Thesis (MScAgric) -- University of Stellenbosch, 2000. / ENGLISH ABSTRACT: Lipids remain one of the most important nutrients required by broilers. The growing awareness that some Western societies have too high a dietary ratio of n-6/n-3 polyunsaturated fatty acids is of direct relevance to broiler nutrition and lipid metabolism. Meaningful quantities of n-3 polyunsaturates have been incorporated into major poultry tissues, so that the production of broiler meat with high n-3 polyunsaturates becomes advantageous for the broiler industry as they are perceived as having a 'healthier' lipid profile. Unfortunately, such broiler meat is rather susceptible to oxidative deterioration, and oxidation often determines shelf life of poultry meat products. The addition of a-tocopherol (vitamin E) to broiler diets is an effective means of improving the oxidative stability of broiler meat. Elevated a-tocopherol levels in broiler feeds increase tissue concentrations thereof resulting in improved stability of membranal structures which may be expected to increase the oxidative stability of broiler meat and meat products. Three investigations were done at Mariendahl Poultry Research Station in Stellenbosch. The broilers were kept in 1 x 0.4 x 0.5 m cages in a broiler rearing house. All the trials started with day-old chicks, except experiment 1 where 3-week old broilers were used. At the end of trials 2 and 3 the 6-week old broilers were slaughtered and the carcasses prepared for chemical analysis. Experiment 1: Metabolisabie energy of Canola acid oil and Famarol acid oil for broiler chickens. In trials with 21-day-old male broilers the true metabolisabie energy value, corrected for nitrogen retention (TMEn) was determined by the balance method for Canala acid oil (CAO) and Famarol acid oil (FAO). The trials were duplicated, each time using different samples of the two oils from the same source (experiment 1 and 2). Each of the two oils were blended in two ratios with a basal diet to form the test diets, viz. 100% Basal; 96% Basal: 4% Oil; 92% Basal: 8% Oil. In experiment 3, 50 % bran was added to the maize to form the basal diet. The balance trials lasted for 3 days after an adaptation period of 4 days. The TMEn values determined by regression for the broilers of CAO did not differ significantly (P>0.05) between experiments 1 and 2. However, the value for experiment 3 was significantly (P<0.05) higher than those for experiments 1 and 2. The TMEn values of FAO also did not differ significantly (P>0.05) between experiments 1 and 2, although the value for experiment 3 was significantly higher than that of experiment 1. The addition of 50 % bran to the basal diet in experiment 3 could have stimulated the digestive breakdown process and hence increase the secretion of digestive enzymes. This could lead to an increase in the utilisation of the test lipid and therefore an increase in the TMEn value. The TMEn values of CAO differed significantly (P<0.05) from those of FAO for all three the experiments (exp. 1:30.6 ± 0.399 MJ/kg for CAO vs. 25.9 ± 0.441 MJ/kg for FAO; expo 2: 31.0 ± 0.633 MJ/kg for CAO vs. 26.1 ± 0.668 MJ/kg for FAO: expo 3: 32.1 ± 0.867 MJ/kg for CAO vs. 27.1 MJ/kg for FAO).Experiment 2: of broilers. The dietary effects of various combinations of Canala acid oil (CAO, a high level of C18:3n-3 and MUFA) and Famarol Effects of various dietary n-6/n-3 fatty acid ratios on the perfonnance and body composition acid oil (FAO, a high level of 18:2n-6 and SFA) on tissue fatty acid composition were studied in broiler carcasses and abdominal fat pads. From day-old to six weeks, chicks were fed one of six diets containing 100% FAO, 80% FAO-20% CAO, 60% FAO-40% CAO, 40% FAO-60% CAO, 20% FAO-80% CAO, 100% CAO. There were no statistical differences (P>0.05) in average daily gain (1.71 ± 0.059 g) or feed conversion ratios (1.97 ± 0.051) among dietary groups. No statistical differences (P>0.05) were found in the chemical proximate composition of the carcasses for the moisture (66.20 ± 0.112 %), protein (17.63 ± 0.484 %), lipid (15.92 ± 1.507 %) and ash (0.95 ± 0.115 %) content