Cardio-respiratory and mechanical work output variables were measured for four F1 crossbred dairy cows (average weight 475 kg) over a range of work levels. Resting (standing prior to exercise) heart rates (average 62 beats per min) and respiratory rates (average 21 breaths per min) were similar to those previously reported for cattle of similar weight. Minute ventilation was 0·146 l/min per kg. Resting oxygen uptake (average 0·0057 l/min per kg) was higher than values that have been reported for cattle under more relaxed conditions.

The cows were exercised on an oval track by undertaking two bouts of activity for 500 m with a 5-min intervening recovery period. Walking increased minute ventilation by approximately 60 I/min and heart rate by 30 beats per min. Pulling a loaded sledge increased these variables further to approximately 200 l/min and 135 beats per min at 32 kg/min (530 W), the highest work level studied. The calculated oxygen pulse was 72 ml per heart beat, with maximum oxygen consumption approximately 9 l/min.

Overall ivorking efficiency increased with work level to a maximum of approximately 26% at the highest work level. At this level the cows were pulling proportionately about 0·14 of their body weight.

During periods of recovery after work, the cardio-respiratory parameters varied as would be expected and recovery was usually complete within 7 min.

Estimates of genetic parameters for test day records of yields of milk, fat and protein and concentrations of fat and protein were obtained on 47 736 British Holstein-Friesian heifers in 7973 herds, progeny of 40 proven (to improve connectedness) and 707 young sires (comprising about one-fifth of the progeny), using multivariate restricted maximum likelihood methods with a sire model.

Heritability estimates for lactation yields of milk, fat and protein and concentrations of fat and protein were 0·49, 0·39, 0·43, 0·63 and 0·47, respectively. Estimates for individual test day records of these traits ranged from 0·27 to 0·43, 0·16 to 0·34, 0·22 to 0·33, 0·11 to 0·48 and 0·21 to 0·43, respectively. Generally, heritability estimates for test day records were lowest at start and highest in mid lactation.

Estimates of genetic correlations among yields of a trait on different test days ranged from 0·57 to 0·99, and for fat and protein concentrations from 0·34 to 0·99, the correlations being highest for adjacent tests. Phenotypic correlations were lower than genetic correlations. Genetic correlations of test day records with corresponding lactation traits were high (0·76 to 0·99), being highest in mid lactation.

Genetic correlations of test day milk yield with test day yields and concentrations of fat and protein throughout the lactation were similar to those for complete lactation.

The high heritabilities of test day yields and their high genetic correlations with complete lactation, except for the first 1 or 2 test days, suggest that lactation performance may be predicted from test days in early and mid lactation.

Monthly and fortnightly milk production records were analysed from 59 autumn-calving Angus and Angus × Holstein crossbred cows. Half the cows had been administered 10 mg thyroxine per day from day 60 to 120 of lactation and half were controls. Four published equations to characterize individual lactation curves were compared. These were: (1) log Y(n) = log –a1 + b1log n – c1n (Wood); (2) equation 1 with each log Y(n)2 weighted by Yin)2 (Wood weighted); (3) log [Y(n)/n7 = log l/a3 – k3n(Jenkins); and (4) log Y(n) = a4 – b4n‘(l + 25·5 n’) + c4n2 = d 4/ n (Morant), where Y(n) is milk yield on day n of lactation, n' is n–110 (the mid point of lactation), and the a, b, c, k and d parameters are estimated from solution of the equations. The lactation curve from the Jenkins equation projected peak milk yield to occur some 30 days later than estimates from the other equations. It underestimated production early and late in lactation and overestimated it during mid lactation. For several cows, the Morant equation projected that peak production occurred at the end of lactation. Also, analysis of variance of milk production variables was less sensitive when the traits were estimated by the Morant equation than when they were estimated by one of the others. The Wood weighted equation resulted in estimates of peak day of lactation and peak yield that were less variable and more realistic than estimates from the Wood equation. Collectively, therefore, the Wood weighted equation was deemed most suitable to characterize variability among and within these beef cows in milk production. All four equations, however, ranked the 59 cows similarly for estimated 220-day yield.

