Printer Friendly
The Free Library
23,383,293 articles and books

Sustainable commercial maggot production (maggotry) for animal & aquafeeds in rivers state, South South Nigeria.


The costs of poultry and fish feeds have continued to increase in recent times. These high feed costs can be attributed to scarcity and high cost of feed ingredients particularly protein supplements. The cost of fish meal, the most guaranteed animal protein source has become prohibitive. Plant sources even though not balanced, are not cheap either. Good quality fish meal costs over $2.1 per kg, about thrice the cost of soyabean meal and four times the cost of groundnut cake (GNC). There is thus need for alternatives to these exorbitant protein sources. The development of non conventional protein supplements such as insect larvae in commercial quantity appears to be possible alternative. House fly larvae meal has been found to be not only rich in limiting essential amino acids, but also highly available to poultry, pig and fish, save that it is not yet available in commercial quantity. In other words, the development of insect larvae in naturally occurring decaying matter, particularly animal manure, and their use as protein sources have been widely reported only at experimental levels [1,2,3,4,5,6,7,8,9,10,11,12,13]. However, information on commercial models is lacking as all known authors and researchers are in agreement that commercial maggot production has not yet been developed and has remained the only bottle neck in the exploitation of this tested feed resource. The low cost protein emanating from this would encourage poultry, livestock and fish farmers, promote fish and poultry industry, and possibly lead to increase in animal production and consequent economic affordability of the needed animal protein. The objective of this study therefore is to develop a commercial model for sustainable maggot meal production via conversion of abattoir and other plant wastes to feed resource - a solid waste management strategy.

Materials and Methods

Daily and annual slaughter figures of two species of animals (cattle and goat) commonly slaughtered in Rivers State were monitored and determined using the Rumueme slaughter slab as a case study for 30 days. Blood potential of the slab was based on the average weight of blood yield per cow/goat from three categories (A,B,C) of each of the animal species. Official record of all registered slaughter slabs and their slaughter figures were obtained from the Rivers State Ministry of Agriculture. The actual blood yield at Rumueme Slaughter slab was used to project the Rivers State yield. Sample collection for substrate mixture (medium for larvae production) was carried out thrice per month for 12 months

Twenty-five kg of whole undiluted blood (WUB) was mixed with five kilogram of each absorbent material namely wheat brain (WB), rice dust (RD) and saw dust (SD) and exposed for biodegradation in an open sided space of 4.32[m.sup.2] demarcated into three equal parts of 1.44[m.sup.2] each. House flies laid eggs in the substrate which hatched into larvae and were harvested on the 5th day of substrate exposure. Altogether, there were three test absorbent materials (Table 1). Each of the three absorbent materials was mixed with WUB to form the substrates (representing three treatments) and were allowed to ferment for 48 hours. The odour of fresh blood and subsequently, the fermenting mixture attracted flies to enter and perch on the mixture through the opened front screen, which was closed on the 2nd day. Samples of the flies were captured and were identified by Entomologist as houseflies. HFLM per quantity of blood was determined from the most efficient treatment. Based on the projected daily and annual slaughter figures in the state, HFL potential in Rivers State was determined. Proximate analysis by [14] was used to determine the nutrient composition of blood and absorbent materials used in the substrate mixture. Data collected were subjected to analyses of variance procedure of [15] and means were separated using [16].


Results of blood yield (Table 2) showed that large cattle yielded significantly (P<0.5) more blood (16.16kg) than medium cattle (12.36kg) and small cattle (9.29kg), while large goats yielded significantly more blood (0.99kg) than both medium and small categories (0.61 & 0.56kg). Based on mean blood yield of 12.6kg and 0.72kg per cattle and goat respectively, the slaughter figures at Rumueme slab and projections made for the state, were 29 cattle and goats/day at Rumueme and 1,040-1,362 cattle and goats/day in Rivers State. The daily blood yield projection at Rumueme slab and Rivers State were 234.72kg and 6,744.2-6,897.5kg respectively (85,673kg and 2.461,633-2,518,000kg respectively per annum).

