Nd–Sr isotopic constraint to the formation of metatexite and diatexite migmatites,Higo metamorphic terrane,central Kyushu,Japan

ABSTRACT

Metatexite and diatexite migmatites are widely distributed within the upper amphibolite and granulite-facies zones of the Higo low-P/high-T metamorphic terrane. Here we report Nd–Sr isotopic and whole rock composition data from an outcrop in the highest-grade part of the granulite-facies zone, in which diatexite occurs as a 3 m-thick layer between 2 m-thick layers of stromatic-structured metatexite within pelitic gneiss. The metatexite has Nd–Sr isotopes and whole rock compositions similar to those of the gneiss, but the diatexite shows the reverse. The diatexite has a higher ε_Nd(t) and ¹⁴⁷Sm/¹⁴⁴Nd ratio (ε_Nd(t) = ?0.5; ¹⁴⁷Sm/¹⁴⁴Nd = 0.1636) than the gneiss (ε_Nd(t) = ?2.1; ¹⁴⁷Sm/¹⁴⁴Nd = 0.1287) and metatexite (ε_Nd(t) = ?3.1; ¹⁴⁷Sm/¹⁴⁴Nd = 0.1188). The (⁸⁷Sr/⁸⁶Sr)_initial and ⁸⁷Rb/⁸⁶Sr of the diatexite ((⁸⁷Sr/⁸⁶Sr)_initial = 0.70568; ⁸⁷Rb/⁸⁶Sr = 0.416) are lower than those of the gneiss ((⁸⁷Sr/⁸⁶Sr)_initial = 0.70857; ⁸⁷Rb/⁸⁶Sr = 1.13) and metatexite ((⁸⁷Sr/⁸⁶Sr)_initial = 0.70792; ⁸⁷Rb/⁸⁶Sr = 1.11). The metatexite and gneiss show enrichment of Th and depletion of P and Eu and have a similar chondrite-normalized REE pattern, which shows steep LREE–MREE-enriched and gently declining HREE patterns and negative Eu anomalies, whereas the diatexite shows enrichment of Sr and depletion of Th and Y, and exhibits gently declining LREE and steeply declining HREE pattern and weak Eu depletion. The metatexite migmatite is interpreted to have formed by in situ partial melting in which the melt did not migrate from the source, whereas the diatexite migmatite included an externally derived melt with a juvenile component. The Cretaceous high-temperature metamorphism of the Higo metamorphic terrane is interpreted to reflect emplacement of mantle-derived basalts under a volcanic arc along the eastern margin of the Eurasian continent, and mass transfer and advection of heat via hybrid silicic melts from the lower crust.     

Multiple mantle metasomatism beneath the Leizhou Peninsula,South China: evidence from elemental and Sr-Nd-Pb-Hf isotope geochemistry of the late Cenozoic volcanic rocks

ABSTRACT

We analysed whole-rock major and trace elements and Sr-Nd-Pb-Hf isotopes of the late Cenozoic volcanic rocks in the Leizhou Peninsula, South China to investigate their mantle source characteristics. These volcanic rocks, collected from Jiujiang, Tianyang and Huoju areas of the Leizhou Peninsula, are characterized by incompatible element enrichment but variable isotopic depletion. The volcanic rocks from Jiujiang and Tianyang show prominent primitive-mantle-normalized positive Nb, Ta and Sr anomalies and depleted Sr-Nd-Pb-Hf isotope compositions, whereas those from Huoju show slight positive to negative Nb and Ta anomalies, a prominent positive Pb anomaly, and more enriched Sr-Nd-Pb-Hf isotope compositions. Two types of mantle metasomatism are required to explain the geochemical characteristics of these rocks. The Jiujiang and Tianyang samples were largely derived from a mantle source metasomatized recently by a low-F melt. Such low-F melt is generated within the asthenospheric mantle, which is enriched in volatiles and incompatible elements with positive Sr anomaly and depleted Sr-Nd-Pb-Hf isotope compositions. The Huoju samples were largely derived from a mantle source metasomatized by recycled upper continental crust material. These two types of mantle metasomatism beneath the Leizhou Peninsula are consistent with trace element characteristics of mantle mineralogy (e.g. clinopyroxene vs. amphibole), which reflects source evolution in space and time (e.g. tectonic setting change).     

