For safe disposal of radioactive wastes, accurate analysis of nuclear isotopes is important. It is known that there are 14 nuclides that have to identify nuclide-specific concentration levels. 63Ni, one of non-volatile nuclear isotopes which is included in those 14 nuclides, has to follow chemical separation for exact analysis. As various analysis methods were developed, various methods for analyzing 63Ni also emerged. Past method has used measurement specimens of 59Ni, after 59Ni measurement has been done. It used HClO4, known as strong oxidizing agent, to dissolve DMG, an organic substance used to form 59Ni precipitates. Nowadays, we analyze 59Ni and 63Ni simultaneously, which enables short analysis time, without use of HClO4. But high accuracy is just as important as short measurement time and efficiency. So, this paper compare 63Ni specific activity value used new method with the value, past method used, using real sample’s data. As a result, all sample data from new method’s relative 63Ni specific activity is within the uncertainty range of past ones based on past specific activity value. Consistency of new method’s result and past method’s data increased the reliability of the data and accuracy of those methods.

This study was conducted aiming to figure out two things. First, knowledge of the change in spatial distribution of Tetranychus urticae depending on how to control it (using pesticide or natural enemy). Second, spatial association of T. urticae and Phytoseiulus persimilis in biocontrol plot (B.P). The data was analyzed by spatial analysis by distance indices (SADIE) using global aggregation index, Ia . Ia values were 0.77-1.37 in conventional plot (C.P) and 0.88-1.68 in B.P, respectively. However, the fluctuation level of Ia in B.P was higher than C.P. Therefore, the results indicated that there was a clear spatial pattern change in B.P, i.e. prey’s spatial distribution is affected by natural enemy. And spatial association analysis showed that T. urticae and P. persimilis have positively associated. It means that T. urticae is relatively low mobile prey, and P. persimilis is relatively high mobile predator.

The aim of the study was to investigate the effects of incentive spirometry and Ujjayi breathing technique on the pulmonary function of smokers. Subjects were individuals who had a smoking habit of at least a year. Subjects were randomly divided into 3 groups: the incentive spirometry group (n=8), Ujjayi breathing technique (n=9), and a group applying both incentive spirometry as well as Ujjayi breathing technique (n=8). Each intervention was performed twice a day, 5 times a week, for a total of 8 weeks whereupon the change in pulmonary function was evaluated. A spirometer was used to measure FVC, FEV1, and FEV1/FVC. The survey used for this study included the Fagerström Test of Nicotine Dependence (FTND) and the Shortness of Breath Questionnaire (SOBQ). Study results for the comparison within groups showed that in the group that performed both the incentive spirometry and Ujjayi breathing technique, FEV1 improved with statistical significance (p<.05). Furthermore, within this comparison the FEV1/FVC improved with statistical significance. Comparison amongst the groups showed no statistically significant differences in all areas. Following, to effectively increase pulmonary function in young adult smokers, both incentive spirometry and Ujjayi breathing technique should be employed together.

This study was performed to investigate how changing the period of light and dark influences the vegetative growth and the photosynthesis of Doritaenopsis Queen Beer ‘Mantefon’. Clones of Dtps. Queen Beer ‘Mantefon’ at 4-month-old stage were grown in a closed-plant factory system with four different light/dark cycles; 06/06 h, 08/08 h, 10/10 h, and 12/12 h. Temperature and relative humidity were set at 28oC and 80%, respectively, with a photosynthetic photon flux density of 160 ± 10 μmol·m-2·s-1. Repetitive measurements showed that the leaf length and the leaf width were the longest under 12/12 h closely followed by 10/10 h. The fresh weight and the dry weight of leaves and roots were the heaviest at 10/10 h treated samples. Different CO2 uptake patterns were observed from different light/dark cycles. Under 10/10 h and 12/12 h treatments, the CO2 uptake started at early dark period. When the light/dark cycles were shortened to 06/06 h and 08/08 h, the CO2 uptake started at the middle of dark period. Total CO2 uptake amounts were the highest under 12/12 h treatment followed by 10/10 h, 06/06 h, and 08/08 h treatments. Quantitative measurements showed that the vegetative growths under 10/10 h treatment were comparable with that of 12/12 h treatment. These studies indicated that manipulating light/dark can modify the photosynthesis patterns and vegetative growth of Dtps. Queen Beer ‘Mantefon’, resulting in the reduction of the production period.

