본 논문에서는 다목적 구조물인 다중연결 해양부유체를 대상으로 변형 기반 모드 차수축소법을 적용하고 차수축소모델의 구조응 답 예측 성능을 향상시키기 위해 유전 알고리즘 기반의 센서 배치 최적화를 수행하였다. 다중연결 해양부유체의 차수축소모델 생성 에 필요한 변형 기반 모드 데이터를 얻기 위해 다양한 규칙파랑하중조건에 대한 유체-구조 연성 수치해석을 수행하고 변형 기반 모드 의 직교성, 자기상관계수를 이용하여 주요 변형 기반 모드를 선정하였다. 다중연결 해양부유체의 경우 차수축소모델의 구조응답 예 측 성능이 계측 및 예측 구조응답 위치에 따라 민감하기 때문에 유전 알고리즘 기반의 최적화를 수행하여 최적의 센서 배치를 도출하 였다. 최적화 결과, 모든 센서 배치 조합에 대한 차수축소모델 생성 및 예측 성능 평가 대비 약 8배의 계산 비용을 절감하였으며, 예측 성능 평가 지표인 평균 제곱근 오차가 초기 센서 배치보다 84% 감소하였다. 또한, 다중연결 해양부유체 모형시험 결과를 이용하여 불 규칙파랑하중에 대한 최적화된 센서 배치의 차수축소모델의 구조응답 예측 성능을 평가 및 검증하였다.

The objectives of this study were to estimate genetic parameters and breeding values of four carcass traits of the Hanwoo cattle breed: carcass weight (CWT), back fat thickness (BFT), eye-muscle area (EMA), and marbling score (MAR). Genetic parameters and breeding values were estimated based on data (“estimating dataset”) collected from September 2004 to March 2019. Predictability of parental breeding value estimates (EBVs) for the performances of progeny of the control group was evaluated on another dataset (“testing dataset”) using linear model equations involving parental EBVs classified into sex and age groups. The parental EBVs of animals in the testing dataset were traced by pedigree relationships of animals in the estimating dataset. Heritability estimates of CWT, BFT, EMA, and MAR were 0.53, 0.43, 0.38, and 0.54, respectively. Genetic correlation coefficients of CWT with BFT, EMA, and MAR were +0.32, +0.59, and +0.11, respectively. Environmental correlation coefficients of CWT with BFT, EMA, and MAR were +0.46, +0.55, and +0.29, respectively. In the testing dataset, partial regression coefficients of phenotypic values of progeny on sire EBVs ranged from +0.43 to +0.60 depending on traits fit into the models, while those on dam EBVs ranged from +0.54 to +0.67. All partial regression coefficients were statistically significant and were approximated to the expected value of +0.5. Together, these values validate the use of parental EBVs for predicting progeny carcass phenotypes in the Hanwoo herd.

Recently there has been an increasing amount of foreign livestock products distributed in the domestic market due to the market opening. Some vicious dealers sell the foreign beef in the trade name of the native beef during the final distribution step to arouse the social criticism frequently. In this report, we investigated a method to distinguish the native beef from the foreign one scientifically using the PCR-RAPD, a recent gene technique. Hygienical safety was also examined using a microbiological test for toxicity of Escherichia coli O157:H7 and the food poisoning bacteria. The conditions of DNA amplification for the PCR analysis were 1 × Taq polymerise buffer, 1.5 mM MgCl₂, 50 uM dNTP, 100 ng primers, 2.5 unit Taq polymerise and 5-20 ng template DNA, with the final volume of 50 Etl. The size of the amplified product was detected mostly in the range of 0.5-2.0 kbp. The size of DNA, gene marking factor, which could be a criterion distinguishing the native beef from the foreign one, appeared approximately 1.2 kbp. The native beef was distinguished from the foreign beef with more than 90% of confidence by the gene marking factor. This method was expected to be useful in the breed discrimination between the native beef and the foreign one. The hygienical test results showed that, fortunately, neither Salmonella spp. and Listeria monocytogenes which form a principal cause of the food poisoning nor Enterohemorrhagic Escherichia coli : EHEC which have provoked a recent social disturbance, were detected at all.

Bulb onion (Allium cepa), which belongs to the family Amaryllidaceae, is one of the oldest vegetative crops known to humans. Despite its high economic value, only a few reports are available on the use of molecular markers in genetic diversity analysis of Allium cepa for its improvement. Molecular genetic markers have been widely used as powerful tools for analyzing the plant genome. In particular, Microsatellites or simple sequence repeats (SSRs) markers are tandem repeats of one to six bp in length and have been proven to be the most powerful polymerase chain reaction (PCR)-based DNA markers in plant diversity analysis. In this study, the genomic DNA was isolated from different Allium cepa lines. The ESTs and gDNA sequences of onion were collected from National Center for Biotechnology information. The SSRs with two to five motifs over a length of 12 bp, were identified using SSRIT (Gramene) software. The PCR products of 100 to 350 bp in length containing SSRs, primers was designed using Primer3 with lengths of 20 to 24 bp and a melting temperature of 60℃. The SSR markers with high polymorphism-information content (PIC) levels was useful for collecting progeny with high genetic homogeneity for onion breeding, and to obtain representative marker sets for genetic tests. The SSR Finder program and the developed SSR markers could be a useful resource for genetic diversity and purity testing in onion.

The cultivated radish (Raphanus sativus L.) is a major vegetable crop in the world wide and fast-growing species that grows inhabitats of six continents. It is very important to determine hybrid seed purity in the production of hybrid Brassica vegetable seeds to avoid unacceptable contamination with self-inbred (sib) seeds. The use of random amplified polymorphic DNA (RAPD) markers for evaluating seed purity in F2 -hybrid radish cultivars demonstrated. One hundred eighty seeds from the F1 male and female harvest were subsequently screened for seed purity using 13 primers. The 13 primers result in 17 cultivar-specific bands and 23 variable RAPD bands scored for cultivar. RAPD analysis of hybrid seeds from the harvest revealed 128 seeds tested except underdevelopment and decayed seeds were sibs. Especially, F2 hybrids of radish, OPC13, OPD20 were presented clear hybrid bands. It maintains higher than average level of genetic diversity compared with their correspondent parents. RAPD amplification of DNA extracted from germinated individuals from the female harvest reveal that 10 of 208 seeds tested were self-inbred (4.8%). RAPD analysis of hybrid seeds from the male harvest revealed 7 of the 208 seeds tested were sibs (3.4%). The RAPD may lead to a better insight in to the hybrid seed purity.