• Title/Summary/Keyword: isotope fractionation

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A Review on Identification Methods for TCE Contamination Sources using Stable Isotope Compositions (안정동위원소 조성을 이용한 TCE 오염원 규명방법 소개)

  • Park, Youngyun;Lee, Jin-Yong;Na, Won Jong;Kim, Rak-Hyeon;Choi, Pil Sung;Jun, Seong-Chun
    • Journal of Soil and Groundwater Environment
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    • v.18 no.3
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    • pp.1-10
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    • 2013
  • This study was performed to summarize application of ${\delta}^{13}C$, ${\delta}^{37}Cl$ and ${\delta}D$ of trichloroethylene (TCE) to studies on environmental forensic field regarding identification of TCE sources and evaluation of contribution of TCE to groundwater using data collected from literatures. ${\delta}^{13}C$, ${\delta}^{37}Cl$ and ${\delta}D$ of TCE give some information regarding sources of TCE because they show specific value according to manufacturing method. Also, TCE do not show a significant isotopic fractionation owing to adsorption and dilution. The isotopic fractionation mainly occurs by biodegradation. In addition, isotopic fractionation factor for TCE is different according to a kind of microorganism participated in biodegradation. However, the isotopic data of TCE have to be applied with chemical compositions of TCE and other hydrogeologic factors because isotopic fractionation of TCE is influenced by various factors.

Variation Pattern of ${\delta}^{13}C_{DIC}$ of the Odaecheon Stream Water

  • Shin, Woo-Jin;Chung, Gong-Soo
    • 한국지구과학회:학술대회논문집
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    • 2005.02a
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    • pp.115-125
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    • 2005
  • Carbon isotopic composition of a stream (Odaecheon Stream) monitored over 7 months from July 2004 to January 2005 in Gangweon Province ranges from -9.24 to -4.69‰. Strong negative correlation between ${\delta}^{13}C_{DIC}$ and water temperature suggests that temperature is a dominant factor controlling ${\delta}^{13}C_{DIC}$ in the Odaecheon Stream. The variation pattern of ${\delta}^{13}C_{DIC}$ was thought to be caused by fractionation of C isotope between stream water and atmosphere and more fractionation at reduced temperature. More fractionation of C isotope between stream water and atmosphere at reduced temperature resulted in increase of ${\delta}^{13}C_{DIC}$ of stream water in winter compared to summer. Photosynthesis and respiration of aqueous biota seem to affect little in ${\delta}^{13}C_{DIC}$ as indicated by little variation of dissolved oxygen and reverse variation pattern of Eh in the stream and scarce aqueous biota in stream water. pH seems to be controlled by $CO_2{2}$ exchange between stream water and atmosphere. During summer more $CO_2{2}$ exchange between stream water and atmosphere resulted in decrease in pH value.

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Quantifying nitrogen source contribution ratios using stable isotope method: Application of Bayesian mixing model (안정동위원소를 이용한 하천에서의 질소오염원 기여율 정량화: Bayesian 혼합모델의 적용)

  • Nam, Tae-Hui;Ryu, Hui-Seoung;Kang, Tae-Woo;Han, Yeong-un;Kim, Jihyun;Lee, Kyounghee;Hwang, Soonhong;Kim, Kyunghyun
    • Journal of Korean Society on Water Environment
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    • v.35 no.6
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    • pp.510-519
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    • 2019
  • The 'Stable Isotope Analysis in R' (SIAR), one of the Bayesian mixing models for stable isotopes, has been proven to be useful for source apportionment of nitrates in rivers. In this study, the contribution ratios of nitrate sources were quantified by using the SIAR based on nitrogen and oxygen stable isotope measurements in the Yeongsan River. From the measurements, it was found that the values of δ15N-NO3 and δ18O-NO3 ranged from -8.2 ‰ to +13.4 ‰ and from +2.2 ‰ to +9.8 ‰, respectively. We further analyzed the contribution ratios of the five nitrate sources by using the SIAR. From the modeling results, the main nitrate source was found to be soil N (29.3 %), followed by sewage (26.7 %), manure (19.6 %), chemical fertilizer (17.9 %) and precipitation (6.3 %). From the results, it was found that the anthropogenic sources, i.e., sewage, manure and chemical fertilizer contribute 64.2% of the total nitrate inflow from the watershed. Due to the significant correlation of δ15N-NO3 and lnNO3- in this study, the fractionation factors reflecting the biogeochemical processes of stable isotope ratios could be directly obtained. This may make the contribution ratios obtained in this study more precise. The fractionation factors were identified as +3.64 ± 0.91 ‰ for δ15N-NO3 (p<0.01) and -5.67 ± 1.73 ‰ for δ18O-NO3(p<0.01), respectively, and were applied in using the SIAR. The study showed that the stable isotope method using the SIAR could be applied to quantitatively calculate the contribution ratios of nitrate sources in the Yeongsan River.

