Method for evaluating resistance of brassica plants on club root
A technology for clubroot and clubroot, applied in botany equipment and methods, horticultural methods, horticulture, etc., can solve the problem of clubroot disease, which is difficult to ensure the consistency of identification conditions, difficult to complete large-scale variety identification, and time-consuming and other problems, to achieve the results of accurate and reliable identification results, strong practicability, and easy operation
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Embodiment 1
[0042] experiment material:
[0043] Varieties to be identified are: Chinese cabbage C09-35, Chinese cabbage C09-36, Chinese cabbage C09-37, Chinese cabbage C09-38,
[0044] The control is: Chinese cabbage 83-1, a high-susceptibility variety known to be susceptible to clubroot;
[0045] The test steps are as follows:
[0046] (1) The identification of mycorrhiza of Plasmodium brassicae, according to the following conventional methods:
[0047] Root swelling caused by clubroot infection only occurs in cruciferous crops. It is mainly distinguished from root swelling caused by root-knot nematodes. The root epidermis enters the cambium, which stimulates the parenchyma cells to divide and expand, and finally causes the root to form a nodule. Root swelling caused by clubroot can occur in both the main and lateral roots of the crop. The nodules on the main root are mostly close to the upper part, round or oval, with uneven and rough surfaces, and may crack or not crack later; the ...
Embodiment 2
[0077] Test materials: Chinese cabbage C10053, Chinese cabbage C10054, Chinese cabbage C10055, Chinese cabbage C10056;
[0078] The control is: Chinese cabbage 83-1, a high-susceptibility variety known to be susceptible to clubroot;
[0079] Test procedure is except that following operational measures are different, and all the other operational measures are identical with embodiment 1:
[0080] (2) Mycorrhizal inoculation method of Plasmodium brassicae in laboratory freezer box
[0081] (1) Preparation of culture substrate
[0082] The perlite is soaked in acidic water with a pH of 5.0 for 96 hours before use, and the culture medium is mixed according to the ratio of perlite and crushed Plasmodium brassica mycorrhizae in a ratio of 1 liter: 15 grams;
[0083] (3) Sowing
[0084] Freezing box 1 is placed in the stainless steel pan;
[0085] (6) Put the stainless steel plate filled with the inoculum solution and the freezing box inside the plate (that is, the freezing box w...
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