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1.
Mudstone xenoliths in a strongly reduced andesitic subaquatic breccia with native iron from the Asuk Member on Disko contain Ti oxides which are oxygen deficient relative to rutile. Ore microscopy reveals that the mudstone xenoliths contain former clastic oxide grains which have equilibrated to blue Ti oxides and grey aluminous Ti oxides. They also contain still immature coal fragments in a glassy matrix with native iron.The blue oxides are compositionally similar to magnéli phases TinO2n–1 within the range n=4 to 7, and several grains contain more than one natural magnéli phase. Two other phases found are 1) pale orange blebs in magnéli phases with a composition approaching Al1Ti 1 3+ Ti 2 4+ O7 (AlTi phase B) and 2) grey oxide rims on magnéli phases or independent grains of the compositional series Al2–x(Ti 0.5 4+ (Mg,Fe)0.5)xTi n–2 4+ O2n–1 with n mostly between 7 and 10 (AlTi phase A). The natural magnéli phases equilibrated at oxygen fugacities 4 to 5 log units below the Fe-W oxygen buffer at igneous temperatures and represent the most reduced high-temperature environment yet recorded among native iron bearing rocks from Disko. The extremely reducing conditions were met in rocks where coal fragments were still in a state of degassing hydrocarbon components at the time of quenching. Field geology and carbon barometry indicate equilibration at pressures of less than 10 bars.  相似文献   

2.
Euhedral crystals of ulvöspinel are found in many of the native-iron-bearing xenoliths from the basalt of Bühl near Kassel (West Germany) and Ovifak on Disko Island (West Greenland). The typical assemblage of these xenoliths at both localities is: native Fe, troilite, cohenite, ulvöspinel, ilmenite, olivine, and plagioclase, as well as silicate glass containing droplets of former Fe and troilite melt. The ulvöspinel subsolidus textures and intergrowths also indicate identical cooling histories for the xenoliths in both cases. Ulvöspinel crystallized after the formation of iron, but still above the Fe-FeS eutectic at 988° C. A subsequent strong drop in oxygen fugacity revealed partial breakdown of ulvöspinel according to the reaction .Microprobe analyses of a Bühl xenolith indicate that ulvöspinel contains up to 4.7 w.t.% MnO, while olivine compositions correspond to Fa64–74Fo12–24Te12–15. The entire xenolith contains 1.9 w.t.% MnO. This fact, together with the geological evidence and the occurrence of corroded quartz relicts within some of the xenoliths provides clear evidence for reduction under near-surface conditions in a blast-furnace-like process. The reducing agent was coal from the Tertiary seams cut by the erupting basalt, while the xenolith source material most probably was spherosiderite, which is very common in the coals and would explain the high MnO content. Consequently, the presence of cohenite is not necessarily an indicator of high pressure.The analogies between the Bühl and Ovifak localities and their xenoliths strongly suggest a similar formation through near surface reduction and not derivation from the mantle.  相似文献   

3.
A strongly reduced native iron-bearing andesite breccia from Disko contains graphite-rich modified shale xenoliths with magnesian spinels. These spinels are free from or very poor in ferric iron and vary considerably within the MgO-FeO-Cr2O3-Al2O3 compositional space. Through a simple substitution of the type 3 (Mg, Fe)2+ ⇆ 2(Al, Cr)3++□vacancy, the spinels vary from stoichiometric (Mg, Fe)2+ (Al, Cr)3+ 2O4 towards (Al, Cr)2O3. The simple substitution of Cr for Al suggests that Cr was accepted into the spinel structure as Cr3+, despite the reduced nature of the enclosing andesite. The most magnesian spinels are cation deficient spinelss in the synthetic systems MgO-Al2O3 and MgO-Al2O3-Cr2O3. The absence of exolved (Al, Cr)2O3-component is probable due to rapid quenching.  相似文献   

