• 한국응용곤충학회지
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• 제30권1호
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• pp.65-79
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• 1991

서울 남산의 식생과 개미군집의 종조성 및 colony 밀도를 구명하기 위하여 1989년 6월부터 1990년 10월 까지 13종의 식생에다 39방형구를 설치하여 443colony를 채집한 결과 4아과 23속 28종의 분포를 확인하였다. 그 중에 배잘록침개미(신칭) Cerapachys humicola $O_{GATA}$는 한국미기록아과인 배잘록침개미아과(신칭) Cerapachinae에 속하는 미기록종이었다. 식생별 개미군집의 종조성은 아카시나무군락에 3아과 14속 15종으로서 남산에서 채집된 전종수인 28종의 53%에 해당되며, 신갈나무에는 3아과 12속 14종이 채집되어 전체종수의 50%로서 비교적 종류조성이 풍부하였고, 버즘나무에 3아과 3속 3종으로 가장 단조로웠다. 식생별 colony 밀도는 산벚나무군락에서 7,875colony/$m^2$로 가장 높고, 버즘나무에서 1,000colony/$\m^2$로서 가장 낮았다. 개미의 종별 상대밀도는 스미드개미가 RD=0.422로 가장 높았다. 배잘록침개미, 장구개미가 RD=0.002로 가장 낮았다. 식생간에 개미군집의 유사도를 Sorensen지수로 분석한 결과는 산벚나무와 팥배나무군락사이에서 0.745, 산벚나무와 소나무군락사이에서 0.736으로 높았고, 산벚나무와 화백군락 그리고 산벚나무와 메타세코이아군락간에서 각각 0.164로 가장 낮았다. 각 식생군락내의 개미의 우점도를 Simpson공식에 의해 분석하여 볼 때 버즘나무군락에 $\lambda$=0.067로 가장 낮았다. 역 Simpson지수에 의하여 분석된 다양도는 메타세코이아 $d_{s}$=14.925 리기다소나무 $d_{s}$=7.874순으로 높았고 버즘나무군락에$d_{s}$=2.545로 가장 낮았다. $d_{s}$와 $d_{max}$를 사용하여 산출한 균등도는 메타세코이아군락에서 $E_{s}$=0.713, 화백군락에서 $E_{s}$=0.624로 높았고, 신갈나무군락에서 $E_{s}$=0.182로 가장 낮았다.

• 한국환경농학회지
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• 제17권2호
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• pp.107-116
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• 1998

광분해 촉진에 의한 작물 및 토양중 잔류농약의 인위적인 경감을 위하여 자연계에 천연적으로 존재하거나 또는 합성화합물중에서 감광작용을 갖을 것으로 예상되는 40여종에 대하여 감광작용을 검정하여 6종의 화합물을 선정하고 고추와 토마토에 사용되는 살균제중 procymidone,vinclozolin 및 carbendazim을 관행법에 따라 상기 작물에 살포한 후 감광제를 처리하여 다음과 같은 결과를 얻었다.1.Acetone에 용해되어 있는 procymidone,vinclozolin, carbendazim의 최대흡장 파장 (${\lambda}$max)은 모두 209nm 이었고,최대 molar absorptivity (${\varepsilon}$max)는 각각 853,853,8740이었다.2.40여종의 자연계에 천연적으로 존재하는 화합물과 합성 유기 및 무기화합물의 감광작용을 탐색하여 방향족 ketone계인 PS-1,방향족 amine계인 PS_2, quinone계인 PS-3,무기화합물인 PS-4,유기염산인 PS-5,광촉매제인 PS-6를 선발하였다.3.감광제 살포에 의한 토양중 농약의 광분해 촉진효과에서 procymidone의 경우에는 감광제 PS-2를 처리 한 후 3일에 대조구 잔류량의 59%로 감소하여 그 효과가 현저하였다.4.토양에서 vinclozolin의 경우에는 감광제 PS-2를 처리 한 후 1일 잔류랑이 된 양이 대구조의 71%로 그리고 15일 후에는 21%로 감소하였다.

• 생명과학회지
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• 제17권2호통권82호
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• pp.266-271
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• 2007

