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1.
Siderophile and lithophile trace element data for 69 samples from the Sudbury impact crater fill (Onaping Formation) and quartz diorite offset dikes help constrain the sources of the established moderately elevated platinum group element signature associated with the impact structure. The siderophile element distribution of the crater fill requires contributions from bulk continental crust, mafic rocks and a chondritic component. A mantle component is absent, but the involvement of mid to lower crust is implied. After considering post‐impact hydrothermal alteration, melt heterogeneity and mafic target admixture, the projectile elemental ratios were determined on a more robust data subset. Chondrite discrimination diagrams of these ratios identify an ordinary or enstatite chondrite as the most probable source of meteoritic material in the Sudbury crater fill. However, the relative and absolute siderophile element distributions within the impact structure as well as bolide size models are congruent with the bolide being a comet that had a chondritic refractory component.  相似文献   

2.
Impact melt samples from drill hole B1-59 at the 3.8 km diameter Brent crater (Ontario) have been analysed for siderophile trace elements indicative of meteoritic contamination. Samples from the basal melt zone at 823–857 m depth are enriched in Ir, Os, Pd, Ni, Co, Cr and Se over basement, with the abundance pattern suggesting a chondritic projectile for Brent. From a Ni-Cr correlation of 10 melt samples an L or LL chondrite is inferred. The contribution of an ultramafic country rock (alnoite) in the melt is too small to significantly influence its NiCr ratio. Glass-rich breccias from the allochthonous breccias filling the crater also contain a meteoritic component. Interelement ratios (e.g. NiCr) are, however, fractionated relative to the melt zone samples. This, as well as the low Au content of all Brent samples, is probably a product of alteration.Additional data on impact melts from the 65 km diameter crater Manicouagan still did not reveal a meteoritic component, as also for the Mistastin crater (28 km diameter) where Cr analyses set an upper limit of 1% of an achondritic projectile component in the melt. Irghizites (tektite like glasses) from the Zhamanshin impact structure have been found to contain high Ni and Co concentrations, and our data show that Ir is also enriched. It is however not possible to define the projectile-type. Enrichment of an Ivory Coast tektite in Ir is confirmed. There are large differences in siderophile element concentrations among tektites, with otherwise similar chemical composition.There are now four known craters formed by chondrites (Clearwater East, Lapparjärvi, Wanapitei, and Brent), with Brent being the smallest of these. For smaller craters the projectiles appear to be limited to iron or stony-iron meteorites, because of atmospheric destruction of relatively small stony meteorites. It appears, however, that all major classes of meteorites are represented among the projectiles at terrestrial impact craters.  相似文献   

3.
Morokweng is a large, 145 Ma impact structure in the Northwest Province of South Africa. The impact origin of this structure and its melt rock has been confirmed by ample evidence of shock metamorphism in clasts within the melt rock and samples from granitoid basement below the melt body. The age of this structure is indistinguishable from the biostratigraphic age of the Jurassic-Cretaceous (J-K) boundary. The size of Morokweng, for which diameters ranging from 70 to 165 kilometers have been quoted before, and which has important implications regarding its relation to the J-K boundary, remains an open question.Here we present new results of a detailed petrographic and chemical investigation of impact melt rock and country rock samples. The granophyric melt rock is mostly unaltered and contains a large number of gabbroic and felsic clasts. The occurrence of baddeleyite, formed from high-temperature dissociation of primary zircon, indicates a high-temperature origin. The impact melt rock body, which in the cores investigated here has a thickness of at least 120 m, shows no statistically significant variation or trend in chemical composition with depth or geographic location. Chemical data for impact melt rock, breccia dike/vein breccia samples, granite, quartzite, and basic to mafic clasts were used in harmonic least squares mixing calculations to determine the source rock types and their proportions involved in the formation of the impact melt rock. Granite is the dominant target rock component (50 to 63% by weight; depending on target composition input to the mixing models), with significant (35 to 50%) mafic contributions, and a (possible) minor contribution of quartzite. New platinum group element (Ru, Rh, Pd, Os, Ir, and Pt), Re, and Au data, as well as data for other siderophile elements (Cr, Co, Ni, and Ir), confirm the presence of up to ∼ 5% of a chondritic component in the melt rock. The indigenous contribution of the PGEs from the target rocks is negligible. Normalized PGE abundance patterns and interelement ratios of Morokweng impact melt rock indicate that the projectile was likely of ordinary chondritic (possibly L chondrite) composition, but the choice of the meteoritic compositional data influences this interpretation.  相似文献   

