• 한국해양환경ㆍ에너지학회지
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• 제13권1호
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• pp.1-11
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• 2010

2012 여수 엑스포 부지인 신항해역의 생물해양학적 환경특성과 이를 조절하는 물리 화학적 요인의 경시적인 변동특성을 파악하기 위해 1개 정점을 대상으로 2006년 4월부터 2007년 12월까지 일주일 간격을 원칙으로 현장조사를 실시하였다. 수온은 표층에서 $6.8{\sim}27.8^{\circ}C$, 저층에서 $6.3{\sim}25.9^{\circ}C$의 범위를, 염분은 표층에서 12.8~33.0 psu의 범위를, 저층에서 25.2~33.6 psu의 범위를 보였다. 강우가 집중된 하계에 급격하게 염분이 낮아지면서 표·저층사이에 강한 염분약층이 형성되었다. 용존무기질소(DIN)는 표층에서 $1.36{\sim}82.7{\mu}M$, 저층에서 $1.27{\sim}25.2{\mu}M$의 범위를, 인산성 인은 표층에서 $0.06{\sim}2.13{\mu}M$, 저층에서 $0.07{\sim}1.38{\mu}M$의 범위를, 규산성 규소는 표층에서 $1.68{\sim}52.0{\mu}M$, 저층에서 $1.37{\sim}30.7{\mu}M$의 범위를 나타내었으며, 영양염류는 계절적으로 강우량이 많은 시기와 저수온기에 높고, 춘계와 추계에 크게 감소하였다. N/P ratio는 표층에서 4.43~325, 저층에서 3.57~321의 범위로 변동하였으며, 강우가 집중되는 시기에 급격히 증가하고, 그 외 시기에는 16 내외의 값을 나타내었다. $Chlorophyll{\alpha}$는 표층에서 $0.46{\sim}65.0{\mu}g$ $L^{-1}$, 저층에서 $0.71{\sim}15.0{\mu}g$ $L^{-1}$의 범위를 나타내었으며, 저수온기에는 낮은 농도로 유지되다 고수온기에 생물량이 급격히 증가하였다. 주성분분석과 중회귀분석 결과, 본 연구해역의 물리 화학적 및 생물학적 요인의 경시적인 변동은 염분의 변화로 표현되는 담수유입에 의해 크게 지배되는 구조를 보이고, 공급된 무기영양염은 식물플랑크톤의 흡수 동화를 통해 비교적 효율적으로 조절되고 있으며, 또한 저수온기에는 무기화과정과 영양염 순환을 통해 재생산된 영양염이 이 해역의 환경구조에 큰 영향을 미치는 것으로 판단되었다.

• 생태와환경
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• 제34권1호통권93호
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• pp.30-44
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• 2001

수자원관리에 중요한 육수학적 정보를 제공하기 위해 1993년 6월에서 1994년 5월까지 주암호에 대하여 월간 조사를 실시하였다. 표층의 투명도, 엽록소 a, 총질소, 총 인농도 및 일차생산력은 조사기간 각각 1.7${\sim}$4.5 m, 0.9${\sim}$12.5 mgChl/m$^{3}$, 0.53${\sim}$1.48 mgN/l, 6${\sim}$29 mgP/m$^{3}$, 304${\sim}$2,549mgCm$^{-2}$day$^{-1}$로 이들의 하계 평균농도로 산정한 주암호의 영양상태는 중영양호로 해당된다. 유역으로부터의 인 유입은 집중호우시에 다량 유입되기 때문에 총인 농도도 하계에 높고 동계에 낮다. 주암호의 연간 수면적당 인부하량은 0.94gPm$^{-2}$yr$^{-1}$로 부영양화 임계부하량(1.0gPm$^{-2}$yr$^{-1}$)에 거의 근접하고 있다. 주암호에서 식물플랑크톤에 대한 제한영양소 조사결과 인과 질소가 동시에 성장을 제한하는 요소로 나타났다. 식물플랑크톤군집의 계절별 천이양상은 온대호수의 일반적 경향과 같이 동계에 춘계에는 규조류(Asterionella formosa, Aulacoseira granulata var. angustissima)가 우점하였고, 하계에는 남조류(Microcystis aeruginosa, M. sp., M. viridis)가 우점하였다. 동물플랑크톤은 요각류 유생이 연중 우점하였고 8월에는 요각류 유생 이외에 지각류인 Bosminopsis longirostris가 각각 우점하였다. 조사기간 주암호 퇴적물의 조사 정점별 유기탄소 및 인, 질소의 평균 함량은 각각 9.5${\sim}$14.0 mgC/g, 1.0${\sim}$1.82mgP/g, 0.51${\sim}$0.65mgN/g의 분포를 보여주었다. 주암호 유역으로부터의 유기물 유입량은 1,222 tonC/yr이며 식물플랑크톤의 일차생산에 의한 자체생성유기물량은 6,718 ton/yr으로 전체 유기물부하량중 자체생성 유기물 비율이 대부분을 차지했다. 주암호의 부영양화를 방지하기 위해 앞으로의 유역관리는 점오염원의 관리와 더불어 비료사용량의 축소, 축산분뇨의 적절한 처리, 토양유실방지등 유역의 비점오염원에 대한 관리에 더욱 집중해야 할 것으로 보인다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.88-89
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• 2013

