绿帘石记录俯冲带变质流体活动

俯冲带是连接地球表生圈层和深部圈层的关键纽带,深刻影响着地球内部的运行方式和人类宜居环境。俯冲板片脱水释放的高压-超高压变质流体控制着俯冲带诸多重要地质过程,如地幔楔交代和部分熔融、岛弧岩浆活动、中/深源地震以及地球内部的元素迁移和分异等等。深入了解这些流体的源区、运移、成分和物理化学条件是理解这些流体性质和行为的前提和关键。绿帘石是俯冲带变质岩中一个常见的含水造岩矿物,具有较宽广的稳定温压范围(绿片岩相-榴辉岩相)、较高的微量元素含量和缓慢的体扩散行为(如Sr、Pb、Th、U、Cr、V和LREE),能够指示俯冲带(多期)变质流体活动和地球化学效应。本文总结了近年来俯冲带变质绿帘石研究的主要进展及其在揭示俯冲带流体活动方面的重要应用,包括探究俯冲带流体的起源、成分特征、运移方式、氧逸度条件、交代效应和多期次结晶行为。这些研究表明绿帘石是一个极好的变质流体活动记录器,能够为理解俯冲带流体活动和深部元素迁移提供关键信息。     

Boron geochemistry from some typical Tibetan hydrothermal systems: Origin and isotopic fractionation

The Tibetan plateau is characterized by intense hydrothermal activity and abnormal enrichment of trace elements in geothermal waters. Hydrochemistry and B isotope samples from geothermal waters in Tibet were systematically measured to describe the fractionation mechanisms and provide constraints on potential B reservoirs. B concentrations range from 0.35 to 171.90 mg/L, and isotopic values vary between −16.57 ‰ and +0.52 ‰. Geothermal fields along the Indus-Yarlung Zangbo suture zone and N–S rifts are observed with high B concentrations and temperatures. The similar hydrochemical compositions of high-B geothermal waters with magmatic fluid and consistent modeling of B isotopic compositions with present δ¹¹B values imply that the B in high-B geothermal waters is mainly contributed by magmatic sources, probably through magma degassing. In contrast, geothermal fields in other regions of the Lhasa block have relatively low B concentrations and temperatures. After considering the small fractionation factor and representative indicators of Na/Ca, Cl/HCO₃, Na + K and Si, the conformity between modeling results and the isotopic compositions of host rocks suggests that the B in low-temperature geothermal fields is mainly sourced from host rocks. According to simulated results, the B in some shallow geothermal waters not only originated from mixing of cold groundwater with deep thermal waters, but it was also contributed by equilibration with marine sedimentary rocks with an estimated proportion of 10%. It was anticipated that this study would provide useful insight into the sources and fractionation of B as well as further understanding of the relationships between B-rich salt lakes and geothermal activities in the Tibetan plateau.     

Boron isotopic variations in tourmaline from metacarbonates and associated calc-silicate rocks from the Bohemian Massif: Constraints on boron recycling in the Variscan orogen

