榴辉岩富铝单斜辉石出溶石榴子石现象研究

本文研究了江苏孟中榴辉岩富铝单斜辉石中出溶石榴子石现象，建立了出溶母体辉石成分，提出了出溶石榴子石的矿物反应。     

孟中榴辉岩形成和演化和P-T轨迹

本文研究了江苏东海县孟中榴辉岩富铝单斜辉石中石榴子石出溶作用,利用温压计对榴辉岩中各阶段矿物组合进行了温压估算,由此建立了孟中榴辉岩形成和演化的P-T轨迹。结果表明,该榴辉岩经历了地幔条件下由于降温和可能的升压作用,富铝单斜辉石中出溶石榴子石并形成榴辉岩;榴辉岩构造侵位到高角闪岩相片麻岩基底中;退化变质这3个阶段的演化过程。      

徐淮地区镁铁质岩石捕虏体单斜辉石中石榴石和石英的出溶

徐淮地区早侏罗世侵入杂岩中榴辉岩,石榴辉石岩和单斜辉石岩捕虏体单斜辉石中可以观察丰富的出溶石英针和石榴石,黝帘石及角闪石的出溶叶片,榴辉岩中出溶石英针的绿辉石核部比其边部相对富含FeO和MgO,贫SiO2,Al2O3和CaO。在石榴辉石岩和单斜辉石岩捕虏体中具有出溶石榴石的单斜辉石。从靠近出溶石榴石的一侧向其核部,Al2O3,Na2O和TiO2含量降低,MgO,SiO2和CaO含量增加,单斜辉石中定向石英针的出溶表明曾经存在有超高压条件下（≥25×10^8Pa)稳定的过硅质绿辉石。单斜辉石中出溶石榴石表明温压条件的降低可能是引起出溶的一个主要原因,捕虏体中的矿物组合和岩相学特征表明它们曾经遭受了榴辉岩相和角闪岩相退化变质作用,这与因压力和温度降低引起矿物出溶的结果相吻合。     

石榴石辉石岩的单斜辉石中韭闪石和钛铁矿出溶结构及地质意义

本文首次报道了在苏鲁超高压变质带胡家岭地区石榴石辉石岩中发现的韭闪石出溶结构。该石榴石辉石岩是由石榴子石、单斜辉石以及镁铝尖晶石、钛铁矿和磁铁矿组成。在石榴子石巨斑晶中有单斜辉石包体，单斜辉石包体中又有石榴子石包体以及大量韭闪石出溶片晶和钛铁矿( 磁铁矿)出溶棒。单斜辉石中韭闪石出溶片晶呈平行条带状，其宽度在1～10μm之间。透射电子显微镜(TEM)观察韭闪石的(010)面平行于主晶透辉石的(010)面，且两者的界面在纳米尺度上是连续过渡的，证明韭闪石是出溶形成的。大量钛铁矿出溶棒的定向排列也显示出它们是自然出溶形成的。从单斜辉石出溶的矿物组合推测其原始单斜辉石成分中应富含H2O、Na和Ti，属高压型单斜辉石。该石榴石辉石岩经历了超高压变质作用后，在抬升减压过程中形成这些出溶结构。大量钛铁矿出溶棒均斜切韭闪石出溶片晶，表明该超高压岩石在减压过程中至少经历了两期以上导致温压明显变化的地质事件。     

雅鲁藏布江缝合带白朗县白岗尖晶石—石榴子石相二辉橄榄岩的相界反应及其意义

西藏白朗县白岗村蛇绿混杂岩中有一罕见的尖晶石石榴子石二辉橄榄岩小岩块,被松软的蛇纹岩化尖晶石二辉橄榄岩包裹其中。岩块中发育有碎基单斜辉石、斜方辉石中出溶单斜辉石、切过出溶单斜辉石的贯入单斜辉石和外来碎粒单斜辉石及钙质辉石+铬尖晶石→钙铁石榴子石相界反应。同时,在岩块和包壳岩石的橄榄石中出现针状硅镁石出溶物。计算这些矿物的温度压力表明,它们的温度压力都处于>800℃,>1.8GPa以上的地幔石榴子石域超高压环境,而且,经历过一个上升→俯冲→上升的"N"字形历程。     