Pluripotent stem cells can be derived from both pre- and post-implantation embryos. Embryonic stem cells (ES cells), derived from inner cell mass (ICM) of blastocyst are naïve pluripotent and epiblast stem cells (EpiSCs) derived from post-implantation epiblast are primed pluripotent. The phenotypes and gene expression patterns of the two pluripotent stem cells are different each other and EpiSCs thought to be in a more advanced pluripotent (primed pluripotent state) than mouse ES cells (naïve pluripotent state). Therefore, we questioned whether EpiSCs are less potential to be differentiated into specialized cell types in vitro. EpiSCs were isolated from 5.5～6.5 day post coitum mouse embryos of the post-implantation epiblast. The EpiSCs could differentiate into all tree germ layers in vivo, and expressed pluripotency markers (Oct4, Nanog). Interestingly, EpiSCs also were able to efficiently differentiate into neural stem cells (NSCs). The NSCs differentiated from EpiSCs (EpiSC-NSCs) expressed NSC markers (Nestin, Sox2, and Musasi), self-renewed over passage 20, and could differentiate into two neural subtypes, neurons, astrocytes and oligodendrocytes. Next, we compared global gene expression patterns of EpiSC-NSCs with that of NSCs differentiated from ES cells and brain tissue. Gene expression pattern of brain tissue derived NSCs were closer to ES cell-derived NSCs than EpiSC-NSCs, indicating that the pluripotent stem cell-derived somatic cells could have different characteristics depending on the origin of pluripotent stem cell types. * This work was supported by the Next Generation Bio-Green 21 Program funded by the Rural Development Administration (Grant PJ 008009).

Pyrifluquinazon, as a quinazinalone chemical group, based on a new mode of biological activity. It is reported that mode of action is modifies insect behavior, rapidly stopping feeding such that insects starve to death. Time-release feature and mortality effect on M. persicae using different pyrifluquinazon nano type and non-nano type were compared. Pyrifluquinazon nano type was formulated with different molecular weight and density of used chitosan (CS 30000 0.1% and CS 3000 0.3%). In the CS 30,000 0.1%, the mortality was weakly occurred at early time, but steadily increased after 4days. Finally, we confirmed more than 70% mortality as a peak at 16days. In CS 3000 0.3%, the mortality showed about 70% until 18days as a effective controlled release. Also, We examine time-release feature and mortality effect on M. persicae according to the different pyrifluquinazon nano type(CS 30000 0.1% and CS 3000 0.3%) of concentrations. The CS 30000 0.1% bioassay results of different concentration were showed that the highest concentration(100ppm) was measured better mortality than other concentration at 0 day, but cannot confirm different effect about dissimilar concentration. However, increasing rates of M. persicae were low as treatment concentrate was high. In CS 3000 0.3% 100ppm concentration bioassay result, aphid mortality reached peak at 24 days and increasing rate also low. Additionally, for the comparing of bioassay and feeding behavior of M. persicae against pyrifluquinazon nano types and non-nano type, EPG technique was carried out. In case of non nano type, feeding inhibition efficacy was showed during 4 days after treatment, but appeared similar level with control after 10days. In CS 3000 0.3% 50ppm, residual efficacy was specially showed until 28days after treatment whereas treatments with CS 30000 0.1% were similar to the control after 22days. These result show that the change of feedinng behavior and motrality of M. persicae is correlated with the change of nano type or non nano type of pyrifluquinazon.

Several species of the genus Aphidius are used in biological control programs against aphid pests throughout the world and their behavior and physiology are well studied. But despite knowing the importance of sensory organs in their behavior, their antennal structure is largely unknown. In this study, the external morphology and distribution of the antennal sensilla on the antennal of both female and male adults of A. colemani were described using scanning electron microscopy (SEM). Generally, the filaform antennae of males (1,515.20±116.48 ㎛) are longer than females (1,275.06±116.42㎛). Antennae of this species is made up of scape, pedicel and flagellomeres. Male and female antennae differed in the total number of flagellomeres as 15 in males and 13 in females. Female and male antennae of A. colemani has samely seven types of sensilla. We classified sensilla placodea, Bohm bristles, 2 types of sensilla coeloconica, , 2 types of sensilla basiconica as with a tip pore and with wall pores, sensilla trichodea. In addition, the possible functions of the above sensilla types are discussed in light of previously published literature; mechanoreception(Bohm bristles, sensilla coeloconicaⅡ and sensilla trichodea) and chemoreception(sensilla coeloconicaⅠ, sensilla basiconicaⅠ,Ⅱ and sensilla placodea). Future studies on the functional morphology of the antennal sensilla of A. colemani using transmission electron microscopy (TEM) coupled with electrophysiological recordings will likely confirm the functions of the different sensilla identified in this study.

