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1.
Chromite deposits in the northern Oman ophiolite: Mineralogical constraints   总被引：1，自引：0，他引：1  
Chromite deposits in the northern Oman ophiolitic complex occur in three structural contexts, i.e., (1) at the base of the cumulate series, (2) in the top kilometer of the mantle sequence, and (3) in the deeper parts of the mantle. Types 1 and 2 are characterized by the diversity of interstitial silicates where in decreasing order of abundance olivine, clinopyroxene, orthopyroxene, plagioclase, and amphibole occur, as opposed to type 3 which contains only olivine. They differ however in ore texture. Similar silicates also occur as euhedral inclusions in chromite crystals, but their proportions are reversed. The composition of the interstitial silicates is comparable to that found in early cumulates. Type-1 and type-2 chromite deposits crystallized from a magma similar to that from which the basal cumulates formed (Al2O3, 15.1–16.1 wt%; FeO/MgO, 0.55–0.60). The type-3 chromites were derived from a magma of much lower Al2O3 content (12.5 wt%). It is considered that they belong to an older episode in the magmatic evolution of the complex.  相似文献   

2.
Summary The Neoproterozoic Bou Azzer ophiolite complex hosts numerous, small lenticular bodies of massive and disseminated chromite. Metallurgical-grade high-Mg and high-Cr spinels (cores with 48–62 wt% Cr2O3) reveal complex alteration patterns of successive Cr and Mn enrichment and loss of Al towards the rims, while the Mg# ratios [(Mg/(Mg + Fe2+)] remain almost constant. Concentration patterns of platinum-group elements are typical for ophiolitic chromitite poor in sulfides, with predominance of the IPGE, variable Rh, and low Pt and Pd. The most abundant platinum-group mineral is Rh-bearing laurite that occurs either included in spinel or in silicate matrix, whereas Os-Ir-Ru alloy is always included in spinel. Laurite inclusions reveal complex intergrowth textures with Rh-Ru-Pt rich alloy, and with Rh-rich sulfide. Most laurites display trends to sulfur-poor compositions leading to local formation of very fine-grained Ru-Os-Ir alloy phases. Ni-Co-Fe sulfides, arsenides and sulfarsenides devoid of PGE are associated with the alteration of chromite. Textural position and chemical composition of the base metal inclusions, as well as comparison of alteration features between chromite and accessory chromian spinel in the Co-Ni-As ores of the Bou Azzer ophiolite indicate a close connection. It is suggested that hydrothermal fluids percolated through the marginal zones of the ophiolite belt during greenschist facies metamorphism and deposited Ni-Co-Fe arsenides, sulfarsenides and minor sulfides as accessories within altered chromitites, and also in structurally favourable zones as Ni-Co-As ores. Author’s address: Dr. Frank Melcher, Federal Institute for Geosciences and Natural Resources, Stilleweg 2, 30655 Hannover, Germany  相似文献   

3.
The chromiferous ultramafic rocks of Sukinda Valley (21°0'–21°5'N:85°43'–86°0'E) of Orissa are intrusive into the Iron-Ore Supergroup (2,950–3,200 Ma) at the eastern periphery of the Indian Precambrian shield. Both laterally and vertically, chromite occurs as persistent layers, lenses or pockets in the serpentinized and silicified dunite-peridotite extending over a strike length of 25 km. The ultramafic rocks and the chromitite layers are cofolded with the Iron-Ore Supergroup into a plunging syncline. Primary layering, ball and pillow structures, cross laminations, graded bedding etc. can also be detected. The different varieties of chromite ore present in the area are massive, banded and spotted, laminated and friable. The grain size of chromite varies between 0.25 and 4 mm, and the fineness of the grain increases from the bottom to the top layers. The cell dimension of chromite (8.23–8.32 Å) decreases with the increase of Al2O3.Cr2O3 in pure chromite varies between 48 to 61 wt. percent, Al2O3 is 7.10–15.09 wt. percent, whereas Fe2O3 is very low (0.03–3.20 wt. percent). The amount of RO to R2O3 varies within a narrow limit of 0.98–1.13, indicating that the chromite is chemically balanced. The FeO to MgO ratio is intermediate between the stratiform and alpine type. Fe3+ and Al3+ increase with respect to Cr3+ and Mg2+ in the upper chromitite layers. TiO2 lacks significant correlation with the major element composition of chromite.It is concluded that the Sukinda Valley chromitites of Orissa are predominantly stratiform in nature and were presumably formed in situ by crystal settling, the layering having been accentuated by the fluctuation of FO2. The geological features suggest a single magmatic cycle.  相似文献   

