Method for identifying infection condition of gall disease of cryptomeria fortunei
A technology for cedar and gall tumor, which is applied in the field of identifying the infection status of cedar gall disease, can solve the problems that have not yet occurred, and achieves the effects of non-destructive detection process, convenient operation, high safety and repeatability
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Embodiment 1
[0034] Example 1 Acquisition of characteristic peaks of cedars infected with galls and uninfected cedars
[0035] 1 Preparation of pellets for infrared analysis
[0036] 1) Sample collection: Branches and needles of Cryptomeria cedar infected with gall tumor and branches and needles of Cryptomeria uninfected with gall tumor were collected in Tianmu Mountain, Zhejiang Province;
[0037] 2) Freeze-drying and grinding: freeze-dry the collected cedar cedar samples at -70°C, and then grind them into sample powders with a particle size of less than 2 μm in a mortar;
[0038] 3) Potassium bromide preparation: put the potassium bromide (KBr) powder in a desktop oven, bake at 120°C for 24 hours for drying treatment, grind the potassium bromide powder in a clean agate mortar and pass it for 200 Mesh sieve, dry under infrared light for 4h, put into desiccator and save for later use;
[0039] 4) Preparation of compressed tablets: Mix 100mg of dried potassium bromide with 1mg of sample p...
Embodiment 2
[0063] Example 2 Identification of gall tumor infection status of cedar to be tested
[0064] Take cedar branch sample D1 known to be infected with gall disease, and cedar branch sample W1, branch sample S1, and needle sample S2 of cedar branch sample S2 with unknown gall disease infection status; The disease infection status of cedar was identified.
[0065] 1 Morphological observation of pathogenic bacteria
[0066] Cut tissue pieces from D1, W1, S1, and S2 samples respectively, disinfect them with sodium hypochlorite for 7 to 8 minutes, rinse them with sterile water for 4 to 5 times, and put the tissue pieces into potato dextrose agar (PDA) containing cedar juice for culture. cultured at a constant temperature of 25°C, and purified after the formation of colonies
[0067] Cultivate, record the characteristics of the colonies and perform microscopic examination. The observation results are shown in Table 3.
[0068] Table 3 Pathogen Morphological Observation Results of Each...
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