The current study investigated the effects of pre-grazing herbage mass (PGHM, 1500 or 2500 kg dry matter (DM)/ha) and post-grazing sward height (PGSH, 4 or 6 cm) on herbage production and its nutritive value and DM intake, grazing behaviour and growth of Charolais steers (n = 96; 12 months of age; 396 ± 19.0 kg) during a 222-day grazing season, and the subsequent effect of an indoor finishing diet (grass silage alone or supplemented with concentrates) for 146 days, on performance and carcass traits. Steers were assigned to one of 12 grazing groups and group was assigned to a 2 (PGHM) × 2 (PGSH) factorial arrangement of treatments. At the end of the grazing season, live-weight was 16 kg heavier for PGHM-1500 than PGHM-2500 and 34 kg heavier for PGSH-6 than PGSH-4. After indoor finishing, there was no difference in carcass weight between PGHM treatments, but PGSH-6 had a 19 kg heavier carcass than PGSH-4. Herbage production was 881 and 517 kg DM/ha greater for PGHM-2500 than PGHM-1500 and for PGSH-4 than PGSH-6, respectively. Grazing stocking rate did not differ between PGHM treatments but PGSH-4 carried 1.35 more steers/ha than PGSH-6. Supplementing concentrates during the indoor period increased carcass weight (42 kg) and fat score (2.10 units). In conclusion, grazing to 6 rather than 4 cm, increased individual carcass weight but not carcass weight gain/ha. Compared to PGHM-2500, grazing PGHM-1500 increased steer live-weight gain at pasture, but did not affect carcass weight following indoor finishing.

The objective was to reduce the incidence of liver abscesses (LAs) in young bulls by reducing the starch content of the concentrate and increasing the straw intake by adding molasses without reducing performance. Eighty-five Danish Friesian bulls (146 ± 2.6 kg live weight (LW)) were allocated to four treatment groups in a 2 × 2 factorial design and were ad libitum fed either a high (H) (43%) or a low (L) (25%) starch concentrate, and either chopped barley straw (S) or a mixture (Sm) of chopped barley straw and sugar-beet molasses (75:25). The bulls were slaughtered at 440 (±4.2) kg LW (11.3 months of age) on average. The concentrate dry-matter intake (DMI) was 7.5% higher (P < 0.001), the roughage DMI was 12% higher (P < 0.01), whereas the total net energy intake was 7% lower (P < 0.001) for the L compared with the H concentrate. By adding molasses to the straw, roughage DMI increased from 0.50 to 0.96 kg/day (P < 0.001). Average daily gain (ADG) was not affected by treatment. Feed conversion efficiency (FCE) for dry matter (FCEDM) was decreased (P < 0.001), whereas FCE for net energy (FCENE) was increased with the L concentrate (P < 0.01), suggesting a lower utilisation of the cell wall fraction with the H starch concentrate. There were no major effects of treatment on carcass characteristics. The higher roughage intake with Sm prevented rumen wall damage, but did not reduce the number of animals with LAs. The L concentrate did not affect the rumen wall but reduced the level of LA (2 v. 9 animals, P < 0.02). There was a higher level of respiratory diseases in animals fed the H concentrate (P < 0.05). The experiment showed that it was possible to maintain performance and reduce LA by using a lower starch content of the concentrate.

