Adequate and appropriate nutrition is essential for the production of high quality commercially farmed animal species. Although South Africa has had a well-established ostrich industry for over a century, little information on ostrich nutrition, in particular the specific nutritional requirements at different stages of production, is available. The industry has consequently relied heavily on data derived from poultry and pigs, but this has often proved to be unsatisfactory for ostriches and has resulted in serious nutritional-related problems. Recent studies on the metabolisable energy of specific components of diet formulations and balanced diets have indicated that ostriches have enhanced digestibility compared with poultry and pigs. At the same time, in the present economic climate, it is necessary to find cost-effective diets for breeding birds without compromising egg and chick production. This study primarily assessed the effect of different dietary protein and energy levels on production parameters and body condition of breeding female and male ostriches. The energy content of the diet appears to be the main constraint to egg production and breeders on low energy diets laid fewer eggs and lost more body condition compared with breeders fed higher energy diets. A diet with 8.5 MJ/kg DM and 10% protein with well balanced amino acids appears to be sufficient for female breeders without compromising production and a diet with 7.5 MJ/kg DM and 10% protein appears suitable for breeding male ostriches. Different dietary energy and protein levels similarly had little or no effect on egg quality and composition. This study also assessed the carry-over effect of the nutritional regime in one year on the production in the following breeding season. Females fed diets as low as 7.5 MJ/kg ME in the previous breeding season produced significantly fewer eggs in the next breeding season, which resulted in lower chick production. Energy had no effect on the percentage infertile eggs or on the initial egg weight. Different levels of dietary protein had no effect on egg production, egg weight, fertility, hatchability and initial chick weight.

Hierdie verhandeling is ‘n samestelling van verskeie studies, elk opgeskryf in die formaat en styl soos vereis deur die Suid-Afrikaanse Vereeniging vir Diereproduksie (South African Society of Animal Science). Hoofstuk 1 is ‘n literatuurstudie bestaande uit ‘n algemene inleiding wat agtergrond oor die studie verskaf en sluit die probleemstelling in, naamlik die swak oorlewing van volstruiskuikens wat onder kunsmatige toestande grootgemaak word. Hoofstukke 2, 3, 4 en 5 bestaan uit die eerste vier studies, waartydens sekere bestuurs-aspekte, wat moontlik oorlewing van volstruiskuikens kan verbeter (nl: populasiedigtheid, tipe vloer-oppervlak, die aanwending van broeipare en die aanwending van peetouers), ondersoek is. Hoofstukke 6, 7, 8 & 9 handel oor studies wat gerig is om voeding meer aanloklik te maak vir volstruiskuikens teneinde voedselinname te stimuleer en sodoende produksie en oorlewing te verbeter (nl: verskaffing van groenvoer, geur van voer, kleur van voer en beligting van voer). Die laaste hoofstuk bestaan uit ‘n algemene gevolgtrekking en aanbevelings. Alhoewel daar gepoog is om herhaling in hoofstukke te beperk, was dit onmoontlik om herhaling van sekere gedeeltes van hoofstukke te voorkom.

