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1.
Metallography, electron microscopy and X-ray diffraction techniques were employed to study a fragment of the Tishomingo iron meteorite. The results suggest the following thermal-mechanical history: The fragment was originally a large crystal of taenite (γ). Cooling through the α + γ phase boundary did not result in accompanying precipitation of kamacite (α). Transformation to a martensitic structure initiated between ? 25 and ?65°C. Transformation continued as the temperature fell to ? 75 to ? 115°C, resulting in approx 80% martensite (α′). Subsequent shock deformation and thermal aging processes substantially modified the taenite and martensite microstructures. Twins in the retained taenite phase are attributed to shock deformation at a pressure estimated for a single event at ~170 kbar. The existing complex, altered martensite structure containing both taenite and kamacite (3–15% Ni) particles was apparently the product of both shock deformation and thermal aging processes. The maximum temperature reached during thermal aging is estimated to be less than 400°C, and perhaps below 310°C.  相似文献   

2.
东乌珠穆沁旗中铁陨石中有二种橄榄石。一种是陨石中基质橄榄石，另一种是镶嵌在陨石表面的角砾状橄榄石。电子探针成分分析结果表明，两种橄榄石中的FeO和MnO比值，包体矿物种类，包体铁纹石和镍纹石中Fe,Ni的含量等，均有较大区别。陨石中基质橄榄石矿物是本陨石中原物质，而角砾状橄榄石是宇宙中物质。他们是两块自由翱于宇宙中的物质碰撞混合而形成的东乌珠穆旗陨石中这种现象。  相似文献   

3.
The fragments of the Chelyabinsk meteorite studied are represented by light-gray granular rock of chondritic structure. The chondrules and their cementing matter are mainly constituted by olivine and orthopyroxene. The matrix consists of a pyroxene-olivine aggregate with plagioclase, apatite, melted glass, and the inclusions of ore minerals: taenite, kamacite, troilite, pyrrhotite and pentlandite (more rarely), and individual grains of chromite and ilmenite. The comparison of the composition of the Chelyabinsk meteorite to the average composition of LL chondrites had shown their complete convergence. The concentrations of sidero- and chalcophile rare elements in the meteorite, normalized to CI chondrites, are much close to the values for LL chondrites and almost reproduce the character of their distribution in the spider diagram. However, some high-charged and lithophile elements (Nb, Zr, Hf, Sr, Ba, Th, and U) not belonging to the mentioned groups are characterized by somewhat increased contents. The enrichment of the samples of the Chelyabinsk meteorite in rare-earth elements compared to LL chondrite (5.18 against 3.58 ppm) is also revealed. This is related to the higher concentrations of light lanthanides in the meteorite samples, which is seen from the increased La/Yb ratio compared to the value for LL chondrite (1.9–2.3 and 1.4, respectively). Iron-nickel alloys are the main magnetism carriers in the Chelyabinsk meteorite. The compositions of kamacite, taenite, chromite, and Fe-sulfides are not much different. The optical and microprobe data are confirmed by the thermomagnetic parameters as well: (1) The specific magnetization of 4–6 Am2/kg points to small variations in the concentrations of magnetic minerals. (2) The M(T) curves for all the samples nearly repeat each other, and the Curie temperatures of 490–520 and 740–770°C are registered in the curves of the first and second heating, hence, these curves correspond to kamacite of various composition, right up to pure iron. (3) The monocline ferrimagnetic pyrrhotite of TC = 320–340°C is registered in the treated fragments in both the M(T) curves of heating and cooling. (4) The concentrations by thermomagnetic analysis amount to 0.6–1.6% (0.9% average) for kamacite, 0.7–1.5% (1.1% average) for taenite, and 0–1.5% (0.4% average) for monocline pyrrhotite. (5) No magnetite was found in the M(T) curve during the first heating of the samples. Hence, the content of magnetite is much below 0.1.  相似文献   

4.
本文对南丹IIICD铁陨石的矿物学特征进行了研究,并与同为铁陨石但化学分类不同的阿根廷IAB铁陨石和西伯利亚IIB铁陨石进行了对比,重点探讨了风化作用对铁陨石矿物学特征的影响.首先用偏光显微镜、静水称重、扫描电镜观察了样品的基本矿物学特征和微形貌特征,然后用振动式样品磁强计、X射线衍射与电子探针能谱半定量测试研究了样品的磁学性质、物相和化学组成.研究结果表明,南丹铁陨石在较强的自然风化作用下,光泽变弱为土状光泽,相对密度降低;风化产生的反铁磁性物质会使陨石的磁性下降;另外,样品表面物相组成也发生较大变化,以针铁矿(FeOOH)和磁铁矿(Fe3O4)等铁的次生矿物为主;但风化壳以下的矿物物相及化学成分均未发生明显变化,以Fe、Ni为主的铁纹石、镍纹石物相存在.  相似文献   

