Determining the energy values of feed ingredients for poultry is of great concern, especially since production efficiency is associated with profit margins. Therefore, accurate, precise, and reproducible energy values for feed ingredients are of the utmost importance in formulating an economical diet. An important aspect in determining the apparent metabolizable energy (AME) of a feed ingredient is the procedure employed in the drying of excreta samples. During sample preparation, substantial grinding losses were incurred amounting to 3.5 to 5.2% of the dried sample weight. Also moisture uptake during sample grinding accounted for a 1.9 to 3.9% increase in sample weight. To properly account for such losses, freshly collected excreta samples should be weighed, oven-dried at 40 C, reweighed, allowed to equilibrate with atmospheric moisture, weighed, ground, reweighed, and stored in air-tight containers for subsequent analyses. From the oven-drying of feed and excreta samples at various temperatures, a linear decrease in sample weight occurred with increasing drying temperatures. When dried at 100 C or less, the energy content of feed and excreta samples remained unchanged, but increased significantly at higher temperatures. The nitrogen composition of feed and excreta samples exhibited a similar trend, but a significant loss of excreta nitrogen (2%) occurred at 100 C. The loss of excreta nitrogen at a temperature of 100 C is of relatively minor consequence in the determination of metabolizable dry matter, but is of major concern in nitrogen balance studies. Extraction of feed and excreta samples with N,N-dimethylformamide and titration with Karl Fischer reagent indicated that significant amounts of water were retained by samples dried at 40, 60, and 80 C. However, at temperatures of 100 C or greater, little water was retained but sample decomposition occurred. A drying temperature of 90 C or the Karl Fischer method may yield a more accurate value for the dry matter of feed or excreta. When seven roosters were subjected to a total collection method for five consecutive days, individual birds were better metabolizers of dry matter and energy than others. By either a voluntary intake method or by a total collection method, values for the nitrogen-corrected metabolizable energy of corn were similar. The total collection method proved to be more reliable since it provided the least amount of variation when <u>ad libitum</u> feed intake and total excreta output were measured over a period of several days. In past experiments, adding fats to a test diet at the expense of cerelose in amounts no greater than 20% of the diet to determine the metabolizable energy of the fat has been associated with a high degree of variability. From the force-feeding of fats at levels to 100%, the variation associated with the metabolizable energy value of a fat was greatly reduced. The methodology presented here provided reliable estimates and detected differences between the metabolizable energy of two feed-grade fats in comparison to previous methods. / Ph. D. / incomplete_metadata

Experiments were conducted to investigate the effects of E. coli and rotavirus as causative agents in producing infectious stunting syndrome of poults. The syndrome, as it occurs commercially, was characterized in two experiments to produce decreased digestible dry matter and nitrogen as well as increased excreta nitrogen and gross energy content of affected poults. The effects of E. coli and rotavirus on the nutritional performance of poults were compared to the commercial syndrome by digestibility trials and assay of intestinal mucosaI enzyme activities. The strain of E. coli used in these experiments was isolated from the yolk sac of stunted poults. Inoculation of day-old poults was done orally in one experiment and via the yolk sac in another series of experiments. Experiments were designed in a factorial arrangement of E. coli inoculation and dietary protein level (28 vs. 22%). Oral administration of the pathogenic E. coli at a low dose (.1 ml of a 10⁻² dilution of a 24-hr culture) to day-old poults produced a significant increase in feed efficiency by 21 days of age for birds fed either 28 or 22°0 protein diets. In this case, E. coli apparently was established as part of the normal intestinal microflora of the turkey without producing a toxic response. Similar concentrations of E. coli (10⁻³ and 10⁻² dilutions) inoculated into the yolk sac of day-old poults resulted in significant mortality and morbidity. The lower dilution (10⁻³) produced the desired response of stunted poults without substantial mortality. Body weight gain and feed consumption were severely decreased by E. coli inoculation at both levels of protein (28 or 22%). The 28% protein diet alleviated the reduction in feed consumption for birds infected with the lower concentration of E. coli. The 10⁻² dilution caused substantial mortality and similar responses on body weight at both levels of protein. A malabsorption of nutrients accompanied E. coli infection in spite of reduced feed consumption as indicated by increased excreta nitrogen and gross energy content for all infected poults. In three experiments, rotavirus was orally inoculated into poults over 21 days of age previously fed either 28 or 22% protein diets. The response of rotavirus was variable in the three experiments, however, the low protein diet (22%) increased the poults susceptibility to rotavirus infection. Serum antibodies to rotavirus were detected in all poults tested prior to inoculation. Ubiquitous in nature, rotavirus appears to produce clinical signs of infection in combination with stress on the poults. Effects of rotavirus on digestibility parameters were inconclusive. In experiments with either rotavirus or E. coli, activities of intestinal mucosal enzymes were found to vary more between poults within a treatment than by any effect of the various treatments. / Ph. D.

