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1.
In northwest Turkey, high-pressure metamorphic rocks occur as exotic blocks within the Çetmi mélange located on the south of the Biga Peninsula. Rutile chemistry and rutile thermometry obtained from the eclogite and associated garnet-mica schist in the Çetmi mélange indicate significant trace element behaviour of subducted oceanic crust and source-rock lithology of detrital rutiles. Cr and Nb contents in detrital rutile from garnet-mica schist vary from 355 to 1026 μg/g and 323 and 3319 μg/g, respectively. According to the Cr-Nb discrimination diagram, the results show that 85% of the detrital rutiles derived from metapelitic and 15% from metamafic rocks. Temperatures calculated for detrital rutiles and rutiles in eclogite range from 540 °C to 624 °C with an average of 586 °C and 611 °C to 659 °C with an average of 630 °C at P = 2.3 GPa, respectively. The calculated formation temperatures suggest that detrital rutiles are derived from amphibolite- and eclogite-facies metamorphic rocks. Amphibolite-facies rocks of the Kazdağ Massif could be the primary source rocks for the rutiles in the garnet-mica schist from the Çetmi mélange. Nb/Ta ratios of metapelitic and metamafic rutiles fall between 7–24 and 11–25, respectively. Nb/Ta characteristics in detrital rutiles may reflect a change in source-rock lithology. However, Nb/Ta ratios of rutiles in eclogite vary from 9 to 22. The rutile grains from eclogites are dominated by subchondritic Nb/Ta ratios. It can be noted that subchondritic Nb/Ta may record rutile growth from local sinks of aqueous fluids from metamorphic dehydration.  相似文献   

2.
The petrogenetic relations among Ti‐rich minerals in high‐grade metabasites is illuminated here through a detailed petrological investigation of an anatectic garnet–clinopyroxene granulite from the Grenville Province, Ontario, Canada containing rutile, titanite and ilmenite in distinct microtextural settings. Garnet porphyroblasts exhibit zoned Ti concentrations (up to 0.15 wt% TiO2 in their cores), as well as a variety of rutile inclusion types, including clusters of small, variably elongate grains and thin (≤1 μm) oriented needles. Calcite inclusions in garnet, commonly observed surrounding garnet cores containing quartz and clinozoisite, indicate the presence of evolving C–O–H fluids during garnet growth and suggest that the rutile clusters may have formed from subsequent Ti diffusion and rutile precipitation within existing fluid inclusions. Titanite forms large subhedral crystals and typically occurs where the primary garnet–clinopyroxene assemblage is in contact with leucosome containing megacrystic hornblende, silvialitic scapolite and calcic plagioclase. Many titanite crystals exhibit marginal subgrains that correspond with sharp changes in their major and trace element composition, likely related to a dissolution–precipitation or recrystallization process following primary crystallization. Clinopyroxene–ilmenite symplectite coronas surround titanite in most locations, likely forming from reaction with the hornblende‐plagioclase matrix (±fluids/melt). Integration of multi‐equilibria thermobarometry and Zr thermometry in rutile and titanite with phase equilibrium modelling allows definition of a clockwise P–T path evolving to peak pressures of ~1.5 GPa at ~750°C during garnet and rutile growth, followed by peak temperature conditions of ~1.2 GPa and ~820–880°C associated with melt‐present titanite growth, and finally cooling and decompression to regional amphibolite facies conditions (~1.0 GPa and ~750°C) associated with the formation of clinopyroxene–ilmenite symplectites surrounding titanite. P–T pseudosections calculated for the pristine (leucosome‐ and titanite ‐free) metabasite bulk composition reproduce much of the prograde phase relations, but predict rutile as the stable Ti‐rich mineral at the peak thermal conditions associated with melt‐present titanite growth. The P–M(CaO) and T–M(CaO) models show that bulk CaO concentrations have a significant effect on the stability ranges of titanite and rutile. Increased bulk CaO tends to stabilize titanite to higher pressure and temperature at the expense of rutile, with a ≥15% increase in CaO producing the observed titanite‐bearing assemblage at high‐P granulite facies conditions. Thus, the model results are consistent with the textural observations, which suggest that titanite stability is associated with a chemical exchange between the host metabasite and a Ca‐rich melt.  相似文献   