among dietary groups. No statistical differences (P>0.05) were found in the chemical proximate composition of the abdominal fat pads for the moisture (28.77 ± 0.112 %), protein (3.03 ± 0.484 %), lipid (63.32 ± 9.789 %) and ash (0.45 ± 0.135 %) content among dietary groups. With the increase in dietary CAO levels, the percentages of C18:2n-6 and C20:4n-6 in the carcasses decreased respectively with 1.78 % from 20.88 % and 0.35 % from 1.05 %, whilst C18:3n-3 and longer chain n-3 fatty acids such as C20:5n-3 and C22:6n-3 increased respectively with 2.25 % from 1 %, 0.1 % from 0.1 % and 0.67 % from 0.2 %. The same tendency was seen in the abdominal fat pads where C18:2n-6 and C20:4n-6 decreased respectively with 1.55 % from 20.75 % and 0.98 % from 1.2 % with an increase in dietary CAO, whilst C18:3n-3, C20:5n-3 and C22:6n-3 increased respectively with 2.13 % from 1.15 %, 0.45 % from 0.03 % and 0.95 % from 0.05 %. The n-3/n-6 ratio in the carcasses and abdominal fat pads increased respectively with 0.16 % from 0.06 % and 0.19 % from 0.06 % with an increase in dietary CAO. These results clearly indicate that dietary CAO enriched with a-linolenic acid lower saturated fatty acids respectively in broiler carcasses and abdominal fat pads with 4.88 % from 31.6 % and 10.63% from 31.1 %, whilst increasing monounsaturated fatty acids with 3.87 % from 44.95 % and 7.25 % from 46.7 % respectively and polyunsaturated fatty acids with 1.02 % from 23.45 % and 2.38 % from 23.2 % respectively. Experiment 3: Effect of dietary vitamin E on the performance of broilers and oxidative stability, colour, microbiological stability, fatty acid composition and pH of broiler meat during refrigerated and frozen storage. Experiment 1 was carried out with 220 one-day-old broiler chicks to evaluate the effect of eleven concentrations of vitamin E (0, 20, 40, 60, 80, 100, 120, 140, 160, 180 and 200 mg a-tocopheryl acetate 1 kg diet) on their production performance and the oxidative stability of their frozen broiler carcasses. The diets with vitamin E levels 0 to 100 mg were fed from day-old to 42 days of age while the diets with vitamin E levels 120 to 200 mg were fed from 21 to 42 days of age. The oxidative stability, evaluated by thiobarbituric acid reactive substances (TBARS) values, was determined after 30, 90, 120 and 150 days of storage at -20°C. There were no statistical differences (P>0.05) in average daily gain (1.85 ± 0.111 g) or feed conversion ratios (2.29 ± 0.397) among dietary groups. TBARS values increased significantly (P<0.05) with increasing time of storage (basal diet: day 30 = 1.71 ± 0.51; day 150 = 4.89 ± 0.51), but decreased significantly (P<0.05) with increasing vitamin E levels (day 150: basal = 4.89 ± 0.51; 100 mg / kg = 1.09 ± 0.27). Experiment 2 was carried out with day-old broiler chicks to evaluate the effect of five concentrations of vitamin E (0, 40, 80, 120 and 160 mg atocopheryl acetate / diet) on their performance and the oxidative stability of their refrigerated carcasses. The experimental diets were fed from day-old to 42 days of age. The oxidative stability, evaluated by TBARS values, colour deterioration and microbiological stability were determined after 0, 4, 8, 10 and 12 days of storage at 4°C. Fatty acid analysis was done on the samples of days 0 and 12. There were no statistical differences (P>0.05) in average daily gain (1.88 ± 0.117 g) or feed conversion ratios (2.37 ± 0.467) among dietary groups. TBARS values increased significantly (P<0.05) with increasing time of storage, but decreased significantly (P<0.05) with increasing vitamin E levels. There were no statistical differences (P>0.05) in colour measurements for L* (44.97 ± 0.662), a* (5.23 ± 0.315) or b* (12.76 ± 0.321) values between treatments. Microbiological counts increased significantly (P<0.05) over time with vitamin E concentration showing no effect. There were no statistical differences (P>0.05) for any of the fatty acid groups measured (SFA: Day 0 = 26.1 ± 1.13%, Day 12 = 26.1 ± 1.17%; MUFA: Day 0 = 41.4 ± 1.46%, Day 12 = 40.2 ± 2.28%; PUFA: Day 0 = 32.4 ± 1.95%, Day 12 = 33.8 ± 