Thesis (MScAgric)--University of Stellenbosch, 2000 / ENGLISH ABSTRACT: A flock of 500 Hybro broiler breeders were employed to study the effect of different levels of protein and energy on production and body composition. The daily lysine intake of the birds were 900, 1050, 1200 and 1350 mg respectively, each fed in diets with a daily energy intake of 1800 and 2000 kJ ME to provide a 4 x 2 factorial design. Lysine was used as the reference amino acid in the experiment and all other amino acids were kept in a constant ratio in every experimental diet. The total production was divided into 3 periods of 13 weeks each (week 23 - 35; week 36 - 48 and week 49 - 61) to determine the effect of the treatments over time. Production was evaluated by hen day production; egg weight (g/egg); egg mass (g/day); fertility; hatchability; chicks/hen/week; feed conversion and day old chick weight. Hen day production was significantly (P < 0,05) lower at the high energy intake for period week 49 to 61. Energy and protein levels significantly increased egg weight. Effect of protein was consistent during all three periods of production. Egg mass output had a significant (P < 0,05) response to increasing levels of protein for the total period of production. The birds on the high energy diet produced a significant higher egg mass per hen during the first period of production (week 23 - 35). Hatchability was reduced (P < 0,05) by the higher energy intake for the total period of production and this effect was very significant (P < 0,01) during the final period of production. Similar to hen day production, the higher energy had a significant (P < 0,05) negative effect on the amount of chicks produced. The well-known correlation between egg weight and chick weight was confirmed with the regression equation: Chick weight = 10,5 + 1,22 x Egg weight. Both energy and protein had a significant (P < 0,01) positive effect on chick weight. The feed conversion was lower at increasing levels of amino acid intake (P < 0,01). Higher energy intake significantly (P < 0,05) increased hen weight and protein had a very significant effect during the first period of production (P < 0,01). The isotope dilution technique (tritiated water) was used to estimate the body composition of the breeders. This was done at 5 different periods (week 27, 35, 43, 52 and 61) of the production period to establish changes in requirements over time. Significant correlation were found between carcass moisture and waterspace (R2 = 0,76); fat % and carcass moisture (R2 = 0,78); protein % and waterspace (R2 = 0,35) and fat % and waterspace (R2 = 0,46). The regression equations obtained from these correlation were employed to determine excess energy and lysine consumed at different ages. Energy requirements were calculated according to the effective energy (EE) system and the conventional ME system. According to effective energy the lower energy intake was not sufficient and the maximum requirement was calculated to be 1942 kj EE/day. The metabolizable energy calculations indicated sufficient intakes at every treatment with the maximum requirement 1746 kj ME/day. The lysine requirement was found to be in excess of 1050 mg lysine per day. The recommendation for daily lysine intake is 1200 mg/day and the energy intake of breeders should be 1900 to 2000 kj ME/day from week 23 to 35 and can be reduced to 1800 kj ME/day in the final period of production. / AFRIKAANSE OPSOMMING: Om die effek van verskillende vlakke energie en proteïen op produksie en liggaamsamestelling te ondersoek is 'n trop van 500 Hybro braaikuiken teelouers gebruik. Die daaglikse lisien inname van die henne was onderskeidelik 900, 1050, 1200 en 1350 mg, wat elk by 'n daaglikse energie inname van 1800 en 2000 kJ ME verskaf is, in 'n 4 x 2 faktoriale ontwerp. Alle aminosure is in 'n konstante verhouding met die verwysings aminosuur lisien in die rantsoen ingesluit. Om te evalueer of daar veranderinge oor 'n tydperk plaasvind weens die verskillende behandelings is die produksie periode in drie periodes van 13 weke elk verdeel (week 23 - 35; week 36 - 48 en week 49 - 61). Die produksie standaarde wat gemeet is, is hen dag produksie, eiergewig (g/eier), eiermassa (g/dag), vrugbaarheid, uitbroeibaarheid, kuikens/hen/week, voeromset en dagoud kuikenmassa. Hen dag produksie was betekenisvol (P < 0,05) laer by die hoër energie innames in die laaste periode van 49 tot 61 weke. Energie en proteïen het eiergewig betekenisvol (P < 0,01) verhoog. Die effek van hoër vlakke proteïen was konstant in alle produksie periodes. Die daaglikse eiermassa (g/dag) het ook saam met stygende vlakke proteïen verhoog en hierdie effek was vir die totale periode van produksie. Energie het die eiermassa in die eerste periode van produksie (week 23 - 35) verhoog. Uitbroeibaarheid is verlaag (P < 0,05) vir die totale periode van produksie deur die hoër energie inname en die effek was selfs groter (P < 0,01) in die finale periode van produksie. In ooreenstemming met die hen dag produksie is die aantal kuikens geproduseer negatief beïnvloed deur die hoër energie inname (P < 0,05). Die korrelasie wat bestaan tussen eiermassa en kuikenmassa is bevestig deur die regressie: Kuikenmassa = 10,5 + 1,22 x Eiermassa. Energie en proteïen het kuikenmassa betekenisvol (P < 0,01) verhoog. Voeromset was laer by stygende vlakke van proteïen inname (P < 0,01). Die hoër energie inname het henmassa ook betekenisvol (P < 0,05) verhoog en proteïen het dieselfde effek slegs in die eerste periode van produksie gehad (P < 0,01). Die liggaamsamestelling van teelhenne is bepaal met behulp van die isotoop verdunnings tegniek (tritium water). Dit is bepaal op 5 verskillende stadiums in die produksie periode (week 27, 35, 43, 52 en 61) om die moontlike verandering in behoeftes oor tyd vas te stel. Betekenisvolle korrelasies is gevind tussen karkasvog en die waterspasie (RZ= 0,76); vet % en karkasvog (R2 = 0,78); proteïen % en waterspasie (R2 = 0,35) en vet % en waterspasie (R2 = 0,46). Die regressie vergelykings van hierdie korrelasies is gebruik om die hoevelheid surplus energie en lisien ingeneem te bepaal. Die" effective energy" sisteem en die konvensionele ME sisteem is gebruik in die bepaling van energie behoeftes. Volgens die " effective energy" was die energie inname nie voldoende by die laer energie innames nie en die maksimum behoefte is bereken as 1942 kJ EE/dag. Die maksimum energie behoefte volgens metaboliseerbare energie is bereken as 1746 kj ME/dag. Die lisien behoefte moet hoër as 1050 mg/dag wees. Die aanbeveling van die daaglikse lisien inname is 1200 mg/dag en die energie inname moet 1900 tot 2000 kj/dag wees tot 35 weke produksie en kan daarna verlaag word na 1800 kJ ME/dag.

