The nutritional value of different categories of peas was measured in mash or pelleted diets using adult cockerels. Twenty-five round and white-flowered peas (feed peas), 12 round and coloured-flowered peas and five wrinkled and white-flowered peas were used in mash diets. From the same batches, 11 feed peas, five coloured peas and four wrinkled peas were tested in pelleted diets.

Mean apparent metabolizable energy (AME) values were 12·02, 11·35 and 10·50 MJ/kg dry matter (DM) for feed peas, coloured peas and wrinkled peas respectively in mash diets and 13·18, 12·72 and 11·63 MJ/kg DM for the same categories in pelleted diets.

Mean starch digestibility was 0·905, 0·887 and 0·802 for feed peas, coloured peas and wrinkled peas respectively in mash diets and 0·985, 0·984 and 0·840 for these categories in pelleted diets.

Mean protein digestibility was 0·788, 0·643 and 0·798 for feed peas, coloured peas and wrinkled peas respectively in mash diets and corresponding values for peas in pelleted diets were 0·855, 0·743 and 0·853.

Pelleting thus had a positive effect on the nutritional value of peas and this improvement was all the more important because the AME and protein digestibility of the pea in mash diets was low.

The nutritional value of feed peas for cockerels was not strongly correlated with chemical composition or to digestibility data obtained in the pig.

Early embryo loss is the major cause of reproductive failure in cattle. The effect of short-term changes in energy intake pre- and post-insemination on embryo survival and systemic progesterone was investigated in heifers. Two pasture allowances (low, L and high, H) were calculated on a dry-matter basis to provide 0⋅8 and 2⋅0 times maintenance requirements, respectively. Following oestrous synchronization, heifers (no. = 296) were allocated to either L or H pasture allowance for a 10 day period before artificial insemination (AI). On the day after AI, heifers (no. = 247) were again randomly allocated to either the L or H pasture allowance until either embryo recovery between days 14 to 16 or pregnancy diagnosis at day 30 (AI = day 0). Hence, there were four nutrition treatments; L-L, L-H, H-H and H-L. Blood samples were collected on days 4, 5, 6 and 7 of the pre- and days 4, 5, 6, 7, 13 and 14 of the post-AI oestrous cycle (oestrus = day 0) for determination of plasma progesterone. Embryo survival rate was significantly lower in the H-L (0⋅38) than in the L-L (0⋅70), L-H (0⋅71; P < 0⋅001) or H-H (0⋅65; P < 0⋅01) treatment groups but there was no evidence that the detrimental effect of reduced energy intake after AI was mediated through changes in systemic progesterone.

Three experiments were conducted to investigate the effect of bag incubation sequence on the degradation of food components in situ in the caecum of mature, caecally fistulated Welsh-cross pony geldings (mean live weight 278 kg) offered hay ad libitum. In experiment 1 a fibre-based commercial horse concentrate was incubated in situ using a forward (3, 5, 16, 8, 24, 48 h) or reverse (48, 24, 8, 16, 5, 3 h) incubation sequence. Dry matter (DM), crude protein (CP), neutral-detergent fibre (NDF) and acid-detergent fibre (ADF) degradation coefficients and calculated effective degradability (ED) values were determined. In experiment 2 unmolassed sugar-beet pulp (USBP), hay cubes (HC), soya hulls (SH) and a 2: 1 mixture of oat hulls: naked oats (OHNO) were incubated in situ as for experiment 1. In experiment 3 unprocessed barley (UB), micronized barley (MB), extruded barley (EB) and dehydrated grass (DHG) were incubated in situ according to slightly different forward or reverse incubation sequences of (2, 4, 6, 12, 8, 24, 48 h) and (48, 24, 8, 4, 12, 6, 2 h) respectively. In experiments 2 and 3 only DM degradation parameters were studied.