2.52%) among dietary groups. Similarly, none of the fatty acids showed statistical significant (P>0.05) concentration changes over time. There were no statistical differences (P>0.05) in pH (6.01 ± 0.206) among dietary groups. / AFRIKAANSE OPSOMMING: Lipiede is steeds een van die mees belangrike voedingstowwe wat deur braakuikens benodig word. Die groeiende bewuswording dat sekere Westerse gemeenskappe 'n te hoë verhouding van n-6/n-3 poli-onversadigde vetsure in hul dieet het, is direk relevant vir braaikuikenvoeding en lipiedmetabolisme. Betekenisvolle hoeveelhede n-3 polionversadigde vetsure is geïnkorporeer in die belangrikste hoendersnitte, met die gevolg dat die produksie van braaikuikenvleis met hoë n-3 poli-onversadigde vetsure voordelig is vir die braaikuikenindustrie en geag word 'n meer "gesonde" beeld te hê. Ongelukkig is sodanige braaikuikenvleis redelik vatbaar vir oksidatiewe bederf, en oksidasie bepaal dikwels die rakleeftyd van hoendervleisprodukte. Die byvoeging van a-tokoferol (vitamine E) by braaikuikendiëte is 'n effektiewe manier om die oksidatiewe stabiliteit van braaikuikenvleis te verbeter. Verhoogde a-tokoferol vlakke in braakuikenvoere verhoog die weefselkonsentrasie wat verhoogde stabiliteit van die membraanstrukture en derhalwe moontlike verhoogde oksidatiewe stabiliteit van braakuikenvleis en -produkte tot gevolg het. Drie ondersoeke is onderneem by Mariendahl Pluimvee Navorsingstasie te Stellenbosch. Die braakuikens is aangehou in 1 x 0.4 x 0.5m hokke in braaikuikenhuise. In al die proewe is dagoud kuikens gebruik, behalwe eksperiment 1 waar drieweek oue kuikens gebruik is. Aan die einde van proewe 2 en 3 is die ses-week oue braaikuikens geslag en die karkasse voorberei vir analise. Eksperiment 1: braaikuikens. Die ware metaboliseerbare energie waarde van Canola voergraadolie (CAO) en Famarol voergraadolie (FAO), Metaboliseerbare energie van Canola voergraadolie en Famarol voergraadolie vir gekorregeer vir stikstof retensie (WMEn), is by wyse van proewe op 21 dae oue braaikuikenhaantjies bepaal deur van die balansrnetode gebruik te maak. Die proewe is tweemaal herhaal vir verhoogde akkuraatheid, met die gebruik van verskillende monsters van die twee olies vanaf dieselfde bron. Die olies is in twee verhoudings met 'n basale diëet gemeng om die proef dieet te vorm, nl. 100% Basaal; 96% Basaal: 4% Olie en 92% Basaal: 8% Olie. Die balans proewe het 3 dae geduur na afloop van 'n aanpassingsperiode van 4 dae. Die WMEn waardes van CAO, bepaal deur middel van regressie analise, het nie betekenisvol verskil (P>0.05) tussen eksperimente 1 en 2 nie. Die waarde van eksperiment 3 was betekenisvol hoër (P<0.05) as die van die eerste twee eksperimente. Die WMEn waardes van FAO het ook nie betekenisvol verskil (P>0.05) tussen eksperimente 1 en 2 nie, maar die waarde vir eksperiment 3 was betekenisvol hoër as dié van eksperiment 1. Die WMEn waardes van COA het betekenisvol verskil (P< 0.05) van dié van FAO vir al die eksperimente (exp. 1: 30.6 ± 0.399 MJ/kg vir CAO vs. 25.9 ± 0.441 MJ/kg vir FAO; expo 2: 31.0 ± 0.633 MJ/kg vir CAO vs. 26.1 ± 0.668 MJ/kg vir FAO: expo 3: 32.1 ± 0.867 MJ/kg vir CAO vs. 27.1 MJ/kg vir FAO). Eksperiment 2: Die invloed van verskeie rantsoen n-6/n3 vetsuurverhoudings op die produksie en liggaamsamestelling van braaikuikens. Die rantsoeneffek van verskeie kombinasies Canola voergraadolie (CAO, 'n hoë vlak van C18:3n-3 en monoonversadigde vetsure) en Famarol voergraadolie (FAO, 'n hoë vlak van 18:2n-6 en versadigde vetsure) op die weefselvetsuursamestelling is bestudeer in braaikuikenkarkasse en abdominale vetneerlegging. Die kuikens is van dagoud to op ses-weke ouderdom een van ses diëte gevoer met die volgende samestellings: 100% FAO, 80% FAO-20% CAO, 60% FAO - 40%CAO, 40% FAO - 60% CAO, 20% FAO - 80% CAO, 100% CAO. Daar was geen statistiese verskil tussen die rantsoengroepe (P>0.05) in die gemiddelde daaglikse toename (1.71 ± 0.059 g) of die voeromsetverhoudings (1.97 ± 0.051) nie. Geen statistiese verskil (P>0.05) is gevind in die chemiese samestelling van die karkasse vir vog (66.20 ± 0.112 %), proteïn (17.63 ± 0.484 %), lipied (15.92 ± 1.507 %) en as (0.95 ± 0.115 %) inhoud tussen die rantsoen groepe nie. Geen statistiese verskille (P>0.05) is gevind in die chemiese samestelling van die abdominale vetneerlegging vir vog (28.77 ± 0.112 %), proteien (3.03 ± 0.484 %), lipied (63.32 ± 9.789 %) en as (0.45 ± 0.135 %) inhoud onder die rantsoengroepe nie. Met die verhoging in die rantsoen CAO vlakke het die persentasie van C18:2n-6 en C20:4n-6 in die karkasse verminder met 1.78 % en 0.35 % respektiewelik, terwyl C18:3n-3 en langer ketting n-3 vetsure soos C20:5n-3 en C22:6n-3 respektiewelik met 2.25 %, 0.1 % en 0.67 % verhoog het. Dieselfde tendens is opgemerk in die abdominale vetneerlegging waar C18:2n-6 en C20:4n-6 afgeneem het met 1.55 % en 0.98 % respektiewelik met die verhoging van rantsoen CAO, terwyl C18:3n-3, C20:5n-3 en C22:6n-3 verhoog het met 2.13 %, 0.45 % en 0.95 % respektiewelik. Die n- 3/n-6 verhouding in die karkasse en abdominale vetneerlegging het verhoog met 0.16 % en 0.19 % respektiewelik met die verhoging van die rantsoen CAO. Die resultate toon onomwonde aan dat rantsoen CAO verryk met c-Iinoletensuur, verlaag versadigde vetsure in braaikuikenkarkasse en -adbdominale vetneerleggings met 4.88 % en 10.63% respektiewelik, terwyl die mono-onversadigde vetsure met 3.87 % en 7.25 % respektiewelik verhoog word en polionversadigde vetsure met 1.02 % en 2.38 % respektiewelik verhoog word. Eksperiment 3: Die invloed van vitamine E op die produksie van braaikuikens en die oksidatiewe stabiliteit, kleur, mikrobiologiese stabilitiet, vetsuursamestelling en pH van braaikuikenvleis gedurende verkoelde en bevrore berging. Eksperiment 1 is uitgevoer met 220 dagoud braaikuikens ten einde die effek van elf konsentrasies van vitamine E (0, 20, 40, 60, 80, 100, 120, 140, 160, 180 en 200 mg a-tokoferyl acetaat / kg voer) op hul produksieprestasie en die oksidatiewe stabiliteit van hul gevriesde braakuikenkarkasse te evalueer. Die diëte met vitamine E vlakke 0 tot 100 mg is vanaf dagoud tot 42-dae-ouderdom gevoer, terwyl die diëte met vitamine E vlakke van 120 tot 200mg gevoer is vanaf 21 tot 42- dae-ouderdom. Die oksidatiewe stabiliteit, soos geëvalueer deur tiobarbituriese suur reaktiewe stowwe (TBARS) waardes, is bepaal na 30, 90, 120 en 150 dae van berging teen -20°C. Daar was geen statistiese verskille (P>0.05) in die gemiddelde daaglikse toename (1.85 ± 0.111 g) of voeromsetverhoudings (2.29 ± 0.397) tussen die rantsoengroepe nie. TBARS waardes het betekenisvol toegeneem (P<0.05) met die verhoging in bergingsperiode, maar het betekenisvol afgeneem (P<0.05) met verhoogde vitamine E vlakke. Eksperiment 2 is uitgevoer met dagoud braaikuikens ten einde die effek van vyf konsentrasies van vitamine E (0, 40, 80, 120 and 160 mg a-tokoferyl acetaat / kg voer) op hul prestasie en die oksidatiewe stabiliteit van hul verkoelde karkasse te evalueer. Die eksperimentele diëte is gevoer vanaf dagoud tot 42- dae-ouderdom. Die oksidatiewe stabiliteit, geëvalueer deur middel van TBARS waardes, kleur afname en mikrobiologiese stabiliteit is bepaal na 0, 4, 8, 10 en 12 dae van berging teen 4°C. Vetsuuranalises is gedoen op die monsters van dae 0 en 12. Daar was geen statistiese verskille (P>0.05) in die gemiddelde daaglikse toename (1.88 ± 0.117 g) of voeromsetverhoudings (2.37 ± 0.467) tussen die rantsoengroepe nie. TBARS waardes het betekenisvol verhoog (P<0.05) met die verlengde bergingsperiode, maar het betekenisvol afgeneem (P<0.05) met verhoogde viatmine E vlakke. Daar was geen statistiese verskille (P>0.05) in kleur metings vir L* (44.97 ± 0.662), a* (5.23 ± 0.315) of b* (12.76 ± 0.321) waardes tussen behandelings nie. Mikrobiologiese tellings het betekenisvol verhoog (P<0.05) oor tyd met die vitamine E konsentrasie wat geen effek getoon het nie. Daar was geen statisties betekenisvolle verskille (P>0.05) vir enige van die vetsuurgroepe tussen die behandelings nie. Soortgelyks het geen van die vetsure statisties betekenisvolle (P>0.05) konsentrasieveranderings oor tyd aangetoon nie. Daar was geen statistiese verskil (P>0.05) in die pH (6.01 ± 0.206) tussen die rantsoengroepe nie.