Leaves of Leucaena leucocephala, Sesbania sesban and Calliandra callothyrsus were harvested in Rwanda from young shoots at 8 weeks after the first cutting. They were dried, ground and incubated at the same time in polyester bags in three non-lactating Holstein-Friesian cows each fitted with a ruminal cannula. The bags were removed at 0, 2, 4, 8, 24, 48, 72 and 144 h after the start of incubations. The different parameters characterizing extent and rate of ruminal degradation of organic matter (OM), neutral-detergent fibre (NDF), and crude protein (CP) were calculated. In vitro digestibility of residual protein after 24 h and 48 h incubation was also determined. Sesbania sesban had lowest cell wall contents and gave highest ruminal degradability for OM, NDF and CP. Leucaena leucocephala was degraded to a lesser extent, but its undegraded protein had a somewhat higher in vitro digestibility. In contrast, protein of Calliandra callothyrsus was poorly degraded and digested. The proportion and composition of cell wall could not explain these differences in digestion characteristics and other measurements, such as tannins, were incriminated. Increased ruminal incubation time augmented the extent of ruminal degradation and reduced in vitro digestibility of undegraded protein but did not affect the undigestible protein fraction.

The effects of a barley beef diet without (control) and with a yeast culture (YC) on rumen fermentation, in vivo diet digestibility, nitrogen retention, live-weight gain and food intake were evaluated using 13 Limousin × British Friesian bulls per treatment. The YC was composed of the yeast species Saccharomyces cerevisiae and its growth medium dried in such a manner that it maintained its fermentative capacity. The addition of YC significantly increased the concentration of acetate (P < 0·05) while propionate concentration tended to be higher for bulls given YC (P > 0·05). The acetate: propionate ratio remained unchanged. Concentration of total volatile fatty acid (VFA) was significantly higher in YC bulls compared with control bulls (P < 0·05). The in vitro studies using the Menke gas test confirmed these findings. Mean in vitro gas production in bulls receiving YC was lower than that in the controls (P < 0·05) and methane production was significantly reduced by the addition of YC after 12h (P < 0·01). Ruminal ammonia concentrations were not affected by treatment but ruminal pH was significantly depressed by the addition of YC (P < 0·05).

Apparent digestibility of dry matter, organic matter, crude protein and neutral-detergent fibre were unaffected by treatment but tended to be higher with the control diet. Nitrogen retention was not affected by the addition of YC and mean values for allantoin excretion and plasma urea were similar.

In a 28-week feeding trial, dry-matter intake was significantly greater for bulls given YC (5·55 kg/day) than for control bulls (5·32 kg/day, P < 0·05) but average daily gain, 1·55 and 1·58 kg/day for control and YC respectively, and food conversion efficiency were not improved significantly by YC (P > 0·05).

An experiment was conducted to examine the effects of body condition at calving and feeding level post partum on the duration of the post-partum anoestrous period in beef cows. Forty-seven cows were used in each of 2 years. Cows were fed differentially before calving to achieve two levels of body condition at calving in November and December and were then fed at one of two levels of feeding post partum in a 2 × 2 factorial experiment. At calving, mean body condition scores were 2·85 (F) and 2·23 (T) (P < 0·001) while live weights were 521 kg and 457 kg (P < 0·001) for F and T cows respectively. After calving metabolizable energy intakes were 111 and 118 MJ/day (H) or 56 and 64 MJ/day (L) in years 1 and 2 respectively. The H cows maintained live weight during the first 61 days of lactation while the L cows lost live weight (0·0 v. -1·1 kg/day, P < 0·001). The number of cows still acyclic on 1 May each year was higher (P < 0·01) on the TL treatment (10/24) compared with the other treatment combinations (FH: 2/22; FL: 5/22; TH: 2/24). The effect of level of feeding on the duration of the anoestrous period was significant in the T cows (89 v. 116 days for TH and TL cows respectively; P < 0·01) but not in the F cows (80 v.89 days for the FH and FL cows respectively; P > 0·05). At 3 weeks post partum LH pulse frequency was higher in F than in T cows and tended to be higher in H than in L cows. At 6 and 9 weeks post partum LH pulse frequency was higher in H than L cows. LH pulse amplitude was higher in F than T cows at 3 weeks post partum and tended to be higher at 6 weeks post partum. It is concluded that both body condition at calving and feeding level after calving influence the duration of the post-partum anoestrous period with the effect of feeding level being particularly pronounced in thin cows.