Of the three starch-based foods studied in experiment 3 (UB, MB and EB), incubation sequence did not significantly P > 0·05) affect any of the degradation parameters examined. Conversely however, of the six fibre-based foods which were examined across the three experiments, incubation sequence did significantly P < 0·05) affect in situ degradation parameters in the commercial horse concentrate in experiment 1, the SH food in experiment 2 and the DHG food in experiment 3. Depending on the food or food constituent studied (i.e. DM, CP, NDF or ADF) degradation coefficients a, b, c and a + b along with ED values calculated at fractional outflow rates of 0·05 and 0·025 could all be statistically different CP < 0·05) according to whether a forward or reverse incubation sequence was used. It is postulated that this effect is related to the basic digestive physiology of the equine caecum which is small, digesta passage rate through it is fast and digesta volumes can vary considerably. These factors may interact to create a considerable degree of non-uniformity within the caecal digesta pool in which in situ bags are incubated. Consequently, it is recommended that in future in situ experiments in the equine hindgut, animals are offered ad libitum diets in an attempt to minimize variation within the caecum. It is also recommended that in situ experimental protocols incorporate more than one incubation sequence when the degradation parameters of fibrous foods are studied in equids.

The live-weight responses, voluntary herbage intakes and diet compositions of two breeds of sheep of different mature live weights, grazing two contrasting hill vegetation communities, were studied over three consecutive grazing seasons. A total of 228 Latxa and 255 Gallega non-lactating ewes, with mature live weights of 42.4 and 33.1 kg respectively, grazed two replicates, each of two 5-ha plots comprising by area either 0⋅3 Calluna vulgaris and 0.7 grass species (Agrostis capillaris, Festuca rubra and Nardus stricta) (treatment C3) or 0.7 C. vulgaris and 0⋅3 of the above grass species (treatment C7).

The Latxa ewes achieved higher rates of live-weight gain than the Gallega ewes under conditions of high availability (sward surface height >3⋅0 cm) of the preferred grass species (A. capillaris and F. rubra) but had lower rates of live-weight gain in the later part of the grazing season when the availability of the preferred grass species was low. In general, the Latxa ewes had higher voluntary herbage intakes per unit live weight and selected a diet of higher digestibility than the Gallega ewes (P < 0⋅001). The composition of the diet was significantly affected by treatment (P < 0⋅001) and was of a higher digestibility in the earlier part of the grazing season (P < 0⋅001).

The results indicate the existence of a significant (P < 0⋅001) genotype × environment interaction affecting diet selection and animal performance. Between-breed differences in diet selection are likely to be important in determining grazing behaviour and thus the suitability of different genotypes for particular environments. Breeds with a small body size are likely to be better suited to the poorer land resources where the availability of preferred species is low.

The purpose of this experiment was to determine whether body temperature is a sensitive parameter to measure long-term effects of stress in pigs. Mixing of unacquainted pigs is a severe stressor that has detrimental effects on health, production and welfare. We measured deep body temperature after mixing growing pigs. Five pigs of 15 weeks of age, each individually housed with a companion pig, were mixed with two unacquainted congeners. Deep body temperature, heart rate and activity were recorded by radiotelemetry 9 days prior to until 8 days after mixing. These parameters were also recorded in five control pigs (individually housed with a companion pig) during the same time span. Behaviour during the light period was recorded on videotape on the day of mixing and on three subsequent days. Mixing induced a significant rise in body temperature that lasted for 8 h after mixing. Although heart rate and general activity level did not significantly differ between mixed and control pigs, mixing significantly increased the frequency of fighting and reduced the frequency of eating. In conclusion, the present experiment shows that mixing induces a long-lasting hyperthermia in pigs. Thus, deep body temperature may be used as a sensitive parameter to measure long-term effects of stress in pigs.

