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1.
对流上地幔Os同位素组成的准确估算是运用Re-Os同位素体系探讨地幔演化的基础。前人研究主要是以地幔橄榄岩为研究对象,由于地幔橄榄岩Os同位素存在明显的不均一性,因而直接影响估算值的准确性。对流上地幔中包含的不同亏损程度的难熔组分在部分熔融过程中难以熔融,对形成的熔体相的Os同位素组成贡献很少或者没有。因此,与对流上地幔具有相同的Os同位素组成初始值的早期分离结晶岩石(如堆晶岩),结合堆晶岩中锆石的准确定年,可以用来估算对流上地幔Os同位素组成。本文根据这一方法测试了那曲地区弧后盆地堆晶岩的Os同位素组成和锆石U-Pb年龄,推测那曲地区新特提斯洋对流上地幔Os同位素组成为碳质球粒陨石型的。根据这一模型,对比了罗布莎和东巧铬铁矿岩、含矿围岩以及不含矿围岩的Os同位素特征,揭示出矿石及围岩均具有古老大陆岩石圈地幔信息,而不含矿围岩(泽当岩体)的Os同位素组成为碳质球粒陨石型的,无古老大陆岩石圈地幔信息。  相似文献   

2.
高山  刘勇胜 《地学前缘》2003,10(3):61-67
测定了辽宁复县奥陶纪金伯利岩和河北汉诺坝与山东栖霞第三纪碱性玄武岩中产出的地幔包体的Re Os同位素组成。金伯利岩中地幔包体的Re贫化Os同位素模式年龄 (TRD)为 2 .5~ 2 .8Ga ,从Re Os同位素定年角度证明了华北克拉通确实存在太古宙岩石圈地幔。对汉诺坝二辉橄榄岩包体获得了 (1.9± 0 .18)Ga的Re Os同位素等时线年龄 ,表明现今保存在那里的地幔主要是古元古代时形成的。汉诺坝地区出露有大量新太古代岩石 ,表明曾存在太古宙地幔。由于缺乏太古宙年龄 ,说明由汉诺坝所代表的克拉通中部曾存在的太古宙地幔在古元古代时已被减薄 ,并被 1.9Ga的新生岩石圈地幔置换。该事件与华北克拉通中部广泛的古元古代碰撞造山过程导致的麻粒岩相变质作用的时代相同 ,说明有关的岩石圈置换作用可能主要与拆沉作用有关。栖霞地幔包体具有与现代对流地幔相同的Os同位素组成 ,且Os同位素组成与Re/Os比值没有明显相关性 ,表明年龄很新。结合其它地质地球化学证据 ,说明克拉通东部的太古宙岩石圈地幔的置换作用主要发生在中生代 ,且可能与三叠纪华北和扬子陆块的陆陆碰撞造山导致的岩石圈地幔和下地壳的拆沉作用有关。本研究表明华北克拉通岩石圈地幔置换作用在时空上的分布是十分不均一的。 2 .5~ 2 .8Ga与 1.9Ga不仅?  相似文献   

3.
支霞臣  秦协 《地球科学》2006,31(1):23-30
Re-Os同位素体系为研究地幔的成分-结构-演化提供了新的地球化学示踪和定年的工具.上地幔Os同位素组成演化的球粒陨石模型是Re-Os体系用于地幔物质定年的基础, 尤其在采用Re亏损模式年龄和Os同位素代理等时线年龄时.综合了铁陨石和各类球粒陨石、地幔橄榄岩包体和蛇绿岩豆荚状铬铁矿的Re-Os同位素体系研究的近期成果, 为认识对流上地幔Os同位素组成的演化提供了制约.对河北遵化蛇绿岩豆荚状铬铁矿岩的研究, 获得新太古代(2.5 Ga)时形成豆荚状铬铁矿的对流上地幔的187Os/188Os=0.110 2, 与球粒陨石型模式的一致.文献中常用的球粒陨石模式的参数如下: 地球形成时(4.558 Ga)初始值187Os/186Os为0.095 31, 现代值分别采用碳质球粒陨石的187Os/186Os比值为0.127 0和原始上地幔(PUM)的187Os/186Os比值为0.129 6, PUM与普通球粒陨石和顽火球粒陨石的187Os/186Os比值接近.   相似文献   

