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1.
Elongated NE-SW trending bodies of iron-rich rock are exposed adjacent to pyroxenite dyke within Sukinda ultramafic complex, Odisha. Field study followed by optical and electron microscopy, XRD and EPMA investigation reveal the rocks to be fine grained, weathered, limonitised; containing quartz, magnetite, hematite/martite and goethite. The rock has suffered from deformation during intrusion of chromiferous magma. It rarely shows banding/lamination, but largely exhibits mylonitic fabric, resulting from magmatic intrusion. The stronger deformation is evident from sub-grain formation, deformed mineral grains; often with orientation, stretching (boudinage) and shortening (folding); presence of porphyroclasts, pull-apart structure, undulose extinction, dynamic recrystallisation etc. From the microstructure and mineral abundance, the rock is designated as “Mylonitic Magentite Quartzite” (MMQ).Enrichment of some elements like Ni, Mg, Cr in the magnetite phase of MMQ is attributed to solid state diffusion of these elements from chromiferous mafic magma during thermal metamorphism. This is determined from electron probe microanalysis of iron-rich phase in MMQ, which is found to contain 88-90 wt% of FeO(t) with ~1%, NiO, ~1%, MgO and 0.1% Cr2O3 having around 3 mole% of trevorite; 4-6% of magnesioferrite; 0.15-0.3% of chromite; 86-87% of magnetite and 3-4% of wustite. Considering presence of wustite as temperature indicator, the temperature of magma envisaged to be around 950-1100°C.In a later period, the MMQ has undergone oxidation and lateritisation owing to its prolonged exposure. During this process, new minerals like hematite and goethite substituted magnetite, resulting leaching of iron (FeO: 62-68%) and magnesium (MgO: 0.1-0.35) and enrichment of chromium (Cr2O3:4-7%) and nickel (NiO: 1.6-2.3%). The silica (SiO2: 4-5%), alumina (Al2O3:~1%) are contributed by kaolinite, formed during lateritisation.The field and laboratory studies confirm these iron-rich exposures to be enclaves of BIFs, banded magnetite quartzite (BMQ) in particular, within the Sukinda chromiferous ultramafic complex. Micro-structural features and microchemical composition of iron minerals in these exposures are interpreted as the influence of forceful ultramafic intrusion into the existing BMQ and effect of thermal metamorphism followed by oxidation, weathering/lateritisation.  相似文献   

2.
Cihai and Cinan are Permian magnetite deposits related to mafic-ultramafic intrusions in the Beishan region, Xinjiang, NW China. The Cihai mafic intrusion is dominantly composed of dolerite, gabbro and fine-grained massive magnetite ore, while gabbro, pyrrhotite + pyrite-bearing clinopyroxenite and magnetite ore comprise the major units in Cinan. Clinopyroxene occurs in both deposits as 0.1–2 mm in diameter subhedral to anhedral grains in dolerite, gabbro and clinopyroxenite. High FeO contents (11.7–28.9 wt%), low SiO2 (43.6–54.3 wt%) and Al2O3 contents (0.15–6.08 wt%), and low total REE and trace element contents of clinopyroxene in the Cinan clinopyroxenite imply crystallization early, at high pressure. This clinopyroxene is FeO-rich and Si and Ti-poor, consistent with the clinopyroxene component of large-scale Cu-Ni sulfide deposits in the Eastern Tianshan and Panxi ares, as well as Tarim mafic intrusion and basalt, implying the Cinan mafic intrusion and sulfide is related to tectonic activity in the Tarim LIP. The similar mineral chemistry of clinopyroxene, apatite and magnetite in the Cihai and Cinan gabbros (e.g., depleted LREE, negative Zr, Hf, Nb and Ta anomalies in clinopyroxene, lack of Eu anomaly in apatite and similarity of oxygen fugacity as indicated by V in magnetite), indicate similar parental magmatic characteristics. Mineral compositions suggest a crystallization sequence of clinopyroxenite/with a small amount of sulfide – gabbro – magnetite ore in the Cinan deposit, and magnetite ore – gabbro – dolerite in Cihai. The basaltic magma was emplaced at depth, with magnetite segregation (and formation of the Cinan magnetite ores) occurring in relatively low fO2 conditions, after clinopyroxenite and gabbro fractional crystallization. The evolved Fe-rich basaltic magma rapidly rose to intermediate or shallow depths, forming an immiscible Fe-Ti oxide magma as fO2 increased and leaving a Fe-poor residual magma in the chamber. The residual magmas was emplaced at different levels in the crust, forming the Cihai gabbro and dolerite, respectively. Finally, the immiscible Fe-Ti oxide magma was emplaced into the earlier formed dolerite because of late magma pulse uplift, resulting in a distinct boundary between the magnetite ores and dolerite.  相似文献   