Various metacarbonate and associated calc-silicate rocks form minor but genetically significant components of the lithological units in the Bohemian Massif of the Variscan orogen in Central Europe.These rocks vary in terms of their lithostratigraphy,chemical composition and mineral assemblage(dolomite/calcite ratio,silicate abundance).Tourmaline is present in five paragenetic settings within the metacarbonate and calc-silicate units.TypeⅠcomprises individual,euhedral,prismatic grains and grain aggregates in a carbonate-dominant(calcite±dolomite)matrix poor in silicates.TypeⅡis characterized by euhedral to subhedral grains and coarse-to fine-grained aggregates in silicate-rich layers/nests within metacarbonate bodies whereas typeⅢoccurs as prismatic grains and aggregates at the contact zones between carbonate and associated silicate host rocks.TypeⅣis in veins crosscutting metacarbonate bodies,and typeⅣtourmaline occurs at the exocontacts of elbaite-subtype granitic pegmatite.Tourmaline from the different settings shows distinctive compositional features.Typical for typeⅠare Mg-rich compositions,with fluor-uvite>dravite>>magnesio-lucchesiite.Tourmalines from typeⅡsilicate-rich layers/nests are highly variable,corresponding to oxy-schorl,magnesio-foitite,Al-rich dravite and fluor-uvite.Typical for typeⅢtourmalines are Ca,Ti-bearing oxy-dravite compositions.The typeⅣveins feature dravite and fluor-uvite tourmaline compositions whereas typeⅤtourmaline is Li,F-rich dravite.Tourmaline is the only Bbearing phase in paragenetic typesⅠ-Ⅳ,where it is characterised by two principal ranges of B-isotope composition(δ^11B=-13‰to-9‰and-18‰to-14‰).These ranges correspond to regionally different units of the Moldanubian Zone.Thus,the Svratka Unit(Moldanubian Zone s.l.)contains only isotopically lighter tourmaline(δ^11B=-18‰to-14‰),whereas metacarbonates in the Poli?ka unit(Teplá-Barrandian Zone)and Olesnice unit(Moravicum of the Moravo-Silesian Zone)has exclusively isotopically heavier tourmaline(δ^11B=-9‰to-13‰).Tourmalines from metacarbonates in the Variegated Unit cover both ranges of isotope composition.The isotopically light end of the B isotope range may indicate the presence of continental evaporites within individual investigated areas.On the other hand,variations in the range of~8δ-units is consistent with the reported shift in B isotopic composition of metasedimentary rocks of the Bohemian Massif due to the prograde metamorphism from very-low grade to eclogite facies.In contrast to the metacarbonate-hosted settings,tourmaline of paragenetic type V from the exocontact of granitic pegmatites displays a significantly heavier range ofδ^11B(as low as-7.7‰to-0.6‰),which is attributed to partitioning of 10 B to cogenetic axinite and/or different B-signature of the source pegmatite containing tourmaline with heavyδ^11B signature.     

Detrital,metamorphic and metasomatic tourmaline in high-pressure metasediments from Syros (Greece): intra-grain boron isotope patterns determined by secondary-ion mass spectrometry

The boron isotopic composition of zoned tourmaline in two metasediments from the island of Syros, determined by secondary-ion mass spectrometry (SIMS), reflects the sedimentary and metamorphic record of the rocks. Tourmaline from a silicate-bearing marble contains small (≤20 μm) detrital cores with highly variable δ ¹¹B values (−10.7 to +3.6‰), pointing to a heterogeneous protolith derived from multiple sources. The sedimentary B isotopic record survived the entire metamorphic cycle with peak temperatures of ∼500°C. Prograde to peak metamorphic rims are homogeneous and similar among all analysed grains (δ ¹¹B ≈ +0.9‰). The varying δ ¹¹B values of detrital cores in the siliceous marble demonstrate that in situ B isotope analysis of tourmaline by SIMS is a potentially powerful tool for provenance studies not only in sediments but also in metasediments. A meta-tuffitic blueschist bears abundant tourmaline with dravitic cores of detrital or authigenic origin (δ ¹¹B ≈ −3.3‰), and prograde to peak metamorphic overgrowth zones (−1.6‰). Fe-rich rims, formed during influx of B-bearing fluids under retrograde conditions, show strongly increasing δ ¹¹B values (up to +7.7‰) towards the margins of the grains. The δ ¹¹B values of metamorphic tourmaline from Syros, formed in mixed terrigenous–marine sediments, reflect the B signal blended from these two different sources, and was probably not altered by dehydration during subduction.     