4.
苏皖地区发育的新生代玄武岩中富含地幔橄榄岩捕虏体,测定了25个橄榄岩全岩的锇同位素组成。结果表明大部分样品呈亏损特征,187Os/188Os=0.119~0.129.Os同位素比值与主量成分之间有显著的相关性.采用187Os/188Os-Al2O3代用等时线方法,由截距得到初始值(187Os/188Os)0=0.109,在对流地幔的187Os/188Os比值演化线上获得模式年龄t=2.5(±0.1)Ga,为晚太古-早元古代。用样品组中最低的锇同位素组成,即187Os/188Os=0.119,计算Re亏损模式年龄,t=1.2Ga,为中元古代。表明苏皖地区新生代玄武岩中的地幔橄榄岩捕虏体具有古老的形成年龄,它们是经过显生宙减薄作用后的残余地幔的碎片。大陆岩石圈地幔的古老形成年龄与上覆地壳克拉通的古老稳定年龄相耦合。  相似文献   

5.
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。  相似文献   

6.
在Re-Os同位素体系应用于蛇绿岩研究之前,一直认为蛇绿岩的地幔橄榄岩是古大洋岩石圈地幔的残留.近年来,随着Re-Os同位素测试技术的提高和广泛运用,在现代大洋以及蛇绿岩中均发现有古老大陆岩石圈地幔(SCLM)的信息.  相似文献   

7.
金宝山铂钯矿是峨眉山大火成岩省具有典型意义的岩浆Ni-Cu-PGE矿床,成矿岩体岩矿石Sm-Nd、Re-Os同位素特征表明为地幔柱成因并受到岩石圈地幔和地壳混染作用的影响.∈Nda=+0.01~+0.89,显著高于大陆岩石圈地幔,而低于软流圈地幔,介于地幔柱与岩石圈地幔之间但明显靠近地幔柱的同位素组成.γOs=20~60,高于任何端员类型的地幔储集库,反映地壳混染作用.混合模型分析表明,成矿岩浆演化经历了10%左右的大陆岩石圈地幔熔体混合并受到下地壳5%~10%的混染.  相似文献   

8.
库地蛇绿岩属于西昆仑早古生代蛇绿岩带,主要由变质橄榄岩、堆晶橄榄岩、基性火山岩和石英岩等组成。库地蛇绿岩体具有较好的岩相分带,其中纯橄岩相与辉橄岩相中产出豆荚状铬铁矿。与其他岩相对比,铬铁矿具有最高的Cr2O3含量、最大的Mg#值和最小的Fe#值,表明铬铁矿形成于富Mg的环境,且经历了更高程度的部分熔融。利用铬铁矿(铬尖晶石)矿物的化学成分,得出铬尖晶石的结晶温度为1366~1404℃,平均1379℃;压力为2.98~3.03GPa,平均3.00GPa;地幔部分熔融程度F为17.33%~18.84%,平均18.28%。结合已有的研究成果,推测库地蛇绿岩的基底橄榄岩单元源区为石榴石二辉橄榄岩,形成于亏损的软流圈地幔,对应的大地构造位置为消减带之上岛弧环境。  相似文献   

