Academic literature on the topic 'Struthio camelus – Feeding and feeds'

The Gompertz equation was used to compute growth curves for three groups of ostriches (Struthio camelus), from Oudtshoorn in South Africa, the Namib desert in Namibia and from Zimbabwe. All were reared under typical intensive farm conditions with ad libitum feeding. There were no significant differences in mature mass between regions but the maximum daily weight gain for males occurred later (day 163) for Oudtshoorn birds, compared with day 121 for Namibian and day 92 for Zimbabwean. Oudtshoorn females reached maximum rate of gain on day 175 compared with day 115 for Namibian and day 114 for Zimbabwean. Comparisons might prove important when planning programmes for the genetic improvement of commercial flocks, but possible influences of food composition and environment should be investigated.

This study was conducted to evaluate captive growerostrich behavioral patterns. The fifteen grower red-necked (Struthiocameluscamelus) flock (2-month age) were stocked at Rajaa Agriculture Scheme 75km. South of Khartoum, White Nile Govern ate and accommodated in pen of dimension’s 9.5x5.5x3.5m with a concrete floor. Feeding plane was at 16.34% crude protein and 10.11 MJ ME/ Kg. Behavior was observed during three consecutive days on grower chicks over three daylight periods, 6:00 -10:00 a.m., 10:00 a.m. - 2:00 p.m. and 2:00 – 6: 00p.m. Walking, sitting, standing, feeding, drinking, pecking, coprophagy, urination and defecation for three consecutive days was observed. The mean daylight time budget of different behavioral attributes of grower ostrich chicks show that 70% of activity was devoted to feeding, drinking, coprophagy and defecation. Resting was less (20% of time). Defecation is less (11.67± 0.1.36 %) in the morning and coprophagy is high (07.36 ±02.27%) in the evening the day.

AbstractIn an experiment involving 30 roosters and 15 mature male ostriches the apparent metabolizable energy (ME) values, corrected for zero nitrogen retention (AMEn), were determined by balance method for maize and lucerne meal. A group of 10 roosters received maize as the sole dietary component. For the second group of 10 roosters a blend of 750 g/kg maize and 250 g/kg lucerne was prepared. The diet of the third group consisted of 500 g/kg maize and 500 g/kg lucerne meal. The ostrich basal diet consisted of 1000 g/kg lucerne, and was blended in the ratios 50 lucerne: 50 maize and 25 lucerne: 75 maize. Each dietary treatment was given to five ostriches, individually housed in metabolism crates. Food intake and excreta collection was carried out over a period of 5 days after the ostriches had been accustomed to the diets for 7 days. For roosters food intake and excreta collection lasted for 72 h after an adaptation period of 24 h.The AMEn value for maize was 14·49 (s.e. 0·046) MJ/kg in roosters while in ostriches AME,, values of 14·3 (s.e. 1·81) and 14·5 (s.e. 0·845) MJ/kg for the 500 g/kg inclusion and 250 g/kg inclusion respectively were found.In roosters lucerne meal yielded AME,, values of 4·49 (s.e. 0·506) and 4·05 (s.e. 0·321) at 250 g/kg and 500 g/kg inclusion levels respectively. For the ostriches a value of 8·9 (s.e. 0·755) Mj/kg was found for lucerne.True ME, corrected for zero nitrogen retention, (TMEJ was computed by regressing gross energy output on gross energy input over all feeding levels. Maize yielded values of 14·65 (s.e. 0·0455) and 14·9 (s.e. 0·351) for roosters and ostriches respectively while corresponding values for lucerne were 4·03 (s.e. 0·118) and 8·6 (s.e. 0·296) MJ/kg.It was concluded that the ostriches were capable of digesting a high starch diet such as maize to the same extent as adult roosters but ostriches were capable of digesting a high fibre ingredient such as lucerne meal much more efficiently.

