Determination of Optimum Dietary Crude Protein Requirement for Maximum Growth of African Catfish (Clarias gariepinus)
Research Article
Determination of Optimum Dietary Crude Protein Requirement for Maximum Growth of African Catfish (Clarias gariepinus)
Muhammad Ramzan Ali1*, Hasina Basharat2, Aziz Ahmed1, Mubeen Fakhar1 and Aleem Khan1
1Aquaculture and Fisheries Program, National Agriculture Research Centre (NARC), Park Road, Islamabad, Pakistan; 2Department of Zoology, PMAS Arid Agriculture University, Rawalpindi, Pakistan.
Abstract | African catfish was introduced in Pakistan due to its high growth and economic importance. The feeding experiment was performed to find out the optimum level of protein in the diet of African catfish formulated from low cost locally available feed ingredients. This feeding trial was performed on African catfish in twelve fiber glass circular tanks (2000 L water capacity) for period of 12 weeks at the stocking rate of 20 fish/ tank. The experimental design was CRD with 4 treatments having 3 replicates. Four experimental diets containing different levels of crude protein (CP: 40%, 35%, 30% and 25%) levels were prepared. The final weight of fish and weight gain was improved by increasing proteins levels in feed. The fish fed with the feed containing 25% CP level showed minimum weight gain (127.69 g), and followed by feed of 30% CP level (142.4 g), 35 % CP level (168.3 g) and 40 % CP level (173.4 g); although growth parameters of fish feed of 35 and 40% CP level did not differ significantly. The results of cost benefit analysis pointed out that 35% protein level is optimum for African catfish as increasing protein levels beyond 35% increases the cost of feed without affecting the growth rate in a significant way thus reducing the net profitability. It was concluded that dietary protein requirement of African catfish ranged between 35-40% CP. For the commercial production of African catfish 35% crude protein level in the feed was optimum.
Received | March 16, 2024; Accepted | April 26, 2024; Published | June 05, 2024
*Correspondence | Muhammad Ramzan Ali, Aquaculture and Fisheries Program, National Agriculture Research Centre (NARC), Park Road, Islamabad, Pakistan; Email: dervashgill@gmail.com
Citation | Ali, M.R., H. Basharat, A. Ahmed, M. Fakhar and A. Khan. 2024. Determination of optimum dietary crude protein requirement for maximum growth of African catfish (Clarias gariepinus). Sarhad Journal of Agriculture, 40(2): 595-602.
DOI | https://dx.doi.org/10.17582/journal.sja/2024/40.2.595.602
Keywords | Clarias gariepinus, Feeding levels, Feed efficiency, Specific growth rate, Feed conversion ratio
Copyright: 2024 by the authors. Licensee ResearchersLinks Ltd, England, UK.
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Introduction
The aquaculture system of Pakistan is mainly extensive and in some areas are semi-intensive having low stocking density, culture of low value fish species and low per unit fish production (2.5 ton per ha). It is high time to move towards intensive aquaculture by introducing high value fish species with high growth and export potential. The African catfish was a potential candidate as it can be stocked at higher densities, can attain maximum weight of 16-40 tons/ha. In addition, they have high consumer preference due to fewer bones, good meat, adaptability to wide range of environmental conditions and disease resistance. The African catfish introduced in Pakistan due to its rapid growth (reaching market size of 1 kg in 5-6 months) and flesh with very few spines.
Fish requires sufficient food supply in the precise proportions and with proper nutritional contents for growth, energy, reproduction, movement and other activities (Umaru et al., 2016). In this scenario, formulation of fish feed is of significance as 40-50% of the production costs is represented by this input (Steven and Louis, 2009).
