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Citation of this paper

Effects of dietary protein levels on performance of African catfish Clarias gariepinus in fertilized and unfertilized earthen ponds

J M Mwangi, J G Maina and C K Gachuiri

University of Nairobi, Department of Animal Production, P O Box 29053-00625, Nairobi, Kenya.
jackson.muchiri85@gmail.com

Abstract

The recommended protein levels in catfish diets aim to maximize growth with little regard to production costs. A study was done in Kirinyaga County, Kenya to evaluate the effects of dietary protein levels on performance of C. gariepinus in fertilized and unfertilized earthen ponds. Two earthen ponds, one fertilized with chicken manure and the other unfertilized, were stocked with C gariepinus fingerlings weighing 3.29±0.329 g, in 2m 2 happas at 10 fish/m2. Four iso-caloric diets (3000 kcal/kg) with varying levels of rice milling byproducts and containing protein levels of 25%, 30%, 35% and a control diet (no rice byproducts and 35%CP) were formulated. The control diet and 25%, 30% and 35% protein level diets cost, 47.8, 34.5, 38.3 and 42.6 KSh/kg of diet respectively. All diets were fed to the fish in triplicate happas for 128 days. The parameters that were monitored were growth, survival, feed utilization and water quality. The average dissolved oxygen content and weight gains of fish in the fertilized pond was higher than the unfertilized pond. The fish fed the diet containing 25% CP had the highest protein efficiency ratio (2.18) in the fertilized pond. The study concluded that the fish fed the low cost 25% CP diet in the fertilized pond had performance parameters close to those fed the other diets and is therefore suitable for C. gariepinus culture in fertilized earthen ponds when considering the production cost.

Key words: cost, growth, production, rice byproducts, water quality


Introduction

Protein content of diets is usually the major consideration during feed formulation due to its nutritional importance and relatively high cost followed by the energy level (Craig and Helfrich 2002; Munguti et al 2012). A standard dietary crude protein level recommendation for African Catfish Clarias gariepinus has not been established. The National Research Council (1993) has established a standard dietary protein requirement for Channel catfish Ictalurus punctatus ranging between 32-36%. These levels have been determined using young fish under optimum environmental and other conditions and are formulated with the objective of maximizing growth with inadequate consideration given to production costs or profit maximization (Parker 2002). The protein levels have also been determined under intensive production systems. As such, there is need to evaluate the performance of C. gariepinus under varying dietary protein content to assess growth and the economics of production in lower level production systems where the ponds are fertilized and water is static.

Clarias gariepinus is an omnivorous fish which has relatively better utilization of high protein than high carbohydrate diets (FAO 2015). This is a challenge to its sustainable culture as the protein fraction of the diet is more expensive compared to carbohydrates (Munguti et al 2012). In this study, rice milling byproducts, which are abundant in the study site in Kirinyaga County (Government of Kenya 2009), were incorporated as cheap sources of energy.

A major challenge encountered in the culture of fish in ponds is the poor water quality (de Graaf and Janssen 1996) resulting from decomposing left over feeds and fecal material which release ammonia from protein decomposition (Parker 2002). Pond fertilization has been used to increase the natural food for the fish and improve pond water quality; it results in growth of algae which increase dissolved oxygen concentration in the pond water during photosynthesis and also assimilate ammonia (Knud-Hansen 1998). Several studies have shown beneficial effects of fertilization in tilapia ponds (Liti et al 2002; Muendo et al 2006, Sorphea 2010; Zahid et al 2013). Studies on effects of pond fertilization for Clarias gariepinus raised in ponds are inadequate (Bok and Jongbloed 1984; Mosha 2015).

The overall objective of this study was to investigate the effects of dietary protein levels on performance of C. gariepinus cultured in fertilized and unfertilized earthen ponds and fed diets based on rice milling byproducts.


Materials and methods

Study site

This study was carried out from 15th February, 2014 to 3 rd July, 2014 at the National Aquaculture Research Development and Training Center, located in Kirinyaga County, Kenya. It is 104 km NE of Nairobi at 0° 39’ S and 37° 12’ E and at an altitude of 1230 meters above sea level.