Influence of igneous processes and serpentinization on geochemistry of the Logatchev Massif harzburgites (14°45′N,Mid-Atlantic Ridge), and comparison with global abyssal peridotites

We acquired bulk-rock analyses of Mid-Atlantic Ridge (MAR) harzburgites in order to understand the influence of submarine igneous and metamorphic processes on the distribution of incompatible elements (especially rare Earth elements or REEs) in abyssal peridotites. The geochemical characteristics of these Logatchev Massif serpentinized and talc-altered harzburgites, and spatially associated metagabbros were then compared with a compilation of global abyssal peridotites. The Logatchev harzburgites show light rare earth element (LREE) enrichments (average La _N /Yb _N = 2.81), positive correlations between LREEs (e.g. La, Ce, Pr, and Nd) and high field strength elements (HFSEs; e.g. Nb and Zr), and positive correlations between HFSEs and Th. Most global abyssal peridotites show similar trends. We suggest that the systematic enrichment of incompatible elements probably reflects a post-partial fusion magmatic refertilization. The compositional scatter exhibited by some serpentinized peridotites in Nb-LREE diagrams is probably due to the elimination of diopside during partial melting and significant impregnation by a melt produced in the Opx–Ol–Sp melting field rather than to later hydrothermal alteration. The correlation between Pb and Nd observed for most global abyssal peridotites, including the Logatchev harzburgites, indicates magmatic generation. The scatter of Pb in some rocks suggests that lead is likely mobile during serpentinization or weathering. Low to moderate water/rock (W/R) ratios in the harzburgites calculated from Sr isotopic compositions (5.98–26.20 for a close system and 1.66–2.72 for an open system), and the low abundance of REEs in Logatchev hydrothermal fluids indicate that the REE contents of abyssal peridotites probably were little influenced by hydrothermal alteration. Compared to this later alteration, the presence of small proportions of gabbroic melt (from 1:30 to 1:3 in our sample) that crystallized in the residual harzburgites modified their REE patterns significantly by elevating the LREEs.     

Eocene mafic volcanism in northern Anatolia: its causes and mantle sources in the absence of active subduction

Eocene mafic volcanic rocks occurring in an E–W-trending, curvilinear belt along and north of the Izmir–Ankara–Erzincan suture zone (IAESZ) in northern Anatolia, Turkey, represent a discrete episode of magmatism following a series of early Cenozoic collisions between Eurasia and the Gondwana-derived microcontinents. Based on our new geochronological, geochemical, and isotope data from the Kartepe volcanic units in northwest Anatolia and the extant data in the literature, we evaluate the petrogenetic evolution, mantle melt sources, and possible causes of this Eocene volcanism. The Kartepe volcanic rocks and spatially associated dikes range from basalt and basaltic andesite to trachybasalt and basaltic trachyandesite in composition, and display calc-alkaline and transitional calc-alkaline to tholeiitic geochemical affinities. They are slightly to moderately enriched in large ion lithophile (LILE) and light rare earth elements (LREE) with respect to high-field strength elements (HFSE) and show negative Nb, Ta, and Ti anomalies reminiscent of subduction-influenced magmatic rocks. The analysed rocks have ⁸⁷Sr/⁸⁶Sr_(i) values between 0.70570 and 0.70399, positive ?_Nd values between 2.7 and 6.6, and Pb isotope ratios of ²⁰⁶Pb/²⁰⁴Pb_(i) = 18.6–18.7, ²⁰⁷Pb/²⁰⁴Pb_(i) = 15.6–15.7, and ²⁰⁸Pb/²⁰⁴Pb_(i) = 38.7–39.1. The ⁴⁰Ar/³⁹Ar cooling ages of 52.7 ± 0.5 and 41.7 ± 0.3 Ma obtained from basaltic andesite and basalt samples indicate middle to late Eocene timing of this volcanic episode in northwest Anatolia. Calculated two-stage Nd depleted mantle model (T_DM) ages of the Eocene mafic lavas range from 0.6 to 0.3 Ga, falling between the T_DM ages of the K-enriched subcontinental lithospheric mantle of the Sakarya Continent (1.0–0.9 Ga) to the north, and the young depleted mantle beneath central Western Anatolia (0.4–0.25 Ga) to the south. These geochemical and isotopic features collectively point to the interaction of melts derived from a sublithospheric, MORB-like mantle and a subduction-metasomatized, subcontinental lithospheric mantle during the evolution of the Eocene mafic volcanism. We infer triggering of partial melting by asthenospheric upwelling beneath the suture zone in the absence of active subduction in the Northern Neotethys. The geochemical signature of the volcanic rocks changed from subduction- and collision-related to intra-plate affinities through time, indicating an increased asthenospheric melt input in the later stages of Eocene volcanism, accompanied by extensional deformation and rifting.     

