변산반도국립공원을 대상으로 식생분포 실태를 파악하고 현존식생도 조사방법 및 작도 기준을 제시하는데 본 연구의 목적이 있다. 과거 국립공원의 식생조사문헌을 검토하고 현존식생 조사 및 작도기준안을 마련하여, 변산반도국립공원의 식생분포조사를 실시하였다. 변산반도국립공원의 현존식생은 총 8개 식물군락과 기타지역으로 구분되었으며, 2차림인 자연림은 소나무군락, 낙엽활엽수림, 굴참나무군락, 침엽수-활엽수혼효림 4개 식생군락으로, 조림지는 리기다소나무림, 곰솔림, 리기테다소나무림, 리기다소나무-곰솔림 4개 수림으로 구분되었다. 변산반도국립공원의 녹지자연도는 7등급 지역이 약 69.1%로 가장 넓었고, 9등급 지역은 0.36%로 매우 희소하였다. 국립공원의 체계적인 식생조사 및 관리를 위해서는 식생조사방법 및 작도 기준이 필요하다고 판단된다.
In order to determine whether green tea tannin ameliorates abnormal arginine metabolism as the result of excessive arginine, we have assessed the effects of the administration of green tea tannin mixture in rats treated 30 days with 2% arginine. In the arginine-treated group, the level of guanidino compounds such as arginine (Arg), guanidinoacetic acid (GAA), creatinine (Cr), methylguanidine (MG) and guanidinosuccinic acid (GSA), nitric oxide, urea, protein and glucose increased significantly in the serum, urine and kidney, whereas the oxygen species-scavenging enzymes of kidney were reduced as compared with the non-argmme-treated group. By way of contrast, the administration of green tea tannin reduced blood urea nitrogen and serum creatinine, and reduced the urinary excretion of guanidinoacetic acid, creatinine, and NO2-+NO3-. The increased levels of urinary urea, protein and glucose in the arginine-treated group were also lowered by the administration of green tea tannin. In these groups, the activities of superoxide dismutase and catalase in the kidneywere increased, thereby suggesting the involvement of radicals in the normalizing of kidney function. These results show that the abnormal renal function induced by the adminstration of excessive arginine in rats may be restored by treatment with green tea tannin.
This study was carried out to investigate the effect of each single component of the synthetic sex pheromone in the rice green caterpillar, Naranga aenescens and rice leaf roller, Cnaphalocrocis medinalis. Trap catches with each single component or binary mixtures of the sex pheromone in N. aenescens were significantly lower than that with an optimum mixture (2: 1: 4) of Z9-14:Ac, Z9-16:Ac and Z11-16:Ac. But only few number of C. medinalis male was caught in trap baited with each component of the sex pheromone excepting Z13-18:Ald. In an optimum composition of the sex pheromone in C. medinalis, trap catches baited with an 11: 100: 11 mixture of Z11-18:Ald, Z13-18:Ald, and Z13-18:Ac without two alcohol components (Z11-18:OH and Z13-18:OH) was higher than that baited with an optimum mixture of Z11-18:Ald, Z13-18:Ald, Z11-18:OH, Z13-18:OH, and Z13-18:Ac. The efficacy of the sex pheromone lure of N. aenescens kept over 4 weeks. The occurrence of N. aenescens caught in trap baited with sex pheromone gave three peaks and C. medinalis showed two distinct peaks throughout the flight season. Therefore, it can be expected that pheromone-baited trap provides a simple tool for monitoring N. aenescens and C. medinalis in Korea.
The purpose of this research was to identify the difference between expected and actual corporate image in the market and to verify the possibility of green-oriented corporate identity (CI) visual design as a useful method for communicating with consumers. In addition, this research suggests how green-oriented CI visual design can effectively convey corporate image to consumers. The methods of research used to achieve this aim were case studies and questionnaire surveys. In regard to the results, the difference between consumers'perceived favourable corporate image and companies' expectation about corporate image was found. Moreover, the results show that green-oriented visual identity (VI) design can improve corporate image. In turn, the gap between the expected and actual perception of corporate image can be decreased through green-oriented design. Based on these results, a method of effective development for green-oriented VI design is recommended.