大别地体超高压变质岩石锆石Lu-Hf同位素研究

对大别山南部超高压变质带双河和黄镇地区的榴辉岩、片麻岩和硬玉石英岩中变质锆石进行了原位LA-MC-ICPMS的Lu-Hf同位素分析.双河和黄镇的榴辉岩及双河的硬玉石英岩有低176Lu/177Hf和低176Hf/177Hf组成,两地的片麻岩有高176Hf/177Hf比和高且分散的176Lu/177Hf组成.锆石Hf同位素分布主要受变质原岩的形成时代控制,增生锆石基本上继承了原岩锆石的Hf同位素特征,既有增生锆石相对有低176Lu/177Hf和高176Hf/177Hf、继承重结晶锆石相对有高176Lu/177Hf和低176Hf/177Hf的特征,也有二者相互重叠没有区别的,它主要受原岩性质和变质过程中锆石遭受的溶蚀程度控制.增生锆石的低Lu/Hf是锆石在变质过程中Lu含量下降和Hf含量增高造成的,增生锆石的高176Hf/177Hf继承自岩石中其它高Lu/Hf比矿物的长期演化.继承锆石的初始Hf同位素组成εHf值和亏损地幔模式年龄TDM示踪表明,各超高压变质原岩的时代和成因是复杂的：双河榴辉岩原岩物质源自25亿年的亏损地幔和至少27亿年以上的古老晚太古地壳混合.双河片麻岩原岩年龄相同,但有不同的壳幔混合物源.黄镇榴辉岩原岩主要源于亏损幔源岩浆形成的初生地壳的重循环,很少的地壳混染.黄镇片麻岩和榴辉岩的物源区年龄相同.两地片麻岩原岩物源主要来自弱亏损地幔,存在古老地壳物质和地幔物质的混合.大别地区超高压变质岩锆石的Lu-Hf同位素特征主要反映了7～8亿年和18～19亿年时扬子克拉通北缘地区的岩浆活动特点和大地构造环境.     

南海珊瑚礁硼同位素组成及其环境意义

采用正热电离质谱方法测定了中国南海诸岛７０００ａ以来的珊瑚礁的硼同位素的硼含量。讨论了珊瑚礁中硼同位素 硼含量,Ｐ不管不顾忻代等参数的关系。结果表明,所测定的珊瑚礁硼同位素组成变化范围为２２．７￣２４．８‰,并且与珊瑚 硼含量呈正相关关系。根据硼同位素与海水ＰＨ值的关系计算出过去７０００ａ南海泊ＰＨ值变化８．１０￣８．４１。初步探讨了硼同位素组成与南海海平面变化的关系。     

Chemical and isotopic (B, Sr) composition of alluvial sediments as archive of a past hydrothermal outflow

The geochemical and isotopic signature of Quaternary alluvial sediments filling a post-orogenic basin along the Tyrrhenian coasts of Italy (Cornia Plain, Tuscany) was investigated to unravel possible interactions with geothermal fluids from the Larderello geothermal field. Two cores located in the upper (UCP) and lower (LCP) sector of the plain were sampled to depths of up to 80 m. A third core in a neighbouring area not affected by geothermal activity was also sampled (Arno plain at Pisa), and its sediment composition was used as reference. The Cornia sediments (fraction < 65 μm) show high B, Cs and Sb concentrations related to a peculiar chemical enrichment of the clay fraction. They also show remarkable enrichments in As (up to 1000 μg g^− 1) reflecting a contribution from local ore deposits.⁸⁷Sr/⁸⁶Sr ratios, ranging from 0.71022 to 0.71698, reveal the nature of the weathered mother rocks of the alluvial sediments, whereas the boron isotopic composition, varying from − 20‰ to − 10‰, suggests an interaction between the clay fraction and boron-rich fluids at temperatures greater than 50 °C. This implies that hydrothermal fluids widely circulated within the Cornia basin in the past, ultimately leading to the geochemical anomalies currently recorded in local sediments.Although natural (geogenic) in origin, these anomalies cause severe problems to the regional water management (groundwater exploitation) through leaching of trace elements into circulating groundwater, a phenomenon which has to be carefully studied and monitored.     

