• Food Science and Preservation
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• v.13 no.6
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• pp.703-707
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• 2006

The propose of this study was to investigate the changes of available components in Chajogi (Perilla sikokiana B.) by different harvest periods. The Chajogi samples were divided into four groups by harvest period. The four groups were divided into I (harvesting sample at 14, July, 2005), II (harvesting sample at 25, July, 2005), III (harvesting sample at 15, Aug, 2005) and IV sample (harvesting sample at 2, Sept, 2005), and then analysed with regard to the content of proximate compositions, minerals, amino acids, perillaldehyde and anthocyanin. The contents of reducing sugar increased with increasing harvesting periods, while those of crude protein, crude lipid and total amino acids decreased for IV sample as compared to the other samples. The levels of heavy metals in all samples were not detected. The Zn, Fe and Mg contents of IV sample decreased sharply. The perilladehyde contents were 0.36%, 0.42% 0.45%, and 0.35% for I, II, III, and IV products, respectively. III sample as contented to the other samples was shown to have the highest anthocyanine content (1.21% in dry basis). In conclusion, the date of harvesting Chajogi affects the contents of available components.

• Economic and Environmental Geology
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• v.29 no.6
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• pp.725-732
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• 1996

To assess soil distribution patterns of heavy metals in agricultural environments, we have measured the concentrations of six metals from surficial soils of three different groups divided on the basis of the surrounding environment: (1) soil group I-cultivated soils within the purely agricultural regions, (2) soil group II-both cultivated and uncultivated soils near various livelihood facilities, and (3) soil group III-mainly cultivated soils near major polluting sources. The mean concentrations for the three soil groups were found in the range as follows: 0.12~0.15 (Cd), 4.94~6.08 (Pb), 0.05~0.11 (Hg), 2.82~3.50 (Cu), 4.69~7.82 (Zn), and 0.36~0.78 (As) ppm. Examination of data distribution trends indicates that the concentrations determined from the relatively unpolluted soil environs (groups I and II) were comparable not only between each other but also with those reported previously in background soil environs of Korea. The concentration data for the soil group III were however found to be much higher than the rest two groups. Unlike the direct comparison of the magnitudes of concentrations, results of a regression analysis exhibited much different patterns: it was seen that the correlation patterns for soil group I were rather analogous to those of soil group III. The similarities in correlation patterns between groups I and III along with the lack of correlations in soil group II suggest that soil characteristics such as whether being cultivated or not are important factors affecting soil distributions of heavy metals.

• Economic and Environmental Geology
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• v.21 no.3
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• pp.287-307
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• 1988

The Cheongju gold-silver mine is located at approximately $36^{\circ}28^{\prime}$north latitude and $127^{\circ}31^{\prime}$ east longitude in the Cheongju City of the Chung cheong bug Do, South Korea. Gold-Silver bearing hydrothermal quartz veins, occur in Cheongju Granit of Jurassic age. K-Ar isotope data for sericite in quartz vein indicate that the Au-Ag mineralization took place in early Cretaceous ($97.5{\pm}2.18$ MA. Park, et ai, 1986). Three stage of mineralization recognized anre, from early to later, (I) Sulide stage: pyrite, arsenopyrite, pyrrhotite (Hpo), sphalerite, chalcopyrite, electrum and quartz (II) Electrum stage: pyrite, sphalerite, galena, chalcopyrite, electrum and quartz. (III) Silver mineral stage: pyrite, marcasite, pyrrhotite (Mpo), sphalerite, galena, electrum, native silver argentite, fluorite, calcite and quartz. In this paper, mode of occurrences and chemical compositions of electum and native silver have been investigated by means of microscope and EPMA. Electron probe microanalysis shows that an individual grain of electrum is almost homogeneous in composition. Silver content of electrum ranges from 44.7-67.1 atom.%. Gold content of native silver ranges below 0.2 atom. %. Vicker's hardness number (VHN) of electrum and native silver ranges $78.2-81.8kg/mm^{2}$ respectively. The filling temperature of fluid inclusions in quartz ranges from $130-280^{\circ}C$. On the basis of arsenpyrite geothemometer, the equilibrium temperature and sulfur fugacity of the pyrite-arsenopyrite-pyrrhotite(Hpo) assemblage is assumed to be in ange from $300-310^{\circ}C$ and $10^{-10}$ to $10^{-11}$ atm. The estimated ore reserviors on Cheongju mine area are calculated to 8000 T/M, averaing 8.6g/t Au, 27.8 g/t Ag, 1.25% Pb, l.65% Zn.

