地幔交代作用的微区微量元素证据——云南双沟蛇绿岩的质子探针研究

用质子探针技术对双沟地幔交代熔融物的微区微量元素进行了测定。研究表明,地幔橄榄岩中的残留矿物橄榄石和斜方辉石仅含Ni和Zn,而Ga、Ge、Sr、Rb、Zr、Y、As、Pb等微量元素主要集中在地幔部分熔融所产生的矿物(尤其是尖晶石和绿泥石)中。微区范围内微量元素的分布表明,尖晶石二辉橄榄岩地幔不均一性的尺度可达微米级,通常解释为尖晶石二辉橄榄岩在开放系统下地幔交代作用的结果。     

大洋橄榄岩岩石学和地球化学研究的前沿信息

大洋橄榄岩和洋中脊玄武岩是地幔熔融和熔体萃取过程中的互补产物 ,地幔熔融和熔体萃取过程形成洋壳 ,因此大洋橄榄岩和洋中脊玄武岩的研究可提供这一过程的独立信息。通过大洋橄榄岩和洋中脊玄武岩的岩石学与地球化学研究 ,特别是痕量元素在熔融和熔体演化过程中地球化学行为的研究 ,对定量描述洋中脊下地幔熔融动力学和认识化学地球动力学模式是十分重要的。目前 ,大洋橄榄岩的研究 ,已成为岩石学研究的前沿领域之一。     

西准噶尔达拉布特地幔橄榄岩弧前成因的矿物地球化学和氧同位素证据

达拉布特蛇绿岩位于中亚造山带西南缘,是古亚洲洋的扩张、俯冲、消减和闭合过程的产物,保留了洋盆形成及构造演化信息。前人对达拉布特蛇绿岩的形成大地构造背景始终未取得统一的认识。为探讨蛇绿岩所代表的构造演化过程,笔者以达拉布特蛇绿岩中的地幔橄榄岩为研究对象,通过详细的矿物地球化学及其氧同位素研究,对达拉布特地幔橄榄岩成因及构造背景提出新的制约。达拉布特方辉橄榄岩中橄榄石Ni/Co值为21~22,Ni/Mn值为3.0~7.8具有部分熔融残余的特征,此外,橄榄石中不相容元素相对于正常地幔橄榄石亏损,表明方辉橄榄岩为部分熔融的残余组分。方辉橄榄岩中尖晶石Cr# 为47~52、TiO2含量0.01%~0.04%,橄榄石Fo为90.34%~90.98%指示方辉橄榄岩经历>20%的部分熔融。方辉橄榄岩中橄榄石δ18 Oolivine值+5.1~+6.2‰、单斜辉石δ18Ocpx值+5.6~+6.9‰,其变化范围较大且整体高于正常地幔中橄榄石和单斜辉石的δ18 O值,矿物间氧同位素分馏系数Δ18OOpx—olivine平均-0.3‰,Δ18OOpx—cpx平均-0.7‰,显著区别于正常地幔中平衡的氧同位素分馏系数,具有明显的交代作用特征。结合方辉橄榄岩橄榄石中亏损的微量元素特征,认为方辉橄榄岩可能受到流体交代作用的影响,俯冲壳源物质脱水形成的高δ18O流体交代地幔橄榄岩导致了矿物与矿物间不平衡的氧同位素特征。通过尖晶石与单斜辉石成分判别,尖晶石与单斜辉石的主量元素具有介于弧前与深海地幔之间的过渡型特征,与俯冲初始阶段形成的地幔橄榄岩相似。综合矿物地球化学与氧同位素特征,笔者认为达拉布特地幔橄榄岩为形成于弧前初始俯冲环境。板块俯冲导致弧前扩张形成新洋壳,上涌的软流圈MORB like熔体与俯冲壳源物质熔融形成熔/流体与地幔橄榄岩相互作用,形成达拉布特地幔橄榄岩。     