3.
In the present study we focused on detrital rutile separated from 12 psammitic samples that belong to three different sedimentary successions (Carboniferous, Permo-Carboniferous, Permo-Triassic) occurring on Chios Island, Greece. The Ti, Cr, Al, Fe, Nb, Zr, Si, and V contents of the rutiles were obtained by electron-microprobe analyses to trace their provenance.The Cr and Nb concentrations of the analysed rutile grains show a wide range and indicate that this mineral in the Carboniferous succession is mainly derived from metamafic rocks, whereas in the Permo-Carboniferous and Permo-Triassic successions stem from a metapelitic source. The calculated formation temperatures using the Zr-in-rutile thermometer range from ca. 520 to 850 °C with “hotter” rutile being encountered in the Permo-Carboniferous and Permo-Triassic successions. This feature together with the rutile chemistry indicate a change in source-rock lithology through time, which could either reflect an increasing depth of erosion of an exhumed ‘Variscan’ nappe pile of heterogeneous composition in the hinterland or a change in the style of accretion and erosion of different terranes at the southern margin of Laurussia during the subduction of a branch of the Palaeotethys Ocean in the Late Palaeozoic. In general, this study underscores the importance of rutile chemistry and thermometry in quantitative single-mineral provenance analysis and in chemostratigraphic analysis of clastic sedimentary rocks.  相似文献   

4.
Fractionation between Nb and Ta, elements generally regarded as geochemical ‘identical twins’, is a key to deciphering the formation of the continental crust (CC). Here we show that Nb/Ta of rutile grains in eclogitic rocks from the Chinese Continental Scientific Drilling (CCSD) project are remarkably heterogeneous but overall subchondritic at core depths of 100–700 m, and are less variable and mainly suprachondritic at core depths of 700–3025 m, indicating clear Nb/Ta fractionation across a subducted slab. To understand the potential mechanism of Nb/Ta fractionation within the subducted plate, we analysed by laser ablation ICPMS a thermal migration experiment in which a wet andesite was placed in a large thermal gradient (300°C/cm with ends ranging from 950–350°C) at 0.5Gpa. Results show that Nb, Ta and Ti, driven by the thermal gradient, preferentially migrate by diffusion through supercritical fluids into the cooler end of the experiment (at 650–350°C). Due to contrasting Nb and Ta thermal migration patterns, dramatic fractionation between Nb, Ta, and Ti took place in the cooler end. Experimental results are consistent with the measured Nb, Ta in rutile from CCSD drillhole samples. We consider that major fractionation between Nb, Ta must occur before rutile appears, most likely during the prograde blueschist to amphibole–eclogite transformation, when Ti is also mobile. Before rutile appears, partitioning between Ti‐rich dominant minerals such as amphiboles and fluids in the hotter region where dehydration preferentially occurs, produces Nb–Ta–Ti‐rich fluids with subchondritic Nb/Ta, and dehydration residues with suprachondritic Nb/Ta. Meanwhile, owing to evolution of the thermal gradient within the subducting slab, thermal migration of Nb, Ta, and Ti in aqueous fluids result in Nb, Ta, and Ti enrichment in the cooler region and depletion in the hotter region. As a result of high‐pressure metamorphism, hydrous rutile‐rich eclogites with overall subchondritic Nb/Ta form in the cooler region, whereas relatively anhydrous rutile‐poor eclogites with suprachondritic Nb/Ta form in the hotter region. Subsequently, partial melting of hydrous rutile‐rich eclogites with initial subchondritic Nb/Ta at deeper levels transfers overall subchondritic Nb/Ta coupled with Nb, Ta, and Ti depletion characteristics to the CC, leaving dry rutile‐poor eclogites with suprachondritic Nb/Ta and rutile‐rich residual eclogites with overall, heterogeneous subchondritic Nb/Ta as a complementary reservoir to the CC.  相似文献   

