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1.
上地幔不相容元素的显交代作用   总被引:2,自引:0,他引:2  
陆琦  周湖云 《地球科学》1996,21(5):553-556,T002
通过矿物微区成分和图象分析,研究了在金伯利岩中发现的多种氧化物矿物的成分、结构特点及其相互关系.指出富含硅酸盐不相容元素的地幔流体交代、熔融先期形成的矿物以及充填作用,形成了近年来我国和南非金伯利岩中发现的多种新矿物相,包括沂蒙矿系列、蒙山矿系列、K-Cr柱红石、阿玛科矿、Zr-Ti氧化物(锆钛矿)、REE-Ti氧化物(铈钛矿)等.这些新矿物高度富集了K,Ba,Ca,Sr,Ti,Zr,REE等不相容元素.研究表明不相容元素的显交代作用可分早、中、晚3个阶段,各阶段不相容元素的富集程度、温压条件及流体的动力学特征等既有明显的差异性,又有一定的继承性  相似文献   

2.
用微束分析和微区图像分析技术,研究了山东金伯利岩中沂蒙矿(系列)、蒙山矿(系列)、桂红石、Zr-REE-Ti氧化物、钛铁矿(富镁)、钙钛矿和亚铁板钛矿的成分、产出特征和相互关系。这些关系包括:①镁钛铁矿-尖晶石的固溶体分离及伴生的交代作用──沂蒙矿的形成;②蒙山矿的熔融交代作用及其形成的亚铁板钛矿;③斑点、微脉交代充填作用及其形成的柱红石、Zr-REE-Ti氧化物等新矿物相。通过研究,总结了上地幔中与氧化物矿物相关的一些显交代作用的规律,提出了上地幔中不相容元素的显交代作用可分为早、中、晚三期。这些为地幔流体交代作用的总成分目录和机理作出了重要的补充。  相似文献   

3.
陆琦  周湖云 《矿物学报》1994,14(4):343-347,T001
本文回顾了国内外金伯利岩及其它地幔岩中发现的K、Ba、Ca、REE的Ti-Cr-Fe-Mg氧化物矿物的研究现状,包括沂蒙矿系列、蒙山矿系列及柱红石系列。在此基础上概括性地总结了笔者近一、二年对山东蒙阴金伯利岩中蒙山矿矿物所进行的微区矿物学方向研究取得的最新进展,包括①揭示了K、Ba、Ca、REE等半径较大的元素在蒙山矿中的不均匀分布特点;②首次在金伯利岩中发现了蒙山矿系列矿物的Ca端元-Ca蒙山矿  相似文献   

4.
我国东部新生代玄武岩中深源岩石包体内的尖晶石类矿物属铬尖晶石和铁尖晶石,金伯利岩及其地幔岩包体和金刚石中的尖晶石类矿物主要为铝铬铁矿。玄武岩中橄榄岩类包体内的尖晶石比其辉石岩类包体中的尖晶石含Cr高,含Al低,这与Cr为相容元素、Al为不相容元素、玄武岩中橄榄岩类包体是上地幔部分熔融出玄武岩浆后的残留物及其上地幔岩石的捕虏体、而辉石岩类是玄武岩浆结晶的产物有关。玄武岩中深源岩石包体中的尖晶石明显地比金伯利岩中的粗晶、地幔岩石包体及金刚石中的尖晶石含Cr低,含Al高,其主要原因是前者比后者形成的压力低  相似文献   

5.
陆琦  周湖云 《矿物学报》1997,17(3):270-275
在研究沂蒙矿,蒙山矿等地幔矿物时,新发现了两种Zr-Ti,REE-Ti氧经物矿物。Zr-Ti氧化物新相6个样品点的探针成分分析:TiO227.756-46.811,ZrO231.724-58.092,TFeO2.75-5.82,Cr2O31.728-4.65,Nb2O51.353-4.357,Ta2O50.155-2.814,SiO20.894-13.749,主次元素的成分变化幅度均较大,但以氧为  相似文献   

