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1.
余淳梅  郑建平 《地球科学》2006,31(1):93-100
橄榄岩成分及其中矿物(如单斜辉石)微量元素组成可以很好地揭示岩石圈地幔性质．在对汉诺坝新生代玄武岩中橄榄岩捕虏体做详细岩相学和岩石化学研究基础上,重点分析了单斜辉石的激光原位微量元素,并探讨了新生代华北克拉通北缘岩石圈地幔特征及地幔演化．汉诺坝地区岩石圈地幔是相当于原始地幔经过不同程度的部分熔融抽取形成的,除个别样品的部分熔融程度为15％-20％外,多数样品<5％．全岩主元素、单斜辉石成分体现出新生代汉诺坝地区的岩石圈地幔是很不均一的:在主体饱满型中有亏损型地幔的残留．这种共存现象可能是软流圈物质对古老地幔进行侵蚀、混合和改造置换的结果．单斜辉石微量元素组成所体现的碳酸岩岩浆交代作用和硅酸盐熔／流体的交代作用也支持这一认识．  相似文献   

2.
橄榄岩-熔体的相互作用:岩石圈地幔组成转变的重要方式   总被引：31，自引：2，他引：31  
张宏福 《地学前缘》2006,13(2):65-75
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。  相似文献   

3.
昌乐方山新生代玄武岩中携带有大量深源捕虏岩,其岩石类型以二辉辉石岩、二辉橄榄岩为主,方辉橄榄岩、单斜辉石岩、单辉橄榄岩少见,未见纯橄岩。二辉辉石岩、二辉橄榄岩、方辉橄榄岩的矿物岩石、地球化学特征和平衡温度压力计算显示为地幔来源,采用地质温度压力计进行计算,获取三者都源于岩石圈地幔,形成的深度范围为41~66.7 km。根据单辉橄榄岩和单斜辉石岩的矿物化学分析,单斜辉石岩和单辉橄榄岩形成深度要低于前三者,且与前三者有密切成因联系。"熔体—岩石"反应在各类深源捕虏岩中广泛存在,除方辉橄榄岩样品不存在明显的"熔体—岩石"反应外,二辉辉石岩、单斜辉石岩、二辉橄榄岩中不同的矿物边缘与玄武质熔体接触部位有着不同类型的反应边和反应矿物出现:橄榄石边部发生(Mg,Fe)_2SiO_4(镁橄榄石)+熔体(原始岩浆)=(Mg,Fe)_2SiO_4(贵橄榄石)+熔体(演化岩浆)反应,使得边部富铁贫镁;单斜辉石与玄武质熔体反应,多具有粉红色反应边,具有富Ti、Al、Fe,贫Si、Mg,较玄武岩基质中单斜辉石斑晶更低Mg~#的特征。斜方辉石与玄武质熔体反应生成复杂的反应带,存在斜方辉石+熔体=橄榄石+SiO_2(熔体)+单斜辉石的反应,反应带内新生成的矿物由内向外具有明显趋向玄武质熔体成分的变化;尖晶石与玄武质熔体反应边缘具有富Fe、Ti,贫Mg、Al,以及更高的Cr~#,趋向于形成钛铁矿的变化特征。二辉橄榄岩中熔体囊和单辉橄榄岩中筛状单斜辉石以及粉红色的反应边都暗示了二者至少经历了两个期次的熔体作用。随着岩石圈地幔的演化,熔体的再富集作用使得难熔的方辉橄榄岩逐渐转变为相对富集的二辉橄榄岩,后期二辉橄榄岩又与玄武质熔体反应,生成更加富集的单辉橄榄岩,而方山方辉橄榄岩也受到了熔体的轻度改造,已不具有难熔古老岩石圈地幔岩石的显著特征,鲁西新生代玄武岩中深源捕虏体与熔体的反应广泛存在,熔体成分以玄武质为主,这可能是华北克拉通岩石圈置换的重要方式之一,导致古老岩石圈地幔的消失。  相似文献   

