Device and method for sargassaceae seaweed germplasm preservation
A technology of sargassum and seaweed, which is applied in the field of algal germplasm resource preservation and cultivation, can solve the problems of lack of intertidal dry dew state, difficult indoor cultivation for a long time, and easy to be polluted by miscellaneous algae, and achieves low investment and resistance to stress. The effect of good sex, simple technique and equipment
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Embodiment 1
[0048] Embodiment 1: Preservation of germplasm resources of Sargassum sargassum
[0049] (1) Turn on the instrument, put an appropriate amount of seawater into the seawater recovery pool 6, turn on the temperature control system to keep the seawater temperature at 16°C; turn on the seawater delivery pump 7 and delivery controller 9, and spray the culture net tray 2 to keep it moist ; Simultaneously, turn on the lighting system LED lamp 12 to control the lighting to 4000lx, and adjust the switch timing controller 13 to control the lighting cycle as: light: dark=12:12h.
[0050] (2) Select a well-grown Sage algae, soak the main branch of the algal strain with alcohol with a volume concentration of 75% for 30 seconds, and quickly wash it with a large amount of sterilized seawater for 3 to 4 times; cut off the main branch of the algal strain, and the length of the fragment is 5 to 6 cm , wash carefully with sterilized seawater, remove the surface attachments, and evenly fix it on ...
Embodiment 2
[0059] Embodiment 2: the preservation of sea millet germplasm resources
[0060] (1) Turn on the instrument, put an appropriate amount of sterilized seawater into the seawater recovery pool 6, open the temperature control system 8, and keep the seawater temperature at 14°C; Wet; at the same time, turn on the lighting system LED light 12 to control the lighting to 3000 lx, and adjust the timer 13 to control the lighting cycle as: light: dark = 12:12h.
[0061] (2) Select an excellent variety of sea millet with strong growth potential and high alginate content, use a brush and tweezers to remove the sundries and attached organisms on the surface, soak the main branch of the algae strain with alcohol with a volume concentration of 75% for 30 seconds, and disinfect it with a large amount of water. Quickly wash the seawater 3 to 4 times; cut off the main branch of the algae strain, the length of the fragment is 5 to 6 cm, and evenly fix it on the culture net plate 2, and the densit...
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