Boron isotope composition of geothermal fluids and borate minerals from salar deposits (central Andes/NW Argentina)

We have measured the boron concentration and isotope composition of regionally expansive borate deposits and geothermal fluids from the Cenozoic geothermal system of the Argentine Puna Plateau in the central Andes. The borate minerals borax, colemanite, hydroboracite, inderite, inyoite, kernite, teruggite, tincalconite, and ulexite span a wide range of δ¹¹B values from −29.5 to −0.3‰, whereas fluids cover a range from −18.3 to 0.7‰. The data from recent coexisting borate minerals and fluids allow for the calculation of the isotope composition of the ancient mineralizing fluids and thus for the constraint of the isotope composition of the source rocks sampled by the fluids. The boron isotope composition of ancient mineralizing fluids appears uniform throughout the section of precipitates at a given locality and similar to values obtained from recent thermal fluids. These findings support models that suggest uniform and stable climatic, magmatic, and tectonic conditions during the past 8 million years in this part of the central Andes. Boron in fluids is derived from different sources, depending on the drainage system and local country rocks. One significant boron source is the Paleozoic basement, which has a whole-rock isotopic composition of δ¹¹B=−8.9±2.2‰ (1 SD); another important boron contribution comes from Neogene-Pleistocene ignimbrites (δ¹¹B=−3.8±2.8‰, 1 SD). Cenozoic andesites and Mesozoic limestones (δ¹¹B≤+8‰) provide a potential third boron source.     

硼同位素分析方法研究进展

硼具有两种稳定同位素10B和11B,其在自然界的丰度分别是19.90%和80.10%。自然界硼同位素组成变化很大, δ11B变化可达90‰以上(－30‰～＋60‰)。硼同位素的分析精度优于0.2‰,因此被广泛应用于多种地质过程的示踪研究。近年来,硼元素的提取、分离纯化和仪器测定技术均取得了可喜的进展,分析精度不断提高,为硼同位素地球化学研究奠定了良好的基础。本文从样品分解、化学分离和仪器测定等方面对硼同位素分析测试方法进行了归纳总结。     

包含变质岩分类三要素的主要变质岩分类表

变质岩分类的三要素是:变质岩的物质成分(化学成分、矿物成分)、变质岩的组构(结构、构造)和变质岩的成因(变质作用类型和形成变质岩的物理化学条件).由于变质岩的化学成分、矿物成分、组构特征和形成变质岩的地质环境十分复杂,致使至今尚无以变质岩分类三要素为基础的、内容比较完善的分类方案.本文中主要变质岩的分类是以其分类三要素为基础编制的,首次将不同成因的变质岩类并列于同一表中、将鉴定变质岩的主要标志性矿物成分和组构特征列入同一分类表中.该分类对鉴定变质岩石具有可操作性和实用性,分类表中涵盖了自然界主要的变质岩石.     

变质流体地球化学：从静态定性“流”向动态定量

对变质岩的矿物学演化研究使岩石学家和地球化学家认识到,流体流动在变质作用过程中发挥着重要的作用。根据变质矿物共生组合、化学和同位素数据能够鉴别流体在变质体中所流经的区域,确定流体的数量、相对于温度和压力梯度以及岩石接触带的流体流动方向,并确定流体活动的时代。仅在特殊的矿物组合、流体成分、温度和压力条件下,流体可能沿矿物颗粒缝隙的网状交叉的显微通道流动。变质流体流动对于研究地壳的热和质量传输及变形机制和速率有着重要的作用。在各种地壳环境中都存在大量的含水流体,区域和接触变质岩石具有的时间积分流量远远大于紧邻岩石脱水所提供的数量。支持高水流量的证据包括不同学科种类,例如岩石学、矿物学、结构和显微构造以及稳定同位素。渗透率增大可能是促使流体流量变大的主要机制。通过同位素地球化学家与构造地质学家和岩石学家们之间的密切合作,直接对变质岩渗透率增大机制进行实验测定和理论模拟,并在野外检验渗透率增大模型,将有助于理解变质作用的热和流体循环与变形作用之间的关系。     

Boron isotope variations in nature: a synthesis

The large relative mass difference between the two stable isotopes of boron, ¹⁰B and ¹¹B, and the high geochemical reactivity of boron lead to significant isotope fractionation by natural processes. Published ¹¹B values (relative to the NBS SRM-951 standard) span a wide range of 90. The lowest ¹¹B values around — 30 are reported for non-marine evaporite minerals and certain tourmalines. The most ¹¹B-enriched reservoir known to date are brines from Australian salt lakes and the Dead Sea of Israel with ¹¹B values up to +59. Dissolved boron in present-day seawater has a constant world-wide ¹¹B value of + 39.5. In this paper, available ¹¹B data of a variety of natural fluid and solid samples from different geological environments are compiled and some of the most relevant aspects, including possible tracer applications of boron-isotope geochemistry, are summarized.