5.
Accessory, homogeneous ilmenite and rutile are important oxide phases in amphibole-rich high-pressure cumulate veins which crosscut the Lherz orogenic lherzolite massif. Those veins crystallized from alkaline melts at P = 1.2–1.5 GPa within the uppermost lithospheric mantle. Transitional basalts contaminated by peridotitic wall-rocks and then uncontaminated alkali basalts (basanites) reused the same vein conduits. Petrographic observations give evidence that Fe–Ti oxide saturation depends on the silica contents of each parental melt. The water-poor silica-rich transitional melts that generated websterites and plagioclase-rich clinopyroxenites reached early Ti-oxide saturation (1,200°C; 1.5 GPa). Rutile is as abundant as ilmenite. It is enriched with Nb–Zr–Hf by a factor of 10–100 relative to either amphibole or ilmenite. The amphibole pyroxenites and hornblendites crystallized from basanites reached late Fe–Ti oxide saturation after precipitation of amphibole, with ilmenite crystallizing along with phlogopite in the latter. The Lherz ilmenites are devoid of exsolution and contain very little trivalent iron. This compositional feature indicates more reducing crystallization conditions than usually inferred for alkali lavas and their megacrysts (FMQ ± 1). The veins incompletely equilibrated for redox conditions with their wall-rock peridotites which record more oxidizing conditions (FMQ ± 1). The veins also exchanged magnesium and chromium, as suggested by Cr-bearing, Mg-rich ilmenite (up to 44 mol% MgTiO3) in veins less than 3–4 cm thick. Mg-rich ilmenite megacrysts occurring in alkali basalts could be actually xenocrysts from veins similar in thickness to those occurring at the Lherz massif, although crystallized from more oxidized magmas.  相似文献   

6.
Spinels, Fe–Ti oxide minerals, apatites, and carbonates hosted in ophiolitic serpentinites and metagabbros of Gabal Garf (southern ED) and Wadi Hammariya (central ED) of Egypt are discussed. Microscopic and electron probe studies on these minerals are made to evaluate their textural and compositional variations. Alteration of chromites led to form ferritchromite and magnetite; rutile–magnetite intergrowths and martite are common in serpentinites. Fine trillis exsolution of ilmenite–magnetite and ilmenite–hematite and intergrowth of rutile–magnetite and ilmenite–sphene are recorded. Composite intergrowth grains of titanomagnetite–ilmenite trellis lamellae are common in metagabbros. The formation of ilmenite trellis and lamellae in magnetite and titanomagnetite indicate an oxidation process due to excess of oxygen contained in titanomagnetite; trapped and external oxidizing agents. This indicates the high P H2O and oxygen fugacity of the parental magma. The sulfides minerals include pyrrhotite, pyrite and chalcopyrite. Based on the chemical characteristics, the Fe–Ti oxide from the ophiolitic metagabbros in both areas corresponds to ilmenite. The patites from the metagabbros are identified as fluor-apatite. Carbonates are represented by dolomites in serpentinites and calcite in metagabbros. Spinel crystals in serpentinites are homogenous or zoned with unaltered cores of Al-spinel to ferritchromit and Cr-magnetite toward the altered rims. Compared to cores, the metamorphic rims are enriched in Cr# (0.87–1.00 vs. 0.83–0.86 for rims and cores, respectively) and impoverished in Mg# (0.26–0.48 vs. 0.56–0.67) due to Mg–Fe and Al (Cr)–Fe3+ exchange with the surrounding silicates during regional metamorphism rather than serpentinization process. The Fe–Ti oxides have been formed under temperature of ~800 °C for ilmenite. Al-spinels equilibrated below 500–550 °C, while the altered spinel rims correspond to metamorphism around 500–600 °C. Geochemical evidence of the podiform Al-spinels suggest a greenschist up to lower amphibolite facies metamorphism (at 500–600 °C), which is isofacial with the host rocks. Al-spinel cores do not appear to have re-equilibrated completely with the metamorphic spinel rims and surrounding silicates, suggesting relic magmatic composition unaffected by metamorphism. The composition of Al-spinel grains suggest an ophiolitic origin and derivation by crystallization of boninitic magma that belonging to a supra-subduction setting could form either in forearcs during an incipient stage of subduction initiation or in back-arc basins.  相似文献   