With the narrow margin of profit in the broiler enterprise, how can producers increase profit potential? It is not an easy task to answer this question since the net financial return depends on many factors; some are related to the animal, some to the feed, some to the environment and others are outside the production system, like availability and cost of labour and capital. Many researchers have attempted to improve the efficiency of the system using alternative management strategies and to develop a unified theory that could simultaneously evaluate all the relevant factors and the interactions between them. Simulation models are seen as the most promising means of moving this subject forward. Geneticists are continually improving the potential growth rate of broilers, yet there has been little change in feed specifications for these birds over the past few decades. Only recently has it been possible to make use of simulation models to optimise the feeds and feeding programs of modern broiler strains at a commercial level, but little testing of these programs has been carried out. What is needed is a thorough investigation of these models, which at present are based on an individual, as opposed to a population response. Modelling plays an increasingly important part in animal science and research as a way of organizing and evaluating the large body of existing knowledge. With the use of an accurate description of the potential growth rates of broiler genotypes, it is possible to make more efficient use of growth models which are becoming more abundant in the industry and which, in turn, enable the nutritionist or producer to predict the performance of animals when subjected to a given feed or feeding programme. The predictions made by most of the growth models now available are based on individual animals, and the results obtained may be inadequate in optimising the nutrient requirements of a broiler population because of the variation that exists in these populations. Variation in performance traits in broilers may be the result of variation in the genotype, in the environmental conditions within the house, and in the composition of the feed offered to the birds, and these sources of variation cannot all be accommodated in a model that simulates the food intake and growth of just one bird. But if variation is to be incorporated into growth models, it is necessary to ascertain the effects of variation in the various genetic parameters on the mean response of the population. A sensitivity analysis is useful in accomplishing this objective. Similarly, it is important to know what the optimum size of a simulated population should be, that takes account both of the accuracy of the simulation and the time taken to complete the exercise. This is especially important when optimisation routines are followed, as such calculations are time consuming. As a means of addressing these issues, simulation exercises were conducted using EFG Broiler Growth Model version 6 and EFG Broiler Optimiser Model version 1 (EFG Software, 2006) to determine: (a) whether it is worth generating a population when optimising feeds and feeding programs for broilers, rather than using the average individual, (b) the size of the population required to obtain an accurate estimate of the population response when optimising the feeding program for different objective functions, (c) the effect of changing the value of genetic parameters such as mature protein weight, rate of maturing, feathering rate and the maximum lipid:protein ratio in the gain on the optimum amino acid contents and nutrient densities of broiler feeds, and (d) the effect of variation in nutrient composition of different batches of feed, which have the same nutrient profile but different qualities of the main protein source, on broiler performance. A review of sources of variation in the nutrient content of poultry feed was conducted, and simulation exercises were carried out to determine to what extent broiler performance is affected by the segregation or breakage of pellets into small pieces at the time of delivery and along the feed conveyor within the broiler house, by the change in nutrient quality that might occur along the conveyor, and by the microclimates that develop in a longitudinally ventilated broiler house. The tendency in broiler marketing in most parts of the world is to sell broilers cut up, as portions or deboned after evisceration, rather than selling whole birds. Estimation of the growth rates of carcass parts is therefore of considerable importance if simulation models are to be useful in optimising the feeds and feeding programmes of broilers under different conditions. Allometric equations are used in the EFG broiler growth model to predict the weights of these carcass parts from the weight of body protein at the time. These equations are based on data collected many years ago, and it would be useful to determine whether they are still relevant in the face of announcements by the major broiler breeding companies that tremendous strides have been made in improving breast meat yield, for example, by judicious selection. For the purpose of this investigation it was important to determine to what extent the weights of the physical parts varied at the same body protein weight, thereby enabling a more accurate estimation of the variation that could be expected in these weights when developing a population response model. Towards this end, experiments were conducted to determine the effect of dietary protein content on the performance of Cobb and Ross broilers, including mortality and uniformity, and on the allometric relationships between the physical and chemical components of the body and body protein. The overall objective of these exercises was to address issues relating to the use of simulation models in predicting food intake and growth of broilers, in optimising the amino acid contents and nutrient densities of feeds for broilers, and in representing a population of broilers when the performance of only one bird is simulated at a time. / Thesis (Ph.D.)-University of KwaZulu-Natal, Pietermaritzburg, 2008.