6.
路迳岩筒属火山通道相,由金伯利质煌斑岩、角砾岩、角砾凝灰岩组成,富含幔源橄榄岩包体、普通辉石巨晶和岩球。造岩矿物是橄榄石、斜方辉石、单斜辉石、角闪石和金云母,深源特征指示矿物有镁铝榴石、铬透辉石、铬尖晶石和镁钛铁矿。岩石化学组成超低SiO2,低MgO,高Al2O3,富碱,富挥发组分。轻稀土元素富集,相容元素贫化,不相容元素明显富集。岩浆起源深度约85km。其中:岩体产状,富含包体、巨晶和岩球,岩石结构和构造,矿物组成,岩石化学组成超低SiO2、富碱、富挥发组分等特征与金伯利岩相似;但岩石化学组成高Al2O3,低MgO,K2O低于Na2O,REE和LREE/HREE偏低,部分微量元素的亏损或富集,金云母成分富TiO2,富TFeO,贫MgO,镁铝榴石、铬透辉石、铬尖晶石和镁钛铁矿的Cr2O3含量偏低,岩浆起源深度较浅,均与金伯利岩有重大差异,而更接近煌斑岩类。研究认为,是幔源岩浆岩的一种新类型,岩石名称界定为金伯利质煌斑岩。  相似文献   

7.
近年来,在我国山东蒙阴及南非,西北澳大利亚的金伯利岩,钾镁煌斑岩等地幔岩中陆续发现了一系列新的钛酸盐矿物,包括蒙山矿系列,沂蒙矿系列,柱红石系列,钾钡石及易解石类矿物新种,它们分别具AM21O38,AM12O19,A1-2B8O16,A2B6O13,AB2O6等化合物的结构,其共同特征是含亲石大阳离子及硅酸盐不相容元素。笔者通过对其中一些矿物的晶体结构测定,综合国内外的有关资料,指出大阳离子在这些  相似文献   

8.
隋延辉  戚长谋 《世界地质》2003,22(4):373-375,403
对华北地台金伯利岩地球化学找矿信息提取表明:铬是判别岩体含矿与否的重要指示元素。铬的相态分属尖晶石、镁铝榴石和镁钛铁矿三类矿物族。研究得出,各矿物指示含矿的化学成分标型为:铬尖晶石Cr2O3>53%,Al2O3<11%,MgO<12%,Cr#值大于0 7。镁铝榴石Cr2O3>5%,Al2O3<19%,Cr#值大于0 2。镁钛铁矿Cr2O3>1%,MgO>11%。由于铬尖晶石相对稳定,其化学组成为提取金伯利岩找矿信息的首选对象。  相似文献   

9.
中国金伯利岩中的钛铁矿   总被引:2,自引:0,他引:2  
董振信 《矿物学报》1991,11(2):141-147
本文研究了金伯利岩中,作为巨晶和粗晶,基质相矿物,与金云母、镁铝榴石、铬尖晶石等矿物的连生体,金刚石中包裹体矿物及金伯利岩地幔岩包裹体矿物产出的钛铁矿的大小,形态、皮壳及化学成分、端元组分、环带及成分变异趋势。并与其他岩类中的钛铁矿作了对比。探讨了不同产状、共生组合类型的钛铁矿的成因。指出了与金刚石紧密伴生的钛铁矿的标型特征及找矿意义。  相似文献   

10.
岚皋金云角闪辉石岩类捕虏体特征   总被引:6,自引:0,他引:6  
陕西岚皋地区碱质基性超基性潜火山杂岩中的金云角闪辉石岩类捕虏体,主要由透辉石、富钛韭闪石、高Ti金云母、磷灰石及钛铁矿组成。捕虏体发育三联晶、碎裂边、扭折变形等固相线下变形变质结构,与正常地幔尖晶石二辉橄榄岩成分相比,捕虏体富TiO2、Fe2O3、CaO、Na2O、K2O,贫MgO;其稀土元素具富集特征,尤其富集LREE;微量元素配分型式显示富亲石不相容元素的特征。岩相学、矿物学及岩石化学特征表明,该类捕虏体为交代地幔捕虏体,它代表了北大巴山早古生代裂谷作用时期的异常地幔。交代营力可能源于地幔热柱的上升,在地幔深处可能以熔体交代作用为主,往上逐渐以流体交代作用为主  相似文献   