Thesis (MSc)--Stellenbosch University, 2015. / ENGLISH ABSTRACT: When modern man assumed the responsibility of domesticating animals for his own purposes, he directly accepted the responsibility associated with feeding and caring for them. Considering intensive production systems, nutrition is one of the most important aspects in maintaining healthy livestock as well as ensuring profitability is achieved. This is due to the fact that the feeding of the livestock is often the most expensive overhead cost encountered. In ostrich production systems, nutrition costs total an estimated 70 – 80% of the costs associated with rearing the birds from chick to slaughter. When dissecting the typical composition of these ostrich diets, it becomes evident energy and protein are two of the most important, and abundant, nutrients found. Therefore, this study was conducted to investigate the effects of different concentrations of protein and energy in the diets of slaughter ostriches, on their production parameters. In the first study (Chapter 3), five diets with different protein concentrations were formulated across the four feeding phases of slaughter ostriches (pre-starter, starter, grower and finisher). Three replications per treatment were conducted resulting in 15 camps of ostriches. Significant differences (P < 0.05) were found in the live weights of the birds at the end of each feeding phase except the finisher phase. In terms of the production parameters, differences (P < 0.05) were found for the dry matter intake (DMI), average daily gain (ADG) and the feed conversion ratio (FCR). Results indicated that the birds on the middle diet (control) and on the diets containing proportionally higher protein concentrations, although not different from each other, consistently outperformed those on diets containing lower concentrations of protein. These trends were also evident when comparing the cold carcass and thigh weights of the treatment birds post-slaughter. Therefore, from a financial standpoint, it could be concluded that increasing the protein content of the diets beyond that level currently used in industry (control) is not sensible. The second study (Chapter 4) was an evaluation on the primary products harvested from the birds utilized in the first study, namely the feathers, skin and meat. The aim of the investigation was to determine if the dietary protein concentrations had any effect on these products. No differences (P > 0.05) were observed across the feather yields or classes measured, except for the ‘tail feathers’, where the birds fed the lowest protein levels in their diets yielded the fewest. Differences (P < 0.05) were however found in selected skin parameters measured. Decreased dietary protein resulted in smaller wet skin size, smaller sizes of the feather nodules, as well as smaller crust size after the tanning process was completed. However, this had no impact (P > 0.05) on the skin grades achieved. Hence it became clear that dietary protein has an impact on the skin size achieved, which did not translate into differences in skin quality. Similarly, it did not affect the feather yields or quality. Energy is the most important nutrient in livestock diets as it is the first limiting nutrient influencing intake. Therefore, in the third study (Chapter 5), treatments in the form of five different levels of energy in the diets of ostriches, were investigated. Structurally, the layout was similar to the first study with three replications per treatment yielding 15 camps of ostriches. Significant differences (P < 0.05) were found between the live weights of the birds after the pre-starter phase, but not overall after the completion of the trial. The middle diet (diet 3) containing 14.5 MJ ME/kg displayed the highest gains per day of 216.0 ± 8.08 g per chick. The results of the growth were mirrored in the production parameters (DMI, ADG, FCR), where no differences (P > 0.05) were found for the rest of the feeding phases. In a follow up investigation of the effects of dietary, this chapter focused on the impact these different energy levels (Chapter 5) had on the primary products harvested after slaughter (Chapter 6). In particular, the feather yield and quality, skin yield and selected quality parameters, as well as the chemical composition of the meat was studied. No differences were found (P > 0.05) across any of the feather yields or classes measured. Concerning the skin yields and quality, similar results were found with no differences (P > 0.05) between the crust sizes or grades. With regards to the proximate composition of the meat, no major effect (P > 0.05) was found as a result of the treatment diets. Therefore, dietary energy content exhibited little influence over the feather, skin and meat parameters measured in this study. / AFRIKAANSE OPSOMMING: Die oomblik toe die nuwerwetse mens die verantwoordelikheid aanvaar het vir die mak maak van diere vir sy eie gebruik, het hy direk die verantwoordelikheid aanvaar wat geassosieer