• Proceedings of the Korea Water Resources Association Conference
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• 2011.05a
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• pp.202-206
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• 2011

본 연구에서는 정체성 수역인 신갈호를 대상으로 저층 퇴적물의 오염물질에 대한 조사를 실시 하였다. 신갈호 저층 퇴적물의 분석 결과, 함수율의 범위는 49.0~68.2%로 조사되었으며, 평균 함수율은 60.8%로 나타났다. 함수비의 경우에는 지점별 96.1~214.6%의 넓은 범위를 보였으며 평균 함수비는 165.8%로 조사되었다. 퇴적물의 pH는 모든 지점에서 산성을 띄었으며, 하류부로 갈수록 더욱 낮아지는 경향을 보였다. 입도분석 결과, 토성은 SL(사양토) 및 SiL(실트질양토)로 나타났으며, 이러한 토성분포는 입자별 침강속도에 의한 것으로 퇴적물의 지점별 이 화학적 특성에 많은 영향을 줄 것으로 판단된다. 유기물 함량 분석결과, 강열감량의 경우 8.22~11.36%로 평균 10.22% 의 유기물 함량을 보였으며, COD는 24,92 mg/kg~27,38 mg/kg의 값으로 평균 26,16 mg/kg로 조사되었다. 영양물질 함량 분석결과, T-N의 경우 신갈호 저층 퇴적물 평균 2,916 mg/kg의 질소 함량을 보였으며, T-P의는 평균 710 mg/kg로 조사되었다. 영양물질 함량 분석결과 하류부로 갈수록 높아지는 경향을 보였으나 총질소의 경우 지점별 비슷한 값을 보인 반면, 총인은 지점별 큰 차이를 보였다. 퇴적물의 중금속 함량은 Cd, Cu, Zn, $Cr^{6+}$, Pb을 분석하였으며, Cd 0.10~0.12 mg/kg, Cu 18.33~20.67 mg/kg, Zn 82.73~110.15 mg/kg, $Cr^{6+}$ 0.78~0.93 mg/kg Pb 11.04~14.53 mg/kg의 범위를 보였으며, 지점별로 큰 차이를 보이지 않았다. 본 연구의 자료는 신갈호 유역의 개발계획 및 준설 검토에 대한 유용한 자료로 활용 가능할 것으로 판단된다.

• Korean Journal of Veterinary Service
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• v.29 no.4
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• pp.459-467
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• 2006

