柴北缘超高压变质带沙柳河蛇绿岩型地幔橄榄岩及其意义

本文报道了柴北缘大陆型超高压变质带沙柳河地区发现的蛇绿岩型地幔橄榄岩,其原始矿物组合为橄榄石 斜方辉石 铬铁矿。方辉橄榄岩中识别出两个世代的橄榄石,第一世代橄榄石(OI~1)残晶发育扭折带,化学成分与现代大洋地幔橄榄岩的橄榄石一致,第二世代橄榄石(OI~2)Fo 值高达94～97,其内部含有细小的流体包裹体,是第一世代橄榄石蛇纹石化后再次变质的产物。斜方辉石残晶的成分具有高 Al 和 Ca 的特征,与大洋地幔橄榄岩中斜方辉石的成分一致。温压条件的估算反映该橄榄岩体属于典型的尖晶石相方辉橄榄岩。其围岩是由堆晶辉长岩变质的条带状蓝晶石榴辉岩,二者构成了大洋蛇绿岩套的下部层位,并且与区内具有 N-MORB 和 OIB 性质的榴辉岩共生。这些特征表明该方辉橄榄岩应代表洋壳下伏地幔橄榄岩,从而揭示大陆造山带从早期的大洋俯冲消亡到大陆俯冲碰撞的完整过程。     

西昆化地区新生代火岩中的深源包体

青藏高原的形成与演化是举世瞩目的现代地学前缘,岩石圈结构及其演变对于探讨高原隆升及其资料环境效应具有重要意义。多年来,对于青藏高原岩石圈结构的认识主要基于地球物理探测结果和地质研究,尚未发现深达地幔的物质。我们在西昆化地区康西瓦新生代火山岩中首次发现了以含金云母方辉橄榄岩为主的深源包体,其主要组成矿物为橄榄石和斜方辉石,含有少量单斜辉石、尖晶石和金云母。橄榄岩为主的深源包体,其主要组成矿物为橄榄     

内蒙古苏尼特左旗乌兰敖包基性-超基性岩的成因及其对含矿性的指示

乌兰敖包基性-超基性岩位于阿拉善北缘兴蒙造山带,由方辉橄榄岩、辉绿岩、辉长岩组成。地球化学分析表明:蛇纹石化橄榄岩为地幔橄榄岩,辉绿岩和辉长岩为拉斑玄武岩系列岩石,均具有与N-MORB相似的微量元素特征,但区别于N-MORB,3种岩石共同组成了蛇绿混杂岩。矿物学分析表明蛇纹石化橄榄岩中橄榄石为地幔橄榄岩中镁橄榄石(Fo=91.10~91.81),铬铁矿为铬尖晶石,具有高的Cr~#和Mg~#值分别为61.04~64.44、50.40~56.37)。单斜辉石出现在方辉橄榄岩、辉长岩及辉绿岩中,而斜方辉石只出现在方辉橄榄岩中,其中方辉橄榄岩中单斜辉石为顽透辉石,辉长岩中为普通辉石,而辉长岩中为次透辉石、贫钙普通辉石、普通辉石,斜方辉石均为斜顽辉石。辉长岩U-Pb年龄为344.5±1.5 Ma,表明该蛇绿混杂岩形成于早石炭世。地球化学及矿物学特征表明乌兰敖包蛇绿岩形成于俯冲早期的弧前环境中,属于SSZ型蛇绿岩。蛇绿混杂岩成因提供铬铁矿形成的有利条件,因此应围绕铬铁矿进行找矿工作。     

女山和盘石山橄榄岩包体中的水: 红外光谱研究

运用傅立叶变换红外光谱技术对来自安徽女山新生代碧玄岩中的6个和江苏盘石山新生代玄武岩中的3个名义上“干”橄榄岩包体中的矿物进行了观察。结果显示:单斜辉石和斜方辉石普遍含有微量的结构水,以OH^-的形式赋存;除1个女山包体外,其余的橄榄石均未探测到结构水;女山1个石榴石橄榄岩中的石榴石未能探测到结构水。单斜辉石中结构水含量>斜方辉石>>橄榄石(石榴石)。结合文献中的资料来看,岩石圈地幔中水的分布可能既具有大尺度不均一性,又具有小尺度不均一性,可能并不具有明显的垂向分带。     