With the worldwide increase in consumption of poultry meat in recent years, the production of hatchable eggs from broiler breeding stock has become a critically important component of the poultry industry. Surprisingly, a perusal of the literature pertaining to broiler breeder nutrition leads to the conclusion that research nutritionists have neglected these birds. It has been assumed in many cases that the research on laying hens is applicable to broiler breeders. However, fundamental differences are apparent between the two strains that should be investigated more comprehensively if the potential of broiler breeder hens is to be achieved. Commercial laying hens have been selected predominantly for increased egg production whereas broilers have been selected for early rapid growth rate. By selecting for improved growth rate, both food consumption and mature weight of these birds has increased (Reddy, 1996), but because of the negative genetic correlation between body weight and egg production (Robinson et al, 1993) reproductive performance has not been improved. Broiler breeder hens differ from commercial laying hens, by their non-normal frequency distribution of egg outputs, their considerable lipid reserves, and by the fact that many do not lay in closed cycle. The practice of restricting feed intake during both the rearing and laying periods has become a standard management procedure in commercial broiler breeder operations and this differs from the manner in which commercial hens are fed. This raises important issues regarding the requirements of these birds for energy, amino acids and other essential nutrients, as the birds do not have the opportunity of meeting their nutrient requirements by adjusting food intake upwards when one or more of these nutrients is deficient in the feed. It is the duty of the nutritionist to provide the correct daily allowance of each nutrient in order to achieve maximum egg output by the flock, but given the variation between hens within a flock, such decisions need to be made on both biological and economic grounds. Improved strains are continually being produced by breeder companies, which exhibit better growth, feed efficiency and productivity. The way in which broiler breeder hens were fed in the past might not be the most effective way to feed the latest strains. Getting the right amount of feed with the right nutrient levels at the right time is the most important part of feeding broiler breeders, and to succeed their daily nutrient requirements need to be known. Information concerning the nutritional requirements of broiler breeder hens is limited in comparison to other types of domesticated poultry. However, enough information is available concerning energy and amino acid nutrition of this type of poultry to enable one to develop models useful for constructing accurate feeding programmes. The most appropriate way of estimating the nutrient requirement of broiler breeder hens during the laying period, or of optimising a feeding strategy, is by the use of simulation models. Emmans and Fisher (1986) suggested that a better approach to the problem of describing requirements and of expressing them quantitatively can be achieved by considering: firstly, the bird’s characteristics, secondly by defining resource scales carefully and thirdly by considering the quantities of each resource needed per unit of function. This approach has a greater chance of success than attempting to measure requirements by direct experimentation. Energy and amino acids are required for growth of tissues, egg production, maintaining normal body temperature, vital life functions and activity. For development of feeding programmes, we are most concerned with the three primary components, maintenance, growth and egg output. There are a number of factors that impact on the total nutrient requirement of the breeder. The maintenance component is affected by body size, environmental temperature, level of activity (housed in floor pens vs. cages) and possibly breed. Regarding the growth component, in the case of broiler breeders during lay the composition of growth needs to be addressed: whether this is only lipid gain or also includes protein gain. Lastly, the egg component is influenced by egg mass and hen age. In order to calculate energy and amino acid requirements, one must have knowledge of the requirements per unit of body protein weight, growth rate and egg mass. By continually monitoring the environmental conditions in the broiler breeder house, as well as body weight, egg weight and egg number, it is possible to estimate the state of the hens at any time and hence the optimum nutrient concentrations that should be fed the next day of the laying period by using the Breeder Model presented in this thesis. Optimising the feeding of broiler breeders during the laying period is made difficult because of the many interacting factors influencing their performance All the hens are not the same, they are not housed in the same environments, and the costs of feeding and the revenue derived from the sale of the product differs from one locality to another. The solution to this problem lies in the use of simulation models to describe the causal relationship between inputs and the predicted responses. This thesis explored new concepts and components for a simulation model to predict the nutrient requirement and performance of broiler breeders after sexual maturity. / Thesis (Ph.D.)-University of KwaZulu-Natal, Pietermaritzburg, 2007.