4.
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   

5.
This paper describes a suite of peridotite xenoliths. some carrying diamonds at high grades, from the richly diamondiferous early Proterozoic (1180 Ma) Argyle (AK1) lamproite pipe, in northwestern Australia. The peridotites are mostly coarse garnet lherzolites but also include garnet harzburgite, chromite — garnet peridotite, a garnet wehrlite, and an altered spinel peridotite with extremely Cr-rich chromite. In all cases the garnet has been replaced by a kelyphite-like, symplectic intergrowth of Alrich pyroxenes, Al-spinel and secondary silicates. The peridotites have refractory compositions characterized by high Mg/(Mg+Fe) and depletion in lithophile elements (Al2O3 and CaO < 1%, Na2O0.03%) and high field strength cations such as Ti, Zr, Y, and Yb. Olivines have high Mg/(Mg+Fe) (Mg 91–93 ) and, like olivine inclusions in diamonds from the Argyle pipe, contain detectable amounts of Cr2O3 (0.03%–0.07%) but have very low CaO contents (typically 0.04%–0.05%). Enstatites (Mg 92–94 ) have comparatively high Cr2O3 (0.2%–0.45%) and Na2O (up to 0.18%) but very low Al2O3 contents (0.5%–0.7%). Diopsides (Mg 92–94 , Ca/(Ca+Mg+Fe)=0.37–0.43) are Cr-rich (0.7%–1.9% Cr2O3) and have low Al2O3 (0.7%–2.2%) and Na2O (0.5%–1.6%) contents. Many have high K2O contents, typically 0.1%–0.4% but up to 1.3% K2O in one xenolith. The chromite coexisting with former garnet is Mg-and Cr-rich [Mg/(Mg+Fe2+)=0.68–0.72, Cr/(Cr+Al)=0.72–0.79] whereas chromite in the spinel peridotite is even more Cr-rich (65% Cr2O3, Cr/(Cr+Al)=0.85, resembling inclusions in diamond. One highly serpentinized former garnet peridotite contains a Cr-rich (up to 13% Cr2O3) titanate resembling armalcolite but containing significant K2O (1%–2.5%), CaO (0.6%–2.2%), ZrO2 (0.1%–0.8%), SrO (0.1%–0.3%), and BaO (up to 0.58%): this appears to have formed as an overprint of the primary mineralogy. Temperatures and pressures estimated from coexisting pyroxenes and reconstructed garnet compositions indicate that the garnet lherzolites equilibrated at 1140°–1290° C and 5.0–5.9 GPa (160–190 km depth), within the stability field of diamond. Oxygen fugacties within the diamond forming environment are estimated from spinel-bearing assemblages to be reducing, with f O2 between MW and IW. The presence of significant K in the diopsides from the peridotite xenoliths and in diopsides from heavy mineral concentrate from the Argyle pipe implies metasomatic enrichment of the subcontinental lithosphere within the diamond stability field. The P-T conditions estimated for the Argyle peridotites demonstrate that diamondiferous lamproite magmas incorporate mantle xenoliths from similar depths to kimberlites in cratonic settings, and imply that Proterozoic cratonized orogenic belts can have lithospheric roots of comparable thickness to beneath Archaean cratons. These roots lie at the base of the lithosphere within the stability field of diamond. The xenoliths, the calcic nature of chrome pyropes from heavy mineral concentrate, and the diamond inclusion assemblage indicate that the lighosphere beneath the Western Australian lamproites is mostly depleted lherozolite rather than the harzburgite commonly found beneath Archaean cratons. Nevertheless, the dominance of eclogitic paragenesis inclusions in Argyle diamonds indicates a significant proportion of diamondiferous eclogite is also present. The form, mineral inclusion assemblage, and the C-isotopic composition of diamonds in the peridotite xenoliths suggest that disaggregated diamondiferous peridotites are the source of the planar octahedral diamonds which constitute a minor component of the Argyle production. These diamonds are believed to have formed from mantle carbon in reduced, refractory peridotite (Iherzolite-harzburgite) in contrast to the predominant strongly 13C-depleted eclogitic suite diamonds which contain a recycled crustal carbon component. The source region of the lamproites has undergone long-term (2 Ga) enrichment in incompatible elements.  相似文献   

