INTRODUCTION
Each group was given the different species of microalgae to be cultured. As mentioned in previous post, Tetraselmis was chosen by our group.
OBJECTIVES
Each group was given the different species of microalgae to be cultured. As mentioned in previous post, Tetraselmis was chosen by our group.
OBJECTIVES
- To differentiate types of algal culture modes and their growth phases
- To differentiate the methods of microalgal growth measurement and harvesting
METHODOLOGY
1)
Prepare
the algal medium in 1L flask
250 ml of F/2 or F/2+Si (depend
on algae sample) was filled in 1 L flask & autoclaved. The appropriate
volume of filtered sterilized vitamin was placed when the media has cooled
down.
2)
Estimation
of microalgal cell densities
A growing culture of microalgae
was provided. A sample was pipetted carefully into the groove of the
haemacytometer.The algal cell were counted under 400× (40× ocular)
magnification.The no. of algal cells was
counted. The counts in the quadrants were averaged and the algal density in the
sample was calculated, taking into the account the dilution factor.
3)
Microalgae
culture
o
Each medium was inoculate with enough volume of
microalgae inoculums to achieve 1×10^5 starting cell densities.
o
Daily, once in the morning and once in the
afternoon,the flasks were shaked gently to aerate and suspend the microalgae.
o
The microalgal cells in flask were counted
daily. Photographs of the progress in colour development was took and
described.
o
A graph was drawn to show the microalgae density
trend and the various phases of development was determined.
RESULTS
AND DISCUSSION
Microalgal species
|
Day
|
Cell density
(cell/ml) |
SGR
|
Doubling time
|
Tetraselmis
|
0 (18/9)
|
426
|
||
1 (19/9)
|
603
|
|||
2 (20/9)
|
700
|
|||
3 (21/9)
|
746
|
|||
4 (22/9)
|
685
|
|||
5 (23/9)
|
681
|
|||
6 (24/9)
|
687
|
|||
7 (25/9)
|
670
|
|||
8 (26/9)
|
557
|
|||
9 (27/9)
|
484
|
|||
10 (28/9)
|
358
|
|||
| 11 (29/9) | 311 |
*Is there any differences between Tetraselmis and Chaetoceros? How about their use in aquaculture?
Tetraselmis
|
Chaetoceros
|
|
Colour
|
Green
|
Brown
|
Shape
|
Cordiform
and almost spherical
|
Elliptic
cylinder
|
Organization
|
Unicellular
|
Simple
colonies or chain of cells,
|
Live
form & its distinctive feature
|
Flagellate
|
Non-flagellate
|
Class of microalgae
|
Chlorophyta
|
Bacillariophyta
|
Both species have been used in aquaculture for feeding of molluscs,penaied shrimp and marine fish.
CONCLUSION
Batch culture is the best way to practice in lab rather than continuos culture. It also can helps maintain their purity so that the growth phases interuption will be reduced.
CONCLUSION
Batch culture is the best way to practice in lab rather than continuos culture. It also can helps maintain their purity so that the growth phases interuption will be reduced.

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