Fish requires sufficient food supply with proper nutritional contents for growth, energy, reproduction, movement and other activities (Umaru et al., 2016). Fish needs maximum level of protein in the diet for better growth performance when compared with other cultured animals and this makes fish feed very expensive. African catfish is omnivore that feeds on fish, invertebrates, reptiles and amphibians (Kadye and Booth, 2012). Commercial feed is usually comprised of expensive and high-quality proteins and in addition, its processing, packaging and transport contributes towards its higher costs. One of the main operational expenditures for the Channel catfish and African catfish farming is the cost of feed (FAO, 2012). The precise knowledge on the protein requirement of fish is therefore important for any aquaculture initiative as high-priced protein ingredients are usually needed in greater amounts for the majority of fish species (NRC, 1993).
Since African catfish requires major portion of protein in feed so, there is need to find out the optimum level of protein in its diet with replacement of low cost locally available feed ingredients. Keeping in view the above facts present study was conducted to determine optimum dietary crude protein requirement for maximum growth of C. gariepinus.
Materials and Methods
The experiment was performed at Aquaculture and Fisheries, National Agricultural Research Centre, Islamabad. This feeding trial was performed on C. gariepinus in twelve fiber glass circular tanks (2000 L water capacity) for period of 12 weeks at the stocking rate of 20 fish/ tank. The experimental design was CRD with 4 treatments having 3 replicates.
Four experimental diets containing different levels of crude protein (CP: 40%, 35%, 30% and 25%) were prepared. The composition and proximate analysis of feeds is shown in Table 1. The fish was fed at the rate of 5% wet fish body weight for four times a day.
Table 1: The composition and proximate analysis of diet used for African catfish in circular tanks.
Feed ingredients |
25% CP |
30% CP |
35% CP |
40% CP |
Fish meal |
30 |
30 |
30 |
30 |
Soybean meal |
2 |
13 |
20 |
25 |
Sunflower meal |
5 |
5 |
5 |
5 |
Canola seed meal |
5 |
5 |
5 |
5 |
Rice Polish |
27 |
17 |
10 |
8 |
Gluten 30% |
5 |
13 |
10 |
0 |
Gluten 60% |
0 |
0 |
6 |
17 |
Wheat bran |
22 |
13 |
10 |
6 |
Vitamin C |
0.5 |
0.5 |
0.5 |
0.5 |
Soybean oil |
2 |
2 |
2 |
2 |
Vitamin premixes |
1.5 |
1.5 |
1.5 |
1.5 |
Total |
100 |
100 |
100 |
100 |
Proximate analysis |
||||
Dry matter |
90.2 |
89.98 |
92.5 |
89.82 |
Crude fat |
2.69 |
3.10 |
3.60 |
4.05 |
Crude protein |
23.94 |
29.84 |
33.68 |
39.25 |
Total ash |
9.14 |
10.4 |
8.56 |
7.33 |
Crude fiber |
14.68 |
12.94 |
15.94 |
13.25 |
At end the experiments, all fish were caught with nets, total fish were counted and final weight were recorded. The growth parameters i.e., Weight gain, Percent weight gain, Feed efficiency, Specific growth rate (SGR), Protein Efficiency Ratio (PER), Feed Conversion Ratio (FCR) and Survival Rate was calculated by following formulae:
Weight Gain = Mean final weight of fish – Mean initial weight of fish
Percent Weight Gain= final weight of fish – initial weight of fish/ Initial weight × 100
Protein Efficiency ratio = Weight gain(g)/Protein fed (g)
Feed Efficiency = (Wt. gain/feed offered × 100)
Food Conversion Ratio = (Feed offered/Weight gain)
Specific Growth Rate (SGR) = {[(ln Wf – ln Wi) × 100]/days}.
Wf: final weight, Wi: initial weight
Survival rate = Total number of fish harvested/ Total number of fingerlings stocked × 100
Results and Discussions
The fortnightly growth trend of African catfish fed on diets containing different levels of crude protein showed that growth performance of fish increases gradually with the passage of time (Figure 1). Maximum growth was observed by fish fed by diet of higher protein level. Our results are in accordance with the studies of Machiels and Henken (1985), who reported that growth rate and protein gain increased as levels of protein in the feed increased. The data on growth parameters i.e., average final weight, weight gain, feed conversion ratio (FCR), specific growth rate (SGR), feed efficiency ratio (FE %) and protein efficiency ratio (PER) of African catfish fed on diet containing varying CP levels, is given in Table 2.
