A method for counting cells of Microcystis population
A technology of Microcystis cells and colony cells, which is applied in the direction of biochemical equipment and methods, and microbial measurement/inspection, can solve the problems of reducing the accuracy of Microcystis colony cells and the damage of Microcystis colony cells, and achieves improved The effect of counting, short time consumption, and simple experimental steps
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Embodiment 1
[0031] Example 1 Example of the method of the present invention being applied to the monitoring of Microcystis cell density in natural water bodies
[0032] Use the present invention to count the number of Microcystis cells when the Microcystis bloom broke out in the Jinhe River Basin, Tianjin City, on July 3, 2013:
[0033] (1) Use a 1L water collector to collect 1L of water samples from natural water bodies during the blooming period of Microcystis Jinhe; (2) Filter the collected Jinhe water samples through a microporous membrane with a pore size of about 0.45 μm , Microcystis samples were attached to the microporous membrane;
[0034] (3) Resuspend the Microcystis colony sample attached to the microporous membrane after filtration in a solution containing 10mL10 -3 mol / LEDTA solution in a 100mL beaker;
[0035] (4) After adding 100 small glass beads to the above 100mL beaker, stir magnetically at 1600rm / min for 90-110min; (see figure 1 )
[0036] (5) Take the microcysti...
Embodiment 2
[0042] Example 2 Example of the method of the present invention being applied to the monitoring of Microcystis cell density in cultured water
[0043] On July 5, 2013, at the Carp Fine Breed Farm of Tianjin Agricultural College, the Microcystis cells (containing Microcystis aeruginosa M. aeruginosa and fish-damaging Microcystis M. ichthyoblabe) with a density of 6.42×10 7 ind / L.
[0044] The method is the same as in Example 1, except that the microporous filter membrane with a pore size of 0.45 μm is replaced with a sieve with a pore size no greater than 2 μm, the results are shown in figure 2 .
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