Replacement of fish meal with maggot meal in African catfish (Clarias gariepinus) diets

 

 
 

 

 

 

 

 

 

 

 

 

 


Revista Científica UDO Agrícola Volumen 9. Número 3. Año 2009. Páginas: 666-671

 

Replacement of fish meal with maggot meal in African catfish (Clarias gariepinus) diets

 

Sustitución de harina de pescado con harina de larvas en dietas para el bagre Africano (Clarias gariepinus)

 

Alphonsus Okey ANIEBO1, Ebere Samuel ERONDU 2 and Onyema Joseph OWEN3

 

1Department of Animal Science, Anambra State University Igbariam, PMB 6059 Awka, Nigeria, 2Department of Animal Science and Fisheries, University of Port Harcourt, Nigeria and 3Department of Animal Science, Rivers State University of Science and Technology, PMB 5080 Port Harcourt, Nigeria

E-mails: okeyphasona@yahoo.com and eserondu@yahoo.com  Corresponding author

 

Received: 04/13/2009

First reviewing ending: 07/15/2009

First review received: 11/10/2009

Accepted: 12/07/2009

 

ABSTRACT

 

Maggot meal produced from maggots grown on a mixture of cattle blood and wheat bran was used in substituting fish meal in African catfish, Clarias gariepinus, diet. A feeding trial was carried out for a period of ten weeks to evaluate the growth and nutrient utilization of catfish juveniles using diets in which fish meal was substituted with maggot meal at the following levels, 0, 50, and 100 %.  Proximate and amino acid analyses of the maggot meal were carried out. Also the proximate composition of the test diets was determined. The results showed that maggot meal has 92.7% dry matter, 47.6% crude protein, 25.3% fat, 7.5% crude fiber, 6.25% ash, and an amino acid profile comparable to fish meal. Maggot meal-based diets compared favourably with fish meal-based diets as there were no significant differences in the growth and nutrient utilization indices (weight gain, length gain, daily growth rate, specific growth rate, feed conversion ratio and protein efficiency ratio). It is concluded that maggot meal is a viable alternative protein source to fish meal in the diet of African catfish. Its utilization is expected to reduce feed cost drastically, thus leading to a viable and sustainable aquaculture industry.

 

Kew words: Maggot meal, Clarias gariepinus, fish meal replacement

 

RESUMEN

 

Se utilizó harina de larvas producida a partir de larvas cultivadas en una mezcla de sangre de ganado y afrecho de trigo en la sustitución de la harina de pescado en dietas pare el bagre Africano (Clarias gariepinus). Se realizó un ensayo de alimentación para investigar el eefcto de la harina de larvas sobre el crecimiento y la utilziación de alimento. Se formularon tres dietas las cuales contenían diferentes concentraciones de harina de larvas como sustituto de la harina de pescado (0, 50 y 100% nivel de sustitución). Después de un periodo de diez semanas, las dietas basadas en harina de larvas se compararon favorablemente con las dietas basadas en harina de pescado debido a que no hubo diferencias significativas en el crecimiento y los índices de utilización del alimento (ganancia de peso, incremento de longitud, tasa de crecimiento específica, relación de conversión de alimento y relación de eficiencia proteica). Se concluye que la harina de larvas es una fuente de proteínas viable y alternativa a la harina de pescado en la dieta del bagre Africano. Se espera que su utilización reduzca drásticamente el costo de alimentación, lo que conduciría a una industria acuicola viable y sustentable.

 

Palabras clave: Harina de larvas, Clarias gariepinus, sustitución de harina de pescado.

 


INTRODUCTION

 

Feed is the single most expensive factor in aquaculture production and the protein component of fish diet constitutes the highest cost. The proportion of protein in fish diets is higher than those of other cultured animals, thus making feeds very exorbitant.  Studies have shown that the African catfish, Clarias gariepinus, requires about 40% crude protein in their diet and best results have been achieved with crude protein values ranging from 35-50% for all African catfish species (Wilson and Moreau 1996; Adebayo and Quadri, 2005).

