Food can be used in an automatic milking system (AMS) to encourage frequent attendance to, and modify behaviour in, an AMS. An AMS was designed such that a cow had to pass from a bedded area through the AMS to enter the feeding area. A visit resulted in milking if the interval since the last milking was greater than 4 h.

Fourteen Holstein-Friesian dairy cows were allowed to attend voluntarily an AMS for 15 h/day for three 8-day periods. In period 1 the cows were given forage in the feeding area and concentrates in the bedded area but in period 2 this was reversed. Period 3 repeated period 1. The cows were also divided into two groups of seven, only one of which was given 1 kg of concentrates when milked in each period in a cross-over design.

Visits per cow per day increased when the cows were given forage in the feeding area (6·0 v. 4·1 (s.e.d. 0·08) P < 0·05) but milkings per cow per day were only slightly different (2·6 v. 2·4 (s.e.d. = 0·02) P = 0·052). Feeding forage in the feeding area modified forage-eating behaviour by reducing the number of bouts (4·9 v. 7·6 bouts per cow per day, P < 0·05) and total forage eating time (209 v. 289 min per cow per day (s.e.d. = 33·6), P < 0·05). The cows also tended to spend less time lying (529 v. 620 min per cow per day (s.e.d. = 43·2) P = 0·051).

There was no effect of feeding/not feeding concentrates in the milking stall on visits per cow per day or milkings per cow per day. However, feeding tended to create more shuffling behaviour during the automatic teat cup attachment process (3·4 v. 6·7 shuffling bouts per milking (s.e.d. 2·07) P = 0·053) but there were no effects on the levels of kicking, successful teat cup attachment rate, vocalization, elimination, hesitations in mounting a step or poor rear leg positions. The cows tended to adjust to a more accessible stance during both the automatic attachment process (from 17% of milkings exhibiting poor leg positions at the start of attachment, to 10% at the end, P < 0·01) and over the course of the experiment (from 26% to 10%, P < 0·02). There was a trend for cows who were not fed to milk out quicker than those who were fed for all milkings per day combined (733 s v. 811 (s.e.d. 43·3) s P = 0·074) but there were no other effects on yield, milk flow rate from the udder or time taken to milk out for all milkings through the day combined or just the first milking of the day.

Feeding concentrates in the feeding area can be used as an alternative to feeding forage in the feeding area, but there is no need to feed concentrates in the milking stall. Feeding cows while they were being milked did not improve their behaviour or milking characteristics.

Two experiments were conducted with dairy cows to examine the effects of including white clover in perennial ryegrass swards and of offering the cows a choice between tall and short mixed perennial ryegrass/white clover swards. In the first experiment, cows grazed a perennial ryegrass sward (treatment Prg); a mixed sward of perennial ryegrass and white clover (treatment WC); treatment Prg during the night and treatment WC during the day (treatment Prg night/WC day); or they were offered a choice between Prg and WC (treatment Prg/WC). Cows in treatment WC produced more milk than cows in treatment Prg, with cows in Prg night/WC day and Prg/WC intermediate. The milk fat content of cows in treatment Prg was greater than in the other three treatments. When cows were offered both mixed grass/clover and pure grass swards (treatments Prg night/WC day and Prg/WC) they exhibited a partial preference for the WC sward and grazed it to a lower herbage height than the pure grass sward. In the second experiment, cows were offered a WC sward at 6 or 3·5 cm sward surface height, or a choice between pastures at the two heights. Cows offered only the tall sward produced most milk, and those offered only the short sward produced the least. Milk fat content was reduced for cows offered only the tall sward. Cows offered a choice of the tall or short swards spent longer grazing in total than the cows offered only tall or only short swards but there was no difference in the time spent grazing the tall and short swards.