The final weight of fish and weight gain was improved by increasing proteins levels in feed. The fish fed with the feed containing 25% CP level showed minimum weight gain (127.69 g), and followed by feed of 30% CP level (142.4 g), 35 % CP level (168.3 g) and 40 % CP level (173.4 g); although growth parameters of fish fed with 35 and 40% CP level did not differ significantly.
The growth rate of African catfish was best in the fish fed with diet of high-protein contents (protein 40%) compared to the diet with low-protein (20%). Faturoti and Lawal (1986) reported that 40% crude protein is suitable for normal growth in Heterobranchus bidorsalis and Clarias gariepinus. The present results revealed that maximum growth rate was achieved at 40 % CP level in terms of weight gain, final weight and specific growth rate. This could be due to the metabolism of excessive amino acids by oxidative deamination which helps in generating energy (Li et al., 2009; Vergara et al., 1996). Similarly, insufficient levels of proteins caused poor growth in various fish species (Giri et al., 2003; Kim and Lee, 2005). The CP levels of 40, 35, 30 and 25% CP in experimental diets did not affect the water quality parameters that continued to remain in appropriate range as described earlier (Buentello et al., 2000).
In terms of specific growth rate (SGR) and feed conversion ratio (FCR), it appears that CP levels in 40% and 35% were better followed by CP levels 30% and 25% CP. Feed efficiency of African catfish fed 40% and 35% CP feed was higher than that of fish fed 30% and 25% CP feed. The best SGR (1.8%/day) was obtained at 40% and 35% CP levels. The relationship of SGR with respect to body weight is shown in Figure 2. The 35% protein was recorded optimal for African catfish as increasing further protein level increases the cost of feed and reducing the profit. Previously, Keremah and Baregha (2014)have reported similar trend whereby final weight gain, percentage weight gain and specific growth rate improved by improving the dietary protein level in feed. Studies on FCR values for all treatments ranges from 2.1-2.4 and did not differ significantly (P<0.05) and these observations are found consistent with the studies on carnivorous fish species such as the estuary
Table 2: Growth parameters of African catfish fed on diet containing varying CP levels (S.D: 20 fish/tank).
Parameters |
25% CP |
30% CP |
35% CP |
40% CP |
Initial weight (g/fish) |
41.82±0.93a |
41.7±0.82a |
41.30±0.96a |
41.10±0.78a |
Final body weight (g/fish) |
169.51±0.90c |
184.1±0.90b |
209.6±0.42a |
214.5±0.87a |
Weight gain (g/fish) |
127.69±0.10c |
142.4±0.65b |
168.3±0.21a |
173.4±0.67a |
Food conversion ratio (FCR) |
2.4±0.45a |
2.3±0.55a |
2.1±0.41a |
2.1±0.48a |
Specific growth rate (SGR) |
1.55±0.25c |
1.67±0.23b |
1.80±0.21a |
1.83±0.22a |
Protein efficiency ratio (PER) |
4.0±0.43a |
3.33±0.41a |
2.85±0.37b |
2.50±0.35b |
Feed efficiency (FE %) |
41.74±0.22b |
43.10±0.31b |
45.67±0.24a |
45.89±0.36a |
Means with different letters differ significantly.
grouper Epinephelus salmoides (Teng et al., 1978) and striped bass, Morone saxatilis (Berger and Halver, 1987) fed with formulated diets. Mohanty and Samantaray (1996) and Lochmann and Phillips (1994) reported similar results for gold fish (Carassius auratus) juveniles fed at protein levels of 21.2-34.5% and snakehead (Chana striata) fry using casein or other varied protein sources having 30-60% CP level. In this study slightly decreasing trend of PER by increasing protein could also accounts for PER to be consistent with other studies on Cyprinus sp. (Ogino and Saito, 1970), gilthead sea bream (Sabaut and Luquet, 1973), Florida red hybrid tilapia species (Clark et al., 1990) and Nile tilapia (Siddiqui et al., 1988).