Melt–peridotite interaction in the shallow lithospheric mantle of the North China Craton: evidence from melt inclusions in the quartz-bearing orthopyroxene-rich websterite from Hannuoba

To better understand the origin, migration, and evolution of melts in the lithospheric mantle and their roles on the destruction of the North China Craton (NCC), we conducted a petrological and geochemical study on a quartz-bearing orthopyroxene-rich websterite xenolith from Hannuoba, the NCC, and its hosted melt and fluid inclusions. Both clinopyroxene and orthopyroxene in the xenolith contain lots of primary and secondary inclusions. High-temperature microthermometry of melt inclusions combined with Raman spectroscopy analyses of coexisting fluid inclusions shows that the entrapment temperature of the densest inclusions was ~1215°C and the pressure ~11.47 kbar, corresponding to a depth of ~38 km, i.e. within the stability of the spinel lherzolite. Intermediate pressure inclusions probably reflect progressive fluid entrapment over a range of depths during ascent, whereas the low-pressure inclusions (P < 2 kbar) may represent decrepitated primary inclusions. In situ laser-ablation ICP-MS analyses of major and trace elements on individual melt inclusions show that the compositions of these silicate melt inclusions in clinopyroxene and orthopyroxene are rich in SiO₂, Al₂O₃, and alkalis but poor in TiO₂ and strongly enriched in light rare earth elements (LREEs) and large ion lithophile elements (LILEs), with negative anomalies of high-field strength elements (HFSEs). These characteristics suggest that the silica-rich melts could be derived from the partial melting of subducted oceanic slab. Therefore, this kind of quartz-bearing orthopyroxene-rich websterite may be produced by interaction between the slab-derived melts with the mantle peridotite. This study provides direct evidence for the origin, migration, and evolution of melts in the lithospheric mantle, which may play an important role in the destruction of the NCC.     

内蒙古二连浩特北部阿仁绍布地区晚石炭世花岗岩Sr-Yb分类及其成因

对分布在内蒙古二连浩特北部阿仁绍布地区的晚石炭世花岗岩类,依据Sr、Yb含量,划分为低Sr高Yb型、极低Sr高Yb型和低Sr低Yb型花岗岩3种类型。低Sr高Yb型花岗岩类相对低Si、富Al,Na2O>K2O,稀土元素分馏中等,有或无负Eu异常,Sr含量低,平均为183×10-6,Ba含量较高,平均585×10-6,Y含量高,平均30.06×10-6,Rb/Sr比值较低,平均0.97;极低Sr高Yb型花岗岩富Si、REE,低Al、Sr、Ba,高的Rb/Sr比值(平均为7.47),具明显的负Eu异常等;低Sr低Yb型花岗岩富Si,贫Al、Ca、Mg,重稀土元素(Y、Yb)含量低,Y含量在(7.26～10.6)×10-6之间,平均9.76×10-6,Yb含量在(1.04～1.89)×10-6之间,平均1.44×10-6,δEu=0.64～0.94,具弱负Eu异常,微量元素Ba含量高,Rb/Sr比值低。3种类型的花岗岩类过铝指数(A/CNK)多小于1.0,说明它们均源自变质火成岩的部分熔融。由于源区的深度不同(pT条件不同)和残留的主要矿物相不同,它们的岩石地球化学特征存在差异。极低Sr高Yb型花岗岩形成深度最浅(中上地壳),熔融残留相以斜长石为主;低Sr高Yb型花岗岩类形成于中下地壳,熔融残留相为斜长石和辉石;低Sr低Yb型花岗岩形成深度最深,推测可能形成于加厚下地壳(>40km)底部,熔融残留相为石榴子石、斜长石和角闪石。     

100MPa、800℃下Mo和W在流体／花岗质熔体相间分配的实验研究

利用“RQV-快速内冷淬火”（外加热冷封式）高温高压实验装置,在100MPa、800℃条件下,以东秦岭地区出露的高钾钙碱性岩浆岩（合峪花岗岩）为实验初始物,实验研究了Mo和W在花岗岩-H2O、花岗岩-NaCl（KCl）-H2O及花岗岩-NaF-H2O体系流体／熔体相间的分配行为。实验结果表明,Mo比W更倾向于分配进入流体相（DMo^流体/溶体〉〉DW^流体/溶体）,相对于纯水体系而言,流体介质中Cl和F的存在均有利于Mo和W向流体相迁移富集,随体系内Cl含量的不断增高,Mo和W的分配系数呈线性增大趋势,而在天然花岗岩可能含有的F含量范围之内,F含量的增高将阻碍Mo、W向流体相迁移,流体介质中Na／K（摩尔比）的变化对Mo和W的分配系数没有明显影响,表明体系碱质（Na或K）类型不是Mo和W在流体／熔体相间分配的主要影响因素。     