A variety of influenza A viruses from animal hosts are continuously prevalent throughout the world which cause human epidemics resulting millions of human infections and enormous industrial and economic damages. Thus, early diagnosis of such pathogen is of paramount importance for biomedical examination and public healthcare screening. To approach this issue, here we propose a fully integrated Rotary genetic analysis system, called Rotary Genetic Analyzer, for on-site detection of influenza A viruses with high speed. The Rotary Genetic Analyzer is made up of four parts including a disposable microchip, a servo motor for precise and high rate spinning of the chip, thermal blocks for temperature control, and a miniaturized optical fluorescence detector as shown Fig. 1. A thermal block made from duralumin is integrated with a film heater at the bottom and a resistance temperature detector (RTD) in the middle. For the efficient performance of RT-PCR, three thermal blocks are placed on the Rotary stage and the temperature of each block is corresponded to the thermal cycling, namely $95^{\circ}C$ (denature), $58^{\circ}C$ (annealing), and $72^{\circ}C$ (extension). Rotary RT-PCR was performed to amplify the target gene which was monitored by an optical fluorescent detector above the extension block. A disposable microdevice (10 cm diameter) consists of a solid-phase extraction based sample pretreatment unit, bead chamber, and 4 ${\mu}L$ of the PCR chamber as shown Fig. 2. The microchip is fabricated using a patterned polycarbonate (PC) sheet with 1 mm thickness and a PC film with 130 ${\mu}m$ thickness, which layers are thermally bonded at $138^{\circ}C$ using acetone vapour. Silicatreated microglass beads with 150~212 ${\mu}L$ diameter are introduced into the sample pretreatment chambers and held in place by weir structure for construction of solid-phase extraction system. Fig. 3 shows strobed images of sequential loading of three samples. Three samples were loaded into the reservoir simultaneously (Fig. 3A), then the influenza A H3N2 viral RNA sample was loaded at 5000 RPM for 10 sec (Fig. 3B). Washing buffer was followed at 5000 RPM for 5 min (Fig. 3C), and angular frequency was decreased to 100 RPM for siphon priming of PCR cocktail to the channel as shown in Figure 3D. Finally the PCR cocktail was loaded to the bead chamber at 2000 RPM for 10 sec, and then RPM was increased up to 5000 RPM for 1 min to obtain the as much as PCR cocktail containing the RNA template (Fig. 3E). In this system, the wastes from RNA samples and washing buffer were transported to the waste chamber, which is fully filled to the chamber with precise optimization. Then, the PCR cocktail was able to transport to the PCR chamber. Fig. 3F shows the final image of the sample pretreatment. PCR cocktail containing RNA template is successfully isolated from waste. To detect the influenza A H3N2 virus, the purified RNA with PCR cocktail in the PCR chamber was amplified by using performed the RNA capture on the proposed microdevice. The fluorescence images were described in Figure 4A at the 0, 40 cycles. The fluorescence signal (40 cycle) was drastically increased confirming the influenza A H3N2 virus. The real-time profiles were successfully obtained using the optical fluorescence detector as shown in Figure 4B. The Rotary PCR and off-chip PCR were compared with same amount of influenza A H3N2 virus. The Ct value of Rotary PCR was smaller than the off-chip PCR without contamination. The whole process of the sample pretreatment and RT-PCR could be accomplished in 30 min on the fully integrated Rotary Genetic Analyzer system. We have demonstrated a fully integrated and portable Rotary Genetic Analyzer for detection of the gene expression of influenza A virus, which has 'Sample-in-answer-out' capability including sample pretreatment, rotary amplification, and optical detection. Target gene amplification was real-time monitored using the integrated Rotary Genetic Analyzer system.

