ABSTRACT
The study was conducted to investigate the effect of replacing soya bean meal with soya bean offal meal in the diet of Nile tilapia O. niloticus fingerlings and to determine its growth performance. Fifteen (15) plastic rearing tanks (30cm x 45cm x 35cm depth) were used for the experiment. Plastic rearing tanks were randomly assigned in three replicates to five treatments. Three hundreds (300) fingerlings of O. niloticus of mixed sexes and sizes of initial mean weight of (6.0±2.04a g) were stocked in fifteen (15) white rectangular plastic tanks of water holding capacity of 50 litres (30cm x 45cm and 35cm depth) with twenty (20) fingerlings per tank and water maintained at 40 litres level for a period of twelve (12) weeks. Soya bean Offal meal (SBOFFM) was used to replace Soya bean meal (SBM) at inclusion levels of 0%, 25%, 50%, 75% and 100% for Diet 1 to 5 respectively. T1- 24.82±0.72b CP, T2- 25.34±1.93a CP, T3- 24.75±1.01b CP, T4- 24.21± 0.43b CP and T5- 25.12±0.70a CP. Total growing period was 97 days (14 days of acclimatization and 83 days of feeding). The results obtained showed T2 (25.34±1.93a) (25%) inclusion Soya bean Offal had the highest Mean Weight Gain (MWG) of (21.97±4.29a g), Mean Length Gain (MLG) of (1.76±0.23a cm), Protein Efficiency Ratio (PER) of 0.867±0.5a g, Net Protein Utilization (NPU) of 150.35± 0.2a %, Feed Efficiency Ratio (FER) of 1.89±0.4a, Gross Feed Conversion Efficiency (GFCE) of 200.00±0.4a and crude protein of O. niltocus carcass (38.1±0.20a g/100g DM). Feed Conversion Ratio (FCR) and Specific Growth Rate showed no significant difference (P≥0.05). Also, pH (1-12), Temperature (T°C), Dissolved Oxygen (DO) (mg/l), Electrical Conductivity (µ/S), and Total Dissolve Solute (TDS) (mg/l) showed no significant difference (P ≥0.05). The study results demonstrate that soybean offal meal could replace the soya bean meal in the diet of Nile tilapia without negative effects on growth, or on total production and even leading to high net economic returns as shown in the diets with 25% CP crude protein from plant source.
TABLE OF CONTENTS
Cover Page i
Title Page ii
Declaration iii
Certification iv
Dedication v
Acknowledgments vi
Abstract vii
Table of Contents ix
List of Tables xiii
List of Figure xiv
List of Appendices xv
CHAPTER ONE 1
1.0 INTRODUCTION 1
1.1 Background of the study 1
1.2 Statement of the Research Problem 2
1.3 Justification 3
1.4 Aim 4
1.5 Objectives 4
1.6 Hypotheses 5
CHAPTER TWO 6
2.0 LITERATURE REVIEW 6
2.1 Non- conventional Feed Ingredients used in Tilapia Diets 6
2.2 Products of Plant Origin 9
2.3 Anti-nutritional Factors Present in the Soya bean Seed 9
2.4 Feeding Habits of Nile Tilapia 10
2.5 Economic Importance of Soya bean (Glycine max. Linn.) 15
2.6 Growth and Nutrient Utilisation of Nile Tilapia 16
2.7 Distribution of Nile Tilapia 17
2.8 The Biology and Ecology of Nile Tilapia 17
2.9 Physico – Chemical Parameters within the Plastic Rearing Tanks 19
CHAPTER THREE 20
3.0 MATERIALS AND METHODS 20
3.1 Proximate Analysis of the Feed 20
3.1.1 Determination of the Moisture Content 20
3.1.2 Determination of Ash Content 21
3.1.3 Determination of Crude Lipid Content 21
3.1.4 Determination of Crude Protein 22
3.1.5 Determination of Carbohydrates 23
3.1.6 Determination of Crude Fibre Content 23
3.2 Anti-nutritional analysis of the experimental feed 24
3.2.1 Determination of oxalate 24
3.2.2 Determination of Tannin 25
3.2.3 Determination of Saponin 26
3.2.4 Determination of phytate 26
3.2.5 Determination of Trypsin Inhibitor (Ti) 27
3.2.6 Determination of Cyanogenic Glycosides 28
3.3 Determination of Growth Performance Parameters 29
3.3.2 Percentage Live Weight Gain (LWG%) 29
3.3.3 Specific Growth Rate (SGR) 29
3.3.4 Feed Conversion Ratio (FCR) 30
3.3.5 Gross Food Conversion Efficiency (GFCE) 30