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Résumé La grande différence relative de masse entre les isotopes stables du bore, ¹⁰B et ¹¹B, et la grande réactivité geochimique du bore ont pour conséquence un fractionnement isotopique naturel important. Les valeurs de ¹¹B publiées (par rapport au standard NBS SRM-951) varient de 90. Les valeurs de ¹¹B les plus basses (–30) correspondent aux evaporites non-marines et à certaines tourmalines. Le réservoir le plus enrichi en ¹¹B est représenté par les saumures des lacs salés d' Australie et par la Mer Morte en Israël, qui ont des valuers de ¹¹B allent jusqu'à + 59. L'eau de mer a une valeur de ¹¹B mondialement constante de + 39.5. Des valeurs de ¹¹B des solutions naturelles ainsi que des roches et minéraux de différentes origines, publiées jusqu'à présent, sont présentées ici. En outre quelques aspects importants concernant la géochimie des isotopes du bore y compris quelques applications sont exposés.

     

Sr isotopic composition of Paleoproterozoic C-rich carbonate rocks: The Tulomozero Formation,SE Fennoscandian Shield

Rb–Sr systematics has been studied in ¹³C-rich carbonate rocks of the Paleoproterozoic (2.09 ± 0.07 Ga) Tulomozero Formation in the northern Onega Lake area, the SE Fennoscandian Shield. The formation is divided into eight members (A–F) consisting of greenschist-facies-grade, variegated sandstones, siltstones, mudstones, stromatolitic dolostones and subordinate crystalline limestones. Samples of carbonate rocks were obtained from two overlapping drillholes intersecting the entire thickness of the Tulomozero Formation. Prior to isotope analysis, the rocks powders were treated with 1N ammonium acetate for partial removal of the late epigenetic carbonate phases. Major resetting of the Rb–Sr systems in the Tulomozero carbonate rocks appears to take place during the Svecofennian regional metamorphic event, and it was screened by using Mn/Sr, Fe/Sr, Mg/Ca, and ¹⁸O/¹⁶O ratios. High Sr content (up to 2080 μg/g in limestones, and 530 μg/g in dolostones) coupled with low Fe/Mn (<0.40) ratios in the Tulomozero carbonate rocks of Members A, B (the lower part), D, F, and E are consistent with accumulation of original carbonate sediments in evaporitic lacustrine, playa, and sabkha environments. A decrease in the Sr content with concurrent increase in the Fe/Mn ratio (>0.40) in dolostones of the upper part of Member B, and of Members G and H is indicative of seawater influxes (sea transgression) into the Tulomozero basin. The ⁸⁷Sr/⁸⁶Sr values in the least altered (Mn/Sr < 2.0) marine dolostones are 0.70418–0.70442 and 0.70343–0.70409 for the earlier and late phases of the marine transgression, respectively. The decrease in the ⁸⁷Sr/⁸⁶Sr ratio in ca. 2.1 Ga seawater is attributable to an increase in hydrothermal flux Sr into the Palaeoproterozoic ocean.     