4.
为完整了解华北克拉通的破坏程度和机制,加深对其西部陆块岩石圈地幔的研究十分重要,而位于华北克拉通西部集宁新生代碱性玄武岩中的地幔橄榄岩包体,为研究人员认识该地区的岩石圈地幔的性质和演化起到指示作用.运用LA-ICP-MS和LA-MC-ICP-MS对集宁地区橄榄岩矿物进行原位微区测试,获得其主量、微量元素和Sr同位素成分的数据.根据矿物组成,可以将集宁地区的橄榄岩分为两类:第一类为贫单斜辉石橄榄岩 (单斜辉石体积分数小于8%),它们经历了高程度的部分熔融,可能是古老难熔岩石圈地幔的残留;第二类为二辉橄榄岩 (单斜辉石体积分数大于13%),其熔融程度低,代表了新生饱满的岩石圈地幔.第一类橄榄岩中单斜辉石REE含量整体偏低且轻微富集LREE,第二类橄榄岩中单斜辉石具有LREE富集和轻微亏损两种配分模式,大部分样品的核边有一定的强不相容元素及Sr同位素组成变化.这些微量元素和同位素特征都表明集宁橄榄岩包体经历过交代作用.(La/Yb)N和Ti/Eu比值特征表明它们经历过多阶段的交代作用,交代介质有硅酸盐、碳酸盐熔/流体,这些交代介质可能为来源于古亚洲洋板块俯冲时释放的熔/流体.   相似文献   

5.
本文对华北克拉通三个不同地区(河北汉诺坝、内蒙古集宁三义堂、河南鹤壁)新发现的含金云母尖晶石二辉橄榄岩和尖晶石橄榄单斜辉石岩捕虏体进行了详细的矿物组成、单斜辉石的微量元素和 Sr-Nd 同位素研究。通过与相同地区不含金云母尖晶石二辉橄榄岩捕虏体的系统对比发现通常含金云母的地幔橄榄岩比不含金云母的地幔橄榄岩岩富 Al_2O_3、CaO、NaO、K_2O、TiO_2,但相对贫镁;其单斜辉石的 LREE 更为富集,但 Sr、Nd 同位素组成则相对亏损。这说明地幔交代作用不仅能够造成地幔橄榄岩的玄武质组分和稀土元素的富集,而且亦能够造成全岩和橄榄石 Mg~#的降低和同位素组成的相对亏损。捕虏体的 Rb-Sr 等时线年龄暗示地幔交代作用发生在中、新生代;其交代熔体来源于软流圈。同时说明华北新生代岩石圈地慢普遍存在的主、微量元素和同位素组成类似于"大洋型"岩石圈地幔的特征很可能是岩石圈地幔橄榄岩与软流圈来源的熔体的大规模反应的结果,而非真正意义上的新增生的岩石圈地幔。  相似文献   

6.
张明  解广轰 《地球化学》1996,25(5):425-444
对中国东部赋存于新生代玄武岩中的地幔岩捕虏体的全岩和单斜辉石等作了主元素和微量元素分析，证实了二辉橄榄岩及其单斜辉石在主元素有连续变化的趋势，反映了具部分熔融后残留相的性质。方辉橄榄岩及其中的单斜辉石的主元素，Ｎｄ／Ｙｂ，Ｔｉ／Ｚｒ和Ｓｒ／Ｚｒ值与二辉橄榄岩的同类矿物是不连续过渡。  相似文献   

7.
江苏盘石山幔源橄榄岩包体成因的地球化学   总被引：8，自引：2，他引：8  
根据主要元素、微量元素，若干矿物相主要元素和单斜辉石微量元素测定认为：盘石山幔源橄榄岩包体是由接近原始地幔源区的地幔经不同比例部分熔融后的残余二辉橄榄岩和方辉橄榄岩组成，基本未受其它过程干扰。由主要元素和ＭｇＯ相关性的回归方程，根据二元混合规律估算了原始熔体的组成范围。计算了包体的平衡温度，认为较亏损的方辉橄榄岩可能位于弱亏损的二辉橄榄岩之上，全岩和单斜辉石中不相容元素含量有可能作为地幔部分熔融和  相似文献   

8.
鲁江姑  郑建平 《地质学报》2011,85(3):330-342
内容提要：在对吉林辉南新生代玄武岩中捕虏体橄榄岩详细的岩相学和矿物主量元素研究基础上,重点分析了单斜辉石激光原位微量元素,并讨论了辉南陆下岩石圈地幔的性质及其在华北克拉通破坏过程中的意义。橄榄石、单斜辉石和尖晶石的Mg#和Cr#均表明该区陆下岩石圈地幔主体是饱满的,同时也存在少量过渡和难熔型地幔。单斜辉石REE配分形式包括LREE亏损、倒U字型REE和LREE富集等不同类型。这些橄榄岩是地幔经历不同程度的部分熔融作用(低于10%)和复杂地幔交代作用的产物。交代介质主体是硅酸盐熔体,但个别样品有碳酸岩熔体交代的残留。橄榄石Mg#和平衡温度无相关性,说明辉南陆下岩石圈地幔不存在明显的分层而是交叉的。这些地幔特征和华北东部其他地区新生代的主体地幔性质相似,是熔-岩反应、侵蚀作用和上涌软流圈物质冷却转变置换的综合结果。  相似文献   