3.3.6 Feed Efficiency (FER) 30
3.3.7 Protein Efficiency Ratio (PER) 30
3.3.8 Apparent Net Protein Utilization (AP1>NPU) 30
3.3.9 Net Protein Utilization (NPU) 30
3.3.10 Productive Protein Value (PPV) 31
3.3.11 Nitrogen Metabolism (Nm) 31
3.3.12 Standard Length Gain 31
3.3.13 Standard Length Gain Percentage 32
3.4 Experimental site 32
3.5 Experimental Design 32
3.6 Experimental feedstuffs 33
3.7 Processing of Feed Ingredients 33
3.8 Feed Formulation 34
3.8.1 Dry and Wet mixing of ingredients 34
3.8.2 Procedures for pelleting of diets 36
3.9 Feeding the Fingerlings 36
3.10 Experimental Set-up 36
3.11 Economic Analyses of Experimental Diets 37
3.12 Monitoring of Physico-Chemical Parameters in the Tanks 37
3.13 Data Analysis 38
CHAPTER FOUR 39
4.0 RESULTS 39
4.1 Proximate Composition of Soya bean offal and Soya bean Meal 39
4.2 Anti-nutritional Factors in Soyabean offal and soya bean meal 39
4.3 Proximate composition of the Experimental diets (g/100g DM) 43
4.5 Carcass Composition of O. niloticus (g/100g DM) 47
4.6 Physico-chemical Parameters of water Monitored in the experimental tanks 47
4.7 Cost and quantity of feed ingredients used in formulating diets 50
4.8 Cost effectiveness of formulated feed 50
CHAPTER FIVE 53
5.0 DISCUSSION 53
5.1 The Proximate and Anti-nutritional Composition of Soya bean and Soya bean offal Meal 53
CHAPTER SIX 60
6.1 SUMMARY, CONCLUSIONS AND RECOMMENDATIONS 60
6.2 SUMMARY 60
6.4 RECOMMENDATIONS 62
REFERENCES 63
APPENDICES 73
LIST OF TABLES
Tables Titles Pages
Table 3. 1: Composition of Experimental Diets used for the feeding Trial 35
Table 4. 1 : Proximate Composition of Soya bean offal Meal and Soya bean Meal 41
Table 4. 2 : Anti-nutritional Factors (mg/g) of Soya bean Offal and Soya bean Meal 42
Table 4. 3 : Proximate Composition of Experimental Diets Fed to Oreochromis niloticus (g/100g DM) 45
Table 4. 4 : Growth Rate and Feed Utilization of O. niloticus Fed at Different Inclusion Levels 46
Table 4. 5 : Carcass Composition of O. niloticus after the experiment ( g/100g DM) 48
Table 4. 6 : Cost effectiveness of feed formulation 52
LIST OF FIGURE
Figure 4.1: Cost and quantity of Feed ingredients used in Formulating of diets for O.niloticus 51
LIST OF APPENDICES
Appendix I : Soya bean plant (Glycine max,Linn) 73
Appendix II : Soya bean seed (Glycine max, Linn) 73
Appendix III : Soya bean offal meal (Glycine max linn). 74
Appendix IV : Pelleted Fish feed Formulated with Soya bean offal Meal 74
Appendix V : Cross section of experimental set-up 75
Appendix VI : Lateral view of O.niloticus after the experiment 75
CHAPTER ONE
1.0 INTRODUCTION
1.1 Background of the study
As aquaculture production becomes more and more intensive in Nigeria, fish feed could be a significant factor in increasing the productivity and profitability of aquaculture as it accounts for at least 60 percent of the cost of fish production (Jamiu and Ayinla, 2003).The need to intensify the culture of the fish, so as to meet the ever increasing demand for fish has made it essential to develop suitable diets either in supplementary forms for ponds or as complete feed in tanks (Olukunle, 2006). For the purpose of nutritional and economic benefits, previous researchers have made attempts at increasing the use of non-conventional plant and animal materials to replace conventional feed ingredients like maize and fish meal in fish feed ration. Nigeria is the second largest producer of farm-raised tilapia in Africa, after Egypt (Fagbenro et al., 2010), however, her contribution to global output is just a meager 28,950 metric tons. One of the greatest advantage of tilapia for aquaculture is that they feed on a low trophic level. The members of the genus Oreochromis are all herbivorous, feeding on algae, aquatic plants, and other, detrital material (Agbo et al., 2015).
