School of Agriculture, Food and Ecosystem Sciences - Theses
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ItemResponses of young sheep to supplements when fed low quality roughages( 1999)The morphological components of which cereal straw is composed vary in composition and nutritive value. In a survey of relevant literature, stem materials (ST) are usually found to be consumed by ruminant animals at a slower rate than leaf material (LF) from the same crop residues when these are fed alone as separated fractions. This is attributed to the higher content of cell wall constituents (CWCs) and often lower content of N of ST. Because ST and LF can vary in proportions in the roughage fed as a basal feed, the response of animals to supplements might also be expected to be variable particularly when the basal feed is offered in excess that permits selection. In particular the response to supplemental N sources varying in ruminai degradability may vary. The objective of this thesis program was to investigate the interactions between the basal roughage and supplement measured as effects on digestion and LW responses of young sheep. The overall hypothesis was that across diets made up of different proportions of LF and ST fractions of cereal straw, the response to N supplements is dependent on CWCs concentration. The program was completed through a series of experiments conducted at the Mt Derrimut Field Satation of the University of Melbourne. In all experiments the animals were fed on a basal feed of LF or ST fractions of barley straw, with supplements including (a) Bar+USS, barley grain (Bar) fortified with urea solution prepared at a ratio of 5:1 (urea plus Na,SO4). (b) USS, urea solution alone added to the basal roughage and (c) FM, fishmeal. With each basal feed one group of lambs did not receive any supplement and served as a control group (CONT). Experiment 1 (Chapter 3) was conducted to evaluate chemical and nutritional characteristics of straw fractions of Parwon cultivar barley. Straw was separated into 4 fractions - stem (ST), leaf blade (LB), leaf sheath (LS) and broken fractions plus weeds (OT). The separated fractions were analysed chemically ( van Soest, 1974) and in vitro digestibility (Tilley and Terry 1964 ) determined. ST was the largest fraction and contained a significantly higher concentration of neutral detergent fibre (NDF; p<0.01) than LB, LS and OT (83.1, 78.6, 76.8,and 71.5 g/100g respectively). ST contained less hemicellulose (HC) than LB but more than LS and OT (37.5, 39.6, 36.3, and 35.7 respectively). N content was lower in ST than in LB, LS and OT fractions (0.4, 0.9, 0.6, and 0.7 respectively). Digestibility in vitro was significantly lower (P<0.001) for ST than for other fractions (38.5, 72.7, 60.1, and 63.0 respectively) while energy required for grinding (Chenost 1966) was much higher (P<0.001) for ST than for other fractions (121, 54.6, 64.2, 56.6 respectivly). In Experiment 2 (Chapter 4) ST and LF fractions of the same Parwon barley straw were fed as the basal feed to lambs and DM intake of ST was 15% lower than for LF (403 vs 473 g/d). When LF feed was supplemented with USS and FM, DM intake was greater by 28% and 25% respectively, while supplementation with Bar+USS resulted in 10% lower LF intake. In contrast, with animals fed ST as the basal roughage, only FM led to an increase in DM intake of only 10%. Supplementation with Bar+US and USS and FM improved overall digestibility, estimated metabolisable energy intake and N intake. Low N intakes on the basal roughages supported low ruminai ammonia-N concentrations (mg/1) immediately before feeding (ST, 20.4 ; LF 35.8), but these were improved where supplements had been fed with each of ST Bar+USS, 263.7; USS, 186.7; and FM, 151) and LF (Bar+USS, 219.5; USS, 62.5; and FM, 150). Six hours after feeding, ammonia-N concentrations (mg/l)were higher for ST (99) still low for LF(35) when fed alone, reduced below the prefeeding levels by supplements of Bar+USS (ST,167; LF 173) but raised by USS (ST, 201; LF 148) and FM (ST, 114; LF, 192). The concentrations of total volatile fatty acids (VFA) in rumen fluid (mMoUl) were not significantly different for ST and LF before feeding except where FM was the supplement, or six hours after feeding except where Bar+USS or USS were fed with LF (before feeding: ST, 51; Bar+USS, 55.7; USS,46.5; FM, 56 ; LF, 42.6; Bar+USS, 53; USS, 55.5; FM, 63.6; 6h after feeding ST, 55.5; Bar+USS, 70.2; USS, 62.1; FM, 50.4 ; LF, 55.7; Bar+USS, 69.5; USS, 60.9; FM, 60.9). Lambs on ST and LF alone lost weight (ST, -105; LF -98 g/d ). Rate of liveweight loss was less when Bar+USS (ST, -32.3; LF -2.4g/d) and USS (ST, -79.8; LF -31.2 g/d) supplements were fed, while FM promoted LW gain (ST, 37.5; LF, 72.4g/d). N retention data was consistent with these LW gains, except where Bar+USS was the supplement, in which case the animals were in positive N balance though losing weight. Wool growth was significantly improved (P<0.001) only by FM on both ST (+47%) and LF (+57%) basal roughages. In Experiments 3 and 4 (Chapter . 