Research Article
Open Access
Evaluation of small barbus silage through
inclusion into commercially formulated
poultry feed
Alemu Lema Abelti*
Batu Fishery and Other Aquatic Life Research Center, Oromia Agricultural Research institute, Ethiopia
*Corresponding author: Alemu Lema Abelti, Batu Fishery and Other Aquatic Life Research Center, Oromia Agricultural Research institute, Associate Researcher of Fish postharvest technology, Ethiopia, , Tel: +251913189100; E-mail:
@
Received: September 25, 2017; Accepted: December 27, 2017; Published: January 5, 2018
Abstract
The aim of the present study was to produce fish silage by formic
acid fermentation and evaluate its use in feeding of Lohman brown.
A total of twenty five 120 day old Lohman brown were used for the
experiment. A 24 weeks experiment was conducted to investigate
the utilization of a diet based on commercial poultry feed and silage.
Five diets containing various levels of fish silage (0, 2, 4, 6 and 8%)
were evaluated. The birds were weighed and allotted to five pens
containing five birds each. Daily feed intake, number and weight of
egg laid were daily measured. Body weight was measured monthly.
The highest average feed intake was recorded in treatment four
(135.89 ± 7.82) g/ poultry in which 6 % of silage was included into
commercial diet. The highest body weight obtained was (1968.00 ±
119.39) during 33rd week in which 6 % of silage was included into
commercial diet. The highest average weight of egg (68.59 ± 4.96)
was observed in T4 (6% silage included). It was concluded that
addition of 6% fish silage into commercial poultry diet increased
early egg laying, feed intake, body weight gain, egg production and
average weight of eggs. Laying hen fed on 6% silage gained average
weight of 649 gram, average egg number (117) and egg weight (60
gram) for feeding period of 24 weeks.
Keywords: Silage; small barbus; poultry; feed intake; weight
gain; egg production;
Introduction
Fish silage is a semi-liquid product resulting from the
preservation of whole fish or parts by the addition of acids
(inorganic or organic) or by bacterial fermentation, adding
latter a carbohydrates source along with lactobacilli species to
convert sugars into lactic acid [4, 13]. Acid silage was developed
in 1920 by A. I. Virtanen, using hydrochloric and sulphuric acid
for the conservation of forages. Experiments with fish began
in Sweden in 1936, using hydrochloric, sulphuric, and formic
acids and sugars [28]. The presence of mineral or organic acids
or the lactic fermentation decreases the pH, which inhibits the
growth of bacteria, and hence enables long-term storage of the
raw material. Fish silage made with organic or mineral acids
is commonly referred to as acid fish silage, while that which
requires the addition of a source of carbohydrates and anaerobic
storage conditions is known as fermented or biological fish
silage [6]. Liquefaction is caused by enzymes present in the fish,
and is accelerated by the acid which in addition to creating the
right conditions for the enzymes to work, helps to break down
bone and limits the growth of spoilage bacteria [30]. When fish
is ensiled with formic acid, the pH is kept under 3.5 [28]. This
preserves the amino acids, but during storage autolysis takes
place so that the protein is broken down to shorter peptides and
free amino acids [6].
Fish silage is used in Norway in feeds for fur animals and
farmed fish and recently it has become permitted for use at a
30 g/kg dry weight basis in feed mixtures for poultry and pigs.
Since then, several scholars have successfully utilized acidpreserved
silage obtained from different raw materials in diets
for different animal species. Fish silage can substitute fish meal
or soybean for quality protein at low cost. Feeding experiments
which substituted fish silage with fish meal/soybean meal in
diets of different animals has been conducted. Some of the
animals used were White leghorn chickens [6]; broiler chickens
[2, 18, 15, 9, 16]; laying hens [16]; Labeo rohita fingerlings [21];
Juvenile Litopenaeus vannamei [24]; Tilapia [8] laying Japanese
quails [15, 31], Common Carp (Cyprinus carpio) fingerlings [25]
and Young rats [6]. The incorporation of fermented fish silage in
dietary feed formulation in poultry may be used as an effective,
suitable and cheaper protein source [31]. Reported that 15% of
a mixture of fish silage-sorghum (70% - 30%) might be included
in the diet without adverse effect on feed intake, weight gain and
feed conversion ratio of broilers [18]. Other research conducted
by [17] reported that chicks (36.3 ± 0.6 g) fed with fish silage
diets (by-products of farmed salmon) at levels of 5 and 10%
had a significant greater weight gain and feed intake. Recently,
[2] reported that fish silage could replace up to 20% of soybean
meal in broiler diets without affecting growth performance and
sensory quality of meat.