word met hul voeding en versorging. Met inagneming van intensiewe produksiestelsels is voeding een van die belangrikste aspekte in die handhawing van gesonde vee asook om winsgewendheid te verseker. Dit is as gevolg van die feit dat die voeding van diere dikwels die grootste oorhoofse uitgawe is. In volstruisproduksiestelsels bereik die voedingskostes ‘n totale geskatte hoeveelheid van 70 – 80% van die kostes wat geassosieer word met die grootmaak van die voëls vanaf kuiken tot slagvoël. Wanneer die tipiese samestelling van hierdie volstruisdiëte ontleed word, is dit duidelik dat energie en proteïene twee van die mees belangrike en volopste voedingstowwe is wat gevind word. Hierdie studie was dus onderneem om die effek van verskillende konsentrasies proteïene en energie in die diëte van slagvoëls en hulle produksieparameters te ondersoek. Vir die eerste studie (Hoofstuk 3) is vyf diëte met verskillende proteïenkonsentrasies geformuleer vir die vier voedingsfases van slagvolstruise (voor-aanvangs, aanvangs, groei en afronding). Drie herhalings per behandeling is gebruik wat 15 volstruiskampe tot gevolg gehad het. Betekenisvolle verskille (P < 0.05) in die lewende gewig van die voëls is aan die einde van elke voedingsfase gevind, behalwe vir die afrondingsfase. In terme van die produksieparameters is verskille (P < 0.05) gevind vir die droë materiaalinname (DMI), gemiddelde daaglikse toename (GDT) en die voeromsetverhouding (VOV). Resultate het getoon dat voëls wat die middelste dieet (kontrole) en diëte wat proporsioneel hoër proteïenkonsentrasies bevat het, alhoewel hulle nie van mekaar verskil nie, konsekwent beter presteer het as die wat diëte met laer proteïenkonsentrasies ontvang het. Hierdie tendense is ook waargeneem toe die koue karkas- en dygewigte van die eksperimentele voëls na-doods vergelyk is. Vanuit ‘n finansiële oogpunt kan daar dus tot die gevolgtrekking gekom word dat dit nie sinvol sal wees om die proteïeninhoud van volstruisdiëte te verhoog bo die vlak wat tans in die industrie (kontrole) gebruik word nie. Tydens die tweede studie (Hoofstuk 4) is die primêre produkte (vere, velle en vleis) wat vanaf die volstruise in die eerste studie geoes is, geëvalueer. Die doel van hierdie studie was om te bepaal of die verskillende proteïenkonsentrasies in die dieet enige effek op hierdie produkte het. Geen verskille (P > 0.05) is by die veeropbrengste of die verskillende veertipes wat gemeet is, waargeneem nie, behalwe vir die stertvere, waar die voëls wat die laagste proteïenvlakke in hulle diëte ontvang het, die laagste opbrengs gelewer het. Verskille (P < 0.05) is egter gevind in die geselekteerde velparameters wat gemeet is. ‘n Vermindering in die proteïenkonsentrasie het ‘n kleiner nat velgrootte tot gevolg gehad, asook ‘n afname in knoppiegrootte nadat die looiproses voltooi is. Hierdie waarneming het egter geen invloed (P > 0.05) op die gradering van die velle gehad nie. Dit het dus duidelik na vore gekom dat die dieetproteïen wel die velgrootte wat bereik is, beïnvloed het, maar nie tot verskille in velkwaliteit gelei het nie. Veeropbrengs en –kwaliteit is ook nie deur die dieetproteïen beïnvloed nie. Energie is die eerste beperkende voedingskomponent wat voerinname bepaal. Gegewe die groot invloed wat dit op voerinname het, is dit dus die mees belangrike komponent in die dieet van vee. Vandaar dan die derde studie (Hoofstuk 5) waar die behandelings in die vorm van vyf verskillende energievlakke in die diëte van volstruise ondersoek is. Die struktuur en uitleg van die studie was soortgelyk aan die eerste studie met drie herhalings per behandeling wat 15 volstruiskampe tot gevolg gehad het. Betekenisvolle verskille (P < 0.05) is gevind tussen die lewende gewigte van die voëls na die voor-aanvangsfase, maar nie nadat die hele proefneming voltooi is nie. Die middelste dieet (dieet 3) wat 14.5 MJ ME/kg bevat het, het die hoogste toename per dag van 216.0 ± 8.08 g per kuiken opgelewer. Groeiresultate is weerspieël in die produksieparameters (DMI, GDT, VOV), waar geen verskille (P > 0.05) in die res van die voedingsfases gevind is nie. Tydens ‘n opvolgondersoek rakende die effek van dieet, het hierdie hoofstuk gefokus op die impak wat die verskillende energievlakke (Hoofstuk 5) op die primêre produkte wat na-doods geoes is. Daar is in besonder na die vere-opbrengs en –kwaliteit, velgrootte en geselekteerde kwaliteitparameters, asook die chemiese samestelling van die vleis gekyk. Geen verskille (P > 0.05) is by die veeropbrengste of die verskillende veertipes wat gemeet is, gevind nie. Met betrekking tot die velgroottes en -kwaliteit, is soortgelyke resultate gevind met geen verskille (P > 0.05) tussen die knoppiegrootte en –gradering nie. Met verwysing na die proksimale samestelling van die vleis is geen betekenisvolle effek (P > 0.05) as gevolg van die eksperimentele diëte waargeneem nie. Die inhoud van die dieetenergie het dus ‘n klein invloed op die vere-, vel- en vleisparameters wat in hierdie studie geëvalueer is, gehad.

