Liquid containing diatom, diatom and method for culturing diatom
A cultivation method and diatom technology, which are applied in seaweed cultivation, botanical equipment and methods, cultivation and other directions, can solve the problems of inability to obtain sufficient cultivation amount and the like
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Embodiment 1
[0118] Culture medium 1 (1.5×10 -3 m 3 )join in Figure 7 Shown laboratory flat culture flask 11 (capacity 1.5 × 10 -3 m 3 ), add sodium bicarbonate to the culture medium 1 until the mass concentration of sodium bicarbonate is 1.0×10 3 ppm. Then, a predetermined amount of Chaetoceros was inoculated into the culture solution 1 . Then, the temperature of the culture solution is maintained at about 25° C. to about 35° C., and a fluorescent lamp or the like is used to make the 2 The culture solution 1 is irradiated with light of / s intensity, and in this state, the air mixed with 3% carbon dioxide is sent into the culture solution 1 through the glass tube 13 connecting the plug 12 of the bottle 11, and the culture solution 1 is ventilated. While stirring, the cultivation test of Chaetoceros was carried out. The time change of the Chaetoceros cell concentration and the time change of the pH in the culture solution 1 were respectively measured.
Embodiment 2
[0120] Culture medium 2 (1.5×10 -3 m 3 ) into the laboratory flat culture flask 11, adding sodium bicarbonate to a mass concentration of sodium bicarbonate is 1.0 × 10 3 ppm. Then, inoculate the chaetoceros of predetermined amount (the same amount with embodiment 1) in culture liquid 2, under the approximately identical condition (the temperature of culture liquid: about 25 ℃~about 35 ℃, photon amount: about 200μmol / m 2 / s, carried out aeration and agitation by air mixed with 3% carbon dioxide), the culture test of Chaetoceros was carried out. The time change of the Chaetoceros cell concentration and the time change of pH in the culture solution 2 were respectively measured.
Embodiment 3
[0122] Culture medium 3 (1.5×10 -3 m 3 ) into the laboratory flat culture flask 11, adding sodium bicarbonate until the mass concentration of sodium bicarbonate is 1.0 × 10 3 ppm. Then, inoculate the chaetoceros of predetermined amount (the same amount with embodiment 1) in culture liquid 3, under the approximately identical condition (culture liquid temperature: about 25 ℃~about 35 ℃, photon amount: about 200 μ mol) with embodiment 1 / m 2 / s, carried out aeration and agitation by air mixed with 3% carbon dioxide), the culture test of Chaetoceros was carried out. The time change of the Chaetoceros cell concentration and the time change of pH in the culture solution 3 were respectively measured.
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