CCSD超高压变质岩绿辉石中的石英出溶体及其大陆动力学意义

单斜辉石中发育石英出溶体是UHP变质作用的典型矿物学标志之一,在世界上著名UHP变质地体中屡有发现。本文利用激光Raman光谱和电子探针分析在中国大陆科学钻探先导孔(CCSD-PP1)榴辉岩岩心的绿辉石中发现了大量石英(棒)出溶现象。通过与CCSD主孔榴辉岩各种赋存形式的绿辉石成分对比,发现含石英出溶体的绿辉石具有超硅特征,这是出溶现象发生的决定性因素之一。结合高压实验岩石学资料,提出在UHP变质的峰值期部分Si进入六次配位的Si-O八面体位置,压力降低这部分Si析出,形成石英出溶体的出溶机制。结合新的矿物学研究进展,认为绿辉石中出溶石英所标志的压力应远大于前人提出的2.5GPa,意味着苏鲁超高压变质带陆壳物质的俯冲深度要大于目前一般认为的80~120km范围。     

海南文昌二辉橄榄岩中辉石出溶结构的结晶学取向分析

本文用电子背散射衍射技术(electron backscatter diffraction,EBSD)测试了海南文昌玄武岩中二辉橄榄岩包体中的辉石主晶与其出溶片晶的结晶学取向关系。结合电子探针成分测试,得出:单斜辉石(透辉石)主晶中出溶了两组不同方向的片晶,一组为斜方辉石(顽火辉石-易变辉石)片晶,另一组为单斜辉石(普通辉石)片晶。由于出溶片晶在EBSD测试切面上体现为以线状体,因此需要找到一种方法将线状体所代表的片晶的晶面符号推算出来。本文介绍了一种利用吴氏网进行坐标系旋转的"晶带相交法",该方法可以作图推算出溶片晶的晶面符号。根据"晶带相交法"得出,斜方辉石(顽火辉石-易变辉石)出溶片晶为(100),单斜辉石(普通辉石)出溶片晶为~(401)。根据前人的研究资料,出溶片晶~(401)可能指示最小出溶压力为9.5~12.5GPa。出溶片晶的结晶学取向涉及到主晶与出溶体的晶体结构匹配关系,并且与出溶温度-压力有关,因此出溶片晶的结晶学取向分析具有晶体化学理论意义和反映地质温压过程的实际意义。这种"晶带相交法"可以推广应用于其他矿物出溶结构的结晶学取向研究中。     

大别山菖蒲—碧溪岭地区高压—超高压榴辉岩相变质岩和有关岩石的岩石类型及其原岩性质

安徽岳西菖蒲—碧溪岭地区出露两条北北西向的高压—超高压变质岩带:西带由土桥冲至菖蒲水电站,该带由层状硬玉石英岩类、大理岩及少量的石英深色榴辉岩以及浅色榴辉岩等组成;东带由小南山岭至碧溪岭,主要由层状的浅色榴辉岩系列和层状深色榴辉岩系列岩石组成。该区发育的层状浅色榴辉岩和层状的深色榴辉岩两种榴辉岩在岩石组合、矿物组合、矿物成分等方面有明显差别。浅色榴辉岩一般由硬玉质绿辉石(Jd 65～45)、+镁铝以及钙铝端元成分(Pyr+Gro,60±)的石榴子石+蓝晶石±多硅白云母±石英及次生的角闪石、绿帘石组成。其中夹有硬玉质绿辉石石英岩、富蓝晶石岩石、石榴子石岩和硬玉石榴白云片岩等岩石薄层。深色榴辉岩由绿辉石(Jd20～50)±富铁铝端元的石榴子石(Alm 50～60)+金红石±石英及次生的角闪石等组成。石英深色榴辉岩由绿辉石(Jd 40～45)+镁铝端元的石榴子石(Pyr 10～30)+石英+金红石及次生的角闪石、长石组成。深色榴辉岩与石榴橄榄岩分布上紧密相随。浅色榴辉岩的原岩为基性凝灰质沉积岩,相伴随的硬玉石英岩、硬玉岩、白云片岩的原岩大致分别为粉砂岩、长石砂岩、泥质粉砂岩;深色榴辉岩为基性凝灰质熔岩。大理岩的原岩为灰岩。同时,本文的研究表明,在相同的变质作用条件下,榴辉岩相岩石中石榴     