3.
岩浆-热液系统中铁的富集机制探讨   总被引:8,自引:17,他引:8  
与岩浆-热液系统有关的铁矿类型有岩浆型钒钛磁铁矿床、玢岩铁矿、矽卡岩型铁矿和海相火山岩型铁矿,与这些铁矿有关的岩浆岩从基性-超基性、中性到中酸性岩均有,其中岩浆型钒钛磁铁矿床与基性-超基性深成侵入岩有关,形成于岩浆阶段,主要与分离结晶作用有关,但是厚大的富铁矿石的形成则可归结于原始的富铁钛苦橄质岩浆、分离结晶作用、多期次的岩浆补充以及流动分异等联合过程。钒钛磁铁矿石产于岩体下部还是上部与母岩浆的氧逸度有关:高的氧逸度导致磁铁矿早期结晶而使得其堆积于岩体的下部,相反,低氧逸度则导致低品位的浸染状矿石产于岩体的上部。虽然野外一些证据表明,元古宙斜长岩中的磷铁矿石可能是不混溶作用形成的,但是目前尚无实验证据。某些玢岩铁矿的一些磷灰石-磁铁矿石可能与闪长质岩浆同化混染了地壳中的磷导致的不混溶作用有关。除此之外,其他各类与岩浆作用有关的铁矿床均与岩浆后期的岩浆-热液作用有关。这些不同类型铁矿床的蚀变和矿化过程具有相似性,反映了它们形成过程具有相似的物理化学条件。成矿实验以及流体包裹体研究表明,岩浆-流体转换过程中出溶流体的数量以及成分受多种因素控制,其中岩浆分离结晶作用以及碳酸盐地层和膏盐层的混染可导致出溶的流体中Cl浓度的升高。早期高氧逸度环境可以使得硫以SO42-形式存在,抑制硫与铁的结合形成黄铁矿,有利于铁在早期以Cl的络合物发生迁移。大型富铁矿的形成需要一个长期稳定的流体对流循环系统,而岩浆的多期侵位或岩浆房以及在相对封闭的环境中(需要一个不透水层)一个有利于流体循环的断裂/裂隙系统是形成一个长期稳定的流体对流循环系统的必要条件。但是由于不同地质环境,流体中铁的卸载方式和位置会有明显差别,由此导致不同的矿石结构构造和不同的矿体产状。  相似文献   

4.
似层状铬铁矿床长期以来被认为是岩浆分异成因,但近年来有学者提出其中个别产在蛇绿岩中。本文选择北京放马峪似层状铬铁矿床中纯橄岩、辉橄岩和辉石岩中不同类型的含铬尖晶石进行了电子探针分析。研究表明,岩浆早期的纯橄岩和辉橄岩中的铬尖晶石富铬(Cr2O3平均43.32%),而岩浆晚期辉石的结晶消耗了大量Cr3+,由于氧逸度的升高,在辉石岩的单斜辉石中出溶贫铬的铬磁铁矿(Cr2O3平均10.32%)和富铝尖晶石(Cr2O3平均15.77%)。与世界上不同类型铬尖晶石的矿物化学特征进行对比,可以认为放马峪铬铁矿床是产在阿拉斯加型岩体中的早期岩浆矿床,而与蛇绿岩无关。本文对放马峪铬铁矿床成因和成矿专属性的限定,为这类镁铁-超镁铁岩体的铬、铜镍、铂族元素的找矿勘查提供了依据。  相似文献   

5.
Composition of chromiferous spinel included in olivines of Mg-rich basalts and gabbros of the Deccan Traps (Gujarat and Western Ghats) are reported here. They vary from Al-rich compositions [Al2O3 = 53wt.%; Cr#, 100Cr/(Cr + Al) = 12] to Cr-rich compositions [Cr2O3 = 51wt.%; Cr# = 84], and from Cr-Al rich compositions towards Cr-rich Ti-magnetite (TiO2 up to 23 wt.%, ulvöspinel up to 67mol.%). The Mg# [100Mg/(Mg + Fe2+)] of spinel decreases from 81 to nearly zero. The highest Cr# has been found in the Bushe Fm., Thakurvadi Fm., and some high-Ti basalts of the Pavagadh section, whereas some of the low-Ti basalts of Saurashtra have Al-rich compositions typical of spinels found in mid-ocean ridge basalts. The chemical composition of the Deccan Trap spinels is completely different compared to that observed in mantle spinel suites, with very few exceptions. The decreasing Al and increasing Fe and Ti of spinel seems to be mainly the result of decrease of Mg in the locally coexisting melts and favourable cationic substitutions in the lattice. There is barely any evidence of general relationships between the composition of the Deccan spinels and inferred mantle sources of the host magmas. Pyroxene inclusions in spinels may witness a high-pressure stage of crystallization, but the possibility of non-equilibrium crystallization, or even magma mixing, cannot be ruled out. Overall, the compositional ranges of chromiferous spinel in the Deccan Traps closely match those observed in the other Large Igneous Provinces having mafic/ultramafic intrusions and mafic magma compositions (e.g., Siberian Traps, Karoo, Emeishan).  相似文献   