软流圈熔体地幔交代作用过程中的铂族元素行为

南美洲南部的Pali Aike火山岩区第四纪碱性玄武岩中普遍发育含石榴石的斜方辉石岩包体。这种斜方辉石岩既作为独立的捕掳体存在又以细脉的形式穿插于橄榄岩捕掳体中。斜方辉石岩普遍含富Ti矿物,并且次生斜方辉石含橄榄石和单斜辉石残晶。与含石榴石橄榄岩中的斜方辉石相比,这种次生的斜方辉石以高TiO2、中等含量的Al2O3以及低Mg#为特征,表明它是在一种高度分异演化的富Ti熔体交代作用下通过消耗橄榄石和单斜辉石方式形成的。斜方辉石岩全岩的Co、Ni略低,Cr和铂族元素(PGE)含量与地幔橄榄岩相当,表明这些元素在交代作用过程中相对稳定,而交代介质带入的组分以碱质(K2O+Na2O)、Ti、Si、Al和S为主。交代的斜方辉石在现代活动岛弧和古克拉通的地幔橄榄岩捕掳体中多有报道。与这些环境中地幔样品的斜方辉石相比,PaliAike地区的次生斜方辉石含有相对高的Ti和Al,以及相对低的Mg。高Ti低Mg属性反映了交代介质可能来源于下伏的软流圈地幔并且经历了高度的分异和演化过程。Pali Aike地区所见到的这种交代斜方辉石和斜方辉石岩在其他被上涌软流圈影响的陆下岩石圈地幔中可能普遍存在。这些研究对了解中国华北-东北中生代以来的岩石圈地幔减薄机制有着重要的借鉴意义。     

蛇纹石化方辉橄榄岩弹性波速实验研究及其在地幔楔中的应用

地幔楔是俯冲带系统的重要组成单元,在地球内部物质循环、壳幔相互作用过程中起着承上启下的关键作用。俯冲板片脱水可以引起上覆地幔楔中橄榄岩类的蛇纹石化,而蛇纹石的波速显著低于地幔橄榄岩,所以不同蛇纹石化程度的地幔楔表现出不同的低速特征。本研究首先利用天然叶蛇纹石热压合成纯的蛇纹岩样品,利用橄榄石和斜方辉石热压合成方辉橄榄岩样品,然后在高压下分别测量合成的方辉橄榄岩和蛇纹岩样品的纵波速度(V_P)和横波速度(V_S),结合Voigt-Reuss-Hill岩石物理模型计算得到不同蛇纹石含量的方辉橄榄岩的波速,最后结合地震波资料,估算出不同俯冲带地幔楔的蛇纹石化程度。研究表明,在地幔楔蛇纹石化程度和含水量的估算中,必须考虑斜方辉石蛇纹石化的影响。相比前人研究,方辉橄榄岩的蛇纹石化可能更接近于实际情况。     

吉林双辽地区橄榄岩包体中熔体-岩石作用特征及其对地幔交代作用的启示

吉林双辽地区古近纪玄武岩中一方辉橄榄岩包体记录了上地幔交代作用的信息。原生斜方辉石被交代成因的单斜辉石和橄榄石所围绕,或形成反应边结构,或斜方辉石残留在次生单斜辉石中。这些反应结构仅出现在尖晶石的周围。电子探针分析表明次生单斜辉石具有高Mg#、Cr#和CaO/Al2O3比值,次生橄榄石高Mg#、CaO和Cr2O3,被交代的尖晶石边部高Cr#、CaO。由于交代作用并未影响橄榄岩体系的Mg#,而且熔体-岩石反应结构指示Opx(斜方辉石) Sp(尖晶石) 熔体(Ⅰ)→Cpx(单斜辉石) Ol(橄榄石) 熔体(Ⅱ),结合实验以及文献资料,认为双辽地区的岩石圈地幔受到了硅酸盐熔体的交代。这种交代导致橄榄岩中斜方辉石逐渐减少,单斜辉石和橄榄石逐渐增加,从而使方辉橄榄岩渐变成易剥橄榄岩。这种交代现象可能发生在软流圈-岩石圈接触带上的熔-岩反应区,暗示了在古近纪双辽地区岩石圈减薄和软流圈上涌导致的软流圈-岩石圈的相互作用仍在继续。     