Experimental diets and design

Rice bran was purchased from a large scale rice miller in Kirinyaga County while other feed ingredients were purchased from suppliers in Nairobi. The raw materials were analyzed for nutrient content at the University of Nairobi, Department of Animal production, before inclusion in fish diets. The analysis of the feed ingredients for DM, CP, EE, CF and ash was done according to the procedures outlined by the Association of Official Analytical Chemists (AOAC 1998) prior to the diet formulations. Four iso-caloric diets (3000 kcal/kg) having protein levels of 35% (Diet 1: control), 25% (Diet 2: Low Protein), 30% (Diet 3: Medium protein), and 35% (Diet 4: High protein) were formulated and used in this study. All diets except Diet 1 (control) contained rice milling byproducts. Other ingredients included maize, wheat pollard, soybean meal and freshwater shrimp (Caridina nilotica) meal as shown in Table 1. The fish were stocked at 10 fish/m2 in happas measuring 2 X 1 m each, placed in two earthen ponds, one fertilized and the other unfertilized, each measuring 150 m2. Each of the four diets was fed to three groups of fish in each pond for a period of 128 days.

Table 1. Composition of the African catfish, Clarias gariepinus (Burchell 1822) diets used in the study

Ingredients, %

Diets

*Control
(Diet 1)

25% CP
(Diet 2)

30% CP
(Diet 3)

35 % CP
(Diet 4)

Maize grain

22.1

10.0

10.0

10.0

Rice bran (fine)

-

20.0

20.0

20.0

Rice grain (chicken/broken rice)

-

15.8

8.54

-

Corn oil

-

4.93

2.18

-

Soybean meal, solvent extracted

15.0

15.0

15.0

15.0

Wheat pollard

10.0

10.0

10.0

10.0

Freshwater Shrimp Meal

45.7

22.0

32.2

42.5

Di-calcium Phosphate

0.20

0.13

0.10

0.10

Limestone

3.33

0.00

0.00

0.00

HCL-Lysine

0.30

0.00

0.00

0.00

DL-Methionine

0.30

0.10

0.00

0.00

Ascorbic acid

2.00

1.00

1.00

1.42

Salt

0.50

0.50

0.50

0.50

§ Vitamin-Mineral premix

0.50

0.50

0.50

0.50

Total

100

100

100

100

Calculated composition (air-dry basis)

Digestible Energy, kcal/kg

3000

3000

3000

3024

Crude Protein, %

35.0

25.0

30.0

35.0

Calcium, %

3.07

0.97

1.36

1.77

Phosphorous, %

0.62

0.50

0.55

0.59

Crude fiber, %

3.80

5.07

5.15

5.17

Lysine, %

2.68

1.55

1.49

2.33

Methionine, %

1.18

0.64

0.70

0.85

Cost/kg, KSh.

47.8

34.5

38.3

42.6

* Control contains 35% protein without inclusion of rice milling byproducts. ‡The cost of corn oil,
ascorbic acid, transport of ingredients, pelleting and packaging of the diets are not included in the total
cost of the diets because they were inflated compared to market prices due to experimental conditions.
§The vitamin-mineral premix provided the following per kg of feed: Vitamin A, 5000 IU; Vitamin D3,
1000 IU; Vitamin E, 150 IU; Vitamin K3, 3 mg; Thiamine, 10 mg; Riboflavin, 15 mg; Pyridoxine and Pyridoxamine, 7.50 mg; Cyanocobalamin, 0.025 mg; Niacin, 100 mg; Pantothenic acid, 27.5 mg; Biotin, 0.50 mg; Folic acid, 3 mg; Choline, 500 mg; Vitamin C, 300 mg; Manganese, 75 mg; Iron, 20 mg; Zinc, 22.5 mg; Copper, 2.50 mg; Cobalt, 0.10 mg; Iodine, 0.70 mg; Selenium, 0.06 mg.

