Method for testing influence of dual stress on physiological characteristics of growth of gentiana straminea
A technology of Gentiana chinensis and physiological characteristics, which is applied in the measurement of color/spectral characteristics, material analysis through observation of the influence of chemical indicators, and testing of plants/trees, etc. It can solve the problems of low germination rate and seedling survival rate, and achieve guarantee Authenticity, yield and quality improvements
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Embodiment 1
[0060] Using NaCl+Na 2 CO 3 Different stress conditions were simulated from PEG-6000. The control group in this experiment was distilled water. The concentration of PEG-6000 was set at 2%, 4%, 6%, 8%, 10%, and 12%, and the concentration of saline-alkali stress was 10+10 .
[0061]
[0062] Table I
Embodiment 2
[0064] A test method for the influence of double stress on the physiological characteristics of the growth of Gentiana quinata, including the combination of N1PI, the concentration of saline-alkali stress 5+10mmol / L, and the PEG-6000 concentration of 2% combined 10ml solution, placed in a petri dish, Then put the petri dish into an artificial climate box for cultivation (60% relative humidity, 16h / d, 25°C), and replace the petri dish every 2 days. The number of seeds germinated was counted daily, and the radicle length > 1mm was taken as the standard, and the statistics were continued for 8 days. The seed germination rate on the 6th day was taken as the final seed germination rate, and the seed germination rate, germination potential, and germination index were calculated in turn, and the stem length, root length, fresh weight and related physiological indicators of the seedlings were measured after the 8th day.
Embodiment 3
[0066] A test method for the influence of double stress on the physiological characteristics of the growth of Gentiana gentiana, including the combination of N3P4, the concentration of saline-alkali stress 25+25mmol / L, and the PEG-6000 concentration of 8% combined 10ml solution, placed in a petri dish, Then put the petri dish into an artificial climate box for cultivation (relative humidity 60%, 16h / d, 25°C), and replace the petri dish every 2 days. Count the number of seeds germinated every day, taking the radicle length > 1mm as the standard, and continue counting for 8 days. The seed germination rate on the 6th day was taken as the final seed germination rate, and the seed germination rate, germination potential, and germination index were calculated in turn, and the stem length, root length, fresh weight and related physiological indicators of the seedlings were measured after the 8th day.
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