6.
Al-spinels in primitive arc volcanics   总被引：1，自引：0，他引：1  
Summary Al-rich spinels (100Cr/(Cr + Al) < 5, Al2O3 > 50 wt%) are common in alpine peridotites, both terrestrial and lunar mafic and ultramafic cumulates, and in certain metamorphic rocks, but they are apparently rare in terrestrial volcanic rocks. Here we describe the occurrence of Al-rich spinel inclusions in olivine phenocrysts in island arc volcanic rocks from five new localities: Bukit Mapas (Sumatra) and eastern Bali in the Sunda arc, and Epi, Merelava, and Ambrym islands in the Vanuatu arc. More commonly, relatively Cr-rich spinels also occur as inclusions in the saine olivine phenocrysts, and it appears that the Cr-poor aluminous spinels must be in disequilibrium with the host basaltic melts. In the rocks studied, Al-rich spinels also coexist with trapped silicate glasses and highly aluminous clinopyroxene in melt inclusions in olivine. This paragenesis suggests an origin involving contamination by localized Al-rich melt pockets as opposed to a xenocrystic origin. Two mechanisms to produce this high-Al melt in basaltic magma chambers are suggested: (1) localized high-Al melt production by complete breakdown of assimilated lower crustal gabbroic rocks. In this model the high-Al melt may crystallise Al-rich spinels which are subsequently trapped as solid inclusions by phenocryst phases of the host basaltic melt or may be trapped as melt inclusions in which Al-rich spinels and Al-rich clinopyroxene crystallise as daughter phases, and (2) in congruent breakdown of amphibole in amphibole-rich cumulates in sub-arc, or sub-OIB volcano magma chambers. The latter reaction produces a melt with 20–22% of Al2O3, aluminous clinopyroxene, Al-rich spinel and olivine. Mixing between these amphibole breakdown products and host basaltic melt may occur throughout the evolution of a magmatic system, but particularly during recharge with hot magnesian basalt batches. Aluminous spinels and aluminous clinopyroxene produced during amphibole breakdown, or perhaps crystallised from aluminous melt produced in the saine reaction, are incorporated into the magma during recharge, and subsequently trapped, together with the coexisting Cr-spinels, by crystallising olivine and clinopyroxene.
Al-Spinelle in primitiven Inselbogen-Vulkaniten
Zusammenfassung Al-reiche Spinelle (100Cr/(Cr + Al) < 5, Al2O3 > 50 Gew.%) sind in alpinen Peridotiten, in terrestrischen und lunaren mafischen und ultramafischen Kumulaten und in manchen metamorphen Gesteinen weit verbreitet, aber sie scheinen in terrestrischen, vulkanischen Gesteinen selten zu sein. Wir beschreiben hier das Vorkommen von Al-reichen Spinell-Inklusionen in Olivinkristallen von Inselbogen-Vulkaniten von 5 neuen Lokalitäten: Bukit Mapas (Sumatra) und Ost-Bali im Sunda-Bogen und die Inseln Epi, Merelava und Ambrym im Vanuatu-Bogen. Relativ Cr-reiche Spinelle kommen häufiger auch als Einschlüsse in denselben Olivin-Kristallen vor, und es scheint, daß Chrom-arme Aluminiumspinelle im Ungleichgewicht mit ihren basaltischen Mutterschmelzen stehen. In den untersuchten Gesteinen kommen Al-reiche Spinelle zusammen mit Silikatgläsern und Aluminium-reichen Klinopyroxenen in Schmelzeinschlüssen in Olivinen vor. Diese Assoziation weist auf einen Ursprung hin, der Kontamination durch lokalisierte Al-reiche pockets von Schmelze involviert; dies steht im Gegensatz zu einem Ursprung als Xenokristalle. Wir schlagen zwei Mechanismen vor, die diese Aluminium-reiche Schmelze in basaltischen Magmakammern erzeugen können: (1) lokalisierte Produktion von Aluminium-reicher Schmelze durch vollkommene Auflösung von assimilierten gabbroischen Gesteinen aus der unteren Kruste. In diesem Modell kann die Aluminium-reiche Schmelze Al-reiche Spinelle kristallisieren, die dann anschließend als feste Einschlüsse von Phenokristallen in der basaltischen Mutterschmelze eingefangen werden oder als Schmelzeinschlüsse, in denen Al-reiche Spinelle und Al-reiche Klinopyroxene als Tochterphasen kristallisieren. (2) Inkongruenter Zerfall von Amphibol in Amphibol-reichen Kumulaten in Magmakammern unter Inselbögen oder unter OIB-Vulkanen. Die letztgenannte Reaktion erzeugt eine Schmelze mit ungefähr 20–22% Al2O3, Aluminium-haltigen Klinopyroxen, Al-reichen Spinell und Olivin. Mischung zwischen diesen Produkten des Zerfalls von Amphibol und basaltischer Mutterschmelze kann während der ganzen Evolution eines magmatischen Systems stattfinden, aber besonders während der Zufuhr neuer heißer Magnesium-reicher Basalte. Aluminium-haltige Spinelle und Klinopyroxene, die während des Zerfalls von Amphibol entstanden sind oder vielleicht aus einer Aluminium-haltigen Schmelze in derselben Reaktion produziert wurden, werden während der Neuzufuhr in das Magma inkorporiert und im Anschluß daran, zusammen mit den koexistierenden Cr-Spinellen, von kristallisierendem Olivin und Klinopyroxen eingefangen.