5 and 6) the objective was to investigate the factors responsible for low feed intake and poor performance of lambs fed ST compred to those on LF. The DMI (g/d) of lambs fed ST and LF were similar to those achieved in experiment 2; and were significantly greater for LF (P<0.001). Likewise supplements of Bar+USS, USS and FM had similar effects to those reported for experiment 2_ Changes in DMI, MEI ruminai environment before feeding or 6 and:12 hours after feeding were consistent with those recorded during experiment 2. However concentration of total VFA was significantly elevated at 12 hours after feeding. Differences in ruminal environment were evident in terms of VFA concentrations and the distribution of rumen digesta particulate material in different size fractions; both variables were affected both by the basal diet and the supplement. For LF, the proportions of particles >2mm and of very fine particles (0.125 mm) were greater and for particles between 0.5 and 1 mm less those for ST in all cases. Further, the proportion of particles >2mm was less where FM was fed than for any other feeding regime. The mean retention times of rumen fluid, measured from CoEDTA dilution rate, and calculated for rumen particulate material was longer (24%, P<0.01) for ST than for LF but there was no significant effect of supplement on this (Experiment 4, Chapter 6). The mean percentage of very fine particles in the faeces of lambs fed on LF was higher than for lambs fed ST alone or with supplements. Rate of ruminai degradation of OM of ST and LF as measured by nylon bag technique ( Experiment 3, Chapter 5) was similar at 12 and 24 hours but greater for LF than for ST at 48 and 96 hours of incubation. Bar (cracked whole grain) was degraded more rapidly and extensiveley than FM; in LF fed sheep this difference was more marked. Rate of degradation of acid detergent fibre (ADF) was influenced by the kind of supplement and was greatest in lambs given FM , and least in lambs given ST with no supplement. Only the FM supplement resulted in LW gains, though rates of LW loss were least and LW gains with FM were greatest with LF as the basal roughage. The responses are interpreted as flowing from the greater proportion of ADF and lignin in the CWCs content and the greater digestibility of ADF in the LF fraction. The ST feed fraction with higher concentrations of cell wall constituents (CWCs) as NDF was eaten at a slower rate (Experiment 5, Chapter 7) and digesta particulate material and, in these experiments, the fluid phase are retained longer in the rumen. LF showed not only an advantage over ST in these respects but also in terms of a number of important digestion parameters supported a greater response to supplements, particularly N supplements of low degradability. Thus FM is these experiments interacted with the roughage component of the diet. It provided more consistent ruminai ammonia concentrations supporting a better environment for microbial activity and growth. Microbial protein together with undegraded dietary protein together provide a balance of nutrients that allows LW gains on otherwise submaintenance basal feeds. The greater enhancement of performance with LF compared to ST and the particle size measurements suggest that greater fragmentability of LF may be a major contributor . In terms of technical improvement of livestock feeding systems, providing the animal with opportunity for selection of more leaf and less stem may improve the likelihood of responses to supplements but this was not demonstrated in Experiment 5. FM was used as the experimental supplement to provide slowly degraded and undegraded dietary protein of high biological value to the animal. FM is expensive and other crop byproducts and local feed materials with properties of slow degradability of protein and good amino acid balance need to be identified. An alternative strategy would be to provide a maximum opportunity for the selection of most digestible parts. If refusals are then collected, quality could be further improved with alkali treatment and necessary supplementation. This would provide a strategy for the use of morphological fractions which could be an economical approach for the efficient utilization of roughages.
