Thirteen dairy cows between 7 and 20 days post partum were fitted with catheters in both the jugular vein and caudal vena cava, the latter with the tips anterior to the junction with the ovarian veins. Blood samples were taken from nine control cows from both sites at 15-min intervals for periods of between 8 and 16 h. Four more cows were sampled for 13 h and given 4 × 2·5 ug GnRH intravenously at 3-h intervals starting 1 h after sampling began. Plasma oestradiol-17(3 concentrations were significantly higher in the vena cava than in the jugular vein in the two cows in which they were compared. Twenty-eight LH pulses occurred in the nine control cows during the sampling periods. These were followed within 1 h by increases in caval oestradiol-17β concentrations in 26 cases. LH pulses occurred after 14 of the 16 GnRH injections and with one exception were associated with oestradiol pulses in the vena cava. Oestradiol concentrations generally peaked 15 to 45 min after each LH peak. It is concluded that ovarian follicles are responsive to LH pulses by releasing oestradiol pulses early in the post-partum period.

The influence of season and management system on the productivity of Friesian cows in a Mediterranean climate was assessed. Intakes of food and water and milk yields were measured in 154 cows over 2·5 years while intensively managed in yards giving access to shelter (free stalls) or that were fully exposed to solar radiation (open lots). Food quality was also monitored to permit estimates of the efficiency of utilization of metabolizable energy for milk production over fortnightly periods.

The highest milk yields and energetic efficiencies were recorded during spring. Energy intakes were highest but energetic efficiencies were lowest during winter. Cows consumed the least food during summer and autumn and drank the most water during summer. The only significant effect of management system was for water intake, which was higher in the open lots than in the free stalls. There was evidence of heat stress in summer and cold stress in winter, but there appeared to be little benefit with milk yields through the provision of shelter.

The work done, distance travelled and body temperature of five teams of oxen ploughing land for winter crops was measured continuously over a 5-h working day. On terraces in East Nepal the cattle worked at slow speeds (about 0·3 m/s). Daily work output was variable and depended on ground and soil conditions and on the man working the team. Estimated daily energy expenditure on working days in October and November was 1·25 to 1·46 × maintenance. Differences between teams were small. No noticeable change in performance occurred over the 5-h work, with the exception of one team which usually worked erratically over the last 2 h. Only one animal showed signs of heat stress during work, when its body temperature increased by 1·8 to 2°C, otherwise body temperature varied little (< 1°C) during work.

Two pairs of cattle and two pairs of buffaloes carted loads, in wooden wheeled local carts, 16 to 17 km over the same flat route on village tracks. One team worked each day in temperatures of 24 to 37°C for a total of 6 days per team.

Body temperature, respiration rate and stepping rate in one animal from each pair and work done and distance travelled were monitored.

Buffaloes and cattle started work at speeds of 1 m/s or more. Cattle kept this up for most of the day whereas the buffaloes showed a steady decrease in speed over the day to speeds of less than 0·9 m/s in the last hour. Body temperature of the buffaloes increased during work. By 3-5 h, increases of up to 3·5°C in starting values could be seen. It was necessary to stop and let the buffaloes wallow for at least 20 min to allow them to cool off before they would continue to work. During wallowing body temperature decreased to or below values seen at the start of the day's work. Unlike the buffaloes, the cattle showed changes of less than 1°C in body temperature during work. Respiration rates of buffaloes increased at least two-fold as they began panting usually after 1·5 to 2·5 h. Respiration rates of the cattle could also increase up to three-fold during work. The results have shown that in well fed animals there is little to choose between buffaloes and oxen in daily work output. Estimated daily energy expenditures by the buffaloes and cattle on working days were similar, 1·75 to 1·79 and 1·74 to 1·78 × maintenance, respectively. However, buffaloes usually took longer to achieve the work, as time had to be allowed for wallowing. This is seen as the main disadvantage of using buffaloes for carting on longer routes.