Six experimental diets with similar contents of macronutrients (450, 300 and 70 g/kg dry matter of protein, carbohydrate and fat, respectively) and, therefore, total energy, hut differing in the composition of lipid component, were each given to three replicate groups of European eel. Different fat mixtures were used to formulate diets with different levels of fatty acids considered as essential for fish: linoleic (18: 2n6), linolenic (18: ЗпЗ) and highly unsaturated fatty acid (HUFA)n3, mainly EPA (20: 5n3) and DHA (22: 6n3). One tested diet contained low levels of all the three components, three diets had a high level of each one of these, the fifth diet contained high levels of both 18C fatty acids and, finally, a sixth diet incorporated simultaneously high amounts of 18: 2n6 and (HUFA)nЗ.

Dietary lipid composition did not significantly affect food intake or protein and fat apparent digestibility. However, growth and food efficiency were the best with the diet containing approximately 5 g/kg of both linoleic and linolenic acids. Although all groups increased their body fat content over the experiment, the fatty acid composition of total muscle lipids was rather insensitive to lipid dietary composition, perhaps due to the high body fat content of the eels prior to the experiment.

The accuracy with which several laboratory-based measurements predict the metabolizable energy (ME) value of whole-crop wheat (WCW) was determined. Twenty-six WCW forages differing in variety (cv. Slepjner, Hussar and Cadenza), maturity at harvest (milk, cheese and dough stages) and treatment applied (urea-treated, untreated or acid-based additive treated) were harvested in 2 years and conserved anaerobically in 200·1 barrels. The forages were then scanned using near infrared reflectance spectroscopy (NIRS) and analysed for chemical composition, in vitro rumen fluid-pepsin digestibility, in vitro neutral detergent-cellulase plus gamannase digestibility, in vitro fermentation gas production and in situ rumen degradability. ME was calculated using measured energy losses in faeces and urine and predicted energy losses as methane. The relationships between ME and the laboratory-based measurements were determined by regression. Gross energy was consistently the best predictor of ME (R2 = 0.53 and 0.86 in years 1 and 2 respectively). However the autocorrelation involved, militates against the prediction of ME from gross energy. None of the chemical constituents or biological techniques gave a good, robust prediction of ME. However, an NIRS calibration developed using the WCW samples was highly correlated (R2 = 0.68) with ME. This work therefore suggests that traditional laboratory-based, food evaluation techniques are unsuitable for predicting the ME content of WCW but that NIRS holds promise.

Two experiments determined the effects of daily oral supplements of vitamin A (retinol) and injected preparations of vitamin A on liver vitamin A concentration and plasma carotenoid (PC) concentration. Vetade is an oily injectable vitamin A preparation, while Nov-a-Vit is an aqueous injectable vitamin A preparation. Angus crossbred heifers were used in experiment 1 and Angus and Simmental crossbred steers were used in experiment 2. All cattle grazed pasture but were given also 1 kg per head of pellets daily and vitamin A supplements were included in the pellets when required. In experiment 1, one group of heifers was given 1 × 106 i.u. vitamin A per head daily for 31 days, while a second group in another part of the paddock was not supplemented with vitamin A. A third group of heifers grazed with this latter group and was injected with 2·5 × 106 i.u. vitamin A (Vetade) three times weekly. The oral vitamin A supplement proportionately reduced plasma and liver carotenoid concentrations by 0·49 and 0·41 respectively, while increasing liver vitamin A concentration three-fold. By contrast, the Vetade failed to increase liver vitamin A concentration or to reduce liver and plasma carotenoid concentrations. In experiment 2, two groups of steers were injected twice weekly for 7 weeks with 2 × 106 i.u. vitamin A as Nov-A-Vit or as Vetade. A third treatment group, grazing with these steers, received no vitamin A injection, while a fourth group grazing in a separate area of the paddock was supplemented daily with 1 × 106 i.u. vitamin A per head in their diet. The injection of Nov-A-Vit and the oral vitamin A supplement decreased PC concentration by a similar amount but the increase in liver vitamin A concentration was larger for steers injected with Nov-A-Vit. Vetade injections failed to increase liver vitamin A concentration and there was no decrease in PC concentration. The plasma cholesterol concentration for the treatment groups varied over the duration of the experiment but could not be related to the vitamin A treatment or to the changes in PC concentration. These results indicate that vitamin A injections can be used to reduce PC concentration provided they increase liver vitamin A concentration.