Background : Cynanchum wilfordi is a typical myocardial medicinal crop. Because it penetrates more than 1m, it requires a lot of labor and harvesting costs. In addition, we needed 4 - 5 times of weeding until July, and in the soil with poor drainage, root rot disease occurs and yield is greatly reduced. Therefore, this study was conducted to develop new cultivation technology that can minimize the effort cost and increase the yield. Methods and Results : As a test material, container standards were used plume tube of diameter 30 ㎝ × height 50 ㎝, 80 ㎝, 100 ㎝. The culture soil manufactured by mixing cokofit 60%, peatmoss 10%, pearlite 6%, vermiculite 10%, zeolite 5%, and charcoal 5%. The compost was made by mixing fowl droppings 45% and cattle manure 5%. The mixing ratio of the culture soil and the compost was 100 : 0, 90 : 10, 80 : 20, 70 : 30, respectively, and the mixture was filled in the container. Cynanchum wilfordi seedling sow raising seedlings during one month seeds become dormancy breaking. Culture soil and container of Cynanchum wilfordi was effective 87% increase (384 ㎏/10 a → 720) in quantity contrast conventional culture in height 50 ㎝ container + culture soil 100 : 0. 80 and 100 ㎝ containers were found to be unsuitable for production throughout the year because of thin thickness of subterranean part and low commercial yield due to the long time required for roots to reach the hardpan layer. The yields of compost mixture decreased from 0% (720 ㎏/10 a) > 10% (642) > 20% (560) > 30% (475) in 50 ㎝ containers. When the compost content was more than 20%, the yield decreased due to physiological damage during the early growth. Conclusion : The culture soil and container cultivate for harvesting ease of Cynanchum wilfordi was effective saving more than 15 times more than the harvest time contrast manpower harvest and the yield was increased by 87%. Also, container cultivation was effective the cost cutting of installation dismantlement and redres since no need to move the cultivation area.

Background : Schisandra chinensis is being weighted difficulties in stable production, there is increasing drought damage caused by climate change as shallow rooted crops. Therefore, the study was performed for water supply capacity and growth characteristics analysis by setting the irrigation method for the drought damage reduction. Methods and Results : Test material was used sophomore V-shaped planting Schisandra chinensis. Irrigation method were surface watering, underground watering, sprinkler and untreated. Underground irrigation was irrigation that buried hose and then dug up the 15㎝. Soil moisture tension was the irrigation after fixed at -30 ㎪(23%). Irrigation timing was performed in June-July that high drought damage and made the most fruit enlargement. The main investigating items were investigated fruit growth, normal fault rate, soil moisture and EC content according to the irrigation method. Normal fruit rate according to irrigation method were appeared in sprinkler(81, 74 %)>underground irrigation(76, 69 %)>surface irrigation(76, 67%)>untreated(66, 52 %). Cluster length of yield component was determined to effective irrigation method in fruit growth the highest in sprinkler. Soil moisture contents was maintained at appropriate level with significant -30㎪(23 %) in the sprinkler. EC content low with a downward trend in underground irrigation and sprinkler. Water supply capacity according to Irrigation Method were sprinkler 40 tons, underground irrigation 85 tons, surface irrigation 138 tons. Conclusion : Appropriate watering methods for drought damage reduction of Schisandra chinensis caused by climate change was determined in the most efficient irrigation method in sprinkler that high fruit growth and normal fruit rate, lower the required of water supply capacity.