To determine effects of photoperiod and ovaries and their interactions on live-weight (LW) gain, carcass composition, growth hormone (GH), insulin (INS) and prolactin (PRL), crossbred beef heifers were utilized. Heifers (no. = 70) were blocked by LW and assigned to a pre-treatment slaughter group for estimation of initial carcass composition or to treatments in a 2 × 2 factorial experiment (no. = 14 per treatment). Main effects were: photoperiod (8 h light (L): 16 h dark (D) v. 16L: 8D) and ovaries (intact (INT) v. ovariectomized (OVX)). Heifers were given a maize-based mixed diet (115 g protein and 11·5 MJ metabolizable energy per kg dry matter) ad libitum once per day at 07.30 h. On days 64 and 138, blood samples were taken every 30 min for 10 h from five heifers in each treatment. On day 144 treated heifers were slaughtered. Relative to OVX heifers, INT heifers had greater (P < 0·01) average LW gain (1·03 v. 1·17 kg/day), carcass weight (252 v. 270 kg) and carcass protein accretion rates (68 v. 82 g/day) but carcass fat accretion was not affected (P < 0·l; 381 v. 399 g/day). Compared with 8L: 16D, exposure to 16L: 8D non-significantly increased LW gain more in OVX heifers (16 kg) than in INT heifers (3 kg). Photoperiod did not significantly influence weight or composition of the carcass. There was no significant interaction between photoperiod and ovaries on carcass composition. Across all heifers GH declined (P < 0·05) and INS and PRL increased (P < 0·05) from day 64 to 138. Compared with 8L: 16D, exposure to 16L: 8D increased PRL on day 64 (P < 0·05; 13·4 v. 28·5 u.g/1) and decreased INS averaged across days 64 and 138 (P = 0·l; 0·71 v. 0·55 u/l) but had no effect on GH. GH, INS and PRL did not differ between INT and OVX heifers. It is concluded that ovariectomy of heifers reduces LW gains, carcass weights and accretion of protein, and that exposure to 16L: 8D partially prevents the loss in LW gain.

The effective degradability (Dg) of dry matter (DM), nitrogen (N) and amino acids (AA) in soya-bean meal (SBM), fish meal (FM), dried brewers' grains (DBG) and ensiled lucerne (EL) was measured using polyester bags suspended in the rumens of six cows given a basal diet of maize silage, hay and concentrate. Rumen outflow rate was measured using chromium-mordanted SBM.

AA were grouped into essential (EAA), non-essential (NEAA) or branched chain (BrAA). The AA concentration in DM varied from 88 g/kg DM for EL to 566 g/kg for FM. The proportion of determined AA in crude protein (CP) was similar for SBM, FM and DBG and always higher than 0·85. EL had the lowest A A concentration in CP, partly due to the presence of ammonia N (170 g/kg total N).

Methionine always had a higher, and threonine a lower Dg than total AA in all foods. Dg of other AA was generally food dependent.

SBM always had the highest EAA, BrAA, NEAA, mean AA and total N degradability, whilst FM always had the lowest Dg for EAA, BrAA, mean AA and total N, and these values were significantly different in comparison with SBM. The effective Dg of BrAA in DBG was significantly lower than in SBM and significantly higher than in FM. In EL, NEAA and mean AA Dg were significantly lower compared with SBM.

Effective Dg of total AA in SBM and EL was significantly lower than the CP Dg; this difference was not apparent in DBG or FM.

The undegraded fraction of FM and EL had a significantly higher proportion of EAA whilst DBG and EL had a higher proportion of BrAA when compared with the unexposed food. Isoleucine concentration, highest in EL, and lysine and methionine contents, highest in FM, differed significantly between the four protein source residues.

The first limiting AA after rumen incubation, in relation to casein and meat, was always methionine. The essential amino acid index of the food residues post incubation, relative to casein and meat, was lower in SBM, DBG and EL but higher in FM.