Twenty-five New Zealand White × Californian lactating doe rabbits were used to study the effect of different dietary fibre concentrations on the amino acid contribution of soft faeces to the total amino acid intake. Five isoenergetic diets containing 312, 334, 360, 384, and 412 g/kg neutral-detergent fibre (DM basis) were formulated. All diets were designed to maintain the same amino acid pattern. Soft faeces production showed a trend to increase (P = 0·07) as dietary fibre increased. The content of isoleucine (P < 0·01), glutamic acid, leucine and alanine (P < 0·05) in soft faeces decreased as the dietary fibre increased. A trend to decrease with the increase of dietary fibre was also observed for aspartic acid (P = 0·06), lysine (P = 0·07), methionine and valine (P = 0·1). As a consequence, the soft faeces contribution to the total intake of individual amino acids did not vary with the type of diet. The average contribution of soft faeces to the total amino acid intake for the most limiting amino acids of lactating doe rabbits under practical conditions, methionine, threonine and lysine, were 0·17 , 0·21 and 0·18 g/g, respectively.

The effects of three fat supplements on milk yield and composition were measured using 12 mid-lactation in-calf Hoistein-Friesian cows in a balanced incomplete change-over design over three periods each of 3 weeks. All cows received a basal diet consisting of 36 kg/day grass silage (dry matter (DM) 270 g/kg, metabolizable energy (ME) 11·6 MJ/kg DM) and 7 kg/day o f a concentrate mixture containing (g/kg) rolled barley (501), molassed sugar-beet pulp shreds (277), soya-bean meal (208) and a standard cow mineral supplement (14). Treatments were CON (control-no supplement); LIN and FISH (250 gl day of either linseed oil or marine oil, providing approximately 0·046 of ME intake) or TOA (95 glday of tuna orbital oil, providing 0·018 of total ME intake).

There were no significant effects on silage DM intake or milk yield (means 9·25 and 17·2 kg/day respectively). The FISH and TOA treatments depressed (F < 0·05) milk fat concentration (45·4, 44·6, 34·5 and 41·6 (s.e.d. 1·08) g/kg for CON, LIN, FISH and TOA respectively; note — the same treatment order is used for all results quoted). Compared with values for CON, yield of f at (glday) was significantly (F < 0·05) greater for LIN and significantly lower for FISH (739, 808, 572 and 732, s.e.d. 28·7). All three oil supplements reduced (F < 0·05) milk protein content (33·6, 32·5, 30·6 and 32·4 (s.e.d. 0·43) g/kg) but, apart from a small increase for LIN, protein yield (glday) was unaffected (545, 586, 510 and 574, s.e.d. 20·2).

The concentrations (g/100 g) of short-chain fatty acids (< C14) and C16 : 0 in milk f at were lower (F < 0·05) for LIN than for the other treatments. All supplements increased the concentrations ofC18:1 (F < 0·05), the value for LIN being greater (F < 0·05) than for the other treatments (21·0, 27·2, 25·3 and 23·7, s.e.d. 0·74). The FISH and TOA treatments increased (F < 0·05) the concentrations of long chain (< C2O) (n-3) poly-unsaturated fatty acids (PUFA), (0·19, 0·17, 0·49 and 0·27, s.e.d. 0·026) but less than proportionately 0·03 of dietary intake of these acids was transferred to milk, probably because they were found to be mostly in the phospholipid and cholesterol ester fractions of plasma. The FISH and TOA treatments increased (F < 0·05) the percentages of total trans fatty acids in milk fat (1·13, 2·19, 10·26 and 3·62, s.e.d. 0·728) whilst a significant (F < 0·05) increase in conjugated linoleic acid (CLA) was observed only for FISH (0·16, 0·28, 1·55, and 0·52, s.e.d. 0·154). Concentrations of CLA and total trans acids in milk were highly correlated (r = 0·91, no. =36, F < 0·001) whilst trans acids in milk were inversely correlated with milk fat content (r = -0·63, no. = 36, F < 0·001) supporting the theory that milk fat depression may be caused by increased supply of trans fatty acids to the mammary gland. The health implications of these changes in milk fat composition are discussed.

