Method for inducing vein burst of Newhall navel orange in magnesium deficiency condition
A technology of hormone umbilicus and magnesium deficiency, applied in the directions of botanical equipment and methods, application, magnesium fertilizer, etc., can solve the problems of leaf loss, leaf yellowing, magnesium deficiency, etc., and achieve the effect of easy to master and simple operation.
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Embodiment 1
[0042] Example 1 Initial Experiment of Magnesium Deficiency Inducing Newhall Navel Orange Leaf Vein Burst
[0043] Select grafted Newhall navel orange seedlings with a diameter of about 0.5 cm and a height of about 30 cm, and cut the aboveground part of the plant to a height of about 20 cm, leaving 5 autumn leaves in 2010, and cutting the main root to about 5 cm. On March 23, 2011, the potted sand cultivation experiment was carried out. One plant per pot was added with 8 kg of quartz sand and perlite (volume ratio 1:1), and a tray was placed on the bottom of the pot. In the early stage, only deionized water was supplied for seedling hardening.
[0044] On April 15, 2011, magnesium deficiency stress culture was carried out. The culture medium uses Hoagland (1 / 2 concentration) and Aron full concentration formula nutrient solution:
[0045] The formula of the normal group is: Ca(NO 3 ) 2 4H 2 O2mmol·L -1 , KNO 3 3mmol·L -1 , NH 4 h 2 PO 4 0.5mmol·L -1 , MgSO 4 ·7H 2...
Embodiment 2
[0054] Example 2 Simple Magnesium Deficiency Induced Newhall Navel Orange Leaf Burst Experiment
[0055] Such as figure 1 As shown, select the 2-year-old Newhall navel orange grafted seedlings with a rootstock diameter of about 1.5cm and a height of about 35cm, and cut the aboveground part of the plant to about 20cm, leaving five 2-year-old leaves (2013 autumn leaves) , The main root is cut to about 5cm. On March 18, 2014, the potted sand culture experiment was carried out. One plant per pot was added with 8 kg of quartz sand and perlite (volume ratio 1:1), a tray was placed on the bottom of the pot, and deionized water was supplied for hardening for 15 days.
[0056] On April 3, 2014, 1 / 4 of the improved Hoagland and Aron formula nutrient solutions were used to culture the grafted seedlings for 30 days. Its formula is: Ca(NO 3 ) 2 4H 2O0.8125mmol·L -1 , KNO 3 0.1575mmol·L -1 , NH 4 NO 3 0.125mmol·L -1 , KH 2 PO 4 0.125mmol·L -1 , MgSO 4 ·7H 2 O0.375mmol·L -1 ...
Embodiment 4
[0068] Example 4 Microscopic changes of leaf main vein and lateral vein tissue structure
[0069] Observation of leaf microstructure: taking the 2-year-old autumn shoot old leaves of Example 2 as objects, the conventional paraffin section method was adopted. The thickness of the main vein slices was 6 μm, and that of the lateral veins was 5 μm; they were counter-stained with safranin and fast green, sealed with neutral resin, and the fiber structure changes of the main veins and lateral veins were observed. The pictures were acquired by OLMPUSBX-51 microscope imaging system.
[0070] Test results such as Figure 4 shown. Among them, A: main vein at the 2nd month; B: main vein at the 4th month; C: primary phloem cell degeneration (red arrow); D: main vein at the 6th month, phloem cells grew significantly (black arrow) ;E: phloem cell enlargement (black arrow), cell disintegration (red arrow); F: main vein burst; G: lateral vein at the second month; H: lateral vein at the fou...
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