Energy and nitrogen balances were carried out with four multi-porous Holstein/Friesian cows offered four diets in a Latin-square experiment to evaluate urea-treated whole-crop wheat as a partial grass silage replacement for lactating dairy cows. Grass silage (GS) was produced from the primary growth of a perennial ryegrass sward. Spring wheat (cv. Axona) was harvested at 603 g dry matter (DM) per kg and preserved with 20 (WCW-20) or 40 (WCW-40)kg urea per t DM. The diets were 6 kg DM of a dairy concentrate daily with one of four forage treatments offered ad libitum. The forage treatments were GS alone, a 2:1 DM ratio of GS with WCW-40 (2:1 40), or a 1:2 DM ratio of GS with WCW-20 (1:2 20) or WCW-40 (1:2 40). Each period lasted 4 weeks with energy and nitrogen balances being carried out in respiration chambers over 6 days in the last week. Replacement of GS by diets containing WCW resulted in significant increases in DM intake (P < 0·01). Changes in milk yield and composition were small and non-significant but yields of milk fat and protein were higher on WCW diets than on GS diets (P< 0·05). With increasing proportions of WCW in the diet there were significant linear falls in apparent digestibility of DM (P < 0·001), organic matter (F < 0·001), neutral-detergent fibre (F < 0·01), acid-detergent fibre (F < 0·01), starch (F < 0·001) and nitrogen (P < 0·01). Gross energy intakes (P < 0·01) and faecal (P < 0·001), methane (P < 0·05) and milk (P < 0·05) energy outputs were higher with the WCW diets than with GS but urine energy and heat losses were unaffected. In consequence there were no significant differences among the diets in digestible or metabolizable energy (ME) intakes. However dietary ME concentrations (MJ ME per kg corrected DM) fell with increasing WCW inclusion from 11·54 on GS to a mean of 9·96 on the 1:2 diets (P < 0·001). It was calculated that the ME concentration of the WCW was only 8·1 MJ/kg corrected DM at maintenance intake, considerably lower than values used conventionally. There were no significant diet effects on the partition of ME or on the partial efficiency of ME utilization for milk production (k1). The increasing inclusion of WCW increased N losses in urine (P < 0·05) and faeces (F < 0·01) with no net effect on N digested or retained though there was a small increase in milk N output (P < 0·01). It is concluded that low digestibility is the major cause of the small milk response to the partial substitution of urea-treated WCW for grass silage with no evidence of a reduction in the efficiency of utilization of ME.

The effects of adrenergic challenge (in order to evaluate the adipose tissue lipolytic potential) and time of challenge relative to feeding on the response curve of plasma non-esterified fatty acids (NEFA) in four underfed or overfed non-lactating non-pregnant cows were studied. Basal NEFA and NEFA response to isoproterenol (ISO; 4 nmol/kg body weight) were higher when challenged before than after feeding and higher in underfed than overfed cows. Interaction between feeding level and time of challenge was significant (P < 0·001) for the rising part of NEFA response. Pooled NEFA response curves from several trials (no. = 63 challenges) were analysed in order to obtain a simplified procedure for the prediction of the NEFA response. High correlations were found between the response area or maximal NEFA response and NEFA response at 15 min (r = 0·95 and 0·98, respectively). This simplified procedure was applied on pooled data from 84 challenges in order to evaluate the effects of energy balance, physiological status, body condition score (BCS) and time of challenge relative to feeding. Energy balance had a significant effect on basal plasma NEFA and NEFA response at 15 min after ISO challenge (–7·6 and –14·2 μmol/l when the daily energy balance increased by 1 MJ, respectively). Time of ISO injection relative to feeding had a greater effect on stimulated NEFA than on basal NEFA (308 v. 239 μmol/l). There was a significant effect of BCS (41 μmol/l per unit of BCS) on the basal plasma NEFA level. The NEFA response at 15 min after ISO challenge was lower (387 μmol/l) in lactating cows than in dry cows. The NEFA response to ISO at 15 min could provide an efficient method of studying the adipose tissue lipolytic potential of cattle in vivo.