Oxygen isotope geothermometers for metamorphic rocks

The Chicago mineral-carbonate oxygen isotope fractionation curves have been combined with mineral-water fractionation data for jadeite, zoisite and rutile and new data for grossular-water to provide a set of self-consistent mineral-pair calibrations. The A coefficients in the equation 1000 In α= A × 10⁶T^-2 of the new mineral-pair fractionations are
Jadeite Zoisite Grossular Rutile
Quartz 1.69 2.00 3.03 5.02
Jadeite 0.31 1.34 3.33
Zoisite 1.03 3.02
Grossular 1.99
The isotopic fractionation properties of natural pyralspite garnet [(Ca, Fe, Mg, Mn)₃Al₂Si₃O₁₂] can be approximated by those of the grossular end-member. Appropriate substitutions also yield coefficients for the solid-solution minerals: sodic pyroxene and epidote, e.g.
A _{quartz-sodic pyroxene}= 2.75 - 1.06X_jd,
A _{quartz-epidote}= 2.00 + 0.75X_ps
where X _Jd and X _Ps are the mole fractions of the jadeite and pistacite components, respectively.
The new data set is particularly suitable for the geothermometry of metamorphic rocks. δ¹⁸O data from minerals of the high-pressure metamorphic rocks of the Sesia Zone of Italy and Cyclades Complex of Greece yield well-constrained mean temperatures of 572 and 478 C, respectively. Type III blueschist metabasalts of the Franciscan Formation of California give mean quartz-garnet temperatures of 354 C.     

Two-dimensional patterns of metamorphic fluid flow and isotopic resetting in layered and fractured rocks'pa

One-dimensional advection-dispersion models predict that characteristic δ¹⁸O vs. distance and δ¹⁸O vs. δ¹³C profiles should be produced during isothermal metamorphic fluid flow under equilibrium conditions. However, the patterns of isotopic resetting in rocks that have experienced fluid flow are often different from the predictions. Two-dimensional advection-dispersion simulations in systems with simple geometries suggest that such differences may be as a result of fluid channelling and need not indicate disequilibrium, high dispersivities, or polythermal flow. The patterns of isotopic resetting are a function of: (1) the permeability contrast between more permeable layers ('channels') and less permeable layers ('matrix'); (2) the width and spacing of the channels; (3) the width and spacing of discrete fractures; and (4) the orientation of the pressure gradient with respect to layering. In fractured systems, the efficiency of isotopic transport depends on the fracture aperture and the permeability of the surrounding rock. Resetting initially occurs along and immediately adjacent to the fractures, but with time isotopic resetting because of flow through the rock as a whole increases in importance. Application of the one-dimensional advection-dispersion equations to metamorphic fluid flow systems may yield incorrect estimates of fluid fluxes, intrinsic permeabilities, dispersivities, and permeability contrasts unless fluid flow occurred through zones of high permeability that were separated by relatively impermeable layers.     

Modeling of subduction components in the Genesis of the Meso-Cenozoic igneous rocks from the South Shetland Arc, Antarctica

Isotope data and trace elements concentrations are presented for volcanic and plutonic rocks from the Livingston, Greenwich, Robert, King George and Ardley islands (South Shetland arc, Antarctica). These islands were formed during subduction of the Phoenix Plate under the Antarctica Plate from Cretaceous to Tertiary. Isotopically (⁸⁷Sr/⁸⁶Sr)_o ratios vary from 0.7033 to 0.7046 and (¹⁴³Nd/¹⁴⁴Nd)_o ratios from 0.5127 to 0.5129. εNd values vary from +2.71 to +7.30 that indicate asthenospheric mantle source for the analysed samples. ²⁰⁸Pb/²⁰⁴Pb ratios vary from 38.12 to 38.70, ²⁰⁷Pb/²⁰⁴Pb ratios are between 15.49 and 15.68, and ²⁰⁶Pb/²⁰⁴Pb from 18.28 to 18.81. The South Shetland rocks are thought to be derived from a depleted MORB mantle source (DMM) modified by mixtures of two enriched mantle components such as slab-derived melts and/or fluids and small fractions of oceanic sediment (EM I and EM II). The isotopic compositions of the subduction component can be explained by mixing between at least 4 wt.% of sediment and 96 wt.% of melts and/or fluids derived from altered MORB.     