With 6 Figures  相似文献   

7.
The mantle section of Al'Ays ophiolite consists of heterogeneously depleted harzburgites, dunites and large-sized chromitite pods. Two chromitite-bearing sites (Site1 and Site2), about 10 km apart horizontally from one another, were examined for their upper mantle rocks. Cr-spinels from the two sites have different chemistry; Cr-rich in Site1 and Al-rich in Site2. The average Cr-ratio = (Cr/(Cr + Al) atomic ratio) of Cr-spinels in harzburgites, dunites and chromitites is remarkably high 0.78, 0.77 and 0.87, respectively, in Site1, compared with those of Site2 which have intermediate ratio averages 0.5, 0.56 and 0.6, respectively. The platinum-group elements (PGE) in chromitites also show contrasting patterns from Site1 to Site2; having elevated IPGE (Os, Ir, Ru) and strongly depleted in PPGE (Rh, Pt, Pd) with steep negative slopes in the former, and gentle negative slopes in the latter. The oxygen fugacity (Δlog fO2) values deduced from harzburgites and dunites of Site1 show a wide variation under reducing conditions, mostly below the FMQ buffer. The Site2 harzburgites and dunites, on the other hand are mostly above the FMQ buffer. Two magmatic stages are suggested for the lithospheric evolution of Al'Ays ophiolite in response to a switch of tectonic setting. The first stage produced a peridotites–chromitites suite with Al-rich Cr-spinels, possibly beneath a mid-ocean ridge setting, or most likely in back-arc rift of a supra-subduction zone setting. The second stage involved higher degrees of partial melting, produced a peridotites–chromitites suite with Cr-rich Cr-spinels, possibly in a fore-arc setting. The coexistence of compositionally different mantle suites with different melting histories in a restricted area of an ophiolite complex may be attributable to a mechanically juxtaposed by mantle convection during recycling. The mantle harzburgites and dunites are apt to be compositionally modified during recycling process; being highly depleted (Site1 case) than their original composition (Site2 case).  相似文献   

8.
西藏罗布莎蛇绿岩中不同产出的纯橄岩及成因探讨   总被引：2，自引：2，他引：0  
罗布莎蛇绿岩中的纯橄岩有三种产出情况,除了与豆荚状铬铁矿伴生的薄壳状纯橄岩外,还有产在方辉橄榄岩底部被认为是堆晶岩的厚层状纯橄岩和方辉橄榄岩中的透镜状纯橄岩。厚层状纯橄岩约700～1000m厚,以橄榄石富镁(Fo93～95),单斜辉石低铝富镁(Al2O30.47%～0.85%,Mg#95～97),铬尖晶石高铬低镁(Cr#值平均77,Mg#平均51)为特征。该纯橄岩中的浸染状铬铁矿也是高铬低镁型,但Mg#值(平均59)高于厚层状纯橄岩的副矿物铬尖晶石。薄壳状纯橄岩与厚层状纯橄岩成分相近,其橄榄石Fo92～94,单斜辉石Al2O3<1%和Mg#95～97;铬尖晶石的Cr#值平均71,Mg#值平均52。与薄壳状纯橄岩伴生的块状铬铁矿为高镁高铬型,但Mg#值(平均68)相对更高些,Cr#值平均79。透镜状纯橄岩的特征是橄榄石Fo(91～92)和铬尖晶石Cr#(60左右)均低于前两类纯橄岩,但单斜辉石的Al2O3(1.41%～1.71%)则高于前两者。透镜状纯橄岩的矿物成分与方辉橄榄岩重叠,两者为渐变过渡关系。研究对比表明,罗布莎厚层状纯橄岩不同于经典的蛇绿岩的超镁铁质堆晶岩,认为将其成因解释为拉斑玄武质熔体与地幔橄榄岩的反应较为合理。透镜状纯橄岩与方辉橄榄岩存在成生联系,可能是地幔橄榄岩高度部分熔融的产物,或熔体和方辉橄榄岩在原位发生反应的产物;薄壳状纯橄岩成因与厚层状纯橄岩相同,但与其相伴的块状铬铁矿是否由拉斑玄武质熔体与方辉橄榄岩反应形成,值得商榷。  相似文献   

9.
东波超镁铁岩体产在雅鲁藏布江缝合带的西段,与周边白垩纪沉积岩地层和火山岩以断层接触.航磁资料显示该岩体约400km2规模,地表出露连续,地下有一定延深.超镁铁岩体由亏损的地幔橄榄岩组成,主要有高镁的方辉橄榄岩、纯橄岩和少量二辉橄榄岩.方辉橄榄岩和二辉橄榄岩中橄榄石和斜方辉石属高镁型,分别为Fo=89.5～91.5和Mg#=90～91.5.但二辉橄榄岩中的Al2O3和CaO含量明显高于方辉橄榄岩.方辉橄榄岩中单斜辉石Mg#=92～95,二辉橄榄岩的Mg#=92～93,两者的值也重叠.二辉橄榄岩中的Al2O3和CaO含量要明显高于方辉橄榄岩.这些均为阿尔卑斯型地幔橄榄岩的典型特征.纯橄岩中的橄榄石Fo=92～93.2,其斜方辉石和单斜辉石的Mg#=～93,但Al2O3和CaO的含量比方辉橄榄岩和二辉橄榄岩的低.三种岩石的成分变化规律,反映了地幔部分熔融程度的差异.二辉橄榄岩铬尖晶石的Cr#值20～30,反映为典型深海橄榄岩特征,指示MOR环境.与其不同的是,方辉橄榄岩的铬尖晶石的Cr#=20～75,指示MOR和SSZ两者兼有环境.岩石的原始地幔标准化的REE和微量元素蛛网图模式支持了上述的认识.东波地幔橄榄岩中的岩石学特征与产有大型铬铁矿床的罗布莎地幔橄榄岩可对比,岩体中已多处发现块状铬铁矿石,其铬铁矿的Cr2O3含量56％～59％,表明东波是寻找铬铁矿大矿和富矿甚具前景的一个超镁铁岩体.  相似文献   