9.
位于安徽省境内的女山新生代碱性玄武岩中含有大量而且类型丰富的地幔橄榄岩包体,主要类型有尖晶石相、石榴石相、尖晶石-石榴子石过渡相二辉橄榄岩以及少量的方辉橄榄岩,其中部分尖晶石二辉橄榄岩样品中出现富含挥发分的角闪石、金云母和磷灰石。本文选择该区的尖晶石二辉橄榄岩和方辉橄榄岩包体进行了较为详细的岩石学、矿物学、地球化学研究工作。结果显示,除2个方辉橄榄岩表现难熔特征外,其它25件尖晶石相二辉橄榄岩均具有饱满的主量元素组成。二辉橄榄岩样品的Sr-Nd-Hf同位素均表现为亏损地幔的性质,不同于古老克拉通型难熔、富集的岩石圈地幔。富含挥发份交代矿物的出现以及轻稀土元素不同程度的富集,表明女山岩石圈地幔经历了较为强烈的交代作用,然而Re-Os同位素及PGE分析结果表明交代作用并没有显著改变Os同位素组成。二辉橄榄岩样品均具有较高的Os同位素组成,结合其饱满的主量元素组成,亏损的同位素特征,表明女山地区岩石圈地幔整体为新生岩石圈地幔。但1个方辉橄榄岩样品给出了较低的Os同位素比值0.1184,其Re亏损年龄为1.5Ga,它可能来自于软流圈中残留的古老难熔地幔。  相似文献   

10.
对华北山东地区不同构造单元中生代白垩纪基性-中基性岩浆岩进行了系统的Re-Os同位素研究.侵入岩样品采自鲁西济南岩体、鲁中沂南岩体和胶东的观水岩墙群, 火山岩样品采自鲁西蒙阴、费县、方城青山群和鲁中安丘青山群.所有样品均以低Re(0.076×10-9~0.711×10-9)和Os(0.006×10-9~1.030×10-9)含量以及高放射成因Os同位素比值为特征, 其相应的初始187Os/188Os比值和γOs(t)值分别为0.131 6~0.529 1和4.30~319.00(安丘粗面安山岩分别高达1.463和1 060.000), 并具有较大变化范围(0.125~2.090 Ga)的Os同位素模式年龄.在Os-Nd和Os-Sr同位素关系图上, 这些样品分布于典型的岩石圈地幔与地壳端元组成之间, 显示壳-幔源岩浆混合特征.然而, 除1件观水岩体(MGS0610)和费县玄武岩之外, 各地质单元样品之间或所有的中生代岩浆岩作为整体, 样品的γOs(t)与(La/Ta)N和(Th/Nb)N比值间缺乏明显的相关关系, 说明样品的混源Os同位素并非来自岩浆作用过程中的地壳围岩混染.区内基性岩浆岩Os同位素模式年龄TMA明显小于古生代地幔橄榄岩包体的Re亏损模式年龄(TRD), 可能为地幔条件下源岩与再循环地壳物质发生交代作用后Re/Os比值升高所致.蒙阴高镁安山岩和沂南闪长岩在Yb-Re/Yb图解中大致位于中生代辉石岩包体与地壳端元之间, 也指示了下地壳拆沉后产生的熔体与地幔岩石可能发生了交代作用.蒙阴安山岩MMY-12(SiO2=56.4%)具有古老壳源特征的Os同位素模式年龄(2.090 Ga)、高Mg#(64.6)和高Os含量(0.089×10-9), 为这一解释提供了有力的佐证.   相似文献   