5.
Phosphorus-bearing Fe and Ni sulfides represent a new type of phosphorus compounds and are characteristic accessory phases of CM chondrites. The proportions of atoms in the sulfides can be approximated by the equation (Fe + Ni)/P = 0.965 ± 0.003 (1σ) · S/P + 1.255 ± 0.036 (1σ). Sulfides with high S/P ratios are systematically richer in Fe and poorer in Ni compared with low-S/P sulfides. Their characteristic minor elements are Cr, Ca, Co, K, and Na. The contents of Cr and Ca may reach several weight percent, but their incorporation does not affect the relation between (Fe + Ni)/P and S/P. This is also true of light elements (O and H), which probably occur in the P-bearing sulfides in certain amounts. The sulfides are usually associated with schreibersite, barringerite, eskolaite, and daubreelite. A negative correlation was observed between the Fe/Ni ratios of coexisting P-bearing sulfides and phosphides. Metallic iron was never found in association with the sulfides. It can be suggested that P-bearing sulfide is a primary phase rather than a secondary alteration product formed under the conditions of the CM chondrite parent body. This phase had to be stable in the solar nebula after the formation of Ca-Al inclusions and before the condensation of Fe-Ni metal. At high temperatures, P-bearing sulfide with low Fe/Ni and S/P ratios coexists with schreibersite in the solar gas. During condensation schreibersite is replaced by barringerite, which is accompanied by a decrease in the Fe/Ni ratio of phosphides and an increase in the S/P and Fe/Ni ratios of P-bearing sulfides. Trace element data suggest that the P-bearing sulfides could be formed in the solar nebula by the sulfidization of a precursor phase of extrasolar origin.  相似文献   

6.
It appears that the highly unequilibrated Bishunpur ordinary chondrite preserves phase relations acquired during solar nebular processes to a relatively high degree; metamorphic temperatures may not have exceeded 300–350°C. The major categories of metal are: 3 kinds of metal in the metal matrix, three kinds in chondrule interiors and 2 kinds in chondrule rims. The fine-grained matrix metal is highly variable in composition: the kamacite Co content (7.8 ± 2.0 mg/g) is within the L-group range (6.7–8.2 mg/g) but extends well above and below; its Ni content (38 ± 5 mg/g) is considerably lower than in more equilibrated chondrites and taenite is Ni-rich ( > 450 mg/g) and unzoned. These compositions imply equilibration at very low temperatures of about 300–350°C. It seems unlikely that volume diffusion could account for the observed relatively unzoned phases; a better model involves mass transport by grain boundary diffusion and grain growth at the indicated temperatures. We find no evidence that the matrix was ever at higher temperatures. Large (50–650 μm) polycrystalline metal aggregates consisting of individually zoned crystals are also found in the matrix; they probably represent clusters formed in the solar nebula. A few large (50–250 μm) round monocrystalline grains are also present in the matrix.Metal-bearing chondrules tend to be highly reduced; they contain low-Ni metal that occasionally contains Si and/or Cr. Silicates in these chondrules tend to have low FeO(FeO + MgO) ratios. The Si-rich metal grains are never in contact with silicates and are always surrounded by troilite with a poorly characterized Ca, Cr-sulfide at the metal-troilite interface; they appear to be high temperature nebular condensates that avoided oxidation even during the chondrule forming process. Silicon contents drop below our detection limit when the sulfide coating is absent. Much more common in chondrule interiors are Si-free spheroidal metal grains not associated with sulfides. These have Ni and Co contents very similar to the Si-bearing grains, and appear to be oxidized variants of the same material. The third class of chondrule metal is fine ( ~1 μm) dusty grains inside individual olivine grains. These seem to reflect high temperature in situ reduction of FeO from the olivine.The composition of kamacite is different in sulfide-rich and sulfide-poor chondrule rims and in both cases it is dissimilar to the compositions in the chondrule interiors and matrix; this indicates that chondrule rims could not have resulted from reactions with the matrix, but are primary features acquired prior to accretton.  相似文献   