This study was designed to investigate if there were groundwater contamination in 17 landfill where slaughtered animals were buried during the crisis of 2002 foot-and-mouth-disease (FMD) outbreaks in Gyeonggi province. From March to August 2005 groundwater was collected once a month from 17 sites, and examined with potential for hydrogen (pH), colour, turbidity, lead (Pb), arsenic (As), mercury (Hg), cadmium (Cd), copper (Cu), zinc (Zn) , iron (Fe), manganese (Mn) , aluminium (Al), nitrate-nitrogen $(NO_3-N)$, ammonia-nitrogen $(NH_3-N)$, microbial pathogen and Escherichia spp. In the examination of $NH_3-N$ which of the mean concentration was from not-detected (ND) to 0.05 mg/l. The range of $NH_3-N$ level was $0.3-24.1mg/{\ell}$. However, groundwater from four sites was to go beyond the drinking water quality standard (DWQS), i.e., the mean concentration of those were $15.5mg/{\ell}\;(site\;1),\;20.7mg/{\ell}\;(site\;9),\;24.1mg/{\ell}\;(site\;13)\;and\;10.6mg/{\ell}\;(site\;17)$. In the investigation of pH, colour and turbidity, all of the pH were below of DWQS (pH 5.8-6.6), but one site in color test and four sites in turbidity test were over the standard level. Among 9 metal ions examined, Mn was in excess of DWQS, and its concentration was $2.4mg/{\ell}$. Pb, Cd, Hg and As were not traced. The contents of Cu, Zn, Fe and Al were $ND-0.22mg/{\ell},\;0.01-0.05mg/{\ell},\;ND-0.05mg/{\ell}\;and\;0.03-0.16mg/{\ell}$, respectively. Escherichiae spp were not identified, but bacterial colonies were detected at 3 groundwater including 2 sites over the DWQS at the level of $491CFU/m{\ell}\;(site\;4)\;and\;217CFU/m{\ell}\;(site\;15)$.

• Analytical Science and Technology
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• v.10 no.3
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• pp.187-195
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• 1997

Chemically modified electrodes(CMEs) for Ag(I) were constructed by incoporating 1,5,9,13-tetrathiacyclohexadecane([16]-ane-$S_4$) with a conventional carbon-paste mixture composed of graphite powder and nujol oil. Ag(I) ion was chemically deposited onto the surface of the modified electrode with [16]-ane-$S_4$ by immersion of the electrode in the acetate buffer solution(pH=4.5) containing $5.0{\times}10^{-4}M$ Ag(I) ion. And then the electrode deposited with Ag(I) was reduced at -0.3V vs. S.C.E. Well-defined stripping voltammetric peaks could be obtained by scanning the potential to the positive direction. The CME surface was regenerated with exposure to 0.1M $HNO_3$ solution and was reused for the determination of Ag(I) ion. When deposition/measurement/regeneration cycles were 10 times, the response could be reproduced with relative standard deviation of 6.08%. In case of differential pulse stripping voltammetry, the calibration curve for Ag(I) was linear over the range of $5.0{\times}10^{-7}{\sim}1.5{\times}10^{-6}M$. And the detection limit was $2.0{\times}10^{-7}M$. Various ions such as Cd(II), Ni(II), Pb(II), Zn(II), Mn(II), Mg(II), EDTA, and oxalate(II) did not influence the determination of Ag(I) ion, except Cu(II) ion.

• Korean Journal of Environmental Agriculture
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• v.4 no.1
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• pp.25-30
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• 1985

In order to characterize relationship between accumulation of cadmium, zinc and lead in soil and soil chemical properties and also to choose a suitable soil extractant for the prediction model of heavy metal content in brown rice, four extractants-0.1 M HCl, 0.1 M $HNO_3$, 0.1 M $NH_4-oxalate$ and 0.001 M 2Na-EDTA, were compared by analyzing 84 soil samples collected from paddy fields adjacent to five zinc-minig sites. Contents of Cd, and Pb in soil increased with Zn content and those of three elements were found to be much higher in surface soil ($0{\sim}15 cm$) than suvsqrface soil ($15{\sim}30 cm$). Contents of these elements in soil were positively correlated with soil pH, but its correlation between extractable heavy metal content and organic matter or CEC varied from region to region. These three elements were negatively correlated with Mg content of soils. The extractability of the metals was in the order 0.1 M $HCI{\geq}0.1 M$ $HNO_3>0.001 M$ 2Na-EDTA>0.1 M $NH_4-oxalate$.