4.
To characterize the compositions of materials accreted to the Earth-Moon system between about 4.5 and 3.8 Ga, we have determined Os isotopic compositions and some highly siderophile element (HSE: Re, Os, Ir, Ru, Pt, and Pd) abundances in 48 subsamples of six lunar breccias. These are: Apollo 17 poikilitic melt breccias 72395 and 76215; Apollo 17 aphanitic melt breccias 73215 and 73255; Apollo 14 polymict breccia 14321; and lunar meteorite NWA482, a crystallized impact melt. Plots of Ir versus other HSE define excellent linear correlations, indicating that all data sets likely represent dominantly two-component mixtures of a low-HSE target, presumably endogenous component, and a high-HSE, presumably exogenous component. Linear regressions of these trends yield intercepts that are statistically indistinguishable from zero for all HSE, except for Ru and Pd in two samples. The slopes of the linear regressions are insensitive to target rock contributions of Ru and Pd of the magnitude observed; thus, the trendline slopes approximate the elemental ratios present in the impactor components contributed to these rocks. The 187Os/188Os and regression-derived elemental ratios for the Apollo 17 aphanitic melt breccias and the lunar meteorite indicate that the impactor components in these samples have close affinities to chondritic meteorites. The HSE in the Apollo 17 aphanitic melt breccias, however, might partially or entirely reflect the HSE characteristics of HSE-rich granulitic breccia clasts that were incorporated in the impact melt at the time of its creation. In this case, the HSE characteristics of these rocks may reflect those of an impactor that predated the impact event that led to the creation of the melt breccias. The impactor components in the Apollo 17 poikilitic melt breccias and in the Apollo 14 breccia have higher 187Os/188Os, Pt/Ir, and Ru/Ir and lower Os/Ir than most chondrites. These compositions suggest that the impactors they represent were chemically distinct from known chondrite types, and possibly represent a type of primitive material not currently delivered to Earth as meteorites.  相似文献   

5.
The composition of the sampled melt rocks at the 22 km diameter E. Clearwater impact structure indicates the presence of 8% C-1 material. The meteoritic component is fractionated with refractory siderophiles, up to 30 times C-1 abundances, concentrated in ten to hundred micron-sized, magnetic particles. These particles consist of the Ni-sulphide, millerite, and what is assumed to be a mixture of refractory silicates and magnetite with grain sizes of <1 m. The larger particles have a core-rim structure with millerite and occasionally very minor galena and possibly pentlandite in the core. An origin as a combination of altered meteoritic metal and condensed meteoritic silicate is favored for the origin of the siderophile-rich particles. If 8% meteoritic material is taken as the average meteoritic contamination in the melt, then the E. Clearwater projectile may have impacted with a velocity of 17 km s–1. Peak shock pressures would have been of the order of 300 GPa, sufficient to vaporize the silicate component but only melt the metal component of the projectile. As the meteoritic material was being driven down into vaporized/ melted target rocks during the initial stages of impact, the melted Fe, Ni metal underwent oxidation, Fe was removed, and meteoritic silicate material recondensed on the cooler, essentially Ni metal. As cavity excavation proceeded, these Ni metal, silicate-oxide particles were incorporated in the melt, their refractory nature prevented thermal digestion and sulphur in the melt reacted with the metal to produce millerite on final equilibration. If this hypothesis is correct, it suggests that the E. Clearwater projectile was a C-2 or C-3 chondrite, both of which are compatible with the trace element composition of the melt rocks. Clearwater Lake is a twin impact structure formed by an asteroid pair. It is still not clear, however, what type of projectile formed the 32 km diameter western structure, where the surface melt rocks contain no identifiable meteoritic signature.  相似文献   