滇西点苍山-哀牢山变质岩系变质时限研究

点苍山-哀牢山变质带沿红河-哀牢山走滑剪切带呈北西-南东向展布,其主体由下元古界苍山群和哀牢山群深变质岩系组成,是滇西最显著的带状变质带之一。点苍山-哀牢山变质带的变质时限和山脉隆升时限由于缺乏精确年代学数据制约,一直存在不同认识。本文选取点苍山花岗闪长质糜棱岩（DCS-1）,哀牢山墨江-元江段黑云母花岗闪长质片麻岩（SM07-1）和其侵位的同变形花岗岩脉（SM07-3）以及元江县城西北山前花岗质片麻岩（YJ）作为研究对象,并挑选出锆石颗粒（SM07-3）、黑云母（SM07-1-Bi,SM07-3-Bi）、白云母（SM07-1-Ms）、钾长石(DCS-1-Kf, SM07-3-Kf)和斜长石（YJ-Pl）以及基质（YJ-ma）进行精确年代学测试。花岗岩脉颗粒锆石U-Pb SHRIMP 加权平均年龄为30.8±0.3Ma（SM07-3, MSWD=3.27）;其它单矿物激光⁴⁰Ar/³⁹Ar等时线年龄分别为13.1±1.5Ma (DCS-1-Kf, MSWD=2.9)、22.3±0.9Ma (SM07-1-Ms, MSWD=1.7)、21.9±0.7Ma (SM07-1-Bi, MSWD=1.3)、21.3±0.7Ma (SM07-3-Kf, MSWD=1.2)、22.7±0.8Ma (SM07-3-Bi, MSWD=2.4)、19.8±1.6Ma (YJ-ma, MSWD=19)和21.57±0.38Ma (YJ-Pl, MSWD=1.5)。结合区域地质背景、地质演化、野外观察和年代学资料,本文研究认为点苍山-哀牢山变质带的峰期变质变形时间为30Ma左右,此时山脉已开始隆升,在约20Ma和13Ma山脉分别经历一期构造热事件作用,揭示山脉经历快速隆升和冷却过程。     

The sulfur isotopic composition of sulfides from ores and host rocks of the Upper Kolyma region,Magadan Oblast

More than 200 analyses of the sulfur isotopic composition of sulfides from various terrigenous and intrusive host rocks, metasomatically altered wall rocks, and gold lodes of the Upper Kolyma region are presented. In accessory pyrite of the metaterrigenous rocks, δ³⁴S varies from ?23.1 to +5.7‰ δ³⁴S of pyrite and arsenopyrite from gold-quartz mineralization is within the range ?10.6 to ?0.4‰ and is close to the average δ³⁴S of pyrite from the metaterrigenous rocks (?4.4‰). In the intrusive rocks, δ³⁴S of pyrite varies from ?3.8 to +2.6‰ (+0.7‰, on average) and drastically differs from δ³⁴S of arsenopyrite from postmagmatic gold-rare-metal mineralization (?7.9 to ?2.7‰; ?5.2‰, on average). The comparison of the δ³⁴S of accessory sulfides from the host rocks with δ³⁴S of sulfides from the gold deposits suggests that sulfur mobilized from the terrigenous sequences participated in the hydrothermal process. The results obtained are consistent with the metamorphic model of the formation of gold-quartz deposits in the Upper Kolyma region.     

Tethyan and Indian subduction viewed from the Himalayan high- to ultrahigh-pressure metamorphic rocks

The Himalayan range is one of the best documented continent-collisional belts and provides a natural laboratory for studying subduction processes. High-pressure and ultrahigh-pressure rocks with origins in a variety of protoliths occur in various settings: accretionary wedge, oceanic subduction zone, subducted continental margin and continental collisional zone. Ages and locations of these high-pressure and ultrahigh-pressure rocks along the Himalayan belt allow us to evaluate the evolution of this major convergent zone.

(1) Cretaceous (80–100 Ma) blueschists and possibly amphibolites in the Indus Tsangpo Suture zone represent an accretionary wedge developed during the northward subduction of the Tethys Ocean beneath the Asian margin. Their exhumation occurred during the subduction of the Tethys prior to the collision between the Indian and Asian continents.