Results of maggot production (Table 3) revealed that WB + WUB (S1) yielded the highest quantity of maggot (7.16kg). the yield was significantly better (P<0.05) than S2 (RD+WUB) and S3 (SD+WUB) that yielded 2.46kg and 0.13kg respectively. Blood yield projection and maggot yield potential in Rivers State showed that 25kg WUB has the potential to yield 7.16kg wet maggot equivalent to 3.2kg dry maggot. Therefore, state daily blood output of 6,744.2-6,897.5kg has the potential to yield 1,932-1,975.2kg wet maggot (863-883kg dry maggot). The annual maggot potential in Rivers State from blood output of 2,461,633-2,518,000kg was 705,012-721,155kg (315,089 322,304kg dry maggot).


The significant (P<O.05) difference observed in the quantity of blood yielded by meat animals of different sizes agrees with the report that blood yield is a percentage of body weight [17]. The total projected blood yield gives an insight of the actual volume of blood that is wasted on daily basis and the pollution load that is exerted on the surface water bodies adjoining slaughter houses in Rivers State. This is consistent with the findings of [18,19,20], that blood and gut contents were discharged directly into nearby water bodies where they constitute pollution threat to aquatic life. This supports the report that facilities for waste recovery, treatment and re-use are non-existent in most Nigeria abattoir [21,20]. This practice undermines the utility of the abundant resources that abound in these "blood wastes" [22].

The choice of fresh animal blood and agro-by products as substrate mixtures is to remove any bias of fish/meat consumers that maggots grow in decomposing waste and animal faeces which are repugnant and distasteful [23,11]. Hence, production of maggots as in this present study is from acceptable substrate. Result showed that WB + WUB supported larval growth more efficiently and was significantly better than RD + WUB and SD + WUB. This confines from the fact that WB has better nutrient composition and availability than RD and SD [24,25,26,27]. The short metamorphic period of maggot (3 - 4 days) could have been too short a time for microbial degradation of cellulose and other fibrous components of SD and to a lesser extent RD. The high density of RD could have decreased aerobic conditions in the substrate mixture which ostensibly affected both survival of eggs and hatched larvae adversely. This view is consistent with the report that anaerobic manure was lethal or at least unsuitable for larval development [28]. The better efficiency of WUB than DB could be attributed to reduced amount of nutrients available to the maggots. In all cases, maggot yield was found to be inversely related to the residual manure after maggot harvesting. This is consistent with the views of [8] who stated that as insect larvae feed on organic materials, they absorb the nutrients and reduce the waste volume significantly. It was also observed that as biodegradation of substrate by maggot progressed, the increasing size and activities of maggot appeared to be aerating the medium and reducing both moisture content and odour emission from the substrate correspondingly with the duration of biodegradation.

The blending of WB and SD was aimed at reducing the cost of WB. The result of 70:30 blend demonstrated that the combination of WB with cheaper saw dust could still support maggot production as efficiently as whole WB. Comparing the best model in this study (WB-WUB) with those reported by previous researchers, it could be seen that one kg of substrate yielded 238.7g maggot against 28.34g maggot per kg manure by [29] and 15.15g per kg manure by [30]. The wide margin of over 230g maggot / kg substrate is proof of its commercial status since blood, and wheat bran and sawdust are available all year round. It could be deduced that the maggot yield is affected negatively by extreme climatic conditions (extreme dry weather and too much rain). This is consistent with the observations [31] that fly breeding cannot be successful at a moisture level of 30% and less and water logging prevents larval development. [32] Also reported that 50% of eggs laid by flies die if exposed to the sun for several hours. However, in a continuous production system these climatic factors could be managed. Substrate could be sprinkled with water in dry weather to prevent dehydration, while moisture level of the substrate could be minimized during mixing in period of heavy rainfall.

It was observed that housefly population in a netted system depleted about the 3rd month in a continuous production system. The depletion of housefly population could be due to expiration of their life span [33,34]. It implies that the continued production and harvesting of larvae which are never allowed to pupate or metamorphose into adult flies has the tendency of bringing a housefly population to extinction. To ensure continuity of the process, intermittent batches of larvae population could be allowed to undergo complete metamorphosis to bring back a new and vibrant generation of houseflies into the system.

It is concluded that the mixture of WUB + WB is the best substrate for maggot production or a combination of WB + SD in a ratio of 70:30 mixed with WUB for further reduction in production cost. Where blood is not available in large quantity, 50% dilution with water will suffice.


We appreciate the following persons who assisted in the course of this study, Chinoso Onyeguili Jonathan Chigbu, Mr. Peter Ajuogu & Mrs Aniebo Grace Chineme, Mr. Friday Owuno and Dr. Okoli I.C and the butchers union of Rumueme slaughter slab for their assistance and understanding.