6.
The abundances of the highly siderophile elements (HSE) Re, Os, Ir, Ru, Pt, Rh, Pd and Au, and 187Os/188Os isotope ratios have been determined for a set of carbonaceous, ordinary, enstatite and Rumuruti chondrites, using an analytical technique that permits the precise and accurate measurement of all HSE from the same digestion aliquot. Concentrations of Re, Os, Ir, Ru, Pt and Pd were determined by isotope dilution ICP-MS and N-TIMS analysis. The monoisotopic elements Rh and Au were quantified relative to the abundance of Ir.Differences in HSE abundances and ratios such as Re/Os, 187Os/188Os, Pd/Ir and Au/Ir between different chondrite classes are further substantiated with new data, and additional Rh and Au data, including new data for CI chondrites. Systematically different relative abundances of Rh between different chondrite classes are reminiscent of the behaviour of Re. Carbonaceous chondrites are characterized by low average Rh/Ir of 0.27 ± 0.03 (1s) which is about 20% lower than the ratio for ordinary (0.34 ± 0.02) and enstatite chondrites (EH: 0.33 ± 0.01; EL: 0.32 ± 0.01). R chondrites show higher and somewhat variable Rh/Ir of 0.37 ± 0.07.Well-defined linear correlations of HSE, in particular for bulk samples of ordinary and EL chondrites, are explained by binary mixing and/or dilution by silicates. The HSE carriers responsible for these correlations have a uniform chemical composition, indicating efficient homogenization of local nebular heterogeneities during or prior to the formation of the host minerals in chondrite components. Excepting Rumuruti chondrites and Au in carbonaceous chondrites, these correlations also suggest that metamorphism, alteration and igneous processes had negligible influence on the HSE distribution on the bulk sample scale.Depletion patterns for Rh, Pd and Au in carbonaceous chondrites other than CI are smoothly related to condensation temperatures and therefore consistent with the general depletion of moderately volatile elements in carbonaceous chondrites. Fractionated HSE abundance patterns of ordinary, enstatite and Rumuruti chondrites, however, are more difficult to explain. Fractional condensation combined with the removal of metal phases at various times, and later mixing of early and late formed metal phases may provide a viable explanation. Planetary fractionation processes that may have affected precursor material of chondrite components cannot explain the HSE abundance patterns of chondrite groups. HSE abundances of some, but not all Rumuruti chondrites may be consistent with solid sulphide-liquid sulphide fractionation processes during impact induced melting.  相似文献   

7.
The composition of the sampled melt rocks at the 22 km diameter E. Clearwater impact structure indicates the presence of ～8% C-1 material. The meteoritic component is fractionated with refractory siderophiles, up to 30 times C-1 abundances, concentrated in ten to hundred micron-sized, magnetic particles. These particles consist of the Ni-sulphide, millerite, and what is assumed to be a mixture of refractory silicates and magnetite with grain sizes of <1 μm. The larger particles have a core-rim structure with millerite and occasionally very minor galena and possibly pentlandite in the core. An origin as a combination of altered meteoritic metal and condensed meteoritic silicate is favored for the origin of the siderophile-rich particles. If 8% meteoritic material is taken as the average meteoritic contamination in the melt, then the E. Clearwater projectile may have impacted with a velocity of 17 km s?1. Peak shock pressures would have been of the order of 300 GPa, sufficient to vaporize the silicate component but only melt the metal component of the projectile. As the meteoritic material was being driven down into vaporized/ melted target rocks during the initial stages of impact, the melted Fe, Ni metal underwent oxidation, Fe was removed, and meteoritic silicate material recondensed on the cooler, essentially Ni metal. As cavity excavation proceeded, these Ni metal, silicate-oxide particles were incorporated in the melt, their refractory nature prevented thermal digestion and sulphur in the melt reacted with the metal to produce millerite on final equilibration. If this hypothesis is correct, it suggests that the E. Clearwater projectile was a C-2 or C-3 chondrite, both of which are compatible with the trace element composition of the melt rocks. Clearwater Lake is a twin impact structure formed by an asteroid pair. It is still not clear, however, what type of projectile formed the 32 km diameter western structure, where the surface melt rocks contain no identifiable meteoritic signature.  相似文献   