Fish silage offers an opportunity to make use of by-catch,
viscera and by-products from the fishing vessels and fish
processing sites. By-catch is often thrown overboard because of
its low price. Preserving and storing as silage is a convenient way
of utilizing such resources. In Lake Ziway, unexploited strait fin
barb, Barbus paludinosus was identified and its MSY (Maximum
Sustainable Yield) is estimated between 0.60 - 0.83 tons per km2.
Considering the total area of the lake (434 km 2) it is estimated that
an annual production of 260.4 to 360.2 with mean of 312 tons per
annum of B. paludinosus can be harvested from Lake Ziway. With
the observed substantial biomass, high productivity, high growth
rate and short generation of B. paludinosus fishery can be started
at pelagic habitats [12]. It is based on this recommendation that,
the by-catch, unexploited strait fin barb (Barbus paludinosus) was
selected as a raw material for silage preparation. The objective of
this study was to determine the chemical composition (Moisture
content, crude protein, Fat and Ash content) of fish silage and
evaluate small barbus silage through inclusion into commercially
formulated poultry diet.
Materials and methods
Experimental site
This trial was conducted at Batu fishery and Other Aquatic
life researcher center. Five houses having an area of 4m2 were
constructed from mud brick; roof was covered with twisted
bamboo, the polyurethane finally thatched by typha. The front
side of the houses was built by 90 cm x 100 cm mesh wire to let
the light enter (Figure 1).
Preparation of silage
A total of 50 kg specimen of Small barbus (Barbus paludinosus)
was harvested from Lake Zeway using a monofilament. The total
length of the specimen ranged from 7.4 to 12.5 cm with mean
length of 8.89 cm, and the weight ranged from 3.9 to 15.1 g with
a mean weight 7.68g. The fish was minced using electric meat
mincer (220 kg/hr) then mixed with 3% by weight solution of
98% formic acid in the ratio of 30L for 1 tone [30] to lower the
pH up to 3.5, then continuously stirred twice a day for ten days.
Initially, the mixture was in semi-solid form but it started to
liquefy on the fourth day. Eventually the silage was placed in acidresistant
container plastic bucket and sealed until fermentation
was completed. The mixture was stored at room temperature for
a period of 120 days (Figure 2).
Figure 1: Poultry house
Figure 2: Small barbus harvested using monofilament
Determination of chemical composition of fish silage
and prepared feed
Proximate composition and anti-nutritional factors of
prepared fish acid silage was determined by standard methods
of Association of Official Analytical Chemists (2005) for moisture,
protein, fat and ash contents.
Moisture determination
Wet silage sample was weighed, placed in crucible and then
dried in oven at 105°C for overnight. Crucible was taken out
the next day and weighed again. The loss in weight represented
the moisture contents and was determined. The percentage is
determined by the following formula:
Where W1 = initial weight of the sample W2 = final weight of
the sample
Protein determination
Five grams of dried fish silage sample was taken in a flask and
mixed with mixture of (Potassium Sulphate + Copper Sulphate)
and transferred to a flask containing 200 mL of concentrated
H2SO4. This flask was placed on a heating block, the heaters were
turned on and the flask was kept there until white fumes stopped
appearing and the solution became clear, indicating completion
of the digestion process. The solution was removed away from
the heater and then cooled. The solution was diluted with the
addition of 60 mL of distilled water and its pH was raised to 6.5–7
by adding 45% NaOH solution. Then five to six drops of indicator
solution was added and the flask was connected with a condenser
with the tip immersed in standard acid and heated until NH3 was
evaporated. The final solution mixture was then titrated using
0.2N HCl against NaOH. Protein contents were then determined
applying the following mathematical formula:
A = volume of 0.2 N HCl used for sample titration
B = volume of 0.2 N HCl used in blank titration
N = normality of HCl
W = weight of sample
14 = atomic weight of nitrogen
6.25 = constant for nitrogen calculation
Ash determination
Ten grams of sample was taken in a crucible and weighed.
Crucible with sample was placed in muffle furnace at a
temperature of 550°C for 5 hours. When the sample turned white,
it was taken out and weighed again. White-colored contents
remaining at the bottom of the crucible represented ash, which
was carefully weighed and its percentage present in the feed was
calculated by the following formula.
Where: W1 = Mass of empty porcelain dish
W2 = Mass of dish with ash
W3 = Mass of original product sample
Lipid determination
The soxhelt apparatus was set and 5 g of sample was placed
in the extraction thimble and transferred to the condenser.
Petroleum ether was filled in a flask and the apparatus was
switched on. This process was continued for 16 hours. Then
turned the heaters were switched off, and the flask was removed
and gently dried on the same heater. When the contents of the
flask smelled oily, they were removed and weighed and the fat
content in the test sample was calculated using the following
formula.