The objective of the study was to evaluate the effect of an exogenous multi-blend enzyme ( -glucanase and xylanase) on the performance of the broiler chickens and laying hens fed diets based on wheat and barley. Experiments were conducted on a flock of broilers and two flocks of laying hens. In both cases feed and water were provided ad libitum. The enzyme effect of enzyme addition on the broiler performance involved 2080 day-old male and female chicks in 48 pens, allocated one of four dietary treatments (0, 50, 100 or 200g/ton enzyme supplementation), to 35 days of age. On day 35, ten birds from each treatment were sacrificed for the analysis of the digestive organs weight (gizzards and livers). The trial was divided into two phases: a starter (1 to 21 d) and grower (22 to 35 d). Feed consumption was measured weekly and birds were also weighed weekly. The investigation of enzyme effect in laying hen diets involved 896 birds for each specific period. Each replicate consisted of four cages (four birds per cage) with a common feeder; 16 hens/pen of 56 pens. Eggs were weighed three times a week, feed consumption weekly and birds every weeks. The addition of a multi-blend enzyme significantly improve body weight, body weight gain, food intake, and feed conversion ratio for both sexes (P<0.05) in broiler chickens. There was a significant improvement in egg production in laying hens (P<0.05). Egg weight and egg mass were not significantly improved. Wheat and barley have cell wall components (arabinoxylans and -glucans respectively) which have a negative effect on the nutritive value of these feeds and therefore performance in poultry fed diets based on these ingredients. Addition of an exogenous multi-blend enzyme( -glucanase and xylanase) could help reduce these effects and improve performance and digestibility values in poultry. The null hypothesis was there will be no difference between supplemented and un-supplemented diets based on wheat and barley in performance of poultry. The results of this study suggest that the inclusion of 50 g/ton enzyme helps improve poultry performance, especially in young birds. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2010.

There are negative influences of selection for broiler growth on the reproductive ability of broiler breeder parents. This is mostly due to problems related to excessive body weight, such as an inability to achieve successful cloacal contact during natural mating. There is also an age-related decline in fertility of broiler breeders. In attempts to prolong the fertile period of the breeders, various forms of management techniques have been employed. These include tools such as feed restriction, photoperiod management, spiking, and possibly even using artificial insemination. The first objective of this thesis was to investigate the possible benefits of feeding broiler breeder males diets containing lower crude protein levels, than given to the females, as a means of possibly tempering growth rate or improving semen quality and fertility. There was a definite improvement in the ability of the spermatozoa of the males on a lower crude protein diet to survive in the female reproductive tract. Males that received higher levels of crude protein were at a disadvantage in that fewer males yielded semen in response to abdominal massage. The second objective of this thesis was to assess the possible benefits in semen quality and fertility, when supplementing the male diets with additional vitamin E or Se in the form of Sel-Plex®. No significant effect of treatment was observed on egg fertility or semen quality. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2008.

Breeding companies advertise their chickens as having been selected for heavier breast meat. However, when comparisons are made between strains, these are normally made at a common age, and under these conditions the heaviest birds will have the heaviest breast meat yield. More meaningful comparisons would be made by relating breast weight to body protein weight, as these are allometrically related. Two experiments were conducted to test the hypothesis that the allometric relationship for each body part is the same irrespective of strain, sex and feed protein content, i.e. that geneticists have not been successful in changing the allometric relationship between breast meat weight and body protein weight. In the first trial, three strains, two sexes and four feed protein levels were used to 6 weeks of age, and in the second, four strains, two sexes and three feed protein levels were used to 12 weeks. Birds were sampled weekly, and the weights of breast meat (no skin or bone) and the meat and skin of the thigh, drum and wing were recorded before determining the body protein content of each of 1526 broilers. The hypothesis could not be corroborated when the data from the two trials were combined so a further trial was conducted to determine the amount of lipid that is deposited in the meat and skin of each of the commercially important parts of the broiler, on the assumption that differences in lipid deposition between strains, sexes and feed protein levels in the various physical parts would assist in explaining the anomalies in the analyses. It was confirmed in the third trial that the small differences between the observed and predicted weights of the physical parts may be accounted for through varying amounts of lipid deposition in these parts, depending on strain, sex and feed protein level, which must be accounted for when using allometry to predict the weights of the physical parts of the broiler at different stages of growth. The data collected in this series of trials may be used to predict the weights of these physical parts more accurately than has been the case to date. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2009.

