 g/day) and protein (130 g/day) whereas animals in the L-H group maintained their lipid reserves but lost 65 g protein per day. This study demonstrates the considerable amounts of lipid and protein which may be mobilized by the sow during lactation to buffer the nutritional stress through a low intake of food. The body composition of the sow during the first lactation can be accurately predicted from live weight and depth of backfat.

The proportion of whole grain consumed that was voided intact in the faeces of ewes in late pregnancy and early lactation was measured for diets based on a range of forages in two experiments. The proportions of grain voided intact varied widely between ewes and was to some extent a characteristic of the individual ewe. During late pregnancy on hay-based diets the mean proportion of grain recovered was 0·053 with a range from 0·042 to 0·063 while on silage-based diets 0·135 (range 0·082 to 0·209) was recovered. On silage-based diets after lambing 0·196 and 0·235 of grain was voided intact in the faeces. The proportion of intact grain voided was affected by forage intake. The estimated increase in the proportion of grain voided intact was 0·012 measured over a range of forages before lambing and 0·021 on silage after lambing per 100 g increase in dry matter intake. However, when the total digestibility was measured, there were no differences between feeding of whole and processed grain where proportionately 0·06 of whole grain consumed was voided intact.

An evaluation of the response to selection for prolificacy within a nucleus sheep flock of a commercial group-breeding scheme is presented. In 1979, the Romney Group Breeders formed a nucleus flock of 120 prolific ewes chosen from 12 contributing flocks. A control flock was established in 1982 from the same source. The analysis was conducted on the trait of litter size. Selection differentials are presented for each year of birth progeny group in both flocks. Expected selection response was calculated from selection differentials and was found to have an average value of 1·5% of parent mean litter size per year. Using least squares procedures the litter size performance of control and nucleus ewes of 2, 3 and 4 years of age was corrected for environmental effects. Realized response was estimated from the differences between corrected litter size means of control and nucleus flocks. Response in litter size was found to be significant within years and within ewe age groups (P < 0·05).

The heritability of growth traits from birth to 6 months of age and the genetic and phenotypic correlations among them were determined from paternal half-sib analyses of 1689 records of D'man lambs. Heritability estimates were 0·34 (s.e. 0·08), 0·23 (s.e. 0·06), 0·52 (s.e. 0·10) and 0·43 (s.e. 0·09) for weights at birth, 30 days, 90 days and 180 days, respectively. Heritabilities for average daily gains from birth to 30 days and from 30 to 90 days were estimated to be 0·12 (s.e. 0·05) and 0·56 (s.e. 0·11), respectively. Genetic and phenotypic correlations among growth traits were all positive and of high magnitude. The former estimates varied from 0·66 to 0·98, the latter estimates ranged from 0·23 to 0·92. Selection for high weight at 90 days would be expected to have large effect on other growth traits as a result of their large positive genetic correlations.

The effects of dietary protein (151 to 282 g crude protein per kg dry matter (DM)) and lysine (8·5 to 16·4 g/kg DM) on the carcass composition and energy metabolism of entire male pigs, given food close to appetite, was studied from 33 to 88 kg. Four replicates (three Landrace and one Duroc) of four littermates were used. Energy and nitrogen (N) balances were conducted at approximately 35 to 43, 58 to 65 and 78 to 85 kg and body composition was determined at slaughter. There was no effect of dietary treatment on the crude protein content of the empty body (EBW) but the DM (P < 0·001), fat (P < 0·001) and ash (P < 0·05) proportions and fat: protein ratio in EBW (P < 0·01) increased with decreasing dietary protein level. The mean maximum protein retention was 183 g/day. Retention of protein (P < 0·05) and proportion of protein energy in the gain (P < 0·01) decreased linearly and fat retention (P < 0·001) and energy content of the gain (P < 001) increased with decreasing dietary protein. The N retention values calculated from balance data were proportionately 0·21 higher at high protein intakes (509 g/day) and 0·056 higher at low protein intakes (329 g/day) than the values obtained by slaughter. Using the ideal protein system the value for the efficiency of utilization of apparently digested ideal protein for protein deposition (a2) fell linearly (P < 0·001), based on the slaughter data, as dietary protein content increased. Heat production, calculated from slaughter data, was proportionately 0·07 higher than that measured by indirect calorimetry and 0·17 higher than the computed value for heat production using the standard values of energy costs for maintenance and for protein and fat deposition.

