INFLUENCE OF DIFFERENT MICROALGAE ... - Marc Lacuisse
used, but in the long term other factors (such as in biochemical composition of algae, algae cell hardness and physico-chemical parameters) also determine ...
INFLUENCE OF DIFFERENT MICROALGAE SPECIES ON SIZE AND GROWTH OF Brachionus plicatilis Marc A. Lacuisse, Rui J. Rocha, Luis E.C. Conceição, Pavlos Makridis, Maria Teresa Dinis
CCMar
Centre of Marine Sciences, Algarve University, Faro, PORTUGAL
Centre of Marine Sciences
Æ Table 1: Average cell diameter and dry weight of algae strains
Introduction: First feeding of fish larvae with a small mouth opening, in species such as groupers, requires the use of rotifers with a maximum body size smaller than 100µm. “Super Small” rotifer strains such as Brachionus rotundiformis Tschugunoff have been applied for this purpose.
Rotifer cultures on microalgae strains with a small cell size have been earlier used to decrease average size of rotifer populations (Knuckey, 2004). ÎThe aim of this work was to determine the influence of different strains of microalgae on average body size of the common rotifer strain Brachionus plicatilis.
However, the size of rotifers depends upon various parameters such as temperature, life stage, and type of food.
Æ Table 2: Experimental setup 5 days 25°C 30 ppm 250 ml Erlenmeyer 10 rotifers/ml None
4.38 2.80 1.65 3.52 3.02
24.11 7.20 7.21 11.08 7.07
Media exchange
100% daily with 30µg algae DW/ml
The microalgae strains used (table 1) were cultured under the following conditions: F2 medium, 30 ppt salinity, 24 hours illumination, 22°C, and harvested only during the exponential phase. Rotifer cultures started using pure strains of Brachionus plicatilis, previously fed ad libidum with Tetraselmis suecica. Experimental cultures were set as describe in table 2. Rotifers were daily filtered using a 35 µm mesh, and daily fed with a constant number of algae cells (30 µg algae DW/ml).
1.00
Micro N gad N occ
Eggs/ind
0.75
150
Rotifers’ loricas length and width were determined at the beginning (day 0) and at the end of the experiment (day 4), using a minimum of 30 egg-carrying rotifers from each culture.
0.50
0.25 Ind/mL
Dry weight (pg per cell) 161.26
Materials and methods:
Experiment duration Temperature Salinity Culture container Initial inoculation Aeration
Population density and egg ratio were daily determined.
100 0.00 0
1
2
3
4
Days
50
ŠEgg ratio and concentration à obtained along the experiment.
0 0
1
2
3
4
Æ
Days
Width and lorica length at the beginning and end of the experiment.
150
225 Lorica width Lorica length (μm)(µm)
50
0
*
*
175
*
*
150 125
53%
Î A 10% decrease in both lorica length (158µm ± 2.4 SD) and width of rotifers (117µm ± 1.6 SD) occurred when feeding M. pusilla. Î A significant change (p
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