6.
武定迤纳厂矿床位于我国云南省中部,在大地位置上处于扬子板块西缘,康滇地轴云南段,是滇中具有代表性的元古代铁-铜-金-稀土矿床.其矿化作用分为岩浆气液期、交代成矿期、热液成矿期和成矿后热液期4个期次,其中前3个期次是铁成矿的主要期次,分别以角砾状磁铁矿、浸染状磁铁矿和粗粒脉状磁铁矿为代表.各类磁铁矿含有一定量的SiO2、Cr2O3、Al2O3、MgO等,角砾状磁铁矿石的主元素成分与铁成分比值最高,其次为浸染状磁铁矿,最低为脉状磁铁矿.不同类型的磁铁矿微量元素变化很大,浸染状磁铁矿稀土配分具四重效应,角砾状磁铁矿和粗粒脉状磁铁矿稀土配分为右倾型.成矿早期磁铁矿的形成受岩浆作用影响强烈,含铁的岩浆导致围岩碎裂,形成了早期角砾状矿石;交代成矿期的铁质主要源于岩浆演化晚期分异形成的富铁流体,富铁流体与围岩发生强烈的物质交换,导致大量铁质沉淀;随着矿化作用的进行,热液作用逐渐增强,加之外界流体的逐渐加入,对之前形成的磁铁矿进行改造,使其具有热液成因的表象特征.从矿物成分体现出的矿床成因上看,该矿床属于岩浆隐爆-交代型成因,与世界知名的IOCG型矿床有相似之处.  相似文献   

7.
产于层状镁铁质-超镁铁质岩体中的太和岩浆型Fe-Ti氧化物矿床是峨眉山大火成岩省内带几个超大型Fe-Ti氧化物矿床之一。太和岩体长超过3km,宽2km,厚约1.2km。根据矿物含量和结构等特征,整个岩体从下向上可划分为下部岩相带、中部岩相带、上部岩相带。下部岩相带主要以(橄榄)辉长岩和厚层不含磷灰石的块状Fe-Ti氧化物矿层组成。中部岩相带韵律旋回发育,(磷灰石)磁铁辉石岩主要位于旋回的底部,旋回上部为(磷灰石)辉长岩。上部岩相带主要是贫Fe-Ti氧化物的磷灰石辉长岩。太和中部岩相带磷灰石磁铁辉石岩含有5%~12%磷灰石、20%~35%Fe-Ti氧化物、50%~60%硅酸盐矿物,且硅酸盐矿物与磷灰石呈堆积结构。磷灰石磁铁辉石岩中磁铁矿显示高TiO2、FeO、MnO、MgO,且变化范围与趋势接近于攀枝花岩体。钛铁矿FeO分别与TiO2、MgO显示负相关,而FeO分别与Fe2O3、MnO显示正的相关,且TiO2、FeO、MnO、MgO含量变化较大,这些特征都暗示磁铁矿和钛铁矿是从富Fe-Ti-P岩浆中分离结晶。因此,可以推断太和磷灰石磁铁矿辉石岩形成于矿物重力分选和堆积。太和下部岩相带包裹在橄榄石中磁铁矿含有相对较高Cr2O3(0.07%~0.21%),而中部岩相带包裹在橄榄石中磁铁矿Cr2O3(0.00%~0.03%)显著降低,且这些磁铁矿Cr2O3含量变化与单斜辉石Cr含量和斜长石An牌号呈正相关。这些特征印证了形成中部岩相带的相对演化的富Fe-Ti-P母岩浆可能是源自中部岩浆房的混合岩浆。上部岩相带磁铁矿和中部岩相带顶部少量磁铁矿显示较低Ti+V可能是由于岩浆房中累积的岩浆热液对磁铁矿成分进行了改造。  相似文献   

8.
Summary Spinel occurs in the pyroxenitic, peridotitic and gabbroic layers of the Ivrea-Verbano layered igneous complex. Its composition varies between picotite and Mg-hercynite. Maximum Cr2O3 contents are found in the spinels of the dunitic cumulitic layers occurring at some height above the base of the complex. Chromium deposits are absent. The lack of chromite and of chromium deposits is attributed to the early fractionation of clinopyroxene (which depleted the residual liquid in chromium) instead of olivine, as a consequence of the relatively high pressure prevailing during crystallization (8 kb). The relationships betweenfO2-composition of spinel-composition of the silicate phases indicate thatfO2 exerted a major control on the internal stratigraphy of the single layers and on the pattern of fractionation. The variation offO2 are on their turn related to accidental variations of the pressure acting on the magma.It is finally suggested that chromium deposits are limited to low pressure layered intrusions, where the magma has been emplaced rapidly into a shallow magma chamber. No chromium concentration is to be expected in those complexes that crystallized into deep-seated magma chambers and that fractionated at relatively high pressure, not markedly different from that at which the magma was produced. One of the major controls on the presence of chromium deposits results, therefore, to be the geotectonic environment of intrusion.
Chrom-Spinell im geschichteten vulkanischen Komplex von Ivrea-Verbano, Westalpen, Italien
Zusammenfassung Für die Spinelle der Pyroxenit-, Peridotit- und Gabbro-Lagen des Ivrea-Verbano-Intrusivkomplexes wurde eine Zusammensetzung im Bereich Picotit und Mg-Herzynit bestimmt. Die Dunit-Lagen im basalen Anteil des Komplexes führen Spinelie mit Cr2O3-Gehalten bis zu 30 Gew-%. Chromerz-Konzentrationen fehlen jedoch, was auf die fraktionierte Kristallisation von Klinopyroxen (und Entstehung Cr-Restschmelzen) an Stelle von Olivin, als Folge der bei relativ hohem Druck (8 kbar) erfolgten Intrusion, zurückzuführen ist. Die Beziehungen zwischen Sauerstoffpartialdruck und Spinell- und Silikat-Zusammensetzung zeigen den bedeutendenfO2-Einfluß auf den stratigraphischen Aufbau der einzelnen Gesteinslagen und auf die fraktionierenden Kristallisationsvorgänge. Die schwankendenfO2-Werter stehen in Zusammenhang mit den ebenfalls variierenden auf das Magma wirkenden Drücken.Es ist anzunehmen, daß Chromerzkonzentrationen nur in geschichteten Intrusivkomplexen vorkommen, die sich unter niederem Druck bzw. in einer oberflächennahen Magma-Kammer bildeten, und nicht in jenen, die tiefer intrudierten und bei hohem Druck kristallisierten. Von großer Bedeutung für die Bildung von Chromerzlagerstätten ist also das geotektonische Milieu der Intrusion.