We have fabricated and evaluated newNew high high-efficiency green green-light light-emitting phosphorescent devices with an emission layer of [TCTA/TCTA1/3TAZ2/3/TAZ] : Ir(ppy)3 were fabricated and evaluated, and compared the electroluminescence characteristics of these devices were compared with the conventional phosphorescent devices with emission layers of (TCTA1/3TAZ2/3) : Ir(ppy)3 and (TCTA/TAZ) : Ir(ppy)3. The current density, luminance, and current efficiency of the a device with an emission layer of (80Å-TCTA/90˚Å-TCTA1/3TAZ2/3/130Å-TAZ) : 10%-Ir(ppy)3 were 95 mA/cm2, 25000 cd/m2, and 27 cd/A at an applied voltage of 10 V, respectively. The maximum current efficiency was 52 cd/A under the a luminance value of 400 cd/m2. The peak wavelength and FWHM (FWHM (full width at half maximum) in the electroluminescence spectral were 513 nm and 65 nm, respectively. The color coordinate was (0.30, 0.62) on the CIE (Commission Internationale de I'Eclairage) chart. Under the a luminance of 15000 cd/m2, the current efficiency of the a device with an emission layer of (80Å-TCTA/90Å-TCTA1/3TAZ2/3/130Å-TAZ) : 10%-Ir(ppy)3 was 34 cd/A, which has beenshowed an improvement of improved 1.7 and 1.4 times compared to those of the devices with emission layers of (300Å-TCTA1/3TAZ2/3) : 10%-Ir(ppy)3 and (100Å-TCTA/200Å-TAZ) : 10%-Ir(ppy)3, respectively.
Recent studies on nuclear transfer and induced pluripotent stem cells have demonstrated that differentiated somatic cells can be returned to the undifferentiated state by reversing their developmental process. These epigenetically reprogrammed somatic cells may again be differentiated into various cell types, and used for cell replacement therapies through autologous transplantation to treat many degenerative diseases. To date, however, reprogramming of somatic cells into undifferentiated cells has been extremely inefficient. Hence, reliable markers to identify the event of reprogramming would assist effective selection of reprogrammed cells. In this study, a transgene construct encoding enhanced green fluorescent protein (EGFP) under the regulation of human Oct4 promoter was developed as a reporter for the reprogramming of somatic cells. Microinjection of the transgene construct into pronuclei of fertilized mouse eggs resulted in the emission of green fluorescence, suggesting that the undifferentiated cytoplasmic environment provided by fertilized eggs induces the expression of EGFP. Next, the transgene construct was introduced into human embryonic fibroblasts, and the nuclei from these cells were transferred into enucleated porcine oocytes. Along with their in vitro development, nuclear transfer embryos emitted green fluorescence, suggesting the reprogramming of donor nuclei in nuclear transfer embryos. The results of the present study demonstrate that expression of the transgene under the regulation of human Oct4 promoter coincides with epigenetic reprogramming, and may be used as a convenient marker that non-invasively reflects reprogramming of somatic cells.
Pyrausta panopealis is the major pest in green perilla. The larva weaves a web on the shoot of green perilla and damages. In case of extreme, The larva cuts the main branch of green perilla and the leaf of green perilla isn’t harvested anymore. A field study was conducted to estimate economic injury levels (EILs) and control thresholds (CTs) for P. panopealis injuring green perilla in green-houses. Different densities of P. panopealis ranged from 1 to 20 crops (2 units per crop) per 100 crops on 13. June, early inoculation. The number of injured leaf and the rate of injured crop were increased by 23. June, on the other hand were decreased after that day. Also, the amount of yield sow the same result above. The economic loss time calculated by the ratio of cost managing this moth to market price (C/V) (C: cost managing a moth, V: Market price) was 4.0%. The economic injury level was 5.1 larval per 100 crops. The control thresholds calculated by 80% level of economic injury level was 4.1 larval per 100 crops.
