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1.
Apollo 15 low-Ti mare basalts have traditionally been subdivided into olivine- and quartz-normative basalt types, based on their different SiO2, FeO, and TiO2 whole-rock compositions. Previous studies have reconciled this compositional diversity by considering the olivine- and quartz-normative basalts as originating from different lunar mantle source regions. To provide new information on the compositions of Apollo 15 low-Ti mare basalt parental magmas, we report a study of major and trace-element compositions of whole rocks, pyroxenes, and other phases in the olivine-normative basalts 15016 and 15555 and quartz-normative basalts 15475 and 15499. Results show similar rare-earth-element patterns in pyroxenes from all four basalts. The estimated equilibrium parental-melt compositions from the trace-element compositions of pyroxenes are similar for 15016, 15555 and 15499. Additionally, an independent set of trace-element distribution coefficients has been determined from measured pyroxene and mesostasis compositions in sample 15499. These data suggest that fractional crystallization may be a viable alternative to compositional differences in the mantle source to explain the 25% difference in whole-rock TiO2, and corresponding differences in SiO2 and FeO between the Apollo 15 olivine- and quartz-normative basalts. In this model, the older (3.35 Ga) quartz-normative basalts, with lower TiO2 experienced olivine, chromite, and Cr-ulvöspinel fractionation at ‘crustal levels’ in magma chambers or dikes, followed by limited near-surface mineral fractionation, within the lava flows. In contrast, the younger (3.25 Ga) olivine-normative basalts experienced only limited magmatic differentiation at ‘crustal-levels’, but extensive near-surface mineral fractionation to produce their evolved mineral compositions. A two-stage mineral-fractionation model is consistent with textural and mineralogical observations, as well as the mineral trace-element constraints developed by this study.  相似文献   

2.
The Grader layered intrusion is part of the Havre-Saint-Pierre anorthosite in the Grenville Province (Quebec, Canada). This intrusion has a basin-like morphology and contains significant resources of Fe–Ti–P in ilmenite and apatite. Outcropping lithologies are massive oxide alternating with anorthosite layers, banded ilmenite–apatite–plagioclase rocks and layered oxide apatite (gabbro-)norites. Drill cores provide evidence for stratigraphic variations of mineral and whole rock compositions controlled by fractional crystallization with the successive appearance of liquidus phases: plagioclase and ilmenite followed by apatite, then orthopyroxene together with magnetite, and finally clinopyroxene. This atypical sequence of crystallization resulted in the formation of plagioclase–ilmenite–apatite cumulates or “nelsonites” in plagioclase-free layers. Fine-grained ferrodiorites that cross-cut the cumulates are shown to be in equilibrium with the noritic rocks. The high TiO2 and P2O5 contents of these assumed liquids explains the early saturation of ilmenite and apatite before Fe–Mg silicates, thus the nelsonites represent cumulates rather than crystallized Fe–Ti–P-rich immiscible melts. The location of the most evolved mineral and whole rock compositions several tens of meters below the top of the intrusion, forming a sandwich horizon, is consistent with crystallization both from the base and top of the intrusion. The concentrations of V and Cr in ilmenite display a single fractionation path for the different cumulus assemblages and define the cotectic proportion of ilmenite to 21 wt.%. This corresponds to bulk cotectic cumulates with ca. 8 wt.% TiO2, which is significantly lower than what is commonly observed in the explored portion of the Grader intrusion. The proposed mechanism of ilmenite-enrichment is the lateral removal of plagioclase due to its relative buoyancy in the dense ferrodiorite melt. This plagioclase has probably accumulated in other portions of the intrusion or has not been distinguished from the host anorthosite.  相似文献   

3.
A comprehensive Zr isotopic study was conducted on eleven lunar basalts and highland rocks to search for evidence of the extinct nuclide 92Nb, which decays to 92Zr with a half-life of 36 Ma. Internal isochrons were determined for two early highland rocks, 77215 and 60025. No resolvable Zr isotopic variations were detected in this wide range of lunar samples and thus there is no evidence for the former existence of live 92Nb on the Moon. The Nb/Zr ratios of lunar ilmenites and bulk rock samples vary by only a factor of two to three relative to the chondritic Nb/Zr ratio. No evidence for larger Nb/Zr fractionation was found. This limited fractionation and late isotopic closure of the source region prevents the formation of measurable 92Zr anomalies in high-Ti mare basalts. As a consequence, it is not possible to draw conclusions from the 92Nb-92Zr chronometer about the timing of early lunar differentiation and to constrain the role of ilmenite in the source region of high-Ti mare basalts. However, the fractionation is still sufficient to deduce an upper limit for the initial 92Nb/93Nb ratio of the solar system of <5 × 10−4.  相似文献   