Although significantly higher rate of growth was observed with 40% levels of CP as compared to other protein levels. However, on the basis of cost calculation, feed having 35% CP was found more economical compared to feed with 40% CP. These results of cost benefit analysis pointed out that 35% protein level is optimum for African catfish as increasing protein levels beyond 35% increases the cost of feed without affecting the growth rate in a significant way thus reducing the net profitability (Figure 3). The present findings were similar to earlier studies on same species using fish meal as a source of protein with 35% CP level (Morenike and Akinola, 2010; Keremah and Baregha, 2014). The lowest cost of production of C. gariepinus at temperature 28°C was achieved at 36% protein level in fish feed (Al- Deghayem et al., 2014).
Table 3: Carcass composition of African catfish fed with diets containing different protein levels. Means with different letter differ significantly (P<0.05).
Parameters |
25% CP |
30% CP |
35% CP |
40% CP |
Carcass (%) |
58.1b |
62.7a |
64.4a |
65.5a |
Moisture (%) |
71.69a |
72.18a |
71.74a |
72.54a |
Dry matter (%) |
28.31a |
27.82a |
28.26a |
27.46a |
Crude protein* |
43.50b |
47.42b |
52.71a |
53.98a |
Crude lipid* |
5.01b |
6.27b |
10.31a |
11.48a |
Ash* |
5.63b |
7.51a |
7.96a |
8.01a |
* Percentage of dry matter.
The data on proximate composition of Carcass of African catfish is given in Table 3. Crude protein in the African catfish fed with diets containing 40% and 35% CP were higher (P<0.05) followed by the fish fed diets with 30 and 25% CP levels, respectively. Various researchers (Faturoti and Lawal, 1986; Faturoti, 2000; Aderoulo and Akenermi, 2009) have reported that carcass proteins and lipids level is increased in African catfish using fishmeal and 40% CP. According to Lin and Shiau (1995), carcass composition should reflect the diets as it was observed from results of present study. The catfish fed with diet having 40 to 44% protein showed significant positive performance as compared with fish offered diets of 32 to 36% CP (Kiriratnikom, 2012). In this study higher levels of crude lipids were observed in fish fed with 35 and 40% CP compared to 25 and 30% CP level which is in disagreement with the findings of Davis et al. (1993) who reported that fish fed with lower levels of proteins have more fatty acid contents than those fed with higher levels of proteins. In addition, ash content in the fish fed at 40% CP was also higher compared to the fish fed with feed at 25% CP level as reported earlier by Ali et al. (2014).
Table 4: Water quality parameters during experimental trial of African catfish.
Parameters |
25% CP |
30% CP |
35% CP |
40% CP |
Temperature (°C) |
28.3±0.7 |
27.2±0.4 |
28.4±0.2 |
28.0±0.2 |
Dissolved oxygen (mg L-1) |
5.7±0.37 |
6.6±0.26 |
5.9±0.34 |
6.0±0.87 |
pH |
7.6±0.02 |
7.2±0.04 |
7.0±0.07 |
7.7±0.09 |
Electrical conductivity (µs/cm) |
154.6±1.32 |
151.1±2.10 |
156.30±1.9 |
158.60±3.6 |
Alkalinity (mg L-1) |
164.3±17.2 |
158.6±16.8 |
161.9±23.4 |
163.8±25.9 |
Hardness (mg L-1) |
170.8±8.75 |
169.5±16.2 |
165.2±13.2 |
168.1±9.5 |
In this study all fish survived easily during the whole experiment. No mortality was observed during the whole experimental trial. The high rate of survival might also be due to the favorable conditions of water body, the good health condition of the fish stocked, the quality and quantity of the feeds used and also, the acceptance of feeds by the fish. The high survival validates the report of Otubusin (2000).
The data on limnological features during farming are given in Table 4. The values were in acceptable range for culture of African catfish (Viveen et al., 1985). In addition, oxygen levels for the size air breathing African catfish used used in this study may not be considered critical (Haylor and Oyegunwa, 1993).