Supplemental diets are usually much less expensive than complete diets and usually high in carbohydrates as well as increasing productivity (Abu et.al., 2010). Tilapia exhibit their best growth rates when they are fed a balanced diet that provides a proper mixture of protein, carbohydrates, lipids, vitamins, mineral and fibre. Krome et.al. (2016) provided excellent reviews that examined the details of tilapia nutrition. The nutritional requirements are slightly different for each species and more importantly vary with life stages. Fry and fingerlings require a diet higher in protein, lipids, vitamins and minerals and lower in carbohydrates as they are developing muscle, internal organs and bone with rapid growth. Sub-adult fish need more calories from fat and carbohydrates for basal metabolism and a smaller percentage of protein for growth. Adult fish need even less protein, however the amino acids that make up that protein need to be available (Agbo et al., 2015). Corn, wheat, rice and a number of agricultural products are typical carbohydrate sources (Agbo et al., 2015). The ratio of energy, lipids and carbohydrates to the proteins available in the diet are often critical measures. Ng and Romano (2013) provided a comprehensive review of carbohydrate and fiber utilization in tilapia. Vitamins and minerals are critical to proper nutrition in tilapia and considerable research has been conducted to determine these requirements (Agbo et al., 2015). Specific nutritional needs vary with species, age of fish, production system, and salinity. According to FAO (2006), fish supplies from capture fisheries will therefore, not be able to meet the growing global demand for aquatic food. There is need for a viable alternative fish production system that can sufficiently meet this demand, and aquaculture fits exactly into this role (Abu et al., 2010). Precocious breeding and high cost of feed are among the militating factors to tilapia production. Although, there has been breakthrough in checking the precocious breeding of tilapia through genetically modified parent stock and administration of Methyl-testosterone (MT) feed, availability of cost effective and highly potent feed still remains a major constraint to tilapia culture.
1.2 Statement of the Research Problem
Fish feed account for about 60% of recurrent cost of aquaculture operation (Eyo, 2013). Expensive feeds could negatively affect the profitability of fish farming through incapacitating the expansion of farms to increase production and consequently, low yield in term of quality and quantity of fishes (Gabriel et al., 2007). Aquaculture has traditionally relied on products from industrial fisheries; namely fish meal and oil which are most expensive global resource. The global fish meal price has increased more than two fold in recent years (FAO, 2013). In Asia alone, the production of fish feed increased from 40% in 2000 to 60% in 2008 while the fish meal consumption for tilapia increased from 0.8 million tons to 1.7 million tons during same period (Tacon and Metian, 2015). Despite the increase in fish feed prices, the farm gate prices of aquaculture products have remained static, literally impinging on the economic viability of thousands of small-scale producers that form the backbone of the aquaculture sector (Rana, 2009). Indeed, the increasing price of feed ingredients (fish meal, fish oil and cereal), energy and transportation costs have complicated the availability of aqua-feeds to many fish farmers worldwide. This global phenomenon could influence small-scale producers to change businesses and/or result to poverty, vulnerability and loss of livelihood especially in developing countries (Rana, 2009). Fish feeds account for the highest operational costs in aquaculture with protein being the most expensive diet (Munguti et al., 2012). Fish Meal (FM) is the most expensive protein source in aquaculture feeds (Amaya et al., 2007). Fish require high proportion of protein in their diet because they metabolize protein as energy source (Aladetohun and Sogbesan, 2013).The development of commercial aqua-feeds has been traditionally based on fish meal as the main protein source with high protein content and balanced Essential Amino Acid (EAA) profile (Agbo et al.,2015).
1.3 Justification
The need to increase food production for the ever-increasing population of people in the world including Nigeria cannot be over emphasized. To solve these problems there is the need to exploit any available food resources. The most important food content that promotes growth and good health is protein. Sources of protein readily available apart from poultry are fish and plant proteins resources. Since fish feed account for 60% of recurrent cost of aquaculture operation, therefore this research may reduce the economic burden to the aquaculturist through finding °cheap and available protein supplement (Omeru and Solomon, 2016). The efficiency of production and growth of fish in the cultural system depends on feeding complete feed at levels not exceeding the dietary requirement of the fish (Krome et al. 2014) .The choice of O .niloticus among other fish species was due to availability of the species in almost all freshwater bodies in Nigeria and also it is among the commonest accepted fish in our local markets. Nile tilapia is highly culturable of a high fecundity, which make it breed even in captivity (FAO, 2013). Oreochromis niloticus is highly palatable. Nile tilapia is among few fish species that are cultured by many aqua-culturists, this is because it is disease resistant, could be cultured in small water bodies and is a good converter of feeds (FAO, 2013).
1.4 Aim
To replace the soya bean meal with soya bean offal meal in the diet of Oreochromis niloticus.
1.5 Objectives
i. To determine the proximate and anti-nutritional composition of soya bean offal meal.
ii. To assess the growth performance of Oreochromis niloticus fed soya bean offal meal at different inclusion levels.
iii. To determine the cost effectiveness of replacing soya bean meal with soya bean offal meal at different inclusion levels.
1.6 Hypotheses
I. There is no significant difference in the proximate and anti-nutritional composition of soya bean meal and soya bean offal meal.
II. The growth response and feed utilization of Oreochromis niloticus fed at different inclusion levels of soya bean offal meal do not differ significantly.
III. There is no significant difference in the cost effectiveness of replacing soya bean meal with soya bean offal meal.
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