9.
本文利用电子背散射衍射(EBSD)技术对河北张家口大麻坪汉诺坝玄武岩橄榄岩捕虏体中斜方辉石与玄武岩反应结构的显微构造进行了详细研究。研究结果表明: ① 其反应边具有复杂的多层筛状结构特征,包括玄武岩层、富橄榄石层以及橄榄石和单斜辉石交生层;② 由外至内,橄榄石的Mg值逐渐升高,而单斜辉石的Mg值变化不大;③ 反应边结构中的单斜辉石与斜方辉石残斑之间存在很好的结晶学拓扑关系,即(100)opx//(100)cpx、(010)opx//(010)cpx、(001)opx//(001)cpx;④ 橄榄石的结晶学取向无序且与斜方辉石和单斜辉石均无关。这个反应过程可以用贫硅熔体先与斜方辉石反应形成单斜辉石,并导致熔体富硅,从而橄榄石从反应熔体中结晶出来合理地解释。相对富硅熔体与橄榄岩的反应,贫硅熔体与橄榄岩的反应过程由于筛状反应边的存在可能更容易进行,筛状结构反应边可以为熔体在橄榄岩中沿颗粒边界运移提供通道,并使橄榄岩主要组成矿物发生细粒化和岩石结构变得松散,可以有效保证熔体上升过程中对橄榄岩的持续侵蚀和破坏,从而可能导致岩石圈地幔性质的迅速转变。  相似文献   

10.
苏鲁造山带中胡家林超镁铁质岩岩石地球化学特征   总被引：1，自引：0，他引：1  
苏鲁造山带中胡家林超镁铁质岩地块主要由两部分组成:南部滑石山以蛇纹岩和蛇纹石化橄榄岩为主,夹薄层状石榴橄辉岩-(石榴)单斜辉石岩;北部胡家林主要由(石榴)单斜辉石岩组成,夹厚层状蛇纹岩。蛇纹岩-蛇纹石化橄榄岩低Al2O3、低Ca O和高Mg O,REE含量低,但LREE稍富集。石榴橄辉岩和(石榴)单斜辉石岩低Mg O和Ca O,高REE含量高,其稀土配分曲线均表现出单斜辉石单矿物的配分特征。这些超镁铁岩块中不同岩石的微量元素均具有Pb的正异常,弱的Nb、Ta的负异常,显示地壳流体交代信息。Nd、Sr、Pb同位素特征显示存在亏损地幔与地壳之间的混合作用。亲石元素含量最低的蛇纹石化石榴橄辉岩的Sr、Nd、Pb同位素组成受交代流体控制明显,而石榴橄辉岩和(石榴)单斜辉石岩不明显。胡家林和滑石山超镁铁岩中所含的交代地壳成分不同,胡家林样品受到含水熔体和富水流体的双重交代,滑石山样品主要受富水流体的交代。  相似文献   

11.
REE abundances in minerals from spinel peridotite xenoliths from West Germany, the south-western U.S. and Mongolia decrease in the order clinopyroxene > orthopyroxene > olivine > spinel. While clinopyroxenes are similar in absolute chondrite-normalized concentrations to those known from other studies, orthopyroxenes and olivines are significantly lower in LREE although comparable in HREE. Spinels are much lower in all REE than any previously reported values and are completely negligible for the REE budget of peridotites.Partition coefficients for most orthopyroxene/clinopyroxene pairs increase systematically from La to Lu. Olivine/clinopyroxene and spinel/clinopyroxene partition coefficients increase from the intermediate rare earth elements to Lu and normally are higher for La compared to Sm.The application of Nagasawa's (1966) elastic lattice model suggests that all heavy but only minor amounts of the light REE substitute into structural positions of orthopyroxene and olivine.Significant differences between orthopyroxene/clinopyroxene partition coefficients for various xenoliths may be assigned to dependences upon equilibration temperature and bulk chemistry.Apart from grain surface contaminations, fluid inclusions which are practically always present in mantle minerals, can highly concentrate light rare earth elements and thus may be responsible for unexpectedly high concentrations of incompatible elements frequently reported for mantle olivines or orthopyroxenes.  相似文献   