[1] Calvert, C.C; Morgan, N.O. and Eby, H.J. (1971).Proceedings of the International Symposium on Livestock Waste Columbus p 319-320.

[2] Teotia, J.S. and Miller, B.F. (1974) British Poultry Sci 155-182.

[3] Gawaard, A.A. and Brune, H. (1979) Tierphysiol Tieremaehr Futternittelkde 42: 261-222.

[4] Atteh, J.O. and Olagbenla, F.D (1993). Nig. J. Anim. Prod. Vol. 20: 44-49.

[5] Atteh, J.O. and Oyedeji, J.O. (1994. Centre Point 4: 39-46.

[6] Sheppard, C. and Newton, L. (1999) Feedstuffs 71 (50):21.

[7] Teguia A; Mpoame, M. and Okourou Mba, J.A. (2002) Tropiculture 4: 187-192.

[8] Sheppard, C. (2002. University of Georgia, Tifton G.A. 31794 USA.

[9] Idowu, A.B; Amusan, A.A.S and Oyediran, A.G. (2003). Nig. J. Anim.Prod. 30(1): 139-144s.

[10] Fasakin E.A.; Balogun, A.M and Ajayi, O.O. (2003) Aquaculture Research. 9(34): 733-738.

[11] Awoniyi, T.A.M; Adebayo, I.A. and Aletor, V. A. (2004 International Journal of Poultry Science 3(6) 386-390. Asian Network for Scientific Information, 2004.

[12] Teguia, A. (2005) Alternatives to animal protein sources in broiler feeds in: alternative feed stuff for broilers in Cameroon. 17039.htm.

[13] Ogunji, J; Slawski, H; Schulz, C; Werner, C. and Wirth, M. (2006) World Aquaculture Society Abstract data. Aqua 2006.--Meeting Abstract 277

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

[15] Steel R.G. D. and Torrie, J.H. (1980). Principles and procedures of statistics A. Biometric approach. 2nd Ed. McGraw Hill. New York.

[16] Duncan, D.B. (1955. Biometrics 11:1-42.

[17] Crawshaw, R. (1994). Blood meal: A review of nutritional qualities for pigs, Poultry and ruminant animals. National Renderers Association, London U.K. 1-6.

[18] Odeyemi, O. (1991 Proceedings of the third National Conference on Water Pollution. June 1991 Port Harcourt, Nigeria.

[19] Abiola, S.S. (1995. Nigeria Journal of Animal Production (5), 54-62.

[20] Olanike, K. A. (2002). AJEAM /RAGEE 4 No (1), 23-28

[21] Aniebo, A.O. (1994) PGD project, University of Agriculture, Makurdi Nigeria

[22] Igene, J.O. (1991). Animal production in Nigeria. In: M Kwanashie (ed)"Training manual on the processing sub-sector". Policy Analysis Department Fed. Min. of Industries Abuja.

[23] Atteh, J.O. and Adedeyin, D.D. (1993). Nig. J. Anim. Prod, 20:50-55.

[24] N.R.C (1977) Nutritional requirements of warm water fishes. National Academy of Science. Washington D.C. 1977 p.46.

[25] McDonald, P; Edward, R. A. and Greenhalgh, J.F.D (1981) Animal nutrition 3rd Edition. Longman Publishers London.

[26] Parr, W. H. (1988) The small-scale manufacture of compound animal feeds. ODNRI. Overseas Development National Resources Institute, Centre Avenue, Kent U.K. Bulletin, No.9 Perspectives 103 (12).

[27] Sowande, O.S; Akinleye, B.S; Ogundipe, B.A. and Idowu, O.M.O. (2002) Proceedings of the 27th Annual Conf. Of Nigeria Society for Anim. Production (NSAP) March 17-21. 2002. Fed University of Tech Akure.

[28] Beard, R. L. and Sands, D.S (1973). Environmental Entomology 2:801-806.

[29] Akpodiete, O.J. Ologhobo, A.D and Oluyemi, J.O. (1993) the production and nutritive value of maggot meal from larvae and pupal in three substrates of poultry droppings. Report to the Dept of Animal Science, University of Ibadan, Nigeria.

[30] Awoniyi, T.A.M, Aletor, V.A. (2002Proc. 29th Ann. Cont. Nig. Soc. of Anim. Prod. NSAP. March 17-21 2002. Fed- University of Tech. Akure Nigeria. Pp 170-173.