The response of Awassi ewes to graded amounts of supplementary concentrate diet was examined for the first 12 weeks of lactation. The growth rate of lambs and their health status were also investigated. Seventy-five ewes were divided into three equal groups and given a basal roughage diet of shredded wheat straw at a rate of 750 g dry matter (DM) per ewe per day supplemented with a concentrate diet at three amounts, 950 g (low), 1150 g (medium) and 1350 g (high) of DM per ewe per day starting at the beginning of lactation. Ewes were adapted to the diet by feeding daily at a rate of 200 g per ewe during the last 6 weeks of pregnancy. The concentrate was estimated to contain 11⋅8 MJ of metabolizable energy and 182 g of crude protein per kg DM. Ewes and their offspring were housed in a partly enclosed yard. Lambs remained with their dams continuously except for the days of milk yield measurements, when they were separated from the dam for 11 or 12 h. The ewes were examined for subclinical mastitis and the incidence of scouring in lambs was recorded.

Ewes given the high level of concentrate produced more (P < 0⋅05) milk but differences between medium and low groups were significant only up to week 4 of lactation. Total milk yields during the 9 weeks test period were 58⋅5, 70⋅4 and 93⋅3 kg for the low, medium and high groups, respectively. Ewes suckling twins produced more (P < 0⋅05) milk than ewes suckling singles. The rate of weight loss was lower (P < 0⋅01) for ewes given the high feeding regime; these regained their immediate post-lambing body weight by week 10. Sex of lambs and litter size had no effect on body weight loss but ewes nursing twins tended to loose more weight during the 12 weeks suckling period. Lamb growth rates were similar (P > 0⋅05) across treatments. The daily intake of concentrate by the ewes did not affect the incidence of scouring in lambs or mastitis in ewes.

On both economical and biological grounds it is recommended to offer concentrate during the first 9 weeks of lactation at levels >950 g per ewe per day in order to produce an appreciable yield of milk and restore a positive energy balance early in the ewe lactation period.

Thermal environment and water supply are factors which are supposed to influence the performance and well being of farm-raised mink but conclusive literature data are still very limited. The present series of experiments was conducted in order to quantify effects of thermal environment on water intake and excretion, urinary solute excretion and estimate possible stress reactions. Water intake and excretion, urinary osmolality and urinary excretion of sodium (Na), potassium (K), cortisol and catecholamines were studied in a balanced Latin-square design experiment with six adult male mink, kept at three different ambient temperatures (Ta); (5°C, 20 °C and close to 35 °C) and given three different water supplies (E: extra water in the food; N: normal ad libitum drinking water supply; R: restricted, free access to drinking water twice daily). The experiment comprised nine periods, each of 3 days. Food apparent digestibility, intake of metabolizable energy (ME), metabolic and evaporative water, oxidation of nutrients and ME requirement for maintenance (MEm) were calculated. Water intake was strongly affected by Ta, with dietary water being the major source at 5°C and 20 °C, its importance being profoundly exceeded by drinking water at 35 °C. Water excretion in urine was highest at the lowest Ta and lowest at the highest Ta. Restriction of access to drinking water resulted in lower total water intake, and excretion, mainly by decreased urinary volume, reflected by increased urinary osmolality and increased solute concentration. ME intake decreased as Ta increased but urinary and total water output per kJ ME was not significantly affected by Ta or water supply. Excretion of Na and К per kJ ME mainly monitored urinary water excretion, being highest under conditions when urine production was highest. Metabolic water made up 0·14 to 0·17 of the total water intake and evaporative loss increased from about 50 to 125 g/kg live weight (M)0·75 as Ta increased. MEm was lowest (534 kJ/kg M0·75) at 20 °C, and highest (647 kJ/kg M0·75) at 35 °C. Cortisol excretion generally tended to increase when water supply was restricted, the increase being significant at 35 °C. This, in combination with outer signs of distress in the animals, emphasized that this high temperature in combination with limited access to drinking water exposed the animals to a very stressful situation but rectal temperature remained normal, indicating intact temperature regulation mechanisms.

