Rapid propagation method of Taishan varbuschianum
A fast and lily technology, applied in the field of plant biology, can solve the problems of limited artificial breeding, self-flowering infertility, slow natural reproduction speed, etc., and achieve the effect of filling the technical gap
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Embodiment approach 1
[0031] Take a single wild lily lily plant under the forest on the sunny slope of Mount Tai at an altitude of about 800m as the test plant. At the initial stage of flowering, collect its complete raceme. The inflorescence has 1-3 unopened flower buds, the smallest flower bud is green, and the length is 3-5cm. The tip of the largest bud is about 1 / 3-1 / 2 red, the length is more than 5cm, and the buds are not open; the height of the inflorescence is 15-30cm, and the isolated inflorescence of wild Lilium variegata is used as the test material for artificial cultivation.
[0032] The isolated inflorescences are cultivated in a closed environment in the cultivation room by means of hydroponics, and there are no flowers of the same type in the cultivation room;
[0033] Taishan natural well water is used for hydroponics, pH is about 6.7, and the temperature is natural water temperature, about 20-25°C; the average daily temperature for cultivation is 18-26°C, and the average daily light...
Embodiment approach 2
[0044] Take a single wild Lilium variegata plant under the forest on the sunny slope of Mount Tai at an altitude of about 800m as the test plant, cut the 15-22d old capsule, peel off the attached perianth, wash the surface with running water, and then carry out aseptic disinfection. First disinfect with 70% alcohol for 20-30s, then disinfect with 0.1% mercuric chloride solution for 8-11min, then rinse with sterile water 3-5 times, absorb excess water on the surface, and use the sterile ovary as the test material.
[0045] Cut the sterile ovary along the dorsal suture to reveal the yellow-white immature embryo. The immature embryos were sowed on the immature embryo culture medium with tweezers, and after 20-30 days of dark culture, the immature immature embryos began to differentiate into green embryogenic callus. Continue to culture this type of embryogenic callus on the same medium, subculture once every 20-30 days, after 2-3 subcultures, the volume of embryogenic callus will...
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