Fish meal and monensin, as supplements to grass silage, were offered either separately or together to Friesian steers from 5 to 9 months of age (period 1). At 9 months, six steers from each of the supplemented treatments were slaughtered to determine body composition. Of the remaining steers, from 9 months of age to slaughter at 490 kg live weight (LW) (period 2), six continued on each of the same treatments, whilst six received silage unsupplemented. A further group of six steers which had received fish meal and monensin during period 1, received monensin only as a supplement to their silage.

During period 1 fish-meal supplementation increased LW, empty body and carcass weight gains, and tissues gains, while monensin had no apparent effect. During period 2, continued supplementation with both fish meal and monensin significantly increased LW, empty body and carcass gains compared with the continuously unsupplemented steers, whilst fish meal and monensin separately produced intermediate increased gains. All three supplement regimes significantly reduced the time taken to reach slaughter.

The only significant effect on body composition was that steers receiving fish meal and monensin had a higher crude protein concentration in the empty body than those receiving only fish meal as a supplement. They also had the highest crude protein concentration in the carcass, although this was not significant. Steers which had their supplements withdrawn after 9 months of age generally maintained gains intermediate between those continuing to receive supplements and those steers unsupplemented throughout. Only those not continuing to receive fish meal and monensin together appeared to perform appreciably worse. Nevertheless, although time taken to reach slaughter from 4 months of age varied by as much as 96 days, there were no other significant differences in body or carcass composition, hi terms of cost effectiveness, use of monensin showed distinct advantages over fish meal.

Ten Holstein bulls, 4 to 5 years old were used to study the effect of cooling the bulls on their semen quality. Five bulls were sprinkled with water for 15 min five times a day throughout a 6-week period of the summer season (hot-dry) in Saudi Arabia, and the other five bulls acted as the control and were not sprinkled with water. Semen quality was improved significantly during the cooling period. This improvement was evident from the significant increase in sperm motility (P < 0·01) and decrease in the percentage of both dead and morphologically abnormal (primary and secondary) spermatozoa per ejaculate of cooled bulls (P < 0·01). The effect of cooling was more marked through the last 3 weeks than during the first 3 weeks of the experimental period. Ejaculate volume, sperm concentration and hence total sperm counts did not differ significantly between the cooled and the non-cooled bulls. Concerning the type of abnormal spermatozoa, the overall secondary abnormality was higher than the primary in both the cooled and the control groups, with higher values for the control (P < 0·01). Only the mid piece showed higher primary defects than the secondary. The pyriform heads, the coiled mid pieces and tails and the bent tails were the main sources of variations (P < 0·01) in the incidence of sperm abnormality between the cooled and the non-cooled bulls. Cooling the bulls during the heat stress period also lowered their rectal temperature and increased blood haemoglobin level without affecting the packed cell volume

With the objective of determining genetic × environmental interaction for beef production under direct grazing conditions, measured as both individual average daily gain (ADG) and per ha (PROD), 160 steers were utilized through 2 years, from two breeds of different growth potential, and four stocking rates (SR) tending to establish different nutritional environments. The breeds were Aberdeen Angus (A) and high-grade Limousin crossbred (L) and the SRs established were 2·25, 2·87, 3-50 and 4·13 steers per ha. The pasture where the steers grazed was Festuca arundinacea. Response variables were analysed by least-squares using a fixed model of year, breed, SR and their two-way interactions. There were highly significant effects (P < 0·01) of the interaction of breed × SR for ADG and PROD. Quadratic and linear regressions (P < 0·01) were adjusted for PROD and ADG on SR respectively using the least-squares means. The proportional superiority of L on A at the lowest SR was 0·27, while at the highest SR the situation was reversed, A gained proportionately 0·32 more weight than L. These results indicated that under limiting conditions of nutrition as generated at the highest SR in this experiment, the small-sized individuals tended to produce meat more efficiently both individually and per ha, the opposite situation being true when nutritional conditions were not restrictive.