11.
Podiform chromite deposits occur in the mantle sequences of many ophiolites that were formed in supra-subduction zone (SSZ) settings. We have measured the Re-Os isotopic compositions of the major chromite deposits and associated mantle peridotites of the Dongqiao Ophiolite in the Bangong-Nujiang suture, Tibet, to investigate the petrogenesis of these rocks and their genetic relationships.The 187Os/188Os ratios of the chromite separates define a narrow range from 0.12318 to 0.12354, less variable than those of the associated peridotites. Previously-reported 187Os/188Os ratios of the Os-rich alloys enclosed in the chromitites define two clusters: 0.12645 ± 0.00004 (2 s; n = 145) and 0.12003 to 0.12194. The ultra-depleted dunites have much lower 187Os/188Os (0.11754, 0.11815), and the harzburgites show a wider range from 0.12107 to 0.12612. The average isotopic composition of the chromitites (187Os/188Os: 0.12337 ± 0.00001) is low compared with the carbonaceous chondrite value (187Os/188Os: 0.1260 ± 0.0013) and lower than the average value measured for podiform chromitites worldwide (0.12809 ± 0.00085). In contrast, the basalts have higher 187Os/188Os, ranging from 0.20414 to 0.38067, while the plagioclase-bearing harzburgite and cumulates show intermediate values of 187Os/188Os (0.12979 ~ 0.14206). Correspondingly, the basalts have the highest 187Re/188Os ratios, up to 45.4 ± 3.2, and the chromites have the lowest 187Re/188Os ratios, down to 0.00113 ± 0.00008. We suggest that melts/fluids, derived from the subducting slab, triggered partial melting in the overlying mantle wedge and added significant amounts of radiogenic Os to the peridotites. Mass-balance calculations indicate that a melt/mantle ratio of approximately 15:1 (melt: 187Re/188Os: 45.4, 187Os/188Os: 0.34484; mantle peridotite: 187Re/188Os: 0.0029, 187Os/188Os: 0.11754) is necessary to increase the Os isotopic composition of the chromitite deposits to its observed average value. This value implies a surprisingly low average melt/mantle ratio during the formation of the chromitite deposits. The percolating melts probably were of variable isotopic composition. However, in the chromitite pods the Os from many melts was pooled and homogenized, which is why the chromitite deposits show such a small variation in their Os isotopic composition. The results of this study suggest that the 187Os/188Os ratios of chromitites may not be representative of the DMM, but only reflect an upper limit. Importantly, the Os-isotope compositions of chromitites strongly suggest that such deposits can be formed by melt/mantle mixing processes.  相似文献   

12.
Re-Os同位素体系在蛇绿岩应用研究中的进展   总被引:2,自引:1,他引:2  
Re-Os不同于由亲石元素构成的同位素体系,在原始上地幔(PUN)部分熔融过程中,母体Re是中等不相容元素,优先进入熔体相,子体Os是强相容元素,富集在残留相中,是研究蛇绿岩的极好示踪剂。在蛇绿岩应用研究中已经取得了4个方面的进展:(1)明确了熔体相的Re/Os和^187Os/^188Os比值高,而残留相的低;(2)铬铁矿中铂族元素矿物(PGM)的Re亏损年龄(TRD)证实了蛇绿岩中复杂的超镁铁岩体是多阶段部分熔融的产物;(3)现代大洋橄榄岩和玄武岩的Re-Os同位素研究表明熔体相和残留相的^187Os/^188Os比值在高于亏损地幔值(DMM)的部分是一致的,而低于DMM的存在不一致性,为研究蛇绿岩中熔体相与残留相是否存在“耦合”关系提供了新的制约因素;(4)揭示了蛇绿岩地幔橄榄岩中含有古大陆岩石圈地幔,这是前所未知的。虽然取得了不少进展,但是由于Re-Os同位素体系用于蛇绿岩研究的时间较短,尚存在一些问题,如显生宙蛇绿岩地幔橄榄岩的定年问题,有待进一步深化研究。  相似文献   

13.
Ultramafic xenoliths entrained in the late Miocene alkali basalts and basanites from NW Turkey include refractory spinel-harzburgites and dunites accompanied by subordinate spinel-lherzolites. Whole-rock major and trace element characteristics indicate that the xenoliths are mostly the solid residues of varying degrees of partial melting (~4–~15%), but some have geochemical signatures reflecting the processes of melt/rock interaction. Mantle-normalized trace element patterns for the peridotites vary from LREE-depleted to strongly LREE-enriched, reflecting multistage mantle processes from simple melt extraction to metasomatic enrichment. Rhenium and platinum group element (PGE) abundances and 187Os/188Os systematics of peridotites were examined in order to identify the nature of the mantle source and the processes effective during variable stages of melt extraction within the sub-continental lithospheric mantle (SCLM). The peridotites are characterized by chondritic Os/Ir and Pt/Ir ratios and slightly supra-chondritic Pd/Ir and Rh/Ir ratios, representing a mantle region similar in composition to the primitive mantle (PM). Moderate enrichment in PPGE (Pd–Pt–Rh)/IPGE (Ir–Os–Ru) ratios with respect to the PM composition in the metasomatized samples, however, reflects compositional modification by sulphide addition during possible post-melting processes. The 187Os/188Os ratios of the peridotites range from 0.11801 to 0.12657. Highly unradiogenic Os isotope compositions (γOs at 10 Ma from –7.0 to –3.2) in the chemically undisturbed mantle residues are accompanied by depletion in Re/Os ratios, suggesting long-term differentiation of SCLM by continuous melt extraction. For the metasomatized peridotites, however, systematic enrichments in PPGE and Re abundances, and the observed positive covariance between 187Re/188Os and γOs can most likely be explained by interaction of solid residues with basaltic melts produced by melting of relatively more radiogenic components in the mantle. Significantly, the wide range of 187Os/188Os ratios characterizing the entire xenolith suite seems to be consistent with multistage evolution of SCLM and suggests that parts of the lithospheric mantle contain materials that have experienced ancient melt removal (~1.3 Ga) which created time-integrated depletion in Re/Os ratios; in contrast, some other parts display evidence indicative of recent perturbation in the Re–Os system by sulphide addition during interaction with metasomatizing melts.  相似文献   