The South African ostrich industry is presently characterised by a drastic decline in the slaughter price of slaughter birds, due to the drop in the price of meat as well as leather. As a result, the economic viability of ostrich farming is severely hampered by these developments, and many generally accepted industry practices have to be reviewed. Among the practices under review is the possibility of slaughtering ostriches at an earlier age than the traditional slaughter age of 12 - 14 months, in order to minimise feed costs and the incidence of damage to the skin. However, little information is available on the effect of the slaughter age on the yield and quality of the economically important end-products. The effect of slaughter age on production and the economic viability of a commercially intensive ostrich production system was consequently evaluated in a completely randomised experimental design involving two batches (n= 81 and n= 94) of ostriches. The experiments took place at Kromme Rhee experimental farm of the Elsenburg Research Centre near Stellenbosch. The birds were subject to experimental treatment at the age of 4 months (n= 81, from May 2004 to March 2005) and 6 months (n= 94, from August 2004 to August 2005) respectively. The ostriches were randomly divided into 10 groups of between 16 and 20 birds per group. Standard production practices, as applied in an intensive ostrich production unit, were implemented. Clean drinking water and self-mixed grower diet (min 15 percent crude protein, 0.68 percent lysine and 11.4 MJ ME per kg feed) and finisher diet (min 14 percent crude protein, 0.55 percent lysine and 9.8 MJ ME per kg feed) were provided ad libitum to the birds. Birds were slaughtered at the ages of 8.5, 10.5, 12.5, 14.5, and 16.5 months respectively. Data on feed intake and yields of cold carcass, crust skin size, skin grade and total feathers was recorded for birds slaughtered at the respective ages. Data was analysed according to the analysis of variances. Values for meat yield, skin size yield and feed intake were predicted by regression analysis based on experimental values. Industry figures and norms were used as proxy for other production inputs and costs. A gross margin type analysis was performed to evaluate the effect of different slaughter ages on the profitability of each production system. There was a positive correlation between age and feed intake (r2= 0.40), slaughter weight (r2= 0.97), cold carcass yield (r2= 0.48), skin surface area (r2= 0.39), skin grade (r2= 0.19) and total yield of feathers (r2= 0.29). The dry skin grade showed deterioration as slaughter age was prolonged. Highly significant differences (P< 0.01) in slaughter weight, cold carcass yield, skin surface area, dry skin grade and total feathers were detected at the different slaughter ages. There were no significant differences (P> 0.05) with respect to gender for slaughter weight, skin surface area and dry skin grade within the different age groups. Males had significantly higher (P< 0.05) cold carcass yield and total feather yield than their female counterparts. From this study it can be concluded that an increase in slaughter age significantly increases feed intake, slaughter weight, cold carcass yield, and skin surface area. It is also clear that an increase in slaughter age can be detrimental to dry skin grade. The relative income contribution of the three main products (skin: meat: feathers) occurred in a ratio of 47:53:0, 52:47:1, 47:50:3, 44:51:5, 39:56:5 at the respective slaughter ages. Total income revealed an increase of 26 percent from 8.5 to 10.5 months slaughtering, an increase of 4 percent between 10.5 and 12.5 months, and an increase of 11 percent between 12.5 and 14.5 months. The income dropped by 0.3 percent between 14.5 and 16.5 months slaughtering. Total costs increased with slaughter age, particularly feed costs which showed an increase (at a decreasing rate) between the different slaughter ages. The margin above specified cost per bird was the highest for birds slaughtered at the age of 10.5 months. The margin above cost showed a steady decline as birds were slaughtered at higher ages. Slaughtering at 16.5 months revealed a negative margin. To compare the effect of differences in time span on different slaughter age regimes, margin above costs for each system over 5 years were discounted to a present value. In this study, with current feed costs and income from end products, slaughtering at 10.5 months revealed the highest present value for the margin above cost. Furthermore, slaughtering at 16.5 months revealed a negative present value on the margin above cost after 5 years. Financial viability calculations are relevant and valid for data obtained in this case study. Financial viability is however case-specific and may vary between producers, depending on their individual management practices, production systems and cost structures. Results from this study may be of significant value to managerial decision-making in the ostrich industry.