The effects of concentrate energy source on feeding behaviour and energy utilization, when offered with grass silages of differing intake characteristics, were studied in lactating dairy cows. A total of five silages, which differed in fermentation and intake characteristics, were prepared. Silages A, B and D and silages C and E were harvested from primary regrowths and secondary regrowths respectively of predominantly perennial ryegrass swards. Herbage was ensiled either pre-wilted or unwilted and either untreated or treated with a bacterial inoculant or formic acid based additives. Five concentrates (0s, 25s, 50s, 75s and 100s) were formulated to contain similar concentrations of crude protein, effective rumen degradable protein and metabolizable energy (ME) but using different carbohydrate sources to achieve a wide range of starch concentrations. The silages were offered ad libitum, supplemented with 10 kg concentrates per head per day. In experiment 1, a partially balanced change-over design experiment involving 50 lactating dairy cows was undertaken to examine the effects of concentrate energy source on silage feeding behaviour. Silages A, B, C, D and E were each supplemented with concentrates Os, 25s, 50s, 75s and 100s. Concentrate energy source did not alter (P > 0·05) silage feeding behaviour. The number of meals per day decreased (P < 0·01) as silage dry-matter concentration increased. Experiment 2, a completely randomized experiment involving 18 lactating dairy cows, was undertaken to examine the effects of concentrate energy source on energy utilization with cows offered silages B, C and D. These were supplemented with 10 kg/day of concentrates Os, 50s and 100s. Concentrate energy source had little effect (P > 0·05) on ME intake, energy output or on the efficiency of utilization of ME for lactation (k1). In experiment 3, the effect of concentrate energy source on silage preference was examined in a factorial design experiment involving 12 lactating dairy cows. Silages B, C and D were supplemented with concentrates Os, 50s and 100s. Concentrate energy source did not alter (P > 0·05) silage preference. It is concluded that with silages of differing fermentation and intake characteristics but of similar digestibility, concentrate energy source had no effect on feeding behaviour, silage preference or energy utilization. Furthermore there was no evidence of concentrate energy source by silage type interactions on silage feeding behaviour and preference, or energy utilization.

The metabolic response of dairy cows to high as opposed to low altitude conditions (2000 m v. 400 m above sea level) was determined. In the first experiment, four cows were subjected to a series of measurements before, during and after transport from lowland to high altitude pasture. During transport, cortisol, l-lactate and non-esterified fatty acids were significantly elevated but decreased within 1 to 3 days to initial levels. After transport, β-hydroxybutyrate and the thyroid hormones immediately increased and returned within 3 weeks to initial levels. Plasma urea increased during transport and subsequently was at an intermediate level due to the different diet. There were no direct carry-over effects of transport on metabolic traits during pasturing.

In the second experiment, three groups of six different dairy cows were either grazed in one of two consecutive years or kept inside (2nd year only). Lowland sojourn lasted for 4 weeks, and high altitude period for 8 weeks. At the end of high altitude sojourn, both outside and inside groups were found still to have significantly higher plasma cortisol values than at lowland. Thyroid hormones and ketosis related metabolites sharply increased at the start of the alpine period and were elevated for 1 to 3 weeks thereafter. According to the hormonal and metabolic profiles, the permanently housed cows did not benefit from the less adverse climatic conditions and the lower physical strain. Plasma urea closely reflected dietary changes in the ratio of nitrogen to fermentable organic matter. Plasma protein, albumin, creatinine, and liver enzyme activities were not affected by transport or high altitude sojourn in both experiments. The results indicate that the metabolic response to transport and high altitude conditions can be mostly explained by the efforts to cover the additional energy requirements. Overall the data suggest a wide but nevertheless limited ability of early-lactating cows to adapt to high altitude conditions.

Parameters based on probabilities of gene origin were used to evaluate the genetic variability of four Austrian cattle breeds. Effective numbers of founders, ancestors and remaining founder genomes showed that all four populations investigated are rather small genetically. Effective numbers of remaining founder genomes were 94 for Simmental, 41 for Braunvieh (Brown Swiss), 32 for Pinzgauer and 21 for Grauvieh (Grey cattle, a small mountain breed). As the value of 94 for Simmental was rather large in comparison with estimates from other populations in previous studies, the effect of population structure was investigated. A cosine measure of similarity based on differences in individual founder contributions to different subpopulations was defined and used for analysis. Subpopulations defined by regions were clearly more distinct for Simmental than for Braunvieh. The size of the cosine values depended on the method of calculating founder contributions and was overestimated when choosing the method not accounting for drift and bottlenecks (effective number of founders).