10.
The Jurassic Bangong Lake ophiolite, NW Tibet, is a key element within the western part of the Bangong–Nujiang suture zone, which marks the boundary between the Lhasa and Qiangtang blocks. It is a tectonic mélange consisting of numerous blocks of peridotite, mafic lavas and dikes. The mantle peridotites include both clinopyroxene-bearing and clinopyroxene-free harzburgites. The Cpx-bearing harzburgite contains Al-rich spinel with low Cr#s (20–25), resembling peridotites formed in mid-ocean ridge settings. On the other hand, the Cpx-free harzburgite is highly depleted with Cr-rich spinel (Cr# = 69–73), typical of peridotites formed in subduction zone environments. Mafic rocks include lavas of N-MORB and E-MORB affinity and boninites. The N-MORB rocks consist of pillow lavas and mafic dikes, whereas the E-MORB rocks are brecciated basalts. The boninites have high SiO2 (53.2–57.9 wt%), MgO (6.5–12.5 wt%), Cr (166–752 ppm) and Ni (63–213 ppm) and low TiO2 (0.22–0.37 wt%) and Y (5.34–8.10 ppm), and are characterized by having U-shaped, chondrite-normalized REE patterns. The N-MORB and E-MORB lavas probably formed by different degrees of partial melting of primitive mantle, whereas the boninites reflect partial melting of depleted peridotite in a suprasubduction zone environment. The geochemistry of the ophiolite suggests that it is a fragment of oceanic lithosphere formed originally at a mid-ocean ridge (MOR) and then trapped above an intraoceanic subduction zone (SSZ), where the mantle peridotites were modified by boninitic melts. The Bangong–Nujiang suture zone is believed to mark the boundary between two blocks within Gondwanaland rather than to separate Gondwanaland from Eurasia.  相似文献   

11.
ABSTRACT

A chromite deposit was discovered in the Kudi ophiolite in the Palaeozoic western Kunlun orogenic belt. Chromite forms elongated (<2 m in width) and banded chromitite bodies (<0.1 m in width for each band) in dunite and podiform chromitite bodies (<1.5 m in width) in harzburgite. Dunite is classified into two types. Type I dunite hosting massive and banded chromitites shows low Fo in olivine (88.1–90.9), moderate Cr# [=Cr/(Cr + Al), 0.47–0.56] in chromite, and a positively sloped primitive mantle-normalized platinum group elements (PGE) pattern, suggesting that it is a cumulate of a mafic melt. Harzburgite and type II dunite show olivine with high Fo (>91.1) and chromite with moderate to high Cr# (0.44–0.61), and flat to negatively sloped primitive mantle-normalized PGE patterns, indicating that they are residual mantle peridotite after partial melting. Chromite in all three types of chromitites has relatively uniform moderate values Cr# ranging from 0.43 to 0.56. Massive chromitite contains euhedral chromite with high TiO2 (0.40–0.43 wt.%) and has a positively sloped primitive mantle-normalized PGE pattern, suggesting that it represents a cumulate of a melt. Rocks containing disseminated and banded chromite show overall low total PGE, < 117 ppb, and a negatively sloped primitive mantle-normalized PGE pattern. Chromite grains in these two types of occurrences are irregular in shape and enclose olivine grains, suggesting that chromite formed later than olivine. We suggest that chromite-oversaturated melt penetrated into the pre-existing dunite and crystallized chromite. The oxygen fugacity (fO2 values of chromitites and peridotites are high, ranging from FMQ+0.8 (0.8 logarithmic unit above the fayalite-magnetite-quartz buffer) to FMQ+2.3 for chromitites and from FMQ+0.9 to FMQ+2.8 for peridotites (dunite and harzburgite). The mineral compositions and high fO2 values as well as estimated parental magma compositions of the chromitites suggest that the Kudi ophiolite formed in a sub-arc setting.  相似文献   

12.
The Bracco–Gabbro Complex (Internal Liguride ophiolite), that intruded subcontinental mantle peridotite, contains layers of chromitite that are associated with ultramafic differentiates. The chromitites and disseminated chromites in the ultramafics have Al contents similar to the Al-rich podiform chromitites [0.40 < Cr# = Cr/(Cr + Al) < 0.55]. TiO2 contents of the chromitites are unusually high and range up to 0.82 wt%. The calculated Al2O3 and TiO2 content of the parental melt suggest that the melt was a MORB type. Geothermobarometrical calculations on few preserved silicate inclusions revealed formation temperatures between 970 and 820 °C under a relatively high oxygen fugacity (ΔlogfO2 at +2.0–2.4). Chromitites were altered during the post-magmatic tectono-metamorphic uplift and the final exposure at the seafloor, as evidenced by the formation of ferrian chromite. The PGE contents of the chromitites and associated ultramafics are unusually low (PGEmax 83 ppb). The chondrite-normalized PGE spidergrams show positive PGE patterns and to some extent similarities with the typical trend of stratiform chromitites. No specific PGM have been found but low concentrations of PPGE (Rh, Pt, and Pd) have been detected in the sulphides that occur interstitially to or enclosed in chromite. Recently, it has been shown that the Internal Liguride gabbroic intrusions have formed by relatively low degrees of partial melting of the asthenospheric mantle. We conclude that the low degree of partial melting might be the main factor to control the unusual low PGE contents and the rather unique PGE distribution in the Bracco chromitites.  相似文献   