7.
The Bovedy L-group chondrite contains a light-colored poikilitic lithic fragment with olivine, low-Ca pyroxene and kamacite compositions characteristic of porphyritic chondrules from unequilibrated ordinary chondrites. Its texture, compositional similarities to porphyritic chondrules, and low Na2O, K2O and P2O5 content indicate that the fragment represents a solidified, slightly fractionated impact melt formed from a source that was rich in porphyritic chondrules. The fragment is heterogeneous, with a progressive increase in the bulk MgOFeO ratio and in MgO content of olivines and low-Ca pyroxenes across its length. 39Ar40Ar analyses of the fragment and host indicate that the meteorite experienced extensive degassing due to reheating. The approximate age of 0.5–0.94 Byr dates the reheating event and not the formation of the lithic fragment or the Bovedy breccia. This reheating event renders the fragment's and host's metallographic cooling rate of ~ 5 C/Myr (through 500°C) imprecise. However, the absence of martensite and the presence of kamacite. zoned taenite and tetrataenite in the fragment and host are consistent with such slow cooling through 500°C. This cooling rate must have resulted from burial of the fragment-host assemblage beneath insulating material on the Bovedy parent body. If the thermal diffusivity (κ) of this overburden was approximately comparable to that of the lunar regolith (10?4cm2/sec), then the fragment was buried at a depth ≌ 6.5 km; if K = 10?2 cm2/sec (similar to chondritic material), then the fragment was buried at a depth ?65 km.  相似文献   

8.
Magnetic properties of the Chelyabinsk meteorite: Preliminary results   总被引：1，自引：0，他引：1  
This paper presents the distribution of magnetic susceptibility, χ0, in fragments of the Chelyabinsk ordinary chondrite (LL5, S4, W0, fall of February 15, 2013) from the collection of the Vernadsky Institute of Geochemistry and Analytical Chemistry, Russian Academy of Sciences, and results obtained by standard magnetic techniques for the meteorite material, including thermomagnetic analysis, measurements of natural remanent magnetization (NRM) and saturation isothermal remanent magnetization (SIRM), as well as the spectra of their alternating field demagnetization at amplitudes up to 170 mT, measurements of hysteresis loops and back-field remanence demagnetization curves at temperatures from 10 K to 700°C etc. The mean logχ0 values for the light-colored (main) lithology of the meteorite material and impact-melt breccia from our collection are 4.54 ± 0.10 (n = 66) and 4.65 ± 0.09 (n = 38) (×10?9 m3/kg), respectively. According to international magnetic classification of meteorites, Chelyabinsk falls within the range of LL5 chondrites. The mean metal content was estimated from the saturation magnetization, M s, of the light- and dark-colored lithologies as 3.7 and 4.1 wt %, respectively. Hence, the dark lithology is richer in metal. The metal grains are multidomain at room temperature and show low coercive force, B c (<2 mT) and remanent coercive force, B cr (15–23 mT). The thermomagnetic analyses of the samples showed that the magnetic properties of the Chelyabinsk meteorite are controlled mainly by taenite and kamacite at temperatures >75 K. In the temperature range below 75 K, magnetic properties are controlled by chromite; the magnetic hardness of the samples is maximal at 10 K and equals to 606 and 157 mT for the light- and dark-colored lithologies, respectively.  相似文献   