7.
对中国大陆科学钻探（CCSD）主孔200~1005m范围内8件榴辉岩样品的金红石进行了LA-ICPMS原位微区微量元素分析,结合前人已发表的全岩和金红石分析数据,研究结果发现：在不同类型榴辉岩中,金红石的微量元素与其全岩成分具有不同的相关关系。金红石中的Nb和Ta元素含量不同程度地受控于全岩Nb和Ta含量。在高钛和低镁钛榴辉岩中,金红石的Cr与全岩Cr/TiO2正相关;在富镁榴辉岩中,金红石的Cr含量受全岩MgO含量的控制;在高钛和富镁榴辉岩中,全岩成分明显影响着金红石的Zr含量,金红石Zr温度计可能不适用。低镁钛榴辉岩的金红石的平衡温度普遍低于榴辉岩峰期变质温度,可能是变质流体参与下的扩散作用和退变质作用所致;多数情况下,单个样品中大部分金红石颗粒的Zr含量是均匀的,金红石Zr温度计所给出的温度可能代表着退变质再平衡的温度;CCSD榴辉岩的全岩Nb/Ta比值普遍低于其中金红石的Nb/Ta比值,不支持金红石榴辉岩可能是地球上超球粒陨石Nb/Ta比值储库的观点。  相似文献   

8.
The lower sill at Benfontein, South Africa, shows a high degree of magmatic sedimentation to kimberlite, oxide-carbonate, and carbonate layers. The iron-titanium oxide minerals are similar in the carbonate-rich and silicate-rich layers and are represented by titaniferous Mg-Al chromite, Mg-Al titanomagnetite, magnesian ilmenite, rutile, and perovskite. The spinel crystallization trend was toward enrichment in Mg and Ti and depletion in Cr; this trend is similar to that observed in many kimberlites. The ilmenite has Mg and Cr contents within the range observed in kimberlites and lacks the Mn enrichment observed in ilmenites from carbonatites. Perovskite in silicate-rich and carbonate-rich layers shows similar total REE contents and LREE enrichment and lacks the remarkable Nb enrichment observed in perovskite from carbonatites. These new data on the iron-titanium oxide minerals in the lower Benfontein sill do not support a genetic relationship between kimberlites and carbonatites.  相似文献   

9.
Integrated petrographic and chemical analysis of zircon, garnet and rutile from ultrahigh‐temperature (UHT) granulites in the Anápolis–Itauçu Complex, Brazil, is used to constrain the significance of zircon ID‐TIMS U–Pb geochronological data. Chondrite‐normalized rare earth element (REE) profiles of zircon cores have positive‐sloping heavy‐REE patterns, commonly inferred to be magmatic, whereas unambiguous metamorphic grains and overgrowths have flat to slightly negatively sloping heavy‐REE patterns. However, in one sample, a core of zircon interpreted as having formed prior to garnet crystallization and a metamorphic zircon formed within microstructures involving garnet breakdown both display elevated heavy‐REE (and Y) with positive‐sloping patterns. DREE(zrc/grt) partition coefficients suggest an approximation to equilibrium between zircon and garnet cores, although progressive enrichment in heavy REE towards garnet rims occurs in two of the samples investigated. Titanium‐in‐zircon thermometry indicates zircon growth during both the prograde and post‐peak evolution, but not at peak temperatures of the UHT metamorphism. By contrast, zirconium‐in‐rutile thermometry of inclusions armoured by garnet records crystallization temperatures, based on the upper end of the interquartile range of the data, of ～890 to 870 °C and maximum temperature around 980 °C, indicating prograde and retrograde growth close to and after peak conditions. Rutile located in retrograde microstructures records crystallization temperatures of 850 to 820 °C. Rutile intergrown with ilmenite and included within orthopyroxene, which is associated with exsolved zircon, records temperatures ～760 °C, consistent with Ti‐in‐zircon crystallization temperatures. ID‐TIMS U–Pb geochronological data from two of the four samples investigated define upper intercept ages of 641.3 ± 8.4 Ma (MSWD 0.91) and 638.8 ± 2.5 Ma (MSWD 1.03) that correlate with periods of zircon growth along the prograde segment of the P–T path. Individual zircon U–Pb dates retrieved from all samples range from 649 to 634 Ma, indicating a maximum duration of c. 15 Myr for the UHT event. This period is interpreted as recording modest thickening of hot backarc lithosphere located behind the Arenópolis Arc at the edge of the São Francisco Craton consequent upon terminal collision of the Parána Block with the arc during the amalgamation of West Gondwana.  相似文献   