青藏高原拉萨地块松多榴辉岩的岩相学特征和变质演化过程

松多榴辉岩出露于拉萨地块的石英片岩中,主要由较为基性的金红石榴辉岩和较为酸性的石英榴辉岩组成。榴辉岩相矿物组合为石榴子石 绿辉石 绿帘石±多硅白云母±石英±金红石。岩石发生了较强烈的退变质作用,退变质矿物有角闪石、绿帘石、石英、钠长石及绿泥石。石榴子石变斑晶具有生长环带结构,变斑晶和基质石榴子石主要落入C类榴辉岩区,少数石榴子石变斑晶边部和基质石榴子石落入B类榴辉岩区;单斜辉石主要为绿辉石,少数Ⅰ世代和Ⅲ世代为普通辉石;角闪石均为钙质角闪石。根据石榴子石-绿辉石-多硅白云母矿物温压计计算,获得的温压范围为630～777℃和2.58～2.70GPa,峰期变质条件接近于石英-柯石英转变线。榴辉岩的原岩经历了从高绿片岩相、角闪岩相、榴辉岩相、角闪岩相到高绿片岩相的变质过程,这反映了与古特提斯洋闭合有关的俯冲进变质作用和随后的折返退变质作用。     

大别山北部榴辉岩的退变质特征及其地质意义

研究了大别山北部榴辉岩的变质岩岩石学。结果表明，该区榴辉岩相变质作用可分为早期(超高压)和晚期(高压)两个阶段，并在折返过程中形成了一系列特征性的退变质显微构造。其中，退变质结构主要包括：(1)由于压力降低而出溶形成的一些定向针状或叶片状矿物包裹体，如钠质单斜辉石中石英及石榴子石中的金红石、单斜辉石和磷灰石等；(2)冠状体或后成合晶，特别是石榴子石外围发育两期(“双层”)后成合晶；(3)反应边或退变边，如绿辉石的透辉石退变边、透辉石的角闪石退变边和金红石的钛铁矿退变边等。这些退变质结构为本区榴辉岩高级变质岩的快速折返过程和抬升历史提供了强有力的岩石学依据；石榴子石中针状矿物出溶体进一步证明研究区榴辉岩早期经历了超高压变质作用，峰期变质压力应大干4．0GPa，甚至可能达到5～7GPa或更高。     

胶东威海地区榴辉岩退变质的地球动力学信息

威海地区榴辉岩退变质过程表现为三个阶段：第一阶段,原生绿辉石分解形成钠质单斜辉石＋斜长石合晶体;第二阶段,原生石榴石及钢质单斜辉石＋斜长石合晶体,周边出现角闪石＋斜长石　状反应边;第三阶段,石榴石及钢质单斜辉石消失。其后榴辉岩相退变质的ｐ－ｔ演化轨迹是压力相对温度快速降低的顺时针形式,反映本区榴辉岩折返的地球动力学过程可能是在经历了快速上升的构造侵位同时,晚元古宙巨量花岗岩浆可将相辉岩块体携带到上部地壳。     

Diffusion gradients in an eclogite xenolith from the Roberts Victor kimberlite pipe: (2) kinetics and implications for petrogenesis