Management of fish

Mixed-sex Clarias gariepinus fingerlings (average weight 1.4± 0.06 g) were bought from Jambo fish farm in Kiambu County in Kenya and transported to the study site. They were acclimatized to pond conditions for a week and during this time, they were fed on the control diet (Diet 1). At the end of the week, the fish (average weight 3.29± 0.329g ) were weighed in groups of 20 fish picked at random and randomly allocated to 12 happas in each of the two ponds which constituted two blocks. The ponds were limed with agricultural lime at the rate of 2,500 kg/ha (Boyd and Massaut 1999; Ngugi et al 2007) two weeks prior to stocking. The fish were fed on the respective diets thrice a day as recommended by Aderolu et al (2010) to reduce cannibalism. This was done at 10% of their body weight when the fish (weighing 1.4± 0.06 g) were bought and was reduced to 3% of their body weight when the fish attained a weight of approximately 36 g. This was according to guidelines by Hogendoorn et al (1983), Hecht et al (1988) and de Graaf and Janssen (1996). The amount of feed was adjusted every two weeks after weighing the fish and was increased as the fish body weight increased.

One pond was fertilized with chicken manure two weeks before stocking at 25 kg dry weight per 100 m˛ of pond and thereafter 3 kg dry weight per 100 m˛ of pond every 10 days (Tacon 1988) while the other pond was left unfertilized. Water quality parameters monitored weekly were: temperature, pH, Dissolved Oxygen (DO), ammonia, nitrates, nitrites, Total Dissolved Solids (TDS), salinity and Electrical Conductivity (EC). The temperature was measured using a thermometer, DO using an oxygen probe, while pH was measured using a pH meter. Ammonia, nitrates, and nitrites were measured using kits manufactured by Colombo Aquatest kits. The TDS, salinity and EC were measured using a multi-parameter probe (HI 98282.2) manufactured by Hanna Instruments.

Data collection and analysis

The weight and length of all the fish were measured in two week intervals in order to adjust the feeding rates and to calculate the weight gain (g), Specific Growth Rate (%/day), feed intake (g), Apparent Feed Conversion Ratio, Fulton’s condition factor (Blackwell et al 2000), Protein Efficiency Ratio and Protein Intake (g). Data on performance were analyzed using two-way Analysis of Variance (ANOVA) in Genstat 13th edition. Differences between treatment means were considered significant at p<0.05 and if found to be significant they were separated using Tukey’s multiple comparison procedure. T-tests were done to compare the water quality parameters of fertilized and unfertilized ponds.


Results and discussion

Ingredient proximate components

The proximate components in the dietary ingredients are shown in Table 2. Rice milling byproducts (bran and chicken rice) were abundant in the study site and were included in the diets. Rice bran (fine) had a CP of 14.4% and CF of 10% which were higher than the CP of 11.9% and 10.8% and CF of 9.1% and 8.32% reported by Njuguna (2007) and Maina et al (2013) respectively in Kenya. However, the CP content was within the range of 13.8-15.4% reported in Uruguay (Gallinger et al 2004) but the CF was higher than that reported (7.4-8.3%) in that study. This is acceptable according to the definition of rice bran by Tacon et al (2009) who stated that it should contain a CF level of less than 13%. Chicken/broken rice, which consists of particles of rice grains that break during the milling process, had a CP of 7.87% which is close to 7.1% reported by Chau Thi Da (2012) in Vietnam.

Table 2. Proximate components (%) of feed ingredients (Dry matter basis)

Feed ingredients

DM

CP

Ether
extract

Ash

CF

Maize grain

90

7.61

0.58

0.98

13.1

Rice bran (fine)

90.2

14.4

1.07

12.3

10

Rice grain (chicken/broken rice)

88.4

7.87

0.77

2.00

6.45

Soybean meal

87.5

45.6

0.58

8.69

11.1

Wheat pollard

90.1

15.5

0.38

4.29

8.26

Freshwater Shrimp Meal

86.2

59.6

0.50

21.3

13.6

Effects of dietary protein levels and pond fertilization on performance of Clarias gariepinus

The effects of protein levels and pond fertilization on various performance indices of Clarias gariepinus were analyzed. For all the parameters, there were no interactions between dietary protein levels and pond fertilization. The weight gain per day of the fish is shown in Figure 1.

Effects of dietary protein levels on performance of Clarias gariepinus

The effects of dietary protein levels on performance of C gariepinus are shown in Table 3. The final weight, weight gain, and Specific Growth Rate (SGR) of the fish increased with increasing protein levels. Several authors, Machiels and Henken (1985), Degani et al (1989), Ali and Jauncey (2005) and Ahmad (2008) also reported that growth of C gariepinus increased with increasing dietary protein levels. The Apparent Feed Conversion Ratio (AFCR) also improved with increasing dietary protein level. This was attributed to the fact that C. gariepinus utilizes high protein diets better than high carbohydrate diets (FAO 2015).