12.
The concentrations of titanium and rare earth elements (REE) in olivines, orthopyroxenes, clinopyroxenes and spinels from four anhydrous, spinel-bearing peridotite xenoliths have been determined. The distribution of titanium (used as an analogue for the high field strength elements: HFSE) relative to the REE between clinopyroxenes and orthopyroxenes varies as a function of the whole rock composition and modal mineralogy. The distribution coefficients for titanium and the REE in these peridotites do not reflect mineral-melt equilibria. It is believed that subsolidus distribution coefficients for HFSE relative to REE vary with temperature. Ratios of various incompatible elements (e.g., Ti/Eu, Zr/Sm, Hf/Sm and P/Nd) in peridotite minerals differ from those in most primary basalts. However, the abundance ratios of incompatible elements in the bulk peridotite are comparable to those found in modern basalts. Given this and the differing contribution of melt from each phase during melting, near constant ratios of such incompatible elements in primary and primitive basalts and komatiites reflect the buffering of the melt by its residue. These ratios are fixed in the magma during the initial stages of melting because of similar and low distribution coefficients between melt and bulk residue for these element pairs. Differences in the relative abundances of titanium and REE in clinopyroxenes and orthopyroxenes demonstrate that mantle normalized abundance patterns for clinopyroxene are not equivalent to those of the whole rock. Therefore, claims of a widespread HFSE-depleted reservoir in the upper mantle base solely on the relative abundances of incompatible elements in peridotitic clinopyroxenes are invalid.  相似文献   

13.
Coarse-grained, granular spinel lherzolites xenoliths from the Premier kimberlite show evidence of melt extraction and metasomatic enrichment, documenting a complex history for the shallow mantle beneath the Bushveld complex. Compositions of orthopyroxene, clinopyroxene and spinel indicate equilibration within the spinel–peridotite facies of the upper mantle, at depths from 80 to 100 km and temperatures from 720 to 850 °C. Bulk compositions have lower Mg-number [atomic 100 Mg/(Mg + Fe*)] than previously studied spinel peridotites from Premier, and have higher Mg/Si than low-temperature coarse grained garnet lherzolites, suggesting shallower melting conditions or metasomatic enrichment. Clinopyroxene in one sample is highly LREE-depleted indicating very minor modification of a residue of 20% melt extraction, whereas the calculated REE pattern for a melt in equilibrium with a mildly LREE-depleted sample is similar to MORB or late Archean basalt, possibly related to the Bushveld Complex. Bulk and mineral compositions suggest minimal refertilization by silicate melts in four out of six samples, but REE patterns indicate introduction of a LIL-enriched component that may be related to kimberlite.  相似文献   

14.
Potassic latite in the transition zone of the Colorado Plateau near Chino Valley, Arizona, contains abundant eclogite and amphibolite xenoliths and minor websterite and pyroxenite xenoliths. One unit contains peridotite xenoliths; analyzed samples have mg-ratios of 68 and 71, 58 and 63 wt% SiO2, and are enriched in potassium and other large ion lithophile (LIL) elements. Rare earth element (REE) patterns are light REE enriched with La greater than 100 times chondritic abundance. The peridotite xenoliths are partly to totally altered, but contain remnant olivine, orthopyroxene, and clinopyroxene; one harzburgite nodule also contains spinel. Mineral compositions from the xenoliths are relatively refractory and similar to those in other spinel peridotite xenoliths from the Colorado Plateau. Geothermometry on olivine-spinel and two-pyroxene pairs indicates equilibration temperatures of less than 800° C for the peridotite nodules. The relatively low temperatures calculated from mineral equilibria are consistent with temperature estimates for other mantle nodules from under the Colorado Plateau.Peridotite xenoliths, mg-ratios, and Ni contents are evidence that the latite magma was derived from mantle peridotite. The potassic nature of the magma probably accounts for its silica-rich composition. The potassic, silica-rich nature of the latite and its enrichment in LREE and other LIL elements are consistent with a source which was metasomatically enriched in these elements either before or during partial melting. The source could have been either spinel or garnet peridotite.  相似文献   

