Abstract:
Oreochromis niloticus fingerlings size ranging from 16 to 17 g
were fed two diets containing 25% and 30% protein. The fish meal
content of each diet was reduced from 25% (control) to 10% and
replaced with graded levels of P_;_ aureus (green gram)and
V.catiang (undudhal) seperately upto an inclusion level of 50%,
for each protein level. Each experiment lasted for 10 weeks, and
growth was measured in terms of percentage weight gain (PWG) and
specific growth rate (SGR). Total, protein and lipid
digestibilities, as well as carcass protein, lipid and energy
deposition were also measured.
After 10 weeks it was revealed that, both PWG and SGR at both
dietary crude protein levels increased upto an inclusion level of
20% and thereafter tended to decrease with increasing inclusion
levels of P^ aureus and catiang. The overall best PWG and SGR
values were recorded for 20% and 30% inclusion levels of these
two ingredients. At the 30% dietary crude protein level, V .
catiang substituted diets performed better than the corresponding
P. aureus substituted diets, where as at the 25% protein level,
both aureus and V_^ catiang performed equally well.
The protein and lipid digestibilities were high for all the
substitution levels of the two diets (25% and 30%), and did not
show a defenite trend in variation. However, the total, protein
and lipid digestibilities tended to increase at a dietary protein level of 25% at all inclusion levels of aureus and V_^ catiang.
Considering the FCR, PER and the growth data of each substitution
level of the two dietary protein levels as a whole, it is
concluded that, both P^ aureus and catiang were equally good
as partial substitutes for fish meal upto an inclusion level of
30% and that a dietary protein level of 25% would suffice for
optimum growth for 0_j_ niloticus of size ranging 16 to 17 g.
Purified casein based diets supplemented with graded levels of
pyridoxine hydrochloride (to supply 0, 2.5, 5.0, 10.0,20.0 and
40.0 mg pyridoxine/kg of diet) were fed to young Atlantic salmon
for 12 weeks. From the results it was seen that the dietary
pyridoxine level required for maximum growth was in the range of
5 to 10 mg/kg of diet. Liver alanine amino transferase activity
increased with dietary pyridoxine intake up to a level of 5 mg/kg
of diet. It was also revealed that liver and kidney deposition of
vitamin C was influenced by dietary pyridoxine intake. The
Vitamin C deposition in the liver of the dietary pyridoxine
deficient groups was minimal, whereas the deposition of vitamin C
in the kidney was elevated.
There were no apperent changes in the haematocrit and haemoglobin
value of the dietary deficient groups. The immuno response
studies indicated higher antibody formation in the dietary
pyridoxine deficient groups. Fish fed unsupplemented diets showed
anorexia, poor growth, hyperirritability, lethargy and erratic
swimming behaviour. Histopathological examination of deficient groups showed degenerative changes in liver, kidney, gill
lamellae and disintegration of erythrocytes. These deficiency
signes were prevented by 2.5 mg pyridoxine/kg of diet.
Sixteen practical diets containing graded levels of vitamin C and
E (to supply 0, 100, 1000 and 3000 mg of vitamin C/kg of diet and
0, 30, 300 and 900 IU of vitamin E/kg of diet), were fed to young
Atlantic salmon of size ranging from 4.4 g to 4.8 g for 30 weeks.
The tissue deposition of vitamin C in the liver was depressed in
the liver and kidney of the dietary deficient groups only after
30 weeks had elapsed. In the fish of the rest of the dietary
vitamin C and E groups, the vitamin C deposition in the liver and
kidney increased with increasing dietary vitamin C and E content.
Dietary vitamin E had no visible effect on the tissue deposition
of vitamin C in liver and kidney of the experimental fish.
Tissue deposition of vitamin E in liver and muscle of the
experimental fish of the dietary vitamin E deficient groups was
depressed at dietary vitamin C levels of 0, 100 and 1000 mg/kg of
diet. However, at a dietary vitamin C level of 3000 mg/kg of
diet, tissue deposition of vitamin E in liver and muscle was
significantly elevated , indicating probable synergistic action
of vitamin C.
The final mean weight tended to decrease in fish fed the
unsupplemented vitamin C diets, but there was no definite trend
in the variation. The study also revealed that there was a significant change in variation of haematocrit levels after 30
weeks of the trial. Haematocrit values were lower in fish fed
diets unsupplemented with dietary vitamin C and E. In fish fed
diets unsupplemented with dietary vitamin C, but supplemented
with vitamin E, the haematocrit values were comparatively lower
than fish of the rest of the diety groups.
Finally there was no definite trend in the variation of antibody
formation in the experimental fish fed the various diets.
However, there was a tendency for a comparative reduction in the
antibody formation in fish fed vitamin C unsupplemented diets.
From this study it could be concluded that, the minimum dietary
requirements of vitamin C and E were 100 mg of vitamin C/kg of
diet and 30 IU of vitamin E/kg of diet. It also demonstrated the
probable synergistic action of vitamin C.
The experiments with 0^ niloticus was carried out at the Fish
Feed Experimental Center and Nutrition Laboratory, Ministry of
Fisheries, Sri Lanka and the experiments with S_i_ salar was
carried out at the Halifax Fisheries Research Laboratory,
Halifax, N.S, Canada