Feed preparation
Feed was prepared by adding fish silage into commercially
formulated poultry feed purchased from Alama koudijs plc.
T1= 0% fish silage + 100% commercially formulated poultry
feed
T2= 2% fish silage + 98 % commercially formulated poultry
feed
T3= 4% fish silage + 96 % commercially formulated poultry
feed
T4= 6 % fish silage + 94 % commercially formulated poultry
feed and
T5= 8% fish silage + 92 % commercially formulated poultry
feed
Poultry management
A total of twenty five 120 day old Lohman brown were used for
the experiment. Twenty five poultry was assigned to five different
silage inclusion rates. Each of five poultry house was equipped
with round feeder and waterier. The birds were weighed and
allotted to five pens containing five birds each. The birds were
maintained under the standard management practices with ad
libitum feeding and clean drinking water throughout the period
of the experiment (24 weeks). The eggs were weighed daily using
an electronic balance to an accuracy of 0.1 g. Every month, the
weight of poultry was recorded using sensitive balance.
Data collected
Body weight, feed intake, Egg production, chemical
composition (Moisture content, crude protein, ash and fat
content) of commercial poultry feed and prepared feed was
measured. Initial body weight and final body weight of each
treatment was compared using ANOVA. Feed offered and refused
was recorded daily to determinate the feed intake. Feed intake
was monitored by feeding weighed quantities of feed daily and
subtracting the left over from the quantity fed the previous day.
The birds were weighed monthly and body weight between two
consecutive weighing was recorded.
Results
Chemical composition of silage and prepared feed
The total chemical composition of silage, commercial feed and
the different formulated feed was reported in Table 1. Silage which
was hygienically prepared from small barbs’ had contain 79.8 ±
0.63 % moisture content, 16 ± 0.47 % crude protein, 0.5 ± 0.02 %
crude fat and 3.5 ± 0.32 % ash. After the chemical composition of
silage was determined, it was added to commercial poultry feed
purchased from Alema Koudijs plc.
Feed intake
Feed intake of egg laying hen was variable, resulting in the
lowest value at first 4 weeks in treatment three (62.80 ± 1.72)
grams per bird in which 4 % of silage was included. The highest
average feed intake was recorded between 25 and 28 weeks in
treatment four (135.89 ± 7.82) gram per bird in which 6 % of
silage was included into commercial diet (Table 2).
Body weight
Supplementation of fish silage in the diet had no significant
(P > 0.05) effect on body weight. However, chickens showed great
feed intake, which was implicated in a rapid increase in weight
from the beginning of the experiment (Table 3). Body weight of
chickens monthly did not show significant difference between
treatments (P > 0.05), although the chicks in treatment with 6
% fish silage included exhibited a slightly higher body weight
(1968.00 ± 119.39 gram) than other treatments.
Egg production
The age at first egg ranged between 149 days to 157 days
(Table 4). Age at first egg was lowest (149 days) in hens feeding
on 6% fish silage and highest (157 dads) in hens fed no fish silage
included diets.
Egg weight
Egg weights recorded at different weeks of age starting from
21 weeks of age are presented in table 5, including the first egg
weight. Significant (P < .05) difference between egg weights at
different weeks of age was observed and is in agreement with the
reports of [19, 20].