9.
We report the results of coordinated ion microprobe and transmission electron microscope (TEM) studies of presolar graphites from the KE3 separate (1.65-1.72 g/cm3) of the Murchison CM2 meteorite. Isotopic analysis of individual graphites (1-12 μm) with the ion microprobe shows many to have large 18O excesses combined with large silicon isotopic anomalies, indicative of a supernova (SN) origin. Transmission electron microscopy (TEM) of ultramicrotome slices of these SN graphites revealed a high abundance (25-2400 ppm) of internal titanium carbides (TiCs), with a single graphite in some cases containing hundreds of TiCs. Isotopic compositions of individual TiCs by nanoscale resolution secondary ion mass spectrometry (NanoSIMS) confirmed their presolar origin. In addition to TiCs, composite TiC/Fe grains (TiCs with attached iron-nickel subgrains) and solitary kamacite internal grains were found. In the composite grains, the attached iron phase (kamacite [0-24 at. % Ni] or taenite [up to 60 at. % Ni]) was epitaxially grown onto one or more TiC faces. In contrast to the denser Murchison KFC1 graphites, no Zr-Ti-Mo carbides were observed. The average TiC diameters were quite variable among the SN graphites, from 30 to 232 nm, and were generally independent of the host graphite size. TiC grain morphologies ranged from euhedral to anhedral, with the grain surfaces exhibiting variable degrees of corrosion, and sometimes partially amorphous rims (3 to 15 nm thick). Partially amorphous rims of similar thickness were also observed on some solitary kamacite grains. We speculate that the rims on the internal grains are most plausibly the result of atom bombardment caused by drift of grains with respect to the ambient gas, requiring relative outflow speeds ∼100 km/s (i.e., a few percent of the SN mass outflow speed).Energy dispersive X-ray spectrometry (EDXS) of TiCs revealed significant V in solid solution, with an average V/Ti ratio over all TiCs of ∼83% of the solar value of 0.122. Significant variations about the mean V/Ti ratio were also seen among TiCs in the same graphite, likely indicating chemical equilibration with the surrounding gas over a range of temperatures. In general, the diversity in internal TiC properties suggests that TiCs formed first and had substantially diverse histories before incorporation into the graphite, implying some degree of turbulent mixing in the SN outflows.In most graphites, there is a decrease in the number density of TiCs as a function of increasing radial dis- tance, caused by either preferential depletion of TiCs from the gas or an acceleration of graphite growth with decreasing ambient temperature. In several graphites, TiCs showed a trend of larger V/Ti ratios with increasing distance from the graphite center, an indication of progressive equilibration with the surrounding gas before they were sequestered in the graphites. In all but one graphite, no trend was seen in the TiC size vs. distance from the graphite center, implying that appreciable TiC growth had effectively stopped before the graphites formed, or else that graphite growth was rapid compared to TiC growth. Taken together, the chemical variations among internal grains as well as the presence of partially amorphous rims and epitaxial Fe phases on some TiCs clearly indicate that the phase condensation sequence was TiC, followed by the iron phases (only found in some graphites) and finally graphite. Since graphite typically condenses at a higher temperature than iron at low pressures (<10−3 bars) in a gas with C > O and otherwise solar composition, the observed condensation sequence implies a relative iron enrichment in the gas or greater supersaturation of graphite relative to iron.The TEM observations allow inferences to be made about the physical conditions in the gas from which the grains condensed. Given the TiC sizes and abundances, the gas was evidently quite dusty. From the observed TiC size range of ∼20 nm to ∼500 nm (assuming ∼1 yr growth time and T ∼ 1800°K), we infer minimum Ti number densities in the gas to be ∼7 × 104 to ∼2 × 106 atoms/cc, respectively. Although the gas composition is clearly not solar, for scale, these number densities would correspond to a pressure range of ∼0.2 μbar to ∼5.0 μbar in a gas of solar composition. They also correspond to minimum TiC grain number densities of ∼3 × 10−4 to ∼0.2 grains/cc, assuming complete condensation of Ti in TiC. We estimate the maximum ratio of mean TiC grain separation distance in the gas to grain diameter from the Ti number densities as ∼3 × 105 to ∼1 × 106.  相似文献   

10.
On September 13, 1976, the Qingzhen enstatite chondrite fell near Qingzhen County, Guizhou Province (26°32′N, 106°28′E). The total mass recovered was 2.6 kg. Phenomena of the meteorite fall were recorded as well. In the present paper some of the significant observations are described. X-ray diffraction analyses and petrologic studies revealed that it is mainly composed of enstatite/clinoenstatite, plagioclase, troilite, kamacite, taenite, quartz and oldhamite. X-ray electron microprobe analyses were performed on orthoenstatite and clinoenstatite. Chemical analysis gave: SiO2-36.48; Al2O3-1.64; TiO2-0.08; Cr2O3-0.28; FeO-0.30; MnO-0.25; MgO-18.19; CaO-1.14; Na2O-1.06; K2O-0.11; H2O+-0.47; H2O?-0.10; P2O5-0.39; FeS-13.35; FeO-22.94; Ni-1.81; Co-0.093; C-0.37; Cu-0.022; Zn-0.027; CaS-0.60; total-99.70 (wt.%). This meteorite has been extremely reduced; all iron is present as FeS and metallic Fe-Ni. The Qingzhen enstatite chondrite is characterized by high ratio, Si/Mg as compared with ordinary chondrites, scarcity of olivine, and enrichment in sulfur and iron. In thin sections, it is observed that round chondrules approximately account for 10–15 per cent, being porphyritic, radial, excentroradial, or excentric fan-shaped. Devitrified chondrules composed of pyroxene were also identified. It is postulated from its mineralogy, chemistry and textural characteristics that the Qingzhen meteorite should be assigned toE 4 orEH chondrites.  相似文献   