In a bimineralic eclogite xenolith (sample JJG41) from the Roberts Victor kimberlite, compositional gradients in clinopyroxene are related to garnet exsolution. Two principal reactions involving clinopyroxene and garnet occur: (i) The net-transfer Al₂Si^-1Mg^-1 which is responsible for garnet growth according to the equation 2Di+Al₂Si^-1Mg^-1=Grossular+MgCa^-1 (reaction 1). This has created substantial compositional gradients in Al, Si and Mg within clinopyroxene. (ii) The exchange of Fe–Mg between garnet and clinopyroxene (reaction 2). During the stage of garnet growth (reaction 1) the lamellae crystallized sequentially as a result of a temperature decrease from around 1400 to 1200° C. This exsolution growth-stage was under the control of Al diffusion in clinopyroxene and at around 1200° C further growth of garnet lamellae became impeded by the sluggishness of Al diffusion in the clinopyroxene host. However, reaction 2 continued during further cooling down to about 1000° C; this temperature being inferred from the constant Fe–Mg partitioning at clinopyroxene-garnet interfaces for the whole set of lamellae. The initial clinopyroxene in JJG41 was probably formed by crystallization from a melt in Archaean time. The cessation of Fe–Mg exchange between garnet and clinopyroxene at about 1000° C may well predate the eruption of the eclogite in kimberlite at around 100 Ma. Kinetic models of reaction are examined for both reactions. Modelling of reaction 1, involving both diffusion and interface migration, allows several means of estimating the diffusion coefficient of Al in clinopyroxene; the estimates are in the range 10^-16-10^-20 cm²/s at 1200° C. These estimates bracket the experimentally determined data for Al diffusion in clinopyroxene, and from these experimental data a preferred cooling rate of about 300° C/Ma is obtained for the period of growth of garnet exsolution lamellae. A geospeedometry approach (Lasaga 1983) suitable for a pure-exchange process (reaction 2) is used to estimate the cooling rate in the later stages of the thermal history (after garnet growth); values 4–40° C/Ma are consistent with the shape of the Fe-diffusion gradients in the clinopyroxene. The extensive thermal history recorded by JJG41, including probable melt involvement at ca. 1400° C, demonstrates the complex evolution of rocks within the mantle. Whilst the notion of formation of mantle eclogites from subducted oceanic crust has become fashionable, it is clear that tracing eclogite geochemical and P-T characteristics backwards from their nature at the time of xenolith eruption, through high-temperature mantle events to the characteristics of the original subducted oceanic crust, will be very complex.     

Petrogenesis and implications of jadeite‐bearing kyanite eclogite from the Sanbagawa belt (SW Japan)

Jadeite‐bearing kyanite eclogite has been discovered in the Iratsu body of the Sanbagawa belt, SW Japan. The jadeite + kyanite assemblage is stable at higher pressure–temperature (P–T) conditions or lower H₂O activity [a(H₂O)] than paragonite, although paragonite‐bearing eclogite is common in the Sanbagawa belt. The newly discovered eclogite is a massive metagabbro with the peak‐P assemblage garnet + omphacite + jadeite + kyanite + phengite + quartz + rutile. Impure jadeite is exclusively present as inclusions in garnet. The compositional gap between the coexisting omphacite (P2/n) and impure jadeite (C2/c) suggests relatively low metamorphic temperatures of 510–620 °C. Multi‐equilibrium thermobarometry for the assemblage garnet + omphacite + kyanite + phengite + quartz gives peak‐P conditions of ~2.5 GPa, 570 °C. Crystallization of jadeite in the metagabbro is attributed to Na‐ and Al‐rich effective bulk composition due to the persistence of relict Ca‐rich clinopyroxene at the peak‐P stage. By subtracting relict clinopyroxene from the whole‐rock composition, pseudosection modelling satisfactorily reproduces the observed jadeite‐bearing assemblage and mineral compositions at ~2.4–2.5 GPa, 570–610 °C and a(H₂O) >0.6. The relatively high pressure conditions derived from the jadeite‐bearing kyanite eclogite are further supported by high residual pressures of quartz inclusions in garnet. The maximum depth of exhumation in the Sanbagawa belt (~80 km) suggests decoupling of the slab–mantle wedge interface at this depth.     