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ItemVariability in the intake of supplements by grazing sheep( 1979)Although the practice of feeding supplements to grazing animals is widespread through the world, its efficiency still deserves further study. Factors associated with the supplements themselves, the animals being fed, the environment, and the grazing diet being supplemented together constitute a set of variables which affects not only acceptance and intake, but also the nutritional and economic efficiencies of supplementary feeding. This study is concerned with the feeding of supplements to grazing sheep under temperate climatic conditions. Oat grain, hay and molasses-urea blocks (Barastoc, KMM Pty. Ltd., Melbourne) were used initially, but subsequent experiments were confined to the utilization of molasses-urea blocks. Only recently have researchers emphasized the importance of variability in supplement intake between individuals within a herd or flock and estimates of intake, with large ranges between animals, have now appeared in the literature. Langlands and Bowles (1976) considered that such wide variabilities in intake, limit the effectiveness of all forms of supplementation. However, little is known about the factors affecting variability in a group situation and few attempts have been made to identify the possible factors inducing such wide ranges of intakes in grazing animals. Arnold and Bush (1968) identified three types. of sheep: "shy-feeders", periodic non-feeders, and over indulgers". In some situations social dominance has been observed to affect responses to supplements (Franklin and Sutton, 1952; Wagnon, 1965; Squires and Daws, 1975) , and Arnold and taller (1974) correlated the intake of supplements with body weights of sheep. Chapter 1 of this thesis reviews the direct and indirect effects on animal performance of the main factors related to the feeding of supplements. Chapter 2 presents estimations of intake of three supplements, oats, hay, molasses-urea block, made with sheep in small paddocks. Results of behavioural observations and body measurements of the sheep are presented and discussed separately in Chapter 3. Chapter 4 provides an assessment of the acceptability of molasses-urea blocks by seven different flocks of grazing sheep on five private properties. The effects of confining sheep in yards on their acceptance of the blocks are also reported. Few studies have sought to determine whether management stratagems may improve the rate of adaptation of sheep to molasses-urea blocks and induce more uniform intakes between animals. Pilot trials described in Chapter 5 were conducted to identify possible management procedures that may be suitable for these purposes. Four such procedures were sufficiently encouraging to justify testing in a replicated experiment, which is described in Chapter 6. These treatments were imposed on sheep confined in yards and fed hay at a submaintenance levels. The investigations described in Chapter 7 utilised a different approach and are concerned with the behavioural aspects of learning, a topic which has been intensively studied with laboratory animals but only rarely with farm animals. The effects of offering molasses-urea blocks to lambs in the pre-weaning period are assessed in terms of their acceptance of blocks in later life. Inevitably only a few experimental possibilities and combinations have been assessed in the work reported in this thesis. Major attention was directed towards molasses-urea blocks because they induced wider variability in the responses by sheep than did hay or grain supplements . The blocks used were those manufactured by KMM Pty. Ltd., Melbourne, had a hard texture for protection against wet weather conditions and required animals to lick them rather than chew them. Variations in block formulation were not studied in the work described in this thesis and it remains possible that other types of block may have produced different results.
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ItemEffects of resistance to prehension and structure of pastures on grazing behaviour and intake of dairy cows( 2000)Pasture intake by dairy cows is affected by plant and sward structural characteristics of the pasture. In the meantime, grazing animals are constrained to gather their food bite by bite removing only a portion of the herbage present at the location which they bite. The extent to which grazing animals overcome the constraints imposed by the plant and structural characteristics of the pasture is the major determinant of herbage intake. The experiments which form the basis of this thesis concentrated on determining the role of sward resistance