钛同位素地球化学综述     

赵新苗  唐索寒  李津  朱祥坤  王辉  李志汉  张宏福 《地学前缘》2020,27(3):68-77

随着分析技术的进步,非传统稳定同位素体系在地球化学、天体化学和生物地球化学等研究领域的应用日益广泛。钛(Ti)是一个非常重要的过渡族金属元素,在地球和其他类地球行星中广泛存在。但是由于Ti是一种难熔的、流体不活动性元素,高温地质过程中Ti同位素分馏很小。人们对Ti同位素体系的地球化学应用的关注相对其他非传统稳定同位非常有限。而近年来,随着化学纯化方案的优化以及双稀释剂方法的改进和仪器质谱性能的提高,Ti同位素组成的高精度测试已经能够实现。天然样品中Ti同位素组成的变化随之得以发现,使得学者们能够利用这一新的稳定同位素体系来解决与高温和低温地球化学相关的问题。很快Ti同位素体系地球化学研究成为当前国际地质学界的前沿研究课题和新的发展方向之一。本文首先在简要介绍Ti元素和Ti同位素体地球化学性质的基础上,介绍了Ti元素化学分离和Ti同位素分析方法。随后笔者总结了已有的不同类型球粒陨石和地球样品的质量相关Ti同位素组成研究结果,对硅酸盐地球的Ti同位素组成做了初步评估。前人对高温地质样品的Ti同位素组成研究初步探明Ti同位素在岩浆演化过程,例如部分熔融和结晶分异等重要地质过程中的分馏行为。笔者在此基础上探讨了结晶分异过程中引起Ti同位素分馏的主要控制因素,指出Ti同位素是潜在的研究岩浆演化过程的新工具。最后笔者探讨了Ti同位素地球化学未来的发展方向,以加速我国在Ti同位素地球化学方面的应用研究。  相似文献   

新疆北部弧-盆转化体系下铁氧化物-铜-金矿床的流体演化特征:来自卤族元素和稀有气体同位素的证据     

梁培  陈华勇  赵联党  Kendrick MARK  江宏君  张维峰  吴超  谢玉玲 《地学前缘》2020,27(3):239-253

东准噶尔北缘和东天山雅满苏带是中国新疆北部地区两个重要的晚古生代铁氧化物-铜-金矿化潜力区,以老山口、乔夏哈拉和黑尖山矿床作为典型矿床代表。研究表明两区域的铁氧化物-铜-金矿床均产出于盆地闭合的弧盆转化体系下,且具有明显的铁、铜-金两阶段矿化。卤族元素和稀有气体同位素作为可靠的流体示踪剂,被应用于探究这一特定构造环境下的铁氧化物-铜-金矿床的流体演化和矿床成因。结果显示老山口、乔夏哈拉和黑尖山矿床的成矿流体具有明显的混合流体端员特征:(1)岩浆流体端员,主要参与黑尖山矿床磁铁矿阶段,I/Cl、Br/Cl和⁴⁰Ar/³⁶Ar比值分别为(16.3~18.0)×10^-6、(1.03~1.06)×10^-3和352~437;(2)海水表源蒸发成因盐卤水端员,主要参与老山口矿床铜-金矿化阶段,I/Cl、Br/Cl和⁴⁰Ar/³⁶Ar比值分别为(77.1~87.7)×10^-6、(1.53~1.80)×10^-3和672~883;(3)蒸发岩溶解或者深度水-岩反应成因的盐卤水/沉积岩地层水端员,主要参与到老山口、乔夏哈拉矿床的磁铁矿阶段以及黑尖山、乔夏哈拉矿床的铜-金矿化阶段,综合I/Cl、Br/Cl和⁴⁰Ar/³⁶Ar比值分别为(477~26 301)×10^-6、(0.39~1.28)×10^-3和288~510。明显的多阶段矿化和铜-金矿化阶段以非岩浆富Ca高盐度卤水为主的特征与世界范围内的IOCG型矿床极为相似,表明新疆北部的铁氧化物-铜-金矿床应为IOCG型矿床。  相似文献   