With 7 Figures  相似文献   

9.
攀枝花岩体钛铁矿成分特征及其成因意义   总被引:2,自引:1,他引:1  
峨眉大火成岩省是全球最大的钒钛磁铁矿床聚集区,攀枝花岩体是其中的典型代表。根据岩性特点,攀枝花岩体主体可划分为上、中、下三个岩相带,其中中部岩相带和下部岩相带岩性旋回非常发育,每个旋回从下向上铁钛氧化物和暗色硅酸盐矿物逐渐减少,块状铁钛氧化物矿石或磁铁矿辉长岩都出现在每个旋回的底部和下部。然而,尽管钛铁矿固相线以下固溶体出溶远弱于磁铁矿,从而能更好地保留成因信息,但其成分变化的成因意义没有受到足够重视。本次研究发现作为主要金属氧化物之一的钛铁矿的成分不仅在不同岩性中有明显差异,同时,中、下部岩相带的各岩性旋回中钛铁矿成分也具有周期性变化。例如,块状矿石中钛铁矿具有最高的MgO和TiO2及最低的FeO、Fe2O3和MnO,而辉长岩中钛铁矿则具有相反的成分特征。同时,钛铁矿的MgO含量与磁铁矿的MgO含量及橄榄石的Fo牌号具有显著的正相关关系。这种规律性变化说明每个旋回可以代表一次比较明显的岩浆补充,每次新岩浆补充后,钛铁矿和磁铁矿及橄榄石都是结晶较早的矿物。与Skaergaard岩体相比,攀枝花岩体钛铁矿的MgO含量较高,表明攀枝花岩体分离结晶过程中铁钛氧化物结晶较早;与挪威Tellnes斜长岩套铁钛矿床中的钛铁矿相比,攀枝花岩体的钛铁矿不仅具有较高的MgO和FeO,还具有极高的TiO2和MnO,但Fe2O3却很低,说明地幔柱背景下形成的钛铁矿与斜长岩套中钛铁矿的成分有显著的区别。  相似文献   

10.
The Sarfartôq carbonatite complex was emplaced in lower Palaeozoic time in a weakness zone within the Precambrian shield. Dolomitic magma intruded in two major stages of activity. In the first stage a steeply dipping conical body of concentric sheets of rauhaugite was formed, while in the second stage several batches of magma were emplaced into the surrounding marginal shock-zone as concentric and radial beforsite dykes and agglomerates. Hydrothermal activity gave rise to several phases of mineralisation in veins and shear zones. The accompanying fenitisation was of the Na-type. The whole complex covers about 90 km2. The main rock-forming minerals are dolomite-ankerite, apatite, orange reversely pleochroic phlogopite, richterite-arfvedsonite and magnetite. Important accessories are pyrochlore, zircon and niobian rutile. A complete mineral list is given, together with microprobe data on mineral chemistry. The dolomitic magmas were poor in SiO2, Al2O3 and K2O in relation to other carbonatites. Nb, U and LREEs are strongly enriched in pyrochloremineralised zones where the Nb content may be up to 40%. Some shear zones are strongly enriched in Th and HREEs (specifically Eu) and lesser Pb and Zn. Niobium, uranium, rare earth elements and phosphorus occur in economically interesting concentrations.  相似文献   