A statistical analysis strategy for the detection of quantitative trait loci (QTLs) in half-sib populations is outlined. The initial exploratory analysis is a multiple regression of the trait score on a subset of markers to allow a rapid identification of possible chromosomal regions of interest. This is followed by multiple marker interval mapping with regression methods within and across families fitting one or two QTLs. Empirical thresholds are determined by experiment-wise permutation tests for different significance levels and empirical confidence intervals for the QTLs' positions are obtained by bootstrapping methods. For traits with evidence for a significant single-QTL effect, an approximate maximum likelihood analysis is performed to obtain estimates of QTL effect and the probability of the QTL genotype for each parent of a group of half-sibs. The strategy is demonstrated in an analysis of previously published data on chromosome 6 and five production traits from a granddaughter design in dairy cattle. The results confirm and extend evidence for QTLs affecting protein percentage. Informativeness of markers limited the possibility of mapping more than one QTL on the same linkage group.

A model which was originally developed to derive the probability density of a calving distribution for beef cows under natural breeding has been modified to incorporate the effects of using oestrous synchronization at the beginning of the breeding period.

The model has been used to investigate five oestrous synchronization strategies over four herds, each with differing calving patterns: no synchronization; every cow in the herd is synchronized; every anoestrous cow is synchronized; every cow calving more than 20 days after the date of the planned start of calving is synchronized; every cow calving 30 days after the date of the planned start of calving is synchronized. Two of the herds previously had long calving periods and two previously had short, compact calving periods.

Model results showed that synchronization improved average herd calf live weight by 21 kg in the two herds with long prior calving periods but showed little effect in the two herds with compact prior calving periods. Synchronizing cows which calved more than 20 days after the start of calving in the herd showed similar results to synchronizing every cow in the herd and thus would be more cost effective. Synchronizing cows which calved more than 30 days after the start of calving in the herd showed a smaller advantage but only in the herds with long prior calving periods. The optimal strategy for oestrous synchronization in a herd will depend on the prior calving distribution and the average duration ofanoestrus in that herd as well as the relative costs of the treatment.

Saliva and faecal samples were collected from hill cattle (no. = 10) given tannin-rich oak (Quercus incana) leaves in the north-west Himalayan region of India. Amino acid composition of the saliva samples after thawing to remove precipitated proteins by centrifugation, and dialysis (molecular weight cut off: 3500) to remove small moieties revealed 6·4 (s.d. 0·6) % proline, 15·6 (s.d. 0·6) % glutamine plus glutamate and 9·2 (s.d. 1·0) % glycine on molar basis. For Holstein Friesian cattle (no. = 4) which had no history of consumption of tannin-containing foods, these values were 6·5 (s.d. 0·4) %, 15·2 (s.d. 0·5) % and 9·8 (s.d. 0·7) % respectively. Proline concentration in the proteins present either as free or as tannin-protein complexes in the lyophilized faecal samples from hill cattle was 4·7 (s.d. 0·2) % (on molar basis) of the total amino acids and 5·3 (s.d. 0·2) % in Holstein Friesian cattle. In the faeces of oak-fed cattle, the tannin and condensed tannin levels on dry-weight basis were 0·81 (s.d. 0·20) % as tannin acid equivalent and 0·06 (s.d. 0·04) % as leucocyanidin equivalent respectively. For tannic acid, the relative affinity of salivary proteins, using the competitive binding assay, was about six-times higher than that of bovine serum albumin (BSA) and was of the same order as that of gelatin. Turbidity of complexes formed between salivary proteins or BSA and tannic acid showed proportionately about 0·50 lower turbidity for salivary proteins in 0-2 mol/I acetate buffer (pH 4·9 containing 0·17 mol/l NaCl) and proportionately about 0·84 lower turbidity in distilled water. The results suggest that unlike rats or mice, the proline-rich proteins do not appear to be of any physiological significance in the adaptation of cattle to tannins. However, the salivary proteins of cattle though not rich in proline, have a high affinity for tannins and these proteins have a high tendency to form soluble tannin-protein complexes.