安徽庐枞盆地泥河玢岩型铁矿床地质-原生晕地球化学找矿模型   总被引：1，自引：1，他引：0  

张赞赞  张舒  吴明安  写熹  吕博  魏国辉 《矿床地质》2020,39(2):305-325

开展长江中下游地区玢岩型铁矿床轴向原生晕地球化学分析及建模,可弥补地球物理勘探结果的多解性及探测精度的局限性,对定位和评价深部盲矿体具有至关重要的作用。文章在以往研究的基础上,开展庐枞盆地泥河玢岩型铁矿床钻孔原生晕的研究工作,采用多元统计分析方法,查明了主要成矿指示元素在不同地质体中的富集和亏损,确定了磁铁矿、硫铁矿和硬石膏矿体的矿中、近矿及远矿指示元素组合,结合矿床成因模型,建立了泥河玢岩型铁矿床地质-原生晕地球化学找矿模型,通过罗河和小包庄玢岩型铁矿床的佐证,认为该模型可以应用于长江中下游成矿带玢岩型铁矿床的勘探工作中。  相似文献   

钾稳定同位素研究综述     

王昆  李伟强  李石磊 《地学前缘》2020,27(3):104-122

钾稳定同位素是重要的非传统稳定同位素体系,也是近年来迅速发展的热门研究课题。对钾同位素研究历史和现状进行综述,具体包括以下内容:(1)总结了钾元素的地球化学和宇宙化学性质,包括钾在主要地质储库(地幔、地壳、海洋)中的丰度及其分配,钾在岩浆演化中的不相容大离子亲石性,常见含钾火成岩/沉积岩矿物以及钾在表生过程中的循环,也包括主要行星物质(球粒陨石、非球粒陨石、火星和灶神星陨石以及月球样品)中钾的含量、赋存状态、主要矿物,钾在太阳星云冷凝、行星积聚以及岩浆海过程中的中等挥发性质;(2)介绍了钾同位素的研究历史,从1922年Dempster利用最早的质谱仪测量钾同位素在自然界的丰度,到Taylor和Urey在1938发表的经典的钾同位素分馏实验,再到Humayun和Clayton在1995年发表的钾同位素领域的经典研究,最后到近几年的进展;(3)介绍了对钾的前处理(离子交换柱法)以及钾同位素的主要测量方法,包括早期热电离质谱仪法(TIMS),二次离子质谱仪法(SIMS)和近十几年以来高速发展的多接收电感耦合等离子体质谱仪法(MC-ICP-MS)及其不同的技术路线;(4)介绍了高精度钾同位素比值在低温地球化学和生物地球化学中的应用,包括钾同位素在地表的风化过程中、海水洋壳的反向风化作用中的分馏及其在示踪全球钾元素循环和洋壳俯冲等过程中的应用;(5)介绍了高精度钾同位素比值在高温地球化学中的应用,包括钾同位素在岩浆分异和矿物结晶过程中的分馏;(6)介绍了高精度钾同位素比值在宇宙化学中的应用,包括在太阳星云冷凝、行星凝聚、月球形成大碰撞、岩浆海、火山喷发去气过程中的分馏作用。  相似文献   

The δ60/58Ni Values of Twenty‐Six Selected Geological Reference Materials     

Weihan Li  Jian‐Ming Zhu  Decan Tan  Guilin Han  Zhouqiao Zhao  Guangliang Wu 《Geostandards and Geoanalytical Research》2020,44(3):523-535