Males and females from Soay, Welsh Mountain, Southdown, Finnish Landrace, Jacob, Wiltshire Horn and Oxford Down sheep breeds and a breed of feral goats were slaughtered when proportionately 0·40, 0·52, 0·64 or 0·76 of mature live weight. On average, carcasses contained 583 g muscle, 243 g fat and 174 g bone per kg. Individual cuts (four commercially higher-valued and six lower-valued cuts of the shoulder, rib, loin and gigot joints) ranged from 375 to 670g muscle, 129 to 625 g fat and 0 to 294 g bone per kg.

Allometric coefficients are given for 32 traits. The distribution of bone in the carcass joints changed little as animals matured but carcass muscle and fat distributions changed significantly.

Breeds differed significantly in proportion of carcass muscle, fat and bone and also in their distribution. Welsh Mountain, Southdown, Wiltshire and Oxford Down all deposited carcass fat about three times more rapidly than did the Soay, goat, Finnish Landrace and Jacob. The Oxford Down had the lowest proportion of muscle (514 g/kg) and most fat (317 g/kg). The Southdown had least bone (148 g/kg) and the feral goat most muscle (662 g/kg). Southdown and Soay had the most muscle in commercially higher-valued cuts and Jacob and feral goat the least. Males had significantly more of their muscle in the neck and shoulder and significantly less in the gigot and flank.

As breed size increased, proportion of carcass muscle and bone decreased and proportion of carcass fat increased. These breed regressions were attributed to the small but exceptionally lean feral Soay and goat breeds, rather than to a failure of genetic size-scaling. There were no significant trends with breed size among the domesticated breeds.

Males and females from Soay, Welsh Mountain, Southdown, Finnish Landrace, Jacob, Wiltshire Horn and Oxford Down sheep breeds and a breed of feral goats were slaughtered when proportionately 0·40, 0·52 0·64 or 0·76 of mature live weight. Lipid concentrations in dried tissue were obtained for perirenal fat, omental plus mesenteric fat, subcutaneous fat, carcass muscle plus associated intermuscular fat, carcass bone and offal (pelt, head, feet and organs). Lipid varied from 260 g/kg dry matter (DM) for bone to 968 g/kg for perirenal fat.

As animals matured, lipid concentration increased in the dry matter of all tissues except bone, most rapidly in offal and least in intra-abdominal fat. The increases were highly correlated with the associated increases in proportion of dissected fat.

Breeds differed significantly in lipid concentration in the DM of all tissues examined. Breeds with a high lipid concentration in DM of one tissue usually had high concentrations in all other tissues. The Oxford Down had the highest concentration, and the Soay and feral goat the lowest. Males had slightly lower concentrations in all tissues except internal fat.

As breed size increased, mean lipid concentration (at the same stage of maturity) also increased in the DM of all tissues except bone. These breed regressions were attributed to the sampling of breeds, the smallest breeds being the exceptionally lean Soay and feral goat. Among the domesticated breeds, there were no signficant trends with breed size.

Breed means are given for 40 traits relating to food conversion efficiency and body composition at the same stage of maturity in seven breeds of sheep and a feral goat breed. In terms of breed means, food intake and food conversion efficiency were genetically correlated, as were most traits associated with fatness or leanness.

Highly inter-correlated measures of breed fatness were proportion of fat in the carcass, proportion of total carcass fat found in the rib plus loin, the fat : muscle ratio and the lipid concentration in the dry matter of all tissues except bone. Dressing proportion was highly correlated with all these measures of fatness.

Breeds with a high proportion of subcutaneous fat did not necessarily have a low proportion of intra-abdominal fat. A low proportion of carcass fat in the rib plus loin was associated with a high proportion in the shoulder (inter-breed correlation —0·7): both were measures of leanness. Muscle : bone ratio was not correlated with fatness or leanness. Slower maturing, larger breeds had slightly more bone, less fat and more lean in their higher-priced cuts. Breeds with heavier fleeces were fatter (0·7). The food conversion efficiency of a breed was largely independent of its body composition.