Constraining the P–T path of a MORB-type eclogite using pseudosections, garnet zoning and garnet-clinopyroxene thermometry: an example from the Bohemian Massif

A mid‐ocean ridge basalt (MORB)‐type eclogite from the Moldanubian domain in the Bohemian Massif retains evidence of its prograde path in the form of inclusions of hornblende, plagioclase, clinopyroxene, titanite, ilmenite and rutile preserved in zoned garnet. Prograde zoning involves a flat grossular core followed by a grossular spike and decrease at the rim, whereas Fe/(Fe + Mg) is also flat in the core and then decreases at the rim. In a pseudosection for H₂O‐saturated conditions, garnet with such a zoning grows along an isothermal burial path at c. 750 °C from 10 kbar in the assemblage plagioclase‐hornblende‐diopsidic clinopyroxene‐quartz, then in hornblende‐diopsidic clinopyroxene‐quartz, and ends its growth at 17–18 kbar. From this point, there is no pseudosection‐based information on further increase in pressure or temperature. Then, with garnet‐clinopyroxene thermometry, the focus is on the dependence on, and the uncertainties stemming from the unknown Fe³⁺ content in clinopyroxene. Assuming no Fe³⁺ in the clinopyroxene gives a serious and unwarranted upward bias to calculated temperatures. A Fe³⁺‐contributed uncertainty of ±40 °C combined with a calibration and other uncertainties gives a peak temperature of 760 ± 90 °C at 18 kbar, consistent with no further heating following burial to eclogite facies conditions. Further pseudosection modelling suggests that decompression to c. 12 kbar occurred essentially isothermally from the metamorphic peak under H₂O‐undersaturated conditions (c. 1.3 mol.% H₂O) that allowed the preservation of the majority of garnet with symplectitic as well as relict clinopyroxene. The modelling also shows that a MORB‐type eclogite decompressed to c. 8 kbar ends as an amphibolite if it is H₂O saturated, but if it is H₂O‐undersaturated it contains assemblages with orthopyroxene. Increasing H₂O undersaturation causes an earlier transition to SiO₂ undersaturation on decompression, leading to the appearance of spinel‐bearing assemblages. Granulite facies‐looking overprints of eclogites may develop at amphibolite facies conditions.     

Phlogopite in mantle xenoliths and kimberlite from the Grib pipe,Arkhangelsk province,Russia:Evidence for multi-stage mantle metasomatism and origin of phlogopite in kimberlite

