Estimation method, information processing apparatus, and non-transitory computer-readable storage medium for estimating motion of animal
US-2018352786-A1 · Dec 13, 2018 · US
US9485970B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9485970-B2 |
| Application number | US-201414911885-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 16, 2014 |
| Priority date | Aug 16, 2013 |
| Publication date | Nov 8, 2016 |
| Grant date | Nov 8, 2016 |
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A selective breeding method of a new strain of Crassostrea gigas with orange left and right shells includes: selecting individuals of C. gigas with purple left shell and black mantle as the male broodstocks and individuals of C. gigas with black left shell and black mantle as the female broodstocks from cultured populations to generate a F1 family by applying single-pair mating strategy; selecting individuals with black purple left and right shells and black mantle from the F1 family as broodstocks to generate F2 families through family selection; selecting individuals with black purple left and right shells and black mantle from the F2 families as broodstocks to generate F3 families through family selection; and selecting individuals with orange left and right shells from the F3 families as broodstocks to propagate to generate a new strain of C. gigas with the stably inherited trait of orange left and right shells.
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We claim: 1. A selective breeding method of a new strain of Crassostrea gigas with orange left and right shells, comprising the following steps: (1) selective breeding of a first generation (F1): selecting individuals of C. gigas with pure purple left shell and black mantle as male broodstocks and individuals of C. gigas with pure black left shell and black mantle as female broodstocks from cultured populations to generate a F1 family by applying single-pair mating strategy; (2) selective breeding of a second generation (F2): selecting individuals with black purple left and right shells and black mantle from the F1 family as broodstocks to generate F2 families through family selection; (3) selective breeding of a third generation (F3): selecting individuals with black purple left and right shells and black mantle from the F2 families as broodstocks to generate F3 families through family selection; and (4) purification of the new strain: selecting individuals with orange left and right shells from the F3 families as broodstocks to propagate to generate a new strain of C. gigas with stably inherited trait of orange left and right shells. 2. The selective breeding method according to the claim 1 , wherein the broodstocks used are one to two years old C. gigas individuals with regular shell ranging from 10 to 12 cm in shell height. 3. The selective breeding method according to the claim 1 , wherein generating the F1 family, the F2 family, the F3 family and the purification of the new strain comprises the following steps: A. single-pair mating and hatching: identifying male and female broodstocks, and separating them into different groups; mating one female with one male to generate full-sib families; putting fertilized eggs obtained from each family separately into 100 L polyethylene plastic buckets filled with filtered seawater; marking on the polyethylene plastic buckets and aerating the seawater slightly; controlling a stocking density at 20-40 eggs/mL and a seawater temperature at 20-24° C., the fertilized eggs developing into D-shaped larvae after 18-20 h incubation, B. larvae culture: selecting the D-shaped larvae with 300 mesh sieve by siphonage and cultivating them in 100 L polyethylene plastic buckets separately, C. spats nursery: cultivating all the families in an outdoor nursery tank after all eyed larvae metamorphose to spats, and D. offshore grow-out: transferring the spats of the families to the same sea area for cultivation after wild C. gigas larvae have finished attaching stage, wherein in the step B, a stocking density is decreased with larval growth, a density being initially set to 10-15 larvae/mL at a stage when a shell height of the larvae is less than 120 μm, controlled at 5-10 larvae/mL when a shell height increases from 120 to 150 μm, maintained at less than 5 larvae/mL when a shell height ranges from 150 to 200 μm, and reduced to 2 larvae/mL when a shell height increases to 250 to 300 μm. 4. The selective breeding method according to the claim 3 , wherein in the step B, a water temperature is controlled from 20 to 24° C., and a salinity is maintained from 28 to 30 psu, wherein in the step B, early larvae with a shell height less than 120 μm are fed with Isochrysis galbana as initial feeds, and larvae at later stages are fed with at least one of Isochrysis galbana, Platymonas helgolandica and Chaetoceros calcitrans , and wherein the step B is free of mutual contamination among different families.
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