• Korean Journal of Materials Research
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• v.15 no.6
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• pp.413-418
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• 2005

Perovskite $Pb(Ni_{1/3}Nb_{2/3})O_3-Pb(Zr,Ti)O_3[PNN-PZT]$ ceramics were synthesized by conventional ceramic processing technique. In order to modify piezoelectric properties for sensor application in this system, NiO addition was considered to provide $Ni^{+2}$ as an acceptor, which was known to occupy with B site in the structure. The effect of NiO addition up to $8\;mol\%$ on the following piezoelectric properties as well as sintering properties was investigated. When NiO added more than $1\;mol\%$, average grain size was decreased and second phase was found to form. Moreover, the second phase caused decrease in relative dielectric constant $(\varepsilon_{33}T/\varepsilon0)$, electro-mechanical coupling factor $(k_p)$, and piezoelectric charge constant $(d_{33})$, while increasing mechanical quality factor $(Q_m)$. When $1\;mol\%$ NiO was added, density, dielectric properties and piezoelectric properties were abruptly increased.

• Korean Journal of Veterinary Research
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• v.40 no.1
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• pp.117-129
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• 2000

This study was carried out to examine proliferative activity and expression of c-myc oncoprotein and p2lras in normal and preneoplastic rat livers induced by an in vivo mid-term chemical carcinogenesis assay. Sixty, six-week-old male specific pathogen free Sprague-Dawley male rats were randomly divided into five groups. Group I was received a single intraperitoneal(IP) dose(200mg/kg) of diethylnitrosamine(DEN). Group 2(10 rats) was operated partial hepatectomy(PH) and Group 3 was received IP(200mg/kg) DEN, fed two weeks later with 500ppm of phenobarbital(PB). Group 4 was received IP(200mg/kg) DEN, fed two weeks later 500ppm(PB) and PH at week 3 after the onset of experiment. While group 5(20 rats) was not treated and used as a control group. All the rats were sacrificed at age 14 weeks except 10 rats from group 5 were sacrificed at the onset of experiment. Livers of all rats were examined for 5-bromo-2'-deoxyuridine(BrdU) incoporation, proliferating cell nuclear antigen(PCNA), silver-binding nucleolar organizer regions(AgNORs) counts per nucleus and expression of c-myc oncoprotein and p21ras. Both the number and area of the preneoplastic lesions were significantly(p<0.01) compared to other groups. A significant(p<0.01) increase in immunoreactive cells were detected in preneoplastic hepatocytes in Groups 3 and 4 by PCNA and BrdU immunohistochemical stain. The number of the positive cells were significantly(p<0.05) lower in normal 14-week-old rats than those of 6-week-old rats. The results showed that proliferative activity of the hepatocytes was increased by treatment with DEN, PH and PB. Meanwhile, AgNORs counts per nucleus were significantly(p<0.05) increased in the preneoplastic hepatocytes of rats in both groups 3 and 4. The expression of c-myc oncoprotein and p21ras were more readily localized within the hepatic preneoplastic lesions such as hyperplastic nodules. Especially, group 4 showed significantly (p<0.05) overexpressed levels compared to groups 1 and 3. These findings suggest that PCNA, BrdU and AgNORs are significantly increased and c-myc oncoprotein and p21ras are significantly overexpressed in hepatic preneoplastic lesions induced by mid-term carcinogenesis. So these parameters can be an effective markers for hepatic prencoplastic lesions.

• Journal of Plant Biology
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• v.28 no.1
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• pp.69-77
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• 1985