11.
Alterations caused by week-long heating of Murchison in a low-pressure environment at 400–1400°C are of two types: thermodynamically-favored, kinetically-controlled or thermodynamicallycontrolled, rapid processes. Kinetically-controlled changes pertinent to chondritic evolution and which vary progressively with temperature in heated Murchison include: chondrule blurring; matrix coarsening; increasing mean Fa and Fs contents of ferromagnesian silicates; equilibration of olivine; increasing Mg/Si, Ca/Si, Ai/Si and Cr/Si and decreasing Fe/Si, Ni/Si and S/Si in matrix; Cr loss from kamacite; homogenization and Ni-zoning in taenite at high temperatures. Low-temperature thermodynamicallycontrolled changes include: transformation of high-Ni troilite to low-Ni and formation of Ni- and Co-rich metal from pentlandite. High-temperature changes include formation of Cr-rich magnetite and formation of a Ni-rich sulfide similar to that found in highly-altered chondrites. Trends resulting from processes of both kinds in Murchison are consistent with characteristics of a postulated C30 metamorphic suite while those changes causes by reactions of the second kind are similar to those in heavily shock-heated, ordinary chondrites and the heavily-metamorphosed C5–6 chondrite. Mulga West. Either our simulations support the metamorphic origin of the C30 suite and other thermally-induced changes or the natural alterations support the utility of laboratory simulations in studying meteoritic evolution.  相似文献   

12.
Pallasites are highly differentiated meteorites and provide a unique sample from the deep interiors of solar system parent bodies. They contain evidence of the former existence of one or more residual melts. Olivine is a major phase. Its primary shape is rounded; the angular crystals in many pallasites are secondary. Tubular inclusions are widespread. They perhaps are the residence of CO2, released during laboratory heating experiments. Phosphoran olivine, a new variety of olivine containing 4–5 wt% P2O5, occurs in a few pallasites. Its Fe/Mg ratio is apparently independent of the host olivine composition.Pyroxene (not previously described from pallasites) occurs in symplectic intergrowths in seven meteorites. Compositionally, it lies in the gap between pyroxenes in chondrites and most irons. There are two groups: Fs11.6 ± 0.2 and Fs16.7 ± 0.2 The pyroxene contains exceptionally low Ca (< 0.1–0.2 wt%) and there is an indication of an inverse relation between Fe and Ca.Modal analyses and density measurements were made on all available specimens and bulk compositions were calculated. The ‘average’ pallasite contains 65 vol. % olivine and 50.5 wt % total Fe. Many of the densities of pallasites cluster around that calculated for close-packed olivine.Pallasites are exotic cumulates. Their textures resemble terrestrial cumulates, as does the presence of olivine and chromite. The metal texture resembles a solidified intercumulus liquid. Those pallasites containing olivine in excess of close-packing were subjected to adcumulus growth, thereby also explaining the widespread mutual borders.There is abundant evidence of deformation. For olivines this includes their fragmental shape and kink banding. Troilite formed a eutectic-like melt with kamacite: pieces of spalled olivine and schreibersite were injected into and captured by this melt. Troilite polycrystallinity resulted from the deformation. This deformation occurred while the pallasites were still deeply buried, resulting in incipient spheroidization of olivine fragments, including the formation of elongate, rounded crystals. A later, lower temperature deformation disrupted plessite.Pallasites formed in multiple parent bodies by processes that recurred in several places within the solar system, as shown by the mineralogical and textural similarities between pallasites that differ in their isotopic and trace element compositions. Type IIIB irons still seem the most likely associated meteorites.Two new pallasites, Dora and Rawlinna, are described briefly.  相似文献   

13.
Mineralogical and mineral chemical evidence for prograde metamorphism is rarely preserved in rocks that have reached ultrahigh‐temperature (UHT) conditions (>900 °C) because high diffusion and reaction rates erase evidence for earlier assemblages. The UHT, high‐pressure (HP) metasedimentary rocks of the Leverburgh belt of South Harris, Scotland, are unusual in that evidence for the prograde history is preserved, despite having reached temperatures of ～955 °C or more. Two lithologies from the belt are investigated here and quantitatively modelled in the system NaO–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O: a garnet‐kyanite‐K‐feldspar‐quartz gneiss (XMg = 37, A/AFM = 0.41), and an orthopyroxene‐garnet‐kyanite‐K‐feldspar quartzite (XMg = 89 A/AFM = 0.68). The garnet‐kyanite gneiss contains garnet porphyroblasts that grew on the prograde path, and captured inclusion assemblages of biotite, sillimanite, plagioclase and quartz (<790 °C, <9.5 kbar). These porphyroblasts preserve spectacular calcium zonation features with an early growth pattern overgrown by high‐Ca rims formed during high‐P metamorphism in the kyanite stability field. In contrast, Fe‐Mg zonation in the same garnet porphyroblasts reflects retrograde re‐equilibration, as a result of the relatively faster diffusivity of these ions. Peak P–T are constrained by the occurrence of coexisting orthopyroxene and aluminosilicate in the quartzite. Orthopyroxene porphyroblasts [y(opx) = 0.17–0.22] contain sillimanite inclusions, indicative of maximum conditions of 955 ± 45 °C at 10.0 ± 1.5 kbar. Subsequently, orthopyroxene, kyanite, K‐feldspar and quartz developed in equilibrated textures, constraining the maximum pressure conditions to 12.5 ± 0.8 kbar at 905 ± 25 °C. P–T–X modelling reveals that the mineral assemblage orthopyroxene‐kyanite‐quartz is compositionally restricted to rocks of XMg > 84, consistent with its very rare occurrence in nature. The preservation of unusual high P–T mineral assemblages and chemical disequilibrium features in these UHT HP rocks is attributed to a rapid tectonometamorphic cycle involving arc subduction and terminating in exhumation.  相似文献   

