Feeding additive for barbus hollandi fry and application of feeding additive in barbus hollandi fry cultivation
A Hastelloy formula and additive technology, applied in the field of aquaculture, can solve problems such as difficult to find traces
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Embodiment 1
[0031] 1. Preparation of Culture Medium
[0032] The present embodiment utilizes the nutrient solution containing different nutrients to cultivate Paramecia, and the specific nutrient solution types involved and their corresponding preparation methods are as follows:
[0033] (1) Brassica napus extract culture solution: take fresh Brassica oleracea leaves, absorb the moisture on the surface of the leaves after cleaning, smash the background of the leaves and fully squeeze out the slurries of the cabbage leaves, filter the extruded slurries with gauze, and collect the filtrate, 15 g of the filtrate was added to 450 mL of water, boiled, cooled to room temperature, and allowed to stand for 1 day to obtain a culture solution for paramecia inoculation.
[0034] (2) Cooked egg yolk culture solution: mash 0.5 g of egg yolk, add 100 mL of cold boiled water to it, stir well to fully mix the egg yolk and water, and let stand for 1 day to obtain a culture solution for paramecium inoculat...
Embodiment 2
[0049] 1. Paramecia culture
[0050] The paramecia culture method adopted in the present embodiment is as follows:
[0051] Take fresh lettuce leaves, clean them, absorb the moisture on the surface of the leaves, smash the background of the leaves and fully squeeze out the pulp of the leaves, filter the extruded pulp with gauze, collect the filtrate, add 15g of the filtrate to 450mL of water, and boil. After cooling, 0.3 g of the freeze-dried powder of bacterial strain is added thereto, and the culture solution for inoculation of paramecium is obtained after the freeze-dried powder of the composite bacterial strain is completely dissolved. Use a capillary pipette to inoculate 20 paramecia into the container containing the above-mentioned culture solution, then cover the opening of the container with gauze, and cultivate the paramecia at a constant temperature of 25°C and pH=6.8±0.2. The culture period was 5 days, and one tenth of the culture medium in the culture vessel was p...
Embodiment 3
[0059] In this example, the paramecia culture system obtained after the culturing period of the seven treatment groups in Example 2 was used as the base liquid, and the influence of the strain regulator on the paramecia culture system was explored. In this example, the same base solution was used to divide into 4 treatment groups, which were specifically marked as treatment group 1, treatment group 2, treatment group 3 and treatment group 4. Bacillus, Escherichia coli and Paramecia were counted.
[0060] Treatment group 1: The ethanol extract of Rhizoma Rhizoma was added to the base solution, and the addition amount of the extract of Rhizoma Rhizoma was 8 wt% of the base solution, and the culture was continued for 8 hours.
[0061] Treatment group 2: The ethanol extract of Rhizoma Imperatae was added to the base solution, and the amount of the extract of Rhizoma Rhizoma was 8 wt% of the base solution, and the culture was continued for 8 hours.
[0062] Treatment 3 groups: the...
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