扬子地块奥陶系碳酸盐岩重磁化机制探讨

碳酸盐岩是记录古地磁场信息的重要载体,然而,广泛存在的重磁化现象制约了碳酸盐岩在古地磁研究中的应用,其重磁化机制亟待解决.本文对采自贵州羊蹬地区的319块奥陶系碳酸盐岩定向样品作了详细的古地磁学和岩石磁学研究,其结果表明,94%样品(A类)记录了单一剩磁分量A,其解阻温度低于450℃;在地理坐标系下的平均方向为Dg/Ig=3.1°/48.1°(α95=2.9°),对应的古地磁极(87.0°N,2.8°E,A95=3.0°)与扬子地块古近纪-第四纪的古地磁极重合.6%样品(B类)记录了两个磁化分量,其高温分量(450℃~585℃)与A分量显著不同,但明显远离扬子块体早古生代古地磁极;低温分量(< 450℃)与A分量类似.说明羊蹬剖面奥陶系碳酸盐岩记录了两期重磁化.A分量和B低温分量的主要载磁矿物为磁黄铁矿(胶黄铁矿),B高温分量的主要载磁矿物为磁铁矿.这些磁性矿物都是成岩后的次生矿物.其中,解阻温度高于450℃的磁铁矿可能受晚燕山期造山运动影响生成;磁黄铁矿(胶黄铁矿)等矿物可能与印度板块与欧亚大陆碰撞引起的喜马拉雅造山运动所产生的流体作用有关,以后一期重磁化为主.新生代早期青藏高原隆升产生的流体在流经东南缘的碳酸盐岩等沉积岩层时,与原岩发生相互作用,使磁黄铁矿、胶黄铁矿、磁铁矿等磁性矿物生长并获得化学剩磁,造成了广泛重磁化.     

祁连山玉石沟橄榄岩显微构造特征及演化

橄榄岩作为上地幔的主要成分,影响着上地幔的流变学行为,其显微构造记录了岩石形成发展过程中所经受的构造事件.通过对祁连山玉石沟橄榄岩样品的镜下显微构造观察、岩石组构测定及TEM位错分析,探讨了与变形相关的温度、围压、含水性和应变速率等因素,总结该岩石的变形机制和变形历史,并推断其形成发展时大地构造环境.研究表明,玉石沟橄榄岩产自上地幔,其变形改造经历了上地幔演化和脆-韧性变形2个阶段.上地幔演化阶段橄榄石发育明显的A型原生组构,电子背散射衍射技术（EBSD）测定的橄榄石显微组构表明,该地区橄榄岩形成于高温（＞ 1200℃）、低应力（＜350 MPa）、低应变速率、低含水量的地幔浅部环境条件下;脆-韧性变形阶段叠加改造了原生A型组构,而发育明显的D型次生组构.橄榄石变形主控因素为动态恢复作用,普遍发育亚晶粒、消光带和扭折显微构造等相关组构,并与透射电镜下所观察到的位错排对应,同时还发育以微破裂为主的一套脆性变形组构,表现出两组共轭剪破裂和另一组张性破裂等现象,揭示出与韧性动态恢复现象一致的应力场方向指示.     

西藏雅鲁藏布江缝合带东波地幔橄榄岩中金刚石的发现及地质意义

本文报道了雅鲁藏布江缝合带西段的东波蛇绿岩地幔橄榄岩中发现与罗布莎和普兰岩体相似的金刚石和特殊地幔矿物群。东波地幔橄榄岩体以方辉橄榄岩为主,含少量二辉橄榄岩和纯橄岩,辉石岩和辉长岩呈脉状产在方辉橄榄岩中。岩石地球化学特征表明东波岩体形成于MOR环境后受到SSZ环境的改造。通过重砂分选实验,在693 kg的地幔橄榄岩大样中发现了金刚石和碳硅石等30余种特殊矿物群,包括金刚石、自然铬、自然金、自然铁、自然硅、自然铜等自然元素矿物类;碳硅石等碳化物;铬尖晶石、金红石、铬铁矿、刚玉、黑钨矿、铌钽铁矿、磁铁矿、赤铁矿、方铁矿、锡石等氧化物;铁铬镍合金、镍铁合金、铜锌合金等合金互化物;辉钼矿、方铅矿、辉铋矿、黄铁矿、黄铜矿、毒砂和闪锌矿等硫化物;橄榄石、辉石、锆石、蓝晶石、白云母、蛇纹石、绿帘石等硅酸岩;萤石等氟化物。该矿物群与雅鲁藏布江缝合带的罗布莎和普兰两个岩体中发现的特殊矿物群非常类似,同时也为蛇绿岩型金刚石这一新类型提供了佐证。     