4.
We have studied a large (12 × 22 × 30 cm) spinel lherzolite xenolith with undeformed margins in alkali basalt (basanite) from the eroded crater of Late Cenozoic Shavaryn Tsaram-1 volcano in western Mongolia. The xenolith was sampled along its median transversal profile, at every 15–20 mm for bulk chemistry of lherzolite and basalt (ICP-MS) and at 4–10 mm for the chemistry of olivine, orthopyroxene, clinopyroxene, and Cr-spinel minerals, and of material filling cracks (LA ICP-MS). Incompatible elements (especially, LREE) are distributed unevenly over the xenolith, both in lherzolite and in its constituent minerals, as well as in crack-filling material, with abnormal LREE enrichment in some specimens. Judging by the measured trace-element spectra compared with the model patterns, incompatible elements reside in different amounts as interstitial impurity in cracks inside and between mineral grains in lherzolite, also being a substitutional impurity in the lherzolite constituent minerals. Experimental acid leaching of specimens from sites of high crack density showed (La/Yb)n ratios in the crack fill to be much higher than in the basalt host and more so in bulk lherzolite (180 against 33 and 1.5–3.6, respectively). The proportional contents of P and Ca in the leaching solution, especially in that from the xenolith’s center mark the presence of an apatite microphase, which can be a LREE repository.The observed patterns of LREE and other incompatible elements in the xenolith and in the host alkali basalt fit a model implying that mobile elements residing as interstitial impurity came with fluids which were released from rising basaltic magma and percolated into the xenolith along cracks.  相似文献   

5.
We investigate the effects of xenolith–host basalt interaction on lower crustal mafic granulite xenoliths from the Central Pannonian Basin. The xenoliths are devoid of any signs of melting, nevertheless various phenomena are identified, which indicate that the original mineralogy and chemistry of the xenoliths was modified during interaction with the host basalt. The rock-forming silicates are only slightly affected by alteration, but the Fe–Ti-oxides are overprinted to a significant extent. Complex chemical zoning patterns are detected using high-resolution element mapping in ilmenites and in lamellar titanomagnetite–ilmenite intergrowths. The chemical alteration of the Fe–Ti-oxides was diffusion-controlled and, hence, time and temperature dependent. On the basis of diffusion profiles in titanomagnetite we estimate the duration of xenolith–host basalt interaction to be at least 9–20 h. This is comparable to the time necessary for the ascent of the host basalt to the surface. It is too short to reflect alteration during granulite facies metamorphism in the deep crust. The chemical alteration of the titanomagnetite thus reflects the total duration of the xenolith–host basalt interaction.  相似文献   

6.
A wide variety of rock types are present in the O'Leary Peak and Strawberry Crater volcanics of the Pliocene to Recent San Francisco Volcanic Field (SFVF), AZ. The O'Leary Peak flows range from andesite to rhyolite (56–72 wt % SiO2) and the Strawberry Crater flows range from basalt to dacite (49–64 wt % SiO2). Our interpretation of the chemical data is that both magma mixing and crustal melting are important in the genesis of the intermediate composition lavas of both suites. Observed chemical variations in major and trace elements can be modeled as binary mixtures between a crustal melt similar to the O'Leary dome rhyolite and two different mafic end-members. The mafic end-member of the Strawberry suite may be a primary mantle-derived melt. Similar basalts have also been erupted from many other vents in the SFVF. In the O'Leary Peak suite, the mafic end-member is an evolved (low Mg/(Mg+ Fe)) basalt that is chemically distinct from the Strawberry Crater and other vent basalts as it is richer in total Fe, TiO2, Al2O3, MnO, Na2O, K2O, and Zr and poorer in MgO, CaO, P2O5, Ni, Sc, Cr, and V. The derivative basalt probably results from fractional crystallization of the more primitive, vent basalt type of magma. This evolved basalt occurs as xenolithic (but originally magmatic) inclusions in the O'Leary domes and andesite porphyry flow. The most mafic xenolith may represent melt that mixed with the O'Leary dome rhyolite resulting in andesite preserved as other xenoliths, a pyroclastic unit (Qoap), porphyry flow (Qoaf) and dacite (Darton Dome) magmas. Thermal constraints on the capacity of a melt to assimilate (and melt) a volume of solid material require that melt mixing and not assimilation has produced the observed intermediate lavas at both Strawberry Crater and O'Leary Peak. Textures, petrography, and mineral chemistry support the magma mixing model. Some of the inclusions have quenched rims where in contact with the host. The intermediate rocks, including the andesite xenoliths, contain xenocrysts of quartz, olivine and oligoclase, together with reversely zoned plagioclase and pyroxene phenocrysts. The abundance of intermediate volcanic rocks in the SFVF, as observed in detail at O'Leary Peak and Strawberry Crater, is due in part to crustal recycling, the result of basalt-driven crustal melting and the subsequent mixing of the silicic melts with basalts and derivative magmas.  相似文献   