Six replicates (five Landrace and one Duroc) of four littermate entire male pigs were used to evaluate the effect of protein level in diets of constant amino acid composition on live-weight gain, efficiency of gain, nitrogen balance and carcass characteristics. The diet contents ranged from 151 to 282 g crude protein (CP) and 8·5 to 16·4 g lysine per kg dry matter (DM) and were studied over two live-weight ranges, 33 to 55 kg and 55 to 88 kg. All the diets had similar metabolizable energy (ME) values (15·0 MJ/kg DM). Pigs were given food twice daily to appetite. Sixteen pigs (four replicates) were used for metabolism trials at 35 to 43, 58 to 65 and 78 to 88 kg live weight and after attaining a live weight of 88 kg they were slaughtered to assess carcass characteristics. Between 33 and 55 kg live weight significantly linear improvements (P < 0·01) in the daily live-weight gain and in the ratio ME: live-weight gain were observed for daily intakes in excess of 300 g ideal protein and 21 g lysine (212 g CP and 12·5 g lysine per kg DM). Between 55 and 88 kg live weight, linear improvements in the same two variables were observed for daily intakes of 395 g ideal protein and 28 g lysine (212 g CP and 12·5 g lysine per kg DM). For the 33 to 88 kg live-weight period the average ME intake was 30 MJ/day and the predicted intakes for maximum growth and food conversion efficiency were in excess of 370 g ideal protein and 26 g lysine. Nitrogen retention improved significantly with increasing dietary crude protein content in all three balance periods. Fat thickness measurements decreased linearly (P < 0·05) and the proportions of lean and fat in rumpback increased and decreased respectively (P < 0·01) as the dietary protein level increased.

In earlier studies with pigs the P-adrenergic agonist Ro 16·8714 ((3-AG) enhanced the efficiency of nitrogen (N) retention. Therefore effects of Ro 16·8714 were studied on growth rate, body composition, N, fat and energy retention in pigs fed isoenergetically, but given different amounts of protein (112 or 138 g/kg diet) without (groups LP and NP) or with 60 mg Ro 16·8714 per kg diet (groups LPP and NPP) from 60 to 100 kg live weight. Weight gain (898, 927, 855 and 810 g/day in NP, NPp, LP and LPp) decreased, whereas food: gain ratio (2·94, 2·82, 3·04 and 3·24 kg/kg in NP, NPP, LP and LPP) was increased by low protein intake (P < 0·05) and both weight gain and food conversion were modified by the interaction (P × P) of protein intake and Ro 16·8714 (P < 0·05). Killing-out proportion (820, 830, 830 and 830 g/kg in groups NP, NPp, LP and LPP) was modified by protein intake and Ro 16·8714 (P < 0·05). Carcass growth rate (760, 814, 748 and 723 g/day in NP, NPP, LP and LPP) was modified by protein intake and by P × p (P < 0·05), while non-carcass growth rate (90, 77, 76 and 56 g/day in NP, NPP, LP and LPP) was changed by protein intake and by Ro 16·8714 (P < 0·05). Compared with NP, weights of kidneys (−0·025 kg), small intestine (−0·26 kg) and large intestine (−0·17 kg) were decreased by low protein feeding, and weights of heart, spleen and stomach decreased in response to Ro 16·8714 (-002, -0·02 and -0·06 kg; P < 0·05) while both low protein intake and Ro 16·8714 reduced liver weight (−0·12 and −0·23 kg, respectively; P < 0·05) and blood volume obtained at slaughter (-0·12 and -0·23 kg; P < 0·05). Carcass N (1813, 1970, 1786 and 1825 g in NP NPp, LP and LPP) increased in response to Ro 16-8714, but was reduced by low protein intake (P < 0·05), while noncarcass N (330, 309, 312 and 285 g in NP, NPp, LP and LPP) was decreased by both low protein intake and Ro 16-8714 (P < 0·01). Carcass and non-carcass fat (22·1, 19·9, 23·4 and 23·0 kg, respectively 1·51, 1·41, 1·59 and 1·68 kg in NP, NPp, LP and LPP) increased with low protein feeding (P < 0·05), but were not significantly influenced by Ro 16·8714. The efficiency of N retention (295, 363, 321 and 327 g/kg N retained: N intake in NP, NPp, LP and LPP) was enhanced by Ro 16·8714 (P > 0·05) whereas the efficiency of energy retention was not influenced by Ro 16·8714 and protein intake. In conclusion, an adequate intake of protein is necessary for optimum expression of many, but not all, effects of the P-adrenergic agonist Ro 16·8714.

Previous investigations have established that supplementing broiler chicken diets with appropriate endosperm cell wall degrading enzymes can improve nutrient digestion, and indicated that this could allow lower protein diets to be used. In this study the effect of enzyme supplementation on the productive value of low (192 g/kg dry matter (DM)) and high (227 g/kg DM) protein diets was studied. The diets employed were based on barley, wheat and rye, and the two enzyme preparations used, Glucanase GP 5000® and Novozym-343®, contained β3-glucanase and arabinoxylanase activities.

The high protein diet gave a higher incidence of sticky droppings, but resulted in a higher growth rate and improved food conversion ratio than the low protein diet. Enzyme supplementation reduced the incidence of sticky droppings and also improved growth rate, food intake and food conversion efficiency for both diets, with the Glucanase GP 5000 preparation generally being more effective. Enzyme supplementation improved growth rate on the low protein diet to a level equal to or better than that on the high protein diet, although this was achieved by a better food intake and an inferior food conversion ratio. This study demonstrated that supplementation with appropriate enzymes could allow a reduction in dietary protein level without affecting broiler growth rate.