8.
Platinum-group element (PGE) geochemistry combined with elemental geochemistry and magnetite compositions are reported for the Mesoproterozoic Zhuqing Fe–Ti–V oxide ore-bearing mafic intrusions in the western Yangtze Block, SW China. All the Zhuqing gabbros display extremely low concentrations of chalcophile elements and PGEs. The oxide-rich gabbros contain relatively higher contents of Cr, Ni, Ir, Ru, Rh, and lower contents of Pt and Pd than the oxide-poor gabbros. The abundances of whole-rock concentrations of Ni, Ir, Ru, and Rh correlate well with V contents in the Zhuqing gabbros, implying that the distributions of these elements are controlled by magnetite. The fractionation between Ir–Ru–Rh and Pt–Pd in the Zhuqing gabbros is mainly attributed to fractional crystallization of chromite and magnetite, whereas Ru anomalies are mainly due to variable degrees of compatibility of PGE in magnetite. The order of relative incompatibility of PGEs is calculated to be Pd?<?Pt?<?Rh?<?Ir?<?Ru. The very low PGE contents and Cu/Zr ratios and high Cu/Pd ratios suggest initially S-saturated magma parents that were highly depleted in PGE, which mainly formed due to low degrees of partial melting leaving sulfides concentrating PGEs behind in the mantle. Moreover, the low MgO, Ni, Ir and Ru contents and high Cu/Ni and Pd/Ir ratios for the gabbros suggest a highly evolved parental magma. Fe–Ti oxides fractionally crystallized from the highly evolved magma and subsequently settled in the lower sections of the magma chamber, where they concentrated and formed Fe–Ti–V oxide ore layers at the base of the lower and upper cycles. Multiple episodes of magma replenishment in the magma chamber may have been involved in the formation of the Zhuqing intrusions.  相似文献   

9.
The emission of platinum group elements (PGE) from automobile catalytic converters has led to enrichment of PGE in road dusts and roadside soils in urban areas that are well above the natural background levels. This paper evaluates the source of contamination of all the PGE and Au in road dusts and roadside soils in the Pearl River Delta region, including three major cities, Shenzhen, Guangzhou and Hong Kong, South China. Samples were digested using Carius tube and analyzed by isotope dilution ICP-MS; Os was separated by distillation and other PGE by Te-coprecipitation. All samples have elevated PGE concentrations above the background values of uncontaminated soils and contain higher Pt, Pd and Rh than other PGE. The maximum values are 181 ng/g Pt, 514 ng/g Pd, 53 ng/g Rh and 1345 ng/g Au. There are clear positive correlations between Pt and Pd, Pt and Rh, and Pd and Rh, indicating that the main emitted of PGE from automobile catalyst are Pt, Pd and Rh. High concentrations of Au were also found in road dust samples from Hong Kong and Shenzhen. Dust samples with higher Os contents have lower 187Os/188Os ratios. Samples from Hong Kong show relatively high Pt/Rh ratios. Positive correlations between Pt and Ru, and Pt and Ir were found in Shenzhen and Hong Kong, but only positive correlations between Pt and Ir were found in Guangzhou. These different characteristics reflect different automobile catalytic systems used in Hong Kong and mainland China.  相似文献   