 

In Nigeria, the bulk of the feed used in fish production, especially for catfishes, is imported and this has led to a high production cost of farmed fish.  Aquafeed production in most African countries is yet to be commercialized due to the ever-rising cost of feed ingredients, especially fish meal which is imported. The rising cost of diet ingredients, especially fish meal, has thus retarded the growth of aquaculture in Africa. With the ever increasing demand for fish meal globally, it is expected that its cost will continue to rise in the world market. In order to stem this trend, scientists are carrying out studies to identify cheaper alternatives with comparable nutritional quality.  Maggot meal has been reported to be a possible alternative (Sheppard 2002; Teguia et al. 2002; Ogunji et al. 2006).

 

It has good nutritional value, cheaper and less tedious to produce than other animal protein sources. It is also produced from wastes, which otherwise would constitute environmental nuisance. The production system thus serves the dual purpose of providing a nutrient-rich resource as well as a source of waste transformation and reduction. However, the production system is yet to be commercialized (Teguia 2005) probably because its utility and value in aquafeeds have not been elucidated. The reported crude protein values range from 43 to 62 % (Awoniyi et al, 2003; Fasakin et al. 2003). As far as we know, there is a dearth of information on the utilization of maggot meal in aquafeeds.

 

The few studies on its utilization in replacing fish meal in fish diets are inconclusive, especially with particular reference to catfishes. This research is therefore, aimed at evaluating for the first time, the substitution of fish meal with maggot meal from a commercial model, in catfish diets. It is believed that this study would provide the springboard for commercialization of maggot meal production process and thus provide an inexpensive animal protein source for aquafeeds.

 

MATERIALS AND METHODS

 

Maggot production and experimental diets

 

One hundred kilogram of cattle blood and 20 kg wheat bran were mixed together and spread on a floor space of 6m2 to a thickness of 3 cm to constitute the substrate. The odor of fresh blood and subsequently, fermenting substrate attracted flies, which later laid eggs on it. The eggs hatched into larvae within two days and were allowed 48 hours to develop further. The mature maggots were harvested, sun dried until a constant weight was achieved. The dried maggots were milled into a meal using a hammer mill.

 

Proximate composition of the maggot meal (Table 1) was determined using the method described in AOAC (1990). Also, amino acid analysis of the maggot meal was carried out using Technicon Sequential Multi sample amino acid analyzer (TSM) as described in AOAC (1990).

 

 

 

 

Table 1. Proximate composition of housefly maggot meal generated from a mixture of cattle blood and wheat bran on dry-matter basis.

 

Nutrient

Composition (%)

Dry matter

72.7

Crude protein

47.6

Fat

25.3

Crude fiber

7.5

Ash

6.25

 

 

 

 

 

 

 

 

 

 

 

 

Three isonitrogenous and isocaloric diets (D) were formulated (Table 2) as follows: DI was a fish meal-based diet (containing 25% fish meal), while D2 was a maggot meal substituted diet (containing 12.5% each of fish and maggot meals), and D3, a maggot meal-based diet (containing 25% maggot). Other ingredients used in the formulation included maize, soya bean meal, blood meal, wheat bran, palm oil, bone meal, vitamin and mineral premix and methionine. This formulation is in conformity with the nutritional requirement of the species as given by Uys (1989). The diets were pelleted using motorized pelleter of 2mm die size. The pellets were subsequently sun-dried. Samples of the three diets were subjected to proximate analysis (AOAC 1990) (Table 2).

 

 

 

Table 2. Formulation and nutritional composition of experimental diets.