The effect of recombinantly derived bovine somatotropin (bST) administration on wool follicle populations, wool growth and body growth was examined in young lambs. Romney × (Border Leicester × Romney) lambs were treated with bST at doses of 0·1 or 0·3 mg/kg live weight per day, or with excipient, commencing on the day of birth and continuing at weekly intervals until the last injection was given at 11 weeks of age. Concentrations of immunoreactive somatotropin in plasma were 19·2 (s.e. 2·1), 65·2 (s.e. 2·8) and 74·7 (s.e. 4·8) μgll in the control, low dose bST and high dose bST groups, respectively. Somatotropin treatment did not alter the density of primary (P) or secondary (S) follicles in the skin, or the S/P ratio, as measured by histological examination of mid-side skin biopsy samples at 14 weeks of age. Mid-side greasy and clean wool growth during weeks 2 to 14 of the study were increased (P < 0·05) in bST-treated lambs but treatment had no effect on wool growth during the immediate post-treatment period (weeks 14 to 22), or on yearling fleece weight or wool quality characteristics. Body growth was not altered by bST administration. It is concluded that bST treatment stimulates wool growth even in very young lambs but, contrary to the results of a previous study, does not alter the development of wool follicle populations.

Development of new systems of lamb finishing for the late winter/spring market involving an extended housed store period on a predominantly straw diet are constrained by unacceptable reduction in muscle mass arising from inadequate protein supply during dietary adaptation from grass to straw. Problems with subsequent finishing on forage brassicas fedin situ arise from carcass contamination due to soiled wool of crossbred lambs which grow long fleeces over the extended store I finishing period. In order to study the effect of fish-meal supplementation on dietary change over from grass to straw 116 Mule wether lambs were allocated to four treatments, three of which received a supplement of 100 glday fish meal for 28 days from housing and introduction of a diet of straw ad libitum and 225 glday grain distillers' dark grains, the fourth group received no fish meal and was unshorn (No F/US). Shearing treatments of shorn (F/S), unshorn (F/US) and crutched (F/C) were applied to fish-meal supplemented group's. After 112 days, the housed lambs were grazed outside on swedes (Brassica napus) and effects of treatments on performance and bacterial contamination of carcasses (shearing treatments only) were studied. Fish-meal supplementation significantly reduced weight loss on dietary change by 2·2 kg after 45 days (P< 0·001). Of fishmeal supplemented lambs 83% eventually ‘finished’ (defined as Meat and Livestock Commission fat class 3LI3H) v. 34% of unsupplemented lambs. Shearing or crutching had little effect on store or finishing performance indicating adequate fleece regrowth for insulation purposes after turn-out. Shorn and crutched lambs had lower levels of bacterial carcass contamination with reductions of 0·06, 0·42 and 0·40 in counts for colony forming units per cm2, coliforms and Escherichia coli on leg sites (P < 0·05). Economic evaluation indicated financial advantage from fish-meal supplementation with an increase in margin over food costs of €3·50 as a result of heavier carcass weight and a reduced need for remedial concentrate feeding in the store period.

Sheep of three hill breeds, Scottish Blackface, Cheviot and Welsh Mountain and the reciprocal crosses among these breeds were inbred (mostly by parent × offspring mating) for four generations to five levels with inbreeding coefficients ofO, 0·25 (I1), 0·38 (I2), 0·50 (I3) and 0·59 (I4). Inbred females were also mated to unrelated inbred males of the same breed type to produce line crosses (LC). Each type of dam (except LC and I4) was mated to produce lambs of up to three different inbreeding levels thus allowing the effects of the individual's own inbreeding to be separately assessed from the effects of maternal inbreeding. This study examined body weight at a sequence of ages from birth to 4 years of age with 2369 animals (ages up to 78 weeks old) or 1062 animals (2 to 4 years old) contributing to the analyses.