7.
Rare dunite and 2-pyroxene gabbro xenoliths occur in banded trachyte at Puu Waawaa on Hualalai Volcano, Hawaii. Mineral compositions suggest that these xenoliths formed as cumulates of tholeiitic basalt at shallow depth in a subcaldera magma reservoir. Subsequently, the minerals in the xenoliths underwent subsolidus reequilibration that particularly affected chromite compositions by decreasing their Mg numbers. In addition, olivine lost CaO and plagioclase lost MgO and Fe2O3 during subsolidus reequilibration. The xenoliths also reacted with the host trachyte to form secondary mica, amphibole, and orthopyroxene, and to further modify the compositions of some olivine, clinopyroxene, and spinel grains. The reaction products indicate that the host trachyte melt was hydrous. Clinopyroxene in one dunite sample and olivine in most dunite samples have undergone partial melting, apparently in response to addition of water to the xenolith. These xenoliths do not contain CO2 fluid inclusions, so common in xenoliths from other localities on Hualalai, which suggests that CO2 was introduced from alkalic basalt magma between the time CO2-inclusion-free xenoliths erupted at 106±6 ka and the time CO2-inclusion-rich xenoliths erupted within the last 15 ka.  相似文献   

8.
Manganiferous quartz-mica schists (4 m in stratigraphic thickness) overlie epidote amphibolite in the Chiroro River area, Hidaka Mountains, Hokkaido. The schist layers have a considerable range of A/F ratios and bulk oxidation ratios which vary from 21.5 to 100. Manganese contents are from 4 to 30 times higher than that of the average shale with 0.09% MnO. The schists are essentially quartz-white mica-biotite-Mn garnet-tourmaline-±epidote-magnetite assemblages. A highly oxidized layer (5–8 cm thick) 95 cm above the epidote amphibolite contact is characterized by viridine-piemontite-spessartine-Mn white mica-Mn tourmaline-Ti-Mn haematite indicative of both high initial manganese content and very high f O2 conditions of recrystallization.Viridine contains up to 17 mol% Mn3+SiO5 and coexists with piemontite with between 13.6 and 15.4 wt% Mn2O3. Mn-poor-Fe-rich (Ps32) epidote occurs in the less oxidized schist enclosing the viridine-piemontite bearing seam. Garnets vary widely in composition with end member variations (mol%) of Spess22.9–80.5; And0.2–11.7; Alm1.1–57.1; Pyr2.0–12.2; Gross7.0–49.0. The more manganiferous garnets occur in rocks with higher oxidation ratios while almandiferous varieties occur in schists with low oxidation ratios. Biotite ranges from green to red-brown varieties (increasing Ti and Fe) with Mg/ (Mg+Fe) ratios varying from 56 to 48. Ten to fifteen percent octahedral R2+ is replaced by Al indicating a trend towards eastonite-siderophyllite. The white micas deviate only slightly from dioctahedral stoichiometry but have up to 25% of octahedral sites occupied by Fe, Mg and to a lesser extent Mn and Ti as R2+ Si4+2Al3+ and in highly oxidized rocks as (Fe,Mn)3+Al3+. The white mica in the highly oxidized viridine-piemontite schist is pale pinkishorange, exhibits reverse pleochroism, and has between 0.30 and 0.43 wt% Mn2O3.There is a close comparison, both in terms of stratigraphic thickness and Fe-Mn variation, between the Chiroro schist sequence and many oceanic cores so that the bulk chemistry and mineralogy of the pelitic schists is largely an extension of the original Eh-pH conditions of hemipelagic sedimentation and post-depositional adjustments during diagenesis. The thin viridine-piemontite bearing schist is correlated with an oxidized, Fe-Mn rich layer commonly found in present day oceanic cores. The viridine presumably formed by reaction of original ferro-manganese microgranules and clay minerals. Halmrolytic alteration of the underlying metabasalt resulted in leaching of Mn and Fe (in particular) into the overlying sediments and the formation of concentrations of haematite — manganese oxide — Mn garnet along the schist-epidote amphibolite contact.Estimation of the P-T conditions of metamorphism from the phase relations and compositions in the epidote amphibolite associated with the manganiferous schist gives T °C = 530560 and a minimum P fluid > 3 kb which corresponds to the epidote amphibolite facies of Barrovian-type terrains.This paper is dedicated to Professor Kenzo Yagi on the occasion of his retirement from the Chair of Mineralogy, Department of Geology and Mineralogy, Hokkaido University, Sapporo, Japan  相似文献   