西准噶尔达拉布特地幔橄榄岩弧前成因的矿物地球化学和氧同位素证据

达拉布特蛇绿岩位于中亚造山带西南缘,是古亚洲洋的扩张、俯冲、消减和闭合过程的产物,保留了洋盆形成及构造演化信息。前人对达拉布特蛇绿岩的形成大地构造背景始终未取得统一的认识。为探讨蛇绿岩所代表的构造演化过程,笔者以达拉布特蛇绿岩中的地幔橄榄岩为研究对象,通过详细的矿物地球化学及其氧同位素研究,对达拉布特地幔橄榄岩成因及构造背景提出新的制约。达拉布特方辉橄榄岩中橄榄石Ni/Co值为21~22,Ni/Mn值为3.0~7.8具有部分熔融残余的特征,此外,橄榄石中不相容元素相对于正常地幔橄榄石亏损,表明方辉橄榄岩为部分熔融的残余组分。方辉橄榄岩中尖晶石Cr# 为47~52、TiO2含量0.01%~0.04%,橄榄石Fo为90.34%~90.98%指示方辉橄榄岩经历>20%的部分熔融。方辉橄榄岩中橄榄石δ18 Oolivine值+5.1~+6.2‰、单斜辉石δ18Ocpx值+5.6~+6.9‰,其变化范围较大且整体高于正常地幔中橄榄石和单斜辉石的δ18 O值,矿物间氧同位素分馏系数Δ18OOpx—olivine平均-0.3‰,Δ18OOpx—cpx平均-0.7‰,显著区别于正常地幔中平衡的氧同位素分馏系数,具有明显的交代作用特征。结合方辉橄榄岩橄榄石中亏损的微量元素特征,认为方辉橄榄岩可能受到流体交代作用的影响,俯冲壳源物质脱水形成的高δ18O流体交代地幔橄榄岩导致了矿物与矿物间不平衡的氧同位素特征。通过尖晶石与单斜辉石成分判别,尖晶石与单斜辉石的主量元素具有介于弧前与深海地幔之间的过渡型特征,与俯冲初始阶段形成的地幔橄榄岩相似。综合矿物地球化学与氧同位素特征,笔者认为达拉布特地幔橄榄岩为形成于弧前初始俯冲环境。板块俯冲导致弧前扩张形成新洋壳,上涌的软流圈MORB like熔体与俯冲壳源物质熔融形成熔/流体与地幔橄榄岩相互作用,形成达拉布特地幔橄榄岩。     

西藏雅鲁藏布江缝合带泽当地幔橄榄岩的矿物化学和铂族元素特征

泽当蛇绿岩位于雅鲁藏布江缝合带东段,由地幔橄榄岩、辉长辉绿岩、火山岩等组成。地幔橄榄岩主要为方辉橄榄岩和二辉橄榄岩,有少量的铬铁矿化方辉橄榄岩和透镜状纯橄岩。地幔橄榄岩中橄榄石的Fo值为89.6~91.8,属镁橄榄石。斜方辉石为顽火辉石,En端员组分变化于87.8~90.3。单斜辉石En组分变化于44.1~50.0,主要为顽透辉石和透辉石。二辉橄榄岩与方辉橄榄岩铬尖晶石的Cr#为17.0~31.8,为富铝型尖晶石。泽当地幔橄榄岩PGE总量为16.67×10-9~32.59×10-9,与原始地幔相似。矿物化学特征显示泽当二辉橄榄岩属于深海型地幔橄榄岩,方辉橄榄岩属于弧前地幔橄榄岩。尖晶石Cr#、橄榄石Mg#的变化以及高Os含量(3.50×10-9~7.75×10-9)表明泽当地幔橄榄岩经历了部分熔融过程;正斜率的PGE配分模式以及较高的Pd/Ir值(1.09~3.94)表明泽当地幔橄榄岩受到了俯冲带环境下地幔交代作用的改造。泽当地幔橄榄岩矿物学特征与铂族元素地球化学特征显示其形成于MOR环境,后受到SSZ环境的改造。     