4.
To investigate the formation and early evolution of the lunar mantle and crust we have analysed the oxygen isotopic composition, titanium content and modal mineralogy of a suite of lunar basalts. Our sample set included eight low-Ti basalts from the Apollo 12 and 15 collections, and 12 high-Ti basalts from Apollo 11 and 17 collections. In addition, we have determined the oxygen isotopic composition of an Apollo 15 KREEP (K - potassium, REE - Rare Earth Element, and P - phosphorus) basalt (sample 15386) and an Apollo 14 feldspathic mare basalt (sample 14053). Our data display a continuum in bulk-rock δ18O values, from relatively low values in the most Ti-rich samples to higher values in the Ti-poor samples, with the Apollo 11 sample suite partially bridging the gap. Calculation of bulk-rock δ18O values, using a combination of previously published oxygen isotope data on mineral separates from lunar basalts, and modal mineralogy (determined in this study), match with the measured bulk-rock δ18O values. This demonstrates that differences in mineral modal assemblage produce differences in mare basalt δ18O bulk-rock values. Differences between the low- and high-Ti mare basalts appear to be largely a reflection of mantle-source heterogeneities, and in particular, the highly variable distribution of ilmenite within the lunar mantle. Bulk δ18O variation in mare basalts is also controlled by fractional crystallisation of a few key mineral phases. Thus, ilmenite fractionation is important in the case of high-Ti Apollo 17 samples, whereas olivine plays a more dominant role for the low-Ti Apollo 12 samples.Consistent with the results of previous studies, our data reveal no detectable difference between the Δ17O of the Earth and Moon. The fact that oxygen three-isotope studies have been unable to detect a measurable difference at such high precisions reinforces doubts about the giant impact hypothesis as presently formulated.  相似文献   

5.
Megacrysts from the Grib kimberlite pipe (Arkhangelsk Province, Russia)   总被引：3，自引：0，他引：3  
The megacryst suite of the Grib kimberlite pipe (Arkhangelsk province, Russia) comprises garnet, clinopyroxene, magnesian ilmenite, phlogopite and garnet-clinopyroxene intergrowths. Crystalline inclusions, mainly of clinopyroxene and picroilmenite, occur in garnet megacrysts. Ilmenite is characterized by a wide range in the contents of MgO (10.6–15.5 wt.%) and Cr2O3 (0.7–8.3 wt.%). Megacryst garnets show wide variations in Cr2O3 (1.3–9.6 wt.%) and CaO (3.6–11.0 wt.%) but relatively constant MgO (15.4–22.3 wt.%) and FeO (5.2–9.9 wt.%). The pyroxenes also show wide variations in such oxides as Cr2O3, Al2O3 and Na2O (0.56–2.95; 0.86–3.25; 1.3–3.0 wt.%, respectively). The high magnesium and chromium content of all these minerals puts them together in one paragenetic group. This conclusion was confirmed by studies of the crystalline inclusions in megacrysts, which demonstrate similar variations in composition. Low concentration of hematite in ilmenite suggests reducing conditions during crystallization. P–T estimates based on the clinopyroxene geothermobarometer (Contrib. Mineral. Petrol. 139 (2000) 541) show wide variations (624–1208 °C and 28.8–68.0 kbars), corresponding to a 40–45 mW/m2 conductive geotherm. The majority of Gar-Cpx intergrowths differ from the corresponding monomineralic megacrysts in having higher Mg contents and relatively low TiO2. The minerals from the megacryst association, as a rule, differ from the minerals of mantle xenoliths, but garnets in ilmenite-bearing peridotite xenoliths are compositionally similar to garnet megacrysts. The common features of trace element composition of megacryst minerals and kimberlite (they are poor in Zr group elements) suggest a genetic relationship. The origin of the megacrysts is proposed to be genetically connected with kimberlite magma-chamber evolution on the one hand and with associated mantle metasomatism on the other. We suggest that, depending on the primary melt composition, different paragenetic associations of macro/megacrysts can be crystallized in kimberlites. They include: (1) Fe–Ti (Mir, Udachnaya pipes); (2) high-Mg, Cr (Zagadochna, Kusova pipes); (3) high-Mg, Cr, Ti (Grib pipe).  相似文献   