Early-cut, precision-chopped (EP) and late-cut, flail-harvested (LF) silages were offered ad libitum to breeding ewes during mid and late pregnancy in two experiments. Silages offered in late pregnancy were factorially arranged with silages offered in mid pregnancy giving four silage treatments. Voluntary drymatter intake, ewe weight change, lamb birth weight and blood levels of 3-hydroxybutyrate (3-OHB) and non-esterifiable free fatty acids (NEFA) were measured. The intake of LF silage was proportionately 0·61 and 0·72 of that of EP silage in mid and late pregnancy respectively. While type of silage given in mid pregnancy did not affect the mean silage intake in weeks 15 to 20 of pregnancy, the rate of decline in intake was higher and the intake during week 20 of pregnancy was lower following the feeding of EP silage in mid pregnancy. Despite a considerably lower level of body reserves associated with LF silage given in mid pregnancy, there was little effect on levels of 3-OHB or NEFA in late pregnancy or on lamb birth weight.

Groups of wether lambs were grown at different rates from about 24 kg live weight to 50 kg, by feeding them different amounts of the same concentrate diet. The slow growing lambs had higher contents of protein, ash, calcium (Ca), and phosphorus (P), and less fat and magnesium (Mg) than other groups. Differences in composition were significant between slow (120 g/day) and fast growth (230 g/day; P < 0-05) but not always between intermediate (160 g/day) and other growth rates. The differences became small and insignificant when data were expressed on a fat-free basis except for Mg which decreased with slow growth. Ash, for example, increased from 47 g/kg fat-free gain with fast growing animals to 54 g/kg with slow growth. Mg decreased from 0·44 g/kg fat-free gain with fast growth to 0·24 g/kg with slow growth. The data support the view that the ratio of ash to fat-free empty-body increases only slightly with age.

The basic diet contained 3·9 g Ca per kg dry matter and the effect of a substantial supplement of calcium carbonate on lambs growing at the fast rate was to increase their retentions of ash, Ca and P by a factor greater than 1·25. There are alternative explanations for this finding. One possibility is that the availability of Ca in the basic diet had been reduced by unknown factors. It is also possible that the supplementary carbonate altered the acid/base status of the animals and resulted in conditions which favoured skeletal mineralization.

The effect of consumption of saltbush and sodium chloride on energy metabolism in sheep was investigated. Twenty-four Awassi wethers were fed at maintenance level and allotted to three treatments: saltbush (Atriplex barclayana), salt (NaCl) and control. Daily mineral intakes with these diets were 149, 158 and 57 g, respectively. The saltbush had been irrigated with an equal-part mixture of seawater and fresh water and contained 15 g nitrogen and 310 g ash per kg. Energy and nitrogen balance were conducted using indirect calorimetry. The disappearance of organic matter and nitrogen from saltbush in the rumen was studied by the polyester bag technique.

Water intake of animals fed a high salt diet was 2·9 times higher and urine excretion was 3·7 times higher than in the control. Digested energy was proportionately 0·616 of dietary gross energy in the saltbush treatment, and 0·700 and 0·707 in the salt and control treatments respectively. Metabolizable energy (ME) was proportionately 0·795, 0·786 and 0·815 of digested energy, and heat production was 1·135, 1·043 and 0·867 of ME in the saltbush, salt and control treatments, respectively. The calculated values for digestible energy, ME, and net energy for maintenance on the saltbush diet were 5·02, 3·77 and 0·54 MJ/kg dry matter.

It is suggested that the low energetic utilization of saltbush is related to its low digestibility and the associated increase in energy expenditure, which are apparently related to mineral metabolism in the rumen. To maintain sheep on saltbush diets efforts should be made to lower the mineral content of this shrub.