to prehension, measured in situ, as an integrating sward characteristic that determines foraging decisions of cows and the extent to which they defoliate pasture swards. Under rotational grazing systems, a cow is offered an area of pasture that is often smaller than the area from which the cow harvests its bites (defoliated area, DA). The cow therefore faces changing sward conditions during the process of grazing down into the sward and removing bites at successive lower defoliation planes. The defoliation pattern in grazing down the sward profile and the consequent herbage intake and diet composition, are examined in this thesis. A novel apparatus was designed to measure the BFF in situ at different sward profile heights. In the initial experiment, changes in BFF down the sward profile of six pasture species were examined in order to evaluate the mechanical efficiency of defoliating bites at different depths, in terms of bite weight:BFF ratio. The hypothesis tested was that cows remove 30 - 40% of the sward height at each bite due to a mechanical advantage in terms of BW:BFF. The BFF varied more between defoliation strata than between pasture species. The bite weight and BFF increased with the depth of defoliation. The mechanical efficiency of defoliating bites estimated as the BW:BFF ratio declined slightly with bite depth until a depth of about 30 - 40% of the sward height is reached, when the ratio declined more rapidly. Based on these results and those of Wade (1991), four theoretical defoliation planes (DPI, DP2, DP3 & DP4) were set each at 35% of the pre-grazing sward heights to estimate the total area defoliated by grazing cows under different sward conditions. DP2 is the plane of removal of a second bite after a first bite has removed DPI. Three spring grazing experiments were conducted to explore relationships between pasture allowance and/or sward structure and intake dynamics. In the first experiment, cows were offered a herbage allowance (HA) of 50 kg DM/cow/day either as one block with continuous access for 24 hours, or as six equal break rations opened at intervals during a 24 hour period. In the two subsequent experiments, different sward types were created in order to alter the BFF. In the second experiment swards were created with two different surface heights (USH) and in a 2 x 2 factorial, cows were offered two HA (35 and 70 kgDM/cow/day). In the third experiment, swards with three different tiller densities were created and cows were offered a similar HA of 8 kg DM/cow/3 hours. The defoliation pattern, BFF at 30, 50 and 70% of USH, DM intake, grazing behaviour and the energetics of grazing were measured. The major conclusions derived from these experiments are as follows. The average depth of defoliation (DD) increased with sward height and fell between DP2 and DP4. However, the proportion of area defoliated at each defoliation plane declined down the profile, at rates that varied with HA and tiller density but was unaffected by sward height. At a HA of 70 kg, cows barely reached DP4. The area defoliated at DP4 increased with decreasing herbage allowance and decreasing tiller density. The initial bulk density and post-grazed bulk density declined with USH, but the grazed-stratum bulk density was not significantly affected by USH. Therefore, it was concluded that the volume of canopy defoliated was the major determinant of intake. With increasing HA, the average bite weight (BW) increased, prehension bite rate declined but the overall intake rate increased. The time cost of a bite increased with BW. However, the energy expenditure on prehending a bite did not show a consistent relationship with BW. The BFF increased with sward height and tiller density. However, BFF in the leafy layer of 70% of the sward height was not affected by initial sward height or tiller density. The increase in BFF with initial sward height and tiller density was greater in the lower stemmy layer of 30% sward height. The average bite area (BA) and BW increased with HA. Intake was positively correlated with HA (R = 0.49), HM (R = 0.65) and tiller density (R = 0.51). Multiple regression analysis with herbage intake as the dependent variable indicated that, in addition to HM and HA (R2 = 0.887) , inclusion of the difference in BFF between that at 30% USH and that at 70% USH (BFFdif) as a sward characteristic provided an equation with a substantially better fit (R2 = 0.956). DMI = -3.47 + 1.80 HM + 0.225 HA R2 = 0.887 DMI = -2.73 I + 2.76 HM + 0.732 HA - 0.0416 BFFdif R2 = 0.956 It is concluded that the BFFdif has a significant value in integrating the changes in sward characteristics down the profile and is useful in improving the intake model.