揭示地质现象的本质与核心

青藏高原的形成与演化是举世瞩目的现代地学前缘 ,岩石圈结构及其演变对于探讨高原隆升及其资源环境效应具有重要意义。多年来 ,对于青藏高原岩石圈结构的认识主要基于地球物理探测结果和地质研究 ,尚未发现深达地幔的物质。我们在西昆仑地区康西瓦新生代火山岩中首次发现了以含金云母方辉橄榄岩为主的深源包体 ,其主要组成矿物为橄榄石和斜方辉石 ,含有少量单斜辉石、尖晶石和金云母。橄榄岩具有平衡粒状变晶结构 ,部分橄榄石颗粒仍保留有扭折带。电子探针分析结果表明 ,尖晶石的x(Cr) /x(Cr +Al)变化为 2 5%～ 8% ,属于尖晶石铬铁矿系列。根据CarrollWebb和Wood(1986 )提出的温压图解 ,橄榄岩形成压力大致为16 0 0MPa ,约相当于深度 56km。据此 ,认为康西瓦新生代玄武岩中产出的橄榄岩包体系岩浆活动过程中从岩石圈地幔携带上来的幔源物质 ,对于探讨青藏高原北部的岩石圈结构及其演化具有重要意义。     

河北阳原新生代玄武岩中橄榄岩捕虏体的含水量研究

为约束华北克拉通岩石圈的流变机制,使用傅立叶变换显微红外光谱仪（FTIR）测量了阳原玄武岩中尖晶石橄榄岩捕虏体的矿物含水量。FTIR光谱结果表明阳原橄榄岩捕虏体的橄榄石、斜方辉石和单斜辉石都有特征的OH吸收峰。橄榄石含有微量的水（4×10-6~9×10-6 H2O）,斜方辉石含水量为（105~201）×10-6,单斜辉石含水量为（260~440）×10-6,计算得出的全岩含水量为（49~75）×10-6。值得注意的是,富流体交代以及后期蚀变作用使得含角闪石的方辉橄榄岩样品中单斜辉石的含水量显著增加。阳原橄榄岩中单斜辉石与斜方辉石的含水量存在明显的正相关关系,水在单斜辉石和斜方辉石中的分配系数D cpx/opxOH =2.4±0.9,与全球橄榄岩样品的平均值基本一致（D cpx/opx OH = 2.2±0.1）。与汉诺坝的橄榄岩捕虏体相比,阳原捕虏体中橄榄石和辉石的结构水含量都明显较高,这可能与阳原橄榄岩经历的上地幔交代作用有关。统计表明全球克拉通玄武岩携带的尖晶石橄榄岩捕虏体中橄榄石的含水量普遍较低（0~10×10-6）,而斜方辉石和单斜辉石的含水量则存在明显的不均一性。金伯利岩携带的石榴石橄榄岩中橄榄石、斜方辉石和单斜辉石的含水量都明显高于玄武岩携带的尖晶石橄榄岩中相应矿物的含水量,这可能与金伯利岩来源深、富流体、上升快的性质相关。     

我国东部某些地幔岩中圆形矿物包裹体及地幔岩退火时间的探讨

我国东部沿海地区新生代碱性玄武岩中,广泛分布尖晶石二辉橄榄岩等地幔岩包体,地幔岩的退火时间和退火温度是岩石圈演化的重要标志。研究表明,地幔橄榄岩是宿主岩石中的异源包体,为先已存在的固态的地幔物质。镜下观察表明,地幔橄榄岩的主要造岩矿物中常含有圆形矿物包裹体,如橄揽石中含有尖晶石和斜方辉石,斜方辉石中含有橄榄石和尖晶石包裹体等。矿物包裹体从原始的多边形转变为球粒状的形态变化是地幔岩在某种退火温     

吉林汪清和龙岗新生代岩石圈地幔的含水性和元素地球化学特征

首次报道了来自东北地区岩石圈地幔水含量的数据。通过对吉林龙岗和汪清新生代玄武岩中的橄榄岩包体矿物进行电子探针(EMP)和激光熔蚀等离子体质谱(LA-ICPMS)的分析,得到了矿物的主量元素和微量元素的数据,结果显示这些橄榄岩是原始地幔经历了不同程度部分熔融的残余,大部分样品的熔融程度可能<10%。橄榄岩样品在后期还经历了地幔交代作用,大部分样品受到硅酸岩熔体的交代,少部分样品受到碳酸岩熔体的交代。显微傅里叶变换红外光谱(FTIR)的分析结果显示,橄榄岩样品中的单斜辉石、斜方辉石均含有以结构羟基形式存在的水,而橄榄石中没有明显的羟基吸收峰。龙岗样品中单斜辉石的水含量为(48~464)×10^-6(H₂O, 质量分数),斜方辉石水含量为(28~104)×10^-6;汪清样品中单斜辉石的水含量为(34~403)×10^-6,斜方辉石的水含量为(13~89)×10^-6;所有样品全岩水含量为(8~92)×10^-6。样品的水含量可以代表龙岗和汪清地区岩石圈地幔的水含量信息,并且水含量变化范围较大,造成这种变化的原因可能是由于地幔源区初始水含量的不均一,以及部分熔融和地幔交代作用叠加的结果。     