 

 

Diets (%)

Ingredients

D1

D2

D3

Corn

11

11

11

Soy bean meal

34

39

43.5

Fish meal

25

12.5

-

Maggot meal (HFLM)

-

12.5

25

Blood meal

10.3

10

10

Wheat bran

11

8.0

6.0

Palm oil

5.2

3.5

1.0

Bone meal

3.0

3.0

3.0

Vitamin/Mineral premix*

0.3

0.3

0.35

DL-Methionine

0.2

0.2

0.15

Total

100

100

100

Nutritional composition (in % of dry matter)

 

 

 

Dry matter

90.45

90.78

90.13

Crude Protein

40.76

40.59

40.74

Ether extract

9.2

8.98

8.51

Crude fiber

4.1

4.87

5.22

Ash

10.59

9.10

8.0

M.E (kcal/kg)

2,795.8

2,794.5

2,737.3

M.E.(MJ/kg)

11.7

11.69

11.45

 

* Biomix fish vitamin/mineral premix providing per kg of diet at 5kg per tonne inclusion: 20,000 i.u, Vitamin A, 2000 i.u,Vit. D3, 200 mg Vit E, 8mg Vit K3, 20mg Vit B1, 30mg Vit B2, 12mg Vit B6, 50 mg Pantothenic acid, 0.8mg Biotin, 150 mg Niacin, 0.05mg Vit B12, 4.0mg Folic acid, 500mg Vit C, 600 mg Choline chloride, 200mg Inositol, 200mg Betaine, 2.0mg Cobalt, 40mg Iron, 5.0mg lodine, 30mg Manganese, 4mg Copper, 40mg Zinc, 0.2mg Selenium, 100mg Lysine, 100mg Methionine, 100mg Anti-oxidant.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Feeding Trial   

 

One hundred and thirty-five catfish juveniles of the same age and uniform size were procured. The fish having an average weight of 10g were divided into three groups of 45 fingerlings each, and each group assigned to a dietary treatment. Each treatment had three replicates, and the fish from each replicate were held in a 1 x 0.5 x 1.2 m concrete tank at a stocking rate of 15 fish/ tank. The fish were fed daily at 5% of their body weight for a period of ten weeks. This feeding rate is adjudged suitable for African catfishes of comparable life history stage as the one used in the present study (Erondu et al., 2006; Sogbesan et al., 2006). Each fish was weighed and total length measured using Ohaus Scouth II digital top loading balance and meter rule, respectively, on a weekly basis.

 

From the data, the following growth and nutrient utilization parameters were computed: weight gain, length increase, daily and specific growth rates, feed conversion ratio and protein efficiency ratio.

 

All the data collected were subjected to Analysis of Variance, using the SAS general linear model, to determine any differences in means among the dietary treatments.

 

RESULTS

 

Proximate composition of housefly maggot meal is shown in Table 1, while Table 3 is a presentation of its amino acid profile. The values recorded indicate that the biomaterial has a good nutrient quality, especially when compared with fish meal (Table 3).

 

 

 

Table 3. Amino acid profile of housefly maggot meal compared with that of fish meal

 

Amino acid                

Housefly maggot meal

Fish meal*

Histidine            

3.09

1.36

Arginin                                    

5.80

3.99

Aspartic acid  

8.25

Not given

Threonine       

2.03

2.60

Serine 

3.23

Not given

Glutamic acid 

15.3

Not given

Proline

2.85

Not given

Glycine                                   

4.11

Not given

Alanine

2.86

Not given

Cystine                                     

0.52

0.82

Valine              

3.61

3.09

Isoleucine                        

3.06

2.97

Leucine

6.35

4.45

Lysine

6.04

4.55

Tyrosine                                  

2.91

1.98

Phenylalanine  

3.96

2.35

Methionine                 

2.28

1.68

Tryptophan

-

0.69

 

*N.R.C. (1977)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

            There were no significant differences (p>0.05) in all the parameters measured in this study (Table 4).

 

 

 

 

Table 4. Growth and nutrient utilization data of Clarias gariepinus juveniles fed on maggot meal substituted diets *. 