13.
鲍佩声 《地质通报》2009,28(12):1941-1961
着重论述了蛇绿岩地幔橄榄岩中豆荚状铬铁矿的成因,并对现今盛行的岩石/熔体反应成矿说提出了质疑。世界含铬铁矿的地幔橄榄岩均显示上部偏基性、下部偏酸性的垂直熔融分带,与蛇绿岩堆晶岩中上部偏酸性、下部偏基性的岩浆分异垂直层序恰恰相反。豆荚状铬铁矿与熔融剖面上部的纯橄岩或纯橄岩-方辉辉橄岩杂岩带紧密伴生。豆荚状铬铁矿是原始地幔岩高度熔融再造的产物,高铬型铬铁矿与PPG型蛇绿岩伴生,形成于岛弧或弧前盆地环境;高铝型铬铁矿与PTG型蛇绿岩伴生,形成于扩张脊（MOR）或弧后盆地环境。玻安岩（boninite）与高铬型豆荚状铬铁矿无成因关系,铬铁矿（或富铬矿浆）的形成反而为boninite提供了其形成所需的残余地幔;高铝型铬铁矿不是地幔橄榄岩/拉斑玄武质熔体反应形成的,而是富铬矿浆与基性熔体发生再平衡的产物。豆荚状铬铁矿中超高压矿物包体的出现为其地幔深部成因提供了佐证,而boninite形成于浅部较低压的条件;豆荚状铬铁矿中富集强相容元素IPGE（Os、Ir、Ru）合金,boninite富集不相容元素PPGE (Pt、Pd)硫（砷）化物, 而亏损IPGE,显示其形成较晚。因此,boninite与铬铁矿无生因关系,两者均受岛弧（或弧前盆地）环境的制约而在空间上相伴产出。  相似文献   

14.
The Mayarí-Baracoa ophiolitic belt in eastern Cuba hosts abundant chromite deposits of historical economic importance. Among these deposits, the chemistry of chromite ore is very variable, ranging from high Al (Cr#=0.43–0.55) to high Cr (Cr#=0.60–0.83) compositions. Platinum-group element (PGE) contents are also variable (from 33 ppb to 1.88 ppm) and correlate positively with the Cr# of the ore. Bulk PGE abundances correlate negatively with the Pd/Ir ratio showing that chromite concentrates mainly Os, Ir and Ru which gives rise to the characteristic negatively sloped, chrondrite-normalized PGE patterns in many chromitites. This is consistent with the mineralogy of PGEs, which is dominated by members of the laurite–erlichmanite solid solution series (RuS2–OsS2), with minor amounts of irarsite (IrAsS), Os–Ir alloys, Ru–Os–Ir–Fe–Ni alloys, Ni–Rh–As, and sulfides of Ir, Os, Rh, Cu, Ni, and/or Pd. Measured 187Os/188Os ratios (from 0.1304 to 0.1230) are among the lower values reported for podiform chromitites. The 187Os/188Os ratios decrease with increasing whole-rock PGE contents and Cr# of chromite. Furthermore, γOs values of all but one of the chromitite samples are negative indicating a subchondiritc mantle source. γOs decrease with increasing bulk Os content and decreasing 187Re/188Os ratios. These mineralogical and geochemical features are interpreted in terms of chromite crystallization from melts varying in composition from back-arc basalts (Al-rich chromite) to boninites (Cr-rich chromite) in a suprasubduction zone setting. Chromite crystallization occurs as a consequence of magma mixing and assimilation of preexisting gabbro sills at the mantle–crust transition zone. Cr#, PGE abundances, and bulk Os isotopic composition of chromitites are determined by the combined effects of mantle source heterogeneity, the degree of partial melting, the extent of melt-rock interactions, and the local sulfur fugacity. Small-scale (μm to cm) chemical and isotopic heterogeneities in the platinum-group minerals are controlled by the mechanism(s) of chromite crystallization in a heterogeneous environment created by the turbulent regime generated by successive inputs of different batches of melt.  相似文献   