6.
我国嫦娥三号着陆于雨海北部的年轻玄武岩熔岩平原上,该区域的物质成分和矿物组成对于理解月球年轻的火山活动具有重要研究价值。月球全球勘探者(Lunar Prospector,LP)探测的元素数据揭示着陆区附近岩石类型主要为高铁中钛玄武岩(19.5%FeO;5.2%TiO_2)。本研究利用月球矿物绘图仪(Moon Mineralogy Mapper,M~3)获取的嫦娥三号着陆区附近的新鲜撞击坑高光谱数据,采用Hapke辐射传输模型和修正高斯模型(MGM)联合分析,对其年轻月海玄武岩铁镁质矿物进行了定量反演。研究表明该区域玄武岩中矿物组成以单斜辉石矿物为主,存在较高比例的橄榄石。基于光谱库匹配方法和MGM优化分析,我们反演出单斜辉石,斜方辉石,橄榄石和钛铁矿四种矿物的相对体积比为57.6:18.0:15.3:9.1,这一研究结果有待于与嫦娥三号玉兔号月球车上搭栽的红外成像光谱仪数据进行比对,以期从遥感和就位探测两个角度获得对于该地区矿物和岩石类型的全面认识。  相似文献   

7.
J.C. Duchesne  B. Charlier 《Lithos》2007,98(1-4):339-343
Merging our data with those of Robins and Chiodoni [Robins, B., Chiodoni, F., 2007. Poles apart: A discussion of the « Geochemistry of cumulates from the Bjerkreim–Sokndal layered intrusion (S. Norway). Part I: Constraints from major elements on the mechanism of cumulate formation and on the jotunite liquid line of descent ». Lithos doi:10.1016/j.lithos.2007.03.007], we examine the major-element compositions of 135 samples of so-called phi-C cumulates of the Bjerkreim–Sokndal layered intrusion. We show the limits of the TiO2/MgO ratio vs. Al2O3 diagram in order to ascertain the proportions of cumulus minerals (ilmenite and orthopyroxene) in the ilmenite leuconorite mafic pole. We also discard anomalous samples as we did in the previous paper. The rest of the samples (124 phi-C, i.e. 92% of the whole population) are then used to confirm the existence of plagioclase and mafic poles. It is shown that the mafic pole is indeed a mixture of ilmenite and orthopyroxene, not induced by “spurious correlation”.  相似文献   

8.
According to palinspastic reconstructions, the Neo-Tethys opening took place during the Permian between the Cimmerian fragments in the north and the Indo-Arabian margin in the south. Igneous remnants of this opening are exposed in Oman within either the Hawasina nappes or the para-autochtonous Arabian platform exposed in the Saih Hatat tectonic window. They consist predominantly of pillowed basaltic flows among which three groups have been distinguished. Group 1 is tholeiitic and characterized by low TiO2 and incompatible trace element contents, and a large range of Ndi values. Group 1 basalts are associated with distal sediments and plot near the boundary of or within the MORB field in the Pb–Pb correlation diagrams and between the MORB and Bulk Silica Earth (BSE) fields in Ndi–(206Pb/204Pb)i diagram. Group 2 basalts are alkaline and differ from Group 1 ones by their higher TiO2, La and Nb contents, and lower and more homogeneous Ndi values (+3 to +5). Group 2 volcanics are similar to alkali basalts from oceanic islands and share with Group 1 similar initial Pb ratios. Group 3 consists of tholeiitic and alkali basalts which are interbedded either with carbonate-platform sediments from the Saih Hatat window or with distal sediments from the Hawasina Nappes. This group differs from Groups 1 and 2 by its low to negative Ndi (+1.6 to −2). Group 1 likely derived from the mixing of depleted and enriched sources while Group 2 derived exclusively from an enriched source. There is no indication that continental crust was involved in the genesis of both Groups 1 and 2. In contrast, the low to negative Ndi values of Group 3 suggest that the magmas of this group were contaminated by the Arabian continental crust during their ascent. The geochemical features of the Middle Permian plume-related basalts suggest thus that the basement of the Hawasina basin was not genuine oceanic crust but either the thinned Arabian rifted continental margin or the continent–ocean transition zone of the Neo-Tethys.  相似文献   