北秦岭松树沟橄榄岩与铬铁矿矿床的成因关系

松树沟橄榄岩体是秦岭造山带中规模最大的赋存铬铁矿床的超基性岩体。松树沟橄榄岩主要由细粒橄榄岩质糜棱岩和中粗粒橄榄岩组成。本文通过对松树沟橄榄岩的岩相学、主微量、稀土元素地球化学的系统研究,认为松树沟细粒方辉橄榄岩为洋脊扩张过程中地幔岩减压-近分离熔融产生的残留体,细粒纯橄岩主要由地幔橄榄岩熔融残留橄榄石、消耗辉石的减压熔融反应:aCpx+bOpx+cSpl=dOl+1Melt生成的橄榄石和少量的地幔方辉橄榄岩残留体组成,但均受到了后期渗滤熔体的再富集作用;中粗粒纯橄岩和方辉橄榄岩主要为上述反应产生的渗滤熔体被圈闭在迁移通道或减压扩容带内在热边界层(TBL)通过反应:MeltA=Ol+MeltB冷凝结晶而成,属堆晶橄榄岩。Pb-Sr-Nd同位素地球化学的证据显示,松树沟橄榄岩与基性岩具有共同的地幔源区,二者同为松树沟蛇绿岩的重要组成部分。通过矿床地质特征及铬铁矿电子探针测试研究,认为松树沟铬铁矿床是产于中粗粒堆晶纯橄岩中的层状铬铁矿床,形成于格林威尔期松树沟洋盆的扩张过程中,是中粗粒纯橄岩在热边界层(TBL)的冷凝结晶过程中岩浆分异作用的产物。     

内蒙古阿尔山——柴河地区陆下岩石圈地幔性质研究——第四纪碱性玄武岩中橄榄岩捕掳体中单斜辉石微量元素证据

阿尔山—柴河第四纪碱性玄武岩中地幔捕掳体为尖晶石相的二辉橄榄岩和方辉橄榄岩,方辉橄榄岩数量略多于二辉橄榄岩。采用激光剥蚀等离子体质谱(LA--ICP--MS)对研究区地幔橄榄岩中的单斜辉石和橄榄石等矿物进行了成分分析,结合橄榄岩包体的岩相学、岩石化学的特征,重点探讨了研究区所经历的部分熔融作用和地幔交代作用。结果显示,少数样品的熔融程度5%,大多数样品熔融程度范围为10%~20%,研究区陆下岩石圈地幔性质以难熔、亏损为主要特征。同时也经历了复杂的交代作用改造,交代介质为富挥发组分的硅酸盐熔/流体。与华北克拉通东北缘陆下岩石圈地幔比较,推测研究区遭受破坏和改造的程度较小,并保留有相当量的古老地幔残余。     

地幔富硅交代与大陆岩石圈的演化

富硅交代是弧下地幔中熔体岩石相互作用的主要表现形式 ,是造成古老克拉通陆下岩石圈地幔富硅的主要机制。在弧下地幔捕掳体中 ,橄榄岩被来自俯冲洋壳物质部分熔融生成的含水富硅熔体交代后 ,斜方辉石含量的增加使全岩富集SiO2 ,斜方辉石显示异常低的Al2 O3和Cr2 O3,微量元素上表现为强烈富集LILE ,强烈亏损Nb ,Ta和Ti。在古老克拉通地幔岩样品中 ,方辉橄榄岩具过剩的斜方辉石 ,橄榄石的Ni含量与斜方辉石的组成含量成正比 ,而和橄榄石的x(Mg) /x(Mg +Fe2 +)值没有正比关系 ,被解释为亏损的地幔橄榄岩和来自俯冲板片的富硅熔体相互作用的结果。熔体岩石相互作用最终导致了陆下岩石圈地幔富集SiO2 ,这种被含水富硅熔体改造后的地幔岩石的部分熔融可能是造成陆壳富硅富镁的主要原因。含水富硅熔体对岩石圈地幔的影响程度也可能是大陆岩石圈增生或裂解、增厚或减薄的关键因素之一。     