The experiment was undertaken to quantify the α and γ-tocopherols accumulation in muscle and backfat from Iberian pigs given food free-range as affected by the time of free-range feeding or the weight gained during the fattening in free-range. Pigs were given their food in a free-range production system with pasture and acorns (Quercus rotundifolia) for different periods of time: 46 days (free-range 3), 83 days (free-range 2) and 111 days (free-range 1). A control was given food free-range for 0 days. In addition another experiment was developed to determinate the effect of the the weight gained on the tocopherols accumulation at a similar period of time (111 days) given food free-range: one group gained 68·7 kg of weight (free-range A) and the other 43·6 kg (free-range B). The concentration of γ-tocopherol significantly (P<0·0001) increased after 83 days of feeding in the longissimus dorsi (LD) and biceps femoris (BF) muscles, and after 111 days in the inner and outer backfat layers. The concentration of α-tocopherol was not statistically affected by the days of free-range feeding in any case. Iberian pigs that put on more weight had significantly (P< 0·0001) higher concentration of α and γ-tocopherols in the inner and outer backfat layers, and α-tocopherol in the BF muscle than those given food free-range B. However, no differences were detected in the proportion of α-tocopherol in the LD and γ-tocopherol in the LD and BF. The γ-tocopherol content of LD and BF muscles depending on the days of feeding were adjusted to linear and quadratic regressions (R2=0·8705 and 0·8697, respectively), while the outer and inner backfat layers were linear equations (R2=0·8480 and 0·8119, respectively). However, the γ-tocopherol concentration as affected by the weight gained in free-range showed in all tissues a linear and a quadratic trend that were adjusted to exponential responses. The α-tocopherol content was affected by the γ-tocopherol concentration in muscle and outer backfat layer. The tocopherol concentration (α and γ-tocopherols) in the backfat layers may discriminate better between the pigs of high quality that were given food free-range for a long period of time and those that stayed an intermediate period. However, to discriminate between the pigs on formulated food and those given food free-range, the quantification of the γ-tocopherol concentration in muscle could be a better indicator.

To evaluate the effect of litter size and littermate weight on low-birth-weight (< 1 kg) piglets that have been cross-fostered, piglets' pre-weaning performance in the following groups were compared. Group A (no. = 10), low-birth-weight piglets raised with equal number of heavy-birth-weight piglets in small (eight piglets) litters; group B (no. = 10), low-birth-weight piglets raised with equal number of heavy-birth-weight piglets in large (12 piglets) litters; group C (no. = 10), low-birth-weight piglets raised with equal number of average-birth-weight piglets in small (eight piglets) litters; D (no. = 10), low-birth-weight piglets raised with equal number of average-birth-weight piglets in large (12 piglets) litters; E (no. = 10), small (eight piglets) low-birth-weight litters; F (no. = 10), large (12 piglets) low-birth-weight litters.

Mortality of low-birth-weight piglets in large litters was greater (P < 0.001) with heavy littermates, but in small litters was no different. Weight gain of piglets until day 3 post partum was not significantly (P > 0.05) affected by littermate weight and litter size, or their interaction. Weight at 21 days post partum was significantly affected by littermate weight, litter size, and their interaction. Low-birth-weight piglets in small litters had significantly higher 21-day weights in large litters (P < 0.01, P < 0.05 and P < 0.05 with littermates of low, average and heavy birth weight respectively). In large but not small litters, low-birth-weight piglets missed more nursing episodes and spent more time in teat disputes than their heavier littermates whether in heavy-birth-weight (P < 0.01), or average-birth-weight (P < 0.05) litters.

Littermate weight may affect the performance of low-birth-weight piglets due to direct competition for access to a functional teat.

Five hundred and eighty-four Pannon White kits of 73 newborn litters were submitted to one of five treatments. Control litters (SS) were nursed once a day for 35 days post partum (traditional method of nursing). DD litters were raised by two does and the kits were nursed both in the morning and in the evening until day 35 post partum. DS litters were nursed twice a day for 23 days, and then once a day until weaning at 35 days. Part of the DS litters were nursed at 08:00 and 20:00 h (i.e. every 12 h, DS12), the rest were nursed at 08:00 and at 16:00 h (DS8). Kits of the fifth treatment (D0) were nursed twice a day until day 23, and then immediately weaned.

