Method for determining floating percentage of microcystis
A microcystis, percentage technology, applied in the field of determining the floating percentage of Microcystis, can solve the problem of limiting the outbreak mechanism of cyanobacteria blooms, achieve the effects of short sinking and floating time, easy operation, and reduced errors
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Embodiment 1
[0049] The culture temperature is 25°C, and the light intensity is 100umol / m 2 Microcystis under the condition of s is transferred to a set temperature of 10°C and a light intensity of 0umol / m 2 • Culture in the light incubator of s, take a sample every two hours, and measure the change of the floating percentage of Microcystis over time. The specific operation is as follows: put the pipette tip in an autoclave, sterilize it at 120°C for 30 minutes, then put it in the ultra-clean workbench, put the pipette tip in the ultra-clean workbench and sterilize it with ultraviolet light for 30 minutes, wait for After the tip of the pipette is cooled, take samples in the ultra-clean workbench according to the method of aseptic operation. Shake the algae well before sampling, then use a pipette to draw a small amount of algae solution, and drop a drop on the cell counting plate (CELL-VU). Cover the edge of the glass to slowly infiltrate the algae liquid, absorb the excess algae liquid w...
Embodiment 2
[0053] The culture temperature is 25°C, and the light intensity is 100umol / m 2 Microcystis under the condition of s is transferred to a set temperature of 20°C and a light intensity of 100umol / m 2 Cultivate in the light incubator of s, take a sample once every two hours, measure the change of the floating percentage of Microcystis over time, the method of measuring the floating percentage is the same as above, the experimental results are shown in Table 3, as can be seen, under this condition , the floating percentage of Microcystis gradually decreased.
[0054] Table 3 Microcystis floating percentage changes
[0055]
Embodiment 3
[0057] The culture temperature is 25°C, and the light intensity is 100umol / m 2 Microcystis under the condition of s is transferred to a set temperature of 20°C and a light intensity of 500umol / m 2 Cultivate in the light incubator of s, take a sample every two hours, measure the change of the floating percentage of Microcystis over time, the method of measuring the floating percentage is the same as above, the experimental results are shown in Table 4, as can be seen, under this condition , the floating percentage of Microcystis decreased rapidly.
[0058] Table 4 Microcystis floating percentage changes
[0059]
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