11.
http://www.sciencedirect.com/science/article/pii/S1674987113000303   总被引:4,自引:0,他引:4  
The Xinjie layered intrusion in the Panxi region,SW China,hosts both Fe-Ti oxide and platinum-group element(PGE) sulfide mineralization.The intrusion can be divided,from the base upward,into UnitsⅠ,ⅡandⅢ,in terms of mineral assemblages.UnitsⅠandⅡare mainly composed of wehrlite and clino-pyroxenite, whereas UnitⅢis mainly composed of gabbro.PGE sulfide-rich layers mainly occur in Unit I, whereas thick Fe-Ti oxide-rich layers mainly occur in UnitⅢ.An ilmenite-rich layer occurs at the top of UnitⅠ.Fe-Ti oxides include magnetite and ilmenite.Small amounts of cumulus and intercumulus magnetite occur in UnitsⅠandⅡ.Cumulus magnetite grains are commonly euhedral and enclosed within olivine and clinopyroxene.They have high Cr2O3 contents ranging from 6.02 to 22.5 wt.%,indicating that they are likely an early crystallized phase from magmas.Intercumulus magnetite that usually displays ilmenite exsolution occupies the interstices between cumulus olivine crystals and coexists with interstitial clinopyroxene and plagioclase.Intercumulus magnetite has Cr2O3 ranging from 1.65 to 6.18 wt.%, lower than cumulus magnetite.The intercumulus magnetite may have crystallized from the trapped liquid.Large amounts of magnetite in UnitⅢcontains Cr2O3(<0.28 wt.%) much lower than magnetite in UnitsⅠandⅡ.The magnetite in UnitⅢis proposed to be accumulated from a Fe-Ti-rich melt.The Fe-Ti-rich melt is estimated to contain 35.9 wt.%of SiO2,26.9 wt.%of FeOt,8.2 wt.%of TiO2,13.2 wt.%of CaO, 8.3 wt.%of MgO,5.5 wt.%of Al2O3 and 1.0 wt.%of P2O5.The composition is comparable with the Fe-rich melts in the Skaergaard and Sept Iles intrusions.Paired non-reactive microstructures,granophyre pockets and ilmenite-rich intergrowths,are representative of Si-rich melt and Fe-Ti-rich melt,and are the direct evidence for the existence of an immiscible Fe-Ti-rich melt that formed from an evolved ferro-basaltic magma.  相似文献   

12.
文章对备战铁矿区内的基性-超基性岩、中基性岩脉、矿体围岩和铁矿石中的辉石、橄榄石、金云母、铁钛氧化物进行了电子探针分析与显微特征研究。金云母辉石橄榄岩中辉石的化学成分在w(SiO_2)-w(Al_2O_3)图中均落于亚碱性系列区域,在w(Al_2O_3)-w(Na_2O)-w(TiO_2)图中,辉石主要落在拉斑玄武岩系列区域,表明该区岩浆经历了拉斑玄武岩系列演化。备战金云母辉石橄榄岩中橄榄石的w(FeO)较低,介于19.22%~23.79%,w(MgO)较高,介于37.35%~41.30%,Fo变化介于0.74~0.79,属于贵橄榄石。橄榄石中较低的w(FeO)表明其形成于较高的氧逸度环境,而岩浆的拉斑玄武岩系列演化一般发生于低氧逸度条件,综合分析岩浆经历了从低氧逸度到高氧逸度变化的过程。随着岩浆的演化,橄榄石Fo与w(Ni)由负相关变为正相关又变为负相关关系,其中负相关关系表明在岩浆演化过程中橄榄石与粒间硫化物熔浆发生过Ni-Fe交换反应,从另一方面可以认为岩浆中含有丰富的硫,岩浆中的高硫特征很可能是备战磁铁矿为较纯磁铁矿(低Ti)的原因之一。此外,成矿岩浆具有高氧逸度特征,铁钛氧化物固溶体在亚固相条件下的氧化作用使固溶体发生分离以及铁磷络合物的发育等因素是造成矿区磁铁矿为较纯磁铁矿(成分接近分子式Fe_3O_4)的原因。金云母辉石橄榄岩和铁矿石中均发育金云母,表明铁矿与基性-超基性岩的源区都是富含挥发分的。该区铁钛氧化物主要有4种:较纯磁铁矿、含钛铬磁铁矿、铬铁矿、钛铁矿。金云母辉石橄榄岩中的较纯磁铁矿(低Ti),与铁矿石中磁铁矿成分类似,表明两者具有成因联系。结合金云母辉石橄榄岩的显微特征分析,在岩浆阶段曾有一期富铁镁岩浆的加入,这很可能为备战铁矿的形成提供了主要的铁质来源。  相似文献   

