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Isotopic analysis of nickel, copper, and zinc in various freshwater samples for source identification 不同淡水样品中镍、铜和锌的同位素分析,用于来源鉴定
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2021-01-01 DOI: 10.2343/GEOCHEMJ.2.0627
S. Takano, Mao Tsuchiya, S. Imai, Yuhei Yamamoto, Y. Fukami, Katsuhiko Suzuki, Y. Sohrin
Nickel (Ni), copper (Cu), and zinc (Zn) are commonly used in human activities and pollute aquatic environments including rivers and oceans. Recently, Ni, Cu, and Zn isotope ratios have been measured to identify their sources and cycles in environments. We precisely determined the Ni, Cu, and Zn isotope ratios in rain, snow, and rime collected from Uji City and Mt. Kajigamori in Japan, and investigated the potential of isotopic ratios as tracers of anthropogenic materials. The isotope and elemental ratios suggested that road dust is the main source of Cu in most rain, snow, and rime samples and that some of the Cu may originate from fossil fuel combustion. Zinc in the rain, snow, and rime samples may be partially attributed to Zn in road dust. Zinc isotope ratios in the Uji rain samples are lower than those in the road dust, which would be emitted via high temperature processes. Nickel isotope ratios are correlated with V/Ni ratios in the rain, snow, and rime samples, suggesting that their main source is heavy oil combustion. Furthermore, we analyzed water samples from the Uji and Tawara Rivers and the Kakita River spring in Japan. Nickel and Cu isotope ratios in the river water samples were significantly heavier than those in rain, snow, and rime samples, while Zn isotope ratios were similar. This is attributed to isotopic fractionation of Cu and Ni between particulate-dissolved phases in river water or soil.
镍(Ni)、铜(Cu)和锌(Zn)是人类活动中常用的物质,对河流和海洋等水生环境造成污染。最近,Ni, Cu和Zn同位素比值被测量以确定它们在环境中的来源和循环。我们精确测定了日本宇治市和鹿城森山雨、雪和白垩的Ni、Cu和Zn同位素比值,并探讨了同位素比值作为人类活动物质示踪剂的潜力。同位素和元素比值表明,在大多数雨、雪和霜样品中,道路粉尘是铜的主要来源,部分铜可能来自化石燃料燃烧。雨、雪和白霜样品中的锌可能部分归因于道路粉尘中的锌。宇治雨样品中的锌同位素比率低于道路尘埃中的锌同位素比率,道路尘埃将通过高温过程排放。镍同位素比值与雨、雪和雾凇样品中的V/Ni比值相关,表明其主要来源是重油燃烧。此外,我们还分析了日本宇治河和田原河以及Kakita河泉水的水样。河流水样中镍、铜同位素比值显著高于雨、雪、水样,锌同位素比值相近。这是由于Cu和Ni在河流水或土壤中颗粒溶解相之间的同位素分馏。
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引用次数: 7
Europium isotope fractionation in highly fractionated igneous rocks with large Eu negative anomaly 具有大Eu负异常的高分选火成岩中铕同位素分选
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2021-01-01 DOI: 10.2343/geochemj.2.0631
Seung-Gu Lee, Tsuyoshi Tanaka
highly fractionated granite is geologically related to postorogenic events and also to mineralization of rare-metals such as W, Sn, Sb, REEs etc. Another one of the geochemical characteristics of such highly fractionated granite is chondrite-normalized REE pattern with large Eu negative anomaly. In addition, the rhyolite is the most evolved volcanic rock. Since the chemical composition of major elements and chondrite-normalized REE patterns in rhyolite are similar to those of highly fractionated granites, rhyolite was considered highly fractionated igneous rock for comparison of Eu isotope ratio in highly fractionated granite. Eu is a very interesting element of REEs because it has two oxidation states (Eu2+ and Eu3+) whereas most of the rare earth elements exist as the trivalent state (3+) in the nature. The divalent