The ostrich oil of Struthio camelus (Ratite) found uses in folk medicine as an anti-inflammatory in eczema and contact dermatitis. The anti-inflammatory effect of a γ-lactone (5-hexyl-3H-furan-2-one) isolated from ostrich oil and its formulated nano-emulsion in formalin-induced paw edema was investigated in this study. Ostrich oil was saponified using a standard procedure; the aqueous residue was fractionated, purified, and characterized as γ-lactone (5-hexyl-3H-furan-2-one) through the interpretation of IR, NMR, and MS analyses. The γ-lactone was formulated as nano-emulsion using methylcellulose (MC) for oral solubilized form. The γ-lactone methylcellulose nanoparticles (γ-lactone-MC-NPs) were characterized for their size, shape, and encapsulation efficiency with a uniform size of 300 nm and 59.9% drug content. The γ-lactone was applied topically, while the formulated nanoparticles (NPs) were administered orally to rats. A non-steroidal anti-inflammatory drug (diclofenac gel) was used as a reference drug for topical use and ibuprofen suspension for oral administration. Edema was measured using the plethysmograph method. Both γ-lactone and γ-lactone-MC-NPs showed reduction of formalin-induced paw edema in rats and proved to be better than the reference drugs; diclofenac gel and ibuprofen emulsion. Histological examination of the skin tissue revealed increased skin thickness with subepidermal edema and mixed inflammatory cellular infiltration, which were significantly reduced by the γ-lactone compared to the positive control (p-value = 0.00013). Diuretic and toxicity studies of oral γ-lactone-MC-NPs were performed. No diuretic activity was observed. However, lethargy, drowsiness, and refusal to feeding observed may limit its oral administration.

AbstractThe knowledge about transport of sugars in animals and birds gastrointestinal tract is very important for science as carbohydrates are the main energy source of food. Since until now there is few information about the localization of glucose transporters - integral membrane proteins that mediate the transport of glucose and related substances across the cellular membranes - in birds gastrointestinal tract, the aim of the present study was to localize glucose transporters-2 and -5 (GLUT-2 and -5) in three parts of the ostriches gastrointestinal tract – proventriculus, duodenum and ileum - comparatively in ostrich chicken in their early ontogenesis period. Material from the superficial gland zone of the proventriculus, duodenum and terminal zone of the ileum were collected from eight female ostriches (Struthio camelus var. Domesticus): two chickens after hatching, three 7 and three 30-days old ostriches. The material was fixed with 10% formalin, embedded into paraffin, slices 7 μm thick were cut followed by immunohistochemical staining with polyclonal primary antibodies Rabbit anti-GLUT-2 and Rabbit anti-GLUT-5, carried out according to the manufacturers guidelines (IHC kit, Abcam, UK). The results showed that the staining for both antibodies was weaker in all parts of the gastrointestinal tract of ostriches after hatching compared to 7 and 30 days old ostriches showing that the gastrointestinal tract of ostriches immediately after hatching is not entirely capable of transportation of carbohydrates. The results of our study may indicate the possibility of a close relationship between feeding and the ability to transport sugars in the gastrointestinal tract.

Thesis (MScAgric (Animal Sciences))--University of Stellenbosch, 2010.
ENGLISH ABSTRACT: The purpose of this study was to evaluate the production of slaughter ostriches in a grazing environment at different levels of supplementary feed. Two grazing trials were conducted. In the first trial, one group of finisher ostriches (six months old) was put into a feedlot and received a complete finisher diet. The other four groups were allowed to graze lucerne pasture (stocking rate of 15 birds/ha) with 1500, 1000, 500, and 0g supplementary feed/bird/day. Pasture production and intake were measured. There was no difference (P >0.05) between the end mean live weights of the feedlot ostriches and those two grazing groups receiving 1500 or 1000g supplementation. The average daily gain (ADG) of the group receiving 1000g supplementation was lower (P <0.05) than the ADG of the group receiving 1500g supplementation, but all three groups reached a mean target slaughter weight of 95kg within the 154 days of the study. Therefore, pastures together with the correct supplementation (at least 1000g/bird/day) can replace complete feeds in the finishing phase of slaughter ostriches and can play an important role in the production of these birds. For lucerne intake, a quadratic relationship (P <0.01) was found between pasture dry matter (DM) intake (g/bird/day) and