Inbreeding of the individual had a highly significant retarding effect on body weight and growth rate up to the I2 level for weights of lambs up to 24 weeks old, with a slight recovery in performance thereafter. For the later ages examined, the maximum depression was reached at the I3 stage. The partial recovery in performance at the higher levels of inbreeding for lambs less than 24 weeks of age was also noted within lines and did not therefore appear to arise only from a loss of lines as inbreeding proceeded. The effect of dam's inbreeding was to depress growth up to the I3 level and at most ages up to I4. Line-cross lambs were generally heavier (but not significantly so) than non-inbred (F2 and the pure equivalent, O2) and progeny of line-cross dams were similar in weight to those from other non-inbred (F1, or F2 and O1, or O2 dams) or slightly better. The more highly inbred the individuals the more, in general, they fell behind the weights of the corresponding non-inbreds as they grew older. Inbreeding may thus have permanently stunted the sheep.

There were no significant differences between purebred and crossbred sheep in the rate of inbreeding depression. Only at the ages of 3 and 6 weeks was there a significant difference between the three pure breeds in the changes in weight attributable to inbreeding. Up to the age of weaning (15 weeks) the changes with inbreeding of individuals could not be explained statistically in terms of dominance effects alone and non-allelic interactions may therefore also be involved. At all ages the effect of inbreeding of the dam was consistent with dominance effects alone.

Sheep of three hill breeds and the crosses among them were closely inbred for four generations to create five levels with inbreeding coefficients 0·0 (F2/O2), 0·25 (I1,), 0·375 (I2), 0·50 (I3), and 0·59 (I4). Inbred females were also mated to unrelated inbred males of the same breed or crossbred type to produce line-crosses (LC). Mating was arranged so that the effects of inbreeding on the individual could be differentiated from maternal inbreeding. A total of 2369 animals were available up to 78 weeks of age and 1062 to the age of 4 years. This study examines the effects on six linear body dimensions and draws comparison with the effects on body weight. There were significant reductions in the size of the body dimensions with increasing inbreeding but the maximum depression was usually at the I2 stage for individual inbreeding and the I3 stage for maternal inbreeding. Most of the linear and many of the non-linear effects of inbreeding of the individual were significant and the effects of maternal inbreeding were also significant in a majority of cases. Inbreeding effects were more marked for relatively late-maturing parts (shoulder and hook widths) than for early-maturing (cannon bone and tibia lengths) with head width and body length intermediate but closer to the early-maturing parts. This was seen separately at each age, and in the effects of advancing age. By 78 weeks of age, the effects of inbreeding of the individual on absolute size had increased with age and by 4 years of age, in spite of a small recovery in size relative to F2/O2, was still greater than in early life. The effects of maternal inbreeding became progressively less with advancing age relative to non-inbreds. The changes with inbreeding could not be explained by dominance effects alone and epistasis is therefore likely also to be involved.

The effects of four generations of inbreeding, to achieve inbreeding coefficients (F) of 0·25, 0·375, 0·50 and 0·59, on conception rate, prolificacy, litter weight at birth and survival of breeding females, have been studied in sheep. Crosses of inbred lines were also examined. Three breeds, Scottish Blackface, Cheviot and Welsh Mountain, and the crosses among these breeds, were involved. Analyses were carried out both for the data overall and within inbred lines.

Conception rate at the first oestrus at which the ewe was mated (in each year) declined almost linearly from 0·71 (F2 generation - inbreeding F = 0·0) to 0·44 (F = 0·59) with line crosses showing 0·78 conception rate. The corresponding results following up to three rounds of services at successive oestrous periods were 0·91, 0·74 and 0·97 respectively. Analyses within lines showed a steeper rate of decline in conception rate to 0·33 (F = 0·59) following first services and 0·63 following up to three successive periods. This indicates that the lines with the best conception rates survived the inbreeding process better.