9.
Mineralogical-geochemical data obtained on a large xenolith of spinel lherzolite from basanites of Shavaryn Tsaram volcano (Middle Pleistocene) provide evidence that the xenolith was affected by heat and fluid that came from the basalt melt and induced geochemical heterogeneity of the xenolith. Olivine crystals from the central portion of the xenolith contain much more CaO than this mineral from the peripheral zones of the xenolith as well as in xenocrystals of the host basalts. The large xenolith was unevenly annealed by the host basalt melt, and this predetermined the heterogeneous diffusion-controlled “purification” of olivine crystals from their CaO admixture. The xenolith is heterogeneously enriched in LREE and some trace elements (Zr, Hf, Nb, Th, and U), and their distribution demonstrates unclearly pronounced concentric zoning: these elements enriched the outer portions of the xenolith. The enrichment of the xenolith in LREE and other mobile trace elements is explained by their occurrence not only as structurally bound (isomorphic) components in minerals but also in the form of nonstructural admixtures (contaminant), as minute grains of compounds hosted in the interstitial space and tiny cracks cutting mineral grains. The enrichment of the xenolith in these admixtures proceeded via their infiltration-controlled introduction with fluid from the basalt along minute cracks.  相似文献   

10.
Spinel-lherzolite xenoliths in alkali basalts from eastern China have porphyroclastic to equigranular textures displaying varying degrees of deformation and subsolidus re-equilibration. The proportions of minerals in these xenoliths vary from 52 to 72% homogeneous olivine (Fo88-91); 11 to 26% orthopyroxene (Wo0.9.1.6; En88-90; Fs8.7.10.7), with minor discontinuous variations of Al2O3, FeO, and CaO; 6 to 19% clinopyroxene (Wo43.47; En49.51; Fs3.7.6.7); and 1 to 5% spinel, with similar Mg# (79.6 to 82.6), but wider variations of Al2O3 and Cr2O3 (100Cr/(Cr + Al + Fe3+) = 8.1 to 23.6). Although previous trace-element and isotopic studies have shown that at least two distinctly different mantle sources were sampled by Cenozoic basalts, mineralogical heterogeneities seem to be minor within the spinel-peridotite-facies lithosphere beneath eastern China.

These xenoliths experienced limited interaction with the host basaltic magma during eruption. Symplectites of secondary, minute silicates, titanomagnetite, and sulfide have replaced orthopyroxene—and to a lesser extent olivine—at the contact with the basalt. The spinel in the margin of the xenolith is continuously zoned by substitutions of Fe3O4 (magnetite) and Fe2TiO4 (ulvospinel) for MgAl2O3 (spinel), and is rimmed by titanomagnetite with a sharp boundary. However, the compositions of the interior clinopyroxenes were commonly modified by metasomatic partial melting, which resulted in “spongy-textured” rinds on primary clinopyroxene. This secondary assemblage is composed mainly of a refractory, jadeite-poor clinopyroxene, which is largely in optica! continuity with the primary clinopyroxene in addition to interstitial feldspars, with minor titanomagnetite and Fe-Ni sulfides. This assemblage was produced by the introduction of K-rich fluids from the enclosing basaltic magma. The intensity of these secondary reactions appears to have been a function of the residence time of the xenolith in the host basalt. Therefore, all secondary alteration of both external and internal primary minerals in these xenoliths are the result of near-surface metasomatic processes, rather than of mantle phenomena.  相似文献   

11.
新疆觉罗塔格地区自然铜矿化玄武岩沿着阿齐库都克深大断裂北侧分布,前人对其成岩年代一直存在争议.本文测得玄武岩条带中部的黑尖山玄武岩同岩浆期锆石SHRIMP U-Pb年龄为306.2±4.0Ma;测得东部东尖峰玄武岩的同岩浆期锆石LA-ICPMS U-Pb年龄为308.9±5.8Ma,确定了玄武岩是晚石炭世的岩浆作用,且归属于晚石炭世马头滩组.与觉罗塔格地区著名的晚石炭世-早二叠世铜镍矿化基性-超基性岩成因对比表明,该晚石炭世玄武岩与之具有共同岩浆源区特征,它们都是觉罗塔格地区晚石炭世-早二叠世岩石圈地幔深部受热熔融而形成岩浆作用.马头滩组玄武岩层是自然铜矿化的重要矿源层.  相似文献   