Background : Cirsium japonicum seeds is the high price, less than 40% germination rate is low. There is a need for a method developed to increase seed germination rate increases consumption. Also, by measuring the harvest season each functional ingredients contents was performed to investigate the optimal timing harvest of ingredients that target. Methods and Results : Test materials were used Cirsium japonicum seeds harvested from late May until mid-June in medicinal testing ground. GA3(0, 25, 50, 100 ppm), Kinetin(0, 25, 50, 100 ppm) and KNO3(0, 25, 50, 100 ppm) of Growth regulator were treated, it examined the population grew more than 1 ㎜. Contents of functional components to harvest season analyzed by HPLC after pre-treatment harvested and drying the leaves and roots in late august until early November. Germination rate of the growth regulator treatment was higher by 52% from the full ripening brown seeds GA3 100 ppm, 56% in the Kinetin 50 ppm, KNO3 treatment in 52% germination in 25 mM. The white seed germination rate was low at less than 10% of all growth regulator treatment. Functional ingredient content of leaf according to harvest time were higher respectively Rutin is 8.61 ug/g in late october, apigenin is 59.6 ug/g in beginning november, quercetin is 8.61 ug/g in beginning september, kaemferol is 32.9 ug/g in late september. Very low content in roots, there was no significant difference. The main ingredient silymarin was highest 4.36 ㎎/g at the late september in case of leaf, and syringin was maintained at a high level from mid-september to early october. Conclusion : Seed germination is thought to be able to increase the germination through the growth regulator treatment and assort brown seed. Functional components according to the harvest time is determined to be able to improve effective component when processing harvest to select a high yield by the component for the purpose.

Background : Aralia cordata and Polygonum multiflorum GAP cultivation requires a stable drying and storage settings after harvesting. therefore, this experiment was performed in order to effectively manage the physical, chemical and biological hazards. Methods and Results : Test materials were used biennial Aralia cordata, Polygonum multiflorum harvested from the medicinal testing ground. The drying temperatures were treated with 40, 50, 6 0℃ and natural drying. Storage containers were stored in plastic boxes, styrofoam boxes and kraft paper containers, examined the color and quality changes for eight months. Aralia cordata and Polygonum multiflorum drying temperature is dry it took natural drying 720 hours, 40℃ hot air drying 180 hours, 50℃ hot air drying 168 hours and 60℃ hot air drying 108 hours. However, the difference chromaticity of the Lab value corresponding to the temperature does not appear, it was good to dry in a short time at 60℃. Aralia cordata and Polygonum multiflorum stored in a styrofoam box storage method but can be stored at room temperature for up to four months, began to decay caused by moisture content it continues to increase. In plastic box in case of Aralia cordata and kraft vessel in case of Polygonum multiflorum can be stored for eight months in room temperature without decay. Styrofoam boxes stored at 5℃ cold storage were higher water absorption such as room temperature, but decay did not occur. Plastic box and styrofoam box were a tendency such as room temperature. Conclusion : Aralia cordata and Polygonum multiflorum are thought that the color change is not large depending on the drying temperature the lower the water content. Styrofoam storage box, the air permeability is higher than plastic boxes and containers Kraft vessel, decay occurs expected increase.

The flower buds of Sophora japonica L (SF), as a well-known traditional Chinese medicinal herb, have been used to treat bleeding-related disorders such as hematochezia, hemorrhoidal bleeding, dysfunctional uterine bleeding, and diarrhea. However, no specific anti-cancer effect and its molecular mechanism of SF have been described. Thus, we performed in vitro study to investigate if treatment of SF affects activating transcription factor 3 (ATF3) expression and ATF3-mediated apoptosis in human colorectal cancer cells. The effects of SF on cell viability and apoptosis were measured by MTT assay and Western blot analysis against cleaved poly (ADP-ribose) polymerase (PARP). ATF3 activation induced by SF was evaluated using Western blot analysis, RT-PCR and ATF3 promoter assay. SF treatment caused decrease of cell viability and increase of apoptosis in a dose-dependent manner in HCT116 and SW480 cells. Exposure of SF activated the levels of ATF3 protein and mRNA via transcriptional regulation in HCT116 and SW480 cells. Inhibition of extracellular signal-regulated kinases (ERK) 1/2 by PD98059 and p38 by SB203580 attenuated SF-induced ATF3 expression and transcriptional activation. Ectopic ATF3 overexpression accelerated SF-induced cleavage of PARP. These findings suggest that SF-mediated apoptosis may be the result of ATF3 expression through ERK1/2 and p38-mediated transcriptional activation.