9.
月海玄武岩与月球演化   总被引：6，自引：0，他引：6  
徐义刚 《地球化学》2010,39(1):50-62
月海玄武岩主要产于月球近边的盆地中,覆盖面积为月球表面的l％,其形成年龄多在39～31亿年之间,是各类月岩中最年轻的。与地球玄武岩相似,月海玄武岩由斜长石、辉石和橄榄石组成,但它们比地球玄武岩具有更低的Mg#、A1：0,、K和Na含量．高的FeO含量（大于16％）和变化范围大的TiO2含量（小于l％到大于13％）。根据TiO2含量的变化,月海玄武岩分成高Ti（〉6％）,低Ti（1．5％〈TiO：〈6％）以及极低Ti（〈1．5％）三类。所有月海玄武岩都具有Eu负异常,并亏损挥发性元素和亲铁元素。月海玄武岩的同位素特征指示其至少为三个组分混合的产物：（1）高：238U／204Pb、高87Sr／86Sr和负εNd组分,可能是岩浆海分异的残余岩浆即KREEP;（2）低：238U／204Pb、低87Sr／86sr和正εNd组分,来源于原始月幔,其熔融产物为低Ⅱ玄武岩;（3）中等87Sr／86Sr和εNd组分,位于月幔的顶部,经历了岩浆海（洋）过程中形成的堆晶物质的再熔融,还可能受到了陨击事件的影响,其熔融产物是高Ti玄武岩。月海玄武岩的元素和同位素地球化学性质支持岩浆海的假说,其源区的形成与岩浆海的分异密切相关,并经历了三个阶段：（a）岩浆海阶段,通过岩浆海的结晶分异形成顶部为斜长岩月壳,中间为高Ⅱ、富钛铁矿层,底部为巨厚的硅酸盐低Ti层的三层壳幔结构;（b）富钛铁矿堆晶岩（携带少量残余熔体）因密度大而下沉至下部的硅酸盐月幔（400km以下）;（C）月幔中这些不同源区的岩石发生减压熔融。早期由较浅的低熔点组分熔融形成低K高Ti玄武岩,之后形成来源较深的高Ti玄武岩和低Ti玄武岩。  相似文献   

10.
Lunar geochemistry as told by lunar meteorites   总被引：7，自引：0，他引：7  
About 36 lunar meteorites have been found in cold and hot deserts since the first one was found in 1979 in Antarctica. All are random samples ejected from unknown locations on the Moon by meteoroid impacts. Lithologically and compositionally there are three extreme types: (1) brecciated anorthosites with high Al2O3 (26–31%), low FeO (3–6%), and low incompatible elements (e.g., <1 μg/g Th), (2) basalts and brecciated basalts with high FeO (18–22%), moderately low Al2O3 (8–10%) and incompatible elements (0.4–2.1 μg/g Th), and (3) an impact-melt breccia of noritic composition (16% Al2O3, 11% FeO) with very high concentrations of incompatible elements (33 μg/g Th), a lithology that is identified as KREEP on the basis of its similarity to Apollo samples of that designation. Several meteorites are polymict breccias of intermediate composition because they contain both anorthosite and basalt. Despite the large range in compositions, a variety of compositional parameters together distinguish lunar meteorites from terrestrial materials. Compositional and petrographic data for lunar meteorites, when combined with mineralogical and compositional data obtained from orbiting spacecraft in the 1990s, suggest that Apollo samples identified with the magnesian (Mg-rich) suite of nonmare rocks (norite, troctolite, dunite, alkali anorthosite, and KREEP) are all products of a small, geochemically anomalous (noritic, high Th) region of crust known as the Procellarum KREEP Terrane and are not, as generally assumed, indigenous to the vast expanse of typical feldspathic crust known as the Feldspathic Highlands Terrane. Magnesian-suite rocks such as those of the Apollo collection do not occur as clasts in the feldspathic lunar meteorites. The misconception is a consequence of four historical factors: (1) the Moon has long been viewed as simply bimodal in geology, mare or highlands, (2) one of the last, large basin-forming bolides impacted in the Procellarum KREEP Terrane, dispersing Th-rich material, (3) although it was not known at the time, the Apollo missions all landed in or near the anomalous Procellarum KREEP Terrane and collected many Th-rich samples formed therein, and (4) the Apollo samples were interpreted and models for lunar crust formation developed without recognition of the anomaly because global data provided by orbiting missions and lunar meteorites were obtained only years later.  相似文献   