Thesis (MScAgric (Animal Sciences))--University of Stellenbosch, 2010. / ENGLISH ABSTRACT: The nutrient requirements for breeding ostriches are currently not well-defined. Quantification of the nutrient requirements will improve the financial wellbeing of the industry. A study of the growth of the reproductive organs and liver, together with various production studies, were therefore undertaken in order to gain knowledge about the nutrition of breeding ostriches, thereby quantifying the nutrient requirements of breeding ostriches. Various studies were conducted to determine the influence of dietary protein, amino acids and energy on production levels of breeding ostriches. In a first study, five diets, varying in crude protein (CP) but with a constant energy content of 9.2 MJ ME/kg feed, were provided at a feed intake level of 2.5 kg/bird/day. The dietary CP levels were 7.5%, 9.1%, 10.8%, 12.3% and 14.0%. No differences (P>0.05) between treatments (total eggs per female per season) were found for number of unfertilized eggs (eggs per female per season; 8.9±0.8), dead-in-shell chicks (8.0±0.5), number of chicks hatched (19.1±1.1) and change in mass of females (-16.2±1.6kg). A tendency was observed for a difference in total egg production (mean and standard error; 39.1±3.6; P=0.08). The 12.3% CP diet caused the lowest (P<0.05) change in live mass (-3.8±2kg) for male birds. No interaction (P>0.05) occurred between the genotype of the bird and the dietary protein concentration for both egg and chick production. In a second study, six diets varying in ME (MJ ME/kg feed), were provided at an average feed intake level of 3.4 kg/bird/day. The levels were 7.5, 8.0, 8.5, 9.0, 9.5 and 10.0 MJ ME/kg feed respectively. No differences (P>0.05) were observed for total eggs produced per female per season (44.8±7.8), number of chicks hatched (15.4±4.1), number of infertile eggs (11.5±3.8), number of dead-in-shell eggs (12.1±3.2) and change in mass of females (10.7±3.6kg). Males increased linearly (y=2.4x + 2.45; R2=0.09; P<0.05) in live mass as the dietary energy content increased. Two eggs per diet per month were analyzed for crude protein, crude fat and trace elements, and one egg per diet per month was analyzed for fatty acid composition. Eggs from the first and last month of the season were subjected to amino acid analysis. Analysis of variance showed no difference in crude protein and fat (P>0.05) content of eggs between the experimental diets, as well as for the calcium content of eggshells. The proline content differed (P<0.05) between the diets. The C18:3n-3 (linoleic acid) content of the eggs increased (P<0.05) amongst the dietary treatments. Crude protein, fat and C18:3n-3 content in eggs increased (P<0.05) for the number of the egg in the laying cycle. In a third study, the feed intake of breeding ostriches, as affected by dietary energy content was investigated. Average feed intake (kg feed/bird/day) was not affected (P>0.05) at any dietary energy level when levels of 8.0, 8.7, 9.4, 10.1, 10.8 and 11.5 MJ ME/kg feed were provided. The mean and standard error was 3.7±0.2kg. The production of breeding female ostriches was not influenced by dietary ME and protein at these feed intake levels. Ostrich birds do not have the ability to regulate their feed intake at any dietary energy level as used in this study. The amount of nutrients deposited in the eggs had no influence on the reproductive efficiency of the breeding female ostrich. The experiments also revealed that female breeding ostriches were independent of dietary energy and protein as used in this study for the mean frequency of egg laying at various dietary protein and energy levels (P>0.05). In a fourth study, the growth and development of the reproductive organs of female birds at the onset of the breeding season were investigated. The amount of nutrients needs to be determined in order to support the growth of the reproductive organs during the breeding season, due to the fact that these organs are linked to egg production. It was thus necessary to investigate whether the reproductive organs grew and developed during a season. The first slaughter interval was conducted at the start of the breeding season. The ovary, oviduct