oxidation state of Eu becomes a cause of elemental fractionation during magma evolution in the Earth and planetary system and can be used as an indicator of oxygen fugacity of magma system (Burnham et al., 2015). Eu has only two isotopes, 151Eu and 153Eu. Though Belli et al. (2007) reported that 151Eu decayed to 147Pm by α decay with the half-life T1/2 = 5 × 10 18 yr, apparently, 151Eu can be considered as a stable isotope in earth and solar system. In addition, Eu isotope ratio in geological rocks may vary due to redox condition in Earth system (Dauphas et al., 2014). Europium isotope fractionation in highly fractionated igneous rocks with large Eu negative anomaly
高分选花岗岩在地质上与造山事件有关,也与W、Sn、Sb、ree等稀有金属的成矿作用有关。高分异花岗岩的另一个地球化学特征是球粒陨石归一化稀土模式,具有较大的Eu负异常。流纹岩是演化最成熟的火山岩。由于流纹岩主要元素化学组成和球粒陨石归一化稀土模式与高分馏花岗岩相似,因此在比较高分馏花岗岩Eu同位素比值时,流纹岩被认为是高分馏火成岩。Eu是一种非常有趣的稀土元素,因为它有两个氧化态(Eu2+和Eu3+),而大多数稀土元素在自然界中以三价态(3+)存在。Eu的二价氧化态成为地球和行星系统岩浆演化过程中元素分馏的原因,可以作为岩浆系统氧逸度的指标(Burnham et al., 2015)。Eu只有两种同位素,151Eu和153Eu。虽然Belli et al.(2007)报道151Eu通过α衰变衰变为147Pm,半衰期T1/2 = 5 × 10 18 yr,但显然151Eu可以被认为是地球和太阳系中的稳定同位素。此外,地质岩石中的Eu同位素比值可能会因地球系统的氧化还原条件而变化(Dauphas et al., 2014)。具有大Eu负异常的高分选火成岩中铕同位素分选
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引用次数: 3
10Be/9Be ratios of phenakite and beryl measured via direct Cs sputtering: Implications for selecting suitable Be carrier minerals for the measurement of low-level 10Be 通过直接Cs溅射测量的苯钠矿和绿柱石的10Be/9Be比率:选择合适的Be载体矿物用于测量低水平10Be的意义
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2021-01-01 DOI: 10.2343/geochemj.2.0630
Atsunori Nakamura, Atsuyuki Ohta, Hiroyuki Matsuzaki, Takashi Okai
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引用次数: 1
Does carbon dioxide storage by cyanobacteria induce biomineralization in presence of basaltic glass? 蓝藻储存二氧化碳是否会在玄武岩玻璃中诱发生物矿化?
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2020-12-17 DOI: 10.2343/GEOCHEMJ.2.0617
Thomas Ferrini, Olivier Grandjouan, O. Pourret, R. Martinez
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引用次数: 0
Constraints on redox conditions in the Japan Sea in the last 47,000 years based on Mo and W as palaeoceanographic proxies 基于Mo和W古海洋学代用物的近47000年来日本海氧化还原条件约束
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2020-01-01 DOI: 10.2343/geochemj.2.0606
M. Tsujisaka, Shinsuke Nishida, S. Takano, M. Murayama, Y. Sohrin
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引用次数: 5
Distribution and geochemical significance of biphenyls and related bicyclic aromatic structures in oils from Ancon oilfield (Tertiary Progreso Basin), Ecuador 厄瓜多尔anon油田石油中联苯及相关双环芳烃结构的分布及其地球化学意义
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2020-01-01 DOI: 10.2343/geochemj.2.0598
Miguel Ángel Martínez, E. Lorenzo, A. Morato, Adriana Gamboa
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引用次数: 0
Comparison of S-type/I-type (Australia) and Ilmenite-series/Magnetite-series (Japan) in terms of gas features occluded in granitoids s型/ i型(澳大利亚)与钛铁矿系列/磁铁矿系列(日本)花岗岩类中封闭气体特征的比较
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2020-01-01 DOI: 10.2343/geochemj.2.0591
Koichiro Nagamine, M. Araki
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引用次数: 1
U-Pb dating of granitic cobble (dropstone) recovered from inner slope of the Chile Trench (48°S): Constraint for its provenance 智利海沟内坡(48°S)花岗岩卵石U-Pb定年:物源约束