11.
The Emeishan continental flood basalt (ECFB) sequence in Dongchuan, SW China comprises a basal tephrite unit overlain by an upper tholeiitic basalt unit. The upper basalts have high TiO2 contents (3.2–5.2 wt.%), relatively high rare-earth element (REE) concentrations (40 to 60 ppm La, 12.5 to 16.5 ppm Sm, and 3 to 4 ppm Yb), moderate Zr/Nb and Nb/La ratios (9.3–10.2 and 0.6–0.9, respectively) and relatively high Nd (t) values, ranging from − 0.94 to 2.3, and are comparable to the high-Ti ECFB elsewhere. The tephrites have relatively high P2O5 (1.3–2.0 wt.%), low REE concentrations (e.g., 17 to 23 ppm La, 4 to 5.3 ppm Sm, and 2 to 3 ppm Yb), high Nb/La (2.0–3.9) ratios, low Zr/Nb ratios (2.3–4.2), and extremely low Nd (t) values (mostly ranging from − 10.6 to − 11.1). The distinct compositional differences between the tephrites and the overlying tholeiitic basalts cannot be explained by either fractional crystallization or crustal contamination of a common parental magma. The tholeiitic basalts formed by partial melting of the Emeishan plume head at a depth where garnet was stable, perhaps > 80 km. We propose that the tephrites were derived from magmas formed when the base of the previously metasomatized, volatile-mineral bearing subcontinental lithospheric mantle was heated by the upwelling mantle plume.  相似文献   

12.
Bauxite exploration involves routine analysis of a large number of samples for a wide range of elements. In Nigeria, though geological field exploration for bauxite started almost three decades ago very little has been achieved, mainly due to the non-availability of facilities for evaluating the dozens of suspected bauxite deposits scattered around the country. In this regard, a procedure for the rapid, accurate and precise measurement of a number of important elements in bauxite has been developed based on the newly acquired radioisotope based EDXRF spectrometer. Elements and oxides analyzed are Al2O3, SiO2, TiO2, Fe2O3, K2O, Mn, Co, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb and Pb. The richest bauxite sample has concentrations of 48.08, 18.90, 1.26, 7.71 and 1.93 wt% for Al2O3, SiO2, TiO2, Fe2O3, and K2O, respectively. The other values in ppm are Mn (3 0 2), Co (5 3 2), Cu (45), Zn (51), Ga (41), Rb (32), Sr (2 2 2), Y (32), Zr (8 4 9), Nb (89) and Pb (72). The measurement errors in terms of accuracy and precision are less than 5% and 10% and 5% and 15% for major and trace elements, respectively. Statistical correlation analysis carried out on the results shows the most significant relationships to be the negative correlations of alumina with silica, iron oxide and titanium. This is believed to be related to the processes of formation of bauxite, with the Si and Fe–Ti being removed as Al was being enriched.  相似文献   

13.
Anders Lindh 《Lithos》1972,5(4):325-343
Phase relations in the system FeO---Fe2O3---TiO2, at temperatures ranging between 300°C and 700°C, have been investigated experimentally with special refference to the reaction Fe3O4 + TiO2 = Fe2O3 + FeTiO3. Pressure was varied between 500 and 2000 bars but its effect was negligible. Magnetite and rutile are the stable assemblage at temperatures above 550 dgC, and hematite and ilmenite are stable for lower temperatures. The equilibrium oxygen fugacity is estimated to be 10−17.5 bars at equilibrium temperature. It is suggested that intermediate hematite-ilmenite solid solutions are inhomogeneous, consisting of ‘domains’ of hematite and ilmenite. The ‘domains’ are too small to be resolved by X-ray diffraction techniques. The top of the solvus curve in the hematite-ilmenite solution corresponds to a temperature of 660°C. Regular solution theory is not applicable to the solid solution.  相似文献   