11.
Hydrous high-pressure veins formed during dehydration of eclogites in two paleo-subduction zones (Trescolmen locality in the Adula nappe, central Alps and Münchberg Gneiss Massif, Variscan fold belt, Germany) constrain the major and trace element composition of solutes in fluids liberated during dehydration of eclogites. Similar initial isotopic compositions of veins and host eclogites at the time of metamorphism indicate that the fluids were derived predominantly from the host rocks. Quartz, kyanite, paragonite, phengite, zoisite and omphacite are the dominant minerals in the veins. The major element compositions of the veins are in agreement with experimental evidence indicating that the composition of solutes in such fluids is dominated by SiO2 and Al2O3. Relative to N-MORB, the veins show enrichments of Cs, Rb, Ba, Pb, and K, comparable or slightly lower abundances of Sr, U, and Th, and very low abundances of Nd, Sm, Zr, Nb, Ti and Y. The differential fractionation of highly incompatible elements such as K, U and Th in the veins, as well as the presence of hydrous minerals in the eclogites rule out partial melting as a cause for vein formation. These results confirm previous suggestions that fluids derived from subducted basalt may have low abundances of high field strength elements, rare earth elements and Y. Variable vein-eclogite enrichment factors of incompatible alkalis and to a lesser extent Pb appear to reflect mineralogical controls (phengite, epidote-group minerals) on partitioning of these elements during dehydration of eclogite in subduction zones. However, abundance variations of incompatible elements in minerals from eclogites suggest that the composition of fluids released from eclogites at temperatures <700°C may not reflect true equilibrium partitioning during dehydration. Simple models for the trace elements U and Th indicate the relative importance of the basaltic and sedimentary portions of subducted oceanic crust in producing the characteristic chemical signatures of these elements in convergent plate margin volcanism.  相似文献   

12.
The results of study of crichtonite group minerals in pyropes from the Internatsionalnaya kimberlite pipe are reported. Most of the studied samples are characterized by high concentrations of Sr, Ca, Na, and LREEs in comparison with minerals of the LIMA series from kimberlites of South Africa, whereas the average concentrations of Ba and K are significantly lower. Crichtonite group minerals in pyropes are characterized by predomination of Na over K in most samples and by a high concentration of Al2O3 (up to 4.5 wt %). Findings of inclusions of crichtonite group minerals with high concentrations of incompatible elements provide evidence for the metasomatic origin of host chromium-rich pyropes.  相似文献   

13.
Spinel peridotite xenoliths from the Atsagin-Dush volcanic centre, SE Mongolia range from fertile lherzolites to clinopyroxene(cpx)-bearing harzburgites. The cpx-poor peridotites typically contain interstitial fine-grained material and silicate glass and abundant fluid inclusions in minerals, some have large vesicular melt pockets that apparently formed after primary clinopyroxene and spinel. No volatile-bearing minerals (amphibole, phlogopite, apatite, carbonate) have been found in any of the xenoliths. Fifteen peridotite xenoliths have been analysed for major and trace elements; whole-rock Sr isotope compositions and O isotope composition of all minerals were determined for 13 xenoliths. Trace element composition and Sr-Nd isotope compositions were also determined in 11 clinopyroxene and melt pocket separates. Regular variations of major and moderately incompatible trace elements (e.g. heavy-rare-earth elements) in the peridotite series are consistent with its formation as a result of variable degrees of melt extraction from a fertile lherzolite protolith. The Nd isotope compositions of LREE (light-rare-earth elements)-depleted clinopyroxenes indicate an old (≥ 1 billion years) depletion event. Clinopyroxene-rich lherzolites are commonly depleted in LREE and other incompatible trace elements whereas cpx-poor peridotites show metasomatic enrichment that can be related to the abundance of fine-grained interstitial material, glass and fluid inclusions in minerals. The absence of hydrous minerals, ubiquitous CO2-rich microinclusions in the enriched samples and negative anomalies of Nb, Hf, Zr, and Ti in primitive mantle-normalized trace element patterns of whole rocks and clinopyroxenes indicate that carbonate melts may have been responsible for the metasomatic enrichment. Low Cu and S contents and high δ34S values in whole-rock peridotites could be explained by interaction with oxidized fluids that may have been derived from subducted oceanic crust. The Sr-Nd isotope compositions of LREE-depleted clinopyroxenes plot either in the MORB (mid-ocean-ridge basalt) field or to the right of the mantle array, the latter may be due to enrichment in radiogenic Sr. The LREE-enriched clinopyroxenes and melt pockets plot in the ocean island-basalt field and have Sr-Nd isotope signatures consistent with derivation from a mixture of the DMM (depleted MORB mantle) and EM (enriched mantle) II sources. Received: 18 January 1996 / Accepted: 23 August 1996  相似文献   