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2020-01-01 DOI: 10.2343/geochemj.2.0602
Y. Orihashi, R. Anma, S. Machida, M. Sasaki, Kaishi Nakao, Y. Takaku, N. Abe
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引用次数: 0
Influence of dual sulfate reduction pathways on pore-fluid chemistry and occurrences of methane hydrate in sediment cores (IODP-353) off Mahanadi basin, Bay of Bengal 双硫酸盐还原途径对孟加拉湾Mahanadi盆地沉积物岩心孔隙流体化学和甲烷水合物赋存的影响(IODP-353
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2020-01-01 DOI: 10.2343/geochemj.2.0576
A. Peketi, A. Mazumdar, S. Pillutla, D. J. Patil
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引用次数: 3
Optimizing the Pratt-type titrimetric method to determine FeO in geochemical reference materials 优化pratt滴定法测定地球化学标准物质中FeO的方法
IF 0.8 4区 地球科学 Q3 Earth and Planetary Sciences Pub Date : 2020-01-01 DOI: 10.2343/geochemj.2.0605
A. Nakamura, Takashi Okai, Atsuyuki Ohta
Copyright © 2020 by The Geochemical Society of Japan. values are validated by comparisons with the measured value of the reference materials. Among various types of wet chemical analyses, titrimetric methods are one of the most classical methods used to measure FeO values. Although titrimetric methods yield accurate FeO values, it is time consuming. Much progress has been made on measuring FeO using analytical instruments; this includes new methods such ion chromatography (Kanai, 1990; le Roex and Watkins, 1995), Mössbauer spectroscopy (Lalonde et al., 1998), phenanthroline spectrophotometry (Husler et al., 2011; Tarafder and Thakur, 2013), X-ray absorption near-edge structure (XANES) spectroscopy (Farges, 2001; Ohta et al., 2006; O’Neill et al., 2006, 2018; Berry et al., 2010, 2018; Cottrell and Kelley, 2011; Zhang et al., 2018), and electron probe microanalysis (EPMA) (Hughes et al., 2018; Li et al., 2019). In each of these developments, it is crucial to compare the results of unknown geological samples with geochemical reference materials; therefore, the importance of geochemical reference materials with certified values is increasing. The certified values of geochemical reference materials have previously been determined mainly by a titrimetric method. During this method, samples are first decomposed by sulphuric acid (H2SO4) and hydrofluoric acid (HF) in crucibles. They are then titrated with a potassium dichromate (K2Cr2O7) solution to allow volumetric calculation of the amounts of FeO. The difficulty arises Optimizing the Pratt-type titrimetric method to determine FeO in geochemical reference materials
日本地球化学学会版权所有©2020。通过与标准物质的测量值进行比较,验证了数值。在各种湿化学分析方法中,滴定法是测量FeO值最经典的方法之一。虽然滴定法能得到准确的FeO值,但耗时长。利用分析仪器测量FeO已取得很大进展;这包括离子色谱等新方法(Kanai, 1990;le Roex和Watkins, 1995), Mössbauer光谱学(Lalonde等人,1998),菲罗啉分光光度法(Husler等人,2011;Tarafder and Thakur, 2013), x射线吸收近边缘结构(XANES)光谱学(Farges, 2001;Ohta等人,2006;O’neill et al., 2006, 2018;Berry等人,2010,2018;Cottrell and Kelley, 2011;Zhang et al., 2018)和电子探针微分析(EPMA) (Hughes et al., 2018;Li等人,2019)。在每一个发展中,将未知地质样品的结果与地球化学参考物质进行比较是至关重要的;因此,具有认证值的地球化学标准物质的重要性日益增加。地球化学标准物质的检定值以前主要是用滴定法测定的。在该方法中,样品首先在坩埚中被硫酸(H2SO4)和氢氟酸(HF)分解。然后用重铬酸钾(K2Cr2O7)溶液滴定,以计算FeO的体积。优化普拉特滴定法测定地球化学标准物质中FeO的方法是一个难点
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引用次数: 0
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Geochemical Journal
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