We present petrography and mineral chemistry for both phlogopite,from mantle-derived xenoliths(garnet peridotite,eclogite and clinopyroxene-phlogopite rocks)and for megacryst,macrocryst and groundmass flakes from the Grib kimberlite in the Arkhangelsk diamond province of Russia to provide new insights into multi-stage metasomatism in the subcratonic lithospheric mantle(SCLM)and the origin of phlogopite in kimberlite.Based on the analysed xenoliths,phlogopite is characterized by several generations.The first generation(Phil)occurs as coarse,discrete grains within garnet peridotite and eclogite xenoliths and as a rock-forming mineral within clinopyroxene-phlogopite xenoliths.The second phlogopite generation(Phl2)occurs as rims and outer zones that surround the Phil grains and as fine flakes within kimberlite-related veinlets filled with carbonate,serpentine,chlorite and spinel.In garnet peridotite xenoliths,phlogopite occurs as overgrowths surrounding garnet porphyroblasts,within which phlogopite is associated with Cr-spinel and minor carbonate.In eclogite xenoliths,phlogopite occasionally associates with carbonate bearing veinlet networks.Phlogopite,from the kimberlite,occurs as megacrysts,macrocrysts,microcrysts and fine flakes in the groundmass and matrix of kimberlitic pyroclasts.Most phlogopite grains within the kimberlite are characterised by signs of deformation and form partly fragmented grains,which indicates that they are the disintegrated fragments of previously larger grains.Phil,within the garnet peridotite and clinopyroxene-phlogopite xenoliths,is characterised by low Ti and Cr contents(TiO_21 wt.%,Cr_2 O_31 wt.% and Mg# = 100 × Mg/(Mg+ Fe)92)typical of primary peridotite phlogopite in mantle peridotite xenoliths from global kimberlite occurrences.They formed during SCLM metasomatism that led to a transformation from garnet peridotite to clinopyroxene-phlogopite rocks and the crystallisation of phlogopite and high-Cr clinopyroxene megacrysts before the generation of host-kimberlite magmas.One of the possible processes to generate low-Ti-Cr phlogopite is via the replacement of garnet during its interaction with a metasomatic agent enriched in K and H_2O.Rb-Sr isotopic data indicates that the metasomatic agent had a contribution of more radiogenic source than the host-kimberlite magma.Compared with peridotite xenoliths,eclogite xenoliths feature low-Ti phlogopites that are depleted in Cr_2O_3 despite a wider range of TiO_2 concentrations.The presence of phlogopite in eclogite xenoliths indicates that metasomatic processes affected peridotite as well as eclogite within the SCLM beneath the Grib kimberlite.Phl2 has high Ti and Cr concentrations(TiO_22 wt.%,Cr_2O_31 wt.% and Mg# = 100× Mg/(Mg + Fe)92)and compositionally overlaps with phlogopite from polymict brecc:ia xenoliths that occur in global kimberlite formations.These phlogopites are the product of kimberlitic magma and mantle rock interaction at mantle depths where Phl2 overgrew Phil grains or crystallized directly from stalled batches of kimberlitic magmas.Megacrysts,most macrocrysts and microcrysts are disintegrated phlogopite fragments from metasomatised peridotite and eclogite xenoliths.Fine phlogopite flakes within kimberlite groundmass represent mixing of high-Ti-Cr phlogopite antecrysts and high-Ti and low-Cr kimberlitic phlogopite with high Al and Ba contents that may have formed individual grains or overgrown antecrysts.Based on the results of this study,we propose a schematic model of SCLM metasomatism involving phlogopite crystallization,megacryst formation,and genesis of kimberlite magmas as recorded by the Grib pipe.     

Diffusion Gradients in an Eclogite Xenolith from the Roberts Victor Kimberlite Pipe: 1. Mechanism and Evolution of Garnet Exsolution in Al2O3-rich Clinopyroxene

Xenolith JJG41 is from the Roberts Victor kimberlite and isa bimineralic eclogite which is striking for its Al- and Ca-richclinopyroxene crystals showing garnet exsolution lamellae. Thedevelopment of the exsolution has been interpreted as a resultof a slow cooling at depth from near-solidus conditions (c.1400?C) towards normal mantle lithosphere temperatures (Harte& Gurney, 1975). The clinopyroxene retains marked compositionalgradients adjacent to the garnet lamellae and the present paperis concerned with the generation and preservation of these diffusiongradients within a rock from the Earth's mantle In order to understand the mechanism of exsolution reactiona re-examination has been made of the microtexture and chemistryof the garnet lamellae in relation to the compositional gradientsin adjacent clinopyroxene. Three sets of garnet lamellae, whichappear to have crystallized in sequence, may be recognised:type A, large lamellae, nucleated first and closest to the transformationtemperature; type B of intermediate size and age; and type C,small lamellae, nucleated last and with the greatest overstepof the transformation temperature. The major compositional zoning in JJG41 clinopyroxene, a decreaseof Al as Si and Mg increase, is consistent with the garnet growthreaction 2Diop+Al₂Si^–1Mg^–1=2Gros, 1Py.Ca, unlikemost of the elements, shows very flat composition profiles,but with a higher concentration than the initial Ca contentof the unexsolved clinopyroxene. Garnet lamellae are individuallyhomogeneous, but Ca contents vary between lamellae as a functionof lamellae size. In contrast the Fe/Mg distribution coefficientsat interfaces between garnet and clinopyroxene are relativelyconstant irrespective of garnet size. The redistribution of the principal cations—Ca, Fe, Mg,Al, Si—between and within the clinopyrox ene and garnet,during garnet exsolution and cooling, obviously proceeded differentlyfor different elements. Two principal stages in the coolinghistory may be identified: (1) The growth of the sets of garnetlamellae controlled by Al₂Mg^–1Si^–1 redistributionin clinopyroxene. This redistribution was both part of the nettransfer reaction creating garnet, and an exchange reactionin clinopyroxene essential for the diffusional transport ofAl to the growing garnet. Al diffusion in clinopyroxene wasprobably the rate-limiting step, and all other cations, Ca andFe as well as Mg and Si, were mobile during this stage. (2)The occurrence, after the cessation of garnet growth, of diffusionof Fe, Mg and Ca in garnet and interdiffusion of Fe-Mg in clinopyroxene.This resulted in the setting of the KD Fe-Mg at the Cpx-Gt interfacesto a roughly constant value equivalent to approximately 1000?C,which is taken to be the final (‘freezing-in’) temperaturefor redistribution of any elements. During this post garnet-growthstage Ca also became homogenized within individual garnet lamellae,but there is no evidence of Ca equilibration with the clinopyroxene.Under the P-T conditions operating, the initial clinopyroxenecomposition probably resulted in a maximum (M2 site fully occupied)Ca content in clinopyroxene during the stage of garnet growth,and this was maintained during the post-growth stage.     