14.
http://www.sciencedirect.com/science/article/pii/S1674987114000565   总被引:1,自引:0,他引:1  
During granulite-facies metamorphism of metasedimentary rocks by the infiltration of carbonic fluids, the disappearance of hydrated minerals leads to the liberation of aqueous fluids. These fluids are strongly enriched in F and C1, and a series of Large-lon-Lithophile (LIL) elements and rare metals, resulting in their depletion in granulites. To sum up the fate of these elements, we focus on three domains representing different crustal levels and showing distinct behaviours with respect to these elements. The Lapland metasedimentary granulites illustrate the behaviour of the LILE and rare metals during lower crustal metamorphism. There is no change in Ba, moderate loss in Rb, and extreme depletion in Cs, Li, and Sn. F and CI contents are also very low compared to the protoliths or average upper continental crust. Biotite and amphibole breakdown leads to the incorporation of their partitioning into a fluid or a melt. The Tranomaro metasomatized marbles recrystallizing under granulite-facies conditions represent a demonstrative example of fluid transfer from granulite-facies supracrustals to traps represented by regional scale skarns. Such fluids may be at the origin of the incompatible element enrichment detected in leucosomes of migmatites from St Malo in Brittany (France) and Black Hills in South Dakota, The northern French Massif Central provides us with an example of a potential association between incompatible element enrichment of granitic melts and granulite-facies metamorphism. U- and F- enriched fine-grained granites are emplaced along a crustal scale shear zone active during the emplacement within the St Sylvestre peraluminous leucogranitic complex, We propose that during granulite-facies metamorphism dominated by carbonic waves in a deep segment of the continental crust, these shear zones control: (i) the percolation of F-, LILE-, rare metal-rich fluids liberated primarily by the breakdown of biotite; (ii) the enhancement of partial melting by F-rich fluids at intermediate crustal lev  相似文献   

15.
Summary The metabasites of Montiggiu Nieddu occur as a lenticular body in the Hercynian migmatite complex of NE Sardinia and consist of two major lithological associations: ultramafic amphibolites and plagioclase-banded amphibolites, which are genetically related by processes of cumulate differentiation of an original tholeiitic magma. The ultramafic amphibolites consist of relics of igneous phases (anorthite, olivine, orthopyroxene, and clinopyroxene) and metamorphic minerals (orthopyroxene, clinopyroxene, plagioclase, garnet, chlorite, and amphibole) in variable proportions. Based on the distribution of the relics of igneous minerals three main compositional layers (A, B, C) have been identified in the ultramafic amphibolites. The plagioclase-banded amphibolites consist of dark-green and white bands made up of plagioclase, amphibole, garnet, and rare pyroxene in variable proportions. No relics of magmatic minerals were observed. The trace element patterns of the Montiggiu Nieddu metabasites are characterised by selective enrichment of incompatible elements of low ionic potential, such as Sr, Rb, Ba, and Th, and low abundance of K, Cr, Ni, and elements of high ionic potential (from Ta to Yb), which define a relatively flat trend similar to MORB composition. Ti, Y, and heavy rare earth elements are all positively correlated with Zr. This correlation suggests that no significant transport of these elements took place during metamorphism. The metabasites of Montiggiu Nieddu are characterised by low Ti, Ti/V, and Ti/Zr content, low rare earth and high-field strength element concentrations, and moderate selective enrichment in large-ion lithophile elements. They also show geochemical features similar to those of supra subduction zone tholeiites. The CaO-MgO diagram displays a segmented trend, which provides powerful evidence in favour of crystal-liquid separation during magmatic evolution. Received December 4, 2000; revised version accepted January 29, 2001  相似文献   

16.
Trace element compositions of submicroscopic inclusions in both the core and the coat of five coated diamonds from the Democratic Republic of Congo (DRC, formerly Zaire) have been analyzed by Laser Ablation Inductively Coupled Mass Plasma Spectrometry (LA-ICP-MS). Both the diamond core and coat inclusions show a general 2-4-fold enrichment in incompatible elements relative to major elements. This level of enrichment is unlikely to be explained by the entrapment of silicate mantle minerals (olivine, garnet, clinopyroxene, phlogopite) alone and thus submicroscopic fluid or glass inclusions are inferred in both the diamond coat and in the gem quality diamond core. The diamond core fluids have elevated High Field Strength Element (Ti, Ta, Zr, Nb) concentrations and are enriched in U relative to inclusions in the diamond coats and relative to chondrite. The core fluids are also moderately enriched in LILE (Ba, Sr, K). Therefore, we suggest that the diamond cores contain inclusions of silicate melt. However, the Ni content and Ni/Fe ratio of the trapped fluid are very high for a silicate melt in equilibrium with mantle minerals; high Ni and Co concentrations in the diamond cores are attributed to the presence of a sulfide phase coexisting with silicate melt in the diamond core inclusions. Inclusions in the diamond coat are enriched in LILE (U, Ba, Sr, K) and La over the diamond core fluids and to chondrite. The coats have incompatible element ratios similar to natural carbonatite (coat fluid: Na/Ba ≈0.66, La/Ta≈130). The coat fluid is also moderately enriched in HFSE (Ta, Nb, Zr) when normalized to chondritic Al. LILE and La enrichment is related to the presence of a carbonatitic fluid in the diamond coat inclusions, which is mixed with a HFSE-rich hydrous silicate fluid similar to that in the core. The composition of the coat fluid is consistent with a genetic link to group 1 kimberlite.  相似文献   