Twenty-eight male fallow deer (Dama dama), 14 entire and 14 castrated (seven each 1- and 2-year-old) were slaughtered and their carcasses jointed. Each joint was separated into venison, trim A (low visible fat, diced pieces), trim B (pieces suitable only for mincing), waste and bone. Castration had a significant and cumulative effect on live and carcass weights. At 1 year of age castrated males were 80 g/kg lighter in live weight; at 2 years this difference had increased to 119 g/kg. The pattern for differences in hot and cold carcass weights was similar, being 66 and 148 g/kg lighter at 1 and 2 years old, respectively.

Castration caused small but significant shifts in the proportions of the primal joints, and the proportions of venison, trim A and trim B. Castrated males had smaller neck (9 g/kg) and saddle (10 g/kg) joints, but 18 g/kg larger legs. In the whole carcass they contained 12 g/kg more venison, but correspondingly less trim A and trim B.

Older animals had higher proportions of venison and lower proportions of bone. Venison distribution altered with age, but this was mainly a reflexion of changes in joint proportions.

The overall effect of castration was to reduce carcass weights (on which producers are paid) and reduce venison production proportionately to 0-97 and 0-88 of that achieved in 1- and 2-year-old entire males respectively. In some market situations castration may be an acceptable method of producing venison outside of the normal peak production, but the reduced production would require higher schedule prices to be economically viable for the producer.

To test the proposition that growing pigs, when given a choice between two foods, are able to select a diet that meets their requirements, and to investigate the rules of diet selection, four foods (L, A, B and H) with similar energy yields, but different concentrations of crude protein (CP) (125, 174, 213 and 267 g CP per kg fresh food respectively) were formulated. The four foods were offered ad libitum either singly, or as a two-way choice using all the six possible pairs, to 40 individually caged pigs from 12 to 30 kg live weight. On the single foods the rate of food intake fell from 1001 to 971 to 961 to 868 (s.e.d. 40) g/day (F < 0·05) as the protein concentration of the foods increased from L to H; the growth rate followed an opposite trend (492, 627, 743 and 693 (s.e.d. 31) g/day respectively; P < 0·01). When the pigs had to select between two foods limiting in protein (L and A) the less limiting one was preferred (710 (s.e. 200) g A per kg total food intake; the protein concentration of the selected diet was 160 (s.e. 10) g CP per kg). On the choice between B and H (a choice between a food with protein concentration close to requirements and a food with protein excess) the lower food was markedly preferred (928 (s.e. 4) g B per kg total food intake; the protein concentration of the selected diet was 218 (s.e. 1) g CP per kg). When the animals were given a choice between two foods, a combination of which was non-limiting (pairs LB, LH, AB and AH), the protein concentrations of the selected diets were not different between treatments (208, 204, 202 and 205 (s.e.d. 13) g CP per kg respectively) and they also declined systematically with time and weight. The growth rate of the animals on these pairs were 752, 768, 769 and 763 (s.e.d. 54) g/day (P > 0·05), which were not significantly different from the highest growth rate achieved on a single food. The results suggest that pigs, when given a choice between a suitable pair of foods, are able to choose a balanced diet and to change its composition to reflect their changing requirements. The choice-feeding method may well be useful as an effective and economic way of estimating and meeting requirements, and of measuring the growth potential of pigs.

Six experiments involving the artificial insemination (AI) of a total of 300 female red deer (hinds) with frozen-thawed red deer semen (collected by electro-ejaculation) were conducted over 3 years. Insemination took place at fixed times following various oestrous synchronization procedures using progesterone withdrawal and treatment with pregnant mare's serum gonadotropin (PMSG). In the 1st year, the experiments evaluated basic AI techniques in which pregnancy rates were 45% in 20 hinds receiving two inseminations per vaginam (PV) and 56% in 27 hinds inseminated by the laparoscopic intrauterine method (IU). In the 2nd year, the experiments involved comparisons of the progesterone regime, one or two PV inseminations, and the timing of a single PV insemination. There was no effect of replacement of the progesterone device after 9 days and withdrawal 3 days later compared with the use of one device for the whole period in two experiments. The pregnancy rate for a double PV insemination was significantly higher than for a single PV insemination (58 and 34%; P < 0·05) and there was also a small effect of timing of insemination relative to the synchronization treatment. In the 3rd year all hinds were inseminated by the IU method. The experiments involved a comparison of various times of AI following progesterone withdrawal and a comparison of the progesterone regime. The overall pregnancy rate for 63 hinds inseminated was 56% with no difference between three times of insemination (48, 52 and 55 h). In the second experiment, the difference in pregnancy rate between treatment with progesterone for 15 days and 12 days (44 and 72% for 18 hinds per group) was not significant, but the interaction between the length of progesterone treatment and insemination time was significant (P < 0·05), with the 12-day progesterone/55 h insemination giving a much higher pregnancy rate than the 15-day/55 h insemination (89 and 20% respectively). Although no experiments involved direct comparisons of the routes of insemination, overall pregnancy rates were 56% for IU, 53% for double PV and 35% for single PV inseminations.