The first objective of this experiment was to investigate the effect of using different bacterial isolates on the estimation of microbial protein production in semi-continuous fermenters (RUSITEC) given four diets, and to test whether a ‘mixed’ bacterial pellet was representative of the whole bacterial population in the fermenters. A second objective was to compare two different microbial markers (nitrogen-fifteen (15N) and purine bases (PB)). Diets consisted of neutral-detergent fibre from grass hay (10 g/day) and sugar-beet pulp (2 g/day) and 280 mg/day of one of four N forms (isolated soya-bean protein, soya-bean peptides, amino acids blended to profile soya-bean protein and NH4Cl). Two 14-day incubation runs were carried out and in each run each of the four different diets were given to two vessels. On days 12 and 13, total digesta (effluent plus nylon bags residues) was collected for analyses of non-ammonia N, 15N enrichment and PB concentration, and for isolation of total mixed bacterial pellets (TB). On the last day of each incubation run, the system was stopped for isolation of liquid- (LAB) and solid-associated (SAB) bacteria. Microbial N flow was estimated from the 15N enrichment and PB concentration in both total digesta and in the three different bacterial pellets (TB, LAB, and SAB). For all diets, LAB presented a greater (P < 005) 15N enrichment and PB: N ratio than SAB, with TB having an intermediate value. For both markers, the use of LAB produced the lowest (P < 005) estimates of microbial N flow and the use of SAB produced the greatest (P < 005) estimates. The use of TB produced intermediate values with all diets, suggesting that TB consisted of SAB and LAB. For all bacterial pellets, PB produced greater (P 005) values of microbial N flow than 15N. However, there was a positive relationship (r = 0·883; P 0001; no. = 15) between the values of microbial N flow determined with the two markers when TB were used as reference.

An experiment was undertaken to compare the productivity of crossbred ewes, produced by crossing Texel sires with Rouge de l’Ouest (Rouge) dams and Rouge sires with Texel dams, relative to purebred Texel and Rouge ewes. The purebred and crossbred ewes were crossed with Rouge and Texel sires. The proportion of productive ewes was similar in the purebred and crossbred ewes with an average figure of 0·92. Irrespective of crossing sire, Rouge ewes produced 0·48 more lambs per ewe lambed than Texel ewes (P < 0·001). The two crossbred ewe types (Texel ✕ Rouge and Rouge ✕ Texel) each produced similar numbers of lambs (on average 1·92 lambs per ewe lambed). Individual heterosis values for ewe fertility and prolificacy were small and not significant (–1·67 for the proportion of productive ewes and –3·14 for the number of lambs born per ewe lambed). Maternal heterosis values were also not significant but were of larger magnitude (6·26 for ewe fertility and 3·12 for prolificacy). Lamb mortality (number of lambs born dead per ewe lambed) at birth was similar for purebred Rouge (0·44) and Texel (0·30) ewes and was significantly reduced by crossbred matings and mating the crossbred ewes (individual heterosis –30·68, P < 0·10; maternal heterosis –80·23, P < 0·001). Individual and maternal heterosis values for lamb growth rate from birth to six weeks were 8 (P < 0·05) and 4 (P > 0·05) respectively. Lamb growth rate from birth to weaning was significantly lower in lambs from Texel ewes compared with those from the other genotypes (P < 0·05). Individual and maternal heterosis values for live-weight gain from birth to weaning were 5 (P < 0·10) and 5 (P < 0·01). The results of the current study demonstrate the superior performance of purebred Rouge ewes compared with purebred Texel ewes in terms of prolificacy and lamb growth rate from birth to weaning. However, both breeds had high lamb mortality at birth. Crossbreeding led to the production of hybrid ewes which had relatively high prolificacy with low levels of dystocia and lamb mortality.