(2) Eclogitic rocks with unknown age are reported at one location in the Indus Tsangpo Suture zone, east of the Nanga Parbat syntaxis. They may represent subducted Tethyan oceanic lithosphere.

(3) Ultrahigh-pressure rocks on both sides of the western syntaxis (Kaghan and Tso Morari massifs) formed during the early stage of subduction/exhumation of the Indian northern margin at the time of the Paleocene–Eocene boundary.

(4) Granulitized eclogites in the Lesser Himalaya Sequence in southern Tibet formed during the Paleogene underthrusting of the Indian margin beneath southern Tibet, and were exhumed in the Miocene.

These metamorphic rocks provide important constraints on the geometry and evolution of the India–Asia convergent zone during the closure of the Tethys Ocean. The timing of the ultrahigh-pressure metamorphism in the Tso Morari massif indicates that the initial contact between the Indian and Asian continents likely occurred in the western syntaxis at 57 ± 1 Ma. West of the western syntaxis, the Higher Himalayan Crystallines were thinned. Rocks equivalent to the Lesser Himalayan Sequence are present north of the Main Central Thrust. Moreover, the pressure metamorphism in the Kaghan massif in the western part of the syntaxis took place later, 7 m.y. after the metamorphism in the eastern part, suggesting that the geometry of the initial contact between the Indian and Asian continents was not linear. The northern edge of the Indian continent in the western part was 300 to 350 km farther south than the area east of the Nanga Parbat syntaxis. Such “en baionnette” geometry is probably produced by north-trending transform faults that initially formed during the Late Paleozoic to Cretaceous Gondwana rifting. Farther east in the southern Tibet, the collision occurred before 50.6 ± 0.2 Ma. Finally, high-pressure to ultrahigh-pressure rocks in the western Himalaya formed and exhumed in steep subduction compared to what is now shown in tomographic images and seismologic data.     

Migmatites from Grenville, Quebec: metamorphic P-T-X conditions in transitional amphibolite/granulite-facies rocks

Migmatitic rocks near Grenville, Quebec, preserve features indicative of reactions at the onset of granulite facies metamorphism. In this area, metapelites and metacarbonates of the classic Grenville Series are spatially associated with granitic gneiss and metabasite, and flank a Paleozoic, Fe-rich syenite stock. Near this intrusion, the metapelite is diatexitic and nearly devoid of biotite, indicating the involvement of biotite during melting in the contact aureole of this intrusion. Outside of the contact aureole, metapelites and associated rocks contain biotite and are metatexitic. These features suggest two episodes of migmatization, the earlier predating the syenite, the later, synchronous with this intrusion.

Hornblende-rich metabasites near the syenite contain a two-part neosome consisting of coarse-grained leucosome veins and patches that are enclosed by fine-grained, pyroxene-rich envelopes. Migmatization is attributed to dehydration melting in the presence of CO₂-rich fluids possibly derived from nearby carbonate rocks prior to and/or during emplacement of the syenite. The occurrence of isolated mafic clots in the mesosome and rarity of melanosome seams on leucosomes suggest that some melts were mobile on an outcrop scale. These observations suggest that the leucosomes formed by the segregation of melts, which, coupled with CO₂ flux, dehydrated the wallrock along narrow margins, forming the pyroxene-rich neosomes. Back-reaction with residual fluids led to the local scapolitization of plagioclase and the concomitant formation of coronal garnet on pyroxene in neosomes. Thermobarometry of corona structures within the contact aureole generates diffusional Mg-Fe blocking temperatures ( 550 °C at 5.5 kbar). Extrapolated up-temperature, P-sensitive equilibria for the coronas yield similar pressures (8–9 kbar) as texturally-equilibrated assemblages for which high temperatures ( 750 ± 50 °C; X_CO2 = 0.90−0.95) were determined for rocks sampled inside and outside of the contact aureole. This suggests that the Grenville migmatites had not been substantially decompressed by the time that the syenite was emplaced.