14.
One characteristic of many subduction-zone garnet peridotites is that they contain titanium-bearing phases not otherwise found in mantle rocks. In particular, titanoclinohumite and/or its breakdown assemblage consisting of symplectic intergrowths of olivine and ilmenite is common in many of these bodies. The Alpe Arami garnet lherzolite of the Swiss Alps, while lacking titanoclinohumite, displays instead large numbers of FeTiO3 rod-shaped precipitates in the oldest generation of olivine, amounting to approximately 1% by volume, indicating that at some time in its past, the peridotite experienced conditions under which the solubility of TiO2 in olivine was >0.6 wt.%. In order to test the hypothesis that the environment of very high solubility of TiO2 in olivine is to be found at very high pressures, we have conducted experiments on lherzolite compositions with added ilmenite at pressures between 5 and 12 GPa and temperatures of 1350–1700 K. Our results on anhydrous compositions show that whereas solubility of TiO2 was not detected in olivine at 5 GPa, 1400 K where it coexists with rutile, when rutile disappeared from the paragenesis, the solubility climbed to 0.4 wt.% at 8 GPa, 0.5 wt.% at 10 GPa and to >1.0 wt.% at 12 GPa, 1700 K. These results support our previous interpretations from titanate morphology and abundance that the Alpe Arami massif has surfaced from P=10 GPa but remove the need to suggest a deeper origin and possible precursor phase such as wadsleyite. They also support the hypothesis that garnet peridotites with unusual Ti-bearing phases reflect a unique mantle environment occurring in the mantle wedge overlying subduction zones.  相似文献   

15.
Reaction rims of titanite on ilmenite are described in samples from four terranes of amphibolite-facies metapelites and amphibolites namely the Tamil Nadu area, southern India; the Val Strona area of the Ivrea-Verbano Zone, northern Italy, the Bamble Sector, southern Norway, and the northwestern Austroalpine Ötztal Complex. The titanite rims, and hence the stability of titanite (CaTiSiO4O) and Al–OH titanite, i.e. vuaganatite (hypothetical end-member CaAlSiO4OH), are discussed in the light of fH2O- and fO2-buffered equilibria involving clinopyroxene, amphibole, biotite, ilmenite, magnetite, and quartz in the systems CaO–FeO/Fe2O3–TiO2–SiO2–H2O–O2 (CFTSH) and CaO–FeO/Fe2O3–Al2O3–SiO2–H2O–O2 (CFASH) present in each of the examples. Textural evidence suggests that titanite reaction rims on ilmenite in rocks from Tamil Nadu, Val Strona, and the Bamble Sector originated most likely due to hydration reactions such as clinopyroxene + ilmenite + quartz + H2O = amphibole + titanite and oxidation reactions such as amphibole + ilmenite + O2 = titanite + magnetite + quartz + H2O during amphibolite-facies metamorphism, or, as in the case of the Ötztal Complex, during a subsequent greenschist-facies overprint. Overstepping of these reactions requires fH2O and fO2 to be high for titanite formation, which is also in accordance with equilibria involving Al–OH titanite. This study shows that, in addition to P, T, bulk–rock composition and composition of the coexisting fluid, fO2 and fH2O also play an important role in the formation of Al-bearing titanite during amphibolite- and greenschist-facies metamorphism.  相似文献   

16.
In 2013, Chang＇E-3 program will develop lunar mineral resources in-situ detection. A Visible and Near-infrared Imaging Spectrometer （VNIS） has been selected as one payload of CE-3 lunar rover to achieve this goal. It is critical and urgent to evaluate VNIS＇ spectrum data quality and validate quantification methods for mineral composition before its launch. Ground validation experiment of VNIS was carried out to complete the two goals, by simulating CE-3 lunar rover＇s detection environment on lunar surface in the laboratory. Based on the hyperspectral reflectance data derived, Correlation Analysis and Partial Least Square （CA-PLS） algorithm is applied to predict abundance of four lunar typical minerals （pyroxene, plagioclase, ilmenite and olivine） in their mixture. We firstly selected a set of VNIS＇ spectral parameters which highly correlated with minerals＇ abundance by correlation analysis （CA）, and then stepwise regression method was used to find out spectral parameters which make the largest contri- butions to the mineral contents. At last, functions were derived to link minerals＇ abundance and spectral parameters by partial least square （PLS） algorithm. Not considering the effect of maturity, agglutinate and Fe~, we found that there are wonderful correlations between these four minerals and VNIS＇ spectral parameters, e.g. the abundance of pyroxene correlates positively with the mixture＇s absorption depth, the value of absorption depth added as the in- creasing of pyroxene＇s abundance. But the abundance of plagioclase correlates negatively with the spectral parame- ters of band ratio, the value of band ratio would decrease when the abundance of plagioclase increased. Similar to plagioclase, the abundance of ilmenite and olivine has a negative correlation with the mixture＇s reflectance data, if the abundance of ilmenite or olivine increase, the reflectance values of the mixture will decrease. Through model validation, better estimates of pyroxene, plagioclase and ilmenite＇s abundances are given. It is concluded that VNIS has the capability to be applied on lunar minerals＇ identification, and CA-PLS algorithm has the potential to be used on lunar surface＇s in-situ detection for minerals＇ abundance prediction.  相似文献   