14.
The Khetri Copper Belt (KCB), a part of the Proterozoic Delhi–Aravalli fold belt in western India, hosts several Cu deposits, which are known to contain considerable Au, Ag, Co and Ni. Although many Co-bearing phases have been reported from the KCB and adjacent areas, detailed textural and geochemical data are either unavailable or scant except for mackinawite. In this study, we describe the textures and compositions (determined by EPMA) of two very rare Co-rich phases, namely cobaltian mackinawite (containing up to 12.68 wt.% Co, 1.90 wt.% Ni and 2.52 wt.% Cu) and cobalt-pentlandite (containing up to 49.30 wt.% Co and 10.19 wt.% Ni), identified based on composition, from the Madan-Kudan deposit. To the best of our knowledge, neither cobalt-pentlandite nor such highly Co-rich mackinawite have previously been reported from this area. The common sulphide minerals viz. chalcopyrite, pyrrhotite and rare pyrite occur in chalcopyrite-pyrrhotite ± pyrite-magnetite-chlorite-blue amphibole (Cl-rich hastingsite-pargasite-sadanagaite) ± marialitic scapolite ± allanite ± uraninite veins in amphibole-bearing feldspathic quartzite and garnetiferous chlorite schist. Cobaltian mackinawite is invariably associated with chalcopyrite and occurs as exsolution and inclusion within chalcopyrite or outside, but at the contact of chalcopyrite. On the other hand, cobalt-pentlandite is invariably associated with pyrrhotite and shows similar textural relation with pyrrhotite as that of mackinawite with chalcopyrite. Mineralogically diverse undeformed sulphide veins comprising Cl-rich amphibole and locally Cl-rich marialitic scapolite suggests epigenetic hydrothermal mineralization involving Cl-rich saline fluid in the Madan-Kudan deposit. Transport of metals, derived from a mafic source rock with high intrinsic Ni:Co ratio, by Cl-rich fluid can suitably explain the high Co:Ni ratio of the studied ore minerals. Presence of such highly Co-rich phases and other circumstantial evidences, enumerated in this work, are consistent with variants of Fe oxide (–Cu–Au) (IOCG) style mineralization, at least for some stages of mineralization in the Madan-Kudan deposit.  相似文献   

15.
Northwest Africa (NWA) 12379 is a new metal-rich chondrite with unique characteristics distinguishing it from all previously described meteorites. It contains high Fe,Ni-metal content (∼ 70 vol.%) and completely lacks interchondrule matrix; these characteristics are typical only for metal-rich carbonaceous (CH and CB) and G chondrites. However, chondrule sizes (60 to 1200 μm; mean = 370 μm), their predominantly porphyritic textures, nearly equilibrated chemical compositions of chondrule olivines (Fa18.1–28.3, average Fa24.9±3.2, PMD = 12.8; Cr2O3 = 0.03 ± 0.02 wt.%; FeO/MnO = 53.2 ± 6.5 (wt.-ratio); n = 28), less equilibrated compositions of low-Ca pyroxenes (Fs3.2–18.7Wo0.2–4.5; average Fs14.7±3.7Wo1.4±1.3; n = 20), oxygen-isotope compositions of chondrule olivine phenocrysts (Δ17O ∼ 0.2–1.4‰, average ∼ 0.8‰), and the presence of coarse-grained Ti-bearing chromite, Cl-apatite, and merrillite, all indicate affinity of NWA 12379 to unequilibrated (type 3.8) ordinary chondrites (OCs). Like most OCs, NWA 12379 experienced fluid-assisted thermal metamorphism that resulted in formation of secondary ferroan olivine (Fa27) that replaces low-Ca pyroxene grains in chondrules and in inclusions in Fe,Ni-metal grains. Δ17O of the ferroan olivine (∼ 4‰) is similar to those of aqueously-formed fayalite in type 3 OCs, but its δ18O is significantly higher (15–19‰, average = 17‰ vs. 3―12‰, average = 8‰, respectively). We suggest classifying NWA 12379 as the ungrouped metal-rich chondrite with affinities of its non-metal fraction to unequilibrated OCs and speculate that it may have formed by a collision between an OC-like body and a metal-rich body and subsequently experienced fluid-assisted thermal metamorphism. Trace siderophile element abundances and isotopic compositions (e.g., Mo, Ni, Fe) of the NWA 12379 metal could help to constrain its origin.  相似文献   