Two in vitro experiments were conducted in order to determine if microbial fermentation of Eragrostis curvula hay is depressed by high levels of added tallow. Two levels of tallow, to reach 0.06 (T6) and 0.12 (T12) of the ether extract (organic matter basis) in food were compared with a control (T0, 25 g ether extract per kg). The first experiment studied the pattern of gas production. From 24 h onwards, gas volume for T0 was higher (P < 0.05) than for T6 and T12. However, lag time was shorter with tallow, probably because of utilization of the released glycerol. Fermentation of a similar amount of fat included in T6 and T12 as the only substrate (fat-6 and fat-12) depressed gas production compared with the blank, irrespective of fat level. In a second experiment, characteristics of microbial fermentation were studied, including volatile fatty acid (VFA) production, bacterial adhesion to fibrous particles (measured according to purine bases concentration) and polysaccharidase and glycosidase activities, at 6, 12, 24 and 48 h incubation. Total VFA was higher (P < 0.05) in T0 compared with T6 but not with T12. Acetate: propionate ratio diminished with tallow in the food. Higher total xylosidase (P > 0⋅05) and glycosidase (P < 0⋅001) activities were observed for T0 than for T6 and T12 and similar responses were observed regarding specific activities. Bacterial adhesion was not different between T0 and T6 but it was smaller in T12. The inhibition of microbial fermentation by tallow addition is more related to specific polysaccharidase and glycosidase activities, rather than to a depressed bacterial adhesion.

The effects of diets formulated to have two rates of organic matter (OM) release and to be either synchronous or asynchronous with respect to their hourly release of OM and nitrogen (N) in the rumen on N retention, microbial N production, growth and metabolism of ram lambs offered food at a restricted level was studied in two experiments. Four diets were formulated to differ in their rate and extent of OM and N release in the rumen based on the sum of in situ degradability data of the ingredients. All diets were formulated to have a similar metabolizable energy (10·4 MJ/kg dry matter (DM)), crude protein (140 g/kg DM) and daily ratio of N : OM released (34 g N per kg OM) and were either synchronous or asynchronous with respect to their hourly N : OM release. The four diets were slow energy, synchronous (SS), slow energy asynchronous (SA), fast energy, synchronous (FS) and fast energy asynchronous (FA). In both experiments the diets were offered at a rate of 1·75 maintenance energy requirements as two equal meals at 09:00 and 17:00 h. In experiment 1 there was no significant effect of diet on OM apparent digestibility or N retention. Lambs given diet FS had the highest daily production of allantoin (7·82 mmol per day; P < 0·05) and microbial N (7·80 g/day; P < 0Ό5). Hourly plasma urea and ß-hydroxy butyrate (3-OHB) concentrations exhibited a cyclical trend between meals with maximum concentrations occurring within 3 h of feeding and were higher in lambs given diet FA.

In experiment 2 the four diets were offered to 32 growing ram lambs. Animals given synchronous diets (SS and FS) had a significantly higher live-weight gain than those given asynchronous diets (SA and FA; (132 g/day v. 107 g/day respectively; P < 0·001). Food conversion efficiency (FCE; kg gain per kg DM intake) was improved proportionately by 0·23 in animals offered synchronous diets compared with asynchronous diets (P < 0·001). There was little effect of diet on carcass composition except kidney fat, which was greater in lambs offered the synchronous diets (P < 0·01). Plasma 3-OHB concentrations were higher throughout the growth period in lambs given diet FA whilst plasma urea concentrations were greater in lambs given the diet SS. In conclusion, greater attention to the formulation of diets to be synchronous for their hourly release of N : OM in the rumen can improve the growth rate and FCE of lambs. This effect may be due to an improvement in energy rather than N metabolism.