12.
Permo-Triassic alkaline dykes in the Sunnhordland region contain angular inclusions of spinellherzolite composed of olivine (Fo89.5), high-alumina pyroxenes, and Al2O3-rich spinel. Mineral chemistry suggests that the lherzolites represent mantle material which equilibrated at temperatures in the ranges 1050 to 1150°C, compatible with an oceanic geotherm. Megacrysts of augite and spinel are associated with the xenoliths, and have compositions which differ from analogous phases occurring both as phenocrysts and as xenolith constituents. Systematic chemical variations in the clinopyroxene megacrysts may reflect magmatic fractionation processes. Megacrysts may represent disaggregated parts of coarsely crystalline polymineralic assemblages precipitated at high pressures, and temperatures above that indicated by the xenoliths, with subsequent exsolution at temperatures of about 1060°C.  相似文献   

13.
广西平南玄武岩的地球化学特征   总被引：4，自引：0，他引：4  
平南碱性玄武岩产于 NE向的区域性断裂中 ,岩石类型有两类 ,一为碧玄岩 ,全岩 K- Ar年龄为 50 .8Ma,含各类包体 ,有以下特征 :1)含地幔岩包体 ,2 ) [Mg]=0 .78,3)在 Fe O/mol- Mgo/mol图解上液相线橄榄石的成分位于 Fo90～ Fo94之间 ,与橄榄岩包体中的橄榄石成分完全一致。4 ) Ni=0 .0 4 ( % ) <0 .0 5( % ) ,5)其熔浆密度为 2 .62 g/cm3,粘度为 2 .52 Pa· s,携带 4 cm直径包体上升的速度为 37.7cm/s,上升的速度较快 ,具原生碧玄岩浆的特点 ,岩浆液相线的温度为12 86℃ ,起源压力为 1.8GPa,玄武岩富集轻稀土可能与地幔性质有关。一为粗面玄武岩 ,不含包体 ,全岩 K- Ar年龄为 4 9.9Ma,岩浆液相线的温度为 1162℃ ,是进化岩浆。玄武岩的 Nd、Sr同位素显示为亏损地幔源区。它们都是大陆拉张环境下的产物 ,与中国东部新生代玄武岩的形成背景一致。  相似文献   

14.
Fresh submarine basalt glasses from Galapagos Ridge, FAMOUS area, Cayman Trough and Kilauea east rift contain 22 to 160 ppm carbon and 0.3 to 2.8 ppm nitrogen, respectively, as the sums of dissolved species and vesicle-filling gases (CO2 and N2). The large range of variation in carbon content is due to combined effect of depth-dependency of the solubility of carbon in basalt melt and varying extents of vapour loss during magma emplacement as well as in sample crushing. The isotopic ratios of indigenous carbon and nitrogen are in very narrow ranges,?6.2 ± 0.2% relative to PDB and +0.2 ± 0.6 %. relative to atmospheric nitrogen, respectively. In basalt samples from Juan de Fuca Ridge, however, isotopically light carbon (δ13C = around ?24%.) predominates over the indigenous carbon; no indigenous heavy carbon was found. Except for Galapagos Ridge samples, these ocean-floor basalts contain 670 to 1100 ppm sulfur, averaging 810 ppm, in the form of both sulfide and sulfate, whereas basalts from Galapagos Ridge are higher in both sulfur (1490 and 1570 ppm) and iron (11.08% total iron as FeO). The δ34S values average +0.3 ± 0.5%. with average fractionation factor between sulfate and sulfide of +7.4 ± 1.6%.. The sulfate/sulfide ratios tend to increase with increasing water content of basalt, probably because the oxygen fugacity increases with increasing water content in basalt melt.  相似文献   