16.
Heavy metal enrichment parity in sandy and shaly mechanic village (MV) soils was studied in order to explain the technical and economic imperatives of setting an environmentally friendly MV on either soil. Okigwe (shaly) and Nekede (sandy) mechanic village soils in the Imo River basin Nigeria were tested and compared. Spectroscopic analysis of the soil samples collected from three surface layers (L), where L1: 0–10 cm; L2: 10–20 cm and L3: 90–100 cm shows that Pb > Cu > Mn in the Okigwe MV, and Mn > Pb > Cu in the Nekede MV. Mean concentration of metals (mg kg−1) in Okigwe MV are Fe: 51,291 ± 18,148, Ni: 22 ± 4, Cd: 20 ± 3, Pb: 500 ± 513, Cu: 616 ± 369, Cr: 16 ± 9, and Mn: 378 ± 207. Similarly, Nekede MV has 22,101 ± 7,273 of Fe; 8 ± 0.8 of Ni; 11 ± 4 of Cd; 320 ± 122 of Pb; 265 ± 145 of Cu; 11 ± 2 of Cr; and 350 ± 191 of Mn. Pollution factor (Pf): Okigwe MV has 0.77, and Nekede has 0.68. Pollution degree: Okigwe MV is greater in L1 and L2, while Nekede is greater in L3, with greater potentials for Pb, and Mn mobility than the Okigwe. Both have similar trends of metal distribution, and significant correlation with their background values. Low clay-silt content in Nekede MV soil suggests low sorption capacity, whereas the high clay-silt content (47–64%) of the Okigwe soil suggests lower bioavailability. Infiltration basin is not recommended in a MV on sandy soil if water table is near surface. In such case, the MV must be moved to a location where water table is >37 m, or have clay-shale material transported to the site to form impervious layer base for detention basin. For groundwater safety and sustainability, shaly soils are most recommended for MVs so that detention basin could be economically used for storm water treatment.  相似文献   

17.
The paper presents the results of study of ferromanganese carbonate rocks in the Sob area (Polar Urals), which is located between the Rai-Iz massif and the Seida–Labytnangi Railway branch. These rocks represent low-metamorphosed sedimentary rocks confined to the Devonian carbonaceous siliceous and clayey–siliceous shales. In terms of ratio of the major minerals, ferromanganese rocks can be divided into three varieties composed of the following minerals: (1) siderite, rhodochrosite, chamosite, quartz, ± kutnahorite, ± calcite, ± magnetite, ± pyrite, ± clinochlore, ± stilpnomelane; (2) spessartite, rhodochrosite, and quartz, ± hematite, ± chamosite; (3) rhodochrosite, spessartite, pyroxmanite, quartz ± tephroite, ± fridelite, ± clinochlore, ± pyrophanite, ± pyrite. In all varieties, the major concentrators of Mn and Fe are carbonates (rhodochrosite, siderite, kutnahorite, Mn-calcite) and chlorite group minerals (clinochlore, chamosite). The chemical composition of rocks is dominated by Si, Fe, Mn, carbon dioxide, and water (L.O.I.): total SiO2 + Fe2O 3 tot + MnO + L.O.I. = 85.6?98.4 wt %. The content of Fe and Mn varies from 9.3 to 55.6 wt % (Fe2O 3 tot + MnO). The Mn/Fe ratio varies from 0.2 to 55.3. In terms of the aluminum module AlM = Al/(Al + Mn + Fe), the major portion of studied samples corresponds to metalliferous sediments. The δ13Ccarb range (–30.4 to–11.9‰ PDB) corresponds to authigenic carbonates formed with carbon dioxide released during the microbial oxidation of organic matter in sediments at the dia- and/or catagenetic stage. Ferromanganese sediments were likely deposited in relatively closed seafloor zones (basin-traps) characterized by periodic stagnation. Fe and Mn could be delivered from various sources: input by diverse hydrothermal solutions, silt waters in the course of diagenesis, river discharges, and others. The diagenetic delivery of metals seems to be most plausible. Mn was concentrated during the stagnation of bottom water in basin-traps. Interruption of stagnation promoted the precipitation of Mn. The presence of organic matter fostered a reductive pattern of postsedimentary transformations of metalliferous sediments. Fe and Mn were accumulated initially in the oxide form. During the diagenesis, manganese and iron oxides reacted with organic matter to make up carbonates. Relative to manganese carbonates, iron carbonates were formed under more reductive settings and higher concentrations of carbon dioxide in the interstitial solution. Crystallization of manganese and iron silicates began already at early stages of lithogenesis and ended during the regional metamorphism of metalliferous sediments.  相似文献   