扬子克拉通东北缘岩石圈地幔的Re-Os同位素地球化学:大陆岩石圈地幔的形成和演化的制约

苏皖地区新生代碱性玄武岩中有丰富的地幔橄榄岩捕虏体 ,测定了 2 0多个样品的Re Os元素丰度和锇同位素组成 ,结果 :Re =0 .0 2 7× 10 - 9～ 0 .375×10 - 9,Os=0 .112×10 - 9～ 3.35× 10 - 9,1 87Os 1 88Os=0 .117～ 0 .134。由代理等时线法1 87Os 1 88Os Yb获得该区岩石圈地幔早期熔体亏损事件的年龄为 1.7Ga(中元古代 )。苏皖地区岩石圈地幔的古老性表明它是元古代后岩石圈拆沉 减薄作用的残余地幔部分。岩石圈地幔经过了亏损 富集多阶段演化。     

江苏东海芝麻房预先导孔（CCSD-PPl）橄榄岩及其反映的上地幔亏损和交代事件

芝麻房预先导孔橄榄岩岩石类型有二辉橄榄岩、方辉橄榄岩、单辉橄榄岩和纯橄榄岩，其中前3种多数含有石榴子石。这些岩石在垂向上显示成层性，没有某种方向的韵律变化，它们之间呈渐变过渡关系。对样品进行主量元素、微量元素、稀土元素和Sr、Nd、O同位素分析表明，随着样品MgO含量的增高，Al2O3、CaO逐渐降低，呈良好的相关关系，并且大致上从石榴橄榄岩类到不含石榴子石的橄榄岩类主量元素的亏损程度增高，两者一般均比原始地幔主量元素亏损。稀土元素配分型式表现为右倾的轻稀土富集型，在微量元素蛛网图上，也表现为强不相容元素和微量元素到适度不相容元素的总体右倾型，与原始地幔相比，均富集强不相容元素。富集程度的不同与主量元素的亏损无对应关系，说明主量元素和微量元素各自的特点不是同一种事件造成的，而是先前地幔部分熔融作用之后又发生了富含不相容元素流体的交代作用。Sr、Nd同位素具有富集特点，变化范围较大，而且主量元素较亏损的岩石更富集Sr同位素，显示了交代富集的特点。稀土元素(Ce／Yb)x比值和εNd之间的负相关关系和Rb丰度与Sr同位素之间的正相关关系表明，富集Sr、Nd同位素的流体和富集不相容微量元素的流体均来自地幔。     

西藏罗布莎地幔橄榄岩变形显微构造特征及其地质意义

地幔橄榄岩是罗布莎蛇绿岩的主要组成成分之一,通过显微构造特征可对其变形特征进行分析,确定流变学参数,探讨地幔橄榄岩的变形历史。以蛇纹石化程度较低的二辉橄榄岩和方辉橄榄岩为研究对象,橄榄石位错特征研究显示,本区橄榄石主要发育了低温常见的直线型自由位错,局部可见位错弓弯、位错环、位错壁等高温位错,反映罗布莎地幔橄榄岩变形以低温塑性流变为主,局部经历了高温塑性流变,主导变形机制为位错蠕变。橄榄石自由位错统计结果表明,二辉橄榄岩中的橄榄石自由位错密度为4.422×107/cm2,方辉橄榄岩中的橄榄石为9.137×107/cm2,变形过程中所受差异应力分别为65MPa和93MPa。橄榄石和斜方辉石显微组构测量采用了电子背散射衍射技术(EBSD),分析结果表明,橄榄石均发育A型组构,为浅部地幔常见的组构类型,该结果与金刚石、柯石英等超高压矿物所指示的形成深度不一致。     