10.
Fourteen peridotite xenoliths collected in the Massif Central neogene volcanic province (France) have been analyzed for platinum-group elements (PGE), Au, Cu, S, and Se. Their total PGE contents range between 3 and 30 ppb and their PGE relative abundances from 0.01 to 0.001 × CI-chondrites, respectively. Positive correlations between total PGE contents and Se suggest that all of the PGE are hosted mainly in base metal sulfides (monosulfide solid solution [Mss], pentlandite, and Cu-rich sulfides [chalcopyrite/isocubanite]). Laser ablation microprobe-inductively coupled plasma mass spectrometry analyses support this conclusion while suggesting that, as observed in experiments on the Cu-Fe-Ni-S system, the Mss preferentially accommodate refractory PGEs (Os, Ir, Ru, and Rh) and Cu-rich sulfides concentrate Pd and Au. Poikiloblastic peridotites pervasively percolated by large silicate melt fractions at high temperature (1200°C) display the lowest Se (<2.3 ppb) and the lowest PGE contents (0.001 × CI-chondrites). In these rocks, the total PGE budget inherited from the primitive mantle was reduced by 80%, probably because intergranular sulfides were completely removed by the silicate melt. In contrast, protogranular peridotites metasomatized by small fractions of volatile-rich melts are enriched in Pt, Pd, and Au and display suprachondritic Pd/Ir ratios (1.9). The palladium-group PGE (PPGE) enrichment is consistent with precipitation of Cu-Ni-rich sulfides from the metasomatic melts. In spite of strong light rare earth element (LREE) enrichments (Ce/YbN < 10), the three harzburgites analyzed still display chondrite-normalized PGE patterns typical of partial melting residues, i.e., depleted in Pd and Pt relative to Ir and Ru. Likewise, coarse-granular lherzolites, a common rock type in Massif Central xenoliths, display Pd/Ir, Ru/Ir, Rh/Ir, and Pt/Ir within the 15% uncertainty range of chondritic meteorites. These rocks do not contradict the late-veneer hypothesis that ascribes the PGE budget of the Earth to a late-accreting chondritic component; however, speculations about this component from the Pd/Ir and Pt/Ir ratios of basalt-borne xenoliths may be premature.  相似文献   

11.
方解石作为木落稀土矿床常见的脉石矿物,其中的铂族元素(简称PGE)地球化学特征有可能记录了地质流体的性质。采用ICP-MS分析木落方解石中PGE的含量,并对铂族元素的分布、相关性、成因进行了探讨。木落方解石可以分为两类:I型方解石和Ⅱ型方解石。I型方解石中∑PGE(不含Os)0.62～1.33ng/g,具相对低的Pd/Pt、Pd/Rh、Pd/Ru、Pd/Ir比值,不太显著的Pt-Pd分配模式,为岩浆成因方解石,与成矿作用密切相关;Ⅱ型方解石中∑PGE(不含Os)1.85～2.97ng/g,具相对高的Pd/Pt、Pd/Rh、Pd/Ru、Pd/Ir比值和显著的Pt-Pd分配模式,为热液成因方解石,代表了成矿作用后的一期地质流体作用,与成矿关系不大,仅局部地区存在改造前次流体作用形成的稀土矿体。富CO2热液具有携带PGE的能力,并能够导致PGE的分异,与富CO2岩浆相比,富CO2热液对铂族元素具有一定程度的富集作用。  相似文献   

12.
Sixteen crater samples were analyzed by radiochemical neutron activation analysis for Ge, Ir, Ni, Os, Pd and Re. Two impact melt rock samples from Clearwater East (22 km) showed strong, uniform enrichments in all elements except Ge, corresponding to 7.4% C1 chondrite material. Interelement ratios suggest that the meteorite was a C1 (or C2) chondrite, not an iron, stony iron, or chondrite of another type. An Ivory Coast tektite (related to the 10 km Bosumtwi crater) was enriched in Ir + Os and Ni to about 0.04 and 1.6% of C1 chondrite levels, but in the absence of data on country rocks, the meteorite cannot yet be characterized.Impact melt rock samples from Clearwater West (32km), Manicouagan (70km), and Mistastin (28 km) showed no detectable meteoritic component. Upper limits, as Cl chondrite equivalent, were Os ≤ 2 × 10?3% (~0.01 ppb), Ni ≤ 2 × 10?1% (~20ppm). Possible causes are high impact velocity and/or a chemically inconspicuous meteorite (achondrite, Ir,Os-poor iron or stony iron). However, a more likely reason is that some fraction of the impact melt remains meteorite-free, especially at craters with central peaks.Clearwater East is the first terrestrial impact crater found to be associated with a stony meteorite. Apparently the consistent absence of stony projectiles at small craters (< 1 km diameter) reflects their destruction in the atmosphere, as proposed by Öpik.  相似文献   

13.
ABUNDANCE AND DISTRIBUTION OF PLATINUM-GROUP ELEMENTS (PGE) IN PERIDOTITE FROM THE DAGZHUKA OPHIOLITE IN TIBET:IMPLICATIONS FOR MANTLE METASOMATISM  相似文献   