15.
 Lherzolite xenoliths in Miocene to Pleistocene basalts from five sites in the Hamar-Daban range in southern Siberia provide sampling of the mantle close to the axis of the Baikal rift. These anhydrous spinel lherzolites commonly have foliated fabrics and spongy rims around clinopyroxene, and many contain accessory feldspar. The feldspar occurs in reaction zones adjacent to spinel and orthopyroxene (where it appears to have been formed by the reaction: spl+opx+cpx+fluid →fs+ol) and less commonly as thin, irregular veins. The feldspars have variable compositions but are generally alkali-rich; their K2O content ranges from 0.3 to 11.2% and is much higher than in plagioclase from orogenic lherzolites (usually <0.1% K2O). The temperature range for the Hamar-Daban xenolith suite (950–1010° C) is more restricted than for spinel peridotite xenoliths from other occurrences in the Baikal area. The feldspar-bearing lherzolites yield equilibration temperatures similar to or slightly lower than feldspar-free ones. The majority of the Hamar-Daban lherzolites are fertile and clinopyroxene-rich, as for most other occurrences in the Baikal region. Trace element compositions of selected xenoliths and their clinopyroxenes were determined by ICP-MS, INAA and proton microprobe. Feldspar-bearing xenoliths are enriched in alkalies indicating that feldspar formation is associated with addition of material and is not simply due to isochemical phase changes. Most xenoliths and their clinopyroxenes studied are depleted in light REE and have contents of Sr, Zr and Y common for fertile or moderately depleted mantle peridotites. Few are moderately enriched in LREE, Sr, Th and U. Sr-Nd isotope compositions of clinopyroxenes indicate long-term depletion in incompatible elements similar to unmetasomatised xenoliths from other occurrences south and east of Lake Baikal. The formation of feldspar and of spongy aggregates after clinopyroxene, and the enrichment in alkalies appear to be recent phenomena related to infiltration of an alkali-rich, H2O-poor fluid into spinel peridotites. Received: 20 March 1995 / Accepted: 26 June 1995  相似文献   

16.
REE partition data between solid phases in nine spinel peridotite xenoliths from Assab (Ethiopia) are presented together with bulk-rock REE composition. REE partitioning between clinopyroxene and other coexisting solid phases varies over a relatively wide range. The largest ranges are for LREE in clinopyroxene/orthopyroxene and clinopyroxene/olivine pairs, while clinopyroxene/spinel partitioning of REE is more restricted. The range of REE partition values between coexisting phases is due to compositional dependency effects and is correlated with systematic variations in major element composition of the bulk rocks. The measured REE concentration in the Assab mantle harzburgites do not match with the compositions calculated by mass balance from the modal proportions and REE analyses in individual phases. Inconsistencies for HREE may be due to variable HREE amounts in the clinopyroxene, orthopyroxene phases within a single specimen, while the high LREE contents in the whole rocks are due to contamination during transport to the surface. A geochemical model based on theoretical treatment of the REE partition data suggests that the Assab harzburgites acquired their residual character during a batch melting episode in the upper mantle under the Afar region.  相似文献   

17.
Patches of glass with a second generation of small crystals of olivine, clinopyroxene, and spinel are abundant in hydrous peridotite mantle xenoliths with tabular equigranular textures from two maar-type volcanoes, Meerfelder Maar and Dreiser Weiher (West Eifel, Germany). The patches are similar in size to the main phases of the hosting peridotite. Their central part is often occupied by relics of pargasitic amphibole. Mass-balance calculations show that the patches were formed by surface controlled incongruent thermal breakdown of amphibole according to the reaction: amphibole olivine + clinopyroxene + spinel + melt. Simultaneously with the decomposition of amphibole, small crystals of olivine, clinopyroxene, and spinel grew radially from the patch/peridotite interface toward the centre of the patch. Apart from sector zoning of clinopyroxene, the crystals are virtually homogeneous and are separated from the amphibole by a seam of melt (glass). Secondary olivines reveal higher Mg-numbers, secondary clinopyroxenes higher Cr2O3 concentrations than olivines and clinopyroxenes, respectively, of the host peridotite. The silica contents of melts produced by the above breakdown reaction range from 48 to 52% SiO2 as a function of the composition of the parent amphiboles. Patches surrounded by primary olivines only reveal no reaction with the host peridotite. The variation of SiO2, MgO and CaO in melts from these patches is the result of minor precipitation of olivine and clinopyroxene during fast cooling. If patches are in contact with primary olivine and orthopyroxene, melts are additionally modified by the reaction liquid 1 + orthopyroxene liquid 2 + olivine + clinopyroxene resulting in more silica-rich compositions between 54 and 58%. For the rare glasses richer in silica, a more complex formation is required. Veinlets along grain boundaries are filled with glasses which are chemically identical to those from nearby patches. This suggests that the veinlets were filled by melts formed by amphibole breakdown during entrainment of the xenoliths to the host magmas.  相似文献   