No description available.

Graduation date: 1993

The objectives of this research were (1) to study the relative ability of genetically different types of domestic chickens to digest and absorb fat of different types, and (2) to relate fat absorbability coefficients to dietary apparent M. E. values obtained with genetically different types of chickens feeding on diets containing the different types of fat, (3) to search for a possible cause of poultry genetic difference in fat absorbability by examining some of the factors most likely to influence fat digestion and absorption in the genetically different types of chickens. Using New Hampshire, White Leghorn and broiler-type birds, it was found that until 6 weeks of age the New Hampshires were significantly (P≤0.05) superior to the others in their ability to utilize animal tallow. Differences among birds in the absorbability of corn oil were small. Differences in dietary M.E. estimates were closely associated with differences in fat absorbability values and on a 12% tallow diet, the R² values computed on a within age between breeds basis, were 0.67, 0.36 and 0.022 at 3, 5, and 9 weeks of age respectively. This general decline in R² values was a reflection of the narrowing of the range of fat absorbability differences among different types of birds as they grew older. The overall conclusion based on these results, is that breed and/or age differences in M.E. estimates are to a large extent attributable to breed and/or age differences in the absorbability of dietary lipid materials. The search for potential causes of the observed breed differences in fat absorbability was therefore the main theme of the subsequent experiments. A study of the feed passage time in birds of different genetic backgrounds failed to provide any conclusive evidence on whether or not breed differences in ingesta transit time are in measureable terms responsible for fat absorbability differences. It was found, however, that with diets containing 12% of animal tallow or corn oil, feed passage time was significantly longer regardless of the type of birds. On the basis of the results of an experiment in which in vitro pancreatic lipase activity was measured, the New Hampshires ranked first followed by Broilers and White Leghorns in that order. However, the magnitude of differences among them was small. Supplementation of the 12% tallow diet with the bile salt, sodium taurocholate, improved fat utilization significantly by the broiler-type and White Leghorn chicks to the extent of 8.6% and 7.2% respectively. The improvement in fat absorbability was associated with a significant reduction in the amount of fecal soap fatty cacids. The effect of the sodium taurocholate suggested that in the Broilers and White Leghorn chicks, the supply of bile salts was below the critical micellar concentration required for efficient tallow fat absorption. Results from a general study on intestinal fatty acid binding protein (FABP) revealed that a fatty acid binding protein in the same molecular weight range as that one demonstrated in the rat, exists in the intestinal mucosa of the adult chickens and in the mesenteric intestine of day-old chicks prior to the ingestion of any feed. / Land and Food Systems, Faculty of / Graduate