Nature of the mantle roots beneath the North American craton: mantle xenolith evidence from Somerset Island kimberlites

The recently discovered Nikos kimberlite on Somerset Island, in the Canadian Arctic, hosts an unusually well preserved suite of mantle xenoliths dominated by garnet–peridotite (lherzolite, harzburgite, dunite) showing coarse and porphyroclastic textures, with minor garnet–pyroxenite. The whole rock and mineral data for 54 Nikos xenoliths indicate a highly refractory underlying mantle with high olivine forsterite contents (ave. Fo=92.3) and moderate to high olivine abundances (ave. 80 wt.%). These characteristics are similar to those reported for peridotites from the Archean Kaapvaal and Siberian cratons (ave. olivine Fo=92.5), but are clearly distinct from the trend defined by oceanic peridotites and mantle xenoliths in alkaline basalts and kimberlites from post-Archean continental terranes (ave. olivine Fo=91.0). The Nikos xenoliths yield pressures and temperatures of last equilibration between 20 and 55 kb and 650 and 1300°C, and a number of the peridotite nodules appear to have equilibrated in the diamond stability field. The pressure and temperature data define a conductive paleogeotherm corresponding to a surface heat flow of 44 mW/m². Paleogeotherms based on xenolith data from the central Slave province of the Canadian craton require a lower surface heat flow (40 mW/m²) indicating a cooler geothermal regime than that beneath the Canadian Arctic. A large number of kimberlite-hosted peridotites from the Kaapvaal craton in South Africa and parts of the Siberian craton are characterized by high orthopyroxene contents (ave. Kaapvaal 32 wt.%, Siberia 20 wt.%). The calculated modal mineral assemblages for the Nikos peridotites show moderate to low contents of orthopyroxene (ave. 12 wt.%), indicating that the orthopyroxene-rich mineralogy characteristic of the Kaapvaal and Siberian cratons is not a feature of the cratonic upper mantle beneath Somerset Island.     

Lithosphere formation in the central Slave Craton (Canada): plume subcretion or lithosphere accretion?

Major-element compositions of minerals in peridotite xenoliths from the Lac de Gras kimberlites provide constraints on the mode of lithosphere formation beneath the central Slave Craton, Canada. Magnesia contents of reconstructed whole rocks correlate positively with NiO and negatively with CaO contents, consistent with variable partial melt extraction. Alumina and Cr₂O₃ contents are broadly positively correlated, suggestive of melt depletion in the absence of a Cr–Al phase. Garnet modes are high at a given Al₂O₃ content (a proxy for melt depletion), falling about a 7 GPa melt depletion model. These observations, combined with high olivine Mg# and major-element relationships of FeO-poor peridotites (<7.5 wt%) indicative of melt loss at pressures >3 GPa (residual FeO content being a sensitive indicator of melt extraction pressure), and similar high pressures of last equilibration (∼4.2 to 5.8 GPa), provide multiple lines of evidence that the mantle beneath the central Slave Craton has originated as a residue from high-pressure melting, possibly during plume subcretion. Apparent low melt depletion pressures for high-FeO peridotites (>7.5 wt%) could suggest formation in an oceanic setting, followed by subduction to their depth of entrainment. However, these rocks, which are characterised by low SiO₂ contents (<43 wt%), are more likely to be the result of post-melting FeO-addition, leading to spuriously low estimates of melt extraction pressures. They may have reacted with a silica-undersaturated melt that dissolved orthopyroxene, or experienced olivine injection by crystallising melts. A secular FeO-enrichment of parts of the deep mantle lithosphere is supported by lower average Mg# in xenolithic olivine (91.7) compared to olivine inclusions in diamond (92.6).     