Digestible (DE) and metabolizable (ME) energy values for five copra meals and a sample of raw copra, with oil contents ranging from 4 to 662 g/kg, were determined with both a high and a low energy basal diet in a metabolism experiment using 16 female pigs. Determined DE values ranged from 12·68 to 29·92 MJ/kg dry matter (DM) and values for ME from 11·95 to 29·08 MJ/kg DM which was a reflexion of their residual oil contents. Regression equations for the six samples were derived with DE and ME as dependent variables and chemical measurements and gross energy as independent variables. The best equation based on a single chemical parameter (ether extract (EE)) was:

Improvements associated with including more than one independent variable in the regression analysis were marginal. The most accurate equation (in terms of minimized residual s.d.) based on EE and crude fibre (CF) was:

Data from two selected lines of pigs in closed herds of a breeding company were collected over a 5-year period. The lines were selected for growth rate and leanness and were housed together in the same environment. Animals were performance tested from 35 kg for about 58 days, and were fed individually according to a scale determined by time on test; the boars were more liberally fed than the gilts. At the end of test, average daily gain (ADG) values were calculated and ultrasonic measures were taken of fat depths at the shoulder (SF), loin (LF) and last rib, 4·5 cm (CF) and 8 cm (KF) off the mid line.

Estimates of heritabilities, phenotypic and genetic correlations were obtained from paternal half-sib analyses. All heritability estimates were significantly different from zero and ranged from 0·18 to 0·42 for ADG and from 0·21 to 0·59 for fat depths. The genetic correlations between ADG and fat measurements in boars of the two lines were not significantly different from zero, averaging 0·08; in the gilts they were negative, averaging –0·39.

After long-term selection, appreciable genetic variation remained in the closed lines studied here for growth rate and fat depths. Although sex and feeding level were confounded, it is likely that the genetic correlation between growth rate and fat depth was influenced by the level of feeding and associated with partitioning of energy between lean and fat deposition.

Phenotypic and genetic analyses of the litter traits total number born, number born alive and total birth weight were conducted on data from two lines of pigs, line A, a synthetic largely of Landrace origin, and line B, derived from the Large White breed. The data were collected from closed herds of the Cotswold Pig Development Company Limited and comprised 1018 litters in line A and 863 litters in line B. Estimates of heritability and repeatability were low for all traits and consistent with other estimates in the literature, for number born alive being respectively, 0·07 (s.e. 0·04) and 0·15 (s.e. 0·04) in line A and 0·12 (s.e. 0·04) and 0·14 (s.e. 0·04) in line B. There was no evidence of an effect of the size of litter into which a female was born on her subsequent reproductive performance.

Three-week old piglets were subjected to two levels of moderate, chronic cold stress immediately post-weaning and inoculated orally or by aerosol with an enterotoxigenic strain of Escherichia coli. Oral challenge, as well as both piglet-produced and artificial aerosols of E. coli were capable of inducing infection. In infected animals, live-weight gain and food conversion efficiency were significantly worse at 15°C than at 20° or 30°C. The incidence and severity of diarrhoea was greatest at 15°C and least at 30°C, but only in those piglets fed ad libitum. Piglets fed at a restricted level kept at 15°C did not become infected or suffer a check in growth after inoculation.

In the absence of other risk factors, piglets kept at thermoneutrality are unlikely to suffer post-weaning diarrhoea even in the presence of an enterotoxigenic strain of E. coli. Diarrhoeic piglets did not exhibit the normal rise in food intake at temperatures below their thermoneutral zone. Traditionally, the design specification and control of the thermal environment in a piggery has been based on the performance of predominantly healthy pigs but the results of this study imply that the additional criterion of health can now be used.

Three replicates of three group sizes (six, 18 and 36) of grower pigs were housed with the same space allocation (0·66 m2 per pig), feeding and drinking space per animal. The animals were mixed and kept together for a period of 22 days. They were given food ad libitum, were weighed weekly and a record kept of the group food intake for the 22-day period. Weight at mixing had a significant effect on weight gains during the 1st week. There was a significant interaction between group size and replicates for weight gains; generally weight gains were lowest in the group size of 36 animals during the first 2 weeks, but in the 3rd week there was no difference between the group sizes. Sex had no effect on weight gains. The variation in weights between group members were significantly greater in the group size of 36 than in the group sizes of six and 18 at the start of the trial, but at the end of the trial there was no difference in the variances of weights in the three group sizes. There was no difference between the group sizes in the variances of the weight gains. There was a significant positive correlation (r = +0·36) between weight at mixing and weight gain for the group size of 18. Group size had no effect on food intake, but the food conversion efficiency of the animals in the group size of 36 was significantly poorer than in the group sizes of six and 18.