14.
Summary The Jinchuan deposit is a platinum group element (PGE)-rich sulfide deposit in China. Drilling and surface sampling show that three categories of platinum group element (PGE) mineralization occur; type I formed at magmatic temperatures, type II occurs in hydrothermally altered zones of the intrusion, and type III in sheared dunite and lherzolite. All ore types were analyzed for Os, Ir, Ru, Rh, Pd, Pt and Au, as well as for Cu, Ni, Co and S. Type I ore has (Pt + Pd)/(Os + Ir + Ru + Rh) ratios of <7 and relatively flat chondrite-normalized noble metal patterns; the platinum group minerals (PGM) are dominated by sperrylite and moncheite associated with chalcopyrite, pyrrhotite and pentlandite. Type II has (Pt + Pd)/(Os + Ir + Ru + Rh) ratios from 40 to 330 and noble metal distribution patterns with a positive slope; the most common PGM are sperrylite and Pd bismuthotelluride phases concentrated mostly at the margins of base metal sulfides. Type III ores have the highest (Pt + Pd)/(Os + Ir + Ru + Rh) ratios from 240 to 710; the most abundant PGM are sperrylite and phases of the Pt–Pd–Te–Bi–As–Cl system. It is concluded that the Jinchuan deposit formed as a result of primary magmatic crystallization followed by hydrothermal remobilization, transport, and deposition of the PGE.  相似文献   

15.
Platinum group elements (PGE) enrichment occurs in Zn–Cu and Ni-rich ophiolities in a number of geological settings. Platinum group elements (PGE) mineralization in Pyroxenite from the Faryab ophiolities of Zagros belt in south Iran was studied. The ophiolite rocks represent blocks of Tethyan oceanic crust that were emplaced on the continental margin during the late Cretaceous period. Much of lower ophiolitic section is composed of homogeneous harzburgite, while upper sections harzburgite interlayer with dunite and pyroxenite are included. This study focused on pyroxenite that includes most of sulfide mineralization in Faryab. More than 500 samples were investigated from polished thin sections; that cover all area of Faryab. The sulfide phases include pyrrhotite, pentlandite, millerite, violarite, smythite, and heazlewoodite. The results show that in almost all the samples Os is below the 2 ppb detection limit, Platinum values vary from <5 to 91 ppb and the light PGE (Ru, Rh, and Pd) relative to the heavy PGE (Os, Ir, and Pt) are more concentrated. Calculation showed that in pyroxenites Pd–Pt is occurring with orthopyroxenite and Rh–Os is occurring in clinopyroxenite. Ni/Pd ratios in Faryab vary between 7 and 356 and Pd/Ir ratio is 0.1–27. This indicates that in Faryab area partial melt of mantle occurred. Pd/Rh ratio in Faryab is 0.1–11, and Pd/Pt varies between 0.2 and 1.5. Pd/Ir ratio in Faryab decreases and shows that PGE in Faryab occurred.  相似文献   