西藏班公湖—怒江缝合带中段蓬湖蛇绿岩中的洋脊型二辉橄榄岩

蓬湖蛇绿岩产于西藏藏北湖区的蓬湖西侧,属班公湖-怒江缝合带中段白拉拉弄-依拉山亚带。该蛇绿岩主要由地幔橄榄岩、堆晶岩和辉绿岩等组成。其中地幔橄榄岩由方辉橄榄岩和二辉橄榄岩组成。蓬湖二辉橄榄岩的橄榄石Fo值介于88.85～90.33之间、斜方辉石的Al2O3含量范围在4.26%～6.60%。与原始地幔相比,蓬湖二辉橄榄岩岩石有较高的MgO含量和较低的Al2O3、CaO和TiO2等易熔组分含量;稀土元素总量介于1.11×10-6～1.53×10-6之间,明显低于原始地幔值,配分模式为轻稀土轻微亏损。在原始地幔微量元素蛛网图中,蓬湖二辉橄榄岩显示Rb、Zr亏损,U、Ta、Sr强烈富集特征。蓬湖二辉橄榄岩的铂族元素总量介于22.9×10-9～27×10-9之间,PGEs球粒陨石标准化图解显示其为接近原始地幔的"平坦型"。以上特征与深海橄榄岩相似,指示它们可能形成于大洋中脊环境。定量模拟估算表明,蓬湖二辉橄榄岩可能来源于地幔中尖晶石相二辉橄榄岩源区,系经历了约5%～10%的部分熔融残余。蓬湖堆晶岩矿物结晶顺序为橄榄石-单斜辉石-斜长石,其中异剥橄榄岩中的单斜辉石Mg#值介于86.92～89.93之间、橄榄石Fo平均值为84.45,明显不同于MOR型蛇绿岩堆晶岩。蓬湖堆晶岩的矿物组成、岩浆结晶顺序和矿物成分均与俯冲带上SSZ型蛇绿岩形成的堆晶岩类似。以上结果表明,蓬湖二辉橄榄岩形成于大洋脊环境,为尖晶石二辉橄榄岩源区经历了不超过10%部分熔融的残余,后期由于洋内俯冲作用经历了岩石-熔体反应,形成了SSZ型堆晶岩和含较高Cr#值尖晶石的方辉橄榄岩。     

地幔中EM1端员成因的锂同位素制约

在四个地幔端员(DMM、HIMU、EM1、EM2)中,EM1的成因一直令人困惑。华北克拉通中部(太行山地区)地幔橄榄岩捕虏体的Li同位素组成特征为探讨这一问题提供了新的制约。橄榄岩捕虏体中主要组成矿物(橄榄石、斜方辉石和单斜辉石)的Li同位素组成特征表明,该区的岩石圈地幔中有再循环的、古老的洋壳物质。结合已有的地幔橄榄岩捕虏体的Sr-Nd同位素数据,可以推测再循环的古老蚀变洋壳对地幔EM1端员组分的产生有重要的作用。     

西藏西南部达巴-休古嘎布蛇绿岩带中地幔橄榄岩的成因

本文报道了西藏西南部达巴-休古嘎布蛇绿岩带中橄榄岩的矿物化学资料.橄榄岩中主要造岩矿物化学成分的分析研究表明,该区橄榄岩为残余地幔成因,但它们不是地幔简单熔化的残余物.尖晶石中Cr#及辉石中Ti的广泛变化表明它们具有复杂的熔融历史及地幔交代作用的印记,其形成过程可能经历了两种构造环境的转变.早期在MORB环境下形成低Cr#(尖晶石)橄榄岩;其后由于洋内俯冲作用,早先形成的低熔橄榄岩被消减到岛弧之下再度发生熔融形成高Cr#(尖晶石)橄榄岩.从而,在古大洋消失之后形成的碰撞带上同时保存了MORB型和SSZ型两类蛇绿岩.     