Conclusions and Recommendations
It was concluded that dietary protein requirement of African catfish ranged between 35-40% CP. For the commercial production of African catfish 35% crude protein level in the feed was optimum.
Novelty Statement
African catfish was indigenized in Pakistan; after the successful transportation and acclimatization of African catfish in local environment; the optimization of dietary crude protein requirement of African Catfish introduced in Pakistan is necessary for efficient management, increase in fish production and to maximize the return on investment.
Author’s Contribution
Hasina Basharat: This paper is a part PhD study; she performed this research study.
Muhammad Ramzan Ali: Supervised research, help in experimental setup and data analysis and manuscript writing.
Aziz Ahmed: Helped in experimental setup and data collection.
Mubeen Fakhar: Helped lab analysis, reviewed and edited the manuscript.
Aleem khan: Reviewed and edited the manuscript.
Conflict of interest
There is no conflict of interest among the authors of the manuscript.
References
Aderolu, A.Z. and O.A. Akinremi. 2009. Dietary effects of coconut oil and peanut oil in improving Biochemical characteristics of Clarias gariepinus juvenile. Turk. J. Fish. Aquat. Sci., 9: 105-110.
Al-Deghayem, W., H.F. Al-Balawi, S. Kandeal and E.M. Suliman. 2014. The effect of different diets and temperatures on growth rate, nutrient utilization and body composition of Clarias gariepinus (Burchell 1822). Life Sci. J., 10(4): 450-456.
Ali, M.R., Naqvi, S.M.H.M. and S Akhtar. 2014. Dietary protein requirement of giant river catfish, Sperata seenghala (Sykes), determined using diets of varying protein level. Pak. J. Nutr., 13(3): 151-156.
AOAC, 2003. Official methods of analysis (17th Ed). Washington, US. Association of Official Analytical Chemists. Histamine in seafood: biological method. In: Official Methods of Analysis of AOAC International. 16th ed. Gaithersburg, Md: AOAC; 1993:sec 35.1.32, method 977.13
Berger, A. and J.E. Halver. 1987. Effect of dietary protein, lipid and carbohydrate content on the growth, feed efficiency and carcass composition of striped bass Morone saxatilis (Walbaum), fingerlings. Aquacult. Res., 18: 345-356. https://doi.org/10.1111/j.1365-2109.1987.tb00323.x
Boyd, C.E., C.S. Tucker and B. Somridhivej. 2016. Alkalinity and hardness: Critical but elusive concepts in aquaculture. J. World Aquacult. Soc., 47(1): 6-41. https://doi.org/10.1111/jwas.12241
Buentello, J.A., D.M. Gatlin and W.H. Neill. 2000. Effects of water temperature and dissolved oxygen on daily feed consumption, feed utilization and growth of channel catfish (Ictalurus punctatus). Aquaculture, 182: 339-352. https://doi.org/10.1016/S0044-8486(99)00274-4
Chou, R.L., B.Y. Her, G. Su, M.S. Hwang, Y.H. Wu and H.Y. Chen. 2003. Substituting fish meal with soybean meal in diets of juvenile cobia Rachycentron canadum. Aquaculture, 229: 325-333. https://doi.org/10.1016/S0044-8486(03)00395-8
Clark, A E., W.O. Watanabe, B.L. Olla and R.I. Wicklund. 1990. Growth, feed conversion and protein utilization of Florida red tilapia fed iso-caloric diets with different protein levels in sea water pools. Aquaculture, 88: 75-85. https://doi.org/10.1016/0044-8486(90)90321-D
Davis, J.T., D.M. Gatlin and M. Alleger. 1993. Channel catfish dietary effects on body composition and storage quality. SRAC Publication No. 186.