The seasonal effects of heat load and photoperiod on yield and composition of milk from primiparous cows in the course of lactation were studied using test day records from 8968 primiparous cows on 76 farms in Georgia, collected from 1990 through 1997. The effect of prepartum photoperiod on milk production in the subsequent lactation of these cows was also evaluated. These estimated seasonal effects were compared with those estimated for 4728 primiparous cows on 13 farms, and for 1538 multiparous cows on three farms during consecutive lactations in Israel from 1994 through 1996. During lactation, the day length had a positive effect on milk yield and negative effects on fat and protein concentrations in the milk, but the daily change in day length had positive effects on milk yield and fat concentration, and a smaller positive effect on protein concentration. The day length during the prepartum period had negative effects on milk yield and fat and protein concentrations. The heat load during lactation had negative effects on milk yield and fat and protein concentrations. Most of the effects were highly (P < 0·001) significant. There was a very good match between the results obtained for primiparous cows in Georgia and Israel, for the combined effects of heat load and photoperiod during lactation on milk yield and protein and fat concentrations. The match between primiparous and multiparous cows in Israel was better for milk yield and protein concentration than for fat concentration. The estimated effects of pre-partum photoperiod were higher for multiparous cows in Israel than for primiparous cows in either country.

Ruminal bacterial counts and in vivo digestibility were determined on four Mediterranean buffalo bulls and four Friesian bulls, all fistulated at the rumen, and given at maintenance level (50 g/kg M0·75 per day of dry matter) four different diets with the same crude protein content (N ✕ 6·25 = 140 g/kg dry matter) and with forage: concentrate ratios as follows: diet D12·5 = 0·875: 0·125; diet D25·0 = 0·75: 0·25; diet D37·5 = 0·625: 0·375; diet D50·0 = 0·5: 0·5. All the animals received the diets during four consecutive periods in a Latin-square design. Buffaloes had higher total microbial counts (10·78 v. 10·08 log10 cells per g dry rumen content, P < 0·01) as compared with cattle; differences in total ruminal bacterial counts among the diets were only observed within the buffalo species (diet D12·5 v. diets D25·0, D37·5, D50·0: 10·04 v. 10·92, 10·98, 11·17 log10 cells per g dry rumen content, P 0·01) and when comparing the two species for each diet, significantly higher values for bacterial counts in buffaloes were found for diets D25·0: 10·92 v. 10·28 (P 0·05), D37·5: 10·98 v. 10·08 (P 0·01) and D50·0: 11·17 v. 9·76 (P 0·01) log10 cells per g dry rumen content. Cattle showed significantly higher digestibility values for: organic matter (0·696 v. 0·676, P 0·05), neutral-detergent fibre (NDF; 0·548 v. 0·511, P 0·05) and cellulose (0·621 v. 0 · 509, P 0·01), while the crude protein digestibility (CPD) values were similar (0·667 and 0·671). Comparing the two species for each diet, cattle showed significantly higher digestibility values for organic matter in diet D50·0 only (0·714 v. 0·688, P 0·01), for NDF in diet D12·5 only (0·578 v. 0·531, P 0·05) and for cellulose in all diets (0·660 v. 0·546, 0·630 v. 0·525, 0·605 v. 0·505, 0·588 v. 0·460, P 0·01); in contrast buffaloes showed higher values of the CPD for diet D12·5 (0·662 v. 0·632, P 0·05).

Twenty-five male Barbarine lambs aged approximately 150 days were divided into five groups. All the animals received 400 g/day of oat hay and Acacia cyanophylla Lindl. foliage ad libitum. Two groups also received 300 g/ day of a mixture (70: 30) of processed barley and wheat bran, with or without 20 g polyethylene glycol 4000 (PEG), groups CPEG and C respectively. The three other groups had free access to feedblocks based on olive cake, and containing urea, urea and PEG, or PEG, groups BU, BUPEG and BPEG respectively. Lambs were slaughtered at age 230 days and meat quality was determined in the longissimus thoracis et lumborum muscle. Lean colour was significantly affected by dietary condensed tannins. Lightness (L*) was higher in those animals that did not receive PEG (P < 0·001) indicating that condensed tannins can cause lighter meat colour. This difference was not due to the ultimate pH, which was not affected by the inclusion of PEG in the diet. Meat from groups that received supplementation of concentrate had lower values of resistance to the Warner-Bratzler shear device compared with those that received feedblocks. This result was confirmed by a taste panel, that found samples from groups C and CPEG more tender than samples from groups BU, BUPEG and BPEG. Inclusion of PEG in the diet increased intensity of flavour (P < 0·05) but had no effect on overall acceptability. Meat from animals that had received the concentrate had higher overall acceptability (P < 0·05) than meat from animals that received the feedblocks. No differences were found in meat chemical composition.