X射线荧光光谱法测定高锶高钡的硅酸盐样品中主量元素

用百分总和检查硅酸盐岩石全分析数据的质量是分析工作者的传统做法,但对于微量元素含量较高的样品,采用X射线荧光光谱法(XRF)进行测定,如果不考虑微量元素的含量及其对主量元素基体效应的影响,往往会使主量元素含量更加偏离真实值。本文针对Sr、Ba含量较高的硅酸盐样品,通过人工配制标准样品,扩大了Sr、Ba校准曲线的定量范围,主量元素校准中加入Sr、Ba的基体校正系数,达到了主量元素定量更加准确可靠的实际效果。采用此方法分析国家标准物质,各主量元素的精密度(RSD)均小于2%;分析不参加回归的标准物质和人工配制的标准样品,主量元素的测量值与标准值(或参考值)基本一致。该方法可以满足硅酸盐的测定要求,主量元素各项结果的加和能够达到《地质矿产实验室测试质量管理规范》的一级标准(99.3%～100.7%)。     

An Optimised 1,10‐Phenanthroline Method for the Determination of Ferrous and Ferric Oxides in Silicate Rocks,Soils and Minerals

A precise, accurate and rapid method for the sequential determination of FeO and Fe₂O₃ in rocks, soils and some non‐refractory minerals by 1,10‐phenanthroline spectrophotometry is described. Fe(II) and Fe(III) were leached from the sample (?200 mesh) using a mixture of NH₄HF₂ and H₂SO₄ at 40–80 °C for 10 min on a hot plate. Both Fe(II) and Fe(III) could be conveniently estimated sequentially from the same reaction mixture at the μg g^?1 to percentage level. The method is better than the existing wet chemical methods, including the commonly used Pratt's titrimetric redox method, for Fe(II) and Fe(III) determinations in rock and soil samples in terms of precision, accuracy and rapidity. The throughput of the method was very high; at least forty to fifty samples could be estimated easily in a day. The results obtained compare favourably with those obtained by Pratt's method, as well as for certified/recommended values of a set of eleven certified reference materials having FeO and Fe₂O₃ contents in the range 0.21–14.63% and 0.58–8.48%, respectively. The optimised 1,10 phenanthroline method was found to be accurate to within 0.21% m/m FeO and 0.30% m/m Fe₂O₃ compared with the literature values of the certified reference materials studied.     

http://www.sciencedirect.com/science/article/pii/S1674987113000595

Magmatic oxide deposits in the～260 Ma Emeishan Large Igneous Province(ELIP),SW China and northern Vietnam,are important sources of Fe,Ti and V.Some giant magmatic Fe-Ti-V oxide deposits, such as the Panzhihua,Hongge,and Baima deposits,are well described in the literature and are hosted in layered mafic-ultramafic intrusions in the Panxi region,the central ELIP.The same type of ELIP- related deposits also occur far to the south and include the Anyi deposit,about 130 km south of Panzhihua,and the Mianhuadi deposit in the Red River fault zone.The Anyi deposit is relatively small but is similarly hosted in a layered mafic intrusion.The Mianhuadi deposit has a zircon U-Pb age of～260 Ma and is thus contemporaneous with the ELIP.This deposit was variably metamorphosed during the Indosinian orogeny and Red River faulting.Compositionally,magnetite of the Mianhuadi deposit contains smaller amounts of Ti and V than that of the other deposits,possibly attributable to the later metamorphism.The distribution of the oxide ore deposits is not related to the domal structure of the ELIP.One major feature of all the oxide deposits in the ELIP is the spatial association of oxide-bearing gabbroic intrusions,syenitic plutons and high-Ti flood basalts.Thus,we propose that magmas from a mantle plume were emplaced into a shallow magma chamber where they were evolved into a field of liquid immiscibility to form two silicate liquids,one with an extremely Fe-Ti-rich gabbroic composition and the other syenitic.An immiscible Fe-Ti-(P) oxide melt may then separate from the mafic magmas to form oxide deposits.The parental magmas from which these deposits formed were likely Fe-Ti-rich picritic in composition and were derived from enriched asthenospheric mantle at a greater depth than the magmas that produced sulfide-bearing intrusions of the ELIP.