14.
Chromitite pods in the Mayarí-Cristal ophiolitic massif (eastern Cuba) were formed in the Late Cretaceous when island arc tholeiites and MORB-like back-arc basin basalts reacted with residual mantle peridotites and generated chromite-rich bodies enclosed in dunite envelopes. Platinum-group minerals (PGM) in the podiform chromitites exhibit important Os-isotope heterogeneities at the kilometric, hand sample and thin section scales. 187Os/188Os calculated at the time of chromitite crystallization (~90 Ma) ranges between 0.1185 and 0.1295 (γOs = −7.1 to +1.6, relative to enstatite chondrite), and all but one PGM have subchondritic 187Os/188Os. Grains in a single hand sample have initial 187Os/188Os that spans from 0.1185 to 0.1274, and in one thin section it varies between 0.1185 and 0.1232 in two PGM included in chromite which are only several millimeters apart. As the Os budget of a single micrometric grain derives from a mantle region that was at least several m3 in size, the variable Os isotopic composition of PGM in the Mayarí-Cristal chromitites probably reflects the heterogeneity of their mantle sources on the 10–100 m scale. Our results show that this heterogeneity was not erased by pooling and mingling of individual melt batches during chromitite crystallization but was transferred to the ore deposits on mineral scale. The distribution of the Os model ages calculated for PGM shows four main peaks, at ~100, 500, 750 and 1,000 Ma. These variable Os model ages reflect the presence of different depleted domains in the oceanic (Pacific-related) upper mantle of the Greater Antilles paleo-subduction zone. The concordance between the age of crystallization of the Mayarí-Cristal chromitites and the most recent peak of the Os model age distribution in PGM supports that Os in several grains was derived from fertile domains of the upper mantle, whose bulk Os isotopic composition is best approximated by that of enstatite chondrites; on the other hand, most PGM are crystallized by melts that tapped highly refractory mantle sources.  相似文献   