15.
The Neoarchean (ca. 2.75 Ga) Luanga Complex, located in the Carajás Mineral Province in Brazil, is a medium-size layered intrusion consisting, from base to top, of ultramafic cumulates (Ultramafic Zone), interlayered ultramafic and mafic cumulates (Transition Zone) and mafic cumulates (Mafic Zone). Chromitite layers in the Luanga Complex occur in the upper portion of interlayered harzburgite and orthopyroxenite of the Transition Zone and associated with the lowermost norites of the Mafic Zone. The stratigraphic interval that hosts chromitites (∼150 meters thick) consists of several cyclic units interpreted as the result of successive influxes of primitive parental magma. The compositions of chromite in chromitites from the Transition Zone (Lower Group Chromitites) have distinctively higher Cr# (100Cr/(Cr + Al + Fe3+)) compared with chromite in chromitites from the Mafic Zone (Upper Group Chromitites). Chromitites hosted by noritic rocks are preceded by a thin layer of harzburgite located 15–20 cm below each chromitite layer. Lower Cr# in chromitites hosted by noritic rocks are interpreted as the result of increased Al2O3 activity caused by new magma influxes. Electron microprobe analyses on line transverses through 35 chromite crystals indicate that they are rimmed and/or extensively zoned. The composition of chromite in chromitites changes abruptly in the outer rim, becoming enriched in Fe3+ and Fe2+ at the expense of Mg, Cr, Al, thus moving toward the magnetite apex on the spinel prism. This outer rim, characterized by higher reflectance, is probably related to the metamorphic replacement of the primary mineralogy of the Luanga Complex. Zoned chromite crystals indicate an extensive exchange between divalent (Mg, Fe2+) cations and minor to none exchange between trivalent cations (Cr3+, Al3+ and Fe3+). This Mg-Fe zoning is interpreted as the result of subsolidus exchange of Fe2+ and Mg between chromite and coexisting silicates during slow cooling of the intrusion. A remarkable feature of chromitites from Luanga Complex is the occurrence of abundant silicate inclusions within chromite crystals. These inclusions show an adjacent inner rim with higher Cr# and lower Mg# (100 Mg/(Mg + Fe2+)) and Al# (100Al/(Cr + Al + Fe3+)). This compositional shift is possibly due to crystallization from a progressively more fractionated liquid trapped in the chromite crystal. Significant modification of primary cumulus composition of chromite, as indicated in our study for the Luanga Complex, is likely to be common in non-massive chromitites and the rule for disseminated chromites in mafic intrusions.  相似文献   

16.
The Xigaze ophiolite in the central part of the Yarlung–Zangbo suture zone, southern Tibet, has a well-preserved sequence of sheeted dykes, basalts, cumulates and mantle peridotites at Jiding and Luqu. Both the basalts and diabases at Jiding have similar compositions with SiO2 ranging from 45.9 to 53.5 wt%, MgO from 3.1 to 6.8 wt% and TiO2 from 0.87 to 1.21 wt%. Their Mg#s [100Mg/(Mg + Fe)] range from 40 to 60, indicating crystallization from relatively evolved magmas. They have LREE-depleted, chondrite-normalized REE diagrams, suggesting a depleted mantle source. These basaltic rocks have slightly negative Nb- and Ti-anomalies, suggesting that the Xigaze ophiolite represents a fragment of mature MORB lithosphere modified in a suprasubduction zone environment. The mantle peridotites at Luqu are high depleted with low CaO (0.3–1.2 wt%) and Al2O3 (0.04–0.42 wt%). They display V-shaped, chondrite-normalized REE patterns with (La/Gd)N ratios ranging from 3.17 to 64.6 and (Gd/Yb)N from 0.02 to 0.20, features reflecting secondary metasomatism by melts derived from the underlying subducted slab. Thus, the geochemistry of both the basaltic rocks and mantle peridotites suggests that the Xigaze ophiolite formed in a suprasubduction zone.Both the diabases and basalts have Pd/Ir ratios ranging from 7 to 77, similar to MORB. However, they have very low PGE abundances, closely approximating the predicted concentration in a silicate melt that has fully equilibrated with a fractionated immiscible sulfide melt, indicating that the rocks originated from magmas that were S-saturated before eruption. Moderate degrees of partial melting and early precipitation of PGE alloys explain their high Pd/Ir ratios and negative Pt-anomalies. The mantle peridotites contain variable amounts of Pd (5.99–13.5 ppb) and Pt (7.92–20.5 ppb), and have a relatively narrow range of Ir (3.47–5.01 ppb). In the mantle-normalized Ni, PGE, Au and Cu diagram, they are relatively rich in Pd and depleted in Cu. There is a positive correlation between CaO and Pd. The Pd enrichment is possibly due to secondary enrichment by metasomatism. Al2O3 and Hf do not correlate with Ir, but show positive variations with Pt, Pd and Au, indicating that some noble metals can be enriched by metasomatic fluids or melts carrying a little Al and Hf. We propose a model in which the low PGE contents and high Pd/Ir ratios of the basaltic rocks reflect precipitation of sulfides and moderate degrees of partial melting. The high Pd mantle peridotites of Xigaze ophiolites were formed by secondary metasomatism by a boninitic melt above a subduction zone.  相似文献   