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ItemNutritional modification of muscle long-chain omega-3 fatty acids in lambs : effects on growth, and composition and quality of meat( 1999)Three experiments were conducted to investigate the effects of dietary supplements rich in omega-3 fatty acid on muscle omega-3 fatty acid deposition. The consequential effects on growth performance of lambs, colour and lipid oxidative stability of muscle over refrigerated display, and the sensory properties of cooked meat were also examined. A mixture of lucerne chaff : oaten chaff was used as basal diet, offered in different proportions were fed to lambs ad libitum (Expt. 1) or at 90% ad libitum (Expts. 2 and 3). Such mixtures of roughage diet support slow growth and provide a feed quality pattern similar to late spring to late summer pasture. In Expt. 1, fish meal (7%), canola meal (8%) and soymeal (7%) as natural feed supplements were compared in lambs fed low quality roughage diet. In Expt. 2, fish meal (9%) and oilseed supplements either in unprotected form (rapeseed - 7%) or in protected form (ground canola seed - 6%) were examined in lambs on medium quality roughage diet. Lipids and the proteins in the ground canola seed were treated (RUMENTEK) with aldehyde to protect them from the rumen microbial activity. Fish meal (9%), fish oil (1.5%), fish oil (1.5%) with sunflower meal protein (9%),' and sunflower meal protein alone (10.5%) (a commercial product of a protein supplement from RUMENTEK) were compared in lambs fed medium quality roughage diet in Expt. 3. Long-chain omega-3 fatty acids (eicosapentaenoic acid + docosahexaenoic acid) in muscle longissimus thoracis was increased modestly and markedly with fish meal and fish oil alone or with sunflower meal protein diet, respectively. These long-chain fatty acids were deposited in the muscle structural phospholipid rather than in storage triglycerides. All the diets mentioned above also significantly reduced omega-6:omega-3 fatty acid ratio in meat which is another beneficial effect, as the dietary recommendation in many countries has been to reduce the ratio of omega-6:omega-3 in human diet. Soymeal diet increased modestly both the omega-3 and omega-6 fatty acid content of muscle longissimus thoracis resulting in no differences in the omega-6:omega-3 ratio of the meat. A supplement of protected canola seed significantly increased the precursors of omega-6 (linoleic) and omega-3 (linolenic) but not the long-chain analogues such as arachidonic acid (omega-6) and eicosapentaenoic, docosahexaenoic acid (omega-3), respectively. The marked increase in linoleic acid content was in both triglyceride and phospholipid fractions of muscle longissimus thoracis but the modest increase in linolenic acid content was only in triglyceride fraction of meat. Supplements of canola meal used in Expt. 1, unprotected rapeseed used in Expt. 2 and protected sunflower meal protein used in Expt. 3 did not alter the fatty acid composition of muscle longissimus thoracis compared with lambs fed the control diet in that particular experiment. The increased level of long-chain omega-3 fatty acid and/or omega-6 fatty acid with the lipid supplements discussed above did not significantly affect the meat colour stability and lipid oxidative stability of fresh and vacuum packaged meat over the storage at refrigerated display. This suggests that the conditions under which the animals are grown (grazing vs grain fed or feedlot) and the species of animal are important in determining the oxidative stabilities of meat by altering the levels of muscle vitamin E concentrations at slaughter. The level of inclusion of lucerne chaff in the basal diet is an important factor in improving the redness of meat indicated by the a*-value; a higher level of lucerne chaff intake is more likely to be associated with increased intake of vitamin E. Thus colour and lipid oxidative stabilities of meat can be improved in red meat animals that are on poor quality diets by the inclusion of lucerne chaff in their diet. The sensory properties of cooked meat evaluated in the present study were not affected by the significant increase in muscle long-chain omega-3 fatty acid or omega-6 fatty acid content with fish oil and protected canola seed supplements, respectively. Addition of protected sunflower meal as a protein supplement together with fish oil significantly lowered the ratings of flavour and overall acceptability of meat compared with the control lambs. The results demonstrate that the common `lamby' and `muttony' flavour and aroma attributes were not hidden by any of the dietary treatments. These two characters associated with the species flavour and aroma were recognised by the panellists as a distinct attribute. Dry matter intake was not adversely affected by any of the lipid supplements used in the present study. Feed conversion efficiency was highest with fish meal diet on both low and medium quality roughage diets. At medium quality roughage-based diet, Feed conversion efficiency was modestly improved by protected canola seed diet but other supplements providing either natural (unprotected rapeseed) or protected protein (protected sunflower meal) did not support significant differences compared with basal diet. The significant increase in liveweight gain with fish meal diet reflected a significant increase in hot carcass weight compared with all other supplemented lambs either on low or on medium quality roughage diet. Protected lipid and protein offered by protected canola seed diet significantly and moderately increased liveweight gain and hot carcass weight from control diet but not different from unprotected rapeseed diet. The greatest muscle deposition was with the fish meal diet and is attributed mainly to the increased amount of protein and energy absorbed from the small intestine of those lambs. In addition to energy and protein absorption, the alteration of omega-3 polyunsaturated fatty acids in muscle membranes may have a further influence in lean meat production. In terms of carcass gain and intramuscular fat deposition of fishmeal and fish oil fed lambs, the results also lead to a hypothesis that modifying omega-3 polyunsaturated fatty acid of muscle membrane phospholipids may have an influence in improved muscle deposition in lambs by improving the insulin action at skeletal muscle site.