and liver were collected, weighed after each slaughter and analyzed. Ovary and oviduct were analyzed for crude protein and fat. No differences (P>0.05) were observed between the different slaughter intervals for the mass, crude protein and fat content of both organs. No trend (P>0.05) in the weight of the oviduct could be observed over the 49-day period, this weight being highly correlated with body weight; whereas the ovary weight tended to be correlated with the time after the onset of the breeding period, although the variation in weights, both within and between weighings, was very high. The variation in the weight of the ovary probably reflects differences in the laying pattern of individuals. The number of follicles were not affected (P>0.05) by the number of days after mating. Livers were assessed for crude protein and fat, but no difference (P>0.05) was detected between the intervals, but the weight difference amongst the slaughter intervals was significant (P<0.05), suggesting that the ostriches used liver reserves to supplement nutrients that obtained from the diet for the development of the reproductive organs. This data will be used in an optimising model (Brand & Gous, 2006) to predict the nutrient requirements of female breeding ostriches. This study suggests that the female breeding ostrich might need additional protein during the first 7 weeks of the breeding season. Results from Chapter 4 and previous studies were used to calculate the energy, protein and amino acid requirements for the egg production and maintenance of the breeding female ostrich. Two methods were used to determine the energy requirement for egg production. The Metabolisable Energy requirement for egg production (MEe) and efficiency of ME utilization for energy deposition in the egg (ko) was calculated as 12.2 MJ (for an average size egg of 1.4kg) and 0.8 respectively. The Effective Energy requirement for egg production (EEe) and maintenance (EEm) was calculated as 15.9 MJ/day and 17.1 MJ/day respectively. Average total daily protein requirement (TPt) was calculated as 175g day. The amino acid requirements for maintenance and egg production is also provided, which is lower than previous studies. This study also provides evidence that the nutrient requirements are different for every month of the breeding season. / AFRIKAANSE OPSOMMING: Tans heers daar onsekerheid oor die voedingsbehoeftes van volstruis broeivolstruise. Kwantifisering van die voedingsbehoeftes sal ‘n finansiële hupstoot aan die industrie gee. ‘n Groeistudie van die reproduksie-organe en lewer, tesame met ‘n aantal produksie-studies, is uitgevoer om inligting oor die voedingsbehoeftes van volstruis broeivoëls te versamel. Daarby is die voedingsbehoeftes teoreties bereken. ‘n Aantal studies was uitgevoer om die invloed van dieët proteïen en aminosure en energie op produksie-data te bepaal. Eerstens is vyf diëte, wisselend in ru-proteïen (RP) en beperk tot ‘n inname van 2.5 kg/voël/dag, aan broeivolstruise gevoer. Die RP van elke dieët was 7.5%, 9.1%, 10.8%, 12.3% en 14.0%. Die energiewaarde van die voer is konstant by 9.2 MJ ME/kg voer gehou. Geen verskille (P>0.05) was tussen die behandelings waargeneem vir aantal geil eiers (totale eiers geproduseer per voël per seisoen; 8.9±0.8), aantal dood-in-dop (8.0±0.5), aantal kuikens (19.1±1.1) en verandering in massa van wyfies (-16.2±1.6kg) nie. ‘n Neiging (P=0.08) is wel waargeneem vir totale aantal eiers geproduseer. Die gemiddelde en standaard fout was 39.1±3.6. Die 12.3% dieët het tot die laagste verandering (P<0.05) in lewendige massa (-3.8±2kg) vir die mannetjies gelei. Geen interaksie (P>0.05) was tussen die genotipe en dieët proteïen konsentrasie vir beide eier- en kuikenproduksie opgemerk nie. In ‘n tweede studie is ses diëte, variërend in ME (MJ ME/kg voer), by ‘n gemiddelde tempo van 3.4 kg/voël/dag gevoer. Die verskillende ME-vlakke was 7.5, 8.0, 8.5, 9.0, 9.5 en 10.0 MJ ME/kg voer. Geen betekenisvolle verskille (P>0.05) is vir totale eiers geproduseer per voël per seisoen (44.8±7.8), aantal kuikens uitgebroei (15.4±4.1), aantal geil eiers (11.5±3.8), aantal dood-in-dop eiers (12.1±3.2) en massa verandering van wyfies (10.7±3.6kg) opgemerk nie. Die mannetjies het toegeneem