Table 1: Chemical composition of fish silage, commercial control feed and formulated diets (%)
Variables |
Fish silage (%) |
T1 (Mean ± Std.error) |
T2(Mean ± Std.error) |
T3(Mean ± Std.error) |
T4(Mean ± Std.error) |
T5(Mean ± Std.error) |
Moisture content |
79.8±0.63 |
6.72± 0.46 |
6.9±0.52 |
7.44±0.59 |
7.51±0.64 |
8.33±0.72 |
Crude protein |
15.9± 0.47 |
16.0± 0.2 |
15.98±0.2 |
15.89±0.1 |
15.85±0.3 |
15.80±0.4 |
Ether extract |
0.5±0.02 |
5.14±0.09 |
4.23±0.08 |
6.18±0.07 |
5.65±0.08 |
5.25±0.06 |
Total ash |
3.5±0.32 |
6.62±0.7 |
7.41±0.5 |
5.1±0.6 |
6.26±0.7 |
8.99±1.2 |
Carbohydrate |
- |
65.52±3.2 |
65.48±2.9 |
65.39±2.3 |
64.73±1.9 |
61.63±0.9 |
Phytate mg/100 g |
- |
151.82±5.6 |
145.68±4.5 |
143.46±4.3 |
95.99±3.8 |
56.6±2.9 |
Tannin mg/100g |
- |
53.13±2.3 |
51.92±2.4 |
46.78±2.1 |
44.72±1.9 |
43.88±1.8 |
Table 2: Feed intake (g/hen) of laying hens fed on diets containing different levels of fish silage)
Age of poultry in weeks |
T1 (Mean ± Std.error) |
T2(Mean ± Std.error) |
T3(Mean ± Std.error) |
T4(Mean ± Std.error) |
T5(Mean ± Std.error) |
p-value |
17-20 |
67.57±2.72 a |
68.91±1.72 a |
62.80±1.72 a |
70.82±3.69 a |
68.32±2.39 a |
0.251 |
21-24 |
103.79±4.10ab |
103.62±5.91ab |
93.16±6.29b |
119.41±6.31a |
110.06±5.61ab |
0.031 |
25-28 |
120.53±5.11a |
115.44±5.83a |
116.70±7.26a |
135.89±7.82a |
118.60±6.39a |
0.264 |
29-32 |
106.36±1.77ab |
105.60±1.96ab |
98.89±4.46b |
110.36±5.71a |
113.86±1.99a |
0.019 |
33-36 |
107.41±1.29c |
113.86±1.33a |
112.95±1.61ab |
109.21±1.18bc |
111.52±1.10ab |
0.003 |
37-40 |
104.49±1.37a |
106.62±1.19a |
104.60±5.13a |
102.05±4.86a |
105.96±1.28a |
0.853 |
Means followed by the same letter with in the column are not statistically significant
Table 3: Body weight (g) of poultry during experimental period
Age of poultry in week |
T1 (Mean ± Std.error) |
T2(Mean ± Std.error) |
T3(Mean ± Std.error) |
T4(Mean ± Std.error) |
T5(Mean ± Std.error) |
17th week body weight |
1191.9 ± 34.26a |
1190.8 ± 19.39a |
1285.2 ± 65.10a |
1337.6 ± 53.11a |
1158.6 ± 59.03a |
21st week body weight |
1619.51±48.90a |
1482.12±51.54a |
1443.98±44.88a |
1627.14±67.70a |
1472.38±74.18a |
25th week body weight |
1728.36±16.06a |
1633.20±42.61a |
1631.40±18.89a |
1725.80±58.95a |
1615.20±55.5 a |
29th week body weight |
1838.60±40.30a |
1818.80±72.90a |
1802.00±66.66a |
1883.80±87.80a |
1719.20±77.10a |
33rd week body weight |
1863.80±35.92a |
1933.20±68.11a |
1923.80±86.62a |
1968.00±119.39a |
1794.40±57.94a |
37th week body weight |
1862.80±36.52a |
1906.60±98.71a |
1896.26±87.80a |
1950.40±113.76a |
1746.40±64.42a |
Means followed by the same letters are not statistically significant
Table 4: Egg number per bird (No.) and Hen-day egg production (%) at 4 weeks interval starting from 21 weeks of age
Age of poultry in weeks |
T1 (Mean ± Std.error) |
T2(Mean ± Std.error) |
T3(Mean ± Std.error) |
T4(Mean ± Std.error) |
T5(Mean ± Std.error) |
21-24 |
11 (36.7) |
8.4(28) |
3.6(12) |
12.2(40.7) |
9.6(32) |
25-28 |
24.6 (82) |
16.6(55.3) |
16.8(56) |
25.4(84.7) |
22.6(75.3) |
29-32 |
24.4(81.7) |
20.2(67.3) |
21.8(72.7) |
26.6(88.7) |
25.4(84.7) |
33-36 |
25.6(85.3) |
22(73.3) |
22(73.7) |
26.2(87.3) |
24.4(81.3) |
37-40 |
26.8(89.3) |
23.2(77.9) |
22.8(76) |
26.4(88) |
25(83.3) |
Total number of egg per bird |
112.4 |
89.6 |
87 |
116.8 |
107 |
Over all hen day egg production (%) |
74.9 |
59.7 |
58 |
77.8 |
71.3 |
Age at start of laying egg (day) |
157 |
154 |
152 |
149 |
152 |
Table 5: Egg weight (g) and egg number per treatment at 4 weeks interval starting from 21 weeks of age
Age of poultry in weeks |
T1 (Mean ± Std.error) |
T2(Mean ± Std.error) |
T3(Mean ± Std.error) |
T4(Mean ± Std.error) |
T5(Mean ± Std.error) |
21-24 |
48.81 ± 0.51a (55) |
49.06 ± 0.94a (42) |
52.58 ± 0.87a (18) |
49.85 ± 0.97a (61) |
50.78 ± 0.80a (48) |
25-28 |
53.76± 0.44c (123) |
53.45±0.38c(83) |
56.73±0.47ab (84) |
56.96±0.62a (127) |
55.42±0.34 b(113) |
29-32 |
57.69±0.41c (122) |
56.77±0.40bc (101) |
58.79±0.35ab (109) |
59.72±0.59a(133) |
59.75±0.44a(127) |
33-36 |
59.32±0.31c(128) |
58.31±0.34c(110) |
61.82±0.37b(110) |
64.79±0.46a(131) |
61.32±0.44b(122) |
37-40 |
60.70±0.21d(134) |
62.20±0.39c(116) |