Faecal nematode egg counts (FECs) were examined in lactating ewes from divergent flocks of Romney sheep which had been selectively bred from 1979 to 1996 for or against FEC in 4 to 7 month old lambs. Faecal samples were obtained from the ewes while under normal grazing management, 1 to 2 months after lambing in spring for each of 6 years between 1987 and 1996 (no. = 785 records; 298 animals). Analyses were carried out on loge (FEC + 100)–transformed data using animal-model maximum likelihood procedures, accounting for repeated records on ewes, within and between lactations. An examination of non-genetic effects indicated that there was no significant effect of age class of ewe on FEC but ewes which gave birth to single lambs had significantly lower post-parturient FECs than those bearing twins (back-transformed means of 184 v. 276 egg per g, respectively; P < 0·001). In relation to genetic effects, post-parturient FECs were significantly lower in ewes from the flock bred for low lamb-FEC than in their counterparts from the flock bred for high lamb-FEC, with ewes from the most recent birth years (1991 to 1994) showing a nine-fold difference (back-transformed means of 33 and 305 eggs per g faeces respectively; P < 0·001). This was equivalent to 69% of the divergence observed between loge (FEC + 100) in their lambs in the same years. Heritability and repeatability estimates for loge (FEC + 100) in ewes were 0·37 (s.e. 0·06) and 0·46 (s.e. 0·03) respectively. Genetic correlation estimates between a ewe's post-parturient loge (FEC + 200) and her loge (FEC + 100) as a lamb, based on analysis of (co)variance or realized responses, were 0·70 or 0·58 respectively. The phenotypic correlation between a ewe's loge (FEC + 100) and that of her lamb(s) in the same lactation was 0·29 (s.e. 0·06) (P < 0·001). From the results it is clear that substantial genetic changes in post-parturient FECs of breeding ewes can be induced through a correlated response to selective breeding for or against reduced FEC in lambs. This may have important implications for the epidemiology of nematode parasite infections in spring-born lambs, a possibility which is currently being investigated.

Data on ovulation rate, embryo survival and litter size have been analysed from the 1988-96 records collected at AgResearch's Woodlands Research Station on 2180 elite (highly prolific) ewes of three breeds: Romney, Coopworth and Perendale. The Romneys included a subgroup found to carry the sex-linked Inverdale high prolificacy gene. Foundation animals for all breeds were screened on high litter size (lambs born, alive or dead, per ewe lambing) from industry flocks. Prior to being transferred to Woodlands between 1979 and 1984, their average litter size was 2·66. Ovulation rates for descendants of the foundation ewes averaged 2·15 (Romney), 2·43 (Coopworth), 2·15 (Perendale) and 2·96 for the Romney subgroup carrying the Inverdale gene. Embryo survival averaged 0·84 except for a low value in Inverdales (0·76). Using a restricted maximum likelihood model, with full relationship matrix, the within-breed heritability of ovulation rate over all ages and breeds (excluding Inverdale) was 0·14 (s.e. 0·03), with repeatability 0·26 (s.e. 0·02). Litter size averaged 1-80 (Romney), 2·05 (Coopworth), 1·76 (Perendale) and 2·17 (Inverdale). The heritability estimate for litter size (excluding Inverdale) was 0·073 (s.e. 0·018), from data for all ages. The genetic correlation between ovulation rate and litter size was 0·91 (s.e. 0·08). The standard deviation for ovulation rate in the Inverdales was 1·75 times as great as the average of the other three breeds. Embryo survival to term for ewes conceiving to two, three or four ovulations averaged 0·89, 0·77 and 0·64, respectively, and was significantly different among breeds fP < 0·001). The greater ovulation rate in Inverdales than Romneys was sufficient to explain the Inverdale effect on reduced embryo survival. The highest embryo survival was observed in the Coopworth breed (P < 0·001).