Chromian spinel as a petrogenetic indicator in abyssal and alpine-type peridotites and spatially associated lavas

The composition of chromian spinel in alpine-type peridotites has a large reciprocal range of Cr and Al, with increasing Cr# (Cr/(Cr+Al)) reflecting increasing degrees of partial melting in the mantle. Using spinel compositions, alpine-type peridotites can be divided into three groups. Type I peridotites and associated volcanic rocks contain spinels with Cr#<0.60; Type III peridotites and associated volcanics contain spinels with Cr#>0.60, and Type II peridotites and volcanics are a transitional group and contain spinels spanning the full range of spinel compositions in Type I and Type II peridotites. Spinels in abyssal peridotites lie entirely within the Type I spinel field, making ophiolites with Type I alpine-type peridotites the most likely candidates for sections of ocean lithosphere formed at a midocean ridge. The only modern analogs for Type III peridotites and associated volcanic rocks are found in arc-related volcanic and intrusive rocks, continental intrusive assemblages, and oceanic plateau basalts. We infer a sub-volcanic arc petrogenesis for most Type III alpine-type peridotites. Type II alpine-type peridotites apparently reflect composite origins, such as the formation of an island-arc on ocean crust, resulting in large variations in the degree and provenance of melting over relatively short distances. The essential difference between Type I and Type III peridotites appears to be the presence or absence of diopside in the residue at the end of melting.Based on an examination of co-existing rock and spinel compositions in lavas, it appears that spinel is a sensitive indicator of melt composition and pressure of crystallization. The close similarity of spinel composition fields in genetically related basalts, dunites and peridotites at localities in the oceans and in ophiolite complexes indicates that its composition reflects the degree of melting in the mantle source region. Accordingly, we infer from the restricted range of spinel compositions in abyssal basalts that the degree of mantle melting beneath mid-ocean ridges is generally limited to that found in Type I alpine-type peridotites. It is apparent, therefore, that the phase boundary OL-EN-DI-SP +meltOL-EN-SP+melt has limited the degree of melting of the mantle beneath mid-ocean ridges. This was clearly not the case for many alpine-type peridotites, implying very different melting conditions in the mantle, probably involving the presence of water.     

The Ronda high temperature peridotite: Geochemistry and petrogenesis

The Ronda peridotite in southern Spain is a large (~300 km²) exposure of upper mantle which provides direct information about mantle processes on a scale much larger than that provided by mantle xenoliths in basalt. Ronda peridotites range from harzburgite to lherzolite, and vary considerably in major element content, e.g., Al₂O₃ from 0.9 to 4.8%, and trace element abundances, e.g., Sr, Zr and La abundances vary by factors of 20 to 40. These compositional variations are systematic and correlate with (pyroxene + garnet)/olivine ratios and olivine compositions. The data are consistent with formation of residual peridotites by variable degrees of melting (~0 to 30%) of a compositionally homogeneous peridotite. None of the peridotites have geochemical characteristics of residues formed by extensive (?5%) fractional melting and the data can be explained by equilibrium (batch) melting, possibly with incomplete melt segregation in some samples. Based on compositional differences between Ronda peridotites, the segregated melts were picritic (12–22% MgO) with relative rare earth element abundances similar to mid-ocean ridge basalt (MORB). Prior to the melting event the Ronda peridotite body was a suitable source for MORB. The compositional characteristics of Ronda peridotites are consistent with diapiric rise of a fertile mantle peridotite with relatively small degrees of melting near the diapir-wall rock interface yielding residues of garnet iherzolite, and larger degrees of melting in the diapir interior yielding residues of garnet-free peridotite. Subsequently these residual rocks were recrystallized at sub-solidus conditions (Obata, 1980), and emplaced in the crust by thrusting (Lundeen, 1978).     