13.
Textural and mineral–chemical characteristics in the Bangriposi wehrlites (Eastern India) provide insight into metamorphic processes that morphologically and chemically modified magmatic spinel during serpentinization of wehrlite. Aluminous chromite included in unaltered magmatic olivine is chemically homogenous. In sub-cm to 10s-of-micron-wide veins, magnetite associated with antigorite and clinochlore comprising the serpentine matrix is near-stoichiometric. But Al–Cr–Fe3+ spinels in the chlorite–magnetite veins are invariably zoned, e.g., chemically homogenous Al-rich chromite interior successively mantled by ferritchromite/Cr-rich magnetite zone and magnetite continuous with vein magnetite in the serpentine matrix. In aluminous chromite, ferritchromite/Cr-rich magnetite zones are symmetrically disposed adjacent to fracture-controlled magnetite veins that are physically continuous with magnetite rim. The morphology of ferritchromite–Cr-rich magnetite mimics the morphology of aluminous chromite interior but is incongruous with the exterior margin of magnetite mantle. Micropores are abundant in magnetite veins, but are fewer in and do not appear to be integral to the adjacent ferritchromite–Cr-rich magnetite zones. Sandwiched between chemically homogenous aluminous chromite interior and magnetite mantle, ferritchromite–Cr-rich magnetite zones show rim-ward decrease in Cr2O3, Al2O3 and MgO and complementary increase in Fe2O3 at constant FeO. In diffusion profiles, Fe2O3–Cr2O3 crossover coincides with Al2O3 decrease to values <0.5 wt% in ferritchromite zone, with Cr2O3 continuing to decrease within magnetite mantle. Following fluid-mediated (hydrous) dissolution of magmatic olivine and olivine + Al–chromite aggregates, antigorite + magnetite and chlorite + magnetite were transported in 10s-of-microns to sub-cm-wide veins and precipitated along porosity networks during serpentinization (T: 550–600 °C, f(O2): ?19 to ?22 log units). These veins acted as conduits for precipitation of magnetite as mantles and veins apophytic in chemically/morphologically modified magmatic Al-rich chromite. Inter-crystalline diffusion induced by chemical gradient at interfaces separating aluminous chromite interiors and magnetite mantles/veins led to the growth of ferritchromite/Cr-rich magnetite zones, mimicking the morphology of chemically modified Al–Cr–Fe–Mg spinel interiors. Inter-crystalline diffusion outlasted fluid-mediated aluminous chromite dissolution, mass transfer and magnetite precipitation.  相似文献   

14.
The V-Ti magnetite layers (lodestone) occur within the layered gabbro-anorthosites-ultramafic rocks emplaced into the migmatitic gneisses close to the high grade Archeaen Sargur supracrustal rocks in the Kurihundi area. The ore petrographic studies of the lodestone reveal the presence of primary Ti-magnetite, ilmenite, ulvospinel, pleonaste, hematite and pyrite, chalcopyrite, pyrrhotite and secondary Ti-maghemite, martite and goethite as well as secondary covellite. These layers contain Ti-magnetite (60%) and ilmenite (30%) with silicates (<5%) exhibiting granular mosaic texture with well-defined triple junctions and are classified as adcumulus rocks. The grain-boundary relationships in the ores indicate considerable postcumulus growth and readjustment due to combined effects of sintering and adcumulus growth. Intergrowth textures (ulvospinel, ilmenite and pleonaste in Ti-magnetite and hematite in ilmenite) reflects exsolution features crystallized from solid-solutions compositions under different conditions of oxygen fugacities. Larger bodies of pleonaste and ilmenite in Ti-magnetite become lensoid or rounded in outline and these morphological modifications took place during the regional upper amphibolite to lower granulite facies metamorphism at 2.6 Ga ago. The lodestone contains high TiO2 (20 to 22.59 wt%), with V2O5 (0.85 to 1.15%) and Fe2O3 t (72.03 to 74.25%). Ti-magnetite shows alteration to Ti-maghemite, martite and goethite due to low temperature oxidation and hydration during weathering.  相似文献   

15.
The exsolutious of diopside and magnetite occur as intergrowth and orient within olivine from the mantle dunite, Luobusa ophiolite, Tibet. The dunite is very fresh with a mineral assemblage of olivine (〉95%) + chromite (1%-4%) + diopside (〈1%). Two types of olivine are found in thin sections: one (Fo = 94) is coarse-grained, elongated with development of kink bands, wavy extinction and irregular margins; and the other (Fo = 96) is fine-grained and poly-angied. Some of the olivine grains contain minor Ca, Cr and Ni. Besides the exsolutions in olivine, three micron-size inclusions are also discovered. Analyzed through energy dispersive system (EDS) with unitary analytical method, the average compositions of the inclusions are: Na20, 3.12%-3.84%; MgO, 19.51%-23.79%; Al2O3, 9.33%-11.31%; SiO2, 44.89%-46.29%; CaO, 11.46%-12.90%; Cr2O3, 0.74%-2.29%; FeO, 4.26%- 5.27%, which is quite similar to those of amphibole. Diopside is anhedral f'dling between olivines, or as micro-inclusions oriented in olivines. Chromite appears euhedral distributed between olivines, sometimes with apparent compositional zone. From core to rim of the chromite, Fe content increases and Cr decreases; and A! and Mg drop greatly on the rim. There is always incomplete magnetite zone around the chromite. Compared with the nodular chromite in the same section, the euhedral chromite has higher Fe3O4 and lower MgCr2O4 and MgAI2O4 end member contents, which means it formed under higher oxygen fugacity environment. With a geothermometer estimation, the equilibrium crystalline temperature is 820℃-960℃ for olivine and nodular chromite, 630℃-770℃ for olivine and euhedral chromite, and 350℃-550℃ for olivine and exsoluted magnetite, showing that the exsolutions occurred late at low temperature. Thus we propose that previously depleted mantle harzburgite reacted with the melt containing Na, Al and Ca, and produced an olivine solid solution added with Na^+, Al^3+, Ca^2+, Fe^3+, Cr^3+. With temperature d  相似文献   