16.
The concentrations of Rh, Au and other highly siderophile elements (HSE: Re, Os, Ir, Ru, Pt, Rh, Pd and Au), and 187Os/188Os isotope ratios have been determined for samples from peridotite massifs and xenoliths in order to further constrain HSE abundances in the Earth's mantle and to place constraints on the distributions processes accounting for observed HSE variations between fertile and depleted mantle lithologies. Concentrations of Re, Os, Ir, Ru, Pt and Pd were determined by isotope dilution ICP-MS and N-TIMS. The monoisotopic elements Rh and Au were quantified by standardization relative to the concentrations of Ru and Ir, respectively, and were determined from the same digestion aliquot as other HSE. The measurement precision of the concentration data under intermediate precision conditions, as inferred from repeated analyses of 2 g test portions of powdered samples, is estimated to be better than 10% for Rh and better than 15% for Au (1 s).Fertile lherzolites display non-systematic variation of Rh concentrations and constant Rh/Ir of 0.34 ± 0.03 (1 s, n = 57), indicating a Rh abundance for the primitive mantle of 1.2 ± 0.2 ng/g. The data also suggest that Rh behaves as a compatible element during low to moderate degrees of partial melting in the mantle or melt–mantle interaction, but may be depleted at higher degrees of melting. In contrast, Au concentrations and Au/Ir correlate with peridotite fertility, indicating incompatible behaviour of Au during magmatic processes in the mantle. Fertile lherzolites display Au/Ir ranging from 0.20 to 0.65, whereas residual harzburgites have Au/Ir < 0.20. Concentrations of Au and Re are correlated with each other and suggest similar compatibility of both elements. The primitive mantle abundance of Au calculated from correlations displayed by Au/Ir with Al2O3 and Au with Re is 1.7 ± 0.5 ng/g (1 s).The depletion of Pt, Pd, Re and Au relative to Os, Ir, Ru and Rh displayed by residual harzburgites, suggests HSE fractionation during partial melting. However, the HSE abundance variations of fertile and depleted peridotites cannot be explained by a simple fractionation process. Correlations displayed by Pd/Ir, Re/Ir and Au/Ir with Al2O3 may reflect refertilization of previously melt depleted mantle rocks due to reactive infiltration of silicate melts.Relative concentrations of Rh and Au inferred for the primitive mantle model composition are similar to values of ordinary and enstatite chondrites, but distinct from carbonaceous chondrites. The HSE pattern of the primitive mantle is inconsistent with compositions of known chondrite groups. The primitive mantle composition may be explained by late accretion of a mixture of chondritic with slightly suprachondritic materials, or alternatively, by meteoritic materials mixed into mantle with a HSE signature inherited from core formation.  相似文献   

17.
Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) was used to measure distributions of the siderophile elements V, Fe, Co, Ni, Mo, Ru, Rh, Pd, W, Re, Os, Ir, Pt, and Au in Fremdlinge with a spatial resolution of 15 to 25 μm. A sulfide vein in a refractory inclusion in Allende (CV3-oxidized) is enriched in Rh, Ru, and Os with no detectable Pd, Re, Ir, or Pt, indicating that Rh, Ru, and Os were redistributed by sulfidation of the inclusion, causing fractionation of Re/Os and other siderophile element ratios in Allende CAIs. Fremdlinge in compact Type-A inclusions from Efremovka (CV3-reduced) exhibit subsolidus exsolution into kamacite and taenite and minimal secondary formation of V-magnetite and schreibersite. Siderophile element partitioning between taenite and kamacite is similar to that observed previously in iron meteorites, while preferential incorporation of the light PGEs (Ru, Rh, Pd) relative to Re, Os, Ir, and Pt by schreibersite was observed. Fremdling EM2 (CAI Ef2) has an outer rim of P-free metal that preserves the PGE signature of schreibersite, indicating that EM2 originally had a phosphide rim and lost P to the surrounding inclusion during secondary processing. Most Fremdlinge have chondrite-normalized refractory PGE patterns that are unfractionated, with PGE abundances derived from a small range of condensation temperatures, ∼1480 to 1468 K at Ptot = 10−3 bar. Some Fremdlinge from the same CAI exhibit sloping PGE abundance patterns and Re/Os ratios up to 2 × CI that likely represent mixing of grains that condensed at various temperatures.  相似文献   