17.
Oxygen and iron isotope analyses of low-Ti and high-Ti mare basalts are presented to constrain their petrogenesis and to assess stable isotope variations within lunar mantle sources. An internally-consistent dataset of oxygen isotope compositions of mare basalts encompasses five types of low-Ti basalts from the Apollo 12 and 15 missions and eight types of high-Ti basalts from the Apollo 11 and 17 missions. High-precision whole-rock δ18O values (referenced to VSMOW) of low-Ti and high-Ti basalts correlate with major-element compositions (Mg#, TiO2, Al2O3). The observed oxygen isotope variations within low-Ti and high-Ti basalts are consistent with crystal fractionation and match the results of mass-balance models assuming equilibrium crystallization. Whole-rock δ56Fe values (referenced to IRMM-014) of high-Ti and low-Ti basalts range from 0.134‰ to 0.217‰ and 0.038‰ to 0.104‰, respectively. Iron isotope compositions of both low-Ti and high-Ti basalts do not correlate with indices of crystal fractionation, possibly owing to small mineral-melt iron fractionation factors anticipated under lunar reducing conditions.The δ18O and δ56Fe values of low-Ti and the least differentiated high-Ti mare basalts are negatively correlated, which reflects their different mantle source characteristics (e.g., the presence or absence of ilmenite). The average δ56Fe values of low-Ti basalts (0.073 ± 0.018‰, n = 8) and high-Ti basalts (0.191 ± 0.020‰, n = 7) may directly record that of their parent mantle sources. Oxygen isotope compositions of mantle sources of low-Ti and high-Ti basalts are calculated using existing models of lunar magma ocean crystallization and mixing, the estimated equilibrium mantle olivine δ18O value, and equilibrium oxygen-fractionation between olivine and other mineral phases. The differences between the calculated whole-rock δ18O values for source regions, 5.57‰ for low-Ti and 5.30‰ for high-Ti mare basalt mantle source regions, are solely a function of the assumed source mineralogy. The oxygen and iron isotope compositions of lunar upper mantle can be approximated using these mantle source values. The δ18O and δ56Fe values of the lunar upper mantle are estimated to be 5.5 ± 0.2‰ (2σ) and 0.085 ± 0.040‰ (2σ), respectively. The oxygen isotope composition of lunar upper mantle is identical to the current estimate of Earth’s upper mantle (5.5 ± 0.2‰), and the iron isotope composition of the lunar upper mantle overlaps within uncertainty of estimates for the terrestrial upper mantle (0.044 ± 0.030‰).  相似文献   

18.
Many continental flood basalts (CFB) have isotope and trace-element signatures that differ from those of oceanic basalts and much interest concerns the extent to which these reflect differences in their upper mantle source regions. A review of selected data sets from the Mesozoic and Tertiary CFB confirms significant differences in their major- and trace-element compositions compared with those of basalts erupted through oceanic lithosphere. In general, those CFB suites characterised by low Nb/La, high (87Sr/86Sr)i and low εNdi tend to exhibit relatively low TiO2, CaO/Al2O3, Na2O and/or Fe2O3, and relatively high SiO2. In contrast, those which have high Nb/La, low (87Sr/86Sr)i and high εNdi ratios, like the upper units in the Deccan Traps, have major- and trace-element compositions similar to oceanic basalts. It would appear that those CFB that have distinctive isotope and trace-element ratios also exhibit distinctive major-element contents, suggesting that major and trace elements have not been decoupled significantly during magma generation and differentiation.

