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.
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