17.
Potential chromite ore deposits of India are situated in Sukinda, Odisha, which may also be considered as a potential resource for platinum group elements (PGEs). This paper reports on PGE geochemistry in twenty six samples covering chromite ores, chromitites and associated ultramafic rocks of the Sukinda ultramafic complex. Platinum group element contents range from 213 to 487 ppb in the chromite ore body, from 63 to 538 ppb in rocks that have chromite dendrites or dissemination and from 38 to 389 ppb in associated olivine–peridotite, serpentinite, pyroxenite and brecciated rocks. The PGEs are divided into two sub‐groups: IPGE (Ir, Os, and Ru) and PPGE (Pd, Pt, and Rh) based on their chemical behaviour. The IPGE and PPGE in these three litho‐members show a contrasting relationship e.g. average IPGE content decreases from chromite to chromitite and associated rocks while PPGE increases in the same order. Appreciable Ag in chromitite (270–842 ppb) is recorded. Positive correlation between IPGE with Cr2O3 and with Al2O3 is observed while these are negatively correlated with MgO. Covariant relationships between Au and Mg in rocks devoid of chromite and between Ag and Fe in chromitite sample are observed. Chromite in all seams and some chromitite samples exhibit an IPGE‐enriched chondrite normalized pattern while PPGE are highly fractionated and show a steep negative slope, thereby indicating that PGE in the parental melt fractionates and IPGE‐compatible elements prefer to settle with chromite. The rocks devoid of chromite and rocks containing accessory chromite exhibit a nearly flat pattern in chondrite‐normalized PGE plots and this suggests a limited fractionation of PGE in these rocks. Variation in the distribution pattern of PGE and Ag in three typical litho‐members of the Sukinda Valley may be related to multiple intrusion of ultramafic magma, containing variable volume percentage of chromite.  相似文献   

18.
The Shergol ophiolitic peridotites along ISZ, Ladakh Himalaya are serpentinized to various degrees and are harzburgite in composition. Electron microprobe analyses of spinels from Shergol Serpentinized Peridotites (SSPs) were carried out in order to evaluate their compositional variation with alteration. Chemical discontinuity was observed from core to rim in analyzed spinel grains with Cr-rich cores rimmed by Cr-poor compositions. From unaltered cores to rims it was observed that Cr3+# and Fe3+# increases while Mg2+# decreases due to Mg2+ − Fe2+ and Al3+ (Cr3+) − Fe3+ exchange with surrounding silicates during alteration. These peridotites contain Al-rich spinels forming subhedral to anhedral grains with lobate and corroded grain boundaries; altered to ferritchromite or magnetite along cracks and boundaries by later metamorphism episode. The unaltered Cr-spinel cores are identified as Al-rich and are characterized by lower values of Cr3+# (0.34–0.40), high Al3+# (0.58–0.68) and Mg2+# (0.52–0.70). Mineral chemistry of these Al-rich Cr-spinels suggest that host peridotites have an affinity to abyssal and alpine-type peridotites. High TiO2 concentration of magmatic Cr-spinel cores are in agreement with MORB melt-residual peridotite interaction. Presence of unaltered magmatic Cr-spinel cores suggest that they do not have re-equilibrated completely with metamorphic spinel rims and surrounding silicates. Cr-spinel core compositions of SSPs suggest an ophiolitic origin derivation by low degrees of melting of a less-moderate depleted peridotite in a mid-ocean ridge tectonic setting. Based on textural and chemical observations the alteration conditions of studied spinel-group minerals match those of transitional greenschist-amphibolite facies metamorphism consistent with estimated metamorphic equilibration temperature of ∼ 500–600 °C.  相似文献   

19.
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   

20.
Chromite mineralization in metamorphosed dunites from the southern Klyuchevskoy dunite-harzburgite ultramafic complex (Central Urals) has been investigated using geomagnetic surveys along with laboratory studies of ore-forming and accessory spinels of the same genetic type. Magnetization in the study area is carried mainly by accessory Fe-Cr-spinel of a variable Fe2 +(Cr2 -xFex3 +)O4 composition. Metamorphism caused changes in element contents and in both crystal and magnetic structure of the primary nonmagnetic accessory spinel, unlike the almost fresh ore-forming spinel. Thus, ore bodies stand against their host rocks, which is a prerequisite for the use of geomagnetic surveys for exploration of podiform chromite deposits in dunite-harzburgite complexes. Ground magnetic surveys at a test site composed of faulted rocks bearing disseminated chromite mineralization in metamorphosed dunites resolved a chromite ore zone and a fault block boundary showing up as geomagnetic anomalies. Laboratory studies using high technologies (thermomagnetic analysis at 4 to 1000 K, as well as magnetic resonance and magnetic force spectroscopy) revealed, for the first time, magnetic clusters (superparamagnetic phases) in primary nonmagnetic accessory spinel, which are responsible for the magnetic properties of the host rocks. Microscale variations in Cr-spinel correlate with the geomagnetic anomalies recorded by field surveys at the test site.© 2015, V.S. Sobolev IGM, Siberian Branch of the RAS. Published by Elsevier B.V. All rights reserved.  相似文献   

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