본 연구는 Lightcycler (Roche)를 이용한 Real-Time PCR(LC-PCR)기법을 통하여 원유시료에서 신속, 정확하게 황색포도상구균을 검출하는 기법을 개발하고자 하였다. coagulase 전구체를 coding하는 113 bp의 coa 유전자의 증폭, melting curve 분석 및 DNA염기서열을 분석하여 황색포도상구균 특유의 유전자 검출하는 기법을 개발하였다. 또한 분리된 균주중 메치실린에 내성을 나타내는 균주를 검출하고자 penicillin-binding protein, PBP2a (mecA)를 coding 하는 209 bp의 mecA 유전자의 증폭, melting curve 분석 및 DNA염기서열을 분석하여 메치실린내성 황색 포도상구균을 real-time PCR 기법으로 검출하는 기술을 개발하였다. 본 실험에 따르면 647개의 원유시료중 6개의 시료에서 황색포도상구균이 검출되었으며 이중 2개의 시료에서 분리된 황생포도상구균이 메치실린내성 황색포도상구균임을 확인하였다. 또한 DNA 검출한계는 10 fg으로 기존 PCR에 비해 매우 감도가 우수한 것을 확인하였다. 또한 3개의 원유시료에서 돼지나 소의 삼출성 피부염의 원인균인 Staphylococcus chromogenes가 분리되었다.
This study was carried out to investigate the optimum composition of sex pheromone of the rice green caterpillar Naranga aenescens and its efficacy was examined in a paddy field. The mating rate of N. aenescens tended to be increased with age, showing the highest rate of mating at age 2. The highest mating showed within 1 h after the scotophase, and also mating took place even during the photophase. A GC-EAD analysis of virgin female extracts showed two EAG-active components. Their chromatographic behavior was coincident with that of an authentic sample of Z9-14:Ac and Z11-16:Ac, respectively. The mass spectrum of two EAG-active components was almost identical to that of the authentic samples. The EAG response to two compounds, Z9-14:Ac and Z11-16:Ac, was significantly dose-dependent, but response to Z9-16:Ac was not dose-dependent. A 2: 1: 4 mixture of Z9-14:Ac, Z9-16:Ac, and Z11-16:Ac was the most effective composition for attracting N. aenescens. The male moths increased in proportion to the pheromone amount impregnated. The sticky-typed wing trap baited with sex pheromone captured significantly more males than the other two type of trap examined. Trap catches within a paddy field were much more than those in perimeter trap. The trap-baited with sex pheromone gave three or four distinct fluctuation peaks of male catches throughout the flight seasons.
High-efficiency phosphorescent organic light emitting diodes using TCTA-TAZ as a double host and Ir(ppy)3 as a dopant were fabricated and their electro-luminescence properties were evaluated. The fabricated devices have the multi-layered organic structure of 2-TNATA/NPB/(TCTA-TAZ) : Ir(ppy)3/BCP/SFC137 between an anode of ITO and a cathode of LiF/AL. In the device structure, 2-TNATA[4,4',4"-tris(2-naphthylphenyl-phenylamino)-triphenylamine] and NPB[N,N'-bis(1-naphthyl)-N,N'-diphenyl-1,1'-biphenyl-4,4'-diamine] were used as a hole injection layer and a hole transport layer, respectively. BCP [2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline] was introduced as a hole blocking layer and an electron transport layer, respectively. TCTA [4,4',4"-tris(N-carbazolyl)-triphenylamine] and TAZ [3-phenyl-4-(1-naphthyl)-5-phenyl-1,2,4-triazole] were sequentially deposited, forming a double host doped with Ir(ppy)3 in the [TCTA-TAZ] : Ir(ppy)3 region. Among devices with different thickness combinations of TCTA (50 Å-200 Å) and TAZ (100 Å-250 Å) within the confines of the total host thickness of 300 Å and an Ir(ppy)3-doping concentration of 7%, the best electroluminescence characteristics were obtained in a device with 100 Å-think TCTA and 200 Å-thick TAZ. The Ir(ppy)3 concentration in the doping range of 4%-10% in devices with an emissive layer of [TCTA (100 Å)-TAZ (200 Å)] : Ir(ppy)3 gave rise to little difference in the luminance and current efficiency.