Du, Z.Y., Y.J. Liu, L.X. Tian, J.G. He, J.M. Cao and G.Y. Liang. 2006. The influence of feeding rate on growth, feed efficiency and body composition of juvenile grass carp (Ctenopharyngodon idella). Aquacult. Int., 14: 247-257. https://doi.org/10.1007/s10499-005-9029-7
Dwyer, K.S., J.A. Brown, C. Parrish and S.P. Lall. 2002. Feeding frequency affects food consumption, feeding pattern and growth of juvenile yellowtail flounder (Limanda ferruginea). Aquaculture, 213: 279-292. https://doi.org/10.1016/S0044-8486(02)00224-7
Ertan, E., N. Agrali and A.S. Tarkan. 2015. The effects of salinity, temperature and feed ratio on growth performance of European sea bass (Dicentrarchus labrax) in the water obtained through reverse osmosis system and a natural river. Pak. J. Zool., 47(3): 625-633.
FAO, 2012. Farming the waters for people and food. (eds. R.P. Subasinghe, J.R. Arthur, D.M. Bartley, S.S. De Silva, M. Halwart, N. Hishamunda, C.V. Mohan and P. Sorgeloos). Proceedings of the Global Conference on Aquaculture 2010, Phuket, Thailand, Bangkok. pp. 896.
Faturoti, E.O. and L.A. Lawal. 1986. Performance of supplementary feeding and organic manuring of the production of Oreochromis niloticus. J. West Afr. Fish., 1: 25-32.
Faturoti, E.O., 2000. Beneath the ripples and sustainable fish production. Inaugural lecture, University of Ibadan, pp. 54.
Fontainhas-Fernandes, A., E. Gomes, M.A. Reis-Henriques and J. Coimbra. 1999. Replacement of fish meal by plant proteins in the diet of Nile tilapia: Digestibility and growth performance. Aquacult. Int., 7(1): 57-67. https://doi.org/10.1023/A:1009296818443
Garciia, Ortega, A., J. Verreth, K. Vermis, H.J. Nelis., P. Sorgeloos and M. Verstegen. 2010. Laboratory investigation of daily food intake and gut evacuation in larvae of African catfish Clarias gariepinus under different feeding conditions. Aquacult. Int., 18: 119-134. https://doi.org/10.1007/s10499-008-9230-6
Giri, S.S., S.K. Sahoo, A.K. Sahu and P.K. Meher. 2003. Effect of dietary protein level on growth, survival, feed utilization and body composition of hybrid Clarias catfish (Clarias batrachus X Clarias gariepinus). Anim. Feed Sci. Technol., 104: 169-178. https://doi.org/10.1016/S0377-8401(02)00295-X
Gokcek, C.K., Y. Mazlum and I. Akyurt. 2008. Effects of feeding frequency on the growth and survival of Himri barbell and Barbus luteus fry under laboratory conditions. Pak. J. Nutr., 7: 66-69. https://doi.org/10.3923/pjn.2008.66.69
Haylor, G. and O. Oyegunwa. 1993. Onset of airbreathing and development of accessory breathing orgains in relation to temperature in African Catfish (Claria gariepinus Burchell). Aquacult. Res., 24(2): 253-260. https://doi.org/10.1111/j.1365-2109.1993.tb00548.x
Hung, S.S.O. and P.B. Lutes. 1987. Optimum feeding rate of hatchery-product juvenile white sturgeon (Acipenser transmontanus) at 20°C. Aquaculture, 65: 307-317. https://doi.org/10.1016/0044-8486(87)90243-2
Jobling, M. and T.G. Reinsnes. 1986. Physiological and social constrains on growth of Arctic charr, Salvelinus alpinus an investigation of factors leading to stunting. J. Fish Biol., 28: 379-384. https://doi.org/10.1111/j.1095-8649.1986.tb05174.x
Jones, P.L., S.S. De Silva and B.D. Mitchell. 1996. Effects of replacement of animal protein by soybean meal on growth and carcass composition in juvenile Australian freshwater crayfish. Aquacult. Int., 4: 339-359. https://doi.org/10.1007/BF00120950
Keremah, R.I. and J. Esquire. 2014. Comparative assessment of growth performance and economics of production of Clarias gariepinus fingerlings in ponds and tanks. Greener J. Agric. Sci., 4(2): 34-38. https://doi.org/10.15580/GJAS.2014.2.041513577
Kadye, W.T. and A.J. Booth. 2012. Integrating stomach content and stable isotope analyses to elucidate the feeding habits of non-native sharp tooth catfish Clarias gariepinus. Biol. Invasions, 14(4): 779-795. https://doi.org/10.1007/s10530-011-0116-6
Keremah, R.I., 2014. Effect of varying dietary protein levels on growth and nutrient utilization of African catfish Clarias gariepinus fingerlings. J. Exp. Biol. Agric. Sci., 2(1): 13-18.