The effects of the halothane gene on growth and performance were estimated from British Landrace positive and negative selection lines and crosses between the lines. A total of 214 full-sib pairs were performance tested from 25 to 85 kg live weight on either ad libitum or scale (0·69 g/g ad libitum food intake) feeding. Half-sides of 45 carcasses were fully dissected.

In the crosses, growth and performance did not depend on whether the sire or the dam was from the positive line. Carcass length, conformation score, eye muscle area and incidence of pale, soft, exudative meat (PSE) were all intermediate in the crosses. Given food ad libitum, the crosses had increased appetite and growth rates which resulted in increased backfat depths. However, in the fully dissected carcasses, the crosses were intermediate for lean proportion. Although the crosses gave a net economic advantage, the incidence of PSE may be unacceptably high for commercial exploitation.

This experiment was designed to study the effects of stocking density in transit and the use of electric goads on pig welfare and subsequent meat quality. Sixty-four pens, totalling 1400 commercial crossbred hybrid pigs, were transported from a farm to a large commercial abattoir at either high (0·3 m2 per pig) or low (>0·4 m2 per pig) stocking densities. The lorry drivers loaded and unloaded the pens of pigs at either end of their journey with, or without, an electric goad. Similarly, lairage men moved groups of pigs from their lairage pens to the stunning and slaughter area with, or without, goads. Consequently, eight possible treatment combinations arose from this 2 × 2 × 2 factorial experiment. About 20 h after slaughter, the fibre optic probe (FOP) value of the longissimus dorsi muscle was recorded and carcasses were scored for the extent of skin blemish. Pigs in high stocking density groups (HSD) had lower FOP values than those on low stocking density groups (LSD) (P < 0·05) and more severe skin blemish (P < 0·001). The effect of goading in transport or in the lairage, had no significant effect on the FOP values. However, the skin blemish data showed a significant interaction between the use of goads during transport and the stocking density treatment (P < 0·05). This interaction implied that the use of goads when loading pigs at a HSD was associated with a reduction in skin blemish. Conversely, the lowest skin blemish frequency was observed in the LSD treatment group handled without the aid of goads. Pigs in the HSD groups were visibly more skin damaged and exhibited evidence of rectal prolapse which was absent in pigs transported at LSD. Lower stocking densities are to be recommended as carcass, meat quality and pig welfare are probably improved. The use of goads is associated with a higher degree of carcass damage unless pigs are to be densely packed during transport.

Mixing pigs from different social groups is known to cause turmoil which often results in skin lacerations as well as dark, firm and dry meat. Nine hundred and sixty commercial crossbred pigs were used for this experiment, divided into eight consignments. Within each consignment the pigs were divided into groups of about 15. The pigs in each group had coexisted for at least 6 weeks prior to slaughter. Thirty min before loading for slaughter, groups of pigs were either mixed with unfamiliar pigs or not mixed. Similarly, on arrival at the abattoir, groups of pigs were either mixed or not mixed. Hence there were four possible treatment combinations: pigs mixed with unfamiliar animals at loading, mixed at unloading, mixed at both points, or pigs which had remained in their social groups for at least 6 weeks prior to slaughter. Carcasses were dressed according to normal practice. After 20 h in the chiller room carcasses were assessed for skin blemish and fibre optic probe (FOP) values were measured in the longissimus dorsi muscle. Mixing pigs at either loading or unloading, or at both points, had no significant effect on the FOP value, but it did have a significant effect on the frequency of skin blemish values. Skin blemish values increased due to mixing at the farm (+0·36, Meat and Livestock Commission scale) however mixing at both places did not have an additive effect. The results indicate that the ideal movement system might be to keep pigs in their farm pen social groups until the point of slaughter.