When compared (at 8% MgO) with oceanic basalt trends, the displacement of many CFB to lower Na2O, Fe2O3*, TiO2 and CaO/Al2O3, but higher SiO2, at similar Mg#, is not readily explicable by crustal contamination. Rather, it reflects source composition and/or the effects of the melting processes. The model compositions of melts produced by decompression of mantle plumes beneath continental lithosphere have relatively low SiO2 and high Fe2O3*. In contrast, the available experimental data indicate that partial melts of peridotite have low TiO2, Na2O and Fe2O3*CaO/Al2O3, if the peridotite has been previously depleted by melt extraction. Moreover, melting of hydrated, depleted peridotite yields SiO2-rich, Fe2O3- and CaO-poor melts. Since anhydrous, depleted peridotite has a high-temperature solidus, it is argued that the source of these CFB was variably melt depleted and hydrated mantle, inferred to be within the lithosphere. Isotope data suggest these source regions were often old and relatively enriched in incompatible trace elements, and it is envisaged that H2O±CO2 were added at the same time as the incompatible elements. An implication is that a significant proportion of the new continental crust generated since the Permian reflected multistage processes involving mobilization of continental mantle lithosphere that was enriched in minor and trace elements during the Proterozoic.  相似文献   


19.
We have determined cooling rates of orthopyroxene crystals from two Mg-suite lunar samples (gabbronorite 76255 and troctolite 76535) and one terrestrial sample (orthopyroxenite SC-936 from the Stillwater Complex), on the basis of their Fe–Mg ordering states. In addition, a cooling rate of 76255 was determined by modeling the formation of exsolution lamellae in pyroxenes. The M1–M2 site occupancies of the orthopyroxene crystals were determined by single crystal X-ray diffraction and the rate constant for the ordering reaction was used along with calibrations of the equilibrium intracrystalline fractionation of Fe and Mg as a function of temperature to calculate cooling rates. The closure temperatures (TC) of cation ordering are 525 °C for 76255, 500 °C for 76535 and 350 °C for SC-936 corresponding to cooling rates of 4 × 10−2 °C/year at the closure temperature for the lunar samples and 10−6 °C/year for the Stillwater sample. A cooling rate for 76255, determined by simulating the exsolution process, is 1.7 × 10−2 °C/year at a closure temperature for exsolution of 700 °C. The Fe–Mg ordering cooling rate determined for 76535 reflects a complex thermal history superimposed on the initial plutonic provenance established for this sample [McCallum, I.S., Schwartz, J.M., 2001. Lunar Mg suite: thermobarometry and petrogenesis of parental magmas. J. Geophys. Res. 106, 27969–27983]. The preservation of a crystallization age of 4.51 Ga and a metamorphic age of 4.25 Ga for 76535 is consistent with a model in which excavation of this sample from the lower lunar crust took place while the sample was at a temperature above the closure temperatures for the Sm–Nd, U–Pb and Ar–Ar isotopic systems. Temperatures in excess of the isotopic closure temperatures (i.e., >600 °C) in the lower lunar crust were maintained by heat diffusing from concentrations of U- and Th-rich KREEP material at the base of the crust. On the other hand, 76255 formed at a much shallower depth in the lunar crust (2 km) and was well below its isotopic closure temperatures at the time of excavation, most likely during the Serenitatis basin-forming impact event. Both lunar samples were reheated during transport to the surface and deposition in hot ejecta blankets. The reheating was short lived but apparently sufficient to redistribute Fe and Mg in M sites in orthopyroxenes. For the lunar samples, the cooling rates based on Fe–Mg ordering represent final stage cooling within an ejecta blanket.  相似文献   

20.
Ilmenite is one of the common kimberlitic indicator minerals recovered during diamond exploration, and its distinction from non-kimberlitic rock types is important. This is particularly true for regions where these minerals are present in relatively low abundance, and they are the dominant kimberlitic indicator mineral recovered. Difficulty in visually differentiating kimberlitic from non-kimberlitic ilmenite in exploration concentrates is also an issue, and distinguishing kimberlitic ilmenite from those derive from other similar rocks, such as ultramafic lamprophyres, is practically impossible. Ilmenite is also the indicator mineral whose compositional variety has the most potential to resolve provenance issues related to mineral dispersions with contributions from multiple kimberlite sources.

Various published data sets from selected kimberlitic (including kimberlites, lamproites, and various ultramafic lamprophyres) and non-kimberlitic rock types have been compiled and evaluated in terms of their major element compositions. Compositional fields and bounding reference lines for ilmenites derived from kimberlites (sensu stricto), ultramafic lamprophyres, and other non-kimberlitic rock types have been defined primarily on MgO–TiO2 graphs as well as MgO–Cr2O3 relationships.  相似文献   


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