15.
St. Kitts lies in the northern Lesser Antilles, a subduction-related intraoceanic volcanic arc known for its magmatic diversity and unusually abundant cognate xenoliths. We combine the geochemistry of xenoliths, melt inclusions and lavas with high pressure–temperature experiments to explore magma differentiation processes beneath St. Kitts. Lavas range from basalt to rhyolite, with predominant andesites and basaltic andesites. Xenoliths, dominated by calcic plagioclase and amphibole, typically in reaction relationship with pyroxenes and olivine, can be divided into plutonic and cumulate varieties based on mineral textures and compositions. Cumulate varieties, formed primarily by the accumulation of liquidus phases, comprise ensembles that represent instantaneous solid compositions from one or more magma batches; plutonic varieties have mineralogy and textures consistent with protracted solidification of magmatic mush. Mineral chemistry in lavas and xenoliths is subtly different. For example, plagioclase with unusually high anorthite content (An≤100) occurs in some plutonic xenoliths, whereas the most calcic plagioclase in cumulate xenoliths and lavas are An97 and An95, respectively. Fluid-saturated, equilibrium crystallisation experiments were performed on a St. Kitts basaltic andesite, with three different fluid compositions (XH2O = 1.0, 0.66 and 0.33) at 2.4 kbar, 950–1025 °C, and fO2 = NNO ? 0.6 to NNO + 1.2 log units. Experiments reproduce lava liquid lines of descent and many xenolith assemblages, but fail to match xenolith and lava phenocryst mineral compositions, notably the very An-rich plagioclase. The strong positive correlation between experimentally determined plagioclase-melt KdCa–Na and dissolved H2O in the melt, together with the occurrence of Al-rich mafic lavas, suggests that parental magmas were water-rich (> 9 wt% H2O) basaltic andesites that crystallised over a wide pressure range (1.5–6 kbar). Comparison of experimental and natural (lava, xenolith) mafic mineral composition reveals that whereas olivine in lavas is predominantly primocrysts precipitated at low-pressure, pyroxenes and spinel are predominantly xenocrysts formed by disaggregation of plutonic mushes. Overall, St. Kitts xenoliths and lavas testify to mid-crustal differentiation of low-MgO basalt and basaltic andesite magmas within a trans-crustal, magmatic mush system. Lower crustal ultramafic cumulates that relate parental low-MgO basalts to primary, mantle -derived melts are absent on St. Kitts.  相似文献   

16.
Pan‐African high‐pressure granulites occur as boudins and layers in the Lurio Belt in north‐eastern Mozambique, eastern Africa. Mafic granulites contain the mineral assemblage garnet + clinopyroxene + plagioclase + quartz ± magnesiohastingsite. Garnet porphyroblasts are zoned with increasing almandine and spessartine contents and decreasing grossular and pyrope contents from core (Alm46Prp32Grs21Sps2) to rim (Alm52Prp26Grs19Sps3). This pattern is interpreted as a retrograde diffusion zoning with the preserved core chemistry representing the peak metamorphic composition. Mineral reaction textures occur in the form of monomineralic and composite plagioclase ± orthopyroxene ± amphibole ± biotite ± magnetite coronas around garnet porphyroblasts. Thermobarometry indicates peak metamorphic conditions of up to 1.57 ± 0.14 GPa and 949 ± 92 °C (stage I), corresponding to crustal depths of ～55 km. Zircon yielded an U–Pb age of 557 ± 16 Ma, inferred to date crystallization of zircon during peak or immediately post‐peak metamorphism. Formation of plagioclase + orthopyroxene‐bearing coronas surrounding garnet indicates a near‐isothermal decompression of the high‐pressure granulites to lower pressure granulite facies conditions (stage II). Development of plagioclase + amphibole‐coronas enclosing the same garnet porphyroblasts shows subsequent cooling into amphibolite facies conditions (stage III). Symplectitic textures of the corona assemblages indicate rapid decompression. The high‐pressure granulite facies metamorphism of the Lurio Belt, followed by near‐isothermal decompression and subsequent cooling, is in accordance with a long‐lived tectonic history accompanied by high magmatic activity in the Lurio Belt during the late Neoproterozoic–early Palaeozoic East‐African–Antarctic orogeny.  相似文献   