Kim, L.E. and S.M. Lee. 2005. Effects of the dietary protein and lipid levels on growth and body composition of bagrid catfish, Pseudobagrus fulvidraco. Aquaculture, 243: 323-329. https://doi.org/10.1016/j.aquaculture.2004.11.003
Kiriratnikom, S., 2012. Growth, feed utilization, survival and body composition of fingerlings of slender walking catfish, Clarias nieuhofii, fed diets containing different protein levels J. Food Sci. Technol., 34: 37-43.
Lee, S.M., U.G. Hwang and S.H. Cho. 2000. Effects of a feeding frequency and dietary moisture content on growth, body composition and gastric evacuation of juvenile Korean rockfish (Sebastes schlegeli). Aquaculture, 187: 399-409. https://doi.org/10.1016/S0044-8486(00)00318-5
Lovell, T., 1989. Nutrition and feeding of fish. New York: Van Nostrand Reinhold. Vol. 260. https://doi.org/10.1007/978-1-4757-1174-5
Li, P., K. Mai., J. Trushenski and G. Wu. 2009. New developments in fish amino acid nutrition: towards functional and environmentally oriented aquafeeds. Amino Acids, 37(1): 43-53. https://doi.org/10.1007/s00726-008-0171-1
Lim, S.R., S.M. Choi, X.J. Wang, K.W. Kim, I.S. Shin, T.S. Min and S.C. Bai. 2004. Effects of dehulled soybean meal as a fish meal replacer in diets for fingerling and growing Korean rockfish Sebastes schlegeli. Aquaculture, 231(1-4): 457-468. https://doi.org/10.1016/j.aquaculture.2003.09.008
Lin, J.H. and S.Y. Shiau. 1995. Hepatic enzyme adaptation to different dietary carbohydrates in juvenile tilapia Oreochromis niloticus X O. aureus. Fish Physiol. Biochem., 14: 165-170. https://doi.org/10.1007/BF00002459
Lochnmann, R.T. and H. Phillips. 1994. Dietary protein requirement of juvenile golden shiner (Notemigonus crysoleucas) and goldfish (Carassius auratus) in aquaria. Aquaculture, 128: 277-285. https://doi.org/10.1016/0044-8486(94)90317-4
Machiels, M.A.M. and A.M. Henken. 1985. The 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. https://doi.org/10.1016/0044-8486(85)90226-1
Mihelakakis, A., C. Tsolkas and T. Yoshimatsu. 2002. Optimization of feeding rate for hatchery-produced juvenile gilthead sea bream Sparus aurata. J. World Aquacult. Soc., 33: 169-175. https://doi.org/10.1111/j.1749-7345.2002.tb00491.x
Mohanty, S.S. and K. Samantaray. 1996. Effect of varying levels of dietary protein on the growth performance and feed conversion efficiency of snakehead Channa striata fry. Aquacult. Nutr., 2: 89-94. https://doi.org/10.1111/j.1365-2095.1996.tb00013.x
Morenike, A.A. and J.A. Akinola. 2010. Effect of mixed feeding of varying dietary crude protein levels on the growth and feed utilization of Clarias gariepinus (Burchell, 1822) fingerlings. J. Anim. Vet. Adv., 9(10): 1415-1419. https://doi.org/10.3923/javaa.2010.1415.1419
National Research Council (NRC), 1993. Nutritional requirements of fish, National Academy Press, Washington, D.C, USA, pp. 114.