The degree of The degree of The degree of ${Zn}^{2+}$ effect on the photosynthetic electron transport and photophosphorylation activities in barley chloroplasts has been tested.${Zn}^{2+}$treatment was done in the 2 ways. One was that it was added into the chloroplasts suspensions isolated from the plants grown under the normal ${Zn}^{2+}$level (10$^{-6}$ M). The other was that the different concentrations of ${Zn}^{2+}$was applied in each growth medium. Then, it was not added into the chloroplasts suspensions isolated from the plants. PS II activity in both way of the treatments was more severely inhibited than PS I by the increment of ${Zn}^{2+}$ concentration. The photophosphorylation activity measured by pH measurement was gradually decreased with the increase of ${Zn}^{2+}$concentration in both ways, too. However, it was shown that M $n^{2+}$ could be near fully overcome the inhibitory effect of ${Zn}^{2+}$in PS II, and $Mg^{2+}$ could also reduce the Z $n^{2+}$ inhibition in the photophosphorylation. In the low concentrations of $Mg^{2+}$ (3 to 5$\times$10$^{-3}$ M) in the suspension, ${Zn}^{2+}$(2$\times$10$^{-5}$ M) could increase the activity of photophosphorylation. As compares to other cations, Z $n^{2+}$ caused less inhibitory effect on the photophosphorylation activity than Cu, Cd, but more than Pb and Ni. It may be assumed that a complex from reaction of Z $n^{2+}$ and mercaptoethanol was produced and it could reduce the stability of CPI band during SDS-PAGE.effect on the photosynthetic electron transport and photophosphorylation activities in barley chloroplasts has been tested. Z $n^{2+}$ treatment was done in the 2 ways. One was that it was added into the chloroplasts suspensions isolated from the plants grown under the normal Z $n^{2+}$ level (10$^{-6}$ M). The other was that the different concentrations of Z $n^{2+}$ was applied in each growth medium. Then, it was not added into the chloroplasts suspensions isolated from the plants. PS II activity in both way of the treatments was more severely inhibited than PS I by the increment of Z $n^{2+}$ concentration. The photophosphorylation activity measured by pH measurement was gradually decreased with the increase of Z $n^{2+}$ concentration in both ways, too. However, it was shown that M $n^{2+}$ could be near fully overcome the inhibitory effect of Z $n^{2+}$ in PS II, and $Mg^{2+}$ could also reduce the Z $n^{2+}$ inhibition in the photophosphorylation. In the low concentrations of $Mg^{2+}$ (3 to 5$\times$10$^{-3}$ M) in the suspension, Z $n^{2+}$ (2$\times$10$^{-5}$ M) could increase the activity of photophosphorylation. As compares to other cations, Z $n^{2+}$ caused less inhibitory effect on the photophosphorylation activity than Cu, Cd, but more than Pb and Ni. It may be assumed that a complex from reaction of Z $n^{2+}$ and mercaptoethanol was produced and it could reduce the stability of CPI band during SDS-PAGE.effect on the photosynthetic electron transport and photophosphorylation activities in barley chloroplasts has been tested. Z $n^{2+}$ treatment was done in the 2 ways. One was that it was added into the chloroplasts suspensions isolated from the plants grown under the normal Z $n^{2+}$ level (10$^{-6}$ M). The other was that the different concentrations of Z $n^{2+}$ was applied in each growth medium. Then, it was not added into the chloroplasts suspensions isolated from the plants. PS II activity in both way of the treatments was more severely inhibited than PS I by the increment of Z $n^{2+}$ concentration. The photophosphorylation activity measured by pH measurement was gradually decreased with the increase of Z $n^{2+}$ concentration in both ways, too. However, it was shown that M $n^{2+}$ could be near fully overcome the inhibitory effect of Z $n^{2+}$ in PS II, and $Mg^{2+}$ could also reduce the Z $n^{2+}$ inhibition in the photophosphorylation. In the low concentrations of $Mg^{2+}$ (3 to 5$\times$10$^{-3}$ M) in the suspension, Z $n^{2+}$ (2$\times$10$^{-5}$ M) could increase the activity of photophosphorylation. As compares to other cations, Z $n^{2+}$ caused less inhibitory effect on the photophosphorylation activity than Cu, Cd, but more than Pb and Ni. It may be assumed that a complex from reaction of Z $n^{2+}$ and mercaptoethanol was produced and it could reduce the stability of CPI band during SDS-PAGE.ld reduce the stability of CPI band during SDS-PAGE.