BPA는 플라스틱 가소제 및 폴리카보네이트 플라스틱 생산의 모노머로 광범위하게 사용되어 왔으며, 년간 세계적으로 640,000톤 이상이 생산되고 있다. 내분비장애활성을 가진 BPA는 수계 및 공업용수에서 흔히 발견되며, 이의 분석은 HPLC 및 GC 등 기기분석에 의존하고 있다. 그러나 본 연구에서는 환경 및 생활용품에 잔류하는 BPA를 신속, 정확하고, 경제적으로 분석할 수 있는 분광학적 정량방법을 개발하고자 하였으며, 이를 위해 $FeCl_3{\cdot}6H_2O$와 $K_3Fe(CN)_6$를 사용한 비색정량법을 확립하였다. 발색반응으로 생성된 청색화합물의 ${\lambda}max$ 및 반응특이성을 조사하였으며, 최적반응조건(시간, 온도, pH, 농도, 부피, 반응안전성)을 검토하였다. 확립된 발색반응조건에서 BPA에 대한 검량곡선(${\lambda}_{750}$=0.61 BPA $[{\mu}M]$+0.07155, $R^{2}$=0.992)을 얻었으며, 신규 확립된 비색정량법을 이용하여 토양, 수계 및 생활용품의 BPA 분석을 시도한 결과, HPLC 분석시스템과 유사한 결과를 얻을 수 있었다. 본 BPA 및 관련물질에 대한 비색정량법은, 기기분석에 비해 빠르고, 경제적이며, 대량의 시료를 일시에 취급할 수 있어 기기분석의 보완분석으로도 우수하며, BPA 분해산물은 발색반응을 나타내지 않아, 자연계로부터 BPA 분해균주 선별 등에 매우 유용하게 이용될 수 있다.

• Food Science and Biotechnology
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• 제17권3호
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• pp.679-682
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• 2008

A lactic acid bacterium producing an antimicrobial substance against Escherichia coli O157:H7 was isolated from raw milk and identified as Lactobacillus amylovorus ME-1. In addition to E. coli O157 :H7, the antimicrobial substance also inhibited the growth of Bacillus cereus, Listeria monocytogenes, Pseudomonas aeruginosa, Salmonella typhimurium, Staphylococcus aureus, Streptococcus agalactiae, Streptococcus pyrogenes, and Yersinia enterocolitica. The antimicrobial substance was stable at pH 2-12 and $121^{\circ}C$ for 15 min and insensitive to proteinase K, protease, amylase, and catalase. Purification of the antimicrobial substance was conducted through methanol and acetonitrile/ethylacetate extraction, ultrafiltration with a 500 Da cutoff, thin layer chromatography (TLC) with silicagel 60, and high performance liquid chromatography (HPLC) with a $C_{18}$ reverse phase column. The ${\lambda}_{max}$ of the purified antimicrobial substance was determined as 192 nm by ultra violet (UV) scanning, while the molecular weight was estimated as 453 Da based on the mass spectrum. Accordingly, the current results suggest that the antimicrobial substance from the L. amylovorus ME-1 was not a bacteriocin, but rather a new non-proteinaceous substance distinct from acidophilin, acidolin, diacetyl, and reuterin.

• Nutrition Research and Practice
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• 제2권1호
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• pp.46-49
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• 2008

Anthocyanin pigments from varieties of black, red and wild rice were identified and quantified to evaluate their potential as nutritional function, natural colorants or functional food ingredients. Anthocyanin extraction was conducted with acidified methanol with 0.1M HCl (85:15, v/v) and identification of anthocyanin, aglycone and sugar moieties was conducted by comparison with purified standards by HPLC, Ultraviolet-Visible absorption spectrophotometer and paper chromatography. Black and wild rice showed three different types of pigments by HPLC whereas red rice variety did not show any anthocyanins. Out of three pigments detected, one (peak 2) was characterized as cyanidin-3-glucoside (C3G) by comparison of spectroscopic and chromatographic properties with an authentic standard, and another (peak 3) was tentatively identified as cyanidin-fructoside on the basis of spectroscopic properties with ${\lambda}_{max}$ of aglycone in 1% HCl methanol at 537 nm, electrospray ionization mass spectra with major ions at 449 and 287 m/z and chromatographic properties. But another pigment (peak 1) has not been characterized. The most abundant anthocyanin in black and wild rice was C3G.

• 한국전기전자재료학회논문지
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• 제28권5호
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• pp.314-319
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• 2015

In this research, we focused on the development of cy3 dye with high thermal stability and good solubility for LCD color filter. Cy3 dyes were prepared through the synthetic procedure of two steps. The synthesized cy3 dyes were characterized by using NMR, FT-IR, UV/Vis spectroscopy, and TGA. These cy3 dyes showed maximum absorption wave length (${\lambda}_{max}$) in the range of 549~555 nm in UV/Vis spectrum. And we confirmed that solubility characteristics and thermal stability of cy3 dyes were dependent on the structure of counter cation. Cy3 dyes with methyl counter cation and ethyl counter cation have good solubility in organic solvents such as chloroform, ethanol, and PGME. Moreover, Cy3 dye with ethyl counter cation gave excellent thermal stability in TGA thermograms. And Cy3 dye with ethyl counter cation showed good result in photoresist film test.