Thesis (MSc. (Animal Production)) -- University of Limpopo, 2016 / This study was conducted to determine the effect of supplementing diets with antimicrobials and effective microorganisms on productivity and carcass characteristics of Ross 308 broiler chickens. The study consisted of two parts. The first part determined the effect of antimicrobial and effective microorganism (EM) supplementations on growth performance of unsexed Ross 308 broiler chickens aged one to 21 days. A complete randomized design was used and 150 unsexed day-old chicks with an initial weight of 42 ± 2g were randomly assigned to five different treatments which were replicated 3 times with each replicate having 10 chicks. The five grower diets had the same nutrients (20% CP and 12MJ/kg) but different supplementation levels of 0g oxytetracycline and 0ml EMs/l of water (UAM0EM0), 0.01g oxytetracycline (UAM0.01EM0), 30ml EMs/l of water (UAM0EM30), 50ml EMs/l of water (UAM0EM50) and 100ml EMs/l of water (UAM0EM100). A quadratic regression model was used to determine dietary effective microorganism supplementation levels for optimal feed intake and live weight of Ross 308 broiler chickens. A linear model was used to determine the relationship between dietary effective microorganism supplementation levels and metabolisable energy intakes. Antimicrobial and effective microorganism supplementations did not have any effect (P>0.05) on growth rate, feed conversion ratio and mortality. Antimicrobial supplementation improved (P<0.05) feed intake and live weight of the chickens. Supplementation with 50ml of EMs/l of water improved (P<0.05) feed intake. Supplementation with 50 or 100ml of EMs per litre of water increased (P<0.05) ME intake of the chickens. Effective microorganism supplementation levels of 72.25 and 48.29ml of drinking water optimized feed intake and live weight, respectively. The second part of the experiment determined the effect of antimicrobials and effective microorganisms on productivity, blood, carcass characteristics and meat quality of male Ross 308 broiler chickens aged 22 to 42 days. The chickens were randomly allocated to five treatments with three replications, each having six chickens. A total of 90 male chickens, with the initial live weight of 452 ± 3g were allocated to the treatments in a complete randomized design. The chickens were fed a grower diet supplemented with 0g oxytetracycline and 0ml EMs/l of water (MAM0EM0), 0.01g oxytetracycline (MAM0.01EM0), 30ml EMs/l of water (MAM0EM30), v 50ml EMs/l of water (MAM0EM50) and 100ml EMs/l of water (MAM0EM100). Antimicrobial and effective microorganism supplementation did not have effect (P>0.05) on feed intake, growth rate, live weight, ME intake, blood glucose and mortality. Poorer (P<0.05) feed conversion ratio was observed with the supplementation of antimicrobial. Blood glucose levels were optimized at an effective microorganism supplementation level of 29.00ml of EM/l of drinking water (Figure 4.05). Supplementing diets with antimicrobials and effective microorganisms did not have effect (P>0.05) on crop, gizzard, proventriculus and large intestine pH values of male chickens. However, supplementation with of 100ml of EMs per litre of drinking water reduced (P<.0.05) the pH of ileum. Effective microorganism supplementation level of 85.00ml per litre of drinking water optimized the crop pH value. Antimicrobial and effective microorganism supplementations did not have influence (P>0.05) on gizzard, proventriculus, small intestine, caecum, large intestine, liver and heart weights of male chickens at 42 days. Effective microorganism supplementation level of 50ml per litre of drinking water reduced (P<.0.05) crop weight. Antimicrobial and effective microorganism supplementations did not have effect (P>0.05) on whole gastro-intestinal tract (GIT), small intestine and caecum length of the chickens. Antimicrobial supplementation reduced (P<0.05) the length of large intestine. Effective microorganism supplementation levels of 41.00, 45.50 and 85.00ml per litre of drinking water optimized crop weights and caecum and large intestine lengths, respectively. Antimicrobial and effective microorganism supplementations did not have any influence (P>0.05) on live weight, carcass weight, breast weight, drumstick weight ad thigh weight. Similarly, antimicrobial and effective microorganism supplementations did not have influence on meat tenderness, juiciness and flavour. There were no antibiotic and effective microbe residues in the meat. It is, therefore, concluded that effective microorganism supplementation did not have much effect on production parameters, carcass characteristics and meat quality of Ross 308 broiler chickens.

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.