supplementary feed intake (g/bird/day). The maximum lucerne intake level (1692.8g/bird/day) was achieved at 619.6g supplementary feed/bird/day. In the second grazing trial, finisher ostriches were allowed to graze lucerne pastures at two different stocking rates (10 and 15 birds/ha) while receiving either 0 or 800g supplementary feed/bird/day. Ostriches receiving supplementation had higher (P <0.05) mean end live weights than ostriches receiving no supplementation. Ostriches receiving supplementation reached a mean target slaughter weight of 95kg within the timespan of the trial, but ostriches receiving no supplementation did not. Stocking rate had no influence on mean end live weight of the birds. An interaction (P <0.05) was found between the level of supplementation and stocking rate for ADG of the birds. Stocking rate influenced ADG only for birds receiving no supplementation. As stocking rate increased, ADG of birds receiving no supplementation declined. Results of the pasture data indicated an increasing level of replacement of grazed lucerne DM by supplementary feed as the trial progressed and this was more pronounced at the higher stocking rate of 15 birds per hectare. A high stocking rate seems to have had a gradual depressing effect on lucerne DM production, while the less severe levels of defoliation at a lower stocking rate promoted lucerne DM production. A digestibility trial was conducted with mature ostriches (12 months old) to investigate the effect of supplementation on intake and digestibility of nutrients, as well as to investigate the substitution effect that ostriches may display when they receive supplementary feed in addition to grazing. The same dietary treatments as in the first grazing study were given to ostriches while they were kept in metabolism crates. These diets were also fed to 20-week old roosters to obtain energy values for these diets for roosters. These energy values would be used to predict ostrich energy values for the same diets by means of a regression equation. For the roosters, each diet treatment was mixed with 50% maize to prevent digestive disorders and ensure maximum feed intake. Ostriches started to substitute supplementary feed for pasture when supplementation was supplied at levels higher than 62% (i.e. 1000g supplementary feed/bird/day) of total feed intake. For each increase of 100g in supplementary feed intake, pasture was replaced at a rate of 4.9%. Higher (P <0.05) total feed intakes were reached by ostriches if they grazed lucerne pastures and received supplementation than if they grazed pasture alone. Pasture grazing alone had lower (P <0.05) dry matter digestibility (DMD) and apparent metabolizable energy (AME) values for both ostriches and roosters than if pastures were supplied with a supplement. A significant stepwise regression could not be computed for the prediction of ostrich AME values from rooster AME values. The economics of different feeding systems (extensive versus intensive) were evaluated with an economic analysis, which was based on the same materials and methods and results of the first grazing trial. A margin above feed cost (MAFC) analysis was performed to evaluate the economic viability of the different feeding systems. The present value (PV) of the MAFC for the pasture-based system with 1000g/bird/day supplementation was only 8.3% lower than that of the feedlot system over a period of six years, while the PV of the cost of the same pasture-based system was 78.4% lower than that of the feedlot system. Birds finished on lucerne pasture with 1000g supplementation led to a saving of 57% in feeding costs if compared to a feedlot system. A sensitivity analysis of the MAFC revealed that the pasture-based system was less sensitive to changes in feeding costs than the feedlot system. Therefore, the unique circumstances of each ostrich producer will play a role in the decision whether to raise ostriches in a feedlot or on pastures.
AFRIKAANSE OPSOMMING: Die produksie van slagvolstruise in ‘n ekstensiewe weidingsstelsel met verskillende vlakke van aanvullende voeding is gedurende hierdie studie ge-evalueer. Twee weidingsstudies is uitgevoer. In die eerste studie is een groep afrondingsvolstruise (ses maande oud) in ‘n voerkraal geplaas en ‘n volledige afrondingsdieet gevoer. Die ander vier groepe is op besproeide lusernweiding geplaas (teen ‘n weidigtheid van 15 voëls/ha) en het onderskeidelik 1500, 1000, 500 en 0g aanvullende voeding/voël/dag ontvang. Weidingproduksie en -inname is gemeet. Daar was geen verskil (P >0.05) tussen die eindgewigte van die voerkraal volstruise en dié van die weidende voëls wat onderskeidelik 1500 en 1000g aanvullende voeding ontvang het nie. Die gemiddelde daaglikse toename (GDT) van die groep weidende voëls wat 1000g aanvullende voeding ontvang