Carbon Stable Isotope Ratios of Phytoplankton and Benthic Diatoms in Lake Katanuma with Reference to Those of Other Lakes

  • Kikuchi, Eisuke;Takagi, Shigeto;Shikano, Shuichi;Hideyuki, Doi
    • Korean Journal of Ecology and Environment
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    • v.38 no.spc
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    • pp.8-11
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    • 2005
  • Carbon stable isotope ratios of producers varied in lake ecosystems. In tile present study, we tried to estimate the seasonal variations of carbon isotope ratios of phytoplankton and benthic diatoms in a strongly acidic lake ecosystem. Lake Katanuma is a volcanic, strongly acidic lake (average pH of 2.2), located in Miyagi, Japan. Only two algal species dominate in Lake Katanuma; Pinnularia acidojaponica as a benthic diatom, and Chlamydomonas acidophila as a green alga. Carbon isotope values of P. acidojaponica varied seasonally, while those of particulate organic matter, which were mainly composed of C. acidophila remained fairly stable. The differences suggested that $CO_2$ gas was more frequently limited for P. acidojaponica than C. acidophila, since high density patches of benthic diatoms were sometimes observed on the lake sediment. Generally, carbon concentration mechanisms (CCMs)of microalgae can fix bicarbonate in lakes, and affect the carbon isotope values of microalgae. While, in Lake Katanuma, CCMs of the microalgae may scarcely function because of high $CO_2$ gas concentration and low pH. This is the reason for low seasonal amplitude of carbon isotope values of phytoplankton relative to those in other lakes.

Oxygen Isotope Study on the Wolf River Batholith, Wisconsin in U.S.A. (미국 위시컨신주의 올프리버 저반에 대한 산소동위원소 연구)

  • Sun-Joon Kim;Yuch-Ning Shieh
    • The Journal of the Petrological Society of Korea
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    • v.4 no.2
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    • pp.124-133
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    • 1995
  • Oxygen isotope compositions have been determined for the granitic and the related rocks from the Wolf River Ratholith, Wisconsin in U.S.A. Plutons which belong to the differentiation trend are almost identical in oxygen isotope fractionation, and plutons of undifferential sequences also show oxygen isotope compositions similar to each other, which show little isotope fractionations at high temperature range. In oxygen osotope composition, the country rocks (the Penokean plutonic rocks), which is higher by 1~2 permil than the batholith are improbable source of the batholith. However, the assimilation of parent magma of lower ${\delta}^{18}O$ values than the batholith with the Penokean plutonic rocks might have produced the batholith.

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Oxygen isotope study on the hydrothermal alteration in the Wolf River Batholith, Wisconsin in U.S.A

  • Kim, Sun-Joon
    • The Journal of the Petrological Society of Korea
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    • v.2 no.1
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    • pp.19-31
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    • 1993
  • Oxygen isotope compositions of whole rock and/or mineral separates (quartz and feldspar) have been determined for the granitic and related rocks from the Wolf River Batholith, Wisconsin. Hydrothermal alteration resulting in the decrease of ${\Delta}_{Q-F}$/ values was obaserved locally throughout the batholith. Feldspars of different colors (pink, gray and red) were separated whenever feasible and analyzed. Most red feldspars (An$_{10-30}$/) show the highest and constant ${\delta}^18O$/ values (9.3~10.0 permil) suggesting nearly complete isotope exchange with hydrothermal fluid. Based on ${\delta}^18O$/ values and the alteration temperatures (260~$350^{\circ}C$) estimated from fluid inclusion study, ${\delta}^18O$/ of fluid is calculated to be $5.0{\pm}1.4$ permil. Phanerozoic sedimentary formation water in Wisconsin is most likely the source of the fluid.

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Chromatographic Separation of Lithum Isotopes by Hydrous Managanese(Ⅳ) Oxide (가수된 산화 망간(Ⅳ)에 의한 리튬 동위원소의 크로마토그래피적 분리)

  • Kim, Dong Won
    • Journal of the Korean Chemical Society
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    • v.45 no.3
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    • pp.219-222
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    • 2001
  • Separation of lithium isotopes was investigated by chemical ion exchange with a hydrous manganese(IV) oxide ion exchanger using an elution chromatography. The capacity of manganese(IV) oxide ion exchanger was 0.5 meq/g. The heavier lithium isotope was enriched in the solution phase, while the lighter isotope was enriched in the ion exchanger phase. The separation factor was determined according to the method of Glueckauf from the elution curve and isotopic assays. The separation factor of $^6Li^+$-$^7Li^+$ isotope pair fractionation was 1.018.

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Use of Magnesium Stable Isotope Signatures for the Petrogenetic Interpretation of Granitic Rocks (화강암류의 성인 해석에 대한 마그네슘 동위원소 자료의 활용)

  • Cheong, Chang-Sik;Ryu, Jong-Sik
    • The Journal of the Petrological Society of Korea
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    • v.23 no.3
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    • pp.221-227
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    • 2014
  • With the advent of multi collector-inductively coupled plasma mass spectrometry, stable isotopic variations of non-traditional metal elements have provided important constraints on the sources of geologic materials. This review introduces the principles of magnesium isotopic fractionation and analytical methods. Recent case studies are also reviewed for the use of magnesium isotope signatures to decipher the source materials of I-, S-, and A-type granitoids in western North America, Australia, and China.