橄榄岩-熔体的相互作用:岩石圈地幔组成转变的重要方式

橄榄岩-熔体/岩浆的相互作用常被用来解释蛇绿岩套橄榄岩、造山带橄榄岩、超镁铁质侵入杂岩体、地幔橄榄岩捕虏体中某些具有不平衡结构和矿物组成的岩石的形成过程。橄榄岩-熔体的反应主要有两种方式,即消耗橄榄石(和单斜辉石)生成斜方辉石或消耗斜方辉石生成橄榄石(和单斜辉石)。反应的结果不仅造成矿物百分含量的变化,而且造成矿物组成的变化;后者更重要但未引起足够的重视。华北东部中生代玄武质岩石中具有环带状结构的橄榄石和辉石捕虏晶,特别是具有环带状结构的地幔橄榄岩捕虏体的发现,暗示这种橄榄岩-熔体的相互作用在华北东南部中生代岩石圈地幔中很可能普遍存在,为岩石圈地幔组成转变和快速富集的重要方式。这是全球首例由橄榄岩-熔体相互反应造成的岩石圈地幔大规模的组成变化。反应熔体来源途径主要有地壳来源和软流圈地幔来源。来源不同的熔体与橄榄岩的反应造成的组成变化完全不同。     

Composition and evolution of the lithospheric mantle beneath the interior of the South China Block: insights from trace elements and water contents of peridotite xenoliths

Major and trace elements and water contents were analyzed in 16 peridotite xenoliths embedded by the Cenozoic basalts in Pingnan (southeastern Guangxi Province), to constrain the chemical composition and evolution of the lithospheric mantle located in the central part of the South China Block (SCB). The peridotites are mainly moderately refractory harzburgites and lherzolites (Mg#-Ol?=?90.3–91.7) and minor fertile lherzolites (Mg#-Ol?=?88.9–89.9). Clinopyroxenes in the peridotites show LREE-depleted pattern, and commonly exhibit negative anomalies in Nb and Ti, suggesting the peridotites probably represent residues after 1–10% of partial melting without significant mantle metasomatism. Water contents range from 146 to 237 ppm wt. H₂O in clinopyroxene, and from 65 to 112 ppm wt. H₂O, in orthopyroxene but are below detection limit (2 ppm wt. H₂O) in olivine. Calculated bulk water contents, based on the mineral modes and partition coefficient, range from 14 to 83 ppm wt. H₂O (average 59 ppm wt. H₂O). There is a correlation between melting indices (such as Mg#-Ol, Yb_n in clinopyroxene) and water contents in clinopyroxene and orthopyroxene, but no correlation is observed between the whole-rock water contents and the redox state (Fe³⁺/∑Fe ratios in spinel), suggesting that water contents in the peridotites are mainly controlled by the degree of partial melting rather than by oxygen fugacity. The lithospheric mantle beneath the interior of the SCB may not be compositionally stratified; fertile and moderately refractory mantle coexist at the similar depths. Geochemical data and water contents of the studied peridotites are similar to the proposed MORB source and indicate that the ancient refractory lithospheric mantle was irregularly eroded or reacted by the upwelling asthenosphere, and eventually replaced by juvenile fertile accreted mantle through the cooling of the asthenosphere.     

The production of iron oxide during peridotite serpentinization: Influence of pyroxene

Serpentinization produces molecular hydrogen(H2)that can support communities of microorganisms in hydrothermal fields;H2 results from the oxidation of ferrous iron in olivine and pyroxene into ferric iron,and consequently iron oxide(magnetite or hematite)forms.However,the mechanisms that control H2 and iron oxide formation are poorly constrained.In this study,we performed serpentinization experiments at 311℃ and 3.0 kbar on olivine(with 5% pyroxene),orthopyroxene,and peridotite.The results show that serpentine and iron oxide formed when olivine and orthopyroxene individually reacted with a saline starting solution.Olivine-derived serpentine had a significantly lower FeO content(6.57±1.30 wt.%)than primary olivine(9.86 wt.%),whereas orthopyroxene-derived serpentine had a comparable FeO content(6.26±0.58 wt.%)to that of primary orthopyroxene(6.24 wt.%).In experiments on peridotite,olivine was replaced by serpentine and iron oxide.However,pyroxene transformed solely to serpentine.After 20 days,olivine-derived serpentine had a FeO content of 8.18±1.56 wt.%,which was significantly higher than that of serpentine produced in olivine-only experiments.By contrast,serpentine after orthopyroxene had a slightly higher FeO content(6.53±1.01 wt.%)than primary orthopyroxene.Clinopyroxene-derived serpentine contained a significantly higher FeO content than its parent mineral.After 120 days,the FeO content of olivine-derived serpentine decreased significantly(5.71±0.35 wt.%),whereas the FeO content of orthopyroxene-derived serpentine increased(6.85±0.63 wt.%)over the same period.This suggests that iron oxide preferentially formed after olivine serpentinization.Pyroxene in peridotite gained some Fe from olivine during the serpentinization process,which may have led to a decrease in iron oxide production.The correlation between FeO content and SiO_2 or AI_2 O_3 content in olivine-and orthopyroxene-derived serpentine indicates that aluminum and silica greatly control the production of iron oxide.Based on our results and data from natural serpentinites reported by other workers,we propose that aluminum may be more influential at the early stages of peridotite serpentinization when the production of iron oxide is very low,whereas silica may have a greater control on iron oxide production during the late stages instead.     