17.
Petrochemistry of eclogites from the Koidu Kimberlite Complex,Sierra Leone   总被引：1，自引：0，他引：1  
Petrography, mineral and bulk chemistry of upper mantle-derived eclogites (garnet and clinopyroxene) from the Koidu Kimberlite Complex, Sierra Leone, are presented in the first comprehensive study of these xenoliths from West Africa. Although peridotite-suite xenoliths are generally more common in kimberlites, the upper mantle sample preserved in Pipe Number 1 at Koidu is exclusively eclogitic, making this the fifth locality in which eclogite is the sole polymineralic xenolith in kimberlite. Over 2000 xenoliths were collected, of which 47 are described in detail that include diamond, graphite, kyanite, corundum, quartz after coesite, and amphibole eclogites. Grossular-pyrope-almandine garnets are chromium-poor (<0.72 wt% Cr2O3) and fall into two distinct groups based on magnesium content. High-MgO garnets have an average composition of Pyr67Alm22Gross11, low-MgO garnets are grossular- and almandine-rich with an average composition of Gross34Pyr33Alm33. Clinopyroxenes are omphacitic with a range in jadeite contents from 7.7 to 70.1 mol%. Three eclogites contain zoned and mantled garnets with almandine-rich cores and pyrope-rich rims, and zoned clinopyroxenes with diopside-rich cores and jadeite-rich rims, and are among a very rare group of eclogites reported on a world-wide basis. The bulk compositions of eclogites have ranges comparable to that of basalts. High-MgO eclogites (16–20 wt% MgO) have close chemical affinities to picrites, whereas low-MgO eclogites (6–13 wt% MgO) are similar to alkali basalts. High-MgO eclogites contain high-MgO garnets and jadeiterich clinopyroxenes. Low-MgO eclogites contain low-MgO garnets, diopside and omphacite, and the group of primary accessory phases (diamond, graphite, quartz after coesite, kyanite, and corundum); grospydites are peraluminous. Estimated temperatures and pressures of equilibration of diamond-bearing eclogites, using the diamond-graphite stability curve and the Ellis and Green (1979) geothermometer, are 1031°–1363° C at 45–50 kb.K D values of Fe-Mg in garnet and clinopyroxene range from 2.3 to 12.2. Diamonds in eclogites are green, yellow, and clear, and range from cube to octahedral morphologies; the entire spectrum in color and morphology is present in a single metasomatized eclogite with zoned garnet and clinopyroxene. Ages estimated from Sm-Nd mineral isochrons range from 92–247 Ma. Nd values range from +4.05 to 5.23. Values of specific gravity range from 3.06–3.60 g/cc, with calculated seismic Vp of 7.4–8.7 km/s. Petrographie, mineral, and bulk chemical data demonstrate an overall close similarity between the Koidu xenolith suite and upper mantle eclogites from other districts in Africa, Siberia and the United States. At least two origins are implied byP-T, bulk chemistry and mineral compositions: low-MgO eclogites, with diamond and other accessory minerals, are considered to have formed from melts trapped and metamorphically equilibrated in the lithosphere; high-MgO eclogites are picritic and are the products of large degrees of partial melting, with equilibration in the asthenosphere. Fluid or diluted melt metasomatism is pervasive and contributed here and elsewhere to the LIL and refractory silicate incompatible element signature in kimberlites and lamproites, and to secondary diamond growth.  相似文献   

18.
Fluid inclusions occur in a composite xenolith from the Lunar Crater Volcanic Field, Nevada, U.S.A. The xenolith is an amphibole-bearing wehrlite that is cut by an andesine-amphibole vein. The compositions of individual fluid inclusions in both portions of the xenolith have been determined using microthermometry and micro Laser-Raman spectroscopy. Fluids in the host wehrlite are nearly pure CO2 (>99 mol%) whereas those in the vein contain from 8.5 to 12.0 mol % CO in CO2. Chemical modelling shows that the composition of the vein fluids at T room is representative of the composition at the high P, T conditions of trapping. Graphite has not been observed by optical microscopy in any of the fluid inclusions. Graphite is probably absent (although stable at T<800° C) most probably because of the kinetically unfavorable CO decomposition reaction and rapid quenching. By combining the measured fluid compositions with fluid P-V-T data and the chemical equilibrium CO2CO +1/2 O2, we have calculated the oxygen fugacity of the fluid inclusions at 1200° C: log 8.6 (vein) and –6 (host). If the of the fluid in the vein represents that in equilibrium with the magma that crystallized to produce the vein, then the of the basalt magma is near QFM at 1200° C and 10.3 kbar. This is similar to values reported for extrusive basaltic lavas. If the much lower intrinsic oxygen fugacity-values for divines and spinels from alkali basalt nodules are representative of upper mantle conditions, then oxidation of basaltic magmas must occur in the upper mantle prior to ascent to the surface. Implications for the origin of CO2-rich fluids and carbon isotope geochemistry are also discussed.  相似文献   