In order to examine the effects of diets, with two hay to concentrate ratios and two forms of concentrates on the rumen fermentation of dry sheep and milk production of lactating ewes, three trials were conducted.

In the first trial, four wether sheep, each fitted with a rumen cannula, were used in a 4 × 4 Latin-square design, by allocating them to one of four diets with different hay to concentrate ratio and concentrate type. The diets consisted of 0·5 kg hay and 0·75 kg either starchy (HRSC) or fibrous (HRFC) concentrates, or 0·25 kg hay and 1·0 kg either starchy (LRSC) or fibrous (LRFC) concentrates. The diets were designed to provide similar intakes of energy and crude protein. Volatile fatty acids (VFA) and ammonia concentrations, pH values and number of protozoa were determined in wether rumen fluid.

Total VFA concentration was not significantly affected by diet but acetate and n-butyrate proportions were higher (P < 0·002) on the higher forage diets and propionate higher (P < 0·002) on the lower forage diets. pH values and number of protozoa in sheep rumen fluid were unaffected by treatment, while ammonia concentration was lower (P < 0·05) on the HRFC diet.

In the second trial, 60 lactating dairy ewes were allocated to one of four diets for weeks 11 to 15 of lactation (period 1). Ewes were given food daily: 0·87 kg hay and 1·3 kg either HRFC or HRSC concentrates, or 0·4 kg hay and 1·6 kg either LRFC or LRSC concentrates. During weeks 16 to 20 of lactation (period 2), the ewes were given the same amount and type of concentrates but hay was supplied ad libitum and this period formed the third trial.

Milk yield and milk composition were affected significantly by hay to concentrate ratio with the lower hay to concentrate ratio resulting in a significant increase in milk yield, milk protein efficiency, protein content and protein and lactose yields. Milk fat content and yield were reduced. Hay intake was proportionately greater (P < 0·002) by 0·15 to 0·20 with starchy than with fibrous concentrate diets in period 2. Problems such as acidosis or ‘off-food’ periods in ewes given the low hay to concentrate ratio diets were not observed, irrespective of concentrate type.

Quantitative water intake and excretion, urinary osmolality and urinary excretion of Na, K and cortisol were studied in an experiment with nine adult male mink. The experiment comprised four periods each of 3 days, and ambient temperature (Ta) was increased from 5°C to 20 °C (periods 1 to 2) and, after an interval of 1 day, continued at 20°C and then decreased to 5°C (periods 3 to 4). Three different water supplies were given, namely E: extra water in the food, N: normal ad libitum water supply or R: restricted, free access to drinking water twice daily. Intake of metabolizable energy (ME) was calculated, and the water intake and excretion data were related to ME intake. The effect of Ta on quantitative water intake and excretion was evident, with the greatest response recorded when Ta was decreased. Intake of drinking water was highest at 20 °C, as well as the total water balance. The water supply had some, but not a profound, influence on water intake and excretion, with tendencies for reduced drinking water intake and water excretion in urine for R mink. Intake of ME decreased during period 3 at 20 °C and then increased when Ta was decreased to 5°C, which was reflected by an increased 24-h excretion of Na and K as well as an increased osmolality of the urine. Therefore, it was concluded that water intake and excretion were affected by combined effects of Ta and ME intake. Generally, it was shown that the mink responded rapidly to changes in Ta, and within 24 h significant effects of the change could be recorded for several of the traits studied.

