Transplanting method of wooly savatier monochasma herb
A velvet antler grass and a transplanted technology are applied in the field of transplanting velvet velvet grass, which can solve the problems that artificial cultivation cannot be fully realized, the development of velvet velvet grass is limited, and there is no breakthrough in the open-air cultivation of test-tube seedlings. The effect of transplanting survival rate, solving bottleneck problems and enhancing adaptability
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Embodiment 1
[0034] Two months after germination, the test-tube seedlings that were tissue-cultured with velvet grass seeds were transplanted and cultured. The medium was 1 / 2MS, pH=7, agar 5g / L, activated carbon 1g / L, and the tissue cultured seedlings had 2 Cotyledons, 2-4 true leaves with white hairs, 3-4 roots over 2cm long.
[0035] Prepare a solution of 0.01% fludioxonil with sterile water, sterilize under high temperature and high pressure at 121°C for 15 minutes to obtain a sterilizing solution, pour the sterilizing solution into the culture bottle of the above-mentioned test tube seedlings, and open the upper cover to cultivate in the tissue culture room for 7 days, keep the liquid The surface height is below 0.3cm.
[0036] After hardening, the seedlings are transplanted in the greenhouse to grow seedlings, prepare the culture medium of leaf humus, peat soil, perlite, and broken sphagnum moss=2.5:2:1:0.5 (volume ratio), and sterilize under high pressure at 121 degrees Celsius for 1...
Embodiment 2
[0040] Three months after germination, the test-tube seedlings that were tissue-cultured with the seeds of velvet grass were transplanted and cultured. The medium was 1 / 2MS, pH=7, agar 5g / L, activated carbon 1g / L, and the tissue cultured seedlings had 2 Cotyledons, 2-6 true leaves with white hairs, 3-4 roots over 2cm long.
[0041]Prepare a solution of 0.01% fludioxonil with sterile water, sterilize under high temperature and high pressure at 121°C for 15 minutes to obtain a sterilizing solution, pour the sterilizing solution into the culture bottle of the above-mentioned test tube seedlings, and open the upper cover to cultivate in the tissue culture room for 7 days, keep the liquid The surface height is below 0.3cm.
[0042] After hardening, the seedlings are transplanted in the greenhouse to grow seedlings, prepare the culture medium of humus, peat soil, perlite, and broken sphagnum moss=3.5:2:1:0.5 (volume ratio), and sterilize under high pressure at 121 degrees Celsius fo...
Embodiment 3
[0047] Three months after germination, the test-tube seedlings that were tissue-cultured with the seeds of velvet grass were transplanted and cultured. The medium was 1 / 2MS, pH=7, agar 5g / L, activated carbon 1g / L, and the tissue cultured seedlings had 2 Cotyledons, 2-6 true leaves with white hairs, 3-4 roots over 2cm long.
[0048] Prepare a solution of 0.01% fludioxonil with sterile water, sterilize under high temperature and high pressure at 121°C for 15 minutes to obtain a sterilizing solution, pour the sterilizing solution into the culture bottle of the above-mentioned test tube seedlings, and open the upper cover to cultivate in the tissue culture room for 7 days, keep the liquid The surface height is below 0.3cm.
[0049] The seedlings after hardening are transplanted in the greenhouse to grow seedlings, prepare the medium of leaf humus, peat soil, perlite, broken sphagnum moss=3:2:1:0.5 (volume ratio), and sterilize by autoclaving at 121 degrees Celsius for 15 minutes t...
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