Theses and Dissertations

Permanent URI for this collectionhttp://hdl.handle.net/20.500.11837/174

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Browsing Theses and Dissertations by Author "Muchenje, V."

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    Effect of Tenebrio molitor larvae as a protein source on growth performance, carcass yield and meat quality of broiler chickens.
    (University of Fort Hare, 2016) Mngqi, Sinethemba Census; Muchenje, V.
    This study was conducted to assess the effect of including Tenebrio molitor larvae (T. molitor L) as a protein source in different diets on broiler performance, carcass characteristics and meat quality. A total of 144 day-old Cobb-500 chicks were randomly allocated into three treatment groups, each was allocated 16 birds and reared in 9 identical pens. Experimental diets used were as follows: T1 Control (no T. molitor L inclusion); T2 and T3 contained levels of T. molitor L at 5% and 10% of dry matter (DM) intake, respectively. Body weights (BW), average daily gain (ADG), feed intake (FI), and Feed conversion ratio (FCR) were measured for the 1st experimental chapter. For the second experimental chapter; live weights (LW) of broilers were recorded before slaughter and thereafter carcass weights (CW), meat yield (weights of breast, thigh, drumstick and wing) were recorded. The dressing percentage (DP %) was also calculated. Breast muscles were sampled for meat pH and colour measurements. The LW of birds from T1 (0% T. molitor L) were significantly different (P<0.05) from both T2 (5% T. molitor L) and T3 (10% T. molitor L) which were similar to each other, with T2 exhibiting the highest live weights (2166g) and the control treatment exhibiting the lowest live weights (2018.3g). In CW, T1 was significantly different (P<0.05) from T2 while it was similar (P>0.05) to T3. The dressing % of T1 was significantly different (P<0.05) from T2 and T3 which were similar to each other, with T2 having the highest dressing percentage (78, 2%) and T1 having the lowest DP% (66%). The breasts in T2 were significantly higher and different (P<0.05) from both T1 and T3 which were similar to each other. The drumsticks in T3 were significantly different (P<0.05) from T1 while they were similar to T2 with values with T2 having highest values. After 45 minutes of slaughter, a significant difference (P<0.05) was observed in L⃰ among all treatments. In redness (a⃰), T3 was significantly different from T1 but was similar to T2 and all treatments in this study exhibited a darker red meat, with T3 muscles exhibiting darker red colour than the other treatments. Similar results were observed in yellowness (b⃰), where the breast muscles from T3 were more yellow than the other treatments. After 24 hours of slaughter, T2 L⃰ values were significantly different (P<0.05) from both T1 and T3 which were similar to each other. It was also found that the broiler chickens given diet with no T. molitor L inclusion (T1) had lower values of BW, FI, ADG and FCR throughout the experiment than those that were in T2 and T3 with 5% and 10 % T. molitor L inclusion levels, respectively. However, it was also found that although broilers with 5% T. molitor L inclusion (T2) in their diet had high ABW and ADG than the broilers with 10% T. molitor L inclusion (T3), the T3 birds compared favourably to T2 birds as they required low feed intake to reach the same slaughter weight due to high FCR. It was, therefore, concluded that T. molitor L meal can be incorporated into the diets of broilers to produce heavy birds either at 5 or 10%. However, although 5% T. molitor L inclusion yields heavier carcasses, the 10% T. molitor L inclusion compared favourably to 5% inclusion since it required low feed intake to reach the same slaughter weights and there were slight differences on meat quality attributes between the two treatments.Thus T. molitor L at 10% inclusion levels was the best inclusion level to enhance broiler growth performance, carcass yield, meat yield and meat quality.
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    Fatty acid composition, colour stability and lipid oxidation of mince produced from fresh and frozen/thawed fallow deer meat.
    (University of Fort Hare, 2016) Chido, Chakanya; Muchenje, V.
    The aim of the study was to determine the fatty acid composition, colour stability and lipid oxidation of fresh mince produced from fallow deer and to evaluate the effect of frozen storage duration on the retail display shelf life of the mince. A total of 31 fallow deer carcasses were used in the study. After cooling for 24hrs, the carcasses were deboned, external fat from the fore and hindquarter muscles removed and individually vacuum packed. For the first trial, seven fallow deer carcasses were used. Meat from the hind and fore-quarters of each carcass was divided into two equal batches per animal. One batch was minced (through a 5 mm die) and packed into oxygen permeable overwraps and refrigerated at 4°C for a period of eight days under retail display conditions. The second batch was vacuum packed and frozen at -20°C for 2 months at the end of which mince was also produced and monitored over an eight day period under the same conditions that were used for the fresh mince. Colour, pH, lipid and myoglobin stability was determined. Proximate and fatty acid composition was also determined. No differences (P>0.05) were noted between proximate composition of fresh and frozen/thawed