16.
Copper–gold mineralization at the world‐class Batu Hijau porphyry deposit, Sumbawa Island, Indonesia, is closely related to the emplacement of multiple stages of tonalite porphyries. Petrographic examination indicates that at least two texturally distinct types of tonalite porphyries are currently recognized in the deposit, which are designated as “intermediate tonalite” and “young tonalite”. They are mineralogically identical, consisting of phenocrysts of plagioclase, hornblende, quartz, biotite and magnetite ± ilmenite, which are set in a medium‐coarse grained groundmass of plagioclase and quartz. The chemical composition of the rock‐forming minerals, including plagioclase, hornblende, biotite, magnetite and ilmenite in the tonalite porphyries was systematically analyzed by electron microprobe. The chemical data of these minerals were used to constrain the crystallization conditions and fluorine–chlorine fugacity of the corresponding tonalitic magma during its emplacement and crystallization. The crystallization conditions, including temperature (T), pressure (P) and oxygen fugacity (fO2), were calculated by applying the hornblende–plagioclase and magnetite–ilmenite thermometers and the Al‐in‐hornblende barometer. The thermobarometric data indicate that the tonalite porphyries were emplaced at 764 ± 22°C and 1.5 ± 0.3 × 105 kPa. If the pressure is assumed to be lithostatic, it is interpreted that the rim of hornblende and plagioclase phenocrysts crystallized at depths of approximately 5.5 km. As estimated from magnetite–ilmenite thermometry, the subsolidus conditions of the tonalite intrusion occurred at temperatures of 540–590°C and log fO2 ranging from ?20 to ?15 (between Ni‐NiO and hematite–magnetite buffers). This occurred at relatively high fO2 (oxidizing) condition. The fluorine–chlorine fugacity in the magma during crystallization was determined on the basis of the chemical composition of magmatic biotite. The calculation indicates that the fluorine–chlorine fugacity, represented by log (fH2O)/(fHF) and (fH2O)/(fHCl) in the corresponding tonalitic magma range from 4.31 to 4.63 and 3.62 to 3.79, respectively. The chlorine fugacity (HCl) to water (H2O) is relatively higher than the fluorine fugacity (HF to water), reflecting a high activity of chlorine in the tonalitic magma during crystallization. The relatively higher activity of chlorine (rather than fluorine) may indicate the significant role of chloride complexes (CuCl2? and AuCl2?) in transporting and precipitating copper and gold at the Batu Hijau deposit.  相似文献   

17.
Primitive CO3.00–3.1 chondrites contain ∼2-8 vol.% magnetite, minor troilite and accessory carbide and chromite; some CO3.1 chondrites have fayalite-rich veins, chondrule rims and euhedral matrix grains. All CO3.00–3.1 chondrites contain little metallic Fe-Ni (0.4–1.2 vol.%). CO3.2–3.7 chondrites contain 1–5 vol.% metallic Fe-Ni, minor troilite, accessory chromite and 0-0.6 vol.% magnetite. Magnetite is formed in primitive CO3 chondrites from metallic Fe by parent-body aqueous alteration, resulting in decreased metallic Fe-Ni and an increase in the proportion of high-Ni metal grains. The paucity or absence of magnetite in CO chondrites of subtype ≥3.2 suggests that magnetite is destroyed during thermal metamorphism; thermochemical calculations from the literature suggest that magnetite is reduced by H2 and reacts with SiO2 to form fayalite and secondary kamacite. Analogous processes of magnetite formation and destruction occur in other chondrite groups: (1) Primitive type-3 OC have opaque assemblages containing magnetite, carbide, Ni-rich metal and Ni-rich sulfide, but OC of subtype >3.4 contain little or no magnetite. (2) Primitive R3 chondrites and clasts (subtype ≲3.5) contain up to 6 vol.% magnetite, but most R chondrites contain no magnetite. The principal exception is magnetite with 9–20 wt.% Cr2O3 in a few R4-6 chondrites. Magnetite grains with high Cr2O3 behave like chromite and are more stable under reducing conditions. (3) CK chondrites average ∼4 vol.% magnetite with substantial Cr2O3 (up to ∼15 wt.%); these magnetite grains also are stable against reduction during metamorphism. (4) The modal abundance of magnetite decreases with metamorphic grade in CV3 chondrites. (5) Chromite occurs instead of magnetite in those rare samples classified CR6, CR7 and CV7.  相似文献   

18.
Petrological characteristics of granitic rocks related to the world large molybdenum deposits are studied. The granitoids are evaluated by Fe2O3+TiO2‐FeO+MnO‐MgO diagrams, and found to all plot to the magnetite‐series field. They are all high silica and high‐K series, but not A‐type, except for the Climax‐type porphyries and some others in the Colorado mineral belt. By‐product molybdenum contained in porphyry copper deposits, lower grade but huge tonnage, occurs with calc‐alkaline I‐type magnetite‐series granodiorite and monzogranite. Felsic intrusive rocks of the Climax mine are A‐type and are exceptionally high in trace elements such as F and Rb, which are generally enriched with W and Sn‐related granitoids that originated in crustal source rocks. The by‐product molybdenites in porphyry copper deposits appear to originate in adakitic granodiorite or monzogranite, having deep origins with the subducted slab or thickened juvenile mafic lower crust. Therefore, there is no single magma type but the magnetite series, which concentrates a large volume of molybdenum in the ore deposits.  相似文献   