The Protein Efficiency Ratio (PER) of the fish decreased with increasing dietary protein levels. This is because the efficiency of utilization of protein decreases with increase in Protein Intake (Ahmad 2008; Schuchardt et al 2008).

Fish fed the low protein diet (25% CP, with rice milling byproducts) had the lowest final weight, weight gain and SGR but these parameters were not different from those of fish fed control (35% CP, without rice milling byproducts).

Figure 1. Average weight gain per day of Clarias gariepinus fingerlings fed varying
protein level diets in fertilized and unfertilized earthen ponds


Table 3. Effects of dietary protein levels onClarias gariepinus performance

Parameters/fish

Protein level

SEM

p

LP

MP

HP

Initial weight, g

3.59

3.01

3.53

0.232

0.192

Final weight, g

200a

250ab

260b

12.8

0.02

Weight gain, g/d

1.54a

1.93ab

2b

0.099

0.019

* SGR, %/day

4.11a

4.30ab

4.32b

0.051

0.034

Feed intake, g

359

410

427

20.3

0.086

** AFCR

1.85ab

1.67a

1.66a

0.054

0.006

*** PI, g

89.7a

123b

150bc

6.58

<0.001

**** PER

2.18c

2.01c

1.73b

0.055

<0.001

***** K

0.75

0.77

0.77

0.010

0.417

Mortality, %

3.62

3.18

3.62

0.678

0.87

* SGR- Specific Growth Rate; ** AFCR- Apparent Feed Conversion Ratio; ***PI- Protein Intake; **** PER- Protein Efficiency Ratio; ***** K- Fulton’s condition factor; LP- Low Protein diet: MP- Medium Protein diet: HP- High Protein diet: Means with different superscripts in a row are different; Means, n= 480 t al

Effects of pond fertilization on performance of Clarias gariepinus

The effects of pond fertilization on C. gariepinus performance are shown in Table 4. Fish reared in the fertilized pond had higher final weights, weight gains and specific growth rates (259g , 1.99 g/d and 4.32%/day respectively) compared to those in the unfertilized pond (209g, 1.62 g/d and 4.15%/day respectively). Feed intake was also higher for fish in the fertilized pond (451g/fish) compared to those in the unfertilized pond (361g/fish). The performance parameters observed are comparable to those by Bok and Jongbloed (1984) and Mosha (2015) on C. gariepinus and studies on other fish species by Suresh Babu et al (2013) and Zahid et al (2013).

Table 4. Effects of pond fertilization onClarias gariepinus performance

Parameters/fish

Pond fertilization

SEM

p

Fertilized 

Unfertilized 

Initial weight, g

4.23

2.36

0.164

<0.001

Final weight, g

259

209

9.02

0.001

Weight gain, g/d

1.99

1.62

0.07

0.002

SGR, %/day

4.32

4.15

0.036

0.005

Feed intake, g

451

361

14.4

<0.001

** AFCR

1.78

1.77

0.039

0.771

***PI, g

143

114

4.65

<0.001

**** PER

1.84

1.85

0.039

0.86

***** K

0.77

0.76

0.007

0.409

Mortality, %

3.45

3.25

0.479

0.773

* SGR- Specific Growth Rate; ** AFCR- Apparent Feed Conversion Ratio; *** PI- Protein Intake; **** PER- Protein Efficiency Ratio; *****K- Fulton’s condition factor; Means, n= 480

Effects of pond fertilization on water quality of Clarias gariepinus ponds

Ammonia, nitrate and nitrite were not detected in the pond water throughout the experimental period. Pond fertilization had no effect on pond water temperature (Table 5). This was in agreement with Suresh Babu et al (2013), Zahid et al (2013) and Mosha (2015). The recommended temperature for catfish culture ranges between 20-30°C (Parker 2002; Isyagi et al 2009; Water Research Commission 2010). Water temperature is important because fish are ectotherms (Castell 2000), and all their metabolic activities are influenced by the water temperatures.