10.
碎屑金红石:沉积物源的一种指针   总被引：3，自引：2，他引：1  
简星  关平  张巍 《地球科学进展》2012,27(8):828-846
近年来,碎屑金红石的研究已成为沉积物源区分析的一个新前沿。金红石的地球化学组成,尤其是Cr,Nb,Zr等微量元素的含量,对其母岩的形成条件和所经历的地质过程都具有重要的指示意义,同时,碎屑金红石在沉积、成岩过程中表现出极高的稳定性,因而是物源分析的理想指针矿物。首先介绍金红石的矿物学和地球化学基本性质,分析不同来源的金红石典型特征,重点阐述碎屑金红石在物源分析中运用的5个方面:①金红石重矿物比值;②金红石矿物化学成分Cr-Nb判别图解;③金红石Zr含量温度计;④金红石的U-Pb和(U-Th)/He定年;⑤金红石Lu-Hf同位素。综合上述5个方面的物源分析研究,可以获取金红石的母岩类型、形成温度及后期所经历的热演化史等信息。碎屑金红石的物源研究处于起步和探索阶段,仍存在一些亟需解决的问题。  相似文献   

11.
Zr-in-rutile thermometry in blueschists from Sifnos, Greece   总被引：1，自引：0，他引：1  
Zr-in-rutile thermometry on samples of blueschist from Sifnos, Greece, yields temperatures that reflect progressive crystallization of rutile from ca. 445 to 505°C with an analytical precision of + 18/−27 and ± 10°C using the electron microprobe and ± 1.5–3.5°C using the ion microprobe. Individual grains are generally homogeneous within analytical uncertainty. Different grains within a single sample record temperature differences as large 55°, although in most samples the range of temperatures is on the order of 25°. In several samples, Zr-in-rutile temperatures from grains within garnet are lower than temperatures from matrix grains, reflecting growth of rutile with increasing temperature of metamorphism. Although the specific rutile-producing reactions have not been identified, it is inferred that rutile grows from either continuous reaction involving the breakdown of lower grade phases (possibly ilmenite), or from pseudomorph reactions involving the breakdown of relic igneous precursors at blueschist-facies conditions. No systematic variation in rutile temperatures was observed across the blueschist belt of northern Sifnos, consistent with the belt having behaved as a coherent block during subduction.  相似文献   

12.
利用LA-ICP-MS对CCSD-MH超高压榴辉岩中金红石进行了详细的原位微区微量元素组成分析.金红石中高场强元素Nb和Ta含量主要受全岩Nb、Ta和TiO2含量控制, Zr、Hf含量比较稳定基本不受全岩含量影响.粒间金红石中, 同一颗粒金红石核部Zr含量系统高于边部, 而边部则出现了明显的Pb和Sr富集特征.CCSD-MH榴辉岩中金红石与全岩的Nb/Ta比值呈现明显的不一致性.全岩Nb/Ta比值明显低于金红石且与全岩TiO2含量负相关, 而金红石的Nb/Ta比值与全岩Nb、Ta含量和Nb/Ta比值没有明显的相关关系.金红石和全岩之间非完全耦合的Nb/Ta组成表明, 金红石并非形成于原岩的结晶过程中而是在超高压变质作用过程中形成, 尽管金红石是榴辉岩中Nb、Ta含量的主要载体矿物, 但金红石的Nb/Ta比值并不一定能完全代表全岩的特征, 而与全岩Nb、Ta和TiO2的含量有关.粒间金红石核部Zr含量所记录的温度与粒径之间具有明显的正相关性, 反映金红石中的Zr在其形成后没有封闭.粒间金红石所表现出的明显的边部富集Pb和Sr的特征, 反映了后期流体活动对金红石组成的影响.这些研究结果为金红石中Zr在高温下的扩散作用和后期流体活动的影响提供了重要证据, 这可能是利用金红石Zr含量地质温度计计算的苏鲁-大别榴辉岩变质温度(598~827℃) 偏低的主要原因.   相似文献   