Prolificacy, the number of lambs born per ewe lambing, dropped from 1·73 (F = 0·0) to 1·37 (F = 0·25) and thereafter more slowly to 1·24 (F = 0·59). Line crosses were no better than the initial non-inbred generation (F2 and the purebred equivalent O2). Within-line analysis gave the same results.

The effects of inbreeding on litter weight at birth mirror closely those for prolificacy.

Ewe survival declined linearly with inbreeding. There was a 1·2-fold increase in the risk of death for every increase in the inbreeding coefficient (F) of 0·1 (analysed by using a proportional hazard model).

In general, there were no significant differences between purebred and crossbred sheep in the effects of inbreeding. For conception rate, prolificacy and litter weight (for which the point was examined) the changes with inbreeding could not be explained, statistically, in terms of dominance alone, suggesting, therefore, that epistasis is also involved.

The relationships between some wool characteristics and blood group genotypes (AaAa, AbAb, AaAC, AAb, AC and AbAc) were studied in Ossimi and Rahmani Egyptian fat-tailed breeds of sheep.

Interrupted medullation and coarse wool percentages and grade of wool were significantly related to blood group genotypes (P < 0·01). Fibre length and diameter and continuous medullation percentage were significantly related to genotype (P < 0·05). Staple length, number of crimps per cm, percentages of kemp, clean wool, impurities, moisture regain and fine wool were not significantly related to blood group genotype (P > 0·05).

The change in the proportional distribution of bone weight within the carcass skeleton from birth to maturity was examined in rams and ewes from flocks of Australian Merino sheep selected for high (weight plus) and low (weight minus) weaning weight and from a randomly selected control flock. Data from 140 animals (106 immature, 34 mature) were used. Shape parameters for the long bones of the limbs in the 34 mature animals were derived by determining the allometric relationship between bone length, diameter and individual bone weight.

Selection for increased and decreased weaning weight resulted in a concomitant increase and decrease in mature size and total bone weight. In the weight plus group, total bone as a proportion of body weight also increased but selection had little effect on the proportional distribution of bone weight within the skeleton at any stage of maturity. This was the product of similar growth patterns within the skeletal system aiming towards a similar mature distribution pattern for each strain.

Within the strains of different mature size there was a difference between mature rams and ewes in both total bone weight as a proportion of body weight and in the proportional distribution of this bone weight. This was associated with differences in the maturing patterns of the bones of the hindlimb and the pelvic girdle.

Neither selection nor sex affected the relationship between bone shape and bone weight, although the difference in bone weight between the strains and sexes at maturity meant that they also differed in bone shape at this point.

In three experiments with 60, 72 and 72 housed Greyface (Border Leicester × Scottish Blackface) and Suffolk × Greyface lambs on silage-based diets, a range of barley and fish-meal supplementation levels was compared. In experiment 1, six barley levels ranging from 0 to 625 glday were offered to lambs on flail-harvested and precision-chopped silages. In each of experiments 2 and 3, three levels of barley, 200, 400 and 600 g/day, were factorially arranged with four levels of fish meal, 0, 40, 80 and 120 g/day. The daily intake of flail-harvested silage was proportionately 0·76 of that of precision-chopped silage but because of a slower rate of gain the total requirement of silage dry matter (DM) per kg carcass gain was greater with flail-harvested than with precision-chopped silage. On average, over all barley supplemented diets in experiment 1, the requirement per kg carcass gain was 9·2 kg silage DM and 4·9 kg barley DM, with flail-harvested silage, compared with 8·2 kg silage DM and 3·4 kg barley DM with precision-chopped silage. Increasing barley supplementation in experiment 1 from 125 to 625 gl day reduced the silage DM requirement for carcass gain by 4·7 kg/kg increase in barley DM given. The corresponding figure over the range 200 to 600 g barley in experiments 2 and 3 was 2·6 kg silage DM per kg increase in barley DM given. The reduction in silage requirement with increasing barley was generally greater at low than at high levels of barley supplementation within the ranges examined. On silage-based diets optimum barley supplementation level was estimated to be in the region of 500 g/day.