63.93±0.45b(114) |
68.59±0.43a(132) |
64.59±0.58b(125) |
Total number of eggs |
562 |
448 |
435 |
584 |
535 |
Discussion
Various factors may modulate feed intake in birds such as
environmental temperature, energetic content of the diet, texture
and palatability of the feed [1, 26]. Feed intake may be increased
due to increased frequency of feeding, feeding at cooler times of
the day and use of longer periods of light (NRC, 1994). Different
scholars supplemented this finding that the inclusion of fish
silage in the diet showed no effect on weight gain in broilers s [1,
6, 11, 18]. However, [17] found better weight gain in broilers by
including 5% fish silage and 0.8 % fish oil in the diet. Reported
that fish silage is a source of highly available amino acids [27].
The results of this study suggested that layers fed containing 6%
biological silage had an acceptable production and egg quality
performance. The age at first egg is lower than the Gramapriya
and Vanaraja as reported by [10] and higher than that reported
in a two-way cross variety by [23]. There exists difference for
the egg production between different four weeks intervals. Egg
production at different weeks of age (Table 4) indicates that
the birds are laying good number of eggs at different weeks of
age and the egg production was better than the report of [23]
in various two way crosses except in Gramapriya, which was
produced 237.35 eggs up to 72 weeks of age. Egg production at
4 weeks of interval starting from 21 to 40 weeks of age indicated
that the peak production was observed between 37 and 40 weeks
of age (Table 4). There were differences between treatments in
egg production; which was highest for the 6 % silage treatment
(116.8 eggs/hen/ five months), followed by 0% silage (112.4
eggs/hen/ five months), 8 % silage (117 eggs/hen/ five months),
2 % silage (89.6 eggs/hen/ five months) and 4% silage ( 87
eggs/hen/ five months), which corresponded to % hen-day egg
production rates for the four groups of 77.8 %, 74.9 %, 71.3%,
59.7 % and 58 % for the 6%, 0%, 8%, 2% and 4% treatments,
respectively. The effect of treatment on mean egg weight for the
whole period was significant (P < 0.05). Egg weight increased
with an increase in the age of birds and between 37-41 weeks
age, mean egg weight was 60.70 ± 0.21, 62.20 ± 0.39, 63.93 ± 0.45,
68.59 ± 0.43 and 64.59 ± 0.58 for treatments 0%, 2%, 4%, 6% and
8%, respectively. This finding is in agreement with the reports of
[19, 20]. The egg weight at 40 weeks of age (68.59 ± 0.43 g) was
better than Vanaraja and Gramapriya as reported by [10]. Egg
weight is correlated with body weight of laying hens. The relative
egg weight during a laying cycle parallels the relative body weight.
Within a flock, heavier birds lay heavier eggs (NRC, 1994). Fish
silage is a versatile animal feed and if correctly made can be safely
stored, even for a year. Inclusion of fish silage into commercial
poultry diet has enormous advantage. It was observed that, age at
first egg laying was 149 days in hens fed on 6% fish silage while
it was 157 days in hens fed on diet which does not contain fish
silage. The average hen day egg production was best for the 6 %
silage diet included (116.8 eggs/hen/ five months) as compared
to diet containing no silage (112.4 eggs/hen/ five months). A
Laying hen fed on 6% silage laid 68.59 gram average weight as
compared to 60.7 gram average weight during feeding period of
five months. Addition of 6% fish silage into commercial poultry
diet increased early egg laying, feed intake, weight gain, egg
production and average weight of eggs. Generally, including 6%
fish silage into commercial poultry diet has increased 2.9 % hen
day’s egg production, decreased 8% age at first egg laying days
and increased 7.89 % in egg weight. Further research needs to be
done on growth performance and meat quality of broilers
Acknowledgement
I am highly indebted to Oromia Agricultural Research
Institute for funding. I acknowledge all technical staff of Batu
Fish and Other Aquatic Life Research Center who involved during
small barbus collection and silage preparation.
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