Method for increasing germinating rate of longan seeds under condition of short-time room temperature storage
A germination rate and seed technology, applied in the field of improving the germination rate of longan seeds stored in short-term room temperature, can solve the problems of low seed germination rate and the like, and achieve the effects of improving the germination rate, strong feasibility, high application and economic value
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Embodiment 1
[0021] A method for improving the germination rate of longan seeds stored at room temperature, the specific steps are:
[0022] 1. Collection and cleaning of longan seeds
[0023] Take the freshly picked "Dongbi" longan fruit, remove the peel and pulp, put the seeds in clean water, remove deformed, germinated, small and light seeds, quickly wash to remove the pulp attached to the seeds, and drain;
[0024] 2. Preparation of Pyromorpha indica Fermented Liquid
[0025] Activate the Pyromorpha indica strain, then pick the aerial hyphae at the edge of the colony and inoculate it on a new PDA solid medium. Place it in an incubator at 28°C for dark culture for 5 days, use a puncher with a diameter of 5 mm to take the bacterial block into a 250 ml Erlenmeyer flask filled with 100 ml of sterilized PDA liquid medium, at a temperature of 28°C, Cultivate in a shaker with a rotation speed of 120 r / min for 2 days, collect the filtrate after filtering through a single layer of gauze, and ...
Embodiment 2
[0032] A method for improving the germination rate of longan seeds stored at room temperature, the specific steps are:
[0033] 1. Collection and cleaning of longan seeds
[0034] Take the freshly picked "Mid-Autumn No. 1" longan fruit, remove the peel and pulp, put the seeds in clean water, remove deformed, germinated, small, and light seeds, quickly wash and remove the pulp attached to the seeds, and drain ;
[0035] 2. Preparation of Pyromorpha indica Fermented Liquid
[0036] Activate the Pyromorpha indica strain, then pick the aerial hyphae at the edge of the colony and inoculate it on a new PDA solid medium. Place it in an incubator at 28°C for dark culture for 5 days, use a puncher with a diameter of 5 mm to take the bacterial block into a 250 ml Erlenmeyer flask filled with 100 ml of sterilized PDA liquid medium, at a temperature of 28°C, Cultivate in a shaker with a rotation speed of 120 r / min for 2 days, collect the filtrate after filtering through a single layer ...
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