13.
Zr-in-rutile thermometry was applied to ultrahigh-temperature (UHT) granulites from three localities, Dongpo, Tuguishan, and Dajing/Tuguiwula of the Khondalite belt, North China Craton. Zr concentrations of analyzed rutiles were detected by LA-ICP-MS and EMP, which display a mutative composition zoning, a large inter-grain variation, a bimodal distribution at around 1,500 and 6,000?ppm, and no relationship with the textural setting (matrix vs. inclusion). These characteristics were likely caused by post-peak diffusional resetting associated with slow cooling rates and the presence of a CO2-rich fluid. The grains with lower Zr concentrations (~500 to ~3,000?ppm) and temperature estimates (~650 to ~850°C) occur close to or in contact with zircon, which was easily affected by post-peak processes (for example: diffusion, dissolution/reprecipitation). The lowest temperatures (~650 to ~700°C) we obtained represent the closure temperature of Zr-in-rutile. Rutiles with higher Zr concentrations (~3,000 to ~8,000?ppm) and calculated temperatures (~850 to ~1,000°C) were least affected by late resetting, giving near-peak metamorphic temperatures. These temperature results higher than 900°C, even in excess of 1,000°C from the three localities, reconfirm the presence of UHT metamorphism. Our results also suggest that Zr-in-rutile thermometry is valid for ultrahigh-temperature estimates. In addition, there are positive correlations between concentrations of Zr and Hf, Nb and Ta of the investigated rutiles, but the correlations weaken as the concentrations increase, especially for Nb and Ta, implying fractionation of Nb and Ta.  相似文献   

14.
Metamorphic rutile from granulite facies metapelitic rocks of the Archean Pikwitonei Granulite Domain (PGD; Manitoba, Canada) provides constraints on the systematics of trace elements in rutile during high‐temperature conditions and subsequent slow cooling. Compositional profiles and maps of the Zr concentrations in rutile grains (120–600 μm) from three metapelitic gneisses were acquired by electron probe micro‐analysis, using a spatial resolution of down to 2 μm. Simultaneously, profiles were analysed for Nb, Cr and V, which have significantly different diffusion characteristics in rutile. The profiles of all elements show relatively homogeneous concentrations within most grains, but significant inter‐grain differences even within a single thin section. Some rutile grains display a slight concentration decrease from a neighbouring garnet towards the matrix for all measured elements. The lack of diffusion profiles for all analysed elements shows that these are highly immobile in rutile and that distributions of these elements are primary and preserve prograde information. The Nb and Cr concentrations overlap with ranges that are ascribed to different provenances indicating that source discrimination based on these elements is not possible in all cases. High retentiveness for Zr implies that the Zr‐in‐rutile geothermometer is highly robust to diffusive re‐equilibration, even during very slow cooling (<2 °C Ma?1) from granulite facies conditions. Most grains have high Zr contents (3000–4600 ppm). Differences between high Zr contents suggest that during growth under vapour‐absent conditions there may not be saturation of Zr in rutile, even if zircon is present. Therefore, several rutile grains need to be analysed in a sample to obtain a useful minimum peak temperature. The highest Zr concentrations correspond to ～900 °C. This is significantly higher than previous peak temperature estimates of 820 °C based on two‐feldspar thermometry. On a regional scale this implies that part of the PGD was affected by ultra‐high temperature (UHT) metamorphism. It also implies that rutile is able to preserve primary compositions even to UHT conditions. This study shows that, if combined with textural information, Zr‐in‐rutile has the potential to be a very useful tool for estimating rutile crystallization temperatures and peak metamorphic conditions. For granulite facies rocks, Zr‐in‐rutile yields more reliable peak metamorphic temperatures than most other exchange geothermometers, which tend to partially re‐equilibrate by diffusion during cooling.  相似文献   

15.
Magnesium ilmenite from discrete nodules and lamellar intergrowths with pyroxene from the Kao, Sekameng, Frank Smith, and Monastery kimberlites has been analysed for Ti, Fe, Mg, Nb, Zr, Cr, Cu, Zn, Mn, Co, and Ni. Each kimberlite contains discrete ilmenites which exhibit a wide compositional range within the ilmenite-geikeilite series. Lamellar ilmenites from Frank Smith and Monastery differ in composition but both show a limited range in composition which lies within the compositional range shown by discrete ilmenites from these pipes. The ilmenites are enriched in Nb, Zr, Cr, Co, and Ni and depleted in Mn, Cu, and Zn relative to Mg-poor ilmenites from basic intrusions. Nb, Zr, and Ni correlate with Fe, Ti and Mg variations but the abundances of the other trace elements are independent of major element variation. R-mode factor analysis is interpreted to imply that the geochemistry cannot be interpreted in terms of a differentiation hypothesis in which trace elements are removed from or concentrated in residua. Factor scores and major element abundances indicate that each pipe is characterized by a particular suite of discrete ilmenite nodules, which are considered to be phenocrysts in a proto-kimberlite magma. Lamellar ilmenite-pyroxene intergrowths are unlikely to have had a eutectic origin, and show no simple relationship to the discrete ilmenites.  相似文献   