The average dissolved oxygen, pH, conductivity, salinity and total dissolved solids of the fertilized pond (2.8 mg/l, 8.08, 226 µS/cm, 0.11 mg/l and 113 ppm respectively) were higher than for the unfertilized pond (2.15 mg/l, 7.85, 124 µS/cm, 0.06 mg/l and 61.8 ppm respectively). These are in agreement with studies done by Charo-Karisa et al (2013), Suresh Babu et al (2013), Zahid et al (2013), Palm et al (2014) and Mosha (2015). The values are within the range of water quality recommendations made for fish production (Britz and Hecht 1989; Wurts and Durborow 1992; Department of Water Affairs and Forestry 1996; Parker 2002; Stone and Thomforde 2006; Weber-Scannell and Duffy 2007; Borode et al 2008; Water Research Commission 2010; Floyd 2014).

Pond fertilization increases algae growth which carry out photosynthesis during the day thus consuming carbon dioxide (in the form of carbonic acid) and releasing oxygen into the pond water (Knud-Hansen, 1998); this increases the pH and dissolved oxygen of the pond water respectively. Pond fertilization using manure also increases the total dissolved solids, salinity and electrical conductivity of the pond water due to mineralization of the manure (release of organic and inorganic compounds into the pond water).

Table 5. Water quality parameters of the fertilized and unfertilized ponds used to culture Clarias gariepinus

Parameter

Treatment
pond

Frequency

Mean

Standard
deviation

p

Temperature, °C

Fertilized

62

23.9

1.82

0.32

Unfertilized

64

23.6

1.77

Dissolved oxygen, mg/l

Fertilized

63

2.8

1.99

0.037

Unfertilized

64

2.15

1.46

pH

Fertilized

62

8.08

0.307

<0.001

Unfertilized

64

7.85

0.274

Conductivity,

µSiemens/cm

Fertilized

62

226

38.4

<0.001

Unfertilized

64

124

23

Salinity, mg/l

Fertilized

62

0.11

0.019

<0.001

Unfertilized

64

0.06

0.011

Total Dissolved Solids, ppm

Fertilized

62

113

19.3

<0.001

Unfertilized

64

61.8

11.4


Conclusions


Acknowledgements

I would like to thank the Partnerships for Enhanced Engagement in Research (PEER) Science program, funded by the National Academy of Sciences through USAID, for funding this project. I also acknowledge the National Aquaculture Research, Training and Development Centre at Sagana for providing research facilities and the University of Nairobi for providing facilities for the analytical work.


References

Aderolu A Z, Seriki B M, Apatira A L and Ajaegbo C U 2010 Effects of feeding frequency on growth, feed efficiency and economic viability of rearing African catfish (Clarias gariepinus, Burchell 1822) fingerlings and juveniles. African Journal of Food Science 4(5): 286-290.

Ahmad M H 2008 Response of African Catfish, Clarias gariepinus, to different dietary protein and lipid levels in practical diets. Journal of the World Aquaculture Society 39: 541-548.

Ali M Z and Jauncey K 2005 Approaches to optimizing dietary protein to energy ratio for African catfish Clarias gariepinus (Burchell, 1822). Aquaculture Nutrition 11: 95-101.

AOAC 1998 Official methods of analysis of AOAC International (16th ed.). AOAC, USA.

Blackwell B G, Brown M L and Willis D W 2000 Relative Weight status and current use in fisheries assessment and management. Reviews in Fisheries Science 8 (1): 1-44

Bok A H and Jongbloed H 1984 Growth and production of sharptooth catfish,Clarias gariepinus (Pisces: Clariidae), in organically fertilized ponds in the Cape Province, South Africa. Aquaculture 36: 141-155.

Borode A O, Balogun A M and Omoyeni B A 2008 Effect of salinity on embryonic development, hatchability, and growth of African Catfish, Clarias gariepinus, eggs and larvae. Journal of Applied Aquaculture 12(4): 89-93.

Boyd C E and Massaut L 1999 Risks associated with the use of chemicals in pond culture. Aquacultural engineering 20: 113-132.

Britz P J and Hecht T 1989 Effects of salinity on growth and survival of African sharptooth catfish (Clarias gariepinus) larvae. Journal of Applied Ichthyology 5(4): 194-202.

Castell J 2000 Farming the waters: Bringing aquatic plant and animal species to agriculture. Canadian Journal of Animal Science 80: 235-243.