minced meat. The lipid content of fallow deer was 2.4% (±0.04). Total n3 fatty acids differed (P<0.05) between treatments and decreased with increased storage and display day. There were significant (P<0.05) treatment and time interactions on all measured colour parameters, TBARS and myoglobin forms. Fresh mince was lighter and had higher redness (a*) and yellowness (b*) values than mince from two months frozen stored meat. Hue angle for fresh mince remained stable throughout display whereas it increased for frozen/thawed mince. Fresh mince had lower TBARS values than frozen/thawed mince. Minced meat produced from frozen/thawed deer meat had higher surface met-myoglobin and total met-myoglobin percentages. Surface and total oxy-myoglobin percentage was higher in fresh mince. The first trial clearly showed colour and lipid stability differences between fresh mince and mince from frozen/thawed meat. It also showed that fresh mince has a longer retail display life than mince produced from frozen/thawed meat (six days and four days, respectively). In the second trial, the effects of frozen storage duration on colour and lipid stability were investigated. Twenty-four fallow deer were used. Twelve were harvested in June (6male 6female) and the other twelve in August (6 male 6female) of the same year.Twenty four hours after harvesting, the fore and hindquarter muscles of the carcasses were deboned, vacuum packed and kept at -20°C until October (i.e. 2months and 4months frozen storage period). Upon thawing, the meat was processed into mince following the same procedure used for the first trialand displayed for a fiveday period under retail display conditions. Frozen duration and gender had no effect (P>0.05) on the proximate composition of fallow deer meat. The total amount of saturated fatty acids (SFA) increased and total amount of poly unsaturated fatty acids (PUFA) decreased as frozen duration and display day increased (P<0.05). Frozen duration affected (P<0.01) lipid oxidation and percentage oxy-myoglobin. Mince pH and all colour parameters (L*, a*, b*,hue and chroma) differed (P<0.05) between treatments on day zero and three. Display day was a significant factor (P<0.05) on all measured parameters. By day three all parameters except pH showed signs of extended oxidation and discolouration as evidenced by reduced redness, decreased colour intensity and high TBARS values. This study showed that prolonged frozen storage negatively affects the colour and lipid stability of meat and increases oxidation of PUFAs during frozen storage. However, the study also suggests that although frozen/thawed meat has a shorter retail display shelf life, the proximate composition of the meat remains unchanged.
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    Glycolytic potential and meat quality from Dorper and Merino sheep.
    (University of Fort Hare, 2015) Stempa, Thuthuzelwa; Muchenje, V.
    The objective of the study was to determine glycolytic potential and meat quality from Dorper and Merino sheep of both sexes slaughtered at a commercial abattoir. Dorper (n=52) and Merino (n= 48) breeds aged eight years, consisting of 50 intact rams and 50 non-pregnant ewes were used in the study. The sheep used in the study were reared, transported and lairised under identical conditions. Blood samples were collected at exsanguination for the measurement of glucose, lactate and cortisol levels. Samples were also collected from the Muscularis longmissius thoracis et lumborum (LTL) for the measurement glycogen, lactate levels, pH decline and colour. Correlations amongst blood stress indicators, muscle metabolites and meat quality attributes were also determined. Sex and breed had no effect on muscle glycolytic potential, glycogen and lactate levels from Dorper and Merino sheep of both sexes at the abattoir. Although sex and breed had an effect on pre-slaughter stress indicators (lactate and cortisol) collected at exsanguination. Ewes had higher levels of blood lactate (7.4 3 ± 0.49 mmol/L) and cortisol (293.92 ± 14.32 nmol/L) than the rams which had (5.19 ± 0.49 mmol/L) and (179.50 ± 14.32 nmol/L) lactate and cortisol levels, respectively. Furthermore, higher levels of lactate were observed in Dorper (7.54 ± 0.42 mmol/L) compared to the Merino sheep (4.97 ± 0.49 mmol/L). Meat pH decline and colour were also significantly affected by sex and breed. Ewes had higher levels of at pH45 minutes post slaughter iii (7.05 ± 0.04), pH3 hours (6.45 ± 0.04) , pH24 hours (6.00 ± 0.03), a* (14.31 ± 0.33) , b* (8.84 ± 0.29), H* (31.47 ± 0.73) and C* (16.75 ± 0.24) compared to the rams which had pH45 minutes (6.44 ± 0.04), pH3 hours (6.12 ± 0.04), pH24 hours (5.88 ± 0.03), a* (12.25 ± 0.33), b* (7.00 ± 0.29), H* (29.36 ± 0.73) and C* (14.15 ± 0.42) values. Moreover, Merino sheep had higher levels of L* (38.17 ± 0.48) and H* (31.59 ± 0.74) compared to the Dorper which had (36.39 ± 0.46) and (29.33 ± 0.71) L* and H* values, respectively. Blood cortisol was also positively correlated (P < 0.05) to glucose (r = 0.27), lactate (r = 0.37) but was negatively correlated (P < 0.001) to meat lightness (r = -0.44). Furthermore, blood cortisol was positively correlated (P < 0.001) to pH45 (r = 0.34), pH24 (r =0.22), meat yellowness (r = 0.24) and chroma (r = 0.37), but was negatively correlated to meat lightness (r = -0.47). Glycolytic potential was positively correlated (P < 0.001) to muscle glycogen levels (r = 0.66) and muscle lactate (r = 0.71).