15.
Initial 187Os/188Os isotopic compositions for geochronologically and geologically well -constrained 3.8-Ga spinel peridotites from the Itsaq Gneiss Complex of southern West Greenland and chromite separates from 3.46-Ga komatiites from the Pilbara region of Western Australia have been determined to investigate the osmium isotopic evolution of the early terrestrial mantle. The measured compositions of 187Os/188Os(0) = 0.10262 ± 2, from an olivine separate, and 0.10329 ± 3, for a spinel separate from ∼3.8-Ga peridotite G93/42, are the lowest yet reported from any terrestrial sample. The corrections for in situ decay over 3.8 Ga for these low Re/Os phases are minimal and change the isotopic compositions by only 0.5 and 2.2% for the spinel and the olivine, respectively, resulting in 187Os/188Os(3.8 Ga) = 0.1021 ± 0.0002 and 0.1009 ± 0.0002, respectively. These data extend direct measurement of Os isotopic compositions to much earlier periods of Earth history than previously documented and provide the best constraints on the Os isotopic composition of the early Archean terrestrial mantle. Analyses of Pilbara chromites yield 3.46-Ga mantle compositions of 0.1042 ± 0.0002 and 0.1051 ± 0.0002.These new data, combined with published initial Os isotopic compositions from late Archean and early Proterozoic samples, are compatible with the mantle, or at least portions of it, evolving from a solar system initially defined by meteorites to a modern composition of 187Os/188Os(0) = 0.1296 ± 0.0008 as previously suggested from peridotite xenolith data ( Meisel et al., 2001); the associated 187Re/188Os(0) = 0.435 ± 0.005. Thus, chondritic 187Os/188Os compositions were a feature of the upper mantle for at least 3.8 billion years, requiring chondritic Re/Os ratios to have been a characteristic of the very early terrestrial mantle. In contrast, nonchondritic initial compositions of some Archean komatiites demonstrate that Os isotopic heterogeneity is an ancient feature of plume materials, reflecting the development of variable Re/Os mantle sources early in Earth history.The lower average 187Os/188Os = 0.1247 for abyssal peridotites (Snow and Reisberg, 1995) indicate that not all regions of the modern mantle have evolved with the same Re/Os ratio. The relative sizes of the various reservoirs are unknown, although mass balance considerations can provide some general constraints. For example, if the unradiogenic 187Os/188Os modern abyssal peridotite compositions reflect the prevalent upper mantle composition, then the complementary high Re/Os basaltic reservoir must represent 20 to 40% by mass of the upper mantle (taken here as 50% of the entire mantle), depending on the mean storage age. The difficulties associated with efficient long-term storage of such large volumes of subducted basalt suggest that the majority of the upper mantle is not significantly Re-depleted. Rather, abyssal peridotites sample anomalous mantle regions.The existence of 3.8-Ga mantle peridotites with chondritic 187Os/188Os compositions and with Os concentrations similar to the mean abundances measured in modern peridotites places an upper limit on the timing of a late accretionary veneer. These observations require that any highly siderophile element -rich component must have been added to the Earth and transported into and grossly homogenized within the mantle by 3.8 Ga. Either large-scale mixing of impact materials occurred on very short (0-100 myr) timescales or (the interpretation preferred here) the late veneer of highly siderophile elements is unrelated to the lunar terminal cataclysm estimated to have occurred at ∼3.8 to 3.9 Ga.  相似文献   

16.
本文对马关地区新生代碱性玄武岩中的地幔包体进行了系统的岩石学和地球化学研究,并首次进行了包体的Re-Os同位素测试。马关地区的橄榄岩包体主量成分上表现为饱满肥沃的特征;具有不同程度的轻稀土亏损特征,亏损Nb、Ti和Zr等高场强元素(HFSE)以及Ba等大离子亲石元素(LILE);橄榄岩包体的Nd同位素特征表明橄榄岩包体代表的是不均一的亏损地幔。5个橄榄岩全岩样品的Re-Os同位素分析结果表明,样品的Os含量总体较高(3.29×10-9~3.78×10-9),接近于造山带橄榄岩体的Os含量,Re含量变化范围较大(0.24×10-9~0.54×10-9),与Re的迁移能力较强有关。样品的187Os/188Os值在0.12295~0.12530之间变化,与187Re/188Os值和Al2O3含量之间都不存在较好的相关性,说明Re-Os体系不单纯由熔体抽取过程所控制。橄榄岩包体的Re亏损年龄tRD为254~604Ma,说明马关地区岩石圈地幔形成的时代应该在新元古代之前。马关地区岩石圈地幔并非是由软流圈上涌新增生的地幔,而是经历了如下演化历史:在新元古代之前,由原始地幔的部分熔融和熔体抽取作用形成了岩石圈地幔,之后经历了熔/流体交代和改造而发生了再富集作用,导致部分地幔橄榄岩逐渐从亏损难熔的特征向饱满肥沃转变,而未遭受熔/流体的改造的橄榄岩仍然保持了难熔亏损的特征。这种熔/流体交代和改造作用很可能与晚二叠纪峨眉山地幔柱的活动有关,而新生代以来印度-亚洲大陆碰撞导致地幔物质向东南方向的侧向流动,诱发软流圈上涌和马关地区的钾质岩浆的活动,也对马关地区岩石圈地幔的改造具有重要的影响,但由于喷发时间较新对Os同位素组成的影响还未显现出来。  相似文献   