 

                                                                                               

Diets

Production parameters

1 (0%)

2 (12,5%)

3 (25%)

Initial weight (g)

10.0±0.0

10.02±0.025

10.0±0.02

Initial length (cm)

8.32±0.009

8.41±0.7

8.36±0.02

Final body weight (g)

258.61±0.15

269.04±19.07

273.98±20.24

Weight gain (g)

248.61±0.10

259.02±24.05

263.98±27.39

 Length increase (cm)

22.71±0.54

22.94±0.087

23.53±0.09

Specific growth rate

2.53±0.09

2.55±0.07

2.56±0.07

Feed conversion ratio

1.15±0.10

1.17±0.095

1.16±0.10

Protein efficiency ratio

2.55±0.53

2.60±0.52

2.60±0.56

 

* The values of the indices among the different treatments were not significantly different (p>0.05)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Fish Growth

 

The values recorded for the growth parameters evaluated are presented in Table 4. Diet 1 recorded an average weight gain of 248.61g and length increase of 22.71cm; D2 weight and length gains of 259.02 g and 22.94 cm; while D3 recorded 263.98g and 23.53cm weight and length gains, respectively. The average DGR values were 0.44g, 0.46g and 0.47g for D1, D2 and D3, respectively while SGR values were 2.53, 2.55 and 2.56 for D1, D2 and D3, respectively. These values were not significantly different (p>0.05) (Table 4).

 

Nutrient Utilization

 

The FCR values were 1.15, 1.17 and 1.16 for D1, D 2 and D3, respectively; while PER for D1 was 2.55; 2.60 for D2 and 2.60 for D3. The differences were not statistically significant (Table 4).

 

DISCUSSION

 

The non significant differences of the evaluated growth and nutrient utilization indices among the three treatments imply that maggot meal can successfully replace the entire fishmeal portion of the fish diet. Other authors have observed a better performance of fish fed diets containing maggot meal over those solely fed on fish meal diets (Ogunji et al., 2006). This is a reflection of the nutritive quality and acceptance of this biomaterial.. The result also corroborates previous observation that maggot meal, like other animal protein sources was well accepted and utilised by fish (Alegbeleye et al. 1991; Idowu et al. 2003).

 

It has been suggested that the good growth and nutrient utilization capacity of fish fed maggot-based diets stem from the high biological value ie nutrient composition and digestibility, of the ingredient (Sogbesan et al., 2006). Jhingram (1983) reported that maggots are easily digested by fish and this has been attributed to its relatively high crude fibre content, which according to Fagbenro and Arowosoge (1991) plays a significant role in feed digestion. The non significant difference in the values of FCR of the treatment diets is possibly indicative that both protein sources compared favourably in feed to flesh conversion. It has been reported that the biological value of maggot meal is equivalent to that of whole fish meal (Ajani et al., 2004). This fact is strengthened by the results obtained in the present study.

 

 The  PER values were good and not significantly different, and this is consistent with the results reported by Atteh and Ologbenla (1993) that amino acid profile of maggot meal is similar to that of fish meal and meat meal, with a positive linear effect on the fish body protein (Adebayo and Quadri 2005). Sheppard and Newton (1999) have also reported that maggot oil is high in desirable medium chain and mono unsaturated fatty acids, and rich in phosphorus, trace elements and B-complex vitamins (Teotia and Miller, 2003). Ogunji et al. (2006) postulated that several other ingredients of animal origin such as feather meal, poultry by-product meal, and also plant protein sources may not successfully replace fish meal in aquafeeds due to their inferior amino acid profile, and nutrient inhibition factors found in the latter class. Utilization of maggot meal will thus pave way for cheaper and nutritionally rich aquafeeds.

 

CONCLUSIONS

 

It is concluded that based on production cost, availability, biological value, growth and nutrient utilization, maggot meal is a viable alternative protein source to fish meal in catfish diets. This is especially so in developing countries like Nigeria where fish meal is imported at an exorbitant cost.  Though there may be slight constraints in commercial production of maggot meal presently, these can be overcome through active and well-directed research. Aquaculture industry can thus benefit from wide availability of local and inexpensive aquafeeds. This is the key to the development of a productive and sustainable aquaculture in developing countries.