Increasing fish-meal supplementation from 0 to 40 g/day, in experiments 2 and 3, reduced the requirement per kg carcass gain by 2·78 kg silage DM and 1·25 kg barley DM for an increase of 0·40 kg in input of fish meal DM. A further increase from 40 to 80 g/day fish meal reduced the silage DM requirement per kg carcass gain by 1·44 kg and the barley DM requirement by 0·50 kg, for an increase in input of 0·26 kg fish meal DM. A further increase to 120 g/day fish meal resulted in increases in both the silage and barley requirement per kg carcass gain. The optimum level of fish-meal supplementation was between 40 and 80 g/day and was not affected by the level of barley given.

There was evidence of an increase in carcass fat at the higher levels of gain achieved through increasing barley supplementation, but no evidence of increase in carcass fat at the higher levels of gain achieved through fish-meal supplementation.

Consumption of solid food before weaning and growth before and after weaning were studied in 24 litters of eight to 13 Yorkshire × Landrace piglets per litter. From day 21 until weaning at day 28,12 litters were provided with a single two-space feeder, while the other 12 litters were provided with four similar feeders. Daily food intake by each litter was recorded throughout this period and feeding behaviour of individual piglets was filmed during the final 24 h. On the one-feeder treatment there were 4·1 (s.e. 0·6) piglets per litter which fed very little on the day before weaning (< 0·005 of sample video frames). These tended to have high birth weights and high growth rates on days 0 to 21, but low growth rates on days 28 to 42. Conversely, piglets which fed most on creep food were often those which had gained least on days 0 to 21. The four-feeder treatment increased average intake in the last 3 days before weaning and reduced the number of piglets which fed very little in the final 24 h to 0·6 (s.e. 0·3) per litter. However, neither average growth after weaning nor the occurrence of poorly performing individuals was different between treatments. Furthermore, regression analysis of factors related to weight gain from days 28 to 42 showed that feeding behaviour proportionately accounted for 0·02 only of within-litter variation and food intake on days 21 to 28 did not contribute significantly to between-Utter variation. These results suggest that low consumption of solid food before weaning is a predictor of poor growth after weaning, but not a cause.

Changes in body composition during lactation in 40 primiparous rabbits were studied by comparative slaughter. The results were used to determine the utilization of digestible energy (DE) and digestible protein (DP) and their partitioning between maternal body, milk and foetal tissues.

Twelve does were slaughtered immediately after their first parturition (first slaughter group) to estimate initial body composition. The 28 remaining does were remated 1 to 3 days after parturition and divided into two groups offered a pelleted diet at different levels: group L, fed ad libitum and group R, fed 0·75 of ad libitum. The 19 does that were pregnant (10 of L group, 9 of R group) were kept in individual metabolism cages until their second parturition. They were then slaughtered with their litters.

Milk yield was higher (147·0 v. 117·2 g/day, P < 0·02) and live-weight loss was lower (–42 v. –294 g) in group L than in group R. The food intakes were 304·7 and 234·4 g/day, respectively. Body composition of the does changed substantially between the first and second parturition, with a considerable loss of fat and some loss of protein. A large decrease in empty body (digesta-free body) weight was observed in both groups. The loss of energy corresponded to proportionately 0·32 and 0·41 of the initial body energy, in L and R groups respectively.

The DE requirement for maintenance was estimated to be 468 kj/day per kg M0·75 and the efficiencies of utilization of DE and body energy for milk production were 0·63 and 0·76, respectively. The efficiency of utilization of DE for foetal tissue synthesis was estimated to be 0·27 throughout pregnancy. The DP requirement for maintenance was 3·80 g/day per kg M0·75 and the efficiency of utilization of DP for milk protein production was 0·76 and of body protein 0·61. The efficiency of utilization of DP for foetal protein synthesis was 0·46.