矿物微量元素组成用于火成岩构造背景判别

火成岩中的矿物,特别是稳定副矿物的微量元素组成可用于火成岩构造–岩浆背景的判别。产于不同构造背景火成岩中单颗粒锆石原位微量元素含量的准确测定,积累了大量资料。本文介绍了用锆石微量元素含量的二维核密度分布投影,构建了U/Yb-Nb/Yb、Sc/Yb-Nb/Yb和U/Yb-Sc/Yb构造背景判别图解,可以区分洋中脊、地幔柱影响的洋岛及俯冲有关的弧(大陆弧)等不同构造背景形成的火成岩。单斜辉石、尖晶石、黑云母和角闪石的微量元素或主量元素组成同样可用于构造背景识别。     

MK‐1 Apatite: A New Potential Reference Material for (U‐Th)/He Dating

The (U‐Th)/He dating technique has been widely used for several decades to constrain the timing of low temperature geological processes. Recent research has shown that the commonly used reference material (the Durango apatite) often yields dispersed fragment dates that are beyond analytical uncertainties. Here, we report a new apatite (U‐Th)/He dating reference material, MK‐1, which was collected from the Mogok metamorphic belt in Burma. Electron probe microanalysis and backscattered electron images of two randomly selected fragments indicate that this apatite is chemically and structurally homogeneous. We performed single‐grain (U‐Th)/He dating on thirty randomly selected fragments of this material. (U‐Th)/He dating results from multiple laboratories show that fragments of the MK‐1 apatite megacryst yielded reproducible results, with a mean date of 18.0 ± 0.2 Ma. The Th/U ratio of this apatite is homogeneous. Nine randomly selected fragments registered a narrow range of effective uranium (eU) mass fractions (326–354 μg g^?1), with a mean value of 336.6 ± 10.3 μg g^?1. Twenty‐four in situ (U‐Th)/He dates yielded a mean value of 18.0 ± 0.2 Ma (MSWD = 0.41), indistinguishable from the results obtained by the conventional method. All the results suggest that this apatite has the potential to become a new reference material for (U‐Th)/He geochronology.     

汉诺坝橄榄岩捕虏体的单斜辉石LAM-ICPMS分析及其岩石圈地幔演化意义

橄榄岩成分及其中矿物(如单斜辉石)微量元素组成可以很好地揭示岩石圈地幔性质．在对汉诺坝新生代玄武岩中橄榄岩捕虏体做详细岩相学和岩石化学研究基础上,重点分析了单斜辉石的激光原位微量元素,并探讨了新生代华北克拉通北缘岩石圈地幔特征及地幔演化．汉诺坝地区岩石圈地幔是相当于原始地幔经过不同程度的部分熔融抽取形成的,除个别样品的部分熔融程度为15％-20％外,多数样品<5％．全岩主元素、单斜辉石成分体现出新生代汉诺坝地区的岩石圈地幔是很不均一的:在主体饱满型中有亏损型地幔的残留．这种共存现象可能是软流圈物质对古老地幔进行侵蚀、混合和改造置换的结果．单斜辉石微量元素组成所体现的碳酸岩岩浆交代作用和硅酸盐熔／流体的交代作用也支持这一认识．     

Accurate Determination of Sr Isotopic Compositions in Clinopyroxene and Silicate Glasses by LA‐MC‐ICP‐MS

The low‐Sr content (generally < 100 μg g^?1) in clinopyroxene from peridotite makes accurate Sr isotopic determination by LA‐MC‐ICP‐MS a challenge. The effects of adding N₂ to the sample gas and using a guard electrode (GE) on instrumental sensitivity for Sr isotopic determination by LA‐MC‐ICP‐MS were investigated. Results revealed no significant sensitivity enhancement of Sr by adding N₂ to the ICP. Although using a GE led to a two‐fold sensitivity enhancement, it significantly increased the yield of polyatomic ion interferences of Ca‐related ions and TiAr⁺ on Sr isotopes. Applying the method established in this work, ⁸⁷Sr/⁸⁶Sr ratios (Rb/Sr < 0.14) of natural clinopyroxene from mantle and silicate glasses were accurately measured with similar measurement repeatability (0.0009–0.00006, 2SE) to previous studies but using a smaller spot size of 120 μm and low‐to‐moderate Sr content (30–518 μg g^?1). The measurement reproducibility was 0.0004 (2s, n = 33) for a sample with 100 μg g^?1 Sr. Destruction of the crystal structure by sample fusion showed no effect on Sr isotopic determination. Synthesised glasses with major element compositions similar to natural clinopyroxene have the potential to be adopted as reference materials for Sr isotopic determination by LA‐MC‐ICP‐MS.