18.
The analysis of texture, major element and oxygen isotope compositions of cloudy garnet crystals from a metapelite sampled on Ikaria Island (Greece) is used to assess the model of growth and re‐equilibration of these garnet crystals and to reconstruct the pressure–temperature–fluid history of the sample. Garnet crystals show complex textural and chemical zoning. Garnet cores (100–200 μm) are devoid of fluid inclusions. They are characterized by growth zoning demonstrated by a bell‐shaped profile of spessartine component (7–3 mol.%), an increase in grossular from 14 to 22 mol.% and δ18O values between 9.5 ± 0.3‰ and 10.4 ± 0.2‰. Garnet inner rims (90–130 μm) are fluid inclusion‐rich and show a decreasing grossular component from 22 to 5 mol.%. The trend of the spessartine component observed in the inner rim allows two domains to be distinguished. In contrast to domain I, where the spessartine content shows the same trend as in the core, the spessartine content of domain II increases outwards from 2 to 14 mol.%. The δ18O values decrease towards the margins of the crystals to a lowest value of 7.4 ± 0.2‰. The outer rims (<10 μm) are devoid of fluid inclusions and have the same chemical composition as the outermost part of domain II of the inner rim. Garnet crystals underwent a four‐stage history. Stage 1: garnet growth during the prograde path in a closed system for oxygen. Garnet cores are remnants of this growth stage. Stage 2: garnet re‐equilibration by coupled dissolution–reprecipitation at the temperature peak (630 < T < 650 °C). This causes the creation of porosity as the coupled dissolution–reprecipitation process allows chemical (Ca) and isotopic (O) exchange between garnet inner rims and the matrix. The formation of the outer rim is related to the closure of porosity. Stage 3: garnet mode decreases during the early retrograde path, but garnet is still a stable phase. The resulting garnet composition is characterized by an increasing Mn content in the inner rim’s domain II caused by intracrystalline diffusion. Stage 4: dissolution of garnet during the late retrograde path as garnet is not a stable phase anymore. This last stage forms corroded garnet. This study shows that coupled dissolution–reprecipitation is a possible re‐equilibration process for garnet in metamorphic rocks and that intra‐mineral porosity is an efficient pathway for chemical and isotopic exchange between garnet and the matrix, even for otherwise slow diffusing elements.  相似文献   

19.
The average Pb/U ratio of the Shea Creek unconformity-type uranium deposit has been estimated at 0.071±0.015. The calculation was performed on a volume enclosing the orebody to take into account the possible radiogenic lead migration within the ore zone. Despite this precaution, this ratio is significantly lower than the expected ratio (0.211) assuming a main U deposition around 1315 Ma, as suggested by previous UPb isotopic dating. Although part of the radiogenic lead can be trapped as galena within the orebody, about 60% of Pb have migrated more than 700 m away from the orebody, preferentially along the unconformity. To cite this article: P. Kister et al., C. R. Geoscience 336 (2004).  相似文献   

20.
《Applied Geochemistry》2004,19(6):947-955
Nine partial decomposition procedures and a total digestion treatment were applied to road-deposited sediments. The objective was to define a parsimonious, time-efficient decomposition procedure that (1) has limited impact on the alumnio-silicate matrix and/or refractory-associated fractions, (2) has metal recoveries independent of CaCO3 content, and (3) produces high anthropogenic signals for known contaminants (e.g., Cu, Pb and Zn). The 9 digestions varied from weak single reagents (0.11 M acetic acid) to strong multi-step procedures (BCR 3-step plus aqua regia). Eight metals were examined: Al, Co, Cu, Fe, Mn, Ni, Pb, and Zn. Cold (room temperature) 0.5 M HCl shaken over a 1-h period with a solid-to-solution ratio of 1 g:20 ml, was judged superior based on the defined criteria. This simple, rapid treatment had limited impact on the residual matrix (mean and 95% confidence interval for Al recovery was 6±1%); recoveries of all elements examined were independent of CaCO3 content; the treatment produced high mean extraction efficiencies for Cu (58±9%), Pb (84±5%), and Zn (73±7%), and produced high anthropogenic signals. Thus, dilute HCl can be widely recommended as an optimal partial decomposition procedure for assessing non-residual fractions of complex solid media.  相似文献   

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