A total of 317 dairy and beef cattle, offered grass silage-based diets, have been subjected to energy metabolism measurements in calorimetric chambers in 11 feeding experiments at this Institute. In addition the silages (no. = 33) were also given individually to sheep as a sole food at maintenance feeding level for measurement of energy intake and outputs (faeces and urine). The digestible (DE) and metabolizable (ME) energy concentrations of mixed diets for sheep at maintenance were estimated using these measured silage data, predicted silage methane energy output and tabulated energy values of concentrates. The objective of the present study was to use treatment mean data (no. = 59), derived from the cattle (production level) (MEprod or DEprod) and the sheep (maintenance level) (MEmaint or DEmaint), to evaluate the combined effects of animal species and level of feeding on dietary ME or DE concentration. The mean-square prediction error technique and the sensitivity test both indicated that there was little bias derived from the deviation of the slope (line bias) when relating MEprod (DEprod) with cattle to MEmaint (DEmaint) with sheep. Relating feeding level to the decline in ME or DE concentration (from maintenance to production level) revealed that the constant had no significant effect on the relationship, suggesting that there was little difference in dietary ME or DE concentration between sheep and cattle when given food at maintenance. ME d and DE d were significantly related to MEmaint and DEmaint (P < 0001) respectively. These two relationships were however influenced (P < 0001) by level of feeding above maintenance (FL-1). There was little effect of silage DM proportion in the total diets (S/T) on the depression of ME concentration from maintenance to production levels, while this effect on the depression of DE concentration was significant (P < 0001). Therefore, the following two equations are recommended to calculate MEprod and DEprod concentrations respectively for cattle using data obtained with sheep at maintenance. Alternatively, with each unit increase in feeding level above maintenance, dietary ME and DE concentrations respectively were reduced by proportionately 0016 and 0025 for grass silage-based diets, irrespective of the effect of forage proportion on the latter. MEprod = [1 068 - 0019 ✕ (FL-1)] ✕ MEmaint - 0·755 DE d = [0·891 + (-0027 + 0018 ✕ S/T) ✕ (FL-1)] ✕ DEmaint + 1·355

Two 4-week experiments were conducted to examine the effect of type of supplement, offered through automatic feeders at pasture, on supplement intake and grazing behaviour by multiparous spring-calving Holstein-Friesian cows grazing continuously stocked grass pastures. Four supplement formulations were used: a dairy concentrate containing 180 g crude protein per kg fresh weight (treatment DC), a high digestible undegraded protein supplement (treatment HP), a high starch, low protein supplement (treatment HS) and a high fibre supplement (treatment HF). In experiment 1, groups of eight cows were provided with access to one of diets DC, HP or HS, with a maximum of 4 kg being available during each of two periods, between 16:00 and 03:30 h and between 03:30 and 14:30 h. During experiment 2, groups of eight cows were provided access to diet DC, HP, HS or HF, up to a maximum of 8 kg between 16:00 and 14:30 h the following day. Detailed measurements of grazing, ruminating and supplement eating behaviour were made using jaw movement recorders and the transponder-controlled out-of-parlour feeder software. Treatment had no effect on intake rate per min or daily intake of supplement in either experiment, but did affect the temporal pattern of concentrate meals. Treatment did not affect grazing bite mass, bite rate or intake rate in either experiment. During experiment 1, compared with treatment DC, treatment HS reduced total eating time, total grazing jaw movements and daily herbage intake and increased ruminative mastications per bolus and ruminative mastications per kg grass OM intake. In experiment 2, compared with treatment DC, only treatment HS reduced total eating time, total grazing jaw movements and daily herbage intake. Treatments HS and HF both increased ruminative mastications per bolus. The results indicate that when supplements are available at pasture there is a conflict between the time required to consume supplements and herbage and that supplement type can affect both the temporal pattern of supplement intake and subsequent grazing activity.