Rabbit kits that were nursed twice a day (DD, DS12, DS8, D0) consumed on average 1·89 more milk compared with SS individuals until day 23 (overall treatment effect P < 0·001). The 21-day body weight of these young was 1·7 times greater than that of the SS kits (overall P < 0·001). D0 rabbits were weaned early and their growth curve showed a slight break at this point. However, they compensated for this lag by the end of the fattening period. SS rabbits and DD ones were respectively the first and the last to start consuming solid food. The food consumption of DS rabbits was similar to that of DD until day 23 and from then until day 35 it was not significantly different from that of SS. After having been weaned on day 23, D0 kits consumed only very small quantities of pellets for 2 days. Afterwards their food intake increased abruptly. Rabbits that were nursed twice a day (DD, DS12, DS8 and D0) consumed more food as compared with the SS individuals throughout the total period of fattening (157 v. 137 g/day; P < 0·05). The weight at 10 weeks of age was 2·49 v. 2·88 kg (overall P < 0·001), respectively for SS and doublenursed (DD, DS, D0) rabbits. Nursing twice a day did not affect dressing proportion but the proportion of the carcass in the front part of the body decreased slightly (318 v. 323 g/kg; P < 0·05) while that in intermediate part increased (321 v. 307 g/kg; P < 0·05). Nevertheless, rabbits that were nursed twice a day had more (P < 0·05) perirenal + scapular fat and produced heavier livers. Total fat content of the empty body, however, was not significantly higher, with the one exception of the DD rabbits which had higher levels than any other group. The results of our experiment show clearly that the growth potential of rabbit kits is strongly limited by the milk availability during the first weeks post partum.

Estimates of genetic parameters for beef production traits were obtained for Piemontese cattle. Data were from 988 young bulls station-tested from 1989 till 1998. Bulls entered the station at 6 to 8 weeks of age and, after an adaptation period of 3 months, were tested for growth, live fleshiness and bone thinness. Length of test was 196 days. Growth traits considered were gain at farm, gain during the adaptation period, gain on test and total gain at the station. Six different fleshiness traits and bone thinness were scored on live animals at the end of the test using a linear system. Live evaluations of fleshiness were adjusted for the weight at scoring in order to provide an assessment of conformation independent of body size. Genetic parameters were estimated using animal models. Heritability of live-weight gain ranged from 0·20 in the adaptation period to 0·60 for total gain at the station. Genetic correlations between gains at station in different periods were high (from 0·63 to 0·97). Residual correlation between gain during the adaptation period and gain during test was negative, probably due to the occurrence of compensatory growth of the animals.

Live fleshiness traits and bone thinness were of moderate to high heritability (from 0·34 to 0·55) and highly correlated indicating that heavy muscled bulls also have thin bones. Accuracy of breeding values and therefore response to selection were improved by multiple trait analysis of the live fleshiness traits and bone thinness. Overall weight gain at the station had a moderate negative genetic correlation with all live fleshiness traits and bone thinness (from –0·11 to –0·39).

The purpose of this study was to estimate the heritabilities and the genetic correlations of osteochondrosis in different joints and to estimate genetic correlations between osteochondrosis, leg weakness and production traits. The humerus condyles, anconeal process, distal ulna growth line, femoral condyles, distal tibia and medial trochlear ridge of talus on both sides of the animals were examined radiologically for osteochondral lesions and scored from 1 to 5 with increasing severity. The boars were also scored for 13 different leg weakness traits on a scale from 1 (normal) to 5 (very severe changes). During a 3-year period, a total of 2042 Landrace boars from 256 sires and 1946 Yorkshire boars from 240 sires were examined at a mean weight of 93 kg. The data were analysed by animal models for each breed. The Landrace was found to be more severely affected than the Yorkshire regarding osteochondrosis in all localities expect the anconeal process. The genetic correlations between left and right side scores of the osteochondral trait were close to 1. This indicates that genetically the same trait is measured in the left and in the right side of the animal. The heritability of average osteochondrosis scores was low to moderate ranging from 0•08 to 0•39 (s.e. between 0•02 and 0•04). The genetic correlations between osteochondrosis in the different body localities were low, indicating that osteochondrosis is not a generalized disease. The Landrace was more severely affected than the Yorkshire regarding all leg weakness symptoms except buck-kneed forelegs, forelegs turned out and weak pasterns on forelegs. The heritability of leg weakness traits ranged from 0•01 to 0•35 (s.e. between 0•01 and 0•04). Genetic correlations between osteochondrosis and leg weakness showed a clear picture for the Yorkshire breed regarding the humeral condyles: positive correlations with buck-kneed forelegs, forelegs turned out, stiff in front and rear. In both breeds osteochondrosis in femoral condyles showed a high positive correlation with hind legs turned out and a lower positive correlation with stiff in front. The sum of osteochondrosis traits (sumost) was unfavourably genetically correlated with daily gain, whereas the sum of leg weakness traits (sumleg) was unfavourably correlated with lean meat percentage in both breeds. The correlation between the summary measures sumost and sumleg was 0•09 (s.e. 0•11) in the Landrace and –0•07 (s.e. 0•12) in the Yorkshire.