Previous research has shown that supplementing the diet of growing lambs with urea enhances their ability to withstand gastrointestinal infection with the nematode Haemonchus contortus. This study compared lambs given two different amounts (χ 1 and χ 1·5) of the same urea-supplemented diet. One dietary allowance was sufficient to allow uninfected lambs to gain approximately 400 g/week without adverse clinical signs. In contrast half of the H. contortus infected lambs on this dietary allowance had to be humanely killed before the end of the experiment due to severe anaemia and anorexia. All infected lambs on this dietary allowance showed decreased mean red cell volumes and decreased plasma albumin concentrations indicating inadequate replacement of red blood cells and plasma proteins lost during the infection. The remaining lambs were offered proportionately 0·5 more of the same dietary allowance. Among lambs on this dietary allowance, there were very few differences between uninfected and infected sheep in clinical signs and growth rate. Therefore, dietary allowances that are adequate for uninfected lambs are not necessarily sufficient for infected lambs. As nearly all grazing lambs are infected with nematodes, dietary recommendations should take parasitic infection and its nutritional demands into account.

The effect of the duration of grazing (experiment 1) and starvation time and placement in the rumen of inert bulk material before grazing (experiment 2), on the rumen content ferment ability, was investigated by means of measuring cumulative gas production. In experiment 1, a comparison was made of four durations of grazing (1, 1·75, 2·50 and 3·25 h) after overnight starvation. Rumen samples taken from the cows after 1 h of grazing had higher values of total accumulated gas with less (P < 0·05) time required to reach the maximum fermentation rate than cows grazed for 3·25 h. Following grazing, a 7·75·h starvation period was imposed on the four treatments. The extent of fermentation was significantly lower (P < 0·01) after starvation than immediately after grazing (49·7 v. 60·8% of incubated dry matter (DM), respectively). Experiment 2 consisted of a factorial combination of two durations of starvation before grazing (16·5 (LS) and 2·5 (SS) h) with the presence or absence in the rumen of 12·5 kg of a synthetic indigestible material. Before grazing the total accumulated gas production was less (P < 0·05) for the LS than for the SS cows. After the grazing session, the total gas of rumen samples from the LS cows was significantly higher (P < 0·05) than for the SS cows.

This was in agreement with the observed higher DM intake during grazing and DM rumen pools after grazing in LS cows. For both starvation periods, the presence of inert rumen bulk led to a higher total gas, a shorter half-time and less DM left unfermented. The measurement of fermentation kinetics by cumulative gas production was suitable to detect changes in rumen content fermentation patterns due to the clearance of material from the rumen (effect of starvation) or DM intake during the grazing sessions.

Relationships between photoperiod and cycles of voluntary food intake (VFI) and maintenance energy requirements (MER) were determined in Soay rams, subjected to a 6-month photoperiodic regime. Food was offered ad libitum (no. = 5) or at a predicted maintenance level (no. = 5). All rams demonstrated 6-month cycles of VFI, growth and reproductive status. Metabolizable energy intake (MEI) was greatest in rams given food ad libitum (666 (s.e. 21.7) kJ/kg metabolic live weight (M0·75) and food-restricted (528 (s.e. 12.2) kJ/kg M0·75) rams during sexual quiescence. Conversely, MEI was minimal (ad libitum, 289 (s.e. 8.4) kJ/kg M0·75; restricted, 428 (s.e. 8.1) kJ/kg M0·75) during the rut. Distinct cycles of heat production (HP) accompanied changes in MEL Changes in HP were similar (P > 0·05) for both groups (ad libitum, 520 (s.e. 22.1) to 394 (s.e. 9.2) kJ/kg M0·75; restricted 503 (s.e. 14.0) to 407 (s.e. 17.5) kJ/kg M0·75) and therefore energy retention varied more (P < 0·015) when rams were given food ad libitum (ad libitum, 131 (s.e. 43-1) to -106 (s.e. 38.2) kJ/kg M0·75; restricted, 78·0 (s.e. 27.1) to -53.0 (s.e. 38.2) kJ/ kg M0·75). Apparent digestibility of dietary energy varied inversely with MEI (P < 0·01). MERs ranged from 524 (s.e. 35.0) kJ/kg M0·75 to 401 (s.e. 27.3) kJ/kg M0·75, a proportional fluctuation of ±0·13. Changes in metabolic rate preceded those in appetite, suggesting a causal relationship.