Ng, W.K., S. Lu, K.R. Hashim and A. Ali. 2000. Effects of feeding rate on growth, feed utilization and body composition of a tropical bagrid catfish. Aquacult. Int., 8(1): 19-29. https://doi.org/10.1023/A:1009216831360
Otubusin, S.O., 2000. The effects of different feedstuff on tilapia, Oreochromis niloticus fry in floating net- hapa. Niger. J. Sci., 34(4): 377- 379.
Ogino, C. and K. Saito. 1970. Protein nutrition in fish: The utilization of dietary protein by young carp. Bull. Jpn. Soc. Sci. Fish., 36: 250-254.
Riche, M., D.I. Haley, M. Oetker, S. Garbrecht and D.L. Garling. 2004. Effect of feeding frequency on gastric evacuation and the return of appetite in tilapia Oreochromis niloticus (L). Aquaculture, 234(1-4): 657-673. https://doi.org/10.1016/j.aquaculture.2003.12.012
Sabaut, J.J. and P. Luquet. 1973. Nutritional requirements of the gilthead bream Chrysophrys aurata. Quantitative protein requirements. J. Mar. Biol., 18: 50-54. https://doi.org/10.1007/BF00347920
Salama, A.J., 2008. Effects of different feeding frequency on the growth, survival and feed conversion ratio of the Asian sea bass Lates calcarifer juveniles reared under hypersaline seawater of the Red Sea. Aquacult. Res., 39(6): 561-567. https://doi.org/10.1111/j.1365-2109.2007.01890.x
Siddiqui, A.Q., M.S. Howlander and A.A. Adam. 1988. Effects of dietary protein levels on growth, feed conversion and protein utilization in fry and young Nile tilapia, Oreochromis niloticus. Aquaculture, 70: 63-73. https://doi.org/10.1016/0044-8486(88)90007-5
Sogbesan, O.A. and A.A.A. Ugwumba. 2008. Nutritional values of some non-conventional animal protein feed stuffs used as fishmeal supplement in aquaculture practices in Nigeria. Turk. J. Fish. Aquat. Sci., 8: 159-164.
Sotolu, A.O. and E.O. Faturoti. 2009. Growth performance and hematology of Clarias gariepinus fed varying inclusions of Leucaena laucocephala leaf meal. Revista UDO Agricola, 9(4): 979-985.
Steven, C. and A. Louis. 2009. Understanding fish nutrition, feeds, and feeding communications and marketing. Virginia Polytechnic Institute and State University: College of Agriculture and Life Sciences.
Storebaken, T. and E. Austreng. 1987. Ration level for salmonids, growth, survival, body composition, and feed conversion in Atlantic salmon fry and fingerlings. Aquaculture, 60: 189-206. https://doi.org/10.1016/0044-8486(87)90287-0
Teng, S., T. Chua and P. Lim. 1978. Preliminary observations on the dietary protein requirement of estuary grouper Epinephelus salmoides (Maxwell), cultured in floating net-cages. Aquaculture, 15: 257-271.
Umaru, J., J. Auta, S.J. Oniye and A.P.I. Bolorunduro. 2016. Growth and economic performance of African catfish, Clarias gariepinus (Burchell, 1822) Juveniles to imported and local feeds in floating bamboo cages. Int. J. Fish. Aquat., 4(2): 221-226.
Vergara, J.M., L. Robaina, M. Izquierdo and M.D.L. Higuera. 1996. Protein sparing effect of lipids in diets for fingerlings of gilthead sea bream. Fish. Sci., 62(4): 624-628.
Viveen, W.J.A.R., C.J.J. Richter, P.G.W.J. Vanoordt, J.A.L. Janssen and E.A. Huisman. 1985. Practical manual for the culture of the African catfish (Clarias gariepinus). Netherl. Ministry Dev. Cooperat. Sect. Res. Technol., pp. 128.
To share on other social networks, click on any share button. What are these?