• 대한전기학회:학술대회논문집
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• 대한전기학회 1999년도 하계학술대회 논문집 D
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• pp.1559-1562
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• 1999

We formed $SiO_2:F$ films by low-temperature process called Liquid Phase Deposition(LPD) and investigated its electrical and physical properties. Because of the use of room-temperature and no special vacuum apparatus for forming $SiO_2:F$ films, this technique can have some advantages related with the application to dielectric interlayer for multilevel structure in ULSI devices. The growth rate 100nm/hr was obtained at the growth solution of 2.5mol/l. The P-etch rate showed a similar or better tendency compared with $SiO_2$ films formed by CVD, Sputter, E-beam evaporator etc.. The fourier transform infrared (FTIR) spectra revealed that the contained fluorine atoms exist uniform throughout the formed $SiO_2$ films. The Scanning Electron Microscope images showed that LPD-$SiO_2$ films could be stably grown on silicon substrates and the good step-coverage could also be obtained, which indicates that the LPD-$SiO_2$ films have some possibility of the application to planarization and interlayer dielectric films which are vitally necessary to achieve the multilevel interconnection in ULSI. The I-V characteristics has some distinct differences according to the concentration of growth solution.

• 대한화학회지
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• 제52권2호
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• pp.124-132
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• 2008

H3SO4(M: 몰농도) 용액에서 탄소강의 부식방지제로 Furfural hydrazone 유도체의 효과를 질량손실법 및 정전류극성법을 사용해 연구하였다. 이들 유도체 존재하에서 탄소강의 부식속도가 급격히 감소함을 관찰하였다. 이 연구로부터 부식방지효율은 부식방지제 농도가 증가함에 따라 증가하였고 I와 SCN을 첨가하면 부식방지효율은 더욱 증가되었다. 질량손실법을 사용해 5×10-6 M의 유도체가 있을 때와 없을 때 30-60oC 사이에서 탄소강 부식에 미치는 온도 효과를 보았다. 부식과정에 대한 활성화에너지(Ea*)와 다른 열역학적 변수들을 계산하였고 이들에 대해 논의하였다. 정전류극성법을 통해 유도체들이 혼합형 방지제로 작용함을 알았고 외부전류를 흘려주었을 때 음극은 더욱 분극되었다. 3M H3SO4 용액에서 탄소강 표면에 이들 유도체들의 흡착은 Frumkin의 흡착등온을 따랐다. 이들 유도체들의 화학구조를 통해 부식방지 메커니즘을 설명하였다.

• 한국재료학회지
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• 제19권9호
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• pp.510-515
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• 2009

The compound of 2,6-Bis[(9-phenylcarbazolyl)ethenyl]naphthalene (BPCEN-1), 2-[6-{1-Cyano-2-(9-phenylcarbazoly)vinyl}naphthyl]-3-(9-phenylcarbazolyl)acrylonitrile (BPCEN-2), 2,6-Bis[{4-(1-naphthy l)phenylamino} styrenyl] naphthalene (BNPASN-1), 2-[6-{1-Cyano-2-(naphthylphenylaminophenyl) vinyl}naphthyl]-3-(naphthylphenylaminophenyl)acrylonitrile (BNPASN-2) was analyzed electrochemically and spectroscopically and can be obtained by bonding phenylcarbazolyl, naphthylphenylaminophenyl and -CN ligands to 2,7-naphthalene. The electrochemical and spectroscopic study resulted in the P-type (BPCEN-1, BNPASN-1) being changed to N-type (BPCEN-2, BNPASN-2) according to -CN bonding despite having the same structure. The value of band gap(Eg) was revealed to be small as HOMO had shifted higher and LUMO lower. The Eg value for naphthylphenylaminophenyl ligand was reduced because it has a smaller HOMO/LUMO value than that of phenylcarbazolyl from a structural perspective. The electrochemical HOMO/LUMO values for BPCEN-1, BPCEN-2, BNPASN-1, BNPASN-2 were measured to be 5.55eV / 2.83eV, 5.73eV / 3.06eV, 5.48eV / 2.78eV, and 5.53eV / 2.98eV, respectively. By -CN ligand, the UV max, Eg and PL max were shifted to longer wavelength in their spectra and the luminescence band could be also confirmed to be broad in the photoluminescence (PL) spectrum.