The high‐precision δ^60/58Ni values of twenty‐six geological reference materials, including igneous rocks, sedimentary rocks, stream sediments, soils and plants are reported. The δ^60/58Ni values of all samples were determined by double‐spike MC‐ICP‐MS (Nu Plasma III). Isotope standard solution (NIST SRM 986) and geological reference materials (BHVO‐2, BCR‐2, JP‐1, PCC‐1, etc.) were used to evaluate the measurement bias and intermediate precision over a period of six months. Our results show that the intermediate precision of Ni isotope determination was 0.05‰ (2s, n = 69) for spiked NIST SRM 986 and typically 0.06‰ for actual samples, and the δ^60/58Ni _{NIST SRM 986} values were in excellent agreement with previous studies. Eighteen high‐precision Ni isotope ratios of geological reference materials are first reported here, and their δ^60/58Ni values varied from ?0.27‰ to 0.52‰, with a mean of 0.13 ± 0.34‰ (2s, n = 18). Additionally, SGR‐1b (0.56 ± 0.04‰, 2s), GSS‐1 (?0.27 ± 0.06‰, 2s), GSS‐7 (?0.11 ± 0.01‰, 2s), GSD‐10 (0.46 ± 0.06‰, 2s) and GSB‐12 (0.52 ± 0.06‰, 2s) could potentially serve as candidate reference materials for Ni isotope fractionation and comparison of Ni isotopic compositions among different laboratories.  相似文献   

地面磁测资料反演与井中磁测联合找矿——以尕林格Ⅱ矿段为例     

汪钟莲  王永国  王智茂  卢学斌 《地质与资源》2020,29(1):61-67

青海省尕林格铁多金属矿区第四系覆盖层近200 m.矿床以铁矿为主，铜、钴、铅锌多金属矿伴生，进行磁法勘探是最直接而有效的方法.通过对尕林格Ⅱ矿段的地面磁测资料分析，采用二度半反演方法，发现深部存在磁性体.经井中三分量磁测资料的处理和分析，为钻孔布设提供依据，指导钻探施工，在深部找矿方面取得了良好的地质效果.  相似文献   

Ressi experimental catchment: Ecohydrological research in the Italian pre-Alps     

Giulia Zuecco  Chiara Marchina  Ylenia Gelmini  Anam Amin  H. J. van Meerveld  Daniele Penna  Marco Borga 《水文研究》2021,35(3):e14095

Ressi is a small (2.4 ha) forested catchment located in the Italian pre-Alps. The site became an experimental catchment to investigate the water fluxes in the soil–plant–atmosphere continuum and the impact of vegetation on runoff generation in 2012. The elevation of the catchment ranges from 598 to 721 m a.s.l. and the climate is humid temperate. The bedrock consists of rhyolites and dacites; the soil is a Cambisol. The catchment is covered by a dense forest, dominated by beech, chestnut, maple, and hazel trees. The field set up includes measurements of the rainfall in an open area, streamflow at the outlet, soil moisture at various depths and locations, and depth to water table in six piezometers at a 5- or 10-min interval. Samples of precipitation, stream water, shallow groundwater and soil water are collected monthly for tracer analysis (stable isotopes (²H and ¹⁸O), electrical conductivity and major ions), and during selected rainfall–runoff events to determine the contribution of the various sources to runoff. Since 2017, soil and plant water samples have been collected to determine the sources of tree transpiration. Data collected in the period 2012–2016 are publicly available. Data collection is ongoing, and the data set is expected to be updated on an annual basis to include the most recent measurements.  相似文献   

Stable carbon isotope signatures of cellulose in macrophytes collected from three eutrophic lakes in China     

《Limnologica》2020

Aquatic plants are essential for maintaining the diversity and stability of a lake ecosystem. Stable carbon isotopes (δ¹³C) of macrophytes have been widely used as a powerful tool to study ecological processes and paleoenvironmental evolution in lakes. Varying results are obtained when using the δ¹³C of macrophytes to study the changes in the lake environment at different spatio-temporal scales. Thus, sample preparation and subsequent laboratory analyses are crucial for studying environmental changes using the isotopic signal retained in the macrophytes, and are essential for the interpretation of isotope-environment relationships. This study analyzed the δ¹³C of different tissue components of macrophytes in three lakes of the lower Yangtze River basin, and a correlation analysis was performed on aquatic environments influencing the δ¹³C values in the different tissue components of macrophytes. The test results showed the difference between the δ¹³C values of the whole sample and cellulose. Relative analyses indicated that the major factors contributing to the δ¹³C variability in macrophytes were pH and the concentration of dissolved inorganic carbon (DIC). The δ¹³C of α-cellulose (δ¹³C_AC) is more sensitive to environmental variables than that of the whole sample (δ¹³C_W) and holocellulose (δ¹³C_HC). The results of this study imply that extraction of α-cellulose is a prerequisite for research on the changes in lake environment using δ¹³C of macrophytes. This study aims to provide theoretical and data basis for further research on the environmental and ecological change using stable carbon isotopes of aquatic plants.  相似文献   