19.
天津蓟县铁岭子村附近新出露的下马岭组下部黑色岩系中富含菱铁矿,本文从野外产出特征、岩石学特征及常量元素特征等3个方面对这一富菱铁矿地层的基本地质特征进行了报道.该剖面地层主要以黑色页岩、粉砂质富铁层/菱铁矿结核层互层产出为特征,夹有少量粉砂岩.部分富铁层由于风化严重,野外露头以褐铁矿层出现.菱铁矿为地层中主要的铁矿物相,可以形成菱铁矿结核,显微镜下具泥晶或微晶结构;也可以与含量相当的石英粉砂一起,构成致密粉砂质富铁层;亦或呈颗粒状零星分布于黑色页岩、粉砂岩中;另外褐铁矿层中亦存在极少量的菱铁矿残余.地层的常量元素特征整体表现为富含SiO2、TFe及有机质,而贫MnO、CaO、MgO、P2O5及S元素,且除风化层位中的铁多呈三价外,其余多呈二价.总有机碳(TOC)含量由高到低依次为菱铁矿结核、粉砂质富铁层、黑色页岩、粉砂岩.TFe与Al2O3含量的相关性图解显示,在富铁地层中,二者呈现出很好的负相关关系,而在正常的黑色页岩和粉砂岩中,二者则呈现一定的正相关关系,表明富铁地层中的铁主要为海洋自身铁的化学沉积,而正常的黑色页岩和粉砂岩中的铁主要源自陆源碎屑.同时新鲜样品中FeO与TOC含量呈现出很好的正相关关系,表明菱铁矿的形成可能与有机质有关.  相似文献   

20.
The Proterozoic Expo Intrusive Suite comprises a series of maficto ultramafic intrusions crosscutting the Povungnituk Groupof the Cape Smith Fold Belt in New Quebec. The intrusions aremainly in the form of blade-shaped dikes that penetrate a sediment-richhorizon in the middle of the Beauparlant Formation and terminatedownward against massive basalts of the lower Beauparlant Formation.Significant accumulations of magmatic sulfide occur at the basalterminations of the dikes. At stratigraphic levels above theBeauparlant Formation the intrusions appear as broad dikes orsills within the Nuvilik Formation, below the mineralized lavaflows and subvolcanic intrusions of the Raglan Formation. TheExpo Intrusive Suite and the mineralized bodies of the RaglanFormation are probably coeval and comagmatic with the overlyingChukotat Group. Post-emplacement folding has exposed the ExpoIntrusive Suite over about 5 km of structural relief, revealingthe basal sulfide concentrations where dike segments terminateon the flanks of anticlines. The parent magma as preserved inchilled margins and narrow dikes was a picrite containing 17wt % MgO (i.e. komatiitic basalt) and slightly depleted in Th,U and Nb relative to middle and heavy rare earth elements. Thecompositions of ultramafic cumulate rocks within the intrusionsare strongly enriched in Th, U and Nb relative to heavy rareearth elements, reflecting assimilation of the enclosing basaltsand metasediments. Modeling of the assimilation process suggeststhat the picritic magma was capable of assimilating masses ofbasalt or sediment up to 50% of the original mass of magma.Assimilation of 10% of a mixture of basalt and sediment causedthe magma to become sulfide-saturated, and was accompanied bythe crystallization of masses of ultramafic cumulates approximatelyequal to the mass of rock assimilated. The presence of dikeswhose chilled margins resemble uncontaminated primary magmasbut that contain abundant cumulates recording wholesale assimilationof host-rocks indicates that the process of assimilation andfractional crystallization required to produce continental tholeiitesfrom picritic parent magmas may not require the presence oflong-lived magma chambers, but can occur during transport alongdikes and reaction with wall-rocks. KEY WORDS: komatiite; Expo Intrusive Suite; assimilation; fractional crystallization; sulfide mineralization  相似文献   

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