Charo-Karisa H, Opiyo M A, Munguti J M, Marijani E and Nzayisenga L 2013 Cost- benefit analysis and growth effects of pelleted and unpelleted on-farm feed on African catfish (Clarias gariepinus Burchell 1822) in earthen ponds. African Journal of Food, Agriculture, Nutrition and Development 13(4): 8019-8033

Chau Thi Da 2012 Evaluation of locally available feed resources for Striped Catfish ( Pangasianodon hypophthalmus). PhD thesis, Uppsala, Sweden, pp 38.

Craig S and Helfrich L A 2002 Understanding fish nutrition, feeds, and feeding. Virginia- Maryland Regional College of Veterinary Medicine, Virginia Tech and Virginia Cooperative Extension, USA, pp 1-9.

De Graaf G J and Janssen J A L 1996 Artificial reproduction and pond rearing of the African catfish Clarias gariepinus in sub-Saharan Africa- A handbook. FAO Fisheries Technical paper #362, FAO, Rome, pp. 1-72 Retrieved June 3, 2015, from www.nefisco.org/downloads/Clarias.PDF

Degani G, Ben-Zvi Y and Levanon D 1989 The effect of different protein levels and temperatures on feed utilization, growth and body composition of Clarias gariepinus (Burchell 1822). Aquaculture 76: 293-301.

Department of Water Affairs and Forestry 1996 South African Water quality guidelines (2nd ed.), Volume 1: Domestic use. Department of Water Affairs and Forestry, South Africa, pp 1-170.

FAO 2015 Cultured aquatic species information programme: Clarias gariepinus (Burchell, 1822). FAO, Rome. Retrieved June 22, 2015, from http://www.fao.org/fishery/culturedspecies/Clarias_gariepinus/en

Floyd R F 2014 Dissolved oxygen for fish production. University of Florida, USA, pp 1-3 Retrieved October 22, 2016, from http://edis.ifas.ufl.edu/fa002

Gallinger C I, Suárez D M and Irazusta A 2004 Effects of rice bran inclusion on performance and bone mineralization in broiler chicks. The Journal of Applied Poultry Research 13: 183-190.

Government of Kenya 2009 National rice development strategy plan (2008- 2018). Ministry of Agriculture, Kenya, pp 4.

Hecht T, Uys W and Britz P J, eds 1988 The culture of sharptooth catfish,Clarias gariepinus in Southern Africa. South African National Scientific programmes report # 153, Council for Scientific and Industrial Research, Pretoria, pp 133.

Heuze’ V and Tran G 2015 Rice bran and other rice byproducts . Feedipedia, a programme by INRA, CIRAD, AFZ and FAO. Retrieved May 11, 2015, from http://www.feedipedia.org/node/750

Hogendoorn H, Jansen J A J, Koops W J, Machiels M A M, van Ewijk P H and van Hees J P 1983 Growth and production of the African catfish, Clarias lazera (C & V). II Effects of body weight, temperature and feeding level in intensive tank culture. Aquaculture 34(3/4): 265-285.

Isyagi N A, Veverica K L, Asiimwe R and Daniels W H 2009 Manual for the commercial pond production of the African catfish in Uganda.Walimi Fish Co-op Society ltd , Uganda, pp 70-119.

Knud-Hansen C F 1998 Pond fertilization: Ecological approach and practical application. Aquaculture Collaborative Research Support Program, Oregon State University, USA, pp 1-50.

Liti D M, Mac'were O E and Veverica K L 2002 Growth performance and economic benefits of Oreochromis niloticus/Clarias gariepinus polyculture fed on three supplementary feeds in fertilized tropical ponds. Ninth Work Plan, Feeds and Fertilizers Research 2 (9FFR2). Final Report In: K McElwee, K Lewis, M Nidiffer and P Buitrago (Eds.), Nineteenth Annual Technical Report. Pond Dynamics/Aquaculture CRSP, Oregon State University, Corvallis, Oregon, USA, pp 11-16.

Machiels M A M and Henken A M 1985 Growth rate, feed utilization and energy metabolism of the African catfish, Clarias gariepinus (Burchell, 1822), as affected by dietary protein and energy content. Aquaculture 44: 271-284.