Calibration method affects the measured δ2H and δ18O in soil water by direct H2Oliquid–H2Ovapour equilibration with laser spectroscopy     

Hongxiu Wang  Bingcheng Si  Dyan Pratt  Han Li  Xiaojun Ma 《水文研究》2020,34(2):506-516

The direct H₂O_liquid–H₂O_vapour equilibration method utilizing laser spectroscopy (DVE-LS) is a way to measure soil pore water stable isotopes. Various equilibration times and calibration methods have been used in DVE-LS. Yet little is known about their effects on the accuracy of the obtained isotope values. The objective of this study was to evaluate how equilibration time and calibration methods affect the accuracy of DVE-LS. We did both spiking and field soil experiments. For the spiking experiment, we applied DVE-LS to four soils of different textures, each of which was subjected to five water contents and six equilibration times. For the field soil experiment, we applied three calibration methods for DVE-LS to two field soil profiles, and the results were compared with cryogenic vacuum distillation (CVD)-LS. Results showed that DVE-LS demonstrated higher δ²H and δ¹⁸O as equilibration time increased, but 12 to 24 hr could be used as optimal equilibration time. For field soil samples, DVE-LS with liquid waters as standards led to significantly higher δ²H and δ¹⁸O than CVD-LS, with root mean square error (RMSE) of 8.06‰ for δ²H and 0.98‰ for δ¹⁸O. Calibration with soil texture reduced RMSE to 3.53‰ and 0.72‰ for δ²H and δ¹⁸O, respectively. Further, calibration with both soil texture and water content decreased RMSE to 3.10‰ for δ²H and 0.73‰ for δ¹⁸O. Our findings conclude that the calibration method applied may affect the measured soil water isotope values from DVE-LS.  相似文献   

Bound and mobile soil water isotope ratios are affected by soil texture and mineralogy,whereas extraction method influences their measurement     

Rachel E. Adams  Ayumi Hyodo  Toby SantaMaria  Cynthia L. Wright  Thomas W. Boutton  Jason B. West 《水文研究》2020,34(4):991-1003

Questions persist about interpreting isotope ratios of bound and mobile soil water pools, particularly relative to clay content and extraction conditions. Interactions between pools and resulting extracted water isotope composition are presumably related to soil texture, yet few studies have manipulated the bound pool to understand its influence on soil water processes. Using a series of drying and spiking experiments, we effectively labelled bound and mobile water pools in soils with varying clay content. Soils were first vacuum dried to remove residual water, which was then replaced with heavy isotope-enriched water prior to oven drying and spiking with heavy isotope-depleted water. Water was extracted via centrifugation or cryogenic vacuum distillation (at four temperatures) and analysed for oxygen and hydrogen isotope ratios via isotope ratio mass spectrometry. Water from centrifuged samples fell along a mixing line between the two added waters but was more enriched in heavy isotopes than the depleted label, demonstrating that despite oven drying, a residual pool remains and mixes with the mobile water. Soils with higher clay + silt content appeared to have a larger bound pool. Water from vacuum distillation samples have a significant temperature effect, with high temperature extractions yielding progressively more heavy isotope-enriched values, suggesting that Rayleigh fractionation occurred at low temperatures in the vacuum line. By distinctly labelling bound and mobile soil water pools, we detected interactions between the two that were dependent on soil texture. Although neither extraction method appeared to completely extract the combined bound and mobile (total water) pool, centrifugation and high temperature cryogenic vacuum distillations were comparable for both δ²H and δ¹⁸O of soil water isotope ratios.  相似文献