17.
Tectonically emplaced peridotites from North Hebei Province, North China Craton, have retained an original harzburgite mineral assemblage of olivine(54%–58%) + orthopyroxene(40%–46%)+minor clinopyroxene(1%)+spinel. Samples with boninite-like chemical compositions also coexist with these peridotites. The spinels within the peridotites have high-Al end-members with Al_2O_3 content of 30 wt % –50 wt %, typical of mantle spinels. When compared with experimentally determined melt extraction trajectories, the harzburgites display a high degree of melting and enrichment of SiO_2, which is typical of cratonic mantle peridotites. The peridotites display variably enriched light rare earth elements(REEs), relatively depleted middle REEs and weakly fractionated heavy REEs, which suggest a melt extraction of over 25% in the spinel stability field. The occurrence of arc-and SSZ-type chromian spinels in the peridotites suggests that melt extraction and metasomatism occurred mostly in a subduction-related setting. This is also supported by the geochemical data of the coexisting boninite-like samples. The peridotites have ~(187)Os/~(188)Os ratios ranging from 0.113–0.122, which is typical of cratonic lithospheric mantle. These ~(187)Os/~(188)Os ratios yield model melt extraction ages(TRD) ranging from 981 Ma to 2054 Ma, which may represent the minimum estimation of the melt extraction age. The Al_2O_3-~(187)Os/~(188)Os-proxy isochron ages of 2.4 Ga–2.7 Ga suggest a mantle melt depletion age between the Late Achaean and Early Paleoproterozoic. Both the peridotites and boninite-like rocks are therefore interpreted as tectonically exhumed continental lithospheric mantle of the North China Craton, which has experienced mantle melt depletion and subduction-related mantle metasomatism during the Neoarchean-Paleoproterozoic.  相似文献   

18.
Studies of mantle xenolith and xenocryst studies have indicated that the subcontinental lithospheric mantle (SCLM) at the Karelian Craton margin (Fennoscandian Shield) is stratified into at least three distinct layers cited A, B, and C. The origin and age of this layering has, however, remained unconstrained. In order to address this question, we have determined Re–Os isotope composition and a comprehensive set of major and trace elements, from xenoliths representing all these three layers. These are the first Re–Os data from the SCLM of the vast East European Craton.

Xenoliths derived from the middle layer B (at  110–180 km depth), which is the main source of harzburgitic garnets and peridotitic diamonds in these kimberlites, are characterised by unradiogenic Os isotopic composition. 187Os/188Os shows a good correlation with indices of partial melting implying an age of  3.3. Ga for melt extraction. This age corresponds with the oldest formation ages of the overlying crust, suggesting that layer B represents the unmodified SCLM stabilised during the Paleoarchean. Underlying layer C (at 180–250 km depths) is the main source of Ti-rich pyropes of megacrystic composition but is lacking harzburgitic pyropes. The osmium isotopic composition of layer C xenoliths is more radiogenic compared to layer B, yielding only Proterozoic TRD ages. Layer C is interpreted to represent a melt metasomatised equivalent to layer B. This metasomatism most likely occurred at ca. 2.0 Ga when the present craton margin formed following continental break-up. Shallow layer A (at  60–110 km depth) has knife-sharp lower contact against layer B indicative of shear zone and episodic construction of SCLM. Layer A peridotites have “ultradepleted” arc mantle-type compositions, and have been metasomatised by radiogenic 187Os/188Os, presumably from slab-derived fluids. Since layer A is absent in the core of the craton, its origin can be related to Proterozoic processes at the craton margin. We interpret it to represent the lithosphere of a Proterozoic arc complex (subduction wedge mantle) that became underthrusted beneath the craton margin crust during continental collision  1.9 Ga ago.  相似文献   


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