het was laer (P <0.05) as die GDT van die groep weidende voëls wat 1500g aanvullende voeding ontvang het, maar al drie hierdie groepe het ‘n gemiddelde teiken slaggewig van 95kg bereik binne die 154 dae van die studie. Weiding, tesame met die korrekte aanvullende voeding (van ten minste 1000g/voël/dag) kan volvoer rantsoene in die afrondingsfase van slagvolstruise vervang en kan dus ‘n belangrike rol speel ten opsigte van die produksie van hierdie voëls. Vir lusern inname is ‘n kwadratiese passing (P <0.01) tussen weiding droë materiaal (DM) inname (g/voël/dag) en aanvullende voeding inname (g/voël/dag) gevind. Die maksimum lusern inname (1692.8g/voël/dag) is bereik wanneer voëls 619.6g aanvullende voeding/voël/dag ingeneem het. In die tweede weidingsstudie, is afrondingsvolstruise (6 maande oud) toegelaat om lusern te bewei teen twee verskillende weidigthede (10 en 15 voëls/ha) en het ook 0 of 800g aanvullende voeding/voël/dag ontvang. Volstruise wat aanvullende voeding ontvang het, het hoër (P <0.05) gemiddelde eindgewigte bereik as volstruise wat geen aanvullende voeding ontvang het nie. Volstruise wat aanvullende voeding ontvang het, het ook die teiken slaggewig van 95kg bereik binne die tydsduur van die studie, terwyl die volstruise wat geen aanvullende voeding ontvang het nie, nie daarin kon slag nie. Weidigtheid het nie ‘n invloed (P >0.05) gehad op die eindgewigte van die voëls nie, maar ‘n interaksie (P <0.05) is gevind tussen vlak van aanvullende voeding en weidigtheid wat GDT van die voëls betref. Weidigtheid het GDT beïnvloed slegs vir volstruise wat geen aanvullende voeding ontvang het nie. Soos die weidigtheid van die voëls wat geen aanvullende voeding ontvang het nie, toegeneem het, het die GDT van hierdie voëls afgeneem. Ontleding van die weidingsdata het ‘n toenemende vlak van verplasing van die weiding met aanvullende voeding getoon soos die studie gevorder het en dit was meer merkbaar by die hoër weidigtheid. Die hoër weidighteid het ook gelei tot ‘n geleidelike afname in lusern DM produksie, terwyl die minder aggressiewe vlakke van ontblaring by die laer weidigtheid lusern DM produksie bevorder het. ‘n Verteringsstudie is gedoen met volwasse volstruise (12 maande oud) om die invloed van aanvullende voeding op inname en verteerbaarheid van nutriente te toets, asook om die substitusie effek wat volstruise mag toon wanneer hulle aanvullende voeding ontvang op weiding, te ondersoek. Dieselfde dieet behandelings as in die eerste weidingsstudie is vir die volstruise gegee terwyl hulle in metabolisme kratte aangehou is. Hierdie diëte is ook aan 20-week oue hane gevoer om die energie waardes van die diete vir hane te verkry. Hierdie energiewaardes sal dan gebruik word om volstruis energiewaardes te voorspel vir dieselfde diëte met behulp van ‘n regressie vergelyking. Vir die hane is elke dieet gemeng met 50% mielies om inname te handhaaf en spysverteringsstoornisse te voorkom. Volstruise het weiding begin verplaas met aanvullende voeding sodra die vlak van aanvullende voeding hoër as 62% (d.i. meer as 1000g aanvullende voeding/voël/dag) van die totale inname van die voëls was. Vir elke 100g toename in aanvullende voeding, word weiding verplaas teen ‘n tempo van 4.9%. Weiding, tesame met aanvullende voeding, het gelei tot hoër totale droë material (DM) voerinnames by volstruise as wanneer weiding alleen beskikbaar was. Wanneer weiding alleen voorsien was, was daar laer (P <0.05) verteerbaarhede van DM en waarskynlike metaboliseerbare energie (WME) waardes vir beide volstruise en hane as wanneer die weiding voorsien word met aanvullende voeding. Geen betekenisvolle stapsgewyse regressie kon gevind word om volstruis energie waardes uit hoender energie waardes te voorspel nie. Die ekonomie van verskillende sisteme (ekstensief versus intensief) is in hierdie studie vergelyk en is gebaseer op dieselfde materiaal en metodes en resultate van die eerste weidingsstudie. ‘n Marge bo voerkoste analise is gebruik om die ekonomiese lewensvatbaarheid van die sisteme met mekaar te vergelyk. Die huidige waarde van die marge bo voerkoste van die weidingssisteem waar 1000g aanvullende voeding gevoer word was 8.3% laer as dié van die voerkraal sisteem oor ‘n periode van ses jaar. Daarteenoor was die huidige waarde van die koste van dieselfde weidingssisteem 78.4% laer as dié van die voerkraal sisteem. Die weidingssisteem waar volstruise 1000g aanvullende voeding ontvang het, het ‘n besparing van 57% in voerkoste getoon wanneer dit met die voerkraal volstruise vergelyk is. ‘n Sensitiwiteitsanalise van die marge bo voerkoste het getoon dat die weidingssisteem minder sensitief is vir wisselende voerkoste as die voerkraal sisteem. Die unieke omstandighede van elke produsent sal ‘n rol speel in sy keuse om volstruise op weiding of in ‘n voerkraal af te rond.