in liggaamsmassa (P<0.05) soos daar ‘n toename was in die energievlak van die dieët. Twee eiers per dieët per maand is vir ru-proteïen, vet en spoorelemente, en een eier per diet per maand vir vetsure ontleed. Eiers van die eerste en laaste maand van die seisoen is ontleed vir aminosure. Analise van variansie het aangetoon dat daar geen verskille (P>0.05) bestaan vir die ru-proteïen en vetinhoud van die eiers by die verskillende eksperimentele diëte, asook die kalsiuminhoud van die eierdoppe. Prolien vlakke het tussen die diëte verskil (P<0.05). Die C18:3n-3 (linoleïensuur) inhoud van die eiers het verskil (P<0.05) tussen die dieët behandelilngs. Vir die hoeveelste eier in die lê siklus het die ru-proteïen-, vet- en C18:3n-3 inhoud van die eiers verhoog (P<0.05). In ‘n derde studie is ondersoek ingestel na die voerinname van die broeivolstruise soos moontlik beïnvloed deur die energievlak van die dieët. Gemiddelde voerinname (kg voer/voël/dag) is nie (P>0.05) deur die verskillende dieët energie vlakke van 8.0, 8.7, 9.4, 10.1, 10.8 en 11.5 MJ ME/kg voer beïnvloed nie. Die gemiddelde en standaardfout was 3.7±0.2kg. Die produksie van broeivolstruise nie deur verskillende dieëtvlakke van proteïen en energie by vlakke soos gevoer in hierdie studie geraak nie. Broeivolstruise in hierdie studie het nie die vermoë gehad om hul voerinname te beheer by enige dieët energievlak soos gebruik nie. Die aantal nutriënte wat in die eiers neergelê is, het geen bydrae tot die reproduksievermoë van die wyfie gehad nie. Die studie het verder bewys dat die gemiddelde frekwensie van eier-lê by wyfies onafhanklik was by dieët-energie en -proteïenvlakke (P>0.05) soos in hierdie studie gebruik. In ‘n vierde studie is die groei en ontwikkeling van die reproduksie-organe van die wyfies bestudeer tydens die aanvang van die broeiseisoen. Die hoeveelheid of konsentrasie van voedingstowwe moes bepaal word om die groei van die reproduksie-organe te ondersteun tydens die broeiseisoen, omdat hierdie organe aan eierproduksie gekoppel is. ‘n Studie is derhalwe uitgevoer om te bepaal tot watter mate die reproduksie organe groei en ontwikkel tydens die broeiseisoen. Die eerste slagting is uitgevoer op die dag van afkamp. Die ovaria, ovidukt en lewer is versamel, geweeg en ontleed. Die ovaria en ovidukt is ontleed vir ru-proteïen en vet. Geen verskille (P>0.05) is tussen die verskillende slagtings vir die gewig, ru-proteïen en vetinhoud vir beide organe opgemerk nie. Geen betekenisvolle tendens in die gewig van die ovidukt is waargeneem oor die 49-dae periode nie, maar die gewig was hoogs gekorreleerd met liggaamsmassa. Ovaria-gewig het geneig om gekorreleerd te wees met die aantal dae na afkamp. Variasie binne en buite die gewigte was baie hoog. Die aantal follikels teenwoordig is nie beïnvloed (P>0.05) deur die aantal dae na paring. Die lewers is ontleed vir ruproteïen en vet, maar geen verskille (P>0.05) is tussen die intervalle opgemerk nie, maar die gewigte van dag 0 en 49 na paring het verskil (P<0.05). Dit kan aangevoer word dat die voëls moontlik lewer reserwes gebruik het om die voedingstowwe van die dieët te supplementeer vir die ontwikkeling van die reproduksie-organe. Data uit hierdie studie kan gebruik word in ‘n optimiseringsmodel (Brand & Gous, 2006) om die voedingsbehoeftes van broeivolstruise te bepaal. Hierdie studie beveel aan dat die broeiwyfie moontlik addisionele proteïen tydens die eerste sewe weke van die broeiseisoen benodig. Resultate van Hoofstuk 4 en vorige studies is gebruik om die energie- proteïen- en aminosuurbehoefte vir eierproduksie en onderhoud van broeivolstruise te bereken. Twee metodes is gebruik om die energiebehoefte vir eierproduksie te bereken. Metaboliseerbare Energie behoefte vir eierproduksie (MEe) en effektiwiteit van ME benutting vir energie deponering in eier (ko) is onderskeidelik as 12.2 MJ (vir ‘n eier wat gemiddeld 1.4kg weeg) en 0.8 bereken. Effektiewe Energie behoefte vir eierproduksie (EEe) en onderhoud (EEm) was onderskeidelik as 15.9 MJ/dag en 17.1 MJ/dag bereken. Die gemiddelde daaglikse proteïenbehoefte (TPt) is as 175g proteïen/dag bereken. ‘n Aanduiding van die aminosuur behoefte vir onderhoud en eierproduksie word ook gegee, wat laer is as vorige studies.