Maina J G, Kamau W N and Kabuage L W 2013 Evaluation of high levels of rice milling byproducts in chicken layer diets: effects on layer performance, egg quality and economic returns. Livestock Research for Rural Development, Volume 25, Article #7 Retrieved September 20, 2015, from http://www.lrrd.org/lrrd25/7/main25119.htm

Mosha S S 2015 Effect of organic and inorganic fertilizers on natural food composition and performance of African catfish (Clarias gariepinus) fry produced under artificial propagation. MSc Thesis, Tanzania, pp 31-36.

Muendo P N, Milstein A, Van dam A A, Gamal E N, Stoorvogel J J and Verdegem M C J 2006 Exploring the trophic structure in organically fertilized and feed-driven tilapia culture environments using multivariate analyses. Aquaculture Research 37: 151-163.

Munguti J, Charo-Karisa H , Opiyo M A, Ogello E O, Marijani E, Nzayisenga L and Liti D 2012 Nutritive value and availability of commonly used feed ingredients for farmed Nile tilapia (Oreochromis niloticus L.) And African catfish (Clarias gariepinus, Burchell) In Kenya, Rwanda And Tanzania. African Journal of Food, Agriculture, Nutrition and Development 12(3): 6135-6155.

National Research Council 1993 Nutrient requirements of fish. National Academies Press, Washington D C, USA, pp 1-56.

Ngugi C C, Bowman J R and Omolo B O 2007 A new guide to fish farming in Kenya. USAID, USA, pp 34-48.

Njuguna K W 2007 Evaluation of rice milling byproducts from Mwea irrigation scheme in layer chicken diets. MSc. Thesis, University of Nairobi, Kenya, pp. 1-91.

Palm H W, Bissa K and Knaus U 2014 Significant factors affecting the economic sustainability of closed aquaponic systems. Part II: Fish and plant growth. Aquaculture, Aquarium, Conservation and Legislation International Journal of the Bioflux Society 7(3): 162-175.

Parker R 2002 Aquaculture Science (2nd ed.). Delmar, Thomson Learning, USA, pp 233-367.

Schuchardt D, Vergara J M, Fernandez-Palacios H, Kalinowski C T, Hernandez-Cruz C M, Izquierdo M S and Robaina L 2008 Effects of different dietary protein and lipid levels on growth, feed utilization and body composition of red porgy (Pagrus pagrus) fingerlings. Aquaculture Nutrition 14: 1-9.

Sorphea S 2010 Effect of stocking density and fertilization on the growth performance of tilapia (Oreochromis spp.) fed rice bran, water spinach and duckweed in pond and paddy field (pp. 10). MSc thesis.

Stone N M and Thomforde H K 2006 Understanding your fish pond water analysis report. Cooperative extension program, University of Arkansas, USA, pp 1-3.

Suresh Babu C H, Shailender M and V 2013 Effect of fertilization and artificial feed on the growth, condition factor and proximate composition of Indian major carp, Catla catla (Hamilton). International Journal of Research in Fisheries and Aquaculture 3(3): 57-62.

Tacon A G J 1988 The nutrition and feeding of farmed fish and shrimp- A training manual. FAO, Italy.

Tacon A G J, Metian M, Hasan M R 2009 Feed ingredients and fertilizers for farmed aquatic animals: sources and composition, FAO Fisheries and Aquaculture Technical Paper #540. FAO, Rome, pp 1-11.

Water Research Commission 2010 A manual for rural freshwater aquaculture. Department of Agriculture, Forestry and Fisheries, South Africa, pp 8-46.

Weber-Scannell P K and Duffy L K 2007 Effects of total dissolved solids on aquatic organisms: A review of literature and recommendation for Salmonid species. American Journal of Environmental Sciences 3(1): 1-6.

Wurts W A and Durborow R M 1992 Interactions of pH, carbon dioxide, alkalinity and hardness in fishponds. Southern Regional Aquaculture Center, USA, Publication #464, pp 1.

Zahid A, Khan N, Nasir M and Ali M W 2013 Effect of artificial feed and fertilization of ponds on growth and body composition of genetically improved farmed Tilapia. Pakistan Journal of Zoology 45(3): 667-671.


Received 17 January 2018; Accepted 14 February 2018; Published 1 March 2018

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