Origin and evolution of Suru Valley ophiolite peridotite slice along Indus suture zone,Ladakh Himalaya,India: Implications on melt-rock interaction in a subduction-zone environment

In this paper, we present whole-rock and mineral geochemistry of serpentinized peridotites from the Suru Valley ophiolite slice Ladakh Himalaya, in an attempt to put constraints on their petrogenesis and tectonic evolution in the context of Mesozoic Neo-Tethys Ocean. On the basis of petrographic study, Suru Valley serpentinized peridotites can be identified as serpentinized harzburgites. Relative to primitive mantle these rocks have depleted major and rare earth element (REE) geochemical characteristics comparable to ocean floor mantle rocks reflecting their mantle residual nature. However, higher abundance of highly incompatible large ion lithophile elements (e.g., Rb, Ba, Th, U, Pb and Sr), reflect metasomatism in a subduction zone environment. The presence of silicate assemblage includes Mg-rich olivine (Fo_90-92) and orthopyroxene (En_91-93 Fs_6.4-8.7) of supra-subduction zone affinity. Evaluation of mineral and whole-rock geochemistry suggests that the Suru Valley ophiolitic peridotites represent residues left after moderate degrees of partial melting thereby underwent metasomatism in a supra-subduction zone environment related to north dipping intra-oceanic island arc during Cretaceous in the context of Mesozoic Neo-Tethys ocean.     

Peridotites from the Mariana Trough: first look at the mantle beneath an active back-arc basin

Two dives of the DSV Shinkai 6500 in the Mariana Trough back-arc basin in the western Pacific sampled back-arc basin mantle exposures. Reports of peridotite exposures in back-arc basin setting are very limited and the lack of samples has hindered our understanding of this important aspect of lithospheric evolution. The Mariana Trough is a slow-spreading ridge, and ultramafic exposures with associated gabbro dykes or sills are located within a segment boundary. Petrological data suggest that the Mariana Trough peridotites are moderately depleted residues after partial melting of the upper mantle. Although some peridotite samples are affected by small-scale metasomatism, there is no evidence of pervasive post-melting metasomatism or melt-mantle interaction. Spinel compositions plot in the field for abyssal peridotites. Clinopyroxenes show depletions in Ti, Zr, and REE that are intermediate between those documented for peridotites from the Vulcan and Bouvet fracture zones (the American-Antarctic and Southwest Indian ridges, respectively). The open-system melting model indicates that the Mariana Trough peridotite compositions roughly correspond to theoretical residual compositions after ~7% near-fractional melting of a depleted MORB-type upper mantle with only little melt or fluid/mantle interactions. The low degree of melting is consistent with a low magma budget, resulting in ultramafic exposure. We infer that the mantle flow beneath the Mariana Trough Central Graben is episodic, resulting in varying magma supply rate at spreading segments.     

Geodynamic Information in Peridotite Petrology

Systematic differences are observed in the petrology and majorelement geochemistry of natural peridotite samples from thesea floor near oceanic ridges and subduction zones, the mantlesection of ophiolites, massif peridotites, and xenoliths ofcratonic mantle in kimberlite. Some of these differences reflectvariable temperature and pressure conditions of melt extraction,and these have been calibrated by a parameterization of experimentaldata on fertile mantle peridotite. Abyssal peridotites are examplesof cold residues produced at oceanic ridges. High-MgO peridotitesfrom the Ronda massif are examples of hot residues producedin a plume. Most peridotites from subduction zones and ophiolitesare too enriched in SiO₂ and too depleted in Al₂O₃ to be residues,and were produced by melt–rock reaction of a precursorprotolith. Peridotite xenoliths from the Japan, Cascades andChile–Patagonian back-arcs are possible examples of arcprecursors, and they have the characteristics of hot residues.Opx-rich cratonic mantle is similar to subduction zone peridotites,but there are important differences in FeO_T. Opx-poor xenolithsof cratonic mantle were hot residues of primary magmas with16–20% MgO, and they may have formed in either ancientplumes or hot ridges. Cratonic mantle was not produced as aresidue of Archean komatiites. KEY WORDS: peridotite; residues; fractional melting; abyssal; cratonic mantle; subduction zone; ophiolite; potential temperature; plumes; hot ridges     