Thesis (MScAgric (Animal Sciences))--University of Stellenbosch, 2005. / The demand for protein for human and animal nutrition in South Africa is increasing and it will continuously increase. The effect of replacing soybean oilcake meal as protein source for broilers and full-fat soybean meal for weaner pigs, with different levels of sweet lupins (Lupinus angustifolius), canola oilcake and full-fat canola was examined. A basal diet with soybean oilcake as protein source was mixed with a diet using either sweet lupins or canola oilcake or full-fat canola in ratios of 100%, 67% and 33% respectively. In the broiler trial the test diets were fed for a period of six weeks with or without the enzyme Vegpro (Alltech). Pigs were fed the test diets, with and without Roxazyme® enzyme, ad libitum from 8.5 to 25 kg live weight. The fatty acid content of the fat pads of the broilers raised on the different diets was determined. The pigs were kept in the trial up to the grower- finisher phase. The fatty acid content of the carcass fat and muscle of pigs raised on the different diets was determined. The inclusion of enzymes had no effect on the growth, feed intake or feed conversion ratio of broilers fed the test diets. The provision of external dietary enzymes to the weaner pig diets failed to improve either dry matter intake or growth rate, but improved the feed conversion ratio. Broiler weights at six weeks of age were significantly higher for the control diet compared to the 20% lupin diet. There was no significant difference in the feed intake as the lupin content of the diets increased. The feed conversion ratio did not differ significantly between the control diet and the 6.6% lupin diet but became significantly poorer as the lupin content increased to 13.2% and 20% of the test diet. There were no significant differences in production performance of the control diet and the canola oilcake containing diet. The broiler weights at six weeks decreased significantly with each increase in the canola oilcake content of the diets. The feed intake of the 20% canola oilcake diet at week six was significantly less than the intake of the control diet, but not significantly less than the 6.6% and 13.2% canola oilcake diets. The feed conversion ratio of the control diet was significantly better than the 13.2% and 20% canola oilcake diets. No significant differences were found in week six between the 6.6% full-fat canola diet and the control diet for broiler weights and feed intake. The feed conversion ratio of the broilers fed the 13.2% and 20% full-fat canola diets was significantly poorer than the control diet. The final body weights of the weaner piglets fed the control diet were significantly higher than the final body weights of weaner piglets fed the lupin containing diets. The average daily gain of the weaner piglets fed the control diet was significantly higher than the gain of the weaner piglets fed the lupin containing diets. No significant differences in the feed intake and feed conversion ratio between the different lupin inclusion levels were detected. There were no significant differences in body weight, feed intake, average daily gain and the feed conversion ratio, between the various full-fat canola containing diets and the control diet. A significant difference in body weight was found between the weaner piglets fed the 20% canola oilcake diet and the weaner piglets fed the control diet. There were no significant differences in feed intake between the various inclusion levels of canola oilcake. The control and 6.6% canola oilcake containing diets had significantly higher average daily gains than the 20% canola oilcake containing diet. In the final trial the finisher pigs fed the test diet containing 25.00% lupins, had a final body weight significantly lighter than the final body weight of the finisher pigs fed the other test diets. The finisher pigs fed the test diet containing 25.00% lupins, also had a significantly reduced average daily gain and feed intake. The feed intake of the 25.00% canola oilcake diet was significantly lees than the feed intake of the 16.75% full-fat canola containing diet. The feed conversion ratio of the 25.00% lupin containing diet was significantly poorer than the feed conversion ratio of the 16.75% lupin containing diet, 8.25% lupin containing diet, 16.75% full-fat canola containing diet, 25.00% canola oilcake containing diet and the control diet. In a choice feeding trial growing pigs were offered four diets with four different protein sources: sweet lupins (25% inclusion level), canola oilcake (25% inclusion level), full-fat canola (25% inclusion level) and soybean oilcake (25% inclusion level), while their daily intakes were recorded. In a second choice feeding trial pigs were offered ten different diets with increasing levels (6.6%, 13.2%, 20%) of either sweet lupins, canola oilcake meal or full-fat canola meal. The pigs consumed significantly more of the soybean oilcake containing diet compared to diets containing the alternative protein sources. Pigs consumed significantly less of the full-fat canola diet compared to the sweet lupin and canola oilcake diets. Ten different canola cultivars were collected from two different locations in the Mediterranean rainfall area of South Africa namely the Western Cape (Swartland) and Southern Cape (Rûens) grain producing areas. The sinapine and glucosinolate content of various canola cultivars was compared and the influence of locality on the sinapine and glucosinolate content of the canola cultivars was determined. There were no significant differences (P < 0.05) in sinapine content when the canola produced in the Western and Southern Cape were compared. Varola 54 and Rainbow cultivars had significantly higher (P < 0.05) sinapine contents compared to the Varola 50 cultivar. Samples of lupins, field peas, faba beans and narbon beans were collected and analysed for amino acids, alkaloids, non-starch polysaccharides, tannin and starch. The digestible energy value of these alternative protein sources for pigs was determined. Significant differences were found in the amino acid content of the various crops. The alkaloid content of the lupins varied significantly between the sweet and bitter lupin varieties. Sweet L. angustifolius cultivars contained ca 50mg/kg and the bitter L. angustifolius cultivars ca 15000mg/kg alkaloids. The mean alkaloid content of L. albus cultivars was ca 1300mg/kg. The faba beans, narbon beans and peas had significantly higher values for tannins and starch, compared to lupins.