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ItemUtilization of protein and energy in growing lambs( 1970)Extensive pasture improvement throughout large areas of Australia in recent years has emphasized the need for more efficient methods of pasture utilization. This has been achieved to some extent by an increase in sheep stocking rates. However, the benefits from high stocking rates are far greater when used for the production of wool from dry sheep than when applied to breeding flocks producing prime lambs. Results from many experiments with wethers (Arnold & McManus, 1960; Drake & Elliott, 1963; Bishop, Birrell & Tew 1966; Morley & Ward, 1966) indicate that as stocking rate is increased total wool production per acre increases substantially. The relationship between total wool production and stocking rate is curvilinear (Bishop et al., 1966) and although the stocking rate which results in the maximum production per acre is higher than that which achieves the greatest economic return (Lloyd, 1966),a considerable increase in farm income can be obtained when the stocking rate of wethers is raised above conventional levels (Chisholm, 1965). The improvement in pasture utilization when wethers are grazed at high stocking rates is brought about by an increase in competition between individual sheep and the consumption of much of the poorer quality and damaged pasture which is otherwise rejected. Increasing competition eventually results in a reduction in feed intake with a concomitant lowering of production. However, the adverse effects of a reduced intake are less for wool growth than for most other forms of production. For example, the results of Bishop et al. (1966) indicate that wool growth of Corriedale - Polwarth cross wethers will continue at a rate of approximately 14 g/day inspite of the fact that feed intake was insufficient to produce a gain in live-weight. A reduction in feed intake has more serious repercussions in a breeding flock. A nutritional stress on the ewe can lead to (a) low live-weight at mating with its effect on ovulation (Edy, 1968) and lambing percentage (Coop, 1962) , (b) small live-weight gains during gestation with low birth weights of lambs from multiple births (Wallace, 1948) and high perinatal mortality (Alexander, 1962), (c) poor lactation and reduced lamb growth rates (Wallace, 1948). The presence of lambs accentuate the decline in food availability and as a result of the low intake of both milk and pasture the lambs grow poorly. Arnold and Bush (1962) found that meat production from a prime lamb flock did not increase when stocking rates were raised from 4 to 7 ewes per acre. In a more recent study (G.W. Arnold, A Axelsen & M.E. Bourke, 1965 - personal communication) it was found that as the ewes were increased from 5 to 7 per acre the number of lambs reared remained constant at 6.2 per acre, but the meat production declined. Many prime lamb producers in southern Australia have attempted to increase stocking rates, but, poor growth of lambs has generally resulted in a large percentage of them remaining unfattened at the end of the period of pasture growth. These lambs are often carried through to the following autumn and further reduce the feed available in the winter. The poor response in meat production associated with increased stocking rates was considered to be of sufficient importance for the Reserve Bank of Australia to provide finance to investigate "the problems of high stocking rates in the prime lamb industry". It seemed logical that the production of meat may be improved if the competition between the ewes and lambs could be reduced. The most common methods by which this is done is to either creep graze or early wean the lambs, thereby giving them access to more pasture of high quality. The results of several studies in England (Spedding & Large, 1959; Dickson, 1959) and Tasmania (Jefferies, Dreaver & Wilson, 1961) suggest that creep grazing systems do produce faster growth rates in lambs when stocking rates are high. However, limited evidence from the Australian mainland (Arnold & Bush, 1962; Fletcher & Geytenbeek, 1968) indicates that the creep feeding of pasture is not advantageous and that the creep feeding of lucerne produces only slight improvements in growth rates. Lambs weaned at 2 to 3 weeks of age can survive at pasture, but their growth is poor (Spedding, Large & Brown, 1961). Wardrop, Tribe & Coombe (1960) found that lambs weaned at 7 weeks of age could grow as well as unweaned controls, but that their response was sensitive to the quality and quantity of feed. However, the results of Cannon & Bath (1967) indicate that, in conditions typical for southern Australia, stocking rates must be raised above 9.6 lambs per acre before any advantage in meat production can be obtained by weaning lambs at 10 weeks of age. Therefore, it seemed that the early weaning of lambs at pasture would not greatly improve production from prime lamb when high stocking rates were used. Because the response to both early weaning and creep feeding was dependent upon the quality and quantity of the pasture, it was reasoned that these systems may be more successful if the lambs were given concentrate diets formulated to meet their nutrient requirements. However, a survey of the literature revealed that there was a dearth of information on the nutrient requirements of lambs and that many recommendations were contradictory. Because concentrate diets which would satisfy the nutrient requirements of lambs could not be formulated with confidence, the major portion of this thesis has been concerned with determining the protein requirements of young, meat producing lambs.