An experimental programme was initiated in 1990 to investigate the consequences of selection for reduced fatness in hill sheep and to estimate genetic parameters for carcass traits in the same class of animal. Thirty-two progeny groups of lambs were born as a result of mating Scottish Blackface rams to ewes of the same breed on two Scottish Agricultural College hill farms in 1991 and 1992. Sires were from two divergent selection lines for subcutaneous back fat depth and were selected under ad libitum feeding conditions on an index combining live weight and ultrasonic fat depth at 20 weeks of age. The index was designed to alter body composition but not body weight. Weaned male progeny (reared extensively) were brought together from both farms in August of each year, reared on grass and finished for slaughter on swedes at a target condition score of 3. Measurements taken at weaning were: live weight, average ultrasonic measurements of average subcutaneous fat depth and muscle depth. At slaughter, traits measured were: pre-slaughter live weight, pre-slaughter condition score, age at slaughter, cold carcass weight, killing-out proportion, Meat and Livestock Commission (MLC) fat class and MLC conformation class. Side and shoulder dissections were made on proportionally 0·2 and 0·8 of lambs respectively and lean tissue, subcutaneous fat, intermuscular fat and bone were measured. Comparisons were made between the two genetic lines and genetic parameters were estimated from data adjusted to three different ‘end-points’: constant dissected subcutaneous fat weight, constant age at slaughter and constant cold carcass weight. Moderate to low heritability estimates were obtained for most traits: pre-slaughter live weight = 0·36, cold carcass weight = 0·39, fat class = 0·13, conformation class = 0·09, lean weight = 0·27, bone weight = 0·36 (constant subcutaneous fatness), intermuscular fat = 0·20, subcutaneous fat = 0·20 (constant cold carcass weight). Correlations between ultrasonic measurements at weaning, and slaughter and dissected carcass components were moderate to weak. However, there is sufficient genetic variation in the carcass traits to warrant inclusion in breeding goals for hill sheep. The results also show that genetic differences obtained by selection under intensive rearing conditions for divergent fatness are also seen in progeny reared under extensive (hill) conditions.

Video image analysis (VIA), carcass shape and colour data were collected for 1211 lambs of known gender, breed type and carcass weight over a 1-week period using the VIAscan® system developed by the Australian Meat Research Corporation. Classification data (thickness of soft tissue over the 12th rib (GR measurement) and subjective conformation scores on a five-point scale of the leg, loin and shoulder) were assessed by an Agriculture and Agri-Food Canada grader after carcasses had chilled at 5°C for 3 to 6 h. Dissections into saleable meat yield (no. = 58) were performed after carcasses had chilled an additional 24 h. The timing of this study, which was dependent on availability of the VIA equipment, influenced the age and type of lambs available for analysis. The majority of lambs evaluated were wool-breed wethers, age > 10 months, of average GR (15·7 (s.d. 0·2) mm) and muscle conformation (3·0, s.d. 0·1). VIA improved the prediction of saleable meat yield (R2 = 0·71, residual s.d. = 14g/kg) compared with the current classification system (R2 = 0·52, residual s.d. = 18 g/kg). Although prediction ofGR measurement by VIA resulted in a large residual error (residual s.d. = 2·4 mm), the proportion of waste fat (perirenal and subcutaneous) and bone dissected from the carcass was accurately predicted (R2 = 0·62, residual s.d. = 11 g/kg). Proportions of leg (R2 = 0·71, residual s.d. = 7 g/kg) and shoulder (R2 = 0·62, residual s.d. = 9 g/kg) primals were also accurately predicted by VIA, although there were no significant predictors for the proportion of the loin (P > 0·15). VIA improved the prediction of saleable meat yield compared with the current classification system. However collection of additional data including some from extremely lean or well muscled animals would be required before VIA could be recommended to classify lamb carcasses

A study was conducted to find early predictors of the Booroola gene in several generations of a crossbred sheep population. Merino carriers of the Booroola gene were mated with Texel sheep to improve prolificacy of the latter. Ovulation rate at 8 months of age, litter size at 1 and 2 years of age and FSH and inhibin levels at 3, 4, 5 and 6 weeks of age were determined in about 700 females.

Gibbs sampling was applied for inference in a mixed inheritance model. Estimates for the gene effect in heterozygous females were +1·5 corpora lutea and +1·3 lambs at 2 years of age. The gene effect on litter size at 1 year was small. The only significant major gene effect for hormone levels found was for lnINH4 (–0·66).

A number of hormone levels and combinations of hormone levels appeared to be useful predictors of carrier status of individual animals. In comparison with a situation where only parents' genotype is known, posterior probabilities for non-carriers were on average increased from 50 to over 95% when FSH levels were used. However, the combined posterior probabilities of carriers and non-carriers increased only up to 67%. So in general, classification with Gibbs sampling resulted in too few animals being identified as carrier. The sum of FSH levels at 3, 4, 5 and 6 weeks of age is proposed as a predictor of presence of the Booroola gene in an animal. Multivariate analysis of mixed inheritance models could help to find more effective combinations.