徐州-宿州地区榴辉岩类捕虏体中角闪石的结构、矿物化学及成因意义

徐州-宿州地区中生代闪长质岩石中存在丰富的榴辉岩类捕虏体。对该类捕虏体的岩相学和矿物化学研究表明,其中的角闪石具有4种产状：1）位于石榴石中的早期角闪石包裹体,为镁质普通角闪石;2）与榴辉岩中矿物平衡存在的原生角闪石,为韭闪石或韭闪石质普通角闪石;3）位于石榴石和单斜辉石周边的退变角闪石,主要为浅闪石质和阳起石质普通角闪石;4）沿单斜辉石解理分布的出溶角闪石,主要为浅闪石、浅闪石质角闪石和含亚铁韭闪石质普通角闪石。不同产状角闪石矿物化学成分的差异和温压估算结果显示,榴辉岩类捕虏体经历了一个顺时针的P—T演化轨迹,进而反映了中生代早期华北克拉通东部造山作用的存在。     

中国大陆科学钻探主孔(CCSD-MH)石榴石橄榄岩:一个经历了深俯冲作用的古生代超镁铁质侵入体

中国大陆科学钻探主孔中的超镁铁岩主要产在603.20～683.53m深度之间。超镁铁岩的上部直接围岩为高Ti-Fe型榴辉岩;内部夹有薄层状含柯石英高镁榴辉岩和厚层状多硅白云母榴辉岩;下部直接围岩为石英榴辉岩和普通榴辉岩。超镁铁岩的主体岩性为石榴石单辉橄榄岩,主要由橄榄石(60%～70%),石榴石(10%～25%),单斜辉石(5%～15%),斜方辉石(1%～5%)和少量金云母和钛铁矿或钛斜硅镁石组成。橄榄石Fo 79～89,其中一些以包裹体形式出现的高MgO橄榄石可能形成较早,主体橄榄石属变质重结晶阶段形成;石榴石以低CaO、高MgO和Cr_2O_3含量高(达3%)为特征,保留较好的进变质成分环带;单斜辉石Na_2O含量达到4%～5%,分为绿辉石和普通辉石类,属变质成因,结合矿物对的温压估算,岩石已经经历超高压变质作用。岩石成分研究表明,石榴石单辉橄榄岩与其顶、底板榴辉岩及其中的榴辉岩夹层有一较大的成分间断,其中MgO含量约相差10%左右,认为超镁铁岩与榴辉岩的原岩不属同一岩浆演化产物。锆石SHRIMP定年表明石榴石单辉橄榄岩原岩时代为古生代346～461Ma,超高压变质作用时代为早中生代220～240Ma。认为CCSD主孔石榴石橄榄岩为古生代的超镁铁质侵入体,在印支期的中国南北板块俯冲折返过程中经历了超高压变质作用。