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ItemEstimation of the available amino acid contents of feeds for pigs with Tetrahymena pyriformis w( 1973)Experiments were conducted to evaluate the usefulness of the Tetrahymena assay for predicting the available amino acid content of feeds for pigs. In collaborative studies the Tetrahymena lysine values were also compared with values from the Silcock technique for a series of feeds and attempts were made to evaluate which technique was more applicable to pigs. The pig experiments were conducted with pigs fed individually once daily during the 20 to 45 kg growth phase. Pig response was assessed in terms of live-weight gain, feed conversion efficiency and carcass lean as estimated by joint dissections. 1) The 4-day incubation period for the assay of proteins by Tetrahymena as recommended by Stott and. Smith (1966) was found to be adequate for buttermilk powder but not for fish meal or meat and bone meal. By extending the incubation of the latter two meals to 7 days, complete hydrolysis was achieved. Experiments with pigs fed diets formulated with values from either the 4-day or the 7.-day incubation periods for fish meal and meat and bone meal indicated that values obtained with the Tetrahymena assay after complete hydrolysis of the meals were more applicable to pigs than were those estimated after 4-days. 2) For cereals a 10-day incubation period for estimates of lysine and tryptophan with Tetrahymena was found necessary for maximum hydrolysis, and there was good agreement between these values and the response in pigs. 3) There was close agreement between Tetrahymena and Silcock estimates for lysine in samples of soyabean meal that were autoclaved for varying times. In a pig experiment the additions of lysine, methionine and tryptophan to diets containing the autoclaved soyabean meal restored only 43% of the effects of the heat damage. 4) This raised the question as to whether the supplements of free amino acids had been efficiently utilised by the pigs. A pig experiment was conducted to examine the effect of feeding a ration containing free lysine either once daily or in six equal portions at three hourly intervals. The results indicated that only 43% of the free lysine was utilised with once daily feeding relative to the frequent feeding regime. Thus the inability of the amino acids added to the autoclaved soyabean meal to compensate for the effects of heat damage may have been due to inefficient utilisation of the added amino ' acids by the pigs and not to inapplicability of the estimates of heat damage. 5) The amount of protein used in the Tetrahymena assay was found to govern the subsequent hydrolysis of the protein. Attempts to promote more vigourous hydrolysis of small amounts of protein by increasing the amount of inoculum were unsuccessful. Vigourous hydrolysis of the protein was obtained by the addition of 0.25 mg L-lysine-HC1 to each assay; this stimulated the initial growth of Tetrahymena, then vigourous hydrolysis resulted. 6) The rate of release of lysine from protein concentrates by Tetrahymena varied. Buttermilk powder and skim milk powder required 2 days, peanut meal 3 days, soyabean meal 4 days, safflower meal 5 days, rapeseed meal 6 days and fishmeal and meat meal 7 to 8 days. Free lysine was utilised within 4 days. 7) The Tetrahymena and Silcock lysine values for different protein concentrates showed no consistent pattern. For soyabean meal the Tetrahymena lysine values were greater than the Silcock values, for peanut meal the estimates were similar, and for the other proteins the Tetrahymena values were lower than the Silcock values. This was particularly so for a meat meal and rapeseed meal where the Tetrahymena values were approximately half the Silcock estimates. 8) An attempt was made to supplement cereal-based diets with protein-bound lysine to achieve diets of similar lysine content; both the Tetrahymena and the Silcock values were used to compute the amount of supplementary protein needed. Diets formulated according to these two values were then fed to pigs in an attempt to decide which value was the better indicator of lysine availability to pigs. This experiment proved inconclusive as factors other than lysine appeared to have influenced the results. This aspect of the comparison of the two methods of assay needs to be examined using feeding trials on a larger scale to eliminate these complicating factors. 9) In Appendix 1, the modifications made to the Tetrahymena assay to allow complete hydrolysis of proteins are Outlined.
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