Fluorine and chlorine in mantle minerals and the halogen budget of the Earth’s mantle

The fluorine (F) and chlorine (Cl) contents of arc magmas have been used to track the composition of subducted components, and the F and Cl contents of MORB have been used to estimate the halogen content of depleted MORB mantle (DMM). Yet, the F and Cl budget of the Earth’s upper mantle and their distribution in peridotite minerals remain to be constrained. Here, we developed a method to measure low concentrations of halogens (≥0.4 µg/g F and ≥0.3 µg/g Cl) in minerals by secondary ion mass spectroscopy. We present a comprehensive study of F and Cl in co-existing natural olivine, orthopyroxene, clinopyroxene, and amphibole in seventeen samples from different tectonic settings. We support the hypothesis that F in olivine is controlled by melt polymerization, and that F in pyroxene is controlled by their Na and Al contents, with some effect of melt polymerization. We infer that Cl compatibility ranks as follows: amphibole > clinopyroxene > olivine ~ orthopyroxene, while F compatibility ranks as follows: amphibole > clinopyroxene > orthopyroxene ≥ olivine, depending on the tectonic context. In addition, we show that F, Cl, Be and B are correlated in pyroxenes and amphibole. F and Cl variations suggest that interaction with slab melts and fluids can significantly alter the halogen content of mantle minerals. In particular, F in oceanic peridotites is mostly hosted in pyroxenes, and proportionally increases in olivine in subduction-related peridotites. The mantle wedge is likely enriched in F compared to un-metasomatized mantle, while Cl is always low (<1 µg/g) in all tectonic settings studied here. The bulk anhydrous peridotite mantle contains 1.4–31 µg/g F and 0.14–0.38 µg/g Cl. The bulk F content of oceanic-like peridotites (2.1–9.4 µg/g) is lower than DMM estimates, consistent with F-rich eclogite in the source of MORB. Furthermore, the bulk Cl budget of all anhydrous peridotites studied here is lower than previous DMM estimates. Our results indicate that nearly all MORB may be somewhat contaminated by seawater-rich material and that the Cl content of DMM could be overestimated. With this study, we demonstrate that the halogen contents of natural peridotite minerals are a unique tool to understand the cycling of halogens, from ridge settings to subduction zones.     

Dunite Formation Processes in Highly Depleted Peridotite: Case Study of the Iwanaidake Peridotite, Hokkaido, Japan

Dunite formation processes in highly depleted peridotites arediscussed based upon a detailed study of the Iwanaidake peridotite,Hokkaido, Japan, which consists mainly of harzburgite with asmall amount of dunite. In the harzburgites, the Mg# [= 100x Mg/(Mg + Fe²⁺)] of olivine ranges from 91·5 to 92·5,and the Cr# [= 100 x Cr/(Cr + Al)] of spinel from 30 to 70;in the dunites, the Mg# of olivine ranges from 92·5 to94 and the Cr# of spinel from 60 to 85, respectively. The NiOwt % of olivine in harzburgites ranges from 0·38 to 0·44,and in dunites from 0·35 to 0·37. The Mg# andCr# are higher and NiO wt % is lower in the dunites than inthe harzburgites surrounding the dunites. The Mg# and Cr# exhibitnormal depletion trends expected from simple partial melting,whereas the NiO wt % shows an abnormal trend. On the basis ofmass balance calculations, dunites are considered to be derivedfrom the harzburgites by a process involving incongruent meltingof orthopyroxene (orthopyroxene olivine + Si-rich melt). Hydrousconditions were necessary to lower the solidus, and thus meltingof harzburgite was probably triggered by the introduction ofhydrous silicate melt. The dunite in this massif may have formedin the mantle wedge above a subduction zone. KEY WORDS: depleted peridotite; hydrous melt; incongruent melting; residual dunite; Iwanaidake peridotite