• 한국의류학회지
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• 제37권6호
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• pp.827-836
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• 2013

Indigotin, indirubin, berberine, palmatine, alizarin, and purpurin are major pigments of indigo plant, Phellodendron bark, and madder. The six pigments were examined using the HPLC-DAD-MS instrument for the purpose of the simultaneous detection of the pigments in a single sample run. The HPLC-DAD-MS method examined the individual pigment solutions in DMSO, a solution containing 6 pigments, and the DMSO extract of the silk dyed with a dye solution of 5 pigments excluding indirubin. The retention times of the HPLC chromatograms, ${\lambda}_{max}$ of the uv-vis absorption bands in the DAD analyses, and the molecular ions detected for the compound peaks in the MSD analyses were consistent throughout the analyses of individual pigment solutions, mixed pigment solutions, and dye extracted from silk dyeing. The developed instrumental method of the simultaneous detection of six pigments can identify dye in an exhumed textile if the textile is dyed using any one (or multiple) pigments of indigo, Phellodendron bark, or madder plant.

• Applied Biological Chemistry
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• 제41권8호
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• pp.595-599
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• 1998

An analytical method was developed to determine tricyclazole residues in rice grain, straw, and soil using high-performance liquid chromatography (HPLC) with ultraviolet absorption detection. Tricyclazole was extracted with methanol from moist rice grain, straw, and soil samples. n-Hexane washing was employed to remove nonpolar co-extractives during liquid-liquid partition. Tricyclazole was then extracted with dichloromethane from alkaline aqueous phase, while acidic interferences remained in the phase. Dichloromethane extract was further purified by silica gel column chromatography prior to HPLC determination. Reverse-phase HPLC using an octadecylsilyl column was successfully applied to separate and quantitate the tricyclazole residue in sample extracts monitored at ${\lambda}_{max}$ 225nm. Recoveries from fortified samples averaged $95.5{\pm}3.0%\;(n=6),\;87.5{\pm}20.%\;(n=6),\;and\;84.3{\pm}2.8%$ (n=12) for rice grain, straw, and soil, respectively. Detection limit of the method was 0.02 mg/kg for rice grain and soil samples while 0.05 mg/kg for rice straw samples. The proposed method was reproducible and sensitive enough to evaluate the safety of tricyclazole residues in rice grain, straw, and soil.

• 천문학회보
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• 제40권2호
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• pp.30.3-31
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• 2015

We present a kinematic analysis of 172 likely member galaxies of the Ursa Major Cluster. In order to understand the dynamical state of the cluster, we investigate the correlation of the cluster morphology with rotation, the velocity dispersion profile, and the rotation amplitude parallel to the global rotation direction. Both the minor axis and the rotation are very well-aligned with the global rotation axis in the outer region at half radius (> 0.5 $R_{max}$), but not in the inner region. The cluster exhibits low velocity dispersion and rotation amplitude profiles in the inner region, but higher in the outer. Both profiles exhibit outwardly increasing trends, suggesting an inside-out transfer of angular momentum of dark matter via violent relaxation, as revealed by a recent off-axis major-merging simulation. From Dressler-Schectman plots in the plane of galactic positions, and velocity versus position angle of galaxy, we are able to divide the Ursa Major Cluster into two substructures: Ursa Major South (UMS) and Ursa Major North (UMN). We derive a mass of $3.2{\times}10^{14}M_{\odot}$ for the cluster through the two-body analysis by the timing argument with the distance information (37 for UMN and 36 for UMS) and the spin parameter of ${\lambda}=0.049$. The two substructures appear to have passed each other 4.4 Gyr ago and are moving away to the maximum separation.

• 한국자기공명학회논문지
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• 제18권2호
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• pp.74-81
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• 2014

The $N_2O_2$ tetradentate Schiff base ligand, N,N'-bis(salicylidene)pentane-1,3-diamine (Salpn), coupled with 1:2 concentration ratio of 1,3-diaminopentane and salicylaldehyde was used to produce a series of macrocyclic Nikel(II) complexes. In the metal complexation, it was observed that Salpn macrocyclic ligand can adopt more than a metal ion giving an unique multinuclear metal complexes including Ni(II)Salpn and $Ni(II)_3(Salpn)_2$. Characteristic IR ${\upsilon}(M-O)$ peaks for Ni(II)Salpn and $Ni(II)_3(Salpn)_2$ were observed to be $1028cm^{-1}$ and $1024cm^{-1}$, respectively. Characteristic UV-Vis absorption ${\lambda}_{max}$ peaks for $Ni(II)_3(Salpn)_2$ were observed to be 241nm and 401 nm. Structural characterization of $Ni(II)_3(Salpn)_2$ by NMR exhibits that the salicylidene ring moiety has two different resonance signals originated from the magnetically asymmetric diligand and trinuclear bis complex. Complete NMR signal assignments and characterizations elucidating structural features of $Ni(II)_3(Salpn)_2$ were described in detail.