Genetic parameters for birth weight were estimated for two sets of spring-born and one set of autumn-born lambs of the same breed composition and genetic origin using a model that included random additive, additive maternal, permanent environmental maternal, litter and residual effects. Litter effects were significant for all data sets, indicating that within-year effects of common environment and (or) non-additive genotype were important for birth weight and should be included in genetic evaluation programmes. Estimates of variance components for autumn-born lambs differed significantly from those obtained from spring-born lambs or from the combined data. In contrast, estimates obtained for the two sets of spring-born lambs did not differ from those obtained when data on all spring-born lambs were pooled. The estimate of h2 for birth weight in spring-born lambs was over twice as large as that obtained for autumn-born lambs (0·26 v. 0·22).In contrast, the across-year repeatability of ewe effects was much larger in autumn lambs (0·41 v. 0·26) as was the full-sib littermate correlation (0·73 v. 0·49). Mean birth weights were also 0·4 to 0·6 kg less in autumn lambs. These results suggest that negative effects on birth weight that have been reported for lambs gestated during summer in equatorial and subtropical regions are also manifested (albeit at reduced levels) in less extreme climates (in this case, 37°, 15' N latitude and 654 m elevation) and that maternal variation exists in the ability of the ewe to maintain adequate lamb birth weights in autumn lambing systems.

Thirty sows were allocated at their first farrowing to five litter size treatments. Litter sizes of six, eight, 10,12 and 14 were established by cross-fostering within 48 h post partum. Milk yield (Y, kg/day) of sows was linearly related to litter size (L) and was described by the equations; Y = 5·98 (s.e. 0·48) + 0·689 (s.e. 0·046)L, R2 = 0·99; residual s.d. = 0·29; P < 0·001 and Y = 8·20 (s.e. 0·46) + 0·324 (s.e. 0·044)1, R2 = 0·95; residual s.d. = 0·28; P < 0·002 for early (day 10 to day 14) and late (day 24 to day 28) lactation, respectively. The composition of milk from sows suckling various litter sizes remained relatively stable but suckling frequency in early lactation increased linearly in response to increased litter size. Litter size significantly affected the average growth rate of individual piglets; piglet growth rate from birth to weaning at 28 days of age decreased from 283 g/day to 202 giday in response to increasing litter size from six to 14. The relationships between milk yield, average piglet growth rate and litter size indicate that the number of functional glands is the major factor influencing milk yield of sows. Increasing the number of functional glands by increasing litter size more than compensates for any decrease in milk output from individual glands.

The aim of the study was to investigate the influence of different energy levels during a 4-week lactation on the regulation of the metabolic hormones somatotropin (GH), prolactin, insulin and insulin-like growth factor-1 (IGF-1). A total of 21 crossbred sows (German Landrace × Duroc) were cannulated for daily blood collection from 3 weeks before parturition until 2 weeks after weaning and for weekly window sampling (every 20 min for 10 h). Nineteen sows were given 2·8 kg food during late gestation, 5·0 kg food during lactation and 2·8 kg food per day after weaning and two sows were given food at a restricted level (3·0 kg) during lactation. In the 19 sows, the different energy balance was induced by allocation of different numbers of sucking piglets to the respective sows. One group of sows suckled seven piglets and served as a control (C; no. = 7) and another group suckled 10 to 12 piglets and was energy deficient (D). After the study, the sows of the deficient group were, based on their litter weight gain from parturition until weaning, divided into low (D-L; no. = 6) or high (D-H; no. = 6) litter weight gain. The D-H sows lost more body weight during lactation than C and had lower glucose and higher nonesterified fatty acids levels before morning feeding. GH and prolactin increased around parturition and their secretory profiles during lactation were altered by the frequent sucking stimulus, whereby the access of the piglets to their dams was not controlled. During lactation, GH and prolactin were highest in D-H sows. The results suggest a possible role of not only GH but also of prolactin in nutrient partitioning to the mammary gland just before the start of lactation and for minimizing the adverse effects of a negative energy balance. Furthermore, insulin and IGF-1 increased around parturition in all sows. Insulin was higher before and after feeding and the highest levels were found in C and D-L sows. The regulation patterns of insulin and IGF-1 indicate that the lactating sow is able to mobilize enough energy from body reserves to prevent metabolic disorders, even during a period with deficient energy supply. This is contrary to the regulation in the dairy cow, where the negative energy balance is coupled with a severe glucose deficit during phases of high milk yield, which causes decreased levels of insulin and IGF-1. In the sow, the glucose intake with the food meets the glucose requirement for metabolic pathways also during a deficient lactational energy intake. Therefore, in sows IGF-1 can be stimulated by increased GH levels via the GH receptor in the liver during a state of nutritional energy deficiency and the fact that sows can compensate a deficient metabolic state much better than cows is also reflected in the respective endocrinology.