 

ACKNOWLEDGMENTS

 

The authors are grateful to the staff of Phasona Fisheries and Plantation Farms, FHE Rumueme (Agip), Port Harcourt, particularly Grace C. Aniebo and Chinonso Onyeguili for their immense help during sample and data collection. We appreciate the contributions made by S. N. Wekhe and N. O. Isirimah.

 

LITERATURE CITED

 

Adebayo, O. T. and I. C. Quadri. 2005. Dietary protein level and Feeding rate for Hybrid Clarid Catfish, Clarias gariepinus x Heterobranus bidorsallis in homestead tanks. Journal of Applied Aquaculture 17 (1): 97-106.

 

Ajani, E. K.; L. C. Nwanna and B. O. Musa. 2004. Replacement of fishmeal with maggot meal in the diets of Nile tilapia, Oreochromis niloticus. World Aquaculture 35 (1): 52-54.

 

Alegbeleye, W. O.; D. F. Anyanwu and A. M. Akeem. 1991. Effect of varying dietary protein levels on the growth and utilization performance of catfish, Clarias gariepinus. Proceedings of the 4th Annual Conference of Nigerian Association of Aquatic Science Ibadan, Nigeria. p 51-53.

 

AOAC. 1990. The Official Method of Analysis, Association of Official Analytical Chemists, 15th Edition.Washington, D.C. USA.

 

Atteh, J. O. and F. D. Ologbenla. 1993. Replacement of fishmeal with maggots in broiler diet:  Effects on performance and nutrient retention. Nigerian Journal of Animal Production 20: 44-49.

 

Awoniyi, T. A. M; V. A. Aletor and  J. M Aina. 2003. Performance of broilers fed on maggot meal in place of fishmeal. International Journal of Poultry Science 2 (4): 271-274.

 

Erondu, E. S.; D. Bekibele and A. T. Gbulubo 2006. Optimum crude protein requirement for the catfish, Chrysichthys nigrodigitatus. J. Fish. Intl. 1 (1-2): 40-43.

 

Fagbenro, O. A. and I. A. Arowosoge, 1991. Utilisation of agricultural wastes and by-products in fish feeds production in Nigeria. Proceedings of the 6th Annual Conference of Fisheries Society of Nigeria, Lagos, pp.121-130

 

Fagbenro, A. O.; A. M. Balogun and A. M. Anyanwu. 1992. Optimal dietary protein levels for Heterobranchus bidorsalis fingerlings fed compound diets. Israeli Journal of Aquaculture (Bamidgeh) 44 (3): 87-92.

 

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Idowu, A. B.; A. A. S. Amusan and A. G. Oyediran. 2003. The response of C. gariepinus (Burchell 1822) to the diet containing housefly maggot, (Musca domestica). Nigerian Journal of Animal Production 30 (1): 139-144.

 

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National Research Council (NRC). 1977. Nutritional requirements of warm water fishes. National Academy of Science. Washington D.C. USA, 78 p.

 

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Teguia A.; M. Mpoame and J. A. Okourou Mba. 2002. The production performance of broiler birds as affected by the replacement of fish meal by maggot meal in the starter and finisher diets. Tropiculture 4: 187-192.

 

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Teotia, J. S. and B. F. Miller. 1991. Fly pupae as a dietary ingredient for starting chicks. Poultry Science 52: 1830-1835.

 

Uys, W. 1989. Aspects of the nutrional physiology and dietary requirements of juvenile and adult sharptooth catfish, Clarias gariepinus. In: Hecht, T., Oellerman, L. and Verheust, L. 1996. Perspectives on clariid catfish culture in Africa. Aquat. Living Resour. 9: 197-206.

 

Wilson, R. P and Y. Moreau. 1996. Nutrient requirements of catfishes (Siluroidei). In: M. Legrende and J. P. Proteau (EDS) Biology and culture of catfishes. Aquatic Living Resources 9, Horse series, p. 103-111.

 

 

 

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