19.
迟广成  伍月 《岩矿测试》2014,33(3):353-358
晶体矿物学理论认为不同成岩环境金伯利岩中尖晶石族矿物由于形成物理化学条件不同,其晶体结构和化学成分会发生明显的变化,通过对无矿、贫矿、富矿金伯利岩岩管中的尖晶石族矿物晶胞参数和化学成分的测定,研究尖晶石族矿物化学成分和晶胞参数变化与无矿、贫矿、富矿金伯利岩的内在关系,可以提高金伯利岩型金刚石矿床找矿效率。为了确定辽宁瓦房店金伯利岩中的尖晶石族矿物种属,探讨辽宁瓦房店金伯利岩中尖晶石族矿物化学成分和晶胞参数与金伯利岩含矿性关系,本文运用电子探针波谱仪对50件尖晶石族矿物中的MgO、FeO、TiO2、Al2O3、MnO及Cr2O3进行微区化学成分分析,运用单晶X射线衍射仪对136个尖晶石族矿物晶胞参数进行测定。数据统计显示:瓦房店金伯利岩中尖晶石族矿物为铬铁矿和镁铬铁矿,以化学分子式中A、B组主要阳离子占位特征为基础,可把矿区的尖晶石族矿物划分为10个亚种;如果用尖晶石族矿物化学成分中Cr2O3与(Cr2O3+Al2O3)含量的比值Cr'来表示尖晶石族矿物与金伯利岩含矿性的关系,金伯利岩岩体含矿性由富矿→中等含矿→贫矿,相应岩体中尖晶石族矿物Cr'值分别为89.5%、83.4%~87.1%和70.2%,逐渐变低;从无矿金伯利岩岩体→贫矿和中等含矿金伯利岩岩体→富矿金伯利岩岩体,金伯利岩体中第一世代尖晶石族矿物晶胞参数分别为0.831~0.832 nm、0.834~0.836 nm、0.837 nm,有逐渐变大的趋势。本文认为,辽宁瓦房店金伯利岩中第一世代尖晶石族矿物晶胞参数大小和Cr'参数可以作为判断辽宁瓦房店金伯利岩含矿性的指示标型。  相似文献   

20.
The processes of differentiation in the magmatic chamber of the Ioko-Dovyren layered dunite-troctolite-gabbro-gabbronorite massif were simulated using the COMAGMAT-3.5 software package, which is based on the convection-accumulation model for the crystallization of magmatic intrusions. The initial magma composition was assumed to be equal to the weighted mean composition of the rocks composing the intrusion (wt %: 43.92 SiO2, 9.72 Al2O3, 10.53 FeO, 27.88 MgO, 6.99 CaO, 0.59 Na2O, 0.07 K2O, and 0.11 TiO2). The results obtained by simulating the crystallization of this composition within a pressure range of 0–10 kbar indicate that the crystallization sequence determined for the rocks Ol + ChrOl+ Pl+ ChrOl + Pl+ CPx → ± Ol + Pl+ CPx + LowCaPx in an anhydrous system takes place under pressures of 0–2 kbar. A series of simulations for a system closed with respect to oxygen yielded estimates for the phase and chemical composition of the emplaced magma and the parameters of the optimum model, which reproduces accurately enough the geochemical structure of the Ioko-Dovyren intrusion: the naturally occurring distributions of minerals and components in its vertical section. The correlation coefficients between the concentrations of oxides determined in the rocks and calculated within the model are \(r_{MgO,Al_2 O_3 ,CaO} \) ≥ 0.9 and \(r_{FeO,SiO_2 ,Na_2 O} \) ≥ 0.6. The simulated phase composition of the magma during its emplacement corresponded to melt + olivine (Fo 89). The crystallinity of the parental magma was determined to have been equal to approximately 40 vol % at an assumed cumulus density of 90% near the lower contact and 70% near the upper one. The temperature of the magma during its emplacement was close to 1340°C at a pressure of 1 kbar. In the model, plagioclase and clinopyroxene appear on the liquidus at T?1255°C at T?1210°C, respectively, and the crystallization sequence of cumulus minerals corresponds to that observed in nature. The liquid phase (melt) of the parental magma during its emplacement had the following composition (wt %): 45.95 SiO2, 15.93 Al2 O3, 14.49 MgO, 10.88 FeO, 11.46 CaO, 0.97 Na2O, 0.11 K2O, and 0.18 TiO2. Our results confirm the plausibility of the hypothesis that the inner structure of the Ioko-Dovyren intrusion was formed by the emplacement and differentiation of a single magma portion with no less than 40 vol % crystallinity.  相似文献   

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