A 3 × 2 factorial experiment was used to investigate the influence of the breed type of gilts (Meishan synthetic 50% (M), purebred Large White (LW) and purebred Landrace (LR)) on response to insoenergetic diets of differing protein levels (180 g crude protein (CP) per kg, 9 g lysine per kg; or 240 g CP per kg, 12 g lysine per kg) offered to appetite over a 28-day lactation. Body fat reserves were adjusted during pregnancy by supplementing a set quantity of basal diet (131 g CP per kg, 12·7 MJ digestible energy (DE) per kg) with an energy source (maize starch + soya oil), to attain a backfat at P2 (6·5 mm off midline at last rib) of 25 mm at farrowing for all breeds. There were no significant diet effects or breed ×diet interactions on lactational performance. On day 1 of lactation, backfat was: M = 25·9, LW = 24·9, LR = 23·9 mm (P < 0·005). M gilts were lighter at farrowing (M = 173, LW = 192, LR = 182 kg; P < 0·001) and had more piglets than LW and LR. LR gilts had heavier piglets at birth (M = 1·13, LW = 1·18, LR = 1·38 kg, P < 0·001) than M and LW gilts. M gilts had a higher food intake (M = 6·4, LW = 5·2, LR = 5·1 kg/day; P < 0·001) but higher fat (M = 4·1, LW = 2·2, LR = 2·9 mm; P < 0·05) and weight (M = 15·9, LW = 1·0, LR = 4·7 kg; P < 0·001) loss over lactation than LW and LR gilts. LW gilts had a lower lactation output as reflected by lower litter weights at weaning than M and LR gilts (M = 73·7, LW = 59·3, LR = 75·2 kg; P < 0·002). It is concluded that lactation of gilts is not improved by provision of a very high protein diet (240 g CP per kg) and that performance still differs between breeds when backfat levels are standardized.

One hundred and twenty crossbred gilts and sows were used in an experiment with three differently composed pregnancy diets in order to study the effects on performance during three reproduction cycles. Treatments during pregnancy were: (1) a standard diet; (2) 500 g sugar-beet pulp per kg diet; (3) 500 g mixture of green grass-meal, wheat bran and oat hulls per kg diet. Sows were given similar levels of estimated daily net energy (NE). All three groups were given the same standard lactation diet semi-ad libitum in two daily meals. Recordings were made of food intake during pregnancy and lactation, body weight of sows at mating, farrowing and weaning, days until first mating, litter size, and mean piglet weight at birth and weaning. Pregnancy food intake (kg) was highest in diet 3 and lowest in diet 1 (P < 0·001). Food intake was lower for sows given diet 2 than for sows given diets 1 and 3, when measured in NEfor pigs (P < 0·001). Food intake during lactation was higher for sows given diet 2, than for sows in the two other diet groups (P < 0·01). Results were consistent during all three experimental rounds. Mean body weight of sows was the same for all diet groups both at mating, farrowing and weaning. Weight gain during pregnancy and weight loss at farrowing was significantly higher in groups 2 and 3 than in group 1 (P < 0·001). Litter size was not affected by the different pregnancy diets, neither total number live born nor weaned. Both mean piglet weight and total mean litter weight at birth were negatively influenced by diet 2 (P < 0·001) and (P < 0·05) respectively. This indicates that a diet with a high content of soluble dietary fibre and a large capacity to induce satiety may have a negative effect on piglet weight at birth. At weaning, however, the mean weights of piglets were the same for the three diet groups. It was concluded, that it is possible to feed pregnant sows very differently composed diets without detrimental effects on performance.