The purpose of this work was to investigate the relationship between individual animal performance and production per unit area of land of steers of different potential growth rate under different grazing stocking rates (SR). The analysis involved 160 steers divided equally between two breeds, over 2 years at four SRfor each breed and two replicates for each SR. Thus there werefive steers per replicate. The breeds were purebred Aberdeen Angus (Angus) and 4 Limousin (Limousin). After weaning steers were grazed for 251 days on a pasture dominated by Festuca arundinacea. Given that equal SR does not equate to equal treament for breeds characterized to be of different size and rate of growth at a given age, the analysis was undertaken on the basis of three categories of metabolic body size per ha (S). The variables analysed were individual live-weight gain (final minus initial weight, kg), relative individual live-weight gain (logefinal weight - loge initial weight) and production (kg/ha). A mixed model was used to examine effects of breed, S, year and the interactions between these variables. In general significant (P < 0·05) differences were found for all factors of classification and interactions. Independent linear regressions were calculated for each breed between absolute live-weight gain, relative live-weight gain, and production on S. It was concluded that there was a genotype × environment interaction, with the Angus breed tending to show a higher production per unit area than the Limousin, especially at high levels of S when scarcity of forage was apparent. Nevertheless Limousin steers had higher absolute individual performance than the Angus. The higher production of the smaller breed may be explained by a higher SR at a given S level and also by its higher relative individual live-weight gain in relation to that of the larger breed. The data were coded to use Mott's model to study the relationship between absolute performance (kg) and production (kg/ha). However this model ignores the existing interaction involving breeds.

The effects of day length, of the daily change in day length and of heat load, together with age effect, on live-weight gain of Holstein-Friesian bull calves, were studied using 8205 gain records of 1019 calves that were maintained in the experimental herd at Newe Ya'ar during a 5-year period (1991 to 1995). The age range of the calves was 150 to 450 days. Effects of day length (h) and of day length change (min/day) were assumed to be linear and effect of age was assumed to be quadratic. Three heat load indexes were calculated, accounting for day temperatures above 27°C, or night temperatures above 18°C, or both, and their effect was assumed to be linear also. Random effect of calf and fixed effect of the year were also accounted for by the regression analysis. The mean gain was 1·274 kg/day. The effect of day length was 0·027 (s.e. 0·003) kg/day per h, and effect of day length change was 0·042 (s.e. 0·003) kg/ay per min/day both effects being highly significant (P < 0·0001). The effects of heat load according to each of the three indexes were either not significant, or tended to be positive, which implies increased gain with increasing heat load. Effect of age was positive (P = 0·0005), and of age2 was negative (P < 0·0001). Based on the regression model that did not include heat load effect, the peak gain was obtained on 19 May, 33 days before the longest day and the trough was obtained on 18 November, with a difference of 0·206 kg/day (proportionately 0·15 of the peak gain) between peak and trough gains. It was calculated by the regression coefficients for the photoperiod effects, that a calf that enters the feedlot at the age of 150 days and a live weight of 180 kg on 1 January, will be 23 kg heavier at the age of 350 days than a calf that enters the feedlot at the same age and weight on 1 July. This difference is reduced to 10 kg at the age of 450 days.

