Portunus trituberculatus release effect evaluation method
A technology of portunus trituberculatus and individuals, which is applied in the field of seawater animal release, can solve the problems of being unable to scientifically evaluate the level of supplementation of wild resources by the released population, and the inability to accurately distinguish the released individuals from the recaptured population from wild individuals and their quantity, achieving obvious survival/ Death advantage, effect of simplified preparation
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Embodiment 1
[0053] Embodiment 1: Establishment of marking and releasing populations and methods
[0054] 1. Tracing of Individuals of Portunus trituberculatus Family with Specific Molecular Fingerprints
[0055] The offspring bred by each pair of parents have a consistent DNA molecular fingerprint, which is unique to the individual / family and is different from other families and individuals and lasts a lifetime. Using this specific molecular fingerprint and referring to the parental genotype, a specific individual / family can be accurately identified from a mixed population.
[0056] The microsatellites of Portunus trituberculatus are widely distributed in the genome, and the level of genetic variation is rich, which has the characteristics of genetic selection neutrality. The molecular fingerprint formed by the combination of different genotypes of microsatellite molecular markers is an ideal tool for individual / family identification. Taking the microsatellite loci of Portunus trituberc...
Embodiment 2
[0071] Example 2: Small scale testing
[0072] In 2014, the method of the present invention was used to conduct a simulation experiment of releasing fish in Haifeng Aquaculture Co., Ltd., Changyi, Weifang City, Shandong Province. The specific implementation method is as follows: in August 2014, the research group used wild individuals of Portunus trituberculatus to construct 6 full-sib families, which were named family A to family F; Muscle samples from the female parent of the family, stored in a -80°C refrigerator; Cultivated to the second stage of juvenile crabs, 200 individuals were randomly selected from each family, and mixed with 6 families of the same specification cultivated by Haifeng Company, and 200 individuals from each family were mixed; By the time of harvest, all individuals took the large claw muscle tissue and extracted DNA; the Portunus trituberculatus SSR primers described in Table 1 were used to form a multiplex PCR reaction system for Portunus trituberculat...
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