Mineralogy,geochemistry, and geotectonic significance of the Neoproterozoic ophiolite of Wadi Arais area,south Eastern Desert,Egypt

ABSTRACT

The dismembered ophiolites in Wadi Arais area of the south Eastern Desert of Egypt are one of a series of Neoproterozoic ophiolites found within the Arabian–Nubian Shield (ANS). We present new major, trace, and rare earth element analyses and mineral composition data from samples of the Wadi Arais ophiolitic rocks with the goal of constraining their geotectonic setting. The suite includes serpentinized ultramafics (mantle section) and greenschist facies metagabbros (crustal section). The major and trace element characteristics of the metagabbro unit show a tholeiitic to calc-alkaline affinity. The serpentinized ultramafics display a bastite, or less commonly mesh, texture of serpentine minerals reflecting harzburgite and dunite protoliths, and unaltered relics of olivine, orthopyroxene, clinopyroxene, and chrome spinel can be found. Bulk-rock chemistry confirms harzburgite as the main protolith. The high Mg# (91.93–93.15) and low Al₂O₃/SiO₂ ratios (0.01–0.02) of the serpentinized peridotite, together with the high Cr# (>0.6) of their Cr-spinels and the high NiO contents (0.39–0.49 wt.%) of their olivines, are consistent with residual mantle rocks that experienced high degrees of partial melt extraction. The high Cr# and low TiO₂ contents (0.02–0.34 wt.%) of the Cr-spinels are most consistent with modern highly refractory fore-arc peridtotites and suggest that these rocks probably developed in a supra-subduction zone environment.     

Geochemistry of arc-related mantle peridotites and gabbros from the Chaldoran ophiolite,NW Iran

ABSTRACT

The Neo-Tethys-related Chaldoran ophiolite peridotites in NW Iran are remnants of mantle lithosphere, exhumed tectonically during the Late Cretaceous. Harzburgite is the predominant peridotite type, associated with oceanic lower crust cumulate gabbros occasionally. The ophiolite rocks are unconformably overlain by Late Cretaceous-Paleocene sediments. New whole-rock geochemistry of the variably serpentinized harzburgites shows a depleted nature, exemplified by low Al₂O₃, CaO, TiO₂, V and Y and high Ni, Cr and Mg and also low rare earth element (REE) contents. The harzburgites present LREE enrichment. Positive correlations between some LREEs and high field strength elements (HFSE) suggest enrichment of LREEs by melt re-fertilization processes. Cr-spinels have Cr number of [Cr# = Cr/(Cr + Al) = 0.53–0.67], showing medium to high degree of partial melting (F = ~17-20%). Both whole-rock and mineral chemistry data show a supra-subduction zone setting and progressive depletion along with increase in spinel Cr# (MOR to fore arc). The cumulate gabbros have high MgO and SiO₂, low TiO₂ and Ti/V < 10 and also low chondrite normalized Dy (<8.5). The gabbro samples show enriched LREEs and LILEs and depleted HREEs and HFSEs with respect to MORBs.

Subduction initiation (SI) model in a fore-arc/proto-fore-arc environment is suggested for the upper mantle evolution of the Chaldoran ophiolite. The rocks have experienced depletion in a second melting process at the later stages of SI and compositions were probably modified by extraction of island arc tholeiitic (IAT) and possibly boninitic (BON) melts. The chemostratigraphic progression for ‘subduction initiation rule (SIR)’ is likely traceable in Chaldoran mafic-ultramafic sequence, which corresponds to the most Neo-Tethyan ophiolites and is similar to MOR to supra-subduction zone (SSZ) evolution of most Iranian ‘Inner’ and ‘Outer Zagros’ ophiolitic peridotites.     