地幔橄榄岩中橄榄石的指示意义

橄榄石是地幔橄榄岩和辉石岩的主要组成矿物,但也经常以斑晶和捕虏晶的形式出现在玄武质岩石中。结合近年来在地幔橄榄岩的主要元素（如Mg和Fe）组成特征以及Li、Mg和Fe稳定同位素地球化学方面的研究成果,重点对橄榄石的地球化学特征与华北克拉通岩石圈地幔演化过程之间的联系进行了讨论,旨在加深对华北克拉通岩石圈地幔演化过程的理解。现有研究表明：地幔橄榄岩中橄榄石的矿物学特征、元素和同位素地球化学组成能够很好地指示岩石圈地幔的特征及其演化过程,因而具有重要的意义。对于克拉通地区的地幔橄榄岩来说,橄榄石的Mg#通常可以指示岩石圈地幔的属性,古老、难熔的地幔橄榄岩中的橄榄石一般具有较高的Mg#（〉92）,而新生的岩石圈地幔橄榄岩中的橄榄石则具有较低的Mg#（〈91）。因此,地幔橄榄岩中橄榄石的Mg#在一定程度上具有年龄意义。橄榄岩中橄榄石的Li、Mg和Fe同位素组成也可以明确指示岩石圈地幔的属性及其所经历的演化过程,正常地幔的δ7Li、δ26Mg和δ57Fe组成相对均一,如果上述同位素组成偏离正常地幔值,则说明岩石圈地幔经历了熔体/流体的交代作用。华北克拉通地区地幔橄榄岩捕虏体中橄榄石的Li、Mg和Fe同位素组成研究表明：该区的岩石圈地幔经历了多个阶段、不同来源的熔体/流体的改造过程。     

Pervasive melt percolation reactions in ultra-depleted refractory harzburgites at the Mid-Atlantic Ridge, 15° 20′N: ODP Hole 1274A

ODP Leg 209 Site 1274 mantle peridotites are highly refractory in terms of lack of residual clinopyroxene, olivine Mg# (up to 0.92) and spinel Cr# (∼0.5), suggesting high degree of partial melting (>20%). Detailed studies of their microstructures show that they have extensively reacted with a pervading intergranular melt prior to cooling in the lithosphere, leading to crystallization of olivine, clinopyroxene and spinel at the expense of orthopyroxene. The least reacted harzburgites are too rich in orthopyroxene to be simple residues of low-pressure (spinel field) partial melting. Cu-rich sulfides that precipitated with the clinopyroxenes indicate that the intergranular melt was generated by no more than 12% melting of a MORB mantle or by more extensive melting of a clinopyroxene-rich lithology. Rare olivine-rich lherzolitic domains, characterized by relics of coarse clinopyroxenes intergrown with magmatic sulfides, support the second interpretation. Further, coarse and intergranular clinopyroxenes are highly depleted in REE, Zr and Ti. A two-stage partial melting/melt–rock reaction history is proposed, in which initial mantle underwent depletion and refertilization after an earlier high pressure (garnet field) melting event before upwelling and remelting beneath the present-day ridge. The ultra-depleted compositions were acquired through melt re-equilibration with residual harzburgites. Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible for authorized users.     

Petrology of peridotite xenolith-bearing basaltic to andesitic lavas from the Shiribeshi Seamount,off northwestern Hokkaido,the Sea of Japan

The Shiribeshi Seamount off northwestern Hokkaido, the Sea of Japan, is a rear-arc volcano in the Northeast Japan arc. This seamount is composed of calc-alkaline and high-K basaltic to andesitic lavas containing magnesian olivine phenocrysts and mantle peridotite xenoliths. Petrographic and geochemical characteristics of the andesite lavas indicate evidence for the reaction with the mantle peridotite xenoliths and magma mixing between mafic and felsic magmas. Geochemical modelling shows that the felsic end-member was possibly derived from melting of an amphibolitic mafic crust. Chemical compositions of the olivine phenocrysts and their chromian spinel inclusions indicate that the Shiribeshi Seamount basalts in this study was derived from a primary magma in equilibrium with relatively fertile mantle peridotites, which possibly represents the mafic end-member of the magma mixing. Trace-element and REE data indicate that the basalts were produced by low degree of partial melting of garnet-bearing lherzolitic source. Preliminary results from the mantle peridotite xenoliths indicate that they were probably originated from the mantle beneath the Sea of Japan rather than beneath the Northeast Japan arc.