Pigs with inbreeding coefficients, ranging from 0·125 to 0·375 were analysed for effect of inbreeding on daily carcass gain, body length and meat proportion in the carcass. The foundation animals were back crosses of a Landrace boar of his daughters which were Yorkshire Landrace hybrids. The statistical model included effect of sex and slaughter weight in addition to the effect of inbreeding. A statistically significant effect of inbreeding on daily carcass gain was found with a linear decline of 1·6 g for 0·1 increase in inbreeding coefficient. There was no effect of inbreeding on body length and meat proportion. Carcass weight had a highly significant effect on body length and daily carcass gain. Effect of sex was statistically significant for meat proportion only.

Seventy-two, 4-month-old, British Friesian steers were used to investigate the effects of feeding a supplement of fish meal on the voluntary intake and live-weight gain by young growing cattle given a well preserved ryegrass silage. The silage was offered either alone or mixed with 50,100 or 150 g fish meal per kg silage dry matter (DM) and the diets were offered either ad libitum or intakes were restricted to 16, 19 or 22 g dietary DM per kg live weight (LW). Intakes were recorded daily, LW weekly and in vivo apparent digestibility over one 7-day period during the 132-day trial.

For animals fed ad libitum, the absolute intake of dietary DM increased linearly with an increase in the level of fish-meal supplementation such that intake when the highest level of fish meal was given was significantly higher (P < 0·01) than when silage was given alone. However, DM intake per unit LW (approx. 24 g DM per kg LW) was not affected significantly (P > 0·05).

Inclusion of fish meal in the diet did not affect the apparent digestibility of dietary DM, organic matter, acid-detergent or neutral-detergent fibre (NDF) although there was a trend for slightly higher (P > 0·05) gross energy apparent digestibility when fish meal was given. Increasing the level of feeding reduced NDF digestibility. The coefficients measured at the 22 g and ad libitum levels of intake were lower (P < 0·01 and P < 0·05 respectively) than that measured at the 16 g DM per kg LW level.

Animals given silage alone to appetite achieved LW gains of 0·6 kg/day. LW gains increased linearly with increasing level of feeding (P < 0·001) and increasing level offish-meal supplementation (P < 0·001).

Since the productivity of farmed red deer is constrained by their inherent seasonal biology, the potential advantages of breeding out-of-season following melatonin administration were investigated. Calves born in February (F; no. = 8) were heavier at weaning in September of the same year than calves born with normal birth dates in June (}; no. = 8) (73·2 v. 441 (s.e.d. 3·59) kg; P < 0·001) and at the end of April of the next year (88·0 v. 67·6 (s.e.d. 6·44) kg; P < 0·02) although their suckled live-weight gain to 100 days of age was lower (304 v. 361 (s.e.d. 21·4) g/day; P < 0·05). After weaning, F calves had higher voluntary food intake than / calves (g dry matter per head per day) from September to November (1643 v. 2224 (s.e.d. 92·6); P < 0·002), November to February (1435 v. 926 (s.e.d. 67·9); P < 0·002), and February to April (1487 v. 2059 (s.e.d. 115·5); P < 0·02).

Unlike J calves, F calves showed puberty in their first autumn. F male calves (no. = 3) grew antlers which hardened in November, whereas J males (no. = 3) did not, and F males, aged 8 months, had significantly higher mean plasma concentrations of testosterone than J males, aged 4 months (1·35 v. 0·28 (s.e.d. 0·154) fj.g/1, P < 0·001). Oestrous cyclicity was observed in 3/5 group F females, aged 9 months, but in 0/5 group ] females, aged 5 months. Although the dams of F and ] calves had similar live weights at mating, birth and 100 days pos t partum, F dams were heavier (P < 0·05) at weaning. Following parturition, F dams had a mean voluntary food intake of 2700 (s.e. 110) g dry matter per head per day from February to April.