17.
Abundant spinel peridotite xenoliths occur in late Cenozoic alkali basaltic rocks in the Sikhote-Alin region at the Pacific margin of the Asian continent. Major- and trace-element compositions of representative peridotite xenolith are documented for four occurrences located in different structural units of the continental margin. In each locality, the majority of xenoliths have distinctive microstructures, modal and chemical compositions that are typical for a given xenolith suite. Significant textural and compositional differences between the four xenolith suites suggest that the upper mantle beneath the Sikhote-Alin consists of distinct domains with contrasting composition. The inferred large-scale mantle heterogeneities may be due to juxtaposition of lithospheric blocks of different provenance during accretion of the Sikhote-Alin to the Asian continent.

Trace-element patterns of the xenoliths and their minerals obtained ICP-MS technique provide evidence of depletion and enrichment events and indicate contrasting behaviour of REE, HFSE and other incompatible trace elements. The HFSE behave non-concordantly, in particular, some xenoliths have highly fractionated Zr/Hf, Ti/Zr, Nb/Ta, La/Nb and U/Th ratios relative to their values in the primitive mantle. The fractionated compositions may be related to the interaction of evolved subduction-related fluids and melts with lithospheric mantle at the Mesozoic-early Cenozoic active continental margin or to metasomatism during later continental rifting.  相似文献   


18.
浙江临安石室寺伟晶岩位于河桥岩体西北面,属于典型的Nb-Y-F (NYF) 型伟晶岩,富含大量稀有稀土矿物。本文在野外考察和显微镜观察的基础上,结合电子探针背散射电子图像观察与矿物化学成分分析,系统鉴定了石室寺NYF 型伟晶岩中的稀有稀土矿物,揭示了稀有稀土元素的富集、迁移、结晶与成矿过程。研究结果表明:(1) 石室寺伟晶岩中的稀有稀土矿物有铌钽矿物(铌铁矿、铌锰矿、重钽铁矿、细晶石等)、钇矿物(褐钇铌矿、黑稀金矿)、钨矿物(黑钨矿、 白钨矿、铌钨矿物)、铈矿物(独居石、氟铈矿、氟碳铈矿) 和钍矿物等。(2) 铌钨系列矿物的WO3含量在8.30~70.51 wt%之间呈规律变化,可能为铌铁矿与黑钨矿之间形成的一系列多体矿物。(3) 铌铁矿LA-ICP-MS U-Pb 定年结果显示,石室寺伟晶岩的形成年龄为133±2 Ma,与河桥花岗岩具有成因联系。(4) 石室寺NYF 型伟晶岩中稀有稀土元素的成矿过程与其岩浆的结晶演化密切相关:岩浆阶段,锆石、钍石与独居石等矿物最早晶出;岩浆—热液阶段,黑稀金矿、铌铁矿、褐钇铌矿、氟铈矿等稀有稀土矿物逐渐结晶;热液阶段,黑钨矿、铌钨矿物相继形成,同时早期的独居石、氟铈矿受晚期热液交代形成次生铈矿物。  相似文献   

19.
The lower sill at Benfontein, South Africa, shows a high degree of magmatic sedimentation to kimberlite, oxide-carbonate, and carbonate layers. The iron-titanium oxide minerals are similar in the carbonate-rich and silicate-rich layers and are represented by titaniferous Mg-Al chromite, Mg-Al titanomagnetite, magnesian ilmenite, rutile, and perovskite. The spinel crystallization trend was toward enrichment in Mg and Ti and depletion in Cr; this trend is similar to that observed in many kimberlites. The ilmenite has Mg and Cr contents within the range observed in kimberlites and lacks the Mn enrichment observed in ilmenites from carbonatites. Perovskite in silicate-rich and carbonate-rich layers shows similar total REE contents and LREE enrichment and lacks the remarkable Nb enrichment observed in perovskite from carbonatites. These new data on the iron-titanium oxide minerals in the lower Benfontein sill do not support a genetic relationship between kimberlites and carbonatites.  相似文献   

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