Fast exhumation of the ultrahigh-pressure Alpe Arami garnet peridotite (Central Alps, Switzerland): constraints from geospeedometry and thermal modelling

Previous studies suggest that the metamorphic evolution of the ultrahigh‐pressure garnet peridotite from Alpe Arami was characterized by rapid subduction to a depth of c. 180 km with partial chemical equilibration at c. 5.9 Gpa/1180 °C and an initial stage of near‐isothermal decompression followed by enhanced cooling. In this study, average cooling rates were constrained by diffusion modelling on retrograde Fe–Mg zonation profiles across garnet porphyroclasts. Considering the effects of temperature, pressure and garnet bulk composition on the Fe–Mg interdiffusion coefficient, cooling rates of 380–1600 °C Myr^?1 for the interval from 1180 to 800 °C were obtained. Similar or even higher average cooling rates resulted from thermal modelling, whereby the characteristics of the calculated temperature‐time path depend on the shape and size of the hot peridotite body and the boundary conditions of the cooling process. The very high cooling rates obtained from both geospeedometry and thermal modelling imply extremely fast exhumation rates of c. 15 mm yr^?1 or more. These results agree with the range of exhumation rates (16–50 mm yr^?1) deduced from geochronological results. It is suggested that the Alpe Arami peridotite passively returned towards the surface as part of a buoyant sliver, caused as a consequence of slab breakoff.     

A TEM study of the oriented orthopyroxene and forsterite inclusions in garnet from Otrøy garnet peridotite,WGR, Norway: new insights on crystallographic characteristics and growth energetics of exsolved pyroxene in relict majoritic garnet

Regularly oriented orthopyroxene (opx) and forsterite (fo) inclusions occur as opx + rutile (rt) or fo + rt inclusion domains in garnet (grt) from Otrøy peridotite. Electron diffraction characterization shows that forsterite inclusions do not have any specific crystallographic orientation relationships (COR) with the garnet host. In contrast, orthopyroxene inclusions have two sets of COR, that is, COR‐I: <111>_grt//<001>_opx and {110}_grt～//～{100}_opx (～13° off) and COR‐II: <111>_grt//<011>_opx and {110}_grt～//～{100}_opx (～14° off), in four garnet grains analysed. Both variants of orthopyroxene have a blade‐like habit with one pair of broad crystal faces parallel/sub‐parallel to {110}_grt plane and the long axis of the crystal, <001>_opx for COR‐I and <011>_opx for COR‐II, along <111>_grt direction. Whereas the lack of specific COR between forsterite and garnet, along with the presence of abundant infiltrating trails/veinlets decorated by fo + rt at garnet edges, provide compelling evidence for the formation of forsterite inclusions in garnet through the sequential cleaving–infiltrating–precipitating–healing process at low temperatures, the origin of the epitaxial orthopyroxene inclusions in garnet is not so obvious. In this connection, the reported COR, the crystal habit and the crystal growth energetics of the exsolved orthopyroxene in relict majoritic garnet were reviewed/clarified. The exsolved orthopyroxene in a relict majoritic garnet follows COR‐III: {112}_grt//{100}_opx and <111>_grt//<001>_opx. Based on the detailed trace analysis on published SEM images, these exsolved orthopyroxene inclusions are shown to have the crystal habit with one pair of broad crystal faces parallel to {112}_grt//{100}_opx and the long crystal axis along <111>_grt//<001>_opx. Such a crystal habit can be rationalized by the differences in oxygen sub‐lattices of both structures and represents the energetically favoured crystal shape of orthopyroxene inclusions in garnet formed by solid‐state exsolution mechanism. Considering the very different COR, crystal habit, as well as crystal growth direction, the orthopyroxene inclusions in garnet of the present sample most likely had been formed by mechanism(s) other than solid‐state exsolution, regardless of their regularly oriented appearance in garnet and the COR specification between orthopyroxene and garnet. In fact, the crystallographic characteristics of orthopyroxene and the similar chemical compositions of garnet at opx + rt inclusion domains, fo + rt inclusion domains/trails and garnet rim suggest that the orthopyroxene inclusions in the garnet are most likely formed by similar cleaving‐infiltration process as forsterite inclusions, though probably at an earlier stage of metamorphism. This work demonstrates that the oriented inclusions in host minerals, with or without specific COR, can arise from mechanism(s) other than solid‐state exsolution. Caution is thus needed in the interpretation of such COR, so that an erroneous identification of exhumation from UHP depths would not be made.