Thesis (Msc Food Sc (Food Science))--University of Stellenbosch, 2006. / The aim of this study is to determine the effect of crossbreeding Zimbabwean Blue (ZB) and South African Black (SAB) ostriches on the morphological, physical, chemical and sensory quality of the meat. However, it is also necessary to determine the reproductive performance of these genotypes to scientifically support decisions made in the ostrich industry. In relation to reproductive traits and body measurements influencing these traits, results from the study suggested that ZB birds are between 9 and 15% heavier than their SAB contemporaries. Regarding SAB females, egg production was 47% higher, levels of shell deaths were lower, percentage of eggs not incubated was lower (P<0.01) and 84% more (P<0.01) chicks were produced in a season compared to their ZB contemporaries. Mates of SAB males produced a higher (P≤0.05) percentage of eggs not incubated and higher shell death percentages than the mates of ZB males. It has to be conceded that ZB females had a lower reproduction than SAB females, limiting the application of this genotype as a dam line in crossbreeding systems. With regard to morphological properties, the pure Blue genotype in comparison to the pure Black genotype differed significantly (P≤0.05), with 16 kg for live weight, 8.3 kg for carcass weight and 3.5 kg for leg weight. However, when comparing carcass yields (expressed as %) there were no significant differences (P>0.05) between genotypes. The M. gastrocnemius, M. femorotibialis accessorius, M. iliotibialis cranialis, M iliotibialis lateralis, M. iliofibularis and M. iliofemoralis showed significant genotype differences (P≤0.05) for individual muscle weight. When comparing the physical meat quality characteristics between the pure Blue genotype and the pure Black genotype, 70% of the muscles were higher (P≤0.05) in pH24, 50% of the muscles were redder (P≤0.05) and significantly less (P≤0.05) saturated in colour, 67% of the muscles had a lower (P≤0.05) percentage drip loss and 50% of the muscles had a lower (P≤0.05) percentage cooking loss. No significant (P>0.05) genotype differences were observed regarding the sensory quality of the meat. Regarding chemical meat quality characteristics, the percentage of moisture was higher and the percentage of lipid was lower for eight of the ten muscle groups from the pure Blue genotype. No significant differences (P>0.05) were found between genotypes or between muscles regarding the percentage of protein present in the meat. The highest (P>0.05) content of soluble collagen, myoglobin and cholesterol was found in the Blue x Black genotype, whereas the lowest percentage of the latter constituents was found in the pure Blue genotype. For the pure Black genotype the concentration of saturated fatty acids in the meat was lower (P≤0.05), the concentrations of total unsaturated fatty acids and desirable fatty acids in the M. illiofibularis were the highest (P≤0.05), while the concentration of monounsaturated fatty acids was also higher (P≤0.05) in both muscles of this genotype compared to the other two genotypes. Regarding both fat depots, the pure Black genotype had a lower (P≤0.05) concentration of saturated fatty acids, a higher (P≤0.05) concentration of monounsaturated fatty acids and total unsaturated fatty acids and a higher (P≤0.05) polyunsaturated:saturated fatty acid ratio. The percentage of desirable fatty acids in the abdominal fat depot was significantly higher (P≤0.05) for the pure Black and the Blue x Black genotype. In conclusion, crossbreeding between SAB and ZB ostriches seems to be a viable option to produce larger birds with more meat, without negatively affecting the overall quality of the meat.