[31] Raph E.W(1995). Zootecnica International, Vol.1:34.

[32] Soukossi, A. (1992). African Network for Rural Poultry Development (ANRPD): News L., 3(2):6.

[33] Powell, P. K. and Barringer, S. (1995). Housefly biology and management. 10629.htm October 1995.

[34] Sarojini, T.R. (2002). Modern biology for senior secondary schools. 3rd Ed. Africa First Publishers - Book House Trust 1, Onitsha, Nigeria

A.O. Aniebo *, S.N. Wekhe *, E.S. Erondu *** O.J Owen *, E.N Ngodigha **** and N.O. Isirimah **

* Department of Animal Science, ** Department of Soil and Environmental Science, Rivers State University of Science and Technology, PMB 5080 Port Harcourt, Nigeria

*** Department of Animal Science and Fisheries, University of Port Harcourt. Nigeria.

**** Department of Animal Science and Fisheries, Niger Delta University, Wilberforce IslandBayelsa State. Nigeria.
Table 1: Characteristics of Substrate Mixtures

            Substrate Characteristics

Treatment   Absorbent material   WUB

S1          5kg Wheat bran       25kg
S2          5kg Rice dust        25kg
S3          5kg Saw dust         25kg

Table 2: Blood Yield Projection Based on Data from Rumueme
Slaughter Slab (Kg)

Parameters               Cattle

Blood yield/animal
from category A          9.29 [+ or -] 0.72 (c)
Blood yield/animal
from Category B          12.36 [+ or -] 0.87 (b)
Blood yield / animal
from category C          16.16 [+ or -] 1.28 (a)

Av. Blood yield /        12.6
Av. Daily slaughter      18
figure at Rumueme
Av. Daily blood
yield at Rumueme         226.8
Projected daily
slaughter figures in     498
Rivers State
Projected annual
blood yield at           82,782
Projected daily
blood yield in Rivers    6,274
Projected annual         2,290,300
blood yield in Rivers

Parameters               Goats                    Total

Blood yield/animal
from category A          0.56 [+ or -] 0.10 (b)   9.85
Blood yield/animal
from Category B          0.61 [+ or -] 0.11 (b)   12.97
Blood yield / animal
from category C          0.99 [+ or -] 0.23 (a)   17.15

Av. Blood yield /        0.72                     13.32
Av. Daily slaughter      11
figure at Rumueme                                 29
Av. Daily blood
yield at Rumueme         7.92                     234.72
Projected daily
slaughter figures in     652-864                  1040-1362
Rivers State
Projected annual
blood yield at           2,891                    85,673
Projected daily          469.44-
blood yield in Rivers    622.5                    6,744-6,897
Projected annual         171,400-                 2,461,633-
blood yield in Rivers    227200                   2,518,000

a,b,c, means within the same column with different superscripts
are significant (P<0.05).

Table 3: Blood Yield Projection and House Fly Larvae Potentials
in Rivers State. (kg)

Parameters                Blood         Fresh maggot         Dry
                                         potential          maggot

Yield from WB+WUB                      7.16+0.82 (a)         3.2

Yield from RD+WUB                       2.46+0.5 (b)         1.1

Yield from SD+WUB                      0.13+0.05 (c)         0.06

Quantity of HFL per
Using WB+WUB               25               7.16

Daily blood yield      6,744-6,898       1,932-1975        863-883
and corresponding
HFL potential in
Rivers State
Annual blood yield      2,461,633     705,012-721,155      315,089-
and corresponding      -2,518,000                          322,304
HFL potential in
Rivers State

A, b, c, means within the same column with different superscripts are
significant (P<0.05)
COPYRIGHT 2008 Research India Publications
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2008 Gale, Cengage Learning. All rights reserved.

 Reader Opinion




Article Details
Printer friendly Cite/link Email Feedback
Author:Aniebo, A.O.; Wekhe, S.N.; Erondu, E.S.; Owen, O.J; Ngodigha, E.N; Isirimah, N.O.
Publication:International Journal of Biotechnology & Biochemistry
Article Type:Report
Date:May 1, 2008
Previous Article:Performance of varying blends of wheat bran and saw dust as absorbent materials for blood waste in commercial maggotry.
Next Article:Phospholipids assay of Daphnia carinata using 1-D and 2-D Nmr techniques.

Terms of use | Copyright © 2014 Farlex, Inc. | Feedback | For webmasters