Shell growth medium and noninvasive conchocelis observation method
A technology of shell filaments and filaments, which is applied in botany equipment and methods, horticulture, agriculture, etc., can solve the problems of filaments not being resistant to water loss, unable to polish shells, and dehydration death of filaments, etc., to achieve It is beneficial to the effect of picking seedlings and cultivating
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Embodiment 1
[0036] Embodiment 1: The method of non-injury observation altar seaweed shell filament
[0037] (1) white scallop shell is selected as the raw material of shell growth base;
[0038] (2) Soak the shell growth medium with 0.5mol / L dilute hydrochloric acid for half an hour, and measure the thickness of the shell edge regularly. Take out the shells whose thickness is reduced to less than 0.15mm, rinse with water 3 times and set aside;
[0039] (3) Soak the shell growth substrate treated with dilute acid in seawater, and boil and sterilize for 10 minutes;
[0040] (4) Spread the sterilized shell growth medium on the bottom of the container, add PES medium, then crush the free filaments of Porphyra alba, add them to the container, stir gently to promote the uniform dispersion of the free filaments.
[0041] (5) Take a small piece of shell regularly, place it in an observation device equipped with seawater culture medium, observe the transparent area of the shell with a microscope...
Embodiment 2
[0043] Embodiment 2: The method of non-injury observation Porphyra zebra shell filaments
[0044] (1) The raw material of the shell growth base is the thin slices (thickness is about 0.5 mm) that are cut from mussel shells;
[0045] (2) Soak the shell growth medium with 0.25mol / L dilute sulfuric acid for half an hour, and measure the shell edge thickness regularly. Take out the shells whose thickness is reduced to less than 0.15mm, rinse with water 3 times and set aside;
[0046] (3) Soak the shell growth base treated with dilute acid in seawater, boil and sterilize for 15 minutes;
[0047] (4) Spread the sterilized shell growth medium on the bottom of the container, add PES medium, then add the Porphyra zebra fruit spore water into the container, stir gently to promote uniform dispersion, and make the seedlings more uniform.
[0048] (5) Take a small piece of shell, scrub the surface with sterile gauze, and then place it in an observation device equipped with seawater cultu...
Embodiment 3
[0049] Embodiment 3: the method for observing red cabbage shell filaments without damage
[0050] (1) white scallop shell is selected as the raw material of shell growth base;
[0051] (2) Soak the shell growth medium with 0.5mol / L dilute hydrochloric acid for half an hour, and measure the thickness of the shell edge regularly. Take out the shells whose thickness is reduced to less than 0.15mm, rinse with water 3 times and set aside;
[0052] (3) Soak the shell growth substrate treated with dilute acid in seawater, and boil and sterilize for 10 minutes;
[0053] (4) Spread the sterilized shell growth base on the bottom of the container, add PES medium, then add the red cabbage fruit spores or crushed free filaments into the container, and gently stir to promote uniform dispersion.
[0054] (5) Take a small piece of shell, scrub the surface with sterile gauze, and then place it in an observation device equipped with seawater culture medium. The transparent area of the shell...
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Abstract
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