• BMB Reports
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• 제43권8호
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• pp.567-572
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• 2010

In this study, we cloned the ERF-B3 subfamily transcription factor gene BnaERF-B3-hy15 from Brassica napus L. Huyou15. This 600 bp gene encodes a 199 amino acid classic ethylene responsive factor (ERF), which shown no binding or very weak binding GCC box-binding activity by the yeast one-hybrid assay. We used gene shuffling and the yeast one-hybrid system to obtain three mutated sequences that can bind to the GCC box. Sequence analysis indicated that two residues, Gly156 in the AP2 domain and Phe62 at the N-terminal domain were mutated to arginine and serine, respectively. Changes of Gly156 to arginine and Phe62 to serine increased the GCC-binding activity of BnaERF-B3-hy15 and the alter of Gly156 to arginine changed the AP2-domain structure of BnaERF-B3-hy15.

• 수산해양기술연구
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• 제42권1호
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• pp.19-29
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• 2006

To investigate the fishery and fishing ground environment of red horsehead (Branchiostegus japonicus), the author analyzed the fishery data and examined the amount of catches and oceanic environment on the adjacent seas of Jeju island and East China Sea. It was turned out that the favourable season of the red horsehead fishery is the month from March to June, the main fishing ground is located in 60 mile radius from the position $32.5^{\circ}N,\;125.7^{\circ}E$. The bottom seawater temperature in fishing ground was shown between $l3^{\circ}C\;and\;16^{\circ}C$, the salinity was appeared between 33.5 and 34.0psu without the seasonal variation of the year. Concentrations of materials(e.g, $NO_3^-\;and\;NO_2^-$) in spring and summer time in main fishing ground were higher than any other seasons, but that of phospheric materials were lower than any other seasons. Concentrations of $chlorophyll\;-\;{\alpha}$ in the main fishing ground was the highest in spring and summer at the surface layer, but the vertical profile of the $chlorophyll\;-\;{\alpha}$ concentrations in all seasons were not variable at bottom layer. Mean density of zooplankton abundance according to the vertical structure was higher and much stable in summer and autumn than spring and winter.

• 한국식품영양과학회지
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• 제26권2호
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• pp.242-247
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• 1997

엉겅퀴 지상부 중 심혈관계에 대한 영향과 활성성분을 구명하기 위하여 S.D.계 흰쥐의 적출한 성장과 혈관에 대한 작용과 혈압을 측정하였고 그 유효성분을 분리하였다. 엉겅퀴 지상부의 MeOH 추출엑스를 계통분획법에 의하여 분획하여 심장과 혈관에 작용하는 BuOH층을 분리, 정제한 후 UV, IR, $^{1}H-NMR$, $^{13}C-NMR$ 등의 분석방법으로 동정한 결과 flavonoid 배당체인 hispidulin $7-0-{\alpha}-L-rhamnopyranosyl(1{\rightarrow}2)-{\beta}-D-glucopyranoside$로 밝혀졌으며 흰쥐의 심박수 증가 및 심근과 흉부대동맥을 수축시켰고 혈압을 상승시키는 효과가 있었다.

• Journal of Ecology and Environment
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• 제40권1호
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• pp.12-19
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• 2016

Background: Direct impact of inorganic carbon (i.e., carbon dioxide ($CO_2$)) on the periphyton community is important to understand how and to what extent atmospheric conditions can affect the structure and dynamics of these communities in lotic systems. We investigated the influence of elevated $CO_2$ concentration on the periphyton community in the artificially constructed channels during the winter period. The channels made of acrylic paneling were continuously supplied with surface water discharged from a small reservoir, which was supported with ground water, at a flow rate of 5 L/min, and water temperature ranging $4-5^{\circ}C$. The effects of elevated $CO_2$ concentrations (790 ppm) were evaluated in comparison with the control (395 ppm $CO_2$) by analyzing pH, water carbon content and nutrients in water, periphyton composition and biomass, chlorophyll-a, ash-free dry-matter at 2-day intervals for 10 days. Results: After the addition of $CO_2$, significant decreases of pH, $NH_3-N$, and $PO_4-P$ (p < 0.05) and increases of chlorophyll-a, ash-free dry-matter, and the cell density of periphyton (p < 0.01) were observed, whereas the species composition of periphyton and water carbon content did not change. Conclusions: These results suggest that elevated $CO_2$ in flowing water system with low temperature could facilitate the growth of periphyton resulting in biomass increase, which could further influence water quality and the consumers throughout the food web.