18.
The crystal chemistry of six clinopyroxenes enclosed in protogranular spinel-peridotite mantle xenoliths from Lake Nji (Cameroon, W Africa) was studied by means of single-crystal X-ray diffraction and electron microprobe. These spinel-peridotite xenoliths are characterised by clinopyroxene contents distinctly higher than those reported by Lee et al. (1996) for spinel-peridotite xenoliths of the same region (19–11% and 15–8% respectively) and by high clinopyroxene/orthopyroxene ratios: 0.7–2.7 (present study) and about 0.4 (Lee et al. 1996). The clinopyroxene crystal chemistry indicates that the xenoliths show the compositional features of a mantle source contaminated by small-volume melts, responsible for the high clinopyroxene content. The protogranular texture of the Cameroon xenoliths (upper portion of lithospheric mantle) testifies that the spinel peridotite and the associated small-volume melts completely re-equilibrated at the spinel-peridotite facies. This is also supported by the petrological and geochemical data of Lee et al. (1996) on the Etinde–Biu Plateau spinel-peridotite xenoliths, which underwent Late Proterozoic–Early Paleozoic enrichment in incompatible trace elements. Received: 6 October 1999 / Accepted: 27 March 2000  相似文献   

19.
张宏福 《地球科学》2006,31(1):31-37
地幔和／或下地壳中存在2类“复杂”橄榄岩捕虏体:一类为“混杂”,即“polymict”橄榄岩捕虏体;另一类为相对常见的“复合”,即“composite”橄榄岩捕虏体．复合橄榄岩捕虏体通常由橄榄岩和辉石岩／麻粒岩或由橄榄岩夹辉石岩脉2部分或多部分组成．岩相学上易于辨认,有时手标本上即可辨认．而混杂橄榄岩捕虏体为各种橄榄岩和／或辉石岩来源的矿物和熔体混杂在一起组成的构造岩,岩相学上很难辨认,只有通过矿物组成分析来判断．混杂橄榄岩捕虏体仅见于南非Kaapvaal 克拉通金伯利岩岩管中,该类捕虏体来源于地幔塑性剪切带,记录了流／熔体参与下的地幔变形和交代作用的全过程．复合橄榄岩捕虏体较常见,出现在全球各类玄武岩和金伯利岩中．复合橄榄岩捕虏体有多种成因,如地幔变形、壳幔过渡带样品、交代作用和堆积成因等等．这些复合橄榄岩捕虏体同样记录了岩石圈地幔和／或下地壳交代作用／改造过程的中间状态．因此,这些罕见而重要的复杂橄榄岩捕虏体为大陆岩石圈动力学演化过程提供了最直接的样品．  相似文献   

20.
WITT  G.; SECK  H. A. 《Journal of Petrology》1987,28(3):475-493
Mantle xenoliths from the West Eifel, West Germany revealingdistinct disequilibrium textures were formed by strong sheardeformation from coarse grained, high temperature spinel peridotites.Foliated structures are caused by the roughly parallel alignmentof elongated orthopyToxenc porphyroclasts up to 8 ? 2 mm insize and streched patches of clinopyroxene and spinel in a matrixof recrystallized olivine, orthopyroxene, clinopyroxene, andspinel. Bulk chemical disequilibrium finds its expression in a highdegree of chemical heterogeneity which is most evident in orthopyroxene.In orthopyroxene porphyroclasts, unmixed lamellae of clinopyroxeneand chromium-aluminium spinel are confined to the grain cores,because concentration gradients of Al, Cr, and Ca existed atthe time of their exsolution. Orthopyroxene neoblasts also revealdiffusion controlled concentration gradients of Al, Cr, andCa, which decrease from core to rim. The temperature historydetermining the orthopyroxene chemistries was derived from Al-solubilitiesin orthopyroxene using an empirical geothermometer. From thetextural relationships, in conjunction with the temperaturehistory, it is inferred that the shear process causing the deformationof the porphyroclastic xenoliths was associated with a temperaturedecrease from at least 1100 to about 800?C. The observed linkage of deformation and cooling in the xenolithsis related to the diapiric uplift of hot mantle material intoa cooler uppermost mantle beneath the West Eifel. It rules outa deformation due to secular mantle flow or movements along‘cold’ shear zones.  相似文献   

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