16.
In pelitic schists of the Sanbagawa metamorphic belt, sphene, rutile, and ilmenite occur as discrete grains, in composite aggregates, and as inclusions in garnets. Textural relationships, disposition of inclusions in garnet, and the compositions of ilmenites suggest that the titanium-bearing accessories stable at the peak metamorphic conditions were as follows: sphene in the chlorite zone, sphene plus rutile in the garnet zone, and ilmenite in the highest grade of the belt, the biotite zone. Rutile appears in the garnet zone as a consequence of Ca incorporation into garnet and a progressive increase in .Retrograde reactions were responsible for the composite aggregates of rutile, sphene and ilmenite and these must be carefully evaluated before prograde relationships between titanium-bearing accessories can be properly understood.  相似文献   

17.
U–Pb zircon dating is combined with petrology, Zr-in-rutile thermometry and mineral equilibria modelling to discuss zircon petrogenesis and the age of metamorphism in three units of the Variscan Vosges Mountains (NE France). The monotonous gneiss unit shows results at 700–500?Ma, but no Variscan ages. The varied gneiss unit preserves ages between 600 and 460?Ma and a Variscan group at 340–335?Ma. Zircon analyses from the felsic granulite unit define a continuous array of ages between 500 and 340?Ma. In varied gneiss samples, zoned garnet includes kyanite and rutile and is surrounded by matrix sillimanite and cordierite. In a pseudosection, it points to peak conditions of?~16 kbar/850?°C followed by isothermal decompression to 8–10 kbar/820–860?°C. In felsic granulite samples, the assemblage K-feldspar–garnet–kyanite–Zr-rich rutile is replaced by sillimanite and Zr-poor rutile. Modelling these assemblages supports minimum conditions of?~13 kbar/925?°C, and a subsequent P–T decrease to 6.5–8.5 kbar/800–820?°C. The internal structure and chemistry of zircons, and modelling of zircon dissolution/growth along the inferred P–T paths are used to discuss the significance of the U–Pb ages. In the monotonous unit, inherited zircon ages of 700–500?Ma point to sedimentation during the Late Cambrian, while medium-grade metamorphism did not allow the formation of Variscan zircon domains. In both the varied gneiss and felsic granulite units, zircons with a blurred oscillatory-zoned pattern could reflect solid-state recrystallization of older grains during HT metamorphism, whereas zircons with a dark cathodoluminescence pattern are thought to derive from crystallization of an anatectic melt during cooling at middle pressure conditions. The present work proposes that U–Pb zircon ages of ca. 340?Ma probably reflect the end of a widespread HT metamorphic event at middle crustal level.  相似文献   

18.
Application of rutile thermometry to eclogites   总被引：5，自引：0，他引：5  
Summary Metamorphic temperatures can be derived from the Zr content in rutiles coexisting with quartz and zircon. To evaluate how well this recently calibrated rutile thermometer can be applied to eclogites, we analysed 8 samples that cover the whole temperature range of naturally-occurring eclogites (400–900 °C). Due to low concentrations expected at only 400 °C, very high precision (better than 5 percent on a 10 ppm level) secondary ion mass spectrometry (SIMS) is used in this study. In general, temperatures calculated from rutiles agree favourably with literature data as well as with our own estimates, based on several geothermobarometers and phase assemblages. However, the most important result of this study is the observation that temperatures calculated from 4–8 rutiles within a single sample always agree to within better than 25 °C, hence enforcing the claim that rutile thermometry is a powerful tool for relative temperature determinations. An erratum to this article is available at .  相似文献   