18.
The major element relationships in ferromanganese (Fe-Mn) crusts from Afanasiy-Nikitin seamount (ANS), eastern equatorial Indian Ocean, appear to be atypical. High positive correlations (r = 0.99) between Mn/Co and Fe/Co ratios, and lack of correlation of those ratios with Co, Ce, and Ce/Co, indicate that the ANS Fe-Mn crusts are distinct from Pacific seamount Fe-Mn crusts, and reflect region-specific chemical characteristics. The platinum group elements (PGE: Ir, Ru, Rh, Pt, and Pd) and Au in ANS Fe-Mn crusts are derived from seawater and are mainly of terrestrial origin, with a minor cosmogenic component. The Ru/Rh (0.5–2) and Pt/Ru ratios (7–28) are closely comparable to ratios in continental basalts, whereas Pd/Ir ratios exhibit values (<2) similar to CI-chondrite (∼1). The chondrite-normalized PGE patterns are similar to those of igneous rocks, except that Pd is relatively depleted. The water depth of Fe-Mn crust formation appears to have a first-order control on both major element and PGE enrichments. These relationships are defined statistically by significant (r > 0.75) correlations between water depth and Mn/Co, Fe/Co, Ce/Co, Co, and the PGEs. Fractionation of the PGE-Au from seawater during colloidal precipitation of the major-oxide phases is indicated by well-defined linear positive correlations (r > 0.8) of Co and Ce with Ir, Ru, Rh, and Pt; Au/Co with Mn/Co; and by weak or no correlations of Pd with water depth, Co-normalized major-element ratios, and with the other PGE (r < 0.5). The strong enrichment of Pt (up to 1 ppm) relative to the other PGE and its positive correlations with Ce and Co demonstrate a common link for the high concentrations of all three elements, which likely involves an oxidation reaction on the Mn-oxide and Fe-oxyhydroxide surfaces. The documented fractionation of PGE-Au and their positive association with redox sensitive Co and Ce may have applications in reconstructing past-ocean redox conditions and water masses.  相似文献   

19.
对1998年7月发现的辽宁岫岩县苏子沟镇罗圈里直径1.8　km的撞击坑构造作了一系列地质、地球化学测试工作。从坑内出露的基岩（下元古界辽河群里尔峪组变质砂岩）与充填碎屑物质界面上取样，经XRD定性分析显示有自然铂、锇铱矿、自然铑、自然铱的存在。进一步对这一类样品作等离子质谱分析（ICP-MS），则发现有PGE异常。特别是Pt，Pd，Ru甚至高于原始地幔的丰度值。进一步淘选坑里重砂样品则发现数颗粗铂矿物。已作电子探针分析表明PGE质量分数Pt为85.30%～98.68%,Pd为0.45%～0.87%,Rh为0.56%～0.74%,Os为0.66%～1.31%,Ir为1.72%～2.43%,Ru为0.16%～0.31%,此外Ni为0.00%～0.50%,Fe为4.98%～5.42%。笔者认为这种PGE元素异常和粗铂矿的发现是陨石及其撞击作用的重要依据之一。  相似文献   

20.
Boninite-norite (BN) suites emplaced in an intracratonic setting in Archaean Cratons, are reported from many parts of the world. Such high-Mg low-Ti siliceous rocks are emplaced during Neoarchaean-Paleoproterozoic. The Archaean central Indian Bastar Craton also contains such a boninite-norite suite, which occurs in the form of dykes and volcanics. The spatial and temporal correlation of these high-Mg low-Ti siliceous rocks with similar rocks occurring around the northern Bastar and Dharwar Cratons probably represent a Bastar-Dharwar Large Igneous Province during the Neoarchaean-Paleoproterozoic. Platinum group element (PGE) abundances in these rocks provide constraints on their geochemical evolution during the Neoarchaean-Paleoproterozoic. The PGE geochemistry of the boninite-norite suite from the southern part of the central Indian Bastar Craton is presented to understand their behaviour during magma fractionation. In primitive mantle-normalized plots all samples have similar PGE fractionated patterns that are enriched in Pd, Pt and Rh relative to Ru. The Pd/Ru ratios for eight samples range from 2.0 to 7.0 which is higher than primitive mantle (primitive mantle Pd/Ru ≈1.2). The Pd/Pt ratios range between 0.2–2.5 with an average value of 0.7 which is near chondritic (primitive mantle Pd/Pt ≈0.5). PGE variations in these rocks together with those of major and other trace elements are consistent with a model involving olivine fractionation along with chromite as a cotectic phase. The Pt fractionation from Pd and Rh is controlled by both olivine and chromite crystallization at an early stage during high temperature crystal fractionation when the Pt was strongly compatible and Pd and Rh were incompatible. Strong negative correlations of the S content with iron and TiO2 plus lithophile element contents of the rock suggest a decrease of the S solubility in the parental high-Mg magma and separation of an immiscible sulfide liquid with decreasing temperature. Palladium plus other available chalcophile elements (e.g., Re, Au, Ag) have been fractionated in this immiscible sulfide liquid after considerable olivine fractionation of the magma.  相似文献   

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