19.
Qara-aghaj and Skandian as hard rock titanium deposit and Kahnooj one as a placer deposit were investigated from applied mineralogical point of view. The mineralogical studies were carried out using XRD, XRF, optical microscopy, scanning electron microscopy and microprobe analysis. These studies indicated that ilmenite and magnetite are main valuable minerals in the studied ores. Pyroxene, olivine and plagioclase are the main gangue minerals in Qara-aghaj ore while chlorite and plagioclase are the major gangue minerals in Skandian ore. Plagioclase, clinopyroxene, amphibole, feldspate and some quartz are the important gangue minerals in kahnooj deposit. In all three ores ilmenite is mainly in the form of ilmenite grains but some lamellae of ilmenite with thickness between 0.1 to 20 μm have been occurred as exsolution textures inside magnetite grains, where the magnetite here can be referred to as ilmenomagnetite. In the hard rock ores some fine ilmenites have been disseminated in silicate minerals. The liberation degree of granular ilmenite was determined 150, 140 and 200 μm for Qara-aghaj, Skandian and Kahnooj, respectively. So, only the granular form of ilmenite is recoverable by physical methods. Some sphene and rutile as titanium containing minerals were observed mainly inside ilmenite phase in kahnooj ore. Some fine rutile was also found inside Skandian ilmenite while there were not any other titanium minerals inside Qara-aghaj ilmenite. Apatite is another valuable mineral which was found only in Qara-aghaj ore. Using SEM and microprobe analysis it was found that there are different amounts of exsolved fine lamellae of hematite inside ilmenite in Qara-aghaj and Kahnooj ores while it was not observed in Sckandian one. The average contents of TiO2 in the lattice of Qara-aghaj, Skandian and Kahnooj ilmenite were determined 51.13, 50.9% and 52.02%, respectively. FeO content of ilmenite lattice for all three samples is clearly lower than the theoretical content. This is due to the substitution of Mg and Mn for some Fe2+ ions in the ilmenite lattice. V2O3 content of magnetite lattice is up to 1%. So, magnetite can be a suitable source for production of vanadium as a by-product in all three deposits.  相似文献   

20.
The Jumping Brook Metamorphic Suite in the western Cape Breton Highlands of Nova Scotia is part of an inverted Barrovian sequence that formed during a Late Silurian–Early Devonian promontory–promontory collision in the Canadian Appalachians. In this study, systematic discrepancies between geochemical observations and thermodynamic model predictions led to the discovery of a systematic relationship linking the style of garnet core isopleth intersection (GCII) to the pyrophanite (MnTiO3) component of co‐existing ilmenite. Samples that yielded tight GCIIs at or near the garnet‐in curve were found to contain ilmenite with negligible pyrophanite components, whereas samples yielding GCIIs far removed (up to 105°C) from the garnet‐in curve were found to contain ilmenite with significant pyrophanite and/or ecandrewsite (ZnTiO3) components. Based on petrographic and geochemical observations, Mn(±Zn)‐rich ilmenite are interpreted to have sequestered Mn throughout prograde metamorphism due to sluggish intracrystalline diffusion. The amount of reactive Mn input into the thermodynamic models from whole‐rock analyses were, in some cases, overestimated, resulting in garnet‐in curve topologies that extend to erroneously low P–T conditions. Modifications to the whole‐rock chemistry that account for Mn sequestration into ilmenite, however, yielded robust model results. Our results show that, in addition to uncertainties in thermodynamic data sets and phenomenon related to reaction kinetics, Mn‐rich ilmenite may superimpose additional complexities related to the interpretation of predicted equilibria involving garnet. Numerical simulations of garnet crystallization were used to infer P–T paths of metamorphism for one sample from the garnet zone (Mn corrected) and two samples from the staurolite zone (Mn uncorrected) of the inverted sequence. Model results are remarkably similar among the three samples and indicate that garnet crystallization occurred along relatively steep (31–37°C/km) clockwise P–T paths. The peak conditions of garnet crystallization and metamorphism (560–590°C, 7.4–8.0 kbar) are interpreted to have been attained approximately simultaneously, such that the paths are characterized by tight prograde‐to‐retrograde transitions. The hairpin nature of the P–T paths is interpreted to represent the onset of thrust‐related exhumation and isograd inversion along ductile shear zones, consistent with available field and geochronological constraints.  相似文献   

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